# Search results of SQL query from the Crystallography Open Database
# Date and time performed: 2026-01-25T12:41:28+01:00
# Query:
# SELECT data.*
# FROM
#  data JOIN jaltnames
#  ON altname = journal
# WHERE
#  (status is null or status != 'retracted') and
#  (journal_id IN (SELECT DISTINCT(journal_id) FROM jaltnames WHERE altname LIKE 'Organic Chemistry Frontiers') AND duplicateof IS NULL AND (status is NULL OR status != 'errors') AND (method is NULL OR method != 'theoretical'))
# ORDER BY file asc
file,a,siga,b,sigb,c,sigc,alpha,sigalpha,beta,sigbeta,gamma,siggamma,vol,sigvol,celltemp,sigcelltemp,diffrtemp,sigdiffrtemp,cellpressure,sigcellpressure,diffrpressure,sigdiffrpressure,thermalhist,pressurehist,compoundsource,nel,sg,sgHall,sgNumber,commonname,chemname,mineral,formula,calcformula,cellformula,Z,Zprime,acce_code,authors,title,journal,year,volume,issue,firstpage,lastpage,doi,method,radiation,wavelength,radType,radSymbol,Rall,Robs,Rref,wRall,wRobs,wRref,RFsqd,RI,gofall,gofobs,gofgt,gofref,duplicateof,optimal,status,flags,svnrevision,date,time,onhold
"1552964","11.2047","0.0016","12.2098","0.0018","13.3534","0.0017","97.661","0.01","96.853","0.008","99.139","0.009","1769","0.4","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C21 H20 O3 -","- C21 H20 O3 -","- C84 H80 O12 -","4","2","","Zhang, Wen-Zhen; Shi, Ling-Long; Liu, Chuang; Yang, Xu-Tong; Wang, Yan-Bo; Luo, Yi; Lu, Xiao-Bing","Sequential carboxylation/intramolecular cyclization reaction of o-alkynyl acetophenone with CO2","Organic Chemistry Frontiers","2014","1","3","275","","10.1039/c3qo00047h","","","0.71073","MoKα","","0.0874","0.0684","","","0.2013","0.217","","","","","","1.076","","","","has coordinates","301780","2025-08-18","21:43:28",""
"1552965","8.0584","0.001","13.7851","0.0014","14.5897","0.0016","107.134","0.007","105.844","0.008","103.626","0.008","1399.1","0.3","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C18 H14 O3 -","- C18 H14 O3 -","- C72 H56 O12 -","4","2","","Zhang, Wen-Zhen; Shi, Ling-Long; Liu, Chuang; Yang, Xu-Tong; Wang, Yan-Bo; Luo, Yi; Lu, Xiao-Bing","Sequential carboxylation/intramolecular cyclization reaction of o-alkynyl acetophenone with CO2","Organic Chemistry Frontiers","2014","1","3","275","","10.1039/c3qo00047h","","","0.71073","MoKα","","0.112","0.0563","","","0.1483","0.1806","","","","","","1.02","","","","has coordinates","301780","2025-08-18","21:43:28",""
"1552981","13.828","0.003","16.821","0.004","15.516","0.002","90","","90.367","0.013","90","","3609","1.3","150","2","150","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","{Bis-(2-phenylpyridine)}{4,4-dimethyl-2,2-dipyridylamine} iridium hexafluorophosphate","","- C34 H29 F6 Ir N5 P -","- C34 H29 F6 Ir N5 P -","- C136 H116 F24 Ir4 N20 P4 -","4","1","","Sauvageot, Elodie; Marion, Ronan; Sguerra, Fabien; Grimault, Adèle; Daniellou, Richard; Hamel, Matthieu; Gaillard, Sylvain; Renaud, Jean-Luc","Iridium(iii) dipyridylamine complexes: synthesis, characterization and catalytic activities in photoredox reactions","Organic Chemistry Frontiers","2014","1","6","639","","10.1039/c4qo00059e","","","0.71073","MoKα","","0.0484","0.0265","","","0.0649","0.0701","","","","","","1.007","","","","has coordinates","232928","2020-10-21","18:00:00",""
"1552982","9.3281","0.0006","15.4516","0.001","23.6282","0.0017","90","","92.742","0.003","90","","3401.7","0.4","150","2","150","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","{Bis-(1-phenylpyrazole)}{4,4-dimethyl-2,2-dipyridylamine} iridium hexafluorophosphate","","- C30 H27 F6 Ir N7 P -","- C30 H27 F6 Ir N7 P -","- C120 H108 F24 Ir4 N28 P4 -","4","1","","Sauvageot, Elodie; Marion, Ronan; Sguerra, Fabien; Grimault, Adèle; Daniellou, Richard; Hamel, Matthieu; Gaillard, Sylvain; Renaud, Jean-Luc","Iridium(iii) dipyridylamine complexes: synthesis, characterization and catalytic activities in photoredox reactions","Organic Chemistry Frontiers","2014","1","6","639","","10.1039/c4qo00059e","","","0.71073","MoKα","","0.0405","0.0311","","","0.0665","0.0691","","","","","","1.066","","","","has coordinates","232928","2020-10-21","18:00:00",""
"1552990","10.2605","0.0006","16.8131","0.0009","17.3175","0.001","101.471","0.005","103.442","0.005","99.53","0.005","2776.4","0.3","180","0.1","180","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C83 H34 Cl6 N2 O6 -","- C83 H32 Cl6 N2 O6 -","- C166 H64 Cl12 N4 O12 -","2","1","","Xu, Liang; Liang, Sisi; Gan, Liangbing","A green fullerene derivative as a fluoride ion sensor","Organic Chemistry Frontiers","2014","1","6","652","","10.1039/c4qo00111g","","","0.7107","MoKα","","0.1254","0.0992","","","0.2565","0.2844","","","","","","1.035","","","","has coordinates","232938","2020-10-21","18:00:00",""
"1552993","6.6455","0.0002","14.068","0.0005","15.4102","0.0005","90","","90","","90","","1440.68","0.08","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C17 H11 Cl F N O3 -","- C17 H11 Cl F N O3 -","- C68 H44 Cl4 F4 N4 O12 -","4","1","","Liu, Yun-Lin; Liao, Fu-Min; Niu, Yan-Fei; Zhao, Xiao-Li; Zhou, Jian","Highly stereoselective construction of adjacent tetrasubstituted carbon stereogenic centres via an organocatalytic Mukaiyama-aldol reaction of monofluorinated silyl enol ethers to isatins","Organic Chemistry Frontiers","2014","1","7","742","","10.1039/C4QO00126E","","","0.71073","MoKα","","0.0426","0.0315","","","0.0651","0.0712","","","","","","1.03","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1552994","8.1719","0.0015","6.8476","0.0012","12.493","0.002","90","","97.076","0.007","90","","693.8","0.2","173","2","173","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C17 H14 F N O3 -","- C17 H14 F N O3 -","- C34 H28 F2 N2 O6 -","2","1","","Liu, Yun-Lin; Liao, Fu-Min; Niu, Yan-Fei; Zhao, Xiao-Li; Zhou, Jian","Highly stereoselective construction of adjacent tetrasubstituted carbon stereogenic centres via an organocatalytic Mukaiyama-aldol reaction of monofluorinated silyl enol ethers to isatins","Organic Chemistry Frontiers","2014","1","7","742","","10.1039/C4QO00126E","","","0.71073","MoKα","","0.1336","0.0627","","","0.1003","0.125","","","","","","1.05","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1552998","8.4091","0.0007","12.2759","0.0012","24.544","0.002","90","","90","","90","","2533.7","0.4","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C34 H23 O3 P -","- C34 H23 O3 P -","- C136 H92 O12 P4 -","4","1","","Yu, Yue-Na; Xu, Ming-Hua","Design of a new series of chiral phosphite–olefin ligands and their application in asymmetric catalysis","Organic Chemistry Frontiers","2014","1","7","738","","10.1039/C4QO00135D","","","0.71073","MoKα","","0.1527","0.0864","","","0.2094","0.2292","","","","","","1.053","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553007","5.1955","0.0001","8.5856","0.0001","32.9171","0.0004","90","","90","","90","","1468.32","0.04","290","2","290","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C17 H18 N2 O -","- C17 H18 N2 O -","- C68 H72 N8 O4 -","4","1","","Wang, Yong; Xu, Jing-Kun; Gu, Yonghong; Tian, Shi-Kai","Catalytic stereospecific allylation of protected hydrazines with enantioenriched primary allylic amines","Organic Chemistry Frontiers","2014","1","7","812","","10.1039/C4QO00155A","","","1.54184","CuKα","","0.0326","0.0316","","","0.1036","0.1062","","","","","","1.077","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553017","8.8435","0.0004","13.8908","0.0007","14.179","0.0006","90","","90","","90","","1741.8","0.14","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C19 H21 N O4 -","- C19 H21 N O4 -","- C76 H84 N4 O16 -","4","1","","Ma, Dengke; Dai, Jianxin; Qiu, Youai; Fu, Chunling; Ma, Shengming","Gram scale synthesis of 7-methoxy-O-methylmukonal, clausine-O, clausine-K, clausine-H, 7-methoxymukonal, and methyl 2-hydroxy-7-methoxy-9H-carbazole-3-carboxylate","Organic Chemistry Frontiers","2014","1","7","782","","10.1039/C4QO00163J","","","1.54184","CuKα","","0.0514","0.0425","","","0.1074","0.117","","","","","","1.094","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553040","18.2388","0.0011","14.6418","0.0008","20.7375","0.0012","90","","90.251","0.002","90","","5537.9","0.6","296","2","296","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C27 H31 N O6 S -","- C27 H31 N O6 S -","- C216 H248 N8 O48 S8 -","8","4","","Liu, Feng; Wang, Yidong; Ye, Weiming; Zhang, Junliang","Gold(i)-catalyzed asymmetric [3 + 2]-cycloadditions of γ-1-ethoxyethoxy-propiolates and aldehydes","Organic Chemistry Frontiers","2015","2","3","221","","10.1039/C4QO00261J","","","0.71073","MoKα","","0.2011","0.0663","","","0.1128","0.1593","","","","","","0.994","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553041","8.893","0.0002","20.6873","0.0004","9.7453","0.0002","90","","105.318","0.001","90","","1729.17","0.06","296","2","296","2","","","","","","","","7","P 1 21 1","P 2yb","4","","","","- C38 H42 Au Cl N O2 P -","- C38 H42 Au Cl N O2 P -","- C76 H84 Au2 Cl2 N2 O4 P2 -","2","1","","Liu, Feng; Wang, Yidong; Ye, Weiming; Zhang, Junliang","Gold(i)-catalyzed asymmetric [3 + 2]-cycloadditions of γ-1-ethoxyethoxy-propiolates and aldehydes","Organic Chemistry Frontiers","2015","2","3","221","","10.1039/C4QO00261J","","","0.71073","MoKα","","0.0281","0.0245","","","0.0557","0.057","","","","","","1.05","","","","has coordinates","232992","2020-10-21","18:00:00",""
"1553042","15.865","0.004","16.43","0.004","14.961","0.004","90","","90","","90","","3899.8","1.7","173","2","173","2","","","","","","","","3","P n n 2","P 2 -2n","34","","","","- C92 H98 N8 -","- C92 H98 N8 -","- C184 H196 N16 -","2","0.5","","Ie, Machiko; Setsune, Jun-ichiro; Eda, Kazuo; Tsuda, Akihiko","Chiroptical sensing of oligonucleotides with a cyclic octapyrrole","Organic Chemistry Frontiers","2015","2","1","29","","10.1039/C4QO00268G","","","0.71073","MoKα","","0.0511","0.0433","","","0.1077","0.1132","","","","","","1.034","","","","has coordinates,has disorder","232994","2020-10-21","18:00:00",""
"1553043","10.255","0.001","10.8108","0.0012","15.4763","0.0016","90","","90","","90","","1715.8","0.3","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C20 H20 N2 O2 -","- C20 H20 N2 O2 -","- C80 H80 N8 O8 -","4","1","","Yin, Xue-Song; Li, Yi-Chen; Yuan, Jun; Gu, Wen-Jia; Shi, Bing-Feng","Copper(ii)-catalyzed methoxylation of unactivated (hetero)aryl C–H bonds using a removable bidentate auxiliary","Organic Chemistry Frontiers","2015","2","2","119","","10.1039/C4QO00276H","","","0.71073","MoKα","","0.0752","0.05","","","0.1129","0.129","","","","","","1.049","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553044","10.5428","0.0012","16.2625","0.0012","10.8624","0.0015","90","","118.846","0.016","90","","1631.3","0.4","293","2","293.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C17 H17 F3 N2 O2 -","- C17 H17 F3 N2 O2 -","- C68 H68 F12 N8 O8 -","4","1","","Yin, Xue-Song; Li, Yi-Chen; Yuan, Jun; Gu, Wen-Jia; Shi, Bing-Feng","Copper(ii)-catalyzed methoxylation of unactivated (hetero)aryl C–H bonds using a removable bidentate auxiliary","Organic Chemistry Frontiers","2015","2","2","119","","10.1039/C4QO00276H","","","0.71073","MoKα","","0.0864","0.0549","","","0.1359","0.1572","","","","","","1.065","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553045","8.0742","0.0005","12.4409","0.001","17.6473","0.0012","71.94","0.007","79.009","0.006","72.177","0.006","1595.4","0.2","293","2","293.15","","","","","","","","","4","P -1","-P 1","2","","","","- C16 H19 N3 O2 -","- C16 H19 N3 O2 -","- C64 H76 N12 O8 -","4","2","","Yin, Xue-Song; Li, Yi-Chen; Yuan, Jun; Gu, Wen-Jia; Shi, Bing-Feng","Copper(ii)-catalyzed methoxylation of unactivated (hetero)aryl C–H bonds using a removable bidentate auxiliary","Organic Chemistry Frontiers","2015","2","2","119","","10.1039/C4QO00276H","","","0.71073","MoKα","","0.0891","0.0554","","","0.1451","0.1689","","","","","","1.027","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553046","9.5524","0.0009","13.2533","0.0012","18.9296","0.0018","101.946","0.001","101.154","0.001","103.248","0.001","2208","0.4","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C44 H33 F10 Ir N11 P -","- C40 H27 F10 Ir N9 P -","- C80 H54 F20 Ir2 N18 P2 -","2","1","","Cai, Rong; Yan, Wuming; Bologna, Matthew G.; de Silva, Kaushalya; Ma, Zhao; Finklea, Harry O.; Petersen, Jeffrey L.; Li, Minyong; Shi, Xiaodong","Synthesis and characterization of N-2-aryl-1,2,3-triazole based iridium complexes as photocatalysts with tunable photoredox potential","Organic Chemistry Frontiers","2015","2","2","141","","10.1039/C4QO00281D","","","0.71073","MoKα","","0.0357","0.0296","","","0.074","0.0763","","","","","","0.88","","","","has coordinates","232998","2020-10-21","18:00:00",""
"1553047","11.0054","0.0012","14.2851","0.0015","21.789","0.002","71.698","0.002","89.997","0.002","67.306","0.002","2971.6","0.5","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C34 H23 F2 Ir N8 O -","- C34 H23 F2 Ir N8 O -","- C136 H92 F8 Ir4 N32 O4 -","4","2","","Cai, Rong; Yan, Wuming; Bologna, Matthew G.; de Silva, Kaushalya; Ma, Zhao; Finklea, Harry O.; Petersen, Jeffrey L.; Li, Minyong; Shi, Xiaodong","Synthesis and characterization of N-2-aryl-1,2,3-triazole based iridium complexes as photocatalysts with tunable photoredox potential","Organic Chemistry Frontiers","2015","2","2","141","","10.1039/C4QO00281D","","","0.71073","MoKα","","0.0479","0.0313","","","0.0754","0.0824","","","","","","1.03","","","","has coordinates","232998","2020-10-21","18:00:00",""
"1553048","10.8466","0.0008","23.0405","0.0016","10.6995","0.0008","90","","102.658","0.001","90","","2608.9","0.3","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C27 H33 N O3 S Si -","- C27 H33 N O3 S Si -","- C108 H132 N4 O12 S4 Si4 -","4","1","","Shen, Kun; Han, Xiuling; Xia, Guoqin; Lu, Xiyan","Cationic Pd(ii)-catalyzed cyclization of N-tosyl-aniline tethered alkynyl ketones initiated by hydropalladation of alkynes: a facile way to 1,2-dihydro or 1,2,3,4-tetrahydroquinoline derivatives","Organic Chemistry Frontiers","2015","2","2","145","","10.1039/C4QO00286E","","","0.71073","MoKα","","0.0638","0.047","","","0.1218","0.1329","","","","","","1.028","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553049","32.673","0.002","12.2122","0.0008","12.9554","0.0009","90","","92.633","0.002","90","","5163.9","0.6","293","2","293","2","","","","","","","","7","C 1 2/c 1","-C 2yc","15","","cd214703","","- C26 H28 Cl N O3 S Si -","- C26 H28 Cl N O3 S Si -","- C208 H224 Cl8 N8 O24 S8 Si8 -","8","1","","Shen, Kun; Han, Xiuling; Xia, Guoqin; Lu, Xiyan","Cationic Pd(ii)-catalyzed cyclization of N-tosyl-aniline tethered alkynyl ketones initiated by hydropalladation of alkynes: a facile way to 1,2-dihydro or 1,2,3,4-tetrahydroquinoline derivatives","Organic Chemistry Frontiers","2015","2","2","145","","10.1039/C4QO00286E","","","0.71073","MoKα","","0.0564","0.0459","","","0.1166","0.1241","","","","","","1.021","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553050","17.5053","0.0019","20.281","0.002","21.1684","0.0018","90","","90","","90","","7515.3","1.3","296","2","296","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C32 H53 B11 N2 -","- C32 H53 B11 N2 -","- C256 H424 B88 N16 -","8","1","","Zheng, Fangrui; Xie, Zuowei","Reaction of N-heterocyclic carbenes with 13-vertex closo-carboranes: synthesis and structural characterization of zwitterionic salts of 13-vertex nido-carboranes","Organic Chemistry Frontiers","2015","2","1","55","","10.1039/C4QO00287C","","","0.71073","MoKα","","0.2374","0.0733","","","0.1637","0.2567","","","","","","0.996","","","","has coordinates","233002","2020-10-21","18:00:00",""
"1553051","17.474","0.002","20.161","0.002","21.123","0.002","90","","90","","90","","7441.5","1.3","293","2","293","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C32 H55 B11 N2 -","- C32 H55 B11 N2 -","- C256 H440 B88 N16 -","8","1","","Zheng, Fangrui; Xie, Zuowei","Reaction of N-heterocyclic carbenes with 13-vertex closo-carboranes: synthesis and structural characterization of zwitterionic salts of 13-vertex nido-carboranes","Organic Chemistry Frontiers","2015","2","1","55","","10.1039/C4QO00287C","","","0.71073","MoKα","","0.1324","0.0646","","","0.1543","0.1982","","","","","","0.948","","","","has coordinates","233002","2020-10-21","18:00:00",""
"1553052","11.591","0.003","15.516","0.004","16.796","0.004","90","","90","","90","","3020.7","1.3","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C26 H43 B11 N2 -","- C26 H43 B11 N2 -","- C104 H172 B44 N8 -","4","1","","Zheng, Fangrui; Xie, Zuowei","Reaction of N-heterocyclic carbenes with 13-vertex closo-carboranes: synthesis and structural characterization of zwitterionic salts of 13-vertex nido-carboranes","Organic Chemistry Frontiers","2015","2","1","55","","10.1039/C4QO00287C","","","0.71073","MoKα","","0.1916","0.0773","","","0.1748","0.2472","","","","","","1.058","","","","has coordinates","233002","2020-10-21","18:00:00",""
"1553053","10.343","0.004","18.963","0.007","22.347","0.009","90","","90","","90","","4383","3","173","2","173","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C41 H63 B11 N2 O -","- C41 H63 B11 N2 O -","- C164 H252 B44 N8 O4 -","4","1","","Zheng, Fangrui; Xie, Zuowei","Reaction of N-heterocyclic carbenes with 13-vertex closo-carboranes: synthesis and structural characterization of zwitterionic salts of 13-vertex nido-carboranes","Organic Chemistry Frontiers","2015","2","1","55","","10.1039/C4QO00287C","","","0.71073","MoKα","","0.1555","0.0834","","","0.1844","0.2188","","","","","","0.908","","","","has coordinates","233002","2020-10-21","18:00:00",""
"1553054","17.5189","0.0009","20.3686","0.0012","21.3348","0.0013","90","","90","","90","","7613","0.8","296","2","296","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C33 H55 B11 N2 -","- C33 H55 B11 N2 -","- C264 H440 B88 N16 -","8","1","","Zheng, Fangrui; Xie, Zuowei","Reaction of N-heterocyclic carbenes with 13-vertex closo-carboranes: synthesis and structural characterization of zwitterionic salts of 13-vertex nido-carboranes","Organic Chemistry Frontiers","2015","2","1","55","","10.1039/C4QO00287C","","","0.71073","MoKα","","0.1259","0.056","","","0.1254","0.1681","","","","","","1.032","","","","has coordinates","233002","2020-10-21","18:00:00",""
"1553055","10.2998","0.0006","16.7445","0.001","19.7479","0.0012","90","","101.979","0.001","90","","3331.7","0.3","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C27 H43 B11 N2 -","- C27 H43 B11 N2 -","- C108 H172 B44 N8 -","4","1","","Zheng, Fangrui; Xie, Zuowei","Reaction of N-heterocyclic carbenes with 13-vertex closo-carboranes: synthesis and structural characterization of zwitterionic salts of 13-vertex nido-carboranes","Organic Chemistry Frontiers","2015","2","1","55","","10.1039/C4QO00287C","","","0.71073","MoKα","","0.0883","0.0653","","","0.2083","0.2231","","","","","","1.096","","","","has coordinates","233002","2020-10-21","18:00:00",""
"1553056","10.4375","0.0006","19.3175","0.0009","22.8874","0.0013","90","","90","","90","","4614.7","0.4","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C39 H59 B11 N2 -","- C39 H59 B11 N2 -","- C156 H236 B44 N8 -","4","1","","Zheng, Fangrui; Xie, Zuowei","Reaction of N-heterocyclic carbenes with 13-vertex closo-carboranes: synthesis and structural characterization of zwitterionic salts of 13-vertex nido-carboranes","Organic Chemistry Frontiers","2015","2","1","55","","10.1039/C4QO00287C","","","0.71073","MoKα","","0.1296","0.0585","","","0.1179","0.1379","","","","","","0.893","","","","has coordinates","233002","2020-10-21","18:00:00",""
"1553057","9.2469","0.0006","12.1137","0.0007","17.1803","0.0011","90","","99.893","0.002","90","","1895.8","0.2","273","2","273","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H23 N3 O2 S -","- C20 H23 N3 O2 S -","- C80 H92 N12 O8 S4 -","4","1","","Zhu, Tong-Hao; Wei, Tian-Qi; Wang, Shun-Yi; Ji, Shun-Jun","NIS/CHP-mediated reaction of isocyanides with hydrazones: access to aminopyrazoles","Organic Chemistry Frontiers","2015","2","3","259","","10.1039/C4QO00289J","","","0.71073","MoKα","","0.0775","0.0485","","","0.1168","0.1333","","","","","","1.05","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553058","10.943","0.003","12.564","0.004","18.454","0.005","90","","90","","90","","2537.2","1.3","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C25 H25 Br N2 O7 -","- C25 H25 Br N2 O7 -","- C100 H100 Br4 N8 O28 -","4","1","","Sun, Qiang-Sheng; Chen, Xiao-Yang; Zhu, Hua; Lin, Hua; Sun, Xing-Wen; Lin, Guo-Qiang","Asymmetric synthesis of poly-substituted spirocyclohexane oxindole via a squaramide catalyzed cascade Michael–Michael–aldol sequence","Organic Chemistry Frontiers","2015","2","2","110","","10.1039/C4QO00299G","","","0.71073","MoKα","","0.0744","0.0488","","","0.1112","0.1222","","","","","","1.024","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553059","6.6023","0.0006","7.8736","0.0007","32.754","0.003","90","","90","","90","","1702.7","0.3","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C17 H18 Br N O5 -","- C17 H18 Br N O5 -","- C68 H72 Br4 N4 O20 -","4","1","","Li, Ying-Zi; Wang, Jie; Sun, Wang-Bin; Shan, Yi-Fan; Sun, Bing-Feng; Lin, Guo-Qiang; Zou, Jian-Ping","Enantioselective synthesis of bicyclo[2.2.2]octane-1-carboxylates under metal free conditions","Organic Chemistry Frontiers","2015","2","3","274","","10.1039/C4QO00311J","","","0.71073","MoKα","","0.0631","0.0453","","","0.1113","0.1189","","","","","","1.061","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553060","8.7741","0.0001","9.7409","0.0001","14.5365","0.0001","90","","90","","90","","1242.4","0.02","100","2","100","2","","","","","","","synthesis as described","5","P 21 21 21","P 2ac 2ab","19","","","","- C12 H17 N O4 S -","- C12 H17 N O4 S -","- C48 H68 N4 O16 S4 -","4","1","","Riaño, Iker; Uria, Uxue; Carrillo, Luisa; Reyes, Efraim; Vicario, Jose L.","4-Alkenyl-5H-1,2,3-oxathiazole 2,2-dioxides in catalytic and enantioselective [4 + 2] cycloaddition through iminium activation. Straightforward access to the trans-decaline framework and to densely functionalized cyclohexanes","Organic Chemistry Frontiers","2015","2","3","206","","10.1039/C4QO00316K","","","1.54184","CuKα","","0.0208","0.0205","","","0.0551","0.0553","","","","","","1.102","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553061","3.9045","0.0001","9.1939","0.0003","22.5383","0.0007","88.422","0.002","88.131","0.001","78.161","0.001","791.26","0.04","153","2","153","2","","","","","","","","3","P -1","-P 1","2","","","","- C8 H10 O3 -","- C8 H10 O3 -","- C32 H40 O12 -","4","2","","Wang, Qiang; Xu, Qin; Shi, Min","Co-catalysis between DABCO and a Brønsted acid in the catalytic [4 + 2] annulation of isatin with but-3-yn-2-one and mechanistic investigations","Organic Chemistry Frontiers","2015","2","3","211","","10.1039/C4QO00323C","","","1.54178","CuKα","","0.0512","0.0481","","","0.1457","0.1504","","","","","","1.071","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553062","8.1086","0.0014","8.8324","0.0016","13.26","0.002","108.838","0.003","97.636","0.004","94.663","0.004","883","0.3","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C21 H19 N O3 -","- C21 H19 N O3 -","- C42 H38 N2 O6 -","2","1","","Wang, Qiang; Xu, Qin; Shi, Min","Co-catalysis between DABCO and a Brønsted acid in the catalytic [4 + 2] annulation of isatin with but-3-yn-2-one and mechanistic investigations","Organic Chemistry Frontiers","2015","2","3","211","","10.1039/C4QO00323C","","","0.71073","MoKα","","0.0869","0.0682","","","0.1926","0.2173","","","","","","1.05","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553063","18.4165","0.0003","18.4165","0.0003","27.9044","0.0007","90","","90","","90","","9464.3","0.3","123.01","0.1","123.01","0.1","","","","","","","","8","P 4/n c c :2","-P 4a 2ac","130","","","","- C77 H89 Br4 Cl3 F8 I4 N4 O8 -","- C76.74 H88.24 Br4 Cl2.22 F8 I4 N4 O8 -","- C306.96 H352.96 Br16 Cl8.88 F32 I16 N16 O32 -","4","0.25","","Beyeh, N. Kodiah; Valkonen, Arto; Bhowmik, Sandip; Pan, Fangfang; Rissanen, K.","N-Alkyl ammonium resorcinarene salts: multivalent halogen-bonded deep-cavity cavitands","Organic Chemistry Frontiers","2015","2","4","340","","10.1039/C4QO00326H","","x-ray","1.54184","CuKα","","0.1264","0.1053","","","0.3","0.3286","","","","","","1.015","","","","has coordinates,has disorder","233014","2020-10-21","18:00:00",""
"1553064","23.3371","0.0003","23.5232","0.0002","27.0473","0.0003","90","","90","","90","","14848","0.3","123.01","0.1","123.01","0.1","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C72 H114 Br4 Cl2 N4 O9 -","- C72 H114 Br4 Cl2 N4 O9 -","- C576 H912 Br32 Cl16 N32 O72 -","8","1","","Beyeh, N. Kodiah; Valkonen, Arto; Bhowmik, Sandip; Pan, Fangfang; Rissanen, K.","N-Alkyl ammonium resorcinarene salts: multivalent halogen-bonded deep-cavity cavitands","Organic Chemistry Frontiers","2015","2","4","340","","10.1039/C4QO00326H","","","1.5418","CuKα","","0.0905","0.0778","","","0.2208","0.2411","","","","","","1.051","","","","has coordinates,has disorder","233014","2020-10-21","18:00:00",""
"1553065","24.849","0.003","4.7231","0.0005","14.8643","0.0017","90","","103.467","0.002","90","","1696.6","0.3","100","2","100.15","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","(3RS, 4RS)-N-methoxy-3-chloro-4-hydroxy-2,3,4,7-tetrahydro-1H-azepine","","- C7 H7 Cl N O2 -","- C7 H12 Cl N O2 -","- C56 H96 Cl8 N8 O16 -","8","1","","Barnes, Korry L.; Chen, Kelly; Catalano, Vincent J.; Jeffrey, Christopher S.","New building blocks for iminosugars: a concise synthesis of polyhydroxylated N-alkoxypiperidines through an intramolecular azepine ring contraction","Organic Chemistry Frontiers","2015","2","5","497","","10.1039/C4QO00330F","","","0.71073","MoKα","","0.0797","0.0562","","","0.1727","0.1969","","","","","","1","","","","has coordinates,has disorder","233017","2020-10-21","18:00:00",""
"1553066","9.9549","0.0004","11.3328","0.0005","11.8818","0.0005","106.461","0.0007","101.618","0.0007","100.174","0.0007","1219.6","0.09","100","2","99.65","","","","","","","","","4","P -1","-P 1","2","","(2RS, 3RS)-N-phenylmethoxy-2-hydroxymethyl-3-hydroxy-1,2,3,6-tetrahydropyridine","","- C13 H17 N O3 -","- C13 H17 N O3 -","- C52 H68 N4 O12 -","4","2","","Barnes, Korry L.; Chen, Kelly; Catalano, Vincent J.; Jeffrey, Christopher S.","New building blocks for iminosugars: a concise synthesis of polyhydroxylated N-alkoxypiperidines through an intramolecular azepine ring contraction","Organic Chemistry Frontiers","2015","2","5","497","","10.1039/C4QO00330F","","","0.71073","MoKα","","0.0618","0.0367","","","0.0677","0.0727","","","","","","1","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553067","5.3906","0.0003","15.9299","0.0009","17.3564","0.001","112.457","0.0011","97.7331","0.0011","99.3952","0.0011","1326.85","0.13","100","2","99.65","","","","","","","","","4","P -1","-P 1","2","","(2RS,3RS,4SR,5RS)-N-phenylmethoxy-2-hydroxymethyl-3,4,5-trihydroxypiperidine","","- C13 H19 N O5 -","- C13 H19 N O5 -","- C52 H76 N4 O20 -","4","2","","Barnes, Korry L.; Chen, Kelly; Catalano, Vincent J.; Jeffrey, Christopher S.","New building blocks for iminosugars: a concise synthesis of polyhydroxylated N-alkoxypiperidines through an intramolecular azepine ring contraction","Organic Chemistry Frontiers","2015","2","5","497","","10.1039/C4QO00330F","","","0.71073","MoKα","","0.0775","0.0467","","","0.1191","0.1352","","","","","","1","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553068","7.1432","0.0004","8.4932","0.0004","10.1874","0.0005","99.388","0.002","97.577","0.002","106.771","0.002","573.27","0.05","193","2","193","2","","","","","","","synthesis as described","4","P -1","-P 1","2","","","","- C15 H11 N O2 -","- C15 H11 N O2 -","- C30 H22 N2 O4 -","2","1","","Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat","Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds","Organic Chemistry Frontiers","2015","2","4","312","","10.1039/C4QO00338A","","x-ray","0.71073","MoKα","","0.0375","0.034","","","0.0871","0.0899","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553069","7.0179","0.0008","4.6365","0.0004","29.074","0.003","90","","92.757","0.003","90","","944.93","0.17","193","2","193","2","","","","","","","synthesis as described","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H20 N2 O4 -","- C22 H20 N2 O4 -","- C44 H40 N4 O8 -","2","0.5","","Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat","Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds","Organic Chemistry Frontiers","2015","2","4","312","","10.1039/C4QO00338A","","x-ray","0.71073","MoKα","","0.0705","0.0445","","","0.0972","0.1093","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553070","18.2723","0.0016","5.5654","0.0004","8.7266","0.0007","90","","103.633","0.004","90","","862.43","0.12","193","2","193","2","","","","","","","synthesis as described","4","P 1 c 1","P -2yc","7","","","","- C21 H21 N3 O -","- C21 H21 N3 O -","- C42 H42 N6 O2 -","2","1","","Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat","Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds","Organic Chemistry Frontiers","2015","2","4","312","","10.1039/C4QO00338A","","x-ray","0.71073","MoKα","","0.0506","0.0412","","","0.1059","0.1114","","","","","","1.039","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553071","11.008","0.003","7.5883","0.0019","19.571","0.005","90","","90.988","0.01","90","","1634.6","0.7","193","2","193","2","","","","","","","synthesis as described","3","P 1 21 1","P 2yb","4","","","","- C23 H16 O -","- C23 H16 O -","- C92 H64 O4 -","4","2","","Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat","Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds","Organic Chemistry Frontiers","2015","2","4","312","","10.1039/C4QO00338A","","x-ray","0.71073","MoKα","","0.1856","0.0704","","","0.1292","0.172","","","","","","0.972","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553072","9.1264","0.0005","9.7169","0.0006","10.2731","0.0007","95.504","0.004","91.157","0.004","101.221","0.004","888.78","0.1","193","2","193","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H23 N O2 -","- C22 H23 N O2 -","- C44 H46 N2 O4 -","2","1","","Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat","Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds","Organic Chemistry Frontiers","2015","2","4","312","","10.1039/C4QO00338A","","","0.71073","MoKα","","0.0822","0.0587","","","0.1776","0.217","","","","","","1.079","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553073","5.6257","0.0007","19.7469","0.0019","23.768","0.002","79.737","0.006","88.28","0.007","82.746","0.007","2577.3","0.5","193","2","193","2","","","","","","","","4","P -1","-P 1","2","","","","- C20 H18 N4 O2 -","- C20 H18 N4 O2 -","- C120 H108 N24 O12 -","6","3","","Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat","Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds","Organic Chemistry Frontiers","2015","2","4","312","","10.1039/C4QO00338A","","","0.71073","MoKα","","0.147","0.0759","","","0.1565","0.1814","","","","","","1.075","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553074","7.1728","0.0002","8.0196","0.0002","12.8455","0.0004","84.142","0.002","89.687","0.002","87.901","0.002","734.56","0.04","193","2","193","2","","","","","","","synthesis as described","4","P -1","-P 1","2","","","","- C20 H13 N O4 -","- C20 H13 N O4 -","- C40 H26 N2 O8 -","2","1","","Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat","Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds","Organic Chemistry Frontiers","2015","2","4","312","","10.1039/C4QO00338A","","x-ray","0.71073","MoKα","","0.0478","0.0379","","","0.0976","0.1044","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553075","9.9162","0.0008","14.8123","0.0011","7.3118","0.0006","90","","90","","90","","1073.97","0.15","200","2","200","2","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C9 H9 N7 O -","- C9 H9 N7 O -","- C36 H36 N28 O4 -","4","1","","Quinodoz, Pierre; Lo, Cheikh; Kletskii, Mikhail; Burov, Oleg; Marrot, Jérôme; Couty, François","Regio- and stereoselective synthesis of α-hydroxy-β-azido tetrazoles","Organic Chemistry Frontiers","2015","2","5","492","","10.1039/C4QO00345D","","","0.71073","MoKα","","0.0476","0.0368","","","0.0819","0.0874","","","","","","1.055","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553076","10.3879","0.0015","10.3879","0.0015","24.218","0.005","90","","90","","120","","2263.2","0.7","296","2","296","2","","","","","","","","5","P 32","P 32","145","","QM-1","","- C15 H13 N O5 S -","- C15 H13 N O5 S -","- C90 H78 N6 O30 S6 -","6","2","","Quan, Mao; Yang, Guoqiang; Xie, Fang; Gridnev, Ilya D.; Zhang, Wanbin","Pd(ii)-catalyzed asymmetric addition of arylboronic acids to cyclic N-sulfonyl ketimine esters and a DFT study of its mechanism","Organic Chemistry Frontiers","2015","2","4","398","","10.1039/C4QO00347K","","","1.54178","CuKα","","0.0328","0.0326","","","0.0873","0.0875","","","","","","1.094","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553095","9.017","0.0007","12.174","0.0009","12.8341","0.0009","108.889","0.002","99.634","0.002","109.852","0.002","1191.34","0.16","273","2","273","2","","","","","","","","3","P -1","-P 1","2","","","","- C14 H16 O3 -","- C14 H16 O3 -","- C56 H64 O12 -","4","2","","Dethe, Dattatraya H.; Boda, Raghavender; Murhade, Ganesh M.","Lewis acid catalyzed Nazarov type cyclization for the synthesis of a substituted indane framework: total synthesis of (±)-mutisianthol","Organic Chemistry Frontiers","2015","2","6","645","","10.1039/C5QO00005J","","","0.71073","MoKα","","0.1523","0.0964","","","0.2295","0.263","","","","","","1.035","","","","has coordinates","275434","2022-05-16","05:31:57",""
"1553096","12.38928","0.00014","20.5595","0.0003","23.639","0.0003","90","","90","","90","","6021.26","0.13","160","1","160","1","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","1,3,5,7,9-pentakis(4,4,5,5-tetramethyl-1,2,3-dioxaborolane)corannulene","","- C56 H79 B5 O10 -","- C50 H65 B5 O10 -","- C200 H260 B20 O40 -","4","1","","Da Ros, Sara; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.","Boronic esters of corannulene: potential building blocks toward icosahedral supramolecules","Organic Chemistry Frontiers","2015","2","6","626","","10.1039/C5QO00009B","","","1.54184","CuKα","","0.1125","0.1047","","","0.3114","0.322","","","","","","1.371","","","","has coordinates,has disorder","233586","2020-10-21","18:00:00",""
"1553097","20.2644","0.0002","13.18215","0.00013","8.2499","0.00008","90","","90","","90","","2203.78","0.04","160","2","160","2","","","","","","","","5","P m n 21","P 2ac -2","31","","1,3,5,7,9-pentakis(boronic acid)corannulene cis-cyclopentanediol ester","","- C46 H46 B5 Cl3 O10 -","- C46 H46 B5 Cl3 O10 -","- C92 H92 B10 Cl6 O20 -","2","0.5","","Da Ros, Sara; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.","Boronic esters of corannulene: potential building blocks toward icosahedral supramolecules","Organic Chemistry Frontiers","2015","2","6","626","","10.1039/C5QO00009B","","","1.5418","CuKα","","0.0536","0.0531","","","0.1436","0.1442","","","","","","1.059","","","","has coordinates,has disorder","233586","2020-10-21","18:00:00",""
"1553098","9.959","0.0011","24.396","0.003","11.0384","0.0012","90","","108.602","0.001","90","","2541.8","0.5","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","2,3-bis(4-chlorophenyl)-1,1-diphenyl-1H-benzo[b]silole","","- C32 H22 Cl2 Si -","- C32 H22 Cl2 Si -","- C128 H88 Cl8 Si4 -","4","1","","Xu, Liang; Zhang, Shuai; Li, Pengfei","Synthesis of silafluorenes and silaindenes via silyl radicals from arylhydrosilanes: intramolecular cyclization and intermolecular annulation with alkynes","Organic Chemistry Frontiers","2015","2","5","459","","10.1039/C5QO00012B","","","0.71073","MoKα","","0.0494","0.0374","","","0.0883","0.0941","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553099","5.572","0.0004","15.48","0.001","25.4858","0.0016","90","","90","","90","","2198.3","0.3","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","tert-Butyl (1R,2S,3R,6R,7S,9S)-6-phenyl-8-oxa-2- azatetracyclo[7.7.0.02,7.011,16]hexadeca-11(16),12,14- triene-3-carboxylate","","- C25 H29 N O3 -","- C25 H29 N O3 -","- C100 H116 N4 O12 -","4","1","","Arena, Giada; Cini, Elena; Petricci, Elena; Randino, Rosario; Taddei, Maurizio","A highly stereo-controlled protocol to prepare pipecolic acids based on Heck and cyclohydrocarbonylation reactions","Organic Chemistry Frontiers","2015","2","5","526","","10.1039/C5QO00025D","","","0.71073","MoKα","","0.1451","0.0382","","","0.0484","0.0582","","","","","","0.69","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553100","22.264","0.004","10.1945","0.0018","30.92","0.005","90","","91.849","0.003","90","","7014","2","193","2","193","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C23 H16 O3.19 -","- C23 H16 O3 -","- C368 H256 O48 -","16","4","","Liu, Tong; Ding, Qiuping; Zong, Qianshou; Qiu, Guanyinsheng","Radical 5-exo cyclization of alkynoates with 2-oxoacetic acids for synthesis of 3-acylcoumarins","Organic Chemistry Frontiers","2015","2","6","670","","10.1039/C5QO00029G","","","0.71073","MoKα","","0.1006","0.0603","","","0.1625","0.1916","","","","","","1.028","","","","has coordinates,has disorder","233594","2020-10-21","18:00:00",""
"1553101","7.159","0.005","9.364","0.005","10.541","0.005","78.846","0.005","82.356","0.005","72.557","0.005","659.3","0.7","153","2","153","2","","","","","","","","4","P -1","-P 1","2","","","","- C18 H13 N O2 -","- C18 H13 N O2 -","- C36 H26 N2 O4 -","2","1","","Dethe, Dattatraya H.; Kumar B, Vijay","Concise asymmetric total synthesis of bruceolline J","Organic Chemistry Frontiers","2015","2","5","548","","10.1039/C5QO00030K","","","0.71069","MoKα","","0.0701","0.0535","","","0.1428","0.1585","","","","","","1.054","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553102","10.786","0.0004","10.786","0.0004","17.286","0.0007","90","","90","","120","","1741.59","0.12","293","2","293","2","","","","","","","","6","P -3 c 1","-P 3 2""c","165","","","","- C30 H24 F12 N6 Ru Sb2 -","- C30 H24 F12 N6 Ru Sb2 -","- C60 H48 F24 N12 Ru2 Sb4 -","2","0.166667","","Gomes, Filipe; Narbonne, Vanessa; Blanchard, Florent; Maestri, Giovanni; Malacria, Max","Formal base-free homolytic aromatic substitutions via photoredox catalysis","Organic Chemistry Frontiers","2015","2","5","464","","10.1039/C5QO00031A","","","0.71073","MoKα","","0.0862","0.0515","","","0.1511","0.1877","","","","","","1.218","","","","has coordinates","233598","2020-10-21","18:00:00",""
"1553103","6.2097","0.0013","11.272","0.002","11.547","0.003","104.782","0.004","101.238","0.004","100.235","0.004","744.1","0.3","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C16 H22 N O3 S -","- C16 H17 N O3 S -","- C32 H34 N2 O6 S2 -","2","1","","Zhang, Yan-Yan; Hao, Jian; Shi, Min","One pot cascade synthesis of fused heterocycles from furan-tethered terminal alkynes and aldehydes in the presence of amines and CuBr","Organic Chemistry Frontiers","2015","2","4","394","","10.1039/C5QO00033E","","","0.71073","MoKα","","0.0709","0.0656","","","0.1786","0.1866","","","","","","1.065","","","","has coordinates","233600","2020-10-21","18:00:00",""
"1553104","8.3878","0.0016","9.8582","0.0018","19.139","0.003","76.354","0.004","84.421","0.004","73.985","0.004","1477.3","0.5","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C16 H17 N O3 S -","- C16 H17 N O3 S -","- C64 H68 N4 O12 S4 -","4","2","","Zhang, Yan-Yan; Hao, Jian; Shi, Min","One pot cascade synthesis of fused heterocycles from furan-tethered terminal alkynes and aldehydes in the presence of amines and CuBr","Organic Chemistry Frontiers","2015","2","4","394","","10.1039/C5QO00033E","","","0.71073","MoKα","","0.0612","0.0513","","","0.1322","0.1397","","","","","","1.059","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553105","14.5933","0.0018","9.6858","0.0012","11.3977","0.0014","90","","92.745","0.003","90","","1609.2","0.3","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C17 H19 N O3 S -","- C17 H19 N O3 S -","- C68 H76 N4 O12 S4 -","4","1","","Zhang, Yan-Yan; Hao, Jian; Shi, Min","One pot cascade synthesis of fused heterocycles from furan-tethered terminal alkynes and aldehydes in the presence of amines and CuBr","Organic Chemistry Frontiers","2015","2","4","394","","10.1039/C5QO00033E","","","0.71073","MoKα","","0.0564","0.0432","","","0.1107","0.1206","","","","","","1.027","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553106","15.713","0.012","28.08","0.02","28.507","0.018","90","","90","","90","","12578","15","293","2","293","2","","","","","","","","5","I 2 2 2","I 2 2","23","","","","- C33 H30 Br N O5 -","- C33 H30 Br N O5 -","- C528 H480 Br16 N16 O80 -","16","2","","Zhang, Jun-Wei; Liu, Xiao-Wei; Gu, Qing; Shi, Xiao-Xin; You, Shu-Li","Enantioselective synthesis of 4,5,6,7-tetrahydroindoles via olefin cross-metathesis/intramolecular Friedel–Crafts alkylation reaction of pyrroles","Organic Chemistry Frontiers","2015","2","5","476","","10.1039/C5QO00034C","","","0.71073","MoKα","","0.1326","0.0686","","","0.1544","0.1759","","","","","","0.891","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553107","5.5881","0.0002","18.985","0.0006","10.6706","0.0004","90","","94.113","0.003","90","","1129.13","0.07","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","diiodide","","- C17 H0 I2 N3 O6 -","- C10 H7 I2 N O -","- C40 H28 I8 N4 O4 -","4","1","","Zhang, Shuo; Chen, Ying; Wang, Jianwu; Pan, Yue; Xu, Zhenghu; Tung, Chen-Ho","An efficient synthesis of gem-diiodoolefins and (E)-iodoalkenes from propargylic amides with a Cu(i)/Cu(iii) cycle","Organic Chemistry Frontiers","2015","2","5","578","","10.1039/C5QO00043B","","","1.54184","CuKα","","0.1236","0.1113","","","0.2803","0.2931","","","","","","1.212","","","","has coordinates","233604","2020-10-21","18:00:00",""
"1553108","9.2215","0.0006","10.9612","0.0007","11.6484","0.0007","87.764","0.002","69.092","0.003","73.409","0.003","1051.48","0.12","296","2","296.15","","","","","","","","","4","P -1","-P 1","2","","zhangshuotrienes","","- C23 H25 N O5 -","- C23 H25 N O5 -","- C46 H50 N2 O10 -","2","1","","Zhang, Shuo; Chen, Ying; Wang, Jianwu; Pan, Yue; Xu, Zhenghu; Tung, Chen-Ho","An efficient synthesis of gem-diiodoolefins and (E)-iodoalkenes from propargylic amides with a Cu(i)/Cu(iii) cycle","Organic Chemistry Frontiers","2015","2","5","578","","10.1039/C5QO00043B","","","1.54178","CuKα","","0.0557","0.0539","","","0.1496","0.1513","","","","","","1.061","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553109","26.291","0.014","8.781","0.005","18.363","0.01","90","","111.863","0.004","90","","3934","4","296","2","296","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C23 H17 I O3 -","- C23 H17 I O3 -","- C184 H136 I8 O24 -","8","1","","Zhu, Hai-Tao; Fan, Ming-Jin; Yang, De-Suo; Wang, Xiao-Ling; Ke, Sen; Zhang, Chao-Yang; Guan, Zheng-Hui","An iodine-promoted Meyer–Schuster rearrangement for the synthesis of α-iodo unsaturated ketones","Organic Chemistry Frontiers","2015","2","5","506","","10.1039/C5QO00048C","","","0.71073","MoKα","","0.0365","0.0247","","","0.0479","0.0529","","","","","","1.055","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553110","12.3535","0.0005","28.8354","0.0012","15.2713","0.0006","90","","99.472","0.002","90","","5365.7","0.4","173","2","173","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C59 H49 Cl4 F6 N P3 Rh -","- C59 H49 Cl4 F6 N P3 Rh -","- C236 H196 Cl16 F24 N4 P12 Rh4 -","4","1","","Chen, Shanshan; Su, Yan; Han, Keli; Li, Xingwei","Mechanistic studies on C‒C reductive coupling of five-coordinate Rh(iii) complexes","Organic Chemistry Frontiers","2015","2","7","783","","10.1039/C5QO00049A","","","0.71073","MoKα","","0.083","0.0648","","","0.1762","0.2067","","","","","","1.063","","","","has coordinates","233607","2020-10-21","18:00:00",""
"1553111","10.8319","0.0004","13.2288","0.0004","22.0889","0.0008","75.156","0.002","79.856","0.002","69.201","0.002","2847.44","0.18","173","2","173","2","","","","","","","","7","P -1","-P 1","2","","","","- C65 H61 F6 N O2 P3 Rh -","- C65 H61 F6 N O2 P3 Rh -","- C130 H122 F12 N2 O4 P6 Rh2 -","2","1","","Chen, Shanshan; Su, Yan; Han, Keli; Li, Xingwei","Mechanistic studies on C–C reductive coupling of five-coordinate Rh(iii) complexes","Organic Chemistry Frontiers","2015","2","7","783","","10.1039/C5QO00049A","","","0.71073","MoKα","","0.0711","0.0586","","","0.1606","0.181","","","","","","1.13","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553112","13.6534","0.0003","25.7008","0.0005","15.5862","0.0003","90","","93.092","0.001","90","","5461.29","0.19","223","2","223","2","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C59 H46 Cl2 F9 N P3 Rh -","- C59 H46 Cl2 F9 N P3 Rh -","- C236 H184 Cl8 F36 N4 P12 Rh4 -","4","1","","Chen, Shanshan; Su, Yan; Han, Keli; Li, Xingwei","Mechanistic studies on C‒C reductive coupling of five-coordinate Rh(iii) complexes","Organic Chemistry Frontiers","2015","2","7","783","","10.1039/C5QO00049A","","","0.71073","MoKα","","0.0764","0.0533","","","0.1514","0.1829","","","","","","1.017","","","","has coordinates,has disorder","233607","2020-10-21","18:00:00",""
"1553113","16.5731","0.0008","19.6848","0.0007","18.1839","0.0009","90","","112.182","0.002","90","","5493.2","0.4","173","2","173","2","","","","","","","","9","P 1 21/n 1","-P 2yn","14","","","","- C58 H52 B Cl6 F4 N O Os P2 -","- C58 H52 B Cl6 F4 N O Os P2 -","- C232 H208 B4 Cl24 F16 N4 O4 Os4 P8 -","4","1","","Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping","Reactions of osmapyridinium with terminal alkynes","Organic Chemistry Frontiers","2015","2","5","560","","10.1039/C5QO00052A","","","0.71073","MoKα","","0.0779","0.0643","","","0.171","0.1873","","","","","","1.084","","","","has coordinates","233608","2020-10-21","18:00:00",""
"1553114","11.9299","0.0003","14.1946","0.0003","33.0235","0.0007","90","","98.576","0.001","90","","5529.7","0.2","153","2","153","2","","","","","","","","9","P 1 21/c 1","-P 2ybc","14","","","","- C56.25 H52.25 B Cl2.75 F4 N O3 Os P2 -","- C56.25 H52.25 B Cl2.75 F4 N O3 Os P2 -","- C225 H209 B4 Cl11 F16 N4 O12 Os4 P8 -","4","1","","Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping","Reactions of osmapyridinium with terminal alkynes","Organic Chemistry Frontiers","2015","2","5","560","","10.1039/C5QO00052A","","","0.71073","MoKα","","0.0694","0.0566","","","0.1635","0.172","","","","","","1.044","","","","has coordinates","233608","2020-10-21","18:00:00",""
"1553115","12.0746","0.0003","18.8448","0.0003","20.9677","0.0004","90","","90.023","0.001","90","","4771.06","0.17","173","2","173","2","","","","","","","","9","P 1 21/c 1","-P 2ybc","14","","","","- C50 H43 B Cl5 F4 N3 O Os P -","- C50 H44 B Cl5 F4 N3 O Os P -","- C200 H176 B4 Cl20 F16 N12 O4 Os4 P4 -","4","1","","Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping","Reactions of osmapyridinium with terminal alkynes","Organic Chemistry Frontiers","2015","2","5","560","","10.1039/C5QO00052A","","","0.71073","MoKα","","0.0723","0.0526","","","0.1396","0.1954","","","","","","1.17","","","","has coordinates","233608","2020-10-21","18:00:00",""
"1553116","19.3445","0.0009","16.8974","0.0006","16.1902","0.0007","90","","111.004","0.001","90","","4940.5","0.4","173","2","173","2","","","","","","","","8","C 1 c 1","C -2yc","9","","","","- C52 H55 B Cl4 F4 N3 Os P -","- C52 H55 B Cl4 F4 N3 Os P -","- C208 H220 B4 Cl16 F16 N12 Os4 P4 -","4","1","","Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping","Reactions of osmapyridinium with terminal alkynes","Organic Chemistry Frontiers","2015","2","5","560","","10.1039/C5QO00052A","","","0.71073","MoKα","","0.0439","0.0344","","","0.0737","0.0858","","","","","","1.091","","","","has coordinates","233608","2020-10-21","18:00:00",""
"1553117","7.2941","0.0002","13.2249","0.0003","17.2264","0.0004","90","","96.919","0.002","90","","1649.62","0.07","130","0.2","130","0.2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H21 N O3 -","- C19 H21 N O3 -","- C76 H84 N4 O12 -","4","1","","Santos, Hugo; Distiller, Amy; D'Souza, Asha M.; Arnoux, Quentin; White, Jonathan M.; Meyer, Adam G.; Ryan, John H.","1,3-Dipolar cycloaddition reactions of phthalic anhydrides with an azomethine ylide","Organic Chemistry Frontiers","2015","2","6","705","","10.1039/C5QO00062A","","x-ray","0.71073","MoKα","","0.0645","0.0461","","","0.1227","0.1369","","","","","","1.05","","","","has coordinates","233610","2020-10-21","18:00:00",""
"1553118","8.592","0.007","10.956","0.009","16.545","0.014","90","","92.673","0.011","90","","1556","2","100","","100","","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C32 H37 N O4 S Sn -","- C32 H37 N O4 S Sn -","- C64 H74 N2 O8 S2 Sn2 -","2","1","","Kamimura, Akio; Yoshinaga, Tatsuro; Noguchi, Fumiaki; Miyazaki, Koichiro; Uno, Hidemitsu","A mechanistic study on the SHi reaction at tin atoms in a radical cascade reaction","Organic Chemistry Frontiers","2015","2","6","713","","10.1039/C5QO00063G","","","0.71075","MoKα","","0.1065","0.0869","","","0.196","0.2108","","","","","","1.096","","","","has coordinates","233611","2020-10-21","18:00:00",""
"1553119","7.6495","0.0006","12.803","0.0013","16.9343","0.0013","90","","90","","90","","1658.5","0.2","173","2","173","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C16 H16 Cl I O S -","- C16 H16 Cl I O S -","- C64 H64 Cl4 I4 O4 S4 -","4","1","","Berthelot-Bréhier, Anaïs; Panossian, Armen; Colobert, Françoise; Leroux, Frédéric R.","Atroposelective synthesis of axially chiral P,S-ligands based on arynes","Organic Chemistry Frontiers","2015","2","6","634","","10.1039/C5QO00067J","","","0.71073","MoKα","","0.0358","0.0271","","","0.0496","0.0525","","","","","","1.083","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553120","9.4309","0.0003","13.5255","0.0004","19.3191","0.0006","90","","90","","90","","2464.3","0.13","173","2","173","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C28 H26 Cl P S -","- C28 H26 Cl P S -","- C112 H104 Cl4 P4 S4 -","4","1","","Berthelot-Bréhier, Anaïs; Panossian, Armen; Colobert, Françoise; Leroux, Frédéric R.","Atroposelective synthesis of axially chiral P,S-ligands based on arynes","Organic Chemistry Frontiers","2015","2","6","634","","10.1039/C5QO00067J","","","1.54178","CuKα","","0.0529","0.0526","","","0.1372","0.1373","","","","","","1.147","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553121","11.8312","0.0003","15.3726","0.0006","17.795","0.0006","90","","90","","90","","3236.49","0.19","173","2","173","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C35 H34 Cl3 P Pd S -","- C35 H34 Cl3 P Pd S -","- C140 H136 Cl12 P4 Pd4 S4 -","4","1","","Berthelot-Bréhier, Anaïs; Panossian, Armen; Colobert, Françoise; Leroux, Frédéric R.","Atroposelective synthesis of axially chiral P,S-ligands based on arynes","Organic Chemistry Frontiers","2015","2","6","634","","10.1039/C5QO00067J","","","0.71073","MoKα","","0.0801","0.043","","","0.0854","0.1102","","","","","","1.061","","","","has coordinates","233613","2020-10-21","18:00:00",""
"1553122","10.4422","0.0003","33.2582","0.001","10.4466","0.0003","90","","114.77","0.002","90","","3294.2","0.17","296","2","296","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C19 H20 F3 N -","- C19 H20 F3 N -","- C152 H160 F24 N8 -","8","4","","Chen, Mu-Wang; Ye, Zhi-Shi; Chen, Zhang-Pei; Wu, Bo; Zhou, Yong-Gui","Enantioselective synthesis of trifluoromethyl substituted piperidines with multiple stereogenic centers via hydrogenation of pyridinium hydrochlorides","Organic Chemistry Frontiers","2015","2","5","586","","10.1039/C5QO00069F","","","1.54178","CuKα","","0.1075","0.0715","","","0.2153","0.2857","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553123","18.029","0.008","9.695","0.004","14.246","0.007","90","","110.517","0.008","90","","2332.1","1.8","153","","153","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","2,2-bis(eta-5-cyclopentadienyl)-3-trimethylsilyl-5-dimethylamino-1-thia-2-zirconacyclopenta-3,4-diene","","- C23 H35 N S Si Ti -","- C23 H35 N S Si Ti -","- C92 H140 N4 S4 Si4 Ti4 -","4","1","","Suzuki, Noriyuki; Asada, Takumi; Kawamura, Akiko; Masuyama, Yoshiro","Sulfur-containing stable five-membered “cycloallene” complexes: 1-thia-2-zircona- and 1-thia-2-titanacyclopenta-3,4-dienes","Organic Chemistry Frontiers","2015","2","6","681","","10.1039/C5QO00072F","","","0.71075","MoKα","","0.0952","0.0619","","","0.1228","0.142","","","","","","1.067","","","","has coordinates","233616","2020-10-21","18:00:00",""
"1553124","18.125","0.005","9.87","0.002","14.346","0.004","90","","110.563","0.004","90","","2402.9","1.1","153","","153","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","2,2-bis(η5-cyclopentadienyl)-3-tert-butyldimethylsilyl- 5-diethylamino-1-thia-2-zirconacyclopenta-3,4-diene","","- C23 H35 N S Si Zr -","- C23 H35 N S Si Zr -","- C92 H140 N4 S4 Si4 Zr4 -","4","1","","Suzuki, Noriyuki; Asada, Takumi; Kawamura, Akiko; Masuyama, Yoshiro","Sulfur-containing stable five-membered “cycloallene” complexes: 1-thia-2-zircona- and 1-thia-2-titanacyclopenta-3,4-dienes","Organic Chemistry Frontiers","2015","2","6","681","","10.1039/C5QO00072F","","","0.71073","MoKα","","0.0367","0.0321","","","0.0716","0.075","","","","","","1.124","","","","has coordinates,has disorder","233616","2020-10-21","18:00:00",""
"1553125","15.471","0.008","9.164","0.004","14.06","0.007","90","","108.282","0.006","90","","1892.8","1.6","153","","153","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","2,2-bis(η5-cyclopentadienyl)-3-trimethylsilyl-5-dimethylamino- 1-thia-2-zirconacyclopenta-3,4-diene","","- C18 H25 N S Si Zr -","- C18 H25 N S Si Zr -","- C72 H100 N4 S4 Si4 Zr4 -","4","1","","Suzuki, Noriyuki; Asada, Takumi; Kawamura, Akiko; Masuyama, Yoshiro","Sulfur-containing stable five-membered “cycloallene” complexes: 1-thia-2-zircona- and 1-thia-2-titanacyclopenta-3,4-dienes","Organic Chemistry Frontiers","2015","2","6","681","","10.1039/C5QO00072F","","","0.71073","MoKα","","0.0606","0.0448","","","0.0838","0.0939","","","","","","1.098","","","","has coordinates,has disorder","233616","2020-10-21","18:00:00",""
"1553126","6.2605","","6.9304","","14.4299","","92.0278","","99.0665","","112.207","","569.305","","93","","93","","","","","","","","","5","P -1","-P 1","2","","(Z)-N,N-diethyl-3-(tert-butylditrimethylsilyl)prop-2-enethioamide","","- C8 H17 N S Si -","- C8 H17 N S Si -","- C16 H34 N2 S2 Si2 -","2","1","","Suzuki, Noriyuki; Asada, Takumi; Kawamura, Akiko; Masuyama, Yoshiro","Sulfur-containing stable five-membered “cycloallene” complexes: 1-thia-2-zircona- and 1-thia-2-titanacyclopenta-3,4-dienes","Organic Chemistry Frontiers","2015","2","6","681","","10.1039/C5QO00072F","","","0.71075","MoKα","","0.0906","0.0737","","","0.2217","0.2447","","","","","","1.096","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553127","8.3022","0.0003","11.1608","0.0004","16.3992","0.0006","90","","94.272","0.001","90","","1515.31","0.1","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C18 H16 O2 S -","- C18 H16 O2 S -","- C72 H64 O8 S4 -","4","1","","Chen, Dianpeng; Xing, Gangdong; Zhou, Hongwei","Sulfone promoted Rh(iii)-catalyzed C–H activation and base assisted 1,5-H shift strategy for the construction of seven-membered rings","Organic Chemistry Frontiers","2015","2","8","947","","10.1039/C5QO00089K","","","0.71073","MoKα","","0.052","0.0449","","","0.1103","0.1159","","","","","","1.003","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553128","8.6808","0.0008","8.9707","0.0006","11.2873","0.001","104.818","0.006","112.003","0.008","92.742","0.006","777.67","0.13","290","2","290","2","","","","","","","","4","P -1","-P 1","2","","","","- C17 H21 N O3 -","- C17 H21 N O3 -","- C34 H42 N2 O6 -","2","1","","Liu, Xianglei; Gu, Zhenhua","Pd-catalyzed Heck cyclization and in situ hydrocarboxylation or hydromethenylation via a hydrogen borrowing strategy","Organic Chemistry Frontiers","2015","2","7","778","","10.1039/C5QO00091B","","","1.54184","CuKα","","0.0609","0.0568","","","0.1606","0.1664","","","","","","1.072","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553129","5.9958","0.0012","13.644","0.003","17.789","0.004","90","","90","","90","","1455.3","0.5","173","2","173","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C16 H25 F O2 -","- C16 H25 F O2 -","- C64 H100 F4 O8 -","4","1","","Zhang, Xiaofei; Guo, Shuo; Tang, Pingping","Transition-metal free oxidative aliphatic C–H fluorination","Organic Chemistry Frontiers","2015","2","7","806","","10.1039/C5QO00095E","","","0.71073","MoKα","","0.0574","0.0549","","","0.1577","0.16","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553130","8.7359","0.0017","12.804","0.003","20.625","0.004","90","","90","","90","","2307","0.8","113","2","113","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C24 H31 F O8 -","- C24 H31 F O8 -","- C96 H124 F4 O32 -","4","1","","Zhang, Xiaofei; Guo, Shuo; Tang, Pingping","Transition-metal free oxidative aliphatic C–H fluorination","Organic Chemistry Frontiers","2015","2","7","806","","10.1039/C5QO00095E","","","0.71073","MoKα","","0.0843","0.0615","","","0.1225","0.1344","","","","","","1.003","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553131","12.1876","0.0018","9.8204","0.0014","15.854","0.002","90","","96.796","0.003","90","","1884.2","0.5","130","","130","","","","","","","","","6","P 1 21 1","P 2yb","4","","(POX)PdCl2","","- C16 H24 Cl2 N2 O Pd -","- C16 H24 Cl2 N2 O Pd -","- C64 H96 Cl8 N8 O4 Pd4 -","4","2","","Yu, Feng; Chen, Pinhong; Liu, Guosheng","Pd(ii)-catalyzed intermolecular enantioselective hydroamination of styrenes","Organic Chemistry Frontiers","2015","2","7","819","","10.1039/C5QO00096C","","","0.71073","MoKα","","0.0974","0.0638","","","0.118","0.1327","","","","","","1.023","","","","has coordinates","233622","2020-10-21","18:00:00",""
"1553132","10.291","0.002","5.9808","0.0012","12.068","0.002","90","","103.531","0.003","90","","722.1","0.2","273","2","273","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C13 H23 N O3 S -","- C13 H23 N O3 S -","- C26 H46 N2 O6 S2 -","2","1","","Ye, Jian-Liang; Zhang, Yu-Feng; Liu, Yang; Zhang, Jin-Yuan; Ruan, Yuan-Ping; Huang, Pei-Qiang","Studies on the asymmetric synthesis of pandamarilactonines: an unexpected syn-selective vinylogous Mannich reaction of N-tert-butanesulfinimines","Organic Chemistry Frontiers","2015","2","6","697","","10.1039/C5QO00098J","","","0.71073","MoKα","","0.0315","0.0314","","","0.088","0.088","","","","","","1.066","","","","has coordinates","300101","2025-06-17","17:58:10",""
"1553133","10.3564","0.0013","12.0563","0.0015","14.1956","0.0018","69.77","0.005","82.139","0.006","68.496","0.005","1547.3","0.3","150","","150","","","","","","","","","6","P -1","-P 1","2","","Benzyl 2-diethoxyphosphoryloxy-2,3-diphenyl-3-(N-tosylamino)propioate","","- C33 H36 N O8 P S -","- C33 H36 N O8 P S -","- C66 H72 N2 O16 P2 S2 -","2","1","","Kondoh, Azusa; Terada, Masahiro","Brønsted base-catalyzed α-oxygenation of carbonyl compounds utilizing the [1,2]-phospha-Brook rearrangement","Organic Chemistry Frontiers","2015","2","7","801","","10.1039/C5QO00108K","","","0.71075","MoKα","","0.073","0.0627","","","0.1554","0.1641","","","","","","1.041","","","","has coordinates","233625","2020-10-21","18:00:00",""
"1553134","7.82043","0.00019","10.2265","0.0003","17.491","0.0004","90","","90","","90","","1398.85","0.06","299","0.4","299","0.4","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C11 H13 N O7 S2 -","- C11 H13 N O7 S2 -","- C44 H52 N4 O28 S8 -","4","1","","Kang, Jian; Zhu, Baofu; Liu, Jiewei; Wang, Bo; Zhang, Li; Su, Cheng-Yong","Chiral dirhodium catalysts derived from l-serine, l-threonine and l-cysteine: design, synthesis and application","Organic Chemistry Frontiers","2015","2","8","890","","10.1039/C5QO00110B","","","1.54184","CuKα","","0.0375","0.0355","","","0.1101","0.1128","","","","","","0.945","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553135","15.41418","0.00014","15.41418","0.00014","5.95145","0.0001","90","","90","","90","","1414.05","0.03","293","2","293","2","","","","","","","","5","P 41","P 4w","76","","","","- C11 H12 N2 O7 S -","- C11 H12 N2 O7 S -","- C44 H48 N8 O28 S4 -","4","1","","Kang, Jian; Zhu, Baofu; Liu, Jiewei; Wang, Bo; Zhang, Li; Su, Cheng-Yong","Chiral dirhodium catalysts derived from l-serine, l-threonine and l-cysteine: design, synthesis and application","Organic Chemistry Frontiers","2015","2","8","890","","10.1039/C5QO00110B","","","1.54178","CuKα","","0.0387","0.0348","","","0.0932","0.095","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553136","12.8276","0.0003","8.4882","0.0002","24.8068","0.0007","90","","91.044","0.002","90","","2700.6","0.12","291","2","291.15","","","","","","","","","4","P 1 2/c 1","-P 2yc","13","","","","- C14 H14 N2 O3 -","- C14 H14 N2 O3 -","- C112 H112 N16 O24 -","8","2","","Zhang, Duo; Cui, Xiuling; Yang, Fangfang; Zhang, Qianqian; Zhu, Yu; Wu, Yangjie","Palladium-catalyzed direct ortho C‒O bond construction of azoxybenzenes with carboxylic acids and alcohols","Organic Chemistry Frontiers","2015","2","8","951","","10.1039/C5QO00120J","","","1.54184","CuKα","","0.0653","0.0478","","","0.1264","0.1417","","","","","","1.026","","","","has coordinates","233629","2020-10-21","18:00:00",""
"1553137","14.4863","0.0004","17.2032","0.0005","11.5651","0.0005","90","","105.969","0.004","90","","2770.93","0.17","291","2","291.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C28 H21 F3 N4 O6 Pd2 -","- C28 H21 F3 N4 O6 Pd2 -","- C112 H84 F12 N16 O24 Pd8 -","4","1","","Zhang, Duo; Cui, Xiuling; Yang, Fangfang; Zhang, Qianqian; Zhu, Yu; Wu, Yangjie","Palladium-catalyzed direct ortho C‒O bond construction of azoxybenzenes with carboxylic acids and alcohols","Organic Chemistry Frontiers","2015","2","8","951","","10.1039/C5QO00120J","","","0.71073","MoKα","","0.0723","0.0518","","","0.1342","0.1466","","","","","","1.05","","","","has coordinates","233629","2020-10-21","18:00:00",""
"1553138","6.8879","0.0009","8.282","0.0009","14.4023","0.001","104.655","0.008","94.121","0.009","91.668","0.01","791.85","0.15","291","2","291.15","","","","","","","","","4","P -1","-P 1","2","","","","- C17 H18 N2 O3 -","- C17 H18 N2 O3 -","- C34 H36 N4 O6 -","2","1","","Zhang, Duo; Cui, Xiuling; Yang, Fangfang; Zhang, Qianqian; Zhu, Yu; Wu, Yangjie","Palladium-catalyzed direct ortho C–O bond construction of azoxybenzenes with carboxylic acids and alcohols","Organic Chemistry Frontiers","2015","2","8","951","","10.1039/C5QO00120J","","","0.71073","MoKα","","0.0839","0.0508","","","0.1181","0.1377","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553139","8.6248","0.0011","9.8158","0.0012","11.6537","0.0014","99.05","0.002","101.411","0.002","96.596","0.002","944.1","0.2","140","2","140","2","","","","","","","","5","P -1","-P 1","2","","","","- C20 H26 N O2 S -","- C20 H26 N O2 S -","- C40 H52 N2 O4 S2 -","2","1","","Pan, Dong; Chen, Gen-Qiang; Tang, Xiang-Ying; Shi, Min","Palladium-catalyzed intramolecular rearrangement of vinylidenecyclopropanes through C‒C bond activation","Organic Chemistry Frontiers","2015","2","7","792","","10.1039/C5QO00127G","","","0.71073","MoKα","","0.0541","0.0433","","","0.1264","0.1398","","","","","","1.053","","","","has coordinates","233631","2020-10-21","18:00:00",""
"1553140","8.5768","0.0009","10.2978","0.0011","28.986","0.003","90","","90.183","0.002","90","","2560.1","0.5","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C30 H31 N O2 S -","- C30 H31 N O2 S -","- C120 H124 N4 O8 S4 -","4","1","","Pan, Dong; Chen, Gen-Qiang; Tang, Xiang-Ying; Shi, Min","Palladium-catalyzed intramolecular rearrangement of vinylidenecyclopropanes through C–C bond activation","Organic Chemistry Frontiers","2015","2","7","792","","10.1039/C5QO00127G","","","0.71073","MoKα","","0.0627","0.049","","","0.1211","0.1312","","","","","","1.021","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553141","9.8915","0.0004","9.4814","0.0004","11.942","0.0005","90","","102.048","0.004","90","","1095.31","0.08","153","2","153","2","","","","","","","","5","P 1 21 1","P 2yb","4","","(3S,8R)-3j'","","- C21 H22 Br N3 O5 -","- C21 H22 Br N3 O5 -","- C42 H44 Br2 N6 O10 -","2","1","","Hu, Ying; Zhou, Zijun; Gong, Lei; Meggers, Eric","Asymmetric aza-Henry reaction to provide oxindoles with quaternary carbon stereocenter catalyzed by a metal-templated chiral Brønsted base","Organic Chemistry Frontiers","2015","2","8","968","","10.1039/C5QO00132C","","","0.71073","MoKα","","0.0403","0.0376","","","0.103","0.1077","","","","","","1","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553142","7.1573","0.0004","21.4898","0.0009","9.4975","0.0004","90","","90","","90","","1460.8","0.12","173","2","173","2","","","","","","","","5","P n a 21","P 2c -2n","33","","(Z)-1j","","- C14 H15 Br N2 O3 -","- C14 H15 Br N2 O3 -","- C56 H60 Br4 N8 O12 -","4","1","","Hu, Ying; Zhou, Zijun; Gong, Lei; Meggers, Eric","Asymmetric aza-Henry reaction to provide oxindoles with quaternary carbon stereocenter catalyzed by a metal-templated chiral Brønsted base","Organic Chemistry Frontiers","2015","2","8","968","","10.1039/C5QO00132C","","","0.71073","MoKα","","0.0376","0.0344","","","0.0787","0.0811","","","","","","0.999","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553143","13.25","0.0002","16.9695","0.0003","23.3436","0.0004","90","","103.948","0.0018","90","","5093.95","0.15","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C70 H66 Cl34 N8 P2 Ru2 -","- C70 H66 Cl34 N8 P2 Ru2 -","- C140 H132 Cl68 N16 P4 Ru4 -","2","0.5","","Mejuto, Carmen; García-Eleno, Marco A.; Guisado-Barrios, Gregorio; Spasyuk, Denis; Gusev, Dmitri; Peris, Eduardo","Ruthenium complexes with an N-heterocyclic carbene NNC-pincer ligand: preparation and catalytic properties","Organic Chemistry Frontiers","2015","2","8","936","","10.1039/C5QO00137D","","x-ray","1.54184","CuKα","","0.0901","0.0721","","","0.1832","0.2154","","","","","","1.127","","","","has coordinates,has disorder","233636","2020-10-21","18:00:00",""
"1553144","18.2792","0.0003","11.74106","0.00011","17.1049","0.0002","90","","117.389","0.0018","90","","3259.49","0.09","199.95","0.1","199.95","0.1","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C32 H35 Cl2 N4 O5 P Ru -","- C32 H35 Cl2 N4 O5 P Ru -","- C128 H140 Cl8 N16 O20 P4 Ru4 -","4","1","","Mejuto, Carmen; García-Eleno, Marco A.; Guisado-Barrios, Gregorio; Spasyuk, Denis; Gusev, Dmitri; Peris, Eduardo","Ruthenium complexes with an N-heterocyclic carbene NNC-pincer ligand: preparation and catalytic properties","Organic Chemistry Frontiers","2015","2","8","936","","10.1039/C5QO00137D","","","1.54184","CuKα","","0.0407","0.0355","","","0.0931","0.0963","","","","","","1.107","","","","has coordinates","233636","2020-10-21","18:00:00",""
"1553145","8.4926","0.0017","12.013","0.002","19.248","0.004","90","","90","","90","","1963.7","0.7","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C26 H17 O3 P -","- C26 H17 O3 P -","- C104 H68 O12 P4 -","4","1","","Xu, Guangqing; Li, Minghong; Wang, Shouliang; Tang, Wenjun","Efficient synthesis of P-chiral biaryl phosphonates by stereoselective intramolecular cyclization","Organic Chemistry Frontiers","2015","2","10","1342","","10.1039/C5QO00142K","","","1.54178","CuKα","","0.0398","0.0394","","","0.1233","0.1239","","","","","","1.098","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553146","32.577","0.006","10.964","0.002","15.077","0.003","90","","101.267","0.006","90","","5281.3","1.7","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C25 H23 Au I N3 O -","- C25 H22 Au I N3 O -","- C200 H176 Au8 I8 N24 O8 -","8","1","","Xu, Qin; Gu, Peng; Wang, Feijun; Shi, Min","Selectfluor promoted NHC‒oxazoline gold(i) complex catalyzed cycloaddition/oxidation reaction of enynones with alkenes","Organic Chemistry Frontiers","2015","2","11","1475","","10.1039/C5QO00155B","","","0.71073","MoKα","","0.0668","0.043","","","0.1081","0.1187","","","","","","0.965","","","","has coordinates,has disorder","233640","2020-10-21","18:00:00",""
"1553147","10.3025","0.0005","16.0231","0.0008","26.3966","0.0014","90","","90","","90","","4357.5","0.4","293","2","293","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C23 H19 Au I N3 O -","- C23 H19 Au I N3 O -","- C184 H152 Au8 I8 N24 O8 -","8","2","","Xu, Qin; Gu, Peng; Wang, Feijun; Shi, Min","Selectfluor promoted NHC‒oxazoline gold(i) complex catalyzed cycloaddition/oxidation reaction of enynones with alkenes","Organic Chemistry Frontiers","2015","2","11","1475","","10.1039/C5QO00155B","","","0.71073","MoKα","","0.0467","0.0368","","","0.0704","0.0742","","","","","","0.924","","","","has coordinates","233640","2020-10-21","18:00:00",""
"1553148","5.8507","0.001","14.177","0.002","30.834","0.004","90","","90","","90","","2557.5","0.7","293","2","293","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C24 H34 O10 -","- C24 H34 O10 -","- C96 H136 O40 -","4","1","","Huang, Xin; Xue, Can; Fu, Chunling; Ma, Shengming","A concise construction of carbohydrate-tethered axially chiral allenes via copper catalysis","Organic Chemistry Frontiers","2015","2","9","1040","","10.1039/C5QO00164A","","","0.71073","MoKα","","0.102","0.08","","","0.2036","0.2267","","","","","","1.094","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553149","10.8569","0.0001","14.913","0.0002","23.1808","0.0016","90","","90","","90","","3753.2","0.3","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C21 H19 N O6 -","- C21 H19 N O6 -","- C168 H152 N8 O48 -","8","2","","Duan, Jindian; Cheng, Jing; Li, Pengfei","Enantioselective construction of spiro-1,3-indandiones with three stereocenters via organocatalytic Michael-aldol reaction of 2-arylideneindane-1,3-diones and nitro aldehydes","Organic Chemistry Frontiers","2015","2","9","1048","","10.1039/C5QO00166H","","","1.54187","CuKα","","0.1036","0.0978","","","0.2475","0.2574","","","","","","1.097","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553150","13.093","0.003","25.621","0.005","27.14","0.005","90","","90","","90","","9104","3","296","2","296","2","","","","","","","","5","P n a 21","P 2c -2n","33","","","","- C72 H74 I2 N36 O16 -","- C72 H74 I2 N36 O16 -","- C288 H296 I8 N144 O64 -","4","1","","Zhou, Tian-You; Qi, Qiao-Yan; Zhang, Ying; Xu, Xiao-Na; Zhao, Xin","A thermally stable pH-responsive “supramolecular buckle” based on the encapsulation of 4-(4-aminophenyl)-N-methylpyridinium by cucurbit[8]uril","Organic Chemistry Frontiers","2015","2","9","1030","","10.1039/C5QO00168D","","","1.54178","CuKα","","0.0868","0.079","","","0.2324","0.2433","","","","","","1.062","","","","has coordinates","233644","2020-10-21","18:00:00",""
"1553151","20.293","0.0002","6.84225","0.00008","22.5979","0.0002","90","","90.8593","0.0009","90","","3137.36","0.06","99.94","0.17","99.94","0.17","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C18 H19 N O2 -","- C18 H19 N O2 -","- C144 H152 N8 O16 -","8","1","","Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.","γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines","Organic Chemistry Frontiers","2015","2","11","1445","","10.1039/C5QO00183H","","x-ray","1.54184","CuKα","","0.0359","0.0343","","","0.1356","0.1396","","","","","","1.301","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553152","7.63367","0.00018","29.2305","0.0005","6.84862","0.00015","90","","102.295","0.002","90","","1493.12","0.06","99.94","0.19","99.94","0.19","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C18 H19 N O2 -","- C18 H19 N O2 -","- C72 H76 N4 O8 -","4","1","","Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.","γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines","Organic Chemistry Frontiers","2015","2","11","1445","","10.1039/C5QO00183H","","x-ray","1.54184","CuKα","","0.0414","0.0367","","","0.0895","0.0934","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553153","12.4972","0.0002","14.1613","0.0002","17.5538","0.0003","90","","90","","90","","3106.61","0.08","100.01","0.1","100.01","0.1","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C19 H21 N O2 -","- C19 H21 N O2 -","- C152 H168 N8 O16 -","8","1","","Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.","γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines","Organic Chemistry Frontiers","2015","2","11","1445","","10.1039/C5QO00183H","","x-ray","1.54184","CuKα","","0.0422","0.0379","","","0.0934","0.0966","","","","","","1.05","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553154","6.86998","0.00008","15.21957","0.0002","27.0563","0.0004","90","","90","","90","","2828.96","0.06","100","0.1","100","0.1","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C16 H17 N O3 -","- C16 H17 N O3 -","- C128 H136 N8 O24 -","8","2","","Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.","γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines","Organic Chemistry Frontiers","2015","2","11","1445","","10.1039/C5QO00183H","","","1.54184","CuKα","","0.0307","0.0289","","","0.069","0.0703","","","","","","1.057","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553155","6.98428","0.00014","15.3845","0.0004","16.6168","0.0004","110.497","0.002","97.0023","0.0018","102.274","0.0019","1596.16","0.07","100","0.1","100","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C19 H21 N O3 -","- C19 H21 N O3 -","- C76 H84 N4 O12 -","4","2","","Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.","γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines","Organic Chemistry Frontiers","2015","2","11","1445","","10.1039/C5QO00183H","","","1.54184","CuKα","","0.0571","0.042","","","0.1573","0.1611","","","","","","1.271","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553156","6.8071","0.0003","15.0202","0.0007","15.8559","0.0008","90.798","0.004","101.156","0.004","100.035","0.004","1564.3","0.13","99.98","0.1","99.98","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C18 H20 N2 O3 -","- C18 H20 N2 O3 -","- C72 H80 N8 O12 -","4","2","","Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.","γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines","Organic Chemistry Frontiers","2015","2","11","1445","","10.1039/C5QO00183H","","x-ray","1.54184","CuKα","","0.0526","0.0391","","","0.0972","0.1067","","","","","","1.013","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553157","7.5414","0.0003","11.8446","0.0005","12.2635","0.0005","80.154","0.004","88.093","0.004","88.519","0.003","1078.48","0.08","100","0.1","100","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C11 H14 N2 O2 -","- C11 H14 N2 O2 -","- C44 H56 N8 O8 -","4","2","","Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.","γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines","Organic Chemistry Frontiers","2015","2","11","1445","","10.1039/C5QO00183H","","","1.54184","CuKα","","0.0469","0.0399","","","0.0984","0.1031","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553158","12.55604","0.00014","15.09459","0.00013","18.9643","0.00017","90","","105.866","0.001","90","","3457.35","0.06","99.9","0.2","99.9","0.2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C46 H42 N2 O -","- C46 H42 N2 O -","- C184 H168 N8 O4 -","4","0.5","","Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.","γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines","Organic Chemistry Frontiers","2015","2","11","1445","","10.1039/C5QO00183H","","x-ray","1.54184","CuKα","","0.0391","0.0364","","","0.0892","0.0919","","","","","","1.038","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553159","10.1705","0.0003","10.2903","0.0003","19.4528","0.0005","99.778","0.002","99.679","0.002","106.888","0.002","1868.04","0.1","99.99","0.11","99.99","0.11","","","","","","","","4","P -1","-P 1","2","","","","- C48 H46 N2 O3 -","- C48 H46 N2 O3 -","- C96 H92 N4 O6 -","2","1","","Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.","γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines","Organic Chemistry Frontiers","2015","2","11","1445","","10.1039/C5QO00183H","","x-ray","1.54184","CuKα","","0.0942","0.0863","","","0.2303","0.2339","","","","","","1.157","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553160","11.9986","0.0002","10.6018","0.00016","20.9045","0.0004","90","","104.851","0.0019","90","","2570.36","0.08","100","0.1","100","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C34 H34 N2 O -","- C34 H34 N2 O -","- C136 H136 N8 O4 -","4","1","","Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S.","γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines","Organic Chemistry Frontiers","2015","2","11","1445","","10.1039/C5QO00183H","","x-ray","1.54184","CuKα","","0.0485","0.0404","","","0.1016","0.11","","","","","","1.03","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553161","18.06936","0.00019","17.802","0.0002","18.2203","0.0002","90","","90.5295","0.001","90","","5860.69","0.11","173","0.14","173","0.14","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H18 N2 O2 -","- C15 H18 N2 O2 -","- C240 H288 N32 O32 -","16","4","","Huang, Pei-Qiang; Ou, Wei; Ye, Jian-Liang","Aza-Knoevenagel-type condensation of secondary amides: direct access to N-monosubstituted β,β-difunctionalized enamines","Organic Chemistry Frontiers","2015","2","9","1094","","10.1039/C5QO00191A","","","1.54184","CuKα","","0.0559","0.0498","","","0.1319","0.1382","","","","","","1.0616","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553162","9.4647","0.0007","5.7312","0.0005","22.1678","0.0018","90","","100.283","0.001","90","","1183.16","0.17","130","","130","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C10 H9 F3 O2 S2 -","- C10 H9 F3 O2 S2 -","- C40 H36 F12 O8 S8 -","4","1","","Yang, Hai-Bin; Fan, Xing; Wei, Yin; Shi, Min","Solvent-controlled nucleophilic trifluoromethylthiolation of Morita–Baylis–Hillman carbonates: dual roles of DABCO in activating the Zard's trifluoromethylthiolation reagent and the MBH carbonates","Organic Chemistry Frontiers","2015","2","9","1088","","10.1039/C5QO00198F","","","0.71073","MoKα","","0.0717","0.0645","","","0.1972","0.2047","","","","","","1.053","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553163","10.695","0.002","21.389","0.004","9.1312","0.0018","90","","99.66","0.03","90","","2059.2","0.7","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C23 H27 N O3 -","- C23 H27 N O3 -","- C92 H108 N4 O12 -","4","1","","Li, Ming; Qiu, Bin; Kong, Xiang-Jing; Wen, Li-Rong","Synthesis of Passerini adducts from aldehydes and isocyanides under the auxiliary of water","Organic Chemistry Frontiers","2015","2","10","1326","","10.1039/C5QO00202H","","","0.71073","MoKα","","0.1696","0.1321","","","0.2121","0.2283","","","","","","1.243","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553164","12.5003","0.0011","9.5999","0.0008","34.846","0.003","90","","90","","90","","4181.6","0.6","298","2","298","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C22 H24 Cl N O4 -","- C22 H24 Cl N O4 -","- C176 H192 Cl8 N8 O32 -","8","1","","Li, Ming; Qiu, Bin; Kong, Xiang-Jing; Wen, Li-Rong","Synthesis of Passerini adducts from aldehydes and isocyanides under the auxiliary of water","Organic Chemistry Frontiers","2015","2","10","1326","","10.1039/C5QO00202H","","","0.71073","MoKα","","0.0973","0.0465","","","0.094","0.1073","","","","","","1.015","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553165","8.8044","0.0012","9.6097","0.0013","13.3333","0.0018","93.346","0.003","95.699","0.003","90.433","0.003","1120.5","0.3","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C30 H23 N O2 -","- C30 H23 N O2 -","- C60 H46 N2 O4 -","2","1","","Guo, Tenglong; Jiang, Quanbin; Yu, Zhengkun","Palladium-catalyzed oxidative annulation of in situ generated enones to pyrroles: a concise route to functionalized indoles","Organic Chemistry Frontiers","2015","2","10","1361","","10.1039/C5QO00203F","","","0.71073","MoKα","","0.0715","0.0548","","","0.1535","0.1704","","","","","","1.024","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553166","7.008","0.002","13.515","0.004","19.467","0.006","90","","90","","90","","1843.8","0.9","296","2","296","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C10 H8 N4 O -","- C10 H8 N4 O -","- C80 H64 N32 O8 -","8","1","","Li, Pan; Zhao, Jingjing; Xia, Chungu; Li, Fuwei","The development of carbene-stabilized N–O radical coupling strategy in metal-free regioselective C–H azidation of quinoline N-oxides","Organic Chemistry Frontiers","2015","2","10","1313","","10.1039/C5QO00204D","","","0.71073","MoKα","","0.0925","0.0571","","","0.1495","0.1799","","","","","","1.025","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553167","10.974","0.009","13.036","0.01","14.337","0.011","68.085","0.014","67.898","0.013","73.316","0.014","1737","2","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","alkyne-phenyl","","- C25 H0 N24 O0.5 -","- C40 H32 O11 -","- C80 H64 O22 -","2","1","","Song, Chuanling; Sun, Yihua; Wang, Jianwu; Chen, Hui; Yao, Jiannian; Tung, Chen-Ho; Xu, Zhenghu","Successive Cu/Pd transmetalation relay catalysis in stereoselective synthesis of tetraarylethenes","Organic Chemistry Frontiers","2015","2","10","1366","","10.1039/C5QO00205B","","","0.71073","MoKα","","0.1091","0.0716","","","0.2036","0.2373","","","","","","1.028","","","","has coordinates","233657","2020-10-21","18:00:00",""
"1553168","8.621","0.0011","21.744","0.003","18.379","0.002","90","","100.954","0.003","90","","3382.5","0.7","298","2","298.15","","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","alkyne-butyle","","- C36 H40 O8 -","- C36 H40 O8 -","- C144 H160 O32 -","4","0.5","","Song, Chuanling; Sun, Yihua; Wang, Jianwu; Chen, Hui; Yao, Jiannian; Tung, Chen-Ho; Xu, Zhenghu","Successive Cu/Pd transmetalation relay catalysis in stereoselective synthesis of tetraarylethenes","Organic Chemistry Frontiers","2015","2","10","1366","","10.1039/C5QO00205B","","","0.71073","MoKα","","0.1231","0.052","","","0.1163","0.1443","","","","","","1","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553169","9.7518","0.0003","17.4971","0.0005","20.0458","0.0007","90","","101.206","0.003","90","","3355.17","0.19","298.5","0.2","298.5","0.2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","alkyne amide","","- C33 H41 N O9 -","- C33 H41 N O9 -","- C132 H164 N4 O36 -","4","1","","Song, Chuanling; Sun, Yihua; Wang, Jianwu; Chen, Hui; Yao, Jiannian; Tung, Chen-Ho; Xu, Zhenghu","Successive Cu/Pd transmetalation relay catalysis in stereoselective synthesis of tetraarylethenes","Organic Chemistry Frontiers","2015","2","10","1366","","10.1039/C5QO00205B","","","1.54184","CuKα","","0.1056","0.0624","","","0.1931","0.206","","","","","","1.226","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553170","8.503","0.0006","10.6762","0.0005","15.8607","0.001","76.75","0.005","81.107","0.005","88.437","0.005","1384.6","0.15","291","2","291.15","","","","","","","","","4","P -1","-P 1","2","","","","- C15 H14 O3 S -","- C15 H14 O3 S -","- C60 H56 O12 S4 -","4","2","","Li, Siyu; Li, Xiang; Yang, Fan; Wu, Yangjie","Copper-catalyzed direct decarboxylative hydrosulfonylation of aryl propiolic acids with sulfonylhydrazides leading to vinylsulfones","Organic Chemistry Frontiers","2015","2","9","1076","","10.1039/C5QO00212E","","","1.54184","CuKα","","0.0743","0.063","","","0.1737","0.1857","","","","","","1.084","","","","has coordinates","233659","2020-10-21","18:00:00",""
"1553171","10.2945","0.0008","18.1137","0.0016","14.6463","0.0012","90","","105.831","0.002","90","","2627.5","0.4","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C28 H29 N3 O4 S2 -","- C28 H29 N3 O4 S2 -","- C112 H116 N12 O16 S8 -","4","1","","Zhang, Yong-Sheng; Tang, Xiang-Ying; Shi, Min","Divergent synthesis of indole-fused polycycles via Rh(ii)-catalyzed intramolecular [3 + 2] cycloaddition and C–H functionalization of indolyltriazoles","Organic Chemistry Frontiers","2015","2","11","1516","","10.1039/C5QO00216H","","","0.71073","MoKα","","0.0787","0.0519","","","0.1435","0.1647","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553172","11.3585","0.001","11.981","0.001","13.438","0.0012","106.42","0.002","108.985","0.002","104.217","0.002","1539.6","0.2","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C27 H24 Cl3 N3 O4 S2 -","- C27 H24 Cl3 N3 O4 S2 -","- C54 H48 Cl6 N6 O8 S4 -","2","1","","Zhang, Yong-Sheng; Tang, Xiang-Ying; Shi, Min","Divergent synthesis of indole-fused polycycles via Rh(ii)-catalyzed intramolecular [3 + 2] cycloaddition and C–H functionalization of indolyltriazoles","Organic Chemistry Frontiers","2015","2","11","1516","","10.1039/C5QO00216H","","","0.71073","MoKα","","0.0669","0.0531","","","0.1487","0.158","","","","","","1.085","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553173","12.89225","0.00014","15.11065","0.00014","24.8076","0.0003","90","","101.997","0.001","90","","4727.22","0.09","100","2","100","2","","","","","","","","6","C 1 c 1","C -2yc","9","","","","- C26 H23 Cl F7 N O -","- C26 H23 Cl F7 N O -","- C208 H184 Cl8 F56 N8 O8 -","8","2","","Lao, Ye-Xing; Wu, Jia-Qiang; Chen, Yunyun; Zhang, Shang-Shi; Li, Qingjiang; Wang, Honggen","Palladium-catalyzed methylene C(sp3)–H arylation of the adamantyl scaffold","Organic Chemistry Frontiers","2015","2","10","1374","","10.1039/C5QO00218D","","x-ray","1.54184","CuKα","","0.0304","0.0289","","","0.0725","0.0738","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553174","11.6048","0.0014","11.0429","0.0014","22.106","0.003","90","","94.237","0.002","90","","2825.2","0.6","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C9 H6 F3 N3 -","- C9 H6 F3 N3 -","- C108 H72 F36 N36 -","12","3","","Wang, Shuai; Yang, Li-Jun; Zeng, Jun-Liang; Zheng, Yan; Ma, Jun-An","Silver-catalyzed [3 + 2] cycloaddition of isocyanides with diazo compounds: new regioselective access to 1,4-disubstituted-1,2,3-triazoles","Organic Chemistry Frontiers","2015","2","11","1468","","10.1039/C5QO00219B","","","0.71073","MoKα","","0.1446","0.0711","","","0.1935","0.2481","","","","","","1.019","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553175","10.63","0.007","8.222","0.005","13.645","0.008","90","","100.814","0.005","90","","1171.4","1.3","294","2","294","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C11 H7 F6 N3 -","- C11 H7 F6 N3 -","- C44 H28 F24 N12 -","4","1","","Wang, Shuai; Yang, Li-Jun; Zeng, Jun-Liang; Zheng, Yan; Ma, Jun-An","Silver-catalyzed [3 + 2] cycloaddition of isocyanides with diazo compounds: new regioselective access to 1,4-disubstituted-1,2,3-triazoles","Organic Chemistry Frontiers","2015","2","11","1468","","10.1039/C5QO00219B","","","0.71073","MoKα","","0.0627","0.0517","","","0.1428","0.1525","","","","","","1.065","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553176","28.386","0.007","9.195","0.002","17.591","0.005","90","","125.324","0.008","90","","3746.1","1.7","296","2","296","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","1-(2-chlorophenyl)-2,5-diphenylpentane-1,5-dione","","- C23 H19 Cl O2 -","- C23 H19 Cl O2 -","- C184 H152 Cl8 O16 -","8","1","","Li, Yang; Liu, Bang; Ouyang, Xuan-Hui; Song, Ren-Jie; Li, Jin-Heng","Alkylation/1,2-aryl migration of α-aryl allylic alcohols with α-carbonyl alkyl bromides using visible-light photoredox catalysis","Organic Chemistry Frontiers","2015","2","11","1457","","10.1039/C5QO00220F","","","0.71073","MoKα","","0.0845","0.0545","","","0.1378","0.1529","","","","","","1.057","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553177","8.8674","0.0018","9.3784","0.0019","16.618","0.003","82.99","0.03","87.24","0.03","62.65","0.03","1218.3","0.5","170","2","170","2","","","","","","","","5","P -1","-P 1","2","","","","- C25 H27 Br2 N5 O2 -","- C25 H27 Br2 N5 O2 -","- C50 H54 Br4 N10 O4 -","2","1","","Zende, V. M.; Schulzke, C.; Kapdi, A. R.","Pincer CNC bis-N-heterocyclic carbenes: robust ligands for palladium-catalysed Suzuki–Miyaura arylation of bromoanthracene and related substrates","Organic Chemistry Frontiers","2015","2","10","1397","","10.1039/C5QO00236B","","","0.71073","MoKα","","0.0702","0.0541","","","0.1482","0.1615","","","","","","1.019","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553178","23.657","0.005","7.2556","0.0015","18.859","0.004","90","","111.31","0.03","90","","3015.7","1.3","170","2","170","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C21 H14 O2 -","- C21 H14 O2 -","- C168 H112 O16 -","8","1","","Zende, V. M.; Schulzke, C.; Kapdi, A. R.","Pincer CNC bis-N-heterocyclic carbenes: robust ligands for palladium-catalysed Suzuki–Miyaura arylation of bromoanthracene and related substrates","Organic Chemistry Frontiers","2015","2","10","1397","","10.1039/C5QO00236B","","","0.71073","MoKα","","0.0854","0.0448","","","0.1102","0.1314","","","","","","0.929","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553179","10.441","0.002","7.4965","0.0015","22.577","0.005","90","","94.06","0.03","90","","1762.7","0.6","170","2","170","2","","","","","","","","2","P 1 21/n 1","-P 2yn","14","","","","- C26 H18 -","- C26 H18 -","- C104 H72 -","4","1","","Zende, V. M.; Schulzke, C.; Kapdi, A. R.","Pincer CNC bis-N-heterocyclic carbenes: robust ligands for palladium-catalysed Suzuki–Miyaura arylation of bromoanthracene and related substrates","Organic Chemistry Frontiers","2015","2","10","1397","","10.1039/C5QO00236B","","","0.71073","MoKα","","0.0821","0.0478","","","0.12","0.1375","","","","","","1.014","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553180","10.596","0.002","13.501","0.003","12.12","0.002","90","","90.38","0.03","90","","1733.8","0.6","170","2","170","2","","","","","","","","2","C 1 2/c 1","-C 2yc","15","","","","- C26 H18 -","- C26 H18 -","- C104 H72 -","4","0.5","","Zende, V. M.; Schulzke, C.; Kapdi, A. R.","Pincer CNC bis-N-heterocyclic carbenes: robust ligands for palladium-catalysed Suzuki–Miyaura arylation of bromoanthracene and related substrates","Organic Chemistry Frontiers","2015","2","10","1397","","10.1039/C5QO00236B","","","0.71073","MoKα","","0.0521","0.0447","","","0.1214","0.127","","","","","","1.053","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553181","10.767","0.0009","11.483","0.0009","19.2866","0.0015","88.719","0.003","87.476","0.003","80.292","0.003","2347.8","0.3","90","2","90","2","","","","","","","","4","P -1","-P 1","2","","","","- C29 H27 N O4 -","- C29 H27 N O4 -","- C116 H108 N4 O16 -","4","2","","Patra, Atanu; Bhunia, Anup; Yetra, Santhivardhana Reddy; Gonnade, Rajesh G.; Biju, Akkattu T.","Diastereoselective synthesis of cyclopentanone-fused spirooxindoles by N-heterocyclic carbene-catalyzed homoenolate annulation with isatilidenes","Organic Chemistry Frontiers","2015","2","12","1584","","10.1039/C5QO00242G","","","0.71073","MoKα","","0.0393","0.0357","","","0.0876","0.0906","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553182","11.3454","0.0004","13.013","0.0005","12.3899","0.0004","90","","91.009","0.002","90","","1828.93","0.11","299","2","299","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H19 N O7 -","- C20 H19 N O7 -","- C80 H76 N4 O28 -","4","1","","Kulkarni, Anand M.; Srinivas, Kolluru; Deshpande, Mukund V.; Ramana, Chepuri V.","Cu-catalyzed sequential C–N bond formations: expeditious synthesis of tetracyclic indoloindol-3-ones","Organic Chemistry Frontiers","2016","3","1","43","","10.1039/C5QO00248F","","","0.71073","MoKα","","0.0518","0.0435","","","0.113","0.1195","","","","","","1.053","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553183","6.3258","0.0002","17.6205","0.0006","20.9213","0.0007","90","","90","","90","","2331.97","0.13","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","scm5-1986","","- C21 H33 N O4 Si -","- C21 H33 N O4 Si -","- C84 H132 N4 O16 Si4 -","4","1","","Si, Chang-Mei; Mao, Zhuo-Ya; Liu, Yi-Wen; Du, Zhen-Ting; Wei, Bang-Guo; Lin, Guo-Qiang","Stereoselective formation of chiral trans-4-hydroxy-5-substituted 2-pyrrolidinones: syntheses of streptopyrrolidine and 3-epi-epohelmin A","Organic Chemistry Frontiers","2015","2","11","1485","","10.1039/C5QO00250H","","","0.71073","MoKα","","0.1041","0.0518","","","0.1285","0.1503","","","","","","0.933","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553184","13.06","0.0008","13.2703","0.0007","29.7423","0.0018","90","","95.06","0.006","90","","5134.6","0.5","180","0.1","180","0.1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C76 H19 N3 O5 -","- C76 H19 N3 O5 -","- C304 H76 N12 O20 -","4","1","","Xu, Liang; Liang, Sisi; Sun, Jiahao; Gan, Liangbing","Open-cage fullerene with a stopper acts as a molecular vial for a single water molecule","Organic Chemistry Frontiers","2015","2","11","1500","","10.1039/C5QO00265F","","","0.71073","MoKα","","0.1583","0.0965","","","0.198","0.2328","","","","","","0.944","","","","has coordinates","233676","2020-10-21","18:00:00",""
"1553185","17.987","0.003","18.451","0.004","19.171","0.004","90","","117.87","0.02","90","","5624","2","180.01","0.1","180.01","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C82 H27 N5 O5 -","- C82 H27 N5 O5 -","- C328 H108 N20 O20 -","4","1","","Xu, Liang; Liang, Sisi; Sun, Jiahao; Gan, Liangbing","Open-cage fullerene with a stopper acts as a molecular vial for a single water molecule","Organic Chemistry Frontiers","2015","2","11","1500","","10.1039/C5QO00265F","","","0.71073","MoKα","","0.2279","0.087","","","0.1789","0.2221","","","","","","0.821","","","","has coordinates","233676","2020-10-21","18:00:00",""
"1553186","12.9202","0.0002","7.9412","0.0001","14.2105","0.0002","90","","91.2584","0.0011","90","","1457.67","0.04","103","2","103","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C16 H8 Br F3 O2 S -","- C16 H8 Br F3 O2 S -","- C64 H32 Br4 F12 O8 S4 -","4","1","","Zeng, Yao-Fu; Tan, Dong-Hang; Chen, Yunyun; Lv, Wen-Xin; Liu, Xu-Ge; Li, Qingjiang; Wang, Honggen","Direct radical trifluoromethylthiolation and thiocyanation of aryl alkynoate esters: mild and facile synthesis of 3-trifluoromethylthiolated and 3-thiocyanated coumarins","Organic Chemistry Frontiers","2015","2","11","1511","","10.1039/C5QO00271K","","x-ray","1.54184","CuKα","","0.0402","0.039","","","0.1079","0.1093","","","","","","1.099","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553187","8.4582","0.0005","11.1421","0.0005","18.5214","0.0012","90","","100.439","0.005","90","","1716.61","0.17","291.73","0.1","291.73","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H16 N2 O -","- C22 H16 N2 O -","- C88 H64 N8 O4 -","4","1","","Li, Yaxuan; Fu, Yajie; Ren, Chaojie; Tang, Dong; Wu, Ping; Meng, Xu; Chen, Baohua","Copper-catalyzed oxidative coupling reaction of α,β-unsaturated aldehydes with amidines: synthesis of 1,2,4-trisubstituted-1H-imidazole-5-carbaldehydes","Organic Chemistry Frontiers","2015","2","12","1632","","10.1039/C5QO00285K","","x-ray","0.71073","MoKα","","0.0863","0.0557","","","0.1205","0.1413","","","","","","1.054","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553188","10.6439","0.0013","11.6245","0.0014","21.782","0.003","90","","100.416","0.002","90","","2650.7","0.6","150","2","150","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C26 H23 F6 N2 O P2 Rh -","- C26 H23 F6 N2 O P2 Rh -","- C104 H92 F24 N8 O4 P8 Rh4 -","4","1","","Tang, Z.; Mandal, S.; Paul, N. D.; Lutz, M.; Li, P.; van der Vlugt, J. I.; de Bruin, B.","Rhodium catalysed conversion of carbenes into ketenes and ketene imines using PNN pincer complexes","Organic Chemistry Frontiers","2015","2","12","1561","","10.1039/C5QO00287G","","","0.71073","MoKα","","0.051","0.0382","","","0.0948","0.1062","","","","","","1.057","","","","has coordinates","233682","2020-10-21","18:00:00",""
"1553189","13.4021","0.0009","10.9937","0.0007","15.6906","0.001","90","","97.462","0.003","90","","2292.3","0.3","150","2","150","2","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C20 H27 F6 N2 O P2 Rh -","- C20 H27 F6 N2 O P2 Rh -","- C80 H108 F24 N8 O4 P8 Rh4 -","4","1","","Tang, Z.; Mandal, S.; Paul, N. D.; Lutz, M.; Li, P.; van der Vlugt, J. I.; de Bruin, B.","Rhodium catalysed conversion of carbenes into ketenes and ketene imines using PNN pincer complexes","Organic Chemistry Frontiers","2015","2","12","1561","","10.1039/C5QO00287G","","","0.71073","MoKα","","0.0675","0.0381","","","0.0833","0.0988","","","","","","1.079","","","","has coordinates","233682","2020-10-21","18:00:00",""
"1553190","9.70447","0.00019","9.77001","0.00015","14.1603","0.0003","83.358","0.001","74.636","0.001","74.636","0.001","1246.84","0.04","150","2","150","2","","","","","","","","7","P -1","-P 1","2","","","","- C22 H25 F6 N2 O2 P2 Rh -","- C22 H25 F6 N2 O2 P2 Rh -","- C44 H50 F12 N4 O4 P4 Rh2 -","2","1","","Tang, Z.; Mandal, S.; Paul, N. D.; Lutz, M.; Li, P.; van der Vlugt, J. I.; de Bruin, B.","Rhodium catalysed conversion of carbenes into ketenes and ketene imines using PNN pincer complexes","Organic Chemistry Frontiers","2015","2","12","1561","","10.1039/C5QO00287G","","","0.71073","MoKα","","0.0243","0.0221","","","0.0567","0.0577","","","","","","1.057","","","","has coordinates,has disorder","233682","2020-10-21","18:00:00",""
"1553191","10.0366","0.0004","10.6641","0.0005","12.3895","0.0005","70.891","0.002","84.601","0.002","64.031","0.002","1124.59","0.09","100","2","100","2","","","","","","","","7","P -1","-P 1","2","","","","- C24 H25 Cl N2 O0.25 Ru S -","- C24 H25 Cl N2 O0.25 Ru S -","- C48 H50 Cl2 N4 O0.5 Ru2 S2 -","2","1","","Xie, Xiaoke; Huynh, Han Vinh","Cyclometallated ruthenium(ii) complexes with ditopic thienyl‒NHC ligands: syntheses and alkyne annulations","Organic Chemistry Frontiers","2015","2","12","1598","","10.1039/C5QO00292C","","","0.71073","MoKα","","0.0285","0.0251","","","0.0631","0.0649","","","","","","1.074","","","","has coordinates","233684","2020-10-21","18:00:00",""
"1553192","10.4555","0.0004","15.1572","0.0005","16.4668","0.0006","90","","94.422","0.002","90","","2601.83","0.16","180","2","180","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C30 H29 Cl N2 Ru S -","- C30 H29 Cl N2 Ru S -","- C120 H116 Cl4 N8 Ru4 S4 -","4","1","","Xie, Xiaoke; Huynh, Han Vinh","Cyclometallated ruthenium(ii) complexes with ditopic thienyl‒NHC ligands: syntheses and alkyne annulations","Organic Chemistry Frontiers","2015","2","12","1598","","10.1039/C5QO00292C","","","0.71073","MoKα","","0.0415","0.0336","","","0.0868","0.0974","","","","","","1.088","","","","has coordinates","233684","2020-10-21","18:00:00",""
"1553193","10.5184","0.0005","10.8146","0.0005","11.5002","0.0005","87.04","0.001","64.781","0.001","69.987","0.001","1105.18","0.09","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C24 H25 Br N2 Ru S -","- C24 H25 Br N2 Ru S -","- C48 H50 Br2 N4 Ru2 S2 -","2","1","","Xie, Xiaoke; Huynh, Han Vinh","Cyclometallated ruthenium(ii) complexes with ditopic thienyl‒NHC ligands: syntheses and alkyne annulations","Organic Chemistry Frontiers","2015","2","12","1598","","10.1039/C5QO00292C","","","0.71073","MoKα","","0.0467","0.0291","","","0.0534","0.057","","","","","","1.074","","","","has coordinates,has disorder","233684","2020-10-21","18:00:00",""
"1553194","14.301","0.004","11.104","0.003","15.932","0.005","90","","108.464","0.006","90","","2399.7","1.2","100","2","100","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C28 H27 Cl N2 Ru S -","- C28 H27 Cl N2 Ru S -","- C112 H108 Cl4 N8 Ru4 S4 -","4","1","","Xie, Xiaoke; Huynh, Han Vinh","Cyclometallated ruthenium(ii) complexes with ditopic thienyl‒NHC ligands: syntheses and alkyne annulations","Organic Chemistry Frontiers","2015","2","12","1598","","10.1039/C5QO00292C","","","0.71073","MoKα","","0.029","0.0271","","","0.0641","0.0651","","","","","","1.064","","","","has coordinates","233684","2020-10-21","18:00:00",""
"1553195","7.6889","0.0002","15.5382","0.0005","16.4272","0.0006","90","","90","","90","","1962.58","0.11","99.8","0.5","99.8","0.5","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C24 H22 N4 O4 -","- C24 H22 N4 O4 -","- C96 H88 N16 O16 -","4","1","","Mao, Zhong-Yi; Geng, Hui; Zhang, Tian-Tian; Ruan, Yuan-Ping; Ye, Jian-Liang; Huang, Pei-Qiang","Stereodivergent and enantioselective total syntheses of isochaetominines A–C and four pairs of isochaetominine C enantiomers: a six-step approach","Organic Chemistry Frontiers","2016","3","1","24","","10.1039/C5QO00298B","","x-ray","1.54184","CuKα","","0.0459","0.0413","","","0.0978","0.1021","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553196","9.32","0.0006","10.5489","0.0006","12.1772","0.0007","95.818","0.005","90.49","0.005","111.805","0.006","1104.44","0.12","173","0.14","173","0.14","","","","","","","","4","P -1","-P 1","2","","","","- C24 H26 N4 O6 -","- C24 H26 N4 O6 -","- C48 H52 N8 O12 -","2","1","","Mao, Zhong-Yi; Geng, Hui; Zhang, Tian-Tian; Ruan, Yuan-Ping; Ye, Jian-Liang; Huang, Pei-Qiang","Stereodivergent and enantioselective total syntheses of isochaetominines A–C and four pairs of isochaetominine C enantiomers: a six-step approach","Organic Chemistry Frontiers","2016","3","1","24","","10.1039/C5QO00298B","","","1.54184","CuKα","","0.05","0.038","","","0.0869","0.0932","","","","","","0.96","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553197","8.8508","0.0008","10.0352","0.0008","10.7879","0.0009","116.066","0.0015","107.114","0.0016","90.5266","0.0017","811.83","0.12","100","2","99.65","","","","","","","","","5","P -1","-P 1","2","20","()-(1S,11S,13R,14R,Z)-14-Bromo-11,13-dimethoxy-15,15-dimethyl-2.5.12-trioxa-4-azatricyclo[9.2.1.13,13]pentadec-3-ene","","- C15 H24 Br N O5 -","- C15 H24 Br N O5 -","- C30 H48 Br2 N2 O10 -","2","1","","Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.","Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates","Organic Chemistry Frontiers","2016","3","3","330","","10.1039/C5QO00315F","","","0.71073","MoKα","","0.0483","0.0365","","","0.0694","0.0722","","","","","","1","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553198","11.7775","0.0008","8.7429","0.0006","16.8595","0.0012","90","","105.852","0.0013","90","","1670","0.2","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","11","()-(1R,11R,12S)-1,12-Dihydroxy-2,2-dimethyl-5.14-dioxa-4-azabicyclo[9.2.1]tetradecan-3-one","","- C14 H23 Cl2 N O5 -","- C14 H23 Cl2 N O5 -","- C56 H92 Cl8 N4 O20 -","4","1","","Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.","Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates","Organic Chemistry Frontiers","2016","3","3","330","","10.1039/C5QO00315F","","","0.71073","MoKα","","0.055","0.0401","","","0.1167","0.124","","","","","","1","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553199","11.3134","0.0005","9.429","0.0004","12.7345","0.0006","90","","110.991","0.0008","90","","1268.29","0.1","100","2","100","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","10","()-10,10-dimethylhexahydro-2H-pyrrolo[1,2-b][1,2]oxazecine-7,9,11(10H)-trione","","- C13 H19 N O4 -","- C13 H19 N O4 -","- C52 H76 N4 O16 -","4","1","","Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.","Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates","Organic Chemistry Frontiers","2016","3","3","330","","10.1039/C5QO00315F","","","0.71073","MoKα","","0.0791","0.0672","","","0.2501","0.2774","","","","","","1","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553200","17.0197","0.0005","16.271","0.0005","10.1414","0.0003","90","","99.0774","0.0005","90","","2773.26","0.14","100","2","100","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","12","12-Acetyl-2,2-Dimethyl-5.14-dioxa-4-azabicyclo[9.2.1]tetradeca-1(13),11-dien-3-one","","- C15 H21 N O4 -","- C15 H21 N O4 -","- C120 H168 N8 O32 -","8","2","","Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.","Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates","Organic Chemistry Frontiers","2016","3","3","330","","10.1039/C5QO00315F","","","0.71073","MoKα","","0.047","0.0362","","","0.1193","0.1275","","","","","","1","","","","has coordinates","273808","2022-03-18","10:32:15",""
"1553201","10.9816","0.0005","9.2222","0.0004","13.0751","0.0006","90","","107.689","0.0008","90","","1261.57","0.1","100","2","100.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","9","()-(1S,11R,12S,14S)-11-Hydroxy-10,10-dimethyl-7,13,15-trioxa-8-azatetracyclo[9.3.1.01,8.012,14]pentadecan-9-one","","- C13 H19 N O5 -","- C13 H19 N O5 -","- C52 H76 N4 O20 -","4","1","","Acharya, A.; Eickhoff, J. A.; Chen, K.; Catalano, V. J.; Jeffrey, C. S.","Access to bicyclic hydroxamate macrocycles via intramolecular aza-(4 + 3) cyloaddition reactions of aza-oxyallylic cation intermediates","Organic Chemistry Frontiers","2016","3","3","330","","10.1039/C5QO00315F","","","0.71073","MoKα","","0.0605","0.043","","","0.1239","0.1382","","","","","","1","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553202","13.083","0.003","9.848","0.002","18.876","0.004","90","","93.26","0.03","90","","2428.1","0.9","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","IrNC","IrNC","","- C25 H32 Cl Ir N2 -","- C25 H32 Cl Ir N2 -","- C100 H128 Cl4 Ir4 N8 -","4","1","","Tang, Guo-Dong; Pan, Cheng-Ling; Li, Xingwei","Iridium(iii)- and rhodium(iii)-catalyzed coupling of anilines with α-diazoesters via chelation-assisted C‒H activation","Organic Chemistry Frontiers","2016","3","1","87","","10.1039/C5QO00316D","","","0.71073","MoKα","","0.0331","0.0232","","","0.0533","0.0575","","","","","","1.016","","","","has coordinates","233690","2020-10-21","18:00:00",""
