# Search results of SQL query from the Crystallography Open Database
# Date and time performed: 2024-06-18T05:38:02+02:00
# 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 'Green Chemistry') 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
"1519680","25.848","0.002","11.2564","0.0005","20.6909","0.0016","90","","122.413","0.011","90","","5082.2","0.9","297","14","297","14","","","","","","","","8","C 1 2/c 1","-C 2yc","15","","3","","- C49 H42 Au2 Cl2 N2 O4 P4 S2 -","- C49 H42 Au2 Cl2 N2 O4 P4 S2 -","- C196 H168 Au8 Cl8 N8 O16 P16 S8 -","4","0.5","","Vidal, C.; Merz, L.; García-Álvarez, J.","Deep eutectic solvents: biorenewable reaction media for Au( <scp>i</scp> )-catalysed cycloisomerisations and one-pot tandem cycloisomerisation/Diels–Alder reactions","Green Chemistry","2015","17","7","3870","3878","10.1039/C5GC00656B","","","1.5418","CuKα","","0.0497","0.0428","","","0.1171","0.1241","","","","","","1.129","","","","has coordinates","282777","2023-04-20","11:56:43",""
"1550815","5.7205","0.0001","19.9636","0.0003","21.5679","0.0003","90","","90","","90","","2463.09","0.07","120.3","0.8","120.3","0.8","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C30 H30 N2 O2 S -","- C30 H30 N2 O2 S -","- C120 H120 N8 O8 S4 -","4","1","","Yao, Wei-Wei; Li, Ran; Li, Jiang-Fei; Sun, Juan; Ye, Mengchun","NHC ligand-enabled Ni-catalyzed reductive coupling of alkynes and imines using isopropanol as a reductant","Green Chemistry","2019","21","9","2240","","10.1039/C9GC00653B","","x-ray","1.54184","CuKα","","0.0492","0.0466","","","0.1137","0.115","","","","","","1.032","","","","has coordinates,has disorder","224626","2020-10-21","18:00:00",""
"1550819","7.5364","0.0003","20.5621","0.0011","11.4782","0.0005","90","","94.877","0.004","90","","1772.27","0.14","295.3","0.4","295.3","0.4","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H19 N O4 -","- C21 H19 N O4 -","- C84 H76 N4 O16 -","4","1","","Li, Qing-Zhu; Zhang, Xiang; Xie, Ke; Dai, Qing-Song; Zeng, Rong; Liu, Yan-Qing; Jia, Zhi-Qiang; Feng, Xin; Li, Jun-Long","Diastereodivergent synthesis of cyclopropanes via on-water [2 + 1] annulations of diazo compounds with electron-deficient alkenes","Green Chemistry","2019","21","9","2375","","10.1039/C9GC00278B","","x-ray","1.54184","CuKα","","0.0739","0.0568","","","0.1572","0.1776","","","","","","1.025","","","","has coordinates,has disorder","224625","2020-10-21","18:00:00",""
"1550820","13.6825","0.001","10.7919","0.0005","14.7575","0.0012","90","","108.476","0.008","90","","2066.8","0.3","293.06","0.1","293.06","0.1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C24 H19 N3 O3 -","- C24 H19 N3 O3 -","- C96 H76 N12 O12 -","4","1","","Li, Qing-Zhu; Zhang, Xiang; Xie, Ke; Dai, Qing-Song; Zeng, Rong; Liu, Yan-Qing; Jia, Zhi-Qiang; Feng, Xin; Li, Jun-Long","Diastereodivergent synthesis of cyclopropanes via on-water [2 + 1] annulations of diazo compounds with electron-deficient alkenes","Green Chemistry","2019","21","9","2375","","10.1039/C9GC00278B","","x-ray","1.54184","CuKα","","0.0817","0.0709","","","0.1951","0.215","","","","","","1.034","","","","has coordinates","224625","2020-10-21","18:00:00",""
"7200176","9.896","0.002","10.256","0.002","11.128","0.002","89.64","0.03","73.71","0.03","82.42","0.03","1074","0.4","293","2","293","2","","","","","","","","7","P -1","-P 1","2","","","","- C22 H13 Cl2 F N2 O S2 -","- C22 H13 Cl2 F N2 O S2 -","- C44 H26 Cl4 F2 N4 O2 S4 -","2","1","","Jian, Fangfang; Zheng, Jian; Li, Yufeng; Wang, Jing","Novel ((3Z,5Z)-3,5-bis(phenylimino)-1,2-dithiolan-4-yl) and 3H-[1,2]dithiolo[3,4-b]quinolin-4(9H)-one heterocycles: an effective and facile green route","Green Chemistry","2009","11","2","215","","10.1039/b808949c","","","0.71073","MoKα","","0.0736","0.0482","","","0.1297","0.1461","","","","","","1.034","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7200177","6.3729","0.0013","12.941","0.003","13.413","0.003","108.64","0.03","96.27","0.03","96.96","0.03","1027.5","0.5","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C23 H17 Br N2 O S2 -","- C23 H17 Br N2 O S2 -","- C46 H34 Br2 N4 O2 S4 -","2","1","","Jian, Fangfang; Zheng, Jian; Li, Yufeng; Wang, Jing","Novel ((3Z,5Z)-3,5-bis(phenylimino)-1,2-dithiolan-4-yl) and 3H-[1,2]dithiolo[3,4-b]quinolin-4(9H)-one heterocycles: an effective and facile green route","Green Chemistry","2009","11","2","215","","10.1039/b808949c","","","0.71073","MoKα","","0.1315","0.0945","","","0.2769","0.3118","","","","","","1.042","","","","has coordinates,has disorder","180332","2020-10-21","18:00:00",""
"7200178","11.497","0.002","7.537","0.0015","22.384","0.005","90","","103.64","0.03","90","","1884.9","0.7","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C22 H13 Cl N2 O S2 -","- C22 H13 Cl N2 O S2 -","- C88 H52 Cl4 N8 O4 S8 -","4","1","","Jian, Fangfang; Zheng, Jian; Li, Yufeng; Wang, Jing","Novel ((3Z,5Z)-3,5-bis(phenylimino)-1,2-dithiolan-4-yl) and 3H-[1,2]dithiolo[3,4-b]quinolin-4(9H)-one heterocycles: an effective and facile green route","Green Chemistry","2009","11","2","215","","10.1039/b808949c","","","0.71073","MoKα","","0.1159","0.0536","","","0.1404","0.17","","","","","","1.013","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7200179","10.084","0.002","10.331","0.002","10.414","0.002","87.6","0.03","85.58","0.03","78.1","0.03","1058.1","0.4","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C22 H14 Cl2 N2 O S2 -","- C22 H14 Cl2 N2 O S2 -","- C44 H28 Cl4 N4 O2 S4 -","2","1","","Jian, Fangfang; Zheng, Jian; Li, Yufeng; Wang, Jing","Novel ((3Z,5Z)-3,5-bis(phenylimino)-1,2-dithiolan-4-yl) and 3H-[1,2]dithiolo[3,4-b]quinolin-4(9H)-one heterocycles: an effective and facile green route","Green Chemistry","2009","11","2","215","","10.1039/b808949c","","","0.71073","MoKα","","0.1616","0.0668","","","0.1577","0.2053","","","","","","0.965","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7200280","17.1392","0.0005","6.0512","0.0002","10.9857","0.0004","90","","93.007","0.002","90","","1137.79","0.07","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C11 H13 N O3 S -","- C11 H13 N O3 S -","- C44 H52 N4 O12 S4 -","4","1","","Hota, Sandip K.; Chatterjee, Amrita; Bhattacharya, Pranab K.; Chattopadhyay, Partha","A green chemical approach for the N-alkylation of aldoximes to form nitrones in organized aqueous media and their in situ cycloaddition with olefins","Green Chemistry","2009","11","2","169","","10.1039/b812290c","","","0.71073","MoKα","","0.0681","0.0456","","","0.15","0.1748","","","","","","1.241","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7200610","8.77","0.008","9.766","0.009","14.282","0.012","90","","95.363","0.012","90","","1217.9","1.9","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C8 H12 F4 N2 O3 S -","- C8 H12 F4 N2 O3 S -","- C32 H48 F16 N8 O12 S4 -","4","1","","Harmer, Mark A.; Junk, Christopher P.; Rostovtsev, Vsevolod V.; Marshall, William J.; Grieco, Liane M.; Vickery, Jemma; Miller, Robert; Work, Stella","Catalytic reactions using superacids in new types of ionic liquids","Green Chemistry","2009","11","4","517","","10.1039/b818788f","","","0.71073","MoKα","","0.0489","0.0417","","","0.1166","0.1231","","","","","","1.078","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7200611","9.178","0.004","34.444","0.013","10.022","0.004","90","","91.711","0.007","90","","3167","2","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C10 H11 F9 N2 O3 S -","- C10 H11 F9 N2 O3 S -","- C80 H88 F72 N16 O24 S8 -","8","2","","Harmer, Mark A.; Junk, Christopher P.; Rostovtsev, Vsevolod V.; Marshall, William J.; Grieco, Liane M.; Vickery, Jemma; Miller, Robert; Work, Stella","Catalytic reactions using superacids in new types of ionic liquids","Green Chemistry","2009","11","4","517","","10.1039/b818788f","","","0.71073","MoKα","","0.1705","0.0916","","","0.2183","0.258","","","","","","1.07","","","","has coordinates","180337","2020-10-21","18:00:00",""
"7201002","8.655","0.002","9.619","0.003","10.727","0.003","83.143","0.005","72.938","0.004","64.907","0.004","773.2","0.4","296","2","296","2","","","","","","","","5","P -1","-P 1","2","oxazinoquinoline","","","- C19 H13 N O2 S2 -","- C19 H13 N O2 S2 -","- C38 H26 N2 O4 S4 -","2","1","","Saha, Pritam; Naskar, Subhendu; Paira, Priyankar; Hazra, Abhijit; Sahu, Krishnendu B.; Paira, Rupankar; Banerjee, Sukdeb; Mondal, Nirup B.","Basic alumina-supported highly effective Suzuki‒Miyaura cross-coupling reaction under microwave irradiation: application to fused tricyclic oxa-aza-quinolones","Green Chemistry","2009","11","7","931","","10.1039/b902916h","","","0.71073","MoKα","","0.0676","0.0481","","","0.1288","0.1416","","","","","","1.085","","","","has coordinates,has disorder","180341","2020-10-21","18:00:00",""
"7201048","11.3034","0.0011","13.2485","0.0013","8.9142","0.0009","90","","97.277","0.002","90","","1324.2","0.2","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","N-Benzyl-1H-indole-1-carboxamide","N-Benzyl-1H-indole-1-carboxamide","","- C16 H14 N2 O -","- C16 H14 N2 O -","- C64 H56 N8 O4 -","4","1","","Ye, Deju; Wang, Jinfang; Zhang, Xu; Zhou, Yu; Ding, Xiao; Feng, Enguang; Sun, Haifeng; Liu, Guannan; Jiang, Hualiang; Liu, Hong","Gold-catalyzed intramolecular hydroamination of terminal alkynes in aqueous media: efficient and regioselective synthesis of indole-1-carboxamides","Green Chemistry","2009","11","8","1201","","10.1039/b904044g","","","0.71073","MoKα","","0.1036","0.0538","","","0.1006","0.1181","","","","","","0.878","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7201240","7.3084","0.0015","10.576","0.002","8.5363","0.0017","90","","102.7","0.03","90","","643.7","0.2","150","0.2","150","0.2","","","","","","","","5","P 1 21/m 1","-P 2yb","11","N/A","","","- C11 H17 Cl2 N Ti -","- C11 H18 Cl2 N Ti -","- C22 H36 Cl4 N2 Ti2 -","2","0.5","","Fletcher, Andrew E.D.; Hyatt, Jonathan D.; Ok, Kang Min; O'Hare, Dermot","Catalytic dechlorination of polychlorinated biphenyls (PCBs) using amine functionalised titanocenes","Green Chemistry","2009","11","9","1343","","10.1039/b906311k","","","0.71073","MoKα","","0.0477","0.0393","","","0.0975","0.1042","","","","","","1.074","","","","has coordinates,has disorder","180343","2020-10-21","18:00:00",""
"7201469","6.985","0.0006","7.315","0.0006","16.94","0.0016","80.825","0.004","81.027","0.004","63.636","0.005","762.05","0.12","150","2","150","2","","","","","","","synthesis","6","P -1","-P 1","2","","","","- C11 H19 Cl2 O5 P Ru -","- C11 H19 Cl2 O5 P Ru -","- C22 H38 Cl4 O10 P2 Ru2 -","2","1","","Lastra-Barreira, Beatriz; Díez, Josefina; Crochet, Pascale","Highly water-soluble arene-ruthenium(ii) complexes: application to catalytic isomerization of allylic alcohols in aqueous medium","Green Chemistry","2009","11","10","1681","","10.1039/b914789f","","","0.71073","MoKα","","0.046","0.0364","","","0.0948","0.0991","","","","","","0.996","","","","has coordinates","180345","2020-10-21","18:00:00",""
"7201470","7.6034","0.0001","14.0769","0.0002","18.318","0.0003","90","","109.371","0.001","90","","1849.63","0.05","150","2","150","2","","","","","","","synthesis","6","P 1 21/c 1","-P 2ybc","14","","","","- C14 H25 Cl2 O5 P Ru -","- C14 H25 Cl2 O5 P Ru -","- C56 H100 Cl8 O20 P4 Ru4 -","4","1","","Lastra-Barreira, Beatriz; Díez, Josefina; Crochet, Pascale","Highly water-soluble arene-ruthenium(ii) complexes: application to catalytic isomerization of allylic alcohols in aqueous medium","Green Chemistry","2009","11","10","1681","","10.1039/b914789f","","","0.71073","MoKα","","0.0381","0.0308","","","0.0871","0.1175","","","","","","1.318","","","","has coordinates","180345","2020-10-21","18:00:00",""
"7201477","8.133","0.0002","10.9315","0.0003","11.3491","0.0004","111.001","0.001","103.328","0.002","103.603","0.003","858.68","0.05","293","2","293","2","","","","","","","synthesis as described","6","P -1","-P 1","2","","","","- C18 H16 F N O2 S2 -","- C18 H16 F N O2 S2 -","- C36 H32 F2 N2 O4 S4 -","2","1","","Cohen, Anita; Crozet, Maxime D.; Rathelot, Pascal; Vanelle, Patrice","An efficient aqueous microwave-assisted Suzuki‒Miyaura cross-coupling reaction in the thiazole series","Green Chemistry","2009","11","11","1736","","10.1039/b916123f","","x-ray","0.71073","MoKα","","0.1008","0.0772","","","0.2084","0.2201","","","","","","1.098","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7201484","7.6593","0.0007","12.5747","0.0011","20.4376","0.0018","90","","90","","90","","1968.4","0.3","293","2","293","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C15 H31 F3 N2 O3 S -","- C15 H31 F3 N2 O3 S -","- C60 H124 F12 N8 O12 S4 -","4","1","","Lin, Jin-Hong; Zhang, Cheng-Pan; Xiao, Ji-Chang","Enantioselective aldol reaction of cyclic ketones with aryl aldehydes catalyzed by a cyclohexanediamine derived salt in the presence of water","Green Chemistry","2009","11","11","1750","","10.1039/b916583e","","","0.71073","MoKα","","0.0521","0.0451","","","0.1018","0.1048","","","","","","0.986","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7201610","13.748","0.002","7.701","0.001","13.781","0.002","90","","110.97","0.01","90","","1362.4","0.3","120","2","120","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","N,N-Diisopropyl-3-fluorobenzylamine-2-boronic acid","N,N-Diisopropyl-3-fluorobenzylamine-2-boronic acid","","- C13 H21 B F N O2 -","- C13 H21 B F N O2 -","- C52 H84 B4 F4 N4 O8 -","4","1","","Arnold, Kenny; Batsanov, Andrei S.; Davies, Bryan; Whiting, Andrew","Synthesis, evaluation and application of novel bifunctional N,N-di-isopropylbenzylamineboronic acid catalysts for direct amide formation between carboxylic acids and amines","Green Chemistry","2008","10","1","124","","10.1039/b712008g","","","0.71073","MoKα","","0.0436","0.0374","","","0.1019","0.107","","","","","","1.033","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7201611","15.4653","0.0018","7.7851","0.0009","13.2548","0.0015","90","","105.71","0.01","90","","1536.2","0.3","120","2","120","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","N,N-Diisopropyl-5-trifluoromethylbenzylamine-2-boronic acid","N,N-Diisopropyl-5-trifluoromethylbenzylamine-2-boronic acid","","- C14 H21 B F3 N O2 -","- C14 H21 B F3 N O2 -","- C56 H84 B4 F12 N4 O8 -","4","1","","Arnold, Kenny; Batsanov, Andrei S.; Davies, Bryan; Whiting, Andrew","Synthesis, evaluation and application of novel bifunctional N,N-di-isopropylbenzylamineboronic acid catalysts for direct amide formation between carboxylic acids and amines","Green Chemistry","2008","10","1","124","","10.1039/b712008g","","","0.71073","MoKα","","0.0563","0.042","","","0.1045","0.1119","","","","","","1.026","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7202028","16.0672","0.0008","14.9408","0.0008","7.1505","0.0003","90","","96.855","0.002","90","","1704.26","0.14","123","2","123","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","(E,E)-2-(3-formylbenzylidene)-6-(4- methoxybenzylidene)cyclohexanone","(E,E)-2-(3-formylbenzylidene)-6-(4-methoxybenzylidene)cyclohexanone","","- C22 H20 O3 -","- C22 H20 O3 -","- C88 H80 O12 -","4","1","","Giarrusso, Marilena A.; Higham, Luke T.; Kreher, Ulf P.; Mohan, Ram S.; Rosamilia, Anthony E.; Scott, Janet L.; Strauss, Christopher R.","Platform technology for dienone and phenol‒formaldehyde architectures","Green Chemistry","2008","10","8","842","","10.1039/b802755b","","","0.71073","MoKα","","0.0769","0.0456","","","0.0966","0.1077","","","","","","1.044","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7202029","11.446","0.002","15.395","0.003","12.411","0.003","90","","92.07","0.03","90","","2185.5","0.8","123","2","123","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","3,3'-(1E,1'E)-(2-oxocyclohexane-1,3-diylidene)bis(methan-1-yl- 1-ylidene)-bis(2-methoxy-5-methylbenzaldehyde)","3,3'-(1E,1'E)-(2-oxocyclohexane-1,3-diylidene)bis(methan-1-yl-1-ylidene)- bis(2-methoxy-5-methylbenzaldehyde)","","- C26 H26 O5 -","- C26 H26 O5 -","- C104 H104 O20 -","4","1","","Giarrusso, Marilena A.; Higham, Luke T.; Kreher, Ulf P.; Mohan, Ram S.; Rosamilia, Anthony E.; Scott, Janet L.; Strauss, Christopher R.","Platform technology for dienone and phenol‒formaldehyde architectures","Green Chemistry","2008","10","8","842","","10.1039/b802755b","","","0.71073","MoKα","","0.0991","0.0469","","","0.1065","0.1243","","","","","","0.951","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7202030","14.1051","0.0005","5.984","0.0002","14.3719","0.0006","90","","114.297","0.002","90","","1105.61","0.07","123","2","123","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","(2E,2'E)-2,2'-(2,2'-(ethane-1,2-diylbis(oxy))bis(2,1-phenylene))- bis(methan-1-yl-1-ylidene)dicyclohexanone","","- C28 H30 O4 -","- C28 H30 O4 -","- C56 H60 O8 -","2","0.5","","Giarrusso, Marilena A.; Higham, Luke T.; Kreher, Ulf P.; Mohan, Ram S.; Rosamilia, Anthony E.; Scott, Janet L.; Strauss, Christopher R.","Platform technology for dienone and phenol‒formaldehyde architectures","Green Chemistry","2008","10","8","842","","10.1039/b802755b","","","0.71073","MoKα","","0.1256","0.0483","","","0.1118","0.1344","","","","","","0.939","","","","has coordinates","180351","2020-10-21","18:00:00",""
"7202031","15.1785","0.0002","15.078","0.0002","16.5313","0.0003","90","","97.645","0.001","90","","3749.75","0.1","123","2","123","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","3,4:9,10:18,19:25,26-Tetrabenzo-5,8,20,24-tetraoxa-tricyclo[26.3.1.1(12,16)] tritriaconta-1,3,9,11,16,18,25,27-octaene-32,33-dione chloroform water solvate","","- C45.5 H44.5 Cl1.5 O7 -","- C45.5 H44.5 Cl1.5 O7 -","- C182 H178 Cl6 O28 -","4","1","","Giarrusso, Marilena A.; Higham, Luke T.; Kreher, Ulf P.; Mohan, Ram S.; Rosamilia, Anthony E.; Scott, Janet L.; Strauss, Christopher R.","Platform technology for dienone and phenol‒formaldehyde architectures","Green Chemistry","2008","10","8","842","","10.1039/b802755b","","","0.71073","MoKα","","0.1278","0.0625","","","0.1308","0.1538","","","","","","1.048","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7202032","12.115","0.0003","22.3638","0.0005","30.838","0.0008","90","","92.377","0.001","90","","8348","0.4","123","2","123","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","3,4:9,10:18,19:27,28-Tetrabenzo-5,8,20,23,26-pentaoxatricyclo[28.3.1.1(12,16)]- pentatriaconta-1(34),3,9,12,14,16(35),18,27,30,32-decaene-34,35-diol chloroform solvate","","- C94 H90 Cl6 O14 -","- C94 H90 Cl6 O14 -","- C376 H360 Cl24 O56 -","4","1","","Giarrusso, Marilena A.; Higham, Luke T.; Kreher, Ulf P.; Mohan, Ram S.; Rosamilia, Anthony E.; Scott, Janet L.; Strauss, Christopher R.","Platform technology for dienone and phenol‒formaldehyde architectures","Green Chemistry","2008","10","8","842","","10.1039/b802755b","","","0.71073","MoKα","","0.2959","0.0939","","","0.1596","0.2157","","","","","","1.009","","","","has coordinates,has disorder","180351","2020-10-21","18:00:00",""
"7202237","10.9047","0.0002","10.0696","0.0002","24.2827","0.0006","90","","90","","90","","2666.39","0.1","296","2","296","2","","","","","","","synthesized","5","P b c a","-P 2ac 2ab","61","","","","- C15 H12 N2 O S -","- C15 H12 N2 O S -","- C120 H96 N16 O8 S8 -","8","1","","Yella, Ramesh; Ghosh, Harisadhan; Patel, Bhisma K.","It is “2-imino-4-thiazolidinones” and not thiohydantoins as the reaction product of 1,3-disubstituted thioureas and chloroacetylchloride","Green Chemistry","2008","10","12","1307","","10.1039/b807775d","","","0.71073","MoKα","","0.0566","0.0344","","","0.086","0.093","","","","","","0.947","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7202238","12.9","0.004","10.035","0.004","24.251","0.008","90","","90","","90","","3139.3","1.9","296","2","296","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C15 H10 Cl2 N2 O S -","- C15 H10 Cl2 N2 O S -","- C120 H80 Cl16 N16 O8 S8 -","8","1","","Yella, Ramesh; Ghosh, Harisadhan; Patel, Bhisma K.","It is “2-imino-4-thiazolidinones” and not thiohydantoins as the reaction product of 1,3-disubstituted thioureas and chloroacetylchloride","Green Chemistry","2008","10","12","1307","","10.1039/b807775d","","","0.71073","MoKα","","0.1194","0.0576","","","0.1633","0.1953","","","","","","0.97","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7202277","10.704","0.003","15.143","0.004","8.924","0.002","90","","100.006","0.003","90","","1424.5","0.6","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C14 H16 Cl N S2 -","- C14 H16 Cl N S2 -","- C56 H64 Cl4 N4 S8 -","4","1","","Bhadra, Sukalyan; Saha, Amit; Ranu, Brindaban C.","One-pot copper nanoparticle-catalyzed synthesis of S-aryl- and S-vinyl dithiocarbamates in water: high diastereoselectivity achieved for vinyl dithiocarbamates","Green Chemistry","2008","10","11","1224","","10.1039/b809200a","","","0.71073","MoKα","","0.0358","0.0321","","","0.0889","0.0924","","","","","","1.037","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7202470","20.45","0.004","7.329","0.002","10.31","0.003","90","","99.28","0.02","90","","1525","0.7","160","2","160","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C18 H52 N6 O16 P4 -","- C18 H52 N6 O16 P4 -","- C36 H104 N12 O32 P8 -","2","0.5","","Shastri, Kirtida; Cheng, Eileen W. C.; Motevalli, Majid; Schofield, John; Wilkinson, Jennifer S.; Watkinson, Michael","Investigations into the efficacy of methyhlphosphonic acid functionalised 1,4,7-triazacyclononane ligands in bleaching catalysis","Green Chemistry","2007","9","9","996","","10.1039/b609710c","","","0.71073","MoKα","","0.0928","0.0402","","","0.0944","0.1099","","","","","","1.016","","","","has coordinates","180355","2020-10-21","18:00:00",""
"7202471","7.603","0.0007","9.1105","0.0009","13.0353","0.0015","89.455","0.004","75.731","0.004","86.145","0.006","873.06","0.16","120","2","120","2","","","","","","","","6","P -1","-P 1","2","","","","- C9 H28 Br2 N3 O5 P -","- C9 H28 Br2 N3 O5 P -","- C18 H56 Br4 N6 O10 P2 -","2","1","","Shastri, Kirtida; Cheng, Eileen W. C.; Motevalli, Majid; Schofield, John; Wilkinson, Jennifer S.; Watkinson, Michael","Investigations into the efficacy of methyhlphosphonic acid functionalised 1,4,7-triazacyclononane ligands in bleaching catalysis","Green Chemistry","2007","9","9","996","","10.1039/b609710c","","","0.71073","MoKα","","0.157","0.1243","","","0.3384","0.3619","","","","","","1.087","","","","has coordinates","180355","2020-10-21","18:00:00",""
"7202474","6.43","0.004","6.715","0.004","11.544","0.007","87.486","0.012","80.11","0.012","80.82","0.01","484.7","0.5","173","2","173","2","","","","","","","","4","P -1","-P 1","2","2-carboxy-1,3-dimethylimidazolium NO3 H2O","","","- C6 H11 N3 O6 -","- C6 H11 N3 O6 -","- C12 H22 N6 O12 -","2","1","","Smiglak, Marcin; Holbrey, John D.; Griffin, Scott T.; Reichert, W. Matthew; Swatloski, Richard P.; Katritzky, Alan R.; Yang, Hongfang; Zhang, Dazhi; Kirichenko, Kostyantyn; Rogers, Robin D.","Ionic liquids via reaction of the zwitterionic 1,3-dimethylimidazolium-2-carboxylate with protic acids. Overcoming synthetic limitations and establishing new halide free protocols for the formation of ILs","Green Chemistry","2007","9","1","90","","10.1039/b610421e","","","0.71073","MoKα","","0.0928","0.0539","","","0.1394","0.1792","","","","","","1.152","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7202475","6.628","0.002","11.91","0.004","11.538","0.004","90","","104.508","0.007","90","","881.8","0.5","173","2","173","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","4-carboxy-1,3-dimethylimidazolium nitrate","","","- C6 H9 N3 O5 -","- C6 H9 N3 O5 -","- C24 H36 N12 O20 -","4","1","","Smiglak, Marcin; Holbrey, John D.; Griffin, Scott T.; Reichert, W. Matthew; Swatloski, Richard P.; Katritzky, Alan R.; Yang, Hongfang; Zhang, Dazhi; Kirichenko, Kostyantyn; Rogers, Robin D.","Ionic liquids via reaction of the zwitterionic 1,3-dimethylimidazolium-2-carboxylate with protic acids. Overcoming synthetic limitations and establishing new halide free protocols for the formation of ILs","Green Chemistry","2007","9","1","90","","10.1039/b610421e","","","0.71073","MoKα","","0.0625","0.0448","","","0.1004","0.1067","","","","","","1.074","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7202477","17.365","0.0017","9.9287","0.001","20.981","0.002","90","","113.4","0.002","90","","3319.9","0.6","297","2","298","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","2-phenyl-4-p-toluoyl-3H-benzo-[b]-1,5-diazepine-4- (4-methyl phenyl-3H-benzo-[b]-1,5-diazepine","","- C22 H18 N2 -","- C22 H18 N2 -","- C176 H144 N16 -","8","2","","Palimkar, Sanjay S.; Lahoti, Rajgopal J.; Srinivasan, Kumar V.","A novel one-pot three-component synthesis of 2,4-disubstituted-3 H-benzo[ b][1,4]diazepines in water","Green Chemistry","2007","9","2","146","","10.1039/b610523h","","","0.71073","MoKα","","0.1434","0.0771","","","0.172","0.2059","","","","","","1.042","","","","has coordinates","198632","2020-10-21","18:00:00",""
"7202516","9.4031","0.0005","9.3855","0.0005","11.006","0.0006","78.01","0.003","84.307","0.003","82.744","0.003","939.84","0.09","173","2","173","2","","","","","","","","4","P -1","-P 1","2","","","","- C21 H26 N2 O3 -","- C21 H26 N2 O3 -","- C42 H52 N4 O6 -","2","1","","Iván Kanizsai; Szilvia Gyónfalvi; Zsolt Szakonyi; Reijo Sillanpää; Ferenc Fülöp","Synthesis of bi- and tricyclic ?-lactam libraries in aqueous medium","Green Chemistry","2007","9","4","357","","10.1039/b613117d","","x-ray","0.71073","MoKα","","0.1134","0.0655","","","0.111","0.1304","","","","","","1.058","","","","has coordinates","180356","2020-10-21","18:00:00",""
"7202585","7.1563","0.001","13.1156","0.0015","27.469","0.003","90","","90","","90","","2578.2","0.5","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","(1R,2R)-1,3-dihydroxy-N,N-dimethyl-1-(4- (methylthio)phenyl)propan-2-aminium (1R,3R)-2,2-dimethyl-3-(2- methylprop-1-enyl)-cyclopropanecarboxylate, methanol solvated","(1R,2R)-1,3-dihydroxy-N,N-dimethyl-1-[4-(methylthio)phenyl]propan- 2-aminium (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-enyl)- cyclopropanecarboxylate, methanol solvated","","- C23 H39 N O5 S -","- C23 H39 N O5 S -","- C92 H156 N4 O20 S4 -","4","1","","Rosini, Goffredo; Ayoub, Claudia; Borzatta, Valerio; Marotta, Emanuela; Mazzanti, Andrea; Righi, Paolo","The same and not the same. Similarities and differences in the resolution of trans-chrysanthemic acid of industrial origin by the enantiomers of some threo-1-aryl-2-dimethylamino-1,3-propanediols","Green Chemistry","2007","9","5","441","","10.1039/b615785h","","","0.71073","MoKα","","0.056","0.047","","","0.1345","0.1434","","","","","","1.026","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7202586","9.994","0.0005","7.8004","0.0004","15.8597","0.0008","90","","106.301","0.001","90","","1186.68","0.1","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","(1R,2R)-1,3-dihydroxy-N,N-dimethyl-1-(4- (methylthio)phenyl)propan-2-aminium (1R,3R)-2,2-dimethyl-3-(2- methylprop-1-enyl)-cyclopropanecarboxylate","(1R,2R)-1,3-dihydroxy-N,N-dimethyl-1-[4-(methylthio)phenyl]propan- 2-aminium (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-enyl)- cyclopropanecarboxylate","","- C22 H35 N O4 S -","- C22 H35 N O4 S -","- C44 H70 N2 O8 S2 -","2","1","","Rosini, Goffredo; Ayoub, Claudia; Borzatta, Valerio; Marotta, Emanuela; Mazzanti, Andrea; Righi, Paolo","The same and not the same. Similarities and differences in the resolution of trans-chrysanthemic acid of industrial origin by the enantiomers of some threo-1-aryl-2-dimethylamino-1,3-propanediols","Green Chemistry","2007","9","5","441","","10.1039/b615785h","","","0.71073","MoKα","","0.0567","0.0528","","","0.1548","0.1599","","","","","","1.089","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7202699","11.6255","0.0013","15.2552","0.0017","15.2882","0.0018","90","","92.341","0.002","90","","2709.1","0.5","294","2","294","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","Tetra-(n-butylpyridinium) Octamolybdate","","- C36 H56 Mo8 N4 O26 -","- C36 H56 Mo8 N4 O26 -","- C72 H112 Mo16 N8 O52 -","2","0.5","","Ming-Lin, Guo; Hui-Zhen, Li","Selective oxidation of benzyl alcohol to benzaldehyde with hydrogen peroxide over tetra-alkylpyridinium octamolybdate catalysts","Green Chemistry","2007","9","5","421","","10.1039/b700534b","","","0.71073","MoKα","","0.0527","0.0446","","","0.1247","0.1319","","","","","","1.088","","","","has coordinates","180357","2020-10-21","18:00:00",""
"7202710","25.39","0.006","5.557","0.002","13.342","0.001","90","","93.826","0.014","90","","1878.3","0.8","100","2","100","2","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C23 H20 N3 O0.5 -","- C23 H19 N3 O0.5 -","- C92 H76 N12 O2 -","4","1","","Smith, Nicole M.; Raston, Colin L.; Smith, Christopher B.; Sobolev, Alexandre N.","PEG mediated synthesis of amino-functionalised 2,4,6-triarylpyridines","Green Chemistry","2007","9","11","1185","","10.1039/b700893g","","","0.71073","MoKα","","0.1599","0.0905","","","0.2019","0.2378","","","","","","1.005","","","","has coordinates","180358","2020-10-21","18:00:00",""
"7202843","8.5166","0.0014","10.879","0.0018","16.006","0.003","90","","103","0.003","90","","1445","0.4","100","2","100","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","3-methyl-1-(tetrahydro-2H-pyran-2-ylmethyl)-1H-imidazol-3-ium trifluoromethanesulfonate","","","- C11 H17 F3 N2 O4 S -","- C11 H17 F3 N2 O4 S -","- C44 H68 F12 N8 O16 S4 -","4","1","","Leclercq, Loïc; Suisse, Isabelle; Nowogrocki, Guy; Agbossou-Niedercorn, Francine","Halide-free highly-pure imidazolium triflate ionic liquids: Preparation and use in palladium-catalysed allylic alkylation","Green Chemistry","2007","9","10","1097","","10.1039/b703096g","","","0.71073","MoKα","","0.0394","0.035","","","0.0933","0.0968","","","","","","1.07","","","","has coordinates","180359","2020-10-21","18:00:00",""
"7202844","8.6516","0.0015","10.1699","0.0017","12.195","0.002","87.354","0.003","85.474","0.003","83.36","0.003","1061.7","0.3","100","2","100","2","","","","","","","","6","P -1","-P 1","2","3-methyl-1-(4-(1-methyl-1H-imidazol-3-ium-3-yl)butyl)-1H- imidazol-3-ium bis(trifluoromethanesulfonate)","","","- C14 H20 F6 N4 O6 S2 -","- C14 H20 F6 N4 O6 S2 -","- C28 H40 F12 N8 O12 S4 -","2","1","","Leclercq, Loïc; Suisse, Isabelle; Nowogrocki, Guy; Agbossou-Niedercorn, Francine","Halide-free highly-pure imidazolium triflate ionic liquids: Preparation and use in palladium-catalysed allylic alkylation","Green Chemistry","2007","9","10","1097","","10.1039/b703096g","","","0.71073","MoKα","","0.0394","0.0341","","","0.089","0.0927","","","","","","1.05","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7202845","9.5883","0.0013","9.7729","0.0013","19.198","0.003","85.627","0.002","88.693","0.002","88.563","0.002","1792.8","0.4","100","2","100","2","","","","","","","","6","P -1","-P 1","2","1-methyl-3-(tetrahydrofuran-3-ylmethyl)-1H-imidazol-3-ium trifluoromethanesulfonate / tetrabuthylammonium trifluoromethanesulfonate","","","- C27 H51 F6 N3 O7 S2 -","- C27 H51 F6 N3 O7 S2 -","- C54 H102 F12 N6 O14 S4 -","2","1","","Leclercq, Loïc; Suisse, Isabelle; Nowogrocki, Guy; Agbossou-Niedercorn, Francine","Halide-free highly-pure imidazolium triflate ionic liquids: Preparation and use in palladium-catalysed allylic alkylation","Green Chemistry","2007","9","10","1097","","10.1039/b703096g","","","0.71073","MoKα","","0.0786","0.0578","","","0.157","0.1722","","","","","","1.124","","","","has coordinates","180359","2020-10-21","18:00:00",""
"7202913","16.035","0.005","19.797","0.005","24.936","0.005","90","0.005","104.979","0.005","90","0.005","7647","3","110","2","110","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C79 H122 Na2 O7 -","- C79 H122 Na2 O7 -","- C316 H488 Na8 O28 -","4","1","","Chen, Hsuan-Ying; Zhang, Jubo; Lin, Chu-Chieh; Reibenspies, Joseph H.; Miller, Stephen A.","Efficient and controlled polymerization of lactide under mild conditions with a sodium-based catalyst","Green Chemistry","2007","9","10","1038","","10.1039/b705622b","","","0.71073","MoKα","","0.0806","0.0631","","","0.1693","0.1963","","","","","","1.099","","","","has coordinates,has disorder","180360","2020-10-21","18:00:00",""
"7202999","8.952","0.002","10.126","0.003","14.757","0.004","70.511","0.01","79.526","0.01","76.96","0.01","1220.2","0.6","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C14 H20 N2 -","- C14 H20 N2 -","- C56 H80 N8 -","4","2","","Waldemar M. Czaplik; Jörg-M. Neudörfl; Axel Jacobi von Wangelin","On the quantitative recycling of Raney‒Nickel catalysts on a lab-scale","Green Chemistry","2007","9","11","1163","","10.1039/b708057c","","","0.71073","MoKα","","0.2461","0.0879","","","0.2204","0.2937","","","","","","0.978","","","","has coordinates","180360","2020-10-21","18:00:00",""
"7203081","9.955","0.009","10.404","0.009","10.839","0.009","97.689","0.009","98.771","0.007","111.382","0.016","1011","1.5","113","2","113","2","","","","","","","","5","P -1","-P 1","2","","","","- C16 H27 N O7 P2 -","- C16 H27 N O7 P2 -","- C32 H54 N2 O14 P4 -","2","1","","Zhang, Jianfeng; Cui, Zhanwei; Wang, Fei; Wang, Yadan; Miao, Zhiwei; Chen, Ruyu","Mannich type reactions of chlorophosphites, phosphoramides and aldehydes (ketones) under solvent-free and catalyst-free conditions—synthesis of N-phosphoramino α-aminophosphonates","Green Chemistry","2007","9","12","1341","","10.1039/b710008f","","","0.7107","MoKα","","0.0725","0.0574","","","0.1303","0.1388","","","","","","1.123","","","","has coordinates","180361","2020-10-21","18:00:00",""
"7203136","9.4647","0.0002","9.9534","0.0002","15.7079","0.0004","90","","98.509","0.001","90","","1463.49","0.06","150","2","150","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","N,N'-Bis(furan-2-ylmethylene)cyclohexane-1,2-diamine","","","- C16 H18 N2 O2 -","- C16 H18 N2 O2 -","- C64 H72 N8 O8 -","4","1","","van den Ancker, Tania R.; Cave, Gareth W. V.; Raston, Colin L.","Benign approaches for the synthesis of bis-imine Schiff bases","Green Chemistry","2006","8","1","50","","10.1039/b513289d","","","0.71073","MoKα","","0.0721","0.0467","","","0.1155","0.1285","","","","","","1.039","","","","has coordinates","180362","2020-10-21","18:00:00",""
"7203137","18.5478","0.0004","8.9189","0.0002","9.2148","0.0002","90","","101.388","0.001","90","","1494.36","0.06","150","2","150","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","N,N'-Bis(1H-pyrrol-2-ylmethylene)cyclohexane-1,2-diamine","","","- C16 H20 N4 -","- C16 H20 N4 -","- C64 H80 N16 -","4","0.5","","van den Ancker, Tania R.; Cave, Gareth W. V.; Raston, Colin L.","Benign approaches for the synthesis of bis-imine Schiff bases","Green Chemistry","2006","8","1","50","","10.1039/b513289d","","","0.71073","MoKα","","0.0402","0.0371","","","0.0989","0.1012","","","","","","1.067","","","","has coordinates","180362","2020-10-21","18:00:00",""
"7203138","35.5824","0.0014","5.701","0.0003","16.8318","0.0009","90","","112.752","0.002","90","","3148.7","0.3","150","2","396","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","(N-Pyridin-4-ylmethylene)(N'-pyridin-2-ylmethylene) cyclohexane-1,2-diamine","","","- C18 H20 N4 -","- C18 H20 N4 -","- C144 H160 N32 -","8","1","","van den Ancker, Tania R.; Cave, Gareth W. V.; Raston, Colin L.","Benign approaches for the synthesis of bis-imine Schiff bases","Green Chemistry","2006","8","1","50","","10.1039/b513289d","","","0.71073","MoKα","","0.1266","0.0665","","","0.1574","0.1844","","","","","","1.02","","","","has coordinates","180362","2020-10-21","18:00:00",""
"7203388","7.925","0.005","10.643","0.006","13.886","0.008","90","","99.478","0.008","90","","1155.2","1.2","193.1","","","","","","","","","","","5","P 1 21/a 1","-P 2yab","14","","","","- C12 H10 F3 N O2 -","- C12 H10 F3 N O2 -","- C48 H40 F12 N4 O8 -","4","1","","Kayaki, Yoshihito; Yamamoto, Masafumi; Suzuki, Tomoyuki; Ikariya, Takao","Carboxylative cyclization of propargylamines with supercritical carbon dioxide","Green Chemistry","2006","8","12","1019","","10.1039/b603700c","","","0.7107","MoKα","","","0.055","","","","0.162","","","","","","0.947","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7203394","7.1209","0.0008","16.3999","0.0019","15.0997","0.0016","90","","92.716","0.004","90","","1761.4","0.3","193","2","193","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","1,8-dioxo-3, 3-dimethyl-9-(4-Chloro-phenyl)- 1,2,3,4,5,6,7,8,9,10-decahydroacridine","","- C21 H22 Cl N O2 -","- C21 H22 Cl N O2 -","- C84 H88 Cl4 N4 O8 -","4","1","","Wang, Guan-Wu; Miao, Chun-Bao","Environmentally benign one-pot multi-component approaches to the synthesis of novel unsymmetrical 4-arylacridinediones","Green Chemistry","2006","8","12","1080","","10.1039/b604064k","","","0.7107","MoKα","","0.0454","0.0412","","","0.0963","0.0986","","","","","","1.099","","","","has coordinates","176432","2020-10-21","18:00:00",""
"7203399","7.936","0.003","10.048","0.004","17.864","0.007","91.753","0.008","102.116","0.007","106.858","0.007","1326.5","0.9","173","2","173","2","","","","","","","","4","P -1","-P 1","2","benzethonium nitrate","","","- C27 H42 N2 O5 -","- C27 H42 N2 O5 -","- C54 H84 N4 O10 -","2","1","","Pernak, Juliusz; Smiglak, Marcin; Griffin, Scott T.; Hough, Whitney L.; Wilson, Timothy B.; Pernak, Anna; Zabielska-Matejuk, Jadwiga; Fojutowski, Andrzej; Kita, Kazimierz; Rogers, Robin D.","Long alkyl chain quaternary ammonium-based ionic liquids and potential applications","Green Chemistry","2006","8","9","798","","10.1039/b604353d","","","0.71073","MoKα","","0.1503","0.1123","","","0.3193","0.3388","","","","","","1.046","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7203438","11.219","0.0003","12.8515","0.0003","14.1651","0.0004","82.272","0.001","88.467","0.001","75.715","0.001","1961.17","0.09","123","2","123","2","","","","","","","","3","P -1","-P 1","2","(E,E)-2-(4-Ethoxy-3-methoxybenzylidene)-6-(4- methoxybenzylidene)cyclohexanone","(E,E)-2-(4-Ethoxy-3-methoxybenzylidene)-6-(4-methoxybenzylidene)cyclohexanone","","- C24 H26 O4 -","- C24 H26 O4 -","- C96 H104 O16 -","4","2","","Rosamilia, Anthony E.; Giarrusso, Marilena A.; Scott, Janet L.; Strauss, Christopher R.","A direct, efficient synthesis of unsymmetrically substituted bis(arylidene)alkanones","Green Chemistry","2006","8","12","1042","","10.1039/b606042k","","","0.71073","MoKα","","0.0655","0.045","","","0.1069","0.1177","","","","","","1.024","","","","has coordinates","180365","2020-10-21","18:00:00",""
"7203439","7.8646","0.0003","9.683","0.0003","11.3746","0.0005","95.587","0.001","102.801","0.001","91.992","0.002","839.25","0.06","123","2","123","2","","","","","","","","4","P -1","-P 1","2","(E,E)-2-(4-Methoxybenzylidene)-6-(4- nitrobenzylidene)cyclohexanone","(E,E)-2-(4-Methoxybenzylidene)-6-(4-nitrobenzylidene)cyclohexanone","","- C21 H19 N O4 -","- C21 H19 N O4 -","- C42 H38 N2 O8 -","2","1","","Rosamilia, Anthony E.; Giarrusso, Marilena A.; Scott, Janet L.; Strauss, Christopher R.","A direct, efficient synthesis of unsymmetrically substituted bis(arylidene)alkanones","Green Chemistry","2006","8","12","1042","","10.1039/b606042k","","","0.71073","MoKα","","0.0658","0.04","","","0.0904","0.1018","","","","","","1.044","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7203440","18.5748","0.0001","6.2641","0.0001","15.9337","0.0001","90","","115.194","0.001","90","","1677.59","0.03","123","2","123","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","(E,E)-2-((6-Bromopyridin-2-yl)methylene)-6-(4- methoxybenzylidene)cyclohexanone","(E,E)-2-((6-Bromopyridin-2-yl)methylene)-6-(4-methoxybenzylidene)cyclohexanone","","- C20 H18 Br N O2 -","- C20 H18 Br N O2 -","- C80 H72 Br4 N4 O8 -","4","1","","Rosamilia, Anthony E.; Giarrusso, Marilena A.; Scott, Janet L.; Strauss, Christopher R.","A direct, efficient synthesis of unsymmetrically substituted bis(arylidene)alkanones","Green Chemistry","2006","8","12","1042","","10.1039/b606042k","","","0.71073","MoKα","","0.0656","0.0371","","","0.0697","0.0763","","","","","","1.027","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7203441","11.5683","0.0004","12.3023","0.0004","13.6088","0.0005","98.825","0.001","110.125","0.002","111.483","0.002","1603.3","0.11","123","2","123","2","","","","","","","","5","P -1","-P 1","2","","(E)-N,N-dimethyl-9-(naphthalen-1-yl)-5-(naphthalen-2-ylmethylene) -2,3,4,4a,5,6,7,8,9,9a-decahydro-1H-xanthen-4a-amine hydrochloride salt","","- C36 H38 Cl N O -","- C36 H38 Cl N O -","- C72 H76 Cl2 N2 O2 -","2","1","","Rosamilia, Anthony E.; Giarrusso, Marilena A.; Scott, Janet L.; Strauss, Christopher R.","A direct, efficient synthesis of unsymmetrically substituted bis(arylidene)alkanones","Green Chemistry","2006","8","12","1042","","10.1039/b606042k","","","0.71073","MoKα","","0.1809","0.0644","","","0.1623","0.2063","","","","","","0.988","","","","has coordinates","180365","2020-10-21","18:00:00",""
"7203442","10.0896","0.0001","13.29","0.0002","16.6649","0.0003","90","","103.981","0.001","90","","2168.41","0.06","123","2","123","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","(E)-N,N-dimethyl-9-(pyridin-4-yl)-5-(pyridin-4-ylmethylene) -2,3,4,4a,5,6,7,8,9,9a-decahydro-1H-xanthen-4a-amine","","- C26 H31 N3 O -","- C26 H31 N3 O -","- C104 H124 N12 O4 -","4","1","","Rosamilia, Anthony E.; Giarrusso, Marilena A.; Scott, Janet L.; Strauss, Christopher R.","A direct, efficient synthesis of unsymmetrically substituted bis(arylidene)alkanones","Green Chemistry","2006","8","12","1042","","10.1039/b606042k","","","0.71073","MoKα","","0.0836","0.0498","","","0.0985","0.1113","","","","","","1.059","","","","has coordinates","180365","2020-10-21","18:00:00",""
"7203443","8.763","0.0002","10.924","0.0002","20.1019","0.0005","90","","90","","90","","1924.29","0.07","123","2","123","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","7a-Dimethylamino-5,6,7,7a-tetrahydro-4H-benzofuran-2-one","","- C10 H15 N O2 -","- C10 H15 N O2 -","- C80 H120 N8 O16 -","8","1","","Rosamilia, Anthony E.; Giarrusso, Marilena A.; Scott, Janet L.; Strauss, Christopher R.","A direct, efficient synthesis of unsymmetrically substituted bis(arylidene)alkanones","Green Chemistry","2006","8","12","1042","","10.1039/b606042k","","","0.71073","MoKα","","0.0935","0.0496","","","0.1182","0.1495","","","","","","1.083","","","","has coordinates","180365","2020-10-21","18:00:00",""
"7203719","11.2787","0.0012","11.699","0.0013","11.696","0.0013","90","","115.519","0.002","90","","1392.7","0.3","150","2","150","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C32 H40 O2 Sn -","- C32 H39 O2 Sn -","- C64 H78 O4 Sn2 -","2","1","","John Fawcett; Eric G. Hope; Alison M. Stuart; Andrew J. West","Recycling of a perfluoroalkylated BINOL ligand using fluorous solid-phase extraction","Green Chemistry","2005","7","5","316","","10.1039/b418039a","","","0.71073","MoKα","","0.0459","0.045","","","0.1199","0.1205","","","","","","1.076","","","","has coordinates","180368","2020-10-21","18:00:00",""
"7203730","18.3353","0.001","7.6965","0.0004","12.7734","0.0007","90","","104.148","0.001","90","","1747.88","0.16","150","2","150","2","","","","","","","","8","P 1 21/c 1","-P 2ybc","14","","","","- C9 H19 Cl2 N2 Na O6 S Zn -","- C9 H19 Cl2 N2 Na O6 S Zn -","- C36 H76 Cl8 N8 Na4 O24 S4 Zn4 -","4","1","","Liang, Hong-Chang; Das, Sanjib K.; Galvan, Juan R.; Sato, Suzanne M.; Zhang, Yonglian; Zakharov, Lev N.; Rheingold, Arnold L.","Syntheses of water-soluble N-donor ligands for aqueous catalysis using green, Michael-type addition reactions","Green Chemistry","2005","7","6","410","","10.1039/b500264h","","","0.71073","MoKα","","0.0348","0.0302","","","0.0723","0.0745","","","","","","1.031","","","","has coordinates","180368","2020-10-21","18:00:00",""
"7203755","19.1098","0.0008","19.1098","0.0008","10.2052","0.0006","90","","90","","120","","3227.5","0.3","90","2","90","2","","","","","","","","4","R 3 c :H","R 3 -2""c","161","ca.02.b33.1","","","- C24 H21 O6 P -","- C24 H21 O6 P -","- C144 H126 O36 P6 -","6","0.333333","","Ablan, Christopher D.; Sheppard, Daniel; Beckman, Eric J.; Olmstead, Marilyn M.; Jessop, Philip G.","Solubility of several analogues of triphenylphosphine in carbon dioxide","Green Chemistry","2005","7","8","590","","10.1039/b502442k","","","0.71073","MoKα","","0.0421","0.0399","","","0.1046","0.1066","","","","","","1.067","","","","has coordinates","180368","2020-10-21","18:00:00",""
"7203759","14.169","0.0008","6.451","0.0004","15.238","0.0011","90","","110.614","0.002","90","","1303.64","0.15","295","2","295","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","4,5-dicyano-2,7-dinitrofluorenone","","","- C15 H4 N4 O5 -","- C15 H4 N4 O5 -","- C60 H16 N16 O20 -","4","1","","Sévignon, Marc; Macaud, Mathieu; Favre-Réguillon, Alain; Schulz, Jürgen; Rocault, Muriel; Faure, René; Vrinat, Michel; Lemaire, Marc","Ultra-deep desulfurization of transportation fuels via charge-transfer complexes under ambient conditions","Green Chemistry","2005","7","6","413","","10.1039/b502672e","","","0.7107","MoKα","","0.0906","0.054","","","0.1332","0.1553","","","","","","1.042","","","","has coordinates","180368","2020-10-21","18:00:00",""
"7203760","7.731","0.0004","15.143","0.0009","21.152","0.0014","90","","98.189","0.002","90","","2451","0.3","295","2","295","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C29 H16 N4 O5 S -","- C29 H16 N4 O5 S -","- C116 H64 N16 O20 S4 -","4","1","","Sévignon, Marc; Macaud, Mathieu; Favre-Réguillon, Alain; Schulz, Jürgen; Rocault, Muriel; Faure, René; Vrinat, Michel; Lemaire, Marc","Ultra-deep desulfurization of transportation fuels via charge-transfer complexes under ambient conditions","Green Chemistry","2005","7","6","413","","10.1039/b502672e","","","0.7107","MoKα","","0.1471","0.0677","","","0.1599","0.2079","","","","","","0.986","","","","has coordinates","180368","2020-10-21","18:00:00",""
"7203761","10.366","0.0002","16.072","0.0005","8.312","0.0002","90","","103.372","0.0018","90","","1347.26","0.06","295","2","295","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","4,5-dibromo-2,7-dinitrofluorenone","","","- C13 H4 Br2 N2 O5 -","- C13 H4 Br2 N2 O5 -","- C52 H16 Br8 N8 O20 -","4","1","","Sévignon, Marc; Macaud, Mathieu; Favre-Réguillon, Alain; Schulz, Jürgen; Rocault, Muriel; Faure, René; Vrinat, Michel; Lemaire, Marc","Ultra-deep desulfurization of transportation fuels via charge-transfer complexes under ambient conditions","Green Chemistry","2005","7","6","413","","10.1039/b502672e","","","0.7107","MoKα","","0.1155","0.0631","","","0.1283","0.144","","","","","","1.064","","","","has coordinates","180368","2020-10-21","18:00:00",""
"7203787","21.1806","0.0015","21.1806","0.0015","5.6912","0.0006","90","","90","","120","","2211.1","0.3","100","2","100","2","","","","","","","","5","P 62","P 62","171","","","","- C12 H22 N Na O6 -","- C12 H22 N Na O6 -","- C72 H132 N6 Na6 O36 -","6","1","","Godinez-Salomon, Fernando; Hallen-Lopez, Jose M.; Höpfl, Herbert; Morales-Pacheco, Adela; Beltrán, Hiram I.; Zamudio-Rivera, Luis S.","Strecker intermediates as non-pollutant scavengers for cyanides","Green Chemistry","2005","7","10","716","","10.1039/b504406e","","","0.71073","MoKα","","0.0538","0.0533","","","0.1293","0.1297","","","","","","1.129","","","","has coordinates","288181","2023-12-08","12:50:43",""
"7203796","10.0665","0.0004","16.6372","0.0007","10.5634","0.0003","90","","107.793","0.002","90","","1684.52","0.11","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H16 Cl2 O -","- C20 H16 Cl2 O -","- C80 H64 Cl8 O4 -","4","1","","Zhang, Lijun; Wang, Shaowu; Sheng, Enhong; Zhou, Shuangliu","A solvent-free synthesis of α,α′-bis(substituted benzylidene) cycloalkanones catalyzed by lanthanide amides [(Me3Si)2N]3Ln(µ-Cl)Li(THF)3 under microwave irradiation","Green Chemistry","2005","7","9","683","","10.1039/b504890g","","","0.71073","MoKα","","0.0967","0.0707","","","0.1275","0.142","","","","","","1.187","","","","has coordinates","180368","2020-10-21","18:00:00",""
"7203832","20.312","0.003","9.9902","0.0015","15.927","0.002","90","","108.289","0.002","90","","3068.7","0.8","150","2","150","2","","","","","","","","4","P 1 c 1","P -2yc","7","","","","- C18 H12 N2 S2 -","- C17.997 H12 N2 S1.99925 -","- C143.976 H96 N16 S15.994 -","8","4","","Smith, Christopher B.; Raston, Colin L.; Sobolev, Alexandre N.","Poly(ethyleneglycol)(PEG): a versatile reaction medium in gaining access to 4′-(pyridyl)-terpyridines","Green Chemistry","2005","7","9","650","","10.1039/b507581p","","","0.71073","MoKα","","0.0886","0.0738","","","0.1835","0.1981","","","","","","1.029","","","","has coordinates,has disorder","180369","2020-10-21","18:00:00",""
"7203907","6.9104","0.0002","15.8694","0.0005","13.2342","0.0004","90","","103.602","0.002","90","","1410.61","0.07","123","2","123","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C18 H16 O3 -","- C18 H16 O3 -","- C72 H64 O12 -","4","1","","Raston, Colin L.; Scott, Janet L.","Chemoselective, solvent-free aldol condensation reaction","Green Chemistry","2000","2","2","49","","10.1039/a907688c","","","0.71073","MoKα","","0.0844","0.0492","","","0.1063","0.1163","","","","","","1.061","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7203908","7.272","0.0003","7.5704","0.0002","12.3802","0.0004","77.14","0.002","89.263","0.002","69.134","0.002","619.23","0.04","123","2","123","2","","","","","","","","3","P -1","-P 1","2","","","","- C18 H14 O -","- C18 H14 O -","- C36 H28 O2 -","2","1","","Raston, Colin L.; Scott, Janet L.","Chemoselective, solvent-free aldol condensation reaction","Green Chemistry","2000","2","2","49","","10.1039/a907688c","","","0.71073","MoKα","","0.0707","0.0466","","","0.1176","0.1345","","","","","","1.078","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7203909","12.2718","0.0002","7.8706","0.0001","16.1076","0.0003","90","","102.299","0.001","90","","1520.07","0.04","123","2","123","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C21 H20 O -","- C21 H20 O -","- C84 H80 O4 -","4","1","","Raston, Colin L.; Scott, Janet L.","Chemoselective, solvent-free aldol condensation reaction","Green Chemistry","2000","2","2","49","","10.1039/a907688c","","","0.71073","MoKα","","0.0641","0.0448","","","0.1089","0.116","","","","","","1.053","","","","has coordinates","180370","2020-10-21","18:00:00",""
"7203969","14.4429","0.0005","8.0609","0.0003","24.3908","0.0007","90","","99.51","0.002","90","","2800.62","0.16","123","2","123","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","tris-(O-allyl)CTV","2,7,12,-trimethoxy-3,8,13-tri(prop-1-enoxy)-10,15-dihydro-5H-tribenzo [a,d,g]cyclononene","","- C33 H36 O6 -","- C33 H36 O6 -","- C132 H144 O24 -","4","1","","Scott, Janet L.; MacFarlane, Douglas R.; Raston, Colin L.; Teoh, Ching Mei","Clean, efficient syntheses of cyclotriveratrylene (CTV) and tris-(O-allyl)CTV in an ionic liquid","Green Chemistry","2000","2","4","123","","10.1039/b000825g","","","0.71073","MoKα","","0.136","0.0689","","","0.1581","0.1946","","","","","","1.031","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7204028","5.9637","0.0002","9.123","0.0006","12.0646","0.0007","99.666","0.003","96.329","0.003","95.837","0.003","638.28","0.06","123","2","123","2","","","","","","","","3","P -1","-P 1","2","","","","- C14 H14 O6 -","- C14 H14 O6 -","- C28 H28 O12 -","2","1","","Scott, Janet L.; Raston, Colin L.","Solvent-free synthesis of 3-carboxycoumarins","Green Chemistry","2000","2","5","245","","10.1039/b006704k","","","0.71073","MoKα","","0.0673","0.0437","","","0.0947","0.1038","","","","","","1.037","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7204029","5.11","0.0002","19.5292","0.0004","9.4299","0.0003","90","","99.909","0.002","90","","927.01","0.05","123","2","123","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","8-methoxy,3-carboxy-coumarin","","- C11 H8 O5 -","- C11 H7 O5 -","- C44 H28 O20 -","4","1","","Scott, Janet L.; Raston, Colin L.","Solvent-free synthesis of 3-carboxycoumarins","Green Chemistry","2000","2","5","245","","10.1039/b006704k","","","0.71073","MoKα","","0.069","0.0437","","","0.104","0.1157","","","","","","1.037","","","","has coordinates","180371","2020-10-21","18:00:00",""
