# Search results of SQL query from the Crystallography Open Database
# Date and time performed: 2026-01-11T11:29:17+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 volume = 2 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
"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",""
"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",""