"1553203","15.5737","0.0005","12.7774","0.0004","11.4615","0.0003","90","","91.399","0.003","90","","2280.06","0.12","298","","298","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","TNY-TE-09","Benzoic acid 2-(cyclohexyl-phenyl-amino)-1-phenyl-ethyl ester","","- C27 H29 N O2 -","- C27 H29 N O2 -","- C108 H116 N4 O8 -","4","1","","Roy, Tony; Bhojgude, Sachin Suresh; Kaicharla, Trinadh; Thangaraj, Manikandan; Garai, Bikash; Biju, Akkattu T.","Employing carboxylic acids in aryne multicomponent coupling triggered by aziridines/azetidines","Organic Chemistry Frontiers","2016","3","1","71","","10.1039/C5QO00328H","","","0.71073","MoKα","","0.118","0.0678","","","0.1884","0.2219","","","","","","1.095","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553204","9.8964","0.0016","7.7982","0.0013","13.421","0.002","90","","91.267","0.002","90","","1035.5","0.3","301","2","301","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","1-((1R*,2R*)-2-Hydroxy-1,2,3,4-tetrahydronaphthalen-1-yl)ethanone","","- C12 H14 O2 -","- C12 H14 O2 -","- C48 H56 O8 -","4","1","","Ling, Jesse; Lam, Sze Kui; Lo, Brian; Lam, Sarah; Wong, Wing-Tak; Sun, Jian; Chen, Guanhua; Chiu, Pauline","Epoxy and aziridinyl enolsilanes in diastereoselective inter- and intramolecular Friedel–Crafts alkylations","Organic Chemistry Frontiers","2016","3","4","457","","10.1039/C5QO00333D","","","0.71073","MoKα","","0.0474","0.0401","","","0.1101","0.1162","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553205","11.4861","0.0004","14.0594","0.0004","13.486","0.0004","90","","111.393","0.004","90","","2027.77","0.12","293","2","293","2","","","","","","","","6","I 1 a 1","I -2ya","9","","","","- C22 H20 Cl N O2 S -","- C22 H20 Cl N O2 S -","- C88 H80 Cl4 N4 O8 S4 -","4","1","","Prabagar, B.; Nayak, Sanatan; Mallick, Rajendra K.; Prasad, Rangu; Sahoo, Akhila K.","Triphenylphosphine promoted regio and stereoselective α-halogenation of ynamides","Organic Chemistry Frontiers","2016","3","1","110","","10.1039/C5QO00345H","","","1.54184","CuKα","","0.0533","0.053","","","0.1449","0.1455","","","","","","1.075","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553206","11.0065","0.0009","8.788","0.0007","14.4392","0.0012","90","","99.424","0.001","90","","1377.78","0.19","173","2","173","2","","","","","","","","6","P 1 21 1","P 2yb","4","","methyl (1S,3R,3aS,8bS)-1-(4-methoxyphenyl)-3-methyl-8b-nitro-4-tosyl-1,2,3,3a,4,8b-hexahydropyrrolo[3,4-b]indole-3-carboxylate","","- C27 H28 Br N3 O7 S -","- C27 H28 Br N3 O7 S -","- C54 H56 Br2 N6 O14 S2 -","2","1","","Gerten, Anthony L.; Stanley, Levi M.","Enantioselective dearomative [3 + 2] cycloadditions of indoles with azomethine ylides derived from alanine imino esters","Organic Chemistry Frontiers","2016","3","3","339","","10.1039/C5QO00346F","","","0.71073","MoKα","","0.0334","0.0275","","","0.0633","0.0814","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553207","6.2154","0.0003","20.2473","0.0013","22.9882","0.0017","90","","90","","90","","2893","0.3","103","2","103","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C36 H29 Cl O6 -","- C36 H29 Cl O6 -","- C144 H116 Cl4 O24 -","4","1","","Fu, Zhenqian; Wu, Xingxing; Chi, Yonggui Robin","Rapid access to bicyclic δ-lactones via carbene-catalyzed activation and cascade reaction of unsaturated carboxylic esters","Organic Chemistry Frontiers","2016","3","2","145","","10.1039/C5QO00348B","","","0.71073","MoKα","","0.0801","0.0507","","","0.1004","0.1167","","","","","","1.021","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553208","7.1121","0.0007","8.5933","0.001","18.426","0.002","94.339","0.01","100.719","0.01","105.418","0.01","1057.3","0.2","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C24 H25 N3 O2 -","- C24 H25 N3 O2 -","- C48 H50 N6 O4 -","2","1","","Yang, Xiu-Long; Long, Yan; Chen, Fei; Han, Bing","Synthesis of isoxazoline-featured oxindoles by iminoxyl radical-promoted cascade oxyalkylation/alkylarylation of alkenes","Organic Chemistry Frontiers","2016","3","2","184","","10.1039/C5QO00352K","","","0.71073","MoKα","","0.1438","0.0566","","","0.1192","0.1338","","","","","","0.85","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553209","15.8733","0.0011","11.8466","0.0006","12.3385","0.0008","90","","99.402","0.006","90","","2289","0.2","293.69","0.1","293.69","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","3-((4,4-dimethyl-3-phenyl-4,5-dihydroisoxazol-5-yl)methyl)-1-methyl-4-phenyl-1-azaspiro[4.5]deca-3,6,9-triene-2,8-dione","","- C28 H26 N2 O3 -","- C28 H26 N2 O3 -","- C112 H104 N8 O12 -","4","1","","Yang, Xiu-Long; Long, Yan; Chen, Fei; Han, Bing","Synthesis of isoxazoline-featured oxindoles by iminoxyl radical-promoted cascade oxyalkylation/alkylarylation of alkenes","Organic Chemistry Frontiers","2016","3","2","184","","10.1039/C5QO00352K","","x-ray","0.71073","MoKα","","0.1327","0.0649","","","0.1287","0.1683","","","","","","1.038","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553210","9.1241","0.0002","10.2171","0.0002","11.3635","0.0008","78.194","0.006","82.379","0.006","72.418","0.005","985.63","0.08","295","2","295","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H24 Br2 N2 -","- C22 H24 Br2 N2 -","- C44 H48 Br4 N4 -","2","1","","Ma, Can-Liang; Li, Xiao-Hua; Yu, Xiao-Long; Zhu, Xiao-Long; Hu, Yong-Zhou; Dong, Xiao-Wu; Tan, Bin; Liu, Xin-Yuan","Gold-catalyzed tandem synthesis of bioactive spiro-dipyrroloquinolines and its application in the one-step synthesis of incargranine B aglycone and seneciobipyrrolidine (I)","Organic Chemistry Frontiers","2016","3","3","324","","10.1039/C5QO00354G","","","1.54178","CuKα","","0.0546","0.0466","","","0.1153","0.1361","","","","","","1.175","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553211","7.4987","0.0001","7.9073","0.0001","14.5997","0.001","77.721","0.006","79.566","0.006","69.529","0.005","787.06","0.06","295","2","295","2","","","","","","","","3","P -1","-P 1","2","","","","- C20 H22 N2 -","- C20 H22 N2 -","- C40 H44 N4 -","2","1","","Ma, Can-Liang; Li, Xiao-Hua; Yu, Xiao-Long; Zhu, Xiao-Long; Hu, Yong-Zhou; Dong, Xiao-Wu; Tan, Bin; Liu, Xin-Yuan","Gold-catalyzed tandem synthesis of bioactive spiro-dipyrroloquinolines and its application in the one-step synthesis of incargranine B aglycone and seneciobipyrrolidine (I)","Organic Chemistry Frontiers","2016","3","3","324","","10.1039/C5QO00354G","","","1.54178","CuKα","","0.0657","0.056","","","0.1397","0.1652","","","","","","1.217","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553212","10.016","0.005","10.025","0.004","21.596","0.01","90","","90","","90","","2168.5","1.7","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C22 H32 N2 O4 -","- C22 H32 N2 O4 -","- C88 H128 N8 O16 -","4","1","","Fu, Jian-Guo; Xu, Guang-Qiang; Ding, Rui; Lin, Guo-Qiang; Sun, Bing-Feng","Asymmetric total synthesis of Lycopodium alkaloids α-obscurine, N-desmethyl-α-obscurine, β-obscurine and N-desmethyl-β-obscurine","Organic Chemistry Frontiers","2016","3","1","62","","10.1039/C5QO00355E","","","0.71073","MoKα","","0.0399","0.0351","","","0.0918","0.0954","","","","","","1.03","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553213","10.351","0.003","11.942","0.003","26.963","0.006","90","","90","","90","","3332.9","1.5","293","2","293","2","","","","","","","","5","C 2 2 21","C 2c 2","20","","","","- C17 H25 Cl N2 O2 -","- C17 H25 Cl N2 O2 -","- C136 H200 Cl8 N16 O16 -","8","1","","Fu, Jian-Guo; Xu, Guang-Qiang; Ding, Rui; Lin, Guo-Qiang; Sun, Bing-Feng","Asymmetric total synthesis of Lycopodium alkaloids α-obscurine, N-desmethyl-α-obscurine, β-obscurine and N-desmethyl-β-obscurine","Organic Chemistry Frontiers","2016","3","1","62","","10.1039/C5QO00355E","","","0.71073","MoKα","","0.0725","0.0543","","","0.1086","0.1165","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553214","12.0005","0.0005","9.4272","0.0004","25.9285","0.0011","90","","101.178","0.001","90","","2877.7","0.2","150","2","150","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C23 H27 Cl6 I N2 -","- C23 H27 Cl6 I N2 -","- C92 H108 Cl24 I4 N8 -","4","1","","Desens, Willi; Kohrt, Christina; Spannenberg, Anke; Werner, Thomas","A novel zinc based binary catalytic system for CO2utilization under mild conditions","Organic Chemistry Frontiers","2016","3","2","156","","10.1039/C5QO00356C","","","0.71073","MoKα","","0.0319","0.0258","","","0.057","0.0603","","","","","","1.03","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553215","8.3061","0.0002","9.701","0.0002","20.7173","0.0006","90","","90","","90","","1669.35","0.07","294.39","0.1","294.39","0.1","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C16 H17 Cl2 N O4 -","- C16 H17 Cl2 N O4 -","- C64 H68 Cl8 N4 O16 -","4","1","","Yang, Li; Song, Liqiang; Huang, Chong; Huang, Mingzheng; Liu, Bo","Exploiting ortho-substitution effect on formation of oxygen-containing [10]paracyclophane through ring-closing metathesis","Organic Chemistry Frontiers","2016","3","3","319","","10.1039/C5QO00373C","","x-ray","1.54184","CuKα","","0.051","0.0478","","","0.1284","0.1329","","","","","","1.022","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553216","8.3327","0.0007","9.5492","0.0009","11.4501","0.001","90","","108.133","0.009","90","","865.84","0.14","292.36","0.1","292.36","0.1","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C16 H17 Br2 N O4 -","- C16 H17 Br2 N O4 -","- C32 H34 Br4 N2 O8 -","2","1","","Yang, Li; Song, Liqiang; Huang, Chong; Huang, Mingzheng; Liu, Bo","Exploiting ortho-substitution effect on formation of oxygen-containing [10]paracyclophane through ring-closing metathesis","Organic Chemistry Frontiers","2016","3","3","319","","10.1039/C5QO00373C","","x-ray","1.54184","CuKα","","0.0479","0.0459","","","0.1264","0.129","","","","","","1.082","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553217","7.1154","0.0003","11.1585","0.0005","11.1645","0.0005","107.811","0.003","95.51","0.003","91.238","0.003","838.83","0.07","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C20 H16 O5 -","- C20 H16 O5 -","- C40 H32 O10 -","2","1","","Zhang, Wen-Zhen; Yang, Ming-Wang; Yang, Xu-Tong; Shi, Ling-Long; Wang, Hui-Bo; Lu, Xiao-Bing","Double carboxylation of o-alkynyl acetophenone with carbon dioxide","Organic Chemistry Frontiers","2016","3","2","217","","10.1039/C5QO00374A","","","0.71073","MoKα","","0.0621","0.0495","","","0.121","0.1331","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553218","8.6446","0.0011","10.8046","0.0015","24.326","0.003","90","","99.922","0.002","90","","2238.1","0.5","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C25 H27 N O2 S -","- C25 H27 N O2 S -","- C100 H108 N4 O8 S4 -","4","1","","Li, Jiawen; Qin, Guiping; Liu, Yang; Huang, Hanmin","Palladium-catalysed coupling reaction of aminals with N-sulfonyl hydrazones to give allylic sulfones","Organic Chemistry Frontiers","2016","3","2","259","","10.1039/C5QO00381D","","","0.71073","MoKα","","0.0589","0.0399","","","0.0707","0.0781","","","","","","1.02","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553219","7.5687","0.0005","30.831","0.002","8.0907","0.0006","90","","90.916","0.002","90","","1887.7","0.2","173","2","173","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H28 O2 Si -","- C20 H28 O2 Si -","- C80 H112 O8 Si4 -","4","1","","Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu","A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures","Organic Chemistry Frontiers","2016","3","3","354","","10.1039/C5QO00392J","","","0.71073","MoKα","","0.0725","0.0535","","","0.13","0.1403","","","","","","1.089","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553220","7.3733","0.0006","11.2959","0.0009","14.9182","0.001","109.524","0.003","92.663","0.003","101.436","0.003","1139.24","0.15","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C14 H11 F3 O -","- C14 H11 F3 O -","- C56 H44 F12 O4 -","4","2","","Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu","A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures","Organic Chemistry Frontiers","2016","3","3","354","","10.1039/C5QO00392J","","","0.71073","MoKα","","0.1258","0.0636","","","0.1493","0.1873","","","","","","1.021","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553221","15.9874","0.0007","10.2887","0.0004","13.7969","0.0006","90","","108.28","0.001","90","","2154.92","0.16","173","2","173","2","","","","","","","","3","P 1 2/c 1","-P 2yc","13","","","","- C14 H12 O3 -","- C14 H12 O3 -","- C112 H96 O24 -","8","2","","Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu","A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures","Organic Chemistry Frontiers","2016","3","3","354","","10.1039/C5QO00392J","","","0.71073","MoKα","","0.0706","0.0506","","","0.1169","0.1317","","","","","","1.022","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553222","34.01","0.05","9.158","0.013","7.196","0.01","90","","90","","90","","2241","6","296","2","296","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","no","3-fluoro-6,7,8,9-tetrahydrobenzo[a]azulen-10(5H)-one","","- C14 H13 F O -","- C14 H13 F O -","- C112 H104 F8 O8 -","8","1","","Cai, Shujun; Xiao, Zheming; Ou, Jinjie; Shi, Yingbo; Gao, Shuanhu","A photo-induced C–C bond formation methodology to construct tetrahydrofluorenones and their related structures","Organic Chemistry Frontiers","2016","3","3","354","","10.1039/C5QO00392J","","","0.71073","MoKα","","0.094","0.047","","","0.1189","0.1405","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553223","9.9764","0.0005","11.8382","0.0006","12.5698","0.0006","115.716","0.002","100.125","0.002","93.876","0.002","1299.22","0.11","298","2","298","2","","","","","","","","4","P -1","-P 1","2","","7-(2-(diphenylphosphino)phenyl)-7H-benzo[c]carbazole","","- C34 H24 N P -","- C34 H24 N P -","- C68 H48 N2 P2 -","2","1","","Fu, Wai Chung; Zhou, Zhongyuan; Kwong, Fuk Yee","A benzo[c]carbazolyl-based phosphine ligand for Pd-catalyzed tetra-ortho-substituted biaryl syntheses","Organic Chemistry Frontiers","2016","3","2","273","","10.1039/C5QO00400D","","","0.71073","MoKα","","0.0766","0.0595","","","0.1549","0.168","","","","","","1.002","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553224","10.342","0.002","12.672","0.003","13.549","0.003","90","","90","","90","","1775.6","0.7","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C19 H16 F N O5 S -","- C19 H16 F N O5 S -","- C76 H64 F4 N4 O20 S4 -","4","1","","Yu, Jin-Sheng; Zhou, Jian","Organocatalytic enantioselective Mukaiyama–Mannich reaction of fluorinated enol silyl ethers and cyclic N-sulfonyl ketimines","Organic Chemistry Frontiers","2016","3","3","298","","10.1039/C5QO00407A","","","0.71073","MoKα","","0.0294","0.0273","","","0.072","0.0739","","","","","","1.029","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553225","7.1956","0.0003","9.6833","0.0003","23.2873","0.0008","90","","90","","90","","1622.59","0.1","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C17 H14 F2 N2 O4 S -","- C17 H14 F2 N2 O4 S -","- C68 H56 F8 N8 O16 S4 -","4","1","","Yu, Jin-Sheng; Zhou, Jian","Organocatalytic enantioselective Mukaiyama–Mannich reaction of fluorinated enol silyl ethers and cyclic N-sulfonyl ketimines","Organic Chemistry Frontiers","2016","3","3","298","","10.1039/C5QO00407A","","","0.71073","MoKα","","0.0337","0.0314","","","0.0781","0.0801","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553226","8.9936","0.0003","20.9137","0.0005","10.6975","0.0004","90","","112.585","0.004","90","","1857.78","0.12","100.01","0.1","100.01","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C23 H14 Cl2 N2 O -","- C23 H14 Cl2 N2 O -","- C92 H56 Cl8 N8 O4 -","4","1","","Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei","Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives","Organic Chemistry Frontiers","2016","3","3","344","","10.1039/C5QO00417A","","","1.54184","CuKα","","0.0479","0.0417","","","0.0991","0.1029","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553227","6.3775","0.0005","12.1686","0.001","13.4121","0.0008","80.819","0.006","88.955","0.005","75.537","0.007","994.7","0.13","291","2","291.15","","","","","","","","","5","P -1","-P 1","2","","","","- C24 H14 Cl2 N2 O2 -","- C24 H14 Cl2 N2 O2 -","- C48 H28 Cl4 N4 O4 -","2","1","","Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei","Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives","Organic Chemistry Frontiers","2016","3","3","344","","10.1039/C5QO00417A","","","1.54184","CuKα","","0.0623","0.0475","","","0.1165","0.1292","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553228","5.2005","0.0005","13.556","0.003","15.6215","0.0013","73.584","0.012","85.49","0.008","87.12","0.012","1052.7","0.3","291","2","291.15","","","","","","","","","5","P -1","-P 1","2","","","","- C24 H14 Cl2 N2 O2 -","- C24 H14 Cl2 N2 O2 -","- C48 H28 Cl4 N4 O4 -","2","1","","Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei","Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives","Organic Chemistry Frontiers","2016","3","3","344","","10.1039/C5QO00417A","","x-ray","1.54184","CuKα","","0.1141","0.0698","","","0.1908","0.2294","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553229","8.0462","0.0005","9.2337","0.0006","26.6656","0.0013","90","","90","","90","","1981.2","0.2","291","2","291.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C24 H17 Cl N2 O2 -","- C24 H17 Cl N2 O2 -","- C96 H68 Cl4 N8 O8 -","4","1","","Zhang, Zhiguo; Qian, Jingjing; Zhang, Guisheng; Ma, Nana; Liu, Qingfeng; Liu, Tongxin; Sun, Kai; Shi, Lei","Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives","Organic Chemistry Frontiers","2016","3","3","344","","10.1039/C5QO00417A","","","1.54184","CuKα","","0.0529","0.0399","","","0.1013","0.1123","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553230","13.6461","0.0019","10.723","0.0015","22.268","0.004","90","","90.915","0.002","90","","3258","0.9","298","2","298","2","","","","","","","","4","I 1 2/a 1","-I 2ya","15","","Wun1m","","- C20 H15 N3 O3 -","- C20 H15 N3 O3 -","- C160 H120 N24 O24 -","8","1","","Nack, W. A.; Wang, B.; Wu, X.; Jiao, R.; He, G.; Chen, G.","Palladium-catalyzed arylation of β-methylene C(sp3)–H bonds at room temperature: desymmetrization of simple cycloalkyl carboxylic acids","Organic Chemistry Frontiers","2016","3","5","561","","10.1039/C5QO00421G","","","0.71073","MoKα","","0.159","0.153","","","0.3373","0.3402","","","","","","2.199","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553231","7.6839","0.0002","11.0556","0.0003","12.4153","0.0004","90","","106.486","0.004","90","","1011.32","0.05","291","2","291.15","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C23 H18 N2 O5 -","- C23 H18 N2 O5 -","- C46 H36 N4 O10 -","2","1","","Jiao, Lihui; Zhao, Xiaowei; Liu, Huixin; Ye, Xinyi; Li, Yun; Jiang, Zhiyong","Organocatalytic asymmetric conjugate addition of diaryloxazolidin-2,4-diones to nitroolefins: an efficient approach to chiral α-aryl-α-hydroxy carboxylic acids","Organic Chemistry Frontiers","2016","3","4","470","","10.1039/C5QO00428D","","","1.54184","CuKα","","0.0443","0.0395","","","0.105","0.1091","","","","","","1.048","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553232","13.83","0.0011","21.2702","0.0018","14.1309","0.0013","90","","119.452","0.003","90","","3619.6","0.5","298","2","298","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C38 H34 N O4 P S -","- C38 H34 N O4 P S -","- C152 H136 N4 O16 P4 S4 -","4","1","","Zhu, Yi-Long; Wang, De-Cai; Jiang, Bo; Hao, Wen-Juan; Wei, Ping; Wang, Ai-Fang; Qiu, Jiang-Kai; Tu, Shu-Jiang","Metal-free oxidative hydrophosphinylation of 1,7-enynes","Organic Chemistry Frontiers","2016","3","3","385","","10.1039/C5QO00430F","","","0.71073","MoKα","","0.2249","0.0994","","","0.2293","0.249","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553233","20.218","0.004","9.2121","0.0019","15.306","0.003","90","","95.315","0.004","90","","2838.5","1","173.15","","173.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C13 H14 Br N O3 S -","- C13 H14 Br N O3 S -","- C104 H112 Br8 N8 O24 S8 -","8","2","","Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei","Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins","Organic Chemistry Frontiers","2016","3","4","447","","10.1039/C5QO00432B","","","0.71073","MoKα","","0.0444","0.038","","","0.0774","0.081","","","","","","1.106","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553234","7.8592","0.0017","9.0905","0.0018","9.748","0.002","79.19","0.007","89.1","0.008","77.31","0.006","667.1","0.2","173.15","","173.15","","","","","","","","","6","P -1","-P 1","2","","","","- C13 H14 Br N O3 S -","- C13 H14 Br N O3 S -","- C26 H28 Br2 N2 O6 S2 -","2","1","","Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei","Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins","Organic Chemistry Frontiers","2016","3","4","447","","10.1039/C5QO00432B","","","0.71073","MoKα","","0.0271","0.0258","","","0.0625","0.0632","","","","","","1.088","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553235","11.83","0.002","9.2659","0.0019","14.59","0.003","90","","97.6","0.03","90","","1585.2","0.5","173.15","","173.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C16 H14 Br N O3 S -","- C16 H14 Br N O3 S -","- C64 H56 Br4 N4 O12 S4 -","4","1","","Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei","Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins","Organic Chemistry Frontiers","2016","3","4","447","","10.1039/C5QO00432B","","","0.71073","MoKα","","0.0436","0.0387","","","0.0787","0.0807","","","","","","1.155","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553236","8.3045","0.0015","9.415","0.002","11.19","0.002","87.089","0.01","73.797","0.009","70.74","0.07","792.3","0.4","173.15","","173.15","","","","","","","","","6","P -1","-P 1","2","","","","- C16 H14 Br N O3 S -","- C16 H14 Br N O3 S -","- C32 H28 Br2 N2 O6 S2 -","2","1","","Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei","Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins","Organic Chemistry Frontiers","2016","3","4","447","","10.1039/C5QO00432B","","","0.71073","MoKα","","0.0361","0.0333","","","0.0834","0.085","","","","","","1.152","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553237","15.825","0.004","8.982","0.003","11.426","0.006","90","","109.905","0.004","90","","1527.1","1","173.15","","173.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C16 H14 Br N O3 S -","- C16 H14 Br N O3 S -","- C64 H56 Br4 N4 O12 S4 -","4","1","","Song, Lu; Luo, Sanzhong; Cheng, Jin-Pei","Visible-light promoted intermolecular halofunctionalization of alkenes with N-halogen saccharins","Organic Chemistry Frontiers","2016","3","4","447","","10.1039/C5QO00432B","","","0.71073","MoKα","","0.0748","0.0663","","","0.1402","0.1474","","","","","","1.126","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553238","8.1343","0.0014","27.626","0.005","8.8172","0.0015","90","","97.223","0.003","90","","1965.7","0.6","296","2","296","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C22 H25 N O3 -","- C22 H25 N O3 -","- C88 H100 N4 O12 -","4","2","","Mu, Yucheng; Tan, Xiaodong; Zhang, Yemin; Jing, Xiaobi; Shi, Zhuangzhi","Pd(ii)-catalyzed β-C–H arylation of O-methyl ketoximes with iodoarenes","Organic Chemistry Frontiers","2016","3","3","380","","10.1039/C5QO00438A","","","0.71073","MoKα","","0.0695","0.0488","","","0.1228","0.1403","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553418","5.9396","0.0012","11.302","0.002","13.413","0.003","96.05","0.03","99.59","0.03","101.21","0.03","862","0.3","173","2","173","2","","","","","","","","6","P -1","-P 1","2","","","","- C21 H15 Br F N O -","- C21 H15 Br F N O -","- C42 H30 Br2 F2 N2 O2 -","2","1","","Sheng, Jinyu; Su, Xiang; Cao, Chengyao; Chen, Chao","Synthesis of benzo[1,3]oxazines via copper(i)-catalyzed cascade annulation of nitriles, aldehydes and diaryliodonium salts","Organic Chemistry Frontiers","2016","3","4","501","","10.1039/C6QO00012F","","","0.71073","MoKα","","0.0534","0.0469","","","0.1183","0.1315","","","","","","1.035","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553419","9.1158","0.0003","9.8126","0.0003","28.3116","0.0009","90","","90","","90","","2532.46","0.14","294.29","0.1","294.29","0.1","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C28 H22 F3 N O5 -","- C28 H22 F3 N O5 -","- C112 H88 F12 N4 O20 -","4","1","","Gao, Tai-Ping; Liu, Dan; Lin, Jun-Bing; Hu, Xiu-Qin; Wang, Zhu-Yin; Xu, Peng-Fei","Direct construction of chiral quaternary dihydropyranones through highly enantioselective organocatalytic hetero-Diels–Alder reactions of olefinic azlactones","Organic Chemistry Frontiers","2016","3","5","598","","10.1039/C6QO00018E","","","1.54184","CuKα","","0.0838","0.0533","","","0.12","0.1481","","","","","","1.013","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553420","12.5809","0.0003","8.9728","0.0002","13.319","0.0003","90","","93.554","","90","","1500.64","0.06","153","2","153","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C25 H48 N2 O5 S Si -","- C25 H48 N2 O5 S Si -","- C50 H96 N4 O10 S2 Si2 -","2","1","","Ye, Jian-Liang; Chen, Hang; Zhang, Yu-Feng; Huang, Pei-Qiang","A versatile access to vicinal diamine motifs by highly anti-selective asymmetric vinylogous Mannich reactions: an efficient total synthesis of (+)-absouline","Organic Chemistry Frontiers","2016","3","6","683","","10.1039/C6QO00022C","","","0.71073","MoKα","","0.1561","0.0612","","","0.1222","0.2001","","","","","","0.9634","","","","has coordinates","300101","2025-06-17","17:58:10",""
"1553421","11.701","0.002","14.628","0.003","25.939","0.005","90","","90","","90","","4439.8","1.5","273","2","273.15","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C20 H28 Cl N2 O4.5 S -","- C20 H28 Cl N2 O4.5 S -","- C160 H224 Cl8 N16 O36 S8 -","8","2","","Ye, Jian-Liang; Chen, Hang; Zhang, Yu-Feng; Huang, Pei-Qiang","A versatile access to vicinal diamine motifs by highly anti-selective asymmetric vinylogous Mannich reactions: an efficient total synthesis of (+)-absouline","Organic Chemistry Frontiers","2016","3","6","683","","10.1039/C6QO00022C","","","0.71073","MoKα","","0.093","0.0653","","","0.1515","0.1711","","","","","","1.0281","","","","has coordinates","300101","2025-06-17","17:58:10",""
"1553422","22.824","0.001","22.583","0.001","47.813","0.001","90","","90","","90","","24644.5","1.6","100","1","100","1","","","","","","","","7","P n n n :2","-P 2ab 2bc","48","","","","- C250 H238 F24 N18 O12 P4 Ru2 -","- C190 H178 F24 N18 O12 P4 Ru2 -","- C760 H712 F96 N72 O48 P16 Ru8 -","4","0.5","","Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.","Conformations of large macrocycles and ring-in-ring complexes","Organic Chemistry Frontiers","2016","3","6","661","","10.1039/C6QO00024J","","","0.8","synchrotronX-rays","","0.175","0.1536","","","0.4615","0.494","","","","","","2.178","","","","has coordinates","234980","2020-10-21","18:00:00",""
"1553423","20.3614","0.0003","15.5902","0.0003","30.5936","0.0005","90","","94.4504","0.0009","90","","9682.3","0.3","160","1","160","1","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C90 H102 F12 N10 O8 P2 Ru -","- C82 H90 F12 N6 O8 P2 Ru -","- C328 H360 F48 N24 O32 P8 Ru4 -","4","1","","Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.","Conformations of large macrocycles and ring-in-ring complexes","Organic Chemistry Frontiers","2016","3","6","661","","10.1039/C6QO00024J","","","0.71073","MoKα","","0.1644","0.1001","","","0.2714","0.3174","","","","","","1.032","","","","has coordinates,has disorder","234980","2020-10-21","18:00:00",""
"1553424","11.0301","0.0002","12.3939","0.0004","21.8715","0.0007","76.878","0.0012","78.788","0.0019","87.305","0.002","2856.3","0.14","160","1","160","1","","","","","","","","7","P -1","-P 1","2","","","","- C102 H130 F12 N10 O26 S4 Zn2 -","- C102 H130 F12 N10 O26 S4 Zn2 -","- C102 H130 F12 N10 O26 S4 Zn2 -","1","0.5","","Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.","Conformations of large macrocycles and ring-in-ring complexes","Organic Chemistry Frontiers","2016","3","6","661","","10.1039/C6QO00024J","","","0.71073","MoKα","","0.0704","0.0495","","","0.115","0.1256","","","","","","1.035","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553425","15.004","0.0005","15.1525","0.0004","21.5611","0.0007","98.4023","0.0018","98.0121","0.0012","108.321","0.002","4512.9","0.3","160","1","160","1","","","","","","","","8","P -1","-P 1","2","","","","- C155 H166 Cl22 F24 N12 O12 P4 Ru2 -","- C144 H144 F24 N12 O12 P4 Ru2 -","- C144 H144 F24 N12 O12 P4 Ru2 -","1","0.5","","Klosterman, Jeremy K.; Veliks, Janis; Frantz, Derik K.; Yasui, Yoshizumi; Loepfe, Michael; Zysman-Colman, Eli; Linden, Anthony; Siegel, Jay S.","Conformations of large macrocycles and ring-in-ring complexes","Organic Chemistry Frontiers","2016","3","6","661","","10.1039/C6QO00024J","","","0.71073","MoKα","","0.0964","0.0627","","","0.1493","0.1674","","","","","","1.023","","","","has coordinates,has disorder","234980","2020-10-21","18:00:00",""
"1553426","14.556","0.001","24.668","0.001","26.949","0.001","90","","93.27","0.01","90","","9660.8","0.9","100","2","100","2","","","","","","","","8","P 1 21/n 1","-P 2yn","14","","","","- C98 H98 Br2 F12 N16 O10 P2 Ru -","- C78 H68 Br2 F12 N6 O10 P2 Ru -","- C312 H272 Br8 F48 N24 O40 P8 Ru4 -","4","1","","Veliks, Janis; Seifert, Helen M.; Frantz, Derik K.; Klosterman, Jeremy K.; Tseng, Jui-Chang; Linden, Anthony; Siegel, Jay S.","Towards the molecular Borromean link with three unequal rings: double-threaded ruthenium(ii) ring-in-ring complexes","Organic Chemistry Frontiers","2016","3","6","667","","10.1039/C6QO00025H","","","0.6916","synchrotronX-rays","","0.0797","0.0693","","","0.2007","0.2072","","","","","","1.054","","","","has coordinates","234983","2020-10-21","18:00:00",""
"1553427","13.6711","0.0002","16.967","0.0002","22.4266","0.0003","71.073","0.001","82.622","0.001","68.288","0.001","4571.45","0.11","160","1","160","1","","","","","","","","7","P -1","-P 1","2","","","","- C180 H194 F24 N22 O18 P4 Ru2 -","- C168 H176 F24 N16 O18 P4 Ru2 -","- C168 H176 F24 N16 O18 P4 Ru2 -","1","0.5","","Veliks, Janis; Seifert, Helen M.; Frantz, Derik K.; Klosterman, Jeremy K.; Tseng, Jui-Chang; Linden, Anthony; Siegel, Jay S.","Towards the molecular Borromean link with three unequal rings: double-threaded ruthenium(ii) ring-in-ring complexes","Organic Chemistry Frontiers","2016","3","6","667","","10.1039/C6QO00025H","","","1.54184","CuKα","","0.0803","0.069","","","0.2021","0.2134","","","","","","1.072","","","","has coordinates,has disorder","234983","2020-10-21","18:00:00",""
"1553428","19.5895","0.001","7.0388","0.0003","9.2405","0.0004","90","","91.626","0.004","90","","1273.63","0.1","100","0.1","100","0.1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C14 H16 O5 -","- C14 H16 O5 -","- C56 H64 O20 -","4","1","","Yu, Jingxun; Ma, Haichen; Yao, Hongliang; Cheng, Hang; Tong, Rongbiao","Diastereoselective and regiodivergent oxa-[3 + 2] cycloaddition of Achmatowicz products and cyclic 1,3-dicarbonyl compounds","Organic Chemistry Frontiers","2016","3","6","714","","10.1039/C6QO00034G","","x-ray","0.71073","MoKα","","0.0674","0.0452","","","0.0972","0.1067","","","","","","1.002","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553429","8.144","0.0006","14.5913","0.001","11.013","0.0007","90","","94.901","0.007","90","","1303.91","0.16","100.01","0.1","100.01","0.1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C14 H16 O5 -","- C14 H16 O5 -","- C56 H64 O20 -","4","1","","Yu, Jingxun; Ma, Haichen; Yao, Hongliang; Cheng, Hang; Tong, Rongbiao","Diastereoselective and regiodivergent oxa-[3 + 2] cycloaddition of Achmatowicz products and cyclic 1,3-dicarbonyl compounds","Organic Chemistry Frontiers","2016","3","6","714","","10.1039/C6QO00034G","","x-ray","0.71073","MoKα","","0.1435","0.0596","","","0.0906","0.1137","","","","","","1.001","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553430","8.1449","0.0002","10.8999","0.0004","16.4545","0.0006","90","","90","","90","","1460.81","0.08","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C17 H16 Cl N O2 -","- C17 H16 Cl N O2 -","- C68 H64 Cl4 N4 O8 -","4","1","","Vyas, Vijyesh K.; Bhanage, Bhalchandra M.","Asymmetric transfer hydrogenation of seven membered tricyclic ketones: N-substituted dibenzo[b,e]azepine-6,11-dione driven by nonclassical CH/O interactions","Organic Chemistry Frontiers","2016","3","5","614","","10.1039/C6QO00036C","","x-ray","1.54184","CuKα","","0.0619","0.05","","","0.1187","0.1301","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553431","9.837","0.002","10.113","0.002","14.456","0.003","90","","106.063","0.008","90","","1382","0.5","173","2","173","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C31 H28 N4 O3 -","- C31 H28 N4 O3 -","- C62 H56 N8 O6 -","2","1","","Zhu, Yi; Li, Yao; Meng, Qingbin; Li, Xin","An organocatalytic enantioselective vinylogous Mannich reaction of α,α-dicyanoolefins with isatin N-Boc ketimines","Organic Chemistry Frontiers","2016","3","6","709","","10.1039/C6QO00038J","","","1.54187","CuKα","","0.0283","0.0278","","","0.0742","0.0783","","","","","","1.069","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553432","7.7032","0.001","16.441","0.002","14.9629","0.0018","90","","90","","90","","1895","0.4","293","2","293","2","","","","","","","","5","P c a 21","P 2c -2ac","29","4a","4a","","- C23 H15 Cl3 N2 O2 -","- C23 H15 Cl3 N2 O2 -","- C92 H60 Cl12 N8 O8 -","4","1","","Zhang, Zeyuan; Dai, Zhen; Ma, Xinkun; Liu, Yihan; Ma, Xiaojun; Li, Wanli; Ma, Chen","Cu-catalyzed one-pot synthesis of fused oxazepinone derivatives via sp2 C–H and O–H cross-dehydrogenative coupling","Organic Chemistry Frontiers","2016","3","7","799","","10.1039/C6QO00040A","","","0.71","MoKα","","0.0947","0.0629","","","0.1296","0.1592","","","","","","1.006","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553433","7.147","0.0016","7.9449","0.0018","16.405","0.004","101.767","0.002","96.018","0.002","106.731","0.0018","859.9","0.3","298","2","298.15","","","","","","","","","5","P -1","-P 1","2","3k","3k","","- C21 H12 Cl N3 O2 -","- C21 H12 Cl N3 O2 -","- C42 H24 Cl2 N6 O4 -","2","1","","Zhang, Zeyuan; Dai, Zhen; Ma, Xinkun; Liu, Yihan; Ma, Xiaojun; Li, Wanli; Ma, Chen","Cu-catalyzed one-pot synthesis of fused oxazepinone derivatives via sp2 C–H and O–H cross-dehydrogenative coupling","Organic Chemistry Frontiers","2016","3","7","799","","10.1039/C6QO00040A","","","0.71","MoKα","","0.0561","0.0422","","","0.141","0.155","","","","","","1.16","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553434","9.986","0.007","15.521","0.011","8.74","0.006","90","","101.027","0.009","90","","1329.6","1.6","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C16 H11 Br O2 -","- C16 H11 Br O2 -","- C64 H44 Br4 O8 -","4","1","","Qiu, Guanyinsheng; Liu, Tong; Ding, Qiuping","Tandem oxidative radical brominative addition of activated alkynes and spirocyclization: switchable synthesis of 3-bromocoumarins and 3-bromo spiro-[4,5] trienone","Organic Chemistry Frontiers","2016","3","4","510","","10.1039/C6QO00041J","","","0.71073","MoKα","","0.0571","0.0369","","","0.0878","0.0934","","","","","","0.896","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553435","6.3266","0.0006","11.3868","0.0011","18.6894","0.0019","94.305","0.002","99.144","0.002","100.166","0.002","1301","0.2","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C37 H24 O3 -","- C37 H24 O3 -","- C74 H48 O6 -","2","1","","Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian","Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes","Organic Chemistry Frontiers","2016","3","5","603","","10.1039/C6QO00045B","","","0.71073","MoKα","","0.0539","0.047","","","0.1316","0.1432","","","","","","1.062","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553436","6.514","0.0009","11.9444","0.0016","17.215","0.002","93.28","0.003","94.949","0.003","104.241","0.003","1289.2","0.3","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C37 H26 O2 -","- C37 H26 O2 -","- C74 H52 O4 -","2","1","","Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian","Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes","Organic Chemistry Frontiers","2016","3","5","603","","10.1039/C6QO00045B","","","0.71073","MoKα","","0.0549","0.045","","","0.1126","0.1179","","","","","","1.045","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553437","12.8713","0.0007","12.9061","0.0008","18.4438","0.0011","83.491","0.001","70.221","0.001","87.197","0.001","2864.3","0.3","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C38 H27 N O3.5 -","- C38 H27 N O3.5 -","- C152 H108 N4 O14 -","4","2","","Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian","Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes","Organic Chemistry Frontiers","2016","3","5","603","","10.1039/C6QO00045B","","","0.71073","MoKα","","0.0783","0.0591","","","0.1486","0.164","","","","","","1.035","","","","has coordinates,has disorder","234995","2020-10-21","18:00:00",""
"1553438","9.5936","0.0012","9.4163","0.0012","34.688","0.005","90","","93.15","0.003","90","","3128.8","0.7","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C41 H34 O6 -","- C41 H34 O6 -","- C164 H136 O24 -","4","1","","Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian","Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes","Organic Chemistry Frontiers","2016","3","5","603","","10.1039/C6QO00045B","","","0.71073","MoKα","","0.068","0.0483","","","0.1235","0.1367","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553439","9.837","0.002","10.766","0.002","13.71","0.003","87.68","0.03","77.4","0.03","71.54","0.03","1343.4","0.6","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C38 H26 O2 -","- C38 H26 O2 -","- C76 H52 O4 -","2","1","","Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian","Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes","Organic Chemistry Frontiers","2016","3","5","603","","10.1039/C6QO00045B","","","0.71073","MoKα","","0.0713","0.0533","","","0.1418","0.1527","","","","","","1.054","","","","has coordinates","234995","2020-10-21","18:00:00",""
"1553440","26.128","0.002","8.1552","0.0008","21.487","0.002","90","","119.724","0.002","90","","3976","0.6","100","2","100","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C29 H20 O -","- C29 H20 O -","- C232 H160 O8 -","8","1","","Wang, Lei; Zhang, Jianwei; Lang, Ming; Wang, Jian","Palladium-catalyzed ring contraction reaction of naphthoquinones upon reaction with alkynes","Organic Chemistry Frontiers","2016","3","5","603","","10.1039/C6QO00045B","","","0.71073","MoKα","","0.0664","0.0532","","","0.1243","0.1312","","","","","","1.065","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553441","19.7803","0.0006","8.925","0.0003","17.1219","0.0005","90","","93.062","0.001","90","","3018.37","0.16","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C71 H64 O24 -","- C71 H64 O24 -","- C142 H128 O48 -","2","0.5","","Leowanawat, Pawaret; Nowak-Król, Agnieszka; Würthner, Frank","Tetramethoxy-bay-substituted perylene bisimides by copper-mediated cross-coupling","Organic Chemistry Frontiers","2016","3","5","537","","10.1039/C6QO00047A","","","1.54178","CuKα","","0.0541","0.0448","","","0.1018","0.108","","","","","","1.081","","","","has coordinates,has disorder","234997","2020-10-21","18:00:00",""
"1553442","13.1094","0.0007","8.943","0.0005","14.6031","0.0009","90","","105.214","0.002","90","","1652.03","0.16","103","2","103","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C20 H24 N2 -","- C20 H24 N2 -","- C80 H96 N8 -","4","1","","Peng, Xingao; Kaga, Atsushi; Hirao, Hajime; Chiba, Shunsuke","Hydroamination of alkenyl N-arylhydrazones mediated by t-BuOK for the synthesis of nitrogen heterocycles","Organic Chemistry Frontiers","2016","3","5","609","","10.1039/C6QO00053C","","","0.71073","MoKα","","0.053","0.0421","","","0.1089","0.1168","","","","","","1.027","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553443","11.6939","0.0007","9.4598","0.0005","16.9069","0.001","90","","91.481","0.003","90","","1869.65","0.19","103","2","103","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C23 H24 N2 S -","- C23 H24 N2 S -","- C92 H96 N8 S4 -","4","1","","Peng, Xingao; Kaga, Atsushi; Hirao, Hajime; Chiba, Shunsuke","Hydroamination of alkenyl N-arylhydrazones mediated by t-BuOK for the synthesis of nitrogen heterocycles","Organic Chemistry Frontiers","2016","3","5","609","","10.1039/C6QO00053C","","","0.71073","MoKα","","0.0851","0.0497","","","0.1172","0.1342","","","","","","1.042","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553444","5.9262","0.0004","8.0475","0.0005","31.957","0.002","90","","90","","90","","1524.06","0.17","294","2","294","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C16 H16 O3 S -","- C16 H16 O3 S -","- C64 H64 O12 S4 -","4","1","","Phanindrudu, Mandalaparthi; Tiwari, Dipak Kumar; Sridhar, B.; Likhar, Pravin R.; Tiwari, Dharmendra Kumar","Magnetically separable nano-copper catalyzed unprecedented stereoselective synthesis of E-vinyl sulfones from tosylmethyl isocyanide and alkynes: TosMIC as a source of the sulfonyl group","Organic Chemistry Frontiers","2016","3","7","795","","10.1039/C6QO00063K","","","0.71073","MoKα","","0.089","0.0663","","","0.1648","0.1804","","","","","","1.117","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553445","13.4028","0.0008","11.2931","0.0006","14.0439","0.0008","90","","91.99","0.002","90","","2124.4","0.2","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C23 H20 Br2 N2 O2 -","- C23 H20 Br2 N2 O2 -","- C92 H80 Br8 N8 O8 -","4","1","","Hu, Haoxiang; Wang, Yidong; Qian, Deyun; Zhang, Zhan-Ming; Liu, Lu; Zhang, Junliang","Enantioselective gold-catalyzed intermolecular [2 + 2]-cycloadditions of 3-styrylindoles with N-allenyl oxazolidinone","Organic Chemistry Frontiers","2016","3","6","759","","10.1039/C6QO00087H","","","0.71073","MoKα","","0.0723","0.0423","","","0.1003","0.116","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553446","12.5457","0.0006","22.382","0.001","12.6621","0.0005","90","","92.052","0.001","90","","3553.2","0.3","173","2","173","2","","","","","","","","8","P 1 21 1","P 2yb","4","","","","- C36 H56 Au Cl N O P S -","- C36 H56 Au Cl N O P S -","- C144 H224 Au4 Cl4 N4 O4 P4 S4 -","4","2","","Hu, Haoxiang; Wang, Yidong; Qian, Deyun; Zhang, Zhan-Ming; Liu, Lu; Zhang, Junliang","Enantioselective gold-catalyzed intermolecular [2 + 2]-cycloadditions of 3-styrylindoles with N-allenyl oxazolidinone","Organic Chemistry Frontiers","2016","3","6","759","","10.1039/C6QO00087H","","","0.71073","MoKα","","0.0372","0.033","","","0.0732","0.0763","","","","","","1.044","","","","has coordinates","235003","2020-10-21","18:00:00",""
"1553447","21.51","0.02","10.73","0.01","19.7","0.019","90","","113.492","0.012","90","","4170","7","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C26 H21 N O3 S -","- C26 H21 N O3 S -","- C208 H168 N8 O24 S8 -","8","1","","Gong, Xinxing; Xia, Hongguang; Wu, Jie","A palladium-catalyzed tandem reaction of 2-alkynylbenzenesulfonamides with 2-(2-bromoarylidene)cyclobutanones","Organic Chemistry Frontiers","2016","3","6","697","","10.1039/C6QO00091F","","","0.71073","MoKα","","0.1656","0.1158","","","0.3092","0.3265","","","","","","1.056","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553448","10.5273","0.0012","11.4221","0.0014","34.217","0.004","90.072","0.003","98.137","0.003","105.697","0.003","3917.7","0.8","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C23 H21 F N4 -","- C23 H21 F N4 -","- C184 H168 F8 N32 -","8","4","","Jiang, Yu; Wang, Qiang; Sun, Run; Tang, Xiang-Ying; Shi, Min","Base-induced synthesis of N-dialkylaminomethyl-2H-1,2,3-triazoles from N-sulfonyl-1,2,3-triazoles","Organic Chemistry Frontiers","2016","3","6","744","","10.1039/C6QO00102E","","","0.71073","MoKα","","0.1396","0.0679","","","0.1742","0.2272","","","","","","0.958","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553449","9.02156","0.00013","9.44417","0.00011","30.948","0.0004","90","","90","","90","","2636.81","0.06","291.29","0.1","291.29","0.1","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C32 H25 N O6 -","- C32 H25 N O5.955 -","- C128 H100 N4 O23.82 -","4","1","","Ran, Guang-Yao; Wang, Pan; Du, Wei; Chen, Ying-Chun","α-Regioselective [3 + 2] annulations with Morita‒Baylis‒Hillman carbonates of isatins and 2-nitro-1,3-enynes","Organic Chemistry Frontiers","2016","3","7","861","","10.1039/C6QO00118A","","x-ray","1.54184","CuKα","","0.0536","0.0532","","","0.1478","0.1485","","","","","","1.029","","","","has coordinates,has disorder","235009","2020-10-21","18:00:00",""
"1553450","7.187","0.003","10.356","0.004","11.075","0.004","66.214","0.01","86.273","0.017","89.284","0.017","752.6","0.5","173.15","","173.15","","","","","","","","","4","P -1","-P 1","2","","","","- C21 H13 N S -","- C21 H13 N S -","- C42 H26 N2 S2 -","2","1","","Wen, Li-Rong; Shen, Qiang-Yu; Guo, Wei-Si; Li, Ming","Copper-catalyzed tandem arylation–cyclization of 2-alkynylaryl isothiocyanates with diaryliodonium salts: an efficient synthesis of thiochromeno[2,3-b]indoles","Organic Chemistry Frontiers","2016","3","7","870","","10.1039/C6QO00133E","","","0.71073","MoKα","","0.0659","0.0583","","","0.1187","0.1224","","","","","","1.176","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553451","11.0789","0.0015","11.6353","0.0015","16.29","0.003","93.084","0.009","106.29","0.01","115.259","0.008","1786.1","0.5","173.15","","173.15","","","","","","","","","5","P -1","-P 1","2","","","","- C22 H17 N O2 S -","- C22 H17 N O2 S -","- C88 H68 N4 O8 S4 -","4","2","","Wen, Li-Rong; Shen, Qiang-Yu; Guo, Wei-Si; Li, Ming","Copper-catalyzed tandem arylation–cyclization of 2-alkynylaryl isothiocyanates with diaryliodonium salts: an efficient synthesis of thiochromeno[2,3-b]indoles","Organic Chemistry Frontiers","2016","3","7","870","","10.1039/C6QO00133E","","","0.71073","MoKα","","0.0546","0.0487","","","0.16","0.1651","","","","","","1.227","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553452","13.5013","0.001","18.6052","0.0013","13.6121","0.0009","90","","106.649","0.008","90","","3275.9","0.4","291","2","291","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C19 H17 N O5 -","- C19 H17 N O5 -","- C152 H136 N8 O40 -","8","2","","Görgen née Boersch, Christina; Lutsenko, Kiril; Merkul, Eugen; Frank, Walter; Müller, Thomas J. J.","Catalytic one-pot synthesis of 4-(hetero)aryl substituted 5-(2-oxoethyl) oxazol-2(3H)-ones by coupling–isomerization–elimination (CIE) sequence","Organic Chemistry Frontiers","2016","3","7","887","","10.1039/C6QO00138F","","","0.71073","MoKα","","0.0705","0.0318","","","0.0553","0.0581","","","","","","0.8","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553453","8.4973","0.001","40.566","0.006","26.516","0.004","90","","97.469","0.004","90","","9063","2","200","2","200","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","ru_nts_coord_diester_7a","","","- C48 H53 Cl2 N3 O6 Ru S -","- C48 H53 Cl2 N3 O6 Ru S -","- C384 H424 Cl16 N24 O48 Ru8 S8 -","8","2","","Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung","Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes","Organic Chemistry Frontiers","2016","3","8","939","","10.1039/C6QO00148C","","","0.71073","","","0.186","0.0803","","","0.1831","0.244","","","","","","1.035","","","","has coordinates","235018","2020-10-21","18:00:00",""
"1553454","16.8326","0.0017","12.2762","0.0018","20.4575","0.0012","90","","90","","90","","4227.3","0.8","200","2","200","2","","","","","","","","7","P n a 21","P 2c -2n","33","","","","- C44 H49 Cl2 N3 O3 Ru S -","- C44 H49 Cl2 N3 O3 Ru S -","- C176 H196 Cl8 N12 O12 Ru4 S4 -","4","1","","Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung","Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes","Organic Chemistry Frontiers","2016","3","8","939","","10.1039/C6QO00148C","","","0.71073","MoKα","","0.0556","0.0353","","","0.0837","0.0953","","","","","","1.084","","","","has coordinates,has disorder","235018","2020-10-21","18:00:00",""
"1553455","11.3136","0.0015","21.889","0.003","16.102","0.003","90","","97.063","0.005","90","","3957.3","1.1","200","2","200","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","vs_nts_vs_oac_2","","","- C40 H47 Cl2 N3 O4 Ru S -","- C40 H47 Cl2 N3 O4 Ru S -","- C160 H188 Cl8 N12 O16 Ru4 S4 -","4","1","","Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung","Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes","Organic Chemistry Frontiers","2016","3","8","939","","10.1039/C6QO00148C","","","0.71073","MoKα","","0.0622","0.0479","","","0.1348","0.1589","","","","","","1.122","","","","has coordinates","235018","2020-10-21","18:00:00",""
"1553456","20.114","0.003","8.8782","0.001","20.665","0.003","90","","105.736","0.004","90","","3552","0.8","300","2","300","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C36 H46 Cl2 N2 O3 Ru -","- C36 H46 Cl2 N2 O3 Ru -","- C144 H184 Cl8 N8 O12 Ru4 -","4","1","","Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung","Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes","Organic Chemistry Frontiers","2016","3","8","939","","10.1039/C6QO00148C","","","0.71073","MoKα","","0.0939","0.0789","","","0.2425","0.253","","","","","","1.218","","","","has coordinates,has disorder","235018","2020-10-21","18:00:00",""
"1553457","12.073","0.0019","18.008","0.003","10.7084","0.0015","90","","90","","90","","2328.1","0.6","199","2","199","2","","","","","","","","6","P 21 21 2","P 2 2ab","18","","","","- C22 H26 Cl3 N2 O Ru -","- C22 H26 Cl2.5 N2 O Ru -","- C88 H104 Cl10 N8 O4 Ru4 -","4","1","","Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung","Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes","Organic Chemistry Frontiers","2016","3","8","939","","10.1039/C6QO00148C","","","0.71073","","","0.0935","0.0548","","","0.1458","0.1765","","","","","","1.085","","","","has coordinates","235018","2020-10-21","18:00:00",""
"1553458","40.354","0.008","40.354","0.008","14.657","0.003","90","","90","","120","","20670","7","200","2","200","2","","","","","","","","7","R -3 :H","-R 3","148","vs_nts_ru2","","","- C42 H43 Cl2 N3 O4 Ru S -","- C42 H43 Cl2 N3 O4 Ru S -","- C756 H774 Cl36 N54 O72 Ru18 S18 -","18","1","","Sabbasani, Venkata R.; Yun, Sang Young; Lee, Daesung","Structure and reactivity of sulfonamide- and acetate-chelated ruthenium alkylidene complexes","Organic Chemistry Frontiers","2016","3","8","939","","10.1039/C6QO00148C","","","0.71073","","","0.0857","0.066","","","0.1839","0.1966","","","","","","1.297","","","","has coordinates","235018","2020-10-21","18:00:00",""
"1553459","10.0639","0.0019","8.163","0.0016","20.469","0.004","90","","101.995","0.003","90","","1644.8","0.6","200","2","200","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","3ak in manuscript","","","- C14 H10 F12 N2 -","- C14 H10 F12 N2 -","- C56 H40 F48 N8 -","4","1","","Xie, Jin; Li, Jian; Wurm, Thomas; Weingand, Vanessa; Sung, Hui-Ling; Rominger, Frank; Rudolph, Matthias; Hashmi, A. Stephen K.","A general photoinduced electron transfer-directed chemoselective perfluoroalkylation of N,N-dialkylhydrazones","Organic Chemistry Frontiers","2016","3","7","841","","10.1039/C6QO00158K","","","0.71073","MoKα","","0.125","0.0629","","","0.1353","0.1556","","","","","","1.053","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553460","16.558","0.003","17.307","0.004","19.571","0.004","90","","90","","90","","5608","2","173.15","","173.15","","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C27 H26 Cl2 F3 N7 S -","- C27 H26 Cl2 F3 N7 S -","- C216 H208 Cl16 F24 N56 S8 -","8","1","","Wang, Fei; Zhao, Liang; You, Jingsong; Wang, Mei-Xiang","Synthesis of trifluoromethylthiolated azacalix[1]arene[3]pyridines from the Cu(ii)-mediated direct trifluoromethylthiolation reaction of arenes via reactive arylcopper(iii) intermediates","Organic Chemistry Frontiers","2016","3","7","880","","10.1039/C6QO00161K","","","0.71073","MoKα","","0.0947","0.0895","","","0.2241","0.2349","","","","","","1.243","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553461","9.817","0.002","11.968","0.002","13.149","0.003","102.73","0.03","99.17","0.03","104.43","0.03","1421.3","0.6","173.15","","173.15","","","","","","","","","5","P -1","-P 1","2","","","","- C27 H23 F6 N7 S2 -","- C27 H23 F6 N7 S2 -","- C54 H46 F12 N14 S4 -","2","1","","Wang, Fei; Zhao, Liang; You, Jingsong; Wang, Mei-Xiang","Synthesis of trifluoromethylthiolated azacalix[1]arene[3]pyridines from the Cu(ii)-mediated direct trifluoromethylthiolation reaction of arenes via reactive arylcopper(iii) intermediates","Organic Chemistry Frontiers","2016","3","7","880","","10.1039/C6QO00161K","","","0.71073","MoKα","","0.0544","0.0491","","","0.1644","0.1691","","","","","","1.29","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553462","14.717","0.003","15.564","0.003","12.282","0.003","90","","103.48","0.03","90","","2735.8","1.1","173.15","","173.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C27 H23 F6 N7 S2 -","- C27 H23 F6 N7 S2 -","- C108 H92 F24 N28 S8 -","4","1","","Wang, Fei; Zhao, Liang; You, Jingsong; Wang, Mei-Xiang","Synthesis of trifluoromethylthiolated azacalix[1]arene[3]pyridines from the Cu(ii)-mediated direct trifluoromethylthiolation reaction of arenes via reactive arylcopper(iii) intermediates","Organic Chemistry Frontiers","2016","3","7","880","","10.1039/C6QO00161K","","","0.71073","MoKα","","0.0733","0.0659","","","0.1403","0.1443","","","","","","1.181","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553463","10.82","0.006","10.975","0.006","11.163","0.006","74.634","0.005","62.808","0.005","65.132","0.005","1065.4","1","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C17 H25 Cl2 N3 O4 S -","- C17 H25 Cl2 N3 O4 S -","- C34 H50 Cl4 N6 O8 S2 -","2","1","","Zhou, Kaida; Xia, Hongguang; Wu, Jie","Generation of (2-oxoindolin-3-yl)methanesulfonohydrazides via a photo-induced reaction of N-(2-iodoaryl)acrylamide, DABSO, and hydrazine","Organic Chemistry Frontiers","2016","3","7","865","","10.1039/C6QO00163G","","","0.71073","MoKα","","0.0899","0.0806","","","0.2404","0.2518","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553464","11.266","0.0013","12.1474","0.0015","16.278","0.0019","73.095","0.003","73.52","0.003","84.96","0.003","2043.8","0.4","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C22 H18 F3 N O6 -","- C22 H18 F3 N O6 -","- C88 H72 F12 N4 O24 -","4","2","","Li, Zong-Rui; Bao, Xing-Xing; Sun, Jian; Shen, Jing; Wu, Dun-Qi; Liu, Yan-Kai; Deng, Qing-Hai; Liu, Feng","Iron-catalyzed trifluoromethylation of vinylcyclopropanes: facile synthesis of CF3–containing dihydronaphthalene derivatives","Organic Chemistry Frontiers","2016","3","8","934","","10.1039/C6QO00166A","","","0.71073","MoKα","","0.0784","0.0537","","","0.1486","0.1685","","","","","","1.014","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553465","25.856","0.0009","5.37038","0.00017","21.5154","0.0007","90","","101.646","0.003","90","","2926.05","0.17","99.98","0.11","99.98","0.11","","","","","","","","5","I 1 2/a 1","-I 2ya","15","","8a","","- C16 H16 B N3 O2 -","- C16 H16 B N3 O2 -","- C128 H128 B8 N24 O16 -","8","1","","Zhai, Wenlei; Chapin, Brette M.; Yoshizawa, Akina; Wang, Hui-Chen; Hodge, Stephen A.; James, Tony D.; Anslyn, Eric V.; Fossey, John S.","“Click-fluors”: triazole-linked saccharide sensors","Organic Chemistry Frontiers","2016","3","8","918","","10.1039/C6QO00171H","","x-ray","0.71073","MoKα","","0.0491","0.0418","","","0.1011","0.1059","","","","","","1.09","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553466","7.1065","0.0004","9.0913","0.0006","17.685","0.0011","81.994","0.005","84.409","0.005","68.79","0.006","1053.43","0.12","99.9","0.2","99.9","0.2","","","","","","","","5","P -1","-P 1","2","","13a","","- C24 H24 B N3 O4 -","- C24 H24 B N3 O4 -","- C48 H48 B2 N6 O8 -","2","1","","Zhai, Wenlei; Chapin, Brette M.; Yoshizawa, Akina; Wang, Hui-Chen; Hodge, Stephen A.; James, Tony D.; Anslyn, Eric V.; Fossey, John S.","“Click-fluors”: triazole-linked saccharide sensors","Organic Chemistry Frontiers","2016","3","8","918","","10.1039/C6QO00171H","","x-ray","1.54184","CuKα","","0.0539","0.0443","","","0.1147","0.1232","","","","","","1.042","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553467","4.4197","0.0005","11.6677","0.0013","22.915","0.002","90","","90","","90","","1181.7","0.2","173","","173","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C14 H10 Br N O2 -","- C14 H10 Br N O2 -","- C56 H40 Br4 N4 O8 -","4","1","","Zhang, Xu; Xu, Bin; Xu, Ming-Hua","Rhodium-catalyzed asymmetric arylation of N- and O-containing cyclic aldimines: facile and efficient access to highly optically active 3,4-dihydrobenzo[1,4]oxazin-2-ones and dihydroquinoxalinones","Organic Chemistry Frontiers","2016","3","8","944","","10.1039/C6QO00191B","","","0.71073","MoKα","","0.1053","0.0562","","","0.0883","0.0994","","","","","","1.021","","","","has coordinates","277994","2022-09-20","08:32:41",""
"1553468","9.4647","0.0007","12.7252","0.0009","11.5908","0.0008","90","","108.624","0.001","90","","1322.9","0.16","100","2","100","2","","","","","","","","5","P 1 c 1","P -2yc","7","","","","- C14 H15 Cl N2 Pd -","- C14 H15 Cl N2 Pd -","- C56 H60 Cl4 N8 Pd4 -","4","2","","Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John","Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle","Organic Chemistry Frontiers","2016","3","8","957","","10.1039/C6QO00198J","","","0.71075","MoKα","","0.0332","0.0331","","","0.0883","0.0884","","","","","","1.097","","","","has coordinates","235032","2020-10-21","18:00:00",""
"1553469","9.6575","0.0007","11.675","0.0008","26.2578","0.0018","90","","92.079","0.001","90","","2958.7","0.4","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H19 Cl N2 Pd -","- C16 H19 Cl N2 Pd -","- C128 H152 Cl8 N16 Pd8 -","8","2","","Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John","Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle","Organic Chemistry Frontiers","2016","3","8","957","","10.1039/C6QO00198J","","x-ray","0.71075","MoKα","","0.0257","0.0229","","","0.0604","0.0616","","","","","","1.067","","","","has coordinates","235032","2020-10-21","18:00:00",""
"1553470","6.9704","0.0005","17.1706","0.0011","12.2014","0.0009","90","","97.943","0.002","90","","1446.33","0.18","100","2","100","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C16 H17 Cl N2 O Pd -","- C16 H17 Cl N2 O Pd -","- C64 H68 Cl4 N8 O4 Pd4 -","4","1","","Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John","Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle","Organic Chemistry Frontiers","2016","3","8","957","","10.1039/C6QO00198J","","x-ray","0.71075","MoKα","","0.0249","0.0229","","","0.0556","0.0562","","","","","","1.187","","","","has coordinates","235032","2020-10-21","18:00:00",""
"1553471","12.2558","0.0003","9.9099","0.0003","17.4367","0.0005","90","","109.768","0.003","90","","1992.95","0.1","100","2","100","2","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C24 H19 Cl N O P Pd -","- C24 H19 Cl N O P Pd -","- C96 H76 Cl4 N4 O4 P4 Pd4 -","4","1","","Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John","Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle","Organic Chemistry Frontiers","2016","3","8","957","","10.1039/C6QO00198J","","x-ray","0.71075","MoKα","","0.0321","0.0268","","","0.0649","0.0673","","","","","","1.038","","","","has coordinates","235032","2020-10-21","18:00:00",""
"1553472","9.0641","0.0002","9.6782","0.0003","12.7031","0.0004","91.535","0.003","108.207","0.003","112.231","0.003","966.47","0.06","100","2","100","2","","","","","","","","7","P -1","-P 1","2","","","","- C23 H17 Cl N O P Pd -","- C23 H17 Cl N O P Pd -","- C46 H34 Cl2 N2 O2 P2 Pd2 -","2","1","","Roffe, Gavin W.; Tizzard, Graham J.; Coles, Simon J.; Cox, Hazel; Spencer, John","Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle","Organic Chemistry Frontiers","2016","3","8","957","","10.1039/C6QO00198J","","x-ray","0.71075","MoKα","","0.0216","0.0201","","","0.0508","0.0514","","","","","","1.029","","","","has coordinates","235032","2020-10-21","18:00:00",""
"1553473","5.4373","0.0006","22.5643","0.0019","15.678","0.003","90","","91.295","0.01","90","","1923","0.5","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C25 H17 N O S -","- C25 H17 N O S -","- C100 H68 N4 O4 S4 -","4","1","","Singh, Radhey M.; Kumar, Ritush; Bharadwaj, Kishor Chandra; Gupta, Tanu","Pd catalyzed facile synthesis of cyclopenta[b]quinolin-1-one via sequential Sonogashira coupling and annulation. An unusual mode of ring closure, using sulphur as a soft nucleophile","Organic Chemistry Frontiers","2016","3","9","1100","","10.1039/C6QO00203J","","","0.71073","MoKα","","0.1745","0.0803","","","0.136","0.1715","","","","","","1.015","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553474","9.2253","0.0012","12.0172","0.0019","12.8207","0.0016","65.023","0.014","76.245","0.011","83.655","0.012","1251.4","0.3","143","","143","","","","","","","","","2","P -1","-P 1","2","","","","- C36 H26 -","- C36 H26 -","- C72 H52 -","2","1","","He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong","Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores","Organic Chemistry Frontiers","2016","3","9","1091","","10.1039/C6QO00204H","","x-ray","1.5418","CuKα","","0.0532","0.0389","","","0.0933","0.0973","","","","","","1.003","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553475","9.4248","0.0007","9.6366","0.0007","25.0543","0.0016","90","","94.474","0.002","90","","2268.6","0.3","173","2","173","2","","","","","","","","2","P 1 21/n 1","-P 2yn","14","","","","- C32 H24 -","- C32 H24 -","- C128 H96 -","4","1","","He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong","Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores","Organic Chemistry Frontiers","2016","3","9","1091","","10.1039/C6QO00204H","","","0.71073","MoKα","","0.0816","0.0469","","","0.0886","0.1","","","","","","1.043","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553476","16.4844","0.0014","9.1722","0.0012","19.225","0.003","90","","107.472","0.012","90","","2772.7","0.6","143","","143","","","","","","","","","2","P 1 21/c 1","-P 2ybc","14","","","","- C40 H28 -","- C40 H28 -","- C160 H112 -","4","1","","He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong","Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores","Organic Chemistry Frontiers","2016","3","9","1091","","10.1039/C6QO00204H","","x-ray","1.5418","CuKα","","0.0563","0.0387","","","0.0832","0.0872","","","","","","1.006","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553477","11.3717","0.0002","15.9519","0.0003","15.1309","0.0003","90","","93.429","0.002","90","","2739.83","0.09","173","2","173","2","","","","","","","","2","P 1 21/n 1","-P 2yn","14","","","","- C40 H28 -","- C40 H28 -","- C160 H112 -","4","1","","He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong","Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores","Organic Chemistry Frontiers","2016","3","9","1091","","10.1039/C6QO00204H","","","1.54178","CuKα","","0.0443","0.036","","","0.0965","0.0995","","","","","","1.023","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553478","9.5798","0.0002","10.2198","0.0003","29.4004","0.0008","90","","96.324","0.002","90","","2860.89","0.13","173","","173","","","","","","","","","2","P 1 21/c 1","-P 2ybc","14","","","","- C42 H28 -","- C42 H28 -","- C168 H112 -","4","1","","He, Bairong; Nie, Han; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong","Synthesis, structure and optical properties of tetraphenylethene derivatives with through-space conjugation between benzene and various planar chromophores","Organic Chemistry Frontiers","2016","3","9","1091","","10.1039/C6QO00204H","","x-ray","1.5418","CuKα","","0.0723","0.0474","","","0.1076","0.1135","","","","","","1.005","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553479","12.766","0.003","16.24","0.003","13.427","0.003","90","","107.96","0.03","90","","2648","1.1","153","2","153","2","","","","","","","","5","P 1 21 1","P 2yb","4","","(5R,8S,9R,10R)-2-(4-Chlorophenyl)-8-(2-methoxyphenyl)-4-methyl-9-nitro-10-(3-nitrophenyl)-2,3-diazaspiro[4.5]dec-3-ene-1,6-dione","","- C28 H23 Cl N4 O7 -","- C28 H23 Cl N4 O7 -","- C112 H92 Cl4 N16 O28 -","4","2","","Li, Jun-Hua; Cui, Zhi-Hao; Du, Da-Ming","Diastereo- and enantioselective construction of cyclohexanone-fused spirospyrazolones containing four consecutive stereocenters through asymmetric sequential reactions","Organic Chemistry Frontiers","2016","3","9","1087","","10.1039/C6QO00208K","","","0.71073","MoKα","","0.0808","0.0718","","","0.1939","0.2157","","","","","","1.11","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553480","11.7876","0.0009","19.8876","0.0014","12.1607","0.0008","90","","94.193","0.007","90","","2843.2","0.4","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C17 H22 O2 -","- C17 H22 O2 -","- C136 H176 O16 -","8","2","","Ondet, Pierrick; Lempenauer, Luisa; Duñach, Elisabet; Lemière, Gilles","Bismuth(iii) triflate-catalysed tandem cyclisations towards complex polycyclic ethers","Organic Chemistry Frontiers","2016","3","8","999","","10.1039/C6QO00212A","","x-ray","0.71073","MoKα","","0.1574","0.0679","","","0.1576","0.2007","","","","","","1.02","","","","has coordinates,has disorder","301780","2025-08-18","21:43:29",""
"1553481","19.1606","0.0011","13.3348","0.0005","23.8068","0.0011","90","","108.315","0.005","90","","5774.6","0.5","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C17 H22 O2 -","- C17 H22 O2 -","- C272 H352 O32 -","16","4","","Ondet, Pierrick; Lempenauer, Luisa; Duñach, Elisabet; Lemière, Gilles","Bismuth(iii) triflate-catalysed tandem cyclisations towards complex polycyclic ethers","Organic Chemistry Frontiers","2016","3","8","999","","10.1039/C6QO00212A","","x-ray","1.54184","CuKα","","0.0707","0.0451","","","0.1126","0.131","","","","","","1.02","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553482","8.2306","0.0009","9.8924","0.0012","26.999","0.004","90","","98.152","0.013","90","","2176.1","0.5","293.78","0.1","293.78","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","(7aR,9aS,11R)-9a-methoxy-4-tosyl-3,4,5,6,9a,11-hexahydro-1H-7a,11-methanobenzofuro[3,3a-e]azonine-7,10(2H,8H)-dione","","- C23 H27 N O6 S -","- C23 H27 N O6 S -","- C92 H108 N4 O24 S4 -","4","1","","Duan, Shuangshuang; Long, Dan; Zhao, Changgui; Zhao, Gaoyuan; Yuan, Ziyun; Xie, Xingang; Fang, Jianguo; She, Xuegong","Efficient construction of the A/C/D tricyclic skeleton of palhinine A","Organic Chemistry Frontiers","2016","3","9","1137","","10.1039/C6QO00222F","","x-ray","0.71","MoKα","","0.2471","0.1529","","","0.3522","0.4085","","","","","","1.054","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553483","10.005","0.002","9.977","0.002","18.125","0.004","90","","92.34","0.03","90","","1807.7","0.7","173","2","173","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C23 H19 Br O -","- C23 H19 Br O -","- C92 H76 Br4 O4 -","4","1","","Liu, Yu; Zhao, Peng; Zhang, Bo; Xi, Chanjuan","MeOTf-catalyzed annulation of aldehydes and arylalkynes leading to 2,3-disubstituted indanones","Organic Chemistry Frontiers","2016","3","9","1116","","10.1039/C6QO00253F","","","0.71073","MoKα","","0.0762","0.0602","","","0.1883","0.2344","","","","","","1.042","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553484","9.756","0.004","10.716","0.005","10.881","0.004","65.921","0.018","68.07","0.016","63.361","0.019","902.7","0.7","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C23 H20 S -","- C23 H20 S -","- C46 H40 S2 -","2","1","","Ramesh, E.; Shankar, Majji; Dana, Suman; Sahoo, Akhila K.","Silver-mediated oxidative annulation of N-arylthio succinimides with alkynes: direct access to benzo[b]thiophenes","Organic Chemistry Frontiers","2016","3","9","1126","","10.1039/C6QO00259E","","","0.71073","MoKα","","0.0664","0.0453","","","0.1129","0.1232","","","","","","1.076","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553485","6.0606","0.0006","13.4845","0.0014","18.39","0.002","90","","91.36","0.004","90","","1502.5","0.3","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H13 F S -","- C20 H13 F S -","- C80 H52 F4 S4 -","4","1","","Ramesh, E.; Shankar, Majji; Dana, Suman; Sahoo, Akhila K.","Silver-mediated oxidative annulation of N-arylthio succinimides with alkynes: direct access to benzo[b]thiophenes","Organic Chemistry Frontiers","2016","3","9","1126","","10.1039/C6QO00259E","","","0.71073","MoKα","","0.1383","0.0626","","","0.1128","0.1349","","","","","","1.012","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553486","31.8","0.014","8.994","0.004","13.605","0.006","90","","110.595","0.005","90","","3642","3","298","2","298","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C20 H17 F3 I N O -","- C20 H17 F3 I N O -","- C160 H136 F24 I8 N8 O8 -","8","1","","An, Yuanyuan; Kuang, Yunyan; Wu, Jie","Synthesis of trifluoromethylated 3,4-dihydroquinolin-2(1H)-ones via a photo-induced radical cyclization of benzene-tethered 1,7-enynes with Togni reagent","Organic Chemistry Frontiers","2016","3","8","994","","10.1039/C6QO00267F","","","0.71073","MoKα","","0.0489","0.0341","","","0.0798","0.0833","","","","","","0.936","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553487","8.4058","0.0003","10.8659","0.0004","21.9188","0.0009","90","","90","","90","","2001.99","0.13","173","2","173","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","(S)-3o","","- C21 H19 Br N2 O4 -","- C21 H19 Br N2 O4 -","- C84 H76 Br4 N8 O16 -","4","1","","Ma, Qiao; Gong, Lei; Meggers, Eric","Enantioselective β-alkylation of pyrroles with the formation of an all-carbon quaternary stereocenter","Organic Chemistry Frontiers","2016","3","10","1319","","10.1039/C6QO00273K","","","0.71073","MoKα","","0.0545","0.0449","","","0.0864","0.0898","","","","","","0.999","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553488","20.5231","0.0017","9.5667","0.0008","20.3255","0.0018","90","","115.091","0.002","90","","3614.1","0.5","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H18 N6 O -","- C20 H18 N6 O -","- C160 H144 N48 O8 -","8","2","","Liu, Hou-Lu; Jiang, Yu; Hao, Jian; Tang, Xiang-Ying; Shi, Min","A new method to access triazole-fused spiro-guanidines from the reaction of isothiocyanates tethered N-sulfonyl-1,2,3-triazoles and amines","Organic Chemistry Frontiers","2016","3","11","1447","","10.1039/C6QO00304D","","","0.71073","MoKα","","0.124","0.0799","","","0.1656","0.1857","","","","","","1.088","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553489","7.504","0.011","8.467","0.012","13.179","0.018","95.607","0.018","102.6","0.02","110.95","0.02","748.8","1.8","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C18 H11 I N2 O -","- C18 H11 I N2 O -","- C36 H22 I2 N4 O2 -","2","1","","Wu, Yan-Dong; Geng, Xiao; Gao, Qinghe; Zhang, Jingjing; Wu, Xia; Wu, An-Xin","Iodine-promoted sequential dual oxidative Csp3–H amination/Csp3–H iodination reactions: efficient synthesis of 1-iodoimidazo[1,5-a]pyridines","Organic Chemistry Frontiers","2016","3","11","1430","","10.1039/C6QO00313C","","","0.71073","MoKα","","0.0428","0.0332","","","0.0994","0.1136","","","","","","1.141","","","","has coordinates","301780","2025-08-18","21:43:29",""
"1553490","20.2007","0.0006","25.2676","0.0007","31.3498","0.0008","90","","90","","90","","16001.7","0.8","113","","113","","","","","","","","","5","P c c n","-P 2ab 2ac","56","2PdNAmX-2","","","- C60 H44 N4 O4 Pd2 -","- C60 H44 N4 O4 Pd2 -","- C720 H528 N48 O48 Pd24 -","12","1.5","","Naito, Masaya; Komiya, Naruyoshi; Naota, Takeshi","Homochiral association of binuclear trans-bis(β-iminoaryloxy)palladium(ii) complexes doubly linked with m-xylylene spacers: drastic linker-dependence of the association chirality of chiral clothespin-shaped molecules","Organic Chemistry Frontiers","2016","3","10","1286","","10.1039/C6QO00315J","","","0.71075","MoKα","","","0.0687","","","","0.1993","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553491","27.6181","0.0017","13.0551","0.0009","30.802","0.002","90","","113.65","0.0017","90","","10173.2","1.2","113","","113","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","2PdNAmX-1","","","- C61 H45 Cl3 N4 O4 Pd2 -","- C61 H45 Cl3 N4 O4 Pd2 -","- C488 H360 Cl24 N32 O32 Pd16 -","8","1","","Naito, Masaya; Komiya, Naruyoshi; Naota, Takeshi","Homochiral association of binuclear trans-bis(β-iminoaryloxy)palladium(ii) complexes doubly linked with m-xylylene spacers: drastic linker-dependence of the association chirality of chiral clothespin-shaped molecules","Organic Chemistry Frontiers","2016","3","10","1286","","10.1039/C6QO00315J","","","0.71075","MoKα","","","0.0732","","","","0.1673","","","","","","1.053","","","","has coordinates","235053","2020-10-21","18:00:00",""
"1553492","11.5223","0.0012","14.9948","0.0015","16.4141","0.0017","90","","90","","90","","2835.9","0.5","110","2","110","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C29 H44 O6 Si -","- C29 H44 O6 Si -","- C116 H176 O24 Si4 -","4","1","","Pérez-Estrada, S.; Sayar, N.; Granja, J. R.","Towards taxane analogues synthesis by dienyne ring closing metathesis","Organic Chemistry Frontiers","2016","3","10","1331","","10.1039/C6QO00321D","","x-ray","0.71073","MoKα","","0.06","0.0423","","","0.0857","0.0937","","","","","","1.019","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553493","27.836","0.004","7.8125","0.001","14.1759","0.0019","90","","92.711","0.002","90","","3079.4","0.7","110","2","110","2","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C29 H40 O5 Si -","- C29 H40 O5 Si -","- C116 H160 O20 Si4 -","4","1","","Pérez-Estrada, S.; Sayar, N.; Granja, J. R.","Towards taxane analogues synthesis by dienyne ring closing metathesis","Organic Chemistry Frontiers","2016","3","10","1331","","10.1039/C6QO00321D","","x-ray","0.71073","MoKα","","0.0526","0.0394","","","0.0845","0.0894","","","","","","1.025","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553494","13.6594","0.0014","5.9624","0.0005","17.4715","0.0018","90","","106.688","0.012","90","","1363","0.2","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C17 H14 O2 -","- C17 H14 O2 -","- C68 H56 O8 -","4","1","","Cui, Fei-Hu; Su, Shi-Xia; Xu, Yan-li; Liang, Ying; Wang, Heng-shan; Pan, Ying-Ming","Capture of CO2 in air for 4,5-disubstituted furan-2(5H)-ones","Organic Chemistry Frontiers","2016","3","10","1304","","10.1039/C6QO00328A","","x-ray","0.71073","MoKα","","0.1445","0.0656","","","0.1364","0.1923","","","","","","1.051","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553495","14.2296","0.0004","6.2823","0.0002","33.8457","0.001","90","","90.358","0.001","90","","3025.56","0.16","123","2","123","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C38 H24 Cl2 N2 O6 -","- C38 H24 Cl2 N2 O6 -","- C152 H96 Cl8 N8 O24 -","4","1","","Wirtanen, T.; Muuronen, M.; Hurmalainen, J.; Tuononen, H. M.; Nieger, M.; Helaja, J.","Intermolecular oxidative dehydrogenative 3,3′-coupling of benzo[b]furans and benzo[b]thiophenes promoted by DDQ/H+: total synthesis of shandougenine B","Organic Chemistry Frontiers","2016","3","12","1738","","10.1039/C6QO00331A","","","1.54178","CuKα","","0.0608","0.0554","","","0.1524","0.1571","","","","","","1.086","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553496","13.909","0.004","20.264","0.002","22.762","0.002","90","","91.41","0.03","90","","6414","2","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C62 H61 N7 O20 S4 -","- C62 H61 N7 O20 S4 -","- C248 H244 N28 O80 S16 -","4","1","","Gaeta, Carmine; Della Sala, Paolo; Talotta, Carmen; De Rosa, Margherita; Soriente, Annunziata; Brancatelli, Giovanna; Geremia, Silvano; Neri, Placido","A tetrasulfate-resorcin[6]arene cavitand as the host for organic ammonium guests","Organic Chemistry Frontiers","2016","3","10","1276","","10.1039/C6QO00336B","","","0.7","","","0.1064","0.1029","","","0.2779","0.2805","","","","","","1.053","","","","has coordinates,has disorder","235062","2020-10-21","18:00:00",""
"1553497","8.125","0.0016","9.328","0.0019","11.408","0.002","90.91","0.03","96.19","0.03","107.69","0.03","817.8","0.3","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C19 H17 N O4 -","- C19 H17 N O4 -","- C38 H34 N2 O8 -","2","1","","Dai, Jie; Ren, Wenlong; Chang, Wenju; Zhang, Ping; Shi, Yian","An effective route to β2-amino acid derivatives via Pd-catalyzed regioselective hydrocarboxylation of 1,2-disubstituted enimides","Organic Chemistry Frontiers","2017","4","2","297","","10.1039/C6QO00353B","","","0.71073","MoKα","","0.1599","0.0691","","","0.1238","0.1481","","","","","","1.001","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553498","7.51038","0.0001","17.3551","0.0002","23.2172","0.0004","90","","90","","90","","3026.21","0.07","100","0.2","100","0.2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","Triple 3c","","- C14 H17 N5 O4 -","- C14 H17 N5 O4 -","- C112 H136 N40 O32 -","8","2","","Naik, Siddhi D.; Chandra, Girish; Sahu, Pramod K.; Kim, Hong-Rae; Qu, Shuhao; Yoon, Ji-seong; Jeong, Lak Shin","Stereo- and regio-selective synthesis of 3′-C-substituted-(N)-methanocarba adenosines as potential anticancer agents","Organic Chemistry Frontiers","2016","3","11","1472","","10.1039/C6QO00358C","","x-ray","1.54184","CuKα","","0.028","0.0264","","","0.067","0.068","","","","","","1.027","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553499","12.057","0.004","8.771","0.002","14.736","0.005","90","","113.287","0.005","90","","1431.4","0.8","93","","93","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","4-(2-Oxo-3-(trifluoromethyl)-1-oxaspiro[4.4]non-3-en-4-yl)benzonitrile","","- C16 H12 F3 N O2 -","- C16 H12 F3 N O2 -","- C64 H48 F12 N4 O8 -","4","1","","Mizuta, Satoshi; Otaki, Hiroki; Kitamura, Kanami; Nishi, Kodai; Watanabe, Ken; Makau, Juliann Nzembi; Hashimoto, Ryo; Usui, Toshiya; Chiba, Kenya","3,3-Dibromo-2-trifluoromethyl acrylic acid ethyl ester: a versatile platform for the stereoselective preparation of functionalized-α-trifluoromethyl α,β-unsaturated lactones and trifluoromethyl pyrazolinones","Organic Chemistry Frontiers","2016","3","12","1661","","10.1039/C6QO00360E","","","0.71075","MoKα","","0.0921","0.0578","","","0.0995","0.1121","","","","","","1.068","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553500","8.165","0.002","9.432","0.002","10.126","0.003","85.485","0.007","83.241","0.008","73.145","0.007","740.3","0.3","296","2","296","2","","","","","","","","6","P -1","-P 1","2","","","","- C17 H10 Cl F3 N2 O -","- C17 H10 Cl F3 N2 O -","- C34 H20 Cl2 F6 N4 O2 -","2","1","","Jin, Li-Kun; Lu, Guo-Ping; Cai, Chun","Copper-catalyzed 8-amido chelation-induced regioselective C–H fluoroalkylation of quinolines","Organic Chemistry Frontiers","2016","3","10","1309","","10.1039/C6QO00369A","","","0.71073","MoKα","","0.0787","0.063","","","0.1666","0.1787","","","","","","1.057","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553501","4.8217","0.0003","10.1093","0.0006","31.14","0.002","90","","90","","90","","1517.89","0.16","193","","","","","","","","","","see text","3","P 21 21 21","P 2ac 2ab","19","","","","- C24 H15 N -","- C24 H15 N -","- C96 H60 N4 -","4","1","","Zagranyarski, Yulian; Skabeev, Artem; Ma, Yingjie; Müllen, Klaus; Li, Chen","Facile synthesis of annulated heterocyclic benzo[kl]acridine derivatives via one-pot N–H/C–H coupling","Organic Chemistry Frontiers","2016","3","11","1520","","10.1039/C6QO00371K","","x-ray","0.71073","MoKα","","","","","","","","","","","","","","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553502","16.3471","0.0009","11.2916","0.0008","8.0242","0.0004","90","","90","","90","","1481.15","0.15","193","","","","","","","","","","see text","4","P c a 21","P 2c -2ac","29","","","","- C22 H13 N S -","- C22 H13 N S -","- C88 H52 N4 S4 -","4","1","","Zagranyarski, Yulian; Skabeev, Artem; Ma, Yingjie; Müllen, Klaus; Li, Chen","Facile synthesis of annulated heterocyclic benzo[kl]acridine derivatives via one-pot N–H/C–H coupling","Organic Chemistry Frontiers","2016","3","11","1520","","10.1039/C6QO00371K","","x-ray","0.71073","MoKα","","","","","","","","","","","","","","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553503","6.202","0.0005","10.169","0.001","14.7158","0.0018","75.057","0.01","85.343","0.008","84.132","0.007","890.56","0.16","283","10","283","10","","","","","","","","3","P -1","-P 1","2","","","","- C23 H24 N2 -","- C23 H24 N2 -","- C46 H48 N4 -","2","1","","Liu, Cheng-Guo; Gu, Zheng-Yang; Bai, Hui-Wen; Wang, Shun-Yi; Ji, Shun-Jun","An isocyanide insertion approach to substituted pyrrolo[2,3-b]quinolines under metal-free and azide-free conditions","Organic Chemistry Frontiers","2016","3","10","1299","","10.1039/C6QO00373G","","","0.7107","MoKα","","0.0777","0.0529","","","0.1261","0.1477","","","","","","1.012","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553504","8.9115","0.0007","11.1099","0.0007","11.8272","0.0009","83.858","0.006","86.228","0.006","67.922","0.006","1078.45","0.14","291","2","291.15","","","","","","","","","5","P -1","-P 1","2","","","","- C22 H25 N2 O4 P -","- C22 H25 N2 O4 P -","- C44 H50 N4 O8 P2 -","2","1","","Sun, Mengmeng; Sun, Suyan; Qiao, Huijie; Yang, Fan; Zhu, Yu; Kang, Jianxun; Wu, Yusheng; Wu, Yangjie","Silver(i)-promoted C5–H phosphonation of 8-aminoquinoline amides with H-phosphonates","Organic Chemistry Frontiers","2016","3","12","1646","","10.1039/C6QO00379F","","x-ray","0.71073","MoKα","","0.1204","0.0776","","","0.2075","0.2482","","","","","","1.054","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553505","15.3031","0.0006","18.1046","0.0006","15.6855","0.0006","90","","90","","90","","4345.8","0.3","293","2","293","2","","","","","","","","5","P c c n","-P 2ab 2ac","56","","","","- C22 H25 N2 O4 P -","- C22 H25 N2 O4 P -","- C176 H200 N16 O32 P8 -","8","1","","Sun, Mengmeng; Sun, Suyan; Qiao, Huijie; Yang, Fan; Zhu, Yu; Kang, Jianxun; Wu, Yusheng; Wu, Yangjie","Silver(i)-promoted C5–H phosphonation of 8-aminoquinoline amides with H-phosphonates","Organic Chemistry Frontiers","2016","3","12","1646","","10.1039/C6QO00379F","","x-ray","0.71073","MoKα","","0.1048","0.0608","","","0.1597","0.1898","","","","","","1.022","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553506","8.681","0.007","17.323","0.014","32.77","0.03","90","","90","","90","","4928","7","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C31 H27 N2 O2 -","- C31 H27 N2 O2 -","- C248 H216 N16 O16 -","8","2","","Chen, Zhen; Huo, Yuwen; An, Ping; Wang, Xichao; Song, Chun; Ma, Yudao","[2.2]Paracyclophane-based N-heterocyclic carbene as efficient catalyst or as ligand for copper catalyst for asymmetric α-silylation of N-tosylaldimines","Organic Chemistry Frontiers","2016","3","12","1725","","10.1039/C6QO00386A","","","0.71073","MoKα","","0.1149","0.0538","","","0.1064","0.1312","","","","","","0.974","","","","has coordinates","275434","2022-05-16","05:31:57",""
"1553507","17.643","0.001","16.144","0.001","6.601","0.001","90","","90","","90","","1880.2","0.3","100","2","100","2","","","","","","","","4","P 21 21 2","P 2 2ab","18","","((3'S,3a'R,4'R,5'R)-4',5'-di-tert-butoxytetrahydro-3'H-spiro[cyclopropane-1,2'-pyrrolo[1,2-b]isoxazol]-3'-yl)methanol","","- C17 H31 N O4 -","- C17 H31 N O4 -","- C68 H124 N4 O16 -","4","1","","Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.","Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines","Organic Chemistry Frontiers","2016","3","12","1651","","10.1039/C6QO00410E","","","1.54178","CuKα","","0.0652","0.0456","","","0.0939","0.1068","","","","","","1.036","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553508","6.03","0.001","16.334","0.001","18.224","0.001","90","","90","","90","","1795","0.3","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","((3'R,3a'R,4'R,5'R)-4',5'-di-tert-butoxytetrahydro-3'H-spiro [cyclopropane-1,2'-pyrrolo[1,2-b]isoxazol]-3'-yl)methanol","","- C17 H31 N O4 -","- C17 H31 N O4 -","- C68 H124 N4 O16 -","4","1","","Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.","Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines","Organic Chemistry Frontiers","2016","3","12","1651","","10.1039/C6QO00410E","","","1.54178","CuKα","","0.041","0.0333","","","0.0786","0.0921","","","","","","1.1","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553509","10.178","0.001","21.78","0.001","11.615","0.001","90","","90.547","0.001","90","","2574.7","0.4","150","2","150","2","","","","","","","","4","P 1 21 1","P 2yb","4","","(3aS,6R,7S,7aR)-7-(tert-butoxy)tetrahydro-3aH-spiro [1,6-methanopyrano[4,3-c]isoxazole-3,1'-cyclopropane]","","- C13 H21 N O3 -","- C13 H21 N O3 -","- C104 H168 N8 O24 -","8","4","","Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.","Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines","Organic Chemistry Frontiers","2016","3","12","1651","","10.1039/C6QO00410E","","","1.54178","CuKα","","0.0535","0.045","","","0.1106","0.117","","","","","","1.064","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553510","6.078","0.0002","10.204","0.0003","19.957","0.0006","90","","90","","90","","1237.73","0.07","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","(4aS,7R,8S,8aR)-8-(tert-butoxy)hexahydro-1,7-methanopyrano [4,3-b]pyridin-4(7H)-one","","- C13 H21 N O3 -","- C13 H21 N O3 -","- C52 H84 N4 O12 -","4","1","","Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.","Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines","Organic Chemistry Frontiers","2016","3","12","1651","","10.1039/C6QO00410E","","","1.54178","CuKα","","0.0518","0.0401","","","0.09","0.0961","","","","","","1.07","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553511","7.252","0.001","25.57","0.001","14.465","0.001","90","","100.17","0.002","90","","2640.2","0.4","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","(3R,4S,4aR,8aS,11R,12S,12aR,16aS)-4,12-di-tert-butoxydodecahydro-3,5:11,13- dimethanodipyrano[4,3-b:4',3'-h][1,7]diazacyclododecine-8,16(3H,11H)-dione","","- C26 H42 N2 O6 -","- C26 H42 N2 O6 -","- C104 H168 N8 O24 -","4","2","","Cordero, F. M.; Vurchio, C.; Faggi, C.; Brandi, A.","Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines","Organic Chemistry Frontiers","2016","3","12","1651","","10.1039/C6QO00410E","","","1.54178","CuKα","","0.0632","0.0492","","","0.1151","0.125","","","","","","1.025","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553512","9.1392","0.0002","13.2716","0.0003","13.7699","0.0003","77.608","0.001","76.026","0.001","84.909","0.001","1581.79","0.06","200","2","200","2","","","","","","","","5","P -1","-P 1","2","","","","- C41 H31 Cl2 N O2 -","- C40.999 H30.998 Cl1.998 N O2 -","- C81.998 H61.996 Cl3.996 N2 O4 -","2","1","","Seifert, Sabine; Schmidt, David; Würthner, Frank","A cross-coupling-annulation cascade from peri-dibromonaphthalimide to pseudo-rylene bisimides","Organic Chemistry Frontiers","2016","3","11","1435","","10.1039/C6QO00421K","","","1.54178","CuKα","","0.0802","0.0737","","","0.2179","0.2253","","","","","","1.035","","","","has coordinates,has disorder","235081","2020-10-21","18:00:00",""
"1553513","13.3641","0.0012","15.796","0.0014","14.8901","0.0013","90","","112.839","0.002","90","","2896.9","0.4","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C79 H66 Cl2 N2 O4 -","- C79 H66 Cl2 N2 O4 -","- C158 H132 Cl4 N4 O8 -","2","0.5","","Seifert, Sabine; Schmidt, David; Würthner, Frank","A cross-coupling-annulation cascade from peri-dibromonaphthalimide to pseudo-rylene bisimides","Organic Chemistry Frontiers","2016","3","11","1435","","10.1039/C6QO00421K","","","0.71073","MoKα","","0.0651","0.0494","","","0.1334","0.1459","","","","","","1.035","","","","has coordinates,has disorder","235081","2020-10-21","18:00:00",""
"1553514","9.2961","0.0002","10.1519","0.0002","20.823","0.0005","90","","102.267","0.001","90","","1920.26","0.07","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C24 H20 O2 S -","- C24 H20 O2 S -","- C96 H80 O8 S4 -","4","1","","Fu, Rong; Hao, Wen-Juan; Wu, Ya-Nan; Wang, Nan-Nan; Tu, Shu-Jiang; Li, Guigen; Jiang, Bo","Sulfonyl radical-enabled 6-endo-trig cyclization for regiospecific synthesis of unsymmetrical diaryl sulfones","Organic Chemistry Frontiers","2016","3","11","1452","","10.1039/C6QO00422A","","","0.71073","MoKα","","0.0569","0.0445","","","0.1197","0.1306","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553515","7.0521","0.0006","28.03","0.002","10.4649","0.0008","90","","100.069","0.001","90","","2036.7","0.3","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C27 H20 O2 S -","- C27 H20 O2 S -","- C108 H80 O8 S4 -","4","1","","Fu, Rong; Hao, Wen-Juan; Wu, Ya-Nan; Wang, Nan-Nan; Tu, Shu-Jiang; Li, Guigen; Jiang, Bo","Sulfonyl radical-enabled 6-endo-trig cyclization for regiospecific synthesis of unsymmetrical diaryl sulfones","Organic Chemistry Frontiers","2016","3","11","1452","","10.1039/C6QO00422A","","","0.71073","MoKα","","0.1316","0.0684","","","0.1143","0.1437","","","","","","0.999","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553516","15.4186","0.0013","11.3388","0.0008","16.9081","0.0014","90","","107.55","0.009","90","","2818.4","0.4","180.01","0.1","180.01","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C33 H35 N O4 S -","- C33 H35 N O4 S -","- C132 H140 N4 O16 S4 -","4","1","","Lv, Leiyang; Bai, Xiaohui; Yan, Xiaoyu; Li, Zhiping","Iron-catalyzed decarbonylation initiated [2 + 2 + m] annulation of benzene-linked 1,n-enynes with aliphatic aldehydes","Organic Chemistry Frontiers","2016","3","11","1509","","10.1039/C6QO00429F","","","0.71073","MoKα","","0.1051","0.0534","","","0.1076","0.1358","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553517","8.3151","0.0007","8.625","0.0007","18.7838","0.0016","99.74","0.001","96.686","0.001","104.017","0.001","1270.61","0.18","294","2","294","2","","","","","","","","5","P -1","-P 1","2","","","","- C29 H26 N2 O5 S -","- C29 H26 N2 O5 S -","- C58 H52 N4 O10 S2 -","2","1","","Sharma, Pankaj; Kumar, Niggula Praveen; Krishna, Namballa Hari; Prasanna, Daasi; Sridhar, Balasubramanian; Shankaraiah, Nagula","Silver(i)-catalysed domino alkyne-annulation/Diels–Alder reaction: a mild synthetic approach to tetrahydrospiro[carbazole-4,3′-indoline] scaffolds","Organic Chemistry Frontiers","2016","3","11","1503","","10.1039/C6QO00430J","","","0.71073","MoKα","","0.061","0.0494","","","0.1373","0.1503","","","","","","1.016","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553518","8.849","0.005","10.773","0.006","17.758","0.009","90","","91.599","0.007","90","","1692.2","1.6","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C14 H17 F3 N2 O3 S -","- C14 H17 F3 N2 O3 S -","- C56 H68 F12 N8 O12 S4 -","4","1","","Li, Yuewen; Xiang, Yuanchao; Li, Zhiming; Wu, Jie","Direct vicinal difunctionalization of alkynes through trifluoromethylation and aminosulfonylation via insertion of sulfur dioxide under catalyst-free conditions","Organic Chemistry Frontiers","2016","3","11","1493","","10.1039/C6QO00434B","","","0.71073","MoKα","","0.0939","0.068","","","0.1757","0.1857","","","","","","0.963","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553519","11.5593","0.0003","14.0068","0.0003","17.8914","0.0004","90","","90","","90","","2896.78","0.12","130","","130","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C36 H32 F2 N2 O2 -","- C36 H32 F2 N2 O2 -","- C144 H128 F8 N8 O8 -","4","1","","Zhu, Zi-Qi; Yin, Lei; Wang, Yang; Shen, Yang; Li, Can; Mei, Guang-Jian; Shi, Feng","Diastereo- and enantioselective construction of biologically important pyrrolo[1,2-a]indole scaffolds via catalytic asymmetric [3 + 2] cyclodimerizations of 3-alkyl-2-vinylindoles","Organic Chemistry Frontiers","2017","4","1","57","","10.1039/C6QO00446F","","","1.54178","CuKα","","0.0409","0.0361","","","0.1029","0.1084","","","","","","0.821","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553520","19.661","0.013","10.71","0.007","17.118","0.011","90","","97.306","0.011","90","","3575","4","130","","130","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C44 H50 N2 -","- C44 H50 N2 -","- C176 H200 N8 -","4","1","","Zhu, Zi-Qi; Yin, Lei; Wang, Yang; Shen, Yang; Li, Can; Mei, Guang-Jian; Shi, Feng","Diastereo- and enantioselective construction of biologically important pyrrolo[1,2-a]indole scaffolds via catalytic asymmetric [3 + 2] cyclodimerizations of 3-alkyl-2-vinylindoles","Organic Chemistry Frontiers","2017","4","1","57","","10.1039/C6QO00446F","","","0.71073","MoKα","","0.1483","0.0877","","","0.1849","0.221","","","","","","1.07","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553521","6.9478","0.0005","9.1969","0.0005","11.8012","0.001","82.206","0.006","81.643","0.007","75.22","0.006","717.55","0.09","100","2","100","2","","","","","","","","4","P -1","-P 1","2","(Ph-CH3)-S-[Ph(OCH3)3]","","","- C16 H18 O3 S -","- C16 H18 O3 S -","- C32 H36 O6 S2 -","2","1","","Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang","Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent","Organic Chemistry Frontiers","2017","4","1","31","","10.1039/C6QO00451B","","","1.54184","CuKα","","0.0488","0.0374","","","0.0923","0.0976","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553522","7.68603","0.00016","23.9176","0.0004","7.76261","0.00017","90","","111.053","0.003","90","","1331.76","0.05","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","(Ph-CH3)-S-(Ph-(OCH3)2)","","","- C15 H16 O2 S -","- C15 H16 O2 S -","- C60 H64 O8 S4 -","4","1","","Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang","Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent","Organic Chemistry Frontiers","2017","4","1","31","","10.1039/C6QO00451B","","","1.54184","CuKα","","0.0309","0.0287","","","0.0772","0.0786","","","","","","1.07","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553523","5.7042","0.0003","25.743","0.002","7.8069","0.0004","90","","94.59","0.005","90","","1142.71","0.12","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","(Ph-CH3)-S-(Ph-CN)","","","- C14 H11 N S -","- C14 H11 N S -","- C56 H44 N4 S4 -","4","1","","Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang","Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent","Organic Chemistry Frontiers","2017","4","1","31","","10.1039/C6QO00451B","","","0.71073","MoKα","","0.049","0.0426","","","0.0937","0.0967","","","","","","1.066","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553524","5.7958","0.0003","25.4544","0.0012","8.3123","0.0004","90","","93.626","0.004","90","","1223.85","0.1","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","(Ph-CH3)-S-(PhCOCH3)","","","- C15 H14 O S -","- C15 H14 O S -","- C60 H56 O4 S4 -","4","1","","Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang","Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent","Organic Chemistry Frontiers","2017","4","1","31","","10.1039/C6QO00451B","","","0.71073","MoKα","","0.0442","0.0359","","","0.0856","0.0903","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553525","5.611","0.0003","25.6833","0.0013","8.991","0.0004","90","","98.982","0.004","90","","1279.8","0.11","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","(Ph-CH3)-S-(PhCOOCH3)","","","- C15 H14 O2 S -","- C15 H14 O2 S -","- C60 H56 O8 S4 -","4","1","","Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang","Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent","Organic Chemistry Frontiers","2017","4","1","31","","10.1039/C6QO00451B","","","1.54184","CuKα","","0.0725","0.0551","","","0.1475","0.1531","","","","","","1.18","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553526","5.67633","0.00018","26.8781","0.0008","7.7875","0.0002","90","","95.042","0.003","90","","1183.53","0.06","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","(Ph-CN)-S-(PhOCH3)","","","- C14 H11 N O S -","- C14 H11 N O S -","- C56 H44 N4 O4 S4 -","4","1","","Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang","Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent","Organic Chemistry Frontiers","2017","4","1","31","","10.1039/C6QO00451B","","","1.54184","CuKα","","0.0356","0.0332","","","0.0883","0.0899","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553527","7.8232","0.0004","11.6428","0.0005","14.5818","0.0007","84.863","0.004","83.654","0.004","73.557","0.004","1263.68","0.11","100","2","100","2","","","","","","","","4","P -1","-P 1","2","(Ph-CN)-S-S-(Ph-CN)","","","- C14 H8 N2 S2 -","- C14 H8 N2 S2 -","- C56 H32 N8 S8 -","4","2","","Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang","Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent","Organic Chemistry Frontiers","2017","4","1","31","","10.1039/C6QO00451B","","","1.54184","CuKα","","0.0784","0.0691","","","0.2121","0.2166","","","","","","1.119","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553528","12.7034","0.0011","11.6077","0.001","28.683","0.005","90","","90","","90","","4229.5","0.9","102.1","","102.1","","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C22 H32 O2 Si -","- C22 H32 O2 Si -","- C176 H256 O16 Si8 -","8","1","","Liu, Zhen; Xia, Ying; Feng, Sheng; Zhang, Yan; Wang, Jianbo","Rh(i)-Catalyzed coupling of 2-bromoethyl aryldiazoacetates with tertiary propargyl alcohols through carbene migratory insertion","Organic Chemistry Frontiers","2016","3","12","1691","","10.1039/C6QO00453A","","","0.71073","MoKα","","0.1939","0.1532","","","0.3787","0.4104","","","","","","1.06","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553529","9.3034","0.0001","9.6541","0.0002","11.6687","0.0008","101.875","0.007","106.962","0.008","96.397","0.007","964.39","0.09","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C24 H19 N O3 -","- C24 H19 N O3 -","- C48 H38 N2 O6 -","2","1","","Duan, Jindian; Cheng, Yuyu; Li, Rou; Li, Pengfei","Synthesis of spiro[indane-1,3-dione-1-pyrrolines] via copper-catalyzed heteroannulation of ketoxime acetates with 2-arylideneindane-1,3-diones","Organic Chemistry Frontiers","2016","3","12","1614","","10.1039/C6QO00454G","","","1.54187","CuKα","","0.0565","0.0529","","","0.1351","0.1403","","","","","","1.094","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553530","7.455","0.0005","11.3624","0.0007","18.4877","0.0013","90","","92.585","0.006","90","","1564.44","0.18","273.77","0.1","273.77","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C35 H53 N O3 -","- C35 H53 N O3 -","- C70 H106 N2 O6 -","2","1","","Li, Zheng-Yu; Qi, Feng-Ming; Zhi, De-Juan; Hu, Qiao-Ling; Liu, Ying-Hong; Zhang, Zhan-Xin; Fei, Dong-Qing","A novel spirocyclic triterpenoid and a new taraxerane triterpenoid from Teucrium viscidum","Organic Chemistry Frontiers","2017","4","1","42","","10.1039/C6QO00460A","","x-ray","1.54184","CuKα","","0.0628","0.0567","","","0.1539","0.1616","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553531","6.52391","0.0001","12.9427","0.0002","31.7963","0.0006","90","","90","","90","","2684.78","0.08","154.89","0.1","293","","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C30 H50 O3 -","- C30 H50 O3 -","- C120 H200 O12 -","4","1","","Li, Zheng-Yu; Qi, Feng-Ming; Zhi, De-Juan; Hu, Qiao-Ling; Liu, Ying-Hong; Zhang, Zhan-Xin; Fei, Dong-Qing","A novel spirocyclic triterpenoid and a new taraxerane triterpenoid from Teucrium viscidum","Organic Chemistry Frontiers","2017","4","1","42","","10.1039/C6QO00460A","","x-ray","1.54184","CuKα","","0.0436","0.0381","","","0.0965","0.1006","","","","","","1.023","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553532","11.1348","0.0009","10.8734","0.001","24.741","0.002","90","","90","","90","","2995.5","0.4","293.26","0.1","293.26","0.1","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C18 H16 O S -","- C18 H16 O S -","- C144 H128 O8 S8 -","8","1","","An, Zhenyu; She, Yue; Yang, Xiaodong; Pang, Xiaobo; Yan, Rulong","Metal-free synthesis of 3-methylthiofurans from homopropargylic alcohols and DMSO via a tandem sulfenylation/cyclization reaction in a one-pot manner","Organic Chemistry Frontiers","2016","3","12","1746","","10.1039/C6QO00462H","","x-ray","0.71073","MoKα","","0.2039","0.0674","","","0.1267","0.1889","","","","","","0.926","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553533","9.2943","0.0019","18.714","0.004","20.557","0.004","90","","95.79","0.03","90","","3557.3","1.3","173.15","","173.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H21 N O -","- C24 H21 N O -","- C192 H168 N8 O8 -","8","2","","Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua","Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling","Organic Chemistry Frontiers","2016","3","12","1668","","10.1039/C6QO00469E","","","0.71073","MoKα","","0.0781","0.07","","","0.1381","0.1456","","","","","","1.038","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553534","11.335","0.002","7.4991","0.0015","37.869","0.008","90","","90","","90","","3219","1.1","173.15","","173.15","","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C24 H19 N -","- C24 H19 N -","- C192 H152 N8 -","8","1","","Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua","Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling","Organic Chemistry Frontiers","2016","3","12","1668","","10.1039/C6QO00469E","","","0.71073","MoKα","","0.0799","0.0693","","","0.1375","0.1441","","","","","","1.172","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553535","10.641","0.002","10.978","0.002","17.744","0.003","100.04","0.03","106.43","0.03","93.41","0.03","1944.7","0.7","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C42 H34 Cl7 N3 Pd -","- C42 H34 Cl7 N3 Pd -","- C84 H68 Cl14 N6 Pd2 -","2","1","","Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua","Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling","Organic Chemistry Frontiers","2016","3","12","1668","","10.1039/C6QO00469E","","","0.71073","MoKα","","0.0811","0.0765","","","0.2212","0.2352","","","","","","1.024","","","","has coordinates","235107","2020-10-21","18:00:00",""
"1553536","36.49","0.005","36.49","0.005","21.305","0.004","90","","90","","120","","24567","7","173.15","","173.15","","","","","","","","","5","R -3 :H","-R 3","148","","","","- C44 H40 Cl N3 Pd -","- C44 H40 Cl N3 Pd -","- C792 H720 Cl18 N54 Pd18 -","18","1","","Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua","Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling","Organic Chemistry Frontiers","2016","3","12","1668","","10.1039/C6QO00469E","","","0.71073","MoKα","","0.0755","0.0652","","","0.2056","0.2162","","","","","","1.072","","","","has coordinates,has disorder","235107","2020-10-21","18:00:00",""
"1553537","11.611","0.002","19.188","0.004","13.466","0.003","90","","113.15","0.03","90","","2758.5","1.1","173.15","","173.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C33 H25 Cl3 N2 O Pd -","- C33 H25 Cl3 N2 O Pd -","- C132 H100 Cl12 N8 O4 Pd4 -","4","1","","Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua","Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling","Organic Chemistry Frontiers","2016","3","12","1668","","10.1039/C6QO00469E","","","0.71073","MoKα","","0.0392","0.0369","","","0.0834","0.085","","","","","","1.107","","","","has coordinates","235107","2020-10-21","18:00:00",""
"1553538","14.187","0.003","12.38","0.003","14.674","0.003","90","","92.59","0.03","90","","2574.6","1","173.15","","173.15","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C34 H27 Cl N2 O Pd -","- C34 H27 Cl N2 O Pd -","- C136 H108 Cl4 N8 O4 Pd4 -","4","1","","Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua","Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling","Organic Chemistry Frontiers","2016","3","12","1668","","10.1039/C6QO00469E","","","0.71073","MoKα","","0.0286","0.0281","","","0.0705","0.0708","","","","","","1.085","","","","has coordinates","235107","2020-10-21","18:00:00",""
"1553539","11.91","0.002","32.793","0.007","9.4655","0.0019","90","","113.37","0.03","90","","3393.6","1.4","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C40 H33 N3 O0 -","- C40 H33 N3 -","- C160 H132 N12 -","4","1","","Mahmood, Qaiser; Yue, Erlin; Zhang, Wenjuan; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua","Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling","Organic Chemistry Frontiers","2016","3","12","1668","","10.1039/C6QO00469E","","","0.71073","MoKα","","0.0814","0.0633","","","0.1406","0.151","","","","","","1.047","","","","has coordinates","235107","2020-10-21","18:00:00",""
"1553540","12.0255","0.0007","18.091","0.0012","10.1121","0.0007","90","","105.935","0.002","90","","2115.4","0.2","100","1","100","1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C50 H50 N2 O6 S2 -","- C50 H50 N2 O6 S2 -","- C100 H100 N4 O12 S4 -","2","0.5","","Michelet, Bastien; Tang, Shun; Thiery, Guillaume; Monot, Julien; Li, Huijing; Guillot, Régis; Bour, Christophe; Gandon, Vincent","Catalytic applications of [IPr·GaX2][SbF6] and related species","Organic Chemistry Frontiers","2016","3","12","1603","","10.1039/C6QO00470A","","x-ray","0.71073","MoKα","","0.0786","0.0468","","","0.1069","0.1223","","","","","","1.023","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553541","7.6825","0.0003","17.5861","0.0008","22.9639","0.0011","90","","90","","90","","3102.5","0.2","100","1","100","1","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C18 H22 O4 -","- C18 H22 O4 -","- C144 H176 O32 -","8","1","","Michelet, Bastien; Tang, Shun; Thiery, Guillaume; Monot, Julien; Li, Huijing; Guillot, Régis; Bour, Christophe; Gandon, Vincent","Catalytic applications of [IPr·GaX2][SbF6] and related species","Organic Chemistry Frontiers","2016","3","12","1603","","10.1039/C6QO00470A","","x-ray","0.71073","MoKα","","0.0669","0.0581","","","0.1538","0.1604","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553542","6.0149","0.0004","13.4117","0.0009","18.2153","0.0012","90","","91.601","0.002","90","","1468.86","0.17","138","2","138","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H13 F S -","- C20 H13 F S -","- C80 H52 F4 S4 -","4","1","","Wang, Xiaoming; Gensch, Tobias; Glorius, Frank","Highly selective synthesis of 6-substituted benzothiophenes by Sc(OTf)3-catalyzed intermolecular cyclization and sulfur migration","Organic Chemistry Frontiers","2016","3","12","1619","","10.1039/C6QO00477F","","","0.71073","MoKα","","0.0566","0.0397","","","0.08","0.0861","","","","","","1.076","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553543","7.348","0.0009","22.781","0.003","11.236","0.0015","90","","101.092","0.013","90","","1845.7","0.4","293","2","293.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H21 N O2 -","- C22 H21 N O2 -","- C88 H84 N4 O8 -","4","1","","Yu, Wenlong; Zhang, Wei; Liu, Yue; Liu, Zhanxiang; Zhang, Yuhong","Cobalt(iii)-catalyzed cross-coupling of enamides with allyl acetates/maleimides","Organic Chemistry Frontiers","2017","4","1","77","","10.1039/C6QO00479B","","","0.71073","MoKα","","0.1248","0.0677","","","0.1801","0.2255","","","","","","1.024","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553544","9.3103","0.0008","4.8793","0.0005","30.741","0.003","90","","96.596","0.008","90","","1387.3","0.2","293","2","293.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H16 N2 O3 -","- C15 H16 N2 O3 -","- C60 H64 N8 O12 -","4","1","","Yu, Wenlong; Zhang, Wei; Liu, Yue; Liu, Zhanxiang; Zhang, Yuhong","Cobalt(iii)-catalyzed cross-coupling of enamides with allyl acetates/maleimides","Organic Chemistry Frontiers","2017","4","1","77","","10.1039/C6QO00479B","","","0.71073","MoKα","","0.0875","0.0562","","","0.1248","0.1436","","","","","","1.043","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553545","33.922","0.006","33.922","0.006","11.008","0.002","90","","90","","120","","10970","3","173","2","173","2","","","","","","","","5","R 3 c :H","R 3 -2""c","161","","","","- C25 H21 N O2 S -","- C25 H21 N O2 S -","- C450 H378 N18 O36 S18 -","18","1","","Gong, Xinxing; Li, Guangming; Wu, Jie","Synthesis of polycyclic sultams via a palladium-catalyzed reaction of 1-bromo-2-(cyclopropylidenemethyl)benzenes with 2-alkynylbenzenesulfonamides","Organic Chemistry Frontiers","2017","4","1","14","","10.1039/C6QO00480F","","","0.71073","MoKα","","0.0953","0.062","","","0.1336","0.1442","","","","","","0.925","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553546","16.1503","0.0018","8.3426","0.0009","18.1574","0.0019","90","","108.184","0.002","90","","2324.3","0.4","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C24 H28 O8 -","- C24 H28 O8 -","- C96 H112 O32 -","4","1","","Cao, Tao; Ma, Shengming","Nickel-catalyzed alkyl-zincation and carboxylation of diynes","Organic Chemistry Frontiers","2016","3","12","1711","","10.1039/C6QO00484A","","","0.71073","MoKα","","0.0716","0.057","","","0.1473","0.1612","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553547","5.3248","0.0004","17.2473","0.001","7.6729","0.0006","90","","96.167","0.006","90","","700.59","0.09","123","","123","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C18 H12 Br2 -","- C18 H12 Br2 -","- C36 H24 Br4 -","2","0.5","","Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.","Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap","Organic Chemistry Frontiers","2017","4","5","658","","10.1039/C6QO00487C","","","0.71073","MoKα","","0.0461","0.0231","","","0.0494","0.0525","","","","","","0.84","","","","has coordinates","235123","2020-10-21","18:00:00",""
"1553548","6.6723","0.0015","8.653","0.002","15.099","0.003","90","","111.66","0.01","90","","810.2","0.3","123","","123.15","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C20 H16 Br2 -","- C20 H16 Br2 -","- C40 H32 Br4 -","2","0.5","","Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.","Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap","Organic Chemistry Frontiers","2017","4","5","658","","10.1039/C6QO00487C","","","0.71073","MoKα","","0.0845","0.0628","","","0.1605","0.1831","","","","","","1.076","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553549","21.802","0.003","4.9336","0.0005","18.875","0.003","90","","90.188","0.013","90","","2030.2","0.5","123","","123","","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C28 H16 Br2 -","- C28 H16 Br2 -","- C112 H64 Br8 -","4","0.5","","Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.","Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap","Organic Chemistry Frontiers","2017","4","5","658","","10.1039/C6QO00487C","","","0.71073","MoKα","","0.1474","0.0681","","","0.157","0.1785","","","","","","0.831","","","","has coordinates,has disorder","235123","2020-10-21","18:00:00",""
"1553550","10.0648","0.0005","11.6684","0.0006","12.2462","0.0006","77.981","0.002","86.017","0.002","79.287","0.002","1381.44","0.12","100","","100","","","","","","","","","3","P -1","-P 1","2","","jm192.1","","- C36 H32 Br2 -","- C36 H32 Br2 -","- C72 H64 Br4 -","2","1","","Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.","Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap","Organic Chemistry Frontiers","2017","4","5","658","","10.1039/C6QO00487C","","","0.71073","MoKα","","0.0695","0.0508","","","0.1308","0.1396","","","","","","1.07","","","","has coordinates,has disorder","235123","2020-10-21","18:00:00",""
"1553551","11.131","0.0004","10.249","0.0003","11.763","0.0004","90","","101.301","0.002","90","","1315.92","0.08","100","2","100","","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C34 H28 Br2 -","- C34 H28 Br2 -","- C68 H56 Br4 -","2","0.5","","Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.","Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap","Organic Chemistry Frontiers","2017","4","5","658","","10.1039/C6QO00487C","","x-ray","1.54178","CuKα","","0.1028","0.0691","","","0.1474","0.1648","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553552","10.8252","0.0008","13.5794","0.001","14.2122","0.001","114.377","0.004","91.316","0.005","95.604","0.004","1889.2","0.2","100","","100","","","","","","","","","2","P -1","-P 1","2","","jm245.3b","","- C50 H38 -","- C50 H38 -","- C100 H76 -","2","1","","Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.","Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap","Organic Chemistry Frontiers","2017","4","5","658","","10.1039/C6QO00487C","","x-ray","1.54178","CuKα","","0.1377","0.1086","","","0.259","0.2735","","","","","","1.09","","","","has coordinates","235123","2020-10-21","18:00:00",""