"7204218","9.1435","0.0002","27.8109","0.0003","5.8488","0.001","90","","90","","90","","1487.3","0.3","123","2","123","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C15 H17 N O5 -","- C15 H17 N O5 -","- C60 H68 N4 O20 -","4","1","","Correa, Waldo H.; Scott, Janet L.","Solvent-free, two-step synthesis of some unsymmetrical 4-aryl-1,4-dihydropyridines","Green Chemistry","2001","3","6","296","301","10.1039/b106397a","","","0.71073","MoKα","","0.0869","0.049","","","0.0883","0.1012","","","","","","1.039","","","","has coordinates","264728","2021-04-30","11:43:03",""
"7204407","24.9478","0.0009","6.0316","0.0002","8.3285","0.0003","90","","98.391","0.001","90","","1239.82","0.08","123","2","123","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","2-(5'-bromo-2'-hydroxyphenyl)-1,2,3,4-tetrahydroquinazoline","2-[(2'-amino-benzylimino)-methyl]-4-bromo-phenol","","- C14 H13 Br N2 O -","- C14 H13 Br N2 O -","- C56 H52 Br4 N8 O4 -","4","1","","Correa, Waldo H.; Papadopoulos, Stavroula; Radnidge, Peta; Roberts, Brett A.; Scott, Janet L.","Direct, efficient, solvent-free synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolines","Green Chemistry","2002","4","3","245","","10.1039/b202729c","","","0.71073","MoKα","","0.0513","0.0422","","","0.106","0.1113","","","","","","1.051","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7204408","9.436","0.0005","10.4454","0.0005","12.0165","0.0008","99.837","0.002","98.858","0.002","101.754","0.004","1120.4","0.11","123","2","123","2","","","","","","","","3","P -1","-P 1","2","2-phenyl-1,2,3,4-tetrahydroquinazoline","2-phenyl-1,2,3,4-tetrahydroquinazoline","","- C14 H14 N2 -","- C14 H13 N2 -","- C56 H52 N8 -","4","2","","Correa, Waldo H.; Papadopoulos, Stavroula; Radnidge, Peta; Roberts, Brett A.; Scott, Janet L.","Direct, efficient, solvent-free synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolines","Green Chemistry","2002","4","3","245","","10.1039/b202729c","","","0.71073","MoKα","","0.1408","0.0822","","","0.2063","0.2397","","","","","","1.032","","","","has coordinates","180375","2020-10-21","18:00:00",""
"7204409","12.1392","0.0002","7.7897","0.0002","13.5753","0.0003","90","","111.14","0.008","90","","1197.3","0.08","123","2","123","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","2-(2'-nitrophenyl)-1,2,3,4-tetrahydroquinazoline","2-(2'-nitrophenyl)-1,2,3,4-tetrahydroquinazoline","","- C14 H13 N3 O2 -","- C14 H13 N3 O2 -","- C56 H52 N12 O8 -","4","1","","Correa, Waldo H.; Papadopoulos, Stavroula; Radnidge, Peta; Roberts, Brett A.; Scott, Janet L.","Direct, efficient, solvent-free synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolines","Green Chemistry","2002","4","3","245","","10.1039/b202729c","","","0.71073","MoKα","","0.0635","0.045","","","0.1307","0.1524","","","","","","1.133","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7204410","11.3431","0.0004","8.7088","0.0002","23.4287","0.0005","90","","90","","90","","2314.4","0.11","123","2","123","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","2-(4'-hydroxyphenyl)-1,2,3,4-tetrahydroquinazoline","4-(1,2,3,4-tetrahydro-quinazolin-2-yl)-phenol","","- C14 H14 N2 O -","- C14 H13.6 N2 O -","- C112 H108.8 N16 O8 -","8","1","","Correa, Waldo H.; Papadopoulos, Stavroula; Radnidge, Peta; Roberts, Brett A.; Scott, Janet L.","Direct, efficient, solvent-free synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolines","Green Chemistry","2002","4","3","245","","10.1039/b202729c","","","0.71073","MoKα","","0.0754","0.0479","","","0.1116","0.1231","","","","","","1.045","","","","has coordinates,has disorder","180375","2020-10-21","18:00:00",""
"7204411","24.8822","0.0008","4.6291","0.0002","16.5755","0.0005","90","","106.263","0.002","90","","1832.81","0.11","123","2","123","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","N-2-[5'-bromosalicylideneimino)benzyl]-5''-bromosalicylideneimine","N-2-[5'-bromosalicylideneimino)benzyl]-5''-bromosalicylideneimine","","- C21 H16 Br2 N2 O2 -","- C21 H16 Br2 N2 O2 -","- C84 H64 Br8 N8 O8 -","4","1","","Correa, Waldo H.; Papadopoulos, Stavroula; Radnidge, Peta; Roberts, Brett A.; Scott, Janet L.","Direct, efficient, solvent-free synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolines","Green Chemistry","2002","4","3","245","","10.1039/b202729c","","","0.71073","MoKα","","0.1609","0.0498","","","0.0758","0.0959","","","","","","0.901","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7204412","20.4722","0.0003","13.2281","0.0002","20.7521","0.0004","90","","90","","90","","5619.84","0.16","123","2","123","2","","","","","","","","4","P n a 21","P 2c -2n","33","2-(veratryl)-1,2,3,4-tetrahydroquinazoline","2-(3',4'-dimethoxyphenyl)-1,2,3,4-tetrahydroquinazoline","","- C16 H18 N2 O2 -","- C16 H18 N2 O2 -","- C256 H288 N32 O32 -","16","4","","Correa, Waldo H.; Papadopoulos, Stavroula; Radnidge, Peta; Roberts, Brett A.; Scott, Janet L.","Direct, efficient, solvent-free synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolines","Green Chemistry","2002","4","3","245","","10.1039/b202729c","","","0.71073","MoKα","","0.1532","0.0639","","","0.0959","0.1197","","","","","","1.014","","","","has coordinates","180375","2020-10-21","18:00:00",""
"7204413","9.72","0.0002","14.037","0.0002","12.2058","0.0001","90","","97.056","0.002","90","","1652.74","0.04","123","2","123","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","N-2[(salicylideneimino)benzyl]-salicylideneimine","N-2[(salicylideneimino)benzyl]-salicylideneimine","","- C21 H18 N2 O2 -","- C21 H18 N2 O2 -","- C84 H72 N8 O8 -","4","1","","Correa, Waldo H.; Papadopoulos, Stavroula; Radnidge, Peta; Roberts, Brett A.; Scott, Janet L.","Direct, efficient, solvent-free synthesis of 2-aryl-1,2,3,4-tetrahydroquinazolines","Green Chemistry","2002","4","3","245","","10.1039/b202729c","","","0.71073","MoKα","","0.0915","0.047","","","0.1074","0.1256","","","","","","0.987","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7204584","8.5187","0.0009","9.8623","0.0011","14.8684","0.0015","90","","90","","90","","1249.2","0.2","150","2","150","2","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C16 H14 N4 -","- C16 H14 N4 -","- C64 H56 N16 -","4","0.5","","Dudd, Lucinda M.; Venardou, Eleni; Garcia-Verdugo, Eduardo; Licence, Peter; Blake, Alexander J.; Wilson, Claire; Poliakoff, Martyn","Synthesis of benzimidazoles in high-temperature waterThis work was presented at the Green Solvents for Catalysis Meeting held in Bruchsal, Germany, 13‒16th October 2002.Electronic supplementary information (ESI) available: analytical data for compounds 3a‒f and 5g‒j. See http://www.rsc.org/suppdata/gc/b2/b212394k/","Green Chemistry","2003","5","2","187","","10.1039/b212394k","","","0.71073","MoKα","","0.0677","0.0379","","","0.0862","0.0999","","","","","","1.025","","","","has coordinates","180376","2020-10-21","18:00:00",""
"7204585","7.5866","0.0011","10.366","0.002","9.7278","0.0015","90","","107.895","0.002","90","","728","0.2","150","2","150","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C20 H14 N4 -","- C20 H14 N4 -","- C40 H28 N8 -","2","0.5","","Dudd, Lucinda M.; Venardou, Eleni; Garcia-Verdugo, Eduardo; Licence, Peter; Blake, Alexander J.; Wilson, Claire; Poliakoff, Martyn","Synthesis of benzimidazoles in high-temperature waterThis work was presented at the Green Solvents for Catalysis Meeting held in Bruchsal, Germany, 13‒16th October 2002.Electronic supplementary information (ESI) available: analytical data for compounds 3a‒f and 5g‒j. See http://www.rsc.org/suppdata/gc/b2/b212394k/","Green Chemistry","2003","5","2","187","","10.1039/b212394k","","","0.71073","MoKα","","0.0627","0.0419","","","0.0912","0.0977","","","","","","0.961","","","","has coordinates","180376","2020-10-21","18:00:00",""
"7204586","17.712","0.002","8.7976","0.0008","9.7375","0.0009","90","","90","","90","","1517.3","0.3","150","2","150","2","","","","","","","","3","P b c n","-P 2n 2ab","60","","","","- C20 H14 N4 -","- C20 H14 N4 -","- C80 H56 N16 -","4","0.5","","Dudd, Lucinda M.; Venardou, Eleni; Garcia-Verdugo, Eduardo; Licence, Peter; Blake, Alexander J.; Wilson, Claire; Poliakoff, Martyn","Synthesis of benzimidazoles in high-temperature waterThis work was presented at the Green Solvents for Catalysis Meeting held in Bruchsal, Germany, 13‒16th October 2002.Electronic supplementary information (ESI) available: analytical data for compounds 3a‒f and 5g‒j. See http://www.rsc.org/suppdata/gc/b2/b212394k/","Green Chemistry","2003","5","2","187","","10.1039/b212394k","","","0.71073","MoKα","","0.0617","0.0387","","","0.0893","0.0974","","","","","","1.03","","","","has coordinates","180376","2020-10-21","18:00:00",""
"7204602","11.761","0.004","16.685","0.006","11.864","0.004","90","","90.504","0.007","90","","2328","1.4","173","2","173","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C14 H24 F12 N4 O2 P2 -","- C14 H24 F12 N4 O2 P2 -","- C56 H96 F48 N16 O8 P8 -","4","1","","Holbrey, John D.; Visser, Ann E.; Spear, Scott K.; Reichert, W. Matthew; Swatloski, Richard P.; Broker, Grant A.; Rogers, Robin D.","Mercury(ii) partitioning from aqueous solutions with a new, hydrophobic ethylene-glycol functionalized bis-imidazolium ionic liquidThis work was presented at the Green Solvents for Catalysis Meeting held in Bruchsal, Germany, 13‒16th October 2002.","Green Chemistry","2003","5","2","129","","10.1039/b300971h","","","0.71073","MoKα","","0.0695","0.0458","","","0.1165","0.1219","","","","","","1.04","","","","has coordinates,has disorder","180377","2020-10-21","18:00:00",""
"7204603","6.4611","0.0002","16.5436","0.0005","12.1828","0.0004","90","","99.445","0.001","90","","1284.56","0.07","173","2","173","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","1,1'-(1,10-decyl)-bis(3-methylimidazolium) hexafluorophosphate","1,1'-(1,10-decyl)-bis(3-methylimidazolium) hexafluorophosphate","","- C18 H32 F12 N4 P2 -","- C18 H32 F12 N4 P2 -","- C36 H64 F24 N8 P4 -","2","0.5","","Holbrey, John D.; Visser, Ann E.; Spear, Scott K.; Reichert, W. Matthew; Swatloski, Richard P.; Broker, Grant A.; Rogers, Robin D.","Mercury(ii) partitioning from aqueous solutions with a new, hydrophobic ethylene-glycol functionalized bis-imidazolium ionic liquidThis work was presented at the Green Solvents for Catalysis Meeting held in Bruchsal, Germany, 13‒16th October 2002.","Green Chemistry","2003","5","2","129","","10.1039/b300971h","","","0.71073","MoKα","","0.0421","0.0364","","","0.0965","0.1015","","","","","","1.069","","","","has coordinates","180377","2020-10-21","18:00:00",""
"7204604","10.086","0.003","12.459","0.003","15.204","0.004","83.209","0.004","84.16","0.004","67.666","0.005","1751.5","0.8","173","2","173","2","","","","","","","","6","P -1","-P 1","2","","","","- C30 H44 Hg N4 O11 S2 -","- C30 H44 Hg N4 O11 S2 -","- C60 H88 Hg2 N8 O22 S4 -","2","1","","Holbrey, John D.; Visser, Ann E.; Spear, Scott K.; Reichert, W. Matthew; Swatloski, Richard P.; Broker, Grant A.; Rogers, Robin D.","Mercury(ii) partitioning from aqueous solutions with a new, hydrophobic ethylene-glycol functionalized bis-imidazolium ionic liquidThis work was presented at the Green Solvents for Catalysis Meeting held in Bruchsal, Germany, 13‒16th October 2002.","Green Chemistry","2003","5","2","129","","10.1039/b300971h","","","0.71073","MoKα","","0.0409","0.0369","","","0.0895","0.0909","","","","","","1.016","","","","has coordinates","180377","2020-10-21","18:00:00",""
"7204671","8.4317","0.0017","10.439","0.002","11.313","0.002","90","","90","","90","","995.8","0.3","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","1-butyl-3-methylimidazolium fluoride monohydrate","","","- C8 H17 F N2 O -","- C8 H17 F N2 O -","- C32 H68 F4 N8 O4 -","4","1","","Swatloski, Richard P.; Holbrey, John D.; Rogers, Robin D.","Ionic liquids are not always green: hydrolysis of 1-butyl-3-methylimidazolium hexafluorophosphate","Green Chemistry","2003","5","4","361","","10.1039/b304400a","","","0.71073","MoKα","","0.0288","0.0253","","","0.0606","0.0631","","","","","","1.007","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7204752","10.771","0.003","11.201","0.003","11.612","0.004","96.211","0.005","111.392","0.005","94.957","0.005","1284.7","0.7","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","1-(2-hydroxypropyl)-3-methylimidazolium tetraphenylborate","","- C31 H33 B N2 O -","- C31 H33 B N2 O -","- C62 H66 B2 N4 O2 -","2","1","","Holbrey, John D.; Turner, Megan B.; Reichert, W. Matthew; Rogers, Robin D.","New ionic liquids containing an appended hydroxyl functionality from the atom-efficient, one-pot reaction of 1-methylimidazole and acid with propylene oxide","Green Chemistry","2003","5","6","731","","10.1039/b311717k","","","0.71073","MoKα","","0.0479","0.0403","","","0.1097","0.1153","","","","","","1.032","","","","has coordinates","180378","2020-10-21","18:00:00",""
"7204761","19.764","0.009","8.877","0.004","15.763","0.007","90","","117.617","0.007","90","","2450.5","1.9","293","2","293","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C12 H14 N2 O2 -","- C12 H14 N2 O2 -","- C96 H112 N16 O16 -","8","1","","Wang, Zhong-Xia; Qin, Hua-Li","Solventless syntheses of pyrazole derivativesElectronic supplementary information (ESI) available: analytical and spectroscopic data. See http://www.rsc.org/suppdata/gc/b3/b312833d/","Green Chemistry","2004","6","2","90","","10.1039/b312833d","","","0.71073","MoKα","","0.0844","0.0518","","","0.1276","0.1482","","","","","","1.02","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7204801","27.15","0.02","14.785","0.012","31.326","0.017","90","","91.02","0.05","90","","12573","15","295","2","295","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C78 H80 O4 -","- C78 H80 O4 -","- C624 H640 O32 -","8","1","","Makha, Mohamed; Raston, Colin L.; Skelton, Brian W.; White, Allan H.","A more benign approach to the synthesis of calixarenes","Green Chemistry","2004","6","3","158","","10.1039/b315204a","","","0.71073","MoKα","","0.144","0.072","","0.098","","0.144","","","1.34","","","1.15","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7205034","6.2418","0.0016","9.747","0.002","15.951","0.004","90","","90","","90","","970.4","0.4","173","2","173","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","1,3-dimethylimidazolium methylsulphate","","","- C6 H12 N2 O4 S -","- C6 H12 N2 O4 S -","- C24 H48 N8 O16 S4 -","4","1","","Holbrey, John D.; Reichert, W. Matthew; Swatloski, Richard P.; Broker, Grant A.; Pitner, William R.; Seddon, Kenneth R.; Rogers, Robin D.","Efficient, halide free synthesis of new, low cost ionic liquids: 1,3-dialkylimidazolium salts containing methyl- and ethyl-sulfate anions","Green Chemistry","2002","4","5","407","","10.1039/b204469b","","","0.71073","MoKα","","0.0347","0.0285","","","0.058","0.0605","","","","","","0.947","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7205539","9.3778","0.001","10.7852","0.001","11.1818","0.0013","101.718","0.005","114.717","0.004","102.712","0.005","944.94","0.18","150","2","150","2","","","","","","","","7","P -1","-P 1","2","","","","- C18 H16 F3 N3 O3 Ru S -","- C18 H16 F3 N3 O3 Ru S -","- C36 H32 F6 N6 O6 Ru2 S2 -","2","1","","Thibault, Michelle E.; DiMondo, Domenico V.; Jennings, Michael; Abdelnur, Patrícia Verardi; Eberlin, Marcos N.; Schlaf, Marcel","Cyclopentadienyl and pentamethylcyclopentadienyl ruthenium complexes as catalysts for the total deoxygenation of 1,2-hexanediol and glycerol","Green Chemistry","2011","13","2","357","","10.1039/c0gc00255k","","","0.71073","MoKα","","0.0574","0.0395","","","0.0854","0.092","","","","","","1.053","","","","has coordinates","180386","2020-10-21","18:00:00",""
"7205540","8.5469","0.0001","15.1743","0.0002","20.6543","0.0002","90","","100.479","0.0011","90","","2634.04","0.05","153","1","153","1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C50 H46 Cl6 O4 P4 Pd2 -","- C50 H46 Cl6 O4 P4 Pd2 -","- C100 H92 Cl12 O8 P8 Pd4 -","2","0.5","","Marziale, Alexander N.; Jantke, Dominik; Faul, Stefan H.; Reiner, Thomas; Herdtweck, Eberhardt; Eppinger, Jörg","An efficient protocol for the palladium-catalysed Suzuki‒Miyaura cross-coupling","Green Chemistry","2011","13","1","169","","10.1039/c0gc00522c","","","0.71073","MoKα","","0.0393","0.032","","","0.0707","0.0773","","","","","","1.084","","","","has coordinates","180386","2020-10-21","18:00:00",""
"7205541","17.6026","0.0006","17.6026","0.0006","23.747","0.0009","90","","90","","90","","7358","0.5","123","1","123","1","","","","","","","","6","P 43","P 4cw","78","","","","- C36 H44 Cl2 O2 P2 Pd2 -","- C36 H44 Cl2 O2 P2 Pd2 -","- C288 H352 Cl16 O16 P16 Pd16 -","8","2","","Marziale, Alexander N.; Jantke, Dominik; Faul, Stefan H.; Reiner, Thomas; Herdtweck, Eberhardt; Eppinger, Jörg","An efficient protocol for the palladium-catalysed Suzuki‒Miyaura cross-coupling","Green Chemistry","2011","13","1","169","","10.1039/c0gc00522c","","","0.71073","MoKα","","0.0287","0.0273","","","0.0688","0.0701","","","","","","1.071","","","","has coordinates","180386","2020-10-21","18:00:00",""
"7205542","12.284","0.0002","13.229","0.0002","18.391","0.0003","90","","90","","90","","2988.63","0.08","293","2","293","2","","","","","","","","5","P b n a","-P 2ac 2b","60","","","","- C13 H24 F3 N O2 -","- C13 H24 F3 N O2 -","- C104 H192 F24 N8 O16 -","8","1","","Belhocine, Tayeb; Forsyth, Stewart A.; Gunaratne, H. Q. Nimal; Nieuwenhuyzen, Mark; Puga, Alberto V.; Seddon, Kenneth R.; Srinivasan, Geetha; Whiston, Keith","New ionic liquids from azepane and 3-methylpiperidine exhibiting wide electrochemical windows","Green Chemistry","2011","13","1","59","","10.1039/c0gc00534g","","","0.71073","MoKα","","0.0911","0.0789","","","0.2211","0.2428","","","","","","1.062","","","","has coordinates,has disorder","180386","2020-10-21","18:00:00",""
"7205907","8.818","0.002","10.459","0.002","16.684","0.004","73.495","0.003","82.566","0.004","65.165","0.003","1338.8","0.5","295","2","295","2","","","","","","","","5","P -1","-P 1","2","","","","- C24 H36 N2 O6 S -","- C24 H36 N2 O6 S -","- C48 H72 N4 O12 S2 -","2","1","","Shaabani, Ahmad; Sarvary, Afshin; Ghasemi, Sabrieh; Rezayan, Ali Hossein; Ghadari, Rahim; Ng, Seik Weng","An environmentally benign approach for the synthesis of bifunctional sulfonamide-amide compounds via isocyanide-based multicomponent reactions","Green Chemistry","2011","13","3","582","","10.1039/c0gc00442a","","","0.71073","MoKα","","0.1706","0.0722","","","0.194","0.2562","","","","","","1.01","","","","has coordinates","180390","2020-10-21","18:00:00",""
"7205908","11.2071","0.0008","23.3231","0.0015","11.1208","0.0008","90","","117.989","0.001","90","","2566.8","0.3","295","2","295","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C24 H30 N2 O7 S -","- C24 H30 N2 O7 S -","- C96 H120 N8 O28 S4 -","4","1","","Shaabani, Ahmad; Sarvary, Afshin; Ghasemi, Sabrieh; Rezayan, Ali Hossein; Ghadari, Rahim; Ng, Seik Weng","An environmentally benign approach for the synthesis of bifunctional sulfonamide-amide compounds via isocyanide-based multicomponent reactions","Green Chemistry","2011","13","3","582","","10.1039/c0gc00442a","","","0.71073","MoKα","","0.0912","0.0618","","","0.1576","0.1768","","","","","","1.079","","","","has coordinates","180390","2020-10-21","18:00:00",""
"7205909","5.6284","0.0002","12.5878","0.0004","15.935","0.0004","90","","98.913","0.002","90","","1115.35","0.06","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C9 H9 Cl2 N3 O2 -","- C9 H9 Cl2 N3 O2 -","- C36 H36 Cl8 N12 O8 -","4","1","","Li, Da-Peng; Zhang, Guang-Liang; An, Li-Tao; Zou, Jian-Ping; Zhang, Wei","Solvent- and catalyst-free synthesis of 2,3-dihydro-1H-benzo[d]imidazoles","Green Chemistry","2011","13","3","594","","10.1039/c0gc00572j","","","0.71073","MoKα","","0.0622","0.0578","","","0.151","0.1552","","","","","","1.086","","","","has coordinates","180390","2020-10-21","18:00:00",""
"7205910","13.622","0.003","7.8211","0.0011","9.8987","0.0017","90","","104.1","0.02","90","","1022.8","0.3","193","2","193","2","","","","","","","","4","C 1 2/m 1","-C 2y","12","","","","- C7 H18 Cl N3 -","- C7 H18 Cl N3 -","- C28 H72 Cl4 N12 -","4","0.5","","Oelkers, Benjamin; Sundermeyer, Jörg","Pentaalkylmethylguanidinium methylcarbonates ‒ versatile precursors for the preparation of halide-free and metal-free guanidinium-based ILs","Green Chemistry","2011","13","3","608","","10.1039/c0gc00698j","","","0.71073","MoKα","","0.0933","0.0701","","","0.2253","0.232","","","","","","1.257","","","","has coordinates","180390","2020-10-21","18:00:00",""
"7206033","7.7534","0.0016","8.0651","0.0016","18.818","0.004","90","","90","","90","","1176.7","0.4","123","2","123","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C10 H18 N2 O6 -","- C10 H18 N2 O6 -","- C40 H72 N8 O24 -","4","1","","Nonappa,; Ahonen, Kari; Lahtinen, Manu; Kolehmainen, Erkki","Cyclic dipeptides: catalyst/promoter-free, rapid and environmentally benign cyclization of free amino acids","Green Chemistry","2011","13","5","1203","","10.1039/c1gc15043j","","","0.71073","MoKα","","0.0557","0.0429","","","0.0841","0.0881","","","","","","1.035","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7206034","10.5612","0.0014","8.4166","0.0005","15.8706","0.0019","90","","107.86","0.004","90","","1342.7","0.3","123","2","123","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C18 H14 N2 O2 -","- C18 H14 N2 O2 -","- C72 H56 N8 O8 -","4","1","","Nonappa,; Ahonen, Kari; Lahtinen, Manu; Kolehmainen, Erkki","Cyclic dipeptides: catalyst/promoter-free, rapid and environmentally benign cyclization of free amino acids","Green Chemistry","2011","13","5","1203","","10.1039/c1gc15043j","","","0.71073","MoKα","","0.1714","0.0734","","","0.1142","0.1447","","","","","","1.031","","","","has coordinates","180391","2020-10-21","18:00:00",""
"7206035","5.8353","0.0003","9.651","0.0006","12.8178","0.001","90","","90","","90","","721.85","0.08","123","2","123","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C7 H10 N2 O2 -","- C7 H10 N2 O2 -","- C28 H40 N8 O8 -","4","1","","Nonappa,; Ahonen, Kari; Lahtinen, Manu; Kolehmainen, Erkki","Cyclic dipeptides: catalyst/promoter-free, rapid and environmentally benign cyclization of free amino acids","Green Chemistry","2011","13","5","1203","","10.1039/c1gc15043j","","","0.71073","MoKα","","0.0637","0.0476","","","0.0991","0.1065","","","","","","1.073","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7206036","6.0475","0.0007","7.8473","0.001","11.2904","0.0012","90","","97.541","0.007","90","","531.17","0.11","123","2","123","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C12 H18 N2 O2 -","- C12 H18 N2 O2 -","- C24 H36 N4 O4 -","2","0.5","","Nonappa,; Ahonen, Kari; Lahtinen, Manu; Kolehmainen, Erkki","Cyclic dipeptides: catalyst/promoter-free, rapid and environmentally benign cyclization of free amino acids","Green Chemistry","2011","13","5","1203","","10.1039/c1gc15043j","","","0.71073","MoKα","","0.0985","0.0637","","","0.1325","0.1458","","","","","","1.056","","","","has coordinates","180391","2020-10-21","18:00:00",""
"7206037","3.9045","0.0004","11.5645","0.0017","5.1679","0.0007","90","","96.461","0.008","90","","231.87","0.05","123","2","123","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C4 H6 N2 O2 -","- C4 H6 N2 O2 -","- C8 H12 N4 O4 -","2","0.5","","Nonappa,; Ahonen, Kari; Lahtinen, Manu; Kolehmainen, Erkki","Cyclic dipeptides: catalyst/promoter-free, rapid and environmentally benign cyclization of free amino acids","Green Chemistry","2011","13","5","1203","","10.1039/c1gc15043j","","","0.71073","MoKα","","0.0417","0.0367","","","0.0852","0.0875","","","","","","1.083","","","","has coordinates","180391","2020-10-21","18:00:00",""
"7206038","4.6835","0.0004","9.2616","0.0008","23.4038","0.0016","90","","90","","90","","1015.18","0.14","130","0.1","130","0.1","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","syn-(3S,4R)-3,4-dihydroxy-4-(4-nitrophenyl)butan-2-one","<i>syn</i>-(3<i>S</i>,4<i>R</i>)-3,4-dihydroxy- 4-(4-nitrophenyl)butan-2-one","","- C10 H11 N O5 -","- C10 H11 N O5 -","- C40 H44 N4 O20 -","4","1","","Czarnecki, Paweł; Plutecka, Agnieszka; Gawroński, Jacek; Kacprzak, Karol","Simple and practical direct asymmetric aldol reaction of hydroxyacetone catalyzed by 9-amino Cinchona alkaloid tartrates","Green Chemistry","2011","13","5","1280","","10.1039/c1gc15064b","","","1.54184","CuKα","","0.0257","0.0256","","","0.0687","0.0688","","","","","","1.088","","","","has coordinates","202017","2020-10-21","18:00:00",""
"7206164","18.7033","0.0013","25.8907","0.0018","9.8896","0.0006","90","","90","","90","","4789","0.6","293","2","293","2","","","","","","","","5","P n a 21","P 2c -2n","33","","","","- C52 H48 N12 O Ru2 -","- C52 H48 N12 O Ru2 -","- C208 H192 N48 O4 Ru8 -","4","1","","Herrero, Santiago; Jiménez-Aparicio, Reyes; Perles, Josefina; Priego, José L.; Saguar, Susana; Urbanos, Francisco A.","Microwave methods for the synthesis of paddlewheel diruthenium compounds with N,N-donor ligands","Green Chemistry","2011","13","7","1885","","10.1039/c0gc00800a","","","0.71073","MoKα","","0.2126","0.0769","","","0.1835","0.2572","","","","","","0.952","","","","has coordinates","180392","2020-10-21","18:00:00",""
"7206165","18.7417","0.0015","25.884","0.002","9.8779","0.0008","90","","90","","90","","4791.9","0.7","293","2","293","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C48 H40 N12 Ru2 -","- C48 H40 N12 Ru2 -","- C192 H160 N48 Ru8 -","4","1","","Herrero, Santiago; Jiménez-Aparicio, Reyes; Perles, Josefina; Priego, José L.; Saguar, Susana; Urbanos, Francisco A.","Microwave methods for the synthesis of paddlewheel diruthenium compounds with N,N-donor ligands","Green Chemistry","2011","13","7","1885","","10.1039/c0gc00800a","","","0.71073","MoKα","","0.1845","0.0759","","","0.175","0.2117","","","","","","0.839","","","","has coordinates","180392","2020-10-21","18:00:00",""
"7206166","15.028","0.002","15.028","0.002","21.962","0.004","90","","90","","90","","4959.9","1.3","293","2","293","2","","","","","","","","6","P 4/n c c :2","-P 4a 2ac","130","","","","- C52 H44 Cl N8 O5.25 Ru2 -","- C52 H44 Cl N8 O4.92 Ru2 -","- C208 H176 Cl4 N32 O19.68 Ru8 -","4","0.25","","Herrero, Santiago; Jiménez-Aparicio, Reyes; Perles, Josefina; Priego, José L.; Saguar, Susana; Urbanos, Francisco A.","Microwave methods for the synthesis of paddlewheel diruthenium compounds with N,N-donor ligands","Green Chemistry","2011","13","7","1885","","10.1039/c0gc00800a","","","0.71073","MoKα","","0.1307","0.0471","","","0.1055","0.1679","","","","","","1.089","","","","has coordinates","180392","2020-10-21","18:00:00",""
"7206167","14.2592","0.0008","14.2608","0.0008","30.4171","0.0018","90","","90","","90","","6185.2","0.6","293","2","293","2","","","","","","","","6","P c c n","-P 2ab 2ac","56","","","","- C60 H60 Cl N8 O8 Ru2 -","- C60 H60 Cl N8 O8 Ru2 -","- C240 H240 Cl4 N32 O32 Ru8 -","4","0.5","","Herrero, Santiago; Jiménez-Aparicio, Reyes; Perles, Josefina; Priego, José L.; Saguar, Susana; Urbanos, Francisco A.","Microwave methods for the synthesis of paddlewheel diruthenium compounds with N,N-donor ligands","Green Chemistry","2011","13","7","1885","","10.1039/c0gc00800a","","","0.71073","MoKα","","0.2048","0.0778","","","0.2314","0.3492","","","","","","0.987","","","","has coordinates","180392","2020-10-21","18:00:00",""
"7206348","8.8589","0.0003","10.2068","0.0004","11.4469","0.0004","64.251","0.004","84.5","0.003","74.527","0.003","898.24","0.07","296","2","296","2","","","","","","","","3","P -1","-P 1","2","pyrrolo(2,1-a)quinoxaline'","","","- C25 H18 N2 -","- C25 H18 N2 -","- C50 H36 N4 -","2","1","","Rustagi, Vineeta; Aggarwal, Trapti; Verma, Akhilesh K.","Highly efficient Ag(i)-catalyzed regioselective tandem synthesis of diversely substituted quinoxalines and benzimidazoles in water","Green Chemistry","2011","13","7","1640","","10.1039/c1gc15346c","","","1.54184","CuKα","","0.0465","0.0419","","","0.1133","0.1171","","","","","","1.045","","","","has coordinates","180394","2020-10-21","18:00:00",""
"7206349","9.309","0.005","28.239","0.005","7.304","0.005","90","0.005","102.501","0.005","90","0.005","1874.5","1.7","296","2","296","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C25 H18 N2 -","- C25 H18 N2 -","- C100 H72 N8 -","4","1","","Rustagi, Vineeta; Aggarwal, Trapti; Verma, Akhilesh K.","Highly efficient Ag(i)-catalyzed regioselective tandem synthesis of diversely substituted quinoxalines and benzimidazoles in water","Green Chemistry","2011","13","7","1640","","10.1039/c1gc15346c","","","0.71073","MoKα","","0.046","0.0395","","","0.1043","0.109","","","","","","1.034","","","","has coordinates","180394","2020-10-21","18:00:00",""
"7206445","9.163","0.003","15.148","0.005","29.339","0.009","90","","90","","90","","4072","2","173","2","173","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C15 H27 Cl3 N4 O2 Pd -","- C15 H23 Cl3 N4 O2 Pd -","- C120 H184 Cl24 N32 O16 Pd8 -","8","1","","Zhou, Chunshan; Wang, Jinyun; Li, Liuyi; Wang, Ruihu; Hong, Maochun","A palladium chelating complex of ionic water-soluble nitrogen-containing ligand: the efficient precatalyst for Suzuki‒Miyaura reaction in water","Green Chemistry","2011","13","8","2100","","10.1039/c1gc15060j","","","0.71073","MoKα","","0.0436","0.0335","","","0.0973","0.1214","","","","","","1.156","","","","has coordinates","180395","2020-10-21","18:00:00",""
"7206446","13.4701","0.0015","3.835","0.0005","25.5","0.002","90","","117.94","0.002","90","","1163.7","0.2","298","2","298","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H7 Cl N2 O -","- C15 H7 Cl N2 O -","- C60 H28 Cl4 N8 O4 -","4","1","","Cheng, Chuang; Jiang, Bo; Tu, Shu-Jiang; Li, Guigen","[4+2+1] Domino cyclization in water for chemo- and regioselective synthesis of spiro-substituted benzo[b]furo[3,4-e][1,4]diazepine derivatives","Green Chemistry","2011","13","8","2107","","10.1039/c1gc15183e","","","0.71073","MoKα","","0.1814","0.1056","","","0.2202","0.2515","","","","","","1.084","","","","has coordinates","180395","2020-10-21","18:00:00",""
"7206447","14.9522","0.0015","18.8553","0.0019","7.6472","0.0006","90","","102.114","0.002","90","","2108","0.3","298","2","298","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H19 N O9 -","- C22 H19 N O9 -","- C88 H76 N4 O36 -","4","1","","Cheng, Chuang; Jiang, Bo; Tu, Shu-Jiang; Li, Guigen","[4+2+1] Domino cyclization in water for chemo- and regioselective synthesis of spiro-substituted benzo[b]furo[3,4-e][1,4]diazepine derivatives","Green Chemistry","2011","13","8","2107","","10.1039/c1gc15183e","","","0.71073","MoKα","","0.1682","0.0583","","","0.0681","0.0812","","","","","","1.014","","","","has coordinates","180395","2020-10-21","18:00:00",""
"7206448","14.9192","0.0014","8.4607","0.0008","34.445","0.003","90","","102.271","0.002","90","","4248.5","0.7","296","2","296","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C24 H60 N8 O24 P4 Zn3 -","- C24 H60 N8 O24 P4 Zn3 -","- C96 H240 N32 O96 P16 Zn12 -","4","0.5","","Huang, Yu-Ting; Lai, Yu-Lun; Lin, Chia-Her; Wang, Sue-Lein","Direct use of waste PET as unfailing source of organic reagents in the synthesis of intrinsic white/yellow luminescent nanoporous zincophosphates","Green Chemistry","2011","13","8","2000","","10.1039/c1gc15427c","","","0.71073","MoKα","","0.0618","0.0573","","","0.1422","0.1446","","","","","","1.21","","","","has coordinates","180395","2020-10-21","18:00:00",""
"7206449","15.0025","0.0005","8.6854","0.0003","30.5449","0.0011","90","","97.181","0.001","90","","3948.9","0.2","296","2","296","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C20 H52 N8 O22 P4 Zn3 -","- C20 H47 N8 O22 P4 Zn3 -","- C80 H188 N32 O88 P16 Zn12 -","4","0.5","","Huang, Yu-Ting; Lai, Yu-Lun; Lin, Chia-Her; Wang, Sue-Lein","Direct use of waste PET as unfailing source of organic reagents in the synthesis of intrinsic white/yellow luminescent nanoporous zincophosphates","Green Chemistry","2011","13","8","2000","","10.1039/c1gc15427c","","","0.71073","MoKα","","0.0617","0.0342","","","0.0623","0.0673","","","","","","0.836","","","","has coordinates,has disorder","180395","2020-10-21","18:00:00",""
"7206450","9.974","0.0005","9.1804","0.0005","27.5385","0.0017","90","","90","","90","","2521.6","0.2","295","2","295","2","","","","","","","","6","P n a 21","P 2c -2n","33","","","","- C21 H22 N2 O12 P2 Zn2 -","- C21 H22 N2 O12 P2 Zn2 -","- C84 H88 N8 O48 P8 Zn8 -","4","1","","Huang, Yu-Ting; Lai, Yu-Lun; Lin, Chia-Her; Wang, Sue-Lein","Direct use of waste PET as unfailing source of organic reagents in the synthesis of intrinsic white/yellow luminescent nanoporous zincophosphates","Green Chemistry","2011","13","8","2000","","10.1039/c1gc15427c","","","0.71073","MoKα","","0.0836","0.0537","","","0.108","0.1146","","","","","","1.042","","","","has coordinates","180395","2020-10-21","18:00:00",""
"7206451","27.6213","0.0012","9.1189","0.0004","9.9954","0.0005","90","","92.211","0.001","90","","2515.7","0.2","295","2","295","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C21 H22 N2 O12 P2 Zn2 -","- C21 H21 N2 O12 P2 Zn2 -","- C84 H84 N8 O48 P8 Zn8 -","4","1","","Huang, Yu-Ting; Lai, Yu-Lun; Lin, Chia-Her; Wang, Sue-Lein","Direct use of waste PET as unfailing source of organic reagents in the synthesis of intrinsic white/yellow luminescent nanoporous zincophosphates","Green Chemistry","2011","13","8","2000","","10.1039/c1gc15427c","","","0.71073","MoKα","","0.0623","0.0513","","","0.1324","0.1361","","","","","","1.191","","","","has coordinates","180395","2020-10-21","18:00:00",""
"7206452","10.8928","0.0002","8.7917","0.0001","27.7665","0.0004","90","","101.051","0.001","90","","2609.79","0.07","296","2","296","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C21 H34 N2 O12 P2 Zn2 -","- C21 H34 N2 O12 P2 Zn2 -","- C84 H136 N8 O48 P8 Zn8 -","4","1","","Huang, Yu-Ting; Lai, Yu-Lun; Lin, Chia-Her; Wang, Sue-Lein","Direct use of waste PET as unfailing source of organic reagents in the synthesis of intrinsic white/yellow luminescent nanoporous zincophosphates","Green Chemistry","2011","13","8","2000","","10.1039/c1gc15427c","","","0.71073","MoKα","","0.0529","0.036","","","0.0786","0.0949","","","","","","1.055","","","","has coordinates","180395","2020-10-21","18:00:00",""
"7206453","6.4801","0.0002","15.4593","0.0008","19.1885","0.0009","90","","90","","90","","1922.26","0.15","180","2","180","2","","","","","","","synthesis as described","4","P 21 21 21","P 2ac 2ab","19","","","","- C25 H22 N2 O2 -","- C25 H22 N2 O2 -","- C100 H88 N8 O8 -","4","1","","El Asri, Zhor; Génisson, Yves; Guillen, Frédéric; Baslé, Olivier; Isambert, Nicolas; del Mar Sanchez Duque, Maria; Ladeira, Sonia; Rodriguez, Jean; Constantieux, Thierry; Plaquevent, Jean-Christophe","Multicomponent reactions in ionic liquids: convenient and ecocompatible access to the 2,6-DABCO core","Green Chemistry","2011","13","9","2549","","10.1039/c1gc15635g","","x-ray","0.71073","MoKα","","0.0457","0.0342","","","0.0731","0.0778","","","","","","1.025","","","","has coordinates","180395","2020-10-21","18:00:00",""
"7206583","9.3488","0.0017","9.504","0.003","13.036","0.003","74.37","0.02","72.819","0.017","84.648","0.018","1065.5","0.5","293","2","293","2","","","","","","","","4","P -1","-P 1","2","4-(4-chlorophenyl)-6-(4-methylphenyl)-2,3,3a, 4-tetrahydro-1H- pyrido(3,2,1-jk)carbazole","4-(4-chlorophenyl)-6-(4-methylphenyl)-2,3,3a, 4-tetrahydro-1H-pyrido[3,2,1-jk]carbazole","","- C28 H24 Cl N -","- C28 H24 Cl N -","- C56 H48 Cl2 N2 -","2","1","","Chitra, Selvam; Paul, Nidhin; Muthusubramanian, Shanmugam; Manisankar, Paramasivam","A facile, water mediated, microwave-assisted synthesis of 4,6-diaryl-2,3,3a,4-tetrahydro-1H-pyrido[3,2,1-jk]carbazoles by a domino Fischer indole reaction‒intramolecular cyclization sequence","Green Chemistry","2011","13","10","2777","","10.1039/c1gc15483d","","","0.71073","MoKα","","0.06","0.0442","","","0.1374","0.1562","","","","","","1.05","","","","has coordinates","180396","2020-10-21","18:00:00",""
"7206768","14.081","0.0002","14.081","0.0002","27.303","0.0004","90","","90","","90","","5413.49","0.13","150","2","150","2","","","","","","","","4","I 41/a :2","-I 4ad","88","","","","- C11 H24 I N -","- C11 H24 I N -","- C176 H384 I16 N16 -","16","1","","Belhocine, Tayeb; Forsyth, Stewart A.; Gunaratne, H. Q. Nimal; Nieuwenhuyzen, Mark; Nockemann, Peter; Puga, Alberto V.; Seddon, Kenneth R.; Srinivasan, Geetha; Whiston, Keith","Azepanium ionic liquids","Green Chemistry","2011","13","11","3137","","10.1039/c1gc15189d","","","0.71073","MoKα","","0.0518","0.0347","","","0.0947","0.1224","","","","","","1.144","","","","has coordinates,has disorder","180398","2020-10-21","18:00:00",""
"7206769","9.7447","0.0015","10.72","0.002","21.453","0.004","90","","101.948","0.01","90","","2192.5","0.7","120","2","120","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C15 H28 F6 N2 O4 S2 -","- C15 H28 F6 N2 O4 S2 -","- C60 H112 F24 N8 O16 S8 -","4","1","","Belhocine, Tayeb; Forsyth, Stewart A.; Gunaratne, H. Q. Nimal; Nieuwenhuyzen, Mark; Nockemann, Peter; Puga, Alberto V.; Seddon, Kenneth R.; Srinivasan, Geetha; Whiston, Keith","Azepanium ionic liquids","Green Chemistry","2011","13","11","3137","","10.1039/c1gc15189d","","","0.71073","MoKα","","0.0851","0.0655","","","0.1558","0.1721","","","","","","1.028","","","","has coordinates,has disorder","180398","2020-10-21","18:00:00",""
"7206770","7.236","0.002","9.233","0.002","12.061","0.003","85.83","0.04","82.48","0.04","73.52","0.04","765.5","0.4","298","2","298","2","","","","","","","","4","P -1","-P 1","2","","","","- C16 H19 N O4 -","- C16 H19 N O4 -","- C32 H38 N2 O8 -","2","1","","Choudhary, Garima; Peddinti, Rama Krishna","Introduction of a clean and promising protocol for the synthesis of β-amino-acrylates and 1,4-benzoheterocycles: an emerging innovation","Green Chemistry","2011","13","11","3290","","10.1039/c1gc15701a","","","0.71073","MoKα","","0.0701","0.0597","","","0.1436","0.1495","","","","","","1.154","","","","has coordinates","180398","2020-10-21","18:00:00",""
"7206771","7.9077","0.001","10.7341","0.0013","17.41","0.002","90","","93.758","0.001","90","","1474.6","0.3","296","2","296","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C18 H16 O3 -","- C18 H16 O3 -","- C72 H64 O12 -","4","1","","Fan, Xuesen; He, Yan; Cui, Liangyan; Zhang, Xinying; Wang, Jianji","Tandem reaction of 1,2-allenic ketone with α-halo ketone or α-halo ester in water: an efficient and sustainable synthesis of 1,3,4′-tricarbonyl compounds","Green Chemistry","2011","13","11","3218","","10.1039/c1gc15707h","","","0.71073","MoKα","","0.0471","0.0379","","","0.109","0.1189","","","","","","1.05","","","","has coordinates","180398","2020-10-21","18:00:00",""
"7206772","10.5755","0.0004","22.6797","0.0009","8.8593","0.0004","90","","100.329","0.004","90","","2090.46","0.15","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C27 H16 F N3 O2 -","- C27 H16 F N3 O2 -","- C108 H64 F4 N12 O8 -","4","1","","Michael Rajesh, Stephen; Bala, Balasubramanian Devi; Perumal, Subbu; Menéndez, J. Carlos","l-Proline-catalysed sequential four-component “on water” protocol for the synthesis of structurally complex heterocyclic ortho-quinones","Green Chemistry","2011","13","11","3248","","10.1039/c1gc15794a","","","0.71073","MoKα","","0.1464","0.0696","","","0.1789","0.2284","","","","","","1.045","","","","has coordinates","180398","2020-10-21","18:00:00",""
"7207279","31.97","0.04","6.334","0.009","20.49","0.03","90","","120.078","0.013","90","","3590","9","150","2","150","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C17 H12 O5.5 Zn -","- C17 H9 O4 Zn -","- C136 H72 O32 Zn8 -","8","1","","Ibarra, Ilich A.; Bayliss, Peter A.; Pérez, Eduardo; Yang, Sihai; Blake, Alexander J.; Nowell, Harriott; Allan, David R.; Poliakoff, Martyn; Schröder, Martin","Near-critical water, a cleaner solvent for the synthesis of a metal‒organic framework","Green Chemistry","2012","14","1","117","","10.1039/c1gc15726d","","","0.6889","synchrotron","","0.194","0.137","","","0.348","0.409","","","","","","1.13","","","","has coordinates","180403","2020-10-21","18:00:00",""
"7207280","9.7477","0.0005","11.3212","0.0006","12.8467","0.0007","72.948","0.001","88.665","0.001","65.903","0.001","1229.69","0.11","100","2","100","2","","","","","","","","7","P -1","-P 1","2","","","","- C26.5 H27 Cl2 N O P Rh -","- C26.5 H27 Cl2 N O P Rh -","- C53 H54 Cl4 N2 O2 P2 Rh2 -","2","1","","Makhubela, Banothile C. E.; Jardine, Anwar; Smith, Gregory S.","Rh(i) complexes supported on a biopolymer as recyclable and selective hydroformylation catalysts","Green Chemistry","2012","14","2","338","","10.1039/c1gc15979h","","","0.71073","MoKα","","0.0288","0.0243","","","0.059","0.0612","","","","","","1.041","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7207690","10.3969","0.0004","10.3969","0.0004","28.4886","0.0015","90","","90","","120","","2666.9","0.2","180","2","180","2","","","","","","","","3","R -3 :H","-R 3","148","","","","- C15 H33 N3 -","- C15 H33 N3 -","- C90 H198 N18 -","6","0.333333","","Mercer, Sean M.; Robert, Tobias; Dixon, Daniel V.; Chen, Chien-Shun; Ghoshouni, Zahra; Harjani, Jitendra R.; Jahangiri, Soran; Peslherbe, Gilles H.; Jessop, Philip G.","Design, synthesis, and solution behaviour of small polyamines as switchable water additives","Green Chemistry","2012","14","3","832","","10.1039/c2gc16240g","","","0.71073","MoKα","","0.0636","0.0482","","","0.1314","0.1464","","","","","","1.053","","","","has coordinates,has disorder","180407","2020-10-21","18:00:00",""
"7207691","8.096","0.003","8.432","0.003","14.387","0.006","85.32","0.018","88.539","0.019","62.728","0.01","870","0.6","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C20 H18 N2 O3 S -","- C20 H18 N2 O3 S -","- C40 H36 N4 O6 S2 -","2","1","","Wen, Li-Rong; Li, Zhao-Rui; Li, Ming; Cao, Han","Solvent-free and efficient synthesis of imidazo[1,2-a]pyridine derivatives via a one-pot three-component reaction","Green Chemistry","2012","14","3","707","","10.1039/c2gc16388h","","","0.71073","MoKα","","0.0546","0.0496","","","0.1179","0.1218","","","","","","1.095","","","","has coordinates","180407","2020-10-21","18:00:00",""
"7207692","10.4","0.001","12.165","0.0015","15.37","0.002","90","","90","","90","","1944.6","0.4","113","2","113","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","Spiro[cyclopentane-1,2'(1'<i>H</i>)-pyrido[2,3-<i>d</i>]pyrimidin]- 4'(3'<i>H</i>)-one","","- C11 H13 N3 O -","- C11 H13 N3 O -","- C88 H104 N24 O8 -","8","1","","Yang, Liupan; Shi, Daxin; Chen, Shu; Chai, Hongxin; Huang, Danfei; Zhang, Qi; Li, Jiarong","Microwave-assisted synthesis of 2,3-dihydropyrido[2,3-d]pyrimidin-4(1H)-ones catalyzed by DBU in aqueous medium","Green Chemistry","2012","14","4","945","","10.1039/c2gc16469h","","","0.71075","MoKα","","0.0427","0.0395","","","0.0999","0.1026","","","","","","1.049","","","","has coordinates","180407","2020-10-21","18:00:00",""
"7207693","10.591","0.003","12.359","0.003","9.116","0.003","90","","97.951","0.004","90","","1181.8","0.6","153","2","153","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C12 H14 Br N3 O -","- C12 H14 Br N3 O -","- C48 H56 Br4 N12 O4 -","4","1","","Yang, Liupan; Shi, Daxin; Chen, Shu; Chai, Hongxin; Huang, Danfei; Zhang, Qi; Li, Jiarong","Microwave-assisted synthesis of 2,3-dihydropyrido[2,3-d]pyrimidin-4(1H)-ones catalyzed by DBU in aqueous medium","Green Chemistry","2012","14","4","945","","10.1039/c2gc16469h","","","0.71073","MoKα","","0.0555","0.0345","","","0.0685","0.0739","","","","","","0.999","","","","has coordinates","198632","2020-10-21","18:00:00",""
"7207694","8.355","0.002","10.746","0.003","12.843","0.004","98.611","0.002","99.924","0.003","110.707","0.003","1034.3","0.5","153","2","153","2","","","","","","","","5","P -1","-P 1","2","","","","- C23 H28 Cl N3 O2 -","- C23 H28 Cl N3 O2 -","- C46 H56 Cl2 N6 O4 -","2","1","","Yang, Liupan; Shi, Daxin; Chen, Shu; Chai, Hongxin; Huang, Danfei; Zhang, Qi; Li, Jiarong","Microwave-assisted synthesis of 2,3-dihydropyrido[2,3-d]pyrimidin-4(1H)-ones catalyzed by DBU in aqueous medium","Green Chemistry","2012","14","4","945","","10.1039/c2gc16469h","","","0.71073","MoKα","","0.0662","0.0464","","","0.1083","0.116","","","","","","1.001","","","","has coordinates","198632","2020-10-21","18:00:00",""
"7207695","9.8188","0.0002","15.916","0.0003","13.4755","0.0003","90","","100.875","0.002","90","","2068.08","0.07","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C26 H17 Cl N2 O2 -","- C26 H17 Cl N2 O2 -","- C104 H68 Cl4 N8 O8 -","4","1","","Gunasekaran, Pethaiah; Balamurugan, Kamaraj; Sivakumar, Sathiyamoorthi; Perumal, Subbu; Menéndez, J. Carlos; Almansour, Abdulrahman I.","Domino reactions in water: diastereoselective synthesis of densely functionalized indolyldihydrofuran derivatives","Green Chemistry","2012","14","3","750","","10.1039/c2gc16517a","","","0.71073","MoKα","","0.0557","0.0451","","","0.1469","0.1598","","","","","","1.254","","","","has coordinates","180407","2020-10-21","18:00:00",""
"7207696","8.715","0.004","11.09","0.004","13.771","0.007","90","","90.303","0.006","90","","1330.9","1","293","","293","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C16 H18 N2 O -","- C16 H18 N2 O -","- C64 H72 N8 O4 -","4","1","","Jida, Mouhamad; Soueidan, Olivier-Mohamad; Deprez, Benoit; Laconde, Guillaume; Deprez-Poulain, Rebecca","Racemic and diastereoselective construction of indole alkaloids under solvent- and catalyst-free microwave-assisted Pictet‒Spengler condensation","Green Chemistry","2012","14","4","909","","10.1039/c2gc16596a","","","0.71073","MoKα","","0.113","0.0718","","0.1143","0.0602","0.0447","","","","","","1.051","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7207697","11.814","0.0005","21.2181","0.0011","14.6684","0.0006","90","","95.337","0.004","90","","3661","0.3","150","2","150","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C40 H58 Br2 N2 O -","- C40 H58 Br2 N2 O -","- C160 H232 Br8 N8 O4 -","4","1","","Doherty, Simon; Knight, Julian G.; Ellison, Jack R.; Weekes, David; Harrington, Ross W.; Hardacre, Christopher; Manyar, Haresh","An efficient recyclable peroxometalate-based polymer-immobilised ionic liquid phase (PIILP) catalyst for hydrogen peroxide-mediated oxidation","Green Chemistry","2012","14","4","925","","10.1039/c2gc16679h","","","0.71073","MoKα","","0.1057","0.0619","","","0.1392","0.1671","","","","","","1.025","","","","has coordinates","180407","2020-10-21","18:00:00",""
"7207893","9.394","0.003","9.114","0.002","16.558","0.004","90","","104.714","0.003","90","","1371.2","0.6","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H13 N O5 -","- C15 H13 N O5 -","- C60 H52 N4 O20 -","4","1","","Li, Jian; Liu, Yuejin; Li, Chunju; Jie, Haohua; Jia, Xueshun","Atom-economical synthesis of the functionalized spirocyclic oxindole-butenolide via three-component [2 + 2 + 1] cycloaddition strategy","Green Chemistry","2012","14","5","1314","","10.1039/c2gc00015f","","","0.71073","MoKα","","0.0502","0.0369","","","0.0893","0.0982","","","","","","1.058","","","","has coordinates","180409","2020-10-21","18:00:00",""
"7207894","8.897","0.011","12.592","0.016","13.863","0.017","99.404","0.016","108.029","0.017","95.241","0.018","1440","3","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C29 H33 Cl N2 O4 -","- C29 H33 Cl N2 O4 -","- C58 H66 Cl2 N4 O8 -","2","1","","Li, Jian; Liu, Yuejin; Li, Chunju; Jie, Haohua; Jia, Xueshun","Atom-economical synthesis of the functionalized spirocyclic oxindole-butenolide via three-component [2 + 2 + 1] cycloaddition strategy","Green Chemistry","2012","14","5","1314","","10.1039/c2gc00015f","","","0.71073","MoKα","","0.1203","0.0708","","","0.1741","0.2046","","","","","","1.036","","","","has coordinates","180409","2020-10-21","18:00:00",""
"7207895","24.11","0.01","17.011","0.009","33.45","0.02","90","","91.57","0.04","90","","13714","12","","","90","","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","1,3,5,7-tetrakis[4-(diacetoxyiodo)phenyl]adamantane","","- C50 H56 I4 O18 -","- C50 H52 I4 O18 -","- C400 H416 I32 O144 -","8","1","","Dohi, Toshifumi; Fukushima, Kei-ichiro; Kamitanaka, Tohru; Morimoto, Koji; Takenaga, Naoko; Kita, Yasuyuki","An excellent dual recycling strategy for the hypervalent iodine/nitroxyl radical mediated selective oxidation of alcohols to aldehydes and ketones","Green Chemistry","2012","14","5","1493","","10.1039/c2gc16632a","","","","","","0.097","0.067","","","","0.181","","","","","","","","","","has coordinates","180409","2020-10-21","18:00:00",""
"7207896","9.4865","0.0004","9.9343","0.0004","10.5514","0.0005","114.009","0.002","113.796","0.002","90.405","0.002","813.5","0.07","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C20 H19 N3 -","- C20 H19 N3 -","- C40 H38 N6 -","2","1","","Das, Paramita; Butcher, Ray J.; Mukhopadhyay, Chhanda","Zinc titanate nanopowder: an advanced nanotechnology based recyclable heterogeneous catalyst for the one-pot selective synthesis of self-aggregated low-molecular mass acceptor‒donor‒acceptor‒acceptor systems and acceptor‒donor‒acceptor triads","Green Chemistry","2012","14","5","1376","","10.1039/c2gc16641k","","","0.71073","MoKα","","0.0697","0.0506","","","0.1486","0.161","","","","","","1.29","","","","has coordinates","180409","2020-10-21","18:00:00",""
"7207897","25.1335","0.0006","12.37744","0.00018","13.4158","0.0003","90","","119.443","0.003","90","","3634.47","0.17","295","2","295","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C19 H15 N5 O2 -","- C19 H15 N5 O2 -","- C152 H120 N40 O16 -","8","1","","Das, Paramita; Butcher, Ray J.; Mukhopadhyay, Chhanda","Zinc titanate nanopowder: an advanced nanotechnology based recyclable heterogeneous catalyst for the one-pot selective synthesis of self-aggregated low-molecular mass acceptor‒donor‒acceptor‒acceptor systems and acceptor‒donor‒acceptor triads","Green Chemistry","2012","14","5","1376","","10.1039/c2gc16641k","","","1.54184","CuKα","","0.0543","0.0445","","","0.1163","0.125","","","","","","1.042","","","","has coordinates","180409","2020-10-21","18:00:00",""
"7207898","20.561","0.002","7.228","0.0008","24.638","0.003","90","","112.873","0.001","90","","3373.7","0.6","296","2","296","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C20 H14 N4 -","- C20 H14 N4 -","- C160 H112 N32 -","8","2","","Das, Paramita; Butcher, Ray J.; Mukhopadhyay, Chhanda","Zinc titanate nanopowder: an advanced nanotechnology based recyclable heterogeneous catalyst for the one-pot selective synthesis of self-aggregated low-molecular mass acceptor‒donor‒acceptor‒acceptor systems and acceptor‒donor‒acceptor triads","Green Chemistry","2012","14","5","1376","","10.1039/c2gc16641k","","","0.71073","MoKα","","0.0746","0.0457","","","0.1508","0.2011","","","","","","0.683","","","","has coordinates","180409","2020-10-21","18:00:00",""