"1553553","5.828","0.0006","8.2327","0.0008","16.8844","0.0016","90","","98.492","0.003","90","","801.23","0.14","296","2","296","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C19 H17 Cl O -","- C19 H17 Cl O -","- C38 H34 Cl2 O2 -","2","1","","Luo, Hongwen; Yu, Yihua; Ma, Shengming","Suzuki coupling for preparation of allenes – ligand effects and chirality transfer","Organic Chemistry Frontiers","2016","3","12","1705","","10.1039/C6QO00489J","","","0.71073","MoKα","","0.0341","0.0314","","","0.0819","0.0839","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553554","20.3","0.005","5.882","0.005","27.651","0.005","90","0.002","94.075","0.003","90","0.001","3293","3","100","2","100","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","iodo methoxy phenyl methyl phenylselenophene","3-iodo-5-(methoxy(phenyl)methyl)-2-phenylselenophene","","- C18 H15 I O Se -","- C18 H15 I O Se -","- C144 H120 I8 O8 Se8 -","8","1","","Pistoia, Renan P.; Roehrs, Juliano A.; Back, Davi F.; Zeni, Gilson","Iodine-mediated regioselective 5-endo-dig electrophilic cyclization reaction of selenoenynes: synthesis of selenophene derivatives","Organic Chemistry Frontiers","2017","4","2","277","","10.1039/C6QO00491A","","","0.71073","MoKα","","0.0854","0.046","","","0.0627","0.0699","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553555","19.0809","0.0007","5.7136","0.0002","17.2112","0.0006","90","","100.175","0.001","90","","1846.87","0.11","100","2","100","2","","","","","","","","5","P 1 2/c 1","-P 2yc","13","3-iodo-5-isopropoxy-2,4-diphenylselenophene","3-iodo-5-isopropoxy-2,4-diphenylselenophene","","- C20 H19 I O Se -","- C20 H19 I O Se -","- C80 H76 I4 O4 Se4 -","4","1","","Pistoia, Renan P.; Roehrs, Juliano A.; Back, Davi F.; Zeni, Gilson","Iodine-mediated regioselective 5-endo-dig electrophilic cyclization reaction of selenoenynes: synthesis of selenophene derivatives","Organic Chemistry Frontiers","2017","4","2","277","","10.1039/C6QO00491A","","","0.71073","MoKα","","0.0243","0.0207","","","0.0482","0.0495","","","","","","1.07","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553556","11.4186","0.0019","9.7011","0.0017","13.152","0.002","90","","92.473","0.004","90","","1455.5","0.4","293","2","293","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C29 H25 Cl N2 O8 S -","- C29 H25 Cl N2 O8 S -","- C58 H50 Cl2 N4 O16 S2 -","2","1","","He, Fu-Sheng; Li, Cong-Shan; Deng, Hua; Zheng, Xing; Yang, Zhong-Tao; Deng, Wei-Ping","The facile and stereoselective synthesis of pyrrolidine β-amino acids via copper(i)-catalyzed asymmetric 1,3-dipolar cycloaddition","Organic Chemistry Frontiers","2017","4","1","52","","10.1039/C6QO00512H","","","0.71073","MoKα","","0.0552","0.0461","","","0.1112","0.1179","","","","","","1","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553557","14.3717","0.0006","5.917","0.0002","21.4597","0.0009","90","","90","","90","","1824.88","0.12","300","","300","","","","","","","","","3","P n 21 a","P -2ac -2n","33","","","","- C25 H18 O2 -","- C25 H18 O2 -","- C100 H72 O8 -","4","1","","Sreenivasulu, Chinnabattigalla; Gopi Krishna Reddy, A.; Satyanarayana, G.","Oxidative annulations triggered by a simple Lewis acid: facile synthesis of benzofurans","Organic Chemistry Frontiers","2017","4","6","972","","10.1039/C6QO00531D","","","1.54184","CuKα","","0.1073","0.0671","","","0.1467","0.1967","","","","","","1.0503","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553558","7.9447","0.0003","10.3826","0.0004","17.0108","0.0007","90","","90","","90","","1403.16","0.1","300","","300","","","","","","","","Synthesized compound","3","P 21 21 21","P 2ac 2ab","19","","2,3-diphenylbenzofuran","","- C20 H14 O -","- C20 H14 O -","- C80 H56 O4 -","4","1","","Sreenivasulu, Chinnabattigalla; Gopi Krishna Reddy, A.; Satyanarayana, G.","Oxidative annulations triggered by a simple Lewis acid: facile synthesis of benzofurans","Organic Chemistry Frontiers","2017","4","6","972","","10.1039/C6QO00531D","","","1.54184","CuKα","","0.0579","0.0502","","","0.1222","0.1338","","","","","","1.0451","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553559","21.226","0.003","8.2493","0.0007","16.985","0.002","90","","109.61","0.014","90","","2801.6","0.6","294.74","0.1","294.74","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C27 H31 N O7 S3 -","- C27 H31 N O7 S3 -","- C108 H124 N4 O28 S12 -","4","1","","Chen, Fei; Zhou, Neng-Neng; Zhan, Jun-Long; Han, Bing; Yu, Wei","tert-Butyl nitrite-mediated vicinal sulfoximation of alkenes with sulfinic acids: a highly efficient approach toward α-sulfonyl ketoximes","Organic Chemistry Frontiers","2017","4","1","135","","10.1039/C6QO00535G","","","0.71073","MoKα","","0.1316","0.0909","","","0.2444","0.2645","","","","","","1.073","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553560","25.961","0.0017","5.793","0.0003","22.2512","0.0017","90","","114.088","0.009","90","","3055","0.4","293.64","0.1","293.64","0.1","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C15 H21 N O3 S -","- C15 H21 N O3 S -","- C120 H168 N8 O24 S8 -","8","1","","Chen, Fei; Zhou, Neng-Neng; Zhan, Jun-Long; Han, Bing; Yu, Wei","tert-Butyl nitrite-mediated vicinal sulfoximation of alkenes with sulfinic acids: a highly efficient approach toward α-sulfonyl ketoximes","Organic Chemistry Frontiers","2017","4","1","135","","10.1039/C6QO00535G","","x-ray","0.71073","MoKα","","0.1117","0.0626","","","0.1415","0.1744","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553561","6.52","0.006","8.149","0.007","18.175","0.015","102.278","0.014","95.21","0.015","97.731","0.016","927.9","1.4","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C18 H16 F3 N O2 S2 -","- C18 H16 F3 N O2 S2 -","- C36 H32 F6 N2 O4 S4 -","2","1","","Chen, Min-Tao; Tang, Xiang-Ying; Shi, Min","A facile approach for the trifluoromethylthiolation of methylenecyclopropanes","Organic Chemistry Frontiers","2017","4","1","86","","10.1039/C6QO00536E","","","0.71073","MoKα","","0.1295","0.0942","","","0.2386","0.2635","","","","","","1.05","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553562","13.451","0.004","14.313","0.004","15.248","0.004","86.714","0.004","63.827","0.003","90.014","0.004","2629.2","1.3","110","","110","","","","","","","","","4","P -1","-P 1","2","","","","- C17 H15 N O2 -","- C17 H15 N O2 -","- C136 H120 N8 O16 -","8","4","","Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai","Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles","Organic Chemistry Frontiers","2017","4","1","124","","10.1039/C6QO00541A","","","0.71073","MoKα","","0.0847","0.0536","","","0.1215","0.1378","","","","","","1.039","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553563","7.3875","0.0004","11.6702","0.0006","13.4944","0.0007","64.647","0.001","82.911","0.001","77.69","0.001","1026.5","0.09","100.01","","100.01","","","","","","","","","5","P -1","-P 1","2","","","","- C26 H20 Cl N O3 -","- C26 H20 Cl N O3 -","- C52 H40 Cl2 N2 O6 -","2","1","","Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai","Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles","Organic Chemistry Frontiers","2017","4","1","124","","10.1039/C6QO00541A","","","0.71073","MoKα","","0.0347","0.0314","","","0.0892","0.0913","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553564","8.5455","0.0004","12.047","0.0006","12.1501","0.0006","60.733","0.001","81.883","0.002","87.112","0.002","1079.97","0.09","100.01","","100.01","","","","","","","","","5","P -1","-P 1","2","","","","- C23 H24 N2 O6 S -","- C23 H24 N2 O6 S -","- C46 H48 N4 O12 S2 -","2","1","","Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai","Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles","Organic Chemistry Frontiers","2017","4","1","124","","10.1039/C6QO00541A","","","0.71073","MoKα","","0.0552","0.0474","","","0.1229","0.1296","","","","","","1.069","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553565","9.3265","0.001","9.7095","0.0009","23.593","0.002","78.225","0.008","84.998","0.008","75.52","0.008","2023.6","0.3","193","2","193","2","","","","","","","","4","P -1","-P 1","2","","","","- C44 H52 N4 S4 -","- C44 H52 N4 S4 -","- C88 H104 N8 S8 -","2","1","","Xia, Debin; Keerthi, Ashok; An, Cunbin; Baumgarten, Martin","Synthesis of a quinoidal dithieno[2,3-d;2′,3′-d]benzo[2,1-b;3,4-b′]-dithiophene based open-shell singlet biradicaloid","Organic Chemistry Frontiers","2017","4","1","18","","10.1039/C6QO00543H","","","1.54178","CuKα","","0.1924","0.0676","","","0.1475","0.2042","","","","","","0.802","","","","has coordinates","235142","2020-10-21","18:00:00",""
"1553566","8.101","0.0016","19.041","0.004","13.693","0.003","90","","107.19","0.03","90","","2017.8","0.8","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H21 N O8 -","- C20 H21 N O8 -","- C80 H84 N4 O32 -","4","1","","Zhang, Li; Zhang, Beichen; Jiang, Teng; Lu, Tao; Zhou, Qingfa","Synthesis of tricyclic 3-hydroxyisoindolin-1-ones via triethylamine-catalyzed domino reactions of electron-deficient alkynes with phthalimidomalonate derivatives","Organic Chemistry Frontiers","2017","4","1","119","","10.1039/C6QO00544F","","","0.71073","MoKα","","0.1304","0.0679","","","0.1552","0.1807","","","","","","1.008","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553567","11.366","0.004","11.305","0.004","14.788","0.006","90","","110.536","0.006","90","","1779.4","1.1","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C22 H16 Cl N O2 -","- C22 H16 Cl N O2 -","- C88 H64 Cl4 N4 O8 -","4","1","","Zhu, Chao-Qun; Deng, Zhuo-Fei; Zhang, Yahong; Wang, You-Qing","Synthesis of 4-substituted 3-(2-hydroxyphenyl)-quinolines through an unexpected iron(iii) chloride promoted reaction of cyclic imine dibenzo[b,f][1,4]oxazepines with alkynes","Organic Chemistry Frontiers","2017","4","2","196","","10.1039/C6QO00545D","","","0.71073","MoKα","","0.0485","0.0359","","","0.11","0.1195","","","","","","0.973","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553568","8.902","0.006","13.209","0.009","12.059","0.008","90","","99.65","0.007","90","","1397.9","1.6","296","2","296","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C33 H30 N4 O3 -","- C33 H30 N4 O3 -","- C66 H60 N8 O6 -","2","1","","Cheng, Cang; Lu, Xuehe; Ge, Luo; Chen, Jie; Cao, Weiguo; Wu, Xiaoyu; Zhao, Gang","Effective asymmetric vinylogous Mannich reaction of isatin imines with α,α-dicyanoolefins in the presence of a simple chiral amide phosphonium bifunctional phase transfer catalyst","Organic Chemistry Frontiers","2017","4","1","101","","10.1039/C6QO00546B","","","0.71073","MoKα","","0.0389","0.0335","","","0.0782","0.0823","","","","","","1.051","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553569","9.662","0.004","12.286","0.006","24.441","0.011","90","","90","","90","","2901","2","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C31 H27 Br N4 O3 -","- C31 H27 Br N4 O3 -","- C124 H108 Br4 N16 O12 -","4","1","","Cheng, Cang; Lu, Xuehe; Ge, Luo; Chen, Jie; Cao, Weiguo; Wu, Xiaoyu; Zhao, Gang","Effective asymmetric vinylogous Mannich reaction of isatin imines with α,α-dicyanoolefins in the presence of a simple chiral amide phosphonium bifunctional phase transfer catalyst","Organic Chemistry Frontiers","2017","4","1","101","","10.1039/C6QO00546B","","","0.71073","MoKα","","0.0536","0.0363","","","0.0791","0.0854","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553570","8.4091","0.0001","8.4091","0.0001","29.3175","0.0006","90","","90","","90","","2073.13","0.05","293","2","293","2","","","","","","","","4","P 41","P 4w","76","","","","- C25 H23 N O3 -","- C25 H23 N O3 -","- C100 H92 N4 O12 -","4","1","","Xu, Meng-Meng; Wang, Hai-Qing; Wan, Ying; He, Guofeng; Yan, Jingjing; Zhang, Shu; Wang, Shu-Liang; Shi, Feng","Catalytic asymmetric substitution of ortho-hydroxybenzyl alcohols with tetronic acid-derived enamines: enantioselective synthesis of tetronic acid-derived diarylmethanes","Organic Chemistry Frontiers","2017","4","3","358","","10.1039/C6QO00549G","","","1.54178","CuKα","","0.0591","0.0574","","","0.1527","0.155","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553571","7.2915","0.0005","12.7983","0.001","15.9552","0.0009","90","","90","","90","","1488.92","0.18","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C15 H17 Cl N2 O3 -","- C15 H17 Cl N2 O3 -","- C60 H68 Cl4 N8 O12 -","4","1","","Peng, Xiao-Jiao; Ho, Yee Ann; Wang, Zhi-Peng; Shao, Pan-Lin; Zhao, Yu; He, Yun","Formal [3 + 2] cycloaddition of α-unsubstituted isocyanoacetates and methyleneindolinones: enantioselective synthesis of spirooxindoles","Organic Chemistry Frontiers","2017","4","1","81","","10.1039/C6QO00555A","","","0.71073","MoKα","","0.071","0.0481","","","0.095","0.1103","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553572","7.74798","0.00019","9.1129","0.0002","21.719","0.0005","90","","90","","90","","1533.5","0.06","293","2","293","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C15 H11 Cl F3 N3 O3 -","- C15 H11 Cl F3 N3 O3 -","- C60 H44 Cl4 F12 N12 O12 -","4","1","","Hao, Xin-Qi; Wang, Cong; Liu, Shuang-Liang; Wang, Xiao; Wang, Li; Gong, Jun-Fang; Song, Mao-Ping","Cobalt(ii)/(imidazoline–oxazoline)-catalyzed enantioselective Michael addition of 2-acetyl azaarenes to β-CF3-β-disubstituted nitroalkenes","Organic Chemistry Frontiers","2017","4","2","308","","10.1039/C6QO00562D","","x-ray","1.54184","CuKα","","0.039","0.0367","","","0.0913","0.094","","","","","","1.069","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553573","7.68","0.005","8.494","0.005","11.449","0.007","85.96","0.007","77.314","0.007","66.467","0.007","667.9","0.7","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C14 H13 N3 O S -","- C14 H13 N3 O S -","- C28 H26 N6 O2 S2 -","2","1","","Chen, Jichao; Wang, Tianyu; Wang, Tong; Lin, Aijun; Yao, Hequan; Xu, Jinyi","Copper-catalyzed C5-selective thio/selenocyanation of 8-aminoquinolines","Organic Chemistry Frontiers","2017","4","1","130","","10.1039/C6QO00590J","","","0.71073","MoKα","","0.0618","0.0458","","","0.1472","0.1661","","","","","","0.986","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553574","9.8916","0.0007","26.4389","0.0019","7.7778","0.0006","90","","90","","90","","2034.1","0.3","133","2","133","2","","","","","","","","6","P 21 21 2","P 2 2ab","18","","","","- C19 H23 Br N O3 P -","- C19 H23 Br N O3 P -","- C76 H92 Br4 N4 O12 P4 -","4","1","","Wang, Xubin; Wang, Xiaoming; Han, Zhaobin; Wang, Zheng; Ding, Kuiling","Palladium-catalyzed asymmetric allylic amination: enantioselective synthesis of chiral α-methylene substituted β-aminophosphonates","Organic Chemistry Frontiers","2017","4","2","271","","10.1039/C6QO00597G","","","0.71073","MoKα","","0.0629","0.0454","","","0.1077","0.1145","","","","","","1.092","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553575","21.2715","0.0003","21.2715","0.0003","64.3247","0.0014","90","","90","","90","","29105.4","0.9","293","2","293","2","","","","","","","","5","P 41 21 2","P 4abw 2nw","92","","azahelicene dimer","","- C153.47 H187.47 Cl4.41 N2 Si8 -","- C153.47 H187.479 Cl4.41 N2 Si8 -","- C1227.76 H1499.83 Cl35.28 N16 Si64 -","8","1","","Ushiyama, Ayako; Hiroto, Satoru; Yuasa, Junpei; Kawai, Tsuyoshi; Shinokubo, Hiroshi","Synthesis of a figure-eight azahelicene dimer with high emission and CPL properties","Organic Chemistry Frontiers","2017","4","5","664","","10.1039/C6QO00629A","","","0.71073","MoKα","","0.1947","0.1475","","","0.3637","0.4128","","","","","","1.172","","","","has coordinates,has disorder","235160","2020-10-21","18:00:00",""
"1553576","9.4639","0.0002","21.8249","0.0005","9.3192","0.0002","90","","104.752","0.003","90","","1861.42","0.07","150","0.1","150","0.1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C21 H21 Cl F N O2 -","- C21 H21 Cl F N O2 -","- C84 H84 Cl4 F4 N4 O8 -","4","1","","Li, Jianxiao; Hu, Weigao; Li, Chunsheng; Yang, Shaorong; Wu, Wanqing; Jiang, Huanfeng","Palladium-catalyzed cascade reaction of haloalkynes with unactivated alkenes for assembly of functionalized oxetanes","Organic Chemistry Frontiers","2017","4","3","373","","10.1039/C6QO00633G","","x-ray","1.54184","CuKα","","0.0476","0.0446","","","0.1182","0.1209","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553577","7.813","0.004","5.321","0.003","15.394","0.008","90","","91.594","0.008","90","","639.7","0.6","173.15","","173.15","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C15 H15 Br O2 -","- C15 H15 Br O2 -","- C30 H30 Br2 O4 -","2","1","","Li, Jing; Li, Zequan; Zhang, Xun; Xu, Bing; Shi, Yian","Catalytic enantioselective bromohydroxylation of aryl olefins with flexible functionalities","Organic Chemistry Frontiers","2017","4","6","1084","","10.1039/C6QO00636A","","","0.71073","MoKα","","0.0582","0.0575","","","0.1494","0.1501","","","","","","1.071","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553578","5.651","0.002","16.364","0.007","38.4918","0.0016","90","","90","","90","","3559","2","173.15","","173.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C11 H14 Br F O2 -","- C11 H14 Br F O2 -","- C132 H168 Br12 F12 O24 -","12","3","","Li, Jing; Li, Zequan; Zhang, Xun; Xu, Bing; Shi, Yian","Catalytic enantioselective bromohydroxylation of aryl olefins with flexible functionalities","Organic Chemistry Frontiers","2017","4","6","1084","","10.1039/C6QO00636A","","","0.71073","MoKα","","0.0824","0.0694","","","0.1075","0.1135","","","","","","1.159","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553579","10.248","0.006","14.634","0.007","11.146","0.005","90","","107.352","0.018","90","","1595.5","1.4","110","","110","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C17 H12 B F2 N5 O -","- C17 H12 B F2 N5 O -","- C68 H48 B4 F8 N20 O4 -","4","0.5","","Barbon, Stephanie M.; Novoa, Samantha; Bender, Desiree; Groom, Hilary; Luyt, Leonard G.; Gilroy, Joe B.","Copper-assisted azide‒alkyne cycloaddition chemistry as a tool for the production of emissive boron difluoride 3-cyanoformazanates","Organic Chemistry Frontiers","2017","4","2","178","","10.1039/C6QO00640J","","","0.71073","MoKα","","0.077","0.0428","","","0.0962","0.1107","","","","","","1.037","","","","has coordinates,has disorder","235166","2020-10-21","18:00:00",""
"1553580","7.3184","0.0002","13.4865","0.0003","17.4149","0.0004","101.672","0.002","94.139","0.002","101.918","0.002","1635.33","0.07","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C16 H10 Br2 Cl F3 -","- C16 H10 Br2 Cl F3 -","- C64 H40 Br8 Cl4 F12 -","4","2","","Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.","Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes","Organic Chemistry Frontiers","2017","4","2","255","","10.1039/C6QO00643D","","","1.54184","CuKα","","0.0611","0.0454","","","0.1445","0.1869","","","","","","1.067","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553581","7.8481","0.0005","10.5581","0.0007","12.2042","0.001","75.472","0.006","72.741","0.006","72.301","0.006","905.55","0.12","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C20 H20 Br F3 O -","- C20 H20 Br F3 O -","- C40 H40 Br2 F6 O2 -","2","1","","Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.","Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes","Organic Chemistry Frontiers","2017","4","2","255","","10.1039/C6QO00643D","","","1.54184","CuKα","","0.0414","0.0388","","","0.1066","0.1098","","","","","","1.022","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553582","8.3533","0.0005","9.4941","0.0004","12.1934","0.0007","100.216","0.004","97.306","0.005","100.289","0.004","923.7","0.09","105","8","105","8","","","","","","","","5","P -1","-P 1","2","","","","- C20 H20 Br F3 O2 -","- C20 H20 Br F3 O2 -","- C40 H40 Br2 F6 O4 -","2","1","","Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.","Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes","Organic Chemistry Frontiers","2017","4","2","255","","10.1039/C6QO00643D","","","0.7107","MoKα","","0.0345","0.0286","","","0.0627","0.0651","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553583","16.4974","0.0002","6.84171","0.0001","28.6498","0.0003","90","","90","","90","","3233.72","0.07","100","2","100","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C18 H15 Br2 F3 -","- C18 H15 Br2 F3 -","- C144 H120 Br16 F24 -","8","1","","Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.","Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes","Organic Chemistry Frontiers","2017","4","2","255","","10.1039/C6QO00643D","","","1.5418","CuKα","","0.0263","0.0232","","","0.0596","0.0612","","","","","","1.055","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553584","7.1399","0.0002","9.7404","0.0003","22.8361","0.0006","97.673","0.002","97.146","0.002","106.455","0.003","1487.32","0.08","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C16 H11 Br2 F3 -","- C16 H11 Br2 F3 -","- C64 H44 Br8 F12 -","4","2","","Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.","Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes","Organic Chemistry Frontiers","2017","4","2","255","","10.1039/C6QO00643D","","","1.54184","CuKα","","0.0498","0.0469","","","0.1234","0.1276","","","","","","1.057","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553585","22.8229","0.0015","7.4881","0.0004","16.5828","0.0011","90","","102.102","0.007","90","","2771","0.3","100","2","100","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C17 H12 Br F3 -","- C17 H12 Br F3 -","- C136 H96 Br8 F24 -","8","1","","Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.","Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes","Organic Chemistry Frontiers","2017","4","2","255","","10.1039/C6QO00643D","","","1.54184","CuKα","","0.0498","0.0379","","","0.0933","0.1027","","","","","","1.044","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553586","8.2233","0.0003","22.8182","0.0007","10.0565","0.0003","90","","109.447","0.004","90","","1779.36","0.11","100","2","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H17 Br Cl F3 -","- C19 H17 Br Cl F3 -","- C76 H68 Br4 Cl4 F12 -","4","1","","Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.","Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes","Organic Chemistry Frontiers","2017","4","2","255","","10.1039/C6QO00643D","","","0.7107","MoKα","","0.0347","0.0266","","","0.0598","0.0631","","","","","","1.011","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553587","6.9379","0.0019","19.798","0.006","17.773","0.004","90","","90","","90","","2441.2","1.1","296","2","296","2","","","","","","","","5","C m c e","-C 2ac 2","64","","","","- C12 H11 I N2 O2 -","- C12 H11 I N2 O2 -","- C96 H88 I8 N16 O16 -","8","0.5","","He, Xin; Xu, Yi-zhu; Kong, Ling-xuan; Wu, Huan-huan; Ji, De-zhong; Wang, Zhi-bin; Xu, Yun-gen; Zhu, Qi-hua","Copper(i) and N-fluorobenzenesulfonimide-mediated direct regioselective halogenation of 8-amidoquinolines on the C5 position","Organic Chemistry Frontiers","2017","4","6","1046","","10.1039/C6QO00644B","","","0.71073","MoKα","","0.044","0.0379","","","0.0866","0.0901","","","","","","1.13","","","","has coordinates","235172","2020-10-21","18:00:00",""
"1553588","10.4263","0.0009","10.2668","0.0009","40.789","0.004","90","","90.6212","0.0014","90","","4366","0.7","193","2","193","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","3,3,3-tris(3,5-di-t-butyl)prop-1-yne, dichloromethane solvate","","- C46 H66 Cl2 -","- C45 H64 -","- C180 H256 -","4","1","","Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R.","Polymerization of acetylene: polyynes, but not carbyne","Organic Chemistry Frontiers","2017","4","5","668","","10.1039/C6QO00648E","","","0.71073","MoKα","","0.0826","0.0607","","","0.1479","0.1593","","","","","","1.065","","","","has coordinates,has disorder","235174","2020-10-21","18:00:00",""
"1553589","10.3367","0.0013","10.4631","0.0013","19.275","0.002","88.5549","0.0018","78.0127","0.0018","88.5903","0.0019","2038.2","0.4","193","2","193","2","","","","","","","","2","P -1","-P 1","2","","5,5,5-tris(3,5-di-t-butylphenyl)penta-1,3-diyne","","- C47 H64 -","- C47 H64 -","- C94 H128 -","2","1","","Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R.","Polymerization of acetylene: polyynes, but not carbyne","Organic Chemistry Frontiers","2017","4","5","668","","10.1039/C6QO00648E","","","0.71073","MoKα","","0.0692","0.0523","","","0.1344","0.1467","","","","","","1.031","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553590","14.154","0.003","14.154","0.003","12.123","0.002","90","","90","","120","","2103.3","0.7","173","2","173","2","","","","","","","","2","P 3 1 c","P 3 -2c","159","","1,1,1-tris(3,5-di-t-butylphenyl)hepta-2,4,6-triyne","","- C49 H64 -","- C49 H64 -","- C98 H128 -","2","0.333333","","Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R.","Polymerization of acetylene: polyynes, but not carbyne","Organic Chemistry Frontiers","2017","4","5","668","","10.1039/C6QO00648E","","","0.71073","MoKα","","0.072","0.0411","","","0.0776","0.0882","","","","","","1.035","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553591","7.858","0.003","26.656","0.008","8.984","0.003","90","","90.001","0.001","90","","1881.8","1.1","296.15","","296.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C20 H13 F7 N2 O -","- C20 H13 F7 N2 O -","- C80 H52 F28 N8 O4 -","4","1","","Xu, Jun; Qiao, Li; Ying, Beibei; Zhu, Xiaolei; Shen, Chao; Zhang, Pengfei","Transition-metal-free direct perfluoroalkylation of quinoline amides at C5 position through radical cross-coupling under mild conditions","Organic Chemistry Frontiers","2017","4","6","1116","","10.1039/C6QO00655H","","","0.71073","MoKα","","0.1144","0.0545","","","0.1328","0.1523","","","","","","0.887","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553592","14.2771","0.0002","14.228","0.0002","22.6224","0.0004","90","","99.427","0.001","90","","4533.33","0.12","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C44 H58 N2 Se2 Si4 -","- C44 H58 N2 Se2 Si4 -","- C176 H232 N8 Se8 Si16 -","4","1","","Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C.","Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties","Organic Chemistry Frontiers","2017","4","5","682","","10.1039/C6QO00662K","","","0.71073","MoKα","","0.1114","0.0471","","","0.094","0.1178","","","","","","1.01","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553593","14.2494","0.0006","14.1245","0.0006","22.4876","0.0009","90","","98.8","0.002","90","","4472.7","0.3","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C44 H58 N2 S2 Si4 -","- C44 H58 N2 S2 Si4 -","- C176 H232 N8 S8 Si16 -","4","1","","Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C.","Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties","Organic Chemistry Frontiers","2017","4","5","682","","10.1039/C6QO00662K","","","0.71073","MoKα","","0.0919","0.0569","","","0.148","0.1716","","","","","","1.023","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553594","10.8503","0.0005","12.4427","0.0005","12.9897","0.0005","100.306","0.002","91.28","0.002","108.652","0.002","1628.82","0.12","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C32 H22 Br8 N2 -","- C32 H22 Br8 N2 -","- C64 H44 Br16 N4 -","2","1","","Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C.","Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties","Organic Chemistry Frontiers","2017","4","5","682","","10.1039/C6QO00662K","","","0.71073","MoKα","","0.0558","0.0405","","","0.099","0.1057","","","","","","1.028","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553595","9.842","0.002","21.609","0.004","25.234","0.005","90","","91.32","0.03","90","","5365.2","1.8","173.15","","173.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C50 H52 N14 O4 -","- C50 H52 N14 O4 -","- C200 H208 N56 O16 -","4","1","","Zhang, Qian; Wang, Mei-Xiang","Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule","Organic Chemistry Frontiers","2017","4","2","283","","10.1039/C6QO00669H","","","0.71073","MoKα","","0.1092","0.0942","","","0.2041","0.2128","","","","","","1.208","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553596","28.402","0.006","9.816","0.002","18.722","0.004","90","","90.7","0.03","90","","5219.2","1.9","173.15","","173.15","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C54.83 H62.12 Cl1.76 N16.83 O2 -","- C54.824 H62.12 Cl1.764 N16.824 O2 -","- C219.296 H248.48 Cl7.056 N67.296 O8 -","4","0.5","","Zhang, Qian; Wang, Mei-Xiang","Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule","Organic Chemistry Frontiers","2017","4","2","283","","10.1039/C6QO00669H","","","0.71073","MoKα","","0.087","0.0805","","","0.2196","0.2259","","","","","","1.088","","","","has coordinates,has disorder","235183","2020-10-21","18:00:00",""
"1553597","9.6636","0.0003","15.1098","0.0006","18.1939","0.0007","69.768","0.004","84.466","0.003","84.513","0.003","2475.53","0.17","150","0.1","150","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C54 H60 N16 O2 -","- C54 H60 N16 O2 -","- C108 H120 N32 O4 -","2","1","","Zhang, Qian; Wang, Mei-Xiang","Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule","Organic Chemistry Frontiers","2017","4","2","283","","10.1039/C6QO00669H","","x-ray","0.71073","MoKα","","0.0858","0.0575","","","0.1283","0.1452","","","","","","1.0409","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553598","7.5051","0.0007","8.6296","0.0007","11.6509","0.0011","73.729","0.005","77.669","0.004","77.532","0.006","697.78","0.11","200","2","200","2","","","","","","","","3","P -1","-P 1","2","","","","- C40 H24 S2 -","- C40 H24 S2 -","- C40 H24 S2 -","1","0.5","","Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung","The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices","Organic Chemistry Frontiers","2017","4","5","675","","10.1039/C6QO00673F","","","0.71073","MoKα","","0.1065","0.0617","","","0.1647","0.1884","","","","","","1.036","","","","has coordinates","235187","2020-10-21","18:00:00",""
"1553599","16.8864","0.0004","7.4906","0.0002","24.7447","0.0007","90","","90","","90","","3129.94","0.14","200","2","200","2","","","","","","","","2","P n a 21","P 2c -2n","33","","","","- C46 H32 -","- C46 H32 -","- C184 H128 -","4","1","","Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung","The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices","Organic Chemistry Frontiers","2017","4","5","675","","10.1039/C6QO00673F","","","0.71073","MoKα","","0.0692","0.0504","","","0.1175","0.1276","","","","","","1.019","","","","has coordinates","235187","2020-10-21","18:00:00",""
"1553600","7.597","0.0004","8.9994","0.0004","11.0344","0.0005","78.931","0.002","75.805","0.002","83.409","0.002","715.94","0.06","200","2","200","2","","","","","","","","2","P -1","-P 1","2","","","","- C44 H28 -","- C44 H28 -","- C44 H28 -","1","0.5","","Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung","The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices","Organic Chemistry Frontiers","2017","4","5","675","","10.1039/C6QO00673F","","","0.71073","MoKα","","0.0955","0.0504","","","0.1131","0.1326","","","","","","0.988","","","","has coordinates","235187","2020-10-21","18:00:00",""
"1553601","26.478","0.002","8.1615","0.0006","23.0582","0.0017","90","","96.411","0.003","90","","4951.7","0.6","296","2","296","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C26 H22 N4 O5 S -","- C26 H22 N4 O5 S -","- C208 H176 N32 O40 S8 -","8","1","","Chen, Dianpeng; Xing, Gangdong; Yao, Jinzhong; Zhou, Hongwei","Applicable β-sulfonium carbanions: facile construction of thiophene derivatives","Organic Chemistry Frontiers","2017","4","6","1042","","10.1039/C6QO00675B","","","0.71073","MoKα","","0.1002","0.055","","","0.1165","0.1398","","","","","","1.003","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553602","7.9629","0.0003","16.9905","0.0006","18.7808","0.0005","90","","90","","90","","2540.92","0.15","294.06","0.1","294.06","0.1","","","","","","","","5","P b c n","-P 2n 2ab","60","","","","- C12 H9 N O S3 -","- C12 H9 N O S3 -","- C96 H72 N8 O8 S24 -","8","1","","Chen, Qiao; Lei, Yingjie; Wang, Yanfang; Wang, Chao; Wang, Yanan; Xu, Zhaoqing; Wang, Huan; Wang, Rui","Direct thiocyanation of ketene dithioacetals under transition-metal-free conditions","Organic Chemistry Frontiers","2017","4","3","369","","10.1039/C6QO00676K","","x-ray","0.71073","MoKα","","0.0697","0.0482","","","0.1129","0.1301","","","","","","1.049","","","","has coordinates","277994","2022-09-20","08:32:41",""
"1553603","12.2302","0.0009","15.3106","0.0011","36.571","0.003","90","","90","","90","","6848","0.9","296","2","296","2","","","","","","","","8","P 21 21 21","P 2ac 2ab","19","","","","- C71 H46 B F24 Ir N O P -","- C71 H46 B F24 Ir N O P -","- C284 H184 B4 F96 Ir4 N4 O4 P4 -","4","1","","Wang, Qian; Zhang, Zongpeng; Chen, Caiyou; Yang, Hailong; Han, Zhengyu; Dong, Xiu-Qin; Zhang, Xumu","Iridium catalysts with modular axial-unfixed biphenyl phosphine‒oxazoline ligands: asymmetric hydrogenation of α,β-unsaturated carboxylic acids","Organic Chemistry Frontiers","2017","4","4","627","","10.1039/C6QO00677A","","","0.71073","MoKα","","0.0652","0.045","","","0.1009","0.1099","","","","","","1.007","","","","has coordinates","235193","2020-10-21","18:00:00",""
"1553604","11.1134","0.0005","21.1702","0.0009","9.8578","0.0004","90","","101.189","0.0013","90","","2275.19","0.17","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C26 H16 Cu N4 O8 -","- C26 H16 Cu N4 O8 -","- C104 H64 Cu4 N16 O32 -","4","1","","Baur, Andreas; Bustin, Katelyn A.; Aguilera, Ellen; Petersen, Jeffrey L.; Hoover, Jessica M.","Copper and silver benzoate and aryl complexes and their implications for oxidative decarboxylative coupling reactions","Organic Chemistry Frontiers","2017","4","4","519","","10.1039/C6QO00678G","","","0.71073","MoKα","","0.0616","0.037","","","0.078","0.0858","","","","","","1.053","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553605","8.269","0.003","9.296","0.004","16.904","0.007","90","","93.281","0.004","90","","1297.3","0.9","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C16 H11 N O3 -","- C16 H11 N O3 -","- C64 H44 N4 O12 -","4","1","","Fang, Xinxin; Gao, Shang; Wu, Zijun; Yao, Hequan; Lin, Aijun","Pd(ii)-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones","Organic Chemistry Frontiers","2017","4","2","292","","10.1039/C6QO00698A","","","0.71073","MoKα","","0.0456","0.0372","","","0.0974","0.1039","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553606","8.874","0.006","13.733","0.009","27.215","0.017","90","","90","","90","","3317","4","296","2","296","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C22 H15 N O2 -","- C22 H15 N O2 -","- C176 H120 N8 O16 -","8","1","","Fang, Xinxin; Gao, Shang; Wu, Zijun; Yao, Hequan; Lin, Aijun","Pd(ii)-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones","Organic Chemistry Frontiers","2017","4","2","292","","10.1039/C6QO00698A","","","0.71073","MoKα","","0.0465","0.0354","","","0.0886","0.0962","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553607","8.066","0.008","8.242","0.008","12.157","0.013","92.727","0.013","102.604","0.012","98.233","0.011","778","1.4","293","2","293","2","","","","","","","","4","P -1","-P 1","2","2-((3-benzoylisoxazol-5-yl)methyl)isoindoline-1,3-dione","","","- C19 H12 N2 O4 -","- C19 H12 N2 O4 -","- C38 H24 N4 O8 -","2","1","","Li, Yingying; Gao, Mingchun; Liu, Bingxin; Xu, Bin","Copper nitrate-mediated chemo- and regioselective annulation from two different alkynes: a direct route to isoxazoles","Organic Chemistry Frontiers","2017","4","3","445","","10.1039/C6QO00704J","","","0.71073","MoKα","","0.0515","0.039","","","0.0985","0.1077","","","","","","1.086","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553608","9.4574","0.0007","9.9936","0.0009","14.0156","0.0013","89.023","0.007","76.071","0.007","71.074","0.008","1213.5","0.2","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C26 H31 F2 N O3 -","- C26 H31 F2 N O3 -","- C52 H62 F4 N2 O6 -","2","1","","Xu, Jian; Song, Qiuling","Synthesis of fully-substituted 1,2,3-triazoles via copper(i)-catalyzed three-component coupling of sulfoximines, alkynes and azides","Organic Chemistry Frontiers","2017","4","6","938","","10.1039/C6QO00725B","","x-ray","0.71073","MoKα","","0.0814","0.0532","","","0.1352","0.156","","","","","","1.031","","","","has coordinates","300101","2025-06-17","17:58:10",""
"1553609","9.7469","0.0007","13.1171","0.0008","17.5212","0.0012","70.806","0.008","75.292","0.008","73.524","0.008","1996.5","0.3","113","2","113","2","","","","","","","","3","P -1","-P 1","2","","","","- C41 H40 O11 -","- C41 H40 O11 -","- C82 H80 O22 -","2","1","","Lu, Kui; Yang, Ke; Jia, Xiaoliang; Gao, Xing; Zhao, Xia; Pan, Guojun; Ma, Yantao; Huang, Qiyao; Yu, Peng","Total synthesis of I3,II8-biapigenin and ridiculuflavone A","Organic Chemistry Frontiers","2017","4","4","578","","10.1039/C6QO00726K","","","0.71073","MoKα","","0.0639","0.0482","","","0.1461","0.1549","","","","","","1.092","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553610","15.1534","0.001","15.8118","0.001","17.7296","0.001","68.774","0.004","76.898","0.005","79.352","0.005","3832","0.4","113","2","113","2","","","","","","","","3","P -1","-P 1","2","","","","- C43 H46 O11 -","- C43 H46 O11 -","- C172 H184 O44 -","4","2","","Lu, Kui; Yang, Ke; Jia, Xiaoliang; Gao, Xing; Zhao, Xia; Pan, Guojun; Ma, Yantao; Huang, Qiyao; Yu, Peng","Total synthesis of I3,II8-biapigenin and ridiculuflavone A","Organic Chemistry Frontiers","2017","4","4","578","","10.1039/C6QO00726K","","","0.71073","MoKα","","0.0567","0.0442","","","0.1178","0.1244","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553611","9.9046","0.0013","10.4946","0.0012","23.736","0.003","90","","90","","90","","2467.2","0.5","297","2","297","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C31 H23 Cl0 N O4 -","- C31 H23 N O4 -","- C124 H92 N4 O16 -","4","1","","Xu, Junyu; Cao, Jing; Fang, Chao; Lu, Tao; Du, Ding","Organocatalytic C‒C bond activation of cyclopropenones for ring-opening formal [3 + 2] cycloaddition with isatins","Organic Chemistry Frontiers","2017","4","4","560","","10.1039/C6QO00734A","","","0.71073","MoKα","","0.1682","0.0492","","","0.0947","0.1414","","","","","","0.943","","","","has coordinates","235205","2020-10-21","18:00:00",""
"1553612","9.263","0.0019","16.211","0.003","15.413","0.003","90","","91.21","0.03","90","","2313.9","0.8","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C30 H21 N O3 -","- C30 H21 N O3 -","- C120 H84 N4 O12 -","4","1","","Xu, Junyu; Cao, Jing; Fang, Chao; Lu, Tao; Du, Ding","Organocatalytic C–C bond activation of cyclopropenones for ring-opening formal [3 + 2] cycloaddition with isatins","Organic Chemistry Frontiers","2017","4","4","560","","10.1039/C6QO00734A","","","0.71073","MoKα","","0.144","0.0673","","","0.155","0.1945","","","","","","1","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553613","12.3342","0.0005","12.422","0.0005","20.4886","0.0009","94.35","0.003","97.642","0.003","100.981","0.003","3037.8","0.2","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C38.5 H33 Cl O3 -","- C38.5 H33 Cl O3 -","- C154 H132 Cl4 O12 -","4","2","","Zhang, Yuexia; Wu, Xingxing; Hao, Lin; Wong, Zeng Rong; Lauw, Sherman J. L.; Yang, Song; Webster, Richard D.; Chi, Yonggui Robin","Trimerization of enones under air enabled by NHC/NaOtBu via a SET radical pathway","Organic Chemistry Frontiers","2017","4","3","467","","10.1039/C6QO00738D","","","0.71073","MoKα","","0.1569","0.0817","","","0.1959","0.2444","","","","","","1.021","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553614","9.077","0.004","10.4","0.004","11.75","0.005","90","","90","","90","","1109.2","0.8","173.15","","173.15","","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C13 H12 N2 O -","- C13 H12 N2 O -","- C52 H48 N8 O4 -","4","1","","Guo, Wei-Si; Wang, Yuan-Chao; Dou, Qian; Wen, Li-Rong; Li, Ming","A copper-catalyzed arylation/nucleophilic addition/fragmentation/C–S bond formation cascade: synthesis of bis(arylthio)imines","Organic Chemistry Frontiers","2017","4","4","510","","10.1039/C6QO00739B","","","0.71073","MoKα","","0.0383","0.0374","","","0.1194","0.1208","","","","","","1.013","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553615","8.189","0.002","14.782","0.004","17.421","0.005","90","","90","","90","","2108.8","1","173.15","","173.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C23 H19 N O2 S2 -","- C23 H19 N O2 S2 -","- C92 H76 N4 O8 S8 -","4","1","","Guo, Wei-Si; Wang, Yuan-Chao; Dou, Qian; Wen, Li-Rong; Li, Ming","A copper-catalyzed arylation/nucleophilic addition/fragmentation/C–S bond formation cascade: synthesis of bis(arylthio)imines","Organic Chemistry Frontiers","2017","4","4","510","","10.1039/C6QO00739B","","","0.71073","MoKα","","0.0577","0.052","","","0.0937","0.0959","","","","","","1.15","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553616","10.5479","0.0013","16.6","0.002","13.9079","0.0017","90","","92.242","0.002","90","","2433.3","0.5","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H24 S4 Si2 -","- C22 H24 S4 Si2 -","- C88 H96 S16 Si8 -","4","1","","Li, Lu; Li, Bingbing; Li, Chunli; Ma, Zhiying; Xu, Li; Wang, Hua","Selective deprotonation of tetra[3,4]thienylene in the presence of n-BuLi","Organic Chemistry Frontiers","2017","4","6","1019","","10.1039/C6QO00754F","","","0.71073","MoKα","","0.0597","0.0447","","","0.1207","0.1333","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553617","20.763","0.003","20.763","0.003","13.7545","0.0018","90","","90","","90","","5929.6","1.4","296","2","296.15","","","","","","","","","6","I 41/a :2","-I 4ad","88","","","","- C44 H72 Li4 O4 S4 Si4 -","- C44 H72 Li4 O4 S4 Si4 -","- C176 H288 Li16 O16 S16 Si16 -","4","0.25","","Li, Lu; Li, Bingbing; Li, Chunli; Ma, Zhiying; Xu, Li; Wang, Hua","Selective deprotonation of tetra[3,4]thienylene in the presence of n-BuLi","Organic Chemistry Frontiers","2017","4","6","1019","","10.1039/C6QO00754F","","","0.71073","MoKα","","0.1222","0.0831","","","0.2424","0.2973","","","","","","1.024","","","","has coordinates","235211","2020-10-21","18:00:00",""
"1553618","5.7832","0.0006","10.4921","0.0011","12.3215","0.0012","90.576","0.003","97.913","0.002","93.157","0.003","739.28","0.13","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C17 H17 N O4 -","- C17 H17 N O4 -","- C34 H34 N2 O8 -","2","1","","Chen, Hui; Lin, Cong; Xiong, Chunhua; Liu, Zhanxiang; Zhang, Yuhong","One-pot synthesis of fluorescent 2,4-dialkenylindoles by rhodium-catalyzed dual C–H functionalization","Organic Chemistry Frontiers","2017","4","3","455","","10.1039/C6QO00755D","","","0.71073","MoKα","","0.1123","0.0541","","","0.1153","0.1708","","","","","","1.002","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553619","13.585","0.004","12.569","0.003","9.741","0.003","90","","106.741","0.006","90","","1592.8","0.8","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H17 F O -","- C21 H17 F O -","- C84 H68 F4 O4 -","4","1","","Cao, Tongxiang; Chen, Kai; Zhu, Shifa","An efficient approach to generate aryl carbenes: gold-catalyzed sequential activation of 1,6-diynes","Organic Chemistry Frontiers","2017","4","3","450","","10.1039/C6QO00769D","","","0.71073","MoKα","","0.1216","0.0562","","","0.1286","0.1552","","","","","","0.984","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553620","12.3103","0.0016","20.299","0.003","6.9248","0.0009","90","","95.884","0.003","90","","1721.3","0.4","130","","130","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C23 H26 O -","- C23 H26 O -","- C92 H104 O4 -","4","1","","Cao, Tongxiang; Chen, Kai; Zhu, Shifa","An efficient approach to generate aryl carbenes: gold-catalyzed sequential activation of 1,6-diynes","Organic Chemistry Frontiers","2017","4","3","450","","10.1039/C6QO00769D","","","0.71073","MoKα","","0.0754","0.0487","","","0.1184","0.133","","","","","","1.023","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553621","12.4994","0.0013","13.1859","0.0014","16.0253","0.0017","102.651","0.005","95.439","0.006","92.29","0.006","2560.5","0.5","180","2","180","2","","","","","","","","5","P -1","-P 1","2","","","","- C60 H28 F20 N6 O2 -","- C60 H28 F20 N6 O2 -","- C120 H56 F40 N12 O4 -","2","1","","Almeida, José; Aguiar, António; Leite, Andreia; Silva, André M. N.; Cunha-Silva, Luís; de Castro, Baltazar; Rangel, Maria; Barone, Giampaolo; Tomé, Augusto C.; Silva, Ana M. G.","1,3-Dipolar cycloadditions with meso-tetraarylchlorins ‒ site selectivity and mixed bisadducts","Organic Chemistry Frontiers","2017","4","4","534","","10.1039/C6QO00771F","","","0.71073","MoKα","","0.1877","0.1387","","","0.4059","0.434","","","","","","1.614","","","","has coordinates","235216","2020-10-21","18:00:00",""
"1553622","15.6516","0.0005","14.7041","0.0004","20.8303","0.0006","90","","90","","90","","4793.9","0.2","180","","180","","","","101","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C23 H30 N4 O2 Si -","- C23 H30 N4 O2 Si -","- C184 H240 N32 O16 Si8 -","8","1","","Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.","Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry","Organic Chemistry Frontiers","2017","4","6","978","","10.1039/C6QO00787B","","","0.71073","MoKα","","0.048","0.0389","","0.1007","0.0942","0.1005","","","","","","1.0233","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553623","9.4684","0.0003","10.4692","0.0004","12.771","0.0004","96.2634","0.0012","95.7478","0.0012","113.644","0.0011","1138.27","0.07","180","","180","","","","101","","","","","5","P -1","-P 1","2","","","","- C20 H21 N5 O2 Si -","- C20 H21 N5 O2 Si -","- C40 H42 N10 O4 Si2 -","2","1","","Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.","Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry","Organic Chemistry Frontiers","2017","4","6","978","","10.1039/C6QO00787B","","","1.54178","CuKα","","0.0524","0.0469","","0.1317","0.1269","0.1317","","","","","","1.0042","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553624","16.2913","0.0007","10.0932","0.0004","19.7897","0.0008","90","","112.895","0.0012","90","","2997.7","0.2","180","","180","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C14 H8 Br3 N3 -","- C14 H8 Br3 N3 -","- C112 H64 Br24 N24 -","8","2","","Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.","Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry","Organic Chemistry Frontiers","2017","4","6","978","","10.1039/C6QO00787B","","","0.71073","MoKα","","0.0659","0.0374","","0.0956","0.0746","0.0956","","","","","","0.9177","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553625","8.9462","0.0005","11.9145","0.0006","43.549","0.002","90","","90","","90","","4641.9","0.4","180","","180","","","","101","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C21 H34 N4 O2 Si -","- C21 H34 N4 O2 Si -","- C168 H272 N32 O16 Si8 -","8","1","","Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.","Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry","Organic Chemistry Frontiers","2017","4","6","978","","10.1039/C6QO00787B","","","1.54178","CuKα","","0.0668","0.0577","","0.1162","0.1136","0.1162","","","","","","0.9617","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553626","11.9761","0.0003","15.4866","0.0004","11.0055","0.0003","90","","106.167","0.001","90","","1960.46","0.09","296","2","296","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C25 H20 O4 -","- C25 H20 O4 -","- C100 H80 O16 -","4","1","","Mao, Wenbin; Zhu, Chen","Efficient synthesis of multiply substituted butenolides from keto acids and terminal alkynes promoted by combined acids","Organic Chemistry Frontiers","2017","4","6","1029","","10.1039/C6QO00820H","","","0.71073","MoKα","","0.0815","0.0435","","","0.1177","0.1338","","","","","","1.066","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553627","8.8576","0.0007","9.515","0.0007","15.8743","0.0012","79.571","0.002","74.479","0.002","86.413","0.002","1267.66","0.17","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C35 H18 Fe O4 -","- C35 H18 Fe O4 -","- C70 H36 Fe2 O8 -","2","1","","Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian","From tetrabenzoheptafulvalene to sp2 carbon nano-rings","Organic Chemistry Frontiers","2017","4","5","699","","10.1039/C6QO00828C","","","0.71073","MoKα","","0.0571","0.0504","","","0.1402","0.1485","","","","","","1.058","","","","has coordinates","235222","2020-10-21","18:00:00",""
"1553628","12.737","0.003","10.827","0.003","15.738","0.004","90","","105.708","0.006","90","","2089.3","0.9","296","2","296","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C32 H18 O -","- C32 H18 O -","- C128 H72 O4 -","4","1","","Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian","From tetrabenzoheptafulvalene to sp2 carbon nano-rings","Organic Chemistry Frontiers","2017","4","5","699","","10.1039/C6QO00828C","","","0.71073","MoKα","","0.1793","0.0997","","","0.2401","0.2908","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553629","10.5417","0.0004","14.8356","0.0005","24.1274","0.0008","90","","90","","90","","3773.3","0.2","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C51 H29 Cl3 O4 -","- C51 H29 Cl3 O4 -","- C204 H116 Cl12 O16 -","4","1","","Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian","From tetrabenzoheptafulvalene to sp2 carbon nano-rings","Organic Chemistry Frontiers","2017","4","5","699","","10.1039/C6QO00828C","","","1.54178","CuKα","","0.0909","0.0536","","","0.1126","0.131","","","","","","1.023","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553630","12.3541","0.0003","20.5251","0.0006","15.593","0.0004","90","","111.562","0.0016","90","","3677.21","0.17","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C51 H30 Cl2 O -","- C51 H30 Cl2 O -","- C204 H120 Cl8 O4 -","4","1","","Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian","From tetrabenzoheptafulvalene to sp2 carbon nano-rings","Organic Chemistry Frontiers","2017","4","5","699","","10.1039/C6QO00828C","","","0.71073","MoKα","","0.1194","0.0675","","","0.1717","0.2047","","","","","","1.017","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553631","12.2233","0.0002","20.4397","0.0003","15.612","0.0002","90","","111.759","0.0009","90","","3622.59","0.09","296","2","296","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C51 H30 Cl2 -","- C51 H30 Cl2 -","- C204 H120 Cl8 -","4","1","","Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian","From tetrabenzoheptafulvalene to sp2 carbon nano-rings","Organic Chemistry Frontiers","2017","4","5","699","","10.1039/C6QO00828C","","","0.71073","MoKα","","0.0755","0.0569","","","0.1481","0.165","","","","","","1.007","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553632","8.8208","0.0003","12.857","0.0004","18.1141","0.0005","90","","90","","90","","2054.3","0.11","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C20 H19 Br N2 O5 S -","- C20 H19 Br N2 O5 S -","- C80 H76 Br4 N8 O20 S4 -","4","1","","Yu, Lu; Cheng, Yuyu; Qi, Fei; Li, Rou; Li, Pengfei","Organocatalytic regioselective, diastereoselective, and enantioselective annulation of cyclic 1-azadienes with γ-nitro ketones via 3,4-cyclization","Organic Chemistry Frontiers","2017","4","7","1336","","10.1039/C6QO00832A","","","0.71073","MoKα","","0.1259","0.0514","","","0.0608","0.0689","","","","","","0.994","","","","has coordinates","235224","2020-10-21","18:00:00",""
"1553633","5.768","0.002","9.924","0.004","20.463","0.007","100.063","0.004","91.086","0.004","92.46","0.004","1151.8","0.7","298","","298","","","","","","","","","3","P -1","-P 1","2","","","","- C29 H25 N3 -","- C29 H25 N3 -","- C58 H50 N6 -","2","1","","Zhao, Fen; Liu, Yaowen; Yang, Shu; Xie, Kai; Jiang, Yubo","Pd-catalyzed selective N(3)-ortho C–H arylation of 1,4-disubstituted 1,2,3-triazoles","Organic Chemistry Frontiers","2017","4","6","1112","","10.1039/C6QO00834H","","","0.71073","MoKα","","0.0692","0.0457","","","0.1142","0.129","","","","","","1.025","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553634","16.003","0.005","7.036","0.002","16.456","0.005","90","","101.876","0.004","90","","1813.2","0.9","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C21 H15 Br2 N O2 -","- C21 H15 Br2 N O2 -","- C84 H60 Br8 N4 O8 -","4","1","","Qiu, Guanyinsheng; Li, Yuewen; Ma, Lele; Zhou, Hongwei","KBr/K2S2O8-mediated dibromohydration of N-(2-alkynylaryl)acetamide","Organic Chemistry Frontiers","2017","4","6","1069","","10.1039/C6QO00840B","","","0.71073","MoKα","","0.0404","0.0328","","","0.0954","0.0996","","","","","","1.069","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553635","15.552","0.005","9.109","0.003","20","0.006","90","","111.508","0.005","90","","2636","1.5","130","","130","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C33 H31 N O3 -","- C33 H31 N O3 -","- C132 H124 N4 O12 -","4","1","","Liu, Feng; Tian, Jiaxin; Liu, Yong; Tao, Chuangan; Zhu, Hao; Zhang, Aina; Xu, Dongfang; Zhao, Baoguo","Decarboxylative Umpolung of conjugated enals to β-carbanions for intramolecular nucleophilic addition to an aldehyde","Organic Chemistry Frontiers","2017","4","8","1586","","10.1039/C6QO00846A","","","0.71073","MoKα","","0.1011","0.0555","","","0.1276","0.1513","","","","","","0.997","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553636","7.7445","0.0012","13.971","0.002","19.15","0.003","90","","90","","90","","2072","0.5","153","2","153","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","(2'R,3'R,4'R)-4'-benzoyl-1-methyl-3'-phenyl-5'-thioxospiro[indoline-3,2'-pyrrolidin]-2-one","","- C25 H20 N2 O2 S -","- C25 H20 N2 O2 S -","- C100 H80 N8 O8 S4 -","4","1","","Lin, Ye; Liu, Lei; Du, Da-Ming","Squaramide-catalyzed asymmetric Michael/cyclization cascade reaction of 3-isothiocyanato oxindoles with chalcones for synthesis of pyrrolidinyl spirooxindoles","Organic Chemistry Frontiers","2017","4","7","1229","","10.1039/C6QO00852F","","","0.71073","MoKα","","0.0394","0.0361","","","0.0806","0.0827","","","","","","1.001","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553637","8.4855","0.0004","15.887","0.0007","25.5299","0.0013","90","","90","","90","","3441.7","0.3","100","0.2","100","0.2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C16 H21 N3 O5 -","- C16 H21 N3 O5 -","- C128 H168 N24 O40 -","8","2","","Deng, Tao; Thota, Ganesh Kumar; Li, Yi; Kang, Qiang","Enantioselective conjugate addition of hydroxylamines to α,β-unsaturated 2-acyl imidazoles catalyzed by a chiral-at-metal Rh(iii) complex","Organic Chemistry Frontiers","2017","4","4","573","","10.1039/C6QO00865H","","","1.54184","CuKα","","0.0489","0.0384","","","0.0804","0.0857","","","","","","1.003","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553638","11.882","0.002","6.1567","0.0013","22.083","0.004","90","","99.617","0.015","90","","1592.8","0.5","273","2","273","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C36 H40 N2 O4 -","- C36 H40 N2 O4 -","- C72 H80 N4 O8 -","2","0.5","","Purc, Anna; Koszarna, Beata; Iachina, Irina; Friese, Daniel H.; Tasior, Mariusz; Sobczyk, Krzysztof; Pędziński, Tomasz; Brewer, Jonathan; Gryko, Daniel T.","The impact of interplay between electronic and steric effects on the synthesis and the linear and non-linear optical properties of diketopyrrolopyrrole bearing benzofuran moieties","Organic Chemistry Frontiers","2017","4","5","724","","10.1039/C6QO00869K","","","1.54178","CuKα","","0.1821","0.0736","","","0.1614","0.1933","","","","","","0.938","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553639","20.477","0.0009","5.2589","0.0002","28.0402","0.0012","90","","101.007","0.0019","90","","2964","0.2","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C32 H38 N2 O2 S3 -","- C32.4 H37.76 N2 O2 S2.908 -","- C129.6 H151.04 N8 O8 S11.632 -","4","1","","Chen, Wangqiao; Nakano, Masahiro; Takimiya, Kazuo; Zhang, Qichun","Selective thionation of naphtho[2,3-b]thiophene diimide: tuning of the optoelectronic properties and packing structure","Organic Chemistry Frontiers","2017","4","5","704","","10.1039/C6QO00871B","","","1.54187","CuKα","","0.1155","0.0889","","","0.2224","0.2399","","","","","","1.277","","","","has coordinates,has disorder","235238","2020-10-21","18:00:00",""
"1553724","10.445","0.002","14.347","0.003","14.407","0.003","82.53","0.03","85.3","0.03","74.55","0.03","2060.7","0.8","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C22 H23 Cl N2 O0 Ru -","- C22 H23 Cl N2 Ru -","- C88 H92 Cl4 N8 Ru4 -","4","2","","Li, Gang; Lv, Xulu; Guo, Kexiao; Wang, Ya; Yang, Suling; Yu, Liuyang; Yu, Yantang; Wang, Junjie","Ruthenium-catalyzed meta-selective C‒H sulfonation of azoarenes with arylsulfonyl chlorides","Organic Chemistry Frontiers","2017","4","6","1145","","10.1039/C7QO00004A","","","0.71073","MoKα","","0.0817","0.0695","","","0.1802","0.1846","","","","","","1.105","","","","has coordinates","235944","2020-10-21","18:00:00",""
"1553725","34.644","0.007","7.0976","0.0014","13.544","0.003","90","","98.63","0.03","90","","3292.6","1.2","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C18 H13 Cl N2 O2 S -","- C18 H13 Cl N2 O2 S -","- C144 H104 Cl8 N16 O16 S8 -","8","1","","Li, Gang; Lv, Xulu; Guo, Kexiao; Wang, Ya; Yang, Suling; Yu, Liuyang; Yu, Yantang; Wang, Junjie","Ruthenium-catalyzed meta-selective C–H sulfonation of azoarenes with arylsulfonyl chlorides","Organic Chemistry Frontiers","2017","4","6","1145","","10.1039/C7QO00004A","","","0.71073","MoKα","","0.0632","0.0409","","","0.1337","0.1539","","","","","","1.002","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553726","11.4884","0.0005","11.9792","0.0005","20.8251","0.0008","90","","90","","90","","2866","0.2","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C16 H15 N O7 -","- C16 H15 N O7 -","- C128 H120 N8 O56 -","8","2","","Wang, Junliang; Li, Jianneng; Shen, Xianwang; Dong, Cong; Lin, Jun; Wei, Kun","Asymmetric total synthesis of (−)-δ-lycorane","Organic Chemistry Frontiers","2017","4","6","1149","","10.1039/C7QO00021A","","","1.54178","CuKα","","0.0535","0.0527","","","0.1534","0.1545","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553727","13.8813","0.0006","14.4392","0.0007","23.5317","0.0011","95.8618","0.0012","105.365","0.0012","91.4814","0.0011","4517.3","0.4","200","2","200","2","","","","","","","","3","P -1","-P 1","2","","","","- C60 H46 N4.5 -","- C60 H46 N4.5 -","- C240 H184 N18 -","4","2","","Kimura, Yosuke; Kawajiri, Ikumi; Ueki, Masanori; Morimoto, Takayuki; Nishida, Jun-ichi; Ikeda, Hiroshi; Tanaka, Mirai; Kawase, Takeshi","A new fluorophore displaying remarkable solvatofluorochromism and solid-state light emission, and serving as a turn-on fluorescent sensor for cyanide ions","Organic Chemistry Frontiers","2017","4","5","743","","10.1039/C7QO00029D","","","0.71075","MoKα","","0.2091","0.0714","","","0.1685","0.2407","","","","","","0.938","","","","has coordinates,has disorder","274176","2022-03-31","10:10:26",""
"1553728","11.5","0.004","10.46","0.004","11.413","0.005","90","","95.06","0.008","90","","1367.5","0.9","130","","130","","","","","","","","","6","C 1 2 1","C 2y","5","","","","- C11 H16 F3 N O2 S2 -","- C11 H16 F3 N O2 S2 -","- C44 H64 F12 N4 O8 S8 -","4","1","","Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong","(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation","Organic Chemistry Frontiers","2017","4","6","1051","","10.1039/C7QO00042A","","","0.71073","MoKα","","0.0455","0.0404","","","0.0934","0.0982","","","","","","1.108","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553729","6.6977","0.0005","8.1914","0.0006","30.513","0.002","90","","90","","90","","1674.1","0.2","130","","130","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C19 H10 F4 O2 S -","- C19 H10 F4 O2 S -","- C76 H40 F16 O8 S4 -","4","1","","Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong","(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation","Organic Chemistry Frontiers","2017","4","6","1051","","10.1039/C7QO00042A","","","0.71073","MoKα","","0.0353","0.0334","","","0.0865","0.0875","","","","","","1.067","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553730","7.5426","0.0006","13.2312","0.001","15.9887","0.0013","90","","90","","90","","1595.6","0.2","130","2","130","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C15 H15 F3 O5 S -","- C15 H15 F3 O5 S -","- C60 H60 F12 O20 S4 -","4","1","","Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong","(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation","Organic Chemistry Frontiers","2017","4","6","1051","","10.1039/C7QO00042A","","","0.71073","MoKα","","0.0307","0.0273","","","0.07","0.0719","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553731","8.5502","0.0008","11.0835","0.0011","16.8212","0.0016","90","","90","","90","","1594.1","0.3","130","","130","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C17 H11 F3 N2 O S -","- C17 H11 F3 N2 O S -","- C68 H44 F12 N8 O4 S4 -","4","1","","Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong","(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation","Organic Chemistry Frontiers","2017","4","6","1051","","10.1039/C7QO00042A","","","0.71073","MoKα","","0.0471","0.0397","","","0.0975","0.1022","","","","","","1.036","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553732","7.7869","0.0006","10.8732","0.0008","8.8809","0.0007","90","","95.062","0.001","90","","749","0.1","130","","130","","","","","","","","","7","P 1 21 1","P 2yb","4","","","","- C11 H14 Cl2 F3 N O2 S2 -","- C11 H14 Cl2 F3 N O2 S2 -","- C22 H28 Cl4 F6 N2 O4 S4 -","2","1","","Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong","(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation","Organic Chemistry Frontiers","2017","4","6","1051","","10.1039/C7QO00042A","","","0.71073","MoKα","","0.0292","0.0285","","","0.072","0.0725","","","","","","1.035","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553733","12.4266","0.0017","8.8229","0.0012","15.107","0.002","90","","105.7","0.003","90","","1594.5","0.4","130","","130","","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C13 H20 F3 N O4 S2 -","- C13 H20 F3 N O4 S2 -","- C52 H80 F12 N4 O16 S8 -","4","2","","Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong","(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation","Organic Chemistry Frontiers","2017","4","6","1051","","10.1039/C7QO00042A","","","0.71073","MoKα","","0.0445","0.0379","","","0.0862","0.0904","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553734","15.566","0.002","15.831","0.0016","17.7553","0.0019","80.813","0.006","89.907","0.011","88.251","0.009","4317.2","0.8","93","2","93","2","","","","","","","","6","P -1","-P 1","2","","","","- C101 H110 N4 Ni P Pt0.5 -","- C101 H110 N4 Ni P Pt0.5 -","- C202 H220 N8 Ni2 P2 Pt -","2","1","","Fukui, Norihito; Jiang, Hua-Wei; Osuka, Atsuhiro","meso-to-meso PtII-bridged NiII-porphyrin dimers","Organic Chemistry Frontiers","2017","4","5","767","","10.1039/C7QO00093F","","","1.54187","CuKα","","0.0341","0.0313","","","0.0799","0.081","","","","","","1.042","","","","has coordinates,has disorder","235954","2020-10-21","18:00:00",""
"1553735","16.142","0.003","21.227","0.004","22.446","0.004","106.1","0.005","92.132","0.001","93.364","0.006","7365","2","93","2","93","2","","","","","","","","6","P -1","-P 1","2","","","","- C162 H174 Cl10 N8 Ni2 Pt -","- C162 H174 Cl10 N8 Ni2 Pt -","- C324 H348 Cl20 N16 Ni4 Pt2 -","2","1","","Fukui, Norihito; Jiang, Hua-Wei; Osuka, Atsuhiro","meso-to-meso PtII-bridged NiII-porphyrin dimers","Organic Chemistry Frontiers","2017","4","5","767","","10.1039/C7QO00093F","","","1.54187","CuKα","","0.0683","0.0581","","","0.1606","0.1669","","","","","","1.054","","","","has coordinates,has disorder","235954","2020-10-21","18:00:00",""
"1553736","13.8397","0.0009","24.2642","0.0013","16.7166","0.0013","90","","109.444","0.008","90","","5293.4","0.7","180","0.1","180","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C76 H38 Br N O8 -","- C76 H38 Br N O8 -","- C304 H152 Br4 N4 O32 -","4","1","","Xu, Dan; Li, Yanbang; Lou, Ning; Gan, Liangbing","Synthesis of homoazafullerene [C59N(CH2)]R and azahomoazafullerene [C59N(NH)]R","Organic Chemistry Frontiers","2017","4","5","750","","10.1039/C7QO00098G","","","0.71073","MoKα","","0.1521","0.0699","","","0.1429","0.1714","","","","","","0.921","","","","has coordinates","235956","2020-10-21","18:00:00",""
"1553737","21.489","0.004","10.179","0.002","22.215","0.004","90","","90","","90","","4859.2","1.6","100","","100","","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C76 H39 N O9 -","- C76 H39 N O9 -","- C304 H156 N4 O36 -","4","1","","Xu, Dan; Li, Yanbang; Lou, Ning; Gan, Liangbing","Synthesis of homoazafullerene [C59N(CH2)]R and azahomoazafullerene [C59N(NH)]R","Organic Chemistry Frontiers","2017","4","5","750","","10.1039/C7QO00098G","","","0.71073","MoKα","","0.0804","0.0656","","","0.1822","0.1998","","","","","","1.054","","","","has coordinates,has disorder","235956","2020-10-21","18:00:00",""
"1553738","17.5147","0.001","7.024","0.003","15.73","0.009","90","","114.033","0.006","90","","1767.4","1.3","150","","150","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","N-(3-(4-bromophenyl)-5-methylene-2-oxooxazolidin-4-yl)-4-methylbenzenesulfonamide","","- C17 H13 Br N2 O4 S -","- C17 H13 Br N2 O4 S -","- C68 H52 Br4 N8 O16 S4 -","4","1","","Pal, Kuntal; Volla, Chandra M. R.","Rhodium-catalyzed denitrogenative transannulation of 1,2,3-triazolyl-carbamates: efficient access to 4-aminooxazolidinones","Organic Chemistry Frontiers","2017","4","7","1380","","10.1039/C7QO00101K","","","0.7107","MoKα","","0.0547","0.0451","","","0.0991","0.1046","","","","","","1.091","","","","has coordinates","235958","2020-10-21","18:00:00",""
"1553741","28.543","0.006","7.309","0.0015","16.361","0.003","90","","105.04","0.03","90","","3296.3","1.2","293","2","293","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C19 H22 O3 -","- C19 H22 O3 -","- C152 H176 O24 -","8","1","","Chang, Wenju; Dai, Jie; Li, Jingfu; Shi, Yuan; Ren, Wenlong; Shi, Yian","A facile approach to ketones via Pd-catalyzed sequential carbonylation of olefins with formic acid","Organic Chemistry Frontiers","2017","4","6","1074","","10.1039/C7QO00111H","","","0.71073","MoKα","","0.1583","0.0639","","","0.1064","0.1411","","","","","","1.002","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553742","5.69674","0.00011","8.92923","0.00016","19.6982","0.0005","90","","94.927","0.002","90","","998.3","0.04","173","0.1","173","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C11 H8 N O2 S -","- C22 H16 N2 O4 S2 -","- C44 H32 N4 O8 S4 -","2","0.5","","Ammon, Felix; Sauer, Stephanie Theresia; Lippert, Rainer; Lungerich, Dominik; Reger, David; Hampel, Frank; Jux, Norbert","Unexpected formation of [5]helicenes from hexaarylbenzenes containing pyrrole moieties","Organic Chemistry Frontiers","2017","4","5","861","","10.1039/C7QO00112F","","x-ray","1.54184","CuKα","","0.0465","0.043","","","0.1146","0.1186","","","","","","1.054","","","","has coordinates","235964","2020-10-21","18:00:00",""
"1553743","14.0225","0.0007","15.4902","0.001","15.6494","0.0005","109.303","0.004","105.791","0.004","106.459","0.005","2814.2","0.3","152.7","1","152.7","1","","","","","","","","6","P -1","-P 1","2","","","","- C67.5 H66 Cl3 N O2 S -","- C67.5 H66 Cl3 N O2 S -","- C135 H132 Cl6 N2 O4 S2 -","2","1","","Ammon, Felix; Sauer, Stephanie Theresia; Lippert, Rainer; Lungerich, Dominik; Reger, David; Hampel, Frank; Jux, Norbert","Unexpected formation of [5]helicenes from hexaarylbenzenes containing pyrrole moieties","Organic Chemistry Frontiers","2017","4","5","861","","10.1039/C7QO00112F","","x-ray","1.54184","CuKα","","0.0797","0.0729","","","0.1995","0.2094","","","","","","1.021","","","","has coordinates,has disorder","235964","2020-10-21","18:00:00",""
"1553744","8.2685","0.0016","13.793","0.003","17.645","0.003","72.588","0.003","88.716","0.003","77.009","0.002","1868.8","0.6","150","","150","","","","","","","","","3","P -1","-P 1","2","","","","- C84 H108 Si4 -","- C84 H108 Si4 -","- C84 H108 Si4 -","1","0.5","","Bettinger, Holger F.; Einholz, Ralf; Göttler, Andreas; Junge, Marc; Sättele, Marie-Sophie; Schnepf, Andreas; Schrenk, Claudio; Schundelmeier, Simon; Speiser, Bernd","6,6′,11,11′-Tetra((triisopropylsilyl)ethynyl)-anti-[2.2](1,4)tetracenophane: a covalently coupled tetracene dimer and its structural, electrochemical, and photophysical characterization","Organic Chemistry Frontiers","2017","4","5","853","","10.1039/C7QO00117G","","","0.8","synchrotron","","0.0904","0.0564","","","0.1314","0.1438","","","","","","1.015","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553745","6.121","0.005","8.835","0.007","13.265","0.012","83.14","0.02","79.6","0.02","72.93","0.02","672.8","1","296","2","296","2","","","","","","","synthesis","5","P -1","-P 1","2","","(E)-6-methyl-N-(1-phenylethylidene)pyridine-2-sulfonamide","","- C14 H14 N2 O2 S -","- C14 H14 N2 O2 S -","- C28 H28 N4 O4 S2 -","2","1","","Wang, Bin; Xu, Tong; Zhu, Lei; Lan, Yu; Wang, Jingdong; Lu, Ning; Wei, Zhonglin; Lin, Yingjie; Duan, Haifeng","Highly enantioselective nitro-Mannich reaction of ketimines under phase-transfer catalysis","Organic Chemistry Frontiers","2017","4","7","1266","","10.1039/C7QO00124J","","","0.71073","MoKα","","0.0942","0.0655","","","0.1851","0.2162","","","","","","0.967","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553746","8.6132","0.0015","7.4744","0.0014","12.867","0.003","90","","109.429","0.005","90","","781.2","0.3","296","2","296","2","","","","","","","synthesis","5","P 1 21 1","P 2yb","4","","(R)-6-methyl-N-(1-nitro-2-phenylpropan-2-yl)pyridine-2-sulfonamide","","- C15 H17 N3 O4 S -","- C15 H17 N3 O4 S -","- C30 H34 N6 O8 S2 -","2","1","","Wang, Bin; Xu, Tong; Zhu, Lei; Lan, Yu; Wang, Jingdong; Lu, Ning; Wei, Zhonglin; Lin, Yingjie; Duan, Haifeng","Highly enantioselective nitro-Mannich reaction of ketimines under phase-transfer catalysis","Organic Chemistry Frontiers","2017","4","7","1266","","10.1039/C7QO00124J","","","0.71073","MoKα","","0.0385","0.0352","","","0.0849","0.0874","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553747","21.7066","0.0008","21.7067","0.0008","20.1949","0.0013","90","","122.509","0.003","90","","8024.4","0.7","213","2","213","2","","","","","","","","2","C 1 c 1","C -2yc","9","","1,4,1',4?-tetramethyl-9,9?-bifluorenylidene","","- C30 H24 -","- C30 H24 -","- C480 H384 -","16","4","","Takai, Atsuro; Freas, Dylan J.; Suzuki, Toshikane; Sugimoto, Manabu; Labuta, Jan; Haruki, Rie; Kumai, Reiji; Adachi, Shin-ichi; Sakai, Hayato; Hasobe, Taku; Matsushita, Yoshitaka; Takeuchi, Masayuki","The effect of a highly twisted CC double bond on the electronic structures of 9,9′-bifluorenylidene derivatives in the ground and excited states","Organic Chemistry Frontiers","2017","4","5","650","","10.1039/C7QO00125H","","","0.71073","MoKα","","0.1838","0.0776","","","0.1578","0.2027","","","","","","0.874","","","","has coordinates","235970","2020-10-21","18:00:00",""
"1553748","7.6834","0.0016","8.0281","0.0017","12.554","0.003","85.471","0.003","73.42","0.003","74.044","0.003","713.6","0.3","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C15 H13 N O4 S2 -","- C15 H13 N O4 S2 -","- C30 H26 N2 O8 S4 -","2","1","","Zhou, Kaida; Xia, Hongguang; Wu, Jie","Generation of benzosultams via a radical process with the insertion of sulfur dioxide","Organic Chemistry Frontiers","2017","4","6","1121","","10.1039/C7QO00127D","","","0.71073","MoKα","","0.0534","0.0396","","","0.1348","0.1787","","","","","","1.22","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553749","8.151","0.01","8.239","0.009","22.94","0.03","90","","100.06","0.02","90","","1517","3","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H13 N O4 S2 -","- C15 H13 N O4 S2 -","- C60 H52 N4 O16 S8 -","4","1","","Zhou, Kaida; Xia, Hongguang; Wu, Jie","Generation of benzosultams via a radical process with the insertion of sulfur dioxide","Organic Chemistry Frontiers","2017","4","6","1121","","10.1039/C7QO00127D","","","0.71073","MoKα","","0.1152","0.0582","","","0.1803","0.2242","","","","","","0.947","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553750","9.0047","0.0003","9.2247","0.0003","9.4826","0.0003","109.875","0.003","108.593","0.003","107.103","0.003","626.45","0.05","100","","100","","","","","","","","","4","P 1","P 1","1","","","","- C26 H31 N3 O6 -","- C26 H31 N3 O6 -","- C26 H31 N3 O6 -","1","1","","Guo, Jing; Lin, Zi-Hui; Chen, Kai-Bin; Xie, Ying; Chan, Albert S. C.; Weng, Jiang; Lu, Gui","Asymmetric amination of 2-substituted indolin-3-ones catalyzed by natural cinchona alkaloids","Organic Chemistry Frontiers","2017","4","7","1400","","10.1039/C7QO00129K","","x-ray","1.54184","CuKα","","0.0421","0.0417","","","0.121","0.122","","","","","","1.0608","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553751","8.9558","0.0013","9.4432","0.0013","13.6247","0.0018","92.926","0.003","95.287","0.004","111","0.003","1066.8","0.3","240","2","240","2","","","","","","","","3","P -1","-P 1","2","10,10""-dioxyl-9,9':10',9""-teranthrylene","","","- C54 H48 O8 -","- C54 H48 O8 -","- C54 H48 O8 -","1","0.5","","Hirao, Yasukazu; Konishi, Akihito; Kubo, Takashi","Anthroxyl-based biradical: toward the construction of highly stable multi-spin systems","Organic Chemistry Frontiers","2017","4","5","828","","10.1039/C7QO00130D","","","0.71075","MoKα","","0.1807","0.076","","","0.1962","0.2698","","","","","","0.968","","","","has coordinates,has disorder","235976","2020-10-21","18:00:00",""
"1553752","11.8673","0.0003","14.8352","0.0003","15.9367","0.0005","90","","102.976","0.0009","90","","2734.08","0.12","120","2","120","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","2,2"",7,7""-tetra-tert-butyl-10,10""-dioxyl-9,9':10',9""-teranthrylene","","","- C66 H72 O6 -","- C66 H68 O6 -","- C132 H136 O12 -","2","0.5","","Hirao, Yasukazu; Konishi, Akihito; Kubo, Takashi","Anthroxyl-based biradical: toward the construction of highly stable multi-spin systems","Organic Chemistry Frontiers","2017","4","5","828","","10.1039/C7QO00130D","","","0.71075","MoKα","","0.0855","0.0637","","","0.1863","0.2067","","","","","","1.103","","","","has coordinates,has disorder","235976","2020-10-21","18:00:00",""
"1553753","23.6823","0.0014","14.1831","0.0008","19.4393","0.001","90","","101.921","0.0017","90","","6388.6","0.6","296","2","296","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C41 H27 O -","- C41 H27 O -","- C328 H216 O8 -","8","1","","Ip, Ho-Wang; Chow, Hak-Fun; Kuck, Dietmar","Electronic and steric effects on the three-fold Scholl-type cycloheptatriene ring formation around a tribenzotriquinacene core","Organic Chemistry Frontiers","2017","4","5","817","","10.1039/C7QO00132K","","","0.71073","MoKα","","0.0864","0.058","","","0.1439","0.1598","","","","","","1.045","","","","has coordinates","235978","2020-10-21","18:00:00",""
"1553754","12.4244","0.0009","8.0614","0.0006","14.7164","0.001","90","","100.607","0.002","90","","1448.78","0.18","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","methyl 2-(3-methyl-11H-benzo[4,5]imidazo[2,1-a]isoindol-11-yl)acetate","","- C18 H16 N2 O2 -","- C18 H16 N2 O2 -","- C72 H64 N8 O8 -","4","1","","Selvaraju, Manikandan; Wang, Ying-Lien; Sun, Chung-Ming","Ruthenium(ii)-catalyzed C–H alkenylation/annulation cascade for the rapid synthesis of benzoimidazoisoindoles","Organic Chemistry Frontiers","2017","4","7","1358","","10.1039/C7QO00136C","","","0.71073","MoKα","","0.0463","0.0376","","","0.0917","0.0982","","","","","","1.03","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553755","8.086","0.005","14.196","0.005","23.304","0.005","90","0.005","90","0.005","90","0.005","2675","2","293","2","293","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C7.75 H7.75 F7.75 N7.75 O7.75 S7.75 -","- C30 H19 F3 N O5 S2 -","- C120 H76 F12 N4 O20 S8 -","4","1","","Pouambeka, Tony Wheellyam; Zhang, Ge; Zheng, Guang-Fan; Xu, Guo-Xing; Zhang, Qian; Xiong, Tao; Zhang, Qian","Copper-catalyzed oxidative amidation of α,β-unsaturated ketones via selective C‒H or C‒C bond cleavage","Organic Chemistry Frontiers","2017","4","7","1420","","10.1039/C7QO00146K","","","0.71069","MoKα","","0.0936","0.064","","","0.1363","0.1534","","","","","","1.03","","","","has coordinates","235982","2020-10-21","18:00:00",""
"1553756","5.9608","0.0004","18.7773","0.0009","20.3817","0.0011","90","","90","","90","","2281.3","0.2","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C27 H21 N O2 S2 -","- C27 H21 N O2 S2 -","- C108 H84 N4 O8 S8 -","4","1","","Shi, Qing; Li, Pinhua; Zhang, Yan; Wang, Lei","Visible light-induced tandem oxidative cyclization of 2-alkynylanilines with disulfides (diselenides) to 3-sulfenyl- and 3-selenylindoles under transition metal-free and photocatalyst-free conditions","Organic Chemistry Frontiers","2017","4","7","1322","","10.1039/C7QO00152E","","","0.71073","MoKα","","0.041","0.0337","","","0.0813","0.0861","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553757","9.0611","0.0006","7.1551","0.0004","20.5051","0.0018","90","","93.684","0.006","90","","1326.66","0.16","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H12 Cl N O -","- C16 H12 Cl N O -","- C64 H48 Cl4 N4 O4 -","4","1","","Zhang, Zhiguo; Zhang, Yongchao; Huang, Guoqing; Zhang, Guisheng","Organoiodine reagent-promoted intermolecular oxidative amination: synthesis of cyclopropyl spirooxindoles","Organic Chemistry Frontiers","2017","4","7","1372","","10.1039/C7QO00156H","","x-ray","1.54184","CuKα","","0.054","0.0443","","","0.1155","0.1246","","","","","","1.039","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553758","8.3955","0.0002","14.09","0.0004","16.7651","0.0005","90","","90","","90","","1983.19","0.09","100","","100","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C17 H18 Br F3 N2 O6 -","- C17 H18 Br F3 N2 O6 -","- C68 H72 Br4 F12 N8 O24 -","4","1","","Liu, Qiang; Zhao, Kun; Zhi, Ying; Raabe, Gerhard; Enders, Dieter","Squaramide-catalyzed domino Michael/aza-Henry [3 + 2] cycloaddition: asymmetric synthesis of functionalized 5-trifluoromethyl and 3-nitro substituted pyrrolidines","Organic Chemistry Frontiers","2017","4","7","1416","","10.1039/C7QO00161D","","","1.54178","CuKα","","0.028","0.028","","0.031","","0.031","","","1.002","","","1.006","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553759","9.593","0.004","15.307","0.007","16.705","0.008","90","","93.785","0.008","90","","2447.6","1.9","100.01","0.1","100.01","0.1","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C23 H22 Br Cl2 N3 O5 -","- C23 H22 Br Cl2 N3 O5 -","- C92 H88 Br4 Cl8 N12 O20 -","4","1","","Chen, Dong-Zhen; Xiao, Wen-Jing; Chen, Jia-Rong","Synthesis of spiropyrazoline oxindoles by a formal [4 + 1] annulation reaction between 3-bromooxindoles and in situ-derived 1,2-diaza-1,3-dienes","Organic Chemistry Frontiers","2017","4","7","1289","","10.1039/C7QO00163K","","","0.71073","MoKα","","0.0598","0.0405","","","0.1088","0.1204","","","","","","1.023","","","","has coordinates,has disorder","235989","2020-10-21","18:00:00",""
"1553760","6.299","0.008","11.774","0.015","14.904","0.019","99.608","0.016","94.163","0.015","96.363","0.016","1078","2","298","2","298.15","","","","","","","","","6","P -1","-P 1","2","","","","- C20 H17 Br Cl3 N3 O3 -","- C20 H17 Br Cl3 N3 O3 -","- C40 H34 Br2 Cl6 N6 O6 -","2","1","","Chen, Dong-Zhen; Xiao, Wen-Jing; Chen, Jia-Rong","Synthesis of spiropyrazoline oxindoles by a formal [4 + 1] annulation reaction between 3-bromooxindoles and in situ-derived 1,2-diaza-1,3-dienes","Organic Chemistry Frontiers","2017","4","7","1289","","10.1039/C7QO00163K","","","0.71073","MoKα","","0.2","0.1125","","","0.2823","0.3492","","","","","","1.051","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553761","7.738","0.0005","11.656","0.0008","14.0895","0.0008","90","","90","","90","","1270.79","0.14","298.84","0.1","298.84","0.1","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","2',3'-dihydrospiro[cyclopentane-1,1'-cyclopenta[a]naphthalen]-2-one","","- C17 H16 O -","- C17 H16 O -","- C68 H64 O4 -","4","1","","Zhang, Bo-Sheng; Hua, Hui-Liang; Gao, Lu-Yao; Liu, Ce; Qiu, Yi-Feng; Zhou, Ping-Xin; Zhou, Zhao-Zhao; Zhao, Jia-Hui; Liang, Yong-Min","Palladium-catalyzed arene C–H activation/ketone C–H functionalization reaction: route to spirodihydroindenones","Organic Chemistry Frontiers","2017","4","7","1376","","10.1039/C7QO00164A","","x-ray","0.71073","MoKα","","0.0845","0.0553","","","0.112","0.1329","","","","","","1.109","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553762","16.382","0.004","18.322","0.004","14.538","0.003","90","","120.472","0.003","90","","3760.9","1.5","","","273.15","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","1-phenyl-2-tosyl-9H-pyrrolo[1,2-a]indole","","- C24 H19 N O2 S -","- C24 H19 N O2 S -","- C192 H152 N8 O16 S8 -","8","1","","Zhang, Pengbo; Gao, Yuzhen; Chen, Su; Tang, Guo; Zhao, Yufen","Direct synthesis of 2-sulfonated 9H-pyrrolo[1,2-a]indoles via NaI-catalyzed cascade radical addition/cyclization/isomerization","Organic Chemistry Frontiers","2017","4","7","1350","","10.1039/C7QO00167C","","","0.71073","MoKα","","0.0751","0.0546","","","0.1568","0.171","","","","","","1.1214","","","","has coordinates","300101","2025-06-17","17:58:10",""
"1553763","7.1026","0.0003","7.8866","0.0003","11.4159","0.0005","92.777","0.002","92.263","0.002","114.968","0.001","577.75","0.04","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C14 H12 N2 O3 -","- C14 H12 N2 O3 -","- C28 H24 N4 O6 -","2","1","","Hong, Longcheng; Ahles, Sebastian; Strauss, Marcel A.; Logemann, Christian; Wegner, Hermann A.","Synthesis of 2,3-diaza-anthraquinones via the bidentate Lewis acid catalysed inverse electron-demand Diels–Alder (IEDDA) reaction","Organic Chemistry Frontiers","2017","4","5","871","","10.1039/C7QO00172J","","","0.71073","MoKα","","0.0557","0.045","","","0.1174","0.1233","","","","","","1.084","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553764","8.7048","0.001","10.5461","0.0013","13.9946","0.0017","82.33","0.002","79.359","0.002","79.1","0.002","1233.4","0.3","293","2","293","2","","","","","","","","7","P -1","-P 1","2","","","","- C25 H22 F I2 N O2 S -","- C25 H22 F I2 N O2 S -","- C50 H44 F2 I4 N2 O4 S2 -","2","1","","Wang, Qiang; Jiang, Bo; Yu, Liu-Zhu; Wei, Yin; Shi, Min","Iron-catalyzed or iodine-induced intramolecular halocyclization of N-vinyl-tethered methylenecyclopropanes: facile access to halogenated 1,2-dihydroquinolines","Organic Chemistry Frontiers","2017","4","7","1294","","10.1039/C7QO00177K","","","0.71073","MoKα","","0.034","0.0293","","","0.0767","0.0796","","","","","","1.045","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553765","13.2671","0.0017","18.296","0.003","19.283","0.003","90","","108.684","0.003","90","","4434","1.2","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C25 H24 Cl N O2 S -","- C25 H24 Cl N O2 S -","- C200 H192 Cl8 N8 O16 S8 -","8","2","","Wang, Qiang; Jiang, Bo; Yu, Liu-Zhu; Wei, Yin; Shi, Min","Iron-catalyzed or iodine-induced intramolecular halocyclization of N-vinyl-tethered methylenecyclopropanes: facile access to halogenated 1,2-dihydroquinolines","Organic Chemistry Frontiers","2017","4","7","1294","","10.1039/C7QO00177K","","","0.71073","MoKα","","0.1036","0.0688","","","0.1689","0.1901","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553766","12.112","0.003","13.064","0.003","13.586","0.003","113.51","0.02","114.37","0.02","96.715","0.018","1690.6","0.9","295","2","295","2","","","","","","","","4","P -1","-P 1","2","","","","- C18 H17 N S3 -","- C18 H17 N S3 -","- C72 H68 N4 S12 -","4","2","","Schneeweis, Arno; Neidlinger, Andreas; Reiss, Guido J.; Frank, Walter; Heinze, Katja; Müller, Thomas J. J.","Radical cation and dication of a 4H-dithieno[2,3-b:3′,2′-e][1,4]-thiazine","Organic Chemistry Frontiers","2017","4","5","839","","10.1039/C7QO00188F","","","0.71073","MoKα","","0.0962","0.0668","","","0.1361","0.1532","","","","","","1.198","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553767","9.3089","0.0019","10.692","0.002","10.826","0.002","98.78","0.004","90.325","0.004","108.111","0.004","1010.5","0.3","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C26 H20 F3 N O -","- C26 H20 F3 N O -","- C52 H40 F6 N2 O2 -","2","1","","An, Yuanyuan; Zhang, Jun; Xia, Hongguang; Wu, Jie","Radical cyclization of benzene-tethered 1,7-enynes with aryldiazonium tetrafluoroborates: a facile route to benzo[j]phenanthridines","Organic Chemistry Frontiers","2017","4","7","1318","","10.1039/C7QO00193B","","","0.71073","MoKα","","0.1156","0.0615","","","0.1912","0.2556","","","","","","0.988","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553768","8.7598","0.0009","25.852","0.003","8.8958","0.0009","90","","96.431","0.002","90","","2001.9","0.4","133","2","133","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C22 H26 F2 N2 O2 -","- C22 H26 F2 N2 O2 -","- C88 H104 F8 N8 O8 -","4","1","","Liu, Kai; Sui, Lin-Chao; Jin, Qiao; Li, Deng-Yuan; Liu, Pei-Nian","CuBr-mediated radical cascade difluoroacetamidation of acrylamides using α,α-difluoro-α-(TMS)-acetamides","Organic Chemistry Frontiers","2017","4","8","1606","","10.1039/C7QO00209B","","","0.71073","MoKα","","0.0599","0.0381","","","0.0827","0.0932","","","","","","1.01","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553769","21.229","0.01","3.919","0.0019","15.628","0.008","90","","105.861","0.011","90","","1250.7","1.1","273","2","273","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H11 F N2 O -","- C16 H11 F N2 O -","- C64 H44 F4 N8 O4 -","4","1","","Ding, Junshuai; Zhang, Yingchao; Li, Jizhen","Nickel-catalyzed selective C-5 fluorination of 8-aminoquinolines with NFSI","Organic Chemistry Frontiers","2017","4","8","1528","","10.1039/C7QO00211D","","","0.71073","MoKα","","0.1172","0.0737","","","0.2007","0.2307","","","","","","0.994","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553770","11.93574","0.00015","7.18231","0.00008","19.3705","0.0002","90","","94.7142","0.0011","90","","1654.94","0.03","150","0.1","150","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H12 Cl3 N O0 -","- C20 H12 Cl3 N -","- C80 H48 Cl12 N4 -","4","1","","Li, Jianxiao; An, Yanni; Li, Jiawei; Yang, Shaorong; Wu, Wanqing; Jiang, Huanfeng","Palladium-catalyzed C‒S bond activation and functionalization of 3-sulfenylindoles and related electron-rich heteroarenes","Organic Chemistry Frontiers","2017","4","8","1590","","10.1039/C7QO00215G","","x-ray","1.54184","CuKα","","0.0414","0.0398","","","0.1081","0.1101","","","","","","1.057","","","","has coordinates","236006","2020-10-21","18:00:00",""
"1553771","9.8942","0.0018","11.644","0.002","20.487","0.004","87.078","0.008","78.302","0.009","68.651","0.006","2152","0.7","173.15","","173.15","","","","","","","","","5","P -1","-P 1","2","","","","- C34 H52 Cl4 N16 O2 -","- C34 H52 Cl4 N16 O2 -","- C68 H104 Cl8 N32 O4 -","2","1","","Liang, Dong-Dong; Wang, Mei-Xiang","Synthesis and conformational structure of hydrazo-bridged homo calix[2]pyridine[2]triazines","Organic Chemistry Frontiers","2017","4","7","1425","","10.1039/C7QO00221A","","","0.71073","MoKα","","0.1208","0.1118","","","0.3058","0.3152","","","","","","1.12","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553772","11.9766","0.0004","19.3355","0.0005","12.7804","0.0004","90","","114.734","0.004","90","","2688.09","0.17","173","0.1","173","0.1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C5.33 H10 Cl0.67 Co0.33 N2.67 O4 -","- C5.33333 H10 Cl0.666667 Co0.333333 N2.66667 O4 -","- C64 H120 Cl8 Co4 N32 O48 -","12","3","","Liang, Dong-Dong; Wang, Mei-Xiang","Synthesis and conformational structure of hydrazo-bridged homo calix[2]pyridine[2]triazines","Organic Chemistry Frontiers","2017","4","7","1425","","10.1039/C7QO00221A","","x-ray","1.54184","CuKα","","0.0713","0.0627","","","0.1679","0.1785","","","","","","1.048","","","","has coordinates","236009","2020-10-21","18:00:00",""
"1553773","13.18","0.003","19.895","0.004","20.59","0.004","108.27","0.03","107.63","0.03","90.48","0.03","4854","2","173.15","","173.15","","","","","","","","","5","P -1","-P 1","2","","","","- C27 H41 N16 O3.5 S1.5 -","- C27 H41 N16 O3.5 S1.5 -","- C108 H164 N64 O14 S6 -","4","2","","Liang, Dong-Dong; Wang, Mei-Xiang","Synthesis and conformational structure of hydrazo-bridged homo calix[2]pyridine[2]triazines","Organic Chemistry Frontiers","2017","4","7","1425","","10.1039/C7QO00221A","","","0.71073","MoKα","","0.1775","0.152","","","0.4104","0.4325","","","","","","1.136","","","","has coordinates","274176","2022-03-31","10:10:26",""
"1553774","9.003","0.01","10.762","0.012","11.631","0.012","73.19","0.06","69.99","0.05","72.45","0.04","987.6","1.9","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C20 H23 B F2 N2 O2 -","- C20 H23 B F2 N2 O2 -","- C40 H46 B2 F4 N4 O4 -","2","1","","Kubota, Yasuhiro; Tsukamoto, Masahiro; Ohnishi, Katsuhiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki","Synthesis and fluorescence properties of novel squarylium–boron complexes","Organic Chemistry Frontiers","2017","4","8","1522","","10.1039/C7QO00225D","","","0.71075","MoKα","","0.0802","0.0596","","","0.1648","0.1833","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553775","8.6045","0.0006","11.4959","0.0007","10.3691","0.0006","90","","114.544","0.002","90","","933","0.1","296","2","296","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C21 H17 Cl F3 N3 -","- C21 H17 Cl F3 N3 -","- C42 H34 Cl2 F6 N6 -","2","1","","Xie, En; Rahman, Abdul; Lin, Xufeng","Asymmetric synthesis of CF3- and indole-containing tetrahydro-β-carbolines via chiral spirocyclic phosphoric acid-catalyzed aza-Friedel–Crafts reaction","Organic Chemistry Frontiers","2017","4","7","1407","","10.1039/C7QO00229G","","","0.71073","MoKα","","0.0749","0.0341","","","0.0633","0.0903","","","","","","1.003","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553776","10.326","0.002","9.584","0.0019","19.601","0.004","90","","104.43","0.03","90","","1878.6","0.7","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H17 I N2 -","- C22 H17 I N2 -","- C88 H68 I4 N8 -","4","1","","Liu, Cheng-Kou; Yang, Zhao; Zeng, Yu; Guo, Kai; Fang, Zheng; Li, Bo","Sodium nitrite-promoted aerobic oxidative coupling of aryl methyl ketones with ammonium under metal-free conditions: a facile access to polysubstitution imidazoles","Organic Chemistry Frontiers","2017","4","8","1508","","10.1039/C7QO00247E","","","0.71073","MoKα","","0.1106","0.0541","","","0.1168","0.137","","","","","","1","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553777","5.7817","0.0012","8.2558","0.001","19.972","0.002","90","","90","","90","","953.3","0.2","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C10 H12 O2 S -","- C10 H12 O2 S -","- C40 H48 O8 S4 -","4","1","","Meng, Ke; Xia, Jingzhao; Wang, Yanzhao; Zhang, Xinghua; Yang, Guoqiang; Zhang, Wanbin","Ir/BiphPHOX-catalyzed asymmetric hydrogenation of 3-substituted 2,5-dihydropyrroles and 2,5-dihydrothiophene 1,1-dioxides","Organic Chemistry Frontiers","2017","4","8","1601","","10.1039/C7QO00248C","","","1.54178","CuKα","","0.0341","0.034","","","0.0898","0.09","","","","","","1.079","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553778","11.3637","0.0004","6.0455","0.0003","11.3636","0.0004","90","","98.45","","90","","772.2","0.05","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C17 H19 N O2 S -","- C17 H19 N O2 S -","- C34 H38 N2 O4 S2 -","2","1","","Meng, Ke; Xia, Jingzhao; Wang, Yanzhao; Zhang, Xinghua; Yang, Guoqiang; Zhang, Wanbin","Ir/BiphPHOX-catalyzed asymmetric hydrogenation of 3-substituted 2,5-dihydropyrroles and 2,5-dihydrothiophene 1,1-dioxides","Organic Chemistry Frontiers","2017","4","8","1601","","10.1039/C7QO00248C","","","1.54178","CuKα","","0.0426","0.0352","","","0.0792","0.083","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553779","11.0348","0.0007","21.2718","0.0012","7.2221","0.0006","90","","90","","90","","1695.2","0.2","184.3","0.3","184.3","0.3","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C21 H16 N2 O3 -","- C21 H16 N2 O3 -","- C84 H64 N8 O12 -","4","1","","Tang, Hai-Tao; Zeng, Jia-Hao; Chen, Jun-Jia; Zhou, Yun-Bing; Li, Ren-Hao; Zhan, Zhuang-Ping","Synthesis of pyrazolo[5,1-a]isoquinolines through copper-catalyzed regioselective bicyclization of N-propargylic sulfonylhydrazones","Organic Chemistry Frontiers","2017","4","8","1513","","10.1039/C7QO00249A","","","0.71073","MoKα","","0.0713","0.061","","","0.1247","0.1292","","","","","","1.161","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553780","17.5265","0.0008","18.9585","0.0009","11.1154","0.0005","90","","120.995","0.002","90","","3166","0.3","298","2","298","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C19 H11 Cl F3 N O -","- C19 H11 Cl F3 N O -","- C152 H88 Cl8 F24 N8 O8 -","8","1","","Mishra, Kalpana; Singh, Jay Bahadur; Gupta, Tanu; Singh, Radhey M.","TBAB-catalyzed cascade reactions: facile synthesis of 1-trifluoromethyl-3-alkylidene-1,3-dihydrofuro[3,4-b]quinolines via 5-exo-dig cyclization of o-arylalkynylquinoline aldehydes","Organic Chemistry Frontiers","2017","4","10","1926","","10.1039/C7QO00273D","","","0.71073","MoKα","","0.0617","0.0439","","","0.1131","0.1244","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553781","5.0951","0.0004","6.0539","0.0006","14.8931","0.0015","90","","90","","90","","459.38","0.07","273","2","273","2","","","","","","","","4","P n m a","-P 2ac 2n","62","N-Methylcarbamoyl","","","- C2 H4 N4 O -","- C2 H4 N4 O -","- C8 H16 N16 O4 -","4","0.5","","Wan, Huabin; Li, Hongmin; Xu, Jian; Wu, Zhuang; Liu, Qifan; Chu, Xianxu; Abe, Manabu; Bégué, Didier; Zeng, Xiaoqing","N-Methylcarbamoyl azide: spectroscopy, X-ray structure and decomposition via methylcarbamoyl nitrene","Organic Chemistry Frontiers","2017","4","9","1839","","10.1039/C7QO00277G","","","0.71073","MoKα","","0.0512","0.0451","","","0.1313","0.1346","","","","","","2.174","","","","has coordinates","236023","2020-10-21","18:00:00",""
"1553782","12.326","0.004","11.032","0.004","13.445","0.005","90","","90","","90","","1828.3","1.1","293","2","293","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C21 H18 F2 O4 -","- C21 H18 F2 O4 -","- C84 H72 F8 O16 -","4","1","","Li, Yuewen; Lu, Yiye; Mao, Runyu; Li, Zhiming; Wu, Jie","A photoinduced reaction of perfluoroalkyl halides with 1,3-diarylprop-2-yn-1-ones catalyzed by DABSO","Organic Chemistry Frontiers","2017","4","9","1745","","10.1039/C7QO00279C","","","0.71073","MoKα","","0.0343","0.0325","","","0.0913","0.0937","","","","","","1.076","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553783","10.7971","0.0008","15.2395","0.0013","26.1285","0.0019","90","","90","","90","","4299.2","0.6","180","0.1","180","0.1","","","","","","","","4","P b c a","-P 2ac 2ab","61","","Ph-4Br-Pyr","","- C22 H18 Br4 N2 -","- C22 H18 Br4 N2 -","- C176 H144 Br32 N16 -","8","1","","Huang, Zhe; Zhan, Ming; Zhang, Shaoguang; Luo, Qian; Zhang, Wen-Xiong; Xi, Zhenfeng","Synthesis of dibromo- and tetrabromo-bipyrrolines and their corresponding 2,6-diazasemibullvalene derivatives","Organic Chemistry Frontiers","2017","4","9","1785","","10.1039/C7QO00287D","","","0.7107","MoKα","","0.0826","0.0529","","","0.0992","0.1106","","","","","","1.065","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553784","6.6642","0.0004","19.8278","0.0016","14.8224","0.001","90","","101.924","0.007","90","","1916.3","0.2","180.01","0.1","180.01","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","tBu-2Br-NSBV-re","","- C18 H26 Br2 N2 -","- C18 H26 Br2 N2 -","- C72 H104 Br8 N8 -","4","1","","Huang, Zhe; Zhan, Ming; Zhang, Shaoguang; Luo, Qian; Zhang, Wen-Xiong; Xi, Zhenfeng","Synthesis of dibromo- and tetrabromo-bipyrrolines and their corresponding 2,6-diazasemibullvalene derivatives","Organic Chemistry Frontiers","2017","4","9","1785","","10.1039/C7QO00287D","","","0.71073","MoKα","","0.0978","0.0537","","","0.1172","0.132","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553785","23.66","0.002","10.2673","0.001","10.5398","0.001","90","","90","","90","","2560.4","0.4","296","2","296","2","","","","","","","","6","P 21 21 2","P 2 2ab","18","","","","- C26 H25 F3 N O S -","- C26 H25 F3 N O S -","- C104 H100 F12 N4 O4 S4 -","4","1","","Liu, Bing; Zhang, Zhan-Ming; Xu, Bing; Xu, Shan; Wu, Hai-Hong; Liu, Yuanyuan; Zhang, Junliang","Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter","Organic Chemistry Frontiers","2017","4","9","1772","","10.1039/C7QO00291B","","","0.71073","MoKα","","0.0783","0.0617","","","0.1818","0.195","","","","","","1.098","","","","has coordinates","236029","2020-10-21","18:00:00",""
"1553786","8.5817","0.0002","10.4128","0.0003","27.6259","0.0007","90","","90","","90","","2468.64","0.11","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C27 H23 Cl F3 N O3 -","- C27 H23 Cl F3 N O3 -","- C108 H92 Cl4 F12 N4 O12 -","4","1","","Liu, Bing; Zhang, Zhan-Ming; Xu, Bing; Xu, Shan; Wu, Hai-Hong; Liu, Yuanyuan; Zhang, Junliang","Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter","Organic Chemistry Frontiers","2017","4","9","1772","","10.1039/C7QO00291B","","","0.71073","MoKα","","0.0445","0.034","","","0.077","0.0828","","","","","","1.054","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553787","6.2282","0.0002","7.0351","0.0002","36.2461","0.0013","90","","90","","90","","1588.16","0.09","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C15 H16 F3 N O2 S -","- C15 H16 F3 N O2 S -","- C60 H64 F12 N4 O8 S4 -","4","1","","Liu, Bing; Zhang, Zhan-Ming; Xu, Bing; Xu, Shan; Wu, Hai-Hong; Liu, Yuanyuan; Zhang, Junliang","Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter","Organic Chemistry Frontiers","2017","4","9","1772","","10.1039/C7QO00291B","","","0.71073","MoKα","","0.0481","0.0415","","","0.1071","0.1119","","","","","","1.06","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553788","12.9056","0.0003","8.981","0.0002","20.4045","0.0005","90","","106.848","0.003","90","","2263.48","0.1","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C28 H21 N2 O2 P -","- C28 H21 N2 O2 P -","- C112 H84 N8 O8 P4 -","4","1","","Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie","Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides","Organic Chemistry Frontiers","2017","4","10","1981","","10.1039/C7QO00305F","","x-ray","1.54184","CuKα","","0.0506","0.0412","","","0.1062","0.1138","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553789","14.3374","0.0005","9.71","0.0004","18.7718","0.0007","90","","105.341","0.004","90","","2520.22","0.17","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C28 H21 N2 O2 P -","- C28 H21 N2 O2 P -","- C112 H84 N8 O8 P4 -","4","1","","Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie","Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides","Organic Chemistry Frontiers","2017","4","10","1981","","10.1039/C7QO00305F","","x-ray","1.54184","CuKα","","0.0561","0.0467","","","0.1343","0.1436","","","","","","1.049","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553790","9.5853","0.0009","9.8739","0.0008","14.7007","0.0014","103.11","0.008","94.035","0.008","114.371","0.008","1213.1","0.2","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C29 H23 N2 O3 P -","- C29 H23 N2 O3 P -","- C58 H46 N4 O6 P2 -","2","1","","Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie","Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides","Organic Chemistry Frontiers","2017","4","10","1981","","10.1039/C7QO00305F","","x-ray","1.54184","CuKα","","0.0583","0.0467","","","0.1246","0.136","","","","","","1.021","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553791","11.9961","0.0005","8.631","0.0003","21.6563","0.0007","90","","95.014","0.004","90","","2233.68","0.14","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C28 H21 N2 O2 P -","- C28 H21 N2 O2 P -","- C112 H84 N8 O8 P4 -","4","1","","Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie","Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides","Organic Chemistry Frontiers","2017","4","10","1981","","10.1039/C7QO00305F","","x-ray","1.54184","CuKα","","0.0494","0.0406","","","0.1051","0.1133","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553792","9.0757","0.0002","10.4623","0.0002","26.2445","0.0005","90","","90","","90","","2491.99","0.09","290","2","290","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C33 H27 O2 P -","- C33 H27 O2 P -","- C132 H108 O8 P4 -","4","1","","Li, Bin; Zhang, Mingkai; Huang, Xulun; Gu, Zhenhua","Synthesis of 2,3-dihydro-1H-phosphindole-1-oxides via the t-BuLi-mediated rearrangement of vinyl bromides and phosphine oxides","Organic Chemistry Frontiers","2017","4","9","1854","","10.1039/C7QO00310B","","","1.54184","CuKα","","0.0326","0.0313","","","0.0828","0.0843","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553793","12.3885","0.0001","18.8197","0.0002","10.4583","0.0001","90","","103.828","0.001","90","","2367.66","0.04","291","2","291","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C32 H25 O P -","- C32 H25 O P -","- C128 H100 O4 P4 -","4","1","","Li, Bin; Zhang, Mingkai; Huang, Xulun; Gu, Zhenhua","Synthesis of 2,3-dihydro-1H-phosphindole-1-oxides via the t-BuLi-mediated rearrangement of vinyl bromides and phosphine oxides","Organic Chemistry Frontiers","2017","4","9","1854","","10.1039/C7QO00310B","","","1.54184","CuKα","","0.0402","0.0375","","","0.1027","0.1053","","","","","","1.056","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553794","10.0442","0.0004","10.4197","0.0004","11.9542","0.0005","84.471","0.002","84.954","0.002","75.059","0.002","1200.58","0.08","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C28 H33 B O4 -","- C28 H33 B O4 -","- C56 H66 B2 O8 -","2","1","","Hsieh, Jen-Chieh; Hong, Ya-Chun; Yang, Chun-Ming; Mannathan, Subramaniyan; Cheng, Chien-Hong","Nickel-catalyzed highly chemo- and stereoselective borylative cyclization of 1,6-enynes with bis(pinacolato)diboron","Organic Chemistry Frontiers","2017","4","8","1615","","10.1039/C7QO00321H","","","0.71073","MoKα","","0.0726","0.052","","","0.1247","0.1392","","","","","","1.046","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553795","22.0623","0.0004","14.5144","0.0003","5.67392","0.0001","90","","90","","90","","1816.91","0.06","294.08","0.1","294.08","0.1","","","","","","","","4","P 21 21 2","P 2 2ab","18","","","","- C19 H19 Br O6 -","- C19 H19 Br O6 -","- C76 H76 Br4 O24 -","4","1","","Hao, Xiaoyu; Lin, Lili; Tan, Fei; Ge, Shulin; Liu, Xiaohua; Feng, Xiaoming","Asymmetric synthesis of chromans via the Friedel–Crafts alkylation–hemiketalization catalysed by an N,N′-dioxide scandium(iii) complex","Organic Chemistry Frontiers","2017","4","8","1647","","10.1039/C7QO00323D","","x-ray","1.54184","CuKα","","0.0429","0.042","","","0.1027","0.1042","","","","","","1.071","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553796","10.4368","0.0004","6.0294","0.0002","15.7294","0.0005","90","","107.537","0.004","90","","943.81","0.06","200","1","200","1","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C21 H18 Br N O3 -","- C21 H18 Br N O3 -","- C42 H36 Br2 N2 O6 -","2","1","","De Munck, Lode; Sukowski, Verena; Vila, Carlos; Muñoz, M. Carmen; Pedro, José R.","Catalytic enantioselective aza-Reformatsky reaction with seven-membered cyclic imines dibenzo[b,f][1,4]oxazepines","Organic Chemistry Frontiers","2017","4","8","1624","","10.1039/C7QO00329C","","","0.71073","MoKα","","0.0494","0.0362","","","0.0782","0.0855","","","","","","0.969","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553797","9.17425","0.00019","7.88736","0.00013","21.7312","0.0004","90","","99.3556","0.0019","90","","1551.57","0.05","100.01","0.1","100.01","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H13 F N2 O -","- C20 H13 F N2 O -","- C80 H52 F4 N8 O4 -","4","1","","Ren, Xuhong; Wang, Qiyang; Yu, Wenjia; Zhan, Xiaoyu; Yao, Yishan; Qin, Bingjie; Dong, Mingxin; He, Xinhua","Photoredox catalytic intramolecular imine C–H bond functionalization using ligand free Cu(ii) salts","Organic Chemistry Frontiers","2017","4","10","2022","","10.1039/C7QO00348J","","x-ray","1.54184","CuKα","","0.0399","0.0374","","","0.0987","0.1009","","","","","","1.051","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553798","7.6272","0.0007","13.3952","0.0013","11.846","0.0012","90","","90.87","0.003","90","","1210.1","0.2","296","2","296","2","","","","","","","","4","C 1 c 1","C -2yc","9","","2,4,9-trinitro-2,4,9-triazaadamantane-7-yl nitrate","","- C7 H9 N7 O9 -","- C7 H9 N7 O9 -","- C28 H36 N28 O36 -","4","1","","Hou, Tianjiao; Zhang, Jian; Wang, Chenjiao; Luo, Jun","A facile method to construct a 2,4,9-triazaadamantane skeleton and synthesize nitramine derivatives","Organic Chemistry Frontiers","2017","4","9","1819","","10.1039/C7QO00357A","","","0.71073","MoKα","","0.0262","0.0256","","","0.0682","0.0686","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553799","15.7593","0.0003","6.7689","0.0002","21.0839","0.0004","90","","104.622","0.001","90","","2176.24","0.09","200","2","200","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H40 O3 Si -","- C21 H40 O3 Si -","- C84 H160 O12 Si4 -","4","1","","Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis","Gold(i)-catalyzed access to neomerane skeletons","Organic Chemistry Frontiers","2017","4","10","1906","","10.1039/C7QO00360A","","","1.54178","CuKα","","0.0464","0.0372","","","0.0941","0.0995","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553800","8.7959","0.0005","10.4916","0.0006","13.2932","0.0008","70.468","0.002","74.252","0.002","71.371","0.002","1076.8","0.11","200","1","200","1","","","","","","","","4","P -1","-P 1","2","","","","- C22 H26 N4 O6 -","- C22 H26 N4 O6 -","- C44 H52 N8 O12 -","2","1","","Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis","Gold(i)-catalyzed access to neomerane skeletons","Organic Chemistry Frontiers","2017","4","10","1906","","10.1039/C7QO00360A","","","0.71073","MoKα","","0.0542","0.0453","","","0.1248","0.1323","","","","","","1.036","","","","has coordinates,has disorder","236048","2020-10-21","18:00:00",""
"1553801","15.8792","0.0005","7.383","0.0003","18.5839","0.0007","90","","94.011","0.002","90","","2173.37","0.14","200","2","200","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H26 N4 O6 -","- C22 H26 N4 O6 -","- C88 H104 N16 O24 -","4","1","","Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis","Gold(i)-catalyzed access to neomerane skeletons","Organic Chemistry Frontiers","2017","4","10","1906","","10.1039/C7QO00360A","","","1.54178","CuKα","","0.063","0.05","","","0.1208","0.1289","","","","","","1.034","","","","has coordinates","236048","2020-10-21","18:00:00",""
"1553802","19.2372","0.0012","19.7853","0.0013","12.577","0.0007","90","","107.983","0.003","90","","4553.1","0.5","200","1","200","1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H26 N4 O6 -","- C22 H26 N4 O6 -","- C176 H208 N32 O48 -","8","2","","Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis","Gold(i)-catalyzed access to neomerane skeletons","Organic Chemistry Frontiers","2017","4","10","1906","","10.1039/C7QO00360A","","","1.54178","CuKα","","0.0851","0.0689","","","0.2013","0.2182","","","","","","1.066","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553803","15.0743","0.0003","6.8149","0.0001","21.2545","0.0004","90","","92.709","0.001","90","","2181.03","0.07","200","2","200","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C21 H38 O3 Si -","- C21 H38 O3 Si -","- C84 H152 O12 Si4 -","4","1","","Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis","Gold(i)-catalyzed access to neomerane skeletons","Organic Chemistry Frontiers","2017","4","10","1906","","10.1039/C7QO00360A","","","0.71073","MoKα","","0.053","0.0386","","","0.1032","0.1112","","","","","","1.027","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553804","12.0087","0.0006","17.7464","0.0007","12.6045","0.0007","90","","103.892","0.005","90","","2607.6","0.2","293","2","293.15","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C28 H29 I O4 S -","- C28 H29 I O4 S -","- C112 H116 I4 O16 S4 -","4","1","","Miao, Maozhong; Xu, Huaping; Luo, Yi; Jin, Mengchao; Chen, Zhengkai; Xu, Jianfeng; Ren, Hongjun","A modular approach to highly functionalized 3-sulfonylfurans via conjugate addition of 3-cyclopropylideneprop-2-en-1-ones with sodium sulfinates and sequential 5-endo-trig iodocyclization","Organic Chemistry Frontiers","2017","4","9","1824","","10.1039/C7QO00362E","","","0.71073","MoKα","","0.0879","0.0665","","","0.1759","0.1906","","","","","","1.049","","","","has coordinates,has disorder","236050","2020-10-21","18:00:00",""
"1553805","9.8395","0.0017","10.7013","0.0019","10.8636","0.0019","114.335","0.002","94.477","0.002","116.312","0.002","885.4","0.3","296.15","","296.15","","","","","","","","","3","P -1","-P 1","2","","","","- C22 H20 O3 -","- C22 H20 O3 -","- C44 H40 O6 -","2","1","","Shi, Xiaonan; He, Yan; Zhang, Xinying; Fan, Xuesen","Selective syntheses of diversely substituted 2-hydroxy-4′-hydroxybenzophenones through [4 + 2] or [3 + 3] annulation of penta-3,4-dien-2-ones with 3-formylchromones","Organic Chemistry Frontiers","2017","4","10","1967","","10.1039/C7QO00366H","","x-ray","0.71073","MoKα","","0.0628","0.0473","","","0.1274","0.1434","","","","","","1.029","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553806","8.8173","0.0004","14.3926","0.0007","15.3659","0.0007","90","","90","","90","","1949.99","0.16","105.8","","105.8","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C22 H19 N O5 S -","- C22 H19 N O5 S -","- C88 H76 N4 O20 S4 -","4","1","","Xie, Lei; Ma, Hongli; Li, Jiaqi; Yu, Yuan; Qin, Zhaohai; Fu, Bin","Ni(ii)-Catalyzed enantioselective Mukaiyama–Mannich reaction between silyl enol ethers and cyclic N-sulfonyl α-ketiminoesters","Organic Chemistry Frontiers","2017","4","9","1858","","10.1039/C7QO00370F","","","1.5418","CuKα","","0.0275","0.0271","","","0.0686","0.0689","","","","","","1.061","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553807","8.2203","0.0005","9.1263","0.0005","13.0906","0.0007","90","","102.302","0.006","90","","959.52","0.1","106.3","","106.3","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C21 H23 N O5 S -","- C21 H23 N O5 S -","- C42 H46 N2 O10 S2 -","2","1","","Xie, Lei; Ma, Hongli; Li, Jiaqi; Yu, Yuan; Qin, Zhaohai; Fu, Bin","Ni(ii)-Catalyzed enantioselective Mukaiyama–Mannich reaction between silyl enol ethers and cyclic N-sulfonyl α-ketiminoesters","Organic Chemistry Frontiers","2017","4","9","1858","","10.1039/C7QO00370F","","","1.5418","CuKα","","0.0372","0.0366","","","0.0978","0.0986","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553808","29.3492","0.0015","12.5025","0.0006","25.3876","0.0013","90","","113.65","0.003","90","","8533.3","0.8","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C62 H102 Cl8 N26 O21 Zn2 -","- C62 H82 Cl8 N26 O12 Zn2 -","- C248 H328 Cl32 N104 O48 Zn8 -","4","0.5","","Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang","Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril","Organic Chemistry Frontiers","2017","4","9","1799","","10.1039/C7QO00376E","","","0.71073","MoKα","","0.0891","0.077","","","0.2427","0.253","","","","","","1.085","","","","has coordinates","236056","2020-10-21","18:00:00",""
"1553809","27.52","0.003","17.25","0.003","18.358","0.003","90","","94.006","0.007","90","","8694","2","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C60 H68 Cl8 N26 O28 Zn2 -","- C60 H70 Cl8 N26 O12 Zn2 -","- C240 H280 Cl32 N104 O48 Zn8 -","4","0.5","","Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang","Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril","Organic Chemistry Frontiers","2017","4","9","1799","","10.1039/C7QO00376E","","","0.71073","MoKα","","0.1071","0.0703","","","0.2108","0.2315","","","","","","1.079","","","","has coordinates","236056","2020-10-21","18:00:00",""
"1553810","12.2894","0.0018","12.4667","0.0017","14.986","0.002","73.289","0.004","84.747","0.004","62.451","0.004","1947.4","0.5","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C58 H94 Cl6 N26 O22 Zn2 -","- C58 H74 Cl6 N26 O14 Zn2 -","- C58 H74 Cl6 N26 O14 Zn2 -","1","0.5","","Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang","Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril","Organic Chemistry Frontiers","2017","4","9","1799","","10.1039/C7QO00376E","","","0.71073","MoKα","","0.076","0.053","","","0.1377","0.1484","","","","","","1.055","","","","has coordinates","236056","2020-10-21","18:00:00",""
"1553811","12.298","0.003","12.903","0.003","15.662","0.003","75.259","0.003","70.211","0.003","76.684","0.003","2233","0.9","273","2","273","2","","","","","","","","6","P -1","-P 1","2","","","","- C60 H112 Cl10 N26 O28 Zn2 -","- C60 H78 Cl10 N26 O12 Zn2 -","- C60 H78 Cl10 N26 O12 Zn2 -","1","0.5","","Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang","Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril","Organic Chemistry Frontiers","2017","4","9","1799","","10.1039/C7QO00376E","","","0.71073","MoKα","","0.0667","0.0576","","","0.1827","0.1918","","","","","","1.007","","","","has coordinates","236056","2020-10-21","18:00:00",""
"1553812","12.315","0.004","12.875","0.004","15.525","0.006","75.131","0.011","70.361","0.011","77.82","0.01","2219.6","1.3","296","2","296","2","","","","","","","","6","P -1","-P 1","2","","","","- C62 H108 Cl10 N26 O28 Zn2 -","- C62 H74 Cl10 N26 O22 Zn2 -","- C62 H74 Cl10 N26 O22 Zn2 -","1","0.5","","Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang","Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril","Organic Chemistry Frontiers","2017","4","9","1799","","10.1039/C7QO00376E","","","0.71073","MoKα","","0.1104","0.0836","","","0.2457","0.2745","","","","","","1.003","","","","has coordinates","236056","2020-10-21","18:00:00",""
"1553813","5.095","0.008","12.261","0.019","17","0.03","73.395","0.018","81.56","0.02","78.69","0.02","993","3","273","2","273","2","","","","","","","","5","P -1","-P 1","2","","","","- C21 H21 Br N2 O2 -","- C21 H19.5 Br N2 O2 -","- C42 H39 Br2 N4 O4 -","2","1","","Yan, Hao; Li, Xincheng; Wang, Chunxiang; Wan, Boshun","Silver-catalyzed cyclization of nitrones with 2-azetine: a radical approach to 2,3-disubstituted quinolines","Organic Chemistry Frontiers","2017","4","9","1833","","10.1039/C7QO00405B","","","0.71073","MoKα","","0.2545","0.0911","","","0.2098","0.2887","","","","","","0.963","","","","has coordinates,has disorder","236058","2020-10-21","18:00:00",""
"1553814","6.1408","0.0017","10.54","0.003","16.567","0.005","87.399","0.007","81.181","0.006","79.922","0.006","1043.1","0.5","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H26 N2 O4 -","- C22 H26 N2 O4 -","- C44 H52 N4 O8 -","2","1","","Yan, Hao; Li, Xincheng; Wang, Chunxiang; Wan, Boshun","Silver-catalyzed cyclization of nitrones with 2-azetine: a radical approach to 2,3-disubstituted quinolines","Organic Chemistry Frontiers","2017","4","9","1833","","10.1039/C7QO00405B","","","0.71073","MoKα","","0.1062","0.0721","","","0.1651","0.1818","","","","","","1.081","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553815","6.82668","0.00015","9.4989","0.0002","34.5079","0.001","90","","90","","90","","2237.7","0.09","293.49","0.15","293.49","0.15","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C23 H23 Cl O7 -","- C23 H23 Cl O7 -","- C92 H92 Cl4 O28 -","4","1","","Yao, Qian; Lin, Lili; Zhang, Hang; Yu, Han; Xiong, Qian; Liu, Xiaohua; Feng, Xiaoming","The asymmetric synthesis of multisubstituted diquinanes via the domino reaction of electron-deficient enynes","Organic Chemistry Frontiers","2017","4","10","2012","","10.1039/C7QO00408G","","x-ray","1.54184","CuKα","","0.0575","0.0535","","","0.1492","0.1553","","","","","","1.044","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553816","7.8333","0.0001","8.7742","0.0002","23.1441","0.0004","90","","95.475","0.001","90","","1583.46","0.05","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C19 H17 N O3 S -","- C19 H17 N O3 S -","- C76 H68 N4 O12 S4 -","4","1","","De Nisi, A.; Sierra, S.; Ferrara, M.; Monari, M.; Bandini, M.","TBAF catalyzed one-pot synthesis of allenyl-indoles","Organic Chemistry Frontiers","2017","4","9","1849","","10.1039/C7QO00414A","","","0.71073","MoKα","","0.0466","0.0328","","","0.0849","0.0909","","","","","","1.235","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553817","8.5679","0.0012","12.3701","0.0014","18.181","0.003","83.843","0.007","89.595","0.012","80.871","0.009","1891.4","0.5","296","2","296","2","","","","","","","","6","P 1","P 1","1","","","","- C20 H16 F3 N O3 S -","- C20 H15 F3 N O3 S -","- C80 H60 F12 N4 O12 S4 -","4","4","","De Nisi, A.; Sierra, S.; Ferrara, M.; Monari, M.; Bandini, M.","TBAF catalyzed one-pot synthesis of allenyl-indoles","Organic Chemistry Frontiers","2017","4","9","1849","","10.1039/C7QO00414A","","","0.71073","MoKα","","0.2446","0.0738","","","0.1707","0.2621","","","","","","0.892","","","","has coordinates","236062","2020-10-21","18:00:00",""
"1553818","14.884","0.002","4.3831","0.0006","27.39","0.003","90","","117.921","0.006","90","","1578.9","0.4","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C15 H10 I2 O4 -","- C15 H10 I2 O4 -","- C60 H40 I8 O16 -","4","1","","Tang, Yang; Yu, Qiong; Ma, Shengming","Efficient trifluoromethylation via the cyclopropanation of allenes and subsequent C–C bond cleavage","Organic Chemistry Frontiers","2017","4","9","1762","","10.1039/C7QO00419B","","","0.71073","MoKα","","0.1052","0.0835","","","0.1766","0.1859","","","","","","1.14","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553819","14.9433","0.0006","9.3141","0.0004","17.6377","0.0006","90","","102.36","0.001","90","","2397.98","0.16","173","2","173","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C25 H26 F3 N O5 -","- C25 H26 F3 N O5 -","- C100 H104 F12 N4 O20 -","4","1","","Tang, Yang; Yu, Qiong; Ma, Shengming","Efficient trifluoromethylation via the cyclopropanation of allenes and subsequent C–C bond cleavage","Organic Chemistry Frontiers","2017","4","9","1762","","10.1039/C7QO00419B","","","0.71073","MoKα","","0.0948","0.0494","","","0.1183","0.1463","","","","","","1.016","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553820","15.6855","0.0006","9.6366","0.0003","13.4345","0.0005","90","","96.4","0.001","90","","2018.03","0.12","173","2","173","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C21 H24 F3 N O4 -","- C21 H24 F3 N O4 -","- C84 H96 F12 N4 O16 -","4","1","","Tang, Yang; Yu, Qiong; Ma, Shengming","Efficient trifluoromethylation via the cyclopropanation of allenes and subsequent C–C bond cleavage","Organic Chemistry Frontiers","2017","4","9","1762","","10.1039/C7QO00419B","","","0.71073","MoKα","","0.0632","0.0424","","","0.1036","0.1171","","","","","","1.021","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553821","8.577","0.0004","11.253","0.0005","11.3999","0.0005","83.261","0.001","69.715","0.001","68.411","0.001","959.58","0.08","173","2","173","2","","","","","","","","4","P -1","-P 1","2","","","","- C19 H21 F3 O5 -","- C19 H21 F3 O5 -","- C38 H42 F6 O10 -","2","1","","Tang, Yang; Yu, Qiong; Ma, Shengming","Efficient trifluoromethylation via the cyclopropanation of allenes and subsequent C–C bond cleavage","Organic Chemistry Frontiers","2017","4","9","1762","","10.1039/C7QO00419B","","","0.71073","MoKα","","0.074","0.0615","","","0.1764","0.1907","","","","","","1.082","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553822","16.2553","0.0002","8.3116","0.0001","24.8996","0.0004","90","","90","","90","","3364.12","0.08","295","2","295","2","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C19 H15 N3 O4 -","- C19 H15 N3 O4 -","- C152 H120 N24 O32 -","8","2","","Krylov, Igor B.; Paveliev, Stanislav A.; Shelimov, Boris N.; Lokshin, Boris V.; Garbuzova, Irina A.; Tafeenko, Viktor A.; Chernyshev, Vladimir V.; Budnikov, Alexander S.; Nikishin, Gennady I.; Terent'ev, Alexander O.","Selective cross-dehydrogenative C–O coupling of N-hydroxy compounds with pyrazolones. Introduction of the diacetyliminoxyl radical into the practice of organic synthesis","Organic Chemistry Frontiers","2017","4","10","1947","","10.1039/C7QO00447H","","","1.54186","CuKα","","0.078","0.0593","","","0.1415","0.1484","","","","","","0.893","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553823","25.317","0.004","8.8649","0.0015","22.042","0.004","90","","120.571","0.002","90","","4259.3","1.3","100","","100","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C24 H21 F2 O3 P -","- C24 H21 F2 O3 P -","- C192 H168 F16 O24 P8 -","8","1","","Zhang, Pengbo; Ying, Jianxi; Tang, Guo; Zhao, Yufen","Phosphinodifluoroalkylation of alkynes using P(O)H compounds and ethyl difluoroiodoacetate","Organic Chemistry Frontiers","2017","4","10","2054","","10.1039/C7QO00466D","","","0.71073","MoKα","","0.054","0.049","","","0.1296","0.1347","","","","","","1.0601","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553824","7.75","0.001","20.882","0.003","14.5149","0.0019","90","","93.914","0.003","90","","2343.5","0.5","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C26 H28 N2 O5 -","- C26 H28 N2 O5 -","- C104 H112 N8 O20 -","4","1","","Yang, Minghua; Zhang, Shusheng; Zhang, Xiang; Wang, Haoyang; Zhang, Fang; Hou, Yuting; Su, Yue; Guo, Yinlong","An unexpected acid-catalyzed decomposition reaction of cilnidipine and pranidipine to the decarboxylative bridged tricyclic products via cascade rearrangements","Organic Chemistry Frontiers","2017","4","11","2163","","10.1039/C7QO00496F","","","0.71073","MoKα","","0.1081","0.0778","","","0.1691","0.1841","","","","","","1.134","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553825","9.6871","0.0007","14.029","0.0007","23.8866","0.0017","90","","90.258","0.006","90","","3246.2","0.4","289.9","0.3","289.9","0.3","","","","","","","","3","I 1 2/a 1","-I 2ya","15","","","","- C18 H22 O5 -","- C18 H22 O5 -","- C144 H176 O40 -","8","1","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel–Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","","0.7107","MoKα","","0.0806","0.0545","","","0.1326","0.1516","","","","","","1.093","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553826","10.2811","0.0005","28.3515","0.0009","12.9191","0.0005","90","","103.741","0.005","90","","3657.9","0.3","291.08","0.1","291.08","0.1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C20 H26 O6 -","- C20 H26 O6 -","- C160 H208 O48 -","8","2","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel–Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","","0.7107","MoKα","","0.1557","0.0668","","","0.1262","0.1747","","","","","","1.026","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553827","22.151","0.0011","9.8005","0.0004","26.0531","0.0013","90","","117.401","0.006","90","","5021.3","0.5","292.59","0.11","292.59","0.11","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C27 H33 N O7 S -","- C27 H33 N O7 S -","- C216 H264 N8 O56 S8 -","8","1","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel–Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","x-ray","0.71073","MoKα","","0.0815","0.0529","","","0.114","0.1334","","","","","","1.038","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553828","8.9279","0.0006","10.0249","0.0007","10.8557","0.001","115.731","0.008","104.925","0.007","90.322","0.006","838","0.13","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C18 H22 O6 -","- C18 H22 O6 -","- C36 H44 O12 -","2","1","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel–Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","x-ray","0.71073","MoKα","","0.0681","0.0495","","","0.1075","0.1189","","","","","","1.03","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553829","5.9908","0.0005","12.2284","0.001","23.731","0.003","90","","90","","90","","1738.5","0.3","293","2","293","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C19 H23 O6 -","- C19 H24 O6 -","- C76 H96 O24 -","4","1","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel‒Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","","0.71073","MoKα","","0.1199","0.0686","","","0.1491","0.1997","","","","","","0.991","","","","has coordinates","236073","2020-10-21","18:00:00",""
"1553830","13.7047","0.0006","15.4463","0.0007","24.0895","0.001","90","","97.806","0.004","90","","5052.2","0.4","290.74","0.1","290.74","0.1","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C27 H33 N O7 S -","- C27 H33 N O7 S -","- C216 H264 N8 O56 S8 -","8","1","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel–Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","","0.7107","MoKα","","0.1132","0.0598","","","0.1021","0.1244","","","","","","1.062","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553831","8.981","0.002","10.331","0.003","10.885","0.003","66.11","0.03","71.31","0.03","87.32","0.02","870.7","0.5","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C19 H24 O5 -","- C19 H24 O5 -","- C38 H48 O10 -","2","1","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel‒Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","","0.71073","MoKα","","0.1259","0.0673","","","0.1341","0.1744","","","","","","1.034","","","","has coordinates,has disorder","236073","2020-10-21","18:00:00",""
"1553832","9.88","0.002","10.9717","0.0017","12.836","0.002","85.382","0.013","71.391","0.017","65.05","0.019","1193.2","0.4","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C25 H29 N O7 S -","- C25 H29 N O7 S -","- C50 H58 N2 O14 S2 -","2","1","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel–Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","","0.71073","MoKα","","0.095","0.057","","","0.1195","0.1501","","","","","","1.036","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553833","7.3052","0.0011","10.5757","0.0016","14.449","0.002","88.853","0.003","83.694","0.003","77.708","0.003","1084.1","0.3","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C23 H19 Cl F3 N O5 -","- C23 H19 Cl F3 N O5 -","- C46 H38 Cl2 F6 N2 O10 -","2","1","","Sun, Yao-Liang; Wei, Yin; Shi, Min","Tunable regiodivergent phosphine-catalyzed [3 + 2] cycloaddition of alkynones and trifluoroacetyl phenylamides","Organic Chemistry Frontiers","2017","4","12","2392","","10.1039/C7QO00512A","","","0.71073","MoKα","","0.0638","0.0465","","","0.1114","0.1227","","","","","","1.015","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553834","11.287","0.002","12.727","0.002","14.808","0.003","90","","103.68","0.004","90","","2066.8","0.6","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C19 H23 Cl F3 N O4 -","- C19 H23 Cl F3 N O4 -","- C76 H92 Cl4 F12 N4 O16 -","4","1","","Sun, Yao-Liang; Wei, Yin; Shi, Min","Tunable regiodivergent phosphine-catalyzed [3 + 2] cycloaddition of alkynones and trifluoroacetyl phenylamides","Organic Chemistry Frontiers","2017","4","12","2392","","10.1039/C7QO00512A","","","0.71073","MoKα","","0.0781","0.0568","","","0.1427","0.1542","","","","","","1.044","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553835","21.872","0.003","7.604","0.001","24.313","0.003","90","","110.597","0.003","90","","3785.1","0.9","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C21 H17 Cl F3 N O3 -","- C21 H17 Cl F3 N O3 -","- C168 H136 Cl8 F24 N8 O24 -","8","1","","Sun, Yao-Liang; Wei, Yin; Shi, Min","Tunable regiodivergent phosphine-catalyzed [3 + 2] cycloaddition of alkynones and trifluoroacetyl phenylamides","Organic Chemistry Frontiers","2017","4","12","2392","","10.1039/C7QO00512A","","","0.71073","MoKα","","0.0662","0.0487","","","0.1124","0.1212","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553836","6.9086","0.0008","9.5831","0.0007","19.453","0.002","90","","96.737","0.01","90","","1279","0.2","120","","120","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C16 H15 N O -","- C16 H15 N O -","- C64 H60 N4 O4 -","4","2","","Zhang, Wei; Yu, Wenlong; Yan, Qiangqiang; Liu, Zhanxiang; Zhang, Yuhong","Synthesis of substituted oxazoles via Pd-catalyzed tandem oxidative cyclization","Organic Chemistry Frontiers","2017","4","12","2428","","10.1039/C7QO00517B","","","0.71073","MoKα","","0.1472","0.1365","","","0.3471","0.3583","","","","","","1.333","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553837","11.7381","0.0004","13.2058","0.0005","14.4879","0.0006","90","","98.487","0.002","90","","2221.19","0.15","150","2","150","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C25 H29 N O5 S -","- C25 H29 N O5 S -","- C100 H116 N4 O20 S4 -","4","1","","Lv, Leiyang; Lu, Shenglin; Chen, Yuanjin; Li, Zhiping","Diastereoselective building up polycyclic tetrahydrofurans via tandem annulation of 1,n-enynes with aliphatic acids","Organic Chemistry Frontiers","2017","4","11","2147","","10.1039/C7QO00527J","","","0.71073","MoKα","","0.0408","0.0347","","","0.0876","0.0914","","","","","","1.027","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553838","8.0159","0.0011","15.545","0.003","21.174","0.003","90","","90","","90","","2638.4","0.7","133","2","133","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C29 H25 N O7 S -","- C29 H25 N O7 S -","- C116 H100 N4 O28 S4 -","4","1","","Li, Shoulei; Zhang, Enge; Feng, Junjun; Li, Xin","An enantioselective conjugate addition reaction of 3-substituted benzothiophen-2-ones and 2-phthalimidoacrylates","Organic Chemistry Frontiers","2017","4","12","2301","","10.1039/C7QO00531H","","","0.71073","MoKα","","0.0315","0.0276","","","0.07","0.072","","","","","","1.014","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553839","9.5214","0.0008","9.6784","0.0008","9.8861","0.0008","114.205","0.008","92.568","0.007","116.743","0.008","712.04","0.14","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C15 H17 F N2 O2 -","- C15 H17 F N2 O2 -","- C30 H34 F2 N4 O4 -","2","1","","Yang, Zi; Lin, Xing; Wang, Lianhui; Cui, Xiuling","Facile synthesis of 1-aminoindoles via Rh(iii)-catalysed intramolecular three-component annulation","Organic Chemistry Frontiers","2017","4","11","2179","","10.1039/C7QO00541E","","x-ray","1.54184","CuKα","","0.044","0.0376","","","0.1015","0.1075","","","","","","1.042","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553840","10.723","0.016","9.856","0.015","20.94","0.03","90","","100.205","0.017","90","","2178","6","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C23 H22 Br N O4 S -","- C23 H22 Br N O4 S -","- C92 H88 Br4 N4 O16 S4 -","4","1","","Wang, Weiyi; He, Qiuqin; Fan, Renhua","PhI(OAc)2-mediated dialkoxylation of 4-aminostyrenes through a dearomatization process under metal-free conditions","Organic Chemistry Frontiers","2017","4","11","2156","","10.1039/C7QO00545H","","","0.71073","MoKα","","0.1743","0.0976","","","0.2577","0.3288","","","","","","0.996","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553841","13.746","0.002","8.2548","0.0013","15.646","0.003","90","","104.468","0.002","90","","1719.1","0.5","223","2","223","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C17 H21 N O4 S -","- C17 H21 N O4 S -","- C68 H84 N4 O16 S4 -","4","1","","Wang, Weiyi; He, Qiuqin; Fan, Renhua","PhI(OAc)2-mediated dialkoxylation of 4-aminostyrenes through a dearomatization process under metal-free conditions","Organic Chemistry Frontiers","2017","4","11","2156","","10.1039/C7QO00545H","","","0.71073","MoKα","","0.0557","0.0433","","","0.1308","0.1447","","","","","","1.103","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553842","11.7394","0.0011","19.838","0.0019","16.5546","0.0012","90","","94.489","0.007","90","","3843.5","0.6","100","0.1","100","0.1","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C40 H48 Cl2 N2 O2 Pd -","- C40 H48 Cl2 N2 O2 Pd -","- C160 H192 Cl8 N8 O8 Pd4 -","4","1","","Chen, Fu-Min; Huang, Fei-Dong; Yao, Xue-Yi; Li, Tian; Liu, Feng-Shou","Direct C‒H heteroarylation by an acenaphthyl-based α-diimine palladium complex: improvement of the reaction efficiency for bi(hetero)aryls under aerobic conditions","Organic Chemistry Frontiers","2017","4","12","2336","","10.1039/C7QO00562H","","x-ray","0.71073","MoKα","","0.1182","0.0986","","","0.2046","0.2146","","","","","","1.185","","","","has coordinates","236088","2020-10-21","18:00:00",""
"1553843","7.973","0.0003","12.9128","0.0005","14.3781","0.0008","90","","90","","90","","1480.28","0.11","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","3a","","- C16 H15 N O4 -","- C16 H15 N O4 -","- C64 H60 N4 O16 -","4","1","","Wu, Qiuju; Li, Chengcheng; Wang, Weihong; Wang, Hongling; Pan, Dingwu; Zheng, Pengcheng","NHC-catalyzed enantioselective synthesis of dihydropyran-4-carbonitriles bearing all-carbon quaternary centers","Organic Chemistry Frontiers","2017","4","12","2323","","10.1039/C7QO00571G","","","1.54178","CuKα","","0.0445","0.0406","","","0.106","0.1097","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553844","11.831","0.0008","8.4718","0.0005","16.4581","0.001","90","","90.759","0.006","90","","1649.45","0.18","293","2","293.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H21 N O2 -","- C20 H21 N O2 -","- C80 H84 N4 O8 -","4","1","","Wu, Shangze; Huang, Xin; Fu, Chunling; Ma, Shengming","Asymmetric SN2′-type C–H functionalization of arenes with propargylic alcohols","Organic Chemistry Frontiers","2017","4","10","2002","","10.1039/C7QO00588A","","","0.71073","MoKα","","0.0821","0.0489","","","0.1144","0.1394","","","","","","1.038","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553845","8.316","0.002","10.229","0.002","13.179","0.003","69.905","0.018","82.818","0.018","72.23","0.019","1002.3","0.4","293","2","293.15","","","","","","","","","4","P -1","-P 1","2","","","","- C24 H27 N O -","- C24 H27 N O -","- C48 H54 N2 O2 -","2","1","","Wu, Shangze; Huang, Xin; Fu, Chunling; Ma, Shengming","Asymmetric SN2′-type C–H functionalization of arenes with propargylic alcohols","Organic Chemistry Frontiers","2017","4","10","2002","","10.1039/C7QO00588A","","","0.71073","MoKα","","0.2693","0.0889","","","0.1758","0.2639","","","","","","0.994","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553846","11.781","0.001","12.2621","0.0007","12.7517","0.001","90","","110.261","0.009","90","","1728.1","0.2","293","2","293.15","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C17 H22 I N O2 -","- C17 H22 I N O2 -","- C68 H88 I4 N4 O8 -","4","1","","Wu, Shangze; Huang, Xin; Fu, Chunling; Ma, Shengming","Asymmetric SN2′-type C–H functionalization of arenes with propargylic alcohols","Organic Chemistry Frontiers","2017","4","10","2002","","10.1039/C7QO00588A","","","0.71073","MoKα","","0.0708","0.046","","","0.0999","0.1149","","","","","","1.054","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553847","20.993","0.007","3.9406","0.0012","12.147","0.004","90","","95.906","0.005","90","","999.5","0.6","296","2","296","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C8 H6 Br F3 O S -","- C8 H6 Br F3 O S -","- C32 H24 Br4 F12 O4 S4 -","4","1","","Zhang, Yunxiao; Wu, Dongping; Weng, Zhiqiang","Synthesis of 1,2,2-trifluorovinyl sulphides and selenides from trifluorovinylation of organic thiocyanates and selenocyanates","Organic Chemistry Frontiers","2017","4","11","2226","","10.1039/C7QO00595D","","","0.71073","MoKα","","0.0616","0.0498","","","0.1371","0.1432","","","","","","1.072","","","","has coordinates","236093","2020-10-21","18:00:00",""
"1553848","9.3385","0.0018","11.1134","0.0014","11.912","0.002","69.983","0.007","88.735","0.008","69.443","0.007","1080.8","0.3","113","2","113","2","","","","","","","","6","P -1","-P 1","2","","","","- C26 H20 Br N O4 S -","- C26 H20 Br N O4 S -","- C52 H40 Br2 N2 O8 S2 -","2","1","","Jin, Hongxing; Li, Erqing; Huang, You","Divergent synthesis of hydropyridine derivatives via nitrogen-containing Lewis base mediated regioselective [4 + 2] cyclizations","Organic Chemistry Frontiers","2017","4","11","2216","","10.1039/C7QO00596B","","","0.71073","MoKα","","0.0323","0.0253","","","0.0686","0.0704","","","","","","1.045","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553849","27.96","0.01","10.908","0.003","16.954","0.006","90","","121.023","0.005","90","","4431","3","113","2","113","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C26 H20 Br N O4 S -","- C26 H20 Br N O4 S -","- C208 H160 Br8 N8 O32 S8 -","8","1","","Jin, Hongxing; Li, Erqing; Huang, You","Divergent synthesis of hydropyridine derivatives via nitrogen-containing Lewis base mediated regioselective [4 + 2] cyclizations","Organic Chemistry Frontiers","2017","4","11","2216","","10.1039/C7QO00596B","","","0.71073","MoKα","","0.0333","0.0258","","","0.0619","0.0643","","","","","","1.025","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553850","9.7797","0.001","10.9021","0.0011","14.8619","0.0015","90","","90","","90","","1584.6","0.3","296.15","","296.15","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C18 H16 O4 S -","- C18 H16 O4 S -","- C72 H64 O16 S4 -","4","1","","Zhao, Wei-Wei; Liu, Yan-Kai","Enantio- and diastereoselective synthesis of tetrahydrofuro[2,3-b]furan-2(3H)-one derivatives and related oxygen heterocycles via an asymmetric organocatalytic cascade process","Organic Chemistry Frontiers","2017","4","12","2358","","10.1039/C7QO00621G","","","0.71073","MoKα","","0.0427","0.034","","","0.086","0.0919","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553851","9.8074","0.0005","13.2321","0.0005","17.7176","0.0007","100.836","0.003","99.601","0.004","93.264","0.003","2217.36","0.17","150","","150","","","","","","","","","5","P -1","-P 1","2","","","","- C100 H96 Cl6 N6 O10 -","- C100 H96 Cl6 N6 O10 -","- C100 H96 Cl6 N6 O10 -","1","0.5","","Zhang, Yuehong; Wang, Chiming; Chen, Xin; Pan, Houhe; Qi, Dongdong; Wang, Kang; Jiang, Jianzhuang","Novel, linear oligoisoindole compounds with a conjugated electronic structure","Organic Chemistry Frontiers","2017","4","12","2364","","10.1039/C7QO00631D","","","1.54178","CuKα","","0.0751","0.0658","","","0.183","0.1934","","","","","","1.018","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553852","8.9041","0.0004","14.0916","0.0007","16.2768","0.0008","104.121","0.004","91.824","0.004","94.954","0.004","1970.23","0.17","150","","150","","","","","","","","","5","P 1","P 1","1","","diisoindole","","- C88 H122 N2 O4 S2 -","- C88 H122 N2 O4 S2 -","- C88 H122 N2 O4 S2 -","1","1","","Zhang, Yuehong; Wang, Chiming; Chen, Xin; Pan, Houhe; Qi, Dongdong; Wang, Kang; Jiang, Jianzhuang","Novel, linear oligoisoindole compounds with a conjugated electronic structure","Organic Chemistry Frontiers","2017","4","12","2364","","10.1039/C7QO00631D","","","1.54178","CuKα","","0.0527","0.0466","","","0.1245","0.1314","","","","","","1.024","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553853","18.0089","0.0005","19.4187","0.0005","29.7417","0.0007","90.357","0.002","95.539","0.002","107.328","0.002","9875.8","0.5","150","","150","","","","","","","","","5","P -1","-P 1","2","","hexaisoindole","","- C202 H249 Cl14 N9 O15 -","- C202 H249 Cl14 N9 O15 -","- C404 H498 Cl28 N18 O30 -","2","1","","Zhang, Yuehong; Wang, Chiming; Chen, Xin; Pan, Houhe; Qi, Dongdong; Wang, Kang; Jiang, Jianzhuang","Novel, linear oligoisoindole compounds with a conjugated electronic structure","Organic Chemistry Frontiers","2017","4","12","2364","","10.1039/C7QO00631D","","","1.54178","CuKα","","0.1424","0.1121","","","0.3263","0.3551","","","","","","1.3","","","","has coordinates","236096","2020-10-21","18:00:00",""
"1553854","9.9153","0.0002","27.367","0.0005","23.7531","0.0004","90","","93.29","0.002","90","","6434.8","0.2","249.9","","249.9","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C132 H154 Cl12 N6 O8 -","- C132 H154 Cl12 N6 O8 -","- C264 H308 Cl24 N12 O16 -","2","0.5","","Zhang, Yuehong; Wang, Chiming; Chen, Xin; Pan, Houhe; Qi, Dongdong; Wang, Kang; Jiang, Jianzhuang","Novel, linear oligoisoindole compounds with a conjugated electronic structure","Organic Chemistry Frontiers","2017","4","12","2364","","10.1039/C7QO00631D","","","1.54178","CuKα","","0.095","0.0802","","","0.2411","0.2554","","","","","","1.063","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553855","5.1621","0.0006","16.3247","0.0018","20.251","0.002","90","","90","","90","","1706.5","0.3","293","2","293","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C18 H16 Cl N O4 S -","- C18 H16 Cl N O4 S -","- C72 H64 Cl4 N4 O16 S4 -","4","1","","Deng, Hua; He, Fu-Sheng; Li, Cong-Shan; Yang, Wu-Lin; Deng, Wei-Ping","Enantioselective construction of tricyclic pyrrolidine-fused benzo[b]thiophene 1,1-dioxide derivatives via copper(i)-catalyzed asymmetric 1,3-dipolar cycloaddition","Organic Chemistry Frontiers","2017","4","12","2343","","10.1039/C7QO00640C","","","0.71073","MoKα","","0.0476","0.042","","","0.1066","0.1107","","","","","","1.035","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553856","12.0438","0.0011","14.5042","0.0014","22.049","0.003","72.623","0.005","76.291","0.005","77.888","0.005","3530.8","0.7","150","2","150","2","","","","","","","","3","P -1","-P 1","2","Benzoxymethoxy Pillerene","","","- C81 H82 O10 -","- C81 H82 O10 -","- C162 H164 O20 -","2","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","0.2028","0.1038","","","0.2834","0.3483","","","","","","1.001","","","","has coordinates,has disorder","236101","2020-10-21","18:00:00",""
"1553857","12.791","0.004","20.978","0.007","14.779","0.004","90","","98.582","0.007","90","","3921","2","150","","150","","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C44 H48 O12 -","- C44 H48 O12 -","- C176 H192 O48 -","4","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","","0.0801","","","","0.232","","","","","","0.967","","","","has coordinates","236101","2020-10-21","18:00:00",""
"1553858","13.633","0.004","15.357","0.004","20.965","0.005","91.591","0.007","94.087","0.007","111.251","0.008","4073.6","1.9","150","","150","","","","","","","","","4","P -1","-P 1","2","","","","- C90 H125 N3 O10 -","- C90 H125 N3 O10 -","- C180 H250 N6 O20 -","2","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","","0.0506","","","","0.1486","","","","","","1.07","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553859","14.289","0.003","23.102","0.006","20.977","0.006","90","","108.428","0.008","90","","6570","3","150","2","150","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C42 H46 O11 -","- C42 H46 O11 -","- C252 H276 O66 -","6","3","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","0.158","0.0925","","","0.2471","0.2924","","","","","","0.855","","","","has coordinates","236101","2020-10-21","18:00:00",""
"1553860","14.89","0.008","18.123","0.008","21.671","0.01","81.371","0.006","82.134","0.009","87.707","0.013","5726","5","150","2","150","2","","","","","","","","4","P -1","-P 1","2","OctoxyBenzoxyPillerene_3","","","- C119 H158 Cl9 O10 -","- C119 H158 Cl9 O10 -","- C238 H316 Cl18 O20 -","2","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","0.1761","0.111","","","0.3038","0.3479","","","","","","1.042","","","","has coordinates","236101","2020-10-21","18:00:00",""
"1553861","43.045","0.01","21.347","0.005","23.043","0.005","90","","104.773","0.007","90","","20474","8","150","2","150","","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C110 H140 O10 -","- C110 H140 O10 -","- C880 H1120 O80 -","8","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","0.2489","0.148","","","0.3802","0.4289","","","","","","1.094","","","","has coordinates","236101","2020-10-21","18:00:00",""
"1553862","16.77","0.04","21.69","0.05","18.89","0.04","90","","93.48","0.04","90","","6858","3","150","","150","","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C82 H85 O12 -","- C82 H85 O12 -","- C328 H340 O48 -","4","2","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","","0.0751","","","","0.2118","","","","","","1.013","","","","has coordinates","273808","2022-03-18","10:32:15",""
"1553863","16.619","0.003","16.686","0.003","16.858","0.003","95.191","0.007","117.822","0.009","114.325","0.008","3527.9","1.3","150","","150","","","","","","","","","3","P -1","-P 1","2","","","","- C75 H110 O10 -","- C75 H110 O10 -","- C150 H220 O20 -","2","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","","0.1159","","","","0.3888","","","","","","0.799","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553864","12.31","0.03","16.48","0.04","18.98","0.04","83.427","0.016","80.887","0.014","69.254","0.017","3548","14","150","","150","","","","","","","","","3","P -1","-P 1","2","","","","- C81 H84 O10 -","- C81 H84 O10 -","- C162 H168 O20 -","2","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","","0.0892","","","","0.3047","","","","","","1.018","","","","has coordinates","236101","2020-10-21","18:00:00",""
"1553865","12.2178","0.001","15.0675","0.0014","20.9593","0.0017","78.186","0.006","85.869","0.006","67.284","0.005","3483.6","0.5","150","","150","","","","","","","","","4","P -1","-P 1","2","","","","- C82 H86 Cl2 O10 -","- C82 H86 Cl2 O10 -","- C164 H172 Cl4 O20 -","2","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","","0.1051","","","","0.3493","","","","","","1.293","","","","has coordinates","236101","2020-10-21","18:00:00",""
"1553866","8.4885","0.0005","10.6796","0.0006","16.8127","0.0009","74.369","0.004","82.265","0.004","75.011","0.005","1414.37","0.14","296","","296.15","","","","","","","","","4","P -1","-P 1","2","","","","- C31 H36 N2 O4 -","- C31 H36 N2 O4 -","- C62 H72 N4 O8 -","2","1","","Wu, Jia-Le; Wang, Jing-Yi; Wu, Ping; Mei, Guang-Jian; Shi, Feng","Catalytic asymmetric C2-nucleophilic substitutions of C3-substituted indoles with ortho-hydroxybenzyl alcohols","Organic Chemistry Frontiers","2017","4","12","2465","","10.1039/C7QO00649G","","","1.54178","CuKα","","0.1161","0.075","","","0.1876","0.2188","","","","","","1.011","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553867","18.5578","0.0009","18.5578","0.0009","9.8682","0.0006","90","","90","","120","","2943.2","0.3","296","","296","","","","","","","","","4","P 61","P 61","169","","","","- C23 H20 N O2 -","- C23 H21 N O2 -","- C138 H126 N6 O12 -","6","1","","Wu, Jia-Le; Wang, Jing-Yi; Wu, Ping; Mei, Guang-Jian; Shi, Feng","Catalytic asymmetric C2-nucleophilic substitutions of C3-substituted indoles with ortho-hydroxybenzyl alcohols","Organic Chemistry Frontiers","2017","4","12","2465","","10.1039/C7QO00649G","","","1.54178","CuKα","","0.0543","0.0434","","","0.1186","0.1284","","","","","","1.015","","","","has coordinates","236104","2020-10-21","18:00:00",""
"1553868","6.0777","0.0007","22.245","0.003","11.8606","0.0015","90","","96.163","0.002","90","","1594.3","0.3","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C17 H22 N2 O2 -","- C17 H22 N2 O2 -","- C68 H88 N8 O8 -","4","1","","Liu, Xueke; Qian, Ping; Wang, Yi; Pan, Yi","Metal-free sequential decarbonylative annulation of N-cyanamides for the construction of 2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-ones","Organic Chemistry Frontiers","2017","4","12","2370","","10.1039/C7QO00677B","","","0.71073","MoKα","","0.1128","0.0778","","","0.2365","0.274","","","","","","1.05","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553869","21.107","0.003","7.3437","0.0011","21.914","0.003","90","","101.993","0.005","90","","3322.6","0.8","296","2","296","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C20 H22 N2 O -","- C20 H22 N2 O -","- C160 H176 N16 O8 -","8","1","","Liu, Xueke; Qian, Ping; Wang, Yi; Pan, Yi","Metal-free sequential decarbonylative annulation of N-cyanamides for the construction of 2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-ones","Organic Chemistry Frontiers","2017","4","12","2370","","10.1039/C7QO00677B","","","0.71073","MoKα","","0.0959","0.0818","","","0.2146","0.2278","","","","","","1.072","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553870","7.9044","0.0001","11.5678","0.0002","15.8146","0.0002","90","","98.267","0.001","90","","1431.01","0.04","290","2","290","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C31 H38 O9 -","- C31 H38 O9 -","- C62 H76 O18 -","2","1","","Luo, Jun; Huang, Wan-Sha; Hu, Sheng-Mou; Zhang, Pan-Pan; Zhou, Xu-Wei; Wang, Xiao-Bing; Yang, Ming-Hua; Luo, Jian-Guang; Wang, Chen; Liu, Chang; Yao, He-Quan; Zhang, Can; Sun, Hong-Bin; Chen, Yi-Jun; Kong, Ling-Yi","Rearranged limonoids with unique 6/5/6/5 tetracarbocyclic skeletons from Toona ciliata and biomimetic structure divergence","Organic Chemistry Frontiers","2017","4","12","2417","","10.1039/C7QO00678K","","","1.54184","CuKα","","0.035","0.0337","","","0.0879","0.0896","","","","","","1.03","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553871","14.6815","0.0001","17.2043","0.0002","23.1115","0.0002","90","","90","","90","","5837.62","0.09","291","2","291","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C31 H38 O9 -","- C31 H38 O9 -","- C248 H304 O72 -","8","2","","Luo, Jun; Huang, Wan-Sha; Hu, Sheng-Mou; Zhang, Pan-Pan; Zhou, Xu-Wei; Wang, Xiao-Bing; Yang, Ming-Hua; Luo, Jian-Guang; Wang, Chen; Liu, Chang; Yao, He-Quan; Zhang, Can; Sun, Hong-Bin; Chen, Yi-Jun; Kong, Ling-Yi","Rearranged limonoids with unique 6/5/6/5 tetracarbocyclic skeletons from Toona ciliata and biomimetic structure divergence","Organic Chemistry Frontiers","2017","4","12","2417","","10.1039/C7QO00678K","","","1.54184","CuKα","","0.0685","0.0635","","","0.1821","0.1891","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553872","12.1518","0.0014","12.3848","0.0015","19.412","0.002","90","","90","","90","","2921.5","0.6","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C30 H30 I N3 O5 -","- C30 H30 I N3 O5 -","- C120 H120 I4 N12 O20 -","4","1","","Zhu, Jing-Yan; Yang, Wu-Lin; Liu, Yang-Zi; Shang, Shao-Jing; Deng, Wei-Ping","A copper(i)-catalyzed asymmetric Mannich reaction of glycine Schiff bases with isatin-derived ketimines: enantioselective synthesis of 3-substituted 3-aminooxindoles","Organic Chemistry Frontiers","2018","5","1","70","","10.1039/C7QO00691H","","","0.71073","MoKα","","0.0383","0.0336","","","0.0775","0.0799","","","","","","1.038","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553873","6.1598","0.0003","8.133","0.0004","31.1006","0.0015","90","","90","","90","","1558.07","0.13","293","2","293.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C13 H23 N O4 S -","- C13 H23 N O4 S -","- C52 H92 N4 O16 S4 -","4","1","","Wang, Zhi-Peng; Wu, Qi; Jiang, Jia; Li, Zi-Rui; Peng, Xiao-Jiao; Shao, Pan-Lin; He, Yun","Catalytic asymmetric synthesis of pyrrolidine derivatives bearing heteroatom-substituted quaternary stereocenters","Organic Chemistry Frontiers","2018","5","1","36","","10.1039/C7QO00692F","","x-ray","0.71073","MoKα","","0.0588","0.0466","","","0.0947","0.1025","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553874","7.9925","0.0003","13.9906","0.0004","19.0487","0.0006","90","","90","","90","","2130.02","0.12","292","2","292","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C21 H24 N2 O6 S -","- C21 H24 N2 O6 S -","- C84 H96 N8 O24 S4 -","4","1","","Wang, Zhi-Peng; Wu, Qi; Jiang, Jia; Li, Zi-Rui; Peng, Xiao-Jiao; Shao, Pan-Lin; He, Yun","Catalytic asymmetric synthesis of pyrrolidine derivatives bearing heteroatom-substituted quaternary stereocenters","Organic Chemistry Frontiers","2018","5","1","36","","10.1039/C7QO00692F","","","0.71073","MoKα","","0.0451","0.0389","","","0.0939","0.098","","","","","","1.113","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553875","8.4549","0.0014","13.872","0.002","14.009","0.002","117.552","0.003","101.368","0.004","92.964","0.004","1408.7","0.4","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C25 H24 Br2 N2 O3 S -","- C25 H24 Br2 N2 O3 S -","- C50 H48 Br4 N4 O6 S2 -","2","1","","Jiang, Bo; Shi, Min","Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene","Organic Chemistry Frontiers","2017","4","12","2459","","10.1039/C7QO00703E","","","0.71073","MoKα","","0.0839","0.0508","","","0.121","0.1326","","","","","","0.919","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553876","13.823","0.002","11.5473","0.0019","30.267","0.005","90","","98.559","0.006","90","","4777.4","1.3","272","2","272.29","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C44 H45 Br2 N3 O6 S2 -","- C44 H45 Br2 N3 O6 S2 -","- C176 H180 Br8 N12 O24 S8 -","4","1","","Jiang, Bo; Shi, Min","Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene","Organic Chemistry Frontiers","2017","4","12","2459","","10.1039/C7QO00703E","","","0.71073","MoKα","","0.154","0.0663","","","0.1613","0.2048","","","","","","0.941","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553877","11.936","0.0015","13.1209","0.0017","13.8558","0.0016","89.702","0.004","84.883","0.003","66.69","0.003","1983.8","0.4","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C43 H38 Br N3 O4 S2 -","- C43 H38 Br N3 O4 S2 -","- C86 H76 Br2 N6 O8 S4 -","2","1","","Jiang, Bo; Shi, Min","Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene","Organic Chemistry Frontiers","2017","4","12","2459","","10.1039/C7QO00703E","","","0.71073","MoKα","","0.1209","0.059","","","0.1505","0.1878","","","","","","0.925","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553878","10.688","0.002","10.745","0.002","11.245","0.002","103.535","0.004","94.412","0.004","96.045","0.004","1241.6","0.4","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C31 H26 N2 O2 S -","- C31 H26 N2 O2 S -","- C62 H52 N4 O4 S2 -","2","1","","Jiang, Bo; Shi, Min","Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene","Organic Chemistry Frontiers","2017","4","12","2459","","10.1039/C7QO00703E","","","0.71073","MoKα","","0.0744","0.0571","","","0.143","0.1554","","","","","","1.015","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553879","24.816","0.003","10.401","0.0011","16.9512","0.0018","90","","96.192","0.002","90","","4349.8","0.8","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C25 H21 Br N2 O2 S -","- C25 H21 Br N2 O2 S -","- C200 H168 Br8 N16 O16 S8 -","8","1","","Jiang, Bo; Shi, Min","Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene","Organic Chemistry Frontiers","2017","4","12","2459","","10.1039/C7QO00703E","","","0.71073","MoKα","","0.0655","0.0429","","","0.0996","0.1099","","","","","","1.016","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553880","3.8516","0.0002","11.2844","0.0004","21.4208","0.0008","90","","89.074","0.003","90","","930.89","0.07","","","","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C10 H8 Cl N O2 -","- C10 H8 Cl N O2 -","- C40 H32 Cl4 N4 O8 -","4","1","","Ledovskaya, Maria S.; Rodygin, Konstantin S.; Ananikov, Valentine P.","Calcium-mediated one-pot preparation of isoxazoles with deuterium incorporation","Organic Chemistry Frontiers","2018","5","2","226","","10.1039/C7QO00705A","","","","","","0.058","","","","","","","","","","","","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553881","24.1839","0.0009","31.5567","0.0009","12.6112","0.0003","90","","104.99","0.003","90","","9296.9","0.5","273","2","273","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C72 H112 Cl2 N28 O26 -","- C72 H84 N28 O22 -","- C288 H336 N112 O88 -","4","0.5","","Xiao, Zhi-You; Lin, Rui-Lian; Tao, Zhu; Liu, Qing-Yun; Liu, Jing-Xin; Xiao, Xin","Multiple noncovalent interaction constructed polymeric supramolecular crystals: recognition of butyl viologen by para-dicyclohexanocucurbit[6]uril and α,α′,δ,δ′-tetramethylcucurbit[6]uril","Organic Chemistry Frontiers","2017","4","12","2422","","10.1039/C7QO00708F","","","0.71073","MoKα","","0.1978","0.1121","","","0.2997","0.347","","","","","","1.005","","","","has coordinates,has disorder","236118","2020-10-21","18:00:00",""
"1553882","12.8381","0.0007","15.6916","0.0009","22.2878","0.0013","92.995","0.002","98.521","0.002","106.862","0.002","4227.9","0.4","273","2","273","2","","","","","","","","6","P -1","-P 1","2","","","","- C108 H176 Cl6 N52 O50 Sr2 -","- C108 H124 Cl4 N52 O40 Sr2 -","- C108 H124 Cl4 N52 O40 Sr2 -","1","0.5","","Xiao, Zhi-You; Lin, Rui-Lian; Tao, Zhu; Liu, Qing-Yun; Liu, Jing-Xin; Xiao, Xin","Multiple noncovalent interaction constructed polymeric supramolecular crystals: recognition of butyl viologen by para-dicyclohexanocucurbit[6]uril and α,α′,δ,δ′-tetramethylcucurbit[6]uril","Organic Chemistry Frontiers","2017","4","12","2422","","10.1039/C7QO00708F","","","0.71073","MoKα","","0.081","0.0615","","","0.1789","0.1905","","","","","","1.014","","","","has coordinates,has disorder","236118","2020-10-21","18:00:00",""
"1553883","10.8597","0.0007","13.0923","0.0008","18.0508","0.0012","75.984","0.002","74.865","0.002","66.722","0.002","2247.6","0.3","273","2","273","2","","","","","","","","6","P -1","-P 1","2","","","","- C43 H60 N2 P Sc Si2 -","- C43 H60 N2 P Sc Si2 -","- C86 H120 N4 P2 Sc2 Si4 -","2","1","","Gao, Hongjie; Su, Jianhong; Xu, Pengfei; Xu, Xin","Scandium-catalyzed C(sp3)‒H alkylation of N,N-dimethyl anilines with alkenes","Organic Chemistry Frontiers","2018","5","1","59","","10.1039/C7QO00718C","","","0.71073","MoKα","","0.09","0.0474","","","0.1213","0.1448","","","","","","1.07","","","","has coordinates","236120","2020-10-21","18:00:00",""
"1553884","8.859","0.0015","21.377","0.004","8.0979","0.0014","90","","106.44","0.004","90","","1470.9","0.5","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C19 H20 O -","- C19 H20 O -","- C76 H80 O4 -","4","1","","Zang, Wenqing; Wei, Yin; Shi, Min","Gold(i) catalyzed cascade cyclization: intramolecular two-fold nucleophilic addition to vinylidenecyclopropanes (VDCPs)","Organic Chemistry Frontiers","2018","5","2","197","","10.1039/C7QO00722A","","","0.71073","MoKα","","0.0664","0.0449","","","0.115","0.1272","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553885","6.059","0.0012","8.893","0.0018","13.346","0.003","91.59","0.03","93.75","0.03","108.42","0.03","679.9","0.3","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C15 H12 Cl2 O2 -","- C15 H12 Cl2 O2 -","- C30 H24 Cl4 O4 -","2","1","","Dai, Jie; Ren, Wenlong; Li, Jingfu; Shi, Yian","An effective approach to aryl-substituted propanoic acids via the Pd-catalyzed hydrocarboxylation of stilbenes","Organic Chemistry Frontiers","2018","5","4","561","","10.1039/C7QO00726D","","","0.71073","MoKα","","0.0734","0.0514","","","0.1484","0.166","","","","","","1.004","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553886","8.26","0.0017","10.221","0.002","10.602","0.002","102.5","0.03","107.52","0.03","109.03","0.03","756.2","0.4","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C18 H20 O2 -","- C18 H20 O2 -","- C36 H40 O4 -","2","1","","Dai, Jie; Ren, Wenlong; Li, Jingfu; Shi, Yian","An effective approach to aryl-substituted propanoic acids via the Pd-catalyzed hydrocarboxylation of stilbenes","Organic Chemistry Frontiers","2018","5","4","561","","10.1039/C7QO00726D","","","0.71073","MoKα","","0.0901","0.0617","","","0.168","0.1912","","","","","","1.001","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553887","17.558","0.0012","9.331","0.0006","9.8891","0.0006","90","","91.367","0.002","90","","1619.71","0.18","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C18 H17 N O3 S -","- C18 H17 N O3 S -","- C72 H68 N4 O12 S4 -","4","1","","Sun, Deli; Zhang, Ronghua","Transition-metal-free, visible-light-induced oxidative cross-coupling for constructing β-acetylamino acrylosulfones from sodium sulfinates and enamides","Organic Chemistry Frontiers","2018","5","1","92","","10.1039/C7QO00729A","","","0.71073","MoKα","","0.067","0.0466","","","0.1158","0.1264","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553888","15.8995","0.0014","8.3725","0.0008","9.9537","0.0009","90","","100.406","0.003","90","","1303.2","0.2","295","2","295","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C13 H15 N O3 S -","- C13 H15 N O3 S -","- C52 H60 N4 O12 S4 -","4","1","","Sun, Deli; Zhang, Ronghua","Transition-metal-free, visible-light-induced oxidative cross-coupling for constructing β-acetylamino acrylosulfones from sodium sulfinates and enamides","Organic Chemistry Frontiers","2018","5","1","92","","10.1039/C7QO00729A","","","0.71073","MoKα","","0.0959","0.0708","","","0.1171","0.1261","","","","","","1.155","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553889","13.2285","0.0011","9.3407","0.0008","14.9536","0.0012","90","","95.087","0.001","90","","1840.4","0.3","298","2","298","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C18 H17 Cl N2 O3 S -","- C18 H17 Cl N2 O3 S -","- C72 H68 Cl4 N8 O12 S4 -","4","1","","Jiang, Dong-Fang; Hu, Jie-Yu; Hao, Wen-Juan; Wang, Shu-Liang; Tu, Shu-Jiang; Jiang, Bo","Tunable Cu(i)-catalyzed site-selective dehydrogenative amination of β,γ-unsaturated hydrazones for divergent synthesis of pyrazol-4-ones and 1,6-dihydropyradazines","Organic Chemistry Frontiers","2018","5","2","189","","10.1039/C7QO00743D","","","0.71073","MoKα","","0.1116","0.0511","","","0.15","0.2046","","","","","","0.943","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553890","11.6687","0.0009","8.7574","0.0006","17.8369","0.0015","90","","96.512","0.001","90","","1810.9","0.2","298","2","298","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C17 H14 Cl2 N2 O2 S -","- C17 H14 Cl2 N2 O2 S -","- C68 H56 Cl8 N8 O8 S4 -","4","1","","Jiang, Dong-Fang; Hu, Jie-Yu; Hao, Wen-Juan; Wang, Shu-Liang; Tu, Shu-Jiang; Jiang, Bo","Tunable Cu(i)-catalyzed site-selective dehydrogenative amination of β,γ-unsaturated hydrazones for divergent synthesis of pyrazol-4-ones and 1,6-dihydropyradazines","Organic Chemistry Frontiers","2018","5","2","189","","10.1039/C7QO00743D","","","0.71073","MoKα","","0.1131","0.0508","","","0.0895","0.1018","","","","","","0.996","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553891","10.5217","0.0013","14.8118","0.0018","29.451","0.003","90","","94.42","0.003","90","","4576.1","0.9","128","2","128","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C27 H35 N O1.5 P -","- C27 H35 N O1.5 P -","- C216 H280 N8 O12 P8 -","8","1","","Wang, Huanan; Li, Shuaiqi; Wang, Baiquan; Li, Bin","The regioselective synthesis of 2-phosphinoylindoles via Rh(iii)-catalyzed C‒H activation","Organic Chemistry Frontiers","2018","5","1","88","","10.1039/C7QO00746A","","","0.71073","MoKα","","0.0427","0.0357","","","0.0934","0.0968","","","","","","1.057","","","","has coordinates","236129","2020-10-21","18:00:00",""
"1553892","24.609","0.006","9.508","0.002","21.415","0.005","90","","115.972","0.004","90","","4504.7","1.8","213","2","213.15","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C28 H24 N O2 P -","- C28 H24 N O2 P -","- C224 H192 N8 O16 P8 -","8","1","","Wang, Huanan; Li, Shuaiqi; Wang, Baiquan; Li, Bin","The regioselective synthesis of 2-phosphinoylindoles via Rh(iii)-catalyzed C–H activation","Organic Chemistry Frontiers","2018","5","1","88","","10.1039/C7QO00746A","","","0.71073","MoKα","","0.0569","0.0471","","","0.132","0.1488","","","","","","1.029","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553893","11.707","0.005","16.717","0.007","15.157","0.007","90","","96.39","0.007","90","","2948","2","296","2","296","2","","","","","","","","8","P 1 21/c 1","-P 2ybc","14","","","","- C30 H23 Au F3 N4 O3 P S -","- C30 H23 Au F3 N4 O3 P S -","- C120 H92 Au4 F12 N16 O12 P4 S4 -","4","1","","Huang, Ronghui; Yang, Yongchun; Wang, Duo-Sheng; Zhang, Liang; Wang, Dawei","Where does Au coordinate to N-(2-pyridiyl)benzotriazole: gold-catalyzed chemoselective dehydrogenation and borrowing hydrogen reactions","Organic Chemistry Frontiers","2018","5","2","203","","10.1039/C7QO00756F","","","0.71073","MoKα","","0.0791","0.046","","","0.1132","0.1336","","","","","","1.027","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553894","10.31419","0.00017","19.2062","0.0003","11.0205","0.0002","90","","109.532","0.002","90","","2057.49","0.07","135","","135","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C24 H20 N2 O5 -","- C24 H20 N2 O5 -","- C96 H80 N8 O20 -","4","2","","Ruan, Sai; Lin, Xiaobin; Xie, Lihua; Lin, Lili; Feng, Xiaoming; Liu, Xiaohua","Asymmetric synthesis of 3-aminodihydrocoumarins via the chiral guanidine catalyzed cascade reaction of azlactones","Organic Chemistry Frontiers","2018","5","1","32","","10.1039/C7QO00768J","","x-ray","1.54184","CuKα","","0.0427","0.0414","","","0.1079","0.1097","","","","","","1.061","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553895","8.7889","0.0018","8.9182","0.0018","22.444","0.005","90","","91.02","0.03","90","","1758.9","0.6","293","2","","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","9b-(2-bromobenzyl)-5-methyl-5,9b-dihydropyrrolizino[3,2-b]indol-10(4aH)-one","","- C21 H17 Br N2 O -","- C21 H17 Br N2 O -","- C84 H68 Br4 N8 O4 -","4","1","","Zhang, Qianqian; Song, Chuanjun; Huang, He; Zhang, Kun; Chang, Junbiao","Cesium carbonate promoted cascade reaction involving DMF as a reactant for the synthesis of dihydropyrrolizino[3,2-b]indol-10-ones","Organic Chemistry Frontiers","2018","5","1","80","","10.1039/C7QO00771J","","","0.71073","MoKα","","0.119","0.0742","","","0.2136","0.2675","","","","","","1.095","","","","has coordinates","300101","2025-06-17","17:58:10",""
"1553896","9.8465","0.0005","26.3558","0.0014","9.9725","0.0005","90","","104.267","0.002","90","","2508.2","0.2","292","2","292","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H14 N2 O -","- C15 H14 N2 O -","- C120 H112 N16 O8 -","8","2","","Zhang, Qianqian; Song, Chuanjun; Huang, He; Zhang, Kun; Chang, Junbiao","Cesium carbonate promoted cascade reaction involving DMF as a reactant for the synthesis of dihydropyrrolizino[3,2-b]indol-10-ones","Organic Chemistry Frontiers","2018","5","1","80","","10.1039/C7QO00771J","","","1.54178","CuKα","","0.0474","0.042","","","0.1109","0.1155","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553897","18.1727","0.0015","10.5743","0.0009","23.813","0.0019","90","","90","","90","","4576","0.7","293","2","293","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C23 H20 Cl F3 N2 O3 -","- C23 H20 Cl F3 N2 O3 -","- C184 H160 Cl8 F24 N16 O24 -","8","1","","Sun, Yao-Liang; Wei, Yin; Shi, Min","Phosphine catalyzed δ-carbon addition and isomerization of alkynones to ketimines: the preparation of 1,3-diene substituted dihydroquinazolinones and 3-aminooxindoles","Organic Chemistry Frontiers","2018","5","2","210","","10.1039/C7QO00772H","","","0.71073","MoKα","","0.1089","0.0596","","","0.1255","0.1478","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553898","18.416","0.005","11.31","0.003","9.759","0.003","90","","93.907","0.007","90","","2027.9","1","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H24 N2 O4 -","- C20 H24 N2 O4 -","- C80 H96 N8 O16 -","4","1","","Sun, Yao-Liang; Wei, Yin; Shi, Min","Phosphine catalyzed δ-carbon addition and isomerization of alkynones to ketimines: the preparation of 1,3-diene substituted dihydroquinazolinones and 3-aminooxindoles","Organic Chemistry Frontiers","2018","5","2","210","","10.1039/C7QO00772H","","","0.71073","MoKα","","0.0672","0.0457","","","0.1271","0.1398","","","","","","1.027","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553899","5.36821","0.00006","11.71337","0.00015","21.6232","0.0003","90","","90","","90","","1359.66","0.03","100","0.1","100","0.1","","","","","","","synthesis as described","5","P 21 21 21","P 2ac 2ab","19","","(2R,4S,5R)-3-(Hydroxymethyl)-8,8-dimethyl-2-(thiophen-2-yl)-7-oxa-1-azaspiro[4.4]nonan-6-one","","- C14 H19 N O3 S -","- C14 H19 N O3 S -","- C56 H76 N4 O12 S4 -","4","1","","Reboredo, Silvia; García-Marijuan, Ainara; Uria, Uxue; Reyes, Efraím; Carrillo, Luisa; Ugarriza, Iratxe; Vicario, Jose L.","Highly diastereoselective C → N acyl rearrangement in polysubstituted pyrrolidine 2,2-dicarboxylates. Stereocontrolled synthesis of densely functionalized prolines","Organic Chemistry Frontiers","2018","5","6","933","","10.1039/C7QO00793K","","x-ray","1.54184","CuKα","","0.0263","0.0254","","","0.0615","0.062","","","","","","1.079","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553900","9.673","0.0007","11.975","0.0008","10.6305","0.0008","90","","96.144","0.002","90","","1224.3","0.15","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C13 H13 Br N2 O -","- C13 H13 Br N2 O -","- C52 H52 Br4 N8 O4 -","4","1","","Zhao, He; Chen, Xiuwen; Jiang, Huanfeng; Zhang, Min","Copper-catalysed dehydrogenative α-C(sp3)–H amination of tetrahydroquinolines with O-benzoyl hydroxylamines","Organic Chemistry Frontiers","2018","5","4","539","","10.1039/C7QO00794A","","","0.71073","MoKα","","0.0725","0.0383","","","0.0891","0.1042","","","","","","1.001","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553901","6.5337","0.0001","8.4509","0.0001","26.0879","0.0003","90","","90","","90","","1440.46","0.03","289","2","289","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","2-((1R,5R)-1-hydroxy-3-oxo-5-phenylcyclohexyl)pyridine 1-oxide","","- C17 H17 N O3 -","- C17 H17 N O3 -","- C68 H68 N4 O12 -","4","1","","Xu, Youguo; Zhang, Sheng; Li, Lijun; Wang, Yukang; Zha, Zhenggen; Wang, Zhiyong","l-Phenylalanine potassium catalyzed asymmetric formal [3 + 3] annulation of 2-enoyl-pyridine N-oxides with acetone","Organic Chemistry Frontiers","2018","5","3","376","","10.1039/C7QO00796E","","","1.54184","CuKα","","0.0349","0.0324","","","0.0876","0.0987","","","","","","1.068","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553902","18.4928","0.0016","11.5835","0.0008","11.4759","0.0008","90","","90","","90","","2458.3","0.3","293","2","293","2","","","","","","","","6","P n n a","-P 2a 2bc","52","","","","- C16 H36 Br Cl3 Fe N -","- C16 H36 Br Cl3 Fe N -","- C64 H144 Br4 Cl12 Fe4 N4 -","4","0.5","","Li, Sanliang; Zhu, Bo; Lee, Richmond; Qiao, Baokun; Jiang, Zhiyong","Visible light-induced selective aerobic oxidative transposition of vinyl halides using a tetrahalogenoferrate(iii) complex catalyst","Organic Chemistry Frontiers","2018","5","3","380","","10.1039/C7QO00798A","","x-ray","1.54184","CuKα","","0.0724","0.0426","","","0.1123","0.1363","","","","","","1.026","","","","has coordinates,has disorder","236146","2020-10-21","18:00:00",""
"1553903","10.4684","0.0007","7.428","0.0004","18.7773","0.0011","90","","90.086","0.003","90","","1460.11","0.15","150","","150","","","","","","","","synthesis as described","3","P 1 21/n 1","-P 2yn","14","","","","- C24 H13 F -","- C24 H13 F -","- C96 H52 F4 -","4","1","","Shi, Xinzhe; Roisnel, Thierry; Soulé, Jean-François; Doucet, Henri","Synthesis of mono- and di-arylated acenaphthylenes and programmed access to dibenzo[j,l]fluoranthenes via palladium-catalysed C‒H bond functionalisation","Organic Chemistry Frontiers","2018","5","3","398","","10.1039/C7QO00799J","","x-ray","0.71073","MoKα","","0.0962","0.0647","","","0.1592","0.1789","","","","","","1.047","","","","has coordinates,has disorder","236148","2020-10-21","18:00:00",""
"1553904","16.8237","0.0012","11.333","0.0007","10.2994","0.0008","90","","114.382","0.003","90","","1788.6","0.2","150","","150","","","","","","","","synthesis as described","3","C 1 2/c 1","-C 2yc","15","","","","- C24 H14 Cl2 -","- C24 H14 Cl2 -","- C96 H56 Cl8 -","4","0.5","","Shi, Xinzhe; Roisnel, Thierry; Soulé, Jean-François; Doucet, Henri","Synthesis of mono- and di-arylated acenaphthylenes and programmed access to dibenzo[j,l]fluoranthenes via palladium-catalysed C‒H bond functionalisation","Organic Chemistry Frontiers","2018","5","3","398","","10.1039/C7QO00799J","","x-ray","0.71073","MoKα","","0.0404","0.0331","","","0.0828","0.0889","","","","","","1.039","","","","has coordinates","236148","2020-10-21","18:00:00",""
"1553905","17.47","0.004","5.702","0.0013","20.396","0.005","90","","114.211","0.004","90","","1853","0.8","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","1-(4-julolidylidene)-4-phenylthiosemicarbazide","","","- C20 H22 N4 S -","- C20 H22 N4 S -","- C80 H88 N16 S4 -","4","1","","Amendola, Valeria; Boiocchi, Massimo; Fabbrizzi, Luigi; La Cognata, Sonia; Legnani, Laura; Lo Presti, Eliana; Mangano, Carlo; Miljkovic, Ana","Anion-induced isomerization of fluorescent semi(thio)carbazones","Organic Chemistry Frontiers","2018","5","3","391","","10.1039/C7QO00805H","","","0.7107","MoKα","","0.1167","0.0691","","","0.1993","0.2389","","","","","","1.004","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553906","17.0278","0.0009","8.4534","0.0005","14.668","0.0008","90","","110.034","0.002","90","","1983.59","0.19","301","2","301.2","","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C23 H25 N O2 -","- C23 H25 N O2 -","- C92 H100 N4 O8 -","4","1","","Shen, Hong-Qiang; Liu, Cong; Zhou, Ji; Zhou, Yong-Gui","Enantioselective palladium-catalyzed C–H functionalization of pyrroles using an axially chiral 2,2′-bipyridine ligand","Organic Chemistry Frontiers","2018","5","4","611","","10.1039/C7QO00815E","","","1.54178","CuKα","","0.0703","0.064","","","0.1766","0.1844","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553907","16.1979","0.0011","9.8887","0.0007","17.2384","0.0015","90","","100.854","0.002","90","","2711.8","0.4","296","2","296","2","","","","","","","","6","P 1 21 1","P 2yb","4","","FeCl2-OIP-iPr","","- C25.5 H35 Cl2 Fe N3 O1.5 -","- C25.5 H35 Cl2 Fe N3 O1.5 -","- C102 H140 Cl8 Fe4 N12 O6 -","4","2","","Chen, Jianhui; Xi, Tuo; Lu, Zhan","10 gram-scale synthesis of a chiral oxazoline iminopyridine ligand and its applications","Organic Chemistry Frontiers","2018","5","2","247","","10.1039/C7QO00816C","","","0.71073","MoKα","","0.1689","0.0788","","","0.1317","0.1638","","","","","","1","","","","has coordinates","275434","2022-05-16","05:31:57",""
"1553908","8.277","0.002","19.206","0.006","11.294","0.004","90","","93.738","0.006","90","","1791.6","1","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C21 H19 Br O2 -","- C21 H19 Br O2 -","- C84 H76 Br4 O8 -","4","1","","Qi, Jifeng; Zheng, Jing; Cui, Sunliang","Facile synthesis of carbo- and heterocycles via Fe(iii)-catalyzed alkene hydrofunctionalization","Organic Chemistry Frontiers","2018","5","2","222","","10.1039/C7QO00817A","","","0.71073","MoKα","","0.1121","0.05","","","0.0829","0.1024","","","","","","1.003","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553909","8.914","0.01","9.542","0.011","13.652","0.015","86.106","0.014","80.322","0.012","67.976","0.012","1061","2","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C26 H28 O2 -","- C26 H28 O2 -","- C52 H56 O4 -","2","1","","Qi, Jifeng; Zheng, Jing; Cui, Sunliang","Facile synthesis of carbo- and heterocycles via Fe(iii)-catalyzed alkene hydrofunctionalization","Organic Chemistry Frontiers","2018","5","2","222","","10.1039/C7QO00817A","","","0.71073","MoKα","","0.1976","0.1187","","","0.312","0.3561","","","","","","1.049","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553910","21.1618","0.0016","11.9414","0.0011","23.2097","0.0017","90","","90","","90","","5865.1","0.8","291","","291","","","","","","","","","4","P b c n","-P 2n 2ab","60","","7,16-[2,2'-(hexano-2,4-diyne-1,6-dioxy)-dibenzoylo]-5,14-dihydrodibenzo[b,i][1,4,8,11]tetraazacyclotetradecine","","- C38 H26 N4 O4 -","- C38 H26 N4 O4 -","- C304 H208 N32 O32 -","8","1","","Zwoliński, K. M.; Sieroń, L.; Eilmes, J.","One-flask synthesis of dibenzotetraaza[14]annulene cyclic congeners bearing buta-1,3-diyne bridges","Organic Chemistry Frontiers","2018","5","2","171","","10.1039/C7QO00821J","","","0.71073","MoKα","","0.0954","0.0404","","","0.0583","0.0619","","","","","","0.954","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553911","11.2639","0.0012","15.6341","0.0017","13.7495","0.0015","90","","110.204","0.002","90","","2272.3","0.4","90","2","90","2","","","","","","","","6","P 1 21 1","P 2yb","4","","{7,16-bis[2-(prop-2-yn-1-yloxy)benzoyl]-5,14-dihydrodibenzo[b,i][1,4,8,11]tetraazacyclotetradecinato(2-)k^4^N} zinc(II)","","- C46 H50 N4 O8 S4 Zn -","- C46 H50 N4 O8 S4 Zn -","- C92 H100 N8 O16 S8 Zn2 -","2","1","","Zwoliński, K. M.; Sieroń, L.; Eilmes, J.","One-flask synthesis of dibenzotetraaza[14]annulene cyclic congeners bearing buta-1,3-diyne bridges","Organic Chemistry Frontiers","2018","5","2","171","","10.1039/C7QO00821J","","","0.71073","MoKα","","0.0275","0.0269","","","0.0703","0.0708","","","","","","1.011","","","","has coordinates,has disorder","236157","2020-10-21","18:00:00",""
"1553912","17.1209","0.001","6.8257","0.0005","14.2218","0.001","90","","100.2","0.003","90","","1635.72","0.19","150","2","150","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H14 Br N O2 -","- C19 H14 Br N O2 -","- C76 H56 Br4 N4 O8 -","4","1","","Chen, Changjun; Pan, Yixiao; Zhao, Haoqiang; Xu, Xin; Xu, Jianbin; Zhang, Zongyao; Xi, Siqi; Xu, Lijin; Li, Huanrong","A versatile rhodium(iii) catalyst for direct acyloxylation of aryl and alkenyl C–H bonds with carboxylic acids","Organic Chemistry Frontiers","2018","5","3","415","","10.1039/C7QO00844A","","","0.71073","MoKα","","0.048","0.0357","","","0.0917","0.0987","","","","","","1.016","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553913","8.581","0.0017","10.888","0.002","11.352","0.002","93.19","0.03","106.92","0.03","90.49","0.03","1012.8","0.4","194","2","194","2","","","","","","","","5","P -1","-P 1","2","","","","- C24 H28 N O2 Rh -","- C24 H28 N O2 Rh -","- C48 H56 N2 O4 Rh2 -","2","1","","Chen, Changjun; Pan, Yixiao; Zhao, Haoqiang; Xu, Xin; Xu, Jianbin; Zhang, Zongyao; Xi, Siqi; Xu, Lijin; Li, Huanrong","A versatile rhodium(iii) catalyst for direct acyloxylation of aryl and alkenyl C‒H bonds with carboxylic acids","Organic Chemistry Frontiers","2018","5","3","415","","10.1039/C7QO00844A","","","0.7201","","","0.0697","0.0601","","","0.1666","0.1888","","","","","","1.105","","","","has coordinates","236159","2020-10-21","18:00:00",""
"1553914","7.1832","0.001","10.3531","0.0016","12.7041","0.0018","99.499","0.006","102.356","0.006","98.881","0.005","892.4","0.2","150","2","150","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H16 N2 O2 -","- C22 H16 N2 O2 -","- C44 H32 N4 O4 -","2","1","","Chen, Changjun; Pan, Yixiao; Zhao, Haoqiang; Xu, Xin; Xu, Jianbin; Zhang, Zongyao; Xi, Siqi; Xu, Lijin; Li, Huanrong","A versatile rhodium(iii) catalyst for direct acyloxylation of aryl and alkenyl C–H bonds with carboxylic acids","Organic Chemistry Frontiers","2018","5","3","415","","10.1039/C7QO00844A","","","0.71073","MoKα","","0.0429","0.0369","","","0.0949","0.0987","","","","","","1.052","","","","has coordinates","300101","2025-06-17","17:58:10",""
"1553915","30.962","0.005","10.076","0.0018","20.18","0.004","90","","121.016","0.004","90","","5395.5","1.7","205","","205","","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C29 H32 O3 -","- C29 H32 O3 -","- C232 H256 O24 -","8","1","","Liu, Lina; Yuan, Zhenbo; Pan, Rui; Zeng, Yuye; Lin, Aijun; Yao, Hequan; Huang, Yue","1,6-Conjugated addition-mediated [4 + 1] annulation: an approach to 2,3-dihydrobenzofurans","Organic Chemistry Frontiers","2018","5","4","623","","10.1039/C7QO00846E","","","0.71073","MoKα","","0.11","0.0602","","","0.1559","0.1836","","","","","","0.962","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553916","10.1754","0.0007","13.7004","0.0008","13.8309","0.001","119.49","0.007","102.929","0.006","92.342","0.005","1609.7","0.2","150","","150","","","","","","","","","5","P -1","-P 1","2","","","","- C17 H13 Cl N2 O4 -","- C17 H13 Cl N2 O4 -","- C68 H52 Cl4 N8 O16 -","4","2","","Daggupati, Ramana V.; Malapaka, Chandrasekharam","Cu(i)-Catalyzed amidation/imidation of N-arylglycine ester derivatives via C–N coupling under mild conditions","Organic Chemistry Frontiers","2018","5","5","788","","10.1039/C7QO00851A","","x-ray","1.54184","CuKα","","0.057","0.0468","","","0.1497","0.1676","","","","","","1.1456","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553917","6.0881","0.0002","7.8709","0.0004","14.5993","0.0007","86.207","0.004","88.891","0.003","76.774","0.004","679.53","0.05","100.01","0.1","100.01","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C16 H15 N3 O2 -","- C16 H15 N3 O2 -","- C32 H30 N6 O4 -","2","1","","Zhu, Chuanle; Zeng, Hao; Chen, Fulin; Liu, Chi; Zhu, Rui; Wu, Wanqing; Jiang, Huanfeng","Copper-catalyzed coupling of oxime acetates and aryldiazonium salts: an azide-free strategy toward N-2-aryl-1,2,3-triazoles","Organic Chemistry Frontiers","2018","5","4","571","","10.1039/C7QO00874K","","x-ray","1.54184","CuKα","","0.0414","0.0396","","","0.1061","0.1077","","","","","","1.069","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553918","6.4301","0.0002","13.8923","0.0003","12.2241","0.0003","90","","103.031","0.002","90","","1063.85","0.05","150","2","150","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C28 H26 N2 -","- C28 H26 N2 -","- C56 H52 N4 -","2","0.5","","Grandl, Markus; Sun, Yu; Pammer, Frank","Electronic and structural properties of N → B-ladder boranes with high electron affinity","Organic Chemistry Frontiers","2018","5","3","336","","10.1039/C7QO00876G","","","1.54184","CuKα","","0.0444","0.0391","","","0.0983","0.1024","","","","","","1.063","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553919","9.0141","0.0007","12.9277","0.001","15.5179","0.0009","111.75","0.006","98.849","0.006","99.031","0.007","1613.9","0.2","150","2","150","2","","","","","","","","4","P -1","-P 1","2","","","","- C40 H54 B2 N2 -","- C40 H54 B2 N2 -","- C80 H108 B4 N4 -","2","1","","Grandl, Markus; Sun, Yu; Pammer, Frank","Electronic and structural properties of N → B-ladder boranes with high electron affinity","Organic Chemistry Frontiers","2018","5","3","336","","10.1039/C7QO00876G","","","0.71073","MoKα","","0.0891","0.0665","","","0.1693","0.1931","","","","","","1.05","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553920","17.2519","0.0002","10.4002","0.0001","18.7527","0.0002","90","","94.829","0.001","90","","3352.73","0.06","150","2","150","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C40 H54 B2 N2 -","- C40 H54 B2 N2 -","- C160 H216 B8 N8 -","4","1","","Grandl, Markus; Sun, Yu; Pammer, Frank","Electronic and structural properties of N → B-ladder boranes with high electron affinity","Organic Chemistry Frontiers","2018","5","3","336","","10.1039/C7QO00876G","","","1.54184","CuKα","","0.0727","0.0611","","","0.1623","0.17","","","","","","1.025","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553921","10.7137","0.0003","14.9388","0.0004","11.2075","0.0004","90","","101.824","0.003","90","","1755.7","0.09","150","2","150","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C44 H56 B2 N2 -","- C44 H56 B2 N2 -","- C88 H112 B4 N4 -","2","1","","Grandl, Markus; Sun, Yu; Pammer, Frank","Electronic and structural properties of N → B-ladder boranes with high electron affinity","Organic Chemistry Frontiers","2018","5","3","336","","10.1039/C7QO00876G","","","0.71073","MoKα","","0.0572","0.0464","","","0.096","0.1036","","","","","","1.039","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553922","13.3636","0.0003","12.765","0.0002","15.0491","0.0003","90","","111.844","0.002","90","","2382.85","0.09","150","2","150","2","","","","","","","","5","P 1 2/n 1","-P 2yac","13","","","","- C50 H29 B2 F20 N3 -","- C50 H29 B2 F20 N3 -","- C100 H58 B4 F40 N6 -","2","0.5","","Grandl, Markus; Sun, Yu; Pammer, Frank","Electronic and structural properties of N →B-ladder boranes with high electron affinity","Organic Chemistry Frontiers","2018","5","3","336","","10.1039/C7QO00876G","","","1.54184","CuKα","","0.0579","0.051","","","0.1688","0.1791","","","","","","1.094","","","","has coordinates","236167","2020-10-21","18:00:00",""
"1553923","11.196","0.005","13.488","0.007","19.102","0.011","102.11","0.02","104.06","0.02","108.18","0.02","2528","2","150","2","150","2","","","","","","","","5","P -1","-P 1","2","","","","- C60 H38 B2 F20 N2 -","- C60 H38 B2 F20 N2 -","- C120 H76 B4 F40 N4 -","2","1","","Grandl, Markus; Sun, Yu; Pammer, Frank","Electronic and structural properties of N → B-ladder boranes with high electron affinity","Organic Chemistry Frontiers","2018","5","3","336","","10.1039/C7QO00876G","","","0.71073","MoKα","","0.0487","0.041","","","0.0998","0.1044","","","","","","1.079","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553924","8.616","0.004","21.777","0.009","18.552","0.008","90","","100.259","0.009","90","","3425","3","296","2","296","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C35 H37 Cl2 N3 O4 S2 -","- C35 H37 Cl2 N3 O4 S2 -","- C140 H148 Cl8 N12 O16 S8 -","4","1","","Cao, Bo; Wei, Yin; Shi, Min","Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons","Organic Chemistry Frontiers","2018","5","3","423","","10.1039/C7QO00882A","","","0.71073","MoKα","","0.1275","0.054","","","0.1211","0.1549","","","","","","1.01","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553925","24.106","0.003","8.4201","0.001","20.584","0.002","90","","90","","90","","4178","0.8","293","2","293","2","","","","","","","","6","P n a 21","P 2c -2n","33","","","","- C8 H12 Cl Cu N4 O4 -","- C8 H12 Cl Cu N4 O4 -","- C96 H144 Cl12 Cu12 N48 O48 -","12","3","","Cao, Bo; Wei, Yin; Shi, Min","Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons","Organic Chemistry Frontiers","2018","5","3","423","","10.1039/C7QO00882A","","","0.71073","MoKα","","0.1417","0.0743","","","0.1769","0.2014","","","","","","0.846","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553926","33.342","0.003","14.1163","0.0013","13.8882","0.0014","90","","113.533","0.002","90","","5993","1","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C33 H33 N3 O4 S2 -","- C33 H33 N3 O4 S2 -","- C264 H264 N24 O32 S16 -","8","1","","Cao, Bo; Wei, Yin; Shi, Min","Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons","Organic Chemistry Frontiers","2018","5","3","423","","10.1039/C7QO00882A","","","0.71073","MoKα","","0.0784","0.0524","","","0.1319","0.1466","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553927","20.618","0.002","12.7286","0.0014","11.5829","0.0013","90","","96.577","0.002","90","","3019.8","0.6","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C33 H33 N3 O4 S2 -","- C33 H33 N3 O4 S2 -","- C132 H132 N12 O16 S8 -","4","1","","Cao, Bo; Wei, Yin; Shi, Min","Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons","Organic Chemistry Frontiers","2018","5","3","423","","10.1039/C7QO00882A","","","0.71073","MoKα","","0.0574","0.0436","","","0.1133","0.1233","","","","","","1.027","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553928","16.4746","0.0007","9.1306","0.0003","19.2167","0.0008","90","","113.764","0.005","90","","2645.5","0.2","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C36 H29 N3 -","- C36 H29 N3 -","- C144 H116 N12 -","4","1","","Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.","A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones","Organic Chemistry Frontiers","2018","5","4","595","","10.1039/C7QO00888K","","","0.71073","MoKα","","0.0512","0.0406","","","0.0952","0.1024","","","","","","1.021","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553929","9.0006","0.0003","13.4106","0.0007","13.9272","0.0004","73.859","0.004","78.251","0.003","71.617","0.004","1519.94","0.11","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C40.35 H35.05 N3 O1.67 -","- C40.3506 H35.053 N3 O1.675 -","- C80.7012 H70.106 N6 O3.35 -","2","1","","Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.","A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones","Organic Chemistry Frontiers","2018","5","4","595","","10.1039/C7QO00888K","","x-ray","1.54184","CuKα","","0.06","0.0478","","","0.1249","0.1337","","","","","","1.04","","","","has coordinates,has disorder","236172","2020-10-21","18:00:00",""
"1553930","9.8591","0.0003","17.6789","0.0006","16.9614","0.0006","90","","96.753","0.003","90","","2935.83","0.17","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C39 H29 N3 O2 -","- C39 H29 N3 O2 -","- C156 H116 N12 O8 -","4","1","","Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.","A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones","Organic Chemistry Frontiers","2018","5","4","595","","10.1039/C7QO00888K","","","0.71073","MoKα","","0.0712","0.052","","","0.1152","0.1249","","","","","","1.021","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1553931","9.7752","0.0005","18.4617","0.0008","18.0848","0.0009","90","","102.389","0.005","90","","3187.7","0.3","100","2","100","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C43 H29 N3 -","- C43 H29 N3 -","- C172 H116 N12 -","4","1","","Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.","A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones","Organic Chemistry Frontiers","2018","5","4","595","","10.1039/C7QO00888K","","","0.71073","MoKα","","0.0534","0.0427","","","0.0926","0.0987","","","","","","1.017","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553932","9.9057","0.0003","18.2185","0.0005","17.9256","0.0005","90","","94.694","0.003","90","","3224.13","0.16","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C44 H31 N3 O -","- C44 H31 N3 O -","- C176 H124 N12 O4 -","4","1","","Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.","A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones","Organic Chemistry Frontiers","2018","5","4","595","","10.1039/C7QO00888K","","","0.71073","MoKα","","0.0596","0.0442","","","0.0951","0.1036","","","","","","1.014","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553933","9.9528","0.001","5.6608","0.0006","10.1737","0.0008","90","","119.444","0.007","90","","499.16","0.09","173","2","173","2","","","","","","","","4","P 1 c 1","P -2yc","7","","","","- C10 H15 N O3 -","- C10 H15 N O3 -","- C20 H30 N2 O6 -","2","1","","Peter, Clovis; Geoffroy, Philippe; Miesch, Michel","Highly diastereoselective access to polyfunctionalized 1,3-oxazines promoted by Brønsted/Lewis acids","Organic Chemistry Frontiers","2018","5","4","566","","10.1039/C7QO00891K","","","0.71073","MoKα","","0.0356","0.0326","","","0.0793","0.0816","","","","","","1.044","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553934","6.934","0.0005","9.4461","0.0008","12.5549","0.0011","77.759","0.001","76.1","0.001","88.981","0.002","779.63","0.11","298","2","298","2","","","","","","","","3","P -1","-P 1","2","","","","- C16 H14 O7 -","- C16 H14 O7 -","- C32 H28 O14 -","2","1","","Xu, Li-Chen; Zhou, Peng; Li, Jia-Zhuo; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo","Thiazolium salt-catalyzed [3 + 2 + 1] cyclization for the synthesis of trisubstituted 2-pyrones using arylglyoxals as a carbonyl source","Organic Chemistry Frontiers","2018","5","5","753","","10.1039/C7QO00899F","","","0.71073","MoKα","","0.1689","0.1071","","","0.2366","0.2612","","","","","","1.071","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553935","14.18","0.002","16.43","0.003","16.973","0.002","65.7","0.012","71.841","0.016","79.491","0.018","3417.8","1","173","2","173","2","","","","","","","","7","P -1","-P 1","2","","","","- C65 H63 F6 N8 O12 P S6 -","- C65 H63 F6 N8 O12 P S6 -","- C130 H126 F12 N16 O24 P2 S12 -","2","1","","Zhao, Meng-Yao; Guo, Qing-Hui; Wang, Mei-Xiang","Understanding the driving force for the molecular recognition of S6-corona[3]arene[3]pyridazine toward organic ammonium cations","Organic Chemistry Frontiers","2018","5","5","760","","10.1039/C7QO00900C","","","0.71073","MoKα","","0.1783","0.1451","","","0.32","0.3417","","","","","","1.207","","","","has coordinates,has disorder","236178","2020-10-21","18:00:00",""
"1553936","8.4287","0.0001","10.7538","0.0001","30.9419","0.0004","90","","90","","90","","2804.59","0.06","293","2","293","2","","","","","","","synthesis","7","P 21 21 21","P 2ac 2ab","19","","","","- C26 H28 Cl2 N3 O5 P Ru -","- C26 H28 Cl2 N3 O5 P Ru -","- C104 H112 Cl8 N12 O20 P4 Ru4 -","4","1","","de Julián, E.; Menéndez-Pedregal, E.; Claros, M.; Vaquero, M.; Díez, J.; Lastra, E.; Gamasa, P.; Pizzano, A.","Practical synthesis of enantiopure benzylamines by catalytic hydrogenation or transfer hydrogenation reactions in isopropanol using a Ru-pybox catalyst","Organic Chemistry Frontiers","2018","5","5","841","","10.1039/C7QO00908A","","","1.5418","CuKα","","0.053","0.0512","","","0.1296","0.1311","","","","","","1.069","","","","has coordinates","236180","2020-10-21","18:00:00",""
"1553937","28.3195","0.0004","28.3195","0.0004","8.539","0.0002","90","","90","","90","","6848.2","0.2","150","2","150","2","","","","","","","","7","P 4","P 4","75","","","","- C33 H30 Cl2 N3 O4 P Ru -","- C33 H30 Cl2 N3 O4 P Ru -","- C264 H240 Cl16 N24 O32 P8 Ru8 -","8","2","","de Julián, E.; Menéndez-Pedregal, E.; Claros, M.; Vaquero, M.; Díez, J.; Lastra, E.; Gamasa, P.; Pizzano, A.","Practical synthesis of enantiopure benzylamines by catalytic hydrogenation or transfer hydrogenation reactions in isopropanol using a Ru-pybox catalyst","Organic Chemistry Frontiers","2018","5","5","841","","10.1039/C7QO00908A","","x-ray","1.5418","CuKα","","0.0515","0.0432","","","0.1131","0.1184","","","","","","1.062","","","","has coordinates","236180","2020-10-21","18:00:00",""
"1553938","31.825","0.009","31.825","0.009","8.303","0.002","90","","90","","90","","8410","4","296","2","296.15","","","","","","","","","4","I 41 c d","I 4bw -2c","110","","","","- C27 H23 N3 O -","- C27 H23 N3 O -","- C432 H368 N48 O16 -","16","1","","Zhang, Chen; Pi, Junxia; Chen, Shu; Liu, Ping; Sun, Peipei","Construction of a 4H-pyrido[4,3,2-gh]phenanthridin-5(6H)-one skeleton via a catalyst-free radical cascade addition/cyclization using azo compounds as radical sources","Organic Chemistry Frontiers","2018","5","5","793","","10.1039/C7QO00926G","","","0.71073","MoKα","","0.0381","0.0329","","","0.0924","0.0969","","","","","","1.126","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553939","8.8464","0.0004","13.6195","0.0006","30.1026","0.0012","90","","90","","90","","3626.9","0.3","180","0.1","180","0.1","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C22 H22 Si -","- C22 H22 Si -","- C176 H176 Si8 -","8","1","","Yang, Qi; Liu, Liang; Chi, Yue; Hao, Wei; Zhang, Wen-Xiong; Xi, Zhenfeng","Rhodium-catalyzed intramolecular carbosilylation of alkynes via C(sp3)–Si bond cleavage","Organic Chemistry Frontiers","2018","5","5","860","","10.1039/C7QO00927E","","x-ray","0.71073","MoKα","","0.04","0.0365","","","0.0977","0.1005","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553940","12.2864","0.0007","9.5206","0.0006","14.4288","0.0008","90","","96.731","0.006","90","","1676.16","0.17","180","0.1","180","0.1","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C21 H20 Si -","- C21 H20 Si -","- C84 H80 Si4 -","4","1","","Yang, Qi; Liu, Liang; Chi, Yue; Hao, Wei; Zhang, Wen-Xiong; Xi, Zhenfeng","Rhodium-catalyzed intramolecular carbosilylation of alkynes via C(sp3)–Si bond cleavage","Organic Chemistry Frontiers","2018","5","5","860","","10.1039/C7QO00927E","","","0.71073","MoKα","","0.0575","0.0407","","","0.0958","0.1069","","","","","","1.074","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553941","9.297","0.007","11.515","0.009","11.957","0.009","61.974","0.007","80.333","0.011","67.602","0.01","1044.6","1.4","296","2","296","2","","","","","","","","4","P 1","P 1","1","","","","- C23 H22 N2 O7 -","- C23 H22 N2 O7 -","- C46 H44 N4 O14 -","2","2","","Han, Jianxin; Niu, Sheng-Tong; Liu, Yushuang; Gan, Lishe; Wang, Tianfu; Lu, Chong-Dao; Yuan, Tao","Robustanoids A and B, two novel pyrrolo[2,3-b]indole alkaloids from Coffea canephora: isolation and total synthesis","Organic Chemistry Frontiers","2018","5","4","586","","10.1039/C7QO00931C","","","0.71073","MoKα","","0.0863","0.0699","","","0.1773","0.2","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553942","7.483","0.002","12.28","0.004","13.156","0.004","73.055","0.004","75.131","0.005","76.779","0.005","1102.1","0.6","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C28 H21 N5 O -","- C28 H21 N5 O -","- C56 H42 N10 O2 -","2","1","","Gao, Qinghe; He, Shuang; Wu, Xia; Zhang, Jingjing; Bai, Suping; Wu, Yandong; Wu, Anxin","Selective access to dipyrazolo-fused pyridines via formal [3 + 2 + 1] heteroannulation of methyl ketones with pyrazol-5-amines","Organic Chemistry Frontiers","2018","5","5","765","","10.1039/C7QO00941K","","","0.71073","MoKα","","0.1131","0.0584","","","0.1352","0.1763","","","","","","0.885","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553943","9.6948","0.0002","10.6078","0.0003","14.8224","0.0004","105.266","0.001","103.77","0.002","93.623","0.002","1415.35","0.07","100","1","100","1","","","","","","","","5","P -1","-P 1","2","","","","- C83 H54 Cl2 N2 O2 -","- C83 H54 Cl2 N2 O2 -","- C83 H54 Cl2 N2 O2 -","1","0.5","","Marin, L.; Guillot, R.; Gandon, V.; Schulz, E.; Lebœuf, D.","A diversity-oriented synthesis of cyclopenta[b]pyrroles and related compounds through a calcium(ii)/copper(ii) catalytic sequence","Organic Chemistry Frontiers","2018","5","4","640","","10.1039/C7QO00948H","","","0.71073","MoKα","","0.0984","0.085","","","0.2379","0.2508","","","","","","1.043","","","","has coordinates","236189","2020-10-21","18:00:00",""
"1553944","14.1223","0.0005","10.4359","0.0003","19.4476","0.0006","90","","97.282","0.002","90","","2843.05","0.16","100","1","100","1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C34 H29 Cl2 N O3 -","- C34 H29 Cl2 N O3 -","- C136 H116 Cl8 N4 O12 -","4","1","","Marin, L.; Guillot, R.; Gandon, V.; Schulz, E.; Lebœuf, D.","A diversity-oriented synthesis of cyclopenta[b]pyrroles and related compounds through a calcium(ii)/copper(ii) catalytic sequence","Organic Chemistry Frontiers","2018","5","4","640","","10.1039/C7QO00948H","","","0.71073","MoKα","","0.1094","0.0556","","","0.1196","0.1434","","","","","","1.022","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1553945","6.18585","0.00012","19.014","0.0005","13.0299","0.0003","90","","104.086","0.0007","90","","1486.46","0.06","173","","173","","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C13 H9 Br Cl F4 N S -","- C13 H9 Br Cl F4 N S -","- C52 H36 Br4 Cl4 F16 N4 S4 -","4","1","","Das, Prajwalita; Takada, Masahiro; Tokunaga, Etsuko; Saito, Norimichi; Shibata, Norio","Synthesis of pyridine trans-tetrafluoro-λ6-sulfane derivatives via radical addition","Organic Chemistry Frontiers","2018","5","5","719","","10.1039/C7QO00994A","","","0.71075","MoKα","","","0.0243","","","","0.0607","","","","","","1.095","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553946","24.908","0.003","13.4385","0.0017","8.7528","0.0013","90","","93.042","0.006","90","","2925.7","0.7","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C16 H12 Cl N O2 S -","- C16 H12 Cl N O2 S -","- C128 H96 Cl8 N8 O16 S8 -","8","1","","Zhao, Lang; Liao, Wei-Wei","Pd-Catalyzed intramolecular C–H addition to the cyano-group: construction of functionalized 2,3-fused thiophene scaffolds","Organic Chemistry Frontiers","2018","5","5","801","","10.1039/C7QO01000A","","","0.71073","MoKα","","0.0507","0.0406","","","0.0937","0.1023","","","","","","1.021","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553947","9.5527","0.0003","12.362","0.0005","12.0679","0.0005","90","","92.577","0.003","90","","1423.66","0.09","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","N-(8-quinolyl)-N-(2-tetrahydrofuranyl)propionamide","","- C16 H18 N2 O2 -","- C16 H18 N2 O2 -","- C64 H72 N8 O8 -","4","1","","Yue, Qiang; Xiao, Zhen; Ran, Ziyao; Yuan, Songdong; Zhang, Qian; Li, Dong","Copper-catalyzed α-C–H amidation of simple ethers through C(sp3)–H/N–H cross dehydrogenative coupling","Organic Chemistry Frontiers","2018","5","6","967","","10.1039/C7QO01003F","","x-ray","1.54184","CuKα","","0.0642","0.048","","","0.1289","0.1442","","","","","","1.04","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1553948","13.1217","0.0007","8.2301","0.0004","15.9865","0.0009","90","","109.525","0.006","90","","1627.15","0.16","298","2","298","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C17 H15.5 N2 O3.5 S -","- C17 H15.5 N2 O3.5 S -","- C68 H62 N8 O14 S4 -","4","2","","Huang, Bing-Bing; Wu, Liang; Liu, Ren-Rong; Xing, Ling-Ling; Liang, Ren-Xiao; Jia, Yi-Xia","Enantioselective Friedel–Crafts C2-alkylation of 3-substituted indoles with trifluoropyruvates and cyclic N-sulfonyl α-ketiminoesters","Organic Chemistry Frontiers","2018","5","6","929","","10.1039/C7QO01014A","","","0.71073","MoKα","","0.0764","0.0593","","","0.1473","0.1627","","","","","","1.015","","","","has coordinates","274567","2022-04-19","14:22:36",""
"1553949","8.0275","0.0005","13.876","0.0008","31.686","0.003","90","","90","","90","","3529.5","0.4","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C19 H17 F3 N O3.5 -","- C19 H17 F3 N O3.5 -","- C152 H136 F24 N8 O28 -","8","2","","Huang, Bing-Bing; Wu, Liang; Liu, Ren-Rong; Xing, Ling-Ling; Liang, Ren-Xiao; Jia, Yi-Xia","Enantioselective Friedel–Crafts C2-alkylation of 3-substituted indoles with trifluoropyruvates and cyclic N-sulfonyl α-ketiminoesters","Organic Chemistry Frontiers","2018","5","6","929","","10.1039/C7QO01014A","","","0.71073","MoKα","","0.0494","0.0384","","","0.1104","0.1192","","","","","","0.853","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553950","10.4482","0.0002","7.41078","0.00018","13.6312","0.0004","90","","105.538","0.003","90","","1016.88","0.05","172.95","0.1","172.95","0.1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C28 H20 N4 -","- C28 H20 N4 -","- C56 H40 N8 -","2","0.5","","Qin, Wen-Bing; Li, Wei-Wei; Zhu, Peng-Fei; Mo, Xiao-Gang; Zhang, Hui-Jun; Wen, Ting-Bin","Rh(iii)-Catalyzed regio- and stereoselective bisindolylation of vinyl acetate: an efficient approach toward (E)-1,2-bis(2-indolyl)ethenes","Organic Chemistry Frontiers","2018","5","7","1096","","10.1039/C7QO01041A","","","1.54184","CuKα","","0.0309","0.03","","","0.0768","0.0778","","","","","","1.07","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553951","8.5997","0.0003","11.3141","0.0005","23.5957","0.0009","89.88","0.003","86.923","0.003","89.086","0.003","2292.21","0.16","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C25 H30 N2 O3.5 Rh -","- C25 H30 N2 O3.5 Rh -","- C100 H120 N8 O14 Rh4 -","4","2","","Qin, Wen-Bing; Li, Wei-Wei; Zhu, Peng-Fei; Mo, Xiao-Gang; Zhang, Hui-Jun; Wen, Ting-Bin","Rh(iii)-Catalyzed regio- and stereoselective bisindolylation of vinyl acetate: an efficient approach toward (E)-1,2-bis(2-indolyl)ethenes","Organic Chemistry Frontiers","2018","5","7","1096","","10.1039/C7QO01041A","","","1.54184","CuKα","","0.0587","0.056","","","0.1369","0.1411","","","","","","1.052","","","","has coordinates","236199","2020-10-21","18:00:00",""
"1553952","31.277","0.009","16.691","0.005","10.668","0.003","90","","93.503","0.006","90","","5559","3","296","2","296","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C24 H22 S6 Si2 -","- C24 H22 S6 Si2 -","- C192 H176 S48 Si16 -","8","1","","Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua","Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene","Organic Chemistry Frontiers","2018","5","8","1257","","10.1039/C7QO01049D","","","0.71073","MoKα","","0.1099","0.0642","","","0.1494","0.1644","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553953","19.71","0.004","13.215","0.003","10.489","0.002","90","","103.753","0.003","90","","2653.7","1","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H20 S7 Si2 -","- C22 H20 S7 Si2 -","- C88 H80 S28 Si8 -","4","1","","Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua","Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene","Organic Chemistry Frontiers","2018","5","8","1257","","10.1039/C7QO01049D","","","0.71073","MoKα","","0.0446","0.0356","","","0.0985","0.1037","","","","","","1.087","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553954","12.594","0.005","7.353","0.003","15.175","0.006","90","","90","","90","","1405.3","1","296","2","296","2","","","","","","","","5","P n m a","-P 2ac 2n","62","","","","- C11 H11 Br S3 Si -","- C11 H11 Br S3 Si -","- C44 H44 Br4 S12 Si4 -","4","0.5","","Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua","Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene","Organic Chemistry Frontiers","2018","5","8","1257","","10.1039/C7QO01049D","","","0.71073","MoKα","","0.0414","0.0314","","","0.0795","0.0832","","","","","","1.018","","","","has coordinates","236200","2020-10-21","18:00:00",""
"1553955","11.5286","0.001","15.8164","0.0013","8.4588","0.0007","90","","110.19","0.001","90","","1447.6","0.2","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C11 H11 Br S3 Si -","- C11 H11 Br S3 Si -","- C44 H44 Br4 S12 Si4 -","4","1","","Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua","Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene","Organic Chemistry Frontiers","2018","5","8","1257","","10.1039/C7QO01049D","","","0.71073","MoKα","","0.0442","0.0296","","","0.0691","0.0751","","","","","","1.024","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553956","11.566","0.001","31.513","0.003","12.0437","0.001","90","","92.279","0.002","90","","4386.2","0.7","150","2","150","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C53 H49 Cl2 N3 O3 -","- C53 H49 Cl2 N3 O3 -","- C212 H196 Cl8 N12 O12 -","4","1","","Krishnan, Jagadeesh; Jose, Anu; Sasidhar, B. S.; Suresh, E.; Menon, Rajeev S.; Nair, Vijay","An uncommon multicomponent reaction involving nucleophilic heterocyclic carbenes: facile synthesis of fully substituted cyclopentanones","Organic Chemistry Frontiers","2018","5","7","1202","","10.1039/C7QO01051F","","","0.71073","MoKα","","0.1575","0.1192","","","0.199","0.2111","","","","","","1.286","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553957","29.069","0.003","16.647","0.0018","23.834","0.003","90","","124.203","0.002","90","","9538.8","1.9","150","2","150","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C50.5 H49 Cl I N3 O5 -","- C50.5 H49 Cl I N3 O5 -","- C404 H392 Cl8 I8 N24 O40 -","8","1","","Krishnan, Jagadeesh; Jose, Anu; Sasidhar, B. S.; Suresh, E.; Menon, Rajeev S.; Nair, Vijay","An uncommon multicomponent reaction involving nucleophilic heterocyclic carbenes: facile synthesis of fully substituted cyclopentanones","Organic Chemistry Frontiers","2018","5","7","1202","","10.1039/C7QO01051F","","","0.71073","MoKα","","0.0456","0.0367","","","0.0878","0.0913","","","","","","1.016","","","","has coordinates","236202","2020-10-21","18:00:00",""
"1553958","13.605","0.003","13.333","0.003","23.507","0.006","90","","101.393","0.006","90","","4180","1.7","150","2","150","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C52 H47 N3 O3 -","- C52 H47 N3 O3 -","- C208 H188 N12 O12 -","4","1","","Krishnan, Jagadeesh; Jose, Anu; Sasidhar, B. S.; Suresh, E.; Menon, Rajeev S.; Nair, Vijay","An uncommon multicomponent reaction involving nucleophilic heterocyclic carbenes: facile synthesis of fully substituted cyclopentanones","Organic Chemistry Frontiers","2018","5","7","1202","","10.1039/C7QO01051F","","","0.71073","MoKα","","0.165","0.0784","","","0.1391","0.1724","","","","","","0.999","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553959","7.6879","0.0003","13.3936","0.0005","15.696","0.0006","90","","103.359","0.001","90","","1572.46","0.1","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H19 N O2 -","- C20 H19 N O2 -","- C80 H76 N4 O8 -","4","1","","Chen, Wei; Zhang, Yicheng; Li, Pinhua; Wang, Lei","tert-Butyl peroxybenzoate mediated formation of 3-alkylated quinolines from N-propargylamines via a cascade radical addition/cyclization reaction","Organic Chemistry Frontiers","2018","5","5","855","","10.1039/C7QO01052D","","","0.71073","MoKα","","0.0535","0.0399","","","0.0985","0.1099","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553960","12.074","0.003","22.964","0.006","17.711","0.005","90","","93.931","0.005","90","","4899","2","100","","100","","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C51 H51 Cl5 N4 O2 P2 Ru -","- C51 H51 Cl5 N4 O2 P2 Ru -","- C204 H204 Cl20 N16 O8 P8 Ru4 -","4","1","","Roy, Bivas Chandra; Debnath, Subhankar; Chakrabarti, Kaushik; Paul, Bhaskar; Maji, Milan; Kundu, Sabuj","ortho-Amino group functionalized 2,2′-bipyridine based Ru(ii) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols","Organic Chemistry Frontiers","2018","5","6","1008","","10.1039/C7QO01061C","","","0.71073","MoKα","","0.1545","0.0865","","","0.1957","0.2339","","","","","","1.137","","","","has coordinates","236206","2020-10-21","18:00:00",""
"1553961","24.447","0.006","12.95","0.003","7.9","0.0019","90","","90","","90","","2501.1","1","100","","100","","","","","","","","","7","P n a 21","P 2c -2n","33","","","","- C22 H28 Cl F6 N4 P Ru -","- C22 H28 Cl F6 N4 P Ru -","- C88 H112 Cl4 F24 N16 P4 Ru4 -","4","1","","Roy, Bivas Chandra; Debnath, Subhankar; Chakrabarti, Kaushik; Paul, Bhaskar; Maji, Milan; Kundu, Sabuj","ortho-Amino group functionalized 2,2′-bipyridine based Ru(ii) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols","Organic Chemistry Frontiers","2018","5","6","1008","","10.1039/C7QO01061C","","","0.71073","MoKα","","0.0411","0.0357","","","0.082","0.0865","","","","","","1.041","","","","has coordinates","236206","2020-10-21","18:00:00",""
"1553962","9.679","0.003","19.168","0.006","21.719","0.007","90","","91.489","0.006","90","","4028","2","100","","100","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C48 H44 Cl2 N4 P2 Ru -","- C48 H44 Cl2 N4 P2 Ru -","- C192 H176 Cl8 N16 P8 Ru4 -","4","1","","Roy, Bivas Chandra; Debnath, Subhankar; Chakrabarti, Kaushik; Paul, Bhaskar; Maji, Milan; Kundu, Sabuj","ortho-Amino group functionalized 2,2′-bipyridine based Ru(ii) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols","Organic Chemistry Frontiers","2018","5","6","1008","","10.1039/C7QO01061C","","","0.71073","MoKα","","0.1188","0.0606","","","0.1423","0.1855","","","","","","0.952","","","","has coordinates","236206","2020-10-21","18:00:00",""
"1553963","8.0484","0.0007","10.6055","0.0009","21.9053","0.0018","90","","90","","90","","1869.8","0.3","100","2","100","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C23 H21 N O2 S -","- C23 H21 N O2 S -","- C92 H84 N4 O8 S4 -","4","1","","Li, Yun; Chen, Jingchao; He, Zhenxiu; Qin, Hongyu; Zhou, Yongyun; Khan, Ruhima; Fan, Baomin","Cobalt-catalyzed asymmetric reactions of heterobicyclic alkenes with in situ generated organozinc halides","Organic Chemistry Frontiers","2018","5","7","1108","","10.1039/C7QO01064H","","","0.71073","MoKα","","0.0286","0.0274","","","0.0727","0.0736","","","","","","1.086","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553964","14.839","0.004","17.596","0.004","8.652","0.002","90","","90","","90","","2259.1","1","173","2","173.15","","","","","","","","","4","P 21 21 2","P 2 2ab","18","","","","- C26 H27 Br O3 -","- C26 H27 Br O3 -","- C104 H108 Br4 O12 -","4","1","","Li, Shoulei; Liu, Bin; Chen, Li; Li, Xin; Cheng, Jin-Pei","N-Heterocyclic carbene promoted enantioselective desymmetrization reaction of diarylalkane-bisphenols","Organic Chemistry Frontiers","2018","5","7","1101","","10.1039/C7QO01083D","","","0.71073","MoKα","","0.055","0.048","","","0.0846","0.0877","","","","","","1.101","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553965","4.3504","0.0004","24.437","0.002","8.5476","0.0007","90","","102.442","0.002","90","","887.36","0.13","153","2","153","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C10 H8 N4 -","- C10 H8 N4 -","- C40 H32 N16 -","4","1","","Qiao, Kai; Zhang, Dong; Zhang, Kai; Yuan, Xin; Zheng, Ming-Wei; Guo, Tian-Fo; Fang, Zheng; Wan, Li; Guo, Kai","Iron(ii)-catalyzed C-2 cyanomethylation of indoles and pyrroles via direct oxidative cross-dehydrogenative coupling with acetonitrile derivatives","Organic Chemistry Frontiers","2018","5","7","1129","","10.1039/C7QO01086A","","","0.71073","MoKα","","0.0481","0.0449","","","0.1151","0.1186","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553966","9.4077","0.0015","9.9254","0.0016","17.562","0.003","90","","90","","90","","1639.9","0.5","293","","293.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","3-n-Butyl-4-phenyl-3,4-dihydro-2H-benzo[e][1,2]thiazine 1,1-dioxide","","- C18 H21 N O2 S -","- C18 H21 N O2 S -","- C72 H84 N4 O8 S4 -","4","1","","Song, Bo; Chen, Mu-Wang; Zhou, Yong-Gui","Synthesis of chiral sultams with two adjacent stereocenters via palladium-catalyzed dynamic kinetic resolution","Organic Chemistry Frontiers","2018","5","7","1113","","10.1039/C7QO01098B","","","0.71073","MoKα","","0.0932","0.0553","","","0.12","0.1375","","","","","","1.014","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553967","8.9388","0.0002","9.7832","0.0002","13.5584","0.0003","90","","107.86","0.003","90","","1128.54","0.05","294.5","0.7","294.5","0.7","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C15 H7 Cl F N O -","- C15 H7 Cl F N O -","- C60 H28 Cl4 F4 N4 O4 -","4","1","","Liu, Jianming; Yan, Xuyang; Liu, Na; Zhang, Yanyan; Zhao, Shufang; Wang, Xiaopei; Zhuo, Kelei; Yue, Yuanyuan","Elemental sulfur accelerated the reactivity of the 3-position of indole for the construction of chromeno[2,3-b]indoles","Organic Chemistry Frontiers","2018","5","6","1034","","10.1039/C7QO01114H","","x-ray","1.54184","CuKα","","0.0585","0.0567","","","0.141","0.1433","","","","","","1.047","","","","has coordinates","236215","2020-10-21","18:00:00",""
"1553968","9.2089","0.0003","10.5763","0.0004","10.9769","0.0004","100.503","0.003","95.221","0.003","91.16","0.003","1046.09","0.07","100","0.1","100","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C26 H27 N O3 -","- C26 H27 N O3 -","- C52 H54 N2 O6 -","2","1","","Luo, Hejiang; Liang, Renxiao; Chen, Lianfen; Jiang, Huanfeng; Zhu, Shifa","A silver-catalyzed three-component reaction via stabilized cation: synthesis of polysubstituted tetrahydronaphthols and tetrahydronaphthylamines","Organic Chemistry Frontiers","2018","5","7","1160","","10.1039/C7QO01122A","","x-ray","1.54184","CuKα","","0.0418","0.0398","","","0.102","0.1039","","","","","","1.044","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553969","8.9683","0.0005","9.8217","0.0005","11.353","0.0007","75.074","0.005","77.458","0.005","63.345","0.005","857.59","0.09","100","0.1","100","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C23 H19 F O2 -","- C23 H19 F O2 -","- C46 H38 F2 O4 -","2","1","","Luo, Hejiang; Liang, Renxiao; Chen, Lianfen; Jiang, Huanfeng; Zhu, Shifa","A silver-catalyzed three-component reaction via stabilized cation: synthesis of polysubstituted tetrahydronaphthols and tetrahydronaphthylamines","Organic Chemistry Frontiers","2018","5","7","1160","","10.1039/C7QO01122A","","x-ray","0.71073","MoKα","","0.0681","0.0489","","","0.1073","0.1198","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553970","29.1539","0.0005","14.0671","0.0003","24.2333","0.0007","90","","126.156","0.001","90","","8024.4","0.3","190","2","190","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C64 H100 N4 Na4 O46 -","- C64 H84 N4 Na4 O46 -","- C256 H336 N16 Na16 O184 -","4","0.5","","Zhang, Yao; Yu, Shang-Bo; Yang, Bo; Wang, Hui; Zhang, Dan-Wei; Li, Zhan-Ting","Ion-pair electrostatic attraction-enhanced donor‒acceptor interactions between the prototypic 1,4-dialkoxybenzene-viologen binding mode in water","Organic Chemistry Frontiers","2018","5","6","1039","","10.1039/C7QO01126A","","","1.54178","CuKα","","0.1207","0.1053","","","0.2954","0.3094","","","","","","1.041","","","","has coordinates","236220","2020-10-21","18:00:00",""
"1553971","8.7382","0.0006","5.8569","0.0004","23.8346","0.0018","90","","91.141","0.001","90","","1219.58","0.15","298","2","298","2","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C10 H9 Br F N O4 S -","- C10 H9 Br F N O4 S -","- C40 H36 Br4 F4 N4 O16 S4 -","4","1","","Wang, Shi-Meng; Li, Chen; Leng, Jing; Bukhari, Syed Nasir Abbas; Qin, Hua-Li","Rhodium(iii)-catalyzed Oxidative Coupling of N-Methoxybenzamides and Ethenesulfonyl fluoride: a C–H Bond Activation Strategy for the Preparation of 2-Aryl ethenesulfonyl fluorides and Sulfonyl fluoride Substituted γ-Lactams","Organic Chemistry Frontiers","2018","5","9","1411","","10.1039/C7QO01128H","","","0.71073","MoKα","","0.0627","0.0397","","","0.0926","0.0996","","","","","","1.043","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553972","8.6492","0.0009","6.7929","0.0008","25.645","0.003","90","","98.112","0.002","90","","1491.6","0.3","298","2","298","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C15 H11 F O5 S -","- C15 H11 F O5 S -","- C60 H44 F4 O20 S4 -","4","1","","Wang, Shi-Meng; Li, Chen; Leng, Jing; Bukhari, Syed Nasir Abbas; Qin, Hua-Li","Rhodium(iii)-catalyzed Oxidative Coupling of N-Methoxybenzamides and Ethenesulfonyl fluoride: a C–H Bond Activation Strategy for the Preparation of 2-Aryl ethenesulfonyl fluorides and Sulfonyl fluoride Substituted γ-Lactams","Organic Chemistry Frontiers","2018","5","9","1411","","10.1039/C7QO01128H","","","0.71073","MoKα","","0.1039","0.0813","","","0.216","0.2291","","","","","","1.053","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553973","12.062","0.003","4.0452","0.0009","21.707","0.005","90","","90.12","0.02","90","","1059.2","0.4","294","2","294","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C12 H10 Br N O -","- C12 H10 Br N O -","- C48 H40 Br4 N4 O4 -","4","1","","Reddy, Ganapam Manohar; Rao, Naidu Sambasiva; Maheswaran, H.","Highly meta-selective halogenation of 2-phenylpyridine with a ruthenium(i) catalyst","Organic Chemistry Frontiers","2018","5","7","1118","","10.1039/C7QO01133D","","","0.71073","MoKα","","0.1009","0.0419","","","0.076","0.0864","","","","","","0.776","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553974","8.799","0.0004","14.7395","0.0006","16.0279","0.0006","90","","90","","90","","2078.7","0.15","200","2","200","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C24 H25 Cl2 N O -","- C24 H25 Cl2 N O -","- C96 H100 Cl8 N4 O4 -","4","1","","Zheng, Long-Sheng; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie","Ruthenium-catalyzed dynamic kinetic asymmetric transfer hydrogenation: stereoselective access to syn 2-(1,2,3,4-tetrahydro-1-isoquinolyl)ethanol derivatives","Organic Chemistry Frontiers","2018","5","8","1366","","10.1039/C7QO01142C","","","1.54178","CuKα","","0.0259","0.0253","","","0.0677","0.0683","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553975","5.6782","0.0002","8.5568","0.0003","38.5091","0.001","90","","90","","90","","1871.05","0.1","200","1","200","1","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C22 H23 N O S -","- C22 H23 N O S -","- C88 H92 N4 O4 S4 -","4","1","","Zheng, Long-Sheng; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie","Ruthenium-catalyzed dynamic kinetic asymmetric transfer hydrogenation: stereoselective access to syn 2-(1,2,3,4-tetrahydro-1-isoquinolyl)ethanol derivatives","Organic Chemistry Frontiers","2018","5","8","1366","","10.1039/C7QO01142C","","","1.54178","CuKα","","0.042","0.0371","","","0.0905","0.0934","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553976","10.5329","0.0009","10.3187","0.0008","18.4305","0.0016","90","","97.847","0.002","90","","1984.4","0.3","120","2","120","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H20 N4 O4 -","- C21 H20 N4 O4 -","- C84 H80 N16 O16 -","4","1","","Cao, Wen-Bin; Liu, Bei-Bei; Xu, Xiao-Ping; Ji, Shun-Jun","Cooperation of copper and dioxygen for the site-selective construction of benzo[1,5]diazocin-6(5H)-ones from indoles and enaminone analogues","Organic Chemistry Frontiers","2018","5","7","1194","","10.1039/C7QO01154G","","","0.71073","MoKα","","0.126","0.065","","","0.1819","0.2811","","","","","","1.003","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553977","11.9446","0.0012","13.7058","0.0014","19.238","0.002","90","","90","","90","","3149.5","0.6","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C34 H28 N O6 P S -","- C34 H28 N O6 P S -","- C136 H112 N4 O24 P4 S4 -","4","1","","Gu, Zheng; Zhou, Ji; Jiang, Guo-Fang; Zhou, Yong-Gui","Synthesis of chiral γ-aminophosphonates through the organocatalytic hydrophosphonylation of azadienes with phosphites","Organic Chemistry Frontiers","2018","5","7","1148","","10.1039/C7QO01158J","","","0.71073","MoKα","","0.0462","0.0322","","","0.0789","0.0874","","","","","","1.038","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553978","7.9384","0.0009","9.9744","0.0012","17.126","0.002","90","","90","","90","","1356","0.3","294","2","294","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C18 H18 O2 -","- C18 H18 O2 -","- C72 H72 O8 -","4","1","","Someswarao, B.; P., Rasvan Khan; Reddy, B. Jagan Mohan; B., Sridhar; B., V. Subba Reddy","Tandem Prins-type cyclization for the stereoselective construction of fused polycyclic ring systems","Organic Chemistry Frontiers","2018","5","8","1320","","10.1039/C7QO01164D","","","0.71073","MoKα","","0.0732","0.0717","","","0.1684","0.1693","","","","","","1.246","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553979","12.6396","0.001","9.6186","0.0008","11.8318","0.0009","90","","103.394","0.001","90","","1399.33","0.19","294","2","294","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C18 H18 O3 -","- C18 H18 O3 -","- C72 H72 O12 -","4","1","","Someswarao, B.; P., Rasvan Khan; Reddy, B. Jagan Mohan; B., Sridhar; B., V. Subba Reddy","Tandem Prins-type cyclization for the stereoselective construction of fused polycyclic ring systems","Organic Chemistry Frontiers","2018","5","8","1320","","10.1039/C7QO01164D","","","0.71073","MoKα","","0.0521","0.0445","","","0.1237","0.1298","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1553980","13.13","0.04","12.87","0.04","7.8","0.02","90","","105.51","0.02","90","","1270","6","294","2","294","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C14 H15 N O4 -","- C14 H15 N O4 -","- C56 H60 N4 O16 -","4","1","","Someswarao, B.; P., Rasvan Khan; Reddy, B. Jagan Mohan; B., Sridhar; B., V. Subba Reddy","Tandem Prins-type cyclization for the stereoselective construction of fused polycyclic ring systems","Organic Chemistry Frontiers","2018","5","8","1320","","10.1039/C7QO01164D","","","0.71073","MoKα","","0.1204","0.067","","","0.1725","0.2015","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554253","8.8119","0.0001","10.4134","0.0001","27.1396","0.0003","90","","90","","90","","2490.38","0.05","293","2","293","2","","","","","","","","7","P 21 21 21","P 2ac 2ab","19","","","","- C25 H21 Br F3 N3 O4 S -","- C25 H21 Br F3 N3 O4 S -","- C100 H84 Br4 F12 N12 O16 S4 -","4","1","","Zhu, Wen-Run; Chen, Qing; Lin, Ning; Chen, Kai-Bin; Zhang, Zhen-Wei; Fang, Gang; Weng, Jiang; Lu, Gui","Organocatalytic Michael/cyclization cascade reactions of 3-isothiocyanato oxindoles with 3-trifluoroethylidene oxindoles: an approach for the synthesis of 3′-trifluoromethyl substituted 3,2′-pyrrolidinyl-bispirooxindoles","Organic Chemistry Frontiers","2018","5","8","1375","","10.1039/C8QO00044A","","","1.54178","CuKα","","0.0329","0.0312","","","0.0763","0.0774","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554254","13.986","0.0008","14.019","0.0008","28.0285","0.0013","98.119","0.003","91.053","0.003","90.157","0.003","5439.5","0.5","273","2","273","2","","","","","","","","3","P 1","P 1","1","","","","- C28 H36 O8 -","- C28 H36 O8 -","- C224 H288 O64 -","8","8","","Yin, Guo-Ping; Wu, Ya-Rong; Han, Chao; Wang, Xiao-Bing; Gao, Hong-Liang; Yin, Yong; Kong, Ling-Yi; Yang, Ming-Hua","Asperones A‒E, five dimeric polyketides with new carbon skeletons from the fungus Aspergillus sp. AWG 1‒15","Organic Chemistry Frontiers","2018","5","16","2432","","10.1039/C8QO00070K","","","1.54178","CuKα","","0.1592","0.1102","","","0.2928","0.3537","","","","","","1.147","","","","has coordinates","237068","2020-10-21","18:00:00",""