"7207899","11.7899","0.0003","14.3124","0.0005","14.5079","0.0004","64.617","0.001","78.242","0.001","76.142","0.001","2133.06","0.11","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C24 H20 N4 O2 -","- C24 H20 N4 O2 -","- C96 H80 N16 O8 -","4","2","","Das, Paramita; Butcher, Ray J.; Mukhopadhyay, Chhanda","Zinc titanate nanopowder: an advanced nanotechnology based recyclable heterogeneous catalyst for the one-pot selective synthesis of self-aggregated low-molecular mass acceptor‒donor‒acceptor‒acceptor systems and acceptor‒donor‒acceptor triads","Green Chemistry","2012","14","5","1376","","10.1039/c2gc16641k","","","0.71073","MoKα","","0.0877","0.0514","","","0.1385","0.1578","","","","","","1.166","","","","has coordinates","180409","2020-10-21","18:00:00",""
"7208024","4.25566","0.0001","10.2167","0.0002","12.2711","0.0003","90","","90","","90","","533.53","0.02","100","","100","","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","2,4,7-trioxa-3-oxy-bicyclo[3.3.0]octane","","- C5 H6 O4 -","- C5 H6 O4 -","- C20 H24 O16 -","4","1","","Tomczyk, Karolina M.; Guńka, Piotr A.; Parzuchowski, Paweł G.; Zachara, Janusz; Rokicki, Gabriel","Intramolecular etherification of five-membered cyclic carbonates bearing hydroxyalkyl groups","Green Chemistry","2012","14","6","1749","","10.1039/c2gc35265f","","","1.5418","CuKα","","0.0236","0.0225","","","0.0574","0.0587","","","","","","1.062","","","","has coordinates","180411","2020-10-21","18:00:00",""
"7208025","7.9412","0.0002","10.0129","0.0003","10.831","0.0003","90","","90","","90","","861.22","0.04","100","","100","","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","6-(1,3-dioxolan-2-one-4-yl)-2,4,7-trioxa-3-oxy-bicyclo[3.3.0]octane","","- C8 H8 O7 -","- C8 H8 O7 -","- C32 H32 O28 -","4","1","","Tomczyk, Karolina M.; Guńka, Piotr A.; Parzuchowski, Paweł G.; Zachara, Janusz; Rokicki, Gabriel","Intramolecular etherification of five-membered cyclic carbonates bearing hydroxyalkyl groups","Green Chemistry","2012","14","6","1749","","10.1039/c2gc35265f","","","0.71073","MoKα","","0.0317","0.0276","","","0.0608","0.0632","","","","","","1.059","","","","has coordinates","180411","2020-10-21","18:00:00",""
"7208130","12.142","0.002","10.509","0.002","13.907","0.003","90","","106.101","0.004","90","","1704.9","0.6","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C18 H14 Ag N5 O5 -","- C18 H14 Ag N5 O5 -","- C72 H56 Ag4 N20 O20 -","4","1","","Sheykhan, Mehdi; Rashidi Ranjbar, Zohreh; Morsali, Ali; Heydari, Akbar","Minimisation of E-Factor in the synthesis of N-hydroxylamines: the role of silver(i)-based coordination polymers","Green Chemistry","2012","14","7","1971","","10.1039/c2gc35076a","","","0.71073","MoKα","","0.0977","0.0421","","","0.0763","0.0956","","","","","","0.985","","","","has coordinates","180412","2020-10-21","18:00:00",""
"7208131","13.6247","0.0014","8.6852","0.0008","17.0833","0.0019","90","","112.949","0.002","90","","1861.5","0.3","273","2","273","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C21 H18 F3 N O4 -","- C21 H18 F3 N O4 -","- C84 H72 F12 N4 O16 -","4","1","","Reddy, T. Ram; Reddy, L. Srinivasula; Reddy, G. Rajeshwar; Yarbagi, Kaviraj; Lingappa, Y.; Rambabu, D.; Krishna, G. Rama; Reddy, C. Malla; Kumar, K. Shiva; Pal, Manojit","Construction of a quinoline ring via a 3-component reaction in water: crystal structure analysis and H-bonding patterns of a 2-aryl quinoline","Green Chemistry","2012","14","7","1870","","10.1039/c2gc35256g","","","0.71073","MoKα","","0.0582","0.0394","","","0.0906","0.1007","","","","","","1.025","","","","has coordinates","180412","2020-10-21","18:00:00",""
"7208410","11.373","0.002","11.8524","0.0015","13.975","0.002","95.484","0.012","112.666","0.017","91.976","0.013","1725.1","0.5","298","2","298","2","","","","","","","","5","P -1","-P 1","2","","","","- C34 H28 Cl6 N2 O5 -","- C34 H28 Cl6 N2 O5 -","- C68 H56 Cl12 N4 O10 -","2","1","","Khurana, Jitender M.; Chaudhary, Ankita; Lumb, Anshika; Nand, Bhaskara","An expedient four-component domino protocol for the synthesis of novel benzo[a]phenazine annulated heterocycles and their photophysical studies","Green Chemistry","2012","14","8","2321","","10.1039/c2gc35644a","","","0.71073","MoKα","","0.1296","0.0871","","","0.2353","0.2639","","","","","","1.055","","","","has coordinates","180415","2020-10-21","18:00:00",""
"7208597","14.933","0.0016","14.933","0.0016","12.2771","0.0016","90","","90","","90","","2737.7","0.5","296","2","296","2","","","","","","","","4","I 41","I 4bw","80","","","","- C15 H13 N2 S -","- C15 H13 N2 S -","- C120 H104 N16 S8 -","8","1","","Rout, Saroj Kumar; Guin, Srimanta; Nath, Jayashree; Patel, Bhisma K.","An “on-water” exploration of CuO nanoparticle catalysed synthesis of 2-aminobenzothiazoles","Green Chemistry","2012","14","9","2491","","10.1039/c2gc35575b","","","0.71073","MoKα","","0.0641","0.0553","","","0.1214","0.1302","","","","","","1.019","","","","has coordinates","180416","2020-10-21","18:00:00",""
"7208598","10.13","0.002","8.1511","0.0015","13.6","0.002","90","","93.902","0.01","90","","1120.4","0.3","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C11 H12 N2 S2 -","- C11 H12 N2 S2 -","- C44 H48 N8 S8 -","4","1","","Rout, Saroj Kumar; Guin, Srimanta; Nath, Jayashree; Patel, Bhisma K.","An “on-water” exploration of CuO nanoparticle catalysed synthesis of 2-aminobenzothiazoles","Green Chemistry","2012","14","9","2491","","10.1039/c2gc35575b","","","0.71073","MoKα","","0.0469","0.0379","","","0.1007","0.1069","","","","","","1.07","","","","has coordinates","180416","2020-10-21","18:00:00",""
"7208599","10.493","0.0002","14.6391","0.0004","9.0779","0.0002","90","","113.021","0.001","90","","1283.39","0.05","180","2","180","2","","","","","","","","5","C 1 c 1","C -2yc","9","N-(4-methoxyphenyl)-N'-(piperidino)thiourea","N-(4-methoxyphenyl)-N'-(piperidino)thiourea","","- C13 H18 N2 O S -","- C13 H18 N2 O S -","- C52 H72 N8 O4 S4 -","4","1","","Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav","A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents","Green Chemistry","2012","14","9","2462","","10.1039/c2gc35799b","","","0.7107","MoKα","","0.0655","0.0441","","","0.1048","0.1198","","","","","","1.121","","","","has coordinates","180416","2020-10-21","18:00:00",""
"7208600","11.5813","0.0003","9.3856","0.0003","10.8926","0.0004","90","","101.21","0.03","90","","1161.41","0.14","180","2","180","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","N-phenyl-N'-(thiomorpholino)thiourea","N-phenyl-N'-(thiomorpholino)thiourea","","- C11 H14 N2 S2 -","- C11 H14 N2 S2 -","- C44 H56 N8 S8 -","4","1","","Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav","A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents","Green Chemistry","2012","14","9","2462","","10.1039/c2gc35799b","","","0.71073","MoKα","","0.0773","0.0472","","","0.0987","0.1109","","","","","","1.029","","","","has coordinates","180417","2020-10-21","18:00:00",""
"7208601","8.3457","0.0001","26.4224","0.0002","5.3071","0.0006","90","","90","","90","","1170.29","0.13","180","2","180","2","","","","","","","","5","P n m a","-P 2ac 2n","62","N,N'-bis(4-fluorophenyl)thiourea","N,N'-bis(4-fluorophenyl)thiourea","","- C13 H10 F2 N2 S -","- C13 H10 F2 N2 S -","- C52 H40 F8 N8 S4 -","4","0.5","","Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav","A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents","Green Chemistry","2012","14","9","2462","","10.1039/c2gc35799b","","","0.71073","MoKα","","0.0559","0.0364","","","0.0856","0.0924","","","","","","1.065","","","","has coordinates","180417","2020-10-21","18:00:00",""
"7208602","10.2252","0.0002","10.5172","0.0003","11.1949","0.0002","90","","90.788","0.002","90","","1203.79","0.05","180","2","180","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","N-(4-nitrophenyl)-N'-(morpholino)thiourea","N-(4-nitrophenyl)-N'-(morpholino)thiourea","","- C11 H13 N3 O3 S -","- C11 H13 N3 O3 S -","- C44 H52 N12 O12 S4 -","4","1","","Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav","A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents","Green Chemistry","2012","14","9","2462","","10.1039/c2gc35799b","","","0.71073","MoKα","","0.0462","0.033","","","0.0957","0.098","","","","","","1.021","","","","has coordinates","180417","2020-10-21","18:00:00",""
"7208603","21.2213","0.001","8.0908","0.0004","28.6471","0.0015","90","","90","","90","","4918.6","0.4","291","2","291","2","","","","","","","","5","P c a 21","P 2c -2ac","29","N-(4-nitrophenyl)-N'-(morpholino)thiourea","N-(4-nitrophenyl)-N'-(morpholino)thiourea","","- C11 H13 N3 O3 S -","- C11 H13 N3 O3 S -","- C176 H208 N48 O48 S16 -","16","4","","Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav","A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents","Green Chemistry","2012","14","9","2462","","10.1039/c2gc35799b","","","0.71073","MoKα","","0.1498","0.0471","","","0.0911","0.1249","","","","","","1.008","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7208604","12.67213","0.00025","9.79731","0.00027","12.10093","0.00031","90","","115.223","0.0014","90","","1359.12","0.06","293","","293","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H16 N2 S -","- C15 H16 N2 S -","- C60 H64 N8 S4 -","4","1","","Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav","A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents","Green Chemistry","2012","14","9","2462","","10.1039/c2gc35799b","powder diffraction","","1.54059","CuKα_1","","","","","","","","0.0123","","0.571","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7208605","28.4936","0.0024","5.55569","0.00033","8.14303","0.00038","90","","90.7479","0.0043","90","","1288.94","0.15","293","","293","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C14 H14 N2 O S -","- C14 H14 N2 O S -","- C56 H56 N8 O4 S4 -","4","1","","Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav","A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents","Green Chemistry","2012","14","9","2462","","10.1039/c2gc35799b","powder diffraction","","1.54059","CuKα_1","","","","","","","","0.0202","","0.975","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7208606","14.50439","0.00092","13.62318","0.00093","7.14076","0.00026","90","","90","","90","","1410.99","0.14","293","","293","","","","","","","","","5","P n a 21","P 2c -2n","33","","","","- C14 H13 N3 O2 S -","- C14 H13 N3 O2 S -","- C56 H52 N12 O8 S4 -","4","1","","Štrukil, Vjekoslav; Igrc, Marina D.; Fábián, László; Eckert-Maksić, Mirjana; Childs, Scott L.; Reid, David G.; Duer, Melinda J.; Halasz, Ivan; Mottillo, Cristina; Friščić, Tomislav","A model for a solvent-free synthetic organic research laboratory: click-mechanosynthesis and structural characterization of thioureas without bulk solvents","Green Chemistry","2012","14","9","2462","","10.1039/c2gc35799b","powder diffraction","","1.54059","CuKα_1","","","","","","","","0.0174","","0.732","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7208607","10.8539","0.0003","11.5075","0.0004","12.5661","0.0004","97.508","0.002","102.88","0.002","113.095","0.002","1365.14","0.08","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C31 H25 Br F N O7 -","- C31 H25 Br F N O7 -","- C62 H50 Br2 F2 N2 O14 -","2","1","","Devi Bala, Balasubramanian; Michael Rajesh, Stephen; Perumal, Subbu","An eco-friendly sequential catalyst- and solvent-free four-component stereoselective synthesis of novel 1,4-pyranonaphthoquinones","Green Chemistry","2012","14","9","2484","","10.1039/c2gc35930h","","","0.71073","MoKα","","0.0773","0.0467","","","0.1145","0.1289","","","","","","1.027","","","","has coordinates","180417","2020-10-21","18:00:00",""
"7208841","10.788","0.0005","16.5308","0.0008","7.1104","0.0003","90","","106.861","0.001","90","","1213.52","0.1","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C11 H10 N2 O5 S -","- C11 H10 N2 O5 S -","- C44 H40 N8 O20 S4 -","4","1","","Paladhi, Sushovan; Chauhan, Ajay; Dhara, Kalyan; Tiwari, Ashwani Kumar; Dash, Jyotirmayee","An uncatalyzed aldol reaction of thiazolidinediones","Green Chemistry","2012","14","11","2990","","10.1039/c2gc35819k","","","0.71073","MoKα","","0.0328","0.029","","","0.0754","0.0787","","","","","","1.069","","","","has coordinates","180419","2020-10-21","18:00:00",""
"7208842","20.804","0.002","11.9934","0.0014","10.9684","0.0011","90","","102.666","0.002","90","","2670.1","0.5","100","","100","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C8 H6 Br2 N2 O4 S2 -","- C8 H6 Br2 N2 O4 S2 -","- C64 H48 Br16 N16 O32 S16 -","8","2","","Paladhi, Sushovan; Chauhan, Ajay; Dhara, Kalyan; Tiwari, Ashwani Kumar; Dash, Jyotirmayee","An uncatalyzed aldol reaction of thiazolidinediones","Green Chemistry","2012","14","11","2990","","10.1039/c2gc35819k","","","0.71073","MoKα","","0.0913","0.084","","","0.2092","0.2132","","","","","","1.149","","","","has coordinates","180419","2020-10-21","18:00:00",""
"7208843","17.188","0.005","14.671","0.005","17.44","0.005","90","0.005","93.406","0.005","90","0.005","4390","2","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C27 H22 N2 O4 -","- C27 H22 N2 O4 -","- C216 H176 N16 O32 -","8","2","","Ghosh, Partha Pratim; Pal, Gargi; Paul, Sanjay; Das, Asish R.","Design and synthesis of benzylpyrazolyl coumarin derivatives via a four-component reaction in water: investigation of the weak interactions accumulating in the crystal structure of a signified compound","Green Chemistry","2012","14","10","2691","","10.1039/c2gc36021g","","","0.71073","MoKα","","0.167","0.129","","","0.3723","0.3982","","","","","","1.076","","","","has coordinates","180419","2020-10-21","18:00:00",""
"7208844","10.017","0.005","7.789","0.004","27.003","0.015","90","","95.507","0.008","90","","2097.1","1.9","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","trans-3-(2,4-Dichlorophenyl)-2-(4-fluorobenzoyl)- 5-methyl-3,5-dihydrofuro-[3,2-c]quinolin-4(2H)-one","trans-3-(2,4-Dichlorophenyl)-2-(4-fluorobenzoyl)- 5-methyl-3,5-dihydrofuro-[3,2-c]quinolin-4(2H)-one","","- C25 H16 Cl2 F N O3 -","- C25 H16 Cl2 F N O3 -","- C100 H64 Cl8 F4 N4 O12 -","4","1","","Indumathi, Sethuraman; Perumal, Subbu; Anbananthan, Natarajan","A facile eco-friendly three-component protocol for the regio- and stereoselective synthesis of functionalized trans-dihydrofuro[3,2-c]-quinolin-4(2H)-ones","Green Chemistry","2012","14","12","3361","","10.1039/c2gc36040c","","","0.71073","MoKα","","0.1226","0.079","","","0.1823","0.2072","","","","","","1.09","","","","has coordinates","180419","2020-10-21","18:00:00",""
"7208845","10.8016","0.0004","23.0207","0.0005","9.9117","0.0003","90","","111.566","0.004","90","","2292.11","0.14","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","(3aS,3cS,6aR,7S,9S,9aR)-methyl 2,5-diethyl-7,9-di(furan-2-yl)- 1,3,4,6-tetraoxododecahydro-1H-dipyrrolo[3,4-a:3',4'-f] pyrrolizine-3b-carboxylate","","- C25 H25 N3 O8 -","- C25 H25 N3 O8 -","- C100 H100 N12 O32 -","4","1","","Lu, Qing; Song, Gonghua; Jasinski, Jerry P.; Keeley, Amanda C.; Zhang, Wei","One-pot double [3 + 2] cycloaddition for diastereoselective synthesis of tetracyclic pyrrolidine compounds","Green Chemistry","2012","14","11","3010","","10.1039/c2gc36066g","","","1.54178","CuKα","","0.0756","0.0537","","","0.1484","0.1588","","","","","","1.067","","","","has coordinates","180419","2020-10-21","18:00:00",""
"7208846","11.5934","0.0004","23.9267","0.0007","12.5474","0.0005","90","","116.043","0.004","90","","3127.1","0.2","173","2","173","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C28 H28 Cl2 N4 O8 S -","- C28 H28 Cl2 N4 O8 S -","- C112 H112 Cl8 N16 O32 S4 -","4","1","","Lu, Qing; Song, Gonghua; Jasinski, Jerry P.; Keeley, Amanda C.; Zhang, Wei","One-pot double [3 + 2] cycloaddition for diastereoselective synthesis of tetracyclic pyrrolidine compounds","Green Chemistry","2012","14","11","3010","","10.1039/c2gc36066g","","","1.5418","CuKα","","0.0608","0.0526","","","0.1436","0.151","","","","","","1.045","","","","has coordinates","180419","2020-10-21","18:00:00",""
"7208847","7.2406","0.0014","6.3111","0.0011","16.211","0.003","90","","98.719","0.007","90","","732.2","0.2","173","2","173","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C13 H7 F4 I N4 O2 -","- C13 H7 F4 I N4 O2 -","- C26 H14 F8 I2 N8 O4 -","2","1","","Chen, Hao; Ni, Ben-Bo; Gao, Fan; Ma, Yuguo","Pressure-accelerated copper-free cycloaddition of azide and alkyne groups pre-organized in the crystalline state at room temperature","Green Chemistry","2012","14","10","2703","","10.1039/c2gc36069a","","","0.71073","MoKα","","0.0265","0.0261","","","0.0618","0.0621","","","","","","1.051","","","","has coordinates","180419","2020-10-21","18:00:00",""
"7208848","5.7206","0.0011","10.897","0.002","12.306","0.003","86.6","0.03","84.86","0.03","80.87","0.03","753.6","0.3","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C15 H10 F4 N4 O3 -","- C15 H10 F4 N4 O3 -","- C30 H20 F8 N8 O6 -","2","1","","Chen, Hao; Ni, Ben-Bo; Gao, Fan; Ma, Yuguo","Pressure-accelerated copper-free cycloaddition of azide and alkyne groups pre-organized in the crystalline state at room temperature","Green Chemistry","2012","14","10","2703","","10.1039/c2gc36069a","","","0.71073","MoKα","","0.0604","0.0532","","","0.1303","0.136","","","","","","1.098","","","","has coordinates","180419","2020-10-21","18:00:00",""
"7208849","9.5984","0.0004","9.3308","0.0007","14.7806","0.0012","90","","100.934","0.004","90","","1299.73","0.15","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H14 F N O2 -","- C16 H14 F N O2 -","- C64 H56 F4 N4 O8 -","4","1","","Griesbeck, Axel G.; Nazarov, Nestor; Neudörfl, Jörg M.; Heffen, Maria","Intermolecular photodecarboxylation of electron-deficient substrates by phthalimides in water: efficiency, selectivity and online monitoring","Green Chemistry","2012","14","11","3004","","10.1039/c2gc36089f","","","0.71073","MoKα","","0.0723","0.0407","","","0.087","0.0951","","","","","","0.998","","","","has coordinates","180419","2020-10-21","18:00:00",""
"7208850","15.6286","0.001","8.625","0.0007","10.8601","0.0005","90","","96.661","0.004","90","","1454.02","0.16","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C17 H14 F3 N O2 -","- C17 H14 F3 N O2 -","- C68 H56 F12 N4 O8 -","4","1","","Griesbeck, Axel G.; Nazarov, Nestor; Neudörfl, Jörg M.; Heffen, Maria","Intermolecular photodecarboxylation of electron-deficient substrates by phthalimides in water: efficiency, selectivity and online monitoring","Green Chemistry","2012","14","11","3004","","10.1039/c2gc36089f","","","0.71073","MoKα","","0.0673","0.0406","","","0.0946","0.1025","","","","","","1.049","","","","has coordinates","180419","2020-10-21","18:00:00",""
"7208851","8.5482","0.001","10.7471","0.0012","9.6662","0.0011","90","","90","","90","","888.02","0.18","296","2","296","2","","","","","","","","3","P c a 21","P 2c -2ac","29","","","","- C10 H10 N2 -","- C10 H10 N2 -","- C40 H40 N8 -","4","1","","Zhang, Chun; Zhang, Liangren; Jiao, Ning","Catalyst free approach to benzimidazoles using air as the oxidant at room temperature","Green Chemistry","2012","14","12","3273","","10.1039/c2gc36416f","","","0.71073","MoKα","","0.0583","0.0475","","","0.1148","0.1237","","","","","","1.073","","","","has coordinates","180419","2020-10-21","18:00:00",""
"7209200","5.955","0.003","7.46","0.003","19.878","0.008","90","","90","","90","","883.1","0.7","93.1","","","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C10 H11 N O2 -","- C10 H11 N O2 -","- C40 H44 N4 O8 -","4","1","","Ueno, Atsushi; Kayaki, Yoshihito; Ikariya, Takao","Cycloaddition of tertiary aziridines and carbon dioxide using a recyclable organocatalyst, 1,3-di-tert-butylimidazolium-2-carboxylate: straightforward access to 3-substituted 2-oxazolidones","Green Chemistry","2013","15","2","425","","10.1039/c2gc36414j","","","0.7107","MoKα","","","0.0299","","","","0.0924","","","","","","1","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7209250","20.8671","0.0008","10.4343","0.0004","18.53","0.0007","90","","101.947","0.002","90","","3947.2","0.3","100","2","100","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","XST-FG-3","","","- C25 H20 N2 O2 -","- C25 H20 N2 O2 -","- C200 H160 N16 O16 -","8","1","","Xu, Shengtao; Zhou, Yu; Xu, Jinyi; Jiang, Hualiang; Liu, Hong","Gold-catalyzed Michael addition/intramolecular annulation cascade: an effective pathway for the chemoselective- and regioselective synthesis of tetracyclic indole derivatives in water","Green Chemistry","2013","15","3","718","","10.1039/c2gc36301a","","","0.71073","MoKα","","0.0419","0.0383","","","0.102","0.1051","","","","","","1.043","","","","has coordinates","180423","2020-10-21","18:00:00",""
"7209293","16.9","0.02","27.54","0.03","8.179","0.01","90","","90","","90","","3807","8","293","2","293","2","","","","","","","","6","P n m a","-P 2ac 2n","62","","","","- C37 H56 Cu I N4 O2 -","- C37 H56 Cu I N4 O2 -","- C148 H224 Cu4 I4 N16 O8 -","4","0.5","","Wang, Wenlong; Zhang, Guodong; Lang, Rui; Xia, Chungu; Li, Fuwei","pH-Responsive N-heterocyclic carbene copper(i) complexes: syntheses and recoverable applications in the carboxylation of arylboronic esters and benzoxazole with carbon dioxide","Green Chemistry","2013","15","3","635","","10.1039/c3gc36830k","","","0.71073","MoKα","","0.182","0.1183","","","0.261","0.2871","","","","","","1.112","","","","has coordinates","180423","2020-10-21","18:00:00",""
"7209840","7.4617","0.0015","7.5189","0.0018","9.84","0.002","109.76","0.02","90.103","0.017","90.706","0.018","519.5","0.2","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C10 H8 N2 O S2 -","- C10 H8 N2 O S2 -","- C20 H16 N4 O2 S4 -","2","1","","Singh, Maya Shankar; Nagaraju, Anugula; Verma, Girijesh Kumar; Shukla, Gaurav; Verma, Rajiv Kumar; Srivastava, Abhijeet; Raghuvanshi, Keshav","Eco-efficient, regioselective and rapid access to 4,5-disubstituted 1,2,3-thiadiazoles via [3 + 2] cycloaddition of α-enolicdithioesters with tosyl azide under solvent-free conditions","Green Chemistry","2013","15","4","954","","10.1039/c3gc37047j","","","0.71073","MoKα","","0.0637","0.0426","","","0.0991","0.1154","","","","","","1.024","","","","has coordinates","211196","2020-10-21","18:00:00",""
"7209841","8.0015","0.0006","8.1903","0.0006","9.1812","0.0006","85.565","0.005","75.327","0.006","86.509","0.006","579.79","0.07","293","2","293","2","","","","","","","","5","P -1","-P 1","2","C11H10N2O2S2","","","- C11 H10 N2 O2 S2 -","- C11 H10 N2 O2 S2 -","- C22 H20 N4 O4 S4 -","2","1","","Singh, Maya Shankar; Nagaraju, Anugula; Verma, Girijesh Kumar; Shukla, Gaurav; Verma, Rajiv Kumar; Srivastava, Abhijeet; Raghuvanshi, Keshav","Eco-efficient, regioselective and rapid access to 4,5-disubstituted 1,2,3-thiadiazoles via [3 + 2] cycloaddition of α-enolicdithioesters with tosyl azide under solvent-free conditions","Green Chemistry","2013","15","4","954","","10.1039/c3gc37047j","","","0.71073","MoKα","","0.0678","0.0453","","","0.1078","0.1238","","","","","","1.016","","","","has coordinates","180429","2020-10-21","18:00:00",""
"7209842","9.5564","0.0013","16.83","0.002","7.9596","0.001","90","","98.532","0.001","90","","1266","0.3","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C16 H12 N2 O -","- C16 H12 N2 O -","- C64 H48 N8 O4 -","4","1","","Shen, Shao-Chun; Sun, Xing-Wen; Lin, Guo-Qiang","An eco-benign and highly efficient access to 3-heterocyclic-substituted isoindolinones in ammonia water","Green Chemistry","2013","15","4","896","","10.1039/c3gc40162f","","","0.71073","MoKα","","0.056","0.0399","","","0.0983","0.11","","","","","","1.031","","","","has coordinates","180429","2020-10-21","18:00:00",""
"7210021","5.569","0.002","24.721","0.01","13.606","0.006","90","","101.183","0.005","90","","1837.6","1.3","296","2","296","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C21 H18 Br N O S -","- C21 H18 Br N O S -","- C84 H72 Br4 N4 O4 S4 -","4","1","","Ray, Suman; Brown, Mike; Bhaumik, Asim; Dutta, Arghya; Mukhopadhyay, Chhanda","A new MCM-41 supported HPF6 catalyst for the library synthesis of highly substituted 1,4-dihydropyridines and oxidation to pyridines: report of one-dimensional packing towards LMSOMs and studies on their photophysical properties","Green Chemistry","2013","15","7","1910","","10.1039/c3gc40441b","","","0.71073","MoKα","","0.1003","0.0703","","","0.1894","0.2097","","","","","","1.027","","","","has coordinates","180431","2020-10-21","18:00:00",""
"7210022","19.1534","0.001","10.4617","0.0005","12.4228","0.0006","90","","104.23","0.002","90","","2412.9","0.2","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C29 H26 N2 O3 -","- C29 H26 N2 O3 -","- C116 H104 N8 O12 -","4","1","","Ray, Suman; Brown, Mike; Bhaumik, Asim; Dutta, Arghya; Mukhopadhyay, Chhanda","A new MCM-41 supported HPF6 catalyst for the library synthesis of highly substituted 1,4-dihydropyridines and oxidation to pyridines: report of one-dimensional packing towards LMSOMs and studies on their photophysical properties","Green Chemistry","2013","15","7","1910","","10.1039/c3gc40441b","","","0.71073","MoKα","","0.0935","0.0517","","","0.1301","0.1553","","","","","","0.993","","","","has coordinates","180431","2020-10-21","18:00:00",""
"7210023","16.0558","0.0004","13.068","0.0004","11.5754","0.0004","90","","122.419","0.002","90","","2050.2","0.12","296","2","296","2","","","","","","","","4","C 1 c 1","C -2yc","9","","","","- C24 H23 N2 O3 -","- C24 H22 N2 O3 -","- C96 H88 N8 O12 -","4","1","","Ray, Suman; Brown, Mike; Bhaumik, Asim; Dutta, Arghya; Mukhopadhyay, Chhanda","A new MCM-41 supported HPF6 catalyst for the library synthesis of highly substituted 1,4-dihydropyridines and oxidation to pyridines: report of one-dimensional packing towards LMSOMs and studies on their photophysical properties","Green Chemistry","2013","15","7","1910","","10.1039/c3gc40441b","","","0.71073","MoKα","","0.0642","0.0554","","","0.1694","0.1855","","","","","","0.839","","","","has coordinates","180431","2020-10-21","18:00:00",""
"7210450","6.4063","0.001","8.1667","0.0013","23.311","0.004","90","","90","","90","","1219.6","0.3","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","(HCaf)(HSO4)","Caffeinium Hydrogensulfate","","- C8 H12 N4 O6 S -","- C8 H12 N4 O6 S -","- C32 H48 N16 O24 S4 -","4","1","","Mottillo, Cristina; Lu, Yuneng; Pham, Minh-Hao; Cliffe, Matthew J.; Do, Trong-On; Friščić, Tomislav","Mineral neogenesis as an inspiration for mild, solvent-free synthesis of bulk microporous metal‒organic frameworks from metal (Zn, Co) oxides","Green Chemistry","2013","15","8","2121","","10.1039/c3gc40520f","","","0.71073","MoKα","","0.0712","0.043","","","0.0897","0.1006","","","","","","0.955","","","","has coordinates,has disorder","180435","2020-10-21","18:00:00",""
"7210451","7.3073","0.0003","7.1368","0.0003","15.6263","0.0007","90","","91.452","0.002","90","","814.66","0.06","180","2","180","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C8 H6 Cl N O2 -","- C8 H6 Cl N O2 -","- C32 H24 Cl4 N4 O8 -","4","1","","Deadman, Benjamin J.; Battilocchio, Claudio; Sliwinski, Eric; Ley, Steven V.","A prototype device for evaporation in batch and flow chemical processes","Green Chemistry","2013","15","8","2050","","10.1039/c3gc40967h","","","0.71073","MoKα","","0.0625","0.0541","","","0.1546","0.1594","","","","","","1.085","","","","has coordinates","180435","2020-10-21","18:00:00",""
"7210452","15.0238","0.0016","11.6122","0.001","20.9195","0.0019","90","","90","","90","","3649.6","0.6","150","","150","","","","","","","","","7","P b c a","-P 2ac 2ab","61","","","","- C9 H14 Cl3 N6 O P S3 -","- C9 H12 Cl3 N6 O P S3 -","- C72 H96 Cl24 N48 O8 P8 S24 -","8","1","","García-Álvarez, Rocío; Zablocka, Maria; Crochet, Pascale; Duhayon, Carine; Majoral, Jean-Pierre; Cadierno, Victorio","Thiazolyl-phosphine hydrochloride salts: effective auxiliary ligands for ruthenium-catalyzed nitrile hydration reactions and related amide bond forming processes in water","Green Chemistry","2013","15","9","2447","","10.1039/c3gc41201f","","","0.71073","MoKα","","0.0953","0.0588","","0.0941","0.0708","0.0708","","","","","","1.1169","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7211311","8.1356","0.0009","10.6065","0.0013","12.462","0.0015","91.571","0.006","105.781","0.006","100.384","0.006","1014.5","0.2","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C21 H21 N4 O5 -","- C21 H21 N4 O5 -","- C42 H42 N8 O10 -","2","1","","Prasanna, Pitchaimani; Perumal, Subbu; Menéndez, J. Carlos","Chemodivergent, multicomponent domino reactions in aqueous media: l-proline-catalyzed assembly of densely functionalized 4H-pyrano[2,3-c]pyrazoles and bispyrazolyl propanoates from simple, acyclic starting materials","Green Chemistry","2013","15","5","1292","","10.1039/c3gc37128j","","","0.71073","MoKα","","0.051","0.0447","","","0.1293","0.1366","","","","","","1.014","","","","has coordinates","180444","2020-10-21","18:00:00",""
"7211312","12.2016","0.0005","13.6995","0.0005","15.4526","0.0005","90","","110.166","0.002","90","","2424.65","0.16","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C24 H23 N4 O4 -","- C24 H23 N4 O4 -","- C96 H92 N16 O16 -","4","1","","Prasanna, Pitchaimani; Perumal, Subbu; Menéndez, J. Carlos","Chemodivergent, multicomponent domino reactions in aqueous media: l-proline-catalyzed assembly of densely functionalized 4H-pyrano[2,3-c]pyrazoles and bispyrazolyl propanoates from simple, acyclic starting materials","Green Chemistry","2013","15","5","1292","","10.1039/c3gc37128j","","","0.71073","MoKα","","0.0799","0.0604","","","0.2001","0.2121","","","","","","1.103","","","","has coordinates","180444","2020-10-21","18:00:00",""
"7211313","9.7594","0.0004","18.5524","0.0006","18.8335","0.0005","90","","90","","90","","3410","0.2","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C30 H36 Cl6 O8 -","- C30 H36 Cl6 O8 -","- C120 H144 Cl24 O32 -","4","1","","Haldar, Saikat; Kolet, Swati P.; Thulasiram, Hirekodathakallu V.","Biocatalysis: fungi mediated novel and selective 12β- or 17β-hydroxylation on the basic limonoid skeleton","Green Chemistry","2013","15","5","1311","","10.1039/c3gc40193f","","","0.71073","MoKα","","0.064","0.0553","","","0.1667","0.1767","","","","","","1.262","","","","has coordinates","180444","2020-10-21","18:00:00",""
"7211314","18.8143","0.0002","18.2714","0.0002","14.9031","0.0002","90","","117.805","0.0004","90","","4531.61","0.09","100","","100","","","","","","","","Synthesized by the authors. See text","6","C 1 2/c 1","-C 2yc","15","","","","- C19 H33 Cl Ni O3 P2 -","- C19 H33 Cl Ni O3 P2 -","- C152 H264 Cl8 Ni8 O24 P16 -","8","1","","Vabre, Boris; Lindeperg, Fabien; Zargarian, Davit","Direct, one-pot synthesis of POCOP-type pincer complexes from metallic nickel","Green Chemistry","2013","15","11","3188","","10.1039/c3gc40968f","","","1.54178","CuKα","","0.0265","0.0253","","","0.0951","0.0984","","","","","","0.918","","","","has coordinates","180444","2020-10-21","18:00:00",""
"7211315","15.908","0.0012","13.0746","0.001","11.134","0.0008","90","","91.464","0.003","90","","2315","0.3","150","","150","","","","","","","","Synthesized by the authors. See text","6","P 1 21/c 1","-P 2ybc","14","","","","- C20 H33 Cl Ni O4 P2 -","- C20 H33 Cl Ni O4 P2 -","- C80 H132 Cl4 Ni4 O16 P8 -","4","1","","Vabre, Boris; Lindeperg, Fabien; Zargarian, Davit","Direct, one-pot synthesis of POCOP-type pincer complexes from metallic nickel","Green Chemistry","2013","15","11","3188","","10.1039/c3gc40968f","","","1.54178","CuKα","","0.0305","0.0304","","","0.0844","0.0845","","","","","","1.004","","","","has coordinates","180444","2020-10-21","18:00:00",""
"7211316","10.4275","0.0004","14.033","0.0005","20.573","0.0007","90","","101.18","0.001","90","","2953.3","0.18","200","2","200","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C26 H47 Cl Ni O2 P2 -","- C26 H47 Cl Ni O2 P2 -","- C104 H188 Cl4 Ni4 O8 P8 -","4","1","","Vabre, Boris; Lindeperg, Fabien; Zargarian, Davit","Direct, one-pot synthesis of POCOP-type pincer complexes from metallic nickel","Green Chemistry","2013","15","11","3188","","10.1039/c3gc40968f","","","1.54178","CuKα","","0.0464","0.0448","","","0.1176","0.1192","","","","","","1.074","","","","has coordinates","180444","2020-10-21","18:00:00",""
"7211317","10.293","0.001","11.524","0.002","15.213","0.002","78.18","0.01","84.68","0.01","76.56","0.01","1715.9","0.4","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C38 H38 O10 -","- C38 H38 O10 -","- C76 H76 O20 -","2","1","","Forsythe, W. Graham; Garrett, Mark D.; Hardacre, Christopher; Nieuwenhuyzen, Mark; Sheldrake, Gary N.","An efficient and flexible synthesis of model lignin oligomers","Green Chemistry","2013","15","11","3031","","10.1039/c3gc41110a","","","0.71073","MoKα","","0.118","0.0749","","","0.2063","0.2511","","","","","","1.045","","","","has coordinates,has disorder","180444","2020-10-21","18:00:00",""
"7211318","16.032","0.004","11.544","0.003","32.695","0.007","90","","90.772","0.004","90","","6050","3","298","2","298","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C33 H27 N9 O3 -","- C33 H27 N9 O3 -","- C264 H216 N72 O24 -","8","2","","Zhao, Chao-Wei; Ma, Jian-Ping; Liu, Qi-Kui; Yu, Yang; Wang, Peng; Li, Yan-An; Wang, Kui; Dong, Yu-Bin","A self-assembled Pd6L8 nanoball for Suzuki‒Miyaura coupling reactions in both homogeneous and heterogeneous formats","Green Chemistry","2013","15","11","3150","","10.1039/c3gc41154k","","","0.71073","MoKα","","0.1221","0.0663","","","0.1361","0.1631","","","","","","1.024","","","","has coordinates","180444","2020-10-21","18:00:00",""
"7211319","17.2201","0.0016","15.7615","0.0014","19.2134","0.0018","90","","90","","90","","5214.8","0.8","100","2","100","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C25 H20 Cl6 Fe N O4 -","- C25 H20 Cl6 Fe N O4 -","- C200 H160 Cl48 Fe8 N8 O32 -","8","1","","Taherimehr, Masoumeh; Al-Amsyar, Syed M.; Whiteoak, Christopher J.; Kleij, Arjan W.; Pescarmona, Paolo P.","High activity and switchable selectivity in the synthesis of cyclic and polymeric cyclohexene carbonates with iron amino triphenolate catalysts","Green Chemistry","2013","15","11","3083","","10.1039/c3gc41303a","","","0.71073","MoKα","","0.0588","0.0381","","","0.0823","0.0925","","","","","","1.04","","","","has coordinates","180444","2020-10-21","18:00:00",""
"7211320","7.7968","0.0002","21.1512","0.0005","9.1046","0.0003","90","","114.189","0.003","90","","1369.63","0.07","120","2","120","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C16 H18 O4 -","- C16 H18 O4 -","- C64 H72 O16 -","4","1","","Mitchell, Lorna J.; Lewis, William; Moody, Christopher J.","Solar photochemistry: optimisation of the photo Friedel‒Crafts acylation of naphthoquinones","Green Chemistry","2013","15","10","2830","","10.1039/c3gc41477a","","x-ray","1.5418","CuKα","K-L~2,3~","0.0378","0.0329","","","0.09","0.0941","","","","","","1.044","","","","has coordinates","180444","2020-10-21","18:00:00",""
"7211321","12.8287","0.0003","7.9789","0.0003","24.2643","0.0009","90","","90","","90","","2483.67","0.14","120","2","120","2","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C15 H16 O4 -","- C15 H16 O4 -","- C120 H128 O32 -","8","1","","Mitchell, Lorna J.; Lewis, William; Moody, Christopher J.","Solar photochemistry: optimisation of the photo Friedel‒Crafts acylation of naphthoquinones","Green Chemistry","2013","15","10","2830","","10.1039/c3gc41477a","","x-ray","1.5418","CuKα","K-L~2,3~","0.0525","0.0438","","","0.1128","0.1191","","","","","","1.032","","","","has coordinates","180444","2020-10-21","18:00:00",""
"7211322","15.7243","0.0011","5.0123","0.0003","18.5815","0.0012","90","","107.285","0.007","90","","1398.36","0.17","120","2","120","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C16 H18 O5 -","- C16 H18 O5 -","- C64 H72 O20 -","4","1","","Mitchell, Lorna J.; Lewis, William; Moody, Christopher J.","Solar photochemistry: optimisation of the photo Friedel‒Crafts acylation of naphthoquinones","Green Chemistry","2013","15","10","2830","","10.1039/c3gc41477a","","x-ray","1.5418","CuKα","K-L~2,3~","0.0436","0.0362","","","0.0987","0.1048","","","","","","1.048","","","","has coordinates","180444","2020-10-21","18:00:00",""
"7211491","29.861","0.003","10.2141","0.0011","21.675","0.002","90","","117.455","0.001","90","","5866.4","1","296","2","296","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C32 H26 Cl N O7 -","- C32 H26 Cl N O7 -","- C256 H208 Cl8 N8 O56 -","8","1","","Wang, Huiyan; Liu, Xuecheng; Feng, Xian; Huang, Zhibin; Shi, Daqing","GAP chemistry for pyrrolyl coumarin derivatives: a highly efficient one-pot synthesis under catalyst-free conditions","Green Chemistry","2013","15","12","3307","","10.1039/c3gc41799a","","","0.71073","MoKα","","0.1042","0.0517","","","0.1258","0.1518","","","","","","1.018","","","","has coordinates,has disorder","180445","2020-10-21","18:00:00",""
"7211496","12.2357","0.0012","7.5855","0.0008","31.232","0.003","90","","90","","90","","2898.8","0.5","293","2","293","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","2-(dimorpholinomethyl)phenol","2-(dimorpholinomethyl)phenol","","- C15 H22 N2 O3 -","- C15 H22 N2 O3 -","- C120 H176 N16 O24 -","8","1","","Hernández-Altamirano, Raúl; Mena-Cervantes, Violeta Y.; Perez-Miranda, Sandra; Fernández, Francisco J.; Flores-Sandoval, Cesar Andres; Barba, Victor; Beltrán, Hiram I.; Zamudio-Rivera, Luis S.","Molecular design and QSAR study of low acute toxicity biocides with 4,4′-dimorpholyl-methane core obtained by microwave-assisted synthesis","Green Chemistry","2010","12","6","1036","","10.1039/b905153h","","","0.71073","MoKα","","0.0792","0.0661","","","0.1404","0.1466","","","","","","1.268","","","","has coordinates","287896","2023-11-30","16:33:03",""
"7211497","7.0621","0.0007","13.9243","0.0014","16.421","0.0016","90","","90","","90","","1614.8","0.3","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","4-bromo-2-(dimorpholinomethyl)phenol","4-bromo-2-(dimorpholinomethyl)phenol","","- C15 H21 Br N2 O3 -","- C15 H21 Br N2 O3 -","- C60 H84 Br4 N8 O12 -","4","1","","Hernández-Altamirano, Raúl; Mena-Cervantes, Violeta Y.; Perez-Miranda, Sandra; Fernández, Francisco J.; Flores-Sandoval, Cesar Andres; Barba, Victor; Beltrán, Hiram I.; Zamudio-Rivera, Luis S.","Molecular design and QSAR study of low acute toxicity biocides with 4,4′-dimorpholyl-methane core obtained by microwave-assisted synthesis","Green Chemistry","2010","12","6","1036","","10.1039/b905153h","","","0.71073","MoKα","","0.0306","0.0266","","","0.0646","0.0664","","","","","","1.06","","","","has coordinates","287896","2023-11-30","16:33:04",""
"7211498","11.637","0.008","10.801","0.007","19.312","0.013","90","","103.443","0.01","90","","2361","3","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","2,4-di-tert-butyl-6-(dimorpholinomethyl)phenol","2,4-di-tert-butyl-6-(dimorpholinomethyl)phenol","","- C23 H38 N2 O3 -","- C23 H38 N2 O3 -","- C92 H152 N8 O12 -","4","1","","Hernández-Altamirano, Raúl; Mena-Cervantes, Violeta Y.; Perez-Miranda, Sandra; Fernández, Francisco J.; Flores-Sandoval, Cesar Andres; Barba, Victor; Beltrán, Hiram I.; Zamudio-Rivera, Luis S.","Molecular design and QSAR study of low acute toxicity biocides with 4,4′-dimorpholyl-methane core obtained by microwave-assisted synthesis","Green Chemistry","2010","12","6","1036","","10.1039/b905153h","","","0.71073","MoKα","","0.0613","0.0504","","","0.1241","0.1313","","","","","","1.049","","","","has coordinates,has disorder","287896","2023-11-30","16:33:04",""
"7211499","15.067","0.003","10.15","0.002","9.665","0.002","90","","104.544","0.004","90","","1430.7","0.5","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","4,4'-(pyridin-2-ylmethylene)dimorpholine","4,4'-(pyridin-2-ylmethylene)dimorpholine","","- C14 H21 N3 O2 -","- C14 H21 N3 O2 -","- C56 H84 N12 O8 -","4","1","","Hernández-Altamirano, Raúl; Mena-Cervantes, Violeta Y.; Perez-Miranda, Sandra; Fernández, Francisco J.; Flores-Sandoval, Cesar Andres; Barba, Victor; Beltrán, Hiram I.; Zamudio-Rivera, Luis S.","Molecular design and QSAR study of low acute toxicity biocides with 4,4′-dimorpholyl-methane core obtained by microwave-assisted synthesis","Green Chemistry","2010","12","6","1036","","10.1039/b905153h","","","0.71073","MoKα","","0.0592","0.0474","","","0.1036","0.1097","","","","","","1.125","","","","has coordinates","287896","2023-11-30","16:33:04",""
"7212125","6.8805","0.0006","11.6254","0.001","11.9614","0.0011","90","","96.229","0.002","90","","951.13","0.15","173","2","173","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","(1,2,3-triMeIM)(MeCO3)","","","- C8 H14 N2 O3 -","- C8 H14 N2 O3 -","- C32 H56 N8 O12 -","4","1","","Smiglak, Marcin; Hines, C. Corey; Rogers, Robin D.","New hydrogen carbonate precursors for efficient and byproduct-free syntheses of ionic liquids based on 1,2,3-trimethylimidazolium and N,N-dimethylpyrrolidinium cores","Green Chemistry","2010","12","3","491","","10.1039/b920003g","","","0.71073","MoKα","","0.051","0.0428","","","0.1044","0.1087","","","","","","1.164","","","","has coordinates","180452","2020-10-21","18:00:00",""
"7212126","7.479","0.002","13.289","0.004","9.636","0.003","90","","95.011","0.005","90","","954","0.5","173","2","173","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","(1,2,3-triMeIM)(HCO3)H2O","","","- C7 H14 N2 O4 -","- C7 H14 N2 O4 -","- C28 H56 N8 O16 -","4","1","","Smiglak, Marcin; Hines, C. Corey; Rogers, Robin D.","New hydrogen carbonate precursors for efficient and byproduct-free syntheses of ionic liquids based on 1,2,3-trimethylimidazolium and N,N-dimethylpyrrolidinium cores","Green Chemistry","2010","12","3","491","","10.1039/b920003g","","","0.71073","MoKα","","0.1822","0.0719","","","0.1097","0.1407","","","","","","1.003","","","","has coordinates","180452","2020-10-21","18:00:00",""
"7212127","6.6199","0.0006","13.9451","0.0012","9.2587","0.0008","90","","101.76","0.002","90","","836.78","0.13","173","2","173","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","(N,N-diMePyr)(HCO3)","","","- C7 H15 N O3 -","- C7 H15 N O3 -","- C28 H60 N4 O12 -","4","1","","Smiglak, Marcin; Hines, C. Corey; Rogers, Robin D.","New hydrogen carbonate precursors for efficient and byproduct-free syntheses of ionic liquids based on 1,2,3-trimethylimidazolium and N,N-dimethylpyrrolidinium cores","Green Chemistry","2010","12","3","491","","10.1039/b920003g","","","0.71073","MoKα","","0.0445","0.0356","","","0.089","0.0937","","","","","","1.029","","","","has coordinates","180452","2020-10-21","18:00:00",""
"7212281","8.4078","0.0008","8.3744","0.0008","11.4399","0.001","90","","98.698","0.004","90","","796.22","0.13","293","","293","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C18 H20 N2 O2 -","- C18 H20 N2 O2 -","- C36 H40 N4 O4 -","2","1","","Jida, Mouhamad; Deprez-Poulain, Rebecca; Malaquin, Sandra; Roussel, Pascal; Agbossou-Niedercorn, Francine; Deprez, Benoit; Laconde, Guillaume","Solvent-free microwave-assisted Meyers’ lactamization","Green Chemistry","2010","12","6","961","","10.1039/b924111f","","","0.71073","MoKα","","0.0506","0.0392","","0.0746","0.0441","0.0431","","","","","","1.1559","","","","has coordinates","181910","2020-10-21","18:00:00",""
"7212282","17.5352","0.0008","7.6758","0.0004","10.0025","0.0004","90","","113.78","0.003","90","","1232","0.1","293","","293","","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C12 H17 N O4 -","- C12 H17 N O4 -","- C48 H68 N4 O16 -","4","1","","Jida, Mouhamad; Deprez-Poulain, Rebecca; Malaquin, Sandra; Roussel, Pascal; Agbossou-Niedercorn, Francine; Deprez, Benoit; Laconde, Guillaume","Solvent-free microwave-assisted Meyers’ lactamization","Green Chemistry","2010","12","6","961","","10.1039/b924111f","","","0.71073","MoKα","","0.1102","0.0448","","0.0747","0.0458","0.0431","","","","","","1.0751","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7212362","22.045","0.0003","9.268","0.0002","17.8038","0.0004","90","","124.751","0.001","90","","2988.74","0.11","293","2","293","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C20 H15 N O2 -","- C20 H15 N O2 -","- C160 H120 N8 O16 -","8","1","","Raihan, Mustafa J.; Kavala, Veerababurao; Kuo, Chun-Wei; Raju, B. Rama; Yao, Ching-Fa","‘On-water’ synthesis of chromeno-isoxazoles mediated by [hydroxy(tosyloxy)iodo]benzene (HTIB)","Green Chemistry","2010","12","6","1090","","10.1039/b926085d","","","0.71073","MoKα","","0.0724","0.0411","","","0.1091","0.1357","","","","","","1.045","","","","has coordinates","180454","2020-10-21","18:00:00",""
"7212363","7.1337","0.0002","26.8903","0.0009","7.6505","0.0003","90","","90.614","0.001","90","","1467.49","0.09","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H17 N O6 -","- C15 H17 N O6 -","- C60 H68 N4 O24 -","4","1","","Raihan, Mustafa J.; Kavala, Veerababurao; Kuo, Chun-Wei; Raju, B. Rama; Yao, Ching-Fa","‘On-water’ synthesis of chromeno-isoxazoles mediated by [hydroxy(tosyloxy)iodo]benzene (HTIB)","Green Chemistry","2010","12","6","1090","","10.1039/b926085d","","","0.71073","MoKα","","0.0945","0.0561","","","0.1623","0.1833","","","","","","1.042","","","","has coordinates","180454","2020-10-21","18:00:00",""
"7212364","9.1168","0.0003","13.8294","0.0004","17.2443","0.0006","90","","90","","90","","2174.16","0.12","293","2","293","2","","","","","","","","4","P c a b","-P 2bc 2ac","61","","","","- C13 H13 N O2 -","- C13 H13 N O2 -","- C104 H104 N8 O16 -","8","1","","Raihan, Mustafa J.; Kavala, Veerababurao; Kuo, Chun-Wei; Raju, B. Rama; Yao, Ching-Fa","‘On-water’ synthesis of chromeno-isoxazoles mediated by [hydroxy(tosyloxy)iodo]benzene (HTIB)","Green Chemistry","2010","12","6","1090","","10.1039/b926085d","","","0.71073","MoKα","","0.1157","0.0557","","","0.1185","0.1488","","","","","","1.022","","","","has coordinates","180454","2020-10-21","18:00:00",""
"7212365","8.449","0.0008","11.2583","0.0012","12.0738","0.0012","90","","90","","90","","1148.5","0.2","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C11 H13 N O5 -","- C11 H13 N O5 -","- C44 H52 N4 O20 -","4","1","","Raihan, Mustafa J.; Kavala, Veerababurao; Kuo, Chun-Wei; Raju, B. Rama; Yao, Ching-Fa","‘On-water’ synthesis of chromeno-isoxazoles mediated by [hydroxy(tosyloxy)iodo]benzene (HTIB)","Green Chemistry","2010","12","6","1090","","10.1039/b926085d","","","0.71073","MoKα","","0.05","0.0366","","","0.0819","0.0885","","","","","","1.044","","","","has coordinates","180454","2020-10-21","18:00:00",""
"7212382","13.286","0.003","5.6083","0.0012","15.808","0.003","90","","95.142","0.004","90","","1173.1","0.4","294","2","294","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C13 H16 O2 -","- C13 H16 O2 -","- C52 H64 O8 -","4","1","","Liu, Pei Nian; Xia, Fei; Wang, Qing Wei; Ren, Yu Jie; Chen, Jun Qin","Triflic acid adsorbed on silica gel as an efficient and recyclable catalyst for the addition of β-dicarbonyl compounds to alcohols and alkenes","Green Chemistry","2010","12","6","1049","","10.1039/b926142g","","","0.71073","MoKα","","0.1829","0.0734","","","0.2234","0.2822","","","","","","1.017","","","","has coordinates","180454","2020-10-21","18:00:00",""
"7212399","5.7313","0.0007","11.8701","0.0014","18.407","0.002","72.324","0.002","85.809","0.002","79.963","0.002","1174.6","0.2","294","2","294","2","","","","","","","","4","P -1","-P 1","2","6-(2-hydroxyphenyl)-2,2-dimethypiperidim-4-one","","","- C13 H17 N O2 -","- C13 H17 N O2 -","- C52 H68 N4 O8 -","4","2","","Feng, Li-Chun; Sun, Ya-Wei; Tang, Wei-Jun; Xu, Li-Jin; Lam, Kim-Lung; Zhou, Zhongyuan; Chan, Albert S. C.","Highly efficient chemoselective construction of 2,2-dimethyl-6-substituted 4-piperidones via multi-component tandem Mannich reaction in ionic liquids","Green Chemistry","2010","12","6","949","","10.1039/b926498a","","","0.71073","MoKα","","0.1233","0.0528","","","0.1274","0.1568","","","","","","1.016","","","","has coordinates","198632","2020-10-21","18:00:00",""
"7212674","9.6596","0.0004","38.8963","0.0017","12.5248","0.0005","90","","102.989","0.001","90","","4585.4","0.3","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C48 H32 F8 N12 Ru2 -","- C48 H32 F8 N12 Ru2 -","- C192 H128 F32 N48 Ru8 -","4","1","","Herrero, Santiago; Jiménez-Aparicio, Reyes; Perles, Josefina; Priego, José L.; Urbanos, Francisco A.","First microwave synthesis of multiple metal-metal bond paddlewheel compounds","Green Chemistry","2010","12","6","965","","10.1039/c003411h","","","0.71073","MoKα","","0.0984","0.0459","","","0.0912","0.1139","","","","","","1.012","","","","has coordinates","180457","2020-10-21","18:00:00",""
"7212698","8.8041","0.0004","12.5714","0.0005","25.282","0.0011","89.005","0.003","89.757","0.003","86.052","0.003","2791.1","0.2","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C48 H93 Cl5 Cu2 N6 -","- C48 H93 Cl5 Cu2 N6 -","- C96 H186 Cl10 Cu4 N12 -","2","1","","Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg","Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation","Green Chemistry","2010","12","9","1589","","10.1039/c003948a","","","0.71073","MoKα","","0.064","0.0399","","","0.0875","0.0914","","","","","","0.815","","","","has coordinates","180457","2020-10-21","18:00:00",""
"7212699","11.7007","0.0014","13.6056","0.0016","21.043","0.003","91.893","0.01","94.239","0.01","100.766","0.01","3278.2","0.7","173","2","173","2","","","","","","","","6","P -1","-P 1","2","","","","- C60 H112 Cu F6 N8 P -","- C60 H112 Cu F6 N8 P -","- C120 H224 Cu2 F12 N16 P2 -","2","1","","Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg","Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation","Green Chemistry","2010","12","9","1589","","10.1039/c003948a","","","0.71073","MoKα","","0.2179","0.0569","","","0.0795","0.1142","","","","","","0.819","","","","has coordinates,has disorder","180457","2020-10-21","18:00:00",""
"7212700","9.7553","0.0012","13.5795","0.0017","20.6572","0.003","106.873","0.016","94.154","0.016","95.814","0.015","2590.3","0.6","193","2","193","2","","","","","","","","5","P -1","-P 1","2","","","","- C90 H168 Cu6 I6 N12 -","- C90 H168 Cu6 I6 N12 -","- C90 H168 Cu6 I6 N12 -","1","0.5","","Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg","Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation","Green Chemistry","2010","12","9","1589","","10.1039/c003948a","","","0.71069","MoKα","","0.0437","0.0309","","","0.0721","0.0787","","","","","","0.88","","","","has coordinates","180458","2020-10-21","18:00:00",""
"7212701","10.3068","0.0013","16.172","0.002","25.595","0.004","73.875","0.017","87.515","0.017","87.742","0.017","4092.9","1","193","2","193","2","","","","","","","","5","P -1","-P 1","2","","","","- C64 H124 Br8 Cu4 N8 -","- C64 H124 Br8 Cu4 N8 -","- C128 H248 Br16 Cu8 N16 -","2","1","","Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg","Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation","Green Chemistry","2010","12","9","1589","","10.1039/c003948a","","x-ray","0.71069","MoKα","","0.2416","0.062","","","0.1339","0.1803","","","","","","0.604","","","","has coordinates","180458","2020-10-21","18:00:00",""