"1554255","8.3949","0.0009","15.0525","0.0016","22.267","0.002","90","","90","","90","","2813.8","0.5","173","","173","","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","15-13","","- C28 H38 O9 -","- C28 H38 O9 -","- C112 H152 O36 -","4","1","","Yin, Guo-Ping; Wu, Ya-Rong; Han, Chao; Wang, Xiao-Bing; Gao, Hong-Liang; Yin, Yong; Kong, Ling-Yi; Yang, Ming-Hua","Asperones A–E, five dimeric polyketides with new carbon skeletons from the fungus Aspergillus sp. AWG 1–15","Organic Chemistry Frontiers","2018","5","16","2432","","10.1039/C8QO00070K","","","1.54178","CuKα","","0.0338","0.0326","","","0.0864","0.0873","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554256","9.34542","0.00007","14.58845","0.00013","24.65138","0.00016","90","","90","","90","","3360.85","0.04","100.01","0.1","100.01","0.1","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","Lithocarpin C","W-55","","- C37 H42 O11 -","- C37 H42 O11 -","- C148 H168 O44 -","4","1","","Xu, Jianlin; Tan, Haibo; Chen, Yuchan; Li, Saini; Huang, Zilei; Guo, Heng; Li, Haohua; Gao, Xiaoxia; Liu, Hongxin; Zhang, Weimin","Lithocarpins A–D: four tenellone-macrolide conjugated [4 + 2] hetero-adducts from the deep-sea derived fungus Phomopsis lithocarpus FS508","Organic Chemistry Frontiers","2018","5","11","1792","","10.1039/C8QO00095F","","x-ray","1.54184","CuKα","","0.0349","0.034","","","0.0889","0.0897","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554257","12.0999","0.0003","8.9388","0.0002","17.0397","0.0004","90","","90.378","0.002","90","","1842.95","0.08","100","0.1","100","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","Lithocarpin A","w-36","","- C38 H43 Cl3 O11 -","- C38 H43 Cl3 O11 -","- C76 H86 Cl6 O22 -","2","1","","Xu, Jianlin; Tan, Haibo; Chen, Yuchan; Li, Saini; Huang, Zilei; Guo, Heng; Li, Haohua; Gao, Xiaoxia; Liu, Hongxin; Zhang, Weimin","Lithocarpins A–D: four tenellone-macrolide conjugated [4 + 2] hetero-adducts from the deep-sea derived fungus Phomopsis lithocarpus FS508","Organic Chemistry Frontiers","2018","5","11","1792","","10.1039/C8QO00095F","","x-ray","1.54184","CuKα","","0.094","0.0906","","","0.2611","0.265","","","","","","1.036","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554258","8.8203","0.0001","9.95","0.0002","11.3663","0.0002","90","","104.882","0.002","90","","964.07","0.03","100","0.1","100","0.1","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C21 H28 O4 -","- C21 H28 O4 -","- C42 H56 O8 -","2","1","","Hu, Li-Jun; Cheng, Min-Jing; Cao, Jia-Qing; Zhong, Li-Ping; Hu, Ya-Jian; Wang, Ying; Wang, Lei; Ye, Wen-Cai; Li, Chuang-Chuang","Asymmetric total syntheses of callistrilones B, G and J","Organic Chemistry Frontiers","2018","5","9","1506","","10.1039/C8QO00130H","","x-ray","1.54178","CuKα","","0.03","0.0298","","","0.0801","0.0804","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554259","9.56","0.001","10.76","0.003","11.542","0.003","89.84","0.03","78.84","0.02","80.4","0.02","1148","0.5","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","{2-[3-Ethoxy-2-(methoxymethoxy)phenyl]cyclopropane-1,1-diyl}bis(phenylmethanone)","","- C27 H26 O5 -","- C27 H26 O5 -","- C54 H52 O10 -","2","1","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","1.54178","CuKα","","0.0904","0.0459","","","0.1151","0.1363","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554260","5.565","0.001","17.417","0.006","19.97","0.005","90","","90","","90","","1935.6","0.9","293","2","293","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","9-Methyl-8,10-dioxatricyclo[7.2.1.02,7]dodeca-2,4,6-trien-4-amine","","- C11 H13 N O2 -","- C11 H13 N O2 -","- C88 H104 N8 O16 -","8","1","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","1.54178","CuKα","","0.0728","0.0429","","","0.102","0.1167","","","","","","1.1","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554261","10.139","0.003","10.399","0.006","14.357","0.005","80.36","0.04","69.86","0.03","89.98","0.04","1398.4","1.1","298","2","298","2","","","","","","","","4","P -1","-P 1","2","","","","- C15 H21 N O2 -","- C15 H21 N O2 -","- C60 H84 N4 O8 -","4","2","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","0.71073","MoKα","","0.141","0.056","","","0.1299","0.1632","","","","","","1.01","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554262","9.9233","0.0007","15.1382","0.001","8.9089","0.0006","90","","105.815","0.001","90","","1287.64","0.15","120","2","120","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","4-Bromo-6-ethoxy-9-methyl-8,10-dioxatricyclo[7.2.1.02,7]dodeca-2,4,6-triene","","- C13 H15 Br O3 -","- C13 H15 Br O3 -","- C52 H60 Br4 O12 -","4","1","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","0.71073","MoKα","","0.0323","0.0251","","","0.0596","0.0618","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554263","8.638","0.003","15.409","0.007","8.594","0.002","90","","111.43","0.02","90","","1064.8","0.7","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","6-Methoxy-9-methyl-8,10-dioxatricyclo[7.2.1.02,7]dodeca-2,4,6-triene","","- C12 H14 O3 -","- C12 H14 O3 -","- C48 H56 O12 -","4","1","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","0.71073","MoKα","","0.072","0.0393","","","0.0928","0.1071","","","","","","1.02","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554264","9.944","0.005","16.675","0.008","15.179","0.007","90","","108.38","0.04","90","","2389","2","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","1-[4-(2-Hydroxyphenyl)-2-methyl-4,5-dihydrofuran-3-yl]ethanone","","- C13 H14 O3 -","- C13 H14 O3 -","- C104 H112 O24 -","8","2","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","1.54178","CuKα","","0.1516","0.0589","","","0.1474","0.1892","","","","","","0.995","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554265","7.1922","0.0006","9.9323","0.0008","16.0391","0.0013","78.066","0.001","84.732","0.001","86.302","0.001","1115.04","0.16","120","2","120","2","","","","","","","","3","P -1","-P 1","2","","{4-[3-Ethoxy-2-(methoxymethoxy)phenyl]-2-phenyl-4,5-dihydrofuran-3-yl}(phenyl)methanone","","- C27 H26 O5 -","- C27 H26 O5 -","- C54 H52 O10 -","2","1","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","0.71073","MoKα","","0.0562","0.0423","","","0.1006","0.109","","","","","","1.029","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554266","9.9599","0.0006","6.7335","0.0004","20.4059","0.0012","90","","93.522","0.001","90","","1365.94","0.14","120","2","120","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","Methyl 4-[2-(methoxymethoxy)phenyl]-2-methyl-4,5-dihydrofuran-3-carboxylate","","- C15 H18 O5 -","- C15 H18 O5 -","- C60 H72 O20 -","4","1","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","0.71073","MoKα","","0.0419","0.0365","","","0.0952","0.0994","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554267","8.2403","0.0004","11.2635","0.0005","11.6154","0.0007","80.692","0.004","75.701","0.005","83.849","0.004","1028.38","0.1","293","2","293.15","","","","","","","","","3","P -1","-P 1","2","","","","- C23 H32 O6 -","- C23 H32 O6 -","- C46 H64 O12 -","2","1","","Liu, Mengchen; Cheng, Chuanxu; Xiong, Weiyan; Cheng, Hang; Wang, Jian-Li; Xu, Liang","Total synthesis of C19-diterpenoid alkaloid: construction of a functionalized ABCDE-ring system","Organic Chemistry Frontiers","2018","5","9","1502","","10.1039/C8QO00143J","","x-ray","0.71073","MoKα","","0.0702","0.0474","","","0.1041","0.1173","","","","","","1.029","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554268","10.8545","0.0006","11.1988","0.0004","10.9655","0.0006","90","","117.846","0.007","90","","1178.59","0.13","293","2","293.15","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C13 H20 O4 -","- C13 H20 O4 -","- C52 H80 O16 -","4","1","","Liu, Mengchen; Cheng, Chuanxu; Xiong, Weiyan; Cheng, Hang; Wang, Jian-Li; Xu, Liang","Total synthesis of C19-diterpenoid alkaloid: construction of a functionalized ABCDE-ring system","Organic Chemistry Frontiers","2018","5","9","1502","","10.1039/C8QO00143J","","","0.7107","MoKα","","0.0516","0.0402","","","0.0916","0.1002","","","","","","1.025","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554269","13.7347","0.0009","21.989","0.0014","13.7372","0.0011","90","","110.63","0.007","90","","3882.8","0.5","150","2","150","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C76 H104 O26 S3 -","- C76 H84 O26 S3 -","- C152 H168 O52 S6 -","2","1","","Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun","Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity","Organic Chemistry Frontiers","2018","5","7","1079","","10.1039/C8QO00154E","","","1.54178","CuKα","","0.1566","0.1161","","","0.2152","0.2368","","","","","","1.02","","","","has coordinates,has disorder","237081","2020-10-21","18:00:00",""
"1554270","10.70154","0.00011","27.4281","0.0003","26.4591","0.0003","90","","90","","90","","7766.35","0.15","150","2","150.15","","","","","","","","","4","C 2 2 21","C 2c 2","20","","","","- C78 H96 N4 O22 -","- C78 H96 N4 O22 -","- C312 H384 N16 O88 -","4","0.5","","Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun","Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity","Organic Chemistry Frontiers","2018","5","7","1079","","10.1039/C8QO00154E","","x-ray","1.54178","CuKα","","0.0776","0.0757","","","0.2014","0.204","","","","","","1.05","","","","has coordinates,has disorder","237081","2020-10-21","18:00:00",""
"1554271","9.18292","0.00014","12.4621","0.0002","28.4369","0.0005","90","","90","","90","","3254.28","0.09","150","2","150","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C35 H44 O12 -","- C35 H44 O12 -","- C140 H176 O48 -","4","1","","Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun","Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity","Organic Chemistry Frontiers","2018","5","7","1079","","10.1039/C8QO00154E","","x-ray","1.54184","CuKα","","0.0272","0.0268","","","0.0674","0.0677","","","","","","1.076","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554272","15.8696","0.0006","16.1185","0.0005","32.0556","0.0007","90","","90","","90","","8199.6","0.4","123","2","123","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C74 H90 Cl12 O24 -","- C74 H90 Cl12 O24 -","- C296 H360 Cl48 O96 -","4","1","","Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun","Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity","Organic Chemistry Frontiers","2018","5","7","1079","","10.1039/C8QO00154E","","","1.54178","CuKα","","0.0957","0.0812","","","0.1738","0.1837","","","","","","1.003","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554273","10.54064","0.00016","14.6009","0.0003","14.9312","0.0002","62.0192","0.0018","84.9082","0.0013","68.8864","0.0016","1884.1","0.07","293","2","293","2","","","","","","","","4","P 1","P 1","1","","","","- C77.37 H93.1 N4 O24 -","- C77.364 H93.132 N4 O24 -","- C77.364 H93.132 N4 O24 -","1","1","","Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun","Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity","Organic Chemistry Frontiers","2018","5","7","1079","","10.1039/C8QO00154E","","","1.54184","CuKα","","0.051","0.0506","","","0.1346","0.135","","","","","","1.02","","","","has coordinates,has disorder","237081","2020-10-21","18:00:00",""
"1554274","15.2487","0.0011","16.1229","0.0011","29.1352","0.0019","90","","90","","90","","7163","0.9","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C74 H91 N2 O24 -","- C74 H91 N2 O24 -","- C296 H364 N8 O96 -","4","1","","Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun","Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity","Organic Chemistry Frontiers","2018","5","7","1079","","10.1039/C8QO00154E","","","0.71073","MoKα","","0.0842","0.0548","","","0.1445","0.1638","","","","","","1.026","","","","has coordinates,has disorder","237081","2020-10-21","18:00:00",""
"1554275","14.7018","0.0001","14.7018","0.0001","53.2893","0.0002","90","","90","","120","","9974.97","0.1","293","2","293","2","","","","","","","","3","P 65","P 65","170","","","","- C70 H84 O24 -","- C70 H84 O24 -","- C420 H504 O144 -","6","1","","Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun","Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity","Organic Chemistry Frontiers","2018","5","7","1079","","10.1039/C8QO00154E","","","1.54178","CuKα","","0.0736","0.0724","","","0.2119","0.2145","","","","","","1.026","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554276","13.3662","0.0008","19.3514","0.0012","18.2778","0.0011","90","","107.451","0.002","90","","4510","0.5","300","2","300.15","","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C42 H49 Cl2 N3 O3 Ru S -","- C42 H49 Cl2 N3 O3 Ru S -","- C168 H196 Cl8 N12 O12 Ru4 S4 -","4","1","","Sabbasani, Venkata R.; Gupta, Saswata; Young Yun, Sang; Lee, Daesung","A general approach for the formation of oxygen-chelated ruthenium alkylidene complexes relying on the Thorpe‒Ingold effect","Organic Chemistry Frontiers","2018","5","9","1532","","10.1039/C8QO00160J","","","0.71073","MoKα","","0.0556","0.0425","","","0.1139","0.1226","","","","","","1.0356","","","","has coordinates","237085","2020-10-21","18:00:00",""
"1554277","14.573","0.01","14.783","0.01","16.116","0.01","90","","104.49","0.02","90","","3361","4","300","2","300.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C33 H46 Cl2 N2 O Ru -","- C33 H46 Cl2 N2 O Ru -","- C132 H184 Cl8 N8 O4 Ru4 -","4","1","","Sabbasani, Venkata R.; Gupta, Saswata; Young Yun, Sang; Lee, Daesung","A general approach for the formation of oxygen-chelated ruthenium alkylidene complexes relying on the Thorpe‒Ingold effect","Organic Chemistry Frontiers","2018","5","9","1532","","10.1039/C8QO00160J","","","0.71073","MoKα","","0.1839","0.1163","","","0.279","0.3651","","","","","","1.281","","","","has coordinates","237088","2020-10-21","18:00:00",""
"1554278","26.317","0.004","17.57","0.002","17.431","0.002","90","","110.1","0.004","90","","7569","1.7","200","2","200.15","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C36 H44 Cl2 N2 O Ru -","- C36 H44 Cl2 N2 O Ru -","- C288 H352 Cl16 N16 O8 Ru8 -","8","1","","Sabbasani, Venkata R.; Gupta, Saswata; Young Yun, Sang; Lee, Daesung","A general approach for the formation of oxygen-chelated ruthenium alkylidene complexes relying on the Thorpe‒Ingold effect","Organic Chemistry Frontiers","2018","5","9","1532","","10.1039/C8QO00160J","","","0.71073","MoKα","","0.0528","0.0417","","","0.1117","0.124","","","","","","1.08","","","","has coordinates","237088","2020-10-21","18:00:00",""
"1554279","17.5111","0.0007","18.0998","0.0006","8.8623","0.0003","90","","98.023","0.004","90","","2781.39","0.17","291.74","0.1","291.74","0.1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C16 H9 N5 -","- C16 H9 N5 -","- C128 H72 N40 -","8","2","","Xin, Jing-Rui; He, Yan-Hong; Guan, Zhi","Metal-free aerobic oxidative direct C–H amination of electron-deficient alkenes via photoredox catalysis","Organic Chemistry Frontiers","2018","5","10","1684","","10.1039/C8QO00161H","","x-ray","1.54184","CuKα","","0.0739","0.0585","","","0.2017","0.2344","","","","","","1.092","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554280","16.9028","0.0008","16.5253","0.0007","9.9901","0.0004","90","","90","","90","","2790.5","0.2","100","2","100","2","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C20 H14 N2 O2 -","- C20 H14 N2 O2 -","- C160 H112 N16 O16 -","8","2","","Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian","Photo-induced C‒H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives","Organic Chemistry Frontiers","2018","5","10","1679","","10.1039/C8QO00183A","","","0.71073","MoKα","","0.0688","0.0592","","","0.1431","0.1482","","","","","","1.597","","","","has coordinates,has disorder","237093","2020-10-21","18:00:00",""
"1554281","13.3145","0.0004","13.4792","0.0004","7.0709","0.0002","90","","93.942","0.001","90","","1266","0.06","100","2","100","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C9 H6 N O -","- C9 H6 N O -","- C72 H48 N8 O8 -","8","1","","Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian","Photo-induced C–H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives","Organic Chemistry Frontiers","2018","5","10","1679","","10.1039/C8QO00183A","","","1.54178","CuKα","","0.0413","0.0383","","","0.1095","0.1143","","","","","","1.092","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554282","17.23","0.003","8.7235","0.0016","9.6499","0.0018","90","","90","","90","","1450.4","0.5","100","2","100","2","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C20 H16 N2 O2 -","- C20 H16 N2 O2 -","- C80 H64 N8 O8 -","4","1","","Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian","Photo-induced C–H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives","Organic Chemistry Frontiers","2018","5","10","1679","","10.1039/C8QO00183A","","","0.71073","MoKα","","0.0518","0.0476","","","0.1125","0.1155","","","","","","1.062","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554283","8.0334","0.0012","24.561","0.004","9.1052","0.0013","90","","105.603","0.002","90","","1730.3","0.5","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C24 H20 N2 O2 -","- C24 H20 N2 O2 -","- C96 H80 N8 O8 -","4","1","","Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian","Photo-induced C–H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives","Organic Chemistry Frontiers","2018","5","10","1679","","10.1039/C8QO00183A","","","0.71073","MoKα","","0.0655","0.0516","","","0.1345","0.1443","","","","","","1.059","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554284","5.3397","0.0005","12.5882","0.001","17.165","0.0013","95.56","0.003","94.461","0.003","101.447","0.003","1119.93","0.16","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C32 H22 N2 O2 -","- C32 H22 N2 O2 -","- C64 H44 N4 O4 -","2","1","","Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian","Photo-induced C–H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives","Organic Chemistry Frontiers","2018","5","10","1679","","10.1039/C8QO00183A","","","0.71073","MoKα","","0.1775","0.1105","","","0.2431","0.2798","","","","","","1.056","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554285","9.533","0.006","17.215","0.01","11.031","0.005","90","","122.95","0.04","90","","1519.1","1.6","294","2","294","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C21 H14 O -","- C21 H14 O -","- C84 H56 O4 -","4","1","","Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo","Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C–C bond activation: divergent synthesis of indenones and quinones","Organic Chemistry Frontiers","2018","5","10","1613","","10.1039/C8QO00186C","","","0.71073","MoKα","","0.081","0.0524","","","0.1141","0.1281","","","","","","1.084","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554286","8.166","0.004","9.066","0.005","9.404","0.006","85.402","0.019","75.824","0.017","71.601","0.017","640.5","0.6","294","2","294","2","","","","","","","","3","P -1","-P 1","2","","","","- C17 H14 O -","- C17 H14 O -","- C34 H28 O2 -","2","1","","Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo","Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C–C bond activation: divergent synthesis of indenones and quinones","Organic Chemistry Frontiers","2018","5","10","1613","","10.1039/C8QO00186C","","","0.71073","MoKα","","0.0621","0.0469","","","0.1187","0.1288","","","","","","1.044","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554287","9.603","0.003","10.694","0.004","10.7294","0.0016","70.55","0.05","64.18","0.05","81.02","0.06","935.2","0.7","128","2","128","2","","","","","","","","3","P -1","-P 1","2","","","","- C27 H18 O -","- C27 H18 O -","- C54 H36 O2 -","2","1","","Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo","Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C–C bond activation: divergent synthesis of indenones and quinones","Organic Chemistry Frontiers","2018","5","10","1613","","10.1039/C8QO00186C","","","0.71073","MoKα","","0.0818","0.0595","","","0.1441","0.1523","","","","","","0.995","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554288","8.4085","0.0015","9.35","0.0016","14.153","0.003","105.907","0.01","95.411","0.018","97.753","0.013","1050.2","0.4","128","2","128","2","","","","","","","","3","P -1","-P 1","2","","","","- C31 H20 O -","- C31 H20 O -","- C62 H40 O2 -","2","1","","Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo","Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C–C bond activation: divergent synthesis of indenones and quinones","Organic Chemistry Frontiers","2018","5","10","1613","","10.1039/C8QO00186C","","","0.71073","MoKα","","0.0583","0.0427","","","0.1172","0.1221","","","","","","1.063","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554289","23.315","0.0015","11.3915","0.0007","18.4957","0.0012","90","","93.135","0.003","90","","4905","0.5","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C30 H25 Br N2 O2 -","- C30 H25 Br N2 O2 -","- C240 H200 Br8 N16 O16 -","8","2","","Wang, Chao-Ming; Song, Dan; Xia, Peng-Ju; Ye, Zhi-Peng; Xiao, Jun-An; Xiang, Hao-Yue; Chen, Xiao-Qing; Yang, Hua","Photoredox-catalyzed direct aminoalkylation of isatins: diastereoselective access to 3-hydroxy-3-aminoalkylindolin-2-ones analogues","Organic Chemistry Frontiers","2018","5","10","1608","","10.1039/C8QO00201K","","","0.71073","MoKα","","0.0723","0.0513","","","0.1258","0.1394","","","","","","1.029","","","","has coordinates","300101","2025-06-17","17:58:10",""
"1554290","7.6842","0.0009","19.978","0.002","13.7517","0.0018","90","","98.473","0.012","90","","2088","0.4","173","0.1","173","0.1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C26 H21 N3 O2 -","- C26 H21 N3 O2 -","- C104 H84 N12 O8 -","4","1","","Chen, Wei; Ji, Dong-Sheng; Luo, Yong-Chun; Wang, Zhu-Yin; Xu, Peng-Fei","Directing group assisted ZnI2-catalyzed cyclopropanation of indoles via 2-furylcarbenoids","Organic Chemistry Frontiers","2018","5","11","1768","","10.1039/C8QO00232K","","","0.7107","MoKα","","0.1502","0.0669","","","0.1133","0.1605","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554291","27.4221","0.0008","5.1994","0.0002","19.0212","0.0006","90","","121.717","0.001","90","","2306.99","0.14","298","2","298","2","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C11 H14 O2 S2 -","- C11 H14 O2 S2 -","- C88 H112 O16 S16 -","8","2","","Liu, Yan; Zeng, Jing; Sun, Jiuchang; Cai, Lei; Zhao, Yueqi; Fang, Jing; Hu, Bo; Shu, Penghua; Meng, Lingkui; Wan, Qian","1,4-Dithiothreitol mediated cleavage of the acetal and ketal type of diol protecting groups","Organic Chemistry Frontiers","2018","5","16","2427","","10.1039/C8QO00247A","","","1.54178","CuKα","","0.0409","0.04","","","0.105","0.1096","","","","","","1.094","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554292","9.0455","0.0008","9.948","0.0009","11.7172","0.0017","94.495","0.01","95.25","0.01","98.331","0.007","1034.4","0.2","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C25 H20 N2 O3 -","- C25 H20 N2 O3 -","- C50 H40 N4 O6 -","2","1","","Li, Bingnan; Mai, Shaoyu; Song, Qiuling","Synthesis of fused benzimidazoles via successive nucleophilic additions of benzimidazole derivatives to arynes under transition metal-free conditions","Organic Chemistry Frontiers","2018","5","10","1639","","10.1039/C8QO00251G","","x-ray","0.71073","MoKα","","0.1661","0.1274","","","0.3304","0.3582","","","","","","1.059","","","","has coordinates","237100","2020-10-21","18:00:00",""
"1554293","10.3357","0.0005","23.6593","0.0011","11.6006","0.0005","90","","104.704","0.002","90","","2743.9","0.2","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C34 H31 N O5 -","- C34 H31 N O5 -","- C136 H124 N4 O20 -","4","1","","Alajarin, Mateo; Bañon, Daniel; Egea, Adrian; Marín-Luna, Marta; Orenes, Raul-Angel; Vidal, Angel","Accessing polysubstituted oxazolidines, pyrrolidines and imidazolidines by regioselective [3 + 2] annulations of ketenimines with donor–acceptor oxiranes and aziridines","Organic Chemistry Frontiers","2018","5","13","2020","","10.1039/C8QO00255J","","","0.71073","MoKα","","0.0635","0.0477","","","0.1065","0.1145","","","","","","1.043","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554294","10.9629","0.0005","9.8209","0.0004","27.4846","0.0012","90","","91.397","0.001","90","","2958.3","0.2","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C36 H36 N2 O4 -","- C36 H36 N2 O4 -","- C144 H144 N8 O16 -","4","1","","Alajarin, Mateo; Bañon, Daniel; Egea, Adrian; Marín-Luna, Marta; Orenes, Raul-Angel; Vidal, Angel","Accessing polysubstituted oxazolidines, pyrrolidines and imidazolidines by regioselective [3 + 2] annulations of ketenimines with donor–acceptor oxiranes and aziridines","Organic Chemistry Frontiers","2018","5","13","2020","","10.1039/C8QO00255J","","","1.54178","CuKα","","0.0398","0.0366","","","0.0937","0.0965","","","","","","1.017","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554295","18.1688","0.0009","18.3501","0.001","11.8464","0.0007","90","","90","","90","","3949.6","0.4","100","2","100","2","","","","","","","","6","P c a 21","P 2c -2ac","29","","","","- C44 H44 Cl2 N2 O6 S -","- C44 H44 Cl2 N2 O6 S -","- C176 H176 Cl8 N8 O24 S4 -","4","1","","Alajarin, Mateo; Bañon, Daniel; Egea, Adrian; Marín-Luna, Marta; Orenes, Raul-Angel; Vidal, Angel","Accessing polysubstituted oxazolidines, pyrrolidines and imidazolidines by regioselective [3 + 2] annulations of ketenimines with donor–acceptor oxiranes and aziridines","Organic Chemistry Frontiers","2018","5","13","2020","","10.1039/C8QO00255J","","","0.71073","MoKα","","0.0631","0.0463","","","0.1027","0.1119","","","","","","0.918","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554296","12.143","0.003","10.204","0.002","18.499","0.004","90","","94.972","0.012","90","","2283.5","0.9","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C23 H24 N2 O4 S2 -","- C23 H24 N2 O4 S2 -","- C92 H96 N8 O16 S8 -","4","1","","Luo, Fan; Lu, Yu; Hu, Mengjie; Tian, Junsong; Zhang, Lei; Bao, Wangzhen; Yan, Chao; Huang, Xin; Wang, Zhi-Xiang; Peng, Bo","Reductive ortho C–H cyanoalkylation of aryl(heteroaryl) sulfoxides: a general approach to α-aryl(heteroaryl) nitriles","Organic Chemistry Frontiers","2018","5","11","1756","","10.1039/C8QO00268A","","","0.71073","MoKα","","","0.0564","","","0.1209","0.1367","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554297","9.0286","0.0006","24.083","0.0016","10.3285","0.0007","90","","114.965","0.003","90","","2036","0.2","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C21 H22 N2 O2 S2 -","- C21 H22 N2 O2 S2 -","- C84 H88 N8 O8 S8 -","4","1","","Luo, Fan; Lu, Yu; Hu, Mengjie; Tian, Junsong; Zhang, Lei; Bao, Wangzhen; Yan, Chao; Huang, Xin; Wang, Zhi-Xiang; Peng, Bo","Reductive ortho C–H cyanoalkylation of aryl(heteroaryl) sulfoxides: a general approach to α-aryl(heteroaryl) nitriles","Organic Chemistry Frontiers","2018","5","11","1756","","10.1039/C8QO00268A","","","0.71073","MoKα","","","0.0439","","","0.1166","0.1287","","","","","","1.065","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554298","10.4066","0.0014","26.417","0.004","12.0692","0.0014","90","","90","","90","","3318","0.8","293","2","293.15","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","ZHY7009","","- C26 H39 Cl2 Co N3 O12 -","- C26 H39 Cl2 Co N3 O12 -","- C104 H156 Cl8 Co4 N12 O48 -","4","1","","Zhang, Heyi; Lu, Zhan","Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation","Organic Chemistry Frontiers","2018","5","11","1763","","10.1039/C8QO00279G","","","0.71073","MoKα","","0.1363","0.0755","","","0.1596","0.1969","","","","","","1.003","","","","has coordinates","237107","2020-10-21","18:00:00",""
"1554299","10.3907","0.0009","11.9429","0.0011","26.537","0.003","90","","90","","90","","3293.1","0.6","293","2","293.15","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","ZHY7163","","- C26 H39 Cl2 N3 Ni O12 -","- C26 H39 Cl2 N3 Ni O12 -","- C104 H156 Cl8 N12 Ni4 O48 -","4","1","","Zhang, Heyi; Lu, Zhan","Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation","Organic Chemistry Frontiers","2018","5","11","1763","","10.1039/C8QO00279G","","","0.71073","MoKα","","0.128","0.0735","","","0.1546","0.1907","","","","","","1.011","","","","has coordinates","237107","2020-10-21","18:00:00",""
"1554300","6.96436","0.00013","7.91974","0.00013","15.2392","0.0003","90","","92.2266","0.0016","90","","839.9","0.03","293","2","293.15","","","","","","","","","3","P 1 21 1","P 2yb","4","","ZHY8126","","- C22 H18 O -","- C22 H18 O -","- C44 H36 O2 -","2","1","","Zhang, Heyi; Lu, Zhan","Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation","Organic Chemistry Frontiers","2018","5","11","1763","","10.1039/C8QO00279G","","","1.54184","CuKα","","0.041","0.0395","","","0.1052","0.1077","","","","","","1.029","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554301","10.3081","0.0003","11.98","0.0002","26.1548","0.0005","90","","90","","90","","3229.88","0.12","100.01","0.1","100.01","0.1","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","zhy8105","","- C26 H41 Cl2 Fe N3 O12 -","- C26 H41 Cl2 Fe N3 O12 -","- C104 H164 Cl8 Fe4 N12 O48 -","4","1","","Zhang, Heyi; Lu, Zhan","Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation","Organic Chemistry Frontiers","2018","5","11","1763","","10.1039/C8QO00279G","","x-ray","1.54184","CuKα","","0.0535","0.0491","","","0.1266","0.1292","","","","","","1.066","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554302","10.0093","0.0002","14.3918","0.0003","10.7208","0.0002","90","","104.176","0.002","90","","1497.32","0.05","100","","100","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H19 N O3 S -","- C15 H19 N O3 S -","- C60 H76 N4 O12 S4 -","4","1","","Yu, Ji-cong; Yu, Le-mao; Zhao, Xiao-yun; Gan, Lu; Zhu, Wei-wei; Wang, Ze-chen; Wang, Rui; Jiang, Xianxing","Organocatalytic asymmetric [3 + 2] annulation of 1,4-dithiane-2,5-diol with azlactones: access to chiral dihydrothiophen-2(3H)-one derivatives","Organic Chemistry Frontiers","2018","5","13","2040","","10.1039/C8QO00305J","","x-ray","1.54184","CuKα","","0.031","0.0297","","","0.0746","0.0756","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554303","6.54242","0.00011","22.4359","0.0003","10.03319","0.00017","90","","102.165","0.0017","90","","1439.65","0.04","100","","100","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H19 N O3 S -","- C15 H19 N O3 S -","- C60 H76 N4 O12 S4 -","4","1","","Yu, Ji-cong; Yu, Le-mao; Zhao, Xiao-yun; Gan, Lu; Zhu, Wei-wei; Wang, Ze-chen; Wang, Rui; Jiang, Xianxing","Organocatalytic asymmetric [3 + 2] annulation of 1,4-dithiane-2,5-diol with azlactones: access to chiral dihydrothiophen-2(3H)-one derivatives","Organic Chemistry Frontiers","2018","5","13","2040","","10.1039/C8QO00305J","","x-ray","1.54184","CuKα","","0.0359","0.0348","","","0.0929","0.094","","","","","","1.057","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554304","5.9758","0.0003","8.5937","0.0004","15.7695","0.0007","90","","93.352","0.002","90","","808.45","0.07","296","2","296","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C17 H18 Cl N O2 -","- C17 H18 Cl N O2 -","- C34 H36 Cl2 N2 O4 -","2","1","","Hu, Yang; Yin, Xuguang; Chen, Ziyi; Dong, Xiu-Qin; Zhang, Xumu","Highly enantioselective Ir/f-amphox-catalyzed hydrogenation of ketoamides: efficient access to chiral hydroxy amides","Organic Chemistry Frontiers","2018","5","12","2000","","10.1039/C8QO00307F","","","1.54178","CuKα","","0.0426","0.0371","","","0.1144","0.1175","","","","","","1.131","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554305","6.4792","0.0004","25.1943","0.0014","10.1094","0.0006","90","","106.673","0.006","90","","1580.87","0.17","180","0.1","180","0.1","","","","","","","","6","P 1 21/m 1","-P 2yb","11","","","","- C32 H7 Cl4 F10 N3 O2 -","- C32 H7 Cl4 F10 N3 O2 -","- C64 H14 Cl8 F20 N6 O4 -","2","0.5","","Wang, Jun-Fei; Yao, Yuhang; Ning, Yingying; Meng, Yin-Shan; Hou, Chun-Liang; Zhang, Jing; Zhang, Jun-Long","The design of rigid cyclic tripyrrins: the importance of intermolecular interactions on aggregation and luminescence","Organic Chemistry Frontiers","2018","5","12","1877","","10.1039/C8QO00313K","","x-ray","0.71073","MoKα","","0.0694","0.0441","","","0.0889","0.1004","","","","","","1.025","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554306","6.3689","0.0005","19.2075","0.001","14.4005","0.0009","90","","96.153","0.007","90","","1751.5","0.2","180.01","0.1","180.01","0.1","","","","","","","","6","P 1 21/m 1","-P 2yb","11","","","","- C36 H11 Cl2 F10 N5 O2.5 -","- C36 H11 Cl2 F10 N5 O2.5 -","- C72 H22 Cl4 F20 N10 O5 -","2","0.5","","Wang, Jun-Fei; Yao, Yuhang; Ning, Yingying; Meng, Yin-Shan; Hou, Chun-Liang; Zhang, Jing; Zhang, Jun-Long","The design of rigid cyclic tripyrrins: the importance of intermolecular interactions on aggregation and luminescence","Organic Chemistry Frontiers","2018","5","12","1877","","10.1039/C8QO00313K","","x-ray","0.71073","MoKα","","0.0931","0.0683","","","0.2181","0.2414","","","","","","1.117","","","","has coordinates","237111","2020-10-21","18:00:00",""
"1554307","18.5573","0.001","18.3335","0.0013","14.8419","0.001","90","","90","","90","","5049.5","0.6","180","0.1","180","0.1","","","","","","","","6","P n m a","-P 2ac 2n","62","","","","- C38 H7 Br2 F10 N5 O3 -","- C38 H7 Br2 F10 N5 O3 -","- C152 H28 Br8 F40 N20 O12 -","4","0.5","","Wang, Jun-Fei; Yao, Yuhang; Ning, Yingying; Meng, Yin-Shan; Hou, Chun-Liang; Zhang, Jing; Zhang, Jun-Long","The design of rigid cyclic tripyrrins: the importance of intermolecular interactions on aggregation and luminescence","Organic Chemistry Frontiers","2018","5","12","1877","","10.1039/C8QO00313K","","x-ray","0.71073","MoKα","","0.0938","0.0702","","","0.1845","0.2056","","","","","","1.065","","","","has coordinates,has disorder","237111","2020-10-21","18:00:00",""
"1554308","8.2423","0.0002","18.2962","0.0006","34.5544","0.0012","90","","90","","90","","5210.9","0.3","117.5","0.3","117.5","0.3","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C28 H26 F N O8 S -","- C28 H26 F N O8 S -","- C224 H208 F8 N8 O64 S8 -","8","1","","Xing, Siyang; Cui, Hong; Qin, Jiajing; Gu, Nan; Zhang, Bowei; Wang, Kui; Wang, Ying; Xia, Li; Wang, Yumeng","Diastereoselective synthesis of cis-1,3-disubstituted isoindolines via a highly site-selective tandem cyclization reaction","Organic Chemistry Frontiers","2018","5","12","1950","","10.1039/C8QO00316E","","x-ray","1.54184","CuKα","","0.0828","0.0624","","","0.1503","0.167","","","","","","1.01","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554309","21.4204","0.0015","21.5628","0.0012","14.5587","0.0008","90","","97.091","0.006","90","","6673","0.7","135","0.1","135","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C28.8 H27.6 N2 O10 S -","- C28.8 H27.6 N2 O10 S -","- C230.4 H220.8 N16 O80 S8 -","8","2","","Xing, Siyang; Cui, Hong; Qin, Jiajing; Gu, Nan; Zhang, Bowei; Wang, Kui; Wang, Ying; Xia, Li; Wang, Yumeng","Diastereoselective synthesis of cis-1,3-disubstituted isoindolines via a highly site-selective tandem cyclization reaction","Organic Chemistry Frontiers","2018","5","12","1950","","10.1039/C8QO00316E","","x-ray","0.71073","MoKα","","0.1508","0.0971","","","0.2658","0.32","","","","","","1.057","","","","has coordinates,has disorder","237113","2020-10-21","18:00:00",""
"1554310","10.5915","0.0002","15.1258","0.0002","9.0257","0.0002","90","","109.468","0.002","90","","1363.29","0.05","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C17 H14 O2 -","- C17 H14 O2 -","- C68 H56 O8 -","4","1","","Zheng, Wei-Feng; Zhang, Wanli; Huang, Jianhao; Yu, Yibo; Qian, Hui; Ma, Shengming","2,3-Allenoic acids via palladium-catalyzed carboxylation of propargylic alcohols","Organic Chemistry Frontiers","2018","5","12","1900","","10.1039/C8QO00318A","","x-ray","1.54184","CuKα","","0.0407","0.0369","","","0.0989","0.1021","","","","","","1.014","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554311","5.6491","0.0004","11.5037","0.0011","11.5175","0.0007","111.795","0.007","99.48","0.006","90.087","0.007","683.87","0.1","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C15 H18 O2 -","- C15 H18 O2 -","- C30 H36 O4 -","2","1","","Zheng, Wei-Feng; Zhang, Wanli; Huang, Jianhao; Yu, Yibo; Qian, Hui; Ma, Shengming","2,3-Allenoic acids via palladium-catalyzed carboxylation of propargylic alcohols","Organic Chemistry Frontiers","2018","5","12","1900","","10.1039/C8QO00318A","","x-ray","1.54184","CuKα","","0.0879","0.068","","","0.2031","0.2213","","","","","","1.06","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554312","10.573","0.004","7.311","0.002","11.35","0.004","90","","115.216","0.005","90","","793.7","0.5","173","2","173.15","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C16 H17 Br O4 -","- C16 H17 Br O4 -","- C32 H34 Br2 O8 -","2","1","","Li, Sujia; Lv, Jian; Luo, Sanzhong","Enantioselective indium(i)-catalyzed [4 + 2] annulation of alkoxyallenes and β,γ-unsaturated α-keto esters","Organic Chemistry Frontiers","2018","5","11","1787","","10.1039/C8QO00319J","","","0.71073","MoKα","","0.0388","0.0359","","","0.077","0.0793","","","","","","1.076","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554313","8.46","0.02","9.59","0.02","11.8","0.03","97.55","0.09","104.24","0.19","108.51","0.13","857","4","293","2","293","2","","","","","","","","4","P -1","-P 1","2","Q3","","","- C20 H18 N4 O2 -","- C20 H18 N4 O2 -","- C40 H36 N8 O4 -","2","1","","Toonchue, Saowanee; Sumunnee, Ladawan; Phomphrai, Khamphee; Yotphan, Sirilata","Metal-free direct oxidative C–C bond coupling of pyrazolones and quinoxalinones","Organic Chemistry Frontiers","2018","5","12","1928","","10.1039/C8QO00328A","","","0.71073","","","0.0784","0.0461","","","0.1022","0.1147","","","","","","1.049","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554314","9.998","0.005","9.281","0.004","14.416","0.006","90","","95.77","0.02","90","","1330.9","1","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","Q5","","","- C15 H16 N4 O2 -","- C15 H16 N4 O2 -","- C60 H64 N16 O8 -","4","1","","Toonchue, Saowanee; Sumunnee, Ladawan; Phomphrai, Khamphee; Yotphan, Sirilata","Metal-free direct oxidative C–C bond coupling of pyrazolones and quinoxalinones","Organic Chemistry Frontiers","2018","5","12","1928","","10.1039/C8QO00328A","","","0.71073","","","0.0416","0.037","","","0.0957","0.0993","","","","","","1.066","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554315","7.3563","0.0012","46.699","0.007","12.909","0.002","90","","92.798","0.004","90","","4429.4","1.2","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C20 H40.5 O3.25 Si -","- C20 H40.5 O3.25 Si -","- C160 H324 O26 Si8 -","8","4","","Santalla, Hugo; Garrido, Fátima; Gómez, Generosa; Fall, Yagamare","A more reliable synthesis of a Gemini vitamin D analog, a potentially effective chemotherapeutic agent for the treatment of colorectal carcinomas","Organic Chemistry Frontiers","2018","5","13","2016","","10.1039/C8QO00338F","","","0.71073","MoKα","","0.2634","0.1846","","","0.3663","0.4018","","","","","","1.088","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554316","10.1535","0.0002","10.5316","0.0002","25.565","0.0006","90","","90","","90","","2733.73","0.1","297.6","0.8","297.6","0.8","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C32 H31 N O5 -","- C32 H31 N O5 -","- C128 H124 N4 O20 -","4","1","","Duan, Chuan-Qi; He, Xiao-Long; Du, Wei; Chen, Ying-Chun","Asymmetric [4 + 2] cycloadditions with 3-furfural derivatives and α-cyano-α,β-unsaturated ketones","Organic Chemistry Frontiers","2018","5","13","2057","","10.1039/C8QO00351C","","x-ray","1.54184","CuKα","","0.0447","0.0432","","","0.1184","0.1208","","","","","","1.0435","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554317","10.0726","0.0019","10.735","0.002","19.604","0.004","82.045","0.004","86.428","0.005","81.212","0.005","2072.9","0.7","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C23 H20 Br N O2 S -","- C23 H20 Br N O2 S -","- C92 H80 Br4 N4 O8 S4 -","4","2","","Jiang, Bo; Wei, Yin; Shi, Min","Gold- and silver-catalyzed intramolecular annulation and rearrangement of aniline-linked 1,6-enynes containing methylenecyclopropanes","Organic Chemistry Frontiers","2018","5","13","2091","","10.1039/C8QO00358K","","","0.71073","MoKα","","0.1374","0.0618","","","0.1248","0.1556","","","","","","0.968","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554318","9.447","0.004","10.559","0.005","12.512","0.006","76.431","0.008","77.755","0.009","64.585","0.007","1087","0.9","296","2","296","","","","","","","","","5","P -1","-P 1","2","","","","- C26 H23 N O2 S -","- C26 H23 N O2 S -","- C52 H46 N2 O4 S2 -","2","1","","Jiang, Bo; Wei, Yin; Shi, Min","Gold- and silver-catalyzed intramolecular annulation and rearrangement of aniline-linked 1,6-enynes containing methylenecyclopropanes","Organic Chemistry Frontiers","2018","5","13","2091","","10.1039/C8QO00358K","","","0.71073","MoKα","","0.1889","0.0964","","","0.2442","0.3157","","","","","","1.014","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554319","11.7526","0.0016","13.4984","0.0019","13.5265","0.0019","90","","92.44","0.004","90","","2143.9","0.5","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C26 H23 N O2 S -","- C26 H23 N O2 S -","- C104 H92 N4 O8 S4 -","4","1","","Jiang, Bo; Wei, Yin; Shi, Min","Gold- and silver-catalyzed intramolecular annulation and rearrangement of aniline-linked 1,6-enynes containing methylenecyclopropanes","Organic Chemistry Frontiers","2018","5","13","2091","","10.1039/C8QO00358K","","","0.71073","MoKα","","0.1633","0.0757","","","0.1824","0.2426","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554320","9.00774","0.00012","11.44511","0.00014","29.0288","0.0003","90","","90","","90","","2992.71","0.06","293.8","0.5","293.8","0.5","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","((1R,2R,3R,3aS)-1'-benzyl-2'-oxo-1,2-dihydro-3aH-spiro[benzo[d]pyrrolo[2,1-b]thiazole-3,3'-indoline]-1,2-diyl)bis(phenylmethanone)","","- C38 H28 N2 O3 S -","- C38 H28 N2 O3 S -","- C152 H112 N8 O12 S4 -","4","1","","Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming","Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives","Organic Chemistry Frontiers","2018","5","13","2126","","10.1039/C8QO00370J","","x-ray","1.54184","CuKα","","0.0518","0.0487","","","0.1321","0.1365","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554321","14.8962","0.0011","11.3205","0.0008","20.153","0.002","90","","102.279","0.009","90","","3320.7","0.5","293","2","293.15","","","","","","","","","5","C 1 2 1","C 2y","5","","","","- C38 H28 N2 O4 S -","- C38 H28 N2 O4 S -","- C152 H112 N8 O16 S4 -","4","1","","Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming","Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives","Organic Chemistry Frontiers","2018","5","13","2126","","10.1039/C8QO00370J","","x-ray","0.71073","MoKα","","0.0546","0.0441","","","0.1095","0.1153","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554322","6.3467","0.00018","16.1435","0.0004","10.7987","0.0003","90","","96.301","0.003","90","","1099.73","0.05","295.97","0.11","295.97","0.11","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C26 H21 N O4 S -","- C26 H21 N O4 S -","- C52 H42 N2 O8 S2 -","2","1","","Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming","Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives","Organic Chemistry Frontiers","2018","5","13","2126","","10.1039/C8QO00370J","","x-ray","1.54184","CuKα","","0.0639","0.0618","","","0.1519","0.1572","","","","","","1.077","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554323","10.4185","0.0009","15.4927","0.0012","15.8277","0.0018","90","","95.756","0.008","90","","2541.9","0.4","293","2","293.15","","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C30 H22 Cl N O2 S -","- C30 H22 Cl N O2 S -","- C120 H88 Cl4 N4 O8 S4 -","4","2","","Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming","Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives","Organic Chemistry Frontiers","2018","5","13","2126","","10.1039/C8QO00370J","","x-ray","0.71073","MoKα","","0.1377","0.1004","","","0.2762","0.3105","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554324","9.2007","0.0002","9.2791","0.0004","14.237","0.0005","97.598","0.003","91.193","0.003","97.349","0.003","1194.02","0.07","139","","139","","","","","","","","","7","P 1","P 1","1","","","","- C31 H56 F6 Mg N4 O14 S2 -","- C31 H56 F6 Mg N4 O14 S2 -","- C31 H56 F6 Mg N4 O14 S2 -","1","1","","Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming","Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives","Organic Chemistry Frontiers","2018","5","13","2126","","10.1039/C8QO00370J","","x-ray","1.54184","CuKα","","0.0653","0.061","","","0.1662","0.1745","","","","","","1.023","","","","has coordinates","237128","2020-10-21","18:00:00",""
"1554325","8.2339","0.0002","14.7918","0.0004","17.1794","0.0005","101.33","0.002","95.203","0.002","106.126","0.002","1947.28","0.1","100.01","0.1","100.01","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C25 H19 N3 O -","- C25 H19 N3 O -","- C100 H76 N12 O4 -","4","2","","Liu, Yun-Lin; Mao, Xiang-Yu; Lin, Xiao-Tong; Chen, Guo-Shu","A Zn(OTf)2 catalyzed Ugi-type reaction of 3-(2-isocyanoethyl)indoles with indole-derived ketimines: rapid access to hexacyclic spiroindolines","Organic Chemistry Frontiers","2018","5","15","2303","","10.1039/C8QO00382C","","x-ray","1.54184","CuKα","","0.0445","0.0407","","","0.0982","0.1005","","","","","","1.03","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554326","19.5242","0.0003","8.4475","0.0001","25.582","0.0004","90","","107.178","0.002","90","","4031.04","0.11","100","10","100","10","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C25 H16 F3 N3 O2 -","- C25 H16 F3 N3 O2 -","- C200 H128 F24 N24 O16 -","8","2","","Liu, Yun-Lin; Mao, Xiang-Yu; Lin, Xiao-Tong; Chen, Guo-Shu","A Zn(OTf)2 catalyzed Ugi-type reaction of 3-(2-isocyanoethyl)indoles with indole-derived ketimines: rapid access to hexacyclic spiroindolines","Organic Chemistry Frontiers","2018","5","15","2303","","10.1039/C8QO00382C","","","1.54178","CuKα","","0.0536","0.0494","","","0.141","0.1456","","","","","","1.057","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554327","18.7671","0.0001","18.7671","0.0001","24.2076","0.0003","90","","90","","90","","8526.01","0.12","100","0.1","100","0.1","","","","","","","","4","I 41/a :2","-I 4ad","88","","","","- C26 H21 F2 N3 -","- C26 H21 F2 N3 -","- C416 H336 F32 N48 -","16","1","","Liu, Yun-Lin; Mao, Xiang-Yu; Lin, Xiao-Tong; Chen, Guo-Shu","A Zn(OTf)2 catalyzed Ugi-type reaction of 3-(2-isocyanoethyl)indoles with indole-derived ketimines: rapid access to hexacyclic spiroindolines","Organic Chemistry Frontiers","2018","5","15","2303","","10.1039/C8QO00382C","","x-ray","1.54184","CuKα","","0.0426","0.0395","","","0.098","0.1","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554328","57.5837","0.0019","5.8021","0.0002","8.0527","0.0003","90","","90","","90","","2690.46","0.16","296","2","296","2","","","","","","","","4","P b c n","-P 2n 2ab","60","","","","- C16 H15 Cl O -","- C16 H15 Cl O -","- C128 H120 Cl8 O8 -","8","1","","Chen, Mintao; Wei, Yin; Shi, Min","A facile method for the synthesis of trifluoromethylthio-/chloro-homoallylic alcohols from methylenecyclopropanes","Organic Chemistry Frontiers","2018","5","13","2030","","10.1039/C8QO00386F","","","0.71073","MoKα","","0.0589","0.0509","","","0.123","0.1297","","","","","","1.067","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554329","10.0641","0.0003","10.4692","0.0002","12.4244","0.0003","90.033","0.001","93.737","0.001","96.649","0.001","1297.46","0.06","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C12 H13 F3 O2 S -","- C12 H13 F3 O2 S -","- C48 H52 F12 O8 S4 -","4","2","","Chen, Mintao; Wei, Yin; Shi, Min","A facile method for the synthesis of trifluoromethylthio-/chloro-homoallylic alcohols from methylenecyclopropanes","Organic Chemistry Frontiers","2018","5","13","2030","","10.1039/C8QO00386F","","","0.71073","MoKα","","0.0544","0.0413","","","0.1119","0.1252","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554330","12.134","0.003","13.857","0.004","17.116","0.004","70.214","0.005","75.507","0.005","73.496","0.005","2558.3","1.1","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C66 H78 O2 -","- C66 H78 O2 -","- C132 H156 O4 -","2","1","","Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A.","Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation","Organic Chemistry Frontiers","2018","5","15","2288","","10.1039/C8QO00389K","","","0.71073","MoKα","","0.1305","0.0604","","","0.1323","0.1658","","","","","","1.006","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554331","9.3311","0.0006","9.8219","0.0006","16.1042","0.001","103.794","0.001","94.992","0.001","112.566","0.001","1297.14","0.14","100","2","100","2","","","","","","","","2","P -1","-P 1","2","","","","- C68 H74 -","- C68 H74 -","- C68 H74 -","1","0.5","","Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A.","Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation","Organic Chemistry Frontiers","2018","5","15","2288","","10.1039/C8QO00389K","","","0.71073","MoKα","","0.0998","0.064","","","0.1856","0.203","","","","","","1.1","","","","has coordinates,has disorder","237134","2020-10-21","18:00:00",""
"1554332","15.3329","0.0008","18.3488","0.001","15.6332","0.0008","90","","99.6319","0.001","90","","4336.2","0.4","293","2","293","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C95.5 H118 Cl4.5 O4.93 -","- C95.5 H118 Cl4.497 O4.855 -","- C191 H236 Cl8.994 O9.71 -","2","1","","Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A.","Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation","Organic Chemistry Frontiers","2018","5","15","2288","","10.1039/C8QO00389K","","","0.71073","MoKα","","0.1041","0.0787","","","0.2132","0.2326","","","","","","1.061","","","","has coordinates,has disorder","237134","2020-10-21","18:00:00",""
"1554333","32.048","0.0019","25.4121","0.0015","26.3829","0.0015","90","","102.865","0.0011","90","","20947","2","100","2","100","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C127.75 H123 O1.75 -","- C127.75 H123 O1.75 -","- C1022 H984 O14 -","8","1","","Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A.","Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation","Organic Chemistry Frontiers","2018","5","15","2288","","10.1039/C8QO00389K","","","0.71073","MoKα","","0.1598","0.0833","","","0.2135","0.244","","","","","","1.025","","","","has coordinates,has disorder","237134","2020-10-21","18:00:00",""
"1554334","9.5467","0.0009","13.5703","0.0018","26.06","0.002","90","","90","","90","","3376.1","0.6","294.24","0.1","294.24","0.1","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C34 H34 Cl3 Fe N3 O4 -","- C34 H34 Cl3 Fe N3 O4 -","- C136 H136 Cl12 Fe4 N12 O16 -","4","1","","Zhang, Yuehua; Wang, Chunting; Huang, Wei; Haruehanroengra, Phensinee; Peng, Cheng; Sheng, Jia; Han, Bo; He, Gu","Application of organocatalysis in bioorganometallic chemistry: asymmetric synthesis of multifunctionalized spirocyclic pyrazolone–ferrocene hybrids as novel RalA inhibitors","Organic Chemistry Frontiers","2018","5","14","2229","","10.1039/C8QO00422F","","x-ray","1.54184","CuKα","","0.079","0.0679","","","0.1643","0.1774","","","","","","1.082","","","","has coordinates","300101","2025-06-17","17:58:10",""
"1554335","12.0535","0.0003","12.0535","0.0003","43.8649","0.0013","90","","90","","90","","6373","0.3","139.05","0.1","139.05","0.1","","","","","","","","6","P 41 21 2","P 4abw 2nw","92","","","","- C34 H35 Cl2 Fe N3 O4 -","- C34 H35 Cl2 Fe N3 O4 -","- C272 H280 Cl16 Fe8 N24 O32 -","8","1","","Zhang, Yuehua; Wang, Chunting; Huang, Wei; Haruehanroengra, Phensinee; Peng, Cheng; Sheng, Jia; Han, Bo; He, Gu","Application of organocatalysis in bioorganometallic chemistry: asymmetric synthesis of multifunctionalized spirocyclic pyrazolone‒ferrocene hybrids as novel RalA inhibitors","Organic Chemistry Frontiers","2018","5","14","2229","","10.1039/C8QO00422F","","x-ray","1.54184","CuKα","","0.0745","0.063","","","0.1467","0.1552","","","","","","1.07","","","","has coordinates","237136","2020-10-21","18:00:00",""
"1554336","18.4603","0.0003","16.6736","0.0003","13.8087","0.001","90","","103.239","0.007","90","","4137.4","0.3","293","2","293","2","","","","","","","","5","C 1 2 1","C 2y","5","","(1R,2R,4aS,12bS)-1-chloro-2-hydroxy-2,5,5,7-tetramethyl-1,2,3,4,4a,5,7,12b-octahydro-12H-isochromeno[3,4-b]quinolin-12-one","","- C20.57 H26.27 Cl N O3.57 -","- C20 H24 Cl N O3 -","- C160 H192 Cl8 N8 O24 -","8","2","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","","1.54187","CuKα","","0.1415","0.0783","","","0.2","0.2755","","","","","","1.043","","","","has coordinates","237138","2020-10-21","18:00:00",""
"1554337","11.4568","0.0005","11.4834","0.0003","14.2866","0.0007","94.508","0.003","106.183","0.004","90.764","0.002","1798.31","0.13","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C20 H24 Cl N O3 -","- C20 H24 Cl N O3 -","- C80 H96 Cl4 N4 O12 -","4","2","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","","0.71073","MoKα","","0.0761","0.0637","","","0.1833","0.1899","","","","","","1.062","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554338","17.0841","0.0012","18.7193","0.0011","11.1858","0.0007","90","","100.62","0.007","90","","3516","0.4","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H25 N O4 -","- C20 H25 N O4 -","- C160 H200 N8 O32 -","8","2","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","","1.54187","CuKα","","0.054","0.0402","","","0.105","0.1242","","","","","","1.135","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554339","11.3027","0.0005","7.2512","0.0002","23.102","0.0016","90","","98.784","0.007","90","","1871.19","0.17","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H24 Cl N O5 -","- C20 H24 Cl N O5 -","- C80 H96 Cl4 N4 O20 -","4","1","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","","1.54187","CuKα","","0.0596","0.0463","","","0.1156","0.1277","","","","","","1.084","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554340","7.508","0.0002","11.2397","0.0003","21.9828","0.0015","90","","90","","90","","1855.08","0.14","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","(6aS,9R,10R,10aS)-10-chloro-9-hydroxy-6,6,9,12-tetramethyl-6,6a,7,8,9,10,10a,12-octahydro-11H-isochromeno[4,3-c]quinolin-11-one)","","- C20 H24 Cl N O3 -","- C20 H24 Cl N O3 -","- C80 H96 Cl4 N4 O12 -","4","1","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","","1.54187","CuKα","","0.1108","0.0543","","","0.0941","0.141","","","","","","1.14","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554341","17.278","0.002","12.6989","0.001","17.255","0.002","90","","102.191","0.013","90","","3700.6","0.7","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H22 Cl N O4 -","- C20 H22 Cl N O4 -","- C160 H176 Cl8 N8 O32 -","8","2","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","","0.71073","MoKα","","0.1125","0.0613","","","0.1331","0.1521","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554342","16.127","0.0008","7.209","0.0004","16.3705","0.0009","90","","91.08","0.005","90","","1902.89","0.18","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H26 Cl N O4 -","- C20 H26 Cl N O4 -","- C80 H104 Cl4 N4 O16 -","4","1","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","x-ray","0.71073","MoKα","","0.0917","0.0692","","","0.1793","0.1929","","","","","","1.066","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554343","10.2096","0.0003","12.8487","0.0004","12.9425","0.0004","90","","107.01","0.004","90","","1623.53","0.09","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H23 N O2 -","- C20 H23 N O2 -","- C80 H92 N4 O8 -","4","1","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","","0.71073","MoKα","","0.0431","0.0379","","","0.1059","0.1095","","","","","","1.069","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554344","5.5872","0.0007","13.9109","0.0013","14.4106","0.0018","112.533","0.01","98.978","0.011","94.422","0.009","1010.3","0.2","100","0.1","100","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C24 H24 O5 S -","- C24 H24 O5 S -","- C48 H48 O10 S2 -","2","1","","Cui, Zhiming; Zhu, Baofu; Li, Xuechen; Cao, Hua","Access to sulfonylated furans or imidazo[1,2-a]pyridines via a metal-free three-component, domino reaction","Organic Chemistry Frontiers","2018","5","14","2219","","10.1039/C8QO00443A","","x-ray","0.71073","MoKα","","0.0762","0.0633","","","0.1555","0.1681","","","","","","1.061","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554345","10.194","0.002","14.232","0.003","12.523","0.003","90","","106.045","0.006","90","","1746.1","0.7","273","2","273.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","3c","","- C20 H19 N O4 -","- C20 H19 N O4 -","- C80 H76 N4 O16 -","4","1","","Jia, Xiaodong; Hou, Wentao; Chen, Qian; Yuan, Yu; Sun, Jing; He, Kaixuan","Oxidation of active sp3C–H bonds initiated consecutive intermolecular/intramolecular cyclization between glycine derivatives ando-vinylphenols: construction of a polycyclic benzofuroquinoline skeleton","Organic Chemistry Frontiers","2018","5","16","2479","","10.1039/C8QO00444G","","","0.71073","MoKα","","0.1014","0.0609","","","0.1599","0.1822","","","","","","1.067","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554346","9.1376","0.0008","9.5813","0.0009","10.8392","0.001","105.957","0.003","95.789","0.003","98.506","0.003","892.32","0.14","273","2","273.15","","","","","","","","","4","P -1","-P 1","2","","","","- C20 H20 N2 O5 -","- C20 H20 N2 O5 -","- C40 H40 N4 O10 -","2","1","","Jia, Xiaodong; Hou, Wentao; Chen, Qian; Yuan, Yu; Sun, Jing; He, Kaixuan","Oxidation of active sp3C–H bonds initiated consecutive intermolecular/intramolecular cyclization between glycine derivatives ando-vinylphenols: construction of a polycyclic benzofuroquinoline skeleton","Organic Chemistry Frontiers","2018","5","16","2479","","10.1039/C8QO00444G","","","0.71073","MoKα","","0.0596","0.0459","","","0.1257","0.1347","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554347","21.194","0.005","8.4619","0.0012","27.57","0.01","90","","109.98","0.03","90","","4647","2","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C11 H10 N O -","- C11.6 H8.6 N0.8 O1.6 -","- C232 H172 N16 O32 -","20","5","","Gong, Hai-Xian; Cao, Zhu; Li, Meng-Hua; Liao, Sai-Hu; Lin, Mei-Jin","Photoexcited perylene diimide radical anions for the reduction of aryl halides: a bay-substituent effect","Organic Chemistry Frontiers","2018","5","15","2296","","10.1039/C8QO00445E","","","0.71073","MoKα","","0.3157","0.1526","","","0.3538","0.4478","","","","","","1.025","","","","has coordinates","237146","2020-10-21","18:00:00",""
"1554348","10.9697","0.0018","16.013","0.003","13.031","0.002","90","","105.898","0.018","90","","2201.4","0.7","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C24 H21 N O2 -","- C24 H21 N O2 -","- C96 H84 N4 O8 -","4","1","","Gong, Hai-Xian; Cao, Zhu; Li, Meng-Hua; Liao, Sai-Hu; Lin, Mei-Jin","Photoexcited perylene diimide radical anions for the reduction of aryl halides: a bay-substituent effect","Organic Chemistry Frontiers","2018","5","15","2296","","10.1039/C8QO00445E","","x-ray","0.71073","MoKα","","0.21","0.1166","","","0.3294","0.3693","","","","","","0.991","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554349","24.1341","0.0014","25.4123","0.0013","26.638","0.0017","90","","90","","90","","16337.2","1.6","173","2","173.15","","","","","","","","","4","F d d d :2","-F 2uv 2vw","70","","","","- C5.5 H5.62 N0.12 O0.5 -","- C5.5 H5.625 N0.125 O0.5 -","- C704 H720 N16 O64 -","128","4","","Gong, Hai-Xian; Cao, Zhu; Li, Meng-Hua; Liao, Sai-Hu; Lin, Mei-Jin","Photoexcited perylene diimide radical anions for the reduction of aryl halides: a bay-substituent effect","Organic Chemistry Frontiers","2018","5","15","2296","","10.1039/C8QO00445E","","","0.71073","MoKα","","0.0942","0.0766","","","0.2293","0.244","","","","","","1.068","","","","has coordinates","237146","2020-10-21","18:00:00",""
"1554350","9.4355","0.0005","10.2231","0.0006","17.9161","0.0011","87.132","0.005","84.213","0.005","68.822","0.005","1603.09","0.17","173","2","173.15","","","","","","","","","4","P -1","-P 1","2","","","","- C34 H33 N O3 -","- C34 H33 N O3 -","- C68 H66 N2 O6 -","2","1","","Gong, Hai-Xian; Cao, Zhu; Li, Meng-Hua; Liao, Sai-Hu; Lin, Mei-Jin","Photoexcited perylene diimide radical anions for the reduction of aryl halides: a bay-substituent effect","Organic Chemistry Frontiers","2018","5","15","2296","","10.1039/C8QO00445E","","","0.71073","MoKα","","0.1162","0.0845","","","0.2197","0.2349","","","","","","1.068","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554351","40.9015","0.0014","40.9015","0.0014","9.3338","0.0005","90","","90","","90","","15614.8","1.1","100","","100","","","","","","","","","4","I 41/a :2","-I 4ad","88","","","","- C45 H68 N2 O2 -","- C45 H68 N2 O2 -","- C720 H1088 N32 O32 -","16","1","","Mahoney, Janell K.; Regnier, Vianney; Romero, Erik A.; Molton, Florian; Royal, Guy; Jazzar, Rodolphe; Martin, David; Bertrand, Guy","The serendipitous discovery of a readily available redox-bistable molecule derived from cyclic(alkyl)(amino)carbenes","Organic Chemistry Frontiers","2018","5","13","2073","","10.1039/C8QO00447A","","x-ray","1.54178","CuKα","","0.053","0.039","","","0.0921","0.1006","","","","","","1.038","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554352","21.6194","0.0008","10.6383","0.0004","26.8304","0.001","90","","95.299","0.002","90","","6144.4","0.4","100","","100","","","","","","","","","7","C 1 2/c 1","-C 2yc","15","","","","- C56 H78 B2 F8 Fe N2 O2 -","- C56 H78 B2 F8 Fe N2 O2 -","- C224 H312 B8 F32 Fe4 N8 O8 -","4","0.5","","Mahoney, Janell K.; Regnier, Vianney; Romero, Erik A.; Molton, Florian; Royal, Guy; Jazzar, Rodolphe; Martin, David; Bertrand, Guy","The serendipitous discovery of a readily available redox-bistable molecule derived from cyclic(alkyl)(amino)carbenes","Organic Chemistry Frontiers","2018","5","13","2073","","10.1039/C8QO00447A","","","0.71073","MoKα","","0.068","0.0546","","","0.1126","0.1185","","","","","","1.039","","","","has coordinates,has disorder","237149","2020-10-21","18:00:00",""
"1554353","21.3381","0.0005","10.2919","0.0003","24.6126","0.0006","90","","111.615","0.001","90","","5025.1","0.2","100","","100","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C47 H71 B2 F8 N3 O2 -","- C47 H71 B2 F8 N3 O2 -","- C188 H284 B8 F32 N12 O8 -","4","1","","Mahoney, Janell K.; Regnier, Vianney; Romero, Erik A.; Molton, Florian; Royal, Guy; Jazzar, Rodolphe; Martin, David; Bertrand, Guy","The serendipitous discovery of a readily available redox-bistable molecule derived from cyclic(alkyl)(amino)carbenes","Organic Chemistry Frontiers","2018","5","13","2073","","10.1039/C8QO00447A","","x-ray","1.54178","CuKα","","0.0641","0.0515","","","0.1361","0.1447","","","","","","1.03","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554354","6.4711","0.0006","15.6577","0.0015","9.2786","0.0009","90","","90.334","0.007","90","","940.12","0.16","100","2","100","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C19 H28 O7 -","- C19 H26 O7 -","- C38 H52 O14 -","2","1","","Hu, Zheng-Xi; Xu, Hou-Chao; Hu, Kun; Liu, Miao; Li, Xiao-Nian; Li, Xing-Ren; Du, Xue; Zhang, Yong-Hui; Puno, Pema-Tenzin; Sun, Han-Dong","Structurally diverse diterpenoids from Isodon pharicus","Organic Chemistry Frontiers","2018","5","15","2379","","10.1039/C8QO00477C","","","1.54178","CuKα","","0.1943","0.1909","","","0.4189","0.4274","","","","","","1.932","","","","has coordinates","237151","2020-10-21","18:00:00",""
"1554355","6.6084","0.0001","11.8396","0.0002","22.9114","0.0004","90","","90","","90","","1792.61","0.05","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C20 H32 O5 -","- C20 H32 O5 -","- C80 H128 O20 -","4","1","","Hu, Zheng-Xi; Xu, Hou-Chao; Hu, Kun; Liu, Miao; Li, Xiao-Nian; Li, Xing-Ren; Du, Xue; Zhang, Yong-Hui; Puno, Pema-Tenzin; Sun, Han-Dong","Structurally diverse diterpenoids from Isodon pharicus","Organic Chemistry Frontiers","2018","5","15","2379","","10.1039/C8QO00477C","","","1.54178","CuKα","","0.0305","0.0305","","","0.0772","0.0772","","","","","","1.131","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554356","7.2615","0.0001","11.8328","0.0002","14.2292","0.0003","90","","94.546","0.002","90","","1218.78","0.04","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C14 H11 N S2 -","- C14 H11 N S2 -","- C56 H44 N4 S8 -","4","1","","Tan, Wei; Wang, Cuihong; Jiang, Xuefeng","Green carbon disulfide surrogateviaa combination of potassium sulfide and chloroform for benzothiazine-thione and benzothiazole-thione construction","Organic Chemistry Frontiers","2018","5","15","2390","","10.1039/C8QO00481A","","x-ray","1.54184","CuKα","","0.0363","0.0343","","","0.094","0.0954","","","","","","1.071","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554357","8.3766","0.0002","6.2895","0.0001","25.7206","0.0006","90","","95.618","0.002","90","","1348.57","0.05","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C15 H13 N S2 -","- C15 H13 N S2 -","- C60 H52 N4 S8 -","4","1","","Tan, Wei; Wang, Cuihong; Jiang, Xuefeng","Green carbon disulfide surrogateviaa combination of potassium sulfide and chloroform for benzothiazine-thione and benzothiazole-thione construction","Organic Chemistry Frontiers","2018","5","15","2390","","10.1039/C8QO00481A","","x-ray","1.54184","CuKα","","0.0488","0.042","","","0.1073","0.1121","","","","","","1.043","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554358","12.874","0.0005","4.9","0.0002","13.9299","0.0006","90","","93.36","0.003","90","","877.22","0.06","100","","100","","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C20 H22 O5 -","- C20 H22 O5 -","- C40 H44 O10 -","2","1","","Cheng, Yuyu; Fang, Zhiqiang; Li, Wenjun; Li, Pengfei","Phosphine-mediated enantioselective [4 + 1] annulations between ortho-quinone methides and Morita–Baylis–Hillman carbonates","Organic Chemistry Frontiers","2018","5","18","2728","","10.1039/C8QO00487K","","x-ray","1.54178","CuKα","","0.079","0.0699","","","0.1821","0.1928","","","","","","1.048","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554359","9.6906","0.0009","10.9669","0.0011","11.5436","0.0013","70.045","0.01","86.183","0.008","84.832","0.008","1147.6","0.2","295.1","0.2","295.1","0.2","","","","","","","","5","P -1","-P 1","2","","","","- C21 H31 B2 N O4 -","- C21 H31 B2 N O4 -","- C42 H62 B4 N2 O8 -","2","1","","Gao, Guoliang; Kuang, Zhijie; Song, Qiuling","Functionalized geminal-diborylalkanes from various electron-deficient alkynes and B2pin2","Organic Chemistry Frontiers","2018","5","14","2249","","10.1039/C8QO00513C","","x-ray","0.71073","MoKα","","0.1265","0.0724","","","0.1726","0.2056","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554360","10.0513","0.0014","15.5408","0.0016","19.0622","0.0018","88.904","0.008","83.3","0.01","87.795","0.01","2954.8","0.6","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C30 H42 B2 O5 -","- C30 H42 B2 O5 -","- C120 H168 B8 O20 -","4","2","","Gao, Guoliang; Kuang, Zhijie; Song, Qiuling","Functionalized geminal-diborylalkanes from various electron-deficient alkynes and B2pin2","Organic Chemistry Frontiers","2018","5","14","2249","","10.1039/C8QO00513C","","","0.71073","MoKα","","0.1816","0.0933","","","0.2566","0.3251","","","","","","1.012","","","","has coordinates","274567","2022-04-19","14:22:36",""
"1554361","10.3174","0.0005","12.4692","0.0006","20.4932","0.001","90","","96.89","0.001","90","","2617.4","0.2","153","2","153","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C28 H31 Cl3 N2 Pd -","- C28 H31 Cl3 N2 Pd -","- C112 H124 Cl12 N8 Pd4 -","4","1","","Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan","Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides","Organic Chemistry Frontiers","2018","5","16","2484","","10.1039/C8QO00517F","","","0.71073","MoKα","","0.0291","0.0258","","","0.0618","0.0636","","","","","","1.023","","","","has coordinates","237157","2020-10-21","18:00:00",""
"1554362","10.0241","0.0006","11.2921","0.0007","11.727","0.0007","92.4","0.002","105.358","0.001","106.802","0.001","1215.24","0.13","296","2","296","2","","","","","","","","6","P -1","-P 1","2","","","","- C28 H31 Cl N2 O Pd -","- C28 H31 Cl N2 O Pd -","- C56 H62 Cl2 N4 O2 Pd2 -","2","1","","Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan","Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides","Organic Chemistry Frontiers","2018","5","16","2484","","10.1039/C8QO00517F","","","0.71073","MoKα","","0.0232","0.0216","","","0.057","0.058","","","","","","1.063","","","","has coordinates","237157","2020-10-21","18:00:00",""
"1554363","18.6245","0.0007","13.7023","0.0006","22.6048","0.0011","90","","90","","90","","5768.7","0.4","153","2","153","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C28 H28 Cl F3 N2 Pd -","- C28 H28 Cl F3 N2 Pd -","- C224 H224 Cl8 F24 N16 Pd8 -","8","1","","Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan","Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides","Organic Chemistry Frontiers","2018","5","16","2484","","10.1039/C8QO00517F","","","0.71073","MoKα","","0.0752","0.0525","","","0.1484","0.1683","","","","","","1.052","","","","has coordinates,has disorder","237157","2020-10-21","18:00:00",""
"1554364","18.9753","0.0007","19.6328","0.0008","20.1865","0.0008","90","","90","","90","","7520.2","0.5","153","2","153","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C48 H39 Cl N2 Pd -","- C48 H39 Cl N2 Pd -","- C384 H312 Cl8 N16 Pd8 -","8","1","","Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan","Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides","Organic Chemistry Frontiers","2018","5","16","2484","","10.1039/C8QO00517F","","","0.71073","MoKα","","0.0436","0.0295","","","0.0645","0.0701","","","","","","1.041","","","","has coordinates","237157","2020-10-21","18:00:00",""
"1554365","12.6497","0.0005","9.0221","0.0002","14.1532","0.0005","90","","113.568","0.004","90","","1480.53","0.1","294.46","0.1","294.46","0.1","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C35 H32 Br N3 O3 -","- C35 H32 Br N3 O3 -","- C70 H64 Br2 N6 O6 -","2","1","","Mei, Hongjiang; Lin, Lili; Shen, Bin; Liu, Xiaohua; Feng, Xiaoming","Highly enantioselective desymmetrization of prochiral cyclic α,α-dicyanoalkenes via the direct vinylogous Michael/cyclization domino reaction","Organic Chemistry Frontiers","2018","5","16","2505","","10.1039/C8QO00545A","","x-ray","1.54184","CuKα","","0.0462","0.0455","","","0.1144","0.1157","","","","","","1.072","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554366","18.6922","0.0009","5.447","0.0003","14.5323","0.0007","90","","92.936","0.004","90","","1477.68","0.13","99.9","0.2","99.9","0.2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","2-(methylsulfonyl)-8-phenyl-2,8-dihydroindeno[1,2-c]pyrrole","","- C18 H15 N O2 S -","- C18 H15 N O2 S -","- C72 H60 N4 O8 S4 -","4","1","","Shen, Wen-Bo; Zhou, Bo; Zhang, Zhi-Xin; Yuan, Han; Fang, Wei; Ye, Long-Wu","Gold-catalyzed cascade cyclization of N-propargyl ynamides: rapid access to functionalized indeno[1,2-c]pyrroles","Organic Chemistry Frontiers","2018","5","16","2468","","10.1039/C8QO00552D","","x-ray","1.54184","CuKα","","0.0473","0.0457","","","0.1183","0.1198","","","","","","1.081","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554367","7.5235","0.0007","5.5446","0.0008","10.2976","0.001","90","","99.85","0.01","90","","423.23","0.08","293","2","293","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C10 H9 N O -","- C10 H9 N O -","- C20 H18 N2 O2 -","2","1","","Wu, Qi; Li, Yabo; Wang, Chenyang; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie","1,4-Refunctionalization of β-diketones to γ-keto nitriles via C–C single bond cleavage","Organic Chemistry Frontiers","2018","5","16","2496","","10.1039/C8QO00556G","","x-ray","1.54184","CuKα","","0.0863","0.0682","","","0.1904","0.2218","","","","","","1.054","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554368","7.933","0.0006","11.1848","0.0007","13.1762","0.001","72.919","0.006","73.841","0.006","84.499","0.005","1073.26","0.14","100","2","100.15","","","","","","","","Synthesis","5","P -1","-P 1","2","5,6-Diphenyl-3-(trifluoromethoxy)indazolo[2,3-a]quinoline","5,6-Diphenyl-3-(trifluoromethoxy)indazolo[2,3-a]quinoline","","- C28 H17 F3 N2 O1.01 -","- C28 H17 F3 N2 O -","- C56 H34 F6 N4 O2 -","2","1","","Vivek Kumar, Sundaravel; Ellairaja, Sundaram; Satheesh, Vanaparthi; Sivasamy Vasantha, Vairathevar; Punniyamurthy, Tharmalingam","Rh-Catalyzed regioselective C‒H activation and C‒C bond formation: synthesis and photophysical studies of indazolo[2,3-a]quinolines","Organic Chemistry Frontiers","2018","5","18","2630","","10.1039/C8QO00557E","","x-ray","0.71073","MoKα","","0.1282","0.0827","","","0.1973","0.2309","","","","","","1.051","","","","has coordinates,has disorder","237163","2020-10-21","18:00:00",""
"1554369","10.757","0.009","12.558","0.01","14.389","0.012","90","","99.306","0.01","90","","1918","3","296","2","296.15","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C43 H37 Cl3 N2 O2 -","- C43 H37 Cl3 N2 O2 -","- C86 H74 Cl6 N4 O4 -","2","1","","Lu, Yi-Nan; Ma, Chun; Lan, Jin-Ping; Zhu, Caiqiang; Mao, Yu-Jia; Mei, Guang-Jian; Zhang, Shu; Shi, Feng","Catalytic enantioselective and regioselective substitution of 2,3-indolyldimethanols with enaminones","Organic Chemistry Frontiers","2018","5","18","2657","","10.1039/C8QO00565F","","","0.71073","MoKα","","0.1189","0.0663","","","0.1372","0.1587","","","","","","0.988","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554370","22.7223","0.0019","5.7888","0.0004","25.159","0.002","90","","95.416","0.008","90","","3294.5","0.4","293","2","293.15","","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C20 H18 O4 -","- C20 H18 O4 -","- C160 H144 O32 -","8","1","","Ma, Dengke; Song, Yulong; Fu, Chunling; Zhang, Fang; Guo, Yinlong; Huang, Xin; Ma, Shengming","E-Selective N-heterocyclic carbene-catalyzed reaction of aldehydes and butadienoates: effect of water and chloroform as the proton shuttle","Organic Chemistry Frontiers","2018","5","17","2560","","10.1039/C8QO00579F","","","0.71073","MoKα","","0.0817","0.0554","","","0.1329","0.1558","","","","","","1.045","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554371","10.2719","0.0007","10.4262","0.0007","11.7012","0.0008","69.168","0.002","73.012","0.002","86.849","0.002","1118.45","0.13","153","2","153","2","","","","","","","","6","P -1","-P 1","2","","","","- C25 H22 Cl N O3 S -","- C25 H22 Cl N O3 S -","- C50 H44 Cl2 N2 O6 S2 -","2","1","","Wang, Hepan; Wang, Bingbing; Sun, Song; Cheng, Jiang","Copper-catalyzed radical Heck type cyclization: a three-component reaction of DABCO·(SO2)2, aryldiazonium tetrafluoroborates and dienes toward sulfonated benzo- seven-membered nitrogen heterocycles","Organic Chemistry Frontiers","2018","5","17","2547","","10.1039/C8QO00615F","","","0.71073","MoKα","","0.0482","0.0415","","","0.1106","0.1153","","","","","","1.021","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554372","9.5372","0.0007","10.0615","0.0008","11.5029","0.0009","74.116","0.002","83.655","0.002","71.87","0.002","1008.56","0.14","120","2","120","2","","","","","","","","6","P -1","-P 1","2","","","","- C21 H19 Cl F N O6 -","- C21 H19 Cl F N O6 -","- C42 H38 Cl2 F2 N2 O12 -","2","1","","Motornov, Vladimir A.; Tabolin, Andrey A.; Novikov, Roman A.; Nelyubina, Yulia V.; Nenajdenko, Valentine G.; Ioffe, Sema L.","Fluoronitroalkenes in tandem [4 + 1]/[3 + 2]-cycloaddition: one-pot three-component assembly of fluorinated bicyclic nitroso acetals","Organic Chemistry Frontiers","2018","5","17","2588","","10.1039/C8QO00623G","","","0.71073","MoKα","","0.0519","0.0403","","","0.0957","0.1035","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554373","16.4649","0.0014","6.9417","0.0006","15.0372","0.0013","90","","93.483","0.002","90","","1715.5","0.3","120","2","120","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C16 H14 Cl F N2 O6 -","- C16 H14 Cl F N2 O6 -","- C64 H56 Cl4 F4 N8 O24 -","4","1","","Motornov, Vladimir A.; Tabolin, Andrey A.; Novikov, Roman A.; Nelyubina, Yulia V.; Nenajdenko, Valentine G.; Ioffe, Sema L.","Fluoronitroalkenes in tandem [4 + 1]/[3 + 2]-cycloaddition: one-pot three-component assembly of fluorinated bicyclic nitroso acetals","Organic Chemistry Frontiers","2018","5","17","2588","","10.1039/C8QO00623G","","","0.71073","MoKα","","0.0624","0.0423","","","0.1111","0.1236","","","","","","1.036","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554374","6.812","0.005","11.371","0.008","13.441","0.009","80.287","0.013","84.84","0.013","77.986","0.012","1002.1","1.2","130","","130","","","","","","","","","5","P -1","-P 1","2","","","","- C23 H31 N O2 S -","- C23 H31 N O2 S -","- C46 H62 N2 O4 S2 -","2","1","","Han, Yulin; Ma, Shengming","Rhodium-catalyzed highly diastereoselective intramolecular [4 + 2] cycloaddition of 1,3-disubstituted allene-1,3-dienes","Organic Chemistry Frontiers","2018","5","18","2680","","10.1039/C8QO00650D","","","0.71073","MoKα","","0.0764","0.055","","","0.1307","0.1388","","","","","","1.071","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554375","10.6868","0.0014","20.2","0.003","8.0112","0.001","90","","101.747","0.003","90","","1693.2","0.4","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C18 H23 N O2 S -","- C18 H23 N O2 S -","- C72 H92 N4 O8 S4 -","4","1","","Han, Yulin; Ma, Shengming","Rhodium-catalyzed highly diastereoselective intramolecular [4 + 2] cycloaddition of 1,3-disubstituted allene-1,3-dienes","Organic Chemistry Frontiers","2018","5","18","2680","","10.1039/C8QO00650D","","","0.71073","MoKα","","0.0611","0.0486","","","0.1232","0.1316","","","","","","1.029","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554376","8.9632","0.001","26.894","0.003","9.2793","0.001","90","","110.151","0.002","90","","2099.9","0.4","130","","130","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C24 H30 O4 -","- C24 H30 O4 -","- C96 H120 O16 -","4","1","","Han, Yulin; Ma, Shengming","Rhodium-catalyzed highly diastereoselective intramolecular [4 + 2] cycloaddition of 1,3-disubstituted allene-1,3-dienes","Organic Chemistry Frontiers","2018","5","18","2680","","10.1039/C8QO00650D","","","0.71073","MoKα","","0.0781","0.0453","","","0.106","0.1227","","","","","","1.013","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554377","11.0672","0.0002","24.0508","0.0005","11.3892","0.0002","90","","91.3083","0.0019","90","","3030.73","0.1","296.31","0.1","296.31","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C36 H34 N O6 -","- C36 H34 N O6 -","- C144 H136 N4 O24 -","4","2","","Yue, Jing-Fei; Ran, Guang-Yao; Yang, Xing-Xing; Du, Wei; Chen, Ying-Chun","Asymmetric Diels–Alder cycloadditions of benzofulvene-based 2,4-dienals via trienamine activation","Organic Chemistry Frontiers","2018","5","18","2676","","10.1039/C8QO00653A","","x-ray","1.54184","CuKα","","0.0565","0.0538","","","0.14","0.145","","","","","","1.02","","","","has coordinates","274567","2022-04-19","14:22:36",""
"1554378","10.2146","0.0004","11.7243","0.0005","10.2644","0.0004","90","","119.315","0.002","90","","1071.84","0.08","170","2","170","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C24 H26 N2 O3 -","- C24 H26 N2 O3 -","- C48 H52 N4 O6 -","2","1","","Zhang, Zi-Jing; Song, Jin","An isothiourea-catalyzed asymmetric formal [4 + 2] cycloaddition of in situ generated azoalkenes with C1 ammonium enolates","Organic Chemistry Frontiers","2018","5","17","2578","","10.1039/C8QO00657A","","","1.34139","GaKα","","0.0428","0.0399","","","0.0983","0.101","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554379","10.276","0.0012","12.5669","0.0014","13.0463","0.0013","66.455","0.01","73.203","0.009","66.317","0.011","1397.8","0.3","268","40","268","40","","","","","","","","5","P -1","-P 1","2","","6o","","- C32 H27 N O5 S -","- C32 H27 N O5 S -","- C64 H54 N2 O10 S2 -","2","1","","Zhang, Changyuan; Chen, Lianfen; Chen, Kai; Wang, Chuntao; Xu, Zurong; Jiang, Huanfeng; Zhu, Shifa","Cu(i)-Catalyzed stereoselective synthesis of trisubstituted Z-enol esters via interrupting the 1,3-O-transposition reaction","Organic Chemistry Frontiers","2018","5","16","2510","","10.1039/C8QO00664D","","x-ray","0.71073","MoKα","","0.1099","0.0613","","","0.1333","0.1707","","","","","","1.064","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554380","8.611","0.0012","11.3415","0.0015","28.819","0.004","90","","90","","90","","2814.5","0.7","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C29 H28 Cl N3 O7 -","- C29 H28 Cl N3 O7 -","- C116 H112 Cl4 N12 O28 -","4","1","","Wei, Qinghua; Ma, Xiaochu; Chen, Jianghui; Niu, Li; Yang, Xi; Xia, Fei; Liu, Shunying","A triple-functionalised metal centre-catalyzed enantioselective multicomponent reaction","Organic Chemistry Frontiers","2018","5","19","2799","","10.1039/C8QO00703A","","","0.71073","MoKα","","0.1382","0.0564","","","0.1135","0.1486","","","","","","1.002","","","","has coordinates","237178","2020-10-21","18:00:00",""
"1554381","8.4477","0.0015","11.883","0.002","15.889","0.003","97.79","0.004","90.12","0.004","96.968","0.004","1568.3","0.5","298","2","298","2","","","","","","","","6","P -1","-P 1","2","","","","- C29 H43 I Mg N2 O -","- C29 H43 I Mg N2 O -","- C58 H86 I2 Mg2 N4 O2 -","2","1","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.0749","0.0511","","","0.1217","0.1345","","","","","","1.02","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554382","12.5799","0.0011","19.2069","0.0016","20.3357","0.0017","90","","102.473","0.002","90","","4797.6","0.7","140","2","140","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C50 H66 Mg2 N4 -","- C50 H66 Mg2 N4 -","- C200 H264 Mg8 N16 -","4","1","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.0853","0.0641","","","0.181","0.1988","","","","","","1.024","","","","has coordinates","300101","2025-06-17","17:58:10",""
"1554383","21.9804","0.0013","19.3508","0.0011","11.283","0.0007","90","","90","","90","","4799.1","0.5","140","2","140","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C50 H66 Mg2 N4 -","- C50 H66 Mg2 N4 -","- C200 H264 Mg8 N16 -","4","1","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.1069","0.0662","","","0.0993","0.1125","","","","","","1.157","","","","has coordinates","300101","2025-06-17","17:58:11",""
"1554384","11.0139","0.0012","11.3202","0.0012","18.565","0.002","75.316","0.003","83.401","0.003","62.905","0.003","1993.3","0.4","140","2","140","2","","","","","","","","4","P -1","-P 1","2","","","","- C46 H58 Mg N4 -","- C46 H58 Mg N4 -","- C92 H116 Mg2 N8 -","2","1","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.1505","0.0747","","","0.1632","0.1991","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554385","11.4271","0.0014","17.954","0.002","20.908","0.003","90","","93.495","0.003","90","","4281.6","0.9","130","2","130","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C54 H53 Mg N2 -","- C54 H53 Mg N2 -","- C216 H212 Mg4 N8 -","4","1","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.0857","0.0559","","","0.1467","0.1664","","","","","","1.023","","","","has coordinates","237180","2020-10-21","18:00:00",""
"1554386","21.607","0.002","13.2782","0.0012","14.0261","0.0013","90","","90","","90","","4024.1","0.6","130","2","130","2","","","","","","","","4","P c c n","-P 2ab 2ac","56","","","","- C48 H49 Cl2 N2 -","- C48 H49 Cl2 N2 -","- C192 H196 Cl8 N8 -","4","0.5","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.0855","0.0641","","","0.1752","0.1939","","","","","","1.033","","","","has coordinates","237180","2020-10-21","18:00:00",""
"1554387","25.689","0.003","11.0511","0.0014","32.698","0.004","90","","105.996","0.003","90","","8923.3","1.9","298","2","298","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C51 H55 I Mg N2 O -","- C51 H55 I Mg N2 O -","- C408 H440 I8 Mg8 N16 O8 -","8","1","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.0857","0.0517","","","0.1234","0.1396","","","","","","1.015","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554388","11.9804","0.0006","15.2444","0.0007","15.0882","0.0007","90","","95.298","0.001","90","","2743.8","0.2","135","2","135","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C58 H76 Cl2 Mg2 N4 -","- C58 H76 Cl2 Mg2 N4 -","- C116 H152 Cl4 Mg4 N8 -","2","0.5","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.0573","0.0406","","","0.0939","0.1047","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554389","13.2295","0.0008","13.2295","0.0008","19.2267","0.0013","90","","90","","90","","3365.1","0.4","140","2","140","2","","","","","","","","6","P -4","P -4","81","","","","- C68 H96 B2 Mg2 N4 O6 -","- C68 H96 B2 Mg2 N4 O6 -","- C136 H192 B4 Mg4 N8 O12 -","2","0.5","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.1547","0.0647","","","0.1293","0.1641","","","","","","0.886","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554390","10.58","0.0007","10.4047","0.0007","10.785","0.0007","90","","118.687","0.002","90","","1041.5","0.12","140","2","140","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C18 H36 B2 O6 -","- C18 H36 B2 O6 -","- C36 H72 B4 O12 -","2","0.5","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.0877","0.0677","","","0.1435","0.1529","","","","","","1.103","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554391","17.7085","0.0009","33.2898","0.0016","17.0054","0.0009","90","","90","","90","","10024.9","0.9","135","2","135","2","","","","","","","","4","P c c n","-P 2ab 2ac","56","","","","- C52 H70 Mg2 N4 -","- C52 H70 Mg2 N4 -","- C416 H560 Mg16 N32 -","8","1","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.1431","0.1024","","","0.1999","0.2137","","","","","","1.236","","","","has coordinates","300101","2025-06-17","17:58:11",""
"1554392","8.5511","0.0003","10.4286","0.0003","14.3935","0.0004","88.875","0.002","87.601","0.002","68.209","0.003","1190.78","0.07","291","2","291","2","","","","","","","","5","P -1","-P 1","2","","","","- C30 H21 Cl N2 O2 -","- C30 H21 Cl N2 O2 -","- C60 H42 Cl2 N4 O4 -","2","1","","Xu, Hui; Chen, Kuan; Liu, Hong-Wei; Wang, Guan-Wu","Solvent-free N-iodosuccinimide-promoted synthesis of spiroimidazolines from alkenes and amidines under ball-milling conditions","Organic Chemistry Frontiers","2018","5","19","2864","","10.1039/C8QO00723C","","","1.54184","CuKα","","0.0501","0.0464","","","0.127","0.1306","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554393","8.1716","0.0004","30.1115","0.0013","10.9853","0.0005","90","","95.159","0.002","90","","2692.1","0.2","100","","100","","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C22 H24 Cl3 F6 N4 P Ru -","- C22 H24 Cl3 F6 N4 P Ru -","- C88 H96 Cl12 F24 N16 P4 Ru4 -","4","1","","Wu, Qiang; Pan, Le; Du, Guangming; Zhang, Chi; Wang, Dawei","Preparation of pyridyltriazole ruthenium complexes as effective catalysts for the selective alkylation and one-pot C‒H hydroxylation of 2-oxindole with alcohols and mechanism exploration","Organic Chemistry Frontiers","2018","5","18","2668","","10.1039/C8QO00725J","","","0.71075","MoKα","","0.049","0.0457","","","0.0973","0.0986","","","","","","1.266","","","","has coordinates,has disorder","237185","2020-10-21","18:00:00",""
"1554394","8.3324","0.0007","18.0049","0.0015","18.9382","0.0019","90","","90","","90","","2841.2","0.4","296.32","0.1","296.32","0.1","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C17 H13 F2 N O2 -","- C17 H13 F2 N O2 -","- C136 H104 F16 N8 O16 -","8","1","","Ma, Xingxing; Deng, Shuilin; Song, Qiuling","Halodifluoroacetates as formylation reagents for various amines via unprecedented quadruple cleavage","Organic Chemistry Frontiers","2018","5","24","3505","","10.1039/C8QO00727F","","x-ray","0.71073","MoKα","","0.0657","0.0445","","","0.1082","0.1237","","","","","","1.0611","","","","has coordinates","237187","2020-10-21","18:00:00",""
"1554395","6.32","0.002","11.047","0.004","16.999","0.006","90.548","0.009","95.825","0.009","90.542","0.009","1180.6","0.7","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C14 H17 N O -","- C14 H17 N O -","- C56 H68 N4 O4 -","4","2","","Liu, Yang; Cerveri, Alessandro; De Nisi, Assunta; Monari, Magda; Nieto Faza, Olalla; Lopez, Carlos Silva; Bandini, Marco","Nickel catalyzed regio- and stereoselective arylation and methylation of allenamides via coupling reactions. An experimental and computational study","Organic Chemistry Frontiers","2018","5","22","3231","","10.1039/C8QO00729B","","","0.71073","MoKα","","0.1543","0.0971","","","0.2356","0.268","","","","","","1.137","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554396","6.9966","0.001","12.0579","0.0017","12.9998","0.0018","63.724","0.003","88.61","0.003","86.344","0.003","981.4","0.2","296","2","296","2","","","","","","","","6","P -1","-P 1","2","","","","- C12 H26 Cl2 N2 Ni O7 -","- C12 H26 Cl2 N2 Ni O7 -","- C24 H52 Cl4 N4 Ni2 O14 -","2","1","","Liu, Yang; Cerveri, Alessandro; De Nisi, Assunta; Monari, Magda; Nieto Faza, Olalla; Lopez, Carlos Silva; Bandini, Marco","Nickel catalyzed regio- and stereoselective arylation and methylation of allenamides via coupling reactions. An experimental and computational study","Organic Chemistry Frontiers","2018","5","22","3231","","10.1039/C8QO00729B","","","0.71073","MoKα","","0.0746","0.0594","","","0.1628","0.1738","","","","","","1.029","","","","has coordinates","237189","2020-10-21","18:00:00",""
"1554397","10.9821","0.0005","9.771","0.0003","21.137","0.0009","90","","119.629","0.003","90","","1971.56","0.15","295","2","295","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","7,8,9,11,12-pentamethoxy-1,2,5,13b-tetrahydrodibenzo[c,e]pyrrolo[1,2-a]azepin-3-one","","- C22 H25 N O6 -","- C22 H25 N O6 -","- C88 H100 N4 O24 -","4","1","","Boichenko, Maksim A.; Ivanova, Olga A.; Andreev, Ivan A.; Chagarovskiy, Alexey O.; Levina, Irina I.; Rybakov, Victor B.; Skvortsov, Dmitriy A.; Trushkov, Igor V.","Convenient approach to polyoxygenated dibenzo[c,e]pyrrolo[1,2-a]azepines from donor–acceptor cyclopropanes","Organic Chemistry Frontiers","2018","5","19","2829","","10.1039/C8QO00742J","","","1.5418","CuKα","","0.0595","0.0486","","","0.1264","0.1338","","","","","","1.004","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554398","7.0556","0.0003","15.3824","0.0005","10.7866","0.0005","90","","108.471","0.003","90","","1110.38","0.08","295","2","295","2","","","","","","","","4","P 1 c 1","P -2yc","7","","1-(3,4,5-trimethoxybenzyl)-5-(3,4,5-trimethoxyphenyl)pyrrolidin-2-one","","- C23 H29 N O7 -","- C23 H29 N O7 -","- C46 H58 N2 O14 -","2","1","","Boichenko, Maksim A.; Ivanova, Olga A.; Andreev, Ivan A.; Chagarovskiy, Alexey O.; Levina, Irina I.; Rybakov, Victor B.; Skvortsov, Dmitriy A.; Trushkov, Igor V.","Convenient approach to polyoxygenated dibenzo[c,e]pyrrolo[1,2-a]azepines from donor–acceptor cyclopropanes","Organic Chemistry Frontiers","2018","5","19","2829","","10.1039/C8QO00742J","","","1.54186","CuKα","","0.0433","0.0421","","","0.1117","0.1128","","","","","","1.043","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554399","15.7969","0.0003","8.7827","0.0002","14.6012","0.0004","90","","103.801","0.002","90","","1967.28","0.08","295","2","295","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","7,8,10,11,12-Pentamethoxy-1,2,5,13b-tetrahydrodibenzo[c,e]pyrrolo[1,2-a]azepin-3-one","","- C22 H25 N O6 -","- C22 H25 N O6 -","- C88 H100 N4 O24 -","4","1","","Boichenko, Maksim A.; Ivanova, Olga A.; Andreev, Ivan A.; Chagarovskiy, Alexey O.; Levina, Irina I.; Rybakov, Victor B.; Skvortsov, Dmitriy A.; Trushkov, Igor V.","Convenient approach to polyoxygenated dibenzo[c,e]pyrrolo[1,2-a]azepines from donor–acceptor cyclopropanes","Organic Chemistry Frontiers","2018","5","19","2829","","10.1039/C8QO00742J","","","1.5418","CuKα","","0.0475","0.0414","","","0.1116","0.1156","","","","","","1.061","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554400","9.516","0.003","11.551","0.006","13.616","0.007","91.24","0.04","106.05","0.04","99.94","0.03","1412.9","1.2","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","5,6-dioxophenanthriporphyrin","","- C43 H26 N2 O2 -","- C43 H26 N2 O2 -","- C86 H52 N4 O4 -","2","1","","Kupietz, Kamil; Białek, Michał J.; Białońska, Agata; Szyszko, Bartosz; Latos-Grażyński, Lechosław","Aromaticity control via modifications of a macrocyclic frame: 5,6-dimethoxyphenanthriporphyrin and 5,6-dioxophenanthriporphyrin","Organic Chemistry Frontiers","2018","5","21","3068","","10.1039/C8QO00751A","","","1.54184","CuKα","","0.3027","0.1221","","","0.2214","0.3452","","","","","","0.895","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554401","14.154","0.003","17.553","0.003","19.832","0.003","90","","106.78","0.03","90","","4717.4","1.6","100","2","100","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","monocation of 5,6-dioxophenanthriporphyrin","","- C61 H45 B F4 N2 O2 -","- C61 H45 B F4 N2 O2 -","- C244 H180 B4 F16 N8 O8 -","4","1","","Kupietz, Kamil; Białek, Michał J.; Białońska, Agata; Szyszko, Bartosz; Latos-Grażyński, Lechosław","Aromaticity control via modifications of a macrocyclic frame: 5,6-dimethoxyphenanthriporphyrin and 5,6-dioxophenanthriporphyrin","Organic Chemistry Frontiers","2018","5","21","3068","","10.1039/C8QO00751A","","","1.54175","CuKα","","0.0708","0.0564","","","0.1492","0.16","","","","","","0.947","","","","has coordinates","237194","2020-10-21","18:00:00",""
"1554402","8.09","0.002","12.074","0.003","24.254","0.003","82.58","0.02","89.11","0.02","70.85","0.03","2218.3","0.9","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C86 H54 B8 F22 N4 O7 -","- C86 H54 B8 F22 N4 O7 -","- C86 H54 B8 F22 N4 O7 -","1","0.5","","Kupietz, Kamil; Białek, Michał J.; Białońska, Agata; Szyszko, Bartosz; Latos-Grażyński, Lechosław","Aromaticity control via modifications of a macrocyclic frame: 5,6-dimethoxyphenanthriporphyrin and 5,6-dioxophenanthriporphyrin","Organic Chemistry Frontiers","2018","5","21","3068","","10.1039/C8QO00751A","","","1.54175","CuKα","","0.2001","0.081","","","0.1883","0.2196","","","","","","0.664","","","","has coordinates,has disorder","237194","2020-10-21","18:00:00",""
"1554403","5.5091","0.0007","7.2665","0.0008","16.992","0.002","80.823","0.005","83.934","0.004","78.863","0.004","656.9","0.14","99","2","99","2","","","","","","","","5","P -1","-P 1","2","","","","- C14 H18 N2 O S -","- C14 H18 N2 O S -","- C28 H36 N4 O2 S2 -","2","1","","Dutta, Soumya; Mondal, Manas; Ghosh, Tubai; Saha, Amit","Unprecedented thiocarbamidation of nitroarenes: a facile one-pot route to unsymmetrical thioureas","Organic Chemistry Frontiers","2019","6","1","70","","10.1039/C8QO00752G","","","0.71073","MoKα","","0.1205","0.1014","","","0.2704","0.2926","","","","","","1.091","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554404","12.2892","0.0006","11.6999","0.0005","19.3795","0.0009","90","","103.521","0.005","90","","2709.2","0.2","293","2","293","2","","","","","","","","4","P 1 21 1","P 2yb","4","","zwm-132","","- C29 H37 N O7 -","- C29 H37 N O7 -","- C116 H148 N4 O28 -","4","2","","Fan, Yaqin; Wang, Yi; Fu, Peng; Chairoungdua, Arthit; Piyachaturawat, Pawinee; Zhu, Weiming","Secopaxilline A, an indole-diterpenoid derivative from an aciduric Penicillium fungus, its identification and semisynthesis","Organic Chemistry Frontiers","2018","5","19","2835","","10.1039/C8QO00756J","","","1.54178","CuKα","","0.0676","0.0491","","","0.1065","0.1205","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554405","9.5523","0.0004","9.8572","0.0003","23.9209","0.0009","90","","99.141","0.004","90","","2223.76","0.14","296.83","0.1","296.83","0.1","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C28 H24 O5 -","- C28 H24 O5 -","- C112 H96 O20 -","4","1","","Zhao, Yinsong; Zheng, Qinze; Yu, Chuangui; Liu, Zheng; Wang, Deping; You, Jingsong; Gao, Ge","Rh(iii)-Catalyzed regioselective C–H [4 + 2] C-annulation of vinyl enaminones with alkynes to form polysubstituted salicylaldehydes","Organic Chemistry Frontiers","2018","5","19","2875","","10.1039/C8QO00759D","","x-ray","1.54184","CuKα","","0.0773","0.0673","","","0.2147","0.2311","","","","","","1.124","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554406","13.248","0.002","7.6262","0.0012","27.213","0.004","90","","97.298","0.003","90","","2727.1","0.7","296.15","","296.15","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C30 H31 Br N2 O3 -","- C30 H31 Br N2 O3 -","- C120 H124 Br4 N8 O12 -","4","2","","Yuan, Yang; Zheng, Zhan-Jiang; Ye, Fei; Ma, Jun-Han; Xu, Zheng; Bai, Xing-Feng; Li, Li; Xu, Li-Wen","Highly efficient desymmetrization of cyclopropenes to azabicyclo[3.1.0]hexanes with five continuous stereogenic centers by copper-catalyzed [3 + 2] cycloadditions","Organic Chemistry Frontiers","2018","5","18","2759","","10.1039/C8QO00761F","","","0.71073","MoKα","","0.1405","0.0694","","","0.179","0.2167","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554407","7.3005","0.0004","12.1224","0.0005","11.9121","0.0006","90","","105.259","0.006","90","","1017.05","0.09","293","2","293","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C23 H28 O6 -","- C23 H28 O6 -","- C46 H56 O12 -","2","1","","Zhang, Xun; Li, Zhongle; Yong, Huaya; Xie, Zhixiang","Biomimetic syntheses of C23 terpenoids: structural revision of salyunnanin A and confirmation of hassanane","Organic Chemistry Frontiers","2018","5","23","3469","","10.1039/C8QO00772A","","","1.54184","CuKα","","0.0514","0.0506","","","0.1379","0.1395","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554408","7.5983","0.0003","16.424","0.0007","20.8458","0.0008","90","","90","","90","","2601.44","0.18","223","2","223","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","Methyl 5-(5-bromo-2-hydroxybenzoyl) nicotinate","","- C14 H10 Br N O4 -","- C14 H10 Br N O4 -","- C112 H80 Br8 N8 O32 -","8","1","","Maezono, Shizuka Mei Bautista; Kim, Sung Hong; Lee, Yong Rok","Copper-catalyzed [3 + 2 + 1] annulation for functionalized pyridines as potent and dynamic UV absorbers","Organic Chemistry Frontiers","2018","5","23","3368","","10.1039/C8QO00782A","","","0.71073","MoKα","","0.0345","0.0252","","","0.0607","0.0658","","","","","","1.055","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554409","9.0575","0.0017","12.288","0.002","12.993","0.003","90","","94.793","0.002","90","","1441","0.5","293","2","293","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C18 H18 O2 -","- C18 H18 O2 -","- C72 H72 O8 -","4","1","","Yang, Binmiao; Zhai, Xuejie; Feng, Shubo; Shao, Zhihui","Dearomatization of naphthols using oxy-allyl cations: efficient construction of α-all-carbon quaternary center-containing 2-(2-oxocycloalkyl)cycloalkyl diketones","Organic Chemistry Frontiers","2018","5","19","2794","","10.1039/C8QO00783G","","","0.71073","MoKα","","0.0735","0.0518","","","0.1412","0.155","","","","","","1.095","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554410","17.135","0.003","17.343","0.003","20.802","0.003","106.696","0.004","98.131","0.004","118.106","0.003","4934.7","1.4","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C44 H42 Cl N5 O8 -","- C44 H42 Cl N5 O8 -","- C176 H168 Cl4 N20 O32 -","4","2","","Yang, Wen-Juan; Sun, Qiu; Sun, Jing; Yan, Chao-Guo","Domino aza/oxa-hetero-Diels–Alder reaction for construction of novel spiro[pyrido[3′,2′:5,6]pyrano[2,3-d]pyrimidine-7,5′-pyrimidine]","Organic Chemistry Frontiers","2018","5","18","2754","","10.1039/C8QO00784E","","","0.71073","MoKα","","0.1882","0.0908","","","0.2191","0.2653","","","","","","1.017","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554411","12.086","0.003","12.455","0.003","17.13","0.004","96.558","0.009","109.996","0.008","107.812","0.009","2236.9","1","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C42 H38 Cl N5 O6 -","- C42 H38 Cl N5 O6 -","- C84 H76 Cl2 N10 O12 -","2","1","","Yang, Wen-Juan; Sun, Qiu; Sun, Jing; Yan, Chao-Guo","Domino aza/oxa-hetero-Diels–Alder reaction for construction of novel spiro[pyrido[3′,2′:5,6]pyrano[2,3-d]pyrimidine-7,5′-pyrimidine]","Organic Chemistry Frontiers","2018","5","18","2754","","10.1039/C8QO00784E","","","0.71073","MoKα","","0.2438","0.1197","","","0.2511","0.3034","","","","","","1.01","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554412","9.7638","0.0005","10.0633","0.0005","10.6246","0.0005","100.341","0.004","103.17","0.004","95.285","0.004","990.28","0.09","122.98","0.13","122.98","0.13","","","","","","","","2","P -1","-P 1","2","tetraarylethene","tetraarylethene","","- C28 H22 -","- C28 H22 -","- C56 H44 -","2","1","","Chuskit, Deachen; Chaudhary, Renu; Venugopalan, Paloth; König, Burkhard; Natarajan, Palani","Oxidative homodimerization of substituted olefins by DDQ visible light photocatalysis","Organic Chemistry Frontiers","2018","5","24","3553","","10.1039/C8QO00792F","","x-ray","1.54184","CuKα","","0.0434","0.0358","","","0.0881","0.0934","","","","","","1.036","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554413","10","0.002","14.827","0.003","13.344","0.003","90","","101.939","0.003","90","","1935.7","0.7","173","2","173","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C18 H25 N O7 S -","- C18 H25 N O7 S -","- C72 H100 N4 O28 S4 -","4","1","","Lei, Meng; Li, Yanjun; Cao, Shi; Hou, Xinyi; Gong, Lei","Alkylation–peroxidation of α-carbonyl imines or ketones catalyzed by a copper salt via radical-mediated Csp3–H functionalization","Organic Chemistry Frontiers","2018","5","21","3083","","10.1039/C8QO00797G","","","0.71073","MoKα","","0.0888","0.0813","","","0.2211","0.2292","","","","","","1.011","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554414","12.1127","0.001","13.1333","0.0012","13.1505","0.0011","76.939","0.007","79.228","0.007","63.194","0.009","1810.2","0.3","173","","173","","","","","","","","","5","P -1","-P 1","2","","7-endo","","- C19 H24 F3 N O2 -","- C19 H24 F3 N O2 -","- C76 H96 F12 N4 O8 -","4","2","","Long, Hao; Song, Jinshuai; Xu, Hai-Chao","Electrochemical synthesis of 7-membered carbocycles through cascade 5-exo-trig/7-endo-trig radical cyclization","Organic Chemistry Frontiers","2018","5","21","3129","","10.1039/C8QO00803E","","x-ray","1.54184","CuKα","","0.0851","0.0762","","","0.2009","0.2149","","","","","","1.035","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554415","8.6306","0.0004","10.9636","0.0006","14.5139","0.0007","90","","90.644","0.002","90","","1373.25","0.12","100","2","100","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C30 H29 N3 O4 S -","- C30 H29 N3 O4 S -","- C60 H58 N6 O8 S2 -","2","1","","Huang, Qiuhong; Cheng, Yuyu; Yuan, Huijun; Chang, Xiaoyong; Li, Pengfei; Li, Wenjun","Organocatalytic enantioselective Mannich-type addition of 5H-thiazol-4-ones to isatin-derived imines: access to 3-substituted 3-amino-2-oxindoles featured by vicinal sulfur-containing tetrasubstituted stereocenters","Organic Chemistry Frontiers","2018","5","22","3226","","10.1039/C8QO00814K","","x-ray","0.71073","MoKα","","0.0375","0.0331","","","0.0767","0.0786","","","","","","1.049","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554416","18.2546","0.0006","9.1982","0.0003","13.3199","0.0004","90","","108.231","0.001","90","","2124.27","0.12","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H22 N4 O4 -","- C24 H22 N4 O4 -","- C96 H88 N16 O16 -","4","1","","Qiu, Shaobing; Guo, Chunlei; Wang, Mingkang; Sun, Zhenglong; Li, Hui; Qian, Xuhong; Yang, Youjun","Mild dealkylative N-nitrosation of N,N-dialkylaniline derivatives for convenient preparation of photo-triggered and photo-calibrated NO donors","Organic Chemistry Frontiers","2018","5","22","3206","","10.1039/C8QO00818C","","","0.71073","MoKα","","0.0736","0.0494","","","0.1184","0.1352","","","","","","1.038","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554417","11.2278","0.0005","13.7389","0.0006","7.4364","0.0003","90","","107.173","0.001","90","","1095.98","0.08","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C12 H12 N2 O3 -","- C12 H12 N2 O3 -","- C48 H48 N8 O12 -","4","1","","Qiu, Shaobing; Guo, Chunlei; Wang, Mingkang; Sun, Zhenglong; Li, Hui; Qian, Xuhong; Yang, Youjun","Mild dealkylative N-nitrosation of N,N-dialkylaniline derivatives for convenient preparation of photo-triggered and photo-calibrated NO donors","Organic Chemistry Frontiers","2018","5","22","3206","","10.1039/C8QO00818C","","","0.71073","MoKα","","0.05","0.0387","","","0.0914","0.0998","","","","","","1.042","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554418","13.145","0.0005","14.0218","0.0006","12.9264","0.0005","90","","114.416","0.001","90","","2169.47","0.15","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H20 N4 O5 -","- C24 H20 N4 O5 -","- C96 H80 N16 O20 -","4","1","","Qiu, Shaobing; Guo, Chunlei; Wang, Mingkang; Sun, Zhenglong; Li, Hui; Qian, Xuhong; Yang, Youjun","Mild dealkylative N-nitrosation of N,N-dialkylaniline derivatives for convenient preparation of photo-triggered and photo-calibrated NO donors","Organic Chemistry Frontiers","2018","5","22","3206","","10.1039/C8QO00818C","","","0.71073","MoKα","","0.0592","0.0411","","","0.0889","0.1004","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554419","15.853","0.003","12.375","0.002","7.3639","0.0012","90","","90","","90","","1444.7","0.4","296","2","296","2","","","","","","","","2","P n a 21","P 2c -2n","33","","","","- C20 H18 -","- C20 H18 -","- C80 H72 -","4","1","","Muthuramalingam, Somasundaram; Garg, Jai Anand; Karthick, R.; Fox, Thomas; Blacque, Olivier; Venkatesan, Koushik; Ramanathan, Saiganesh; Kabilan, Senthamaraikannan; Balasubramanian, K. K.","Nickel catalyzed synthesis of 4,4′-bichromenes/4,4′-bithiochromenes and their Atropisomerism","Organic Chemistry Frontiers","2019","6","1","134","","10.1039/C8QO00820E","","","0.71073","MoKα","","0.0757","0.0456","","","0.0892","0.1032","","","","","","1.011","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554420","8.0844","0.0004","19.8817","0.001","10.2123","0.0005","90","","109.061","0.002","90","","1551.44","0.13","298","2","298","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C20 H14 O4 -","- C20 H14 O4 -","- C80 H56 O16 -","4","1","","Muthuramalingam, Somasundaram; Garg, Jai Anand; Karthick, R.; Fox, Thomas; Blacque, Olivier; Venkatesan, Koushik; Ramanathan, Saiganesh; Kabilan, Senthamaraikannan; Balasubramanian, K. K.","Nickel catalyzed synthesis of 4,4′-bichromenes/4,4′-bithiochromenes and their Atropisomerism","Organic Chemistry Frontiers","2019","6","1","134","","10.1039/C8QO00820E","","","0.71073","MoKα","","0.0722","0.0486","","","0.1072","0.1218","","","","","","0.988","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554421","5.628","0.002","19.385","0.004","17.569","0.004","90","0.03","91.36","0.03","90","0.03","1916.2","0.9","173","2","173","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C24 H19 Cl N2 O -","- C24 H19 Cl N2 O -","- C96 H76 Cl4 N8 O4 -","4","1","","Tong, Mengchao; Zhang, Yong; Qin, Cong; Fu, Yiwei; Liu, Yonghai; Li, Hao; Wang, Wei","Alkenylazaarenes as dipolarophiles in 1,3-dipolar cycloaddition of nitrones: regioselectivity-switchable and highly diastereoselective synthesis of multisubstituted isoxazolidines","Organic Chemistry Frontiers","2018","5","20","2945","","10.1039/C8QO00826D","","","1.54178","CuKα","","0.0357","0.03","","","0.0779","0.0819","","","","","","1.015","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554422","5.7976","0.0009","9.4263","0.0014","17.097","0.003","87.715","0.003","87.737","0.003","86.465","0.003","931.2","0.3","130","","130","","","","","","","","","5","P -1","-P 1","2","","","","- C24 H19 Cl N2 O -","- C24 H19 Cl N2 O -","- C48 H38 Cl2 N4 O2 -","2","1","","Tong, Mengchao; Zhang, Yong; Qin, Cong; Fu, Yiwei; Liu, Yonghai; Li, Hao; Wang, Wei","Alkenylazaarenes as dipolarophiles in 1,3-dipolar cycloaddition of nitrones: regioselectivity-switchable and highly diastereoselective synthesis of multisubstituted isoxazolidines","Organic Chemistry Frontiers","2018","5","20","2945","","10.1039/C8QO00826D","","","0.71073","MoKα","","0.1002","0.0533","","","0.107","0.1273","","","","","","1.005","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554423","6.229","0.0001","13.6065","0.0002","14.6177","0.0003","90","","90","","90","","1238.92","0.04","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C17 H0.25 N O -","- C17 H11 N O -","- C68 H44 N4 O4 -","4","1","","Xu, Xin-Ming; Lei, Chuan-Hu; Tong, Shuo; Zhu, Jieping; Wang, Mei-Xiang","Lewis acid catalyst-steered divergent synthesis of functionalized vicinal amino alcohols and pyrroles from tertiary enamides","Organic Chemistry Frontiers","2018","5","21","3138","","10.1039/C8QO00839F","","","1.54184","CuKα","","0.0369","0.0343","","","0.0834","0.0862","","","","","","1.11","","","","has coordinates","237224","2020-10-21","18:00:00",""