"7212702","9.002","0.003","9.454","0.003","20.757","0.006","85.74","0.02","87.75","0.03","78.95","0.03","1728.4","1","193","2","193","2","","","","","","","","5","P -1","-P 1","2","","","","- C30 H56 Br2 Cu2 N4 -","- C30 H56 Br2 Cu2 N4 -","- C60 H112 Br4 Cu4 N8 -","2","1","","Stricker, Marion; Linder, Thomas; Oelkers, Benjamin; Sundermeyer, Jörg","Cu(i)/(ii) based catalytic ionic liquids, their metallo-laminate solid state structures and catalytic activities in oxidative methanol carbonylation","Green Chemistry","2010","12","9","1589","","10.1039/c003948a","","","0.71073","MoKα","","0.1405","0.081","","","0.1996","0.2386","","","","","","0.991","","","","has coordinates","180458","2020-10-21","18:00:00",""
"7212731","9.2376","0.001","14.5788","0.0016","14.9383","0.0017","66.775","0.002","74.994","0.002","74.785","0.002","1756.3","0.3","293","2","293","2","","","","","","","","4","P -1","-P 1","2","2,3-dibenzyl-3-hydroxyisoindolin-1-one","2,3-dibenzyl-3-hydroxyisoindolin-1-one","","- C22 H19 N O2 -","- C22 H19 N O2 -","- C88 H76 N4 O8 -","4","2","","Zhou, Yu; Zhai, Yun; Li, Jian; Ye, Deju; Jiang, Hualiang; Liu, Hong","Metal-free tandem reaction in water: An efficient and regioselective synthesis of 3-hydroxyisoindolin-1-ones","Green Chemistry","2010","12","8","1397","","10.1039/c004745g","","","0.71073","MoKα","","0.122","0.0516","","","0.0884","0.1038","","","","","","0.844","","","","has coordinates","180458","2020-10-21","18:00:00",""
"7212732","13.8004","0.0008","11.5529","0.0006","9.8253","0.0006","90","","93.005","0.001","90","","1564.34","0.15","296","2","296","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C14 H14 B Bi F4 O S -","- C14 H14 B Bi F4 O S -","- C56 H56 B4 Bi4 F16 O4 S4 -","4","1","","Qiu, Renhua; Qiu, Yimiao; Yin, Shuangfeng; Song, Xingxing; Meng, Zhengong; Xu, Xinhua; Zhang, Xiaowen; Luo, Shenglian; Au, Chak-Tong; Wong, Wai-Yeung","Facile separation catalyst system: direct diastereoselective synthesis of (E)-α,β-unsaturated ketones catalyzed by an air-stable Lewis acidic/basic bifunctional organobismuth complex in ionic liquids","Green Chemistry","2010","12","10","1767","","10.1039/c004940a","","","0.71073","MoKα","","0.0399","0.039","","","0.1081","0.1089","","","","","","1.047","","","","has coordinates","180458","2020-10-21","18:00:00",""
"7212907","9.3439","0.0008","13.2412","0.0011","15.8279","0.0013","90","","90","","90","","1958.3","0.3","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C20 H26 O4 S -","- C20 H26 O4 S -","- C80 H104 O16 S4 -","4","1","","Rosini, Goffredo; Paolucci, Claudio; Boschi, Francesca; Marotta, Emanuela; Righi, Paolo; Tozzi, Francesco","Acid promoted CIDT for the deracemization of dihydrocinnamic aldehydes with Betti's base","Green Chemistry","2010","12","10","1747","","10.1039/c0gc00013b","","","0.71073","MoKα","","0.0406","0.0355","","","0.0934","0.0988","","","","","","1.095","","","","has coordinates","180460","2020-10-21","18:00:00",""
"7212908","14.6241","0.0013","20.681","0.002","8.745","0.0011","90","","90.538","0.001","90","","2644.7","0.5","298","2","298","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C26 H26 F2 N2 O6 S -","- C26 H26 F2 N2 O6 S -","- C104 H104 F8 N8 O24 S4 -","4","1","","Ma, Ning; Jiang, Bo; Zhang, Ge; Tu, Shu-Jiang; Wever, Walter; Li, Guigen","New multicomponent domino reactions (MDRs) in water: highly chemo-, regio- and stereoselective synthesis of spiro{[1,3]dioxanopyridine}-4,6-diones and pyrazolo[3,4-b]pyridines","Green Chemistry","2010","12","8","1357","","10.1039/c0gc00073f","","","0.71073","MoKα","","0.2589","0.0896","","","0.1396","0.1761","","","","","","1.038","","","","has coordinates,has disorder","180460","2020-10-21","18:00:00",""
"7212909","10.4612","0.0002","11.6733","0.0002","15.4745","0.0002","80.696","0.001","70.225","0.001","83.182","0.001","1750.69","0.05","293","2","293","2","","","","","","","synthesis","8","P -1","-P 1","2","","","","- C20 H44 Cu F6 N8 O4 P5 S2 -","- C20 H44 Cu F6 N8 O4 P5 S2 -","- C40 H88 Cu2 F12 N16 O8 P10 S4 -","2","1","","García-Álvarez, Joaquín; Díez, Josefina; Gimeno, José","A highly efficient copper(i) catalyst for the 1,3-dipolar cycloaddition of azides with terminal and 1-iodoalkynes in water: regioselective synthesis of 1,4-disubstituted and 1,4,5-trisubstituted 1,2,3-triazoles","Green Chemistry","2010","12","12","2127","","10.1039/c0gc00342e","","","0.71073","MoKα","","0.0516","0.042","","","0.1269","0.1444","","","","","","1.166","","","","has coordinates","180460","2020-10-21","18:00:00",""
"7212910","14.5177","0.0002","7.2359","0.0001","14.3593","0.0002","90","","101.588","0.002","90","","1477.68","0.04","100","2","100","2","","","","","","","synthesis","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H12 I N3 S -","- C15 H12 I N3 S -","- C60 H48 I4 N12 S4 -","4","1","","García-Álvarez, Joaquín; Díez, Josefina; Gimeno, José","A highly efficient copper(i) catalyst for the 1,3-dipolar cycloaddition of azides with terminal and 1-iodoalkynes in water: regioselective synthesis of 1,4-disubstituted and 1,4,5-trisubstituted 1,2,3-triazoles","Green Chemistry","2010","12","12","2127","","10.1039/c0gc00342e","","","1.54184","CuKα","","0.043","0.0357","","","0.0959","0.1016","","","","","","1.038","","","","has coordinates","180460","2020-10-21","18:00:00",""
"7212911","35.238","0.003","35.238","0.003","8.3319","0.0015","90","","90","","120","","8959.8","1.9","298","2","298","2","","","","","","","","5","R -3 :H","-R 3","148","Ethyl 10-benzoyl-7-hydroxy-7-(trifluoromethyl)- 1,2,3,4,5,7,8,9-octahydropyrido (1,2-a)(1,3)diazepine-8-carboxylate","Ethyl 10-benzoyl-7-hydroxy-7-(trifluoromethyl)-1,2,3,4,5,7,8,9-octahydropyrido [1,2-a][1,3]diazepine-8-carboxylate","","- C20 H22 F3 N2 O4.5 -","- C20 H22 F3 N2 O4.5 -","- C360 H396 F54 N36 O81 -","18","1","","Yan, Shengjiao; Chen, Yulan; Liu, Lin; He, Nengqin; Lin, Jun","Three-component solvent-free synthesis of highly substituted bicyclic pyridines containing a ring-junction nitrogen","Green Chemistry","2010","12","11","2043","","10.1039/c0gc00373e","","","0.71073","MoKα","","0.1294","0.056","","","0.1364","0.176","","","","","","0.952","","","","has coordinates,has disorder","176453","2020-10-21","18:00:00",""
"7212939","3.970162","0.000095","5.67111","0.00019","5.69467","0.00019","90","","90","","90","","128.217","0.007","300","","","","","","","","","","","4","A m m 2","A 2 -2","38","","Sodium Potassium Niobate","Niobate Perovskite","- K0.7 Na0.3 Nb O3 -","- K0.7016 Na0.2984 Nb0.5 O3 -","- K1.4032 Na0.5968 Nb O6 -","2","0.25","","Handoko, Albertus D.; Goh, Gregory K. L.","Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C","Green Chemistry","2010","12","4","680","","10.1039/b923840a","powder diffraction","","1.78899","CoKα","","","","","","","","","1.277","2.12","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7212940","3.96867","0.00014","5.67069","0.00028","5.69626","0.00029","90","","90","","90","","128.195","0.01","300","","","","","","","","","","","4","A m m 2","A 2 -2","38","","Sodium Potassium Niobate","Niobate Perovskite","- K0.7 Na0.3 Nb O3 -","- K0.832 Na0.168 Nb0.5 O3 -","- K1.664 Na0.336 Nb O6 -","2","0.25","","Handoko, Albertus D.; Goh, Gregory K. L.","Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C","Green Chemistry","2010","12","4","680","","10.1039/b923840a","powder diffraction","","1.78899","CoKα","","","","","","","","","1.243","1.78","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7212941","3.97024","0.00026","5.662","0.00055","5.68624","0.00056","90","","90","","90","","127.82","0.02","300","","","","","","","","","","","4","A m m 2","A 2 -2","38","","Sodium Potassium Niobate","Niobate Perovskite","- K0.7 Na0.3 Nb O3 -","- K0.713 Na0.287 Nb O3 -","- K1.426 Na0.574 Nb2 O6 -","2","0.25","","Handoko, Albertus D.; Goh, Gregory K. L.","Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C","Green Chemistry","2010","12","4","680","","10.1039/b923840a","powder diffraction","","1.78899","CoKα","","","","","","","","","1.582","1.42","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7212942","3.96136","0.00046","5.65428","0.00076","5.68474","0.00086","90","","90","","90","","127.33","0.03","300","","","","","","","","","","","4","A m m 2","A 2 -2","38","","Sodium Potassium Niobate","Niobate Perovskite","- K0.7 Na0.3 Nb O3 -","- K0.76 Na0.24 Nb O3 -","- K1.52 Na0.48 Nb2 O6 -","2","0.25","","Handoko, Albertus D.; Goh, Gregory K. L.","Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C","Green Chemistry","2010","12","4","680","","10.1039/b923840a","powder diffraction","","1.78899","CoKα","","","","","","","","","1.285","1.49","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7212943","3.98381","0.00011","5.689","0.00019","5.70757","0.00019","90","","90","","90","","129.356","0.007","300","","","","","","","","","","","4","A m m 2","A 2 -2","38","","Sodium Potassium Niobate","Niobate Perovskite","- K0.93 Na0.07 Nb O3 -","- K0.999489 Na0.000511376 Nb O3 -","- K1.99898 Na0.00102275 Nb2 O6 -","2","0.25","","Handoko, Albertus D.; Goh, Gregory K. L.","Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C","Green Chemistry","2010","12","4","680","","10.1039/b923840a","powder diffraction","","1.78899","CoKα","","","","","","","","","2.441","1.97","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7212944","3.981973","0.00008","5.68731","0.00014","5.70733","0.00014","90","","90","","90","","129.252","0.005","300","","","","","","","","","","","4","A m m 2","A 2 -2","38","","Sodium Potassium Niobate","Niobate Perovskite","- K0.903 Na0.097 Nb O3 -","- K0.8745 Na0.1255 Nb O2.8642 -","- K1.749 Na0.251 Nb2 O5.7284 -","2","0.25","","Handoko, Albertus D.; Goh, Gregory K. L.","Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C","Green Chemistry","2010","12","4","680","","10.1039/b923840a","powder diffraction","","1.78899","CoKα","","","","","","","","","2.293","3.05","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7212945","3.977443","0.000091","5.68725","0.00017","5.70678","0.00016","90","","90","","90","","129.091","0.006","300","","","","","","","","","","","4","A m m 2","A 2 -2","38","","Sodium Potassium Niobate","Niobate Perovskite","- K0.86 Na0.14 Nb O3 -","- K0.8578 Na0.1422 Nb O2.806 -","- K1.7156 Na0.2844 Nb2 O5.612 -","2","0.25","","Handoko, Albertus D.; Goh, Gregory K. L.","Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C","Green Chemistry","2010","12","4","680","","10.1039/b923840a","powder diffraction","","1.78899","CoKα","","","","","","","","","1.67","1.72","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7212946","3.973479","0.000059","5.68046","0.00011","5.70266","0.00011","90","","90","","90","","128.716","0.004","300","","","","","","","","","","","4","A m m 2","A 2 -2","38","","Sodium Potassium Niobate","Niobate Perovskite","- K0.84 Na0.16 Nb O3 -","- K0.8393 Na0.1607 Nb O2.806 -","- K1.6786 Na0.3214 Nb2 O5.612 -","2","0.25","","Handoko, Albertus D.; Goh, Gregory K. L.","Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C","Green Chemistry","2010","12","4","680","","10.1039/b923840a","powder diffraction","","1.78899","CoKα","","","","","","","","","1.805","1.91","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7212947","3.973479","0.000059","5.68046","0.00011","5.70266","0.00011","90","","90","","90","","128.716","0.004","300","","","","","","","","","","","4","A m m 2","A 2 -2","38","","Sodium Potassium Niobate","Niobate Perovskite","- K0.83 Na0.17 Nb O3 -","- K0.8354 Na0.1746 Nb O3 -","- K1.6708 Na0.3492 Nb2 O6 -","2","0.25","","Handoko, Albertus D.; Goh, Gregory K. L.","Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C","Green Chemistry","2010","12","4","680","","10.1039/b923840a","powder diffraction","","1.78899","CoKα","","","","","","","","","1.833","1.91","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7212948","3.972623","0.000059","5.68015","0.0001","5.7037","0.0001","90","","90","","90","","128.705","0.004","300","","","","","","","","","","","4","A m m 2","A 2 -2","38","","Sodium Potassium Niobate","Niobate Perovskite","- K0.77 Na0.23 Nb O3 -","- K0.7714 Na0.2285 Nb O3 -","- K1.5428 Na0.457 Nb2 O6 -","2","0.25","","Handoko, Albertus D.; Goh, Gregory K. L.","Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C","Green Chemistry","2010","12","4","680","","10.1039/b923840a","powder diffraction","","1.78899","CoKα","","","","","","","","","1.842","2.81","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7212949","3.97304","0.00011","5.67576","0.0002","5.69703","0.00019","90","","90","","90","","128.468","0.007","300","","","","","","","","","","","4","A m m 2","A 2 -2","38","","Sodium Potassium Niobate","Niobate Perovskite","- K0.73 Na0.27 Nb O3 -","- K0.7619 Na0.2381 Nb0.5 O3 -","- K1.5238 Na0.4762 Nb O6 -","2","0.25","","Handoko, Albertus D.; Goh, Gregory K. L.","Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C","Green Chemistry","2010","12","4","680","","10.1039/b923840a","powder diffraction","","1.78899","CoKα","","","","","","","","","1.523","1.25","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7212950","3.970626","0.000088","5.67573","0.00017","5.69855","0.00017","90","","90","","90","","128.424","0.006","300","","","","","","","","","","","4","A m m 2","A 2 -2","38","","Sodium Potassium Niobate","Niobate Perovskite","- K0.75 Na0.25 Nb O3 -","- K0.7549 Na0.245 Nb0.5 O3 -","- K1.5098 Na0.49 Nb O6 -","2","0.25","","Handoko, Albertus D.; Goh, Gregory K. L.","Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C","Green Chemistry","2010","12","4","680","","10.1039/b923840a","powder diffraction","","1.78899","CoKα","","","","","","","","","1.604","1.24","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7212951","3.96953","0.00011","5.6731","0.00021","5.69719","0.00021","90","","90","","90","","128.298","0.008","300","","","","","","","","","","","4","A m m 2","A 2 -2","38","","Sodium Potassium Niobate","Niobate Perovskite","- K0.72 Na0.28 Nb O3 -","- K0.725 Na0.275 Nb0.5 O3 -","- K1.45 Na0.55 Nb O6 -","2","0.25","","Handoko, Albertus D.; Goh, Gregory K. L.","Hydrothermal synthesis of sodium potassium niobate solid solutions at 200 °C","Green Chemistry","2010","12","4","680","","10.1039/b923840a","powder diffraction","","1.78899","CoKα","","","","","","","","","1.411","1.32","","","","","","","has coordinates","176453","2020-10-21","18:00:00",""
"7214116","20.6371","0.0005","11.0516","0.0004","20.5751","0.0006","90","","119.356","0.001","90","","4090","0.2","298","2","298","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C25 H19 N O5 -","- C25 H19 N O5 -","- C200 H152 N8 O40 -","8","2","","Muthusaravanan, Sivasubramanian; Sasikumar, Chinnathambi; Devi Bala, Balasubramanian; Perumal, Subbu","An eco-friendly three-component regio- and stereoselective synthesis of highly functionalized dihydroindeno[1,2-b]pyrroles under grinding","Green Chemistry","2014","16","3","1297","","10.1039/c3gc42150c","","","0.71073","MoKα","","0.0723","0.0511","","","0.1399","0.1589","","","","","","1.022","","","","has coordinates","176432","2020-10-21","18:00:00",""
"7214117","14.5983","0.0015","20.935","0.002","8.5228","0.0009","90","","90","","90","","2604.7","0.5","180","2","180","2","","","","","","","","4","P c c n","-P 2ab 2ac","56","","","","- C9 H21 N O3 -","- C9 H21 N O3 -","- C72 H168 N8 O24 -","8","1","","Vanderveen, Jesse R.; Durelle, Jeremy; Jessop, Philip G.","Design and evaluation of switchable-hydrophilicity solvents","Green Chemistry","2014","16","3","1187","","10.1039/c3gc42164c","","","0.71073","MoKα","","0.0883","0.0614","","","0.1413","0.1531","","","","","","1.075","","","","has coordinates","206958","2020-10-21","18:00:00",""
"7214118","9.0629","0.0011","11.2174","0.0014","16.215","0.002","90","","104.835","0.001","90","","1593.5","0.3","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H14 N2 O3 -","- C20 H14 N2 O3 -","- C80 H56 N8 O12 -","4","1","","Das, Paramita; Dutta, Arghya; Bhaumik, Asim; Mukhopadhyay, Chhanda","Heterogeneous ditopic ZnFe2O4 catalyzed synthesis of 4H-pyrans: further conversion to 1,4-DHPs and report of functional group interconversion from amide to ester","Green Chemistry","2014","16","3","1426","","10.1039/c3gc42095g","","","0.71073","MoKα","","0.0437","0.0356","","","0.1085","0.1196","","","","","","0.843","","","","has coordinates","180472","2020-10-21","18:00:00",""
"7214119","10.0929","0.0003","6.337","0.0002","12.8314","0.0004","90","","100.192","0.001","90","","807.73","0.04","296","2","296","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C21 H16 N2 O -","- C21 H16 N2 O -","- C42 H32 N4 O2 -","2","1","","Das, Paramita; Dutta, Arghya; Bhaumik, Asim; Mukhopadhyay, Chhanda","Heterogeneous ditopic ZnFe2O4 catalyzed synthesis of 4H-pyrans: further conversion to 1,4-DHPs and report of functional group interconversion from amide to ester","Green Chemistry","2014","16","3","1426","","10.1039/c3gc42095g","","","0.71073","MoKα","","0.0558","0.0485","","","0.1422","0.1582","","","","","","0.785","","","","has coordinates","180472","2020-10-21","18:00:00",""
"7214120","6.937","0.005","11.638","0.009","13.019","0.01","75.535","0.008","89.874","0.009","76.165","0.008","986.4","1.3","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C26 H17 N O5 -","- C26 H17 N O5 -","- C52 H34 N2 O10 -","2","1","","Das, Paramita; Dutta, Arghya; Bhaumik, Asim; Mukhopadhyay, Chhanda","Heterogeneous ditopic ZnFe2O4 catalyzed synthesis of 4H-pyrans: further conversion to 1,4-DHPs and report of functional group interconversion from amide to ester","Green Chemistry","2014","16","3","1426","","10.1039/c3gc42095g","","","0.71073","MoKα","","0.0998","0.0635","","","0.1788","0.2145","","","","","","0.931","","","","has coordinates","180472","2020-10-21","18:00:00",""
"7214121","8.6867","0.0005","11.0032","0.0007","12.0059","0.0007","70.06","0.002","84.209","0.002","76.001","0.002","1046.5","0.11","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H27 N3 O3 -","- C22 H27 N3 O3 -","- C44 H54 N6 O6 -","2","1","","Das, Paramita; Dutta, Arghya; Bhaumik, Asim; Mukhopadhyay, Chhanda","Heterogeneous ditopic ZnFe2O4 catalyzed synthesis of 4H-pyrans: further conversion to 1,4-DHPs and report of functional group interconversion from amide to ester","Green Chemistry","2014","16","3","1426","","10.1039/c3gc42095g","","","0.71073","MoKα","","0.0653","0.0542","","","0.1683","0.1864","","","","","","0.961","","","","has coordinates","180472","2020-10-21","18:00:00",""
"7214122","6.892","0.003","8.967","0.003","8.538","0.003","90","","112.7","0.004","90","","486.8","0.3","571","2","571","2","","","","","","","","5","P 1 21/m 1","-P 2yb","11","dia-2","dia-cyclopentadienyldibromodicarbonyl Re(III)","","- C7 H5 Br2 O2 Re -","- C7 H5 Br2 O2 Re -","- C14 H10 Br4 O4 Re2 -","2","0.5","","Hernández, José G.; Macdonald, Neil A. J.; Mottillo, Cristina; Butler, Ian S.; Friščić, Tomislav","A mechanochemical strategy for oxidative addition: remarkable yields and stereoselectivity in the halogenation of organometallic Re(i) complexes","Green Chemistry","2014","16","3","1087","","10.1039/c3gc42104j","","","0.71073","MoKα","","0.0507","0.0319","","","0.0718","0.0778","","","","","","1.015","","","","has coordinates,has disorder","180472","2020-10-21","18:00:00",""
"7214123","6.34","0.0011","12.504","0.002","6.4937","0.0011","90","","109.161","0.002","90","","486.27","0.14","296","2","296","2","","","","","","","","5","P 1 21/m 1","-P 2yb","11","lat-2","lat-cyclopentadienyldibromodicarbonyl Re(III)","","- C7 H5 Br2 O2 Re -","- C7 H5 Br2 O2 Re -","- C14 H10 Br4 O4 Re2 -","2","0.5","","Hernández, José G.; Macdonald, Neil A. J.; Mottillo, Cristina; Butler, Ian S.; Friščić, Tomislav","A mechanochemical strategy for oxidative addition: remarkable yields and stereoselectivity in the halogenation of organometallic Re(i) complexes","Green Chemistry","2014","16","3","1087","","10.1039/c3gc42104j","","","0.71073","MoKα","","0.0441","0.0391","","","0.1058","0.1087","","","","","","1.043","","","","has coordinates","180472","2020-10-21","18:00:00",""
"7214124","6.2456","0.0009","12.2155","0.0017","6.2656","0.0009","90","","106.932","0.001","90","","457.3","0.11","293","2","293","2","","","","","","","","5","P 1 21/m 1","-P 2yb","11","lat-CpRe(CO)2Cl2","lat-cyclopentadienyldichlorodicarbonyl Re(III)","","- C7 H5 Cl2 O2 Re -","- C7 H5 Cl2 O2 Re -","- C14 H10 Cl4 O4 Re2 -","2","0.5","","Hernández, José G.; Macdonald, Neil A. J.; Mottillo, Cristina; Butler, Ian S.; Friščić, Tomislav","A mechanochemical strategy for oxidative addition: remarkable yields and stereoselectivity in the halogenation of organometallic Re(i) complexes","Green Chemistry","2014","16","3","1087","","10.1039/c3gc42104j","","","0.71073","MoKα","","0.0165","0.0163","","","0.0395","0.0396","","","","","","1.129","","","","has coordinates","180472","2020-10-21","18:00:00",""
"7214125","13.389","0.005","9.29","0.004","9.128","0.004","90","","107.669","0.004","90","","1081.8","0.8","293","2","293","2","","","","","","","","5","C 1 2/m 1","-C 2y","12","dia-CpRe(CO)2I2","dia-cyclopentadienyldiiododicarbonyl Re(III)","","- C7 H5 I2 O2 Re -","- C7 H5 I2 O2 Re -","- C28 H20 I8 O8 Re4 -","4","0.5","","Hernández, José G.; Macdonald, Neil A. J.; Mottillo, Cristina; Butler, Ian S.; Friščić, Tomislav","A mechanochemical strategy for oxidative addition: remarkable yields and stereoselectivity in the halogenation of organometallic Re(i) complexes","Green Chemistry","2014","16","3","1087","","10.1039/c3gc42104j","","","0.71073","MoKα","","0.0479","0.0414","","","0.102","0.1076","","","","","","1.052","","","","has coordinates","180472","2020-10-21","18:00:00",""
"7214126","10.2819","0.0009","10.7707","0.0009","15.6284","0.0014","90","","90","","90","","1730.7","0.3","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C23 H20 N2 -","- C23 H20 N2 -","- C92 H80 N8 -","4","1","","Solan, Agnes; Nişanci, Bilal; Belcher, Miranda; Young, Jonathon; Schäfer, Christian; Wheeler, Kraig A.; Török, Béla; Dembinski, Roman","Catalyst-free chemo-/regio-/stereo-selective amination of alk-3-ynones. Synthesis of 1,5-benzodiazepines and 3-amino-2-alkenones","Green Chemistry","2014","16","3","1120","","10.1039/c3gc41898g","","","1.54178","CuKα","","0.0568","0.0521","","","0.1401","0.1445","","","","","","1.032","","","","has coordinates","180472","2020-10-21","18:00:00",""
"7214127","5.7713","0.0009","16.573","0.002","25.145","0.004","90","","92.354","0.008","90","","2403","0.6","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","(Z)-3-[(2-amino-4,5-dimethylphenyl)amino]-4- (4-tert-butylphenyl)-1-(4-chlorophenyl)but-2-en-1-one","","- C28 H31 Cl N2 O -","- C28 H31 Cl N2 O -","- C112 H124 Cl4 N8 O4 -","4","1","","Solan, Agnes; Nişanci, Bilal; Belcher, Miranda; Young, Jonathon; Schäfer, Christian; Wheeler, Kraig A.; Török, Béla; Dembinski, Roman","Catalyst-free chemo-/regio-/stereo-selective amination of alk-3-ynones. Synthesis of 1,5-benzodiazepines and 3-amino-2-alkenones","Green Chemistry","2014","16","3","1120","","10.1039/c3gc41898g","","","1.54178","CuKα","","0.0753","0.0403","","","0.0874","0.0997","","","","","","1.026","","","","has coordinates","180472","2020-10-21","18:00:00",""
"7214128","11.0906","0.0003","14.6981","0.0005","7.6029","0.0008","90","","90","","90","","1239.35","0.14","250","2","250","2","","","","","","","","4","P n a 21","P 2c -2n","33","(pa)2(ox)","1-propylammonium oxalate","","- C8 H20 N2 O4 -","- C8 H20 N2 O4 -","- C32 H80 N8 O16 -","4","1","","Qi, Feng; Stein, Robin S.; Friščić, Tomislav","Mimicking mineral neogenesis for the clean synthesis of metal‒organic materials from mineral feedstocks: coordination polymers, MOFs and metal oxide separation","Green Chemistry","2014","16","1","121","","10.1039/c3gc41370e","","","0.71073","MoKα","","0.1177","0.0807","","","0.2215","0.2622","","","","","","1.05","","","","has coordinates","180472","2020-10-21","18:00:00",""
"7214305","9.7003","0.0003","10.0807","0.0004","26.1807","0.001","88.397","0.002","82.073","0.001","69.855","0.001","2379.99","0.15","298","2","298","2","","","","","","","","5","P -1","-P 1","2","","","","- C40 H86 Mo N2 O10 -","- C40 H86 Mo N2 O10 -","- C80 H172 Mo2 N4 O20 -","2","1","","Chakravarthy, Rajan Deepan; Ramkumar, Venkatachalam; Chand, Dillip Kumar","A molybdenum based metallomicellar catalyst for controlled and selective sulfoxidation reactions in aqueous medium","Green Chemistry","2014","16","4","2190","","10.1039/c3gc42245c","","","0.71073","MoKα","","0.0551","0.0396","","","0.1233","0.1433","","","","","","1.046","","","","has coordinates","180474","2020-10-21","18:00:00",""
"7214306","10.7382","0.0003","10.2853","0.0003","11.9959","0.0003","90","","114.837","0.001","90","","1202.35","0.06","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C10 H16 N2 O S2 -","- C10 H16 N2 O S2 -","- C40 H64 N8 O4 S8 -","4","1","","Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing","Alkoxide-functionalized imidazolium betaines for CO2 activation and catalytic transformation","Green Chemistry","2014","16","4","2266","","10.1039/c3gc42346h","","","0.71073","MoKα","","0.0384","0.0345","","","0.0969","0.1","","","","","","1.051","","","","has coordinates","198633","2020-10-21","18:00:00",""
"7214307","7.0242","0.0004","15.4761","0.0009","11.2508","0.0007","90","","92.082","0.001","90","","1222.24","0.13","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C10 H16 N2 O S2 -","- C10 H16 N2 O S2 -","- C40 H64 N8 O4 S8 -","4","1","","Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing","Alkoxide-functionalized imidazolium betaines for CO2 activation and catalytic transformation","Green Chemistry","2014","16","4","2266","","10.1039/c3gc42346h","","","0.71073","MoKα","","0.1003","0.0518","","","0.1151","0.134","","","","","","1.028","","","","has coordinates","198633","2020-10-21","18:00:00",""
"7214308","12.1669","0.0007","12.065","0.0007","19.2806","0.0011","90","","90","","90","","2830.3","0.3","296","2","296","2","","","","","","","","4","P b c n","-P 2n 2ab","60","","","","- C10 H19 N2 O5 -","- C10 H19 N2 O4.5 -","- C80 H152 N16 O36 -","8","1","","Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing","Alkoxide-functionalized imidazolium betaines for CO2 activation and catalytic transformation","Green Chemistry","2014","16","4","2266","","10.1039/c3gc42346h","","","0.71073","MoKα","","0.1244","0.108","","","0.3651","0.4047","","","","","","0.933","","","","has coordinates","198633","2020-10-21","18:00:00",""
"7214309","22.439","0.005","5.3555","0.0011","13.393","0.003","90","","90","","90","","1609.5","0.6","298","2","298","2","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C23 H15 N O -","- C23 H15 N O -","- C92 H60 N4 O4 -","4","1","","Rao, Yin; Li, Zhexian; Yin, Guodong","Clean and efficient assembly of functionalized benzofuro[2,3-c]pyridines via metal-free one-pot domino reactions","Green Chemistry","2014","16","4","2213","","10.1039/c3gc42234h","","","0.71073","MoKα","","0.076","0.0469","","","0.114","0.1293","","","","","","1.037","","","","has coordinates","180474","2020-10-21","18:00:00",""
"7215076","11.9856","0.0003","18.2571","0.0003","9.0361","0.0002","90","","94.463","0.001","90","","1971.3","0.07","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","3-[(1H-indol-3-yl)(phenyl)methylene]-3H-indol","3-[(1H-indol-3-yl)(phenyl)methylene]-3H-indole","","- C23 H21 Cl N2 O2 -","- C23 H21 Cl N2 O2 -","- C92 H84 Cl4 N8 O8 -","4","0.5","","Silveira, Claudio C.; Mendes, Samuel R.; Villetti, Marcos A.; Back, Davi F.; Kaufman, Teodoro S.","CeIII-promoted oxidation. Efficient aerobic one-pot eco-friendly synthesis of oxidized bis(indol-3-yl)methanes and cyclic tetra(indolyl)dimethanes","Green Chemistry","2012","14","10","2912","","10.1039/c2gc36131k","","","0.71073","MoKα","","0.0632","0.0528","","","0.157","0.1681","","","","","","1.068","","","","has coordinates","176432","2020-10-21","18:00:00",""
"7215077","20.704","0.0005","12.3263","0.0003","21.8634","0.0005","90","","113.463","0.001","90","","5118.3","0.2","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","Tetra(indolyl)dimethane derivative","Tetra(indolyl)dimethane derivative 2 DMSO","","- C28 H30 N2 O2 S2 -","- C28 H30 N2 O2 S2 -","- C224 H240 N16 O16 S16 -","8","1","","Silveira, Claudio C.; Mendes, Samuel R.; Villetti, Marcos A.; Back, Davi F.; Kaufman, Teodoro S.","CeIII-promoted oxidation. Efficient aerobic one-pot eco-friendly synthesis of oxidized bis(indol-3-yl)methanes and cyclic tetra(indolyl)dimethanes","Green Chemistry","2012","14","10","2912","","10.1039/c2gc36131k","","","0.71073","MoKα","","0.0654","0.0496","","","0.1351","0.1466","","","","","","1.045","","","","has coordinates","176432","2020-10-21","18:00:00",""
"7215078","9.7499","0.0004","30.5632","0.0013","8.5329","0.0003","90","","101.967","0.002","90","","2487.44","0.17","180","","180","","","","","","","","synthesis as described","6","P 1 21/c 1","-P 2ybc","14","","","","- C27 H28 N3 O2 P S -","- C27 H28 N3 O2 P S -","- C108 H112 N12 O8 P4 S4 -","4","1","","Keller, Michel; Hameau, Aurélien; Spataro, Grégory; Ladeira, Sonia; Caminade, Anne-Marie; Majoral, Jean-Pierre; Ouali, Armelle","An efficient and recyclable dendritic catalyst able to dramatically decrease palladium leaching in Suzuki couplings","Green Chemistry","2012","14","10","2807","","10.1039/c2gc35832h","","","0.71073","MoKα","","0.0649","0.0413","","","0.0927","0.1032","","","","","","1.019","","","","has coordinates","180481","2020-10-21","18:00:00",""
"7215079","16.0609","0.001","18.7305","0.0013","8.9676","0.0006","90","","98.481","0.006","90","","2668.2","0.3","180","2","180","2","","","","","","","synthesis as described","6","P 1 21/c 1","-P 2ybc","14","","","","- C28 H30 N3 O2 P S -","- C28 H30 N3 O2 P S -","- C112 H120 N12 O8 P4 S4 -","4","1","","Keller, Michel; Hameau, Aurélien; Spataro, Grégory; Ladeira, Sonia; Caminade, Anne-Marie; Majoral, Jean-Pierre; Ouali, Armelle","An efficient and recyclable dendritic catalyst able to dramatically decrease palladium leaching in Suzuki couplings","Green Chemistry","2012","14","10","2807","","10.1039/c2gc35832h","","x-ray","0.71073","MoKα","","0.121","0.0393","","","0.0432","0.0497","","","","","","0.664","","","","has coordinates","180481","2020-10-21","18:00:00",""
"7215080","8.7642","0.0009","10.8437","0.0011","12.1558","0.0012","94.396","0.005","106.808","0.005","109.396","0.005","1023.87","0.19","180","","180","","","","","","","","synthesis as described","6","P -1","-P 1","2","","","","- C21 H23 N2 O2 P S -","- C21 H23 N2 O2 P S -","- C42 H46 N4 O4 P2 S2 -","2","1","","Keller, Michel; Hameau, Aurélien; Spataro, Grégory; Ladeira, Sonia; Caminade, Anne-Marie; Majoral, Jean-Pierre; Ouali, Armelle","An efficient and recyclable dendritic catalyst able to dramatically decrease palladium leaching in Suzuki couplings","Green Chemistry","2012","14","10","2807","","10.1039/c2gc35832h","","x-ray","0.71073","MoKα","","0.0346","0.0324","","","0.0819","0.0837","","","","","","1.048","","","","has coordinates","180481","2020-10-21","18:00:00",""
"7215081","12.8415","0.0005","13.0797","0.0005","28.1381","0.0012","90","","109.006","0.001","90","","4468.5","0.3","150","2","150","2","","","","","","","synthesis","8","P 1 21/c 1","-P 2ybc","14","","","","- C25 H56 Cl6 N8 O5 P4 Pd2 S2 -","- C25 H56 Cl6 N8 O5 P4 Pd2 S2 -","- C100 H224 Cl24 N32 O20 P16 Pd8 S8 -","4","1","","García-Álvarez, Joaquín; Díez, Josefina; Vidal, Cristian","Pd(ii)-catalyzed cycloisomerisation of γ-alkynoic acids and one-pot tandem cycloisomerisation/CuAAC reactions in water","Green Chemistry","2012","14","11","3190","","10.1039/c2gc36176k","","","0.71073","MoKα","","0.0826","0.0459","","","0.129","0.158","","","","","","0.946","","","","has coordinates","180481","2020-10-21","18:00:00",""
"7215082","11.6784","0.0002","5.6853","0.0001","23.4754","0.0003","90","","96.479","0.001","90","","1548.7","0.04","110","2","110","2","","","","","","","synthesis","4","P 1 21/n 1","-P 2yn","14","","","","- C17 H17 N3 O4 -","- C17 H17 N3 O4 -","- C68 H68 N12 O16 -","4","1","","García-Álvarez, Joaquín; Díez, Josefina; Vidal, Cristian","Pd(ii)-catalyzed cycloisomerisation of γ-alkynoic acids and one-pot tandem cycloisomerisation/CuAAC reactions in water","Green Chemistry","2012","14","11","3190","","10.1039/c2gc36176k","","","1.54184","CuKα","","0.046","0.0389","","","0.0984","0.1055","","","","","","1.045","","","","has coordinates","180481","2020-10-21","18:00:00",""
"7215777","9.893","0.002","10.366","0.002","10.379","0.002","102.062","0.017","105.681","0.017","103.638","0.017","952.6","0.4","295","2","295","2","","","","","","","","5","P -1","-P 1","2","","","","- C18 H24 N2 O3 Si -","- C18 H24 N2 O3 Si -","- C36 H48 N4 O6 Si2 -","2","1","","Bellachioma, Gianfranco; Castrica, Luca; Fringuelli, Francesco; Pizzo, Ferdinando; Vaccaro, Luigi","Catalyst- and solvent-free conditions as an environmentally benign approach to 4-aryl-3-cyano-hexahydro-4H-1,2-benzoxazine-2-oxides","Green Chemistry","2008","10","3","327","","10.1039/b712858d","","","0.71073","MoKα","","0.2485","0.0409","","","0.055","0.0772","","","","","","0.876","","","","has coordinates","180488","2020-10-21","18:00:00",""
"7215778","14.092","0.003","8.462","0.003","11.276","0.003","90","","96.819","0.016","90","","1335.1","0.7","295","2","295","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C15 H16 N2 O2 -","- C15 H16 N2 O2 -","- C60 H64 N8 O8 -","4","1","","Bellachioma, Gianfranco; Castrica, Luca; Fringuelli, Francesco; Pizzo, Ferdinando; Vaccaro, Luigi","Catalyst- and solvent-free conditions as an environmentally benign approach to 4-aryl-3-cyano-hexahydro-4H-1,2-benzoxazine-2-oxides","Green Chemistry","2008","10","3","327","","10.1039/b712858d","","","0.71073","MoKα","","0.1538","0.0467","","","0.0535","0.0826","","","","","","0.809","","","","has coordinates","180488","2020-10-21","18:00:00",""
"7215812","12.936","0.003","12.022","0.002","14.578","0.003","90","","90","","90","","2267.1","0.8","298","2","298","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C11 H10 Br N O3 -","- C11 H10 Br N O3 -","- C88 H80 Br8 N8 O24 -","8","1","","Zou, You-Quan; Guo, Wei; Liu, Feng-Lei; Lu, Liang-Qiu; Chen, Jia-Rong; Xiao, Wen-Jing","Visible-light-induced photocatalytic formyloxylation reactions of 3-bromooxindoles with water and DMF: the scope and mechanism","Green Chemistry","2014","16","8","3787","","10.1039/C4GC00647J","","","0.71073","MoKα","","0.0491","0.0346","","","0.1023","0.1224","","","","","","1.053","","","","has coordinates","180489","2020-10-21","18:00:00",""
"7216184","9.2869","0.0019","9.636","0.002","11.202","0.002","84.187","0.003","72.065","0.003","64.104","0.003","857.3","0.3","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C23 H19 N -","- C23 H19 N -","- C46 H38 N2 -","2","1","","Taheri, Amir; Liu, Changhui; Lai, Bingbing; Cheng, Cheng; Pan, Xiaojuan; Gu, Yanlong","Brønsted acid ionic liquid catalyzed facile synthesis of 3-vinylindoles through direct C3 alkenylation of indoles with simple ketones","Green Chemistry","2014","16","8","3715","","10.1039/C4GC00840E","","","0.71073","MoKα","","0.0436","0.0394","","","0.0969","0.0998","","","","","","0.995","","","","has coordinates","180492","2020-10-21","18:00:00",""
"7216185","7.859","0.004","7.981","0.004","23.406","0.012","90","","92.401","0.009","90","","1466.8","1.3","296","2","296","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C20 H19 N -","- C20 H19 N -","- C80 H76 N4 -","4","2","","Taheri, Amir; Liu, Changhui; Lai, Bingbing; Cheng, Cheng; Pan, Xiaojuan; Gu, Yanlong","Brønsted acid ionic liquid catalyzed facile synthesis of 3-vinylindoles through direct C3 alkenylation of indoles with simple ketones","Green Chemistry","2014","16","8","3715","","10.1039/C4GC00840E","","","0.71073","MoKα","","0.1756","0.1541","","","0.498","0.5295","","","","","","1","","","","has coordinates","180492","2020-10-21","18:00:00",""
"7216460","10.7001","0.0008","11.3758","0.0008","17.0795","0.0012","90","","103.62","0.001","90","","2020.5","0.3","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","ethyl3-(4-bromophenyl)-2-cyano-6,6-dimethyl-4-oxo- 2,3,4,5,6,7-hexahydrobenzofuran-2-carboxylate","","- C20 H20 Br N O4 -","- C20 H20 Br N O4 -","- C80 H80 Br4 N4 O16 -","4","1","","Chennapuram, Madhu; Emmadi, Narender Reddy; Bingi, Chiranjeevi; Nanubolu, Jagadeesh Babu; Atmakur, Krishnaiah","Group-assisted purification (GAP) chemistry for dihydrofurans: water as a medium for catalyst free synthesis in a one pot four component reaction","Green Chemistry","2014","16","6","3237","","10.1039/c4gc00388h","","","0.71073","MoKα","","0.0568","0.043","","","0.1097","0.1207","","","","","","1.027","","","","has coordinates,has disorder","180495","2020-10-21","18:00:00",""
"7216461","11.2762","0.0007","13.0441","0.0008","12.5041","0.0007","90","","112.669","0.001","90","","1697.12","0.18","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","3-(4-bromophenyl)-2-cyano-6,6-dimethyl-4-oxo- 2,3,4,5,6,7-hexahydro-1-benzofuran-2-carboxamide","","- C18 H18 N2 O3 -","- C18 H18 N2 O3 -","- C72 H72 N8 O12 -","4","1","","Chennapuram, Madhu; Emmadi, Narender Reddy; Bingi, Chiranjeevi; Nanubolu, Jagadeesh Babu; Atmakur, Krishnaiah","Group-assisted purification (GAP) chemistry for dihydrofurans: water as a medium for catalyst free synthesis in a one pot four component reaction","Green Chemistry","2014","16","6","3237","","10.1039/c4gc00388h","","","0.71073","MoKα","","0.04","0.036","","","0.1018","0.1061","","","","","","1.072","","","","has coordinates","180495","2020-10-21","18:00:00",""
"7216462","14.9957","0.0012","7.6225","0.0006","11.9828","0.001","90","","91.022","0.003","90","","1369.47","0.19","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","LWJ-161C","","","- C17 H15 N3 O -","- C17 H15 N3 O -","- C68 H60 N12 O4 -","4","1","","Li, Wenjun; Du, Zhiyun; Huang, Jiayao; Jia, Qianfa; Zhang, Kun; Wang, Jian","Direct access to 1,2,3-triazoles through organocatalytic 1,3-dipolar cycloaddition reaction of allyl ketones with azides","Green Chemistry","2014","16","6","3003","","10.1039/c4gc00406j","","","0.71073","MoKα","","0.0472","0.0381","","","0.0883","0.0941","","","","","","1.032","","","","has coordinates","180495","2020-10-21","18:00:00",""
"7216643","7.4217","0.0003","23.8402","0.0008","11.7942","0.0004","90","","99.776","0.004","90","","2056.5","0.13","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C27 H26 N2 -","- C27 H26 N2 -","- C108 H104 N8 -","4","1","","Yasmin, Lyzu; Eggers, Paul K.; Skelton, Brian W.; Stubbs, Keith A.; Raston, Colin L.","Thin film microfluidic synthesis of fluorescent highly substituted pyridines","Green Chemistry","2014","16","7","3450","","10.1039/c4gc00881b","","","0.71073","MoKα","","0.1015","0.0824","","","0.1897","0.2007","","","","","","1.143","","","","has coordinates","180497","2020-10-21","18:00:00",""
"7216644","11.8935","0.0005","13.1976","0.0006","33.9681","0.0016","90","","90","","90","","5331.8","0.4","293","2","293","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C28 H30 Cl2 N3 P Ru -","- C28 H30 Cl2 N3 P Ru -","- C224 H240 Cl16 N24 P8 Ru8 -","8","1","","Li, Wei; Xie, Jian-Hua; Yuan, Ming-Lei; Zhou, Qi-Lin","Ruthenium complexes of tetradentate bipyridine ligands: highly efficient catalysts for the hydrogenation of carboxylic esters and lactones","Green Chemistry","2014","16","9","4081","","10.1039/C4GC00835A","","","0.71075","MoKα","","0.0705","0.0659","","","0.1255","0.1273","","","","","","1.293","","","","has coordinates,has disorder","180497","2020-10-21","18:00:00",""
"7218341","10.118","0.003","11.051","0.003","21.051","0.005","90","","99.029","0.005","90","","2324.6","1.1","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C26 H18 Cu N2 O10 -","- C26 H18 Cu N2 O10 -","- C104 H72 Cu4 N8 O40 -","4","0.5","","Kathalikkattil, Amal Cherian; Kim, Dong-Woo; Tharun, Jose; Soek, Han-Geul; Roshan, Roshith; Park, Dae-Won","Aqueous-microwave synthesized carboxyl functional molecular ribbon coordination framework catalyst for the synthesis of cyclic carbonates from epoxides and CO2","Green Chemistry","2014","16","3","1607","","10.1039/c3gc41833b","","","0.71073","MoKα","","0.0851","0.0525","","","0.1152","0.1316","","","","","","1.048","","","","has coordinates","180514","2020-10-21","18:00:00",""
"7229415","14.0947","0.0004","5.86763","0.00014","18.4634","0.0005","90","","97.511","0.003","90","","1513.87","0.07","293","2","293","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H19 N O -","- C19 H19 N O -","- C76 H76 N4 O4 -","4","1","","Karu, Ramesh; Gedu, Satyanarayana","Microwave assisted domino heck cyclization and alkynylation: synthesis of alkyne substituted dihydrobenzofurans","Green Chemistry","2018","20","2","369","","10.1039/C7GC02606D","","x-ray","1.54184","CuKα","","0.0832","0.0581","","","0.1844","0.2002","","","","","","1.2425","","","","has coordinates","230098","2020-10-21","18:00:00",""
"7229581","15.2479","0.0004","5.5541","0.0001","16.8079","0.0003","90","","95.501","0.002","90","","1416.88","0.05","292","2","292","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","(E)-1-phenyl-2-tosylethanone oxime","","- C15 H15 N O3 S -","- C15 H15 N O3 S -","- C60 H60 N4 O12 S4 -","4","1","","Wang, Bin; Tang, Lin; Liu, Liyan; Li, Yanan; Yu, Yang; Wang, Zhiyong","Base-mediated tandem sulfonylation and oximation of alkenes in water","Green Chemistry","2017","","","","","10.1039/C7GC03051G","","","1.54184","CuKα","","0.0407","0.0375","","","0.1044","0.1077","","","","","","1.048","","","","has coordinates","203227","2020-10-21","18:00:00",""
"7229599","9.3104","0.0005","10.7032","0.0004","21.2565","0.0012","86.197","0.004","78.5","0.004","88.333","0.003","2070.87","0.18","173","2","173","2","","","","","","","","8","P -1","-P 1","2","","","","- C82 H78 F12 N2 O P6 Pd2 S4 -","- C78 H68 F12 N2 P6 Pd2 S4 -","- C78 H68 F12 N2 P6 Pd2 S4 -","1","0.5","","Jantan, Khairil Anuar; Kwok, Chuek Yee; Chan, Kuang Wen; Marchiò, Luciano; White, Andrew J. P.; Deplano, Paola; Serpe, Angela; Wilton-Ely, James","From recovered metal waste to high-performance palladium catalysts","Green Chemistry","2017","","","","","10.1039/C7GC02678A","","","1.54184","CuKα","","0.0514","0.039","","","0.0964","0.1041","","","","","","1.024","","","","has coordinates,has disorder","203408","2020-10-21","18:00:00",""
"7229600","20.6104","0.0005","15.5218","0.0004","26.8129","0.0009","90","","107.289","0.003","90","","8190.2","0.4","173","2","173","2","","","","","","","","8","P 1 21/n 1","-P 2yn","14","","","","- C82 H78 F12 N2 O P6 Pd2 S4 -","- C82 H78 F12 N2 O P6 Pd2 S4 -","- C328 H312 F48 N8 O4 P24 Pd8 S16 -","4","1","","Jantan, Khairil Anuar; Kwok, Chuek Yee; Chan, Kuang Wen; Marchiò, Luciano; White, Andrew J. P.; Deplano, Paola; Serpe, Angela; Wilton-Ely, James","From recovered metal waste to high-performance palladium catalysts","Green Chemistry","2017","","","","","10.1039/C7GC02678A","","","0.71073","MoKα","","0.0697","0.0466","","","0.0969","0.1084","","","","","","1.039","","","","has coordinates,has disorder","203408","2020-10-21","18:00:00",""
"7229601","33.0045","0.0005","10.85381","0.00018","26.7343","0.0004","90","","106.511","0.0016","90","","9182","0.3","173","2","173","2","","","","","","","","8","I 1 a 1","I -2ya","9","","","","- C94 H88 F12 N2 O P6 Pd2 S4 -","- C90 H78 F12 N2 P6 Pd2 S4 -","- C360 H312 F48 N8 P24 Pd8 S16 -","4","1","","Jantan, Khairil Anuar; Kwok, Chuek Yee; Chan, Kuang Wen; Marchiò, Luciano; White, Andrew J. P.; Deplano, Paola; Serpe, Angela; Wilton-Ely, James","From recovered metal waste to high-performance palladium catalysts","Green Chemistry","2017","","","","","10.1039/C7GC02678A","","","1.54184","CuKα","","0.0402","0.0373","","","0.0954","0.0986","","","","","","1.041","","","","has coordinates","203408","2020-10-21","18:00:00",""
"7229614","7.4889","0.0007","8.9633","0.0008","12.2743","0.0011","98.953","0.003","106.482","0.003","98.679","0.003","763.71","0.12","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C16 H15 N3 O5 -","- C16 H15 N3 O5 -","- C32 H30 N6 O10 -","2","1","","Qiao, Kai; Yuan, Xin; Wan, Li; Zheng, Mingwei; Zhang, Dong; Fan, Bingbing; Di, Zhechen; Fang, Zheng; Guo, Kai","Highly efficient synthesis of β-nitrate ester carboxamides through the ring-opening of 2-oxazolines","Green Chemistry","2017","","","","","10.1039/C7GC02682J","","","0.71073","MoKα","","0.0803","0.0461","","","0.0917","0.1041","","","","","","1.051","","","","has coordinates","203474","2020-10-21","18:00:00",""
"7229619","7.3712","0.0004","10.3338","0.0006","13.8683","0.0008","90","","93.683","0.003","90","","1054.2","0.1","100","2","100","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C9 H8 Cl2 O2 S -","- C9 H8 Cl2 O2 S -","- C36 H32 Cl8 O8 S4 -","4","2","","Pye, Scott J.; Dalgarno, Scott J.; Chalker, Justin M.; Raston, Colin L.","Organic oxidations promoted in vortex driven thin films under continuous flow","Green Chemistry","2018","20","1","118","","10.1039/C7GC03352D","","","0.71073","MoKα","","0.0257","0.0239","","","0.0569","0.058","","","","","","1.069","","","","has coordinates","230088","2020-10-21","18:00:00",""
"7229620","7.8477","0.0005","7.955","0.0005","20.8582","0.0011","90","","96.801","0.002","90","","1292.98","0.13","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C14 H18 O2 S -","- C14 H18 O2 S -","- C56 H72 O8 S4 -","4","1","","Pye, Scott J.; Dalgarno, Scott J.; Chalker, Justin M.; Raston, Colin L.","Organic oxidations promoted in vortex driven thin films under continuous flow","Green Chemistry","2018","20","1","118","","10.1039/C7GC03352D","","","0.71073","MoKα","","0.0315","0.0283","","","0.0735","0.0755","","","","","","1.046","","","","has coordinates","230088","2020-10-21","18:00:00",""
"7229621","19.293","0.004","7.2555","0.0014","23.177","0.005","90","","90","","90","","3244.3","1.2","296","2","296","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C22 H16 F N -","- C22 H16 F N -","- C176 H128 F8 N8 -","8","1","","Ahmed, Waqar; Zhang, Sheng; Yu, Xiaoqiang; Yamamoto, Yoshinori; Bao, Ming","Brønsted acid-catalyzed metal- and solvent-free quinoline synthesis fromN-alkyl anilines and alkynes or alkenes","Green Chemistry","2018","20","1","261","","10.1039/C7GC03175K","","","0.71073","MoKα","","0.1207","0.0506","","","0.1157","0.1482","","","","","","1.008","","","","has coordinates","276332","2022-06-28","15:25:32",""
"7229669","11.651","0.004","11.814","0.003","23.05","0.007","90","","101.391","0.004","90","","3110.2","1.6","173.15","","173.15","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C39 H31 N O2 P2 -","- C39 H31 N O2 P2 -","- C156 H124 N4 O8 P8 -","4","1","","Wen, Li-Rong; Sun, Yong-Xu; Zhang, Jin-Wei; Guo, Wei-Si; Li, Ming","Catalyst- and solvent-free bisphosphinylation of isothiocyanates: a practical method for the synthesis of bisphosphinoylaminomethanes","Green Chemistry","2018","20","1","125","","10.1039/C7GC03101G","","","0.71073","MoKα","","0.0812","0.0718","","","0.1217","0.1258","","","","","","1.23","","","","has coordinates","230090","2020-10-21","18:00:00",""
"7229731","6.2278","0.0006","37.44","0.004","7.3546","0.0006","90","","90","","90","","1714.9","0.3","293","2","293","2","","","","","","","","4","P n m a","-P 2ac 2n","62","","","","- C20 H20 O2 S -","- C20 H20 O2 S -","- C80 H80 O8 S4 -","4","0.5","","Nguyen, Thanh Binh; Retailleau, Pascal","Sulfurative self-condensation of ketones and elemental sulfur: a three-component access to thiophenes catalyzed by aniline acid‒base conjugate pairs","Green Chemistry","2018","20","2","387","","10.1039/C7GC03437G","","","1.54187","CuKα","","0.0954","0.0639","","","0.1663","0.2021","","","","","","0.926","","","","has coordinates,has disorder","230099","2020-10-21","18:00:00",""
"7229831","10.822","0.003","12.45","0.003","13.434","0.004","68.323","0.006","84.539","0.007","77.041","0.007","1639","0.8","297","1","297","1","","","","","","","","4","P -1","-P 1","2","(E)-3-[1-(dibenzylamino)-3-phenylindolizin-7-yl]-3-phenyl-1-(pyridin-2-yl)prop-2-en-1-one","","","- C42 H33 N3 O -","- C42 H33 N3 O -","- C84 H66 N6 O2 -","2","1","","Albaladejo, María José; González-Soria, María José; Alonso, Francisco","Metal-free remote-site C‒H alkenylation: regio- and diastereoselective synthesis of solvatochromic dyes","Green Chemistry","2018","20","3","701","","10.1039/C7GC03436A","","","0.71073","MoKα","","0.1985","0.0598","","","0.1747","0.2945","","","","","","0.751","","","","has coordinates","230127","2020-10-21","18:00:00",""
"7229832","12.1335","0.0016","12.3113","0.0016","12.6442","0.0017","87.101","0.003","86.513","0.003","69.271","0.003","1762.4","0.4","297","2","297","1","","","","","","","","4","P -1","-P 1","2","(E)-3-[1-(dibenzylamino)-3-(4-methoxyphenyl)indolizin-7-yl]-3-(4-methoxyphenyl)-1-(pyridin-2-yl)prop-2-en-1-one","","","- C44 H37 N3 O3 -","- C44 H37 N3 O3 -","- C88 H74 N6 O6 -","2","1","","Albaladejo, María José; González-Soria, María José; Alonso, Francisco","Metal-free remote-site C‒H alkenylation: regio- and diastereoselective synthesis of solvatochromic dyes","Green Chemistry","2018","20","3","701","","10.1039/C7GC03436A","","","0.71073","MoKα","","0.1904","0.0669","","","0.1245","0.1668","","","","","","0.962","","","","has coordinates","230127","2020-10-21","18:00:00",""
"7229843","3.7722","0.0003","8.864","0.0007","25.643","0.002","86.384","0.007","89.405","0.007","81.479","0.007","846.27","0.12","120","10","120","10","","","","","","","","3","P -1","-P 1","2","","","","- C11 H6 O2 -","- C11 H6 O2 -","- C44 H24 O8 -","4","2","","Chen, Jing-Huo; Deng, Cheng-Hua; Fang, Sheng; Ma, Jian-Gong; Cheng, Peng","Binuclear molybdenum alkoxide as the versatile catalyst for the conversion of carbon dioxide","Green Chemistry","2018","20","5","989","","10.1039/C7GC03372A","","","0.71073","MoKα","","0.106","0.0806","","","0.1831","0.1991","","","","","","1.11","","","","has coordinates","230093","2020-10-21","18:00:00",""
"7229844","3.8398","0.0008","6.201","0.003","35.222","0.007","90","","91.034","0.017","90","","838.5","0.5","120","10","120","10","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C11 H5 O2 -","- C11 H5 O2 -","- C44 H20 O8 -","4","1","","Chen, Jing-Huo; Deng, Cheng-Hua; Fang, Sheng; Ma, Jian-Gong; Cheng, Peng","Binuclear molybdenum alkoxide as the versatile catalyst for the conversion of carbon dioxide","Green Chemistry","2018","20","5","989","","10.1039/C7GC03372A","","x-ray","0.71073","MoKα","","0.1045","0.089","","","0.1873","0.1961","","","","","","1.168","","","","has coordinates","230093","2020-10-21","18:00:00",""
"7229845","17.114","0.004","11.241","0.003","18.622","0.004","90","","116.978","0.004","90","","3192.6","1.3","296","2","296.15","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C32 H25 N O4 S2 Se3 -","- C32 H25 N O4 S2 Se3 -","- C128 H100 N4 O16 S8 Se12 -","4","1","","Wang, Ying-chun; Liu, Li-qiu; Wang, Guang-mang; Ouyang, Hui; Li, You-ji","Catalyst-free room-temperature decarboxylative tri- or tetrafunctionalization of alkynyl carboxylic acids with N-fluorobenzenesulfonimide (NFSI) and diselenides","Green Chemistry","2018","20","3","604","","10.1039/C7GC03267F","","","0.71073","MoKα","","0.0622","0.0365","","","0.0931","0.105","","","","","","1.022","","","","has coordinates","230126","2020-10-21","18:00:00",""
"7229846","9.3039","0.0006","11.2838","0.0009","15.363","0.0008","110.126","0.006","99.341","0.005","93.707","0.006","1481.6","0.18","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C32 H25 N O4 S2 Se2 -","- C32 H25 N O4 S2 Se2 -","- C64 H50 N2 O8 S4 Se4 -","2","1","","Wang, Ying-chun; Liu, Li-qiu; Wang, Guang-mang; Ouyang, Hui; Li, You-ji","Catalyst-free room-temperature decarboxylative tri- or tetrafunctionalization of alkynyl carboxylic acids with N-fluorobenzenesulfonimide (NFSI) and diselenides","Green Chemistry","2018","20","3","604","","10.1039/C7GC03267F","","x-ray","0.71073","MoKα","","0.0601","0.0396","","","0.0877","0.099","","","","","","1.034","","","","has coordinates","230126","2020-10-21","18:00:00",""