"1554424","13.42","0.002","5.3749","0.0008","17.821","0.003","90","","105.381","0.005","90","","1239.4","0.3","296","2","296","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C27 H25 F N2 O5 S -","- C27 H25 F N2 O5 S -","- C54 H50 F2 N4 O10 S2 -","2","1","","Cao, Zhong-Yan; Wang, Wenmin; Liao, Kui; Wang, Xiaoming; Zhou, Jian; Ma, Jing","Catalytic enantioselective synthesis of cyclopropanes featuring vicinal all-carbon quaternary stereocenters with a CH2F group; study of the influence of C–F⋯H–N interactions on reactivity","Organic Chemistry Frontiers","2018","5","20","2960","","10.1039/C8QO00842F","","","0.71073","MoKα","","0.1349","0.0661","","","0.1551","0.1967","","","","","","1.024","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554425","6.6841","0.0006","8.7074","0.0008","14.4482","0.0013","87.391","0.003","81.591","0.002","78.532","0.003","815.14","0.13","296","2","296","2","","","","","","","","5","P 1","P 1","1","","","","- C18 H16 Br F O2 -","- C18 H16 Br F O2 -","- C36 H32 Br2 F2 O4 -","2","2","","Cao, Zhong-Yan; Wang, Wenmin; Liao, Kui; Wang, Xiaoming; Zhou, Jian; Ma, Jing","Catalytic enantioselective synthesis of cyclopropanes featuring vicinal all-carbon quaternary stereocenters with a CH2F group; study of the influence of C–F⋯H–N interactions on reactivity","Organic Chemistry Frontiers","2018","5","20","2960","","10.1039/C8QO00842F","","","0.71073","MoKα","","0.0577","0.0518","","","0.1409","0.1463","","","","","","1.065","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554426","10.0137","0.0006","10.3706","0.0006","11.987","0.0007","90","","109.801","0.002","90","","1171.23","0.12","150","2","150","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C14 H13 N O3 -","- C14 H13 N O3 -","- C56 H52 N4 O12 -","4","2","","Kim, Simon J.; Batey, Robert A.","Enantioselective isoquinuclidine synthesis via sequential Diels–Alder/visible-light photoredox C–C bond cleavage: a formal synthesis of the indole alkaloid catharanthine","Organic Chemistry Frontiers","2018","5","20","2934","","10.1039/C8QO00849C","","","1.54178","CuKα","","0.0278","0.0276","","","0.0695","0.0697","","","","","","1.09","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554427","7.6019","0.0006","7.7795","0.0007","17.7908","0.0015","94.036","0.005","92.577","0.005","114.867","0.004","948.98","0.14","296","2","296","2","","","","","","","","4","P -1","-P 1","2","Organic Compound","","","- C42 H50 O2 Si2 -","- C42 H50 O2 Si2 -","- C42 H50 O2 Si2 -","1","0.5","","Ozdemir, Resul; Park, Sangyun; Deneme, İbrahim; Park, Yonghan; Zorlu, Yunus; Alidagi, Husniye Ardic; Harmandar, Kevser; Kim, Choongik; Usta, Hakan","Triisopropylsilylethynyl-substituted indenofluorenes: carbonyl versus dicyanovinylene functionalization in one-dimensional molecular crystals and solution-processed n-channel OFETs","Organic Chemistry Frontiers","2018","5","20","2912","","10.1039/C8QO00856F","","","0.71073","MoKα","","0.0982","0.086","","","0.2596","0.2746","","","","","","1.078","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554428","39.755","0.005","10.0294","0.0012","11.4351","0.0014","90","","102.874","0.008","90","","4444.8","1","296","2","296","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","Organic Compound","","","- C48 H50 N4 Si2 -","- C48 H50 N4 Si2 -","- C192 H200 N16 Si8 -","4","0.5","","Ozdemir, Resul; Park, Sangyun; Deneme, İbrahim; Park, Yonghan; Zorlu, Yunus; Alidagi, Husniye Ardic; Harmandar, Kevser; Kim, Choongik; Usta, Hakan","Triisopropylsilylethynyl-substituted indenofluorenes: carbonyl versus dicyanovinylene functionalization in one-dimensional molecular crystals and solution-processed n-channel OFETs","Organic Chemistry Frontiers","2018","5","20","2912","","10.1039/C8QO00856F","","","0.71073","MoKα","","0.202","0.1097","","","0.3031","0.373","","","","","","1.016","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554429","17.45405","0.00014","8.11896","0.00007","19.929","0.00015","90","","91.5647","0.0007","90","","2823.06","0.04","100","","100","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C33 H35 N O6 -","- C33 H35 N O6 -","- C132 H140 N4 O24 -","4","1","","Yi, Xiao; Tang, Hongxia; Chen, Jing; Xu, Xiuling; Ma, Yongmin","Facile one-pot synthesis of a 3-azabicyclo[3.3.1]nonane scaffold by a tandem Mannich reaction","Organic Chemistry Frontiers","2018","5","20","3003","","10.1039/C8QO00870A","","","1.54184","CuKα","","0.042","0.0402","","0.1087","0.1047","0.101","","","","","","1.021","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554430","11.083","0.007","21.629","0.013","12.241","0.007","90","","116.92","","90","","2616","3","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C30 H26 Cl3 N O3 -","- C30 H26 Cl3 N O3 -","- C120 H104 Cl12 N4 O12 -","4","1","","Yi, Xiao; Tang, Hongxia; Chen, Jing; Xu, Xiuling; Ma, Yongmin","Facile one-pot synthesis of a 3-azabicyclo[3.3.1]nonane scaffold by a tandem Mannich reaction","Organic Chemistry Frontiers","2018","5","20","3003","","10.1039/C8QO00870A","","","0.71073","MoKα","","0.1545","0.0998","","","0.2507","0.2824","","","","","","0.952","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554431","8.7333","0.001","32.515","0.005","11.3552","0.0017","90","","92.555","0.004","90","","3221.3","0.8","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","(E)-(1-(2-cyclopropyl-3-tosylprop-1-en-1-yl)-2-(4-methoxyphenyl)-2-methylcyclopropyl)diphenylphosphine oxide","","- C36 H37 O4 P S -","- C36 H37 O4 P S -","- C144 H148 O16 P4 S4 -","4","1","","Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei","Transition-metal-free radical cleavage of a hydrazonyl N–S bond: tosyl radical-initiated cascade C(sp3)–OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation","Organic Chemistry Frontiers","2018","5","24","3567","","10.1039/C8QO00873F","","","0.71073","MoKα","","0.1292","0.0566","","","0.1176","0.1417","","","","","","1.015","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554432","10.244","0.0003","13.1272","0.0005","15.4443","0.0005","85.216","0.001","77.319","0.001","69.981","0.001","1903.71","0.11","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","(E)-(1-(2-([1,1'-biphenyl]-4-yl)-3-tosylprop-1-en-1-yl)-2-(4-methoxyphenyl)-2-methylcyclopropyl)diphenylphosphine oxide","","- C45 H41 O4 P S -","- C45 H41 O4 P S -","- C90 H82 O8 P2 S2 -","2","1","","Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei","Transition-metal-free radical cleavage of a hydrazonyl N–S bond: tosyl radical-initiated cascade C(sp3)–OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation","Organic Chemistry Frontiers","2018","5","24","3567","","10.1039/C8QO00873F","","","0.71073","MoKα","","0.0945","0.0539","","","0.1232","0.1402","","","","","","1.024","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554433","10.9576","0.0005","24.0001","0.0011","13.0509","0.0006","90","","94.036","0.002","90","","3423.7","0.3","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","(E)-(2,2-dibenzyl-1-(2-methyl-3-tosylprop-1-en-1-yl)cyclopropyl)diphenylphosphine oxide","","- C40 H39 O3 P S -","- C40 H39 O3 P S -","- C160 H156 O12 P4 S4 -","4","1","","Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei","Transition-metal-free radical cleavage of a hydrazonyl N–S bond: tosyl radical-initiated cascade C(sp3)–OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation","Organic Chemistry Frontiers","2018","5","24","3567","","10.1039/C8QO00873F","","","0.71073","MoKα","","0.0969","0.0501","","","0.1136","0.1315","","","","","","1.018","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554434","12.3705","0.0006","13.8788","0.0008","19.1238","0.001","90","","106.702","0.001","90","","3144.8","0.3","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","(E)-(2-methyl-1-(2-methyl-3-tosylprop-1-en-1-yl)-2-(naphthalen-2-yl)cyclopropyl)diphenylphosphine oxide","","- C37 H35 O3 P S -","- C37 H35 O3 P S -","- C148 H140 O12 P4 S4 -","4","1","","Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei","Transition-metal-free radical cleavage of a hydrazonyl N–S bond: tosyl radical-initiated cascade C(sp3)–OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation","Organic Chemistry Frontiers","2018","5","24","3567","","10.1039/C8QO00873F","","","0.71073","MoKα","","0.0729","0.0464","","","0.1122","0.1237","","","","","","1.021","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554435","22.09","0.006","8.574","0.002","9.447","0.003","90","","101.6","0.02","90","","1752.7","0.8","296","2","296","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C22 H24 N2 -","- C22 H24 N2 -","- C88 H96 N8 -","4","1","","Liu, Siyuan; Zhang, Wenzhu; Qu, Jingping; Wang, Baomin","Engaging 2-methyl indolenines in a tandem condensation/1,5-hydride transfer/cyclization process: construction of a novel indolenine–tetrahydroquinoline assembly","Organic Chemistry Frontiers","2018","5","20","3008","","10.1039/C8QO00875B","","","0.71073","MoKα","","0.0935","0.0493","","","0.1018","0.119","","","","","","1.025","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554436","8.8385","0.0005","14.3341","0.0009","17.8495","0.0011","90","","90","","90","","2261.4","0.2","100","2","100","2","","","","","","","","7","P 21 21 21","P 2ac 2ab","19","","","","- C21 H21 Br N O7 P S -","- C21 H21 Br N O7 P S -","- C84 H84 Br4 N4 O28 P4 S4 -","4","1","","Sun, Jun; Mou, Chengli; Liu, Changyi; Huang, Ruoyan; Zhang, Shupeng; Zheng, Pengcheng; Chi, Yonggui Robin","Enantioselective access to multi-cyclic α-amino phosphonates via carbene-catalyzed cycloaddition reactions between enals and six-membered cyclic imines","Organic Chemistry Frontiers","2018","5","20","2992","","10.1039/C8QO00877A","","","0.71073","MoKα","","0.0765","0.0451","","","0.0859","0.0981","","","","","","0.948","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554437","9.1009","0.0001","17.5658","0.0002","8.1862","0.0001","90","","103.294","0.001","90","","1273.61","0.03","296","1","296","1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","Methyl 4-hydroxy-7-methoxy-2-(methylthio)quinoline-3-carboxylate","","- C13 H13 N O4 S -","- C13 H13 N O4 S -","- C52 H52 N4 O16 S4 -","4","1","","Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung","Structural assignment of the enol–keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones","Organic Chemistry Frontiers","2019","6","2","183","","10.1039/C8QO00884A","","","0.71073","MoKα","","0.0726","0.0558","","","0.1285","0.1368","","","","","","1.079","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554438","7.2268","0.0003","9.0737","0.0004","10.4696","0.0004","80.813","0.002","84.674","0.002","88.958","0.003","674.8","0.05","296","1","296","1","","","","","","","","5","P -1","-P 1","2","","Methyl 8-methoxy-2-(methylthio)-4-oxo-1,4-dihydroquinoline-3-carboxylate","","- C13 H15 N O5 S -","- C13 H15 N O5 S -","- C26 H30 N2 O10 S2 -","2","1","","Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung","Structural assignment of the enol–keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones","Organic Chemistry Frontiers","2019","6","2","183","","10.1039/C8QO00884A","","","0.71073","MoKα","","0.0589","0.0511","","","0.1476","0.1552","","","","","","1.054","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554439","7.2412","0.0009","9.7236","0.0012","11.4552","0.0015","85.64","0.006","87.406","0.006","77.183","0.006","783.86","0.17","296","1","296","1","","","","","","","","5","P -1","-P 1","2","","Methyl 8-methoxy-2-(methylsulfinyl)-4-oxo-1,4-dihydroquinoline-3-carboxylate","","- C13 H19 N O8 S -","- C13 H19 N O8 S -","- C26 H38 N2 O16 S2 -","2","1","","Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung","Structural assignment of the enol–keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones","Organic Chemistry Frontiers","2019","6","2","183","","10.1039/C8QO00884A","","","0.71073","MoKα","","0.0509","0.0429","","","0.1227","0.1289","","","","","","1.077","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554440","6.6266","0.0006","18.2993","0.0015","11.8645","0.001","90","","99.67","0.006","90","","1418.3","0.2","296","1","296","1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","Methyl 5-methoxy-2-(methylsulfinyl)-4-oxo-1,4-dihydroquinoline-3-carboxylate","","- C16 H13 N O5 S -","- C16 H13 N O5 S -","- C64 H52 N4 O20 S4 -","4","1","","Kang, On-Yu; Park, Seong Jun; Ahn, Hyojung; Jeong, Kyung Chae; Lim, Hwan Jung","Structural assignment of the enol‒keto tautomers of one-pot synthesized 4-hydroxyquinolines/4-quinolones","Organic Chemistry Frontiers","2019","6","2","183","","10.1039/C8QO00884A","","","0.71073","MoKα","","0.0963","0.0785","","","0.2396","0.2512","","","","","","1.103","","","","has coordinates","237237","2020-10-21","18:00:00",""
"1554441","9.0319","0.0004","18.9034","0.0009","14.4632","0.0007","90","","96.64","0.002","90","","2452.8","0.2","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C28 H29 Co P S -","- C28 H29 Co P S -","- C112 H116 Co4 P4 S4 -","4","1","","Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang","Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives","Organic Chemistry Frontiers","2018","5","20","2997","","10.1039/C8QO00887F","","","0.71","MoKα","","0.0352","0.0285","","","0.0704","0.074","","","","","","1.042","","","","has coordinates","237239","2020-10-21","18:00:00",""
"1554442","12.766","0.0003","7.3952","0.0002","18.2702","0.0004","90","","103.067","0.002","90","","1680.17","0.07","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H18 N O2 -","- C22 H18 N O2 -","- C88 H72 N4 O8 -","4","1","","Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang","Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives","Organic Chemistry Frontiers","2018","5","20","2997","","10.1039/C8QO00887F","","x-ray","1.54184","CuKα","","0.0807","0.0707","","","0.1844","0.1974","","","","","","1.187","","","","has coordinates,has disorder","237239","2020-10-21","18:00:00",""
"1554443","7.3192","0.0006","11.4476","0.0007","14.2878","0.0011","109.541","0.006","103.435","0.007","90.85","0.006","1091.7","0.15","173","0.1","173","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C30 H23 N O2 -","- C30 H23 N O2 -","- C60 H46 N2 O4 -","2","1","","Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang","Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives","Organic Chemistry Frontiers","2018","5","20","2997","","10.1039/C8QO00887F","","x-ray","1.54184","CuKα","","0.0655","0.0504","","","0.1343","0.1468","","","","","","1.065","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554444","7.4718","0.0009","10.17","0.0013","13.6849","0.0015","80.313","0.01","76.092","0.01","74.405","0.011","966.3","0.2","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C26 H21 N O2 -","- C26 H21 N O2 -","- C52 H42 N2 O4 -","2","1","","Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang","Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives","Organic Chemistry Frontiers","2018","5","20","2997","","10.1039/C8QO00887F","","","0.71073","MoKα","","0.0706","0.0523","","","0.1325","0.1454","","","","","","1.079","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554445","16.6717","0.0015","10.051","0.002","14.516","0.006","90","","90","","90","","2432.4","1.1","172.99","0.1","172.99","0.1","","","","","","","","6","P n a 21","P 2c -2n","33","","","","- C28 H29 Br Co P S -","- C28 H29 Br Co P S -","- C112 H116 Br4 Co4 P4 S4 -","4","1","","Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang","Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives","Organic Chemistry Frontiers","2018","5","20","2997","","10.1039/C8QO00887F","","x-ray","0.71073","MoKα","","0.0588","0.048","","","0.0977","0.1016","","","","","","1.044","","","","has coordinates","237239","2020-10-21","18:00:00",""
"1554446","10.9778","0.0007","16.148","0.001","17.5888","0.0011","90","","106.231","0.0016","90","","2993.7","0.3","230","2","230","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C31 H44 N3 P2 Rh -","- C31 H44 N3 P2 Rh -","- C124 H176 N12 P8 Rh4 -","4","1","","Zhou, Chunhui; Hu, Jinsong; Wang, Yuan; Yao, Changguang; Chakraborty, Priyanka; Li, Huaifeng; Guan, Chao; Huang, Mei-Hui; Huang, Kuo-Wei","Selective carbonylation of benzene to benzaldehyde using a phosphorus‒nitrogen PN3P‒rhodium(i) complex","Organic Chemistry Frontiers","2019","6","6","721","","10.1039/C8QO00892B","","","1.54178","CuKα","","0.0345","0.0339","","","0.0932","0.0937","","","","","","1.047","","","","has coordinates,has disorder","237242","2020-10-21","18:00:00",""
"1554447","29.2408","0.0009","13.8295","0.0004","25.4214","0.0007","90","","120.925","0.001","90","","8818.6","0.5","200","2","200","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C92 H120 N6 O3 P4 Rh2 -","- C92 H120 N6 O3 P4 Rh2 -","- C368 H480 N24 O12 P16 Rh8 -","4","0.5","","Zhou, Chunhui; Hu, Jinsong; Wang, Yuan; Yao, Changguang; Chakraborty, Priyanka; Li, Huaifeng; Guan, Chao; Huang, Mei-Hui; Huang, Kuo-Wei","Selective carbonylation of benzene to benzaldehyde using a phosphorus‒nitrogen PN3P‒rhodium(i) complex","Organic Chemistry Frontiers","2019","6","6","721","","10.1039/C8QO00892B","","","1.54178","CuKα","","0.0288","0.0276","","","0.0752","0.0763","","","","","","1.015","","","","has coordinates","237242","2020-10-21","18:00:00",""
"1554448","26.357","0.0008","7.5712","0.0003","24.9141","0.0008","90","","92.458","0.003","90","","4967.1","0.3","293","2","293","2","","","","","","","","4","I 1 2 1","I 2y","5","","","","- C28 H33 Br O3 -","- C28 H33 Br O3 -","- C224 H264 Br8 O24 -","8","2","","Liu, Lin; Song, Huayue; Chen, Peng; Yuan, Ziyun; Feng, Shangbiao; Zhang, Weiwei; Fang, Bowen; Xie, Xingang; She, Xuegong","Total synthesis of (−)-8-epi-chromazonarol enabled by a unique N2H4·H2O promoted intramolecular oxa-Michael cyclization reaction","Organic Chemistry Frontiers","2018","5","20","3013","","10.1039/C8QO00901E","","","1.54184","CuKα","","0.0497","0.0468","","","0.1352","0.1402","","","","","","0.974","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554449","12.2395","0.0019","14.363","0.002","18.399","0.003","89.442","0.003","89.312","0.002","88.419","0.003","3232.9","0.9","296","2","296.15","","","","","","","","","5","P -1","-P 1","2","","","","- C30 H37 I N2 Ru -","- C30 H37 I N2 Ru -","- C120 H148 I4 N8 Ru4 -","4","2","","Wu, Xuan-Jun; Wang, Hua-Jing; Yang, Zhao-Qi; Tang, Xiao-Sheng; Yuan, Ye; Su, Wei; Chen, Cheng; Verpoort, Francis","Efficient and phosphine-free bidentate N-heterocyclic carbene/ruthenium catalytic systems for the dehydrogenative amidation of alcohols and amines","Organic Chemistry Frontiers","2019","6","5","563","","10.1039/C8QO00902C","","","0.71073","MoKα","","0.0941","0.0641","","","0.1851","0.2175","","","","","","1.002","","","","has coordinates","237246","2020-10-21","18:00:00",""
"1554450","15.329","0.002","7.7727","0.001","21.254","0.003","90","","95.269","0.002","90","","2521.7","0.6","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C27 H31 I N2 Ru -","- C27 H31 I N2 Ru -","- C108 H124 I4 N8 Ru4 -","4","1","","Wu, Xuan-Jun; Wang, Hua-Jing; Yang, Zhao-Qi; Tang, Xiao-Sheng; Yuan, Ye; Su, Wei; Chen, Cheng; Verpoort, Francis","Efficient and phosphine-free bidentate N-heterocyclic carbene/ruthenium catalytic systems for the dehydrogenative amidation of alcohols and amines","Organic Chemistry Frontiers","2019","6","5","563","","10.1039/C8QO00902C","","","0.71073","MoKα","","0.0375","0.0299","","","0.0729","0.0763","","","","","","1.036","","","","has coordinates","237246","2020-10-21","18:00:00",""
"1554451","12.1152","0.0014","14.1577","0.0018","24.768","0.003","90","","93.519","0.002","90","","4240.3","0.9","296","2","296","2","","","","","","","","5","C 1 c 1","C -2yc","9","","","","- C26 H23 N O2 S -","- C26 H23 N O2 S -","- C208 H184 N8 O16 S8 -","8","2","","Zhang, Jia-hao; Wei, Yin; Shi, Min","Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes","Organic Chemistry Frontiers","2018","5","20","2980","","10.1039/C8QO00907D","","","0.71073","MoKα","","0.0513","0.0373","","","0.0883","0.0965","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554452","10.875","0.012","11.83","0.014","16.54","0.02","90","","98.8","0.02","90","","2103","4","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C26 H23 N O2 S -","- C26 H23 N O2 S -","- C104 H92 N4 O8 S4 -","4","1","","Zhang, Jia-hao; Wei, Yin; Shi, Min","Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes","Organic Chemistry Frontiers","2018","5","20","2980","","10.1039/C8QO00907D","","","0.71073","MoKα","","0.0859","0.043","","","0.1015","0.1208","","","","","","1.009","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554453","20.5631","0.0007","27.2351","0.0011","9.3277","0.0003","90","","92.088","0.001","90","","5220.4","0.3","296","2","296","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C26 H23 N O4 S -","- C26 H23 N O4 S -","- C208 H184 N8 O32 S8 -","8","1","","Zhang, Jia-hao; Wei, Yin; Shi, Min","Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes","Organic Chemistry Frontiers","2018","5","20","2980","","10.1039/C8QO00907D","","","0.71073","MoKα","","0.0932","0.0673","","","0.2068","0.2299","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554454","15.787","0.009","10.811","0.006","13.977","0.008","90","","112.816","0.007","90","","2199","2","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","1,1-phenylenedioxa-5-phenyl-3,3,7,7-tetrakis(trifluoromethyl)-1-phospha-2,6,8-trioxabicyclo[4.3.2(1,5)]octane","","- C20 H11 F12 O5 P -","- C20 H11 F12 O5 P -","- C80 H44 F48 O20 P4 -","4","1","","Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.","Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes","Organic Chemistry Frontiers","2018","5","21","3113","","10.1039/C8QO00915E","","x-ray","0.71073","MoKα","","0.0611","0.0444","","","0.1116","0.1226","","","","","","1.028","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554455","7.266","0.003","11.409","0.005","8.573","0.004","90","","96.695","0.006","90","","705.8","0.5","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","triethylammonium oxabenzo-1,3,2-dioxaphosphol-2-oate","","- C12 H20 N O4 P -","- C12 H20 N O4 P -","- C24 H40 N2 O8 P2 -","2","1","","Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.","Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes","Organic Chemistry Frontiers","2018","5","21","3113","","10.1039/C8QO00915E","","x-ray","0.71073","MoKα","","0.0589","0.0429","","","0.0846","0.0915","","","","","","1.038","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554456","4.6005","0.0004","10.122","0.0008","16.4334","0.0014","90","","90","","90","","765.24","0.11","150","2","150","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","2-hydroxyphenyl phosphoric acid","","- C6 H7 O5 P -","- C6 H7 O5 P -","- C24 H28 O20 P4 -","4","1","","Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.","Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes","Organic Chemistry Frontiers","2018","5","21","3113","","10.1039/C8QO00915E","","x-ray","0.71073","MoKα","","0.044","0.0387","","","0.0831","0.0859","","","","","","1.045","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554457","10.7892","0.0006","11.1562","0.0006","11.7122","0.0006","101.788","0.003","99.647","0.003","106.558","0.003","1283.93","0.12","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","1,1- phenylenedioxa-5-phenyl-3,7-bis(ethoxycarbonyl)-3,7-bis(trifluoromethyl)-1-phospha-2,6,8-trioxabicyclo[4.3.2(1,5)]octane","","- C24 H21 F6 O9 P -","- C24 H21 F6 O9 P -","- C48 H42 F12 O18 P2 -","2","1","","Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.","Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes","Organic Chemistry Frontiers","2018","5","21","3113","","10.1039/C8QO00915E","","x-ray","0.71073","MoKα","","0.0813","0.0442","","","0.1057","0.1222","","","","","","1.027","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554458","27.972","0.006","27.972","0.006","11.844","0.003","90","","90","","90","","9267","4","293","2","293","2","","","","","","","","5","I 41/a :2","-I 4ad","88","","1,1-phenylenedioxa-5-phenyl-3,7-bis(trichloromethyl)-1-phospha-2,6,8-trioxabicyclo[4.3.2(1,5)]octane","","- C18 H13 Cl6 O5 P -","- C18 H13 Cl6 O5 P -","- C288 H208 Cl96 O80 P16 -","16","1","","Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.","Tandem dihetero-Diels–Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes","Organic Chemistry Frontiers","2018","5","21","3113","","10.1039/C8QO00915E","","x-ray","0.71073","MoKα","","0.05","0.0399","","","0.0929","0.099","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554459","8.8009","0.0008","12.3786","0.0018","16.3465","0.0019","102.889","0.012","95.068","0.009","108.26","0.011","1624.3","0.4","100","0.2","100","0.2","","","","","","","","5","P -1","-P 1","2","","","","- C40 H40 N O2 S -","- C40 H40 N O2 S -","- C80 H80 N2 O4 S2 -","2","1","","Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang","Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells","Organic Chemistry Frontiers","2018","5","22","3324","","10.1039/C8QO00934A","","x-ray","1.54184","CuKα","","0.1733","0.1048","","","0.2799","0.3361","","","","","","1.039","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554460","7.1299","0.0011","14.678","0.0013","17.037","0.002","74.911","0.009","81.895","0.013","89.178","0.01","1703.8","0.4","102","4","102","4","","","","","","","","5","P -1","-P 1","2","","","","- C44 H42 N O2 S -","- C44 H42 N O2 S -","- C88 H84 N2 O4 S2 -","2","1","","Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang","Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells","Organic Chemistry Frontiers","2018","5","22","3324","","10.1039/C8QO00934A","","x-ray","1.54184","CuKα","","0.2244","0.0946","","","0.2156","0.2882","","","","","","0.948","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554461","13.5245","0.0006","24.687","0.003","20.6534","0.0009","90","","102.064","0.004","90","","6743.4","0.9","100","0.13","100","0.13","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C84 H80 N2 O4 S4 -","- C84 H80 N2 O4 S4 -","- C336 H320 N8 O16 S16 -","4","1","","Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang","Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells","Organic Chemistry Frontiers","2018","5","22","3324","","10.1039/C8QO00934A","","x-ray","1.54184","CuKα","","0.21","0.1447","","","0.3854","0.4192","","","","","","1.061","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554462","14.3142","0.001","16.7266","0.0012","18.5616","0.0011","105.723","0.006","109.469","0.006","90.336","0.006","4010.6","0.5","99.98","0.17","99.98","0.17","","","","","","","","5","P -1","-P 1","2","","","","- C92 H81 N2 O4 S4 -","- C92 H81 N2 O4 S4 -","- C184 H162 N4 O8 S8 -","2","1","","Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang","Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells","Organic Chemistry Frontiers","2018","5","22","3324","","10.1039/C8QO00934A","","x-ray","1.54184","CuKα","","0.2041","0.1084","","","0.318","0.3849","","","","","","1.051","","","","has coordinates","237251","2020-10-21","18:00:00",""
"1554463","8.892","0.012","9.668","0.01","13.91","0.02","86.33","0.05","86.29","0.04","67.91","0.04","1105","2","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C27 H25 N O3 S -","- C27 H25 N O3 S -","- C54 H50 N2 O6 S2 -","2","1","","Beltran, Frédéric; Andna, Lucile; Miesch, Laurence","Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts","Organic Chemistry Frontiers","2019","6","3","373","","10.1039/C8QO00937F","","","0.71073","MoKα","","0.0862","0.0477","","","0.1076","0.1226","","","","","","1.029","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554464","7.6023","0.0004","7.8229","0.0004","16.7412","0.0009","85.307","0.002","84.129","0.002","85.07","0.002","984.06","0.09","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C22 H25 N O3 S -","- C22 H25 N O3 S -","- C44 H50 N2 O6 S2 -","2","1","","Beltran, Frédéric; Andna, Lucile; Miesch, Laurence","Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts","Organic Chemistry Frontiers","2019","6","3","373","","10.1039/C8QO00937F","","","0.71073","MoKα","","0.0583","0.0456","","","0.1183","0.1267","","","","","","1.001","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554465","10.5059","0.0006","11.5524","0.0005","19.3292","0.0009","90","","99.812","0.002","90","","2311.6","0.2","173","2","173","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C28 H27 N O3 S -","- C28 H27 N O3 S -","- C112 H108 N4 O12 S4 -","4","1","","Beltran, Frédéric; Andna, Lucile; Miesch, Laurence","Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts","Organic Chemistry Frontiers","2019","6","3","373","","10.1039/C8QO00937F","","","0.71073","MoKα","","0.0784","0.0505","","","0.1215","0.1379","","","","","","1.035","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554466","8.6751","0.0005","21.9074","0.0013","12.355","0.0005","90","","107.893","0.001","90","","2234.5","0.2","173","2","173","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C25 H29 N O3 S -","- C25 H29 N O3 S -","- C100 H116 N4 O12 S4 -","4","1","","Beltran, Frédéric; Andna, Lucile; Miesch, Laurence","Spirocyclization of keto-ynesulfonamides promoted by quaternary ammonium salts","Organic Chemistry Frontiers","2019","6","3","373","","10.1039/C8QO00937F","","","0.71073","MoKα","","0.0905","0.0654","","","0.1575","0.1784","","","","","","1.012","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554467","9.7218","0.0008","7.7915","0.0006","24.097","0.002","90","","99.734","0.008","90","","1799","0.3","155.9","","155.9","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H16 N2 O6 S -","- C19 H16 N2 O6 S -","- C76 H64 N8 O24 S4 -","4","1","","Shen, Yangyong; Wang, Chaorong; Chen, Wei; Cui, Sunliang","Cascade reaction involving Diels–Alder cascade: modular synthesis of amino α-pyrones, indolines and anilines","Organic Chemistry Frontiers","2018","5","24","3574","","10.1039/C8QO00939B","","","0.71073","MoKα","","0.0666","0.0484","","","0.1183","0.1359","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554468","6.4452","0.0007","11.7323","0.0011","12.5163","0.0012","105.865","0.008","90.612","0.008","93.872","0.008","907.9","0.16","293","2","293.15","","","","","","","","","5","P -1","-P 1","2","","","","- C20 H19 N O4 S -","- C20 H19 N O4 S -","- C40 H38 N2 O8 S2 -","2","1","","Shen, Yangyong; Wang, Chaorong; Chen, Wei; Cui, Sunliang","Cascade reaction involving Diels–Alder cascade: modular synthesis of amino α-pyrones, indolines and anilines","Organic Chemistry Frontiers","2018","5","24","3574","","10.1039/C8QO00939B","","","0.71073","MoKα","","0.0762","0.0508","","","0.1158","0.1339","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554469","10.2302","0.0008","24.9417","0.0018","10.532","0.0007","90","","94.66","0.006","90","","2678.4","0.3","293","2","293.15","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C33 H26 Cl N O2 S -","- C33 H26 Cl N O2 S -","- C132 H104 Cl4 N4 O8 S4 -","4","1","","Shen, Yangyong; Wang, Chaorong; Chen, Wei; Cui, Sunliang","Cascade reaction involving Diels–Alder cascade: modular synthesis of amino α-pyrones, indolines and anilines","Organic Chemistry Frontiers","2018","5","24","3574","","10.1039/C8QO00939B","","","0.71073","MoKα","","0.0692","0.0439","","","0.0958","0.1088","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554470","9.9349","0.0009","5.4755","0.0005","25.351","0.003","90","","101.162","0.01","90","","1353","0.2","292.9","0.8","292.9","0.8","","","","","","","","4","I 1 2 1","I 2y","5","","","","- C26 H30 N4 O9 -","- C26 H30 N4 O9 -","- C52 H60 N8 O18 -","2","0.5","","Chen, Jinhong; Li, Junfang; Zhu, Longqing; Peng, Xue; Feng, Yiyue; Lu, Yingmei; Hu, Xiaoling; Liang, Jianpin; Zhao, Quanyi; Wang, Zhen","Total synthesis and structure revision of chrysamide B","Organic Chemistry Frontiers","2018","5","23","3402","","10.1039/C8QO00949J","","x-ray","0.71073","MoKα","","0.0558","0.0439","","","0.0971","0.1064","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554471","11.6963","0.0014","8.9597","0.0008","23.096","0.002","90","","90.67","0.001","90","","2420.2","0.4","293","2","293","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C26 H30 O6 -","- C26 H30 O6 -","- C104 H120 O24 -","4","1","","Xiong, Yan-Jie; Shi, Shao-Qing; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo","A new dehydrogenative [4 + 1] annulation between para-quinone methides (p-QMs) and iodonium ylides for the synthesis of 2,3-dihydrobenzofurans","Organic Chemistry Frontiers","2018","5","23","3483","","10.1039/C8QO00950C","","","1.54178","CuKα","","0.119","0.0723","","","0.1786","0.2119","","","","","","1.081","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554472","10.805","0.0008","11.7571","0.0009","12.8689","0.0011","106.048","0.002","95.01","0.001","114.103","0.003","1396.3","0.2","298","2","298","2","","","","","","","","6","P -1","-P 1","2","","","","- C27 H28 Cl I N2 O5 -","- C27 H28 Cl I N2 O5 -","- C54 H56 Cl2 I2 N4 O10 -","2","1","","Xiong, Yan-Jie; Shi, Shao-Qing; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo","A new dehydrogenative [4 + 1] annulation between para-quinone methides (p-QMs) and iodonium ylides for the synthesis of 2,3-dihydrobenzofurans","Organic Chemistry Frontiers","2018","5","23","3483","","10.1039/C8QO00950C","","","0.71073","MoKα","","0.0829","0.0495","","","0.1228","0.1373","","","","","","1.039","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554473","8.4088","0.0005","17.398","0.0011","12.1982","0.0008","90","","101.318","0.001","90","","1749.85","0.19","90","","90","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","2-(3-methyl-1-phenyl-1H-pyrazol-2-ium-4-yl)-1,1-bis((trifluoromethyl)sulfonyl)ethan-1-ide","","- C14 H12 F6 N2 O4 S2 -","- C14 H12 F6 N2 O4 S2 -","- C56 H48 F24 N8 O16 S8 -","4","1","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0469","0.0381","","","0.0886","0.0948","","","","","","1.032","","","","has coordinates","237261","2020-10-21","18:00:00",""
"1554474","12.6441","0.0009","11.3643","0.0008","16.2034","0.0011","90","","111.751","0.001","90","","2162.5","0.3","90","","90","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","2-(2,2-bis((trifluoromethyl)sulfonyl)ethyl)-1-(phenylethynyl)-1,5,6,7-tetrahydro-4H-indol-4-one","","- C20 H15 F6 N O5 S2 -","- C20 H15 F6 N O5 S2 -","- C80 H60 F24 N4 O20 S8 -","4","1","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0363","0.0308","","","0.0755","0.0789","","","","","","1.025","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554475","13.0371","0.0009","14.5605","0.001","14.0643","0.001","90","","113.617","0.001","90","","2446.2","0.3","90","","90","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","2-(2,4-diphenyloxazol-3-ium-5-yl)-1,1-bis((trifluoromethyl)sulfonyl)ethan-1-ide","","- C21 H19 F6 N O6 S3 -","- C21 H19 F6 N O6 S3 -","- C84 H76 F24 N4 O24 S12 -","4","1","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0493","0.041","","","0.0957","0.1007","","","","","","1.042","","","","has coordinates,has disorder","237261","2020-10-21","18:00:00",""
"1554476","31.442","0.002","7.7594","0.0005","16.3435","0.0011","90","","91.74","0.001","90","","3985.5","0.4","90","","90","","","","","","","","","7","C 1 2/c 1","-C 2yc","15","","2-(1-(4-chlorophenyl)-5-hydroxy-3-methyl-1H-pyrazol-2-ium-4-yl)-1,1-bis((trifluoromethyl)sulfonyl)ethan-1-ide","","- C14 H11 Cl F6 N2 O5 S2 -","- C14 H11 Cl F6 N2 O5 S2 -","- C112 H88 Cl8 F48 N16 O40 S16 -","8","1","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0329","0.029","","","0.0722","0.0748","","","","","","1.03","","","","has coordinates","237261","2020-10-21","18:00:00",""
"1554477","5.7308","0.0005","13.6484","0.0013","21.184","0.002","90","","95.748","0.001","90","","1648.6","0.3","90","","90","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","3-(2,2-Bis((trifluoromethyl)sulfonyl)ethyl)-4-hydroxy-2H-chromen-2-one","","- C13 H8 F6 O7 S2 -","- C13 H8 F6 O7 S2 -","- C52 H32 F24 O28 S8 -","4","1","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0334","0.0292","","","0.071","0.0735","","","","","","1.023","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554478","14.266","0.002","6.0883","0.0009","18.922","0.003","90","","94.123","0.002","90","","1639.2","0.4","90","","90","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","2-(1-phenyl-1H-pyrazol-2-ium-2-yl)-1,1-bis((trifluoromethyl)sulfonyl)ethan-1-ide","","- C13 H10 F6 N2 O4 S2 -","- C13 H10 F6 N2 O4 S2 -","- C52 H40 F24 N8 O16 S8 -","4","1","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0461","0.0361","","","0.0846","0.0903","","","","","","1.029","","","","has coordinates","237261","2020-10-21","18:00:00",""
"1554479","17.2641","0.001","14.8304","0.0008","23.9088","0.0014","90","","90","","90","","6121.5","0.6","90","","90","","","","","","","","","6","P b c a","-P 2ac 2ab","61","","2-(5-hydroxy-1,3-dimethyl-1H-pyrazol-2-ium-4-yl)- 1,1-bis((trifluoromethyl)sulfonyl)ethan-1-ide","","- C9 H10 F6 N2 O5 S2 -","- C9 H10 F6 N2 O5 S2 -","- C144 H160 F96 N32 O80 S32 -","16","2","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0451","0.0373","","","0.0889","0.0929","","","","","","1.064","","","","has coordinates","237261","2020-10-21","18:00:00",""
"1554480","27.2048","0.0018","18.3507","0.0012","12.2694","0.0008","90","","90","","90","","6125.2","0.7","90","","90","","","","","","","","","6","P n a 21","P 2c -2n","33","","2-(5-hydroxy-2,3-dimethyl-1-phenyl-1H-pyrazol-2-ium-4-yl)- 1,1-bis((trifluoromethyl)sulfonyl)ethan-1-ide","","- C15 H14 F6 N2 O5 S2 -","- C15 H14 F6 N2 O5 S2 -","- C180 H168 F72 N24 O60 S24 -","12","3","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0291","0.0264","","","0.0653","0.0671","","","","","","1.008","","","","has coordinates","237261","2020-10-21","18:00:00",""
"1554481","17.607","0.0012","5.4871","0.0004","25.7682","0.0017","90","","106.169","0.0015","90","","2391","0.3","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C29 H28 N2 O S2 -","- C29 H28 N2 O S2 -","- C116 H112 N8 O4 S8 -","4","1","","Weldeab, Asmerom O.; Li, Lei; Cekli, Seda; Abboud, Khalil A.; Schanze, Kirk S.; Castellano, Ronald K.","Pyridine-terminated low gap π-conjugated oligomers: design, synthesis, and photophysical response to protonation and metalation","Organic Chemistry Frontiers","2018","5","21","3170","","10.1039/C8QO00963E","","","0.71073","MoKα","","0.0677","0.0456","","","0.1154","0.1232","","","","","","1.008","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554482","11.2685","0.0006","18.6581","0.0007","12.8795","0.0008","90","","111.426","0.007","90","","2520.8","0.3","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C26 H22 Br N O9 -","- C26 H22 Br N O9 -","- C104 H88 Br4 N4 O36 -","4","1","","Agafonova, Anastasiya V.; Smetanin, Ilia A.; Rostovskii, Nikolai V.; Khlebnikov, Alexander F.; Novikov, Mikhail S.","Expedient synthesis of 3-hydroxypyrroles via Bu3SnH-triggered ionic 5-exo-trig-cyclization of 5-chloro-3-azamuconoate derivatives","Organic Chemistry Frontiers","2018","5","23","3396","","10.1039/C8QO00982A","","","0.71073","MoKα","","0.0592","0.0388","","","0.0764","0.0845","","","","","","1.03","","","","has coordinates","237266","2020-10-21","18:00:00",""
"1554483","15.569","0.002","29.973","0.004","7.0564","0.001","90","","90","","90","","3292.9","0.8","293","2","293","2","","","","","","","","7","I b a 2","I 2 -2c","45","","","","- C16 H9 Cl F3 N O3 S -","- C16 H9 Cl F3 N O3 S -","- C128 H72 Cl8 F24 N8 O24 S8 -","8","1","","Yi, Ruxia; Li, Xincheng; Wan, Boshun","Ring-opening and cyclization of aziridines with aryl azides: metal-free synthesis of 6-(triflyloxy)quinolines","Organic Chemistry Frontiers","2018","5","23","3488","","10.1039/C8QO00984H","","","0.71073","MoKα","","0.0547","0.0494","","","0.118","0.1234","","","","","","1.115","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554484","4.9693","0.0003","5.8579","0.0003","31.3863","0.0017","90","","90","","90","","913.64","0.09","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C11 H9 F O2 -","- C11 H9 F O2 -","- C44 H36 F4 O8 -","4","1","","Han, Sang Hoon; Pandey, Ashok Kumar; Lee, Heeyoung; Kim, Saegun; Kang, Dahye; Jung, Young Hoon; Kim, Hyung Sik; Hong, Sungwoo; Kim, In Su","One-pot synthesis of 2-naphthols from nitrones and MBH adducts via decarboxylative N–O bond cleavage","Organic Chemistry Frontiers","2018","5","22","3210","","10.1039/C8QO00988K","","","0.71073","MoKα","","0.069","0.0506","","","0.0992","0.106","","","","","","1.064","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554485","6.1036","0.0004","12.5506","0.0007","21.976","0.0013","90","","90","","90","","1683.45","0.18","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C20 H24 O5 -","- C20 H24 O5 -","- C80 H96 O20 -","4","1","","Yang, Qian; Hu, Kun; Yan, Bing-Chao; Liu, Miao; Li, Xiao-Nian; Sun, Han-Dong; Puno, Pema-Tenzin","Maoeriocalysins A–D, four novel ent-kaurane diterpenoids from Isodon eriocalyx and their structure determination utilizing quantum chemical calculation in conjunction with quantitative interproton distance analysis","Organic Chemistry Frontiers","2019","6","1","45","","10.1039/C8QO01007B","","","1.54178","CuKα","","0.0356","0.0353","","","0.0939","0.0942","","","","","","1.072","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554486","5.7918","0.0006","13.738","0.0014","13.4519","0.0013","90","","101.436","0.004","90","","1049.09","0.18","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C14 H8 N3 O -","- C14 H8 N3 O -","- C56 H32 N12 O4 -","4","1","","Li, Ping-Gui; Yan, Cheng; Zhu, Shuai; Liu, Shu-Hui; Zou, Liang-Hua","Direct construction of benzimidazo[l,2-c]quinazolin-6-ones via metal-free oxidative C‒C bond cleavage","Organic Chemistry Frontiers","2018","5","23","3464","","10.1039/C8QO01039K","","","0.71073","MoKα","","0.0831","0.0547","","","0.1246","0.1389","","","","","","1.042","","","","has coordinates","237273","2020-10-21","18:00:00",""
"1554487","13.6363","0.0006","8.5322","0.0003","15.2209","0.0008","90","","116.205","0.001","90","","1588.9","0.12","296","2","296","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C37 H31 N3 O4 S -","- C37 H31 N3 O4 S -","- C74 H62 N6 O8 S2 -","2","1","","Gu, Bo-Qi; Yang, Wu-Lin; Wu, Shu-Xiao; Wang, Yan-Bing; Deng, Wei-Ping","Organocatalytic asymmetric synthesis of tetrahydrocarbazoles via an inverse-electron-demand Diels–Alder reaction of 2,3-indole-dienes with enals","Organic Chemistry Frontiers","2018","5","23","3430","","10.1039/C8QO01042K","","","0.71073","MoKα","","0.0513","0.0388","","","0.0783","0.0857","","","","","","1.063","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554488","9.5039","0.0007","10.0075","0.0008","10.6869","0.0008","64.045","0.002","69.351","0.002","83.294","0.002","854.35","0.11","291","2","291","2","","","","","","","","5","P -1","-P 1","2","","","","- C17 H18 N O5 P -","- C17 H18 N O5 P -","- C34 H36 N2 O10 P2 -","2","1","","Wang, Jie; Li, Jun; Wei, Yuanyuan; Yang, Jingya; Huo, Congde","Copper-catalyzed oxidative phosphonation of 3,4-dihydro-1,4-benzoxazin-2-ones","Organic Chemistry Frontiers","2018","5","24","3534","","10.1039/C8QO01049H","","","1.54178","CuKα","","0.0828","0.082","","","0.1885","0.1899","","","","","","1.081","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554489","7.4865","0.0008","11.7277","0.0013","20.913","0.003","90","","90","","90","","1836.1","0.4","293","2","293","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C10 H8 F N3 -","- C10 H8 F N3 -","- C80 H64 F8 N24 -","8","1","","Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming","Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives","Organic Chemistry Frontiers","2019","6","4","426","","10.1039/C8QO01054D","","","0.71073","MoKα","","0.0552","0.0436","","","0.0997","0.108","","","","","","1.106","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554490","8.4745","0.0007","13.483","0.0013","12.5515","0.0012","90","","96.566","0.003","90","","1424.7","0.2","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H12 F N5 O2 -","- C16 H12 F N5 O2 -","- C64 H48 F4 N20 O8 -","4","1","","Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming","Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives","Organic Chemistry Frontiers","2019","6","4","426","","10.1039/C8QO01054D","","","0.71073","MoKα","","0.0581","0.0443","","","0.1115","0.1196","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554491","6.185","0.002","7.487","0.002","18.728","0.006","90","","96.138","0.011","90","","862.3","0.5","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C10 H8 F N3 -","- C9 H7 F N4 -","- C36 H28 F4 N16 -","4","1","","Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming","Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives","Organic Chemistry Frontiers","2019","6","4","426","","10.1039/C8QO01054D","","","0.71073","MoKα","","0.0746","0.0546","","","0.1129","0.1211","","","","","","1.05","","","","has coordinates","237278","2020-10-21","18:00:00",""
"1554492","27.38","0.03","26.9","0.03","24.03","0.03","90","","90","","90","","17699","4","296","2","296","2","","","","","","","","6","A e a 2","A 2 -2ab","41","","","","- C70 H56 Ag5 Cl2 N6 P4 -","- C70 H56 Ag5 Cl2 N6 P4 -","- C560 H448 Ag40 Cl16 N48 P32 -","8","1","","Zhao, Mingzhu; Cai, Juewang; Zhao, Xiaoming","Silver-promoted selective fluorination of 2-aminopyrimidines: synthesis of 5-fluoro-2-aminopyrimidine derivatives","Organic Chemistry Frontiers","2019","6","4","426","","10.1039/C8QO01054D","","","0.71073","MoKα","","0.0794","0.0647","","","0.1672","0.1826","","","","","","1.112","","","","has coordinates,has disorder","237278","2020-10-21","18:00:00",""
"1554493","3.9188","0.0004","12.5127","0.0013","15.3057","0.0015","101.08","0.005","96.416","0.005","92.665","0.005","730.13","0.13","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C20 H14 N2 -","- C20 H14 N2 -","- C40 H28 N4 -","2","1","","Chang, Yu-Che; Prakash, Sekar; Cheng, Chien-Hong","ReI-Catalyzed highly regio- and stereoselective C–H addition to terminal and internal alkynes","Organic Chemistry Frontiers","2019","6","4","432","","10.1039/C8QO01068D","","","0.71073","MoKα","","0.0531","0.0459","","","0.1268","0.1325","","","","","","1.064","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554494","10.5762","0.0007","7.8869","0.0006","19.9879","0.0016","90","","91.535","0.003","90","","1666.7","0.2","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C22 H19 N3 -","- C22 H19 N3 -","- C88 H76 N12 -","4","1","","Chang, Yu-Che; Prakash, Sekar; Cheng, Chien-Hong","ReI-Catalyzed highly regio- and stereoselective C–H addition to terminal and internal alkynes","Organic Chemistry Frontiers","2019","6","4","432","","10.1039/C8QO01068D","","","0.71073","MoKα","","0.048","0.0377","","","0.0832","0.0897","","","","","","1.05","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554495","9.1577","0.0009","10.7173","0.0007","13.3021","0.001","106.893","0.003","91.497","0.004","91.349","0.003","1248.12","0.18","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C25 H20 N4 O2 -","- C25 H20 N4 O2 -","- C50 H40 N8 O4 -","2","1","","Chang, Yu-Che; Prakash, Sekar; Cheng, Chien-Hong","ReI-Catalyzed highly regio- and stereoselective C–H addition to terminal and internal alkynes","Organic Chemistry Frontiers","2019","6","4","432","","10.1039/C8QO01068D","","","0.71073","MoKα","","0.1257","0.1087","","","0.2187","0.2278","","","","","","1.101","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554496","8.5256","0.0003","16.9053","0.0005","8.9274","0.0003","90","","112.31","0.004","90","","1190.37","0.08","293","2","293","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C30 H25 N O3 -","- C30 H25 N O3 -","- C60 H50 N2 O6 -","2","1","","Xu, Jianfeng; Peng, Jingyi; He, Chonglong; Ren, Hongjun","N-Heterocyclic carbene catalyzed chemo- and enantioselective cross-benzoin reaction of aldehydes with isatins","Organic Chemistry Frontiers","2019","6","2","172","","10.1039/C8QO01085D","","","1.54184","CuKα","","0.0359","0.0348","","","0.0962","0.0974","","","","","","1.045","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554497","12.268","0.002","8.6753","0.0017","37.965","0.007","90","","92.878","0.003","90","","4035.5","1.3","273.15","","273.15","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C18 H12 Cl3 O P S3 -","- C18 H12 Cl3 O P S3 -","- C144 H96 Cl24 O8 P8 S24 -","8","1","","Lu, Guozhang; Chen, Jun; Huangfu, Xinlei; Li, Xueyan; Fang, Meijuan; Tang, Guo; Zhao, Yufen","Visible-light-mediated direct synthesis of phosphorotrithioates as potent anti-inflammatory agents from white phosphorus","Organic Chemistry Frontiers","2019","6","2","190","","10.1039/C8QO01087K","","","0.71073","MoKα","","0.0596","0.0534","","","0.1351","0.139","","","","","","1.148","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554498","25.2058","0.0019","7.2704","0.0006","19.2306","0.0015","90","","105.306","0.002","90","","3399.1","0.5","100","","100","","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C38 H42 Cl2 O7 -","- C38 H42 Cl2 O7 -","- C152 H168 Cl8 O28 -","4","1","","Fan, Jian-Hong; Hu, Ya-Jian; Guo, Qiang; Li, Shaoping; Zhao, Jing; Li, Chuang-Chuang","Asymmetric synthesis of the tetracyclic core of bufogargarizin C by an intramolecular [5 + 2] cycloaddition","Organic Chemistry Frontiers","2019","6","1","22","","10.1039/C8QO01089G","","x-ray","0.71073","MoKα","","0.0433","0.0408","","","0.0936","0.0945","","","","","","1.107","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554499","7.8836","0.0005","12.2399","0.0008","11.1988","0.0008","90","","90.174","0.002","90","","1080.62","0.13","120","2","120","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C27 H22 N O2 P -","- C27 H22 N O2 P -","- C54 H44 N2 O4 P2 -","2","1","","Zhang, Dong-Liang; Li, Cheng-Kun; Zeng, Run-Sheng; Shoberu, Adedamola; Zou, Jian-Ping","Manganese(iii)-mediated selective phosphorylation of enamides: direct synthesis of β-phosphoryl enamides","Organic Chemistry Frontiers","2019","6","2","236","","10.1039/C8QO01098F","","","0.71073","MoKα","","0.0275","0.0269","","","0.0732","0.0738","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554500","6.0253","0.0006","9.0011","0.0009","10.3679","0.0011","75.005","0.003","76.437","0.003","89.09","0.003","527.4","0.09","120","2","120","2","","","","","","","","5","P 1","P 1","1","","","","- C27 H22 N O2 P -","- C27 H22 N O2 P -","- C27 H22 N O2 P -","1","1","","Zhang, Dong-Liang; Li, Cheng-Kun; Zeng, Run-Sheng; Shoberu, Adedamola; Zou, Jian-Ping","Manganese(iii)-mediated selective phosphorylation of enamides: direct synthesis of β-phosphoryl enamides","Organic Chemistry Frontiers","2019","6","2","236","","10.1039/C8QO01098F","","","0.71073","MoKα","","0.0488","0.0427","","","0.085","0.0879","","","","","","1.067","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554501","23.47","0.002","9.9387","0.0006","17.2934","0.0012","90","","123.484","0.007","90","","3364.4","0.5","293","2","293","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C19 H15 F3 O4 -","- C19 H15 F3 O4 -","- C152 H120 F24 O32 -","8","1","","Chen, Yueji; You, Yi; Weng, Zhiqiang","Syntheses of 2-(2,2,2-trifluoroethylidene)/(2,2-difluoroethyl)-1,3-dicarbonyl compounds and their fungicidal activities","Organic Chemistry Frontiers","2019","6","2","213","","10.1039/C8QO01118D","","","0.71073","MoKα","","0.0537","0.0407","","","0.1194","0.1456","","","","","","1.13","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554502","13.7491","0.0016","5.8303","0.0005","21.42","0.003","90","","105.814","0.012","90","","1652.1","0.3","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C17 H12 Br2 F2 O2 -","- C17 H12 Br2 F2 O2 -","- C68 H48 Br8 F8 O8 -","4","1","","Chen, Yueji; You, Yi; Weng, Zhiqiang","Syntheses of 2-(2,2,2-trifluoroethylidene)/(2,2-difluoroethyl)-1,3-dicarbonyl compounds and their fungicidal activities","Organic Chemistry Frontiers","2019","6","2","213","","10.1039/C8QO01118D","","","0.71073","MoKα","","0.1837","0.0882","","","0.1408","0.1687","","","","","","1.017","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554503","21.2879","0.0007","7.5138","0.0004","11.5723","0.0006","90","","90","","90","","1851.02","0.15","100","2","100","2","","","","","","","","4","P 21 21 2","P 2 2ab","18","","","","- C22 H21 N O5 -","- C22 H21 N O5 -","- C88 H84 N4 O20 -","4","1","","Shoji, Taku; Araki, Takanori; Iida, Nanami; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Okujima, Tetsuo","Synthesis of azulenophthalimides by phosphine-mediated annulation of 1,2-diformylazulenes with maleimides","Organic Chemistry Frontiers","2019","6","2","195","","10.1039/C8QO01121D","","","0.71075","MoKα","","0.0612","0.0492","","","0.1036","0.1087","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554504","25.2081","0.0012","25.2081","0.0012","30.11","0.0016","90","","90","","120","","16570","1.4","101","2","101","2","","","","","","","","6","R -3 :H","-R 3","148","","","","- C68 H68 Cl6 N4 O10 P2 -","- C68 H68 Cl6 N4 O10 P2 -","- C612 H612 Cl54 N36 O90 P18 -","9","0.5","","Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan","Anion–π and anion–π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts","Organic Chemistry Frontiers","2019","6","1","110","","10.1039/C8QO01122B","","","1.54178","CuKα","","0.0688","0.0656","","","0.1913","0.1949","","","","","","0.996","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554505","19.7346","0.0013","19.9943","0.0012","14.9829","0.0007","90","","110.36","0.002","90","","5542.6","0.6","100","2","100","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C66 H66 I N2 O4 P2 -","- C66 H66 I N2 O4 P2 -","- C264 H264 I4 N8 O16 P8 -","4","0.5","","Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan","Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts","Organic Chemistry Frontiers","2019","6","1","110","","10.1039/C8QO01122B","","","0.71073","MoKα","","0.0664","0.0566","","","0.1493","0.1555","","","","","","1.039","","","","has coordinates,has disorder","237297","2020-10-21","18:00:00",""
"1554506","10.967","0.0006","15.8648","0.001","20.3172","0.0011","90","","105.084","0.003","90","","3413.2","0.3","100","2","100","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C34 H34 Br Cl3 N O2 P -","- C34 H34 Br Cl3 N O2 P -","- C136 H136 Br4 Cl12 N4 O8 P4 -","4","1","","Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan","Anion–π and anion–π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts","Organic Chemistry Frontiers","2019","6","1","110","","10.1039/C8QO01122B","","","1.54178","CuKα","","0.0818","0.063","","","0.1632","0.1801","","","","","","1.042","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554507","19.664","0.0005","19.9512","0.0006","15.5025","0.0004","90","","111.125","0.001","90","","5673.2","0.3","100","2","100","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C66 H66 F6 N2 O4 P3 -","- C66 H66 F6 N2 O4 P3 -","- C264 H264 F24 N8 O16 P12 -","4","0.5","","Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan","Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts","Organic Chemistry Frontiers","2019","6","1","110","","10.1039/C8QO01122B","","","1.54178","CuKα","","0.0587","0.0565","","","0.154","0.1587","","","","","","1.066","","","","has coordinates,has disorder","237297","2020-10-21","18:00:00",""
"1554508","24.8062","0.0009","24.8062","0.0009","30.0418","0.0011","90","","90","","120","","16009.5","1","100","2","100","2","","","","","","","","6","R -3 :H","-R 3","148","","","","- C66 H66 Cl N2 O7.33 P2 -","- C66 H66 Cl1.00013 N2 O7.33333 P2 -","- C594 H594 Cl9.0012 N18 O66 P18 -","9","0.5","","Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan","Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts","Organic Chemistry Frontiers","2019","6","1","110","","10.1039/C8QO01122B","","","1.54178","CuKα","","0.1453","0.1377","","","0.4022","0.4169","","","","","","2.015","","","","has coordinates,has disorder","237297","2020-10-21","18:00:00",""
"1554509","15.5817","0.0005","20.6208","0.0006","22.0566","0.0007","90","","90","","90","","7086.9","0.4","100","2","100","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C74 H86 F12 N2 O6 P4 -","- C74 H86 F12 N2 O6 P4 -","- C296 H344 F48 N8 O24 P16 -","4","0.5","","Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan","Anion–π and anion–π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts","Organic Chemistry Frontiers","2019","6","1","110","","10.1039/C8QO01122B","","","1.54178","CuKα","","0.1075","0.1029","","","0.2711","0.2756","","","","","","1.046","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554510","14.2234","0.0009","15.5567","0.0011","12.5242","0.0008","90","","108.744","0.002","90","","2624.2","0.3","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C66 H66 N2 O4 P2 -","- C66 H66 N2 O4 P2 -","- C132 H132 N4 O8 P4 -","2","0.5","","Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan","Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts","Organic Chemistry Frontiers","2019","6","1","110","","10.1039/C8QO01122B","","","1.54178","CuKα","","0.0775","0.0711","","","0.2076","0.2176","","","","","","1.119","","","","has coordinates,has disorder","237297","2020-10-21","18:00:00",""
"1554511","24.7543","0.0007","24.7543","0.0007","30.0212","0.0009","90","","90","","120","","15931.6","0.8","100","","99.99","","","","","","","","","6","R -3 :H","-R 3","148","","","","- C66 H66 Br N2 O4 P2 -","- C66 H66 Br0.990667 N2 O4 P2 -","- C594 H594 Br8.916 N18 O36 P18 -","9","0.5","","Ng, Chee Koon; Tam, Teck Lip Dexter; Wei, Fengxia; Lu, Xuefeng; Wu, Jishan","Anion‒π and anion‒π-radical interactions in bis(triphenylphosphonium)-naphthalene diimide salts","Organic Chemistry Frontiers","2019","6","1","110","","10.1039/C8QO01122B","","","1.54184","CuKα","","0.1455","0.1345","","","0.3998","0.4175","","","","","","2.005","","","","has coordinates","237297","2020-10-21","18:00:00",""
"1554512","6.3585","0.0005","10.945","0.0011","17.5672","0.0013","90","","92.051","0.007","90","","1221.78","0.18","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C12 H17 N S -","- C12 H17 N S -","- C48 H68 N4 S4 -","4","1","","Lai, Miao; Wu, Zhiyong; Wang, Yizhi; Zheng, Ying; Zhao, Mingqin","Selective synthesis of aryl thioamides and aryl-α-ketoamides from α-oxocarboxylic acids and tetraalkylthiuram disulfides: an unexpected chemoselectivity from aryl sulfonyl chlorides","Organic Chemistry Frontiers","2019","6","4","506","","10.1039/C8QO01127C","","x-ray","1.54184","CuKα","","0.076","0.0566","","","0.1577","0.1751","","","","","","1.039","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554513","10.687","0.008","12.035","0.009","14.902","0.011","90","","90","","90","","1917","2","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C21 H19 Br O3 -","- C21 H19 Br O3 -","- C84 H76 Br4 O12 -","4","1","","Huang, Huicai; Lu, Xue; Mao, Yukang; Ye, Jinxing","Asymmetric synthesis of highly functionalized furanones via direct Michael reactions mediated by a bulky primary amine","Organic Chemistry Frontiers","2019","6","8","1080","","10.1039/C8QO01132J","","","0.71073","MoKα","","0.0873","0.0517","","","0.1255","0.1398","","","","","","1.008","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554514","10.4344","0.0002","11.4942","0.0002","11.5277","0.0002","90","","90","","90","","1382.58","0.04","288.3","0.1","288.3","0.1","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C17 H20 O3 -","- C17 H20 O3 -","- C68 H80 O12 -","4","1","","Xu, Weici; Li, Yuanzhen; Liu, Rui; Yang, Shuang; Liu, Jian; Fang, Xinqiang","Kinetic resolution of 2,2-disubstituted-1,3-diketones via carbene catalysis","Organic Chemistry Frontiers","2019","6","3","290","","10.1039/C8QO01137K","","","1.54184","CuKα","","0.0333","0.0312","","","0.0783","0.0804","","","","","","1.062","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554515","8.431","0.0006","8.6965","0.0005","11.7742","0.0005","80.603","0.004","87.055","0.004","65.92","0.006","777.47","0.09","100","0.1","100","0.1","","","","","","","","3","P -1","-P 1","2","","","","- C20 H20 O3 -","- C20 H20 O3 -","- C40 H40 O6 -","2","1","","Xu, Weici; Li, Yuanzhen; Liu, Rui; Yang, Shuang; Liu, Jian; Fang, Xinqiang","Kinetic resolution of 2,2-disubstituted-1,3-diketones via carbene catalysis","Organic Chemistry Frontiers","2019","6","3","290","","10.1039/C8QO01137K","","","1.54184","CuKα","","0.0425","0.0362","","","0.0912","0.0961","","","","","","1.045","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554516","9.8733","0.0007","10.3877","0.0007","37.781","0.002","90","","96.893","0.006","90","","3846.8","0.4","100","0.6","100","0.6","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C25 H21 F O3 -","- C25 H21 F O3 -","- C200 H168 F8 O24 -","8","2","","Xu, Weici; Li, Yuanzhen; Liu, Rui; Yang, Shuang; Liu, Jian; Fang, Xinqiang","Kinetic resolution of 2,2-disubstituted-1,3-diketones via carbene catalysis","Organic Chemistry Frontiers","2019","6","3","290","","10.1039/C8QO01137K","","","1.54184","CuKα","","0.1466","0.0889","","","0.1572","0.1914","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554517","23.63","0.002","42.848","0.004","5.8546","0.0005","90","","90","","90","","5927.8","0.9","293","2","293","2","","","","","","","","3","F d d 2","F 2 -2d","43","","","","- C19 H16 O2 -","- C19 H16 O2 -","- C304 H256 O32 -","16","1","","Fan, Jian; Wang, Shengke; Chen, Jiahui; Wu, Manyi; Zhang, Jitan; Xie, Meihua","Synthesis of 2-acetyl trisubstituted furans via copper-mediated deacylation cleavage of unstrained C(sp3)–C(sp2) bonds","Organic Chemistry Frontiers","2019","6","4","437","","10.1039/C8QO01139G","","","0.71073","MoKα","","0.0497","0.0396","","","0.0922","0.0979","","","","","","1.073","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554518","10.476","0.011","15.249","0.018","11.317","0.013","90","","116.28","0.03","90","","1621","3","273","2","273","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C20 H18 O3 -","- C20 H18 O3 -","- C80 H72 O12 -","4","1","","Fan, Jian; Wang, Shengke; Chen, Jiahui; Wu, Manyi; Zhang, Jitan; Xie, Meihua","Synthesis of 2-acetyl trisubstituted furans via copper-mediated deacylation cleavage of unstrained C(sp3)‒C(sp2) bonds","Organic Chemistry Frontiers","2019","6","4","437","","10.1039/C8QO01139G","","","0.71073","MoKα","","0.0851","0.0682","","","0.1841","0.2064","","","","","","1.054","","","","has coordinates,has disorder","237304","2020-10-21","18:00:00",""
"1554519","8.3257","0.0007","15.1988","0.0012","16.3404","0.0013","90","","95.005","0.004","90","","2059.8","0.3","303","2","303","2","","","","","","","","5","I 1 a 1","I -2ya","9","","","","- C23 H21 N O3 S -","- C23 H21 N O3 S -","- C92 H84 N4 O12 S4 -","4","1","","Zhu, Tong-Hao; Zhang, Xiao-Chen; Zhao, Kai; Loh, Teck-Peng","Cu(OTf)2-mediated C(sp2)–H arylsulfonylation of enamides via the insertion of sulfur dioxide","Organic Chemistry Frontiers","2019","6","1","94","","10.1039/C8QO01144C","","","0.71073","MoKα","","0.0487","0.045","","","0.131","0.1373","","","","","","0.898","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554520","11.8106","0.0004","12.5767","0.0004","26.9924","0.001","90","","90","","90","","4009.4","0.2","100","0.3","100","0.3","","","","","","","Marine Sponge-Derived Fungus Aspergillus versicolor SCSIO 41016","4","P 21 21 21","P 2ac 2ab","19","(1R,4R)-4-benzyl-1-((S)-sec-butyl)-1-methoxy-1,2-dihydro-6H-pyrazino[2,1-b]quinazoline-3,6(4H)-dione","Brevianamide Y","","- C23 H25 N3 O3 -","- C23 H25 N3 O3 -","- C184 H200 N24 O24 -","8","2","","Luo, Xiaowei; Chen, Chunmei; Tao, Huaming; Lin, Xiuping; Yang, Bin; Zhou, Xuefeng; Liu, Yonghong","Structurally diverse diketopiperazine alkaloids from the marine-derived fungus Aspergillus versicolor SCSIO 41016","Organic Chemistry Frontiers","2019","6","6","736","","10.1039/C8QO01147H","","x-ray","1.54184","CuKα","","0.063","0.0501","","","0.1333","0.1414","","","","","","1.029","","","","has coordinates","277994","2022-09-20","08:32:41",""
"1554521","9.115","0.003","9.448","0.002","11.944","0.003","101.46","0.02","91.031","0.006","106.62","0.007","962.9","0.5","173","","173","","","","","","","","","5","P -1","-P 1","2","","","","- C20 H23 N2 O3 P -","- C20 H23 N2 O3 P -","- C40 H46 N4 O6 P2 -","2","1","","Yang, Qiaolan; Wu, Chenglin; Zhou, Jianhui; He, Guoxue; Liu, Hong; Zhou, Yu","Highly selective C–H bond activation of N-arylbenzimidamide and divergent couplings with diazophosphonate compounds: a catalyst-controlled selective synthetic strategy for 3-phosphorylindoles and 4-phosphorylisoquinolines","Organic Chemistry Frontiers","2019","6","3","393","","10.1039/C8QO01148F","","","0.71073","MoKα","","0.0985","0.0841","","","0.2742","0.2831","","","","","","1.17","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554522","7.6453","0.0019","11.642","0.003","9.808","0.003","90","","102.969","0.008","90","","850.7","0.4","173","","173","","","","","","","","","5","P 1 c 1","P -2yc","7","","","","- C18 H20 N O3 P -","- C18 H20 N O3 P -","- C36 H40 N2 O6 P2 -","2","1","","Yang, Qiaolan; Wu, Chenglin; Zhou, Jianhui; He, Guoxue; Liu, Hong; Zhou, Yu","Highly selective C–H bond activation of N-arylbenzimidamide and divergent couplings with diazophosphonate compounds: a catalyst-controlled selective synthetic strategy for 3-phosphorylindoles and 4-phosphorylisoquinolines","Organic Chemistry Frontiers","2019","6","3","393","","10.1039/C8QO01148F","","","0.71073","MoKα","","0.0904","0.0586","","","0.1416","0.1677","","","","","","0.883","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554523","27.337","0.003","6.1593","0.0004","20.343","0.002","90","","106.22","0.01","90","","3288.9","0.6","100","","100","","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C30 H40 N6 O12 -","- C30 H36 N6 O12.004 -","- C120 H144 N24 O48.016 -","4","0.5","","Savastano, Matteo; Bazzicalupi, Carla; García-Gallarín, Celeste; López de la Torre, Maria Dolores; Bianchi, Antonio; Melguizo, Manuel","Supramolecular forces and their interplay in stabilizing complexes of organic anions: tuning binding selectivity in water","Organic Chemistry Frontiers","2019","6","1","75","","10.1039/C8QO01152D","","","1.5418","CuKα","","0.0568","0.0466","","","0.1386","0.1599","","","","","","0.807","","","","has coordinates","237310","2020-10-21","18:00:00",""
"1554524","6.8698","0.0001","14.4541","0.0003","14.7842","0.0003","90","","95.204","0.002","90","","1461.97","0.05","100","","100","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C30 H36 N6 O10 -","- C30 H36 N6 O10 -","- C60 H72 N12 O20 -","2","0.5","","Savastano, Matteo; Bazzicalupi, Carla; García-Gallarín, Celeste; López de la Torre, Maria Dolores; Bianchi, Antonio; Melguizo, Manuel","Supramolecular forces and their interplay in stabilizing complexes of organic anions: tuning binding selectivity in water","Organic Chemistry Frontiers","2019","6","1","75","","10.1039/C8QO01152D","","","1.54184","CuKα","","0.0702","0.0513","","","0.1411","0.1714","","","","","","1.081","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554525","15.1627","0.0005","6.4915","0.0004","29.4057","0.0009","90","","90","","90","","2894.4","0.2","100","","100","","","","","","","","","5","P n a 21","P 2c -2n","33","","","","- C26 H38 N6 O9 S2 -","- C26 H38 N6 O9 S2 -","- C104 H152 N24 O36 S8 -","4","1","","Savastano, Matteo; Bazzicalupi, Carla; García-Gallarín, Celeste; López de la Torre, Maria Dolores; Bianchi, Antonio; Melguizo, Manuel","Supramolecular forces and their interplay in stabilizing complexes of organic anions: tuning binding selectivity in water","Organic Chemistry Frontiers","2019","6","1","75","","10.1039/C8QO01152D","","","1.54184","CuKα","","0.0311","0.0287","","","0.0741","0.0755","","","","","","0.973","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554526","11.4833","0.0006","7.3773","0.0005","13.116","0.0007","90","","96.533","0.004","90","","1103.92","0.11","173","2","173","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C21 H28 N2 O8 -","- C21 H28 N2 O8 -","- C42 H56 N4 O16 -","2","1","","Ma, Qiaoning; Yang, Xiaodi; Lei, Xinsheng; Lin, Guo-Qiang","A highly enantioselective synthetic method towards the α2c-adrenoceptor antagonist ORM-10921","Organic Chemistry Frontiers","2019","6","6","773","","10.1039/C8QO01166D","","","1.54178","CuKα","","0.1605","0.1491","","","0.3396","0.3552","","","","","","1.408","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554527","6.1903","0.0012","13.744","0.003","32.103","0.006","90","","90","","90","","2731.3","0.9","294","2","294","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C32 H34 Br0 Cl N O4 -","- C32 H34 Cl N O4 -","- C128 H136 Cl4 N4 O16 -","4","1","","Ma, Qiaoning; Yang, Xiaodi; Lei, Xinsheng; Lin, Guo-Qiang","A highly enantioselective synthetic method towards the α2c-adrenoceptor antagonist ORM-10921","Organic Chemistry Frontiers","2019","6","6","773","","10.1039/C8QO01166D","","","1.54178","CuKα","","0.0353","0.034","","","0.0874","0.0887","","","","","","1.062","","","","has coordinates","237312","2020-10-21","18:00:00",""
"1554528","7.976","0.003","8.218","0.003","15.344","0.006","94.059","0.008","104.85","0.007","97.364","0.008","958.5","0.6","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C5 H4 F N5 O6 -","- C5 H4 F N5 O6 -","- C20 H16 F4 N20 O24 -","4","2","","Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B.","N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design","Organic Chemistry Frontiers","2019","6","2","249","","10.1039/C8QO01173G","","","0.71073","MoKα","","0.0853","0.0448","","","0.0884","0.1034","","","","","","1.009","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554529","5.4659","0.0012","10.477","0.002","8.1322","0.0017","90","","94.857","0.004","90","","464.03","0.17","100","2","100","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C5 H4 F N5 O6 -","- C5 H4 F N5 O6 -","- C10 H8 F2 N10 O12 -","2","1","","Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B.","N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design","Organic Chemistry Frontiers","2019","6","2","249","","10.1039/C8QO01173G","","","0.71073","MoKα","","0.0763","0.0431","","","0.0688","0.0781","","","","","","0.987","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554530","11.4331","0.0011","5.7212","0.0006","11.2434","0.0011","90","","90","","90","","735.44","0.13","100","2","100","2","","","","","","","","5","P n a 21","P 2c -2n","33","","","","- C3 H3 F N6 O4 -","- C3 H3 F N6 O4 -","- C12 H12 F4 N24 O16 -","4","1","","Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B.","N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design","Organic Chemistry Frontiers","2019","6","2","249","","10.1039/C8QO01173G","","","0.71073","MoKα","","0.033","0.0289","","","0.0628","0.0648","","","","","","1.045","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554531","6.6055","0.0003","11.5186","0.0005","23.4809","0.001","90","","90","","90","","1786.57","0.14","100","2","100","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C5 H4 F N5 O6 -","- C5 H4 F N5 O6 -","- C40 H32 F8 N40 O48 -","8","1","","Palysaeva, Nadezhda V.; Gladyshkin, Aleksei G.; Vatsadze, Irina A.; Suponitsky, Kyrill Yu.; Dmitriev, Dmitry E.; Sheremetev, Aleksei B.","N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design","Organic Chemistry Frontiers","2019","6","2","249","","10.1039/C8QO01173G","","","0.71073","MoKα","","0.0368","0.0317","","","0.0837","0.0878","","","","","","1.039","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554532","14.3845","0.0014","4.3448","0.0004","23.199","0.002","90","","90","","90","","1449.9","0.2","100","2","100","2","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C19 H15 N O3 -","- C19 H15 N O3 -","- C76 H60 N4 O12 -","4","1","","Wagh, Sachin Bhausaheb; Sharma, Pankaj; Patil, Manoj D.; Liu, Rai-Shung","Gold-catalyzed oxidative cycloalkenations of alkynes with quinoline N-oxides","Organic Chemistry Frontiers","2019","6","2","226","","10.1039/C8QO01175C","","","0.71073","MoKα","","0.051","0.0375","","","0.0747","0.0802","","","","","","1.035","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554533","21.0827","0.0015","8.2829","0.0006","8.2169","0.0004","90","","95.222","0.002","90","","1428.93","0.16","200","2","200","2","","","","","","","","4","P 1 c 1","P -2yc","7","","","","- C19 H15 N O2 -","- C19 H15 N O2 -","- C76 H60 N4 O8 -","4","2","","Wagh, Sachin Bhausaheb; Sharma, Pankaj; Patil, Manoj D.; Liu, Rai-Shung","Gold-catalyzed oxidative cycloalkenations of alkynes with quinoline N-oxides","Organic Chemistry Frontiers","2019","6","2","226","","10.1039/C8QO01175C","","","0.71073","MoKα","","0.0603","0.0448","","","0.1034","0.1156","","","","","","1.013","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554534","9.2179","0.0004","10.4777","0.0005","14.2247","0.0007","100.062","0.002","92.031","0.002","103.287","0.002","1312.41","0.11","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C28 H33 Au Cl O2 P -","- C28 H33 Au Cl O2 P -","- C56 H66 Au2 Cl2 O4 P2 -","2","1","","Wagh, Sachin Bhausaheb; Sharma, Pankaj; Patil, Manoj D.; Liu, Rai-Shung","Gold-catalyzed oxidative cycloalkenations of alkynes with quinoline N-oxides","Organic Chemistry Frontiers","2019","6","2","226","","10.1039/C8QO01175C","","","0.71073","MoKα","","0.0196","0.0186","","","0.0442","0.048","","","","","","1.137","","","","has coordinates","237315","2020-10-21","18:00:00",""
"1554535","11.0158","0.0017","12.13","0.0016","23.587","0.003","90","","90","","90","","3151.7","0.8","295.19","0.1","295.19","0.1","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C33 H32 Cl N O9 -","- C33 H32 Cl N O9 -","- C132 H128 Cl4 N4 O36 -","4","1","","Cao, Jian; Liu, Jin-Yu; Zhang, Yi-Ming; Wang, Zhu-Yin; Xu, Peng-Fei","Synergistic promotion by intramolecular hydrogen bonding: a bi-functionally catalyzed cascade reaction for the synthesis of enantiopure chromenopyrrolidines","Organic Chemistry Frontiers","2019","6","5","674","","10.1039/C8QO01208C","","","0.71073","MoKα","","0.1754","0.0917","","","0.2117","0.2924","","","","","","0.989","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554536","7.0667","0.0003","23.0878","0.001","21.9663","0.0007","90","","90","","90","","3583.9","0.2","150.01","0.1","150.01","0.1","","","","","","","","5","P c a 21","P 2c -2ac","29","","","","- C20 H15 Br2 N O2 -","- C20 H15 Br2 N O2 -","- C160 H120 Br16 N8 O16 -","8","2","","Liu, Zhenhua; Zhu, Guangyu; Gao, Wen; Yang, Lin; Ji, Huimin; Tong, Lili; Tang, Bo","Copper-catalyzed regioselective cyclization of vinyl azides by gem-difluoromethylene for trisubstituted pyridines","Organic Chemistry Frontiers","2019","6","4","468","","10.1039/C8QO01212A","","x-ray","1.54178","CuKα","","0.048","0.0415","","","0.1039","0.1129","","","","","","1.042","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554537","5.2572","0.001","12.458","0.003","13.205","0.003","69.94","0.03","83.57","0.03","89.74","0.03","806.7","0.3","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C17 H17 Br N4 O -","- C17 H17 Br N4 O -","- C34 H34 Br2 N8 O2 -","2","1","","Lemport, Pavel S.; Smolyar, Ivan V.; Khrustalev, Victor N.; Roznyatovsky, Vitaly A.; Popov, Alexander V.; Kobelevskaya, Valentina A.; Rozentsveig, Igor B.; Nenajdenko, Valentine G.","3,3-Diazidoenones – new types of highly reactive bis-azides. Preparation and synthetic transformations","Organic Chemistry Frontiers","2019","6","3","335","","10.1039/C8QO01214H","","","0.9626","synchrotron","","0.0871","0.0615","","","0.1321","0.1567","","","","","","1.057","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554538","12.429","0.003","10.415","0.002","37.841","0.008","90","","90.13","0.03","90","","4898.4","1.8","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C27 H21 N2 O P -","- C27 H21 N2 O P -","- C216 H168 N16 O8 P8 -","8","2","","Lemport, Pavel S.; Smolyar, Ivan V.; Khrustalev, Victor N.; Roznyatovsky, Vitaly A.; Popov, Alexander V.; Kobelevskaya, Valentina A.; Rozentsveig, Igor B.; Nenajdenko, Valentine G.","3,3-Diazidoenones – new types of highly reactive bis-azides. Preparation and synthetic transformations","Organic Chemistry Frontiers","2019","6","3","335","","10.1039/C8QO01214H","","","0.9626","synchrotron","","0.0717","0.0524","","","0.1369","0.1567","","","","","","1.057","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554539","8.8134","0.0002","10.3559","0.0003","18.035","0.0004","100.993","0.002","95.022","0.002","92.933","0.002","1605.78","0.07","293","2","293","","","","","","","","","5","P -1","-P 1","2","","","","- C34 H44 N2 O Si -","- C34 H44 N2 O Si -","- C68 H88 N4 O2 Si2 -","2","1","","Chen, Cui-Hong; Chai, Yun; Zhou, Zheng-Xin; Rao, Wei-Hao; Liu, Bin; Liu, Li; Xu, Ran; Liu, Yue-Jin; Zeng, Ming-Hua","Room-temperature Pd(ii)-catalyzed direct C–H TIPS-ethynylation of phenylacetic amides with terminal alkynes","Organic Chemistry Frontiers","2019","6","4","442","","10.1039/C8QO01215F","","x-ray","1.54184","CuKα","","0.0943","0.0837","","","0.2634","0.2881","","","","","","1.199","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554540","44.902","0.003","11.1591","0.001","10.6337","0.0007","90","","90","","90","","5328.2","0.7","293","2","293.15","","","","","","","","","2","P m n 21","P 2ac -2","31","","","","- C35 H30 -","- C35 H30 -","- C280 H240 -","8","2","","Liu, Peiren; Li, Qi; Zeng, Hong; Shi, Bingbing; Liu, Jiyong; Huang, Feihe","[15]Paracyclophane and [16]paracyclophane: facile syntheses, crystal structures and selective complexation with cesium cations in the gas phase","Organic Chemistry Frontiers","2019","6","3","309","","10.1039/C8QO01218K","","","0.71073","MoKα","","0.1151","0.0659","","","0.1395","0.1705","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554541","11.372","0.0004","13.1796","0.0006","24.509","0.001","105.144","0.004","93.375","0.003","90.36","0.003","3538.8","0.3","296","2","296.15","","","","","","","","","2","P -1","-P 1","2","","","","- C42 H36 -","- C42 H36 -","- C168 H144 -","4","2","","Liu, Peiren; Li, Qi; Zeng, Hong; Shi, Bingbing; Liu, Jiyong; Huang, Feihe","[15]Paracyclophane and [16]paracyclophane: facile syntheses, crystal structures and selective complexation with cesium cations in the gas phase","Organic Chemistry Frontiers","2019","6","3","309","","10.1039/C8QO01218K","","","0.71073","MoKα","","0.1065","0.0559","","","0.1406","0.1715","","","","","","1.019","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554542","14.2625","0.0006","18.0213","0.0012","31.3062","0.0019","86.466","0.005","83.674","0.005","83.298","0.005","7933.2","0.8","173","1","173","1","","","","","","","","5","P -1","-P 1","2","2S1Se","2S1Se","","- C42 H54 O6 S2 Se -","- C42 H54 O6 S2.0001 Se0.9999 -","- C336 H432 O48 S16.0008 Se7.9992 -","8","4","","Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng","Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity","Organic Chemistry Frontiers","2019","6","2","263","","10.1039/C8QO01220B","","","0.71073","MoKα","","0.3577","0.1279","","","0.2179","0.3316","","","","","","0.978","","","","has coordinates,has disorder","237326","2020-10-21","18:00:00",""
"1554543","17.4194","0.0002","8.2052","0.0001","28.3968","0.0004","90","","90.166","0.001","90","","4058.73","0.09","290","1","290","1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","2S1Se_Ester","2S1Se_Ester","","- C42 H54 O8 S2 Se -","- C42 H53.2 O8 S2 Se -","- C168 H212.8 O32 S8 Se4 -","4","1","","Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng","Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity","Organic Chemistry Frontiers","2019","6","2","263","","10.1039/C8QO01220B","","","1.54184","CuKα","","0.1591","0.1451","","","0.4154","0.4404","","","","","","1.954","","","","has coordinates,has disorder","237326","2020-10-21","18:00:00",""
"1554544","12.1441","0.0008","16.8305","0.0009","20.8669","0.0013","98.844","0.005","91.448","0.005","102.981","0.005","4098.7","0.4","174","2","174","2","","","","","","","","5","P -1","-P 1","2","2Te1se","2Te1Se","","- C42 H54 O6 Se Te2 -","- C42 H54 O6 Se0.9999 Te2.0001 -","- C168 H216 O24 Se3.9996 Te8.0004 -","4","2","","Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng","Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity","Organic Chemistry Frontiers","2019","6","2","263","","10.1039/C8QO01220B","","","0.71073","MoKα","","0.222","0.1224","","","0.2831","0.3567","","","","","","1.05","","","","has coordinates,has disorder","237326","2020-10-21","18:00:00",""
"1554545","14.2879","0.0004","18.0394","0.0007","31.4094","0.0008","86.414","0.002","83.365","0.002","83.373","0.002","7977.7","0.4","174","2","174","2","","","","","","","","5","P -1","-P 1","2","2Se1S","2Se1S","","- C42 H54 O6 S Se2 -","- C42 H54 O6 S0.9999 Se2.0001 -","- C336 H432 O48 S7.9992 Se16.0008 -","8","4","","Wang, Shitao; Shang, Jihai; Yan, Chaoxian; Wang, Wenbo; Yuan, Chengshan; Zhang, Hao-Li; Shao, Xiangfeng","Trichalcogenasumanenes containing various chalcogen atoms: synthesis, structure, properties, and chemical reactivity","Organic Chemistry Frontiers","2019","6","2","263","","10.1039/C8QO01220B","","","0.71073","MoKα","","0.147","0.0737","","","0.1493","0.1919","","","","","","1.024","","","","has coordinates,has disorder","237326","2020-10-21","18:00:00",""
"1554546","13.0718","0.0011","15.5471","0.0013","10.5005","0.0009","90","","113.181","0.001","90","","1961.7","0.3","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C24 H19 Br N2 O -","- C24 H19 Br N2 O -","- C96 H76 Br4 N8 O4 -","4","1","","Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying","Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles","Organic Chemistry Frontiers","2019","6","2","256","","10.1039/C8QO01222A","","","0.71073","MoKα","","0.0703","0.043","","","0.0855","0.0951","","","","","","1.005","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554547","12.9966","0.0015","15.5319","0.0017","10.522","0.0012","90","","113.397","0.002","90","","1949.3","0.4","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C24 H19 Cl N2 O -","- C24 H19 Cl N2 O -","- C96 H76 Cl4 N8 O4 -","4","1","","Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying","Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles","Organic Chemistry Frontiers","2019","6","2","256","","10.1039/C8QO01222A","","","0.71073","MoKα","","0.1316","0.0594","","","0.1392","0.1615","","","","","","0.835","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554548","9.5976","0.0009","10.3316","0.0009","13.9249","0.0013","90","","90","","90","","1380.8","0.2","100","2","100","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C16 H14 Cl N O2 -","- C16 H14 Cl N O2 -","- C64 H56 Cl4 N4 O8 -","4","1","","Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying","Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles","Organic Chemistry Frontiers","2019","6","2","256","","10.1039/C8QO01222A","","","0.71073","MoKα","","0.0261","0.0251","","","0.0706","0.0713","","","","","","1.064","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554549","8.802","0.0005","9.9463","0.0007","10.213","0.0008","116.522","0.007","100.853","0.006","103.243","0.005","734.13","0.11","100","0.1","100","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C19 H16 N2 O -","- C19 H16 N2 O -","- C38 H32 N4 O2 -","2","1","","Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying","Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles","Organic Chemistry Frontiers","2019","6","2","256","","10.1039/C8QO01222A","","x-ray","0.71073","MoKα","","0.0591","0.048","","","0.1137","0.123","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554550","33.58","0.005","13.96","0.002","8.0737","0.0013","90","","100.506","0.003","90","","3721.3","1","100","2","100","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C19 H19 Cl2 N O4 -","- C19 H19 Cl2 N O4 -","- C152 H152 Cl16 N8 O32 -","8","1","","Liu, Xiong-Li; Yue, Jing; Chen, Shuang; Liu, Huan-Huan; Yang, Kai-Mo; Feng, Ting-Ting; Zhou, Ying","Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles","Organic Chemistry Frontiers","2019","6","2","256","","10.1039/C8QO01222A","","","0.71073","MoKα","","0.1178","0.0945","","","0.257","0.2749","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554551","11.8513","0.0006","8.0917","0.0004","24.6768","0.0012","90","","90","","90","","2366.4","0.2","295.38","0.1","295.38","0.1","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C13 H22 O2 -","- C13 H22 O2 -","- C104 H176 O16 -","8","1","","He, Min; Yi, Jiuzhou; Zhao, Gaoyuan; Chen, Peiqi; Long, Dan; Hu, Xiaojun; Li, Huilin; Xie, Xingang; Wang, Xiaolei; She, Xuegong","A concise approach to the tricyclic framework of longipinane- and ent-longipinane-type sesquiterpenoids","Organic Chemistry Frontiers","2019","6","3","383","","10.1039/C8QO01235K","","","0.71073","MoKα","","0.0908","0.0642","","","0.152","0.1749","","","","","","1.066","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554552","9.1789","0.0003","10.574","0.0003","11.4116","0.0004","90","","91.684","0.003","90","","1107.11","0.06","292","2","292","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C25 H24 O5 S -","- C25 H24 O5 S -","- C50 H48 O10 S2 -","2","1","","Zhang, Nan; He, Tingting; Liu, Yidong; Li, Shan; Tan, Yu; Peng, Lei; Li, Dongmei; Shan, Chunhui; Yan, Hailong","Organocatalytic atropo- and E/Z-selective Michael addition reaction of ynones with α-amido sulfones as sulfone-type nucleophile","Organic Chemistry Frontiers","2019","6","4","451","","10.1039/C8QO01241E","","","0.71073","MoKα","","0.0639","0.0464","","","0.0909","0.1016","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554553","9.809","0.008","9.877","0.008","9.925","0.008","66.084","0.014","65.463","0.014","64.347","0.015","758.1","1.1","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C12 H10 F3 N O6 Se -","- C12 H10 F3 N O6 Se -","- C24 H20 F6 N2 O12 Se2 -","2","1","","Ge, Hangming; Shen, Qilong","Trifluoromethyl-substituted selenium ylide: a broadly applicable electrophilic trifluoromethylating reagent","Organic Chemistry Frontiers","2019","6","13","2205","","10.1039/C8QO01249K","","","0.71073","MoKα","","0.0583","0.0435","","","0.093","0.0982","","","","","","1.001","","","","has coordinates","237335","2020-10-21","18:00:00",""
"1554554","10.5315","0.0008","7.0899","0.0004","12.4878","0.0012","90","","105.29","0.008","90","","899.43","0.13","113","2","113","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C20 H29 N O S -","- C20 H29 N O S -","- C40 H58 N2 O2 S2 -","2","1","","Qin, Shuanglin; Liu, Tongtong; Luo, Yunhao; Jiang, Shende; Yang, Guang","Diastereoselective Rh-catalyzed decarboxylative allylation to form quaternary stereocenters using sulfinimine as the directing group","Organic Chemistry Frontiers","2019","6","6","732","","10.1039/C8QO01258J","","","0.71073","MoKα","","0.0454","0.0372","","","0.0829","0.0865","","","","","","1.027","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554555","41.982","0.002","8.4505","0.0002","16.3226","0.0009","90","","123.085","0.008","90","","4851.8","0.6","100","0.1","100","0.1","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C26 H31 N3 Si -","- C26 H31 N3 Si -","- C208 H248 N24 Si8 -","8","1","","Wu, Wanqing; Fang, Songjia; Jiang, Guangbin; Li, Meng; Jiang, Huanfeng","Palladium-catalyzed regioselective C–H alkynylation of indoles with bromoalkynes in water","Organic Chemistry Frontiers","2019","6","13","2200","","10.1039/C8QO01261J","","x-ray","0.71073","MoKα","","0.104","0.0955","","","0.2461","0.2565","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554556","5.7768","0.0005","26.401","0.002","15.2336","0.0014","90","","95.248","0.002","90","","2313.6","0.3","298","2","298","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C30 H25 N O2 -","- C30 H25 N O2 -","- C120 H100 N4 O8 -","4","1","","Ji, Cheng-Long; Pan, Yao; Geng, Fang-Zhou; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo","Synergistic silver/scandium catalytic spiroketalization of β-alkynyl ketones for the atom economical synthesis of skeletally diverse spirocyclic isochromenes","Organic Chemistry Frontiers","2019","6","4","474","","10.1039/C8QO01277F","","","0.71073","MoKα","","0.1742","0.0652","","","0.069","0.0817","","","","","","1.006","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554557","31.1655","0.0005","8.4946","0.0001","13.3472","0.0002","90","","98.752","0.002","90","","3492.37","0.09","100","0.1","100","0.1","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C21 H21 N O2 S -","- C21 H21 N O2 S -","- C168 H168 N8 O16 S8 -","8","1","","Wu, Feng; Chen, Lianfen; Wang, Yongdong; Zhu, Shifa","Gold-catalyzed generation of azafulvenium from an enyne sulfonamide: rapid access to fully substituted pyrroles","Organic Chemistry Frontiers","2019","6","4","480","","10.1039/C8QO01278D","","x-ray","1.54184","CuKα","","0.0434","0.0423","","","0.1101","0.1111","","","","","","1.082","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554558","8.6549","0.0005","18.21","0.0011","11.9124","0.0006","90","","94.769","0.005","90","","1870.96","0.18","172.95","0.1","172.95","0.1","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C21 H18 Br N O3 S -","- C21 H18 Br N O3 S -","- C84 H72 Br4 N4 O12 S4 -","4","1","","Wu, Feng; Chen, Lianfen; Wang, Yongdong; Zhu, Shifa","Gold-catalyzed generation of azafulvenium from an enyne sulfonamide: rapid access to fully substituted pyrroles","Organic Chemistry Frontiers","2019","6","4","480","","10.1039/C8QO01278D","","x-ray","1.54184","CuKα","","0.0832","0.0759","","","0.2101","0.2302","","","","","","1.017","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554559","9.7904","0.0003","10.7882","0.0004","12.3517","0.0004","83.891","0.001","69.723","0.001","84.499","0.001","1214.36","0.07","150","2","150","2","","","","","","","","5","P -1","-P 1","2","","","","- C28 H36 N2 O2 Si -","- C28 H36 N2 O2 Si -","- C56 H72 N4 O4 Si2 -","2","1","","Kong, De-Shen; Wang, Yi-Fan; Tan, Yun-Xuan; Zhang, Jun-Li; Zhang, Jian-Ge; Tian, Ping; Lin, Guo-Qiang","Trisannulation of benzamides and cyclohexadienone-tethered 1,1-disubstituted allenes initiated by Cp*Rh(iii)-catalyzed C–H activation","Organic Chemistry Frontiers","2019","6","5","699","","10.1039/C8QO01279B","","","1.54178","cukα","","0.037","0.0364","","","0.0926","0.093","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554560","9.9601","0.0004","10.6766","0.0003","11.8691","0.0004","74.393","0.001","85.571","0.001","88.958","0.001","1211.99","0.07","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C27 H31 N O4 Si -","- C27 H31 N O4 Si -","- C54 H62 N2 O8 Si2 -","2","1","","Kong, De-Shen; Wang, Yi-Fan; Tan, Yun-Xuan; Zhang, Jun-Li; Zhang, Jian-Ge; Tian, Ping; Lin, Guo-Qiang","Trisannulation of benzamides and cyclohexadienone-tethered 1,1-disubstituted allenes initiated by Cp*Rh(iii)-catalyzed C–H activation","Organic Chemistry Frontiers","2019","6","5","699","","10.1039/C8QO01279B","","","0.71073","MoKα","","0.0708","0.0582","","","0.1647","0.1781","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554561","8.24","0.0004","10.3859","0.0004","17.7438","0.0008","90","","95.373","0.004","90","","1511.84","0.12","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C31 H26 Cl2 N4 O4 S2 -","- C31 H24 Cl2 N4 O4 S2 -","- C62 H48 Cl4 N8 O8 S4 -","2","0.5","","Han, Shuaijun; Gao, Xianying; Wu, Qingsong; Li, Jingya; Zou, Dapeng; Wu, Yusheng; Wu, Yangjie","Nickel-promoted C(2)‒H amidation of quinoline N-oxides with N-fluorobenzenesulfonimide","Organic Chemistry Frontiers","2019","6","6","830","","10.1039/C8QO01281D","","x-ray","1.54184","CuKα","","0.0771","0.0642","","","0.1813","0.1981","","","","","","1.049","","","","has coordinates","237344","2020-10-21","18:00:00",""
"1554562","25.795","0.004","9.144","0.0015","21.256","0.004","90","","90","","90","","5013.6","1.5","100","2","100","2","","","","","","","","6","P n a 21","P 2c -2n","33","","","","- C25.5 H28 Cl N4 O2.5 Pd -","- C25.5 H25 Cl N4 O2.5 Pd -","- C204 H200 Cl8 N32 O20 Pd8 -","8","2","","Sun, Wen-Wu; Liu, Ji-Kai; Wu, Bin","Practical synthesis of polysubstituted unsymmetric 1,10-phenanthrolines by palladium catalyzed intramolecular oxidative cross coupling of C(sp2)–H and C(sp3)–H bonds of carboxamides","Organic Chemistry Frontiers","2019","6","4","544","","10.1039/C8QO01290C","","","0.71073","MoKα","","0.0827","0.072","","","0.2088","0.2181","","","","","","1.088","","","","has coordinates","274176","2022-03-31","10:10:26",""
"1554563","26.203","0.004","10.644","0.0015","30.852","0.004","90","","106.633","0.002","90","","8245","2","100","2","100","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C18 H11 Br N2 -","- C18 H11 Br N2 -","- C432 H264 Br24 N48 -","24","3","","Sun, Wen-Wu; Liu, Ji-Kai; Wu, Bin","Practical synthesis of polysubstituted unsymmetric 1,10-phenanthrolines by palladium catalyzed intramolecular oxidative cross coupling of C(sp2)–H and C(sp3)–H bonds of carboxamides","Organic Chemistry Frontiers","2019","6","4","544","","10.1039/C8QO01290C","","","0.71073","MoKα","","0.0794","0.0469","","","0.098","0.1102","","","","","","1.022","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554564","5.712","0.004","15.28","0.013","8.28","0.005","90","","104.192","0.015","90","","700.6","0.9","100","","100","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C16 H18 O2 S -","- C16 H18 O2 S -","- C32 H36 O4 S2 -","2","1","","Sun, Yongjie; Jiang, Jun; Guo, Xiaochong; Wen, Jialin; Zhang, Xumu","Asymmetric hydrogenation of α,β-unsaturated sulfones by a rhodium/thiourea–bisphosphine complex","Organic Chemistry Frontiers","2019","6","9","1438","","10.1039/C8QO01291A","","x-ray","0.71073","MoKα","","0.0256","0.0246","","","0.0619","0.0623","","","","","","1.043","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554565","13.6813","0.0019","13.6813","0.0019","29.053","0.006","90","","90","","90","","5438.1","1.5","173","2","173.15","","","","","","","","","5","P 43 21 2","P 4nw 2abw","96","","","","- C32 H27 N O4 S -","- C32 H27 N O4 S -","- C256 H216 N8 O32 S8 -","8","1","","Chen, Kun-Quan; Gao, Zhong-Hua; Ye, Song","Bifunctional N-heterocyclic carbene catalyzed [3 + 4] annulation of enals with azadienes: enantioselective synthesis of benzofuroazepinones","Organic Chemistry Frontiers","2019","6","3","405","","10.1039/C8QO01302K","","","0.71073","MoKα","","0.0573","0.0562","","","0.1116","0.1119","","","","","","1.238","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554566","11.043","0.003","14.753","0.005","17.258","0.005","90","","90","","90","","2811.6","1.5","173","2","173.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C33 H29 N O4 S -","- C33 H29 N O4 S -","- C132 H116 N4 O16 S4 -","4","1","","Chen, Kun-Quan; Gao, Zhong-Hua; Ye, Song","Bifunctional N-heterocyclic carbene catalyzed [3 + 4] annulation of enals with azadienes: enantioselective synthesis of benzofuroazepinones","Organic Chemistry Frontiers","2019","6","3","405","","10.1039/C8QO01302K","","","0.71073","MoKα","","0.0804","0.0755","","","0.1196","0.1217","","","","","","1.27","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554567","9.1375","0.0001","13.1527","0.0002","16.354","0.0003","95.187","0.001","95.294","0.001","103.04","0.001","1894.04","0.05","100","0.18","100","0.18","","","","","","","","3","P -1","-P 1","2","","","","- C22 H24 O7 -","- C22 H24 O7 -","- C88 H96 O28 -","4","2","","Liu, Hongxin; Tan, Haibo; Wang, Wenxuan; Zhang, Wenge; Chen, Yuchan; Li, Saini; Liu, Zhaoming; Li, Haohua; Zhang, Weimin","Cytorhizophins A and B, benzophenone-hemiterpene adducts from the endophytic fungus Cytospora rhizophorae","Organic Chemistry Frontiers","2019","6","5","591","","10.1039/C8QO01306C","","x-ray","1.54184","CuKα","","0.0398","0.0375","","","0.0984","0.1009","","","","","","1.049","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554568","13.8718","0.0006","9.6965","0.0005","13.8978","0.0007","90","","92.204","0.004","90","","1867.98","0.16","99.9","0.3","99.9","0.3","","","","","","","","4","P 1 2 1","P 2y","3","","","","- C18 H17 Cl3 O5 -","- C18 H17 Cl3 O5 -","- C72 H68 Cl12 O20 -","4","2","","Liu, Hongxin; Tan, Haibo; Wang, Wenxuan; Zhang, Wenge; Chen, Yuchan; Li, Saini; Liu, Zhaoming; Li, Haohua; Zhang, Weimin","Cytorhizophins A and B, benzophenone-hemiterpene adducts from the endophytic fungus Cytospora rhizophorae","Organic Chemistry Frontiers","2019","6","5","591","","10.1039/C8QO01306C","","x-ray","1.54184","CuKα","","0.0925","0.0821","","","0.2023","0.2154","","","","","","1.063","","","","has coordinates","237352","2020-10-21","18:00:00",""
"1554569","21.469","0.004","29.096","0.006","28.543","0.006","90","","95.17","0.03","90","","17757","6","100","","100","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C172 H203 N13 O10 P2 -","- C172 H203 N13 O10 P2 -","- C688 H812 N52 O40 P8 -","4","0.5","","Lee, Chaeeun; Lee, Hyemi; Lee, Seungwon; Jeon, Hae-Geun; Jeong, Kyu-Sung","Encapsulation of dihydrogenphosphate ions as a cyclic dimer to the cavities of site-specifically modified indolocarbazole-pyridine foldamers","Organic Chemistry Frontiers","2019","6","3","299","","10.1039/C8QO01307A","","","0.7","synchrotron","","0.1761","0.0712","","","0.1519","0.1857","","","","","","0.828","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554570","21.505","0.004","29.114","0.006","28.751","0.006","90","","94.83","0.03","90","","17937","6","100","","100","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","Inverted_pyridine_heptamer","","- C173 H203 N13 O10 P2 -","- C173 H203 N13 O10 P2 -","- C692 H812 N52 O40 P8 -","4","0.5","","Lee, Chaeeun; Lee, Hyemi; Lee, Seungwon; Jeon, Hae-Geun; Jeong, Kyu-Sung","Encapsulation of dihydrogenphosphate ions as a cyclic dimer to the cavities of site-specifically modified indolocarbazole-pyridine foldamers","Organic Chemistry Frontiers","2019","6","3","299","","10.1039/C8QO01307A","","","0.7","synchrotron","","0.1314","0.0904","","","0.2576","0.2822","","","","","","1.017","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554571","8.968","0.0015","9.084","0.0016","14.804","0.002","90","","105.357","0.004","90","","1163","0.3","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C12 H12 N2 O2 S -","- C12 H12 N2 O2 S -","- C48 H48 N8 O8 S4 -","4","1","","Zu, Weisai; Liu, Shuai; Jia, Xin; Xu, Liang","Chemoselective N-arylation of aminobenzene sulfonamides via copper catalysed Chan–Evans–Lam reactions","Organic Chemistry Frontiers","2019","6","9","1356","","10.1039/C8QO01313F","","","0.71073","MoKα","","0.0587","0.0416","","","0.0921","0.1012","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554572","8.0275","0.0015","8.0254","0.0017","12.699","0.003","90","","101.787","0.007","90","","800.9","0.3","296","2","296","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C19 H15 N O2 S -","- C19 H15 N O2 S -","- C38 H30 N2 O4 S2 -","2","1","","Zhao, Zi-Biao; Shi, Lei; Meng, Fan-Jie; Li, Yaming; Zhou, Yong-Gui","Synthesis of chiral seven-membered cyclic sulfonamides through palladium-catalyzed arylation of cyclic imines","Organic Chemistry Frontiers","2019","6","10","1572","","10.1039/C8QO01323C","","","0.71073","MoKα","","0.0292","0.0285","","","0.0777","0.0784","","","","","","1.056","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554573","6.9308","0.0008","6.9507","0.0008","11.8464","0.0014","84.194","0.006","79.023","0.006","64.094","0.006","503.84","0.11","293","2","293","2","","","","","","","","4","P 1","P 1","1","","","","- C10 H13 N O3 -","- C10 H13 N O3 -","- C20 H26 N2 O6 -","2","2","","Yang, Wu-Lin; Sun, Zhong-Tao; Zhang, Jian; Li, Zhong; Deng, Wei-Ping","Enantioselective synthesis of 3-amino-hydrobenzofuran-2,5-diones via Cu(i)-catalyzed intramolecular conjugate addition of imino esters","Organic Chemistry Frontiers","2019","6","5","579","","10.1039/C8QO01335G","","","1.54178","CuKα","","0.0598","0.0514","","","0.1367","0.1453","","","","","","1.068","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554574","15.1538","0.0003","13.5668","0.0003","27.2737","0.0005","90","","92.794","0.002","90","","5600.5","0.2","150","2","150","2","","","","","","","","5","P 1 21 1","P 2yb","4","Mikki_PCM2_09_04_17","","","- C116 H162 Br F3 O12 -","- C116 H162 Br F3 O12 -","- C232 H324 Br2 F6 O24 -","2","1","","Al-Azemi, Talal F.; Vinodh, Mickey; Alipour, Fatemeh H.; Mohamod, Abdirahman A.","Chiral discrimination of 2-heptlyaminium salt by planar-chiral monohydroxy-functionalized pillar[5]arenes","Organic Chemistry Frontiers","2019","6","5","603","","10.1039/C8QO01343H","","","1.54178","CuKα","","0.1467","0.1071","","","0.2924","0.3259","","","","","","1.079","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554575","15.0627","0.0008","13.3599","0.0007","27.1554","0.0019","90","","94.396","0.007","90","","5448.6","0.6","150","2","150","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C116 H162 Br F3 O12 -","- C116 H162 Br F3 O12 -","- C232 H324 Br2 F6 O24 -","2","1","","Al-Azemi, Talal F.; Vinodh, Mickey; Alipour, Fatemeh H.; Mohamod, Abdirahman A.","Chiral discrimination of 2-heptlyaminium salt by planar-chiral monohydroxy-functionalized pillar[5]arenes","Organic Chemistry Frontiers","2019","6","5","603","","10.1039/C8QO01343H","","","0.71075","MoKα","","0.1679","0.1101","","","0.2937","0.338","","","","","","1.112","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554576","7.15","0.005","11.643","0.007","12.098","0.008","90","","95.268","0.013","90","","1002.9","1.1","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C10 H8 N2 Se -","- C10 H8 N2 Se -","- C40 H32 N8 Se4 -","4","1","","Cao, Yuan; Liu, Jie; Liu, Fanmin; Jiang, Lvqi; Yi, Wenbin","Copper-catalyzed direct and odorless selenylation with a sodium selenite-based reagent","Organic Chemistry Frontiers","2019","6","6","825","","10.1039/C8QO01355A","","","0.71073","MoKα","","0.0668","0.0388","","","0.0928","0.1044","","","","","","1.051","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554577","5.799","0.003","7.486","0.004","10.479","0.006","90","","104.17","0.04","90","","441.1","0.4","293","2","293","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C9 H9 F3 N2 -","- C9 H9 F3 N2 -","- C18 H18 F6 N4 -","2","1","","Chen, Mu-Wang; Deng, Zhihong; Yang, Qin; Huang, Jian; Peng, Yiyuan","Enantioselective synthesis of trifluoromethylated dihydroquinoxalinones via palladium-catalyzed hydrogenation","Organic Chemistry Frontiers","2019","6","6","746","","10.1039/C8QO01361F","","","1.54178","CuKα","","0.2357","0.0964","","","0.2635","0.3757","","","","","","1.398","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554578","9.1297","0.0008","10.326","0.0009","24.127","0.0018","90","","90","","90","","2274.5","0.3","123.2","0.2","123.2","0.2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C29 H24 N2 O2 -","- C29 H24 N2 O2 -","- C116 H96 N8 O8 -","4","1","","Xu, Lubin; Chen, Haohua; Liu, Jian; Zhou, Lan; Liu, Qing; Lan, Yu; Xiao, Jian","Chiral phosphoric acid-catalyzed asymmetric C(sp3)–H functionalization of biomass-derived 2,5-dimethylfuran via two sequential Cope-type rearrangements","Organic Chemistry Frontiers","2019","6","8","1162","","10.1039/C8QO01375F","","","1.54184","CuKα","","0.0767","0.0574","","","0.1248","0.1388","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554579","32.1461","0.0004","11.483","0.0001","8.0162","0.0001","90","","90","","90","","2959.05","0.06","293","2","293","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C31 H42 O11 -","- C31 H42 O11 -","- C124 H168 O44 -","4","1","","Zhang, Jia; He, Jun; Cheng, Yung-Chi; Zhang, Pei-Cheng; Yan, Yu; Zhang, Hao-Jun; Zhang, Wei-Ku; Xu, Jie-Kun","Fischernolides A–D, four novel diterpene-based meroterpenoid scaffolds with antitumor activities from Euphorbia fischeriana","Organic Chemistry Frontiers","2019","6","14","2312","","10.1039/C8QO01379A","","","1.54184","CuKα","","0.0384","0.0379","","","0.1","0.1004","","","","","","1.1","","","","has coordinates","300101","2025-06-17","17:58:11",""
"1554580","11.351","0.002","11.9996","0.0017","21.215","0.003","90","","90","","90","","2889.6","0.8","296","2","296.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C35 H26 Cl N5 O -","- C35 H26 Cl N5 O -","- C140 H104 Cl4 N20 O4 -","4","1","","Sun, Bing-Bing; Zhang, Jun-Qi; Chen, Jun-Bo; Fan, Wei-Tai; Yu, Jie-Qiang; Hu, Jia-Ming; Wang, Xing-Wang","Stereoselective synthesis of spirocyclohexadiene-pyrazolones via organic base and/or hydrogen bonding assisted [3 + 3] annulation reactions","Organic Chemistry Frontiers","2019","6","11","1842","","10.1039/C8QO01391H","","","0.71073","MoKα","","0.0864","0.064","","","0.1786","0.192","","","","","","1.078","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554581","9.3289","0.0004","10.9229","0.0005","12.8668","0.0006","87.237","0.001","78.614","0.001","85.681","0.001","1280.91","0.1","120","2","120","2","","","","","","","","5","P -1","-P 1","2","","","","- C33 H23 Cl N4 O -","- C33 H23 Cl N4 O -","- C66 H46 Cl2 N8 O2 -","2","1","","Sun, Bing-Bing; Zhang, Jun-Qi; Chen, Jun-Bo; Fan, Wei-Tai; Yu, Jie-Qiang; Hu, Jia-Ming; Wang, Xing-Wang","Stereoselective synthesis of spirocyclohexadiene-pyrazolones via organic base and/or hydrogen bonding assisted [3 + 3] annulation reactions","Organic Chemistry Frontiers","2019","6","11","1842","","10.1039/C8QO01391H","","","0.71073","MoKα","","0.0479","0.0369","","","0.1022","0.1242","","","","","","1.148","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554582","7.9193","0.0001","15.3744","0.0002","16.4929","0.0002","90","","90","","90","","2008.08","0.04","291","2","291","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C16 H14 F3 N O4 S -","- C16 H14 F3 N O4 S -","- C64 H56 F12 N4 O16 S4 -","4","1","","Gui, Yang; Liang, Xinping; Li, Yanan; Li, Kuiliang; Zha, Zhenggen; Wang, Zhiyong","Asymmetric synthesis of fluoroalkylated N,O-ketals via an organocatalytic dehydration/aminalization/aza-Michael desymmetrization","Organic Chemistry Frontiers","2019","6","7","942","","10.1039/C8QO01397G","","","1.54184","CuKα","","0.0407","0.0401","","","0.1113","0.1125","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554583","28.168","0.003","11.3424","0.0013","10.2126","0.0012","90","","90","","90","","3262.9","0.6","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C36 H32 Br N O4 P2 -","- C36 H32 Br N O4 P2 -","- C144 H128 Br4 N4 O16 P8 -","4","1","","Liu, Bing; Li, Wenbo; Wu, Hai-Hong; Zhang, Junliang","Enantiodivergent synthesis of 1,2-bis(diphenylphosphino)ethanes via asymmetric [3 + 2]-cycloaddition","Organic Chemistry Frontiers","2019","6","5","694","","10.1039/C8QO01404C","","","0.71073","MoKα","","0.0996","0.0581","","","0.1202","0.1385","","","","","","1.011","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554584","9.2282","0.0014","9.1743","0.0014","12.829","0.002","90","","109.724","0.003","90","","1022.4","0.3","120.15","","120.15","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C22 H20 Br N3 O4 -","- C22 H20 Br N3 O4 -","- C44 H40 Br2 N6 O8 -","2","1","","Xie, Chao-Chao; Tan, Rui; Liu, Yan-Kai","Asymmetric construction of polycyclic indole derivatives with different ring connectivities by an organocatalysis triggered two-step sequence","Organic Chemistry Frontiers","2019","6","7","919","","10.1039/C8QO01406J","","","0.71073","MoKα","","0.0514","0.0326","","","0.066","0.073","","","","","","0.839","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554585","9.6264","0.0013","10.858","0.0014","11.2163","0.0014","90","","113.736","0.002","90","","1073.2","0.2","120.15","","120.15","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C21 H24 N2 O7 -","- C21 H24 N2 O7 -","- C42 H48 N4 O14 -","2","1","","Xie, Chao-Chao; Tan, Rui; Liu, Yan-Kai","Asymmetric construction of polycyclic indole derivatives with different ring connectivities by an organocatalysis triggered two-step sequence","Organic Chemistry Frontiers","2019","6","7","919","","10.1039/C8QO01406J","","","0.71073","MoKα","","0.0865","0.0496","","","0.0988","0.1161","","","","","","1.057","","","","has coordinates,has disorder","301780","2025-08-18","21:43:31",""
"1554586","11.431","0.006","5.931","0.003","25.849","0.014","90","","94.751","0.01","90","","1746.5","1.6","293","2","293","2","","","","","","","see text","5","P 1 21/c 1","-P 2ybc","14","","","","- C17 H20 F3 N O3 -","- C17 H20 F3 N O3 -","- C68 H80 F12 N4 O12 -","4","1","","Gupta, Ekta; Zaheer, Mohd Khalid; Kant, Ruchir; Mohanan, Kishor","Additive-free regio- and diastereoselective construction of fully-substituted isoxazolidines employing diazo compounds","Organic Chemistry Frontiers","2019","6","8","1109","","10.1039/C8QO01421C","","","0.71075","MoKα","","0.1224","0.0596","","","0.1498","0.1776","","","","","","0.912","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554587","11.218","0.003","12.296","0.003","16.82","0.005","108.32","0.02","101.98","0.03","102.65","0.02","2051.1","1.1","293","2","293","2","","","","","","","see text","5","P -1","-P 1","2","","","","- C14 H14 F3 N O2 -","- C14 H14 F3 N O2 -","- C84 H84 F18 N6 O12 -","6","3","","Gupta, Ekta; Zaheer, Mohd Khalid; Kant, Ruchir; Mohanan, Kishor","Additive-free regio- and diastereoselective construction of fully-substituted isoxazolidines employing diazo compounds","Organic Chemistry Frontiers","2019","6","8","1109","","10.1039/C8QO01421C","","","0.71075","MoKα","","0.1716","0.0555","","","0.1396","0.1588","","","","","","0.595","","","","has coordinates","301780","2025-08-18","21:43:31",""
"1554694","38.372","0.011","43.842","0.012","41.771","0.012","90","","101.834","0.003","90","","68778","3","123","2","123","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C260 H202 Cu4 N16 O23 -","- C260 H202 Cu4 N16 O23 -","- C2080 H1616 Cu32 N128 O184 -","8","2","","Maehara, Takeshi; Sekiya, Ryo; Harada, Kentaro; Haino, Takeharu","Tunable enforced cavities inside self-assembled capsules","Organic Chemistry Frontiers","2019","6","10","1561","","10.1039/C9QO00010K","","","0.71073","MoKα","","0.4241","0.2119","","","0.4543","0.5367","","","","","","1.066","","","","has coordinates","274567","2022-04-19","14:22:36",""
"1554695","10.7588","0.0007","13.1415","0.0008","15.339","0.001","106.956","0.001","100.938","0.001","91.717","0.001","2028.3","0.2","123","2","123","2","","","","","","","","7","P -1","-P 1","2","","","","- C40 H40 B Cl4 Cu F4 N4 -","- C40 H40 B Cl4 Cu F4 N4 -","- C80 H80 B2 Cl8 Cu2 F8 N8 -","2","1","","Maehara, Takeshi; Sekiya, Ryo; Harada, Kentaro; Haino, Takeharu","Tunable enforced cavities inside self-assembled capsules","Organic Chemistry Frontiers","2019","6","10","1561","","10.1039/C9QO00010K","","","0.71073","MoKα","","0.0384","0.034","","","0.0882","0.0912","","","","","","1.01","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554696","9.0064","0.0003","9.7885","0.0003","30.9078","0.0011","90","","90","","90","","2724.81","0.16","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","(R)-4-benzyl-4-((S)-(4-chlorophenyl)(2-hydroxy-3-methoxyphenyl)methyl)-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one","(R)-4-benzyl-4-((S)-(4-chlorophenyl)(2-hydroxy-3-methoxyphenyl)methyl)-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one","","- C31 H29 Cl N2 O4 -","- C31 H29 Cl N2 O4 -","- C124 H116 Cl4 N8 O16 -","4","1","","Chu, Ming-Ming; Qi, Suo-Suo; Ju, Wan-Zhen; Wang, Yi-Feng; Chen, Xue-Yang; Xu, Dan-Qian; Xu, Zhen-Yuan","Asymmetric organocatalytic conjugated addition of pyrazolin-5-ones to ortho-quinomethanes: construction of vicinal tertiary and all-carbon quaternary stereocenters","Organic Chemistry Frontiers","2019","6","8","1140","","10.1039/C9QO00011A","","","0.71073","MoKα","","0.0615","0.0448","","","0.1069","0.1185","","","","","","1.083","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554697","36.594","0.002","7.353","0.003","28.802","0.003","90","","123.87","0.03","90","","6435","4","90","2","90","2","","","","","","","","4","C 1 c 1","C -2yc","9","","","","- C63.5 H60 N6 O14.5 -","- C63.5 H60 N6 O14.5 -","- C254 H240 N24 O58 -","4","1","","Ren, Demin; Liu, Bin; Li, Xiaofang; Koniarz, Sebastian; Pawlicki, Miłosz; Chmielewski, Piotr J.","Reactions of 2-aza-21-carbaporphyrin with aniline derivatives","Organic Chemistry Frontiers","2019","6","7","908","","10.1039/C9QO00024K","","","0.71073","MoKα","","0.0922","0.0634","","","0.1522","0.1703","","","","","","1.036","","","","has coordinates,has disorder","238060","2020-10-21","18:00:00",""