"7230013","14.9687","0.0005","15.0798","0.0005","21.8498","0.0008","86.944","0.002","88.681","0.002","85.622","0.002","4909.8","0.3","193","2","193","2","","","","","","","","6","P -1","-P 1","2","","","","- C18 H33 Mo12 N6 O40 P -","- C18 H33 Mo12 N6 O40 P -","- C72 H132 Mo48 N24 O160 P4 -","4","2","","Megías-Sayago, Cristina; Álvarez, Eleuterio; Ivanova, Svetlana; Odriozola, José Antonio","Epimerization of glucose over ionic liquid/phosphomolybdate hybrids: structure‒activity relationship","Green Chemistry","2018","20","5","1042","","10.1039/C7GC03738D","","","0.71073","MoKα","","0.1035","0.08","","","0.1907","0.2023","","","","","","1.08","","","","has coordinates","230092","2020-10-21","18:00:00",""
"7230014","12.9158","0.0005","21.2163","0.0008","21.6946","0.0008","95.876","0.002","105.285","0.002","101.08","0.002","5553.7","0.4","193","2","193","2","","","","","","","","6","P -1","-P 1","2","","","","- C24 H45 Mo12 N6 O40 P -","- C24 H45 Mo12 N6 O40 P -","- C96 H180 Mo48 N24 O160 P4 -","4","2","","Megías-Sayago, Cristina; Álvarez, Eleuterio; Ivanova, Svetlana; Odriozola, José Antonio","Epimerization of glucose over ionic liquid/phosphomolybdate hybrids: structure‒activity relationship","Green Chemistry","2018","20","5","1042","","10.1039/C7GC03738D","","","0.71073","MoKα","","0.0664","0.0538","","","0.1109","0.1156","","","","","","1.17","","","","has coordinates","230092","2020-10-21","18:00:00",""
"7230015","22.3846","0.0003","20.969","0.0004","26.0718","0.0005","90","","90","","90","","12237.7","0.4","193","2","193","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C30 H57 Mo12 N6 O40 P -","- C30 H57 Mo12 N6 O40 P -","- C240 H456 Mo96 N48 O320 P8 -","8","1","","Megías-Sayago, Cristina; Álvarez, Eleuterio; Ivanova, Svetlana; Odriozola, José Antonio","Epimerization of glucose over ionic liquid/phosphomolybdate hybrids: structure‒activity relationship","Green Chemistry","2018","20","5","1042","","10.1039/C7GC03738D","","","0.71073","MoKα","","0.0433","0.0352","","","0.0769","0.0817","","","","","","1.051","","","","has coordinates","230092","2020-10-21","18:00:00",""
"7230209","17.5199","0.0018","17.5199","0.0018","10.0567","0.0014","90","","90","","90","","3086.9","0.6","230","","230","","","","","","","","","4","P -4 21 c","P -4 2n","114","","","","- C7 H22 O3 Si3 -","- C7 H22 O3 Si3 -","- C56 H176 O24 Si24 -","8","1","","Arzumanyan, Ashot V.; Goncharova, Irina K.; Novikov, Roman A.; Milenin, Sergey A.; Boldyrev, Konstantin L.; Solyev, Pavel N.; Tkachev, Yaroslav V.; Volodin, Alexander D.; Smol'yakov, Alexander F.; Korlyukov, Alexander A.; Muzafarov, Aziz M.","Aerobic Co or Cu/NHPI-catalyzed oxidation of hydride siloxanes: synthesis of siloxanols","Green Chemistry","2018","20","7","1467","","10.1039/C8GC00424B","","x-ray","0.71073","MoKα","","0.1323","0.05","","","0.1118","0.1359","","","","","","0.945","","","","has coordinates","230108","2020-10-21","18:00:00",""
"7230285","9.4619","0.0004","9.7534","0.0004","10.5387","0.0005","68.185","0.004","78.205","0.004","88.782","0.004","882.26","0.07","150","0.1","150","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C24 H19 N O -","- C24 H19 N O -","- C48 H38 N2 O2 -","2","1","","Teng, Qing-Hu; Peng, Xiang-Jun; Mo, Zu-Yu; Xu, Yan-Li; Tang, Hai-Tao; Wang, Heng-Shan; Sun, Hong-Bin; Pan, Ying-Ming","Transition-metal-free C‒N and C‒C formation: synthesis of benzo[4,5]imidazo[1,2-a]pyridines and 2-pyridones from ynones","Green Chemistry","2018","20","9","2007","","10.1039/C8GC00069G","","x-ray","1.54184","CuKα","","0.0444","0.0421","","","0.1111","0.1132","","","","","","1.031","","","","has coordinates","230111","2020-10-21","18:00:00",""
"7230286","10.6279","0.001","15.8991","0.001","13.4801","0.001","90","","100.33","0.009","90","","2240.9","0.3","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C25 H19 Cl3 N2 -","- C25 H19 Cl3 N2 -","- C100 H76 Cl12 N8 -","4","1","","Teng, Qing-Hu; Peng, Xiang-Jun; Mo, Zu-Yu; Xu, Yan-Li; Tang, Hai-Tao; Wang, Heng-Shan; Sun, Hong-Bin; Pan, Ying-Ming","Transition-metal-free C‒N and C‒C formation: synthesis of benzo[4,5]imidazo[1,2-a]pyridines and 2-pyridones from ynones","Green Chemistry","2018","20","9","2007","","10.1039/C8GC00069G","","x-ray","0.71073","MoKα","","0.1164","0.084","","","0.2101","0.2443","","","","","","1.049","","","","has coordinates","230111","2020-10-21","18:00:00",""
"7230301","6.0145","0.0003","8.0625","0.0005","16.0814","0.0009","96.122","0.002","94.613","0.002","100.073","0.002","759.5","0.07","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C16 H24 O3 -","- C16 H24 O3 -","- C32 H48 O6 -","2","1","","Wang, Yanliang; Guo, Xiangguang; Bi, Yanfeng; Su, Jia; Kong, Weichang; Sun, Xiaoqi","Enrichment of trace rare earth elements from the leaching liquor of ion-absorption minerals using a solid complex centrifugal separation process","Green Chemistry","2018","20","9","1998","","10.1039/C7GC03674D","","","0.71073","MoKα","","0.0731","0.0484","","","0.12","0.1334","","","","","","1.04","","","","has coordinates","230110","2020-10-21","18:00:00",""
"7230302","15.6175","0.0013","8.4961","0.0007","12.67","0.001","90","","96.193","0.002","90","","1671.3","0.2","296","2","296","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C17 H26 O3 -","- C17 H26 O3 -","- C68 H104 O12 -","4","1","","Wang, Yanliang; Guo, Xiangguang; Bi, Yanfeng; Su, Jia; Kong, Weichang; Sun, Xiaoqi","Enrichment of trace rare earth elements from the leaching liquor of ion-absorption minerals using a solid complex centrifugal separation process","Green Chemistry","2018","20","9","1998","","10.1039/C7GC03674D","","","0.71073","MoKα","","0.1022","0.0614","","","0.1201","0.1374","","","","","","0.994","","","","has coordinates","230110","2020-10-21","18:00:00",""
"7230303","12.9802","0.0006","8.6558","0.0004","32.2944","0.0013","90","","94.115","0.001","90","","3619.1","0.3","296","2","296","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C36 H56 O6 -","- C36 H56 O6 -","- C144 H224 O24 -","4","1","","Wang, Yanliang; Guo, Xiangguang; Bi, Yanfeng; Su, Jia; Kong, Weichang; Sun, Xiaoqi","Enrichment of trace rare earth elements from the leaching liquor of ion-absorption minerals using a solid complex centrifugal separation process","Green Chemistry","2018","20","9","1998","","10.1039/C7GC03674D","","","0.71073","MoKα","","0.1159","0.0761","","","0.1965","0.2222","","","","","","1.014","","","","has coordinates,has disorder","230110","2020-10-21","18:00:00",""
"7230313","9.1521","0.0012","9.681","0.0012","11.7658","0.0015","88.195","0.002","86.069","0.002","89.089","0.002","1039.4","0.2","130","","130","","","","","","","","","6","P -1","-P 1","2","","","","- C18 H29 Cl2 Ir N4 O2 -","- C18 H29 Cl2 Ir N4 O2 -","- C36 H58 Cl4 Ir2 N8 O4 -","2","1","","Lu, Sheng-Mei; Wang, Zhijun; Wang, Jijie; Li, Jun; Li, Can","Hydrogen generation from formic acid decomposition on a highly efficient iridium catalyst bearing a diaminoglyoxime ligand","Green Chemistry","2018","20","8","1835","","10.1039/C8GC00495A","","","0.71073","MoKα","","0.0506","0.0358","","","0.0818","0.0883","","","","","","1.006","","","","has coordinates","230091","2020-10-21","18:00:00",""
"7230342","9.324","0.003","9.76","0.003","12.772","0.004","75.736","0.006","70.173","0.005","77.227","0.005","1047.6","0.6","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H25 N5 O4 -","- C22 H25 N5 O4 -","- C44 H50 N10 O8 -","2","1","","Zhang, Furen; Li, Chunmei; Liang, Xuezheng","Solid acid-catalyzed domino cyclization reaction: regio- and diastereoselective synthesis of pyrido[2,3-d]pyrimidine derivatives bearing three contiguous stereocenters","Green Chemistry","2018","20","9","2057","","10.1039/C7GC03812G","","","0.71073","MoKα","","0.0664","0.05","","","0.1226","0.1333","","","","","","1.056","","","","has coordinates","230109","2020-10-21","18:00:00",""
"7230380","43.317","0.009","23.984","0.004","28.932","0.007","90","","117.762","0.004","90","","26598","10","100","2","100","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C116 H88 Cl6 N8 -","- C116 H88 Cl6 N8 -","- C928 H704 Cl48 N64 -","8","1","","Ishizuka, Tomoya; Ohkawa, Shumpei; Ochiai, Hidemi; Hashimoto, Muneaki; Ohkubo, Kei; Kotani, Hiroaki; Sadakane, Masahiro; Fukuzumi, Shunichi; Kojima, Takahiko","A supramolecular photocatalyst composed of a polyoxometalate and a photosensitizing water-soluble porphyrin diacid for the oxidation of organic substrates in water","Green Chemistry","2018","20","9","1975","","10.1039/C8GC00295A","","","0.71073","MoKα","","0.1566","0.111","","","0.3221","0.3485","","","","","","1.077","","","","has coordinates,has disorder","230112","2020-10-21","18:00:00",""
"7230471","9.1495","0.0007","11.0385","0.0008","11.775","0.001","68.418","0.007","81.041","0.007","68.191","0.007","1026.46","0.16","293","2","293.15","","","","","","","","","5","P -1","-P 1","2","","","","- C23 H18 N2 O5 S -","- C23 H18 N2 O5 S -","- C46 H36 N4 O10 S2 -","2","1","","Yao, Xinghui; Weng, Xin; Wang, Kaixuan; Xiang, Haifeng; Zhou, Xiangge","Transition metal free oxygenation of 8-aminoquinoline amides in water","Green Chemistry","2018","20","11","2472","","10.1039/C8GC00191J","","x-ray","0.71073","MoKα","","0.0649","0.0454","","","0.1058","0.1201","","","","","","1.036","","","","has coordinates","230122","2020-10-21","18:00:00",""
"7230499","12.105","0.002","7.6772","0.0015","11.507","0.002","90","","97.73","0.03","90","","1059.7","0.3","153","2","153.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C14 H10 N2 O -","- C14 H10 N2 O -","- C56 H40 N8 O4 -","4","1","","Yu, Wenjia; Zhang, Xianwei; Qin, Bingjie; Wang, Qiyang; Ren, Xuhong; He, Xinhua","Furan-2-carbaldehydes as C1 building blocks for the synthesis of quinazolin-4(3H)-ones via ligand-free photocatalytic C‒C bond cleavage","Green Chemistry","2018","20","11","2449","","10.1039/C8GC00079D","","","0.71073","MoKα","","0.0695","0.0617","","","0.1437","0.15","","","","","","1.152","","","","has coordinates","230121","2020-10-21","18:00:00",""
"7230500","10.351","0.002","11.378","0.002","12.992","0.003","90","","106.17","0.03","90","","1469.6","0.6","153","2","153.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H14 N2 O2 -","- C19 H14 N2 O2 -","- C76 H56 N8 O8 -","4","1","","Yu, Wenjia; Zhang, Xianwei; Qin, Bingjie; Wang, Qiyang; Ren, Xuhong; He, Xinhua","Furan-2-carbaldehydes as C1 building blocks for the synthesis of quinazolin-4(3H)-ones via ligand-free photocatalytic C‒C bond cleavage","Green Chemistry","2018","20","11","2449","","10.1039/C8GC00079D","","","0.71073","MoKα","","0.0602","0.0553","","","0.1266","0.1302","","","","","","1.143","","","","has coordinates","230121","2020-10-21","18:00:00",""
"7230578","5.8802","0.0004","25.3608","0.0019","8.2156","0.0006","90","","109.663","0.002","90","","1153.72","0.14","296","2","296","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C12 H14 O4 -","- C12 H14 O4 -","- C48 H56 O16 -","4","1","","Yang, Da; Liu, Huan; Wang, Dong-Liang; Luo, Zhoujie; Lu, Yong; Xia, Fei; Liu, Ye","Co-catalysis over a bi-functional ligand-based Pd-catalyst for tandem bis-alkoxycarbonylation of terminal alkynes","Green Chemistry","2018","20","11","2588","","10.1039/C8GC00754C","","","0.71073","MoKα","","0.0629","0.0514","","","0.1301","0.1389","","","","","","1.048","","","","has coordinates","230123","2020-10-21","18:00:00",""
"7230581","29.72","0.04","5.675","0.007","7.425","0.009","90","","95.29","0.02","90","","1247","3","293.15","","293.15","","","","","","","","","5","C 1 c 1","C -2yc","9","","","","- C15 H0 Br N O -","- C15 H12 Br N O -","- C60 H48 Br4 N4 O4 -","4","1","","Chen, Chun-Hua; Wu, Qing-Yan; Wei, Cui; Liang, Cui; Su, Gui-Fa; Mo, Dong-Liang","Iron(iii)-catalyzed selective N‒O bond cleavage to prepare tetrasubstituted pyridines and 3,5-disubstituted isoxazolines from N-vinyl-α,β-unsaturated ketonitrones","Green Chemistry","2018","20","12","2722","","10.1039/C8GC00630J","","","0.71073","MoKα","","0.0988","0.0727","","","0.1964","0.2171","","","","","","1.055","","","","has coordinates","230125","2020-10-21","18:00:00",""
"7230582","8.585","0.0015","9.869","0.0017","10.0994","0.0017","91.079","0.003","103.819","0.003","90.728","0.003","830.6","0.2","296.15","","296.15","","","","","","","","","4","P -1","-P 1","2","","","","- C20 H16 F3 N -","- C20 H16 F3 N -","- C40 H32 F6 N2 -","2","1","","Chen, Chun-Hua; Wu, Qing-Yan; Wei, Cui; Liang, Cui; Su, Gui-Fa; Mo, Dong-Liang","Iron(iii)-catalyzed selective N‒O bond cleavage to prepare tetrasubstituted pyridines and 3,5-disubstituted isoxazolines from N-vinyl-α,β-unsaturated ketonitrones","Green Chemistry","2018","20","12","2722","","10.1039/C8GC00630J","","","0.71073","MoKα","","0.1308","0.1156","","","0.3948","0.4283","","","","","","1.928","","","","has coordinates","230125","2020-10-21","18:00:00",""
"7230705","10.4863","0.0002","9.6208","0.0002","12.383","0.0002","90","","111.484","0.002","90","","1162.48","0.04","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C13 H10 Cl N O S -","- C13 H10 Cl N O S -","- C52 H40 Cl4 N4 O4 S4 -","4","1","","Ma, Yan-Na; Guo, Chen-Yang; Zhao, Qianyi; Zhang, Jie; Chen, Xuenian","Synthesis of dibenzothiazines from sulfides by one-pot N,O-transfer and intramolecular C‒H amination","Green Chemistry","2018","20","13","2953","","10.1039/C8GC01057A","","x-ray","1.54184","CuKα","","0.0528","0.0454","","","0.1406","0.1462","","","","","","1.155","","","","has coordinates","230103","2020-10-21","18:00:00",""
"7230721","21.758","0.005","50.304","0.005","13.416","0.005","90","","90","","90","","14684","7","173","2","173","2","","","","","","","","5","F d d 2","F 2 -2d","43","","","","- C80 H70 Cl2 N6 O11 -","- C80 H70 Cl2 N6 O11 -","- C640 H560 Cl16 N48 O88 -","8","0.5","","Wang, Dong; Li, Linna; Feng, Hairong; Sun, Hua; Almeida-Veloso, Fabrice; Charavin, Marine; Yu, Peng; Désaubry, Laurent","Catalyst-free three-component synthesis of highly functionalized 2,3-dihydropyrroles","Green Chemistry","2018","20","12","2775","","10.1039/C8GC00987B","","","0.71073","MoKα","","0.0607","0.0527","","","0.1321","0.1378","","","","","","1.082","","","","has coordinates","230124","2020-10-21","18:00:00",""
"7230722","12.043","0.003","13.174","0.004","13.616","0.004","98.819","0.009","97.641","0.006","98.079","0.005","2087","1","113","","113","","","","","","","","","5","P -1","-P 1","2","","","","- C48 H49 Cl2 N3 O4 -","- C48 H49 Cl2 N3 O4 -","- C96 H98 Cl4 N6 O8 -","2","1","","Wang, Dong; Li, Linna; Feng, Hairong; Sun, Hua; Almeida-Veloso, Fabrice; Charavin, Marine; Yu, Peng; Désaubry, Laurent","Catalyst-free three-component synthesis of highly functionalized 2,3-dihydropyrroles","Green Chemistry","2018","20","12","2775","","10.1039/C8GC00987B","","","0.71075","MoKα","","0.0874","0.0568","","","0.1415","0.1572","","","","","","1.056","","","","has coordinates","230124","2020-10-21","18:00:00",""
"7230738","7.22158","0.00015","9.60997","0.00016","13.4791","0.0003","90","","90","","90","","935.44","0.03","109.95","0.1","109.95","0.1","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C11 H10 O4 -","- C11 H10 O4 -","- C44 H40 O16 -","4","1","","Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.","Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)","Green Chemistry","2018","20","19","4423","","10.1039/C8GC01227J","","x-ray","1.54184","CuKα","","0.0256","0.0247","","","0.0639","0.0646","","","","","","1.075","","","","has coordinates","230100","2020-10-21","18:00:00",""
"7230739","8.36693","0.00018","7.08624","0.00014","19.5336","0.0004","90","","93.2815","0.0018","90","","1156.25","0.04","110.05","0.1","110.05","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C13 H11 N O5 -","- C13 H11 N O5 -","- C52 H44 N4 O20 -","4","2","","Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.","Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)","Green Chemistry","2018","20","19","4423","","10.1039/C8GC01227J","","x-ray","1.54184","CuKα","","0.0381","0.0334","","","0.0811","0.0846","","","","","","1.051","","","","has coordinates","230100","2020-10-21","18:00:00",""
"7230740","13.5583","0.0002","13.5583","0.0002","45.7998","0.0006","90","","90","","120","","7291.3","0.18","110.05","0.1","110.05","0.1","","","","","","","","3","P 65","P 65","170","","","","- C15 H14 O3 -","- C15 H14 O3 -","- C360 H336 O72 -","24","4","","Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.","Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)","Green Chemistry","2018","20","19","4423","","10.1039/C8GC01227J","","x-ray","1.54184","CuKα","","0.0914","0.0909","","","0.2298","0.2302","","","","","","1.072","","","","has coordinates","230100","2020-10-21","18:00:00",""
"7230741","6.32713","0.00007","10.32552","0.0001","15.23806","0.00018","90","","90","","90","","995.516","0.019","110","0.1","110","0.1","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C11 H10 O3 S -","- C11 H10 O3 S -","- C44 H40 O12 S4 -","4","1","","Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.","Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)","Green Chemistry","2018","20","19","4423","","10.1039/C8GC01227J","","x-ray","1.54184","CuKα","","0.021","0.0209","","","0.0563","0.0563","","","","","","1.046","","","","has coordinates","230100","2020-10-21","18:00:00",""
"7230742","9.50457","0.00013","9.59528","0.00011","11.4776","0.00013","90","","90","","90","","1046.75","0.02","110.1","0.14","110.1","0.14","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C13 H12 O4 -","- C13 H12 O4 -","- C52 H48 O16 -","4","1","","Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.","Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)","Green Chemistry","2018","20","19","4423","","10.1039/C8GC01227J","","x-ray","1.54184","CuKα","","0.0257","0.0244","","","0.0604","0.0615","","","","","","1.084","","","","has coordinates","230100","2020-10-21","18:00:00",""
"7230743","6.47958","0.00016","7.89044","0.00019","22.4589","0.0006","90","","90","","90","","1148.25","0.05","109.9","0.2","109.9","0.2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C14 H14 O3 -","- C14 H14 O3 -","- C56 H56 O12 -","4","1","","Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.","Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)","Green Chemistry","2018","20","19","4423","","10.1039/C8GC01227J","","x-ray","1.54184","CuKα","","0.036","0.0334","","","0.0839","0.0864","","","","","","1.067","","","","has coordinates","230100","2020-10-21","18:00:00",""
"7230744","5.94601","0.00013","5.17983","0.00013","18.2456","0.0005","90","","94.739","0.002","90","","560.03","0.02","110","0.1","110","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C13 H11 Cl O3 -","- C13 H11 Cl O3 -","- C26 H22 Cl2 O6 -","2","1","","Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.","Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)","Green Chemistry","2018","20","19","4423","","10.1039/C8GC01227J","","x-ray","1.54184","CuKα","","0.0371","0.0358","","","0.092","0.0934","","","","","","1.038","","","","has coordinates","230100","2020-10-21","18:00:00",""
"7230745","11.11016","0.0001","9.04172","0.00009","15.58673","0.00013","90","","95.3028","0.0008","90","","1559.06","0.02","110.05","0.1","110.05","0.1","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C13 H12 O3 -","- C13 H12 O3 -","- C78 H72 O18 -","6","3","","Hughes, Liam; McElroy, Con R.; Whitwood, Adrian C.; Hunt, Andrew J.","Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen‒Schmidt reactions of dihydrolevoglucosenone (Cyrene®)","Green Chemistry","2018","20","19","4423","","10.1039/C8GC01227J","","x-ray","1.54184","CuKα","","0.03","0.0277","","","0.0673","0.0692","","","","","","1.06","","","","has coordinates","230100","2020-10-21","18:00:00",""
"7230820","7.7651","0.0006","16.4066","0.0012","14.1404","0.0015","90","","90","","90","","1801.5","0.3","173","2","173","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C22 H16 O5 S -","- C22 H16 O5 S -","- C88 H64 O20 S4 -","4","1","","Chen, Zhengkai; Liu, Nai-Wei; Bolte, Michael; Ren, Hongjun; Manolikakes, Georg","Visible-light mediated 3-component synthesis of sulfonylated coumarins from sulfur dioxide","Green Chemistry","2018","20","13","3059","","10.1039/C8GC00838H","","","0.71073","MoKα","","0.0359","0.0299","","","0.0632","0.0647","","","","","","0.976","","","","has coordinates","230102","2020-10-21","18:00:00",""
"7230821","12.8859","0.0012","5.6317","0.0003","25.025","0.002","90","","92.804","0.008","90","","1813.9","0.2","173","2","173","2","","","","","","","","5","P 1 c 1","P -2yc","7","","","","- C21 H13 Cl O4 S -","- C21 H13 Cl O4 S -","- C84 H52 Cl4 O16 S4 -","4","2","","Chen, Zhengkai; Liu, Nai-Wei; Bolte, Michael; Ren, Hongjun; Manolikakes, Georg","Visible-light mediated 3-component synthesis of sulfonylated coumarins from sulfur dioxide","Green Chemistry","2018","20","13","3059","","10.1039/C8GC00838H","","","0.71073","MoKα","","0.086","0.0708","","","0.1858","0.1986","","","","","","0.954","","","","has coordinates","230102","2020-10-21","18:00:00",""
"7230882","8.9159","0.0018","9.228","0.0019","10.159","0.002","105.035","0.005","98.43","0.005","102.959","0.005","767.8","0.3","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C18 H19 N O2 S -","- C18 H19 N O2 S -","- C36 H38 N2 O4 S2 -","2","1","","Herold, Sebastian; Bafaluy, Daniel; Muñiz, Kilian","Anodic benzylic C(sp3)‒H amination: unified access to pyrrolidines and piperidines","Green Chemistry","2018","20","14","3191","","10.1039/C8GC01411F","","","0.71073","MoKα","","0.0476","0.0389","","","0.1008","0.1063","","","","","","1.066","","","","has coordinates","230107","2020-10-21","18:00:00",""
"7230883","39.756","0.004","6.2412","0.0007","31.125","0.003","90","","123.261","0.002","90","","6457.7","1.2","100","2","100","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C14 H15 F6 N O3 S -","- C14 H15 F6 N O3 S -","- C224 H240 F96 N16 O48 S16 -","16","2","","Herold, Sebastian; Bafaluy, Daniel; Muñiz, Kilian","Anodic benzylic C(sp3)‒H amination: unified access to pyrrolidines and piperidines","Green Chemistry","2018","20","14","3191","","10.1039/C8GC01411F","","","0.71073","MoKα","","0.1017","0.0641","","","0.1453","0.1599","","","","","","1.071","","","","has coordinates","230107","2020-10-21","18:00:00",""
"7230887","8.9121","0.0004","10.6028","0.0006","10.607","0.0006","107.362","0.002","95.433","0.002","110.176","0.002","875.81","0.08","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C18 H21 N O6 -","- C18 H21 N O6 -","- C36 H42 N2 O12 -","2","1","","Wang, Yinling; Du, Yiman; He, Jianghua; Zhang, Yuetao","Transformation of lignin model compounds to N-substituted aromatics via Beckmann rearrangement","Green Chemistry","2018","20","14","3318","","10.1039/C8GC00920A","","","0.71073","MoKα","","0.0617","0.0476","","","0.1139","0.1232","","","","","","1.017","","","","has coordinates","230105","2020-10-21","18:00:00",""
"7230903","14.081","0.0014","14.4862","0.0011","16.112","0.0015","90","","113.689","0.012","90","","3009.6","0.5","297","2","297","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C20 H18 O -","- C20 H18 O -","- C160 H144 O8 -","8","1","","Senadi, Gopal Chandru; Wang, Jeh-Jeng","p-TsOH promoted synthesis of benzo-fused O-heterocycles from alkynolsviaring contraction and C‒O scission strategy","Green Chemistry","2018","20","15","3420","","10.1039/C8GC00749G","","x-ray","0.71073","MoKα","","0.1185","0.0714","","","0.1846","0.2261","","","","","","1.03","","","","has coordinates","230113","2020-10-21","18:00:00",""
"7230904","6.3828","0.0008","10.3101","0.0016","11.896","0.002","104.198","0.014","100.779","0.012","97.652","0.012","732.2","0.2","297","2","297","2","","","","","","","","3","P -1","-P 1","2","","","","- C19 H16 O2 -","- C19 H16 O2 -","- C38 H32 O4 -","2","1","","Senadi, Gopal Chandru; Wang, Jeh-Jeng","p-TsOH promoted synthesis of benzo-fused O-heterocycles from alkynolsviaring contraction and C‒O scission strategy","Green Chemistry","2018","20","15","3420","","10.1039/C8GC00749G","","x-ray","0.71073","MoKα","","0.1215","0.0636","","","0.182","0.2617","","","","","","0.867","","","","has coordinates","230113","2020-10-21","18:00:00",""
"7230905","9.52","0.0017","13.2012","0.002","8.3853","0.0014","90","","112.716","0.019","90","","972.1","0.3","297","2","297","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C12 H10 O3 -","- C12 H10 O3 -","- C48 H40 O12 -","4","1","","Senadi, Gopal Chandru; Wang, Jeh-Jeng","p-TsOH promoted synthesis of benzo-fused O-heterocycles from alkynolsviaring contraction and C‒O scission strategy","Green Chemistry","2018","20","15","3420","","10.1039/C8GC00749G","","x-ray","0.71073","MoKα","","0.0995","0.0549","","","0.117","0.1454","","","","","","1.046","","","","has coordinates","230113","2020-10-21","18:00:00",""
"7230906","28.6436","0.0009","28.6436","0.0009","13.5364","0.0005","90","","90","","90","","11106","0.6","100","","100","","","","","","","","","7","I -4","I -4","82","","","","- C53 H44 Cl F6 N4 P3 Ru -","- C53 H44 Cl F6 N4 P3 Ru -","- C424 H352 Cl8 F48 N32 P24 Ru8 -","8","1","","Chakrabarti, Kaushik; Mishra, Anju; Panja, Dibyajyoti; Paul, Bhaskar; Kundu, Sabuj","Selective synthesis of mono- and di-methylated amines using methanol and sodium azide as C1 and N1 sources","Green Chemistry","2018","20","14","3339","","10.1039/C8GC00863A","","","0.71073","MoKα","","0.1039","0.0714","","","0.1913","0.2157","","","","","","1.119","","","","has coordinates","230104","2020-10-21","18:00:00",""
"7230942","10.1352","0.0005","13.2429","0.0007","16.5954","0.0008","110.962","0.005","96.295","0.004","91.276","0.004","2062.93","0.19","293","2","293","2","","","","","","","","7","P -1","-P 1","2","","(3S,10aS)-1-((4-bromophenyl)sulfonyl)-7-methyl-3,4-diphenyl-9-tosyl-3,9,10,10a-tetrahydropyrrolo[2,3-b]carbazol-2(1H)-one","","- C42 H36 Br Cl2 N2 O5.5 S2 -","- C40 H31 Br N2 O5 S2 -","- C80 H62 Br2 N4 O10 S4 -","2","1","","Wang, Cai-Ming; Qi, Lin-Jun; Sun, Qing; Zhou, Bo; Zhang, Zhi-Xin; Shi, Zai-Fa; Lin, Shui-Chao; Lu, Xin; Gong, Lei; Ye, Long-Wu","Transition-metal-free oxidative cyclization of N-propargyl ynamides: stereospecific construction of linear polycyclic N-heterocycles","Green Chemistry","2018","20","14","3271","","10.1039/C8GC01534A","","x-ray","1.54184","CuKα","","0.2899","0.1978","","","0.4901","0.5161","","","","","","1.981","","","","has coordinates","230106","2020-10-21","18:00:00",""
"7230943","18.5095","0.0015","10.9007","0.0008","10.3745","0.0008","90","","103.857","0.008","90","","2032.3","0.3","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","(3R,3aS,4R,9aS)-1-(methylsulfonyl)-3,4-diphenyl-3a,4,9,9a-tetrahydro-1H-benzo[f]indol-2(3H)-one","","- C25 H23 N O3 S -","- C25 H23 N O3 S -","- C100 H92 N4 O12 S4 -","4","1","","Wang, Cai-Ming; Qi, Lin-Jun; Sun, Qing; Zhou, Bo; Zhang, Zhi-Xin; Shi, Zai-Fa; Lin, Shui-Chao; Lu, Xin; Gong, Lei; Ye, Long-Wu","Transition-metal-free oxidative cyclization of N-propargyl ynamides: stereospecific construction of linear polycyclic N-heterocycles","Green Chemistry","2018","20","14","3271","","10.1039/C8GC01534A","","x-ray","1.54184","CuKα","","0.0881","0.0583","","","0.1418","0.1675","","","","","","1.028","","","","has coordinates","230106","2020-10-21","18:00:00",""
"7230944","11.7246","0.0004","12.2563","0.0006","16.5665","0.0007","90","","98.55","0.004","90","","2354.15","0.17","99.97","0.1","99.97","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","(3R,9aS)-3,4-diphenyl-1-tosyl-9,9a-dihydro-1H-benzo[f]indol-2(3H)-one","","- C31 H25 N O3 S -","- C31 H25 N O3 S -","- C124 H100 N4 O12 S4 -","4","1","","Wang, Cai-Ming; Qi, Lin-Jun; Sun, Qing; Zhou, Bo; Zhang, Zhi-Xin; Shi, Zai-Fa; Lin, Shui-Chao; Lu, Xin; Gong, Lei; Ye, Long-Wu","Transition-metal-free oxidative cyclization of N-propargyl ynamides: stereospecific construction of linear polycyclic N-heterocycles","Green Chemistry","2018","20","14","3271","","10.1039/C8GC01534A","","x-ray","1.54184","CuKα","","0.0498","0.043","","","0.1092","0.1149","","","","","","1.035","","","","has coordinates","230106","2020-10-21","18:00:00",""
"7230945","17.0463","0.0015","11.4307","0.0011","18.4621","0.0016","90","","107.898","0.002","90","","3423.3","0.5","298","2","298","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C21 H18 O4 -","- C21 H18 O4 -","- C168 H144 O32 -","8","1","","Sha, Hong-Kai; Liu, Feng; Lu, Juan; Liu, Zhang-Qin; Hao, Wen-Juan; Tang, Jia-Le; Tu, Shu-Jiang; Jiang, Bo","Metal-free benzannulation of yne-allenone esters for atom economical synthesis of functionalized 1-naphthols","Green Chemistry","2018","20","15","3476","","10.1039/C8GC01034J","","","0.71073","MoKα","","0.1499","0.0645","","","0.1741","0.2243","","","","","","0.993","","","","has coordinates","230115","2020-10-21","18:00:00",""
"7230946","14.9117","0.0012","9.0532","0.0008","16.0374","0.0014","90","","99.025","0.002","90","","2138.2","0.3","298","2","298","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C27 H23 N O3 -","- C27 H23 N O3 -","- C108 H92 N4 O12 -","4","1","","Sha, Hong-Kai; Liu, Feng; Lu, Juan; Liu, Zhang-Qin; Hao, Wen-Juan; Tang, Jia-Le; Tu, Shu-Jiang; Jiang, Bo","Metal-free benzannulation of yne-allenone esters for atom economical synthesis of functionalized 1-naphthols","Green Chemistry","2018","20","15","3476","","10.1039/C8GC01034J","","","0.71073","MoKα","","0.2188","0.1367","","","0.3854","0.4177","","","","","","1.138","","","","has coordinates","230115","2020-10-21","18:00:00",""
"7231095","9.7181","0.0005","11.6016","0.0007","12.0845","0.0007","69.98","0.004","78.308","0.004","71.223","0.004","1205.45","0.12","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","1-(1-cyclohexyl-1H-tetrazol-5-yl)-2-(9H-fluoren-9-yl)-1,2,3,4-tetrahydroisoquinoline","","- C29 H29 N5 -","- C29 H29 N5 -","- C58 H58 N10 -","2","1","","Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K.","C‒H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines","Green Chemistry","2018","20","15","3463","","10.1039/C8GC01544A","","","0.71073","MoKα","","0.0888","0.0599","","","0.1354","0.1544","","","","","","0.978","","","","has coordinates","230114","2020-10-21","18:00:00",""
"7231096","8.154","0.0014","14.767","0.002","16.628","0.003","90.056","0.011","100.409","0.011","90.188","0.011","1969.2","0.6","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","5-(1-(9H-fluoren-9-yl)pyrrolidin-2-yl)-1-tert-butyl-1H-tetrazole","","- C22 H25 N5 -","- C22 H25 N5 -","- C88 H100 N20 -","4","2","","Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K.","C‒H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines","Green Chemistry","2018","20","15","3463","","10.1039/C8GC01544A","","","0.71073","MoKα","","0.1677","0.1109","","","0.2542","0.3007","","","","","","0.931","","","","has coordinates","230114","2020-10-21","18:00:00",""
"7231097","9.5211","0.001","11.9295","0.0007","20.9205","0.0017","90","","100.11","0.008","90","","2339.3","0.3","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","((2S,5R)-5-(1-(4-chlorobenzyl)-1H-tetrazol-5-yl)-1-(9H-fluoren-9-yl)pyrrolidin-2-yl)methanol","","- C26 H24 Cl N5 O -","- C26 H24 Cl N5 O -","- C104 H96 Cl4 N20 O4 -","4","2","","Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K.","C‒H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines","Green Chemistry","2018","20","15","3463","","10.1039/C8GC01544A","","","0.71073","MoKα","","0.1806","0.0723","","","0.0854","0.1282","","","","","","0.961","","","","has coordinates","230114","2020-10-21","18:00:00",""
"7231098","10.7702","0.0004","13.9788","0.0004","15.802","0.0006","90","","109.391","0.004","90","","2244.11","0.15","296","2","296","2","","","","","","","","3","C 1 c 1","C -2yc","9","","5-(1-(9H-fluoren-9-yl)pyrrolidin-2-yl)-1-(2,6-dimethylphenyl)-1H-tetrazole","","- C26 H25 N5 -","- C26 H25 N5 -","- C104 H100 N20 -","4","1","","Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K.","C‒H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines","Green Chemistry","2018","20","15","3463","","10.1039/C8GC01544A","","","0.71073","MoKα","","0.0788","0.0536","","","0.1447","0.1626","","","","","","1.002","","","","has coordinates","230114","2020-10-21","18:00:00",""
"7231099","13.8953","0.0007","9.4127","0.0005","16.851","0.0008","90","","97.186","0.004","90","","2186.67","0.19","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","5-((R)-1-(9H-fluoren-9-yl)pyrrolidin-2-yl)-1-((R)-1-phenylethyl)-1H-tetrazole","","- C26 H25 N5 -","- C26 H25 N5 -","- C104 H100 N20 -","4","1","","Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K.","C‒H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines","Green Chemistry","2018","20","15","3463","","10.1039/C8GC01544A","","","0.71073","MoKα","","0.1018","0.0786","","","0.22","0.2368","","","","","","0.979","","","","has coordinates","230114","2020-10-21","18:00:00",""
"7231100","11.3769","0.0003","17.6453","0.0005","11.4216","0.0003","90","","96.532","0.002","90","","2277.99","0.11","296","2","296","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","1-(1-tert-butyl-1H-tetrazol-5-yl)-2-(9H-fluoren-9-yl)-1,2,3,4-tetrahydroisoquinoline","","- C1.61 H1.61 N0.3 -","- C1.61194 H1.61194 N0.298507 -","- C108 H108 N20 -","67","16.75","","Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K.","C‒H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines","Green Chemistry","2018","20","15","3463","","10.1039/C8GC01544A","","","0.71073","MoKα","","0.0622","0.0492","","","0.1581","0.1694","","","","","","1.442","","","","has coordinates","230114","2020-10-21","18:00:00",""
"7231101","9.5012","0.001","15.8064","0.0015","18.7456","0.0017","90","","90","","90","","2815.2","0.5","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","(S)-2-(9H-fluoren-9-yl)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-(1-((R)-1-phenylethyl)-1H-tetrazol-5-yl)isoquinoline","","- C33 H31 N5 O2 -","- C33 H31 N5 O2 -","- C132 H124 N20 O8 -","4","1","","Haldar, Surajit; Saha, Subhajit; Mandal, Sumana; Jana, Chandan K.","C‒H functionalization enabled stereoselective Ugi-azide reaction to α-tetrazolyl alicyclic amines","Green Chemistry","2018","20","15","3463","","10.1039/C8GC01544A","","","0.71073","MoKα","","0.067","0.0434","","","0.088","0.0972","","","","","","0.95","","","","has coordinates","230114","2020-10-21","18:00:00",""
"7231208","8.4181","0.001","9.1433","0.0007","10.4688","0.0009","74.013","0.007","72.64","0.009","69.444","0.009","706.85","0.13","170","","170","","","","","","","","","5","P -1","-P 1","2","","","","- C17 H14 N2 O2 S -","- C17 H14 N2 O2 S -","- C34 H28 N4 O4 S2 -","2","1","","Chen, En; Shao, Jiaan; Tang, Pai; Shu, Ke; Chen, Wenteng; Yu, Yongping","Catalyst-free three-component sequencing for efficient assembly of [1,3] oxazine N-fused imidazole-2-thiones","Green Chemistry","2018","20","16","3696","","10.1039/C8GC01766B","","","0.71073","MoKα","","0.0622","0.048","","","0.1078","0.1218","","","","","","1.063","","","","has coordinates","230101","2020-10-21","18:00:00",""
"7231242","5.8293","0.0003","9.3602","0.0005","10.5304","0.0006","77.907","0.001","80.183","0.001","78.031","0.001","544.74","0.05","293","2","293","2","","","","","","","synthesis as described","4","P -1","-P 1","2","","","","- C12 H14 N2 O -","- C12 H14 N2 O -","- C24 H28 N4 O2 -","2","1","","Pelliccia, Sveva; Abbate, Vincenzo; Meneghetti, Fiorella; Frascione, Nunzianda; Hider, Robert Charles; Novellino, Ettore; Tron, Gian Cesare; Giustiniano, Mariateresa","On-water pyrrolidine-mediated domino synthesis of 2-iminoisatins","Green Chemistry","2018","20","17","3912","","10.1039/C8GC01090K","","x-ray","0.71073","MoKα","","0.0549","0.0462","","","0.1311","0.1414","","","","","","1.061","","","","has coordinates","230094","2020-10-21","18:00:00",""
"7231243","22.8345","0.0007","15.0703","0.0005","27.8444","0.0009","90","","92.926","0.001","90","","9569.4","0.5","150","2","150.01","","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C90 H78 Cl N9 O5 P6 Ru2 -","- C90 H78 Cl N9 O5 P6 Ru2 -","- C360 H312 Cl4 N36 O20 P24 Ru8 -","4","1","","Guan, Chao; Pan, Yupeng; Ang, Eleanor Pei Ling; Hu, Jinsong; Yao, Changguang; Huang, Mei-Hui; Li, Huaifeng; Lai, Zhiping; Huang, Kuo-Wei","Conversion of CO2 from air into formate using amines and phosphorus-nitrogen PN3P-Ru(ii) pincer complexes","Green Chemistry","2018","20","18","4201","","10.1039/C8GC02186D","","","1.54178","CuKα","","0.0679","0.0597","","","0.1731","0.1793","","","","","","1.081","","","","has coordinates","230116","2020-10-21","18:00:00",""
"7231244","12.2479","0.0014","20.634","0.002","25.309","0.003","106.192","0.004","93.516","0.004","106.236","0.004","5829.8","1.1","180","","180","","","","","","","","","6","P -1","-P 1","2","","","","- C48 H40 N3 O P3 Ru -","- C48 H40 N3 O P3 Ru -","- C192 H160 N12 O4 P12 Ru4 -","4","2","","Guan, Chao; Pan, Yupeng; Ang, Eleanor Pei Ling; Hu, Jinsong; Yao, Changguang; Huang, Mei-Hui; Li, Huaifeng; Lai, Zhiping; Huang, Kuo-Wei","Conversion of CO2 from air into formate using amines and phosphorus-nitrogen PN3P-Ru(ii) pincer complexes","Green Chemistry","2018","20","18","4201","","10.1039/C8GC02186D","","","0.71073","MoKα","","0.099","0.077","","","0.1976","0.2072","","","","","","1.06","","","","has coordinates","230116","2020-10-21","18:00:00",""
"7231311","5.6803","0.0005","22.15","0.002","23.2022","0.0016","90","","90.281","0.007","90","","2919.2","0.4","173","2","173","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H14.5 F3 N3 O0.25 -","- C16 H14.5 F3 N3 O0.25 -","- C128 H116 F24 N24 O2 -","8","2","","Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia","Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents","Green Chemistry","2018","20","17","4023","","10.1039/C8GC01797B","","","1.54184","CuKα","","0.1511","0.0915","","","0.2392","0.2987","","","","","","1.028","","","","has coordinates,has disorder","230095","2020-10-21","18:00:00",""
"7231312","5.35503","0.00014","10.169","0.0002","32.73","0.0007","90","","92.72","0.002","90","","1780.31","0.07","173","2","173","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C18 H23 N3 O4 -","- C18 H23 N3 O4 -","- C72 H92 N12 O16 -","4","2","","Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia","Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents","Green Chemistry","2018","20","17","4023","","10.1039/C8GC01797B","","","1.54184","CuKα","","0.0606","0.0493","","","0.1235","0.1355","","","","","","1.072","","","","has coordinates,has disorder","230095","2020-10-21","18:00:00",""
"7231313","27.0703","0.0018","5.7522","0.0004","8.0156","0.0005","90","","90","","90","","1248.14","0.14","173","2","173","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C15 H12 F3 N -","- C15 H12 F3 N -","- C60 H48 F12 N4 -","4","1","","Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia","Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents","Green Chemistry","2018","20","17","4023","","10.1039/C8GC01797B","","","0.71073","MoKα","","0.0536","0.0489","","","0.1187","0.1228","","","","","","1.136","","","","has coordinates","230095","2020-10-21","18:00:00",""
"7231314","12.8362","0.0005","11.1053","0.0004","11.7668","0.0004","90","","92.584","0.004","90","","1675.65","0.11","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C18 H23 N3 O2 -","- C18 H23 N3 O2 -","- C72 H92 N12 O8 -","4","1","","Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia","Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents","Green Chemistry","2018","20","17","4023","","10.1039/C8GC01797B","","","0.71073","MoKα","","0.0659","0.0431","","","0.0875","0.0989","","","","","","1.014","","","","has coordinates","230095","2020-10-21","18:00:00",""
"7231315","5.66625","0.00019","18.3197","0.0005","17.6253","0.0006","90","","90.314","0.003","90","","1829.55","0.1","173","2","173","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C23 H21 N O2 -","- C23 H21 N O2 -","- C92 H84 N4 O8 -","4","2","","Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia","Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents","Green Chemistry","2018","20","17","4023","","10.1039/C8GC01797B","","","0.71073","MoKα","","0.0544","0.0421","","","0.0743","0.0791","","","","","","1.046","","","","has coordinates,has disorder","230095","2020-10-21","18:00:00",""
"7231316","12.8553","0.0005","5.5968","0.0002","24.4632","0.0009","90","","92.11","0.003","90","","1758.9","0.11","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H19 N3 O2 -","- C21 H19 N3 O2 -","- C84 H76 N12 O8 -","4","1","","Sebest, Filip; Casarrubios, Luis; Rzepa, Henry S.; White, Andrew J. P.; Díez-González, Silvia","Thermal azide‒alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-triazolines in deep eutectic solvents","Green Chemistry","2018","20","17","4023","","10.1039/C8GC01797B","","","1.54184","CuKα","","0.0587","0.0421","","","0.1036","0.1185","","","","","","1.037","","","","has coordinates,has disorder","230095","2020-10-21","18:00:00",""
"7231346","11.2915","0.0004","16.6242","0.0006","32.7927","0.0012","90","","90","","90","","6155.6","0.4","199.9","0.4","199.9","0.4","","","","","","","","7","P b c a","-P 2ac 2ab","61","","","","- C18 H26 Cl9 Ir N2 O4 S -","- C18 H26 Cl9 Ir N2 O4 S -","- C144 H208 Cl72 Ir8 N16 O32 S8 -","8","1","","Borja, Pilar; Vicent, Cristian; Baya, Miguel; García, Hermenegildo; Mata, Jose A.","Iridium complexes catalysed the selective dehydrogenation of glucose to gluconic acid in water","Green Chemistry","2018","20","17","4094","","10.1039/C8GC01933A","","x-ray","0.71073","MoKα","","0.0386","0.0325","","","0.0791","0.0845","","","","","","1.065","","","","has coordinates","230096","2020-10-21","18:00:00",""
"7231347","8.592","0.0002","10.2464","0.0003","12.6648","0.0003","78.655","0.002","82.445","0.002","67.017","0.003","1004.56","0.05","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C22 H27 Ir N2 O2 -","- C22 H27 Ir N2 O2 -","- C44 H54 Ir2 N4 O4 -","2","1","","Borja, Pilar; Vicent, Cristian; Baya, Miguel; García, Hermenegildo; Mata, Jose A.","Iridium complexes catalysed the selective dehydrogenation of glucose to gluconic acid in water","Green Chemistry","2018","20","17","4094","","10.1039/C8GC01933A","","x-ray","0.71073","MoKα","","0.0494","0.0399","","","0.094","0.1087","","","","","","1.141","","","","has coordinates,has disorder","230096","2020-10-21","18:00:00",""
"7231348","11.2529","0.0005","21.6653","0.0007","12.9575","0.0005","90","","111.582","0.005","90","","2937.5","0.2","200","0.1","200","0.1","","","","","","","","8","P 1 21/c 1","-P 2ybc","14","","","","- C18 H29 Cl2 F6 Ir N2 O8 S2 -","- C18 H29 Cl2 F6 Ir N2 O8 S2 -","- C72 H116 Cl8 F24 Ir4 N8 O32 S8 -","4","1","","Borja, Pilar; Vicent, Cristian; Baya, Miguel; García, Hermenegildo; Mata, Jose A.","Iridium complexes catalysed the selective dehydrogenation of glucose to gluconic acid in water","Green Chemistry","2018","20","17","4094","","10.1039/C8GC01933A","","x-ray","0.71073","MoKα","","0.0343","0.0302","","","0.0739","0.0769","","","","","","1.059","","","","has coordinates","230096","2020-10-21","18:00:00",""
"7231363","6.7038","0.0011","9.1027","0.0015","21.146","0.003","90","","91.335","0.002","90","","1290","0.4","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C8 H19 N3 Si2 -","- C8 H19 N3 Si2 -","- C32 H76 N12 Si8 -","4","1","","Roshandel, Sahar; Suri, Suresh C.; Marcischak, Jacob C.; Rasul, Golam; Surya Prakash, G. K.","Catalyst and solvent free microwave-assisted synthesis of substituted 1,2,3-triazoles","Green Chemistry","2018","20","16","3700","","10.1039/C8GC01516C","","","0.71073","MoKα","","0.0685","0.0655","","","0.1652","0.1665","","","","","","1.046","","","","has coordinates","209659","2020-10-21","18:00:00",""
"7231382","13.274","0.003","14.344","0.003","6.1256","0.0012","90","","101.518","0.009","90","","1142.8","0.4","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C14 H7 F4 N -","- C14 H7 F4 N -","- C56 H28 F16 N4 -","4","1","","Charpe, Vaibhav Pramod; Hande, Aniket A.; Sagadevan, Arunachalam; Hwang, Kuo Chu","Visible-light induced copper(i)-catalysed denitrogenative oxidative coupling of hydrazinylpyridines with terminal alkynes","Green Chemistry","2018","20","21","4859","","10.1039/C8GC01180J","","","0.71073","MoKα","","0.0735","0.046","","","0.1159","0.1476","","","","","","1.111","","","","has coordinates","230119","2020-10-21","18:00:00",""
"7231389","15.459","","9.19","","23.79","","90","","95.25","","90","","3365.62","","123","2","123","2","","","","","","","","6","C 1 c 1","C -2yc","9","","Choline trichlorostanate","","- C15 H45 Cl9 N3 O4.5 Sn3 -","- C15 H42 Cl9 N3 O4.5 Sn3 -","- C60 H168 Cl36 N12 O18 Sn12 -","4","1","","Bayu, Asep; Yoshida, Akihiro; Karnjanakom, Surachai; Kusakabe, Katsuki; Hao, Xiaogang; Prakoso, Tirto; Abudula, Abuliti; Guan, Guoqing","Catalytic conversion of biomass derivatives to lactic acid with increased selectivity in an aqueous tin(ii) chloride/choline chloride system","Green Chemistry","2018","20","17","4112","","10.1039/C8GC01022F","","","0.71075","MoKα","","0.1029","0.0904","","","0.2148","0.2223","","","","","","1.022","","","","has coordinates","230097","2020-10-21","18:00:00",""
"7231395","19.911","0.003","20.945","0.003","23.811","0.004","106.471","0.003","107.031","0.003","108.096","0.003","8223","2","173","2","173.15","","","","","","","","","4","P -1","-P 1","2","","","","- C90 H101 N6 O12 -","- C90 H101 N6 O12 -","- C360 H404 N24 O48 -","4","2","","Zhu, Xin-Qi; Yuan, Han; Sun, Qing; Zhou, Bo; Han, Xiao-Qin; Zhang, Zhi-Xin; Lu, Xin; Ye, Long-Wu","Benign catalysis with zinc: atom-economical and divergent synthesis of nitrogen heterocycles by formal [3 + 2] annulation of isoxazoles with ynol ethers","Green Chemistry","2018","20","18","4287","","10.1039/C8GC02051E","","","0.71073","MoKα","","0.1043","0.0635","","","0.1576","0.1816","","","","","","1.024","","","","has coordinates","230117","2020-10-21","18:00:00",""
"7231603","11.0544","0.0015","13.3742","0.0018","14.3388","0.0019","84.204","0.002","84.669","0.002","72.812","0.002","2010.4","0.5","100","2","100","2","","","","","","","","8","P -1","-P 1","2","","","","- C40 H45 B Cl2 F4 Ir N3 P2 -","- C40 H45 B Cl2 F4 Ir N3 P2 -","- C80 H90 B2 Cl4 F8 Ir2 N6 P4 -","2","1","","Iturmendi, Amaia; Iglesias, Manuel; Munarriz, Julen; Polo, Victor; Passarelli, Vincenzo; Pérez-Torrente, Jesús J.; Oro, Luis A.","A highly efficient Ir-catalyst for the solventless dehydrogenation of formic acid: the key role of an N-heterocyclic olefin","Green Chemistry","2018","20","21","4875","","10.1039/C8GC02794C","","","0.71073","MoKα","","0.0618","0.0463","","","0.1093","0.1174","","","","","","1.058","","","","has coordinates,has disorder","230120","2020-10-21","18:00:00",""
"7231604","15.5008","0.0017","11.5673","0.0013","21.116","0.002","90","","97.583","0.001","90","","3753","0.7","100","2","100","2","","","","","","","","8","P 1 21/n 1","-P 2yn","14","","","","- C38 H41 B Cl2 F4 Ir N3 P2 -","- C38 H41 B Cl2 F4 Ir N3 P2 -","- C152 H164 B4 Cl8 F16 Ir4 N12 P8 -","4","1","","Iturmendi, Amaia; Iglesias, Manuel; Munarriz, Julen; Polo, Victor; Passarelli, Vincenzo; Pérez-Torrente, Jesús J.; Oro, Luis A.","A highly efficient Ir-catalyst for the solventless dehydrogenation of formic acid: the key role of an N-heterocyclic olefin","Green Chemistry","2018","20","21","4875","","10.1039/C8GC02794C","","","0.71073","MoKα","","0.102","0.0788","","","0.1478","0.1577","","","","","","1.194","","","","has coordinates","230120","2020-10-21","18:00:00",""
"7231651","8.318","0.0017","11.515","0.002","11.539","0.002","61.6","0.03","78.05","0.03","75.08","0.03","934.8","0.4","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C20 H22 F3 N O3 -","- C20 H22 F3 N O3 -","- C40 H44 F6 N2 O6 -","2","1","","He, Yu-Tao; Kang, Dahye; Kim, Inwon; Hong, Sungwoo","Metal-free photocatalytic trifluoromethylative pyridylation of unactivated alkenes","Green Chemistry","2018","20","22","5209","","10.1039/C8GC02782J","","","0.7","synchrotron","","0.0686","0.0624","","","0.1866","0.1927","","","","","","1.125","","","","has coordinates","230086","2020-10-21","18:00:00",""
"7231666","8.6319","0.0006","18.0068","0.0013","7.8624","0.0004","90","","99.001","0.006","90","","1207.03","0.14","291.5","0.3","291.5","0.3","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C13.75 H12.5 N1.25 O1.25 S0.25 -","- C12 H11 O2 S2 -","- C48 H44 O8 S8 -","4","1","","Xing, Zhimin; Yang, Mingyang; Sun, Haiyu; Wang, Zemin; Chen, Peng; Liu, Lin; Wang, Xiaolei; Xie, Xingang; She, Xuegong","Visible-light promoted dithioacetalization of aldehydes with thiols under aerobic and photocatalyst-free conditions","Green Chemistry","2018","20","22","5117","","10.1039/C8GC02237B","","","0.71073","MoKα","","0.0842","0.0596","","","0.1438","0.1639","","","","","","1.056","","","","has coordinates","230087","2020-10-21","18:00:00",""
"7231667","27.538","0.0019","7.887","0.0006","23.328","0.0016","90","","99.24","0.001","90","","5000.9","0.6","150","2","150","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C51 H37 F12 N5 O9 Zn2 -","- C51 H37 F12 N5 O9 Zn2 -","- C204 H148 F48 N20 O36 Zn8 -","4","0.5","","Joharian, Monika; Morsali, Ali; Azhdari Tehrani, Alireza; Carlucci, Lucia; Proserpio, Davide M.","Water-stable fluorinated metal‒organic frameworks (F-MOFs) with hydrophobic properties as efficient and highly active heterogeneous catalysts in aqueous solution","Green Chemistry","2018","20","23","5336","","10.1039/C8GC02367K","","","0.71073","MoKα","","0.1107","0.0568","","","0.1279","0.147","","","","","","1.033","","","","has coordinates","230118","2020-10-21","18:00:00",""
"7231688","17.8928","0.0005","17.8928","0.0005","69.099","0.002","90","","90","","120","","19158.4","0.9","290.83","0.1","290.83","0.1","","","","","","","","6","R -3 c","-R 3 2""c","167","","","","- C114 H126 N24 Nd4 O42 Zn3 -","- C114 H126 N24 Nd4 O42 Zn3 -","- C684 H756 N144 Nd24 O252 Zn18 -","6","","","Wang, Li; Zhang, Ruilian; Han, Qing-Xin; Xu, Cong; Chen, Wan-Min; Yang, Huan; Gao, Guoshu; Qin, Wenwu; Liu, Wei-Sheng","Amide-functionalized heterometallic helicate cages as highly efficient catalysts for CO2 conversion under mild condition","Green Chemistry","2018","","","","","10.1039/C8GC02645A","","x-ray","0.71073","MoKα","","0.1179","0.0489","","","0.0974","0.1245","","","","","","1.007","","","","has coordinates","211611","2020-10-21","18:00:00",""
"7231689","17.8497","0.0005","17.8497","0.0005","68.762","0.002","90","","90","","120","","18973.2","0.9","290.83","0.1","290.83","0.1","","","","","","","","6","R -3 c","-R 3 2""c","167","","","","- C114 H126 Eu4 N24 O42 Zn3 -","- C114 H126 Eu4 N24 O42 Zn3 -","- C684 H756 Eu24 N144 O252 Zn18 -","6","","","Wang, Li; Zhang, Ruilian; Han, Qing-Xin; Xu, Cong; Chen, Wan-Min; Yang, Huan; Gao, Guoshu; Qin, Wenwu; Liu, Wei-Sheng","Amide-functionalized heterometallic helicate cages as highly efficient catalysts for CO2 conversion under mild condition","Green Chemistry","2018","","","","","10.1039/C8GC02645A","","x-ray","0.71","MoKα","","0.0825","0.042","","","0.0829","0.1021","","","","","","1.033","","","","has coordinates","211611","2020-10-21","18:00:00",""
"7231775","11.1231","0.0002","11.9525","0.0002","8.5577","0.0001","90","","99.993","0.002","90","","1120.48","0.03","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C12 H11 N O2 S -","- C12 H11 N O2 S -","- C48 H44 N4 O8 S4 -","4","1","","Wang, Ming; Fan, Qiaoling; Jiang, Xuefeng","Metal-free construction of primary sulfonamides through three diverse salts","Green Chemistry","2018","20","24","5469","","10.1039/C8GC03014F","","x-ray","1.54184","CuKα","","0.0412","0.0395","","","0.1061","0.1078","","","","","","1.041","","","","has coordinates","230085","2020-10-21","18:00:00",""
"7231898","3.9878","0.0002","12.0606","0.0007","24.7189","0.0014","90","","93.93","0.003","90","","1186.07","0.11","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C16 H12 N2 O -","- C16 H12 N2 O -","- C64 H48 N8 O4 -","4","2","","Mishra, Manisha; Twardy, Dylan; Ellstrom, Clifford; Wheeler, Kraig A.; Dembinski, Roman; Török, Béla","Catalyst-free ambient temperature synthesis of isoquinoline-fused benzimidazoles from 2-alkynylbenzaldehydes via alkyne hydroamination","Green Chemistry","2019","21","1","99","","10.1039/C8GC02520G","","","1.54178","CuKα","","0.0439","0.0386","","","0.0935","0.0966","","","","","","1.053","","","","has coordinates","224598","2020-10-21","18:00:00",""
"7231899","13.2669","0.0008","11.5841","0.0007","16.4623","0.0011","90","","100.794","0.004","90","","2485.2","0.3","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C17 H14 N2 -","- C17 H14 N2 -","- C136 H112 N16 -","8","2","","Mishra, Manisha; Twardy, Dylan; Ellstrom, Clifford; Wheeler, Kraig A.; Dembinski, Roman; Török, Béla","Catalyst-free ambient temperature synthesis of isoquinoline-fused benzimidazoles from 2-alkynylbenzaldehydes via alkyne hydroamination","Green Chemistry","2019","21","1","99","","10.1039/C8GC02520G","","","1.54178","CuKα","","0.1097","0.0861","","","0.2373","0.2635","","","","","","1.065","","","","has coordinates","224598","2020-10-21","18:00:00",""
"7231952","10.651","0.005","12.816","0.005","14.137","0.005","100.211","0.005","107.686","0.005","101.151","0.005","1745.4","1.2","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C40 H36 N8 O4 S2 -","- C40 H36 N8 O4 S2 -","- C80 H72 N16 O8 S4 -","2","1","","Deb, Mohit L.; Borpatra, Paran J.; Baruah, Pranjal K.","A one-pot catalyst/external oxidant/solvent-free cascade approach to pyrimidines via a 1,5-hydride transfer","Green Chemistry","2019","21","1","69","","10.1039/C8GC03507E","","","0.71069","MoKα","","0.1249","0.1044","","","0.3581","0.3836","","","","","","1.604","","","","has coordinates","224597","2020-10-21","18:00:00",""
"7231953","20.3152","0.0009","14.7532","0.0006","16.39","0.0007","90","","110.119","0.002","90","","4612.6","0.3","296","2","296","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C26 H26 N4 O2 -","- C26 H26 N4 O2 -","- C208 H208 N32 O16 -","8","1","","Deb, Mohit L.; Borpatra, Paran J.; Baruah, Pranjal K.","A one-pot catalyst/external oxidant/solvent-free cascade approach to pyrimidines via a 1,5-hydride transfer","Green Chemistry","2019","21","1","69","","10.1039/C8GC03507E","","","0.71073","MoKα","","0.1311","0.0772","","","0.2099","0.2566","","","","","","1.05","","","","has coordinates","224597","2020-10-21","18:00:00",""
"7231954","10.9372","0.0007","9.1286","0.0005","35.781","0.002","90","","95.129","0.003","90","","3558.1","0.4","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H20 N4 O2 -","- C22 H20 N4 O2 -","- C176 H160 N32 O16 -","8","2","","Deb, Mohit L.; Borpatra, Paran J.; Baruah, Pranjal K.","A one-pot catalyst/external oxidant/solvent-free cascade approach to pyrimidines via a 1,5-hydride transfer","Green Chemistry","2019","21","1","69","","10.1039/C8GC03507E","","","0.71073","MoKα","","0.1091","0.0706","","","0.1879","0.2219","","","","","","1.038","","","","has coordinates,has disorder","224597","2020-10-21","18:00:00",""
"7231992","13.5409","0.0007","12.9814","0.0008","13.6168","0.0008","90","","90","","90","","2393.6","0.2","293","2","293","","","","","","","","","8","P n m a","-P 2ac 2n","62","","","","- C20 H26 Cl F6 Ir N3 O P -","- C20 H26 Cl F6 Ir N3 O P -","- C80 H104 Cl4 F24 Ir4 N12 O4 P4 -","4","0.5","","Huang, Ming; Li, Yinwu; Liu, Jiahao; Lan, Xiao-Bing; Liu, Yan; Zhao, Cunyuan; Ke, Zhuofeng","A bifunctional strategy for N-heterocyclic carbene-stabilized iridium complex-catalyzed N-alkylation of amines with alcohols in aqueous media","Green Chemistry","2019","21","2","219","","10.1039/C8GC02298D","","","0.71073","MoKα","","0.0475","0.0405","","","0.1057","0.1115","","","","","","1.052","","","","has coordinates,has disorder","224608","2020-10-21","18:00:00",""
"7231993","26.6194","0.0004","26.6194","0.0004","27.22","0.0005","90","","90","","120","","16703.8","0.5","200","","200","","","","","","","","","6","R -3 c :H","-R 3 2""c","167","","","","- C37 H54 Cl N2 P2 Rh -","- C37 H54 Cl N2 P2 Rh -","- C666 H972 Cl18 N36 P36 Rh18 -","18","0.5","","Lam, Raphael H.; McQueen, Caitlin M. A.; Pernik, Indrek; McBurney, Roy T.; Hill, Anthony F.; Messerle, Barbara A.","Selective formylation or methylation of amines using carbon dioxide catalysed by a rhodium perimidine-based NHC complex","Green Chemistry","2019","21","3","538","","10.1039/C8GC03094D","","","0.71073","MoKα","","0.063","0.0499","","0.1208","0.1103","0.1208","","","","","","0.9753","","","","has coordinates","224636","2020-10-21","18:00:00",""
"7232134","13.4813","0.0004","8.2397","0.0003","6.9346","0.0002","90","","90","","90","","770.31","0.04","100","2","100","","","","","","","","","4","P c a 21","P 2c -2ac","29","","DBN-CO2","","- C8 H12 N2 O2 -","- C8 H12 N2 O2 -","- C32 H48 N8 O8 -","4","1","","Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian","Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts","Green Chemistry","2019","21","3","640","","10.1039/C8GC02952K","","","0.71073","MoKα","","0.0459","0.0448","","","0.1153","0.1162","","","","","","1.12","","","","has coordinates","224637","2020-10-21","18:00:00",""
"7232135","10.9982","0.0001","9.2785","0.0001","14.3717","0.0002","90","","105.714","0.001","90","","1411.77","0.03","100","2","100","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C13 H23 N3 O2 -","- C13 H23 N3 O2 -","- C52 H92 N12 O8 -","4","1","","Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian","Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts","Green Chemistry","2019","21","3","640","","10.1039/C8GC02952K","","","0.71073","MoKα","","0.0547","0.0398","","","0.0956","0.1038","","","","","","1.054","","","","has coordinates","224637","2020-10-21","18:00:00",""
"7232136","9.3632","0.0001","18.2488","0.0002","8.129","0.0001","90","","114.812","0.0007","90","","1260.76","0.03","100","2","100","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C12 H21 N3 O2 -","- C12 H21 N3 O2 -","- C48 H84 N12 O8 -","4","1","","Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian","Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts","Green Chemistry","2019","21","3","640","","10.1039/C8GC02952K","","","0.71073","MoKα","","0.0475","0.0417","","","0.1073","0.1115","","","","","","1.096","","","","has coordinates,has disorder","224637","2020-10-21","18:00:00",""
"7232137","9.9385","0.0002","10.0425","0.0002","24.7502","0.0004","90","","90","","90","","2470.25","0.08","100","2","100","","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C13 H19 N3 -","- C13 H19 N3 -","- C104 H152 N24 -","8","2","","Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian","Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts","Green Chemistry","2019","21","3","640","","10.1039/C8GC02952K","","","0.71073","MoKα","","0.046","0.0446","","","0.1198","0.1212","","","","","","1.064","","","","has coordinates","224637","2020-10-21","18:00:00",""
"7232138","7.7428","0.0006","11.1556","0.0009","10.4925","0.0008","90","","98.844","0.001","90","","895.52","0.12","100","2","100","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","[DBNH][HCO3]","","- C8 H14 N2 O3 -","- C8 H14 N2 O3 -","- C32 H56 N8 O12 -","4","1","","Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian","Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts","Green Chemistry","2019","21","3","640","","10.1039/C8GC02952K","","","0.71073","MoKα","","0.0412","0.0385","","","0.0956","0.0977","","","","","","1.043","","","","has coordinates","224637","2020-10-21","18:00:00",""
"7232139","8.1469","0.0001","10.0659","0.0001","12.9174","0.0002","90","","104.799","0.001","90","","1024.16","0.02","100","2","100","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","[MTBDH][HCO3]","","- C9 H17 N3 O3 -","- C9 H17 N3 O3 -","- C36 H68 N12 O12 -","4","1","","Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian","Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts","Green Chemistry","2019","21","3","640","","10.1039/C8GC02952K","","","0.71073","MoKα","","0.0448","0.0382","","","0.0959","0.0999","","","","","","1.038","","","","has coordinates","224637","2020-10-21","18:00:00",""
"7232140","12.5296","0.0002","8.0939","0.0001","19.7181","0.0004","90","","98.5378","0.0012","90","","1977.52","0.06","100","2","100","","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C23 H29 N3 -","- C23 H29 N3 -","- C92 H116 N12 -","4","1","","Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian","Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts","Green Chemistry","2019","21","3","640","","10.1039/C8GC02952K","","","0.71073","MoKα","","0.0665","0.0499","","","0.1284","0.1379","","","","","","1.032","","","","has coordinates,has disorder","224637","2020-10-21","18:00:00",""
"7232141","14.3302","0.0002","9.2194","0.0001","12.9756","0.0002","90","","104.588","0.0006","90","","1659.02","0.04","100","2","100","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C16 H29 N3 O2 -","- C16 H29 N3 O2 -","- C64 H116 N12 O8 -","4","1","","Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian","Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts","Green Chemistry","2019","21","3","640","","10.1039/C8GC02952K","","","0.71073","MoKα","","0.0387","0.0368","","","0.1011","0.1027","","","","","","1.057","","","","has coordinates","224637","2020-10-21","18:00:00",""
"7232142","10.3765","0.0001","13.1188","0.0002","11.2806","0.0002","90","","114.605","0.0006","90","","1396.17","0.04","100","2","100","2","","","","","","","","4","C 1 c 1","C -2yc","9","","","","- C13 H23 N3 O2 -","- C13 H23 N3 O2 -","- C52 H92 N12 O8 -","4","1","","Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian","Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts","Green Chemistry","2019","21","3","640","","10.1039/C8GC02952K","","","0.71073","MoKα","","0.0426","0.042","","","0.1128","0.1135","","","","","","1.06","","","","has coordinates","224637","2020-10-21","18:00:00",""
"7232143","15.2506","0.0003","10.8267","0.0002","10.8569","0.0002","90","","90.09","0.001","90","","1792.62","0.06","100","2","100","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H30 B F4 N3 -","- C15 H30 B F4 N3 -","- C60 H120 B4 F16 N12 -","4","1","","Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian","Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts","Green Chemistry","2019","21","3","640","","10.1039/C8GC02952K","","","0.71073","MoKα","","0.0437","0.0416","","","0.1054","0.1065","","","","","","1.085","","","","has coordinates","224637","2020-10-21","18:00:00",""
"7232144","6.6679","0.0003","14.6889","0.0005","9.6025","0.0004","90","","104.13","0.0018","90","","912.05","0.06","100","2","100.01","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C8 H13 N3 O2 -","- C8 H13 N3 O2 -","- C32 H52 N12 O8 -","4","1","","Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian","Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts","Green Chemistry","2019","21","3","640","","10.1039/C8GC02952K","","","0.71073","MoKα","","0.0416","0.0391","","","0.1085","0.111","","","","","","1.052","","","","has coordinates","224637","2020-10-21","18:00:00",""
"7232145","14.6071","0.0002","41.9109","0.0007","14.5422","0.0002","90","","117.159","0.001","90","","7921.1","0.2","100","2","100","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19.5 H31.5 N3 O2 -","- C19.5 H31.5 N3 O2 -","- C312 H504 N48 O32 -","16","4","","Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian","Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts","Green Chemistry","2019","21","3","640","","10.1039/C8GC02952K","","","0.71073","MoKα","","0.0577","0.0497","","","0.1188","0.1241","","","","","","1.057","","","","has coordinates,has disorder","224637","2020-10-21","18:00:00",""
"7232146","11.8565","0.0005","11.8565","0.0005","24.0309","0.0013","90","","90","","90","","3378.2","0.3","100","2","100","","","","","","","","","4","P 41","P 4w","76","","","","- C16 H29 N3 O2 -","- C16 H29 N3 O2 -","- C128 H232 N24 O16 -","8","2","","Wilm, Lukas F. B.; Eder, Tobias; Mück-Lichtenfeld, Christian; Mehlmann, Paul; Wünsche, Marius; Buß, Florenz; Dielmann, Fabian","Reversible CO2 fixation by N-heterocyclic imines forming water-stable zwitterionic nitrogen-base‒CO2 adducts","Green Chemistry","2019","21","3","640","","10.1039/C8GC02952K","","","0.71073","MoKα","","0.0418","0.0366","","","0.0741","0.0763","","","","","","1.072","","","","has coordinates,has disorder","224637","2020-10-21","18:00:00",""
"7232175","10.8693","0.0008","19.0667","0.0016","11.8343","0.0009","90","","102.11","0.002","90","","2398","0.3","298","2","298","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C27 H31 N O3 -","- C27 H31 N O3 -","- C108 H124 N4 O12 -","4","1","","Chen, Ke; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo","Metal-free synthesis of triarylated (Z)-nitrones via H2O-mediated 1,3-dipolar transfer under aerobic conditions","Green Chemistry","2019","21","3","675","","10.1039/C8GC03593H","","","0.71073","MoKα","","0.0863","0.0432","","","0.0886","0.0986","","","","","","1.021","","","","has coordinates","224638","2020-10-21","18:00:00",""
"7232200","9.594","0.0002","11.0586","0.0003","21.6374","0.0005","90","","93.293","0.002","90","","2291.86","0.09","173","","173","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","((5-chloro-1H-indol-3-yl)(4-chlorophenyl)methyl)diphenylphosphine oxide","","- C27 H20 Cl2 N O P -","- C27 H20 Cl2 N O P -","- C108 H80 Cl8 N4 O4 P4 -","4","1","","Pan, Jiaoting; Zhao, Runmin; Guo, Jiami; Ma, Dumei; Xia, Ying; Gao, Yuxing; Xu, Pengxiang; Zhao, Yufen","Three-component 3-(phosphoryl)methylindole synthesis from indoles, H-phosphine oxides and carbonyl compounds under metal-free conditions","Green Chemistry","2019","21","4","792","","10.1039/C8GC03530J","","x-ray","1.54184","CuKα","","0.053","0.0484","","","0.1261","0.1323","","","","","","1.04","","","","has coordinates","224606","2020-10-21","18:00:00",""
"7232201","8.6081","0.0001","16.0745","0.0002","18.0657","0.0002","90","","99.465","0.001","90","","2465.74","0.05","100.01","0.1","100.01","0.1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","(5-chloro-3-(1-phenylbutyl)-1H-indol-2-yl)diphenylphosphine oxide","","- C30 H27 Cl N O P -","- C30 H27 Cl N O P -","- C120 H108 Cl4 N4 O4 P4 -","4","1","","Pan, Jiaoting; Zhao, Runmin; Guo, Jiami; Ma, Dumei; Xia, Ying; Gao, Yuxing; Xu, Pengxiang; Zhao, Yufen","Three-component 3-(phosphoryl)methylindole synthesis from indoles, H-phosphine oxides and carbonyl compounds under metal-free conditions","Green Chemistry","2019","21","4","792","","10.1039/C8GC03530J","","x-ray","1.54184","CuKα","","0.0817","0.0738","","","0.1859","0.2001","","","","","","1.0309","","","","has coordinates","224606","2020-10-21","18:00:00",""
"7232299","12.1056","0.0008","7.802","0.0005","11.6256","0.0006","90","","97.574","0.005","90","","1088.43","0.12","297","2","297","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C14 H10 N2 O -","- C14 H10 N2 O -","- C56 H40 N8 O4 -","4","1","","Senadi, Gopal Chandru; Kudale, Vishal Suresh; Wang, Jeh-Jeng","Sustainable methine sources for the synthesis of heterocycles under metal- and peroxide-free conditions","Green Chemistry","2019","21","5","979","","10.1039/C8GC03839B","","x-ray","0.71073","MoKα","","0.0957","0.0537","","","0.1163","0.1399","","","","","","1.012","","","","has coordinates","224605","2020-10-21","18:00:00",""
"7232300","12.4895","0.0009","7.7667","0.0005","11.5802","0.0006","90","","96.718","0.006","90","","1115.59","0.12","297","2","297","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C14 H9 F N2 O -","- C14 H9 F N2 O -","- C56 H36 F4 N8 O4 -","4","1","","Senadi, Gopal Chandru; Kudale, Vishal Suresh; Wang, Jeh-Jeng","Sustainable methine sources for the synthesis of heterocycles under metal- and peroxide-free conditions","Green Chemistry","2019","21","5","979","","10.1039/C8GC03839B","","x-ray","0.71073","MoKα","","0.0998","0.0659","","","0.1548","0.1854","","","","","","1.028","","","","has coordinates","224605","2020-10-21","18:00:00",""
"7232306","6.561","0.0003","7.0809","0.0004","12.0629","0.0006","89.067","0.004","87.281","0.003","78.757","0.003","549.03","0.05","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C13 H9 N O3 -","- C13 H9 N O3 -","- C26 H18 N2 O6 -","2","1","","Zhou, Hui; Mu, Sen; Ren, Bai-Hao; Zhang, Rui; Lu, Xiao-Bing","Organocatalyzed carboxylative cyclization of propargylic amides with atmospheric CO2 towards oxazolidine-2,4-diones","Green Chemistry","2019","21","5","991","","10.1039/C8GC03929A","","","0.71073","MoKα","","0.0861","0.0683","","","0.2015","0.218","","","","","","1.086","","","","has coordinates","224604","2020-10-21","18:00:00",""
"7232307","6.7109","0.0007","9.819","0.0013","12.7318","0.0014","75.919","0.008","82.43","0.009","80.639","0.009","799.18","0.16","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C18 H12 F3 N O3 -","- C18 H12 F3 N O3 -","- C36 H24 F6 N2 O6 -","2","1","","Zhou, Hui; Mu, Sen; Ren, Bai-Hao; Zhang, Rui; Lu, Xiao-Bing","Organocatalyzed carboxylative cyclization of propargylic amides with atmospheric CO2 towards oxazolidine-2,4-diones","Green Chemistry","2019","21","5","991","","10.1039/C8GC03929A","","","0.71073","MoKα","","0.1175","0.0621","","","0.1651","0.2018","","","","","","1.039","","","","has coordinates","224604","2020-10-21","18:00:00",""
"7232308","6.04","0.002","19.12","0.007","26.355","0.009","90","","90","","90","","3043.6","1.8","296","2","296","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C18 H15 N O4 -","- C18 H15 N O4 -","- C144 H120 N8 O32 -","8","1","","Zhou, Hui; Mu, Sen; Ren, Bai-Hao; Zhang, Rui; Lu, Xiao-Bing","Organocatalyzed carboxylative cyclization of propargylic amides with atmospheric CO2 towards oxazolidine-2,4-diones","Green Chemistry","2019","21","5","991","","10.1039/C8GC03929A","","","0.71073","MoKα","","0.1022","0.0548","","","0.132","0.1544","","","","","","1.038","","","","has coordinates","224604","2020-10-21","18:00:00",""
"7232363","8.2387","0.0014","9.1226","0.0015","15.647","0.003","78.884","0.002","77.335","0.002","63.875","0.002","1023.9","0.3","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C21 H14 F5 N3 O4 -","- C21 H14 F5 N3 O4 -","- C42 H28 F10 N6 O8 -","2","1","","Du, Xuan-Xuan; Zi, Quan-Xing; Wu, Yu-Meng; Jin, Yi; Lin, Jun; Yan, Sheng-Jiao","An environmentally benign multi-component reaction: regioselective synthesis of fluorinated 2-aminopyridines using diverse properties of the nitro group","Green Chemistry","2019","21","6","1505","","10.1039/C8GC03698E","","","0.71073","MoKα","","0.0658","0.0501","","","0.1497","0.1619","","","","","","1.094","","","","has coordinates","224609","2020-10-21","18:00:00",""
"7232364","8.6308","0.0016","9.4049","0.0018","13.955","0.003","78.895","0.002","81.887","0.002","74.726","0.002","1067.4","0.4","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C23 H19 F5 N2 O2 -","- C23 H19 F5 N2 O2 -","- C46 H38 F10 N4 O4 -","2","1","","Du, Xuan-Xuan; Zi, Quan-Xing; Wu, Yu-Meng; Jin, Yi; Lin, Jun; Yan, Sheng-Jiao","An environmentally benign multi-component reaction: regioselective synthesis of fluorinated 2-aminopyridines using diverse properties of the nitro group","Green Chemistry","2019","21","6","1505","","10.1039/C8GC03698E","","","0.71073","MoKα","","0.0861","0.0512","","","0.1386","0.1679","","","","","","1.022","","","","has coordinates","224609","2020-10-21","18:00:00",""
"7232431","20.733","0.009","26.304","0.012","28.112","0.013","90","","90","","90","","15331","12","223","2","223","2","","","","","","","","6","P c a b","-P 2bc 2ac","61","","","","- C52 H28 Br16 N4 O9 V -","- C52 H28 Br16 N4 O9 V -","- C416 H224 Br128 N32 O72 V8 -","8","1","","Dar, Tawseef Ahmad; Uprety, Bhawna; Sankar, Muniappan; Maurya, Mannar R.","Robust and electron deficient oxidovanadium(iv) porphyrin catalysts for selective epoxidation and oxidative bromination reactions in aqueous media","Green Chemistry","2019","21","7","1757","","10.1039/C8GC03909G","","","0.71073","MoKα","","0.2234","0.0783","","","0.2369","0.3034","","","","","","1.024","","","","has coordinates","224622","2020-10-21","18:00:00",""
"7232432","13.829","0.005","14.439","0.005","26.153","0.005","90","0.005","90","0.005","90","0.005","5222","3","293","2","293","2","","","","","","","","5","P c c n","-P 2ab 2ac","56","","","","- C27.5 H22 N3 O5 V0.5 -","- C27.5 H22 N3 O5 V0.5 -","- C220 H176 N24 O40 V4 -","8","1","","Dar, Tawseef Ahmad; Uprety, Bhawna; Sankar, Muniappan; Maurya, Mannar R.","Robust and electron deficient oxidovanadium(iv) porphyrin catalysts for selective epoxidation and oxidative bromination reactions in aqueous media","Green Chemistry","2019","21","7","1757","","10.1039/C8GC03909G","","","0.71073","MoKα","","0.2466","0.1927","","","0.5193","0.5556","","","","","","2.181","","","","has coordinates","224622","2020-10-21","18:00:00",""
"7232441","11.954","0.002","7.454","0.002","15.468","0.003","90","","95.33","0.03","90","","1372.3","0.5","294","2","294","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H14 N2 O2 -","- C17 H14 N2 O2 -","- C68 H56 N8 O8 -","4","1","","Botla, Vinayak; Pilli, NavyaSree; Malapaka, Chandrasekharam","Uncatalyzed, on water oxygenative cleavage of inert C‒N bond with concomitant 8,7-amino shift in 8-aminoquinoline derivatives","Green Chemistry","2019","21","7","1735","","10.1039/C9GC00289H","","","0.71073","MoKα","","0.0749","0.0696","","","0.2049","0.2126","","","","","","1.06","","","","has coordinates","224624","2020-10-21","18:00:00",""
"7232442","6.294","0.0003","10.6563","0.0007","5.5677","0.0004","90","","95.069","0.005","90","","371.97","0.04","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C2 H4 N8 O4 Zn -","- C2 H4 N8 O4 Zn -","- C4 H8 N16 O8 Zn2 -","2","0.5","","Zhang, Qi; Chen, Dong; Jing, Dong; Fan, Guijuan; He, Liu; Li, Hongzhen; Wang, Wentao; Nie, Fude","Access to green primary explosives via constructing coordination polymers based on bis-tetrazole oxide and non-lead metals","Green Chemistry","2019","21","8","1947","","10.1039/C8GC03973A","","","0.71073","MoKα","","0.0533","0.0412","","","0.1183","0.1304","","","","","","1.113","","","","has coordinates","224602","2020-10-21","18:00:00",""
"7232466","9.6376","0.0009","8.3094","0.0008","14.8885","0.0014","90","","92.042","0.001","90","","1191.6","0.2","296","2","296","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C15 H12 O2 -","- C15 H12 O2 -","- C60 H48 O8 -","4","1","","Tang, Zhi; Tong, Zhou; Xu, Zhihui; Au, Chak-Tong; Qiu, Renhua; Yin, Shuang-Feng","Recyclable nickel-catalyzed C‒H/O‒H dual functionalization of phenols with mandelic acids for the synthesis of 3-aryl benzofuran-2(3H)-ones under solvent-free conditions","Green Chemistry","2019","21","8","2015","","10.1039/C9GC00305C","","","0.71073","MoKα","","0.0481","0.0407","","","0.1062","0.1111","","","","","","1.071","","","","has coordinates","224600","2020-10-21","18:00:00",""
"7232467","12.768","0.003","14.165","0.003","13.588","0.003","90","","111.994","0.006","90","","2278.7","0.9","100","","100","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C19 H26 Cl4 Ir N3 O -","- C19 H26 Cl4 Ir N3 O -","- C76 H104 Cl16 Ir4 N12 O4 -","4","1","","Chakrabarti, Kaushik; Maji, Milan; Kundu, Sabuj","Cooperative iridium complex-catalyzed synthesis of quinoxalines, benzimidazoles and quinazolines in water","Green Chemistry","2019","21","8","1999","","10.1039/C8GC03744B","","","0.71073","MoKα","","0.0257","0.0228","","","0.0573","0.0591","","","","","","1.069","","","","has coordinates","224603","2020-10-21","18:00:00",""
"7232468","9.9995","0.0003","10.3691","0.0003","12.6092","0.0003","90","","101.192","0.001","90","","1282.53","0.06","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C13 H17 N2 O3 -","- C13 H17 N2 O3 -","- C52 H68 N8 O12 -","4","1","","Sun, Zhen; Li, Zheng; Liao, Wei-Wei","An organocatalytic hydroalkoxylation/Claisen rearrangement/Michael addition tandem sequence: divergent synthesis of multi-substituted 2,3-dihydrofurans and 2,3-dihydropyrroles from cyanohydrins","Green Chemistry","2019","21","7","1614","","10.1039/C8GC03978J","","","0.71073","MoKα","","0.0602","0.0589","","","0.1366","0.1374","","","","","","1.09","","","","has coordinates","224623","2020-10-21","18:00:00",""
"7232495","5.01554","0.00007","7.52021","0.00007","15.90107","0.00016","90","","90","","90","","599.755","0.012","150","1","150","1","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C5 H10 O4 -","- C5 H10 O4 -","- C20 H40 O16 -","4","1","","Benhamou, Laure; Foster, Robert W.; Ward, David P.; Wheelhouse, Katherine; Sloan, Lisa; Tame, Christopher J.; Bučar, Dejan-Krešimir; Lye, Gary J.; Hailes, Helen C.; Sheppard, Tom D.","Functionalised tetrahydrofuran fragments from carbohydrates or sugar beet pulp biomass","Green Chemistry","2019","21","8","2035","","10.1039/C9GC00448C","","x-ray","1.54184","CuKα","","0.0271","0.0267","","","0.0658","0.0662","","","","","","0.911","","","","has coordinates","224599","2020-10-21","18:00:00",""
"7232496","22.3597","0.0005","5.5295","0.0002","9.5976","0.0002","90","","90.661","0.002","90","","1186.55","0.06","150","0.1","150","0.1","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C12 H13 Br O4 -","- C12 H13 Br O4 -","- C48 H52 Br4 O16 -","4","1","","Benhamou, Laure; Foster, Robert W.; Ward, David P.; Wheelhouse, Katherine; Sloan, Lisa; Tame, Christopher J.; Bučar, Dejan-Krešimir; Lye, Gary J.; Hailes, Helen C.; Sheppard, Tom D.","Functionalised tetrahydrofuran fragments from carbohydrates or sugar beet pulp biomass","Green Chemistry","2019","21","8","2035","","10.1039/C9GC00448C","","x-ray","1.54184","CuKα","","0.0227","0.0224","","","0.0599","0.0604","","","","","","1.021","","","","has coordinates","224599","2020-10-21","18:00:00",""
"7232514","7.1261","0.0004","8.1012","0.0006","18.5115","0.0009","90","","90","","90","","1068.67","0.11","100","0.1","100","0.1","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C12 H13 Cl O2 -","- C12 H13 Cl O2 -","- C48 H52 Cl4 O8 -","4","1","","Kassin, Victor-Emmanuel H.; Gérardy, Romaric; Toupy, Thomas; Collin, Diégo; Salvadeo, Elena; Toussaint, François; Van Hecke, Kristof; Monbaliu, Jean-Christophe M.","Expedient preparation of active pharmaceutical ingredient ketamine under sustainable continuous flow conditions","Green Chemistry","2019","21","11","2952","","10.1039/C9GC00336C","","x-ray","1.54184","CuKα","","0.0452","0.034","","","0.0753","0.0882","","","","","","1.084","","","","has coordinates","224633","2020-10-21","18:00:00",""
"7232515","6.7087","0.0003","8.9522","0.0003","10.805","0.0004","76.216","0.003","82.767","0.003","72.956","0.003","601.45","0.04","100","0.1","100","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C13 H16 Cl N O -","- C13 H16 Cl N O -","- C26 H32 Cl2 N2 O2 -","2","1","","Kassin, Victor-Emmanuel H.; Gérardy, Romaric; Toupy, Thomas; Collin, Diégo; Salvadeo, Elena; Toussaint, François; Van Hecke, Kristof; Monbaliu, Jean-Christophe M.","Expedient preparation of active pharmaceutical ingredient ketamine under sustainable continuous flow conditions","Green Chemistry","2019","21","11","2952","","10.1039/C9GC00336C","","x-ray","1.54184","CuKα","","0.0503","0.0448","","","0.1192","0.1236","","","","","","1.075","","","","has coordinates","224633","2020-10-21","18:00:00",""
"7232516","10.0679","0.0003","8.2104","0.0003","28.6875","0.0009","90","","98.842","0.003","90","","2343.17","0.13","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C13 H16 Cl N O -","- C13 H16 Cl N O -","- C104 H128 Cl8 N8 O8 -","8","2","","Kassin, Victor-Emmanuel H.; Gérardy, Romaric; Toupy, Thomas; Collin, Diégo; Salvadeo, Elena; Toussaint, François; Van Hecke, Kristof; Monbaliu, Jean-Christophe M.","Expedient preparation of active pharmaceutical ingredient ketamine under sustainable continuous flow conditions","Green Chemistry","2019","21","11","2952","","10.1039/C9GC00336C","","x-ray","1.54184","CuKα","","0.0485","0.0423","","","0.1183","0.1261","","","","","","1.048","","","","has coordinates","224633","2020-10-21","18:00:00",""
"7232523","9.13","0.011","10.446","0.01","11.101","0.009","90","","106.63","0.04","90","","1014.4","1.8","100","2","100","2","","","","","","","","5","C 1 2/m 1","-C 2y","12","","","","- C7 H32 B18 Co N -","- C7 H32 B18 Co N -","- C14 H64 B36 Co2 N2 -","2","0.25","","Bennour, Ines; Cioran, Ana M.; Teixidor, Francesc; Viñas, Clara","3,2,1 and stop! An innovative, straightforward and clean route for the flash synthesis of metallacarboranes","Green Chemistry","2019","21","8","1925","","10.1039/C8GC03943G","","","0.71073","MoKα","","0.0694","0.0676","","","0.1723","0.1741","","","","","","1.154","","","","has coordinates","224601","2020-10-21","18:00:00",""
"7232541","12.469","0.004","6.265","0.002","17.738","0.006","90","","96.553","0.018","90","","1376.6","0.8","273","2","273","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C15 H12 Br N Se -","- C15 H12 Br N Se -","- C60 H48 Br4 N4 Se4 -","4","1","","Rathore, Vandana; Kumar, Sangit","Visible-light-induced metal and reagent-free oxidative coupling of sp2 C‒H bonds with organo-dichalcogenides: synthesis of 3-organochalcogenyl indoles","Green Chemistry","2019","21","10","2670","","10.1039/C9GC00007K","","","0.71073","MoKα","","0.0825","0.0487","","","0.1036","0.1188","","","","","","1.016","","","","has coordinates","224595","2020-10-21","18:00:00",""
"7232571","5.9656","0.0001","12.4421","0.0001","16.3174","0.0002","90","","90","","90","","1211.15","0.03","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","(Methyl 1-(4-bromobenzyl)-1H-1,2,3-triazole-4-carboxylate)","","- C11 H10 Br N3 O2 -","- C11 H10 Br N3 O2 -","- C44 H40 Br4 N12 O8 -","4","1","","Yadav, Dolly; Singh, Nem; Kim, Tae Wu; Kim, Jae Young; Park, No-Joong; Baeg, Jin-Ook","Highly regioselective and sustainable solar click reaction: a new post-synthetic modified triazole organic polymer as a recyclable photocatalyst for regioselective azide‒alkyne cycloaddition reaction","Green Chemistry","2019","21","10","2677","","10.1039/C9GC00894B","","","0.71073","MoKα","","0.0599","0.046","","","0.1173","0.1298","","","","","","1.054","","","","has coordinates","224596","2020-10-21","18:00:00",""
"7232637","17.2098","0.0011","8.7962","0.0005","12.4668","0.0007","90","","112.273","0.002","90","","1746.43","0.18","100","2","100","2","","","","","","","","6","C 1 2/m 1","-C 2y","12","","","","- C30 H40 Cl4 N8 Ni2 O2 -","- C30 H40 Cl4 N8 Ni2 O2 -","- C60 H80 Cl8 N16 Ni4 O4 -","2","0.25","","Angamuthu, Raja; Raje, Sakthi","Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride","Green Chemistry","2019","","","","","10.1039/C8GC04058C","","","0.71073","MoKα","","0.0636","0.0416","","","0.0825","0.0896","","","","","","1.069","","","","has coordinates","214697","2020-10-21","18:00:00",""
"7232638","15.1186","0.0006","18.4249","0.0007","23.5902","0.001","90","","90","","90","","6571.3","0.5","100","2","100","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C28 H34 I2 N8 Ni2 -","- C28 H34 I2.003 N8 Ni2 -","- C224 H272 I16.024 N64 Ni16 -","8","1","","Angamuthu, Raja; Raje, Sakthi","Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride","Green Chemistry","2019","","","","","10.1039/C8GC04058C","","","0.71073","MoKα","","0.0979","0.0601","","","0.1353","0.151","","","","","","1.062","","","","has coordinates,has disorder","214697","2020-10-21","18:00:00",""
"7232639","15.109","0.003","15.035","0.003","10.6611","0.0019","90","","116.24","0.006","90","","2172.2","0.7","100","2","100","2","","","","","","","","5","C 1 2/m 1","-C 2y","12","","","","- C28 H32 Br4 N8 Ni2 -","- C28 H32 Br4 N8 Ni2 -","- C56 H64 Br8 N16 Ni4 -","2","0.25","","Angamuthu, Raja; Raje, Sakthi","Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride","Green Chemistry","2019","","","","","10.1039/C8GC04058C","","","0.71073","MoKα","","0.0833","0.0576","","","0.1555","0.1679","","","","","","1.037","","","","has coordinates","214697","2020-10-21","18:00:00",""
"7232640","19.061","0.004","10.993","0.002","19.32","0.004","90","","112.098","0.005","90","","3750.9","1.3","100","2","100","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C30 H40 I4 N8 Ni2 O2 -","- C30 H40 I4 N8 Ni2 O2 -","- C120 H160 I16 N32 Ni8 O8 -","4","1","","Angamuthu, Raja; Raje, Sakthi","Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride","Green Chemistry","2019","","","","","10.1039/C8GC04058C","","","0.71073","MoKα","","0.1494","0.1157","","","0.3284","0.37","","","","","","1.459","","","","has coordinates","214697","2020-10-21","18:00:00",""
"7232641","11.5825","0.0005","13.5215","0.0006","19.6576","0.0008","98.75","0.001","101.464","0.001","103.617","0.001","2867.7","0.2","100","2","100","","","","","","","","","5","P -1","-P 1","2","","","","- C68 H65 B2 N7 Ni -","- C68 H65 B2 N7 Ni -","- C136 H130 B4 N14 Ni2 -","2","1","","Angamuthu, Raja; Raje, Sakthi","Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride","Green Chemistry","2019","","","","","10.1039/C8GC04058C","","","0.71073","MoKα","","0.0588","0.0419","","","0.1188","0.1326","","","","","","0.964","","","","has coordinates","214697","2020-10-21","18:00:00",""
"7232642","11.1094","0.0007","15.0969","0.0009","18.9302","0.0012","90","","90","","90","","3174.9","0.3","100","2","100","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","Olex2 1.2(compiled 2018.05.29 svn.r3508 for OlexSys, GUI svn.r5506)","","- C38 H40 B2 N4 Ni -","- C38 H40 B2 N4 Ni -","- C152 H160 B8 N16 Ni4 -","4","1","","Angamuthu, Raja; Raje, Sakthi","Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride","Green Chemistry","2019","","","","","10.1039/C8GC04058C","","","0.71073","MoKα","","0.0762","0.0508","","","0.0918","0.1005","","","","","","1.028","","","","has coordinates","214697","2020-10-21","18:00:00",""
"7232643","16.7786","0.0013","11.9023","0.0009","21.251","0.0019","90","","105.676","0.002","90","","4086.1","0.6","100","2","100","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C88 H92 B2 N12 Ni2 O4 -","- C88 H92 B2 N12 Ni2 O4 -","- C176 H184 B4 N24 Ni4 O8 -","2","0.5","","Angamuthu, Raja; Raje, Sakthi","Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride","Green Chemistry","2019","","","","","10.1039/C8GC04058C","","","0.71073","MoKα","","0.085","0.0564","","","0.135","0.1483","","","","","","1.037","","","","has coordinates","214697","2020-10-21","18:00:00",""
"7232644","21.7139","0.0016","11.0715","0.0008","16.0808","0.0012","90","","100.803","0.002","90","","3797.4","0.5","100","2","100","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C14 H21 N4 Ni O9 S1.5 -","- C14 H21 N4 Ni O9 S1.5 -","- C112 H168 N32 Ni8 O72 S12 -","8","1","","Angamuthu, Raja; Raje, Sakthi","Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride","Green Chemistry","2019","","","","","10.1039/C8GC04058C","","","0.71","MoKα","","0.0965","0.0592","","","0.1214","0.1367","","","","","","1.019","","","","has coordinates","214697","2020-10-21","18:00:00",""
"7232645","10.8252","0.0014","11.8798","0.0016","17.529","0.003","70.982","0.004","72.243","0.003","78.092","0.003","2015.3","0.5","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C96 H94 B2 N12 Ni2 S2 -","- C96 H94 B2 N12 Ni2 S2 -","- C96 H94 B2 N12 Ni2 S2 -","1","0.5","","Angamuthu, Raja; Raje, Sakthi","Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride","Green Chemistry","2019","","","","","10.1039/C8GC04058C","","","0.71073","MoKα","","0.178","0.0791","","","0.1532","0.1849","","","","","","1.004","","","","has coordinates","214697","2020-10-21","18:00:00",""
"7232646","30.9603","0.001","30.9603","0.001","11.4869","0.0005","90","","90","","120","","9535.5","0.6","100","2","100.2","","","","","","","","","5","R -3","-R 3","148","","","","- C15 H16 N4 Ni O3 -","- C15 H16 N4 Ni O3 -","- C270 H288 N72 Ni18 O54 -","18","","","Angamuthu, Raja; Raje, Sakthi","Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride","Green Chemistry","2019","","","","","10.1039/C8GC04058C","","","0.71073","MoKα","","0.0565","0.0429","","","0.1145","0.1283","","","","","","1.139","","","","has coordinates","214697","2020-10-21","18:00:00",""
"7232647","42.319","0.003","22.6","0.0014","15.7228","0.0009","90","","93.976","0.004","90","","15001.2","1.7","100","2","100.2","","","","","","","","","6","C 1 2 1","C 2y","5","","","","- C163 H151 B3 N12 Ni3 O7 -","- C163 H151 B3 N12 Ni3 O7 -","- C652 H604 B12 N48 Ni12 O28 -","4","1","","Angamuthu, Raja; Raje, Sakthi","Solvent-Free Synthesis and Reactivity of Nickel(II) Borohydride and Nickel(II) Hydride","Green Chemistry","2019","","","","","10.1039/C8GC04058C","","","0.71","MoKα","","0.0649","0.0531","","","0.1309","0.1403","","","","","","1.021","","","","has coordinates","214697","2020-10-21","18:00:00",""
"7232648","9.9687","0.0008","14.9432","0.0011","24.3238","0.0017","92.312","0.002","97.145","0.002","107.847","0.002","3410.4","0.4","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C40 H26 Cl2 N2 O5 -","- C40 H26 Cl2 N2 O5 -","- C160 H104 Cl8 N8 O20 -","4","2","","Shafiee, Behnaz; Duffield, Joseph; Timm, Rudy; Liyanage, Rohana; Lay, Jackson O.; Khosropour, Ahmad R.; Amiri Rudbari, Hadi; Beyzavi, M. Hassan","Metal-free and benign approach for the synthesis of dihydro-5′H-spiro[benzo[c]chromene-8,4′-oxazole]-5′,6(7H)-dione scaffolds as masked amino acids","Green Chemistry","2019","21","10","2656","","10.1039/C9GC00428A","","","0.71073","MoKα","","0.1961","0.0641","","","0.1412","0.2183","","","","","","0.999","","","","has coordinates","224594","2020-10-21","18:00:00",""
"7232653","10.393","0.005","18.063","0.009","12.568","0.006","90","","99.096","0.01","90","","2330","2","296","2","296","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C26 H24 N O4 P S -","- C26 H24 N O4 P S -","- C104 H96 N4 O16 P4 S4 -","4","1","","Liu, Teng; Li, Yongqin; Cheng, Feixiang; Shen, Xianfu; Liu, Jianjun; Lin, Jun","Highly chemo- and regioselective C‒P cross-coupling reaction of quinone imine ketals with Ar2P(O)H to construct ortho-amino triarylphosphine derivatives","Green Chemistry","2019","21","13","3536","","10.1039/C9GC00989B","","","0.71073","MoKα","","0.222","0.1215","","","0.3121","0.3678","","","","","","1.038","","","","has coordinates","224617","2020-10-21","18:00:00",""
"7232654","10.82","0.0009","17.6091","0.0015","14.0022","0.0013","90","","105.494","0.002","90","","2570.9","0.4","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C27 H26 N O5 P S -","- C27 H26 N O5 P S -","- C108 H104 N4 O20 P4 S4 -","4","1","","Liu, Teng; Li, Yongqin; Cheng, Feixiang; Shen, Xianfu; Liu, Jianjun; Lin, Jun","Highly chemo- and regioselective C‒P cross-coupling reaction of quinone imine ketals with Ar2P(O)H to construct ortho-amino triarylphosphine derivatives","Green Chemistry","2019","21","13","3536","","10.1039/C9GC00989B","","","0.71073","MoKα","","0.0982","0.0557","","","0.1316","0.1547","","","","","","1.016","","","","has coordinates","224617","2020-10-21","18:00:00",""
"7232700","6.7747","0.0003","6.9936","0.0002","10.2745","0.0004","90","","99.508","0.004","90","","480.11","0.03","293","2","293","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C12 H12 O2 -","- C12 H12 O2 -","- C24 H24 O4 -","2","1","","Zhang, Ying-Qi; Zhu, Xin-Qi; Xu, Yin; Bu, Hao-Zhen; Wang, Jia-Le; Zhai, Tong-Yi; Zhou, Jin-Mei; Ye, Long-Wu","Synthesis of functionalized 3-isochromanones via metal-free intramolecular alkoxylation-initiated cascade cyclization","Green Chemistry","2019","21","11","3023","","10.1039/C9GC01030K","","","1.54184","CuKα","","0.0313","0.0308","","","0.0776","0.0782","","","","","","1.079","","","","has coordinates","224634","2020-10-21","18:00:00",""
"7232726","20.2486","0.001","6.7682","0.0002","20.858","0.001","90","","118.296","0.006","90","","2517","0.2","","","","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C33 H27 N3 O2 -","- C33 H27 N3 O2 -","- C132 H108 N12 O8 -","4","1","","Li, Chunmei; Zhang, Furen; Qi, Chenze","A multicomponent two-step strategy for the synthesis of polysubstituted pyrrolo[3,2-c]pyridin-4-ones using a solid acid as a recyclable catalyst","Green Chemistry","2019","21","11","3109","","10.1039/C9GC01120J","","","","","","0.061","","","","","","","","","","","","","","","has coordinates","224632","2020-10-21","18:00:00",""
"7232772","10.5578","0.0011","7.5212","0.0016","15.993","0.002","90","","108.303","0.011","90","","1205.7","0.3","295","2","295","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C13 H15 Br O -","- C13 H15 Br O -","- C52 H60 Br4 O4 -","4","1","","Chen, Chao; Kang, Jun-Chen; Mao, Chen; Dong, Jia-Wei; Xie, Yu-Yang; Ding, Tong-Mei; Tu, Yong-Qiang; Chen, Zhi-Min; Zhang, Shu-Yu","Electrochemical halogenation/semi-pinacol rearrangement of allylic alcohols using inorganic halide salt: an eco-friendly route to the synthesis of β-halocarbonyls","Green Chemistry","2019","21","15","4014","","10.1039/C9GC01152H","","","1.54178","CuKα","","0.057","0.0543","","","0.1928","0.1968","","","","","","1.121","","","","has coordinates","224628","2020-10-21","18:00:00",""
"7232793","21.525","0.001","9.597","0.0005","14.745","0.0006","90","","121.67","0.03","90","","2592.4","0.9","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C12 H11 Br F3 N O2 -","- C12 H11 Br F3 N O2 -","- C96 H88 Br8 F24 N8 O16 -","8","1","","Zou, Long; Li, Pinhua; Wang, Bin; Wang, Lei","Visible-light-induced radical cyclization of N-allylbenzamides with CF3SO2Na to trifluoromethylated dihydroisoquinolinones in water at room temperature","Green Chemistry","2019","21","12","3362","","10.1039/C9GC00938H","","","0.71073","MoKα","","0.1948","0.0612","","","0.0886","0.1127","","","","","","0.859","","","","has coordinates","224635","2020-10-21","18:00:00",""
"7232836","12.3821","0.0005","8.3089","0.0004","21.5533","0.0008","90","","105.353","0.004","90","","2138.3","0.16","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H29 N O3 -","- C24 H29 N O3 -","- C96 H116 N4 O12 -","4","1","","Gong, Ming; Kim, Jung Keun; Zhao, Xiuli; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Wu, Yangjie","Visible-light-induced α-oxyamination of 1,3-dicarbonyls with TEMPO via a photo(electro)catalytic process applying a DSSC anode or in a DSSC system","Green Chemistry","2019","21","13","3615","","10.1039/C9GC01154D","","x-ray","1.54184","CuKα","","0.0681","0.0479","","","0.1208","0.1402","","","","","","1.016","","","","has coordinates","224615","2020-10-21","18:00:00",""
"7232870","14.2456","0.0008","11.4003","0.0006","15.7834","0.0009","90","","104.488","0.006","90","","2481.8","0.2","100.01","0.1","100.01","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C29 H23 F3 O2 Se2 -","- C29 H23 F3 O2 Se2 -","- C116 H92 F12 O8 Se8 -","4","1","","Ma, Xian-Li; Wang, Qian; Feng, Xi-Yuan; Mo, Zu-Yu; Pan, Ying-Ming; Chen, Yan-Yan; Xin, Mao; Xu, Yan-Li","Metal-free visible-light induced cyclization/substitution cascade reaction of alkyne-tethered cyclohexadienones and diselenides: access to 5-hydroxy-3-selenyl-4a,8a-dihydro-2H-chromen-6(5H)-ones","Green Chemistry","2019","21","13","3547","","10.1039/C9GC00570F","","x-ray","0.71073","MoKα","","0.0538","0.0377","","","0.0759","0.0822","","","","","","1.025","","","","has coordinates","224616","2020-10-21","18:00:00",""
"7232871","11.2346","0.0008","13.8269","0.0005","13.8545","0.0008","90","","112.472","0.007","90","","1988.7","0.2","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C23 H19 F3 O3 Se -","- C23 H19 F3 O3 Se -","- C92 H76 F12 O12 Se4 -","4","1","","Ma, Xian-Li; Wang, Qian; Feng, Xi-Yuan; Mo, Zu-Yu; Pan, Ying-Ming; Chen, Yan-Yan; Xin, Mao; Xu, Yan-Li","Metal-free visible-light induced cyclization/substitution cascade reaction of alkyne-tethered cyclohexadienones and diselenides: access to 5-hydroxy-3-selenyl-4a,8a-dihydro-2H-chromen-6(5H)-ones","Green Chemistry","2019","21","13","3547","","10.1039/C9GC00570F","","x-ray","0.71073","MoKα","","0.0596","0.0452","","","0.0993","0.1063","","","","","","1.054","","","","has coordinates","224616","2020-10-21","18:00:00",""
"7232918","11.1568","0.0015","17.163","0.002","9.1319","0.0015","90","","90","","90","","1748.6","0.4","293","2","293","2","","","","","","","","5","P n a 21","P 2c -2n","33","","","","- C16 H24 Cl2 N2 O3 -","- C16 H24 Cl2 N2 O3 -","- C64 H96 Cl8 N8 O12 -","4","1","","Wu, Han-Qing; Yang, Kai; Chen, Xiao-Yun; Arulkumar, Mani; Wang, Neng; Chen, Si-Hong; Wang, Zhao-Yang","A 3,4-dihalo-2(5H)-furanone initiated ring-opening reaction of DABCO in the absence of a metal catalyst and additive and its application in a one-pot two-step reaction","Green Chemistry","2019","21","14","3782","","10.1039/C9GC01740B","","x-ray","0.71073","MoKα","","0.1346","0.0613","","","0.0862","0.104","","","","","","0.892","","","","has coordinates","224620","2020-10-21","18:00:00",""
"7232949","11.4902","0.0002","9.6989","0.0002","15.4453","0.0003","90","","91.189","0.001","90","","1720.89","0.06","170","2","169.98","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H19 N O2 -","- C22 H19 N O2 -","- C88 H76 N4 O8 -","4","1","","Kong, Xianqiang; Liu, Yulong; Lin, Long; Chen, Qianjin; Xu, Bo","Electrochemical synthesis of enaminones via a decarboxylative coupling reaction","Green Chemistry","2019","21","14","3796","","10.1039/C9GC01098J","","","1.34139","GaKα","","0.0463","0.0392","","","0.0916","0.0964","","","","","","1.059","","","","has coordinates","224619","2020-10-21","18:00:00",""
"7232950","12.0153","0.001","12.5845","0.001","15.2028","0.0009","77.758","0.006","85.3","0.006","72.021","0.007","2136.5","0.3","293.75","0.1","293.75","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C22 H21 N3 O4 S2 -","- C22 H21 N3 O4 S2 -","- C88 H84 N12 O16 S8 -","4","2","","Zhang, Yu-Zhen; Mo, Zu-Yu; Wang, Heng-Shan; Wen, Xiao-An; Tang, Hai-Tao; Pan, Ying-Ming","Electrochemically enabled chemoselective sulfonylation and hydrazination of indoles","Green Chemistry","2019","21","14","3807","","10.1039/C9GC01201J","","x-ray","1.54184","CuKα","","0.087","0.074","","","0.1433","0.1891","","","","","","1.051","","","","has coordinates","224621","2020-10-21","18:00:00",""
"7232995","15.4104","0.0004","18.6531","0.0005","15.4547","0.0004","90","","96.747","0.001","90","","4411.7","0.2","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H35 Al N2 -","- C22 H35 Al N2 -","- C176 H280 Al8 N16 -","8","2","","Liu, Wenqing; Ding, Yi; Jin, Da; Shen, Qiumiao; Yan, Ben; Ma, Xiaoli; Yang, Zhi","Organic aluminum hydrides catalyze nitrile hydroboration","Green Chemistry","2019","21","14","3812","","10.1039/C9GC01659G","","","0.71073","MoKα","","0.1105","0.0522","","","0.1188","0.1412","","","","","","1.019","","","","has coordinates","224618","2020-10-21","18:00:00",""
"7232996","27.963","0.005","16.952","0.003","12.983","0.002","90","","107.713","0.005","90","","5862.6","1.7","296","2","296","2","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C31 H47 Al N2 -","- C31 H47 Al N2 -","- C248 H376 Al8 N16 -","8","2","","Liu, Wenqing; Ding, Yi; Jin, Da; Shen, Qiumiao; Yan, Ben; Ma, Xiaoli; Yang, Zhi","Organic aluminum hydrides catalyze nitrile hydroboration","Green Chemistry","2019","21","14","3812","","10.1039/C9GC01659G","","","0.71073","MoKα","","0.0711","0.0511","","","0.123","0.1333","","","","","","1.012","","","","has coordinates","224618","2020-10-21","18:00:00",""
"7233001","3.9198","0.0002","25.3323","0.0011","7.1542","0.0003","90","","97.305","0.005","90","","704.63","0.06","100","0.1","100","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C19 H15 N O2 -","- C19 H15 N O2 -","- C38 H30 N2 O4 -","2","1","","Liang, Yaofeng; Teng, Lili; Wang, Yajun; He, Qiuxing; Cao, Hua","A visible-light-induced intermolecular [3 + 2] alkenylation‒cyclization strategy: metal-free construction of pyrrolo[2,1,5-cd]indolizine rings","Green Chemistry","2019","21","15","4025","","10.1039/C9GC01766F","","x-ray","1.54184","CuKα","","0.0385","0.0367","","","0.0949","0.0966","","","","","","1.067","","","","has coordinates","224627","2020-10-21","18:00:00",""
"7233071","10.5391","0.0009","9.15","0.0014","19.861","0.002","90","","90","","90","","1915.3","0.4","173","2","173.15","","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C10 H9 N3 O -","- C10 H9 N3 O -","- C80 H72 N24 O8 -","8","1","","Zhang, Dongsheng; Fan, Yingzhu; Yan, Zhongliang; Nie, Yi; Xiong, Xingquan; Gao, Lizhu","Reactions of α-haloacroleins with azides: highly regioselective synthesis of formyl triazoles","Green Chemistry","2019","21","15","4211","","10.1039/C9GC01129C","","x-ray","0.71073","MoKα","","0.0629","0.0452","","","0.141","0.1777","","","","","","0.683","","","","has coordinates","224629","2020-10-21","18:00:00",""
"7233234","17.9538","0.0002","13.0669","0.0002","21.0038","0.0003","90","","96.8682","0.0013","90","","4892.14","0.12","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H16 N2 O2 -","- C19 H16 N2 O2 -","- C228 H192 N24 O24 -","12","3","","Kong, Yanyan; Li, Yabo; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie","An electrochemical off‒on method for pyrimidin-2(1H)-one synthesis via three-component cyclization","Green Chemistry","2019","21","16","4495","","10.1039/C9GC02005E","","x-ray","1.54184","CuKα","","0.0729","0.0511","","","0.1457","0.166","","","","","","1.033","","","","has coordinates","224613","2020-10-21","18:00:00",""
"7233311","7.9403","0.0007","17.1323","0.0014","14.1867","0.0012","90","","103.315","0.003","90","","1878","0.3","193","2","193","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C23 H16 O3 Se -","- C23 H16 O3 Se -","- C92 H64 O12 Se4 -","4","1","","Hua, Jiawei; Fang, Zheng; Xu, Jia; Bian, Mixue; Liu, ChengKou; He, Wei; Zhu, Ning; Yang, Zhao; Guo, Kai","Electrochemical oxidative cyclization of activated alkynes with diselenides or disulfides: access to functionalized coumarins or quinolinones","Green Chemistry","2019","21","17","4706","","10.1039/C9GC02131K","","","1.34139","GaKα","","0.0406","0.0383","","","0.1009","0.102","","","","","","1.173","","","","has coordinates","224607","2020-10-21","18:00:00",""
"7233375","19.766","0.0014","19.766","0.0014","7.7429","0.0006","90","","90","","90","","3025.1","0.4","296","2","296","2","","","","","","","","4","P 4/n :2","-P 4a","85","","","","- C15 H13 N3 O4 -","- C15 H13 N3 O4 -","- C120 H104 N24 O32 -","8","1","","Shi, Taoda; Teng, Shenghan; Wei, Yajie; Guo, Xin; Hu, Wenhao","Synthesis of spiro[2,3-dihydrofuran-3,3′-oxindole] derivatives via a multi-component cascade reaction of α-diazo esters, water, isatins and malononitrile/ethyl cyanoacetate","Green Chemistry","2019","21","18","4936","","10.1039/C9GC01751H","","","0.71073","MoKα","","0.0414","0.0379","","","0.0976","0.1001","","","","","","1.036","","","","has coordinates","224631","2020-10-21","18:00:00",""
"7233403","9.5181","0.0002","21.4287","0.0004","7.5942","0.0002","90","","111.404","0.003","90","","1442.09","0.06","169.99","0.1","169.99","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H14 F3 N O -","- C19 H14 F3 N O -","- C76 H56 F12 N4 O4 -","4","1","","Gao, Cai; Li, Bin; Geng, Xueyang; Zhou, Qianting; Zhang, Xinying; Fan, Xuesen","Two birds with one stone: one-pot simultaneous synthesis of 2,2,2-trifluoroethylphenanthridines and benzochromenones featuring the utilization of the byproduct of Togni's reagent","Green Chemistry","2019","21","18","5113","","10.1039/C9GC02001B","","x-ray","1.54184","CuKα","","0.0583","0.0527","","","0.1379","0.1404","","","","","","1.242","","","","has coordinates","224630","2020-10-21","18:00:00",""