"1554698","33.74","0.002","12.9479","0.0008","14.8229","0.0008","90","","100.325","0.006","90","","6370.7","0.7","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C79 H72 N6 O6 -","- C79 H72 N6 O6 -","- C316 H288 N24 O24 -","4","1","","Ren, Demin; Liu, Bin; Li, Xiaofang; Koniarz, Sebastian; Pawlicki, Miłosz; Chmielewski, Piotr J.","Reactions of 2-aza-21-carbaporphyrin with aniline derivatives","Organic Chemistry Frontiers","2019","6","7","908","","10.1039/C9QO00024K","","","1.54184","CuKα","","0.1186","0.0678","","","0.1572","0.1707","","","","","","0.867","","","","has coordinates,has disorder","238060","2020-10-21","18:00:00",""
"1554699","6.9921","0.0003","11.2113","0.0006","12.4434","0.0007","96.443","0.002","95.376","0.002","95.626","0.002","959.19","0.09","296","2","296","2","","","","","","","","7","P -1","-P 1","2","","","","- C18 H16 Br2 F N O3 S -","- C18 H16 Br2 F N O3 S -","- C36 H32 Br4 F2 N2 O6 S2 -","2","1","","Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.","Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation","Organic Chemistry Frontiers","2019","6","8","1133","","10.1039/C9QO00027E","","","0.71073","MoKα","","0.0551","0.0479","","","0.1414","0.1485","","","","","","0.897","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554700","18.258","0.002","13.081","0.0013","15.4466","0.0014","90","","91.845","0.003","90","","3687.2","0.6","300","2","300","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C19 H20 Cl N O3 S -","- C19 H20 Cl N O3 S -","- C152 H160 Cl8 N8 O24 S8 -","8","1","","Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.","Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation","Organic Chemistry Frontiers","2019","6","8","1133","","10.1039/C9QO00027E","","","0.71073","MoKα","","0.0535","0.0488","","","0.139","0.1434","","","","","","1.123","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554701","7.4466","0.0005","24.7338","0.0015","9.6421","0.0005","90","","104.56","0.002","90","","1718.87","0.18","298","2","298","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C17 H14 N2 O7 S -","- C17 H14 N2 O7 S -","- C68 H56 N8 O28 S4 -","4","1","","Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.","Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation","Organic Chemistry Frontiers","2019","6","8","1133","","10.1039/C9QO00027E","","","0.71073","MoKα","","0.0624","0.0435","","","0.1037","0.1128","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554702","10.994","0.013","12.052","0.015","16.9","0.02","95.131","0.011","99.76","0.011","103.107","0.011","2130","4","273","2","273","2","","","","","","","","5","P -1","-P 1","2","","","","- C21 H25 N O4 S -","- C21 H25 N O4 S -","- C84 H100 N4 O16 S4 -","4","2","","Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.","Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation","Organic Chemistry Frontiers","2019","6","8","1133","","10.1039/C9QO00027E","","","0.71073","MoKα","","0.2175","0.0973","","","0.2554","0.3338","","","","","","0.929","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554703","8.2985","0.0003","12.4303","0.0006","19.4432","0.0008","90","","101.322","0.001","90","","1966.59","0.14","300","2","300","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C17 H16 Br3 N O2 S -","- C17 H16 Br3 N O2 S -","- C68 H64 Br12 N4 O8 S4 -","4","1","","Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.","Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation","Organic Chemistry Frontiers","2019","6","8","1133","","10.1039/C9QO00027E","","","0.71073","MoKα","","0.047","0.0394","","","0.0993","0.1036","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554704","6.9458","0.0002","10.9848","0.0002","12.6203","0.0004","95.166","0.002","94.677","0.002","97.68","0.002","946.11","0.04","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C17 H14 Br3 N O3 S -","- C17 H14 Br3 N O3 S -","- C34 H28 Br6 N2 O6 S2 -","2","1","","Anitha, Mandala; Shankar, Mallepalli; Kumara Swamy, K. C.","Reactivity of epoxy-ynamides with metal halides: nucleophile (Br/Cl/OH)-assisted tandem intramolecular 5-exo-dig or 6-endo-dig cyclisation and AgF2-promoted oxidation","Organic Chemistry Frontiers","2019","6","8","1133","","10.1039/C9QO00027E","","","0.71073","MoKα","","0.0809","0.0509","","","0.1129","0.1223","","","","","","1.071","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554705","6.5927","0.0001","24.4163","0.0004","9.1339","0.0002","90","","108.268","0.002","90","","1396.18","0.05","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H11 F3 N2 O -","- C16 H11 F3 N2 O -","- C64 H44 F12 N8 O4 -","4","1","","Zhu, Chuanle; Liu, Chi; Zeng, Hao; Chen, Fulin; Jiang, Huanfeng","Transition-metal free selective C(α)–C(β) bond cleavage of trifluoromethyl ketones with amidines under air: facile access to 5-trifluoromethylated Imidazol-4-ones","Organic Chemistry Frontiers","2019","6","6","858","","10.1039/C9QO00029A","","x-ray","1.54184","CuKα","","0.0517","0.047","","","0.1251","0.1316","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554706","25.9456","0.0005","8.8451","0.0003","23.3704","0.0007","90","","101.146","0.003","90","","5262.1","0.3","293","1","293","1","","","","","","","","5","C 1 2 1","C 2y","5","","","","- C21 H22 Cl N5 O8 -","- C21 H22 Cl N5 O8 -","- C168 H176 Cl8 N40 O64 -","8","2","","Hao, Er-Jun; Fu, Dan-Dan; Wang, Dong-Chao; Zhang, Tao; Qu, Gui-Rong; Li, Gong-Xin; Lan, Yu; Guo, Hai-Ming","Chemoselective asymmetric dearomative [3 + 2] cycloaddition reactions of purines with aminocyclopropanes","Organic Chemistry Frontiers","2019","6","6","863","","10.1039/C9QO00039A","","x-ray","1.54184","CuKα","","0.0667","0.0641","","","0.1749","0.1781","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554707","14.6444","0.0002","19.027","0.0003","9.2992","0.0001","90","","98.115","0.001","90","","2565.17","0.06","291.42","0.1","291.42","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C22 H26 Cl N5 O9 -","- C22 H26 Cl N5 O9 -","- C88 H104 Cl4 N20 O36 -","4","1","","Hao, Er-Jun; Fu, Dan-Dan; Wang, Dong-Chao; Zhang, Tao; Qu, Gui-Rong; Li, Gong-Xin; Lan, Yu; Guo, Hai-Ming","Chemoselective asymmetric dearomative [3 + 2] cycloaddition reactions of purines with aminocyclopropanes","Organic Chemistry Frontiers","2019","6","6","863","","10.1039/C9QO00039A","","x-ray","1.54184","CuKα","","0.0747","0.0664","","","0.185","0.1976","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554708","8.9522","0.0004","12.3288","0.0005","12.6211","0.0005","103.938","0.003","101.104","0.004","102.417","0.004","1275.71","0.1","291.69","0.1","291.69","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C25 H22 Cl N5 O8 -","- C25 H22 Cl N5 O8 -","- C50 H44 Cl2 N10 O16 -","2","1","","Hao, Er-Jun; Fu, Dan-Dan; Wang, Dong-Chao; Zhang, Tao; Qu, Gui-Rong; Li, Gong-Xin; Lan, Yu; Guo, Hai-Ming","Chemoselective asymmetric dearomative [3 + 2] cycloaddition reactions of purines with aminocyclopropanes","Organic Chemistry Frontiers","2019","6","6","863","","10.1039/C9QO00039A","","x-ray","0.71073","MoKα","","0.0608","0.0503","","","0.1244","0.1314","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554709","9.4007","0.0002","10.8468","0.0002","21.7267","0.0005","90","","90","","90","","2215.42","0.08","100","2","100","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C21 H23 Br N2 O4 S -","- C21 H23 Br N2 O4 S -","- C84 H92 Br4 N8 O16 S4 -","4","1","","Shen, Guoli; Khan, Ruhima; Lv, Haiping; Yang, Yong; Zhang, Xia; Zhan, Yong; Zhou, Yongyun; Fan, Baomin","Palladium/silver co-catalyzed syn-stereoselective asymmetric ring-opening reactions of azabenzonorbornadienes with amides","Organic Chemistry Frontiers","2019","6","9","1423","","10.1039/C9QO00041K","","","1.54178","CuKα","","0.0365","0.0364","","","0.0944","0.0946","","","","","","1.087","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554710","7.4893","0.0009","3.8493","0.0004","19.835","0.002","90","","94.273","0.004","90","","570.23","0.11","110","","110","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C14 H8 F2 S2 -","- C14 H8 F2 S2 -","- C28 H16 F4 S4 -","2","0.5","","Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed","Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives","Organic Chemistry Frontiers","2019","6","6","780","","10.1039/C9QO00044E","","x-ray","0.71073","MoKα","","0.0902","0.0787","","","0.1626","0.1703","","","","","","1.342","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554711","5.9315","0.0006","4.9497","0.0005","18.794","0.002","90","","95.89","0.004","90","","548.86","0.1","100","","100","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C12 H6 F N2 S2 -","- C12 H6 F N2 S2 -","- C24 H12 F2 N4 S4 -","2","0.5","","Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed","Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives","Organic Chemistry Frontiers","2019","6","6","780","","10.1039/C9QO00044E","","x-ray","0.71073","MoKα","","0.0928","0.0818","","","0.1515","0.159","","","","","","1.174","","","","has coordinates,has disorder","238072","2020-10-21","18:00:00",""
"1554712","5.7427","0.0003","5.5541","0.0003","17.1753","0.0008","90","","90.509","0.002","90","","547.79","0.05","100","","100","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C12 H6 F2 N2 S2 -","- C12 H6 F2 N2 S2 -","- C24 H12 F4 N4 S4 -","2","0.5","","Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed","Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives","Organic Chemistry Frontiers","2019","6","6","780","","10.1039/C9QO00044E","","x-ray","1.54178","CuKα","","0.035","0.0315","","","0.0832","0.085","","","","","","1.092","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554713","6.2999","0.0003","5.0655","0.0003","18.6515","0.0011","90","","90.341","0.002","90","","595.2","0.06","100","","100","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C14 H6 F4 S2 -","- C14 H6 F4 S2 -","- C28 H12 F8 S4 -","2","0.5","","Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed","Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives","Organic Chemistry Frontiers","2019","6","6","780","","10.1039/C9QO00044E","","","1.54178","CuKα","","0.0472","0.0429","","","0.1048","0.107","","","","","","1.147","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554714","9.3302","0.0004","12.3529","0.0005","14.5826","0.0005","90","","106.185","0.001","90","","1614.11","0.11","100","","100","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C30 H46 F N2 S2 Si2 -","- C30 H46 F N2 S2 Si2 -","- C60 H92 F2 N4 S4 Si4 -","2","0.5","","Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed","Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives","Organic Chemistry Frontiers","2019","6","6","780","","10.1039/C9QO00044E","","","1.54178","CuKα","","0.0331","0.0296","","","0.0737","0.0757","","","","","","1.085","","","","has coordinates","238072","2020-10-21","18:00:00",""
"1554715","9.2882","0.0002","12.3511","0.0003","14.5307","0.0004","90","","105.826","0.001","90","","1603.77","0.07","100","","100","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C30 H48 N2 S2 Si2 -","- C30 H48 N2 S2 Si2 -","- C60 H96 N4 S4 Si4 -","2","0.5","","Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed","Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives","Organic Chemistry Frontiers","2019","6","6","780","","10.1039/C9QO00044E","","","1.54178","CuKα","","0.0422","0.0363","","","0.0877","0.0915","","","","","","1.056","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554716","5.0225","0.0008","7.1949","0.0014","17.29","0.003","84.549","0.003","83.096","0.002","70.873","0.002","584.99","0.18","110","","110","","","","","","","","","5","P -1","-P 1","2","","","","- C12 H4 F4 N2 S2 -","- C12 H4 F4 N2 S2 -","- C24 H8 F8 N4 S4 -","2","1","","Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed","Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives","Organic Chemistry Frontiers","2019","6","6","780","","10.1039/C9QO00044E","","","0.71073","MoKα","","0.0294","0.0266","","","0.066","0.0681","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554717","9.3622","0.0003","12.3591","0.0004","14.6437","0.0004","90","","106.674","0.001","90","","1623.15","0.09","100","","100","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C30 H46 F2 N2 S2 Si2 -","- C30 H46 F2 N2 S2 Si2 -","- C60 H92 F4 N4 S4 Si4 -","2","0.5","","Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed","Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives","Organic Chemistry Frontiers","2019","6","6","780","","10.1039/C9QO00044E","","","1.54178","CuKα","","0.0311","0.0282","","","0.0717","0.0738","","","","","","1.075","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554718","3.8093","0.0003","6.6644","0.0004","21.5126","0.0015","90","","94.338","0.004","90","","544.57","0.07","100","","100","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C12 H5 F N2 S2 -","- C12 H5 F N2 S2 -","- C24 H10 F2 N4 S4 -","2","0.5","","Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed","Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives","Organic Chemistry Frontiers","2019","6","6","780","","10.1039/C9QO00044E","","","1.54178","CuKα","","0.0979","0.0846","","","0.1564","0.1609","","","","","","1.314","","","","has coordinates,has disorder","238072","2020-10-21","18:00:00",""
"1554719","19.9633","0.0007","12.2859","0.0004","13.3676","0.0005","90","","90","","90","","3278.6","0.2","100","","100","","","","","","","","","6","P n a 21","P 2c -2n","33","","","","- C30 H44 F4 N2 S2 Si2 -","- C30 H44 F4 N2 S2 Si2 -","- C120 H176 F16 N8 S8 Si8 -","4","1","","Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed","Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives","Organic Chemistry Frontiers","2019","6","6","780","","10.1039/C9QO00044E","","","1.54178","CuKα","","0.0235","0.0222","","","0.0557","0.0563","","","","","","1.068","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554720","6.6214","0.0004","25.6046","0.0015","7.2049","0.0004","90","","116.456","0.004","90","","1093.59","0.12","110","","110","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C12 H6 F2 N2 S2 -","- C12 H6 F2 N2 S2 -","- C48 H24 F8 N8 S8 -","4","1","","Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed","Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives","Organic Chemistry Frontiers","2019","6","6","780","","10.1039/C9QO00044E","","","1.54178","CuKα","","0.0631","0.0591","","","0.1451","0.1468","","","","","","1.244","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554721","3.8531","0.0006","23.868","0.003","6.121","0.0009","90","","95.29","0.003","90","","560.53","0.14","110","","110","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C12 H4 F4 N2 S2 -","- C12 H4 F4 N2 S2 -","- C24 H8 F8 N4 S4 -","2","0.5","","Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed","Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives","Organic Chemistry Frontiers","2019","6","6","780","","10.1039/C9QO00044E","","","0.71073","MoKα","","0.032","0.0301","","","0.0761","0.0773","","","","","","1.079","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554722","15.9825","0.0007","9.7302","0.0004","13.6524","0.0004","90","","90","","90","","2123.12","0.14","100","","100","","","","","","","","","4","F d d 2","F 2 -2d","43","","","","- C12 H8 N2 S2 -","- C12 H8 N2 S2 -","- C96 H64 N16 S16 -","8","0.5","","Barłóg, Maciej; Kulai, Ihor; Ji, Xiaozhou; Bhuvanesh, Nattamai; Dey, Somnath; Sliwinski, Eric Pierre; Bazzi, Hassan S.; Fang, Lei; Al-Hashimi, Mohammed","Synthesis, characterization and crystal structures of novel fluorinated di(thiazolyl)benzene derivatives","Organic Chemistry Frontiers","2019","6","6","780","","10.1039/C9QO00044E","","","1.54178","CuKα","","0.0265","0.0256","","","0.0616","0.0621","","","","","","1.104","","","","has coordinates,has disorder","238072","2020-10-21","18:00:00",""
"1554723","10.2239","0.0005","11.009","0.0006","11.0538","0.0006","73.729","0.005","86.05","0.005","65.798","0.005","1087.85","0.11","100","0.1","100","0.1","","","","","","","","3","P -1","-P 1","2","","","","- C29 H28 O2 -","- C29 H28 O2 -","- C58 H56 O4 -","2","1","","Zhang, He; Cao, Tongxiang; Luo, Hejiang; Chen, Lianfen; Zhu, Shifa","Enynone-enabled migratory insertion and Schmittel cyclization cascade for the synthesis of furan-fused fluorenes","Organic Chemistry Frontiers","2019","6","8","1118","","10.1039/C9QO00045C","","x-ray","0.71073","MoKα","","0.0577","0.0458","","","0.1096","0.1198","","","","","","1.043","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554724","11.5269","0.0006","6.9766","0.0004","23.812","0.0012","90","","98.369","0.005","90","","1894.54","0.18","100.01","0.1","100.01","0.1","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C26 H20 O3 -","- C26 H20 O3 -","- C104 H80 O12 -","4","1","","Zhang, He; Cao, Tongxiang; Luo, Hejiang; Chen, Lianfen; Zhu, Shifa","Enynone-enabled migratory insertion and Schmittel cyclization cascade for the synthesis of furan-fused fluorenes","Organic Chemistry Frontiers","2019","6","8","1118","","10.1039/C9QO00045C","","x-ray","0.71073","MoKα","","0.0474","0.0398","","","0.0945","0.0991","","","","","","1.084","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554725","22.035","0.012","15.426","0.007","17.593","0.01","90","","121.518","0.007","90","","5098","5","273","2","273","2","","","","","","","synthesis as described","4","C 1 2/c 1","-C 2yc","15","","C60(OCH2CH2F)8","","- C76 H32 F8 O8 -","- C76 H32 F8 O8 -","- C304 H128 F32 O32 -","4","0.5","","Ma, Yue; Uchiyama, Kouya; Ueno, Hiroshi; Okada, Hiroshi; Moriyama, Hiroshi; Matsuo, Yutaka","Highly soluble C2v-symmetrical fullerene derivatives: efficient synthesis, characterization, and electrochemical study","Organic Chemistry Frontiers","2019","6","9","1372","","10.1039/C9QO00056A","","x-ray","0.71073","MoKα","","0.1435","0.0915","","","0.1406","0.1721","","","","","","1.054","","","","has coordinates","238077","2020-10-21","18:00:00",""
"1554726","21.782","","13.957","","24.511","","90","","110.66","","90","","6972.41","","293","2","293","2","","","","","","","synthesis as described","4","P 1 21/n 1","-P 2yn","14","","C60(OCH2CCl3)8","","- C76 H16 Cl24 O8 -","- C76 H16 Cl24 O8 -","- C304 H64 Cl96 O32 -","4","1","","Ma, Yue; Uchiyama, Kouya; Ueno, Hiroshi; Okada, Hiroshi; Moriyama, Hiroshi; Matsuo, Yutaka","Highly soluble C2v-symmetrical fullerene derivatives: efficient synthesis, characterization, and electrochemical study","Organic Chemistry Frontiers","2019","6","9","1372","","10.1039/C9QO00056A","","x-ray","0.71073","MoKα","","0.1543","0.1397","","","0.318","0.3292","","","","","","1.1","","","","has coordinates,has disorder","238077","2020-10-21","18:00:00",""
"1554727","5.0429","0.001","11.88","0.002","25.83","0.005","90","","90","","90","","1547.5","0.5","173.15","","173.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C15 H18 Br N O4 -","- C15 H18 Br N O4 -","- C60 H72 Br4 N4 O16 -","4","1","","Hu, Hui-Juan; Chen, Peng; Ao, Yu-Fei; Wang, Qi-Qiang; Wang, De-Xian; Wang, Mei-Xiang","Highly efficient biocatalytic desymmetrization of meso carbocyclic 1,3-dicarboxamides: a versatile route for enantiopure 1,3-disubstituted cyclohexanes and cyclopentanes","Organic Chemistry Frontiers","2019","6","6","808","","10.1039/C9QO00069K","","","0.710747","MoKα","","0.0274","0.026","","","0.0573","0.0583","","","","","","1.066","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554728","6.5631","0.0014","12.796","0.003","18.385","0.004","90","","90","","90","","1544","0.6","173","2","173.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C15 H18 Br N O4 -","- C15 H18 Br N O4 -","- C60 H72 Br4 N4 O16 -","4","1","","Hu, Hui-Juan; Chen, Peng; Ao, Yu-Fei; Wang, Qi-Qiang; Wang, De-Xian; Wang, Mei-Xiang","Highly efficient biocatalytic desymmetrization of meso carbocyclic 1,3-dicarboxamides: a versatile route for enantiopure 1,3-disubstituted cyclohexanes and cyclopentanes","Organic Chemistry Frontiers","2019","6","6","808","","10.1039/C9QO00069K","","","0.71073","MoKα","","0.0529","0.0457","","","0.0763","0.0794","","","","","","1.147","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554729","16.191","0.002","17.7337","0.0007","8.5986","0.0011","90","","137.72","0.03","90","","1661","1","293","2","293","2","","","","","","","","4","C 1 c 1","C -2yc","9","","","","- C20 H17 O2 P -","- C20 H17 O2 P -","- C80 H68 O8 P4 -","4","1","","Zhao, Xiuli; Huang, Mengmeng; Li, Yabo; Zhang, Jianye; Kim, Jung Keun; Wu, Yangjie","Stepwise photosensitized C(sp3)–C(CO) bond cleavage and C–P bond formation of 1,3-dicarbonyls with arylphosphine oxides","Organic Chemistry Frontiers","2019","6","9","1433","","10.1039/C9QO00075E","","x-ray","1.54184","CuKα","","0.0405","0.0374","","","0.0923","0.0969","","","","","","1.072","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554730","12.1117","0.001","15.5259","0.0012","21.575","0.0018","95.307","0.003","97.116","0.003","101.212","0.002","3920.6","0.6","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C34 H25 Cl O2 -","- C34 H25 Cl O2 -","- C204 H150 Cl6 O12 -","6","3","","Sun, Jing; Jiang, Wang; Yan, Chao-Guo","Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes","Organic Chemistry Frontiers","2019","6","9","1428","","10.1039/C9QO00079H","","","0.71073","MoKα","","0.1596","0.0874","","","0.2316","0.267","","","","","","1.056","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554731","10.7141","0.0009","20.1653","0.0017","12.3094","0.0013","90","","107.329","0.003","90","","2538.8","0.4","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C32 H20 N2 O6 -","- C32 H20 N2 O6 -","- C128 H80 N8 O24 -","4","1","","Sun, Jing; Jiang, Wang; Yan, Chao-Guo","Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes","Organic Chemistry Frontiers","2019","6","9","1428","","10.1039/C9QO00079H","","","0.71073","MoKα","","0.1205","0.0617","","","0.1276","0.1499","","","","","","1.02","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554732","10.602","0.0012","20.505","0.002","12.2951","0.0013","90","","114.94","0.003","90","","2423.6","0.4","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C32 H21 Br O2 -","- C32 H21 Br O2 -","- C128 H84 Br4 O8 -","4","1","","Sun, Jing; Jiang, Wang; Yan, Chao-Guo","Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes","Organic Chemistry Frontiers","2019","6","9","1428","","10.1039/C9QO00079H","","","0.71073","MoKα","","0.0894","0.0454","","","0.0939","0.1076","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554733","9.998","0.007","15.063","0.011","15.716","0.011","63.252","0.013","83.527","0.015","76.536","0.016","2055","3","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C26 H19 Cl O -","- C26 H19 Cl O -","- C104 H76 Cl4 O4 -","4","2","","Sun, Jing; Jiang, Wang; Yan, Chao-Guo","Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes","Organic Chemistry Frontiers","2019","6","9","1428","","10.1039/C9QO00079H","","","0.71073","MoKα","","0.4157","0.1326","","","0.2689","0.3894","","","","","","1.006","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554734","13.3814","0.001","10.6318","0.0008","19.2274","0.0016","90","","92.604","0.003","90","","2732.6","0.4","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C34 H25 Br O4 -","- C34 H25 Br O4 -","- C136 H100 Br4 O16 -","4","1","","Sun, Jing; Jiang, Wang; Yan, Chao-Guo","Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes","Organic Chemistry Frontiers","2019","6","9","1428","","10.1039/C9QO00079H","","","0.71073","MoKα","","0.1384","0.0531","","","0.1044","0.1301","","","","","","1.006","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554735","9.3743","0.0005","13.379","0.0007","14.9327","0.0008","81.008","0.001","89.658","0.001","80.276","0.001","1822.85","0.17","120","","120","","","","","","","","","6","P 1","P 1","1","","","","- C32 H33 Cl3 N4 Ni O4 -","- C32 H33 Cl3 N4 Ni O4 -","- C64 H66 Cl6 N8 Ni2 O8 -","2","2","","Larionov, Vladimir A.; Stoletova, Nadezhda V.; Kovalev, Vladislav I.; Smol'yakov, Alexander F.; Savel'yeva, Tat'yana F.; Maleev, Victor I.","A general synthesis of unnatural α-amino acids by iron-catalysed olefin‒olefin coupling via generated radicals","Organic Chemistry Frontiers","2019","6","8","1094","","10.1039/C9QO00108E","","","0.71073","MoKα","","0.0609","0.0545","","","0.146","0.1513","","","","","","1.037","","","","has coordinates,has disorder","238086","2020-10-21","18:00:00",""
"1554736","9.846","0.0004","12.0451","0.0005","14.2648","0.0006","90","","110.181","0.001","90","","1587.89","0.11","120","","120","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C37 H39 N3 Ni O4 -","- C37 H39 N3 Ni O4 -","- C74 H78 N6 Ni2 O8 -","2","1","","Larionov, Vladimir A.; Stoletova, Nadezhda V.; Kovalev, Vladislav I.; Smol'yakov, Alexander F.; Savel'yeva, Tat'yana F.; Maleev, Victor I.","A general synthesis of unnatural α-amino acids by iron-catalysed olefin–olefin coupling via generated radicals","Organic Chemistry Frontiers","2019","6","8","1094","","10.1039/C9QO00108E","","","0.71073","MoKα","","0.045","0.0372","","","0.0864","0.0899","","","","","","1.005","","","","has coordinates,has disorder","300101","2025-06-17","17:58:11",""
"1554737","11.452","0.0009","13.8346","0.0012","22.8016","0.0019","90","","90","","90","","3612.5","0.5","120","","120","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C36 H39 Cl4 N3 Ni O3 -","- C36 H39 Cl4 N3 Ni O3 -","- C144 H156 Cl16 N12 Ni4 O12 -","4","1","","Larionov, Vladimir A.; Stoletova, Nadezhda V.; Kovalev, Vladislav I.; Smol'yakov, Alexander F.; Savel'yeva, Tat'yana F.; Maleev, Victor I.","A general synthesis of unnatural α-amino acids by iron-catalysed olefin‒olefin coupling via generated radicals","Organic Chemistry Frontiers","2019","6","8","1094","","10.1039/C9QO00108E","","","0.71073","MoKα","","0.0869","0.0634","","","0.1587","0.1773","","","","","","1.031","","","","has coordinates","238086","2020-10-21","18:00:00",""
"1554738","5.459","0.0003","7.8884","0.0003","51.7461","0.0018","90","","90","","90","","2228.33","0.17","295","2","295.15","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C24 H27 Br O3 -","- C24 H27 Br O3 -","- C96 H108 Br4 O12 -","4","1","","Xin, Xiaodong; Pan, Xinhui; Meng, Zhilin; Liu, Xigong; Liu, Lei","Catalytic enantioselective cross-dehydrogenative coupling of 3,6-dihydro-2H-pyrans with aldehydes","Organic Chemistry Frontiers","2019","6","9","1448","","10.1039/C9QO00123A","","x-ray","1.54184","CuKα","","0.0752","0.068","","","0.1962","0.2027","","","","","","1.055","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554739","12.1948","0.0012","18.8246","0.001","10.1822","0.0008","90","","105.486","0.009","90","","2252.6","0.3","293","2","293.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C23 H19 Br N2 O3 S -","- C23 H19 Br N2 O3 S -","- C92 H76 Br4 N8 O12 S4 -","4","1","","Xu, Ze-Feng; Shan, Lihong; Zhang, Wan; Cen, Mengjie; Li, Chuan-Ying","Synthesis of α-aminoketones from N-sulfonyl-1,2,3-triazoles via N-sulfinyl imines generated by intramolecular oxygen transfer","Organic Chemistry Frontiers","2019","6","9","1391","","10.1039/C9QO00126C","","","0.71073","MoKα","","0.0601","0.041","","","0.0929","0.1025","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554740","17.41181","0.00011","27.6471","0.00016","17.61491","0.00011","90","","90","","90","","8479.57","0.09","100","0.1","100","0.1","","","","","","","","4","C 2 2 21","C 2c 2","20","","","","- C43 H36 N4 O9 -","- C43 H36 N4 O9 -","- C344 H288 N32 O72 -","8","1","","Liu, Xiong-Li; Gong, Yi; Chen, Shuang; Zuo, Xiong; Yao, Zhen; Zhou, Ying","Bifunctional oxindole-chromone 4C building block directed asymmetric synthesis of bispirocyclic hexahydroxanthones featuring five contiguous stereocenters and two side-by-side oxindoles","Organic Chemistry Frontiers","2019","6","10","1603","","10.1039/C9QO00127A","","x-ray","1.54184","CuKα","","0.0335","0.0331","","","0.0899","0.0905","","","","","","1.057","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554741","29.1304","0.0003","17.2687","0.0001","17.7328","0.0001","90","","103.665","0.001","90","","8667.88","0.12","100","0.1","100","0.1","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C40 H37.5 N4 O9 -","- C40 H37.5 N4 O9 -","- C320 H300 N32 O72 -","8","2","","Liu, Xiong-Li; Gong, Yi; Chen, Shuang; Zuo, Xiong; Yao, Zhen; Zhou, Ying","Bifunctional oxindole-chromone 4C building block directed asymmetric synthesis of bispirocyclic hexahydroxanthones featuring five contiguous stereocenters and two side-by-side oxindoles","Organic Chemistry Frontiers","2019","6","10","1603","","10.1039/C9QO00127A","","x-ray","1.54184","CuKα","","0.0509","0.0499","","","0.1465","0.1481","","","","","","1.08","","","","has coordinates","238091","2020-10-21","18:00:00",""
"1554742","8.1722","0.0005","16.0848","0.0007","9.1272","0.0006","90","","95.0903","0.0016","90","","1195.02","0.12","123","","123","","","","","","","","","4","P 1 21/m 1","-P 2yb","11","","","","- C31 H26 Cl2 Hf -","- C31 H26 Cl2 Hf -","- C62 H52 Cl4 Hf2 -","2","0.5","","Amaya, Toru; Katoh, Shun; Moriuchi, Toshiyuki; Hirao, Toshikazu","Synthesis of a sumanenyl hafnocene complex","Organic Chemistry Frontiers","2019","6","7","1032","","10.1039/C9QO00140A","","","0.71075","MoKα","","0.0464","0.0326","","","0.0619","0.0847","","","","","","1.234","","","","has coordinates","238093","2020-10-21","18:00:00",""
"1554743","7.272","0.0015","12.369","0.003","12.296","0.003","90","","105.99","0.03","90","","1063.2","0.5","293","2","293","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C24 H34 O6 -","- C24 H34 O6 -","- C48 H68 O12 -","2","1","","Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei","Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate","Organic Chemistry Frontiers","2019","6","6","868","","10.1039/C9QO00144A","","","0.71073","MoKα","","0.1439","0.0602","","","0.0651","0.0808","","","","","","0.954","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554744","17.407","0.003","17.407","0.003","17.977","0.004","90","","90","","120","","4717.3","1.6","293","2","293","2","","","","","","","","4","P 65","P 65","170","","","","- C30 H43 N O7 -","- C30 H43 N O7 -","- C180 H258 N6 O42 -","6","1","","Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei","Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate","Organic Chemistry Frontiers","2019","6","6","868","","10.1039/C9QO00144A","","","0.71073","MoKα","","0.2159","0.0896","","","0.1926","0.2444","","","","","","1.08","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554745","7.323","0.0015","12.384","0.003","12.233","0.002","90","","106.42","0.03","90","","1064.1","0.4","293","2","293","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C24 H34 O5 -","- C24 H34 O5 -","- C48 H68 O10 -","2","1","","Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei","Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate","Organic Chemistry Frontiers","2019","6","6","868","","10.1039/C9QO00144A","","","0.71073","MoKα","","0.0928","0.059","","","0.1519","0.1751","","","","","","1.027","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554746","10.391","0.002","12.429","0.003","18.269","0.004","90","","90","","90","","2359.4","0.9","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C28 H35 N O3 -","- C28 H35 N O3 -","- C112 H140 N4 O12 -","4","1","","Xu, Pengfei; Luan, Hongyu; Yu, Bin; Tu, Yongrui; Sun, Yongqiang; Chen, Wei; Xu, Xi; Ge, Raoling; Wang, Jubo; Li, Zhiyu; Bian, Jinlei","Synthesis and characterization of potential stereoisomeric and degradation impurities of ulipristal acetate","Organic Chemistry Frontiers","2019","6","6","868","","10.1039/C9QO00144A","","","0.71073","MoKα","","0.1157","0.0623","","","0.139","0.1676","","","","","","1.003","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554747","13.0109","0.0008","11.5329","0.0005","16.1284","0.0009","90","","109.629","0.006","90","","2279.5","0.2","150","2","150","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C25 H17 Cl3 N2 O2 S -","- C25 H17 Cl3 N2 O2 S -","- C100 H68 Cl12 N8 O8 S4 -","4","1","","Wang, Shengzheng; Guo, Zhongjie; Wu, Ying; Liu, Wei; Liu, Xueying; Zhang, Shengyong; Sheng, Chunquan","Organocatalytic asymmetric synthesis of highly functionalized spiro-thiazolone–cyclopropane-oxindoles bearing two vicinal spiro quaternary centers","Organic Chemistry Frontiers","2019","6","9","1442","","10.1039/C9QO00145J","","","1.54184","CuKα","","0.1366","0.1264","","","0.3338","0.338","","","","","","1.073","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554748","13.41045","0.0001","13.41045","0.0001","40.0935","0.0005","90","","90","","90","","7210.42","0.12","120","0.16","120","0.16","","","","","","","","4","P 41 21 2","P 4abw 2nw","92","","","","- C40 H34 I3 N3 -","- C40 H34 I3 N3 -","- C320 H272 I24 N24 -","8","1","","Anhäuser, J.; Puttreddy, R.; Lorenz, Y.; Schneider, A.; Engeser, M.; Rissanen, K.; Lützen, A.","Chiral self-sorting behaviour of [2.2]paracyclophane-based bis(pyridine) ligands","Organic Chemistry Frontiers","2019","6","8","1226","","10.1039/C9QO00155G","","x-ray","0.71073","MoKα","","0.0551","0.0448","","","0.1136","0.1189","","","","","","1.106","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554749","32.9899","0.0005","32.9899","0.0005","14.3593","0.0004","90","","90","","90","","15627.7","0.5","120.01","0.1","120.01","0.1","","","","","","","","6","P 42 21 2","P 4n 2n","94","","","","- C152 H120 B4 F16 N8 Pd2 -","- C152 H120 B4 F16 N8 Pd2 -","- C608 H480 B16 F64 N32 Pd8 -","4","0.5","","Anhäuser, J.; Puttreddy, R.; Lorenz, Y.; Schneider, A.; Engeser, M.; Rissanen, K.; Lützen, A.","Chiral self-sorting behaviour of [2.2]paracyclophane-based bis(pyridine) ligands","Organic Chemistry Frontiers","2019","6","8","1226","","10.1039/C9QO00155G","","x-ray","1.54184","CuKα","","0.0997","0.0861","","","0.2445","0.2598","","","","","","1.031","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554750","46.6905","0.0008","26.3232","0.0003","31.9982","0.0005","90","","97.75","0.002","90","","38968","1","120.01","0.1","120.01","0.1","","","","","","","","8","C 1 2/c 1","-C 2yc","15","","","","- C280 H248 F24 N8 O27 P8 Pd4 S8 -","- C280 H248 F24 N8 O27 P8 Pd4 S8 -","- C1120 H992 F96 N32 O108 P32 Pd16 S32 -","4","0.5","","Anhäuser, J.; Puttreddy, R.; Lorenz, Y.; Schneider, A.; Engeser, M.; Rissanen, K.; Lützen, A.","Chiral self-sorting behaviour of [2.2]paracyclophane-based bis(pyridine) ligands","Organic Chemistry Frontiers","2019","6","8","1226","","10.1039/C9QO00155G","","x-ray","1.54184","CuKα","","0.0992","0.0815","","","0.2423","0.2681","","","","","","1.033","","","","has coordinates,has disorder","238098","2020-10-21","18:00:00",""
"1554751","12.4931","0.0005","18.1989","0.0007","20.9673","0.0008","89.537","0.002","87.89","0.003","72.498","0.002","4543.3","0.3","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C62 H74 N22 Na O21 S2 -","- C62 H74 N22 Na O21 S2 -","- C124 H148 N44 Na2 O42 S4 -","2","1","","Bauer, Daniel; Andrae, Beatrice; Gaß, Patrick; Trenz, Danjano; Becker, Sabine; Kubik, Stefan","Functionalisable acyclic cucurbiturils","Organic Chemistry Frontiers","2019","6","10","1555","","10.1039/C9QO00156E","","","1.54178","CuKα","","0.189","0.1246","","","0.282","0.3217","","","","","","1.037","","","","has coordinates,has disorder","238100","2020-10-21","18:00:00",""
"1554752","19.1042","0.0009","43.808","0.002","23.0275","0.0011","90","","90","","90","","19272.1","1.6","100","2","100","2","","","","","","","","7","P b c n","-P 2n 2ab","60","","","","- C64 H72 Cl2 N18 Na2 O19 S2 -","- C64 H72 Cl2 N18 Na2 O19 S2 -","- C512 H576 Cl16 N144 Na16 O152 S16 -","8","1","","Bauer, Daniel; Andrae, Beatrice; Gaß, Patrick; Trenz, Danjano; Becker, Sabine; Kubik, Stefan","Functionalisable acyclic cucurbiturils","Organic Chemistry Frontiers","2019","6","10","1555","","10.1039/C9QO00156E","","","1.54178","CuKα","","0.1383","0.1112","","","0.3068","0.3181","","","","","","2.172","","","","has coordinates,has disorder","238100","2020-10-21","18:00:00",""
"1554754","17.6358","0.0009","25.0174","0.0012","26.064","0.0013","90","","109.616","0.002","90","","10832.1","0.9","100","","100","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C108 H150 F12 N2 O18 P2 -","- C108 H150 F12 N2 O18 P2 -","- C432 H600 F48 N8 O72 P8 -","4","1","","Li, Dong-Hao; Yang, Liu-Pan; Chai, Hongxin; Jia, Fei; Ke, Hua; Jiang, Wei","Temperature-induced large amplitude conformational change in the complex of oxatub[4]arene revealed via rotaxane synthesis","Organic Chemistry Frontiers","2019","6","7","1027","","10.1039/C9QO00159J","","","1.54178","CuKα","","0.0681","0.0598","","","0.1741","0.1847","","","","","","1.052","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554757","12.1293","0.0006","8.5068","0.0004","15.8667","0.0009","90","","92.925","0.005","90","","1635.02","0.15","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H11 F5 N2 O2 -","- C19 H11 F5 N2 O2 -","- C76 H44 F20 N8 O8 -","4","1","","Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun","Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides","Organic Chemistry Frontiers","2019","6","10","1613","","10.1039/C9QO00170K","","x-ray","0.71073","MoKα","","0.0718","0.0499","","","0.1058","0.1188","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554758","7.886","0.0004","9.5658","0.0007","11.4661","0.0007","86.429","0.005","79.097","0.005","77.958","0.006","830.42","0.09","100","0.1","100","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C19 H20 N4 O3 -","- C19 H20 N4 O3 -","- C38 H40 N8 O6 -","2","1","","Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun","Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides","Organic Chemistry Frontiers","2019","6","10","1613","","10.1039/C9QO00170K","","x-ray","1.54184","CuKα","","0.041","0.0396","","","0.1037","0.1047","","","","","","1.088","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554759","8.0444","0.001","10.7234","0.0012","11.5467","0.0013","71.104","0.01","70.41","0.011","73.474","0.01","870.38","0.19","100","0.1","100","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C21 H16 Cl N3 O3 -","- C21 H16 Cl N3 O3 -","- C42 H32 Cl2 N6 O6 -","2","1","","Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun","Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides","Organic Chemistry Frontiers","2019","6","10","1613","","10.1039/C9QO00170K","","x-ray","0.71073","MoKα","","0.0759","0.0561","","","0.1276","0.1414","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554760","7.7358","0.0005","9.6039","0.0006","11.631","0.0007","85.647","0.005","76.146","0.005","78.816","0.005","822.65","0.09","100","0.1","100","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C19 H20 N4 O3 -","- C19 H20 N4 O3 -","- C38 H40 N8 O6 -","2","1","","Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun","Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides","Organic Chemistry Frontiers","2019","6","10","1613","","10.1039/C9QO00170K","","x-ray","0.71073","MoKα","","0.0588","0.0458","","","0.1048","0.1137","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554761","8.7562","0.0001","23.4732","0.0003","8.8632","0.0002","90","","92.21","0.002","90","","1820.35","0.05","150","0.1","150","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H19 N3 O4 -","- C22 H19 N3 O4 -","- C88 H76 N12 O16 -","4","1","","Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun","Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides","Organic Chemistry Frontiers","2019","6","10","1613","","10.1039/C9QO00170K","","x-ray","1.54184","CuKα","","0.0435","0.0382","","","0.0967","0.099","","","","","","1.094","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554762","7.3959","0.0004","19.3566","0.0012","12.7098","0.0009","90","","91.147","0.006","90","","1819.2","0.2","99.99","0.1","99.99","0.1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C21 H15 Cl F N3 O3 -","- C21 H15 Cl F N3 O3 -","- C84 H60 Cl4 F4 N12 O12 -","4","1","","Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun","Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides","Organic Chemistry Frontiers","2019","6","10","1613","","10.1039/C9QO00170K","","x-ray","0.71073","MoKα","","0.0575","0.0445","","","0.1002","0.1079","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554763","15.9357","0.0008","13.7866","0.0008","11.8725","0.0007","90","","93.908","0.005","90","","2602.3","0.3","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C29 H19 F6 N3 O4 -","- C29 H19 F6 N3 O4 -","- C116 H76 F24 N12 O16 -","4","1","","Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun","Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides","Organic Chemistry Frontiers","2019","6","10","1613","","10.1039/C9QO00170K","","x-ray","0.71073","MoKα","","0.0902","0.0643","","","0.15","0.1664","","","","","","1.071","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554766","15.267","0.009","19.087","0.01","24.39","0.015","87.94","0.03","83.839","0.018","73.08","0.02","6760","7","150","2","150","2","","","","","","","","5","P -1","-P 1","2","","","","- C60 H78 Cl2 N4 O16 -","- C60 H78 Cl2 N4 O16 -","- C240 H312 Cl8 N16 O64 -","4","2","","Jordan, Jacobs H.; Wishard, Anthony; Mague, Joel T.; Gibb, Bruce C.","Binding properties and supramolecular polymerization of a water-soluble resorcin[4]arene","Organic Chemistry Frontiers","2019","6","8","1236","","10.1039/C9QO00182D","","","1.54184","CuKα","","0.1896","0.1646","","","0.4164","0.4366","","","","","","2.916","","","","has coordinates,has disorder","279649","2022-11-30","18:17:27",""
"1554768","9.9983","0.0002","16.3521","0.0004","19.4651","0.0005","102.163","0.001","90.869","0.001","105.091","0.001","2995.41","0.12","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C6.21 H2.28 Cl0.48 N0.07 O0.28 S0 -","- C6.2069 H2.27586 Cl0.482759 N0.0689655 O0.275862 -","- C180 H66 Cl14 N2 O8 -","29","14.5","","Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing","Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium","Organic Chemistry Frontiers","2019","6","9","1397","","10.1039/C9QO00188C","","","0.6525","synchrotron","","0.0567","0.0545","","","0.1567","0.1595","","","","","","1.104","","","","has coordinates,has disorder","238110","2020-10-21","18:00:00",""
"1554769","10.4701","0.0003","25.097","0.0011","16.2566","0.0006","90","","91.218","0.003","90","","4270.8","0.3","179.98","0.11","179.98","0.11","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C143 H54 N2 O10 S2 -","- C143 H54 N2 O10 S2 -","- C286 H108 N4 O20 S4 -","2","0.5","","Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing","Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium","Organic Chemistry Frontiers","2019","6","9","1397","","10.1039/C9QO00188C","","","0.71073","MoKα","","0.0873","0.0613","","","0.1482","0.1617","","","","","","1.001","","","","has coordinates,has disorder","238110","2020-10-21","18:00:00",""
"1554770","14.4203","0.0002","27.3088","0.0004","10.3569","0.0001","90","","94.182","0.001","90","","4067.7","0.09","180","0.1","180","0.1","","","","","","","","5","C 1 c 1","C -2yc","9","","","","- C70 H22.75 N O4.88 S2 -","- C70 H22.734 N O4.867 S2 -","- C280 H90.936 N4 O19.468 S8 -","4","1","","Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing","Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium","Organic Chemistry Frontiers","2019","6","9","1397","","10.1039/C9QO00188C","","x-ray","0.71073","MoKα","","0.0451","0.0433","","","0.1187","0.1202","","","","","","1.026","","","","has coordinates","238110","2020-10-21","18:00:00",""
"1554771","10.4366","0.0001","16.3952","0.0003","16.824","0.0003","110.869","0.001","99.019","0.001","100.619","0.001","2565.14","0.08","180","0.1","180","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C81 H42.7 N O5.85 S2 -","- C81 H42.7 N O5.85 S2 -","- C162 H85.4 N2 O11.7 S4 -","2","1","","Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing","Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium","Organic Chemistry Frontiers","2019","6","9","1397","","10.1039/C9QO00188C","","x-ray","0.71073","MoKα","","0.0856","0.0773","","","0.1924","0.197","","","","","","1.01","","","","has coordinates,has disorder","238110","2020-10-21","18:00:00",""
"1554772","10.4595","0.0004","25.0584","0.001","16.2556","0.0007","90","","91.316","0.004","90","","4259.4","0.3","179.99","0.1","179.99","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C143 H57.4 N2 O11.7 S2 -","- C143 H57.404 N2 O11.702 S2 -","- C286 H114.808 N4 O23.404 S4 -","2","0.5","","Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing","Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium","Organic Chemistry Frontiers","2019","6","9","1397","","10.1039/C9QO00188C","","x-ray","0.71073","MoKα","","0.0924","0.0681","","","0.1553","0.1679","","","","","","1.027","","","","has coordinates","238110","2020-10-21","18:00:00",""
"1554775","13.3462","0.0004","10.2259","0.0003","12.0633","0.0004","90","","96.466","0.001","90","","1635.89","0.09","161","2","161","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H20 N2 Se -","- C19 H20 N2 Se -","- C76 H80 N8 Se4 -","4","1","","Guo, Tao; Wei, Xu-Ning; Liu, Yu; Zhang, Pan-Ke; Zhao, Yun-Hui","Oxidative dual C–H selenation of imidazoheterocycles with ethers or alkanes using selenium powder via a radical pathway","Organic Chemistry Frontiers","2019","6","9","1414","","10.1039/C9QO00198K","","","1.54178","cukα","","0.0273","0.0261","","","0.0699","0.0712","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554777","8.4621","0.0005","19.7458","0.001","21.2129","0.001","90","","90","","90","","3544.5","0.3","173","2","173","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C21 H18 N O3 P -","- C21 H18 N O3 P -","- C168 H144 N8 O24 P8 -","8","2","","Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.","Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones","Organic Chemistry Frontiers","2019","6","8","1257","","10.1039/C9QO00199A","","","1.54178","CuKα","","0.0849","0.0738","","","0.1871","0.1949","","","","","","1.066","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554778","18.5757","0.0004","6.176","0.0002","18.9148","0.0005","90","","98.809","0.002","90","","2144.38","0.1","173","2","173","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C25 H23 N2 O2 P -","- C25 H23 N2 O2 P -","- C100 H92 N8 O8 P4 -","4","1","","Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.","Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones","Organic Chemistry Frontiers","2019","6","8","1257","","10.1039/C9QO00199A","","","1.54178","CuKα","","0.0564","0.0408","","","0.0999","0.1093","","","","","","1.022","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554779","29.394","0.003","6.3419","0.0005","28.119","0.003","90","","121.188","0.004","90","","4484.2","0.8","173","2","173","2","","","","","","","","7","C 1 2/c 1","-C 2yc","15","","","","- C22.5 H14.5 Cl1.5 F3 N2 O2 P -","- C22.5 H14 Cl1.5 F3 N2 O2 P -","- C180 H112 Cl12 F24 N16 O16 P8 -","8","1","","Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.","Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones","Organic Chemistry Frontiers","2019","6","8","1257","","10.1039/C9QO00199A","","","1.54178","CuKα","","0.1045","0.0849","","","0.2236","0.2386","","","","","","1.086","","","","has coordinates","238115","2020-10-21","18:00:00",""
"1554780","24.331","0.004","10.2408","0.0018","14.54","0.003","90","","102.686","0.003","90","","3534.5","1.1","173","2","173","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C21 H15 N2 O2 P -","- C21 H15 N2 O2 P -","- C168 H120 N16 O16 P8 -","8","1","","Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.","Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones","Organic Chemistry Frontiers","2019","6","8","1257","","10.1039/C9QO00199A","","","0.71073","MoKα","","0.0568","0.0369","","","0.0955","0.1104","","","","","","1.049","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554781","26.4131","0.0008","9.7872","0.0003","14.9148","0.0005","90","","115.7","0.001","90","","3474.22","0.19","173","2","173","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C21 H15 N2 O2 P -","- C21 H15 N2 O2 P -","- C168 H120 N16 O16 P8 -","8","1","","Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.","Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones","Organic Chemistry Frontiers","2019","6","8","1257","","10.1039/C9QO00199A","","","1.54178","CuKα","","0.0385","0.0346","","","0.093","0.0967","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554784","14.1538","0.0012","10.7714","0.0008","20.0319","0.0019","90","","90","","90","","3054","0.4","173","2","173","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C13 H18 N2 O2 S2 -","- C13 H18 N2 O2 S2 -","- C104 H144 N16 O16 S16 -","8","1","","Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry","Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters","Organic Chemistry Frontiers","2019","6","8","1244","","10.1039/C9QO00202B","","","0.71073","MoKα","","0.1567","0.0652","","","0.124","0.1493","","","","","","0.927","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554785","5.1535","0.0002","7.3073","0.0003","16.2864","0.0007","81.694","0.002","82.41","0.002","74.561","0.001","582.16","0.04","109","2","109","2","","","","","","","","4","P -1","-P 1","2","KH-195","","","- C11 H12 O4 S2 -","- C11 H12 O4 S2 -","- C22 H24 O8 S4 -","2","1","","Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry","Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters","Organic Chemistry Frontiers","2019","6","8","1244","","10.1039/C9QO00202B","","","0.71073","MoKα","","0.0459","0.0367","","","0.0941","0.0995","","","","","","1.076","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554786","19.6986","0.0013","10.9502","0.0008","16.5805","0.0011","90","","122.988","0.0017","90","","2999.9","0.4","100","2","100","2","","","","","","","","4","C 1 c 1","C -2yc","9","","","","- C36 H38 O2 S2 -","- C36 H38 O2 S2 -","- C144 H152 O8 S8 -","4","1","","Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry","Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters","Organic Chemistry Frontiers","2019","6","8","1244","","10.1039/C9QO00202B","","","0.71073","MoKα","","0.0457","0.0369","","","0.088","0.0921","","","","","","1.043","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554787","9.4599","0.0007","10.4995","0.0008","17.9405","0.0013","82.254","0.002","86.522","0.003","88.292","0.002","1762","0.2","103","2","103","2","","","","","","","","4","P -1","-P 1","2","KH-11","","","- C40 H46 O2 S2 -","- C40 H46 O2 S2 -","- C80 H92 O4 S4 -","2","1","","Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry","Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters","Organic Chemistry Frontiers","2019","6","8","1244","","10.1039/C9QO00202B","","","0.71073","MoKα","","0.066","0.0501","","","0.1333","0.1452","","","","","","1.045","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554788","11.3446","0.0008","17.747","0.0013","17.3945","0.0012","90","","97.039","0.002","90","","3475.7","0.4","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C41 H48 O2 S2 -","- C41 H48 O2 S2 -","- C164 H192 O8 S8 -","4","1","","Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry","Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters","Organic Chemistry Frontiers","2019","6","8","1244","","10.1039/C9QO00202B","","","0.71073","MoKα","","0.0798","0.0463","","","0.0976","0.1098","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554789","10.5966","0.0004","11.0075","0.0004","13.0168","0.0005","90","","103.286","0.0013","90","","1477.67","0.1","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C13 H18 N2 O2 S2 -","- C13 H18 N2 O2 S2 -","- C52 H72 N8 O8 S8 -","4","1","","Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry","Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters","Organic Chemistry Frontiers","2019","6","8","1244","","10.1039/C9QO00202B","","","0.71073","MoKα","","0.0505","0.0407","","","0.0965","0.1012","","","","","","1.101","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554790","14.4032","0.0007","9.233","0.0005","24.7181","0.0015","90","","93.6338","0.0015","90","","3280.5","0.3","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C37 H40 O2 S2 -","- C37 H40 O2 S2 -","- C148 H160 O8 S8 -","4","1","","Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry","Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters","Organic Chemistry Frontiers","2019","6","8","1244","","10.1039/C9QO00202B","","","0.71073","MoKα","","0.0599","0.0426","","","0.1038","0.1143","","","","","","1.051","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554792","12.234","0.0011","10.9831","0.0011","14.6454","0.0014","90","","111.492","0.003","90","","1831","0.3","150","2","150","2","","","","","","","synthesis as described","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H12 F6 Se -","- C24 H12 F6 Se -","- C96 H48 F24 Se4 -","4","1","","Shi, Xinzhe; Mao, Shuxin; Roisnel, Thierry; Doucet, Henri; Soulé, Jean-François","Palladium-catalyzed successive C–H bond arylations and annulations toward the π-extension of selenophene-containing aromatic skeletons","Organic Chemistry Frontiers","2019","6","14","2398","","10.1039/C9QO00218A","","x-ray","0.71073","MoKα","","0.0331","0.0256","","","0.0625","0.0672","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554795","11.6434","0.0005","14.186","0.0005","17.6525","0.0006","90","","90","","90","","2915.72","0.19","150","2","150","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C36 H23 Br F3 N2 O3 -","- C36 H23 Br F3 N2 O3 -","- C144 H92 Br4 F12 N8 O12 -","4","1","","Li, Boyu; Gao, Fengyun; Feng, Xing; Sun, Mengmeng; Guo, Yifei; Wen, Dongwa; Deng, Yabo; Huang, Jinqi; Wang, Kairong; Yan, Wenjin","Highly efficient enantioselective synthesis of bispiro[benzofuran-oxindole-pyrrolidine]s through organocatalytic cycloaddition","Organic Chemistry Frontiers","2019","6","10","1567","","10.1039/C9QO00241C","","","1.54178","CuKα","","0.0321","0.0315","","","0.0782","0.0786","","","","","","1.001","","","","has coordinates","238123","2020-10-21","18:00:00",""
"1554799","9.8327","0.0003","16.984","0.0006","16.2007","0.0005","90","","101.138","0.001","90","","2654.54","0.15","100","2","100","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C27 H40 O6 -","- C27 H40 O6 -","- C108 H160 O24 -","4","2","","Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui","The absolute configurations of hyperilongenols A–C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv.","Organic Chemistry Frontiers","2019","6","9","1491","","10.1039/C9QO00245F","","","1.54178","CuKα","","0.0628","0.0615","","","0.1752","0.1773","","","","","","1.031","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554800","12.0011","0.0003","13.3921","0.0003","17.7454","0.0004","90","","90","","90","","2852.04","0.12","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C29 H44 O6 -","- C29 H44 O6 -","- C116 H176 O24 -","4","1","","Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui","The absolute configurations of hyperilongenols A–C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv.","Organic Chemistry Frontiers","2019","6","9","1491","","10.1039/C9QO00245F","","","1.54178","CuKα","","0.0316","0.0316","","","0.0813","0.0814","","","","","","1.072","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554801","9.6691","0.0001","16.4235","0.0001","15.94","0.0001","90","","101.09","","90","","2484.01","0.03","100","2","100","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C26 H38 O6 -","- C26 H38 O6 -","- C104 H152 O24 -","4","2","","Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui","The absolute configurations of hyperilongenols A–C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv.","Organic Chemistry Frontiers","2019","6","9","1491","","10.1039/C9QO00245F","","","1.54178","CuKα","","0.0395","0.0391","","","0.1027","0.103","","","","","","1.035","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554805","12.983","0.003","13.401","0.003","29.22","0.006","81.31","0.03","77.62","0.03","61.97","0.03","4376","2","301","2","301","2","","","","","","","synthesis as described","6","P -1","-P 1","2","","","","- C162 H174 Au4 Cl16 O8 P4 -","- C162 H174 Au4 Cl16 O8 P4 -","- C162 H174 Au4 Cl16 O8 P4 -","1","0.5","","Hau, Franky Ka-Wah; Cheung, Kai-Leung; Zhu, Nianyong; Yam, Vivian Wing-Wah","Calixarene-based alkynyl-bridged gold(i) isocyanide and phosphine complexes as building motifs for the construction of chemosensors and supramolecular architectures","Organic Chemistry Frontiers","2019","6","8","1205","","10.1039/C9QO00258H","","x-ray","0.71073","MoKα","","0.1285","0.0751","","","0.2182","0.2492","","","","","","0.97","","","","has coordinates","238128","2020-10-21","18:00:00",""
"1554807","10.4979","0.0007","10.7112","0.0007","10.8365","0.0007","60.7986","0.0016","76.2796","0.0017","71.3801","0.0017","1003.08","0.12","200","2","200","2","","","","","","","","4","P -1","-P 1","2","5a in manuscript","","","- C27 H23 N O -","- C27 H23 N O -","- C54 H46 N2 O2 -","2","1","","Lustosa, Danilo M.; Cieslik, Patrick; Hartmann, Deborah; Bruckhoff, Tim; Rudolph, Matthias; Rominger, Frank; Hashmi, A. Stephen K.","Direct access to benzo[b]fluorenes via a gold-catalysed A3-coupling strategy","Organic Chemistry Frontiers","2019","6","10","1655","","10.1039/C9QO00260J","","","0.71073","MoKα","","0.0956","0.0551","","","0.1259","0.1418","","","","","","1.023","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554808","6.7344","0.0004","18.9552","0.0012","15.1244","0.0008","90","","90.856","0.004","90","","1930.4","0.2","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","6a in manuscript","","","- C27 H23 N O -","- C27 H23 N O -","- C108 H92 N4 O4 -","4","2","","Lustosa, Danilo M.; Cieslik, Patrick; Hartmann, Deborah; Bruckhoff, Tim; Rudolph, Matthias; Rominger, Frank; Hashmi, A. Stephen K.","Direct access to benzo[b]fluorenes via a gold-catalysed A3-coupling strategy","Organic Chemistry Frontiers","2019","6","10","1655","","10.1039/C9QO00260J","","","1.54178","CuKα","","0.1004","0.0799","","","0.2324","0.2432","","","","","","1.578","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554811","9.7212","0.0001","10.3208","0.0001","28.5171","0.0003","90","","90","","90","","2861.14","0.05","100","0.1","100","0.1","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C34 H30 N2 O7 -","- C34 H30 N2 O7 -","- C136 H120 N8 O28 -","4","1","","Liu, Xiong-Li; Zuo, Xiong; Wang, Jun-Xin; Chang, Shun-qin; Wei, Qi-Di; Zhou, Ying","A bifunctional pyrazolone–chromone synthon directed organocatalytic double Michael cascade reaction: forging five stereocenters in structurally diverse hexahydroxanthones","Organic Chemistry Frontiers","2019","6","9","1485","","10.1039/C9QO00265K","","x-ray","1.54184","CuKα","","0.0327","0.0323","","","0.081","0.0813","","","","","","1.084","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554812","11.7466","0.0001","12.2636","0.0002","22.7319","0.0002","90","","93.091","0.001","90","","3269.89","0.07","100","0.1","100","0.1","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C36 H32 F N3 O7 -","- C36 H32 F N3 O7 -","- C144 H128 F4 N12 O28 -","4","2","","Liu, Xiong-Li; Zuo, Xiong; Wang, Jun-Xin; Chang, Shun-qin; Wei, Qi-Di; Zhou, Ying","A bifunctional pyrazolone–chromone synthon directed organocatalytic double Michael cascade reaction: forging five stereocenters in structurally diverse hexahydroxanthones","Organic Chemistry Frontiers","2019","6","9","1485","","10.1039/C9QO00265K","","x-ray","1.54184","CuKα","","0.0353","0.0345","","","0.0958","0.0964","","","","","","1.035","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554816","6.2353","0.0004","7.7873","0.0004","17.3098","0.001","90","","90.759","0.003","90","","840.42","0.08","170","2","169.99","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C17 H16 Br F3 O2 -","- C17 H16 Br F3 O2 -","- C34 H32 Br2 F6 O4 -","2","1","","Chen, Daoqian; Lu, Long; Shen, Qilong","[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates","Organic Chemistry Frontiers","2019","6","11","1801","","10.1039/C9QO00278B","","","1.34139","GaKα","","0.0375","0.0343","","","0.0841","0.0874","","","","","","1.064","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554817","10.6202","0.0004","6.377","0.0002","16.3385","0.0006","90","","98.252","0.001","90","","1095.07","0.07","296","2","296","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C23 H21 N O7 S -","- C23 H21 N O7 S -","- C46 H42 N2 O14 S2 -","2","1","","Chen, Daoqian; Lu, Long; Shen, Qilong","[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates","Organic Chemistry Frontiers","2019","6","11","1801","","10.1039/C9QO00278B","","","0.71073","MoKα","","0.054","0.0385","","","0.0991","0.1128","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554818","6.4981","0.0003","15.2542","0.0006","17.146","0.0006","90","","90","","90","","1699.57","0.12","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C18 H17 F3 O3 -","- C18 H17 F3 O3 -","- C72 H68 F12 O12 -","4","1","","Chen, Daoqian; Lu, Long; Shen, Qilong","[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates","Organic Chemistry Frontiers","2019","6","11","1801","","10.1039/C9QO00278B","","","1.54178","CuKα","","0.0469","0.0445","","","0.1257","0.1298","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554819","15.277","0.0004","8.0788","0.0002","21.7171","0.0005","90","","98.481","0.001","90","","2651.01","0.11","170","2","169.96","","","","","","","","","6","P 1 c 1","P -2yc","7","","","","- C24 H31 Ag F6 N2 P2 -","- C24 H31 Ag F6 N2 P2 -","- C96 H124 Ag4 F24 N8 P8 -","4","2","","Chen, Daoqian; Lu, Long; Shen, Qilong","[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates","Organic Chemistry Frontiers","2019","6","11","1801","","10.1039/C9QO00278B","","","1.34139","GaKα","","0.0435","0.0405","","","0.0968","0.0997","","","","","","1.036","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554820","12.7111","0.0004","17.36","0.0006","15.7081","0.0005","90","","105.588","0.001","90","","3338.73","0.19","170","2","170.02","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C31 H41 Ag F6 N4 P2 -","- C31 H41 Ag F6 N4 P2 -","- C124 H164 Ag4 F24 N16 P8 -","4","1","","Chen, Daoqian; Lu, Long; Shen, Qilong","[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates","Organic Chemistry Frontiers","2019","6","11","1801","","10.1039/C9QO00278B","","","1.34139","GaKα","","0.0437","0.0429","","","0.1263","0.1278","","","","","","1.108","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554821","11.3702","0.0003","12.6386","0.0003","17.83","0.0005","90","","103.361","0.001","90","","2492.88","0.11","173","2","173","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C25 H31 Ag F3 N2 O P -","- C25 H31 Ag F3 N2 O P -","- C100 H124 Ag4 F12 N8 O4 P4 -","4","1","","Chen, Daoqian; Lu, Long; Shen, Qilong","[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates","Organic Chemistry Frontiers","2019","6","11","1801","","10.1039/C9QO00278B","","","0.71073","MoKα","","0.0284","0.026","","","0.0875","0.0904","","","","","","1.011","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554823","8.061","0.0002","10.8588","0.0002","27.7356","0.0006","90","","90","","90","","2427.77","0.09","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C27 H40 O4 -","- C27 H40 O4 -","- C108 H160 O16 -","4","1","","Xu, Hou-Chao; Hu, Kun; Shi, Xiao-Huo; Tang, Jian-Wei; Li, Xiao-Nian; Sun, Han-Dong; Puno, Pema-Tenzin","Synergistic use of NMR computation and quantitative interproton distance analysis in the structural determination of neokadcoccitane A, a rearranged triterpenoid featuring an aromatic ring D from Kadsura coccinea","Organic Chemistry Frontiers","2019","6","10","1619","","10.1039/C9QO00281B","","","1.54178","CuKα","","0.036","0.0358","","","0.0981","0.0984","","","","","","1.085","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554825","5.4882","0.0007","11.1825","0.0015","11.6413","0.0016","62.292","0.014","80.059","0.011","76.727","0.011","613.82","0.16","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C15 H13 N3 -","- C15 H13 N3 -","- C30 H26 N6 -","2","1","","Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz","A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons","Organic Chemistry Frontiers","2019","6","16","2825","","10.1039/C9QO00294D","","","1.54184","CuKα","","0.1177","0.0956","","","0.2368","0.2677","","","","","","1.009","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554826","15.105","0.0005","12.8664","0.0004","15.5822","0.0005","90","","91.952","0.003","90","","3026.6","0.17","293","2","293","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C17 H17 N3 O2 -","- C17 H17 N3 O2 -","- C136 H136 N24 O16 -","8","1","","Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz","A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons","Organic Chemistry Frontiers","2019","6","16","2825","","10.1039/C9QO00294D","","","0.71073","MoKα","","0.1063","0.0658","","","0.1466","0.1757","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554827","7.1859","0.0004","12.0427","0.0007","12.0895","0.0009","93.791","0.005","100.927","0.005","98.538","0.005","1011.05","0.11","100","0.1","100","0.1","","","","","","","","6","P -1","-P 1","2","","","","- C19 H17 B F2 N4 O2 -","- C19 H17 B F2 N4 O2 -","- C38 H34 B2 F4 N8 O4 -","2","1","","Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz","A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons","Organic Chemistry Frontiers","2019","6","16","2825","","10.1039/C9QO00294D","","x-ray","0.71073","MoKα","","0.0683","0.0479","","","0.1168","0.1299","","","","","","1.018","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554828","10.668","0.0014","24.498","0.004","11.286","0.003","90","","93.034","0.012","90","","2945.4","1","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H16 N3 O2.5 -","- C17 H16 N3 O2.5 -","- C136 H128 N24 O20 -","8","2","","Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz","A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons","Organic Chemistry Frontiers","2019","6","16","2825","","10.1039/C9QO00294D","","","0.71073","MoKα","","0.2527","0.0753","","","0.0943","0.1374","","","","","","0.799","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554829","11.1306","0.0003","11.7622","0.0003","24.0194","0.0007","90","","91.217","0.002","90","","3143.92","0.15","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C17.14 H14.5 B F2 N3 O2 -","- C17 H16 B F2 N3 O2 -","- C136 H128 B8 F16 N24 O16 -","8","2","","Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz","A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons","Organic Chemistry Frontiers","2019","6","16","2825","","10.1039/C9QO00294D","","","0.71073","MoKα","","0.0798","0.0599","","","0.1524","0.173","","","","","","1.04","","","","has coordinates,has disorder","238142","2020-10-21","18:00:00",""
"1554836","9.5782","0.0006","11.765","0.0004","20.2153","0.0009","90","","90","","90","","2278.01","0.19","295","2","295","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C22 H26 N4 O5 -","- C22 H26 N4 O5 -","- C88 H104 N16 O20 -","4","1","","Dai, Chuan; Ma, Jun; Li, Min; Wu, Wen; Xia, Xuefeng; Zhang, Jinqiang","Diversity-oriented submonomer synthesis of azapeptides mediated by the Mitsunobu reaction","Organic Chemistry Frontiers","2019","6","14","2529","","10.1039/C9QO00296K","","","0.71073","MoKα","","0.0883","0.0601","","","0.1385","0.1634","","","","","","1.072","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554843","10.7226","0.0003","12.3939","0.0003","15.6108","0.0004","90","","92.991","0.003","90","","2071.77","0.09","123","40","123","40","","","","","","","","7","C 1 c 1","C -2yc","9","1a","","","- C16 H23 Cl F6 N3 O2 P -","- C16 H23 Cl F6 N3 O2 P -","- C64 H92 Cl4 F24 N12 O8 P4 -","4","1","","Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David","Stable dicationic dioxoliums and fate of their dioxolyl radicals","Organic Chemistry Frontiers","2019","6","18","3184","","10.1039/C9QO00298G","","x-ray","0.71073","MoKα","","0.0509","0.0434","","","0.1061","0.1107","","","","","","1.038","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554844","11.8795","0.0005","14.5176","0.0005","12.6593","0.0006","90","","102.138","0.004","90","","2134.44","0.16","149","2","149","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C17 H23 Cl2 F6 N2 O2 P -","- C17 H23 Cl2 F6 N2 O2 P -","- C68 H92 Cl8 F24 N8 O8 P4 -","4","1","","Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David","Stable dicationic dioxoliums and fate of their dioxolyl radicals","Organic Chemistry Frontiers","2019","6","18","3184","","10.1039/C9QO00298G","","x-ray","0.71073","MoKα","","0.0571","0.04","","","0.0888","0.0979","","","","","","1.035","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554845","36.485","0.007","10.158","0.002","16.856","0.003","90","","92.44","0.03","90","","6241","2","200","","200","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C28 H41 F6 N4 O2 P -","- C28 H41 F6 N4 O2 P -","- C224 H328 F48 N32 O16 P8 -","8","1","","Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David","Stable dicationic dioxoliums and fate of their dioxolyl radicals","Organic Chemistry Frontiers","2019","6","18","3184","","10.1039/C9QO00298G","","x-ray","0.71073","MoKα","","0.0861","0.0524","","","0.1225","0.1496","","","","","","1.096","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554846","24.915","0.002","8.8562","0.0007","19.8464","0.0018","90","","105.666","0.009","90","","4216.5","0.6","150","0.1","150","0.1","","","","","","","","6","I 1 2/a 1","-I 2ya","15","","","","- C34 H49 F12 N7 O4 P2 -","- C34 H49 F12 N7 O4 P2 -","- C136 H196 F48 N28 O16 P8 -","4","0.5","","Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David","Stable dicationic dioxoliums and fate of their dioxolyl radicals","Organic Chemistry Frontiers","2019","6","18","3184","","10.1039/C9QO00298G","","x-ray","0.71073","MoKα","","0.138","0.0803","","","0.1669","0.196","","","","","","1.048","","","","has coordinates,has disorder","238151","2020-10-21","18:00:00",""
"1554847","10.7516","0.0004","12.0558","0.0006","14.8348","0.0006","107.62","0.004","93.413","0.003","109.731","0.004","1696.8","0.14","150","0.14","150","0.14","","","","","","","","7","P -1","-P 1","2","6c","","","- C26 H39.5 F9 N4.5 O5 P S -","- C26 H39.5 F9 N4.5 O5 P S -","- C52 H79 F18 N9 O10 P2 S2 -","2","1","","Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David","Stable dicationic dioxoliums and fate of their dioxolyl radicals","Organic Chemistry Frontiers","2019","6","18","3184","","10.1039/C9QO00298G","","x-ray","0.71073","MoKα","","0.0828","0.0612","","","0.1572","0.1736","","","","","","1.04","","","","has coordinates,has disorder","238151","2020-10-21","18:00:00",""
"1554848","7.59057","0.00019","26.3895","0.0007","12.488","0.0003","90","","107.133","0.003","90","","2390.48","0.11","149.95","0.1","149.95","0.1","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C19 H29 Cl F6 N3 O2 P -","- C19 H29 Cl F6 N3 O2 P -","- C76 H116 Cl4 F24 N12 O8 P4 -","4","1","","Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David","Stable dicationic dioxoliums and fate of their dioxolyl radicals","Organic Chemistry Frontiers","2019","6","18","3184","","10.1039/C9QO00298G","","x-ray","0.71073","MoKα","","0.0593","0.0449","","","0.0993","0.1058","","","","","","1.064","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554849","12.3903","0.001","16.1931","0.001","13.6174","0.0011","90","","113.783","0.01","90","","2500.1","0.4","149.95","0.1","149.95","0.1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","9b","","","- C21 H32 F6 N4 O2 P -","- C21 H32 F6 N4 O2 P -","- C84 H128 F24 N16 O8 P4 -","4","1","","Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David","Stable dicationic dioxoliums and fate of their dioxolyl radicals","Organic Chemistry Frontiers","2019","6","18","3184","","10.1039/C9QO00298G","","x-ray","0.71073","MoKα","","0.0871","0.058","","","0.131","0.1473","","","","","","1.017","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554850","10.5891","0.0002","16.2883","0.0004","13.903","0.0003","90","","102.985","0.002","90","","2336.65","0.09","150","0.14","150","0.14","","","","","","","","6","P 1 21/n 1","-P 2yn","14","6a","","","- C16 H23 F12 N3 O2 P2 -","- C16 H23 F12 N3 O2 P2 -","- C64 H92 F48 N12 O8 P8 -","4","1","","Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David","Stable dicationic dioxoliums and fate of their dioxolyl radicals","Organic Chemistry Frontiers","2019","6","18","3184","","10.1039/C9QO00298G","","x-ray","0.71073","MoKα","","0.0846","0.053","","","0.1114","0.1245","","","","","","1.044","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554851","18.6093","0.0007","10.778","0.0003","15.4265","0.0006","90","","101.706","0.004","90","","3029.76","0.19","149","3","149","3","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C26 H41 Cl2 F6 N2 O2 P -","- C26 H41 Cl2 F6 N2 O2 P -","- C104 H164 Cl8 F24 N8 O8 P4 -","4","1","","Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David","Stable dicationic dioxoliums and fate of their dioxolyl radicals","Organic Chemistry Frontiers","2019","6","18","3184","","10.1039/C9QO00298G","","x-ray","0.71073","MoKα","","0.0973","0.0544","","","0.1016","0.117","","","","","","1.01","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554852","9.5322","0.0004","18.6061","0.0007","21.1198","0.0011","83.275","0.004","88.086","0.004","80.993","0.003","3673.7","0.3","150","0.14","150","0.14","","","","","","","","7","P -1","-P 1","2","","","","- C30.33 H52.53 Cl2.12 F6 N3 O2.44 P -","- C30.323 H52.528 Cl2.118 F6 N3 O2.441 P -","- C121.292 H210.112 Cl8.472 F24 N12 O9.764 P4 -","4","2","","Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David","Stable dicationic dioxoliums and fate of their dioxolyl radicals","Organic Chemistry Frontiers","2019","6","18","3184","","10.1039/C9QO00298G","","x-ray","0.71073","MoKα","","0.1554","0.1108","","","0.2715","0.2951","","","","","","1.105","","","","has coordinates,has disorder","238151","2020-10-21","18:00:00",""
"1554853","12.7678","0.0013","11.6389","0.001","36.278","0.003","90","","94.051","0.007","90","","5377.6","0.8","150","0.14","150","0.14","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C22 H35 Cl F6 N3 O2 P -","- C22 H35 Cl F6 N3 O2 P -","- C176 H280 Cl8 F48 N24 O16 P8 -","8","2","","Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David","Stable dicationic dioxoliums and fate of their dioxolyl radicals","Organic Chemistry Frontiers","2019","6","18","3184","","10.1039/C9QO00298G","","x-ray","0.71073","MoKα","","0.2373","0.0847","","","0.1418","0.2095","","","","","","0.929","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554854","12.1931","0.0003","15.3991","0.0004","22.7102","0.0005","95.65","0.002","102.392","0.002","94.7722","0.0019","4120.61","0.18","149.95","0.1","149.95","0.1","","","","","","","","6","P -1","-P 1","2","","","","- C33 H47.66 F12 N6.5 O4.08 P2 -","- C33 H47.659 F12 N6.5 O4.0795 P2 -","- C132 H190.636 F48 N26 O16.318 P8 -","4","2","","Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David","Stable dicationic dioxoliums and fate of their dioxolyl radicals","Organic Chemistry Frontiers","2019","6","18","3184","","10.1039/C9QO00298G","","x-ray","0.71073","MoKα","","0.0807","0.0581","","","0.1262","0.137","","","","","","1.02","","","","has coordinates,has disorder","238151","2020-10-21","18:00:00",""
"1554857","6.9512","0.0002","8.6039","0.0003","15.1128","0.0004","102.337","0.001","92.466","0.001","108.002","0.001","833.95","0.04","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C19 H20 O3 S -","- C19 H20 O3 S -","- C38 H40 O6 S2 -","2","1","","He, Fu-Sheng; Wu, Youqian; Li, Xiaofang; Xia, Hongguang; Wu, Jie","Photoredox-catalyzed sulfonylation of alkenylcyclobutanols with the insertion of sulfur dioxide through semipinacol rearrangement","Organic Chemistry Frontiers","2019","6","11","1873","","10.1039/C9QO00300B","","","1.34138","GaKα","","0.044","0.0415","","","0.1121","0.1148","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554859","6.0877","0.0011","10.8073","0.0014","26.052","0.004","90","","93.948","0.006","90","","1709.9","0.5","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C17 H23 N O5 S -","- C17 H23 N O5 S -","- C68 H92 N4 O20 S4 -","4","1","","Xu, Dongyang; Wei, Hongbo; Zhen, Yanxia; Gao, Yu-Qi; Li, Ruoxin; Li, Xingzhou; He, Yupeng; Zhang, Zhong; Xie, Weiqing","Carboxylate phosphabetaine as a bifunctional organocatalyst for the intramolecular ring opening of oxetane","Organic Chemistry Frontiers","2019","6","10","1681","","10.1039/C9QO00304E","","","0.71073","","","0.0465","0.0383","","","0.0902","0.0943","","","","","","1.085","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554861","6.4968","0.0013","22.26","0.005","7.1909","0.0014","90","","116.2","0.03","90","","933.1","0.4","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C9 H11 B0.75 O2.25 -","- C9 H11 B O3 -","- C36 H44 B4 O12 -","4","1","","Bhavanarushi, Sangepu; Xu, Yin; Khan, Imran; Luo, Zhibin; Liu, Bin; Xie, Jimin","Transition-metal-free borylation of propargylic alcohols: structurally variable synthesis in ionic liquid medium","Organic Chemistry Frontiers","2019","6","11","1895","","10.1039/C9QO00322C","","","0.71073","MoKα","","0.0449","0.0385","","","0.136","0.1423","","","","","","1.105","","","","has coordinates","238158","2020-10-21","18:00:00",""
"1554863","5.41","0.002","17.433","0.007","11.237","0.004","90","","93.29","0.007","90","","1058","0.7","100","","100","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C11 H7 F3 N2 O2 -","- C11 H7 F3 N2 O2 -","- C44 H28 F12 N8 O8 -","4","1","","Peng, Xiaofeng; Zhang, Xiaofei; Li, Shunyao; Lu, Yunfu; Lan, Lefu; Yang, Chunhao","Silver-mediated synthesis of novel 3-CF3/CN/phosphonate-substituted pyrazoles as pyrrolomycin analogues from 3-formylchromones and diazo compounds","Organic Chemistry Frontiers","2019","6","11","1775","","10.1039/C9QO00324J","","","0.71073","MoKα","","0.1046","0.0595","","","0.1375","0.1599","","","","","","1.019","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554865","12.2161","0.0005","12.5468","0.0005","16.7879","0.0007","90","","90","","90","","2573.13","0.18","273","2","273.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C24 H22 N2 O9 S -","- C24 H22 N2 O9 S -","- C96 H88 N8 O36 S4 -","4","1","","Zhou, Qing; Chen, Bo; Huang, Xiao-Bing; Zeng, Ya-Li; Chu, Wen-Dao; He, Long; Liu, Quan-Zhong","Palladium-catalyzed diastereo- and enantioselective formal [3 + 2] cycloaddition of vinyl cyclopropanes with cyclic 1-azadienes","Organic Chemistry Frontiers","2019","6","11","1891","","10.1039/C9QO00325H","","","1.54178","CuKα","","0.072","0.0579","","","0.1392","0.1531","","","","","","1.088","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554866","10.3133","0.0004","11.2328","0.0004","19.0954","0.0008","90","","99.604","0.002","90","","2181.14","0.15","293","2","293.15","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C24 H24 O6 -","- C24 H24 O6 -","- C96 H96 O24 -","4","1","","Zhou, Qing; Chen, Bo; Huang, Xiao-Bing; Zeng, Ya-Li; Chu, Wen-Dao; He, Long; Liu, Quan-Zhong","Palladium-catalyzed diastereo- and enantioselective formal [3 + 2] cycloaddition of vinyl cyclopropanes with cyclic 1-azadienes","Organic Chemistry Frontiers","2019","6","11","1891","","10.1039/C9QO00325H","","","1.54178","CuKα","","0.054","0.0499","","","0.1332","0.1372","","","","","","1.038","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554868","5.9309","0.0006","17.47","0.002","19.675","0.003","90","","90","","90","","2038.6","0.4","173","2","173","2","","","","","","","synthesis","5","P 21 21 21","P 2ac 2ab","19","4-spiropyrazolone","3-(4-chlorophenyl)-7-methoxy-3'-methyl-1'-phenyl-3H-spiro[benzofuran-2,4'-pyrazol]-5'(1'H)-one","","- C24 H19 Cl N2 O3 -","- C24 H19 Cl N2 O3 -","- C96 H76 Cl4 N8 O12 -","4","1","","Chu, Ming-Ming; Qi, Suo-Suo; Wang, Yi-Feng; Wang, Biao; Jiang, Zhen-Hui; Xu, Dan-Qian; Xu, Zhen-Yuan","Organocatalytic asymmetric [4 + 1] annulation of in situ generated ortho-quinomethanes with 4-halo pyrazolones: straightforward access to chiral spiro-benzofuran pyrazolones","Organic Chemistry Frontiers","2019","6","12","1977","","10.1039/C9QO00332K","","","0.71073","MoKα","","0.0663","0.0585","","","0.1544","0.1624","","","","","","1.085","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554870","9.3579","0.0019","12.566","0.003","29.371","0.006","90","","96.6","0.03","90","","3430.9","1.3","113","2","113","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H18 N2 O4 -","- C19 H18 N2 O4 -","- C152 H144 N16 O32 -","8","2","","Zhang, Wei; Zheng, Han-Liang; Liu, Yang; Yu, Ao; Yang, Chen; Li, Xin; Cheng, Jin-Pei","Catalyst-free amination of α-cyanoarylacetates enabled by single-electron transfer","Organic Chemistry Frontiers","2019","6","11","1900","","10.1039/C9QO00346K","","","0.71073","MoKα","","0.0772","0.0543","","","0.1222","0.1366","","","","","","1.053","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554872","7.807","0.0003","15.9924","0.0005","10.5193","0.0004","90","","109.003","0.004","90","","1241.79","0.08","293","2","293","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C28 H29 N3 O4 -","- C28 H29 N3 O4 -","- C56 H58 N6 O8 -","2","1","","Zhang, Yan-Ping; You, Yong; Zhao, Jian-Qiang; Zhou, Xiao-Jian; Zhang, Xiao-Mei; Xu, Xiao-Ying; Yuan, Wei-Cheng","A AgOAc/quinine-derived aminophosphine complex as an efficient catalyst for diastereo- and enantioselective 1,3-dipolar cycloaddition of α,β-unsaturated 7-azaindoline amides and azomethine ylides","Organic Chemistry Frontiers","2019","6","11","1879","","10.1039/C9QO00347A","","x-ray","1.54184","CuKα","","0.0442","0.0395","","","0.1007","0.106","","","","","","1.042","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554874","8.0029","0.0001","15.3468","0.0003","17.8042","0.0003","90","","90","","90","","2186.69","0.06","299.44","0.1","299.44","0.1","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C23 H30 O8 -","- C23 H30 O8 -","- C92 H120 O32 -","4","1","","Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong","Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018","Organic Chemistry Frontiers","2019","6","17","3053","","10.1039/C9QO00351G","","x-ray","1.54184","CuKα","","0.0361","0.0333","","","0.0883","0.0915","","","","","","1.081","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554876","14.3037","0.0001","14.0845","0.0001","23.7866","0.0002","90","","91.922","0.001","90","","4789.36","0.06","104","7","104","7","","","","","","","","4","C 1 c 1","C -2yc","9","","","","- C29 H27 N2 O4.5 -","- C29 H27 N2 O4.5 -","- C232 H216 N16 O36 -","8","2","","Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong","Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018","Organic Chemistry Frontiers","2019","6","17","3053","","10.1039/C9QO00351G","","x-ray","1.54184","CuKα","","0.0433","0.0414","","","0.1125","0.1141","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554879","8.09067","0.00008","25.4976","0.0003","41.3088","0.0004","90","","90","","90","","8521.7","0.15","101","2","101","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C28.33333 H40.33333 N O9.33333 -","- C28.3333 H40.3333 N O9.33333 -","- C340 H484 N12 O112 -","12","3","","Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong","Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018","Organic Chemistry Frontiers","2019","6","17","3053","","10.1039/C9QO00351G","","x-ray","1.54184","CuKα","","0.0426","0.037","","","0.0941","0.0974","","","","","","1.046","","","","has coordinates","275856","2022-06-07","07:08:27",""
"1554881","12.0924","0.001","16.7422","0.0011","8.278","0.0007","90","","107.825","0.009","90","","1595.5","0.2","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H23 N O4 -","- C17 H23 N O4 -","- C68 H92 N4 O16 -","4","1","","Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua","Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds","Organic Chemistry Frontiers","2019","6","13","2275","","10.1039/C9QO00353C","","","0.71073","MoKα","","0.0862","0.0579","","","0.1284","0.1514","","","","","","1.051","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554882","6.4241","0.0006","10.1906","0.0011","11.3167","0.0014","68.951","0.011","83.144","0.009","83.818","0.008","684.79","0.14","294.9","0.7","294.9","0.7","","","","","","","","4","P -1","-P 1","2","","","","- C14 H13 F3 O5 -","- C14 H13 F3 O5 -","- C28 H26 F6 O10 -","2","1","","Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua","Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds","Organic Chemistry Frontiers","2019","6","13","2275","","10.1039/C9QO00353C","","","1.54184","CuKα","","0.0494","0.0415","","","0.1124","0.122","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554883","12.1636","0.0011","10.2486","0.0007","12.3402","0.0011","90","","110.011","0.01","90","","1445.5","0.2","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C17 H20 O4 -","- C17 H20 O4 -","- C68 H80 O16 -","4","1","","Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua","Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds","Organic Chemistry Frontiers","2019","6","13","2275","","10.1039/C9QO00353C","","","0.71073","MoKα","","0.0858","0.0532","","","0.1195","0.1438","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554884","7.6075","0.001","9.2096","0.0012","19.424","0.003","90","","98.561","0.002","90","","1345.7","0.3","296","2","296","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C16 H18 O4 -","- C16 H18 O4 -","- C64 H72 O16 -","4","1","","Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua","Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds","Organic Chemistry Frontiers","2019","6","13","2275","","10.1039/C9QO00353C","","","0.71073","MoKα","","0.0541","0.0419","","","0.1348","0.1506","","","","","","0.998","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554886","10.9357","0.0005","11.7723","0.0006","24.8931","0.0009","90","","90","","90","","3204.7","0.2","293","2","293","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C33 H27 Cl3 N2 O5 S -","- C33 H27 Cl3 N2 O5 S -","- C132 H108 Cl12 N8 O20 S4 -","4","1","","Ren, Xiao-Rui; Lin, Jun-Bing; Hu, Xiu-Qin; Xu, Peng-Fei","Bifunctional Brønsted base catalyzed inverse-electron-demand aza-Diels–Alder reactions of saccharin-derived 1-azadienes with azlactones","Organic Chemistry Frontiers","2019","6","13","2280","","10.1039/C9QO00357F","","","0.71073","MoKα","","0.0793","0.056","","","0.1179","0.1352","","","","","","1.048","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554888","5.4632","0.0004","16.8139","0.0011","10.7302","0.0007","90","","98.574","0.002","90","","974.64","0.12","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C10 H9 N O Se -","- C10 H9 N O Se -","- C40 H36 N4 O4 Se4 -","4","1","","Xiao, Jun-An; Li, Yu-Chun; Cheng, Xiu-Liang; Chen, Wen-Qiang; Cui, Jian-Guo; Huang, Yan-Min; Huang, Jun; Xiao, Qi; Su, Wei; Yang, Hua","Selenocyanobenziodoxolone: a practical electrophilic selenocyanation reagent and its application for solid-state synthesis of α-carbonyl selenocyanates","Organic Chemistry Frontiers","2019","6","12","1967","","10.1039/C9QO00358D","","","0.71073","MoKα","","0.0768","0.0387","","","0.0749","0.0859","","","","","","1.026","","","","has coordinates","300101","2025-06-17","17:58:11",""
"1554889","10.1323","0.0006","7.4394","0.0005","15.4852","0.001","90","","100.787","0.002","90","","1146.62","0.13","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C24 H33 N O3 Se -","- C24 H33 N O3 Se -","- C48 H66 N2 O6 Se2 -","2","1","","Xiao, Jun-An; Li, Yu-Chun; Cheng, Xiu-Liang; Chen, Wen-Qiang; Cui, Jian-Guo; Huang, Yan-Min; Huang, Jun; Xiao, Qi; Su, Wei; Yang, Hua","Selenocyanobenziodoxolone: a practical electrophilic selenocyanation reagent and its application for solid-state synthesis of α-carbonyl selenocyanates","Organic Chemistry Frontiers","2019","6","12","1967","","10.1039/C9QO00358D","","","0.71073","MoKα","","0.0547","0.0362","","","0.0786","0.0849","","","","","","1.023","","","","has coordinates","300101","2025-06-17","17:58:11",""
"1554891","7.229","0.004","11.212","0.006","22.921","0.012","90","","90","","90","","1857.8","1.7","296.15","","296.15","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C21 H21 Cl O5 -","- C21 H21 Cl O5 -","- C84 H84 Cl4 O20 -","4","1","","Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai","Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways","Organic Chemistry Frontiers","2019","6","12","1972","","10.1039/C9QO00366E","","","0.71073","MoKα","","0.1004","0.0738","","","0.1835","0.2015","","","","","","1.002","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554892","10.3231","0.0013","8.3376","0.001","10.651","0.0013","90","","116.926","0.002","90","","817.35","0.17","100.15","","100.15","","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C20 H18 O4 -","- C20 H18 O4 -","- C40 H36 O8 -","2","1","","Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai","Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways","Organic Chemistry Frontiers","2019","6","12","1972","","10.1039/C9QO00366E","","","0.71073","MoKα","","0.0432","0.0357","","","0.0852","0.0905","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554893","10.5134","0.0013","7.5193","0.0009","22.921","0.003","90","","90","","90","","1812","0.4","296.15","","296.15","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C21 H19 Cl O4 -","- C21 H19 Cl O4 -","- C84 H76 Cl4 O16 -","4","1","","Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai","Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways","Organic Chemistry Frontiers","2019","6","12","1972","","10.1039/C9QO00366E","","","0.71073","MoKα","","0.0627","0.0472","","","0.1089","0.119","","","","","","1.036","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554895","14.05","0.0011","8.3338","0.0006","14.2852","0.0011","90","","101.509","0.001","90","","1639","0.2","273","2","273","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","6-ethyl-3-nitro-1-tosyl-1H-indazole","","- C16 H15 N3 O4 S -","- C16 H15 N3 O4 S -","- C64 H60 N12 O16 S4 -","4","1","","Wang, Guodong; Sun, Jian; Wang, Kai; Han, Junfen; Li, Hongshuang; Duan, Guiyun; You, Guirong; Li, Furong; Xia, Chengcai","Palladium-catalyzed direct C–H nitration and intramolecular C–H functionalization for the synthesis of 3-nitro-1-(phenylsulfonyl)-1H-indazole derivatives","Organic Chemistry Frontiers","2019","6","10","1608","","10.1039/C9QO00367C","","","0.71073","MoKα","","0.0499","0.0408","","","0.1057","0.1132","","","","","","1.042","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554897","7.9218","0.0011","6.5193","0.0008","13.434","0.0016","90","","101.58","0.004","90","","679.67","0.15","173","1","173","1","","","","","","","","4","P 1 21 1","P 2yb","4","","Benzyl 8-azaspiro[bicyclo[3.2.1]octane-(exo)-3,2?-oxirane]-8-carboxylate","","- C16 H19 N O3 -","- C16 H19 N O3 -","- C32 H38 N2 O6 -","2","1","","Mandzhulo, Aleksandr; Vashchenko, Iryna; Gerasov, Andrii; Vovk, Mykhaylo; Rusanov, Eduard; Fetyukhin, Volodymyr; Lukin, Oleg; Shivanyuk, Alexander","Selective synthesis of N-protected exo-spiro[oxirane-3,2′-tropanes]","Organic Chemistry Frontiers","2019","6","10","1692","","10.1039/C9QO00377K","","","0.71073","MoKα","","0.0391","0.0337","","","0.0751","0.0772","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554899","8.9194","0.0008","12.8315","0.0012","18.5057","0.0018","90","","90","","90","","2118","0.3","293","2","293.15","","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C24 H36 O3 -","- C24 H36 O3 -","- C96 H144 O12 -","4","1","","Zhao, Nan; Xie, Shengling; Tian, Peilin; Tong, Rongbiao; Ning, Chengqing; Xu, Jing","Asymmetric total synthesis of (+)-astellatol and (−)-astellatene","Organic Chemistry Frontiers","2019","6","12","2014","","10.1039/C9QO00384C","","","1.54184","CuKα","","0.0724","0.0659","","","0.1672","0.1734","","","","","","1.069","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554901","9.9964","0.0003","10.5385","0.0003","17.4587","0.0005","90","","90","","90","","1839.22","0.09","100.01","0.1","100.01","0.1","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C20 H30 O4 -","- C20 H30 O4 -","- C80 H120 O16 -","4","1","","Zhang, Jing; Tang, Xuli; Han, Xiao; Feng, Danqing; Luo, Xiangchao; Ofwegen, Leen van; Li, Pinglin; Li, Guoqiang","Sarcoglaucins A-I, new antifouling cembrane-type diterpenes from the South China Sea soft coral Sarcophyton glaucum","Organic Chemistry Frontiers","2019","6","12","2004","","10.1039/C9QO00386J","","x-ray","1.54184","CuKα","","0.042","0.0365","","","0.0822","0.0857","","","","","","1.039","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554903","6.5666","0.0003","16.4713","0.0006","8.0376","0.0004","90","","111.405","0.005","90","","809.39","0.07","180","0.1","180","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C19 H20 N2 O3 -","- C19 H20 N2 O3 -","- C38 H40 N4 O6 -","2","1","","Wang, Bo; Wang, Yuankai; Wang, Zixuan; Wang, Jianbo","Rh(i)-Catalyzed intramolecular [2 + 2 + 1] cycloaddition of diynes with the N-terminal of the diazo group","Organic Chemistry Frontiers","2019","6","14","2329","","10.1039/C9QO00403C","","","0.71073","MoKα","","0.0377","0.0347","","","0.0855","0.088","","","","","","1.057","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554905","15.1446","0.0014","24.455","0.002","20.982","0.003","90","","93.45","0.003","90","","7756.8","1.5","150","2","150","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C45 H42 F4 O7 -","- C45 H42 F4 O7 -","- C360 H336 F32 O56 -","8","1","","Wu, Tuoqi; Senior, James; Bremner, Glen; Finden, Jeremy; Branda, Neil R.","Unusual structural changes as a result of weathering benzofuran-based diarylethenes in simulated sunlight","Organic Chemistry Frontiers","2019","6","12","1961","","10.1039/C9QO00409B","","","0.71073","MoKα","","0.0658","0.0493","","","0.129","0.1405","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554906","11.4709","0.0017","13.897","0.002","14.895","0.002","107.986","0.004","112.427","0.004","96.387","0.005","2015.5","0.5","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C47 H45 F4 O7 -","- C47 H45 F4 O7 -","- C94 H90 F8 O14 -","2","1","","Wu, Tuoqi; Senior, James; Bremner, Glen; Finden, Jeremy; Branda, Neil R.","Unusual structural changes as a result of weathering benzofuran-based diarylethenes in simulated sunlight","Organic Chemistry Frontiers","2019","6","12","1961","","10.1039/C9QO00409B","","","0.71073","MoKα","","0.1248","0.0777","","","0.2288","0.2729","","","","","","1.082","","","","has coordinates","238196","2020-10-21","18:00:00",""
"1554908","10.273","0.004","10.178","0.004","16.954","0.007","90","","99.61","0.006","90","","1747.8","1.2","296","2","296.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H19 N O -","- C24 H19 N O -","- C96 H76 N4 O4 -","4","1","","Zhao, Hong-Ping; Ma, Xiao-Pan; Nie, Shu-Min; Xiao, Yuhong; Mo, Dong-Liang","Synthesis of chromeno[4,3-b]quinolines and spirobenzofuran-3,3′-quinolines through silver-mediated Appel reaction/C–Br bond cleavage/double selective rearrangement sequence","Organic Chemistry Frontiers","2019","6","14","2334","","10.1039/C9QO00417C","","","0.71073","MoKα","","0.0504","0.0408","","","0.1109","0.1202","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554910","10.5982","0.0007","10.2369","0.0007","20.9415","0.0014","90","","99.629","0.001","90","","2240","0.3","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C30 H21 N O2 -","- C30 H21 N O2 -","- C120 H84 N4 O8 -","4","1","","Wang, Jian; Cai, Panyuan; He, Yimiao; Liu, Yuan; Zhong, Ling; Ding, Shumin; Shang, Yongjia","Tuneable access to isoquinolines via a transition-metal-free C(sp3)–C(sp3) bond cleavage rearrangement reaction","Organic Chemistry Frontiers","2019","6","14","2430","","10.1039/C9QO00427K","","","0.71073","MoKα","","0.062","0.0426","","","0.0977","0.1085","","","","","","1.02","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554911","10.7138","0.0003","10.8978","0.0003","12.099","0.0003","92.748","0.001","96.702","0.001","90.476","0.001","1401.24","0.07","296","2","296","2","","","","","","","","7","P -1","-P 1","2","","","","- C27 H29 F6 N2 O P Ru -","- C27 H29 F6 N2 O P Ru -","- C54 H58 F12 N4 O2 P2 Ru2 -","2","1","","Hong, Xi; Zhou, Quan; Huang, Shuang; Cui, He-Zhen; Li, Zhi-Ming; Hou, Xiu-Feng","Transition metal catalysed C7 and ortho-selective halogenation of 2-arylbenzo[d]oxazoles","Organic Chemistry Frontiers","2019","6","13","2226","","10.1039/C9QO00429G","","","1.34138","GaKα","","0.0258","0.0242","","","0.0648","0.0659","","","","","","1.053","","","","has coordinates,has disorder","238201","2020-10-21","18:00:00",""
"1554913","6.8959","0.0008","7.1261","0.0006","24.02","0.003","90","","90","","90","","1180.4","0.2","296","","296","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C14 H12 N2 O -","- C14 H12 N2 O -","- C56 H48 N8 O4 -","4","1","","Feng, Guang-Shou; Zhao, Zi-Biao; Shi, Lei; Zhou, Yong-Gui","Iridium-catalyzed asymmetric hydrogenation of quinazolinones","Organic Chemistry Frontiers","2019","6","13","2250","","10.1039/C9QO00443B","","","1.54178","CuKα","","0.1156","0.0683","","","0.1729","0.2048","","","","","","0.912","","","","has coordinates","238203","2020-10-21","18:00:00",""
"1554918","8.4795","0.0001","18.0358","0.0001","21.5437","0.0001","90","","90","","90","","3294.78","0.05","100","0.1","100","0.1","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C35 H27 Br F3 N3 O3 -","- C35 H27 Br F3 N3 O3 -","- C140 H108 Br4 F12 N12 O12 -","4","1","","Zhao, Xiaoyun; Xiong, Jiale; An, Junkai; Yu, Jicong; Zhu, Liping; Feng, Xing; Jiang, Xianxing","Diastereodivergent construction of bispiro[oxindole-bi-pyrrolidine]s with four consecutive stereocenters via asymmetric [3 + 2] cycloaddition of 2,3-dioxopyrrolidines using identical catalysts","Organic Chemistry Frontiers","2019","6","12","1989","","10.1039/C9QO00452A","","x-ray","1.54184","CuKα","","0.0591","0.0577","","","0.1511","0.1528","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554919","11.9726","0.0002","16.0021","0.0003","18.2529","0.0004","90","","90","","90","","3497.01","0.12","149.99","0.1","149.99","0.1","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C40 H31 Cl2 F4 N2 O3 -","- C40 H32 Cl2 F3 N3 O3 -","- C160 H128 Cl8 F12 N12 O12 -","4","1","","Zhao, Xiaoyun; Xiong, Jiale; An, Junkai; Yu, Jicong; Zhu, Liping; Feng, Xing; Jiang, Xianxing","Diastereodivergent construction of bispiro[oxindole-bi-pyrrolidine]s with four consecutive stereocenters via asymmetric [3 + 2] cycloaddition of 2,3-dioxopyrrolidines using identical catalysts","Organic Chemistry Frontiers","2019","6","12","1989","","10.1039/C9QO00452A","","x-ray","1.54184","CuKα","","0.0556","0.0528","","","0.1401","0.1448","","","","","","1.026","","","","has coordinates,has disorder","238208","2020-10-21","18:00:00",""
"1554922","21.4324","0.0012","13.5256","0.0008","8.8733","0.0005","90","","90","","90","","2572.2","0.3","292.94","0.1","292.94","0.1","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C31 H28 N2 O5 -","- C31 H28 N2 O5 -","- C124 H112 N8 O20 -","4","1","","Zhang, Si-Chen; Lei, Xin-Xin; Yang, Yong-jian; Luo, Yong-Chun; Zhang, Huan-Huan; Xu, Peng-Fei","Palladium catalysed [3 + 2]-annulation reaction of vinylcyclopropanes with pentafulvenes: synthesis of polysubstituted spiro[4,4]nona-6,8-dienes","Organic Chemistry Frontiers","2019","6","14","2415","","10.1039/C9QO00467J","","","0.71073","MoKα","","0.0811","0.0502","","","0.0894","0.1086","","","","","","1.055","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554923","8.9859","0.0013","10.004","0.002","15.8029","0.0018","97.57","0.013","90.211","0.011","115.564","0.017","1267.4","0.4","293","0.1","293","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C30 H25 N3 O3 -","- C30 H25 N3 O3 -","- C60 H50 N6 O6 -","2","1","","Zhang, Si-Chen; Lei, Xin-Xin; Yang, Yong-jian; Luo, Yong-Chun; Zhang, Huan-Huan; Xu, Peng-Fei","Palladium catalysed [3 + 2]-annulation reaction of vinylcyclopropanes with pentafulvenes: synthesis of polysubstituted spiro[4,4]nona-6,8-dienes","Organic Chemistry Frontiers","2019","6","14","2415","","10.1039/C9QO00467J","","x-ray","1.54184","CuKα","","0.0585","0.0458","","","0.1141","0.1273","","","","","","1.029","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554925","9.1965","0.0003","9.694","0.0004","38.3086","0.0014","90","","90","","90","","3415.2","0.2","100","2","100","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C38 H31 Br Cl3 N3 O4 -","- C38 H31 Br Cl3 N3 O4 -","- C152 H124 Br4 Cl12 N12 O16 -","4","1","","Zhang, Jing; Chan, Wai-Lun; Chen, Ligong; Ullah, Nisar; Lu, Yixin","Creation of bispiro[pyrazolone-3,3′-oxindoles] via a phosphine-catalyzed enantioselective [3 + 2] annulation of the Morita–Baylis–Hillman carbonates with pyrazoloneyldiene oxindoles","Organic Chemistry Frontiers","2019","6","13","2210","","10.1039/C9QO00471H","","","1.54178","CuKα","","0.0252","0.0249","","","0.0597","0.0599","","","","","","1.082","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554927","20.961","0.008","20.961","0.008","7.086","0.003","90","","90","","120","","2696.2","1.8","273","2","273.15","","","","","","","","","3","R 3 :H","R 3","146","","","","- C16 H18 O -","- C16 H18 O -","- C144 H162 O9 -","9","1","","Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong","Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F","Organic Chemistry Frontiers","2019","6","15","2771","","10.1039/C9QO00477G","","","0.71073","MoKα","","0.1082","0.0714","","","0.1619","0.1846","","","","","","0.936","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554928","42.742","0.003","10.4771","0.0009","10.9037","0.0009","90","","93.609","0.006","90","","4873.1","0.7","293","2","293","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C27 H34 O3 Si -","- C27 H33.992 O3 Si -","- C216 H271.936 O24 Si8 -","8","1","","Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong","Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F","Organic Chemistry Frontiers","2019","6","15","2771","","10.1039/C9QO00477G","","","0.71073","MoKα","","0.0939","0.0697","","","0.1464","0.1574","","","","","","1.105","","","","has coordinates,has disorder","238215","2020-10-21","18:00:00",""
"1554929","7.3423","0.001","8.4321","0.0009","10.4623","0.0011","85.681","0.008","85.985","0.01","78.332","0.01","631.55","0.13","185.1","0.6","185.1","0.6","","","","","","","","3","P -1","-P 1","2","","","","- C14 H18 O5 -","- C14 H18 O5 -","- C28 H36 O10 -","2","1","","Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong","Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F","Organic Chemistry Frontiers","2019","6","15","2771","","10.1039/C9QO00477G","","","0.71073","MoKα","","0.0525","0.0443","","","0.1051","0.11","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554931","17.4772","0.0006","10.488","0.0005","19.6463","0.0005","90","","90","","90","","3601.2","0.2","296.8","0.2","296.8","0.2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C18 H19 N O4 S -","- C18 H19 N O4 S -","- C144 H152 N8 O32 S8 -","8","1","","Huang, Guofei; Ren, Xiaoyu; Jiang, Chunhui; Wu, Jia-Hong; Gao, Guowei; Wang, Tianli","Efficient synthesis of (E)-2-nitromethylcinnamates via phosphine-catalyzed tandem α-addition and 1,3-rearrangement","Organic Chemistry Frontiers","2019","6","16","2872","","10.1039/C9QO00478E","","x-ray","1.54184","CuKα","","0.0659","0.056","","","0.1629","0.1792","","","","","","0.903","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554933","15.971","0.004","4.2214","0.0011","13.319","0.003","90","","90","","90","","898","0.4","173","2","173","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C10 H8 N2 S -","- C10 H8 N2 S -","- C40 H32 N8 S4 -","4","1","","Peng, Yingyuan; He, Qian; Zhang, Xiaofei; Yang, Chunhao","Pd-Catalyzed intramolecular C–H activation and C–S formation to synthesize pyrazolo[5,1-b]benzothiazoles without an additional oxidant","Organic Chemistry Frontiers","2019","6","18","3234","","10.1039/C9QO00484J","","","0.71073","MoKα","","0.0485","0.0387","","","0.0807","0.0848","","","","","","0.991","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554936","10.8238","0.0004","10.3557","0.0003","17.8199","0.0007","90","","96.908","0.003","90","","1982.9","0.12","295.91","0.1","295.91","0.1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H21 N3 O4 -","- C20 H21 N3 O4 -","- C80 H84 N12 O16 -","4","1","","Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei","Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates","Organic Chemistry Frontiers","2019","6","19","3321","","10.1039/C9QO00509A","","x-ray","1.54184","CuKα","","0.0737","0.0671","","","0.1697","0.18","","","","","","1.072","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554938","21.7832","0.0003","21.7832","0.0003","8.49552","0.00015","90","","90","","90","","4031.19","0.11","297.8","0.2","297.8","0.2","","","","","","","","4","P 42 b c","P 4c -2ab","106","","","","- C20 H21 N3 O4 -","- C20 H21 N3 O4 -","- C160 H168 N24 O32 -","8","1","","Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei","Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates","Organic Chemistry Frontiers","2019","6","19","3321","","10.1039/C9QO00509A","","x-ray","1.54184","CuKα","","0.0659","0.0634","","","0.151","0.1561","","","","","","1.063","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554939","6.9944","0.0003","7.8586","0.0004","26.1858","0.0011","85.696","0.004","89.837","0.004","79.658","0.004","1411.87","0.11","296.9","0.6","296.9","0.6","","","","","","","","4","P -1","-P 1","2","","","","- C15 H13 N3 O2 -","- C15 H13 N3 O2 -","- C60 H52 N12 O8 -","4","2","","Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei","Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates","Organic Chemistry Frontiers","2019","6","19","3321","","10.1039/C9QO00509A","","x-ray","1.54184","CuKα","","0.0788","0.0706","","","0.1941","0.2078","","","","","","1.019","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554940","9.69927","0.00009","10.835","0.00009","16.94975","0.00013","90","","90","","90","","1781.28","0.03","150","0.1","150","0.1","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C22 H18 F3 N O3 -","- C22 H18 F3 N O3 -","- C88 H72 F12 N4 O12 -","4","1","","Rabasa-Alcañiz, Fernando; Hammerl, Daniel; Sánchez-Merino, Anabel; Tejero, Tomás; Merino, Pedro; Fustero, Santos; del Pozo, Carlos","Asymmetric synthesis of polycyclic 3-fluoroalkylproline derivatives by intramolecular azomethine ylide cycloaddition","Organic Chemistry Frontiers","2019","6","16","2916","","10.1039/C9QO00525K","","x-ray","1.54184","CuKα","","0.0275","0.0271","","","0.0688","0.0691","","","","","","1.076","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554942","15.5529","0.0006","7.3629","0.0003","19.8862","0.0006","90","","90","","90","","2277.26","0.15","170","2","170.01","","","","","","","","","5","P b c n","-P 2n 2ab","60","","","","- C26 H20 Cu F6 P -","- C26 H20 Cu F6 P -","- C104 H80 Cu4 F24 P4 -","4","0.5","","Liu, He; Shen, Qilong","Bistrifluoromethylated organocuprate [Ph4P]+[Cu(CF3)2]−: synthesis, characterization and its application for trifluoromethylation of activated heteroaryl bromides, chlorides and iodides","Organic Chemistry Frontiers","2019","6","14","2324","","10.1039/C9QO00527G","","","0.71073","MoKα","","0.057","0.0459","","","0.1394","0.15","","","","","","1.057","","","","has coordinates","238227","2020-10-21","18:00:00",""