"7233413","16.7161","0.0002","13.9805","0.0001","19.1927","0.0002","90","","105.636","0.001","90","","4319.34","0.08","100","0.1","100","0.1","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C42 H38 Cl2 O4 P2 Pd S -","- C42 H38 Cl2 O4 P2 Pd S -","- C168 H152 Cl8 O16 P8 Pd4 S4 -","4","1","","Yang, Da; Liu, Huan; Liu, Lei; Guo, Wen-Di; Lu, Yong; Liu, Ye","Co-catalysis over a tri-functional ligand modified Pd-catalyst for hydroxycarbonylation of terminal alkynes towards α,β-unsaturated carboxylic acids","Green Chemistry","2019","21","19","5336","","10.1039/C9GC01887E","","x-ray","1.54184","CuKα","","0.0503","0.0469","","","0.1156","0.1177","","","","","","1.044","","","","has coordinates","224612","2020-10-21","18:00:00",""
"7233576","7.308","0.006","7.452","0.006","7.833","0.007","96.059","0.014","108.374","0.013","117.853","0.014","341.3","0.5","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","4-methylbenzoic acid","","- C8 H8 O2 -","- C8 H8 O2 -","- C16 H16 O4 -","2","1","","Hwang, Kuo Chu; Sagadevan, Arunachalam; Kundu, Pradip","Sustainable Room Temperature Conversion of p-Xylene to Terephthalic Acid using Ozone and UV Irradiation","Green Chemistry","2019","","","","","10.1039/C9GC02095K","","","0.71073","MoKα","","0.0949","0.0602","","","0.1514","0.1717","","","","","","1.038","","","","has coordinates","217859","2020-10-21","18:00:00",""
"7233577","4.206","0.002","15.399","0.009","9.109","0.005","90","","92.854","0.01","90","","589.2","0.5","296","2","296","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","diethyl terephthalate","","- C12 H14 O4 -","- C12 H14 O4 -","- C24 H28 O8 -","2","0.5","","Hwang, Kuo Chu; Sagadevan, Arunachalam; Kundu, Pradip","Sustainable Room Temperature Conversion of p-Xylene to Terephthalic Acid using Ozone and UV Irradiation","Green Chemistry","2019","","","","","10.1039/C9GC02095K","","","0.71073","MoKα","","0.1046","0.0536","","","0.1257","0.1521","","","","","","1.021","","","","has coordinates","217859","2020-10-21","18:00:00",""
"7233620","9.2617","0.0004","17.7294","0.0009","11.9398","0.0005","90","","100.901","0.002","90","","1925.19","0.15","193","2","193","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C23 H22 O3 -","- C23 H22 O3 -","- C92 H88 O12 -","4","1","","Xie, Peizhong; Wo, Xiangyang; Yang, Xiaobo; Cai, Xinying; Li, Shuangshuang; Gao, Cuiqing; Fu, Weishan; Sun, Zuolian; Loh, Teck-Peng","Calcium-catalyzed regioselective dehydrative cross-coupling of propargylic alcohols with 1,3-dicarbonyl compounds","Green Chemistry","2019","21","19","5207","","10.1039/C9GC02635E","","","0.71073","MoKα","","0.0807","0.0642","","","0.1117","0.1218","","","","","","1.024","","","","has coordinates,has disorder","224611","2020-10-21","18:00:00",""
"7233621","11.367","0.0007","15.8302","0.001","11.4198","0.0007","90","","114.025","0.002","90","","1876.9","0.2","193","2","193","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C23 H22 O3 -","- C23 H22 O3 -","- C92 H88 O12 -","4","1","","Xie, Peizhong; Wo, Xiangyang; Yang, Xiaobo; Cai, Xinying; Li, Shuangshuang; Gao, Cuiqing; Fu, Weishan; Sun, Zuolian; Loh, Teck-Peng","Calcium-catalyzed regioselective dehydrative cross-coupling of propargylic alcohols with 1,3-dicarbonyl compounds","Green Chemistry","2019","21","19","5207","","10.1039/C9GC02635E","","","1.34139","GaKα","","0.044","0.04","","","0.1061","0.1103","","","","","","1.042","","","","has coordinates","224611","2020-10-21","18:00:00",""
"7233731","4.8349","0.0003","5.364","0.0003","16.1843","0.001","81.706","0.002","89.469","0.003","86.953","0.003","414.75","0.04","147","2","147","2","","","","","","","","3","P 1","P 1","1","(S,S,S)-arabitol monocaprate","(2S,3S,4S)-2,3,4,5-tetrahydroxypentyl decanoate","","- C15 H30 O6 -","- C15 H30 O6 -","- C15 H30 O6 -","1","1","","Manhas, Sanjay; Lin, Yu Chen; Wang, Grace; Kyne, Luke T.; Taylor, Mark S.","Boronic acid-promoted site-selective Fischer esterifications of sugar alcohols","Green Chemistry","2019","21","19","5363","","10.1039/C9GC00901A","","","1.54178","CuKα","","0.0331","0.0328","","","0.0849","0.0851","","","","","","1.05","","","","has coordinates","224610","2020-10-21","18:00:00",""
"7233764","18.5772","0.0013","6.9751","0.0005","19.5651","0.0014","90","","90.586","0.002","90","","2535.1","0.3","283","2","283.47","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C31 H24 N2 O4 -","- C31 H24 N2 O4 -","- C124 H96 N8 O16 -","4","1","","Zhou, Yuanyuan; Chen, Xianxiao; Ling, Xiangxiang; Rao, Weidong","Catalyst- and additive-free Baeyer‒Villiger-type oxidation of α-iodocyclopentenones to α-pyrones: using air as the oxidant","Green Chemistry","2019","21","20","5611","","10.1039/C9GC02725D","","","0.71073","MoKα","","0.1699","0.0758","","","0.1065","0.1311","","","","","","1.063","","","","has coordinates","224614","2020-10-21","18:00:00",""
"7234157","13.123","0.014","11.404","0.012","16.76","0.018","90","","109.759","0.017","90","","2361","4","296","2","296.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C29 H25 N O2 -","- C29 H25 N O2 -","- C116 H100 N4 O8 -","4","1","","Liao, Jun-Yi; Wu, Qing-Yan; Lu, Xiuqiang; Zou, Ning; Pan, Cheng-Xue; Liang, Cui; SU, Guifa; Mo, Dong-Liang","Copper-Catalyzed Diastereoselective O-Transfer Reaction of N-Vinyl-α,β-Unsaturated Nitrones with Ketenes into γ-Lactones through [5+2] Cycloaddition and N-O Bond Cleavage","Green Chemistry","2019","","","","","10.1039/C9GC01811E","","","0.71073","MoKα","","0.0826","0.0656","","","0.1798","0.1981","","","","","","1.035","","","","has coordinates","218849","2020-10-21","18:00:00",""
"7234611","27.313","0.008","9.409","0.003","24.649","0.007","90","","107.956","0.004","90","","6026","3","123","2","123","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C26 H36 Cl2 Cu N10 O -","- C26 H36 Cl2 Cu N10 O -","- C208 H288 Cl16 Cu8 N80 O8 -","8","1","","Chahal, Manoj; Raje, Sakthi; Kotana, Gopichand; Angamuthu, Raja","Binding Enabled Catalytic Activation of SO2 by Copper Koneramine Complexes at Ambient Conditions","Green Chemistry","2019","","","","","10.1039/C9GC02647A","","","0.71073","MoKα","","0.1146","0.0595","","","0.1358","0.1876","","","","","","1.06","","","","has coordinates,has disorder","219349","2020-10-21","18:00:00",""
"7234612","21.678","0.002","11.7948","0.0013","17.695","0.003","90","","90","","90","","4524.4","1","298","2","298","2","","","","","","","","3","I b a 2","I 2 -2c","45","","","","- C23 H31 N9 -","- C23 H31 N9 -","- C184 H248 N72 -","8","1","","Chahal, Manoj; Raje, Sakthi; Kotana, Gopichand; Angamuthu, Raja","Binding Enabled Catalytic Activation of SO2 by Copper Koneramine Complexes at Ambient Conditions","Green Chemistry","2019","","","","","10.1039/C9GC02647A","","","0.71073","MoKα","","0.0604","0.0469","","","0.1038","0.1129","","","","","","1.098","","","","has coordinates,has disorder","219349","2020-10-21","18:00:00",""
"7234613","14.918","0.001","11.9455","0.0008","16.2476","0.0011","90","","110.94","0.002","90","","2704.1","0.3","173","2","173","","","","","","","","","8","P 1 21/n 1","-P 2yn","14","","","","- C18 H31 Cl2 Cu F3 N8 O5 S -","- C18 H31 Cl2 Cu F3 N8 O5 S -","- C72 H124 Cl8 Cu4 F12 N32 O20 S4 -","4","1","","Chahal, Manoj; Raje, Sakthi; Kotana, Gopichand; Angamuthu, Raja","Binding Enabled Catalytic Activation of SO2 by Copper Koneramine Complexes at Ambient Conditions","Green Chemistry","2019","","","","","10.1039/C9GC02647A","","","0.71073","MoKα","","0.0742","0.0471","","","0.128","0.161","","","","","","1.123","","","","has coordinates","219349","2020-10-21","18:00:00",""
"7234614","8.4954","0.0008","11.7314","0.0011","19.281","0.0018","100.763","0.002","99.35","0.002","108.877","0.002","1734.2","0.3","100","","100","","","","","","","","","8","P -1","-P 1","2","","","","- C25 H32 Cl Cu F6 N9 O6 S2 -","- C25 H32 Cl Cu F6 N9 O6 S2 -","- C50 H64 Cl2 Cu2 F12 N18 O12 S4 -","2","1","","Chahal, Manoj; Raje, Sakthi; Kotana, Gopichand; Angamuthu, Raja","Binding Enabled Catalytic Activation of SO2 by Copper Koneramine Complexes at Ambient Conditions","Green Chemistry","2019","","","","","10.1039/C9GC02647A","","","0.71073","MoKα","","0.1196","0.0819","","","0.2246","0.2612","","","","","","1.053","","","","has coordinates","219349","2020-10-21","18:00:00",""
"7234615","8.1817","0.0003","15.7088","0.0007","24.5591","0.0011","90","","95.921","0.001","90","","3139.6","0.2","273","2","273","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C25 H39 Cl2 Cu N9 O2 -","- C25 H39 Cl2 Cu N9 O2 -","- C100 H156 Cl8 Cu4 N36 O8 -","4","1","","Chahal, Manoj; Raje, Sakthi; Kotana, Gopichand; Angamuthu, Raja","Binding Enabled Catalytic Activation of SO2 by Copper Koneramine Complexes at Ambient Conditions","Green Chemistry","2019","","","","","10.1039/C9GC02647A","","","0.71073","MoKα","","0.0667","0.0486","","","0.1375","0.1548","","","","","","1.055","","","","has coordinates","219349","2020-10-21","18:00:00",""
"7234673","12.018","0.004","22.054","0.006","9.3","0.003","90","","101.617","0.005","90","","2414.4","1.3","296","2","296.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C18 H34 N10 S2 -","- C18 H34 N10 S2 -","- C72 H136 N40 S8 -","4","1","","de Sousa Carvalho, Jr., Paulo de Sousa; Guimarães, Gelton Geraldo Fernandes; Diniz, Luan Farinelli; Ellena, Javier A.; Ribeiro, Caue","High water soluble agrichemicals by engineered organic salts for reducing adverse environmental impacts","Green Chemistry","2019","","","","","10.1039/C9GC02439E","","","0.71073","MoKα","","0.0943","0.0561","","","0.1373","0.1604","","","","","","1.022","","","","has coordinates,has disorder","219394","2020-10-21","18:00:00",""
"7234674","18.132","0.003","11.105","0.002","16.92","0.003","90","","95.693","0.003","90","","3390.1","1","120","","120","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C26 H42 N10 O8 S2 -","- C26 H42 N10 O8 S2 -","- C104 H168 N40 O32 S8 -","4","1","","de Sousa Carvalho, Jr., Paulo de Sousa; Guimarães, Gelton Geraldo Fernandes; Diniz, Luan Farinelli; Ellena, Javier A.; Ribeiro, Caue","High water soluble agrichemicals by engineered organic salts for reducing adverse environmental impacts","Green Chemistry","2019","","","","","10.1039/C9GC02439E","","","0.71073","MoKα","","0.1004","0.095","","","0.2327","0.2364","","","","","","1.082","","","","has coordinates,has disorder","219394","2020-10-21","18:00:00",""
"7234675","8.53","0.0003","9.831","0.0003","22.657","0.0008","90","","111.574","0.001","90","","1766.87","0.1","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C13 H21 N5 O4 S -","- C13 H21 N5 O4 S -","- C52 H84 N20 O16 S4 -","4","1","","de Sousa Carvalho, Jr., Paulo de Sousa; Guimarães, Gelton Geraldo Fernandes; Diniz, Luan Farinelli; Ellena, Javier A.; Ribeiro, Caue","High water soluble agrichemicals by engineered organic salts for reducing adverse environmental impacts","Green Chemistry","2019","","","","","10.1039/C9GC02439E","","","0.71073","MoKα","","0.0789","0.059","","","0.1761","0.1934","","","","","","1.011","","","","has coordinates","219394","2020-10-21","18:00:00",""
"7234676","8.825","0.0004","9.764","0.0005","12.08","0.0006","107.075","0.004","100.749","0.003","96.427","0.003","962.04","0.09","298","2","298","2","","","","","","","","5","P -1","-P 1","2","","","","- C13 H24 N5 O5.5 S -","- C13 H24 N5 O5.5 S -","- C26 H48 N10 O11 S2 -","2","1","","de Sousa Carvalho, Jr., Paulo de Sousa; Guimarães, Gelton Geraldo Fernandes; Diniz, Luan Farinelli; Ellena, Javier A.; Ribeiro, Caue","High water soluble agrichemicals by engineered organic salts for reducing adverse environmental impacts","Green Chemistry","2019","","","","","10.1039/C9GC02439E","","","0.71073","MoKα","","0.1097","0.067","","","0.1827","0.2178","","","","","","1.032","","","","has coordinates,has disorder","219394","2020-10-21","18:00:00",""
"7234677","13.495","0.003","16.262","0.003","23.781","0.005","90","","99.226","0.004","90","","5151.4","1.8","120","2","120","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C39 H63 N15 O12 S3 -","- C39 H63 N15 O12 S3 -","- C156 H252 N60 O48 S12 -","4","1","","de Sousa Carvalho, Jr., Paulo de Sousa; Guimarães, Gelton Geraldo Fernandes; Diniz, Luan Farinelli; Ellena, Javier A.; Ribeiro, Caue","High water soluble agrichemicals by engineered organic salts for reducing adverse environmental impacts","Green Chemistry","2019","","","","","10.1039/C9GC02439E","","x-ray","0.71073","MoKα","","0.0671","0.0545","","","0.1436","0.1531","","","","","","1.028","","","","has coordinates,has disorder","219394","2020-10-21","18:00:00",""
"7234745","17.2218","0.0006","13.242","0.0004","17.2998","0.0005","90","","90","","90","","3945.2","0.2","293.8","0.2","293.8","0.2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C23 H17 F3 O3 -","- C23 H17 F3 O3 -","- C184 H136 F24 O24 -","8","1","","Peng, Fu; Zhao, Qian; Huang, Wei; Liu, Shuai-Jiang; Zhong, Ya-Jun; Mao, Qing; Zhang, Nan; He, Gu; Han, Bo","Amine-catalyzed and functional group-controlled chemo- and regioselective synthesis of multi-functionalized CF3-benzene via a metal-free process","Green Chemistry","2019","","","","","10.1039/C9GC02694K","","x-ray","1.54184","CuKα","","0.0739","0.065","","","0.1607","0.1709","","","","","","1.085","","","","has coordinates","219460","2020-10-21","18:00:00",""
"7234746","7.9917","0.0005","8.305","0.0006","11.875","0.0007","107.623","0.006","97.098","0.005","91.682","0.005","743.55","0.09","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C17 H12 F3 N O2 -","- C17 H12 F3 N O2 -","- C34 H24 F6 N2 O4 -","2","1","","Peng, Fu; Zhao, Qian; Huang, Wei; Liu, Shuai-Jiang; Zhong, Ya-Jun; Mao, Qing; Zhang, Nan; He, Gu; Han, Bo","Amine-catalyzed and functional group-controlled chemo- and regioselective synthesis of multi-functionalized CF3-benzene via a metal-free process","Green Chemistry","2019","","","","","10.1039/C9GC02694K","","x-ray","1.54184","CuKα","","0.0624","0.057","","","0.1626","0.1702","","","","","","1.038","","","","has coordinates","219460","2020-10-21","18:00:00",""
"7234747","15.884","0.0006","7.23","0.0002","32.8613","0.0011","90","","90.675","0.003","90","","3773.6","0.2","292.4","0.5","292.4","0.5","","","","","","","","5","I 1 2/a 1","-I 2ya","15","","","","- C22 H15 Br N O2 -","- C22 H15 Br N O2 -","- C176 H120 Br8 N8 O16 -","8","1","","Peng, Fu; Zhao, Qian; Huang, Wei; Liu, Shuai-Jiang; Zhong, Ya-Jun; Mao, Qing; Zhang, Nan; He, Gu; Han, Bo","Amine-catalyzed and functional group-controlled chemo- and regioselective synthesis of multi-functionalized CF3-benzene via a metal-free process","Green Chemistry","2019","","","","","10.1039/C9GC02694K","","x-ray","1.54184","CuKα","","0.0641","0.0582","","","0.1593","0.1688","","","","","","1.022","","","","has coordinates","219460","2020-10-21","18:00:00",""
"7234809","14.095","0.002","9.4714","0.0014","11.1536","0.0018","90","","102.69","0.009","90","","1452.6","0.4","296","2","296.15","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C13 H16 O10 -","- C13 H16 O10 -","- C52 H64 O40 -","4","1","","Zhou, Hui; Zhang, Hui; Mu, Sen; Zhang, Wen-Zhen; Ren, Wei-Min; Lu, Xiaobing","Highly Regio- and Stereoselective Synthesis of Cyclic Carbonates from Biomass-derived Polyols via Organocatalytic Cascade Reaction","Green Chemistry","2019","","","","","10.1039/C9GC03013A","","","0.71073","MoKα","","0.1396","0.108","","","0.3398","0.3577","","","","","","1.172","","","","has coordinates","220348","2020-10-21","18:00:00",""
"7234810","5.709","0.004","12.143","0.008","14.775","0.009","90","","90","","90","","1024.3","1.2","100","2","100.15","","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C9 H8 O9 -","- C9 H8 O9 -","- C36 H32 O36 -","4","1","","Zhou, Hui; Zhang, Hui; Mu, Sen; Zhang, Wen-Zhen; Ren, Wei-Min; Lu, Xiaobing","Highly Regio- and Stereoselective Synthesis of Cyclic Carbonates from Biomass-derived Polyols via Organocatalytic Cascade Reaction","Green Chemistry","2019","","","","","10.1039/C9GC03013A","","","0.71073","MoKα","","0.0664","0.0373","","","0.079","0.09","","","","","","0.989","","","","has coordinates","220348","2020-10-21","18:00:00",""
"7234811","10.764","0.008","11.06","0.008","25.394","0.019","90","","90","","90","","3023","4","296.15","","296.15","","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C13 H16 O10 -","- C13 H16 O10 -","- C104 H128 O80 -","8","1","","Zhou, Hui; Zhang, Hui; Mu, Sen; Zhang, Wen-Zhen; Ren, Wei-Min; Lu, Xiaobing","Highly Regio- and Stereoselective Synthesis of Cyclic Carbonates from Biomass-derived Polyols via Organocatalytic Cascade Reaction","Green Chemistry","2019","","","","","10.1039/C9GC03013A","","","0.71073","MoKα","","0.1538","0.0942","","","0.1967","0.2404","","","","","","1.021","","","","has coordinates","220348","2020-10-21","18:00:00",""
"7234812","11.6926","0.001","5.2936","0.0005","12.0745","0.0011","90","","118.255","0.001","90","","658.31","0.1","200","2","200","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C6 H6 O6 -","- C6 H6 O6 -","- C24 H24 O24 -","4","1","","Zhou, Hui; Zhang, Hui; Mu, Sen; Zhang, Wen-Zhen; Ren, Wei-Min; Lu, Xiaobing","Highly Regio- and Stereoselective Synthesis of Cyclic Carbonates from Biomass-derived Polyols via Organocatalytic Cascade Reaction","Green Chemistry","2019","","","","","10.1039/C9GC03013A","","","0.71073","MoKα","","0.0409","0.038","","","0.1399","0.1448","","","","","","1.298","","","","has coordinates","220348","2020-10-21","18:00:00",""
"7234813","8.238","0.007","13.923","0.012","17.649","0.015","90","","90","","90","","2024","3","293","","293","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C15 H17 Cl3 O10 -","- C15 H17 Cl3 O10 -","- C60 H68 Cl12 O40 -","4","1","","Zhou, Hui; Zhang, Hui; Mu, Sen; Zhang, Wen-Zhen; Ren, Wei-Min; Lu, Xiaobing","Highly Regio- and Stereoselective Synthesis of Cyclic Carbonates from Biomass-derived Polyols via Organocatalytic Cascade Reaction","Green Chemistry","2019","","","","","10.1039/C9GC03013A","","","0.71073","MoKα","","0.1207","0.0658","","","0.1611","0.1913","","","","","","1.031","","","","has coordinates","220348","2020-10-21","18:00:00",""
"7235236","12.012","0.003","9.465","0.003","15.801","0.005","90","","91.447","0.005","90","","1795.9","0.9","296","2","296.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C23 H19 N O -","- C23 H19 N O -","- C92 H76 N4 O4 -","4","1","","Zhao, Hong-Ping; Liang, Gui-Chao; Nie, Shu-Min; Lu, Xiuqiang; Pan, Cheng-Xue; Zhong, Xin-Xian; Su, Gui-Fa; Mo, Dong-Liang","Metal-free graphene oxide-catalyzed aza-semipinacol rearrangement to prepare 2-(indol-2-yl)phenols and benzofuro[3,2-b]indolines containing quaternary carbon centers","Green Chemistry","2020","22","2","404","410","10.1039/C9GC03345A","","","0.71073","MoKα","","0.075","0.0448","","","0.116","0.1352","","","","","","1.032","","","","has coordinates","257595","2020-10-21","18:00:00",""
"7235247","11.241","0.003","5.7323","0.0017","17.696","0.005","90","","97.712","0.005","90","","1130","0.6","100","2","100","2","","","","","","","","4","P 1 n 1","P -2yac","7","","","","- C14 H13 N O2 -","- C14 H13 N O2 -","- C56 H52 N4 O8 -","4","2","","Pampana, V. Kishore Kumar; Sagadevan, Arunachalam; Ragupathi, Ayyakkannu; Hwang, Kuo Chu","Visible light-promoted copper catalyzed regioselective acetamidation of terminal alkynes by arylamines","Green Chemistry","2020","22","4","1164","1170","10.1039/C9GC03608C","","","0.71073","MoKα","","0.047","0.0397","","","0.0945","0.0981","","","","","","1.059","","","","has coordinates","257588","2020-10-21","18:00:00",""
"7235248","12.2746","0.0008","9.2499","0.0006","14.751","0.0009","90","","100.612","0.002","90","","1646.17","0.18","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C18 H15 N O2 -","- C18 H15 N O2 -","- C72 H60 N4 O8 -","4","1","","Pampana, V. Kishore Kumar; Sagadevan, Arunachalam; Ragupathi, Ayyakkannu; Hwang, Kuo Chu","Visible light-promoted copper catalyzed regioselective acetamidation of terminal alkynes by arylamines","Green Chemistry","2020","22","4","1164","1170","10.1039/C9GC03608C","","","0.71073","MoKα","","0.0781","0.0592","","","0.1182","0.1274","","","","","","1.029","","","","has coordinates","257588","2020-10-21","18:00:00",""
"7235249","14.568","0.002","5.0757","0.0008","16.496","0.003","90","","102.818","0.005","90","","1189.4","0.3","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C13 H13 N O2 S -","- C13 H13 N O2 S -","- C52 H52 N4 O8 S4 -","4","1","","Pampana, V. Kishore Kumar; Sagadevan, Arunachalam; Ragupathi, Ayyakkannu; Hwang, Kuo Chu","Visible light-promoted copper catalyzed regioselective acetamidation of terminal alkynes by arylamines","Green Chemistry","2020","22","4","1164","1170","10.1039/C9GC03608C","","","0.71073","MoKα","","0.0944","0.0441","","","0.0762","0.0901","","","","","","1.011","","","","has coordinates,has disorder","257588","2020-10-21","18:00:00",""
"7235256","8.6559","0.0005","15.6308","0.0009","16.2787","0.0008","90","","90","","90","","2202.5","0.2","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C96 H56 Br12 N12 O5 -","- C96 H56 Br12 N12 O5 -","- C96 H56 Br12 N12 O5 -","1","0.25","","Gohain, Shivanee Borpatra; Basumatary, Monika; Boruah, Purna K.; Das, Manash R.; Thakur, Ashim Jyoti","Nano Au/Pd-catalysed ‘on-water’ synthesis of C3‒C3′ diaryl-oxindole scaffolds via N2-selective dearomatization of indole","Green Chemistry","2020","22","1","170","179","10.1039/C9GC02370D","","","0.71073","MoKα","","0.1928","0.0596","","","0.1108","0.1538","","","","","","0.94","","","","has coordinates","257573","2020-10-21","18:00:00",""
"7235257","14.8779","0.0007","25.5062","0.0007","15.6343","0.0005","90","","104.511","0.002","90","","5743.6","0.4","296","2","296","2","","","","","","","","7","C 1 2/c 1","-C 2yc","15","","","","- C52 H46 Br2 F6 Ir N4 P -","- C52 H46 Br2 F6 Ir N4 P -","- C208 H184 Br8 F24 Ir4 N16 P4 -","4","0.5","","Xu, Zi-Yue; Luo, Yi; Zhang, Dan-Wei; Wang, Hui; Sun, Xing-Wen; Li, Zhan-Ting","Iridium complex-linked porous organic polymers for recyclable, broad-scope photocatalysis of organic transformations","Green Chemistry","2020","22","1","136","143","10.1039/C9GC03688A","","","1.34138","GaKα","","0.0526","0.0485","","","0.1336","0.1375","","","","","","1.07","","","","has coordinates","257576","2020-10-21","18:00:00",""
"7235258","11.3884","0.0014","14.5156","0.0018","14.8459","0.0017","90","","105.062","0.005","90","","2369.9","0.5","173","2","173","2","","","","","","","","8","P 1 2/n 1","-P 2yac","13","","","","- C40 H38 Br2 Cl0.5 F9 Ir N4 P1.5 -","- C40 H38 Br2 Cl0.5 F9 Ir N4 P1.5 -","- C80 H76 Br4 Cl F18 Ir2 N8 P3 -","2","0.5","","Xu, Zi-Yue; Luo, Yi; Zhang, Dan-Wei; Wang, Hui; Sun, Xing-Wen; Li, Zhan-Ting","Iridium complex-linked porous organic polymers for recyclable, broad-scope photocatalysis of organic transformations","Green Chemistry","2020","22","1","136","143","10.1039/C9GC03688A","","","1.34138","GaKα","","0.0762","0.0623","","","0.1864","0.2044","","","","","","1.018","","","","has coordinates,has disorder","257576","2020-10-21","18:00:00",""
"7235259","12.1698","0.0005","14.9926","0.0006","16.2329","0.0007","78.079","0.001","89.769","0.002","77.466","0.002","2826.3","0.2","173","2","173","2","","","","","","","","6","P -1","-P 1","2","","","","- C64 H56 F6 Ir N4 P -","- C64 H56 F6 Ir N4 P -","- C128 H112 F12 Ir2 N8 P2 -","2","1","","Xu, Zi-Yue; Luo, Yi; Zhang, Dan-Wei; Wang, Hui; Sun, Xing-Wen; Li, Zhan-Ting","Iridium complex-linked porous organic polymers for recyclable, broad-scope photocatalysis of organic transformations","Green Chemistry","2020","22","1","136","143","10.1039/C9GC03688A","","","1.34138","GaKα","","0.0447","0.0375","","","0.092","0.0955","","","","","","1.122","","","","has coordinates,has disorder","257576","2020-10-21","18:00:00",""
"7237090","14.87","0.003","8.115","0.0018","15.295","0.004","90","","106.026","0.003","90","","1773.9","0.7","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H16 Br O3 P -","- C19 H16 Br O3 P -","- C76 H64 Br4 O12 P4 -","4","1","","Shen, Ruwei; Zhang, Ming; Xiao, Jing; Dong, Chao; Han, Li-Biao","Ph3P-mediated highly selective C(α)‒P coupling of quinone monoacetals with R2P(O)H: convenient and practical synthesis of ortho-phosphinyl phenols","Green Chemistry","2018","20","22","5111","","10.1039/C8GC02918K","","","0.71073","MoKα","","0.0395","0.0291","","","0.0756","0.0791","","","","","","1.033","","","","has coordinates","236864","2020-10-21","18:00:00",""
"7237091","32.26","0.03","16.224","0.015","7.12","0.007","90","","90","","90","","3727","6","296","2","296","2","","","","","","","","4","A e a 2","A 2 -2ab","41","","","","- C21 H21 O3 P -","- C21 H21 O3 P -","- C168 H168 O24 P8 -","8","1","","Shen, Ruwei; Zhang, Ming; Xiao, Jing; Dong, Chao; Han, Li-Biao","Ph3P-mediated highly selective C(α)‒P coupling of quinone monoacetals with R2P(O)H: convenient and practical synthesis of ortho-phosphinyl phenols","Green Chemistry","2018","20","22","5111","","10.1039/C8GC02918K","","","0.71073","MoKα","","0.0355","0.0325","","","0.0835","0.0851","","","","","","1.049","","","","has coordinates","236864","2020-10-21","18:00:00",""
"7237092","12.451","0.0007","18.5872","0.001","7.9138","0.0005","90","","90","","90","","1831.48","0.18","293","2","293.15","","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C20 H19 O5 P -","- C20 H19 O5 P -","- C80 H76 O20 P4 -","4","1","","Shen, Ruwei; Zhang, Ming; Xiao, Jing; Dong, Chao; Han, Li-Biao","Ph3P-mediated highly selective C(α)‒P coupling of quinone monoacetals with R2P(O)H: convenient and practical synthesis of ortho-phosphinyl phenols","Green Chemistry","2018","20","22","5111","","10.1039/C8GC02918K","","","0.71073","MoKα","","0.0429","0.0362","","","0.0867","0.0919","","","","","","1.041","","","","has coordinates","236864","2020-10-21","18:00:00",""
"7237093","11.472","0.009","17.116","0.013","18.24","0.014","90","","90","","90","","3582","5","296","2","296","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C19 H16 Br O3 P -","- C19 H16 Br O3 P -","- C152 H128 Br8 O24 P8 -","8","1","","Shen, Ruwei; Zhang, Ming; Xiao, Jing; Dong, Chao; Han, Li-Biao","Ph3P-mediated highly selective C(α)‒P coupling of quinone monoacetals with R2P(O)H: convenient and practical synthesis of ortho-phosphinyl phenols","Green Chemistry","2018","20","22","5111","","10.1039/C8GC02918K","","","0.71073","MoKα","","0.1216","0.0705","","","0.1681","0.1873","","","","","","1.064","","","","has coordinates","236864","2020-10-21","18:00:00",""
"7237094","18.086","0.01","11.245","0.006","17.491","0.01","90","","98.109","0.007","90","","3522","3","296","2","296","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C20 H19 O3 P -","- C20 H19 O3 P -","- C160 H152 O24 P8 -","8","1","","Shen, Ruwei; Zhang, Ming; Xiao, Jing; Dong, Chao; Han, Li-Biao","Ph3P-mediated highly selective C(α)‒P coupling of quinone monoacetals with R2P(O)H: convenient and practical synthesis of ortho-phosphinyl phenols","Green Chemistry","2018","20","22","5111","","10.1039/C8GC02918K","","","0.71073","MoKα","","0.0805","0.0478","","","0.1161","0.1287","","","","","","1.053","","","","has coordinates","236864","2020-10-21","18:00:00",""
"7238046","6.4219","0.0012","10.741","0.002","13.507","0.003","90","","95.887","0.003","90","","926.8","0.3","293","2","293.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C9 H12 N2 O -","- C9 H12 N2 O -","- C36 H48 N8 O4 -","4","1","","Kong, Lingbin; Huang, Rong; He, Haodan; Fan, Yunxiang; Lin, Jun; Yan, Shengjiao","Multi-component solvent-free cascade reaction of 2-cyanoacetamides: regioselective synthesis of pyridin-2-ones bearing quaternary centers","Green Chemistry","2020","22","1","256","264","10.1039/C9GC03692J","","","0.71073","MoKα","","0.1226","0.05","","","0.1048","0.1279","","","","","","0.9","","","","has coordinates","257574","2020-10-21","18:00:00",""
"7238047","7.3319","0.0011","11.5409","0.0016","16.169","0.002","90","","99.147","0.002","90","","1350.8","0.3","296.15","","296.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C15 H16 N2 O -","- C15 H16 N2 O -","- C60 H64 N8 O4 -","4","1","","Kong, Lingbin; Huang, Rong; He, Haodan; Fan, Yunxiang; Lin, Jun; Yan, Shengjiao","Multi-component solvent-free cascade reaction of 2-cyanoacetamides: regioselective synthesis of pyridin-2-ones bearing quaternary centers","Green Chemistry","2020","22","1","256","264","10.1039/C9GC03692J","","","0.71073","MoKα","","0.0799","0.0473","","","0.1176","0.1354","","","","","","1.02","","","","has coordinates","257574","2020-10-21","18:00:00",""
"7238048","4.7211","0.0018","13.737","0.005","15.384","0.006","77.216","0.014","86.717","0.015","85.596","0.018","969.3","0.6","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C46 H54 N8 O4 -","- C46 H54 N8 O4 -","- C46 H54 N8 O4 -","1","0.5","","Huang, Yunping; Liu, Yun; Sommerville, Parker J. W.; Kaminsky, Werner; Ginger, David S.; Luscombe, Christine K.","Theobromine and direct arylation: a sustainable and scalable solution to minimize aggregation caused quenching","Green Chemistry","2019","","","","","10.1039/C9GC03391B","","x-ray","0.71073","MoKα","","0.2578","0.0753","","","0.14","0.1999","","","","","","0.915","","","","has coordinates","242692","2020-10-21","18:00:00",""
"7238049","21.6","0.0016","12.9539","0.001","8.945","0.0006","90","","90.508","0.004","90","","2502.8","0.3","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C31 H32 N4 O2 -","- C31 H32 N4 O2 -","- C124 H128 N16 O8 -","4","1","","Huang, Yunping; Liu, Yun; Sommerville, Parker J. W.; Kaminsky, Werner; Ginger, David S.; Luscombe, Christine K.","Theobromine and direct arylation: a sustainable and scalable solution to minimize aggregation caused quenching","Green Chemistry","2019","","","","","10.1039/C9GC03391B","","x-ray","0.71073","MoKα","","0.0687","0.0442","","","0.1041","0.1184","","","","","","1.02","","","","has coordinates","242692","2020-10-21","18:00:00",""
"7238050","11.4759","0.0007","23.1694","0.0015","14.5016","0.001","90","","111.004","0.003","90","","3599.6","0.4","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C76 H98 N16 O8 -","- C76 H98 N16 O8 -","- C152 H196 N32 O16 -","2","0.5","","Huang, Yunping; Liu, Yun; Sommerville, Parker J. W.; Kaminsky, Werner; Ginger, David S.; Luscombe, Christine K.","Theobromine and direct arylation: a sustainable and scalable solution to minimize aggregation caused quenching","Green Chemistry","2019","","","","","10.1039/C9GC03391B","","x-ray","0.71073","MoKα","","0.0784","0.0451","","","0.104","0.1212","","","","","","1.021","","","","has coordinates","242692","2020-10-21","18:00:00",""
"7239605","22.7662","0.0011","12.1453","0.0005","24.9282","0.0011","90","","98.796","0.002","90","","6811.6","0.5","298","","294.9","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C20 H30 Cu2 N8 O14 V5 -","- C20 H30 Cu2 N8 O14 V5 -","- C160 H240 Cu16 N64 O112 V40 -","8","1","","Tian, Hong-Rui; Liu, Yi-Wei; Zhang, Zhong; Liu, Shu-Mei; Dang, Tian-Yi; Li, Xiao-Hui; Sun, Xiu-Wei; Lu, Ying; Liu, Shu-Xia","A multicentre synergistic polyoxometalate-based metal‒organic framework for one-step selective oxidative cleavage of β-O-4 lignin model compounds","Green Chemistry","2020","22","1","248","255","10.1039/C9GC03626A","","","0.71073","MoKα","","0.06","0.0455","","","0.0971","0.1034","","","","","","1.095","","","","has coordinates,has disorder","257575","2020-10-21","18:00:00",""
"7239670","9.0134","0.0004","9.0528","0.0004","9.6602","0.0005","70.923","0.002","76.94","0.002","75.474","0.002","712.15","0.06","273","2","273.15","","","","","","","","","4","P -1","-P 1","2","","2-amino-4-(3-nitrophenyl)-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile","","- C16 H13 N3 O4 -","- C16 H13 N3 O4 -","- C32 H26 N6 O8 -","2","1","","Saini, Sanjeev; Mayank,; Kaur, Navneet; Singh, Narinder","A cytochrome c-urea functionalized dipeptide conjugate: an efficient HBD framework to synthesize 4H-pyrans via one-pot multicomponent reaction","Green Chemistry","2020","22","3","956","968","10.1039/C9GC03512E","","","0.71073","MoKα","","0.0559","0.044","","","0.1111","0.1239","","","","","","1.096","","","","has coordinates","257626","2020-10-21","18:00:00",""
"7239713","8.486","0.001","15.1787","0.0018","16.604","0.002","90","","97.43","0.004","90","","2120.7","0.4","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C23 H20 O4 S Se -","- C23 H20 O4 S Se -","- C92 H80 O16 S4 Se4 -","4","1","","Chen, Shihao; Li, Yaping; Wang, Ming; Jiang, Xuefeng","General sulfone construction via sulfur dioxide surrogate control","Green Chemistry","2020","22","2","322","326","10.1039/C9GC03841H","","","0.71073","MoKα","","0.0582","0.0437","","","0.1134","0.1229","","","","","","1.03","","","","has coordinates","257593","2020-10-21","18:00:00",""
"7239714","11.2374","0.0001","10.3578","0.0001","16.9587","0.0001","90","","90","","90","","1973.9","0.03","292.7","0.6","292.7","0.6","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C11 H10 O2 S -","- C11 H10 O2 S -","- C88 H80 O16 S8 -","8","1","","Chen, Shihao; Li, Yaping; Wang, Ming; Jiang, Xuefeng","General sulfone construction via sulfur dioxide surrogate control","Green Chemistry","2020","22","2","322","326","10.1039/C9GC03841H","","x-ray","1.54184","CuKα","","0.0351","0.034","","","0.0916","0.0927","","","","","","1.031","","","","has coordinates","257593","2020-10-21","18:00:00",""
"7239715","15.4973","0.0003","10.5001","0.0002","9.92584","0.00018","90","","90.3156","0.0016","90","","1615.14","0.05","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H16 F3 N O2 -","- C19 H16 F3 N O2 -","- C76 H64 F12 N4 O8 -","4","1","","Xu, Zhongnan; Huang, Zhixing; Li, Yueheng; Kuniyil, Rositha; Zhang, Chao; Ackermann, Lutz; Ruan, Zhixiong","Catalyst-free, direct electrochemical synthesis of annulated medium-sized lactams through C‒C bond cleavage","Green Chemistry","2020","22","4","1099","1104","10.1039/C9GC03901E","","x-ray","1.54184","CuKα","","0.0418","0.0392","","","0.104","0.1068","","","","","","1.053","","","","has coordinates","257589","2020-10-21","18:00:00",""
"7239716","20.3378","0.001","20.3378","0.001","18.3367","0.0011","90","","90","","90","","7584.5","0.7","100.01","0.1","100.01","0.1","","","","","","","","4","I 41/a :2","-I 4ad","88","","","","- C21 H22 N2 O2 -","- C21 H22 N2 O2 -","- C336 H352 N32 O32 -","16","1","","Li, Jianxiao; Yu, Junsheng; Xiong, Wenfang; Tang, Hao; Hu, Miao; Wu, Wanqing; Jiang, Huanfeng","A palladium-catalyzed oxidative aminocarbonylation reaction of alkynone O-methyloximes with amines and CO in PEG-400","Green Chemistry","2020","22","2","465","470","10.1039/C9GC03562A","","x-ray","0.71073","MoKα","","0.0805","0.0598","","","0.141","0.1522","","","","","","1.063","","","","has coordinates","257594","2020-10-21","18:00:00",""
"7239730","7.1396","0.0018","15.021","0.004","17.652","0.005","90","","96.825","0.004","90","","1879.7","0.9","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H24 N4 O7 -","- C17 H24 N4 O7 -","- C68 H96 N16 O28 -","4","1","","Appiagyei, Benjamin; Bhatia, Souful; Keeney, Gabriela L.; Dolmetsch, Troy; Jackson, James E.","Electroactivated alkylation of amines with alcohols via both direct and indirect borrowing hydrogen mechanisms","Green Chemistry","2020","22","3","860","869","10.1039/C9GC03747K","","","0.71073","MoKα","","0.1038","0.0637","","","0.1688","0.2027","","","","","","1.028","","","","has coordinates,has disorder","257628","2020-10-21","18:00:00",""
"7239750","10.51","0.003","11.377","0.003","32.058","0.009","90","","93.828","0.007","90","","3824.7","1.8","123","2","123","2","","","","","","","synthesis as described","4","P 1 21/c 1","-P 2ybc","14","","","","- C40 H58 O4 Si2 -","- C40 H58 O4 Si2 -","- C160 H232 O16 Si8 -","4","1","","Ohno, Shohei; Avena, Ramon Francisco; Aoyama, Hiroshi; Fujioka, Hiromichi; Arisawa, Mitsuhiro","Thermal [2 + 2]-cycloaddition between silylalkynes and allenylphenols followed by the nucleophilic addition of water: metal-free and economical synthesis of arylcyclobutenals","Green Chemistry","2020","22","4","1220","1228","10.1039/C9GC04184B","","x-ray","1.54178","CuKα","","0.1053","0.0689","","","0.2056","0.2602","","","","","","1.039","","","","has coordinates","257586","2020-10-21","18:00:00",""
"7239751","6.2629","0.0011","18.353","0.003","22.063","0.005","90","","92.471","0.007","90","","2533.6","0.8","100","2","100","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C30 H25 N O2 S Se -","- C30 H25 N O2 S Se -","- C120 H100 N4 O8 S4 Se4 -","4","1","","Dutta, Shubham; Prabagar, B.; Vanjari, Rajeshwer; Gandon, Vincent; Sahoo, Akhila K.","An unconventional sulfur-to-selenium-to-carbon radical transfer: chemo-and regioselective cyclization of yne-ynamides","Green Chemistry","2020","22","4","1113","1118","10.1039/C9GC03745D","","","0.71073","MoKα","","0.0794","0.0523","","","0.1495","0.1677","","","","","","0.909","","","","has coordinates,has disorder","257585","2020-10-21","18:00:00",""
"7239763","8.4738","0.0002","24.4748","0.0006","11.8708","0.0003","90","","91.051","0.001","90","","2461.53","0.1","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C27 H25 Cl O4 -","- C27 H25 Cl O4 -","- C108 H100 Cl4 O16 -","4","1","","Zhang, Zhipeng; Yu, Yang; Huang, Fei; Yi, Xiangyan; Xu, Yao; He, Yide; Baell, Jonathan B.; Huang, He","Catalytic O‒H bond insertion reactions using surface modified sewage sludge as a catalyst","Green Chemistry","2020","22","5","1594","1604","10.1039/C9GC03428E","","","0.71073","MoKα","","0.09","0.0684","","","0.1953","0.2209","","","","","","1.046","","","","has coordinates,has disorder","257583","2020-10-21","18:00:00",""
"7239764","15.0906","0.0005","7.9886","0.0002","15.7975","0.0005","90","","95.544","0.001","90","","1895.52","0.1","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C23 H22 O4 -","- C23 H22 O4 -","- C92 H88 O16 -","4","1","","Zhang, Zhipeng; Yu, Yang; Huang, Fei; Yi, Xiangyan; Xu, Yao; He, Yide; Baell, Jonathan B.; Huang, He","Catalytic O‒H bond insertion reactions using surface modified sewage sludge as a catalyst","Green Chemistry","2020","22","5","1594","1604","10.1039/C9GC03428E","","","0.71073","MoKα","","0.0531","0.0421","","","0.1089","0.1192","","","","","","1.013","","","","has coordinates","257583","2020-10-21","18:00:00",""
"7239784","7.594","0.0014","8.5623","0.0016","13.088","0.003","97.266","0.003","95.849","0.003","95.577","0.003","834.5","0.3","150","2","150","2","","","","","","","","5","P -1","-P 1","2","","","","- C12 H10 Mn N3 O5 -","- C12 H10 Mn N3 O5 -","- C24 H20 Mn2 N6 O10 -","2","1","","Léval, Alexander; Agapova, Anastasiya; Steinlechner, Christoph; Alberico, Elisabetta; Junge, Henrik; Beller, Matthias","Hydrogen production from formic acid catalyzed by a phosphine free manganese complex: investigation and mechanistic insights","Green Chemistry","2020","22","3","913","920","10.1039/C9GC02453K","","","0.71073","MoKα","","0.0384","0.0346","","","0.1035","0.1074","","","","","","1.066","","","","has coordinates","257627","2020-10-21","18:00:00",""
"7239785","7.9845","0.0013","12.118","0.002","14.112","0.002","90","","100.181","0.003","90","","1343.9","0.4","150","2","150","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C11 H9 Br Mn N3 O3 -","- C11 H9 Br Mn N3 O3 -","- C44 H36 Br4 Mn4 N12 O12 -","4","1","","Léval, Alexander; Agapova, Anastasiya; Steinlechner, Christoph; Alberico, Elisabetta; Junge, Henrik; Beller, Matthias","Hydrogen production from formic acid catalyzed by a phosphine free manganese complex: investigation and mechanistic insights","Green Chemistry","2020","22","3","913","920","10.1039/C9GC02453K","","","0.71073","MoKα","","0.0239","0.0201","","","0.0507","0.0525","","","","","","1.049","","","","has coordinates","257627","2020-10-21","18:00:00",""
"7239835","8.6772","0.0008","9.0145","0.0009","9.9691","0.0009","110.22","0.004","107.146","0.003","97.596","0.002","674.97","0.11","298","2","298","2","","","","","","","","5","P -1","-P 1","2","","","","- C15 H13 F N2 S -","- C15 H13 F N2 S -","- C30 H26 F2 N4 S2 -","2","1","","Wen, Jiangwei; Niu, Cong; Yan, Kelu; Cheng, Xingda; Gong, Ruike; Li, Mengqian; Guo, Yongqiang; Yang, Jianjing; Wang, Hua","Electrochemical-induced regioselective C-3 thiomethylation of imidazopyridines via a three-component cross-coupling strategy","Green Chemistry","2020","22","4","1129","1133","10.1039/C9GC04068D","","","0.71073","MoKα","","0.0578","0.0427","","","0.1159","0.1272","","","","","","1.06","","","","has coordinates","257587","2020-10-21","18:00:00",""
"7239951","12.6327","0.0006","15.2434","0.0007","15.98","0.0007","102.027","0.002","105.432","0.002","112.595","0.002","2566.4","0.2","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C33 H27 N O6 -","- C33 H27 N O6 -","- C132 H108 N4 O24 -","4","2","","Largeron, Martine; Deschamps, Patrick; Hammad, Karim; Fleury, Maurice-Bernard","A dual biomimetic process for the selective aerobic oxidative coupling of primary amines using pyrogallol as a precatalyst. Isolation of the [5 + 2] cycloaddition redox intermediates","Green Chemistry","2020","22","6","1894","1905","10.1039/C9GC03992A","","","1.54178","CuKα","","0.0427","0.0375","","","0.0998","0.1045","","","","","","1.011","","","","has coordinates,has disorder","257598","2020-10-21","18:00:00",""
"7239952","5.6742","0.0002","8.7921","0.0004","13.5713","0.0005","103.259","0.001","95.099","0.001","95.624","0.001","651.48","0.04","100","2","100","1","","","","","","","","3","P -1","-P 1","2","(E)-N-(2,3-dihydro-1H-inden-2-yl)-1(p-tolyl)methanimine","","","- C17 H17 N -","- C17 H17 N -","- C34 H34 N2 -","2","1","","Largeron, Martine; Deschamps, Patrick; Hammad, Karim; Fleury, Maurice-Bernard","A dual biomimetic process for the selective aerobic oxidative coupling of primary amines using pyrogallol as a precatalyst. Isolation of the [5 + 2] cycloaddition redox intermediates","Green Chemistry","2020","22","6","1894","1905","10.1039/C9GC03992A","","","1.54178","CuKα","","0.0464","0.0439","","","0.1096","0.1122","","","","","","1.072","","","","has coordinates","257598","2020-10-21","18:00:00",""
"7239953","10.388","0.0004","10.8621","0.0004","11.9356","0.0004","103.368","0.001","111.316","0.001","90.267","0.001","1214.77","0.08","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","2-cyclopropyl-1-phenyl-1H-benzoimidazole","","- C16 H14 N2 -","- C16 H14 N2 -","- C64 H56 N8 -","4","2","","Largeron, Martine; Deschamps, Patrick; Hammad, Karim; Fleury, Maurice-Bernard","A dual biomimetic process for the selective aerobic oxidative coupling of primary amines using pyrogallol as a precatalyst. Isolation of the [5 + 2] cycloaddition redox intermediates","Green Chemistry","2020","22","6","1894","1905","10.1039/C9GC03992A","","","1.54178","CuKα","","0.0327","0.0314","","","0.0776","0.0784","","","","","","1.099","","","","has coordinates","257598","2020-10-21","18:00:00",""
"7239961","8.398","0.005","7.421","0.005","13.749","0.007","90","","99.9","0.05","90","","844.1","0.9","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C9 H5 N O S -","- C9 H5 N O S -","- C36 H20 N4 O4 S4 -","4","1","","He, Dongdong; Yao, Jiaojiao; Ma, Boling; Wei, Jinghao; Hao, Guangguo; Tuo, Xun; Guo, Shengmei; Fu, Zhengjiang; Cai, Hu","An electrochemical method for deborylative seleno/thiocyanation of arylboronic acids under catalyst- and oxidant-free conditions","Green Chemistry","2020","22","5","1559","1564","10.1039/C9GC03797G","","","0.71073","MoKα","","0.1066","0.0905","","","0.1814","0.1828","","","","","","3.633","","","","has coordinates","257584","2020-10-21","18:00:00",""
"7239973","11.3479","0.0005","10.0774","0.0005","11.9461","0.0006","90","","98.694","0.004","90","","1350.43","0.11","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H13 Cl N2 O -","- C15 H13 Cl N2 O -","- C60 H52 Cl4 N8 O4 -","4","1","","Yue, Jing; Ma, Xi-Tao; Liu, Xiong-Li; Wang, Jun-Xin; Liu, Xiong-Wei; Zhou, Ying","Ammonium hydroxide as the ultimate amino source for the synthesis of N-unprotected 3-tetrasubstituted aminooxindoles via catalyst-free direct amination","Green Chemistry","2020","22","6","1837","1841","10.1039/D0GC00130A","","x-ray","0.71073","MoKα","","0.0561","0.0457","","","0.1136","0.122","","","","","","1.07","","","","has coordinates","257597","2020-10-21","18:00:00",""
"7239974","12.8233","0.0013","10.2114","0.0007","12.0326","0.0013","90","","116.906","0.013","90","","1405","0.3","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H15 Cl N2 O -","- C16 H15 Cl N2 O -","- C64 H60 Cl4 N8 O4 -","4","1","","Yue, Jing; Ma, Xi-Tao; Liu, Xiong-Li; Wang, Jun-Xin; Liu, Xiong-Wei; Zhou, Ying","Ammonium hydroxide as the ultimate amino source for the synthesis of N-unprotected 3-tetrasubstituted aminooxindoles via catalyst-free direct amination","Green Chemistry","2020","22","6","1837","1841","10.1039/D0GC00130A","","x-ray","0.71073","MoKα","","0.0562","0.0437","","","0.0944","0.1027","","","","","","1.022","","","","has coordinates","257597","2020-10-21","18:00:00",""
"7239983","11.7246","0.0003","8.3285","0.0002","16.9656","0.0005","90","","90","","90","","1656.66","0.08","106","7","106","7","","","","","","","","4","P b c a","-P 2ac 2ab","61","","TR67.0U","","- C8 H11 N O3 -","- C8 H11 N O3 -","- C64 H88 N8 O24 -","8","1","","Pham, Thuy Trang; Chen, Xi; Söhnel, Tilo; Yan, Ning; Sperry, Jonathan","Haber-independent, diversity-oriented synthesis of nitrogen compounds from biorenewable chitin","Green Chemistry","2020","22","6","1978","1984","10.1039/D0GC00208A","","x-ray","1.54184","CuKα","","0.0425","0.0375","","","0.0945","0.0977","","","","","","1.085","","","","has coordinates","257596","2020-10-21","18:00:00",""
"7239984","7.1931","0.0003","7.0581","0.0004","8.4454","0.0004","90","","92.515","0.004","90","","428.36","0.04","107","4","107","4","","","","","","","","4","P 1 21/m 1","-P 2yb","11","","","","- C10 H11 N O2 -","- C10 H11 N O2 -","- C20 H22 N2 O4 -","2","0.5","","Pham, Thuy Trang; Chen, Xi; Söhnel, Tilo; Yan, Ning; Sperry, Jonathan","Haber-independent, diversity-oriented synthesis of nitrogen compounds from biorenewable chitin","Green Chemistry","2020","22","6","1978","1984","10.1039/D0GC00208A","","x-ray","1.54184","CuKα","","0.0387","0.0348","","","0.0907","0.0936","","","","","","1.057","","","","has coordinates","257596","2020-10-21","18:00:00",""
"7239985","7.1964","0.0001","11.9878","0.0003","14.751","0.0003","90","","90","","90","","1272.55","0.04","107","5","107","5","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","TR205","","- C14 H13 N O5 -","- C14 H13 N O5 -","- C56 H52 N4 O20 -","4","1","","Pham, Thuy Trang; Chen, Xi; Söhnel, Tilo; Yan, Ning; Sperry, Jonathan","Haber-independent, diversity-oriented synthesis of nitrogen compounds from biorenewable chitin","Green Chemistry","2020","22","6","1978","1984","10.1039/D0GC00208A","","x-ray","1.54184","CuKα","","0.029","0.0277","","","0.0719","0.0728","","","","","","1.047","","","","has coordinates","257596","2020-10-21","18:00:00",""
"7239986","24.7484","0.0003","10.706","0.0001","26.2577","0.0003","90","","115.723","0.001","90","","6267.71","0.13","103","2","103","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C60 H84 N4 O24 -","- C60 H84 N4 O24 -","- C240 H336 N16 O96 -","4","1","","Pham, Thuy Trang; Chen, Xi; Söhnel, Tilo; Yan, Ning; Sperry, Jonathan","Haber-independent, diversity-oriented synthesis of nitrogen compounds from biorenewable chitin","Green Chemistry","2020","22","6","1978","1984","10.1039/D0GC00208A","","x-ray","1.54184","CuKα","","0.0489","0.0428","","","0.112","0.1162","","","","","","1.027","","","","has coordinates,has disorder","257596","2020-10-21","18:00:00",""
"7240053","8.4606","0.0004","16.9137","0.0008","35.129","0.003","90","","90.02","0.02","90","","5027","0.5","100.01","0.1","100.01","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H19 N O4 -","- C20 H19 N O4 -","- C240 H228 N12 O48 -","12","3","","Zhao, Yong-Long; Tang, Yong-Qin; Fei, Xing-Hai; Yang, Fen-Fen; Cao, Zhuo-Xian; Duan, Dong-Zhu; Zhao, Qing-Jie; Yang, Yuan-Yong; Zhou, Meng; He, Bin","Direct C(sp3)‒H acyloxylation of indolin-3-ones with carboxylic acids catalysed by KI","Green Chemistry","2020","22","8","2354","2358","10.1039/C9GC04446A","","x-ray","0.71073","MoKα","","0.0779","0.0515","","","0.1179","0.1354","","","","","","1.027","","","","has coordinates","257581","2020-10-21","18:00:00",""
"7240065","8.43","0.006","17.184","0.013","9.073","0.007","90","","93.26","0.04","90","","1312.2","1.7","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","4',6'-dihydroxy-3-(morpholino-4-ium)-3H-spiro[benzo[d][1,2]oxaborole-2,2'-[1,3,5,2,4,6]trioxatriborinan]-2-uide","","- C11 H16 B3 N O7 -","- C11 H16 B3 N O7 -","- C44 H64 B12 N4 O28 -","4","1","","Ming, Wenbo; Liu, Xiaocui; Friedrich, Alexandra; Krebs, Johannes; Budiman, Yudha P.; Huang, Mingming; Marder, Todd B.","Concise synthesis of α-amino cyclic boronates via multicomponent coupling of salicylaldehydes, amines, and B2(OH)4","Green Chemistry","2020","22","7","2184","2190","10.1039/D0GC00346H","","","0.71073","MoKα","","0.066","0.0472","","","0.1103","0.1188","","","","","","1.032","","","","has coordinates","257615","2020-10-21","18:00:00",""
"7240066","9.549","0.005","11.307","0.002","13.26","0.003","100.88","0.03","92.261","0.011","105.79","0.03","1346.6","0.8","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","3-(dibenzylammonio)-4',6'-dihydroxy-3H-spiro[benzo[d][1,2]oxaborole-2,2'-[1,3,5,2,4,6]trioxatriborinan]-2-uide","","- C27 H34 B3 N O8 -","- C27 H34 B3 N O8 -","- C54 H68 B6 N2 O16 -","2","1","","Ming, Wenbo; Liu, Xiaocui; Friedrich, Alexandra; Krebs, Johannes; Budiman, Yudha P.; Huang, Mingming; Marder, Todd B.","Concise synthesis of α-amino cyclic boronates via multicomponent coupling of salicylaldehydes, amines, and B2(OH)4","Green Chemistry","2020","22","7","2184","2190","10.1039/D0GC00346H","","","0.71073","MoKα","","0.0534","0.0415","","","0.1006","0.1076","","","","","","1.048","","","","has coordinates,has disorder","257615","2020-10-21","18:00:00",""
"7240067","11.314","0.007","11.98","0.008","17.961","0.01","72.586","0.009","79.494","0.013","72.755","0.019","2207","2","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","5,7-di-tert-butyl-4',6'-dihydroxy-3-(morpholino-4-ium)-3H-spiro[benzo[d][1,2]oxaborole-2,2'-[1,3,5,2,4,6]trioxatriborinan]-2-uide","","- C19 H32 B3 N O7 -","- C19 H32 B3 N O7 -","- C76 H128 B12 N4 O28 -","4","2","","Ming, Wenbo; Liu, Xiaocui; Friedrich, Alexandra; Krebs, Johannes; Budiman, Yudha P.; Huang, Mingming; Marder, Todd B.","Concise synthesis of α-amino cyclic boronates via multicomponent coupling of salicylaldehydes, amines, and B2(OH)4","Green Chemistry","2020","22","7","2184","2190","10.1039/D0GC00346H","","x-ray","0.71073","MoKα","","0.1549","0.0718","","","0.1277","0.1569","","","","","","1.016","","","","has coordinates","257615","2020-10-21","18:00:00",""
"7240089","12.8944","0.0011","12.8937","0.0011","12.963","0.0012","82.985","0.002","66.987","0.001","88.659","0.002","1968.1","0.3","298","2","298","2","","","","","","","","7","P -1","-P 1","2","","","","- C36 H28 Cl2 F12 N6 P2 Ru -","- C36 H28 Cl2 F12 N6 P2 Ru -","- C72 H56 Cl4 F24 N12 P4 Ru2 -","2","1","","Dong, Wenjin; Tang, Jie; Zhao, Lijun; Chen, Fushan; Deng, Li; Xian, Mo","The visible-light-driven transfer hydrogenation of nicotinamide cofactors with a robust ruthenium complex photocatalyst","Green Chemistry","2020","22","7","2279","2287","10.1039/D0GC00331J","","","0.71073","MoKα","","0.1263","0.098","","","0.2296","0.2467","","","","","","1.095","","","","has coordinates","257614","2020-10-21","18:00:00",""