"1554943","10.5905","0.0002","16.0282","0.0004","11.3851","0.0003","90","","116.637","0.001","90","","1727.47","0.07","135","2","135","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","ORGANIC","","","- C20 H22 N2 O4 -","- C20 H22 N2 O4 -","- C80 H88 N8 O16 -","4","1","","Yakkala, Prasanna Anjaneyulu; Giri, Deepesh; Chaudhary, Bharatkumar; Auti, Prashant; Sharma, Satyasheel","Regioselective C–H alkylation and alkenylation at the C5 position of 2-amino-1,4-naphthoquinones with maleimides under Rh(iii) catalysis","Organic Chemistry Frontiers","2019","6","14","2441","","10.1039/C9QO00538B","","","0.71073","MoKα","","0.0488","0.0397","","","0.1057","0.1129","","","","","","1.051","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554945","7.5896","0.0008","10.9767","0.0011","11.9609","0.0013","110.338","0.004","100.049","0.004","106.048","0.004","856.49","0.16","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C17 H15 Br2 N O2 -","- C17 H15 Br2 N O2 -","- C34 H30 Br4 N2 O4 -","2","1","","Wang, Yu-Chao; Wang, Rui-Xiang; Qiu, Guanyinsheng; Zhou, Hongwei; Xie, Wenlin; Liu, Jin-Biao","ortho-Amide-directed 2,4-dibromohydration of conjugated enynes","Organic Chemistry Frontiers","2019","6","14","2471","","10.1039/C9QO00540D","","","1.34138","GaKα","","0.0566","0.0484","","","0.1295","0.1367","","","","","","1.05","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554946","7.2536","0.0006","9.2341","0.0009","9.3515","0.001","85.065","0.008","81.059","0.008","68.355","0.008","574.85","0.1","295.25","0.1","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C14 H12 N2 O -","- C14 H12 N2 O -","- C28 H24 N4 O2 -","2","1","","Su, Han; Bao, Ming; Pei, Chao; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang","Gold-catalyzed dual annulation of azide-tethered alkynes with nitriles: expeditious synthesis of oxazolo[4,5-c]quinolines","Organic Chemistry Frontiers","2019","6","14","2404","","10.1039/C9QO00568D","","","0.71073","MoKα","","0.0923","0.0533","","","0.1358","0.1669","","","","","","1.016","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554947","9.8811","0.0007","14.4238","0.0007","13.7948","0.0009","90","","109.258","0.007","90","","1856.1","0.2","279","7","279","7","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C25 H15 N3 O -","- C25 H15 N3 O -","- C100 H60 N12 O4 -","4","1","","Su, Han; Bao, Ming; Pei, Chao; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang","Gold-catalyzed dual annulation of azide-tethered alkynes with nitriles: expeditious synthesis of oxazolo[4,5-c]quinolines","Organic Chemistry Frontiers","2019","6","14","2404","","10.1039/C9QO00568D","","x-ray","0.71073","MoKα","","0.0735","0.0468","","","0.1073","0.1255","","","","","","1.0655","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554949","8.0332","0.0002","8.5272","0.0002","16.9075","0.0004","99.329","0.002","99.436","0.002","101.204","0.002","1097.99","0.05","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C25 H23 F2 N O3 S -","- C25 H23 F2 N O3 S -","- C50 H46 F4 N2 O6 S2 -","2","1","","Hu, Xiao-Si; Ding, Pei-Gang; Yu, Jin-Sheng; Zhou, Jian","A Sc(OTf)3 catalyzed Mukaiyama–Mannich reaction of difluoroenoxysilanes with unactivated ketimines","Organic Chemistry Frontiers","2019","6","14","2500","","10.1039/C9QO00577C","","x-ray","1.54184","CuKα","","0.0419","0.0391","","","0.106","0.108","","","","","","1.073","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554951","23.8323","0.0016","5.5909","0.0004","15.658","0.0011","90","","103.617","0.007","90","","2027.7","0.3","100","2","100","2","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C24 H24 O2 S2 -","- C24 H24 O2 S2 -","- C96 H96 O8 S8 -","4","1","","Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo","Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties","Organic Chemistry Frontiers","2019","6","15","2801","","10.1039/C9QO00593E","","","0.71075","MoKα","","0.0959","0.0709","","","0.1475","0.1599","","","","","","1.022","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554952","6.07714","0.00018","13.1618","0.0003","27.1117","0.0008","90","","90","","90","","2168.56","0.1","100","2","100","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C25 H25 N O2 S -","- C25 H25 N O2 S -","- C100 H100 N4 O8 S4 -","4","1","","Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo","Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties","Organic Chemistry Frontiers","2019","6","15","2801","","10.1039/C9QO00593E","","","0.71073","MoKα","","0.0467","0.0402","","","0.0867","0.0895","","","","","","1.03","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554953","13.9336","0.0007","19.7182","0.0009","20.3209","0.0011","90","","103.298","0.005","90","","5433.4","0.5","100","2","100","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C32 H30.52 O4.26 S -","- C32 H30.516 O4.258 S -","- C256 H244.128 O34.064 S8 -","8","1","","Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo","Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties","Organic Chemistry Frontiers","2019","6","15","2801","","10.1039/C9QO00593E","","","0.71073","MoKα","","0.1375","0.0847","","","0.207","0.2401","","","","","","1.025","","","","has coordinates,has disorder","238235","2020-10-21","18:00:00",""
"1554954","28.3482","0.0011","19.5347","0.0007","7.5873","0.0003","90","","90","","90","","4201.6","0.3","100","2","100","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C27 H24 Fe O2 S -","- C27 H24 Fe O2 S -","- C216 H192 Fe8 O16 S8 -","8","1","","Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo","Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties","Organic Chemistry Frontiers","2019","6","15","2801","","10.1039/C9QO00593E","","","0.71073","MoKα","","0.0768","0.0497","","","0.0928","0.1026","","","","","","1.046","","","","has coordinates","238235","2020-10-21","18:00:00",""
"1554957","10.1603","0.0005","10.173","0.0004","23.5179","0.001","90","","90","","90","","2430.83","0.18","100","2","100.1","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C27 H22 Cl N O5 S -","- C27 H22 Cl N O5 S -","- C108 H88 Cl4 N4 O20 S4 -","4","1","","Lin, Wei; Lin, Xiao; Cheng, Yuyu; Chang, Xiaoyong; Zhou, San; Li, Pengfei; Li, Wenjun","Organocatalytic enantioselective direct vinylogous Michael addition of γ-substituted deconjugate butenolides to azadienes","Organic Chemistry Frontiers","2019","6","14","2452","","10.1039/C9QO00597H","","x-ray","0.71073","MoKα","","0.03","0.0274","","","0.0661","0.0674","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554958","10.0757","0.0011","10.4448","0.0009","10.8094","0.0012","90","","92.786","0.003","90","","1136.2","0.2","100","2","100","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C27 H23 N O5 S -","- C27 H23 N O5 S -","- C54 H46 N2 O10 S2 -","2","1","","Lin, Wei; Lin, Xiao; Cheng, Yuyu; Chang, Xiaoyong; Zhou, San; Li, Pengfei; Li, Wenjun","Organocatalytic enantioselective direct vinylogous Michael addition of γ-substituted deconjugate butenolides to azadienes","Organic Chemistry Frontiers","2019","6","14","2452","","10.1039/C9QO00597H","","x-ray","0.71073","MoKα","","0.0293","0.028","","","0.0705","0.0714","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554961","9.8296","0.0013","13.4413","0.0017","22.608","0.003","90","","94.433","0.003","90","","2978.1","0.7","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C30 H29 N O3 S -","- C30 H29 N O3 S -","- C120 H116 N4 O12 S4 -","4","1","","Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min","Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter","Organic Chemistry Frontiers","2019","6","14","2506","","10.1039/C9QO00611G","","","0.71073","MoKα","","0.1107","0.0682","","","0.1582","0.1781","","","","","","1.042","","","","has coordinates","238241","2020-10-21","18:00:00",""
"1554962","5.8832","0.0002","8.7875","0.0002","37.5443","0.0011","90","","90","","90","","1940.99","0.1","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C20 H27 N O2 S -","- C20 H27 N O2 S -","- C80 H108 N4 O8 S4 -","4","1","","Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min","Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter","Organic Chemistry Frontiers","2019","6","14","2506","","10.1039/C9QO00611G","","","0.71073","MoKα","","0.052","0.0415","","","0.1086","0.1175","","","","","","1.024","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554963","8.87","0.0016","10.6671","0.0018","21.508","0.004","90","","90","","90","","2035","0.6","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C22 H29 N O2 S -","- C22 H29 N O2 S -","- C88 H116 N4 O8 S4 -","4","1","","Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min","Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter","Organic Chemistry Frontiers","2019","6","14","2506","","10.1039/C9QO00611G","","","0.71073","MoKα","","0.0781","0.0496","","","0.1022","0.1128","","","","","","0.959","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554964","35.164","0.003","8.6573","0.0006","11.5114","0.0009","90","","94.241","0.002","90","","3494.8","0.5","298","2","298","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C19 H23 N O2 S -","- C19 H23 N O2 S -","- C152 H184 N8 O16 S8 -","8","1","","Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min","Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter","Organic Chemistry Frontiers","2019","6","14","2506","","10.1039/C9QO00611G","","","0.71073","MoKα","","0.0964","0.0583","","","0.1308","0.1549","","","","","","1.054","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554965","19.505","0.003","8.6857","0.0013","13.1687","0.0016","90","","92.309","0.004","90","","2229.2","0.5","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C23 H33 N O2 S -","- C23 H33 N O2 S -","- C92 H132 N4 O8 S4 -","4","1","","Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min","Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter","Organic Chemistry Frontiers","2019","6","14","2506","","10.1039/C9QO00611G","","","0.71073","MoKα","","0.1115","0.0661","","","0.1559","0.1912","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554966","10.888","0.003","8.651","0.002","10.91","0.003","90","","97.5","0.005","90","","1018.8","0.5","293","2","293","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C21 H26 Br N O2 S -","- C21 H26 Br N O2 S -","- C42 H52 Br2 N2 O4 S2 -","2","1","","Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min","Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter","Organic Chemistry Frontiers","2019","6","14","2506","","10.1039/C9QO00611G","","","0.71073","MoKα","","0.0658","0.0461","","","0.1074","0.1167","","","","","","1.029","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554967","12.551","0.003","11.012","0.002","14.276","0.003","90","","113.904","0.005","90","","1803.9","0.7","296","2","296","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C18 H22 Br N O2 S -","- C18 H22 Br N O2 S -","- C72 H88 Br4 N4 O8 S4 -","4","1","","Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min","Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter","Organic Chemistry Frontiers","2019","6","14","2506","","10.1039/C9QO00611G","","","0.71073","MoKα","","0.1743","0.0841","","","0.1987","0.2575","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554970","10.013","0.005","12.073","0.006","12.827","0.006","111.893","0.015","107.027","0.017","93.776","0.019","1348.7","1.2","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C17 H14 Cl -","- C17 H14 Cl -","- C68 H56 Cl4 -","4","2","","Fan, Xing; Liu, Ruixing; Wei, Yin; Shi, Min","Rh-Catalyzed intramolecular decarbonylative cyclization of ortho-formyl group tethered alkylidenecyclopropanes (ACPs) for the construction of 2-methylindenes","Organic Chemistry Frontiers","2019","6","15","2667","","10.1039/C9QO00614A","","","0.71073","MoKα","","0.1127","0.0594","","","0.1447","0.1823","","","","","","1.036","","","","has coordinates","238244","2020-10-21","18:00:00",""
"1554972","14.5964","0.0005","13.9382","0.0005","14.6669","0.0005","90","","90","","90","","2983.94","0.18","194","2","194","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C20 H17 N O -","- C20 H17 N O -","- C160 H136 N8 O8 -","8","1","","Hu, Xiaoping; Wang, Gaonan; Qin, Chunxiang; Xie, Xin; Zhang, Chunli; Xu, Wei; Liu, Yuanhong","Ligandless nickel-catalyzed transfer hydrogenation of alkenes and alkynes using water as the hydrogen donor","Organic Chemistry Frontiers","2019","6","15","2619","","10.1039/C9QO00616H","","","0.71073","MoKα","","0.0422","0.0359","","","0.088","0.0931","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554974","14.929","0.0003","5.74297","0.00008","27.7627","0.0005","90","","104.785","0.0018","90","","2301.48","0.07","100","2","100","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","aminopyrimidine.toluene","","","- C30 H27 N3 -","- C30 H27 N3 -","- C120 H108 N12 -","4","1","","Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang","Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons","Organic Chemistry Frontiers","2019","6","17","3071","","10.1039/C9QO00619B","","","1.54184","CuKα","","0.0428","0.0395","","","0.1034","0.1066","","","","","","1.069","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554975","15.534","0.0013","6.291","0.0003","15.0837","0.001","90","","113.849","0.009","90","","1348.18","0.18","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C17 H16 N2 -","- C17 H16 N2 -","- C68 H64 N8 -","4","1","","Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang","Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons","Organic Chemistry Frontiers","2019","6","17","3071","","10.1039/C9QO00619B","","","0.71073","MoKα","","0.0533","0.0451","","","0.1086","0.1147","","","","","","1.057","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554976","12.9687","0.0003","13.0705","0.0003","7.18","0.0002","90","","90","","90","","1217.06","0.05","100","2","100","2","","","","","","","","3","P c a 21","P 2c -2ac","29","","","","- C15 H13 N3 -","- C15 H13 N3 -","- C60 H52 N12 -","4","1","","Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang","Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons","Organic Chemistry Frontiers","2019","6","17","3071","","10.1039/C9QO00619B","","","1.54184","CuKα","","0.0291","0.0286","","","0.0755","0.0758","","","","","","1.075","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554977","8.8058","0.0008","10.1568","0.0009","10.8636","0.001","112.118","0.009","90.659","0.008","106.96","0.008","852.87","0.15","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C22 H17 N3 -","- C22 H17 N3 -","- C44 H34 N6 -","2","1","","Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang","Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons","Organic Chemistry Frontiers","2019","6","17","3071","","10.1039/C9QO00619B","","","1.54184","CuKα","","0.0765","0.0533","","","0.1464","0.1545","","","","","","1.178","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554979","14.1655","0.0013","22.469","0.002","16.419","0.0015","90","","98.419","0.001","90","","5169.6","0.8","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C30 H24 F2 O5 -","- C30 H24 F2 O5 -","- C240 H192 F16 O40 -","8","2","","Liu, Baohua; Mao, Chunyan; Hu, Qiong; Yao, Liangliang; Hu, Yimin","Direct methylation and carbonylation of in situ generated arynes via HDDA-Wittig coupling","Organic Chemistry Frontiers","2019","6","15","2788","","10.1039/C9QO00621D","","","0.71073","MoKα","","0.1689","0.1089","","","0.3402","0.3959","","","","","","1.349","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554980","9.9135","0.0004","11.2232","0.0004","13.3885","0.0005","94.007","0.002","107.02","0.001","109.916","0.001","1315.15","0.09","273","2","273","2","","","","","","","","4","P -1","-P 1","2","","","","- C15 H12 F O3 -","- C15 H12 F O3 -","- C60 H48 F4 O12 -","4","2","","Liu, Baohua; Mao, Chunyan; Hu, Qiong; Yao, Liangliang; Hu, Yimin","Direct methylation and carbonylation of in situ generated arynes via HDDA-Wittig coupling","Organic Chemistry Frontiers","2019","6","15","2788","","10.1039/C9QO00621D","","","0.71073","MoKα","","0.084","0.0692","","","0.2028","0.2261","","","","","","0.987","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1554983","17.251","0.002","12.1706","0.0017","26.112","0.004","90","","91.879","0.003","90","","5479.4","1.3","113","2","113.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H19 B11 Cl6 O -","- C19 H19 B11 Cl6 O -","- C152 H152 B88 Cl48 O8 -","8","2","","Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.","Peraryl-X-onium ions of nitrogen and oxygen","Organic Chemistry Frontiers","2019","6","15","2640","","10.1039/C9QO00633H","","","0.71073","MoKα","","0.0697","0.0467","","","0.0989","0.1119","","","","","","1.083","","","","has coordinates","238253","2020-10-21","18:00:00",""
"1554984","19.0146","0.0006","13.8372","0.0003","21.2518","0.0005","90","","90","","90","","5591.5","0.3","113.15","","113.15","","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C20 H21 B11 Cl6 O -","- C20 H21 B11 Cl6 O -","- C160 H168 B88 Cl48 O8 -","8","1","","Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.","Peraryl-X-onium ions of nitrogen and oxygen","Organic Chemistry Frontiers","2019","6","15","2640","","10.1039/C9QO00633H","","x-ray","0.71073","MoKα","","0.0452","0.0392","","","0.1062","0.1098","","","","","","1.043","","","","has coordinates","238253","2020-10-21","18:00:00",""
"1554985","18.70332","0.00019","18.4574","0.0003","18.4002","0.00017","90","","90","","90","","6352.02","0.14","160","2","160.15","","","","","","","","","5","P b c n","-P 2n 2ab","60","","","","- C25 H22 B11 Cl6 N -","- C25 H22 B11 Cl6 N -","- C200 H176 B88 Cl48 N8 -","8","1","","Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.","Peraryl-X-onium ions of nitrogen and oxygen","Organic Chemistry Frontiers","2019","6","15","2640","","10.1039/C9QO00633H","","","0.71073","MoKα","","0.0396","0.0307","","","0.0779","0.0833","","","","","","1.024","","","","has coordinates","238253","2020-10-21","18:00:00",""
"1554986","18.015","0.0002","14.8013","0.0002","23.3476","0.0002","90","","90","","90","","6225.53","0.12","160","2","160","2","","","","","","","","5","P b c n","-P 2n 2ab","60","","","","- C25 H22 B11 Cl6 N -","- C25 H22 B11 Cl6 N -","- C200 H176 B88 Cl48 N8 -","8","1","","Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.","Peraryl-X-onium ions of nitrogen and oxygen","Organic Chemistry Frontiers","2019","6","15","2640","","10.1039/C9QO00633H","","","0.71073","MoKα","","0.0534","0.0396","","","0.0966","0.1059","","","","","","1.024","","","","has coordinates","238253","2020-10-21","18:00:00",""
"1554987","31.445","0.002","13.6072","0.0008","32.634","0.002","90","","116.666","0.001","90","","12478.2","1.3","113","","113","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C25 H24 B11 Cl6 N -","- C25 H24 B11 Cl6 N -","- C400 H384 B176 Cl96 N16 -","16","4","","Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.","Peraryl-X-onium ions of nitrogen and oxygen","Organic Chemistry Frontiers","2019","6","15","2640","","10.1039/C9QO00633H","","","0.71073","MoKα","","0.1074","0.0711","","","0.1348","0.1534","","","","","","1.179","","","","has coordinates","238253","2020-10-21","18:00:00",""
"1554989","9.943","","19.423","","27.408","","90","","94.84","","90","","5274.24","","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C27 H24 N4 O4 S2 -","- C27 H24 N4 O4 S2 -","- C216 H192 N32 O32 S16 -","8","2","","Wang, Lihong; Wang, Xiaomin; Zhang, Ge; Yang, Shengbiao; Li, Yan; Zhang, Qian","Copper-catalyzed 1,3-aminoazidation of arylcyclopropanes: a facile access to 1,3-diamine derivatives","Organic Chemistry Frontiers","2019","6","16","2934","","10.1039/C9QO00638A","","","0.71073","MoKα","","0.0899","0.0549","","","0.1647","0.2051","","","","","","0.819","","","","has coordinates","274176","2022-03-31","10:10:26",""
"1554991","9.4606","0.0016","8.7844","0.0015","13.698","0.002","90","","91.45","0.004","90","","1138","0.3","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C13 H11 N O3 -","- C13 H11 N O3 -","- C52 H44 N4 O12 -","4","1","","Sun, Yao-Liang; Wei, Yin; Shi, Min","Phosphine-catalyzed fixation of CO2 with γ-hydroxyl alkynone under ambient temperature and pressure: kinetic resolution and further conversion","Organic Chemistry Frontiers","2019","6","14","2420","","10.1039/C9QO00642G","","","0.71073","MoKα","","0.0639","0.0434","","","0.1065","0.1177","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554992","5.2776","0.0001","10.8907","0.0002","22.1326","0.0004","90","","90","","90","","1272.11","0.04","170","2","170.01","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C15 H13 N O3 -","- C15 H13 N O3 -","- C60 H52 N4 O12 -","4","1","","Sun, Yao-Liang; Wei, Yin; Shi, Min","Phosphine-catalyzed fixation of CO2 with γ-hydroxyl alkynone under ambient temperature and pressure: kinetic resolution and further conversion","Organic Chemistry Frontiers","2019","6","14","2420","","10.1039/C9QO00642G","","","1.34139","GaKα","","0.0331","0.0327","","","0.0874","0.0878","","","","","","1.066","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554993","11.0859","0.0016","9.2256","0.0013","12.6525","0.0018","90","","101.245","0.003","90","","1269.2","0.3","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C14 H11 N O5 -","- C14 H11 N O5 -","- C56 H44 N4 O20 -","4","1","","Sun, Yao-Liang; Wei, Yin; Shi, Min","Phosphine-catalyzed fixation of CO2 with γ-hydroxyl alkynone under ambient temperature and pressure: kinetic resolution and further conversion","Organic Chemistry Frontiers","2019","6","14","2420","","10.1039/C9QO00642G","","","0.71073","MoKα","","0.0519","0.0416","","","0.1097","0.1174","","","","","","1.049","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554995","9.2832","0.0007","10.0044","0.0007","11.107","0.0009","87.027","0.006","65.546","0.008","82.335","0.006","930.61","0.14","173","13","173","13","","","","","","","","5","P -1","-P 1","2","","","","- C23 H18 Cl N O2 -","- C23 H18 Cl N O2 -","- C46 H36 Cl2 N2 O4 -","2","1","","Yao, Yongqi; Yang, Wen; Lin, Qifu; Yang, Weitao; Li, Huanyong; Wang, Lin; Gu, Fenglong; Yang, Dingqiao","1,3-Dipolar cycloaddition of nitrones to oxa(aza)bicyclic alkenes","Organic Chemistry Frontiers","2019","6","19","3360","","10.1039/C9QO00660E","","x-ray","0.71073","MoKα","","0.0775","0.0584","","","0.1265","0.1381","","","","","","1.038","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1554997","6.0211","0.0002","16.1241","0.0005","20.634","0.0005","90","","90","","90","","2003.25","0.1","127","2","127","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C21 H18 N4 O4 S -","- C21 H18 N4 O4 S -","- C84 H72 N16 O16 S4 -","4","1","","Li, Shi-Wu; Du, Yu; Kang, Qiang","A chiral-at-metal asymmetric catalyzed vinylogous Michael addition of ortho-methyl aromatic nitro compounds for isoxazole derivative synthesis","Organic Chemistry Frontiers","2019","6","15","2775","","10.1039/C9QO00676A","","","1.54184","CuKα","","0.104","0.0916","","","0.2275","0.2394","","","","","","1.064","","","","has coordinates","238261","2020-10-21","18:00:00",""
"1554999","10.438","0.005","10.7","0.005","15.172","0.007","80.197","0.009","70.129","0.009","79.638","0.009","1556.7","1.3","296","2","296.15","","","","","","","","","3","P -1","-P 1","2","","","","- C40 H32 O6 -","- C40 H32 O6 -","- C80 H64 O12 -","2","1","","Wang, Wenli; Tang, Yingzhan; Liu, Yongxiang; Yuan, Lei; Wang, Jian; Lin, Bin; Zhou, Di; Sun, Lu; Huang, Renbin; Chen, Gang; Li, Ning","Isolation, structure elucidation, and synthesis of (±)-millpuline A with a suppressive effect in miR-144 expression","Organic Chemistry Frontiers","2019","6","16","2850","","10.1039/C9QO00678H","","","0.71073","MoKα","","0.1055","0.0518","","","0.1228","0.1488","","","","","","1.011","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555001","19.861","0.008","13.383","0.005","18.29","0.007","90","","117.363","0.011","90","","4318","3","296","2","296","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C44 H40 N4 Ni O2 -","- C44 H40 N4 Ni O2 -","- C176 H160 N16 Ni4 O8 -","4","1","","Ren, Demin; Fu, Xinliang; Li, Xiaofang; Koniarz, Sebastian; Chmielewski, Piotr J.","Reaction of antiaromatic porphyrinoid with active methylene compounds","Organic Chemistry Frontiers","2019","6","16","2924","","10.1039/C9QO00679F","","","0.71073","MoKα","","0.1009","0.0543","","","0.1273","0.1625","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555002","14.1112","0.001","4.6513","0.0003","21.124","0.0014","90","","99.827","0.002","90","","1366.14","0.16","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C15 H16 N2 O4 -","- C15 H16 N2 O4 -","- C60 H64 N8 O16 -","4","1","","Mei, Xiangui; Lan, Mengmeng; Cui, Guodong; Zhang, Hongwei; Zhu, Weiming","Caerulomycins from Actinoalloteichus cyanogriseus WH1-2216-6: isolation, identification and cytotoxicity","Organic Chemistry Frontiers","2019","6","20","3566","","10.1039/C9QO00685K","","","1.54178","CuKα","","0.0757","0.0542","","","0.1284","0.1494","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555009","15.8263","0.0007","7.7607","0.0003","15.9189","0.0008","90","","106.393","0.002","90","","1875.73","0.15","273","2","273","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C24 H20 O S -","- C24 H20 O S -","- C96 H80 O4 S4 -","4","1","","Liu, Changqing; Wang, Bo; Guo, Ziyi; Zhang, Jitan; Xie, Meihua","Metal-free cascade rearrangement/radical addition/oxidative C–H annulation of propargyl alcohols with sodium sulfinates: access to 2-sulfenylindenones","Organic Chemistry Frontiers","2019","6","15","2796","","10.1039/C9QO00688E","","","0.71073","MoKα","","0.1035","0.0665","","","0.1751","0.2046","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555010","7.3464","0.0002","8.5371","0.0003","15.0907","0.0005","95.337","0.001","91.518","0.001","104.361","0.001","911.69","0.05","273","2","273","2","","","","","","","","6","P -1","-P 1","2","","","","- C22 H14 Cl F O S -","- C22 H14 Cl F O S -","- C44 H28 Cl2 F2 O2 S2 -","2","1","","Liu, Changqing; Wang, Bo; Guo, Ziyi; Zhang, Jitan; Xie, Meihua","Metal-free cascade rearrangement/radical addition/oxidative C–H annulation of propargyl alcohols with sodium sulfinates: access to 2-sulfenylindenones","Organic Chemistry Frontiers","2019","6","15","2796","","10.1039/C9QO00688E","","","0.71073","MoKα","","0.0517","0.0415","","","0.1053","0.1133","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555013","23.94","0.011","28.05","0.013","23.991","0.011","90","","119.85","0.008","90","","13973","11","150","2","150","2","","","","","","","","5","P 1 21/a 1","-P 2yab","14","","","","- C147 H132 N16 O27 Zn -","- C147 H132 N16 O27 Zn -","- C588 H528 N64 O108 Zn4 -","4","1","","Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad","Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms","Organic Chemistry Frontiers","2019","6","18","3192","","10.1039/C9QO00695H","","","0.71075","MoKα","","0.1687","0.1287","","","0.3375","0.3647","","","","","","1.259","","","","has coordinates,has disorder","238272","2020-10-21","18:00:00",""
"1555014","12.6219","0.0011","16.3765","0.0013","16.6547","0.0014","90","","100.607","0.004","90","","3383.7","0.5","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C38 H32 N2 O6 -","- C38 H32 N2 O6 -","- C152 H128 N8 O24 -","4","1","","Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad","Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms","Organic Chemistry Frontiers","2019","6","18","3192","","10.1039/C9QO00695H","","","1.54178","CuKα","","0.114","0.0825","","","0.1806","0.2071","","","","","","1.132","","","","has coordinates,has disorder","238272","2020-10-21","18:00:00",""
"1555015","4.6619","0.0004","23.4349","0.0019","12.2946","0.0013","90","","97.466","0.006","90","","1331.8","0.2","296","2","296","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C15 H16 O3 -","- C15 H16 O3 -","- C60 H64 O12 -","4","1","","Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad","Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms","Organic Chemistry Frontiers","2019","6","18","3192","","10.1039/C9QO00695H","","","1.54178","CuKα","","0.0936","0.0531","","","0.1186","0.1434","","","","","","1.036","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555016","12.8844","0.0013","13.9073","0.0013","20.6328","0.0019","98.862","0.007","106.525","0.007","94.899","0.007","3469.4","0.6","150","2","150","2","","","","","","","","5","P -1","-P 1","2","","","","- C152 H128 N8 O24 Zn -","- C152 H128 N8 O24 Zn -","- C152 H128 N8 O24 Zn -","1","0.5","","Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad","Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms","Organic Chemistry Frontiers","2019","6","18","3192","","10.1039/C9QO00695H","","","0.71075","MoKα","","0.1869","0.138","","","0.384","0.42","","","","","","1.446","","","","has coordinates","238272","2020-10-21","18:00:00",""
"1555017","12.8709","0.0004","15.6947","0.0004","16.5272","0.0005","90","","92.507","0.002","90","","3335.38","0.17","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C36 H30 N4 O6 -","- C36 H30 N4 O6 -","- C144 H120 N16 O24 -","4","1","","Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad","Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms","Organic Chemistry Frontiers","2019","6","18","3192","","10.1039/C9QO00695H","","","1.54178","CuKα","","0.1505","0.0713","","","0.1979","0.2596","","","","","","0.997","","","","has coordinates","238272","2020-10-21","18:00:00",""
"1555020","42.263","0.003","7.4986","0.0007","12.0012","0.001","90","","93.813","0.003","90","","3794.9","0.5","296","2","296","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","5,6,15,16-Tetrahydro-5,16-epoxyhexacene","","- C26 H18 O -","- C26 H18 O -","- C208 H144 O8 -","8","1","","Han, Jian; Liu, Xinbang; Li, Yu; Lou, Zihao; Yi, Mingdong; Kong, Huihui; Luo, Jun","New synthetic approaches for hexacene and its application in thin-film transistors","Organic Chemistry Frontiers","2019","6","16","2839","","10.1039/C9QO00708C","","","0.71073","MoKα","","0.0784","0.058","","","0.1579","0.1726","","","","","","1.022","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555023","11.0804","0.0003","12.2799","0.0005","13.6018","0.0004","75.764","0.003","84.604","0.003","89.194","0.003","1785.88","0.11","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C24 H17 N O2 -","- C24 H17 N O2 -","- C96 H68 N4 O8 -","4","2","","Yang, Zhijia; Pi, Chao; Cui, Xiuling; Wu, Yangjie","One-pot synthesis of pyranoquinolin-1-ones via Rh(iii)-catalysed redox annulation of 3-carboxyquinolines and alkynes","Organic Chemistry Frontiers","2019","6","16","2897","","10.1039/C9QO00710E","","x-ray","0.71073","MoKα","","0.0668","0.0441","","","0.0931","0.1062","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555024","8.5534","0.0008","5.4976","0.0002","37.5979","0.0018","90","","93.982","0.006","90","","1763.7","0.2","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H17 N O2 -","- C24 H17 N O2 -","- C96 H68 N4 O8 -","4","1","","Yang, Zhijia; Pi, Chao; Cui, Xiuling; Wu, Yangjie","One-pot synthesis of pyranoquinolin-1-ones via Rh(iii)-catalysed redox annulation of 3-carboxyquinolines and alkynes","Organic Chemistry Frontiers","2019","6","16","2897","","10.1039/C9QO00710E","","x-ray","1.54184","CuKα","","0.0824","0.0571","","","0.1361","0.1614","","","","","","1.016","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555025","6.4787","0.0005","10.7989","0.0007","16.2052","0.0006","79.201","0.004","85.566","0.005","73.057","0.007","1065.03","0.12","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C26 H18 F3 N O2 -","- C26 H18 F3 N O2 -","- C52 H36 F6 N2 O4 -","2","1","","Yang, Zhijia; Pi, Chao; Cui, Xiuling; Wu, Yangjie","One-pot synthesis of pyranoquinolin-1-ones via Rh(iii)-catalysed redox annulation of 3-carboxyquinolines and alkynes","Organic Chemistry Frontiers","2019","6","16","2897","","10.1039/C9QO00710E","","x-ray","1.54184","CuKα","","0.1246","0.0857","","","0.2528","0.2922","","","","","","1.06","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1555027","10.465","0.002","9.797","0.002","22.032","0.005","90","","95.834","0.003","90","","2247.1","0.8","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C28 H22 O3 S -","- C28 H22 O3 S -","- C112 H88 O12 S4 -","4","1","","Yang, Tao; Kou, Peihao; Jin, Fengyan; Song, Xian-Rong; Bai, Jiang; Ding, Haixin; Xiao, Qiang; Liang, Yong-Min","TFA-promoted sulfonation/cascade cyclization of 2-propynolphenols with sodium sulfinates to 4-sulfonyl 2H-chromenes under metal-free conditions","Organic Chemistry Frontiers","2019","6","17","3162","","10.1039/C9QO00712A","","","0.71073","MoKα","","0.0562","0.0448","","","0.1104","0.1194","","","","","","1.093","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555029","5.9669","0.0002","11.4767","0.0003","21.9463","0.0007","90","","96.78","0.001","90","","1492.38","0.08","173","2","173","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C17 H15 N O3 S -","- C17 H15 N O3 S -","- C68 H60 N4 O12 S4 -","4","1","","Zhu, Cheng-Zhi; Wei, Yin; Shi, Min","Rhodium(ii)-catalyzed divergent intramolecular tandem cyclization of N- or O-tethered cyclohexa-2,5-dienones with 1-sulfonyl-1,2,3-triazole: synthesis of cyclopropa[cd]indole and benzofuran derivatives","Organic Chemistry Frontiers","2019","6","16","2884","","10.1039/C9QO00714H","","","0.71073","MoKα","","0.0367","0.0331","","","0.086","0.0891","","","","","","1.062","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555030","7.1629","0.0002","10.9804","0.0004","12.5285","0.0004","102.431","0.001","97.658","0.001","98.768","0.001","936.85","0.05","296","2","296","2","","","","","","","","6","P -1","-P 1","2","","","","- C21 H16 Br N O4 S -","- C21 H16 Br N O4 S -","- C42 H32 Br2 N2 O8 S2 -","2","1","","Zhu, Cheng-Zhi; Wei, Yin; Shi, Min","Rhodium(ii)-catalyzed divergent intramolecular tandem cyclization of N- or O-tethered cyclohexa-2,5-dienones with 1-sulfonyl-1,2,3-triazole: synthesis of cyclopropa[cd]indole and benzofuran derivatives","Organic Chemistry Frontiers","2019","6","16","2884","","10.1039/C9QO00714H","","","0.71073","MoKα","","0.0411","0.0368","","","0.1009","0.1042","","","","","","1.055","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555032","9.0601","0.0008","9.927","0.0009","13.5869","0.0012","82.759","0.002","78.19","0.001","83.39","0.002","1181.56","0.18","298","2","298","2","","","","","","","","5","P -1","-P 1","2","","","","- C27 H20 N2 O4 S -","- C27 H20 N2 O4 S -","- C54 H40 N4 O8 S2 -","2","1","","Zhang, Tian-Shu; Wang, Rong; Cai, Pei-Jun; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo","Silver-catalyzed nitration/annulation of 2-alkynylanilines for a tunable synthesis of nitrated indoles and indazole-2-oxides","Organic Chemistry Frontiers","2019","6","16","2968","","10.1039/C9QO00715F","","","0.71073","MoKα","","0.1066","0.0529","","","0.1289","0.1465","","","","","","1.056","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555033","12.7222","0.0013","31.291","0.003","7.7018","0.0007","90","","104.211","0.003","90","","2972.2","0.5","298","2","298","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C29.25 H25.5 Cl0.5 N3 O6 S2 -","- C29.25 H25.5 Cl0.5 N3 O6 S2 -","- C117 H102 Cl2 N12 O24 S8 -","4","1","","Zhang, Tian-Shu; Wang, Rong; Cai, Pei-Jun; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo","Silver-catalyzed nitration/annulation of 2-alkynylanilines for a tunable synthesis of nitrated indoles and indazole-2-oxides","Organic Chemistry Frontiers","2019","6","16","2968","","10.1039/C9QO00715F","","","0.71073","MoKα","","0.1485","0.0679","","","0.1797","0.2115","","","","","","1.034","","","","has coordinates,has disorder","238282","2020-10-21","18:00:00",""
"1555035","17.9223","0.0005","20.5932","0.0006","21.0729","0.0007","90","","100.834","0.003","90","","7638.9","0.4","151","2","151","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C88 H73 Cl10 N3 Pd -","- C88 H73 Cl10 N3 Pd -","- C352 H292 Cl40 N12 Pd4 -","4","0.5","","Zhang, Fei-Yi; Lan, Xiao-Bing; Xu, Chang; Yao, Hua-Gang; Li, Tian; Liu, Feng-Shou","Rigid hindered N-heterocyclic carbene palladium precatalysts: synthesis, characterization and catalytic amination","Organic Chemistry Frontiers","2019","6","18","3292","","10.1039/C9QO00726A","","","1.54184","CuKα","","0.0821","0.075","","","0.2099","0.2229","","","","","","1.089","","","","has coordinates,has disorder","238284","2020-10-21","18:00:00",""
"1555036","17.6466","0.0004","20.7167","0.0005","20.3473","0.0008","90","","95.896","0.003","90","","7399.2","0.4","281.05","0.1","281.05","0.1","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C84 H65 Cl2 N3 O2 Pd -","- C84 H65 Cl2 N3 O2 Pd -","- C336 H260 Cl8 N12 O8 Pd4 -","4","0.5","","Zhang, Fei-Yi; Lan, Xiao-Bing; Xu, Chang; Yao, Hua-Gang; Li, Tian; Liu, Feng-Shou","Rigid hindered N-heterocyclic carbene palladium precatalysts: synthesis, characterization and catalytic amination","Organic Chemistry Frontiers","2019","6","18","3292","","10.1039/C9QO00726A","","","1.54178","CuKα","","0.0542","0.0384","","","0.0838","0.0909","","","","","","0.995","","","","has coordinates","238284","2020-10-21","18:00:00",""
"1555038","8.3117","0.0002","17.2043","0.0004","8.3018","0.0002","90","","103.231","0.001","90","","1155.62","0.05","130","","130","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C9 H13 N5 O4 -","- C9 H13 N5 O4 -","- C36 H52 N20 O16 -","4","1","","Guo, Xiaowei; Wang, Jidong; Su, Can; Liu, Chongxi; Ma, Xiao-Yan; Yu, Zhiyin; Li, Jiansong; Wang, Xiangjing; Xiang, Wensheng; Huang, Sheng-Xiong","A unique spiro-β-triazinedione-γ-hydantoin type alkaloid with antiviral activity against tobacco mosaic virus from Streptomyces gamaensis","Organic Chemistry Frontiers","2019","6","18","3215","","10.1039/C9QO00742C","","","1.54178","CuKα","","0.0485","0.0477","","","0.1252","0.126","","","","","","0.674","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555040","9.3448","0.0005","11.2047","0.0008","12.9889","0.0008","106.439","0.006","97.223","0.005","112.631","0.006","1160.92","0.15","100","0.1","100","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C23 H25 N O9 S -","- C23 H25 N O9 S -","- C46 H50 N2 O18 S2 -","2","1","","Xing, Siyang; Xia, Hanyu; Wang, Xin; Wu, Die; Xu, Xinrui; Su, Yunran; Wang, Kui; Zhu, Bolin; Guo, Junshuo","Diastereoselective access to 2-aminoindanones via the rhodium(ii)-catalyzed tandem reaction involving O–H insertion and Michael addition","Organic Chemistry Frontiers","2019","6","17","3121","","10.1039/C9QO00765B","","x-ray","0.71073","MoKα","","0.0626","0.0482","","","0.114","0.1288","","","","","","1.061","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555042","9.1302","0.0003","9.1578","0.0005","10.226","0.0004","108.986","0.004","98.417","0.003","114.037","0.004","698.83","0.07","373","2","373","2","","","","","","","","4","P 1","P 1","1","","","","- C33 H38 N O5 -","- C33 H38 N O5 -","- C33 H38 N O5 -","1","1","","Freeman, Jared L.; Brimble, Margaret A.; Furkert, Daniel P.","A chiral auxiliary-based synthesis of the C5‒C17 trans-decalin framework of anthracimycin","Organic Chemistry Frontiers","2019","6","16","2954","","10.1039/C9QO00769E","","","1.54184","CuKα","","0.0448","0.0436","","","0.1154","0.1169","","","","","","1.054","","","","has coordinates","238290","2020-10-21","18:00:00",""
"1555043","11.9189","0.0004","6.5987","0.0002","26.7335","0.001","90","","100.124","0.004","90","","2069.83","0.12","100","0.1","100","0.1","","","","","","","","3","I 1 2 1","I 2y","5","","","","- C25 H28 O10 -","- C25 H28 O10 -","- C100 H112 O40 -","4","1","","Pan, Dongyan; Zhang, Xuexia; Zheng, Haizhou; Zheng, Zhihui; Nong, Xuhua; Liang, Xiao; Ma, Xuan; Qi, Shuhua","Novel anthraquinone derivatives as inhibitors of protein tyrosine phosphatases and indoleamine 2,3-dioxygenase 1 from the deep-sea derived fungus Alternaria tenuissima DFFSCS013","Organic Chemistry Frontiers","2019","6","18","3252","","10.1039/C9QO00775J","","x-ray","1.54184","CuKα","","0.0344","0.0329","","","0.0901","0.0909","","","","","","1.0239","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555046","7.7957","0.0007","10.1827","0.0006","12.7574","0.0008","79.033","0.005","76.634","0.007","77.369","0.006","950.96","0.12","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C23 H20 O6 -","- C23 H20 O6 -","- C46 H40 O12 -","2","1","","Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie","A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate","Organic Chemistry Frontiers","2019","6","18","3238","","10.1039/C9QO00795D","","x-ray","0.71073","MoKα","","0.0829","0.053","","","0.1189","0.1395","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555047","10.0036","0.0011","15.567","0.0013","8.7599","0.0011","90","","100.953","0.011","90","","1339.3","0.3","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C16 H11 Br O2 -","- C16 H11 Br O2 -","- C64 H44 Br4 O8 -","4","1","","Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie","A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate","Organic Chemistry Frontiers","2019","6","18","3238","","10.1039/C9QO00795D","","x-ray","1.54184","CuKα","","0.0661","0.0403","","","0.0957","0.1132","","","","","","1.025","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555048","25.676","0.002","4.1792","0.0004","24.335","0.003","90","","112.38","0.014","90","","2414.6","0.5","293","2","293","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C16 H12 O2 -","- C16 H12 O2 -","- C128 H96 O16 -","8","1","","Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie","A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate","Organic Chemistry Frontiers","2019","6","18","3238","","10.1039/C9QO00795D","","x-ray","0.71073","MoKα","","0.1134","0.0687","","","0.1635","0.2052","","","","","","1.05","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555049","14.7414","0.0004","8.7416","0.0003","16.409","0.0005","90","","104.242","0.003","90","","2049.53","0.11","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C23 H22 O6 -","- C23 H22 O6 -","- C92 H88 O24 -","4","1","","Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie","A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate","Organic Chemistry Frontiers","2019","6","18","3238","","10.1039/C9QO00795D","","x-ray","1.54184","CuKα","","0.0794","0.0626","","","0.1809","0.2038","","","","","","1.051","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555050","14.6483","0.0003","17.4042","0.0004","15.2455","0.0004","90","","94.817","0.002","90","","3872.99","0.16","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H17 Cl O6 -","- C22 H17 Cl O6 -","- C176 H136 Cl8 O48 -","8","2","","Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie","A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate","Organic Chemistry Frontiers","2019","6","18","3238","","10.1039/C9QO00795D","","x-ray","1.54184","CuKα","","0.0746","0.0613","","","0.169","0.1846","","","","","","1.028","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1555054","8.8935","0.0001","14.433","0.0001","15.7451","0.0001","90","","92.016","0.001","90","","2019.79","0.03","286","5","286","5","","","","","","","fungus","3","P 1 21/c 1","-P 2ybc","14","","","","- C21 H22 O10 -","- C21 H22 O10 -","- C84 H88 O40 -","4","1","","Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui","Canescones A‒E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens","Organic Chemistry Frontiers","2019","6","18","3274","","10.1039/C9QO00820A","","x-ray","1.54184","CuKα","","0.0425","0.0413","","","0.1123","0.1134","","","","","","1.083","","","","has coordinates,has disorder","238298","2020-10-21","18:00:00",""
"1555055","9.016","0.0002","9.3778","0.0002","10.636","0.0002","93.717","0.002","90.826","0.002","92.317","0.002","896.52","0.03","100.01","0.1","100.01","0.1","","","","","","","fungus","3","P -1","-P 1","2","","","","- C20 H20 O10 -","- C20 H20 O10 -","- C40 H40 O20 -","2","1","","Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui","Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens","Organic Chemistry Frontiers","2019","6","18","3274","","10.1039/C9QO00820A","","x-ray","1.54184","CuKα","","0.0357","0.0326","","","0.0822","0.084","","","","","","1.05","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555056","8.33914","0.00003","13.29606","0.00005","18.06836","0.00008","90","","90","","90","","2003.38","0.014","100","0.1","100","0.1","","","","","","","fungus","3","P c a 21","P 2c -2ac","29","","","","- C21 H22 O11 -","- C21 H22 O11 -","- C84 H88 O44 -","4","1","","Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui","Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens","Organic Chemistry Frontiers","2019","6","18","3274","","10.1039/C9QO00820A","","x-ray","1.54184","CuKα","","0.0219","0.0218","","","0.0559","0.0559","","","","","","1.067","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555057","8.2302","0.0004","14.4554","0.0006","16.2394","0.0007","90","","90","","90","","1932.01","0.15","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C21 H22 O11 -","- C21 H22 O11 -","- C84 H88 O44 -","4","1","","Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui","Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens","Organic Chemistry Frontiers","2019","6","18","3274","","10.1039/C9QO00820A","","","1.54178","CuKα","","0.04","0.0382","","","0.116","0.1193","","","","","","1.019","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555058","8.26703","0.00005","13.79202","0.00008","17.73644","0.0001","90","","102.392","0.0006","90","","1975.18","0.02","99.99","0.1","99.99","0.1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H23 N O9 -","- C22 H23 N O9 -","- C88 H92 N4 O36 -","4","1","","Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui","Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens","Organic Chemistry Frontiers","2019","6","18","3274","","10.1039/C9QO00820A","","x-ray","1.54184","CuKα","","0.0351","0.0331","","","0.0899","0.0913","","","","","","1.065","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555062","10.7304","0.0004","18.6098","0.0005","9.9301","0.0004","90","","115.595","0.004","90","","1788.36","0.12","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C23 H19 F3 -","- C23 H19 F3 -","- C92 H76 F12 -","4","1","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","x-ray","1.54184","CuKα","","0.0447","0.0395","","","0.1059","0.1107","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555063","9.28774","0.00013","13.98378","0.00018","16.25245","0.00018","94.589","0.001","106.279","0.0011","98.2135","0.0011","1989.34","0.05","100","5","100","5","","","","","","","","4","P -1","-P 1","2","","","","- C24 H21 F3 O2 -","- C24 H21 F3 O2 -","- C96 H84 F12 O8 -","4","2","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","x-ray","1.54184","CuKα","","0.0393","0.0384","","","0.0955","0.0962","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555064","8.7646","0.0001","10.6788","0.0002","20.8962","0.0003","90","","94.821","0.001","90","","1948.87","0.05","100","3","100","3","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C24 H20 F4 O2 -","- C24 H20 F4 O2 -","- C96 H80 F16 O8 -","4","1","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","x-ray","1.54184","CuKα","","0.0406","0.0367","","","0.0976","0.101","","","","","","1.077","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555065","9.7671","0.0005","10.3099","0.0004","19.8876","0.0007","92.41","0.003","96.248","0.004","107.45","0.004","1893.23","0.15","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C24 H21 F3 -","- C24 H21 F3 -","- C96 H84 F12 -","4","2","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","","0.71073","MoKα","","0.0722","0.0529","","","0.1186","0.1314","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555066","8.8501","0.0009","10.1181","0.0012","11.7209","0.001","98.214","0.009","105.322","0.009","103.258","0.009","961.85","0.19","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C24 H21 F3 O2 -","- C24 H21 F3 O2 -","- C48 H42 F6 O4 -","2","1","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","x-ray","1.54184","CuKα","","0.1198","0.0868","","","0.2319","0.2604","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555067","9.9918","0.0002","10.2089","0.0002","10.5751","0.0002","91.174","0.002","116.274","0.002","107.926","0.002","904.65","0.04","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C23 H19 F3 O -","- C23 H19 F3 O -","- C46 H38 F6 O2 -","2","1","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","x-ray","1.54184","CuKα","","0.0344","0.033","","","0.0884","0.0897","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555068","8.9463","0.0003","10.2875","0.0003","11.0964","0.0003","70.184","0.002","86.437","0.002","76.947","0.002","935.84","0.05","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C24 H21 F3 -","- C24 H21 F3 -","- C48 H42 F6 -","2","1","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","x-ray","1.54184","CuKα","","0.0536","0.0464","","","0.1316","0.1375","","","","","","1.072","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555069","9.0216","0.0004","9.9831","0.0004","11.9107","0.0005","77.527","0.004","82.086","0.004","74.544","0.004","1005.86","0.08","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C24 H20 Cl F3 O2 -","- C24 H20 Cl F3 O2 -","- C48 H40 Cl2 F6 O4 -","2","1","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","x-ray","1.54184","CuKα","","0.0419","0.0388","","","0.0981","0.1008","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555070","10.5544","0.0004","15.4584","0.0006","12.2743","0.0004","90","","102.702","0.004","90","","1953.59","0.13","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C25 H23 F3 -","- C25 H23 F3 -","- C100 H92 F12 -","4","1","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","","0.71073","MoKα","","0.0489","0.0398","","","0.0928","0.0984","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555071","11.6641","0.0003","9.1396","0.0002","17.3076","0.0004","90","","95.883","0.002","90","","1835.36","0.08","100","3","100","3","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C24 H21 F3 -","- C24 H21 F3 -","- C96 H84 F12 -","4","1","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","x-ray","1.54184","CuKα","","0.0429","0.0377","","","0.1012","0.1051","","","","","","1.055","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555072","9.02917","0.0002","9.25385","0.00019","11.1048","0.0002","87.5911","0.0016","80.5904","0.0018","78.3143","0.0018","896.36","0.03","100","3","100","3","","","","","","","","4","P -1","-P 1","2","","","","- C22 H16 Br F3 -","- C22 H16 Br F3 -","- C44 H32 Br2 F6 -","2","1","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","x-ray","1.54184","CuKα","","0.0267","0.0247","","","0.0604","0.0615","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555073","9.2224","0.0005","10.2968","0.0005","11.9735","0.0005","74.791","0.004","80.463","0.004","72.449","0.005","1041.48","0.09","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C24 H19 Cl2 F3 O2 -","- C24 H19 Cl2 F3 O2 -","- C48 H38 Cl4 F6 O4 -","2","1","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","x-ray","1.54184","CuKα","","0.055","0.0484","","","0.1495","0.1574","","","","","","1.059","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555074","21.8668","0.0005","10.36934","0.00016","18.0539","0.0004","90","","113.947","0.003","90","","3741.25","0.16","100","2","100","2","","","","","","","","4","I 1 2/c 1","-I 2yc","15","","","","- C22 H15 Cl2 F3 -","- C22 H15 Cl2 F3 -","- C176 H120 Cl16 F24 -","8","1","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","","0.71073","MoKα","","0.0502","0.0428","","","0.102","0.1068","","","","","","1.03","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555075","10.1714","0.0003","36.8462","0.001","10.1929","0.0003","90","","103.732","0.003","90","","3710.88","0.19","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C24 H21 F3 -","- C24 H21 F3 -","- C192 H168 F24 -","8","2","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","x-ray","1.54184","CuKα","","0.0618","0.0545","","","0.1489","0.1543","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555076","11.5733","0.0002","18.729","0.0004","19.4741","0.0004","90","","105.635","0.002","90","","4064.94","0.14","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C25 H23 F3 O2 -","- C25 H23 F3 O2 -","- C200 H184 F24 O16 -","8","2","","Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.","TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes","Organic Chemistry Frontiers","2019","6","18","3264","","10.1039/C9QO00822E","","x-ray","1.54184","CuKα","","0.0398","0.0354","","","0.0901","0.0928","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555079","14.099","0.002","5.2916","0.0009","9.1495","0.0016","90","","101.496","0.007","90","","668.92","0.19","273","2","273","2","","","","","","","","4","P 1 c 1","P -2yc","7","","","","- C16 H13 N O3 -","- C16 H13 N O3 -","- C32 H26 N2 O6 -","2","1","","He, Guangke; Li, Yuan; Yu, Zilun; Chen, Zhaoqiang; Tang, Yongming; Song, Guangliang; Loh, Teck-Peng","Selectfluor™-catalyzed oxidative cyclization of ynamides enables facile synthesis of oxazolidine-2,4-diones","Organic Chemistry Frontiers","2019","6","21","3644","","10.1039/C9QO00845D","","","0.71073","MoKα","","0.0506","0.041","","","0.1183","0.1268","","","","","","1.067","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1555081","4.12","0.0005","14.2279","0.0012","26.763","0.002","90","","94.268","0.008","90","","1564.5","0.3","295","2","295","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C17 H12 I N3 S -","- C17 H12 I N3 S -","- C68 H48 I4 N12 S4 -","4","1","","Zhou, Yao; Lou, Yixian; Wang, Ya; Song, Qiuling","Oxidant-controlled divergent transformations of 3-aminoindazoles for the synthesis of pyrimido[1,2-b]-indazoles and aromatic nitrile-derived dithioacetals","Organic Chemistry Frontiers","2019","6","19","3355","","10.1039/C9QO00847K","","","0.71073","MoKα","","0.0518","0.0463","","","0.0962","0.0989","","","","","","1.124","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555082","10.1327","0.001","12.0719","0.0014","28.967","0.003","90","","90","","90","","3543.3","0.7","298","","298","","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C19 H17 N O S2 -","- C19 H17 N O S2 -","- C152 H136 N8 O8 S16 -","8","1","","Zhou, Yao; Lou, Yixian; Wang, Ya; Song, Qiuling","Oxidant-controlled divergent transformations of 3-aminoindazoles for the synthesis of pyrimido[1,2-b]-indazoles and aromatic nitrile-derived dithioacetals","Organic Chemistry Frontiers","2019","6","19","3355","","10.1039/C9QO00847K","","x-ray","0.71073","MoKα","","0.1198","0.0634","","","0.1463","0.1848","","","","","","0.8505","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555084","6.1329","0.0008","40.065","0.005","10.6098","0.0015","90","","103.811","0.004","90","","2531.6","0.6","273","2","273","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C26 H16 F9 N O4 -","- C26 H16 F9 N O4 -","- C104 H64 F36 N4 O16 -","4","1","","He, Wei; Yu, Jipan; Wang, Dawei; Ran, Guoxia; Xia, Xiao-Feng","Synthesis of tri-substituted allyl alcohols via a copper/iron co-catalyzed cascade perfluoroalkylation/rearrangement of aryl propynyl ethers","Organic Chemistry Frontiers","2019","6","20","3575","","10.1039/C9QO00848A","","","0.71073","MoKα","","0.195","0.0971","","","0.2449","0.304","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555085","11.543","0.005","10.4","0.002","32.618","0.006","90","","90","","90","","3916","2","300","2","300.09","","","","","","","","","5","P c a 21","P 2c -2ac","29","","","","- C19 H12 Cl F9 O -","- C19 H10 Cl F9 O -","- C152 H80 Cl8 F72 O8 -","8","2","","He, Wei; Yu, Jipan; Wang, Dawei; Ran, Guoxia; Xia, Xiao-Feng","Synthesis of tri-substituted allyl alcohols via a copper/iron co-catalyzed cascade perfluoroalkylation/rearrangement of aryl propynyl ethers","Organic Chemistry Frontiers","2019","6","20","3575","","10.1039/C9QO00848A","","","1.54178","CuKα","","0.0854","0.0712","","","0.2132","0.2395","","","","","","1.065","","","","has coordinates","300101","2025-06-17","17:58:11",""
"1555087","7.1385","0.0009","7.5039","0.001","19.126","0.003","90","","90","","90","","1024.5","0.2","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C10 H9 F3 N2 O -","- C10 H9 F3 N2 O -","- C40 H36 F12 N8 O4 -","4","1","","Wang, Xiaonan; Gao, Yuan; Wei, Zhonglin; Cao, Jungang; Liang, Dapeng; Lin, Yingjie; Duan, Haifeng","An enantioselective aza-Henry reaction of trifluoromethyl ketimines catalyzed by phase-transfer catalysts","Organic Chemistry Frontiers","2019","6","18","3269","","10.1039/C9QO00850K","","","0.71073","MoKα","","0.0883","0.0458","","","0.0892","0.1034","","","","","","0.933","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555088","7.2179","0.001","17.509","0.002","18.867","0.003","90","","100.172","0.008","90","","2346.9","0.6","293","2","293","2","","","","","","","","6","C 1 c 1","C -2yc","9","","","","- C26 H20 Cl F3 N2 O2 -","- C26 H20 Cl F3 N2 O2 -","- C104 H80 Cl4 F12 N8 O8 -","4","1","","Yu, Yang; Zhang, Yan; Wang, Zhuo; Liang, Yong-Xin; Zhao, Yu-Long","A rhodium-catalyzed three-component reaction of arylisocyanides, trifluorodiazoethane, and activated methylene isocyanides or azomethine ylides: an efficient synthesis of trifluoroethyl-substituted imidazoles","Organic Chemistry Frontiers","2019","6","21","3657","","10.1039/C9QO00856J","","","1.54178","CuKα","","0.0619","0.042","","","0.0952","0.1026","","","","","","1.091","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555092","10.1647","0.0009","17.2468","0.0015","20.8692","0.0018","90","","101.136","0.002","90","","3589.7","0.5","150","2","150.15","","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C46 H40 O8 -","- C46 H40 O8 -","- C184 H160 O32 -","4","1","","Bolshchikov, Boris; Volkov, Sergey; Sokolova, Daria; Gorbunov, Alexander; Serebryannikova, Alina; Gloriozov, Igor; Cheshkov, Dmitry; Bezzubov, Stanislav; Chung, Wen-Sheng; Kovalev, Vladimir; Vatsouro, Ivan","Constructing bridged multifunctional calixarenes by intramolecular indole coupling","Organic Chemistry Frontiers","2019","6","19","3327","","10.1039/C9QO00859D","","x-ray","0.71073","MoKα","","0.0665","0.0432","","","0.0905","0.1004","","","","","","1.02","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555093","16.5782","0.0011","28.2895","0.0019","17.3002","0.0011","90","","93.414","0.002","90","","8099.2","0.9","150","2","150.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C72 H64 N10 O6 -","- C72 H64 N10 O6 -","- C288 H256 N40 O24 -","4","1","","Bolshchikov, Boris; Volkov, Sergey; Sokolova, Daria; Gorbunov, Alexander; Serebryannikova, Alina; Gloriozov, Igor; Cheshkov, Dmitry; Bezzubov, Stanislav; Chung, Wen-Sheng; Kovalev, Vladimir; Vatsouro, Ivan","Constructing bridged multifunctional calixarenes by intramolecular indole coupling","Organic Chemistry Frontiers","2019","6","19","3327","","10.1039/C9QO00859D","","","0.71073","MoKα","","0.2255","0.1582","","","0.4204","0.4539","","","","","","1.472","","","","has coordinates,has disorder","238316","2020-10-21","18:00:00",""
"1555094","30.104","0.003","23.487","0.002","26.09","0.004","90","","121.557","0.001","90","","15719","3","150","2","150.15","","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C76 H68 N8 O8 -","- C76 H68.052 N8.052 O8 -","- C608 H544.416 N64.416 O64 -","8","1","","Bolshchikov, Boris; Volkov, Sergey; Sokolova, Daria; Gorbunov, Alexander; Serebryannikova, Alina; Gloriozov, Igor; Cheshkov, Dmitry; Bezzubov, Stanislav; Chung, Wen-Sheng; Kovalev, Vladimir; Vatsouro, Ivan","Constructing bridged multifunctional calixarenes by intramolecular indole coupling","Organic Chemistry Frontiers","2019","6","19","3327","","10.1039/C9QO00859D","","","0.71073","MoKα","","0.2181","0.164","","","0.3643","0.3949","","","","","","1.034","","","","has coordinates,has disorder","238316","2020-10-21","18:00:00",""
"1555097","14.445","0.0009","6.6377","0.0003","15.6545","0.0006","90","","94.414","0.005","90","","1496.53","0.13","297.4","0.6","297.4","0.6","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C18 H14 Cl N3 -","- C18 H14 Cl N3 -","- C72 H56 Cl4 N12 -","4","1","","Surendra Reddy, G.; Ramachary, Dhevalapally B.","Reaction engineering and photophysical studies of fully enriched C-vinyl-1,2,3-triazoles","Organic Chemistry Frontiers","2019","6","21","3620","","10.1039/C9QO00864K","","x-ray","0.71073","MoKα","","0.1144","0.0775","","","0.2213","0.2595","","","","","","1.046","","","","has coordinates","300101","2025-06-17","17:58:11",""
"1555098","13.055","0.005","13.601","0.005","10.697","0.005","90","0.005","100.788","0.005","90","0.005","1865.8","1.3","293","2","293","2","","","","","","","","3","C 1 c 1","C -2yc","9","","","","- C23 H16 N4 -","- C23 H16 N4 -","- C92 H64 N16 -","4","1","","Surendra Reddy, G.; Ramachary, Dhevalapally B.","Reaction engineering and photophysical studies of fully enriched C-vinyl-1,2,3-triazoles","Organic Chemistry Frontiers","2019","6","21","3620","","10.1039/C9QO00864K","","","0.71073","MoKα","","0.077","0.0668","","","0.1683","0.1755","","","","","","1.071","","","","has coordinates","277994","2022-09-20","08:32:41",""
"1555099","9.293","0.005","13.946","0.005","16.068","0.005","114.567","0.005","99.86","0.005","93.392","0.005","1846.1","1.3","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C23 H14 F N3 O2 -","- C23 H14 F N3 O2 -","- C92 H56 F4 N12 O8 -","4","2","","Surendra Reddy, G.; Ramachary, Dhevalapally B.","Reaction engineering and photophysical studies of fully enriched C-vinyl-1,2,3-triazoles","Organic Chemistry Frontiers","2019","6","21","3620","","10.1039/C9QO00864K","","","0.71073","MoKα","","0.0733","0.0461","","","0.1047","0.1164","","","","","","1.057","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555101","8.9187","0.0005","14.6101","0.0009","16.5218","0.0009","90","","90","","90","","2152.8","0.2","293","","293","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","BM6","","- C25 H22 F N O5 -","- C25 H22 F N O5 -","- C100 H88 F4 N4 O20 -","4","1","","Bhattacharya, Aditya; mani Shukla, Pushpendra; Kumar Kaushik, Lalit; Maji, Biswajit","Synthesis of chromans and kinetic resolution of 2-aryl-3-nitro-2H-chromenes via the NHC-bound azolium homoenolate pathway","Organic Chemistry Frontiers","2019","6","20","3523","","10.1039/C9QO00868C","","x-ray","0.71073","MoKα","","0.0976","0.0578","","","0.1202","0.1502","","","","","","1.072","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555103","19.5977","0.0012","8.1238","0.0004","23.2996","0.0012","90","","90.182","0.005","90","","3709.5","0.3","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C22 H21 N O3 S -","- C22 H21 N O3 S -","- C176 H168 N8 O24 S8 -","8","1","","Chen, Xiaoyan; Zhou, Hao; Chen, Zhiyuan","Pd/P/dba-Promoted cascade annulations to produce fused medium-sized sulfoximine polyheterocycles","Organic Chemistry Frontiers","2019","6","19","3415","","10.1039/C9QO00880B","","","0.71073","MoKα","","0.0458","0.0412","","","0.1085","0.1121","","","","","","1.007","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555104","8.199","0.0007","11.3055","0.0013","14.2419","0.0011","100.441","0.008","100.282","0.007","91.136","0.008","1275.6","0.2","293","2","293","2","","","","","","","","7","P -1","-P 1","2","","","","- C23 H22 Br3 Cl2 N O3 S -","- C23 H22 Br3 Cl2 N O3 S -","- C46 H44 Br6 Cl4 N2 O6 S2 -","2","1","","Chen, Xiaoyan; Zhou, Hao; Chen, Zhiyuan","Pd/P/dba-Promoted cascade annulations to produce fused medium-sized sulfoximine polyheterocycles","Organic Chemistry Frontiers","2019","6","19","3415","","10.1039/C9QO00880B","","","0.71073","MoKα","","0.2451","0.1666","","","0.2851","0.3351","","","","","","1.094","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555110","7.9759","0.0004","16.1628","0.0008","31.7213","0.0015","90","","90","","90","","4089.3","0.3","120","2","120","2","","","","","","","synthesized by the authors","4","P 21 21 21","P 2ac 2ab","19","","","","- C26 H20 O3 S -","- C26 H20 O3 S -","- C208 H160 O24 S8 -","8","2","","Dočekal, Vojtěch; Formánek, Bedřich; Císařová, Ivana; Veselý, Jan","A formal [4 + 2] cycloaddition of sulfur-containing alkylidene heterocycles with allenic compounds","Organic Chemistry Frontiers","2019","6","18","3259","","10.1039/C9QO00886A","","","0.71073","MoKα","","0.0458","0.0383","","","0.0854","0.089","","","","","","1.086","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555111","5.7472","0.0002","16.912","0.0006","22.0104","0.0008","90","","90","","90","","2139.34","0.13","120","2","120","2","","","","","","","synthesized by the authors","5","P 21 21 21","P 2ac 2ab","19","","","","- C27 H21 N O3 S -","- C27 H21 N O3 S -","- C108 H84 N4 O12 S4 -","4","1","","Dočekal, Vojtěch; Formánek, Bedřich; Císařová, Ivana; Veselý, Jan","A formal [4 + 2] cycloaddition of sulfur-containing alkylidene heterocycles with allenic compounds","Organic Chemistry Frontiers","2019","6","18","3259","","10.1039/C9QO00886A","","","1.54178","CuKα","","0.0265","0.0255","","","0.0627","0.0633","","","","","","1.075","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555113","10.596","0.0005","11.6796","0.0005","12.6988","0.0006","69.855","0.004","70.549","0.004","88.791","0.004","1383.42","0.12","293","2","293","2","","","","","","","","5","P 1","P 1","1","","","","- C33 H25 Cl N2 O5 -","- C33 H25 Cl N2 O5 -","- C66 H50 Cl2 N4 O10 -","2","2","","Wang, Zhen-Hua; Lei, Chuan-Wen; Zhang, Xia-Yan; You, Yong; Zhao, Jian-Qiang; Yuan, Wei-Cheng","Asymmetric domino 1,6-addition/annulation reaction of 3-cyano-4-alkenyl-2H-chromen-2-ones with isatin-derived MBH carbonates: enantioselective synthesis of 3,3′-cyclopentenylspirooxindoles bearing 2H-chromen-2-ones","Organic Chemistry Frontiers","2019","6","19","3342","","10.1039/C9QO00890J","","x-ray","1.54184","CuKα","","0.0499","0.0449","","","0.1108","0.1165","","","","","","1.051","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555115","17.7343","0.0017","13.4538","0.0011","24.68","0.002","90","","94.67","0.003","90","","5868.9","0.9","273","2","273","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C33 H29 Cl N2 O3 -","- C33 H29 Cl N2 O3 -","- C264 H232 Cl8 N16 O24 -","8","2","","Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo","Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction","Organic Chemistry Frontiers","2019","6","20","3530","","10.1039/C9QO00891H","","","0.71073","MoKα","","0.1516","0.0662","","","0.1679","0.2067","","","","","","1.016","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555116","9.853","0.0014","14.0452","0.0018","15.201","0.002","111.663","0.004","93.543","0.005","102.84","0.004","1882","0.4","273","2","273","2","","","","","","","","4","P -1","-P 1","2","","","","- C44 H39 N3 O7 -","- C44 H39 N3 O7 -","- C88 H78 N6 O14 -","2","1","","Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo","Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction","Organic Chemistry Frontiers","2019","6","20","3530","","10.1039/C9QO00891H","","","0.71073","MoKα","","0.1855","0.0718","","","0.1451","0.1845","","","","","","1.006","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555117","12.847","0.003","12.739","0.003","20.208","0.004","90","","96.73","0.006","90","","3284.4","1.3","273","2","273","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C33 H29 N3 O5 -","- C33 H29 N3 O5 -","- C132 H116 N12 O20 -","4","1","","Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo","Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction","Organic Chemistry Frontiers","2019","6","20","3530","","10.1039/C9QO00891H","","","0.71073","MoKα","","0.1512","0.0833","","","0.2481","0.2858","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555118","10.1992","0.001","17.1094","0.0019","33.448","0.003","90","","90","","90","","5836.7","1","273","2","273","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C34 H28 Cl2 N2 O3 -","- C34 H28 Cl2 N2 O3 -","- C272 H224 Cl16 N16 O24 -","8","1","","Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo","Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction","Organic Chemistry Frontiers","2019","6","20","3530","","10.1039/C9QO00891H","","","0.71073","MoKα","","0.1643","0.0727","","","0.1324","0.1624","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555120","9.2786","0.0006","9.5213","0.0006","15.4265","0.0006","75.673","0.004","76.438","0.004","71.3","0.005","1232.75","0.13","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C20 H40 N3 O5 P -","- C20 H40 N3 O5 P -","- C40 H80 N6 O10 P2 -","2","1","","Audran, Gérard; Bosco, Lionel; Brémond, Paul; Jugniot, Natacha; Marque, Sylvain R. A.; Massot, Philippe; Mellet, Philippe; Moussounda Moussounda Koumba, Tataye; Parzy, Elodie; Rivot, Angélique; Thiaudière, Eric; Voisin, Pierre; Wedl, Carina; Yamasaki, Toshihide","Enzymatic triggering of C–ON bond homolysis of alkoxyamines","Organic Chemistry Frontiers","2019","6","21","3663","","10.1039/C9QO00899C","","x-ray","1.54184","CuKα","","0.0601","0.0522","","","0.1447","0.1561","","","","","","1.053","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555121","8.8282","0.0006","22.0666","0.0014","12.5309","0.0006","90","","96.936","0.005","90","","2423.3","0.3","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C20 H38 N3 O4 P -","- C20 H38 N3 O4 P -","- C80 H152 N12 O16 P4 -","4","1","","Audran, Gérard; Bosco, Lionel; Brémond, Paul; Jugniot, Natacha; Marque, Sylvain R. A.; Massot, Philippe; Mellet, Philippe; Moussounda Moussounda Koumba, Tataye; Parzy, Elodie; Rivot, Angélique; Thiaudière, Eric; Voisin, Pierre; Wedl, Carina; Yamasaki, Toshihide","Enzymatic triggering of C–ON bond homolysis of alkoxyamines","Organic Chemistry Frontiers","2019","6","21","3663","","10.1039/C9QO00899C","","x-ray","1.54184","CuKα","","0.0584","0.0477","","","0.1301","0.143","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555123","10.22","0.002","9.55","0.002","20.071","0.005","90","","93.737","0.013","90","","1954.8","0.7","273","2","273.15","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C25 H24 O -","- C25 H24 O -","- C100 H96 O4 -","4","1","","Li, Hexin; Zhang, Mengru; Mehfooz, Haroon; Zhu, Dongxia; Zhao, Jinbo; Zhang, Qian","Highly convergent modular access to poly-carbon substituted cyclopropanes via Cu(i)-catalyzed three-component cyclopropene carboallylation","Organic Chemistry Frontiers","2019","6","19","3387","","10.1039/C9QO00902G","","","1.54178","CuKα","","0.0749","0.0624","","","0.1446","0.153","","","","","","1.081","","","","has coordinates","238334","2020-10-21","18:00:00",""
"1555125","13.3229","0.0003","6.2024","0.0001","15.4655","0.0004","90","","115.145","0.003","90","","1156.87","0.05","293","2","293","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C22 H18 Br Cl3 N2 O4 -","- C22 H18 Br Cl3 N2 O4 -","- C44 H36 Br2 Cl6 N4 O8 -","2","1","","Zhao, Mei-Xin; Liu, Qiang; Yu, Kun-Ming; Zhao, Xiao-Li; Shi, Min","Organocatalyzed asymmetric formal [3 + 2] cycloaddition of isocyanoacetates with N-itaconimides: facile access to optically active spiropyrroline succinimide derivatives","Organic Chemistry Frontiers","2019","6","23","3879","","10.1039/C9QO00939F","","x-ray","1.54184","CuKα","","0.0443","0.0424","","","0.1096","0.1112","","","","","","1.093","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555127","5.0942","0.0009","9.6532","0.0013","11.935","0.002","91.045","0.013","91.275","0.014","101.201","0.013","575.43","0.16","293.6","0.3","293.6","0.3","","","","","","","","5","P -1","-P 1","2","","","","- C13 H10 F3 N O -","- C13 H10 F3 N O -","- C26 H20 F6 N2 O2 -","2","1","","Lu, Kui; Wei, Xianfu; Li, Quan; Li, Yuxuan; Ji, Liangshuo; Hua, Erbing; Dai, Yujie; Zhao, Xia","Synthesis of α-trifluoromethyl ethanone oximes via the three-component reaction of aryl-substituted ethylenes, tert-butyl nitrite, and the Langlois reagent","Organic Chemistry Frontiers","2019","6","22","3766","","10.1039/C9QO00940J","","x-ray","0.71073","MoKα","","0.1682","0.0938","","","0.2251","0.2822","","","","","","1.005","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555129","7.0302","0.0007","7.6119","0.0008","7.7844","0.0009","94.191","0.009","109.731","0.01","97.56","0.009","385.61","0.08","293","2","293","2","","","","","","","","3","P 1","P 1","1","","","","- C15 H30 O4 -","- C15 H30 O4 -","- C15 H30 O4 -","1","1","","Song, Yin-Ping; Miao, Feng-Ping; Yin, Xiu-Li; Ji, Nai-Yun","Nitrogenous cyclonerane sesquiterpenes from an algicolous strain of Trichoderma asperellum","Organic Chemistry Frontiers","2019","6","21","3698","","10.1039/C9QO00942F","","","1.54178","CuKα","","0.0322","0.0315","","","0.0858","0.0865","","","","","","1.092","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555131","5.168","0.0004","15.6589","0.0007","15.9344","0.0011","90","","90","","90","","1289.49","0.15","200","2","200","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C16 H9 N3 O2 S -","- C16 H9 N3 O2 S -","- C64 H36 N12 O8 S4 -","4","1","","Recio, Javier; Pérez-Redondo, Adrián; Alvarez-Builla, Julio; Burgos, Carolina","Access to 2-substituted 1-pyridin-3-yl-β-carboline derivatives by intramolecular radical cyclization-ring opening-SNAr substitution","Organic Chemistry Frontiers","2019","6","18","3300","","10.1039/C9QO00944B","","x-ray","0.71073","MoKα","","0.0688","0.0445","","","0.0842","0.0938","","","","","","1.087","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555132","8.3252","0.0006","9.8395","0.0012","11.1869","0.0013","65.08","0.009","71.705","0.009","67.231","0.006","753.73","0.15","200","2","200","2","","","","","","","","6","P -1","-P 1","2","","","","- C16 H10 Br N3 O2 S -","- C16 H10 Br N3 O2 S -","- C32 H20 Br2 N6 O4 S2 -","2","1","","Recio, Javier; Pérez-Redondo, Adrián; Alvarez-Builla, Julio; Burgos, Carolina","Access to 2-substituted 1-pyridin-3-yl-β-carboline derivatives by intramolecular radical cyclization-ring opening-SNAr substitution","Organic Chemistry Frontiers","2019","6","18","3300","","10.1039/C9QO00944B","","x-ray","0.71073","MoKα","","0.047","0.036","","","0.082","0.0882","","","","","","1.087","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555136","7.8518","0.0006","10.3592","0.0007","14.2099","0.0011","80.043","0.002","83.223","0.002","82.438","0.002","1123.12","0.14","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C27 H25 N O3 S -","- C27 H25 N O3 S -","- C54 H50 N2 O6 S2 -","2","1","","Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo","Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones","Organic Chemistry Frontiers","2019","6","20","3555","","10.1039/C9QO00951E","","","0.71073","MoKα","","0.0961","0.0492","","","0.11","0.1265","","","","","","1.018","","","","has coordinates,has disorder","238346","2020-10-21","18:00:00",""
"1555137","5.9034","0.0005","21.165","0.002","21.6677","0.0019","90","","91.308","0.003","90","","2706.6","0.4","296","2","296","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C26 H22 Cl N O3 S -","- C26 H22 Cl N O3 S -","- C104 H88 Cl4 N4 O12 S4 -","4","1","","Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo","Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones","Organic Chemistry Frontiers","2019","6","20","3555","","10.1039/C9QO00951E","","","0.71073","MoKα","","0.1789","0.0779","","","0.1912","0.2261","","","","","","1.035","","","","has coordinates","238346","2020-10-21","18:00:00",""
"1555138","9.3704","0.0005","10.2251","0.0006","11.2595","0.0006","76.2532","0.0018","78.5679","0.0016","75.2513","0.0017","1002.43","0.1","296","2","296","2","","","","","","","","6","P -1","-P 1","2","","","","- C24 H18 Cl N O3 S -","- C24 H18 Cl N O3 S -","- C48 H36 Cl2 N2 O6 S2 -","2","1","","Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo","Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones","Organic Chemistry Frontiers","2019","6","20","3555","","10.1039/C9QO00951E","","","0.71073","MoKα","","0.0459","0.038","","","0.0971","0.1024","","","","","","1.021","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555139","7.8538","0.0006","13.4956","0.001","17.2047","0.0016","90","","101.145","0.003","90","","1789.2","0.3","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C23 H17 N O4 S -","- C23 H17 N O4 S -","- C92 H68 N4 O16 S4 -","4","1","","Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo","Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones","Organic Chemistry Frontiers","2019","6","20","3555","","10.1039/C9QO00951E","","","0.71073","MoKα","","0.0785","0.0505","","","0.1115","0.1231","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555140","13.0035","0.0011","15.8463","0.0012","9.5395","0.0009","90","","101.719","0.003","90","","1924.7","0.3","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C23 H16 N2 O5 S -","- C23 H16 N2 O5 S -","- C92 H64 N8 O20 S4 -","4","1","","Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo","Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones","Organic Chemistry Frontiers","2019","6","20","3555","","10.1039/C9QO00951E","","","0.71073","MoKα","","0.0768","0.047","","","0.104","0.1169","","","","","","1.02","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555141","7.3838","0.0011","11.2551","0.0015","24.298","0.003","90","","90","","90","","2019.3","0.5","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C24 H21 N O3 S -","- C24 H21 N O3 S -","- C96 H84 N4 O12 S4 -","4","1","","Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo","Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones","Organic Chemistry Frontiers","2019","6","20","3555","","10.1039/C9QO00951E","","","0.71073","MoKα","","0.1009","0.0506","","","0.0889","0.1005","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555142","9.2819","0.0008","23.5334","0.0017","10.2751","0.0007","90","","111.152","0.003","90","","2093.2","0.3","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C24 H21 N O3 S2 -","- C24 H21 N O3 S2 -","- C96 H84 N4 O12 S8 -","4","1","","Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo","Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones","Organic Chemistry Frontiers","2019","6","20","3555","","10.1039/C9QO00951E","","","0.71073","MoKα","","0.1492","0.0716","","","0.1659","0.1995","","","","","","1.017","","","","has coordinates","238346","2020-10-21","18:00:00",""
"1555143","8.2024","0.0004","10.5566","0.0005","11.0975","0.0005","68.8504","0.0013","79.7504","0.0014","71.2427","0.0014","846.51","0.07","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C20 H15 N O5 S -","- C20 H15 N O5 S -","- C40 H30 N2 O10 S2 -","2","1","","Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo","Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones","Organic Chemistry Frontiers","2019","6","20","3555","","10.1039/C9QO00951E","","","0.71073","MoKα","","0.043","0.0349","","","0.0879","0.092","","","","","","1.051","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555144","11.095","0.003","12.561","0.004","24.147","0.007","90","","93.088","0.009","90","","3360.3","1.7","296","2","296","2","","","","","","","","5","P 1 2/n 1","-P 2yac","13","","","","- C37 H30 N2 O3 S2 -","- C37 H30 N2 O3 S2 -","- C148 H120 N8 O12 S8 -","4","1","","Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo","Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones","Organic Chemistry Frontiers","2019","6","20","3555","","10.1039/C9QO00951E","","","0.71073","MoKα","","0.1246","0.0827","","","0.228","0.2418","","","","","","1.084","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555145","8.9049","0.0008","14.0612","0.0012","22.343","0.002","90","","93.263","0.003","90","","2793.1","0.4","273","2","273","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C31 H26 N2 O4 S2 -","- C31 H26 N2 O4 S2 -","- C124 H104 N8 O16 S8 -","4","1","","Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo","Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones","Organic Chemistry Frontiers","2019","6","20","3555","","10.1039/C9QO00951E","","","0.71073","MoKα","","0.2165","0.093","","","0.2271","0.2662","","","","","","1.055","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555146","18.289","0.001","13.2118","0.0008","24.2095","0.0013","90","","91.165","0.0019","90","","5848.5","0.6","296","2","296","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C35 H22 Cl2 N2 O3 S2 -","- C35 H22 Cl2 N2 O3 S2 -","- C280 H176 Cl16 N16 O24 S16 -","8","1","","Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo","Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones","Organic Chemistry Frontiers","2019","6","20","3555","","10.1039/C9QO00951E","","","0.71073","MoKα","","0.1565","0.0735","","","0.1527","0.1821","","","","","","1.025","","","","has coordinates","238346","2020-10-21","18:00:00",""
"1555147","7.6623","0.0005","10.2269","0.0007","19.008","0.0013","102.84","0.002","91.559","0.002","103.009","0.002","1410.29","0.17","273","2","273","2","","","","","","","","5","P -1","-P 1","2","","","","- C32 H28 N2 O4 S2 -","- C32 H28 N2 O4 S2 -","- C64 H56 N4 O8 S4 -","2","1","","Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo","Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones","Organic Chemistry Frontiers","2019","6","20","3555","","10.1039/C9QO00951E","","","0.71073","MoKα","","0.092","0.0706","","","0.178","0.1879","","","","","","1.042","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555150","20.6626","0.0008","10.3356","0.0004","13.6724","0.0005","90","","123.325","0.002","90","","2439.76","0.17","100","2","100","2","","","","","","","","5","C 1 2 1","C 2y","5","","","","- C25 H34.5 F3 N O1.25 -","- C25 H34 F3 N O4.25 -","- C100 H136 F12 N4 O17 -","4","1","","Sampaio-Dias, Ivo E.; Silva-Reis, Sara C.; Pinto da Silva, Luís; García-Mera, Xerardo; Maestro, Miguel A.; Rodríguez-Borges, José E.","Mechanistic insights for the transprotection of tertiary amines with Boc2O via charged carbamates: access to both enantiomers of 2-azanorbornane-3-exo-carboxylic acids","Organic Chemistry Frontiers","2019","6","20","3540","","10.1039/C9QO00957D","","","0.71073","MoKα","","0.0434","0.041","","","0.1123","0.1181","","","","","","1.083","","","","has coordinates","279649","2022-11-30","18:17:27",""
"1555152","33.942","0.004","11.5163","0.0011","9.4629","0.0009","90","","99.03","0.004","90","","3653.1","0.7","270","","270","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C20 H21 N O3 S -","- C20 H21 N O3 S -","- C160 H168 N8 O24 S8 -","8","1","","Cecchini, Chiara; Cera, Gianpiero; Lanzi, Matteo; Marchiò, Luciano; Malacria, Max; Maestri, Giovanni","Diastereoselective bicyclization of enynols via gold catalysis","Organic Chemistry Frontiers","2019","6","20","3584","","10.1039/C9QO00963A","","","0.71073","MoKα","","0.1147","0.0516","","","0.1011","0.1309","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555153","7.3872","0.0002","10.8747","0.0003","16.4977","0.0004","90","","90","","90","","1325.32","0.06","200","","200","","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C17 H16 O2 -","- C17 H16 O2 -","- C68 H64 O8 -","4","1","","Cecchini, Chiara; Cera, Gianpiero; Lanzi, Matteo; Marchiò, Luciano; Malacria, Max; Maestri, Giovanni","Diastereoselective bicyclization of enynols via gold catalysis","Organic Chemistry Frontiers","2019","6","20","3584","","10.1039/C9QO00963A","","","1.54184","CuKα","","0.0307","0.0306","","","0.0833","0.0835","","","","","","1.059","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555156","11.8298","0.0002","17.6502","0.0003","13.5929","0.0002","90","","90.058","0.001","90","","2838.17","0.08","298","2","298","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C30 H38 O7 -","- C30 H38 O7 -","- C120 H152 O28 -","4","1","","Feng, Ziwen; Yuan, Zhenbo; Zhao, Xiaobin; Huang, Yue; Yao, Hequan","A [4 + 1] annulation of ortho-electrophile-substituted para-quinone methides for the synthesis of indanes and isoindolines","Organic Chemistry Frontiers","2019","6","20","3535","","10.1039/C9QO00977A","","","1.54178","CuKα","","0.0809","0.0702","","","0.1876","0.2034","","","","","","1.068","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555157","11.2677","0.0001","10.9396","0.0001","24.121","0.0003","90","","93.117","0.001","90","","2968.86","0.05","298","2","298","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C31 H38 N2 O6 -","- C31 H38 N2 O6 -","- C124 H152 N8 O24 -","4","1","","Feng, Ziwen; Yuan, Zhenbo; Zhao, Xiaobin; Huang, Yue; Yao, Hequan","A [4 + 1] annulation of ortho-electrophile-substituted para-quinone methides for the synthesis of indanes and isoindolines","Organic Chemistry Frontiers","2019","6","20","3535","","10.1039/C9QO00977A","","","1.54178","CuKα","","0.0543","0.0487","","","0.1368","0.143","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555159","10.0737","0.0005","6.1334","0.00019","13.8766","0.0006","90","","107.776","0.005","90","","816.45","0.06","109.2","0.5","109.2","0.5","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C20 H19 N O5 -","- C20 H19 N O5 -","- C40 H38 N2 O10 -","2","1","","Sun, Zhaocui; Zhu, Nailiang; Zhou, Man; Huo, Xiaowei; Wu, Haifeng; Tian, Yu; Yang, Junshan; Ma, Guoxu; Yang, Yan-Long; Xu, Xudong","Clavipines A–C, antiproliferative meroterpenoids with a fused azepine skeleton from the basidiomycete Clitocybe clavipes","Organic Chemistry Frontiers","2019","6","22","3759","","10.1039/C9QO01005J","","x-ray","1.54184","CuKα","","0.0376","0.037","","","0.0938","0.0945","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555160","8.594","0.0003","11.8962","0.0008","13.1105","0.0005","90","","90","","90","","1340.36","0.11","109.65","0.1","109.65","0.1","","","","","","","Clitocybe Clavipes","3","P 21 21 21","P 2ac 2ab","19","clavilactone A","","","- C16 H14 O5 -","- C16 H14 O5 -","- C64 H56 O20 -","4","1","","Sun, Zhaocui; Zhu, Nailiang; Zhou, Man; Huo, Xiaowei; Wu, Haifeng; Tian, Yu; Yang, Junshan; Ma, Guoxu; Yang, Yan-Long; Xu, Xudong","Clavipines A‒C, antiproliferative meroterpenoids with a fused azepine skeleton from the basidiomycete Clitocybe clavipes","Organic Chemistry Frontiers","2019","6","22","3759","","10.1039/C9QO01005J","","x-ray","1.54184","CuKα","","0.0389","0.0384","","","0.0986","0.0991","","","","","","1.09","","","","has coordinates","238356","2020-10-21","18:00:00",""
"1555164","11.6812","0.0011","6.6839","0.001","13.6312","0.001","90","","90","","90","","1064.3","0.2","293","2","293","2","","","","","","","","5","P n m a","-P 2ac 2n","62","","","","- C11 H6 Cl2 O S -","- C11 H6 Cl2 O S -","- C44 H24 Cl8 O4 S4 -","4","0.5","","Wang, Ting; An, Zhenyu; Qi, Zhenjie; Zhuang, Daijiao; Chang, Aosheng; Yang, Yunxia; Yan, Rulong","Ring-opening/annulation reaction of cyclopropyl ethanols: concise access to thiophene aldehydes via C–S bond formation","Organic Chemistry Frontiers","2019","6","21","3705","","10.1039/C9QO01014A","","","0.71073","MoKα","","0.0773","0.0459","","","0.1039","0.1271","","","","","","1.053","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555166","9.5954","0.0004","12.6894","0.0004","11.2412","0.0004","90","","112.927","0.004","90","","1260.6","0.09","100","0.3","100","0.3","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C28 H24 Cl N3 O4 S -","- C28 H24 Cl N3 O4 S -","- C56 H48 Cl2 N6 O8 S2 -","2","1","","Zhang, Haoran; Li, Shiwu; Kang, Qiang; Du, Yu","Chiral-at-metal rhodium(iii) complex catalyzed enantioselective synthesis of C2-substituted benzofuran derivatives","Organic Chemistry Frontiers","2019","6","21","3683","","10.1039/C9QO01022J","","","1.54184","CuKα","","0.0477","0.0402","","","0.089","0.0936","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555168","10.8289","0.0002","10.4035","0.0002","17.1866","0.0003","90","","103.19","0.002","90","","1885.14","0.06","120","2","120","2","","","","","","","","5","C 1 c 1","C -2yc","9","","","","- C19 H18 N2 O6 Si -","- C19 H18 N2 O6 Si -","- C76 H72 N8 O24 Si4 -","4","1","","Vale, João R.; Valkonen, Arto; Afonso, Carlos A. M.; Candeias, Nuno R.","Synthesis of silacyclopent-2-en-4-ols via intramolecular [2 + 2] photocycloaddition of benzoyl(allyl)silanes","Organic Chemistry Frontiers","2019","6","22","3793","","10.1039/C9QO01028A","","","1.54184","CuKα","","0.0279","0.0274","","","0.0735","0.0741","","","","","","1.025","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555169","5.9864","0.0001","18.2027","0.0004","21.5323","0.0004","90","","90","","90","","2346.35","0.08","120","2","120","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C25 H22 N2 O6 Si -","- C25 H22 N2 O6 Si -","- C100 H88 N8 O24 Si4 -","4","1","","Vale, João R.; Valkonen, Arto; Afonso, Carlos A. M.; Candeias, Nuno R.","Synthesis of silacyclopent-2-en-4-ols via intramolecular [2 + 2] photocycloaddition of benzoyl(allyl)silanes","Organic Chemistry Frontiers","2019","6","22","3793","","10.1039/C9QO01028A","","","1.54184","CuKα","","0.0383","0.0344","","","0.0848","0.0875","","","","","","1.022","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555173","25.9119","0.0007","7.4654","0.0002","11.5725","0.0003","90","","107.999","0.001","90","","2129.06","0.1","100","2","100","2","","","","","","","","3","C 1 2 1","C 2y","5","","","","- C24 H32 O5 -","- C24 H32 O5 -","- C96 H128 O20 -","4","1","","Wang, Jia-Peng; Shu, Yan; Liu, Shi-Xi; Hu, Jun-Tao; Sun, Cheng-Tong; Zhou, Hao; Gan, Dong; Cai, Xue-Yun; Pu, Wei; Cai, Le; Ding, Zhong-Tao","Expanstines A–D: four unusual isoprenoid epoxycyclohexenones generated by Penicillium expansum YJ-15 fermentation and photopromotion","Organic Chemistry Frontiers","2019","6","23","3839","","10.1039/C9QO01076A","","","1.54178","CuKα","","0.053","0.0525","","","0.1389","0.1396","","","","","","1.06","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555174","12.7263","0.0005","18.5197","0.0007","24.0727","0.0009","90","","90","","90","","5673.6","0.4","100","2","100","2","","","","","","","Penicillium expansum YJ-15","3","P 21 21 21","P 2ac 2ab","19","","expanstine D","","- C22 H30.66667 O4.33333 -","- C22 H30.6667 O4.33333 -","- C264 H368 O52 -","12","3","","Wang, Jia-Peng; Shu, Yan; Liu, Shi-Xi; Hu, Jun-Tao; Sun, Cheng-Tong; Zhou, Hao; Gan, Dong; Cai, Xue-Yun; Pu, Wei; Cai, Le; Ding, Zhong-Tao","Expanstines A–D: four unusual isoprenoid epoxycyclohexenones generated by Penicillium expansum YJ-15 fermentation and photopromotion","Organic Chemistry Frontiers","2019","6","23","3839","","10.1039/C9QO01076A","","","1.54178","CuKα","","0.0494","0.0427","","","0.1223","0.1322","","","","","","0.987","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555176","20.3875","0.0007","20.3875","0.0007","7.4174","0.0003","90","","90","","120","","2669.99","0.17","100","2","100","2","","","","","","","Fungal Co-culture of Epicoccum sp. and Armillaria sp.","3","P 65","P 65","170","","Epicorpenoid A","","- C18 H26 O6 -","- C18 H26 O6 -","- C108 H156 O36 -","6","1","","Li, Hong-Tao; Tang, Linhuan; Liu, Tao; Yang, Ruining; Yang, Yabin; Zhou, Hao; Ding, Zhong-Tao","Polyoxygenated meroterpenoids and a bioactive illudalane derivative from a co-culture of Armillaria sp. and Epicoccum sp.","Organic Chemistry Frontiers","2019","6","23","3847","","10.1039/C9QO01087D","","","1.54178","CuKα","","0.0256","0.0254","","","0.0844","0.0852","","","","","","0.831","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555178","10.4723","0.0007","12.7127","0.0009","12.7391","0.0009","113.157","0.007","97.019","0.006","110.996","0.006","1385.7","0.2","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C34 H27.62 N2 O6 -","- C34 H26.08 N2 O6 -","- C68 H52.16 N4 O12 -","2","1","","Chen, Meng-Ting; Zhang, Yang; Vysotsky, Myroslav O.; Lindner, Joachim O.; Li, Meng-Hua; Lin, Mei-Jin; Würthner, Frank","1,1′-Bi(2-naphthol-4,5-dicarboximide)s: blue emissive axially chiral scaffolds with aggregation-enhanced emission properties","Organic Chemistry Frontiers","2019","6","22","3731","","10.1039/C9QO01090D","","x-ray","0.71073","MoKα","","0.1197","0.0784","","","0.2369","0.2764","","","","","","1.071","","","","has coordinates,has disorder","238371","2020-10-21","18:00:00",""
"1555179","12.287","0.0013","13.2979","0.0016","27.85","0.004","86.66","0.013","90","","90","","4542.7","1","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C51 H52 N2 O7 -","- C51 H52 N2 O7 -","- C204 H208 N8 O28 -","4","2","","Chen, Meng-Ting; Zhang, Yang; Vysotsky, Myroslav O.; Lindner, Joachim O.; Li, Meng-Hua; Lin, Mei-Jin; Würthner, Frank","1,1′-Bi(2-naphthol-4,5-dicarboximide)s: blue emissive axially chiral scaffolds with aggregation-enhanced emission properties","Organic Chemistry Frontiers","2019","6","22","3731","","10.1039/C9QO01090D","","","0.71073","MoKα","","0.2354","0.107","","","0.2667","0.349","","","","","","1.008","","","","has coordinates,has disorder","279649","2022-11-30","18:17:27",""
"1555180","32.9549","0.0008","12.7486","0.0002","24.5123","0.0006","90","","90","","90","","10298.3","0.4","100","0.1","100","0.1","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C32 H28 N2 O6 -","- C31.4775 H25.2 N2 O6 -","- C503.64 H403.2 N32 O96 -","16","4","","Chen, Meng-Ting; Zhang, Yang; Vysotsky, Myroslav O.; Lindner, Joachim O.; Li, Meng-Hua; Lin, Mei-Jin; Würthner, Frank","1,1′-Bi(2-naphthol-4,5-dicarboximide)s: blue emissive axially chiral scaffolds with aggregation-enhanced emission properties","Organic Chemistry Frontiers","2019","6","22","3731","","10.1039/C9QO01090D","","x-ray","1.54184","CuKα","","0.1779","0.1534","","","0.3425","0.3669","","","","","","1.351","","","","has coordinates,has disorder","279649","2022-11-30","18:17:27",""
"1555182","11.6007","0.0008","5.7368","0.0005","15.0074","0.001","90","","101.62","0.007","90","","978.29","0.13","293.8","0.4","293.8","0.4","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C25 H18 O5 -","- C25 H18 O5 -","- C50 H36 O10 -","2","1","","Zhang, Song; Yu, Xiaojun; Pan, Jianke; Jiang, Chunhui; Zhang, Hongsu; Wang, Tianli","Asymmetric synthesis of spiro-structural 2,3-dihydrobenzofurans via the bifunctional phosphonium salt-promoted [4 + 1] cyclization of ortho-quinone methides with α-bromoketones","Organic Chemistry Frontiers","2019","6","22","3799","","10.1039/C9QO01096C","","x-ray","1.54184","CuKα","","0.0635","0.0579","","","0.1605","0.1702","","","","","","1.039","","","","has coordinates","238373","2020-10-21","18:00:00",""
"1555184","11.4043","0.0011","9.8807","0.001","25.367","0.003","90","","93.04","0.003","90","","2854.4","0.5","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C16 H19 N O3 -","- C16 H19 N O3 -","- C128 H152 N8 O24 -","8","2","","Zhong, Jiaxin; He, Haibing; Gao, Shuanhu","Exploration of 1,3-dipolar cycloaddition reactions to construct the core skeleton of Calyciphylline A-type alkaloids","Organic Chemistry Frontiers","2019","6","22","3781","","10.1039/C9QO01111K","","","0.71073","MoKα","","0.1091","0.0465","","","0.0967","0.1238","","","","","","1.001","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555185","24.4812","0.0004","7.9863","0.0001","25.3899","0.0003","90","","103.221","0.001","90","","4832.51","0.12","100","0.1","100","0.1","","","","","","","","4","C 1 c 1","C -2yc","9","","","","- C26 H37 N O8 -","- C26 H37 N O8 -","- C208 H296 N8 O64 -","8","2","","Zhong, Jiaxin; He, Haibing; Gao, Shuanhu","Exploration of 1,3-dipolar cycloaddition reactions to construct the core skeleton of Calyciphylline A-type alkaloids","Organic Chemistry Frontiers","2019","6","22","3781","","10.1039/C9QO01111K","","x-ray","1.54184","CuKα","","0.0582","0.0577","","","0.1522","0.1526","","","","","","1.068","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555186","8.3885","0.0001","24.6653","0.0002","19.7148","0.0001","90","","97.294","0.001","90","","4046.08","0.06","100","0.1","100","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H29 N O5 -","- C22 H29 N O5 -","- C176 H232 N8 O40 -","8","2","","Zhong, Jiaxin; He, Haibing; Gao, Shuanhu","Exploration of 1,3-dipolar cycloaddition reactions to construct the core skeleton of Calyciphylline A-type alkaloids","Organic Chemistry Frontiers","2019","6","22","3781","","10.1039/C9QO01111K","","x-ray","1.54184","CuKα","","0.0458","0.0435","","","0.1068","0.1084","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555189","11.1372","0.0011","8.2426","0.0008","12.2345","0.0012","90","","110.187","0.001","90","","1054.13","0.18","296.15","","296.15","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C25 H23 N O3 S -","- C25 H23 N O3 S -","- C50 H46 N2 O6 S2 -","2","1","","Chen, Ying-Han; Lv, Xue-Jiao; You, Zhi-Hao; Liu, Yan-Kai","Asymmetric organocatalyzed reaction sequence of 2-hydroxy cinnamaldehydes and acyclic N-sulfonyl ketimines to construct diverse chiral bridged polycyclic aminals","Organic Chemistry Frontiers","2019","6","22","3725","","10.1039/C9QO01116A","","","0.71073","MoKα","","0.0434","0.0336","","","0.0807","0.086","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555190","26.476","0.004","9.6581","0.0015","9.1391","0.0014","90","","98.974","0.003","90","","2308.3","0.6","296.15","","296.15","","","","","","","","","5","C 1 2 1","C 2y","5","","","","- C25 H25 N O4 S -","- C25 H25 N O4 S -","- C100 H100 N4 O16 S4 -","4","1","","Chen, Ying-Han; Lv, Xue-Jiao; You, Zhi-Hao; Liu, Yan-Kai","Asymmetric organocatalyzed reaction sequence of 2-hydroxy cinnamaldehydes and acyclic N-sulfonyl ketimines to construct diverse chiral bridged polycyclic aminals","Organic Chemistry Frontiers","2019","6","22","3725","","10.1039/C9QO01116A","","","0.71073","MoKα","","0.0634","0.0416","","","0.0848","0.095","","","","","","1.017","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555191","8.784","0.003","9.976","0.003","12.349","0.004","90","","90.656","0.005","90","","1082.1","0.6","296.15","","296.15","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C25 H23 N O3 S -","- C25 H23 N O3 S -","- C50 H46 N2 O6 S2 -","2","1","","Chen, Ying-Han; Lv, Xue-Jiao; You, Zhi-Hao; Liu, Yan-Kai","Asymmetric organocatalyzed reaction sequence of 2-hydroxy cinnamaldehydes and acyclic N-sulfonyl ketimines to construct diverse chiral bridged polycyclic aminals","Organic Chemistry Frontiers","2019","6","22","3725","","10.1039/C9QO01116A","","","0.71073","MoKα","","0.0609","0.0472","","","0.1244","0.1376","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555193","13.65","0.003","9.7451","0.0019","19.194","0.004","90","","105.2","0.03","90","","2463.9","1","293","2","293","2","","","","","","","Synthetic","5","P 1 21/c 1","-P 2ybc","14","","7-(2H-Indazol-2-yl)-11-tosyl-6a,11a-dihydro-11H-benzo[a]carbazole","","- C30 H23 N3 O2 S -","- C30 H23 N3 O2 S -","- C120 H92 N12 O8 S4 -","4","1","","Vivek Kumar, Sundaravel; Banerjee, Sonbidya; Punniyamurthy, Tharmalingam","Rh-Catalyzed C–C/C–N bond formation via C–H activation: synthesis of 2H-indazol-2-yl-benzo[a]carbazoles","Organic Chemistry Frontiers","2019","6","23","3885","","10.1039/C9QO01120J","","","0.71073","MoKα","","0.0793","0.053","","","0.1282","0.1483","","","","","","1.023","","","","has coordinates,has disorder","301780","2025-08-18","21:43:32",""
"1555195","9.8054","0.0005","11.1916","0.0005","13.8588","0.0006","102.001","0.002","100.882","0.001","107.337","0.001","1367.85","0.11","296","2","296.15","","","","","","","","","5","P -1","-P 1","2","","","","- C31 H29 N3 O3 S -","- C31 H29 N3 O3 S -","- C62 H58 N6 O6 S2 -","2","1","","Wang, Fei; Xu, Pei; Liu, Bei-Bei; Wang, Shun-Yi; Ji, Shun-Jun","Pd-Catalyzed multicomponent reaction of sulfonyl azides, primary amines and methyl α-isocyanoacetates: highly efficient synthesis of tetrasubstituted imidazolone derivatives","Organic Chemistry Frontiers","2019","6","22","3754","","10.1039/C9QO01122F","","","0.71073","MoKα","","0.1029","0.0647","","","0.1392","0.1555","","","","","","1.039","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555198","8.4028","0.0002","8.4685","0.0002","18.8231","0.0005","90","","91.121","0.002","90","","1339.18","0.06","100","2","100.01","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H14 N2 O2 -","- C17 H14 N2 O2 -","- C68 H56 N8 O8 -","4","1","","Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit","Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part","Organic Chemistry Frontiers","2019","6","21","3649","","10.1039/C9QO01134J","","","0.71073","MoKα","","0.0432","0.0365","","","0.0881","0.0926","","","","","","1.03","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555199","28.7181","0.0008","16.094","0.0004","7.4702","0.0002","90","","90","","90","","3452.65","0.16","100","2","99.98","","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C23 H18 N2 O2 -","- C23 H18 N2 O2 -","- C184 H144 N16 O16 -","8","2","","Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit","Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part","Organic Chemistry Frontiers","2019","6","21","3649","","10.1039/C9QO01134J","","","0.71073","MoKα","","0.0623","0.047","","","0.0946","0.1004","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555200","8.899","0.008","16.027","0.013","21.774","0.019","90","","90","","90","","3106","5","100","2","100.01","","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C21 H16 N2 O2 -","- C21 H16 N2 O2 -","- C168 H128 N16 O16 -","8","1","","Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit","Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part","Organic Chemistry Frontiers","2019","6","21","3649","","10.1039/C9QO01134J","","x-ray","0.71073","MoKα","","0.1027","0.0676","","","0.1251","0.1376","","","","","","1.104","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555201","14.7127","0.0013","13.2097","0.0016","27.114","0.003","90","","97.327","0.009","90","","5226.6","1","100","","100.01","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C35 H24 N4 O3 -","- C35 H24 N4 O3 -","- C280 H192 N32 O24 -","8","2","","Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit","Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part","Organic Chemistry Frontiers","2019","6","21","3649","","10.1039/C9QO01134J","","x-ray","0.71073","MoKα","","0.092","0.0563","","","0.1316","0.1489","","","","","","1.061","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555202","16.535","0.0007","8.4288","0.0004","22.1228","0.0009","90","","90","","90","","3083.3","0.2","100","","100.16","","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C21 H16 N2 O2 -","- C21 H16 N2 O2 -","- C168 H128 N16 O16 -","8","1","","Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit","Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part","Organic Chemistry Frontiers","2019","6","21","3649","","10.1039/C9QO01134J","","x-ray","0.71073","MoKα","","0.0729","0.0557","","","0.1381","0.1519","","","","","","1.061","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555203","8.36","0.005","9.772","0.004","13.225","0.006","79.646","0.011","71.931","0.019","81.249","0.016","1005","0.9","100","2","99.96","","","","","","","","","4","P -1","-P 1","2","","","","- C28 H19 N3 O2 -","- C28 H19 N3 O2 -","- C56 H38 N6 O4 -","2","1","","Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit","Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part","Organic Chemistry Frontiers","2019","6","21","3649","","10.1039/C9QO01134J","","x-ray","0.71073","MoKα","","0.0594","0.0511","","","0.1406","0.1468","","","","","","1.071","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555204","14.667","0.004","9.231","0.003","15.139","0.004","90","","107.187","0.008","90","","1958.2","1","100","","100.03","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C23 H16 Br2 N2 O2 -","- C23 H16 Br2 N2 O2 -","- C92 H64 Br8 N8 O8 -","4","1","","Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit","Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part","Organic Chemistry Frontiers","2019","6","21","3649","","10.1039/C9QO01134J","","x-ray","0.71073","MoKα","","0.0254","0.0212","","","0.0497","0.051","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555205","18.714","0.003","15.974","0.003","12.0964","0.0018","90","","90","","90","","3616.1","1","100","2","99.99","","","","","","","","","4","P b c n","-P 2n 2ab","60","","","","- C25 H18 N2 O2 -","- C25 H18 N2 O2 -","- C200 H144 N16 O16 -","8","1","","Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit","Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part","Organic Chemistry Frontiers","2019","6","21","3649","","10.1039/C9QO01134J","","x-ray","0.71073","MoKα","","0.0605","0.0423","","","0.0983","0.109","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555209","28.8585","0.0006","28.8585","0.0006","37.617","0.0004","90","","90","","120","","27130.8","0.8","100","2","100","","","","","","","","","4","P 62 2 2","P 62 2 (0 0 4)","180","","","","- C44.4 H38.4 N1.2 S1.8 -","- C44.4 H38.4 N1.2 S1.8 -","- C888 H768 N24 S36 -","20","1.66667","","Ghosh, Arindam; Dash, Syamasrit; Srinivasan, A.; Suresh, C. H.; Peruncheralathan, S.; Chandrashekar, Tavarekere K.","Core-modified 48π and 42π decaphyrins: syntheses, properties and structures","Organic Chemistry Frontiers","2019","6","22","3746","","10.1039/C9QO01162E","","","1.54184","CuKα","","0.0697","0.0421","","","0.0947","0.1041","","","","","","0.828","","","","has coordinates","238390","2020-10-21","18:00:00",""
"1555210","8.69725","0.00017","10.9283","0.0002","20.5323","0.0005","84.0758","0.0017","88.6243","0.0018","67.6514","0.0018","1795.05","0.07","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C42 H34 N4 S3 -","- C42 H34 N4 S3 -","- C84 H68 N8 S6 -","2","1","","Ghosh, Arindam; Dash, Syamasrit; Srinivasan, A.; Suresh, C. H.; Peruncheralathan, S.; Chandrashekar, Tavarekere K.","Core-modified 48π and 42π decaphyrins: syntheses, properties and structures","Organic Chemistry Frontiers","2019","6","22","3746","","10.1039/C9QO01162E","","x-ray","1.54184","CuKα","","0.0852","0.0779","","","0.2323","0.2367","","","","","","1.092","","","","has coordinates","300101","2025-06-17","17:58:11",""
"1555212","10.0558","0.0007","10.1395","0.0005","18.5575","0.001","90","","98.819","0.006","90","","1869.77","0.19","292.9","0.1","292.9","0.1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C24 H24 O3 -","- C24 H24 O3 -","- C96 H96 O12 -","4","1","","Jiao, Meng-Jie; Liu, Dan; Hu, Xiu-Qin; Xu, Peng-Fei","Photocatalytic decarboxylative [2 + 2 + 1] annulation of 1,6-enynes with N-hydroxyphthalimide esters for the synthesis of indene-containing polycyclic compounds","Organic Chemistry Frontiers","2019","6","23","3834","","10.1039/C9QO01166H","","x-ray","0.71073","MoKα","","0.1486","0.1088","","","0.2683","0.3231","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555215","9.2204","0.0018","24.665","0.005","11.584","0.002","90","","105.11","0.03","90","","2543.4","0.9","113","2","113.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C26 H22 Br F3 N4 O4 -","- C26 H22 Br F3 N4 O4 -","- C104 H88 Br4 F12 N16 O16 -","4","1","","Zhao, Hong-Wu; Guo, Jia-Ming; Wang, Li-Ru; Ding, Wan-Qiu; Tang, Zhe; Song, Xiu-Qing; Wu, Hui-Hui; Fan, Xiao-Zu; Bi, Xiao-Fan","Diastereoselective formal [3 + 3] cycloaddition of isatin-based α-(trifluoromethyl)imines with N,N′-dialkyloxyureas","Organic Chemistry Frontiers","2019","6","23","3891","","10.1039/C9QO01181A","","","0.71073","MoKα","","0.0779","0.0556","","","0.1249","0.137","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:32",""
"1555217","12.15","0.002","12.226","0.0015","26.113","0.004","99.044","0.006","97.039","0.018","99.079","0.011","3739.3","1","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C63.25 H86 Na5 O29.95 S5 -","- C63.25 H86 Na5 O29.95 S5 -","- C126.5 H172 Na10 O59.9 S10 -","2","1","","Pisagatti, Ilenia; Barbera, Lucia; Gattuso, Giuseppe; Parisi, Melchiorre F.; Geremia, Silvano; Hickey, Neal; Notti, Anna","Guest-length driven high fidelity self-sorting in supramolecular capsule formation of calix[5]arenes in water","Organic Chemistry Frontiers","2019","6","22","3804","","10.1039/C9QO01188A","","x-ray","0.7","Synchrotron","","0.1558","0.1449","","","0.37","0.3778","","","","","","1.036","","","","has coordinates,has disorder","238397","2020-10-21","18:00:00",""
"1556394","5.8858","0.0003","9.0384","0.0004","23.4473","0.0011","91.943","0.002","92.404","0.001","99.656","0.002","1227.54","0.1","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C25 H23 Br2 N O4 -","- C25 H23 Br2 N O4 -","- C50 H46 Br4 N2 O8 -","2","1","","Xu, Xinfang; Guo, Xin; Han, Xingchun; Yang, Liping; Hu, Wenhao","Highly diasteroselective intermolecular 1,3-dipolar cycloaddition reactions of carbonyl ylides with aldimines to afford sterically disfavored cis-oxazolidines","Organic Chemistry Frontiers","2014","1","2","181","","10.1039/c3qo00040k","","","0.71073","MoKα","","0.0711","0.051","","","0.1304","0.1452","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:35",""
"1556395","17.548","0.004","24.274","0.005","14.468","0.003","90","","90","","90","","6163","2","173","2","173","2","","","","","","","","3","P c c n","-P 2ab 2ac","56","","","","- C74 H72 O12 -","- C74 H72 O12 -","- C296 H288 O48 -","4","0.5","","Xia, Yu-Xiang; Xie, Tao; Han, Ying; Chen, Chuan-Feng","Triptycene-derived calix[6]arene analogues: synthesis, structure and complexation with paraquat derivatives","Organic Chemistry Frontiers","2014","1","2","140","","10.1039/c3qo00055a","","","0.71073","MoKα","","0.1395","0.1251","","","0.3265","0.3503","","","","","","1.336","","","","has coordinates,has disorder","244433","2020-10-21","18:00:00",""
"1556396","11.466","0.002","11.708","0.002","13.256","0.003","69.828","0.009","73.892","0.009","72.609","0.009","1563.5","0.5","173","2","173","2","","","","","","","","4","P -1","-P 1","2","","","","- C68 H62 Cl6 O8 -","- C68 H62 Cl6 O8 -","- C68 H62 Cl6 O8 -","1","0.5","","Xia, Yu-Xiang; Xie, Tao; Han, Ying; Chen, Chuan-Feng","Triptycene-derived calix[6]arene analogues: synthesis, structure and complexation with paraquat derivatives","Organic Chemistry Frontiers","2014","1","2","140","","10.1039/c3qo00055a","","","0.71073","MoKα","","0.0925","0.0849","","","0.2311","0.2403","","","","","","1.028","","","","has coordinates,has disorder","301780","2025-08-18","21:43:35",""
"1556397","11.429","0.002","11.955","0.002","12.714","0.003","72.18","0.03","70.44","0.03","70.84","0.03","1508.2","0.6","173","2","173","2","","","","","","","","3","P -1","-P 1","2","","","","- C66 H60 O10 -","- C66 H60 O10 -","- C66 H60 O10 -","1","0.5","","Xia, Yu-Xiang; Xie, Tao; Han, Ying; Chen, Chuan-Feng","Triptycene-derived calix[6]arene analogues: synthesis, structure and complexation with paraquat derivatives","Organic Chemistry Frontiers","2014","1","2","140","","10.1039/c3qo00055a","","","0.71073","MoKα","","0.1111","0.0974","","","0.2766","0.2907","","","","","","1.099","","","","has coordinates","301780","2025-08-18","21:43:35",""
"1556398","11.493","0.002","11.851","0.002","12.708","0.003","71.48","0.03","71.12","0.03","72.93","0.03","1517.4","0.6","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C66 H58 Br2 Cl4 O8 -","- C66 H58 Br2 Cl4 O8 -","- C66 H58 Br2 Cl4 O8 -","1","0.5","","Xia, Yu-Xiang; Xie, Tao; Han, Ying; Chen, Chuan-Feng","Triptycene-derived calix[6]arene analogues: synthesis, structure and complexation with paraquat derivatives","Organic Chemistry Frontiers","2014","1","2","140","","10.1039/c3qo00055a","","","0.71073","MoKα","","0.11","0.092","","","0.2566","0.2809","","","","","","1.138","","","","has coordinates,has disorder","301780","2025-08-18","21:43:35",""
"1556399","21.999","0.004","19.134","0.004","33.115","0.007","90","","98.09","0.03","90","","13800","5","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C67 H57 Cl15 O8 -","- C67 H57 Cl15 O8 -","- C536 H456 Cl120 O64 -","8","2","","Xia, Yu-Xiang; Xie, Tao; Han, Ying; Chen, Chuan-Feng","Triptycene-derived calix[6]arene analogues: synthesis, structure and complexation with paraquat derivatives","Organic Chemistry Frontiers","2014","1","2","140","","10.1039/c3qo00055a","","","0.71073","MoKα","","0.1855","0.1658","","","0.3414","0.3536","","","","","","1.303","","","","has coordinates","301780","2025-08-18","21:43:35",""
"1556400","6.427","0.0007","24.105","0.002","8.3807","0.0008","90","","98.77","0.008","90","","1283.2","0.2","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C10 H18 O2 Si -","- C10 H18 O2 Si -","- C40 H72 O8 Si4 -","4","1","","Zhang, Xiaobing; Qiu, Youai; Fu, Chunling; Ma, Shengming","Highly selective 4-alkynoic acids synthesis via iron-mediated complete inversion of stereogenic carbon centers","Organic Chemistry Frontiers","2014","1","3","247","","10.1039/c3qo00066d","","","0.71073","MoKα","","0.1246","0.1016","","","0.2706","0.2869","","","","","","1.098","","","","has coordinates,has disorder","301780","2025-08-18","21:43:35",""