"7240090","11.159","0.0011","12.3059","0.0012","14.8631","0.0013","67.875","0.001","68.045","0.001","86.116","0.003","1747.3","0.3","298","2","298","2","","","","","","","","7","P -1","-P 1","2","","","","- C37 H31 F6 N5 O2 P Ru -","- C37 H31 F6 N5 O2 P Ru -","- C74 H62 F12 N10 O4 P2 Ru2 -","2","1","","Dong, Wenjin; Tang, Jie; Zhao, Lijun; Chen, Fushan; Deng, Li; Xian, Mo","The visible-light-driven transfer hydrogenation of nicotinamide cofactors with a robust ruthenium complex photocatalyst","Green Chemistry","2020","22","7","2279","2287","10.1039/D0GC00331J","","","0.71073","MoKα","","0.1327","0.0942","","","0.2165","0.237","","","","","","1.136","","","","has coordinates,has disorder","257614","2020-10-21","18:00:00",""
"7240091","13.592","0.0011","13.6081","0.0011","14.0589","0.0012","64.306","0.002","73.922","0.004","64.168","0.003","2096.6","0.3","298","2","298","2","","","","","","","","7","P -1","-P 1","2","","","","- C43 H34 Cl3 F6 N5 P Ru -","- C43 H34 Cl3 F6 N5 P Ru -","- C86 H68 Cl6 F12 N10 P2 Ru2 -","2","1","","Dong, Wenjin; Tang, Jie; Zhao, Lijun; Chen, Fushan; Deng, Li; Xian, Mo","The visible-light-driven transfer hydrogenation of nicotinamide cofactors with a robust ruthenium complex photocatalyst","Green Chemistry","2020","22","7","2279","2287","10.1039/D0GC00331J","","","0.71073","MoKα","","0.1117","0.0635","","","0.1569","0.185","","","","","","1.046","","","","has coordinates,has disorder","257614","2020-10-21","18:00:00",""
"7240126","24.951","0.003","24.951","0.003","34.647","0.005","90","","90","","90","","21570","5","100","2","100","2","","","","","","","","4","P 43 21 2","P 4nw 2abw","96","","","","- C84 H90 N12 O6 -","- C84 H90 N12 O6 -","- C672 H720 N96 O48 -","8","1","","Zhang, Lei; Liang, Rongran; Hang, Cheng; Wang, Haiying; Sun, Lin; Xu, Lei; Liu, Dairong; Zhang, Zhenyi; Zhang, Xingmin; Chang, Feifan; Zhao, Shengyu; Huang, Wei","A facile solution-phase synthetic approach for constructing phenol-based porous organic cages and covalent organic frameworks","Green Chemistry","2020","22","8","2498","2504","10.1039/C9GC04033A","","","0.71073","synchrotronMonochr","","0.1283","0.1126","","","0.2724","0.2831","","","","","","1.076","","","","has coordinates","257580","2020-10-21","18:00:00",""
"7240127","18.197","0.002","18.1795","0.0016","23.1831","0.0019","90","","100.957","0.006","90","","7529.4","1.2","123","2","123","2","","","","","","","","4","I 1 2 1","I 2y","5","","","","- C124 H144 N16 O8 -","- C124 H144 N16 O8 -","- C248 H288 N32 O16 -","2","0.5","","Zhang, Lei; Liang, Rongran; Hang, Cheng; Wang, Haiying; Sun, Lin; Xu, Lei; Liu, Dairong; Zhang, Zhenyi; Zhang, Xingmin; Chang, Feifan; Zhao, Shengyu; Huang, Wei","A facile solution-phase synthetic approach for constructing phenol-based porous organic cages and covalent organic frameworks","Green Chemistry","2020","22","8","2498","2504","10.1039/C9GC04033A","","","0.71073","MoKα","","0.1025","0.0656","","","0.1575","0.1698","","","","","","1.012","","","","has coordinates","257580","2020-10-21","18:00:00",""
"7240128","15.7706","0.0004","15.7706","0.0004","23.9901","0.0014","90","","90","","90","","5966.6","0.4","100","2","100","2","","","","","","","","4","P 43 21 2","P 4nw 2abw","96","","","","- C62 H80 N8 O8 -","- C62 H80 N8 O8 -","- C248 H320 N32 O32 -","4","0.5","","Zhang, Lei; Liang, Rongran; Hang, Cheng; Wang, Haiying; Sun, Lin; Xu, Lei; Liu, Dairong; Zhang, Zhenyi; Zhang, Xingmin; Chang, Feifan; Zhao, Shengyu; Huang, Wei","A facile solution-phase synthetic approach for constructing phenol-based porous organic cages and covalent organic frameworks","Green Chemistry","2020","22","8","2498","2504","10.1039/C9GC04033A","","","0.71073","MoKα","","0.0579","0.0474","","","0.1117","0.1167","","","","","","1.052","","","","has coordinates","257580","2020-10-21","18:00:00",""
"7240160","10.1043","0.0008","12.8257","0.0009","12.9176","0.0009","90","","104.397","0.008","90","","1621.5","0.2","100","","100","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C30 H26 Cl7 N O2 -","- C30 H26 Cl7 N O2 -","- C60 H52 Cl14 N2 O4 -","2","1","","Mandal, Susanta; Chhetri, Karan; Bhuyan, Samuzal; Roy, Biswajit G.","Efficient iron catalyzed ligand-free access to acridines and acridinium ions","Green Chemistry","2020","22","10","3178","3185","10.1039/D0GC00617C","","x-ray","0.71073","MoKα","","0.107","0.0895","","","0.2242","0.2535","","","","","","1.047","","","","has coordinates","257572","2020-10-21","18:00:00",""
"7240161","8.2718","0.0008","10.4182","0.0009","13.163","0.0011","113.112","0.008","93.907","0.007","91.575","0.008","1039.06","0.17","","","","","","","","","","","","5","P -1","-P 1","2","","","","- C27 H22 F N O2 -","- C27 H22 F N O2 -","- C54 H44 F2 N2 O4 -","2","1","","Mandal, Susanta; Chhetri, Karan; Bhuyan, Samuzal; Roy, Biswajit G.","Efficient iron catalyzed ligand-free access to acridines and acridinium ions","Green Chemistry","2020","22","10","3178","3185","10.1039/D0GC00617C","","","1.54184","CuKα","","0.1112","0.0926","","","0.2442","0.2934","","","","","","1.0727","","","","has coordinates","257572","2020-10-21","18:00:00",""
"7240203","15.6052","0.0005","15.8374","0.0006","18.1718","0.0005","90","","90","","90","","4491.1","0.3","293","2","293","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","ZIF-62","Zn(Im)1.72(bIm)0.28","","- C16.69 H18.62 N8 O0.83 Zn2 -","- C16.774 H19.807 N8 O0.827 Zn2 -","- C134.192 H158.456 N64 O6.616 Zn16 -","8","1","","Thorne, Michael F.; Gómez, María Laura Ríos; Bumstead, Alice M.; Li, Shichun; Bennett, Thomas D.","Mechanochemical synthesis of mixed metal, mixed linker, glass-forming metal–organic frameworks","Green Chemistry","2020","22","8","2505","2512","10.1039/D0GC00546K","","x-ray","1.54184","CuKα","","0.0503","0.045","","","0.1313","0.1374","","","","","","1.054","","","","has coordinates,has disorder","288248","2023-12-12","12:55:28",""
"7240256","9.563","0.0006","12.5988","0.0007","25.0296","0.0014","81.062","0.003","88.375","0.003","88.956","0.003","2977.5","0.3","200","2","200","2","","","","","","","","5","P 1","P 1","1","","","","- C33 H48 Cl N O -","- C33 H48 Cl N O -","- C132 H192 Cl4 N4 O4 -","4","4","","Xu, Biping; Shang, Yaping; Jie, Xiaoming; Zhang, Xiaofeng; Kan, Jian; Yedage, Subhash Laxman; Su, Weiping","Synthesis of α-enaminones from cyclic ketones and anilines using oxoammonium salt as an oxygen transfer reagent","Green Chemistry","2020","22","6","1827","1831","10.1039/C9GC03845K","","","0.71073","MoKα","","0.0679","0.0503","","","0.1271","0.1453","","","","","","1.076","","","","has coordinates","257599","2020-10-21","18:00:00",""
"7240266","13.2745","0.0008","7.8001","0.0002","24.2247","0.0014","90","","129.278","0.01","90","","1941.6","0.3","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H23 N O4 -","- C22 H23 N O4 -","- C88 H92 N4 O16 -","4","1","","Gu, Guangmiao; Huang, Mengmeng; Kim, Jung Keun; Zhang, Jianye; Li, Yabo; Wu, Yangjie","Visible-light-induced photocatalyst-free C-3 functionalization of indoles with diethyl bromomalonate","Green Chemistry","2020","22","8","2543","2548","10.1039/D0GC00292E","","x-ray","1.54184","CuKα","","0.063","0.049","","","0.125","0.1387","","","","","","1.04","","","","has coordinates","257579","2020-10-21","18:00:00",""
"7240283","9.7382","0.0014","10.0324","0.0013","11.2964","0.0015","73.551","0.007","87.711","0.007","74.719","0.007","1020.3","0.2","120","2","120","2","","","","","","","","5","P -1","-P 1","2","","","","- C20 H18 I N6 O2 -","- C20 H18 I N6 O2 -","- C40 H36 I2 N12 O4 -","2","1","","Liu, Lang; She, Mengyao; Zhang, Jun; Wang, Zhaohui; Liu, Hua; Tang, Mi; Liu, Ping; Zhang, Shengyong; Li, Jianli","A practical strategy for construction and regulation of multi-functional triazepinium salts via highly efficient I2-catalyzed cyclization","Green Chemistry","2020","22","10","3111","3116","10.1039/C9GC04328D","","","0.71073","MoKα","","0.0532","0.0466","","","0.1191","0.124","","","","","","1.065","","","","has coordinates","257571","2020-10-21","18:00:00",""
"7240284","7.6849","0.0004","11.331","0.0005","14.1776","0.0007","94.684","0.002","94.245","0.002","106.982","0.002","1170.56","0.1","297.99","","297.99","","","","","","","","","7","P -1","-P 1","2","","","","- C22 H20 Cl I N6 O S -","- C22 H20 Cl I N6 O S -","- C44 H40 Cl2 I2 N12 O2 S2 -","2","1","","Liu, Lang; She, Mengyao; Zhang, Jun; Wang, Zhaohui; Liu, Hua; Tang, Mi; Liu, Ping; Zhang, Shengyong; Li, Jianli","A practical strategy for construction and regulation of multi-functional triazepinium salts via highly efficient I2-catalyzed cyclization","Green Chemistry","2020","22","10","3111","3116","10.1039/C9GC04328D","","","0.71073","MoKα","","0.022","0.0193","","","0.0469","0.0481","","","","","","1.095","","","","has coordinates","257571","2020-10-21","18:00:00",""
"7240285","21.618","0.003","7.8792","0.001","23.619","0.003","90","","90","","90","","4023.1","0.9","296","2","296.15","","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C22 H16 I N7 -","- C22 H16 I N7 -","- C176 H128 I8 N56 -","8","1","","Liu, Lang; She, Mengyao; Zhang, Jun; Wang, Zhaohui; Liu, Hua; Tang, Mi; Liu, Ping; Zhang, Shengyong; Li, Jianli","A practical strategy for construction and regulation of multi-functional triazepinium salts via highly efficient I2-catalyzed cyclization","Green Chemistry","2020","22","10","3111","3116","10.1039/C9GC04328D","","","0.71073","MoKα","","0.1005","0.0487","","","0.1005","0.1206","","","","","","1.021","","","","has coordinates","257571","2020-10-21","18:00:00",""
"7240286","8.0435","0.0006","11.5711","0.001","27.338","0.002","90","","95.054","0.005","90","","2534.5","0.3","293","","293","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C20 H15 I N6 O -","- C20 H15 I N6 O -","- C80 H60 I4 N24 O4 -","4","1","","Liu, Lang; She, Mengyao; Zhang, Jun; Wang, Zhaohui; Liu, Hua; Tang, Mi; Liu, Ping; Zhang, Shengyong; Li, Jianli","A practical strategy for construction and regulation of multi-functional triazepinium salts via highly efficient I2-catalyzed cyclization","Green Chemistry","2020","22","10","3111","3116","10.1039/C9GC04328D","","","0.71073","MoKα","","0.1421","0.0722","","","0.1699","0.1942","","","","","","1.041","","","","has coordinates","257571","2020-10-21","18:00:00",""
"7240295","4.1648","0.0003","10.9613","0.0006","12.044","0.0007","105.854","0.005","90.015","0.006","94.64","0.006","527.04","0.06","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C12 H11 N O3 -","- C12 H11 N O3 -","- C24 H22 N2 O6 -","2","1","","Guo, Weiwei; Zhang, Qi; Cao, Yang; Cai, Kaihua; Zhang, Shengyong; Chai, Yonghai","Environmentally benign access to isoindolinones: synthesis, separation and resource recycling","Green Chemistry","2020","22","9","2873","2878","10.1039/D0GC00957A","","","1.54184","CuKα","","0.0548","0.042","","","0.1076","0.1181","","","","","","1.03","","","","has coordinates","257616","2020-10-21","18:00:00",""
"7240308","8.802","0.0009","9.0045","0.0008","10.8415","0.0011","83.765","0.004","86.631","0.004","72.048","0.004","812.31","0.14","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C15 H16 Cl N3 O4 -","- C15 H16 Cl N3 O4 -","- C30 H32 Cl2 N6 O8 -","2","1","","Annes, Sesuraj Babiola; Saritha, Rajendhiran; Subramanian, Saravanan; Shankar, Bhaskaran; Ramesh, Subburethinam","Solvent-free and montmorillonite K10-catalyzed domino reactions for the synthesis of pyrazoles with alkynylester as a dual synthon","Green Chemistry","2020","22","8","2388","2393","10.1039/D0GC00162G","","","0.71073","MoKα","","0.048","0.0395","","","0.0999","0.1057","","","","","","1.036","","","","has coordinates","257577","2020-10-21","18:00:00",""
"7240309","5.6602","0.0005","19.0351","0.0018","10.7528","0.001","90","","102.926","0.001","90","","1129.18","0.18","153","2","153","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C12 H12 N2 O2 -","- C12 H12 N2 O2 -","- C48 H48 N8 O8 -","4","1","","Annes, Sesuraj Babiola; Saritha, Rajendhiran; Subramanian, Saravanan; Shankar, Bhaskaran; Ramesh, Subburethinam","Solvent-free and montmorillonite K10-catalyzed domino reactions for the synthesis of pyrazoles with alkynylester as a dual synthon","Green Chemistry","2020","22","8","2388","2393","10.1039/D0GC00162G","","","0.71073","MoKα","","0.0434","0.0398","","","0.11","0.1143","","","","","","1.07","","","","has coordinates","257577","2020-10-21","18:00:00",""
"7240310","6.7032","0.0006","8.5139","0.0009","22.447","0.002","90","","90","","90","","1281.1","0.2","298","2","298","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C13 H14 N2 O S -","- C13 H14 N2 O S -","- C52 H56 N8 O4 S4 -","4","1","","Gan, Ziyu; Li, Guoqing; Yan, Qiuli; Deng, Weiseng; Jiang, Yuan-Ye; Yang, Daoshan","Visible-light-promoted oxidative desulphurisation: a strategy for the preparation of unsymmetrical ureas from isothiocyanates and amines using molecular oxygen","Green Chemistry","2020","22","9","2956","2962","10.1039/D0GC00070A","","","0.71073","MoKα","","0.1043","0.0537","","","0.0972","0.1177","","","","","","1.125","","","","has coordinates,has disorder","257617","2020-10-21","18:00:00",""
"7240311","8.1026","0.0007","15.7929","0.0013","8.4783","0.0008","90","","104.183","0.003","90","","1051.84","0.16","298","2","298","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C11 H14 N2 O2 -","- C11 H14 N2 O2 -","- C44 H56 N8 O8 -","4","1","","Gan, Ziyu; Li, Guoqing; Yan, Qiuli; Deng, Weiseng; Jiang, Yuan-Ye; Yang, Daoshan","Visible-light-promoted oxidative desulphurisation: a strategy for the preparation of unsymmetrical ureas from isothiocyanates and amines using molecular oxygen","Green Chemistry","2020","22","9","2956","2962","10.1039/D0GC00070A","","","0.71073","MoKα","","0.0504","0.0371","","","0.0929","0.1027","","","","","","1.039","","","","has coordinates","257617","2020-10-21","18:00:00",""
"7240411","6.0178","0.0013","10.934","0.002","22.509","0.005","90","","95.035","0.004","90","","1475.3","0.5","100","2","100","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C20 H14 N2 -","- C20 H14 N2 -","- C80 H56 N8 -","4","1","","Charpe, Vaibhav Pramod; Sagadevan, Arunachalam; Hwang, Kuo Chu","Visible light-induced aerobic oxidation of diarylalkynes to α-diketones catalyzed by copper-superoxo at room temperature","Green Chemistry","2020","22","14","4426","4432","10.1039/D0GC00975J","","","0.71073","MoKα","","0.0571","0.0452","","","0.1197","0.1278","","","","","","1.055","","","","has coordinates","257606","2020-10-21","18:00:00",""
"7240412","8.3601","0.0007","8.3601","0.0007","13.3968","0.0012","90","","90","","120","","810.88","0.12","100","2","100","2","","","","","","","","3","P 32 2 1","P 32 2""","154","","","","- C14 H10 O2 -","- C14 H10 O2 -","- C42 H30 O6 -","3","0.5","","Charpe, Vaibhav Pramod; Sagadevan, Arunachalam; Hwang, Kuo Chu","Visible light-induced aerobic oxidation of diarylalkynes to α-diketones catalyzed by copper-superoxo at room temperature","Green Chemistry","2020","22","14","4426","4432","10.1039/D0GC00975J","","","0.71073","MoKα","","0.0313","0.0295","","","0.0685","0.0695","","","","","","1.105","","","","has coordinates","257606","2020-10-21","18:00:00",""
"7240413","19.711","0.002","7.4314","0.0009","20.568","0.002","90","","90","","90","","3012.8","0.6","100","2","100","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C21 H15 N O -","- C21 H15 N O -","- C168 H120 N8 O8 -","8","1","","Charpe, Vaibhav Pramod; Sagadevan, Arunachalam; Hwang, Kuo Chu","Visible light-induced aerobic oxidation of diarylalkynes to α-diketones catalyzed by copper-superoxo at room temperature","Green Chemistry","2020","22","14","4426","4432","10.1039/D0GC00975J","","","0.71073","MoKα","","0.1048","0.0611","","","0.1553","0.2427","","","","","","1.156","","","","has coordinates","257606","2020-10-21","18:00:00",""
"7240414","23.502","0.002","3.9358","0.0003","15.1235","0.0012","90","","105.082","0.002","90","","1350.72","0.19","100","2","100","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C17 H14 O4 -","- C17.024 H14 O4 -","- C68.096 H56 O16 -","4","0.5","","Charpe, Vaibhav Pramod; Sagadevan, Arunachalam; Hwang, Kuo Chu","Visible light-induced aerobic oxidation of diarylalkynes to α-diketones catalyzed by copper-superoxo at room temperature","Green Chemistry","2020","22","14","4426","4432","10.1039/D0GC00975J","","","0.71073","MoKα","","0.0537","0.0379","","","0.0865","0.0944","","","","","","1.044","","","","has coordinates,has disorder","257606","2020-10-21","18:00:00",""
"7240415","9.3322","0.0005","10.0321","0.0005","11.8425","0.0006","95.845","0.002","105.956","0.002","109.513","0.002","981.56","0.09","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C23 H22 N2 O2 S -","- C23 H22 N2 O2 S -","- C46 H44 N4 O4 S2 -","2","1","","Charpe, Vaibhav Pramod; Sagadevan, Arunachalam; Hwang, Kuo Chu","Visible light-induced aerobic oxidation of diarylalkynes to α-diketones catalyzed by copper-superoxo at room temperature","Green Chemistry","2020","22","14","4426","4432","10.1039/D0GC00975J","","","0.71073","MoKα","","0.0566","0.0397","","","0.1006","0.1081","","","","","","1.139","","","","has coordinates","257606","2020-10-21","18:00:00",""
"7240416","8.2958","0.0008","7.8128","0.0007","14.5059","0.0016","90","","98.757","0.003","90","","929.22","0.16","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C11 H9 F O2 -","- C11 H9 F O2 -","- C44 H36 F4 O8 -","4","1","","Zhang, Zhipeng; Yu, Yang; Xie, Yuxing; Hughes, Timothy; Xu, Jun; Huang, Fei; Huang, He","Catalytic C‒C coupling of diazo compounds with arylboronic acids: using surface modified sewage sludge as catalyst","Green Chemistry","2020","22","13","4165","4173","10.1039/D0GC00317D","","","0.71073","MoKα","","0.0586","0.0487","","","0.1343","0.1458","","","","","","1.031","","","","has coordinates","257603","2020-10-21","18:00:00",""
"7240443","38.544","0.004","5.1102","0.0009","11.6487","0.0018","90","","90","","90","","2294.4","0.6","293","2","293","2","","","","","","","","5","P n a 21","P 2c -2n","33","","","","- C11 H11 N O4 S -","- C11 H11 N O4 S -","- C88 H88 N8 O32 S8 -","8","2","","Hadian, Mojgan; Shaabani, Shabnam; Patil, Pravin; Shishkina, Svitlana V.; Böltz, Harry; Dömling, Alexander","Sustainability by design: automated nanoscale 2,3,4-trisubstituted quinazoline diversity","Green Chemistry","2020","22","8","2459","2467","10.1039/D0GC00363H","","","0.71073","MoKα","","0.1406","0.0712","","","0.1668","0.2128","","","","","","0.934","","","","has coordinates","257582","2020-10-21","18:00:00",""
"7240444","20.486","0.002","3.9298","0.0004","13.6374","0.0012","90","","90","","90","","1097.89","0.18","293","2","293","2","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C11 H11 N O5 -","- C11 H11 N O5 -","- C44 H44 N4 O20 -","4","1","","Hadian, Mojgan; Shaabani, Shabnam; Patil, Pravin; Shishkina, Svitlana V.; Böltz, Harry; Dömling, Alexander","Sustainability by design: automated nanoscale 2,3,4-trisubstituted quinazoline diversity","Green Chemistry","2020","22","8","2459","2467","10.1039/D0GC00363H","","","0.71073","MoKα","","0.0852","0.0542","","","0.1367","0.1603","","","","","","1.004","","","","has coordinates","257582","2020-10-21","18:00:00",""
"7240445","11.864","0.003","11.162","0.003","13.889","0.005","90","","99.31","0.03","90","","1815","0.9","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H23 N3 O3 -","- C19 H23 N3 O3 -","- C76 H92 N12 O12 -","4","1","","Hadian, Mojgan; Shaabani, Shabnam; Patil, Pravin; Shishkina, Svitlana V.; Böltz, Harry; Dömling, Alexander","Sustainability by design: automated nanoscale 2,3,4-trisubstituted quinazoline diversity","Green Chemistry","2020","22","8","2459","2467","10.1039/D0GC00363H","","","0.71073","MoKα","","0.2181","0.0746","","","0.1287","0.1705","","","","","","0.884","","","","has coordinates","257582","2020-10-21","18:00:00",""
"7240446","20.522","0.005","3.8101","0.0012","26.193","0.008","90","","102.39","0.03","90","","2000.4","1","293","2","293","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C11 H9 N O4 -","- C11 H9 N O4 -","- C88 H72 N8 O32 -","8","1","","Hadian, Mojgan; Shaabani, Shabnam; Patil, Pravin; Shishkina, Svitlana V.; Böltz, Harry; Dömling, Alexander","Sustainability by design: automated nanoscale 2,3,4-trisubstituted quinazoline diversity","Green Chemistry","2020","22","8","2459","2467","10.1039/D0GC00363H","","","0.71073","MoKα","","0.2002","0.0758","","","0.1904","0.247","","","","","","0.858","","","","has coordinates","257582","2020-10-21","18:00:00",""
"7240449","9.3207","0.0008","10.8786","0.0012","14.8658","0.001","95.037","0.007","96.282","0.006","100.049","0.008","1466.5","0.2","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C35 H35 N O5 -","- C35 H35 N O5 -","- C70 H70 N2 O10 -","2","1","","Ma, Xiao-Pan; Nong, Cai-Mei; Liang, Yu-Feng; Xu, Pei-Pei; Guo, Xiu-Yun; Liang, Cui; Pan, Cheng-Xue; Su, Gui-Fa; Mo, Dong-Liang","An Yb(OTf)3 and visible light relay catalyzed [3 + 2] cycloaddition/[3,3]-rearrangement/[4 + 2] cycloaddition in one pot to prepare oxazonine-fused endoperoxides","Green Chemistry","2020","22","12","3827","3834","10.1039/D0GC00929F","","","0.71073","MoKα","","0.1101","0.0581","","","0.1216","0.1575","","","","","","1.057","","","","has coordinates","257622","2020-10-21","18:00:00",""
"7240489","9.0093","0.0002","9.0093","0.0002","11.2503","0.0004","90","","90","","120","","790.82","0.04","293","","293","","","","","","","","","4","P 62 2 2","P 62 2 (0 0 4)","180","catena-(ammonium bis(m2-oxalato)-scandium dihydrate)","","","- C4 N O10 Sc -","- C4 N O10 Sc -","- C12 N3 O30 Sc3 -","3","0.25","","Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav","Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium","Green Chemistry","2020","22","13","4364","4375","10.1039/D0GC00454E","powder diffraction","","1.5418","CuKα~1~","","","","","","","","","0.029","9.801","","","","","","","has coordinates","257604","2020-10-21","18:00:00",""
"7240490","17.851","0.002","11.0413","0.0007","18.2806","0.0013","90","","104.189","0.002","90","","3493.2","0.5","253","2","253","","","","","","","","synthetic","5","I 1 2/a 1","-I 2ya","15","","Sodium scandium oxalate hexahydrate","","- C6 H10 Na3 O18 Sc -","- C6 H10 Na3 O18 Sc -","- C48 H80 Na24 O144 Sc8 -","8","1","","Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav","Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium","Green Chemistry","2020","22","13","4364","4375","10.1039/D0GC00454E","","x-ray","0.71073","MoKα","","0.0596","0.0373","","","0.0829","0.0915","","","","","","1.033","","","","has coordinates,has disorder","257604","2020-10-21","18:00:00",""
"7240491","15.8839","0.0014","11.4558","0.001","22.7314","0.0019","90","","92.19","0.004","90","","4133.2","0.6","273","2","273","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C7 H12 K3.5 O20 Sc -","- C7 H12 K3.5 O20 Sc -","- C56 H96 K28 O160 Sc8 -","8","1","","Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav","Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium","Green Chemistry","2020","22","13","4364","4375","10.1039/D0GC00454E","","x-ray","1.54178","CuKα","","0.0606","0.0481","","","0.1263","0.1425","","","","","","1.052","","","","has coordinates,has disorder","257604","2020-10-21","18:00:00",""
"7240492","9.0427","0.0002","6.09117","0.00012","7.8999","0.0002","90","","90.182","0.003","90","","435.129","0.017","293","","293","","","","","","","","","4","P 1 2/n 1","-P 2yac","13","catena-(ammonium bis(m2-oxalato)-ytterbium hydrate)","","","- C4 N O9 Yb -","- C4 N O9 Yb -","- C8 N2 O18 Yb2 -","2","0.5","","Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav","Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium","Green Chemistry","2020","22","13","4364","4375","10.1039/D0GC00454E","powder diffraction","","1.5418","CuKα~1~","","","","","","","","","0.015","3.396","","","","","","","has coordinates","257604","2020-10-21","18:00:00",""
"7240493","8.4883","0.0002","9.3894","0.0003","9.7552","0.0002","98.255","0.002","91.154","0.002","96.544","0.003","763.89","0.03","293","","293","","","","","","","","","4","P -1","-P 1","2","catena-(potassium bis(m2-oxalato)-europium hydrate)","","","- C6 Eu K3 O15 -","- C6 Eu K3 O15 -","- C12 Eu2 K6 O30 -","2","1","","Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav","Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium","Green Chemistry","2020","22","13","4364","4375","10.1039/D0GC00454E","powder diffraction","","1.5418","CuKα~1~","","","","","","","","","0.023","2.282","","","","","","","has coordinates","257604","2020-10-21","18:00:00",""
"7240494","8.4795","0.0008","9.3708","0.0009","9.7323","0.0009","98.377","0.004","91.097","0.004","96.629","0.004","759.45","0.12","100","2","100","","","","","","","","synthetic","5","P -1","-P 1","2","","Tripotassium gadolinium oxalate trihydrate","","- C6 H6 Gd K3 O15 -","- C6 H6 Gd K3 O15 -","- C12 H12 Gd2 K6 O30 -","2","1","","Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav","Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium","Green Chemistry","2020","22","13","4364","4375","10.1039/D0GC00454E","","","0.71073","MoKα","","0.021","0.0174","","","0.0369","0.0379","","","","","","1.046","","","","has coordinates","257604","2020-10-21","18:00:00",""
"7240495","9.5867","0.0002","6.64358","0.00016","6.25859","0.00016","98.1966","0.0017","99.4509","0.0019","75.113","0.002","377.889","0.016","293","","293","","","","","","","","","3","P -1","-P 1","2","catena-(tetra-aqua-tris(m2-oxalato-O,O',O'',O''')-di-lutecium(iii)) dihydrate","","","- C3 Lu O9 -","- C3 Lu O9 -","- C6 Lu2 O18 -","2","1","","Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav","Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium","Green Chemistry","2020","22","13","4364","4375","10.1039/D0GC00454E","powder diffraction","","1.5418","CuKα~1~","","","","","","","","","0.027","5.391","","","","","","","has coordinates","257604","2020-10-21","18:00:00",""
"7240496","11.4151","0.0008","12.6781","0.0009","11.4093","0.0008","90","","111.9","0.002","90","","1532.02","0.19","100","2","100","","","","","","","","synthetic","5","C 1 2/c 1","-C 2yc","15","","Potassium scandium oxalate","","- C6 H8 K3 O16 Sc -","- C6 H8 K3 O16 Sc -","- C24 H32 K12 O64 Sc4 -","4","0.5","","Huskić, Igor; Arhangelskis, Mihails; Friščić, Tomislav","Solvent-free ageing reactions of rare earth element oxides: from geomimetic synthesis of new metal‒organic materials towards a simple, environmentally friendly separation of scandium","Green Chemistry","2020","22","13","4364","4375","10.1039/D0GC00454E","","x-ray","0.71073","MoKα","","0.0184","0.018","","","0.0474","0.0478","","","","","","1.102","","","","has coordinates","257604","2020-10-21","18:00:00",""
"7240578","12.2892","0.0004","20.1324","0.0004","18.9867","0.0005","90","","102.411","0.003","90","","4587.7","0.2","123","2","123","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C96 H80 O28 P4 V10 -","- C96 H80 O28 P4 V10 -","- C192 H160 O56 P8 V20 -","2","0.5","","Li, Chifeng; Mizuno, Noritaka; Murata, Kei; Ishii, Kazuyuki; Suenobu, Tomoyoshi; Yamaguchi, Kazuya; Suzuki, Kosuke","Selectivity switch in the aerobic oxygenation of sulfides photocatalysed by visible-light-responsive decavanadate","Green Chemistry","2020","22","12","3896","3905","10.1039/D0GC01500H","","","0.71073","MoKα","","0.0796","0.0521","","","0.1163","0.1285","","","","","","1.017","","","","has coordinates","257624","2020-10-21","18:00:00",""
"7240659","7.8705","0.0005","10.1489","0.0007","23.9418","0.0013","90","","93.881","0.002","90","","1908","0.2","120","2","120","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","trans-Spirodiol (CHCl3)","3-trans","","- C20 H34 O6 -","- C20 H34 O6 -","- C80 H136 O24 -","4","1","","Bonjour, Olivier; Liblikas, Ilme; Pehk, Tõnis; Khai-Nghi, Truong; Rissanen, Kari; Vares, Lauri; Jannasch, Patric","Rigid biobased polycarbonates with good processability based on a spirocyclic diol derived from citric acid","Green Chemistry","2020","22","12","3940","3951","10.1039/D0GC00849D","","","0.71073","MoKα","","0.1292","0.0997","","","0.2398","0.2549","","","","","","1.096","","","","has coordinates,has disorder","257623","2020-10-21","18:00:00",""
"7240671","9.15686","0.00013","13.9511","0.0002","14.2096","0.0002","90","","101.125","0.0014","90","","1781.14","0.04","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C22 H19 N O3 S -","- C22 H19 N O3 S -","- C88 H76 N4 O12 S4 -","4","1","","Wang, Ze-Shu; Chen, Yang-Bo; Wang, Kun; Xu, Zhou; Ye, Long-Wu","One-pot synthesis of 2-hydroxymethylindoles via photoredox-catalyzed ketyl‒ynamide coupling/1,3-allylic alcohol transposition","Green Chemistry","2020","22","14","4483","4488","10.1039/D0GC01522A","","","1.54184","CuKα","","0.0377","0.0335","","","0.0822","0.0886","","","","","","1.12","","","","has coordinates","257607","2020-10-21","18:00:00",""
"7240672","25.4166","0.0016","16.5833","0.001","14.6422","0.0008","90","","105.981","0.002","90","","5933","0.6","150","2","150","2","","","","","","","","7","C 1 c 1","C -2yc","9","","","","- C69 H56 Cu F6 N2 O3 P3 -","- C69 H56 Cu F6 N2 O3 P3 -","- C276 H224 Cu4 F24 N8 O12 P12 -","4","1","","Forero-Cortés, Paola A.; Marx, Maximilian; Moustakas, Nikolaos G.; Brunner, Fabian; Housecroft, Catherine E.; Constable, Edwin C.; Junge, Henrik; Beller, Matthias; Strunk, Jennifer","Transferring photocatalytic CO2 reduction mediated by Cu(N^N)(P^P)+ complexes from organic solvents into ionic liquid media","Green Chemistry","2020","22","14","4541","4549","10.1039/D0GC01627F","","","0.71073","MoKα","","0.0368","0.0343","","","0.0851","0.0867","","","","","","1.038","","","","has coordinates","257608","2020-10-21","18:00:00",""
"7240682","10.3143","0.0011","13.9869","0.0012","20.0442","0.0009","90","","99.155","0.018","90","","2854.8","0.4","296","2","296.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C33 H33 Cl N2 O4 -","- C33 H33 Cl N2 O4 -","- C132 H132 Cl4 N8 O16 -","4","1","","Lei, Jie; Li, Yong; Xu, Jia; Tang, Dian-Yong; Shao, Jing-Wei; Li, Hong-yu; Chen, Zhong-Zhu; Xu, Zhi-Gang","An acid-catalyzed 1,4-addition isocyanide-based multicomponent reaction in neat water","Green Chemistry","2020","22","12","3716","3720","10.1039/D0GC00652A","","","0.71073","MoKα","","0.1463","0.0607","","","0.1123","0.1398","","","","","","1.1102","","","","has coordinates","257625","2020-10-21","18:00:00",""
"7240708","9.783","0.0009","12.3051","0.0011","12.3219","0.0012","62.429","0.001","66.999","0.002","79.648","0.003","1210.3","0.2","298","2","298","2","","","","","","","","5","P -1","-P 1","2","","","","- C27 H26 I O3.5 S -","- C27 H26 I O3.5 S -","- C54 H52 I2 O7 S2 -","2","1","","Zhang, Tian-Shu; Hao, Wen-Juan; Wang, Rong; Wang, Shi-Chao; Tu, Shu-Jiang; Jiang, Bo","Electrocatalytic three-component annulation-halosulfonylation of 1,6-enynes toward 1-indanones using sodium halides as both halogen sources and electrolytes","Green Chemistry","2020","22","13","4259","4269","10.1039/D0GC00771D","","","0.71073","MoKα","","0.1054","0.09","","","0.2178","0.2273","","","","","","1.058","","","","has coordinates","257605","2020-10-21","18:00:00",""
"7240736","13.6722","0.0004","21.2561","0.0006","8.9159","0.0002","90","","95.877","0.001","90","","2577.5","0.12","223","2","223","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","3-(2-hydroxy-5-methylbenzoyl)-5-methylbenzaldehyde","","- C16 H14 O3 -","- C16 H14 O3 -","- C128 H112 O24 -","8","2","","Akhtar, Muhammad Saeed; Thombal, Raju S.; Inductivo Tamargo, Ramuel John; Yang, Won-Guen; Kim, Sung Hong; Lee, Yong Rok","Eco-friendly organocatalyst- and reagent-controlled selective construction of diverse and multifunctionalized 2-hydroxybenzophenone frameworks for potent UV-A/B filters by cascade benzannulation","Green Chemistry","2020","22","14","4523","4531","10.1039/D0GC01011A","","","0.71073","MoKα","","0.058","0.0499","","","0.1428","0.1507","","","","","","1.067","","","","has coordinates","257611","2020-10-21","18:00:00",""
"7240737","7.3618","0.0003","7.4104","0.0002","25.4612","0.0009","90","","95.2808","0.0014","90","","1383.11","0.08","223","2","223","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","3-(2-hydroxy-5-methylbenzoyl)-1-naphthaldehyde","","- C19 H14 O3 -","- C19 H14 O3 -","- C76 H56 O12 -","4","1","","Akhtar, Muhammad Saeed; Thombal, Raju S.; Inductivo Tamargo, Ramuel John; Yang, Won-Guen; Kim, Sung Hong; Lee, Yong Rok","Eco-friendly organocatalyst- and reagent-controlled selective construction of diverse and multifunctionalized 2-hydroxybenzophenone frameworks for potent UV-A/B filters by cascade benzannulation","Green Chemistry","2020","22","14","4523","4531","10.1039/D0GC01011A","","","0.71073","MoKα","","0.0504","0.0429","","","0.1088","0.1157","","","","","","1.069","","","","has coordinates","257611","2020-10-21","18:00:00",""
"7240755","11.8025","0.0004","6.6554","0.0002","19.9584","0.0008","90","","90.687","0.002","90","","1567.63","0.09","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C18 H20 N2 O2 -","- C18 H20 N2 O2 -","- C72 H80 N8 O8 -","4","1","","Liu, Yi; Meng, Ya-Nan; Huang, Xun-Jie; Qin, Fu-Hua; Wu, Dapeng; Shao, Qianjun; Guo, Zhiyong; Li, Qiang; Wei, Wen-Ting","Radical cyclization of 1,6-dienes with azobis(alkylcarbonitriles) on water under additive-free conditions","Green Chemistry","2020","22","14","4593","4596","10.1039/D0GC00140F","","","1.54178","CuKα","","0.0698","0.0482","","","0.1227","0.1363","","","","","","1.024","","","","has coordinates","257609","2020-10-21","18:00:00",""
"7240759","16.882","0.002","16.882","0.002","16.323","0.002","90","","90","","90","","4652.1","1","100","","100","","","","","","","","see text","3","I 41/a :2","-I 4ad","88","","","","- C40 H84 Si5 -","- C40 H84 Si5 -","- C160 H336 Si20 -","4","0.25","","Herz, Fabian A. D.; Nobis, Matthias; Wendel, Daniel; Pahl, Philipp; Altmann, Philipp J.; Tillmann, Jan; Weidner, Richard; Inoue, Shigeyoshi; Rieger, Bernhard","Application of multifunctional silylenes and siliranes as universal crosslinkers for metal-free curing of silicones","Green Chemistry","2020","22","14","4489","4497","10.1039/D0GC00272K","","x-ray","0.71073","MoKα","","0.0496","0.0431","","","0.1071","0.1125","","","","","","1.035","","","","has coordinates","257610","2020-10-21","18:00:00",""
"7240768","7.145","0.0006","10.3161","0.0009","12.2769","0.0011","101.41","0.003","103.927","0.003","93.498","0.002","855.32","0.13","298","2","298.15","","","","","","","","","6","P -1","-P 1","2","","","","- C17 H15 F3 N3 O S2 -","- C17 H15 F3 N3 O S2 -","- C34 H30 F6 N6 O2 S4 -","2","1","","Li, Xiao-Yun; Liu, Yan; Chen, Xiao-Lan; Lu, Xin-Yuan; Liang, Xing-Xing; Zhu, Shan-Shan; Wei, Chuan-Wan; Qu, Ling-Bo; Yu, Bing","6π-Electrocyclization in water: microwave-assisted synthesis of polyheterocyclic-fused quinoline-2-thiones","Green Chemistry","2020","22","14","4445","4449","10.1039/C9GC04445K","","","0.71073","MoKα","","0.0629","0.052","","","0.1399","0.1501","","","","","","1.029","","","","has coordinates","257612","2020-10-21","18:00:00",""
"7240806","8.616","0.004","8.888","0.004","17.715","0.008","90","","96.499","0.009","90","","1347.9","1.1","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C6 H3 Co N18 -","- C6 H3 Co N18 -","- C24 H12 Co4 N72 -","4","1","","Wu, Shuo; Li, Min; Yang, Zhengyi; Xia, Zhengqiang; Liu, Bin; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Gao, Shengli; Lu, Jack Y.","Synthesis and characterization of a new energetic metal‒organic framework for use in potential propellant compositions","Green Chemistry","2020","22","15","5050","5058","10.1039/D0GC01594F","","","0.71073","MoKα","","0.1007","0.053","","","0.1249","0.1496","","","","","","0.999","","","","has coordinates","257619","2020-10-21","18:00:00",""
"7240807","11.2054","0.0001","11.2054","0.0001","83.0175","0.0009","90","","90","","90","","10423.8","0.17","200","2","200","2","","","","","","","","5","P 43 21 2","P 4nw 2abw","96","","","","- C22 H35 Cl2 N4 O2.5 -","- C22 H35 Cl2 N4 O2.5 -","- C352 H560 Cl32 N64 O40 -","16","2","","Esteve, Ferran; Altava, Belén; Burguete, M. Isabel; Bolte, Michael; García-Verdugo, Eduardo; Luis, Santiago V.","Pseudopeptidic macrocycles as cooperative minimalistic synzyme systems for the remarkable activation and conversion of CO2 in the presence of the chloride anion","Green Chemistry","2020","22","14","4697","4705","10.1039/D0GC01449D","","","1.54184","CuKα","","0.0748","0.07","","","0.1758","0.1783","","","","","","1.108","","","","has coordinates,has disorder","257613","2020-10-21","18:00:00",""
"7240814","4.352","0.0008","10.59","0.002","14.532","0.003","90","","98.269","0.002","90","","662.8","0.2","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C7 H5 F2 N O -","- C7 H5 F2 N O -","- C28 H20 F8 N4 O4 -","4","1","","Jiang, Xiaolin; Huang, Zijun; Makha, Mohamed; Du, Chen-Xia; Zhao, Dongmei; Wang, Fang; Li, Yuehui","Tetracoordinate borates as catalysts for reductive formylation of amines with carbon dioxide","Green Chemistry","2020","22","16","5317","5324","10.1039/D0GC01741H","","","0.71073","MoKα","","0.0474","0.0407","","","0.1345","0.1444","","","","","","0.999","","","","has coordinates","257602","2020-10-21","18:00:00",""
"7240863","10.4389","0.0002","21.5791","0.0004","14.669","0.0003","90","","109.581","0.002","90","","3113.27","0.11","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C26 H18 F12 N2 O4 Se2 -","- C26 H18 F12 N2 O4 Se2 -","- C104 H72 F48 N8 O16 Se8 -","4","1","","Lei, Yingjie; Yang, Ju; Wang, Yawen; Wang, Hongying; Zhan, Yue; Jiang, Xianxing; Xu, Zhaoqing","Metal-free fluoroalkylfluoroalkylselenolation of unactivated alkenes: incorporation of two photoinduced processes","Green Chemistry","2020","22","15","4878","4883","10.1039/C9GC03936H","","x-ray","1.54184","CuKα","","0.0685","0.0574","","","0.1539","0.1635","","","","","","1.036","","","","has coordinates","257618","2020-10-21","18:00:00",""
"7240906","18.731","0.008","16.579","0.007","21.872","0.01","90","","100.786","0.006","90","","6672","5","296.15","","296.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C71 H76 O15 Ti4 -","- C71 H75.9999 O15 Ti4 -","- C284 H304 O60 Ti16 -","4","1","","Li, Ning; Liu, Jing-Jing; Sun, Jia-Wei; Dong, Bao-Xia; Dong, Long-Zhang; Yao, Su-Juan; Xin, Zhifeng; Li, Shun-Li; Lan, Ya-Qian","Calix[8]arene-constructed stable polyoxo-titanium clusters for efficient CO2 photoreduction","Green Chemistry","2020","22","16","5325","5332","10.1039/D0GC01497D","","","0.71073","MoKα","","0.1416","0.0677","","","0.1446","0.1765","","","","","","1.028","","","","has coordinates,has disorder","257601","2020-10-21","18:00:00",""
"7240907","24.63","0.03","19.1","0.03","14.9","0.02","90","","90","","90","","7009","17","296.15","","296.15","","","","","","","","","4","C m c 21","C 2c -2","36","","","","- C68 H76 O24 Ti7 -","- C68 H76 O24 Ti7 -","- C272 H304 O96 Ti28 -","4","0.5","","Li, Ning; Liu, Jing-Jing; Sun, Jia-Wei; Dong, Bao-Xia; Dong, Long-Zhang; Yao, Su-Juan; Xin, Zhifeng; Li, Shun-Li; Lan, Ya-Qian","Calix[8]arene-constructed stable polyoxo-titanium clusters for efficient CO2 photoreduction","Green Chemistry","2020","22","16","5325","5332","10.1039/D0GC01497D","","","0.71073","MoKα","","0.1629","0.0852","","","0.169","0.2079","","","","","","1.122","","","","has coordinates,has disorder","257601","2020-10-21","18:00:00",""
"7240916","9.1551","0.0002","11.365","0.0002","18.1448","0.0004","90","","94.124","0.001","90","","1883.04","0.07","124","2","124.58","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","(E)-N-benzyl-N-(3-oxo-1,3-diphenylprop-1-en-1-yl)acetamide","","- C24 H21 N O2 -","- C24 H21 N O2 -","- C96 H84 N4 O8 -","4","1","","Zhao, Kai; Zhang, Xiao-Chen; Tao, Ji-Yu; Wu, Xian-Dan; Wu, Jia-Xu; Li, Wei-Ming; Zhu, Tong-Hao; Loh, Teck-Peng","Regio- and stereoselective C(sp2)‒H acylation of enamides with aldehydes via transition-metal-free photoredox catalysis","Green Chemistry","2020","22","16","5497","5503","10.1039/D0GC01947J","","","1.34139","GaKα","","0.0497","0.0385","","","0.089","0.0961","","","","","","1.07","","","","has coordinates","257600","2020-10-21","18:00:00",""
"7240917","14.3957","0.0007","9.8622","0.0005","14.7627","0.0007","90","","100.8","0.002","90","","2058.78","0.18","170","2","170","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C24 H18 F3 N O2 -","- C24 H18 F3 N O2 -","- C96 H72 F12 N4 O8 -","4","1","","Zhao, Kai; Zhang, Xiao-Chen; Tao, Ji-Yu; Wu, Xian-Dan; Wu, Jia-Xu; Li, Wei-Ming; Zhu, Tong-Hao; Loh, Teck-Peng","Regio- and stereoselective C(sp2)‒H acylation of enamides with aldehydes via transition-metal-free photoredox catalysis","Green Chemistry","2020","22","16","5497","5503","10.1039/D0GC01947J","","","1.34139","GaKα","","0.0478","0.0439","","","0.1192","0.1234","","","","","","1.044","","","","has coordinates","257600","2020-10-21","18:00:00",""
"7240918","10.6923","0.0001","11.1552","0.0002","15.2475","0.0002","90","","97.358","0.001","90","","1803.67","0.04","170","2","170.02","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","1-(4-benzoyl-3-phenylisoquinolin-2(1H)-yl)ethan-1-one","","- C24 H19 N O2 -","- C24 H19 N O2 -","- C96 H76 N4 O8 -","4","1","","Zhao, Kai; Zhang, Xiao-Chen; Tao, Ji-Yu; Wu, Xian-Dan; Wu, Jia-Xu; Li, Wei-Ming; Zhu, Tong-Hao; Loh, Teck-Peng","Regio- and stereoselective C(sp2)‒H acylation of enamides with aldehydes via transition-metal-free photoredox catalysis","Green Chemistry","2020","22","16","5497","5503","10.1039/D0GC01947J","","","1.34139","GaKα","","0.0454","0.0371","","","0.0872","0.0933","","","","","","1.039","","","","has coordinates","257600","2020-10-21","18:00:00",""
"7240919","12.9186","0.0012","11.6675","0.001","13.3986","0.0012","90","","109.007","0.004","90","","1909.4","0.3","185","2","185.32","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H25 N O2 -","- C22 H25 N O2 -","- C88 H100 N4 O8 -","4","1","","Zhao, Kai; Zhang, Xiao-Chen; Tao, Ji-Yu; Wu, Xian-Dan; Wu, Jia-Xu; Li, Wei-Ming; Zhu, Tong-Hao; Loh, Teck-Peng","Regio- and stereoselective C(sp2)‒H acylation of enamides with aldehydes via transition-metal-free photoredox catalysis","Green Chemistry","2020","22","16","5497","5503","10.1039/D0GC01947J","","","1.34139","GaKα","","0.1023","0.0778","","","0.2161","0.2502","","","","","","1.074","","","","has coordinates","257600","2020-10-21","18:00:00",""
"7240920","14.5135","0.0006","11.7884","0.0004","18.8103","0.0007","90","","108.09","0.002","90","","3059.2","0.2","170","2","169.99","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H15 N O -","- C21 H15 N O -","- C168 H120 N8 O8 -","8","2","","Zhao, Kai; Zhang, Xiao-Chen; Tao, Ji-Yu; Wu, Xian-Dan; Wu, Jia-Xu; Li, Wei-Ming; Zhu, Tong-Hao; Loh, Teck-Peng","Regio- and stereoselective C(sp2)‒H acylation of enamides with aldehydes via transition-metal-free photoredox catalysis","Green Chemistry","2020","22","16","5497","5503","10.1039/D0GC01947J","","","1.34139","GaKα","","0.097","0.0731","","","0.1901","0.2147","","","","","","1.031","","","","has coordinates","257600","2020-10-21","18:00:00",""
"7240963","12.0991","0.0002","12.9247","0.0002","10.4969","0.0002","90","","100.474","0.0007","90","","1614.13","0.05","294","2","294","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C15 H13 F3 N2 O2 S -","- C15 H13 F3 N2 O2 S -","- C60 H52 F12 N8 O8 S4 -","4","1","","Nadiveedhi, Maheshwara Reddy; Cirandur, Suresh Reddy; Akondi, Srirama Murthy","Visible-light-promoted photocatalyst- and additive-free intermolecular trifluoromethyl-thio(seleno)cyanation of alkenes","Green Chemistry","2020","22","17","5589","5593","10.1039/D0GC01726D","","","0.71073","MoKα","","0.0924","0.0619","","","0.157","0.1791","","","","","","1.054","","","","has coordinates","257591","2020-10-21","18:00:00",""
"7241038","8.6346","0.0001","11.4963","0.0001","11.874","0.0002","65.995","0.001","87.948","0.001","71.81","0.001","1017.27","0.03","170","","170","","","","","","","","","5","P -1","-P 1","2","","","","- C18 H30 Au Cl2 P -","- C18 H30 Au Cl2 P -","- C36 H60 Au2 Cl4 P2 -","2","1","","Ingner, Fredric J. L.; Giustra, Zachary X.; Novosedlik, Sebastian; Orthaber, Andreas; Gates, Paul J.; Dyrager, Christine; Pilarski, Lukasz T.","Mechanochemical synthesis of (hetero)aryl Au(i) complexes","Green Chemistry","2020","22","17","5648","5655","10.1039/D0GC02263B","","x-ray","0.71073","MoKα","","0.0552","0.0538","","","0.1384","0.1395","","","","","","1.127","","","","has coordinates","257592","2020-10-21","18:00:00",""
"7241039","8.6986","0.001","18.586","0.002","12.1084","0.0013","90","","90.975","0.002","90","","1957.3","0.4","170","","170","","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C17 H29 Au Cl F N P -","- C17 H29 Au Cl F N P -","- C68 H116 Au4 Cl4 F4 N4 P4 -","4","1","","Ingner, Fredric J. L.; Giustra, Zachary X.; Novosedlik, Sebastian; Orthaber, Andreas; Gates, Paul J.; Dyrager, Christine; Pilarski, Lukasz T.","Mechanochemical synthesis of (hetero)aryl Au(i) complexes","Green Chemistry","2020","22","17","5648","5655","10.1039/D0GC02263B","","","0.71073","MoKα","","0.0441","0.0322","","","0.0719","0.0745","","","","","","1.067","","","","has coordinates","257592","2020-10-21","18:00:00",""
"7241086","5.923","0.003","8.454","0.004","10.773","0.005","78.722","0.006","76.248","0.006","86.236","0.006","513.8","0.4","296","2","296.15","","","","","","","","","4","P -1","-P 1","2","","","","- C13 H13 N O -","- C13 H13 N O -","- C26 H26 N2 O2 -","2","1","","Bi, Hong-Yan; Li, Cheng-Jing; Wei, Cui; Liang, Cui; Mo, Dong-Liang","Copper-catalyzed tri- or tetrafunctionalization of alkenylboronic acids to prepare tetrahydrocarbazol-1-ones and indolo[2,3-a]carbazoles","Green Chemistry","2020","22","17","5815","5821","10.1039/D0GC01514H","","","0.71073","MoKα","","0.0549","0.0507","","","0.139","0.1435","","","","","","1.082","","","","has coordinates","257590","2020-10-21","18:00:00",""
"7241087","10.3801","0.0006","12.7791","0.0007","22.1745","0.0012","92.814","0.002","92.689","0.002","104.376","0.002","2840.6","0.3","100","2","100","2","","","","","","","","7","P -1","-P 1","2","","","","- C44 H36 Ir2 N8 Na2 O23 S4 -","- C44 H36 Ir2 N8 Na2 O23 S4 -","- C88 H72 Ir4 N16 Na4 O46 S8 -","2","1","","Ainembabazi, Diana; Wang, Kai; Finn, Matthew; Ridenour, James; Voutchkova-Kostal, Adelina","Efficient transfer hydrogenation of carbonate salts from glycerol using water-soluble iridium N-heterocyclic carbene catalysts","Green Chemistry","2020","22","18","6093","6104","10.1039/D0GC01958E","","x-ray","0.71073","MoKα","","0.079","0.0554","","","0.1176","0.1275","","","","","","1.057","","","","has coordinates,has disorder","257621","2020-10-21","18:00:00",""
"7241129","11.37","0.0004","10.2878","0.0004","14.5801","0.0006","90","","97.519","0.004","90","","1690.8","0.11","100","0.1","100","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C21 H18 N2 O S -","- C21 H18 N2 O S -","- C84 H72 N8 O4 S4 -","4","1","","Zhong, Ping-Fu; Lin, Hong-Min; Wang, Lin-Wei; Mo, Zu-Yu; Meng, Xiu-Jin; Tang, Hai-Tao; Pan, Ying-Ming","Electrochemically enabled synthesis of sulfide imidazopyridines via a radical cyclization cascade","Green Chemistry","2020","22","19","6334","6339","10.1039/D0GC02125C","","x-ray","0.71073","MoKα","","0.0462","0.0382","","","0.0847","0.0901","","","","","","1.048","","","","has coordinates","258874","2020-11-06","12:32:13",""
"7241130","4.9241","0.0018","14.209","0.004","15.299","0.0016","90.853","0.015","96.934","0.019","99.1","0.03","1048.6","0.5","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C22.75 H22 N3 O1.75 S -","- C22.75 H22 N3 O1.75 S -","- C45.5 H44 N6 O3.5 S2 -","2","1","","Zhong, Ping-Fu; Lin, Hong-Min; Wang, Lin-Wei; Mo, Zu-Yu; Meng, Xiu-Jin; Tang, Hai-Tao; Pan, Ying-Ming","Electrochemically enabled synthesis of sulfide imidazopyridines via a radical cyclization cascade","Green Chemistry","2020","22","19","6334","6339","10.1039/D0GC02125C","","x-ray","0.71073","MoKα","","0.2222","0.107","","","0.2312","0.3136","","","","","","0.89","","","","has coordinates","258874","2020-11-06","12:32:14",""
"7241131","5.6915","0.0002","12.7636","0.0006","26.8264","0.0012","90","","90","","90","","1948.78","0.14","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C25 H20 N2 S -","- C25 H20 N2 S -","- C100 H80 N8 S4 -","4","1","","Zhong, Ping-Fu; Lin, Hong-Min; Wang, Lin-Wei; Mo, Zu-Yu; Meng, Xiu-Jin; Tang, Hai-Tao; Pan, Ying-Ming","Electrochemically enabled synthesis of sulfide imidazopyridines via a radical cyclization cascade","Green Chemistry","2020","22","19","6334","6339","10.1039/D0GC02125C","","x-ray","0.71073","MoKα","","0.0804","0.052","","","0.1068","0.1254","","","","","","1.042","","","","has coordinates","258874","2020-11-06","12:32:14",""
"7241146","8.5574","0.0002","9.8938","0.0002","14.8351","0.0004","91.403","0.001","93.658","0.001","97.92","0.001","1240.8","0.05","100","2","100","2","","","","","","","","5","P 1","P 1","1","","","","- C54 H52 F4 N4 O12 -","- C54 H52 F4 N4 O12 -","- C54 H52 F4 N4 O12 -","1","1","","Babij, Nicholas R.; Choy, Nakyen; Cismesia, Megan A.; Couling, David J.; Hough, Nicole M.; Johnson, Peter L.; Klosin, Jerzy; Li, Xiaoyong; Lu, Yu; McCusker, Elizabeth O.; Meyer, Kevin G.; Renga, James M.; Rogers, Richard B.; Stockman, Kenneth E.; Webb, Nicola J.; Whiteker, Gregory T.; Zhu, Yuanming","Design and synthesis of florylpicoxamid, a fungicide derived from renewable raw materials","Green Chemistry","2020","22","18","6047","6054","10.1039/D0GC02063J","","","0.71073","MoKα","","0.036","0.0327","","","0.089","0.0973","","","","","","1.09","","","","has coordinates","257620","2020-10-21","18:00:00",""
"7241147","8.3081","0.0003","11.7497","0.0004","26.4644","0.0008","90","","90","","90","","2583.39","0.15","100","2","100","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C24 H36 Cl F2 N O4 -","- C24 H36 Cl F2 N O4 -","- C96 H144 Cl4 F8 N4 O16 -","4","1","","Babij, Nicholas R.; Choy, Nakyen; Cismesia, Megan A.; Couling, David J.; Hough, Nicole M.; Johnson, Peter L.; Klosin, Jerzy; Li, Xiaoyong; Lu, Yu; McCusker, Elizabeth O.; Meyer, Kevin G.; Renga, James M.; Rogers, Richard B.; Stockman, Kenneth E.; Webb, Nicola J.; Whiteker, Gregory T.; Zhu, Yuanming","Design and synthesis of florylpicoxamid, a fungicide derived from renewable raw materials","Green Chemistry","2020","22","18","6047","6054","10.1039/D0GC02063J","","","0.71073","MoKα","","0.0463","0.0373","","","0.0827","0.0865","","","","","","1.035","","","","has coordinates","257620","2020-10-21","18:00:00",""
"7241185","8.1097","0.0012","14.367","0.0019","16.622","0.002","90","","98.194","0.002","90","","1916.9","0.4","296.15","","296.15","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C19 H15 Cl F N O8 -","- C19 H15 Cl F N O8 -","- C76 H60 Cl4 F4 N4 O32 -","4","1","","Chen, Li; Huang, Rong; Li, Kun; Yun, Xing-Han; Yang, Chang-Long; Yan, Sheng-Jiao","An environmentally benign cascade reaction of chromone-3-carboxaldehydes with ethyl 2-(pyridine-2-yl)acetate derivatives for highly site-selective synthesis of quinolizines and quinolizinium salts in water","Green Chemistry","2020","22","20","6943","6953","10.1039/D0GC02460K","","","0.71073","MoKα","","0.0628","0.0431","","","0.1061","0.1193","","","","","","1.034","","","","has coordinates","258879","2020-11-06","12:33:30",""
"7241224","9.61101","0.00018","10.7261","0.0002","15.5952","0.0003","90","","90","","90","","1607.69","0.05","296.63","0.16","296.63","0.16","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C21 H17 N O2 -","- C21 H17 N O2 -","- C84 H68 N4 O8 -","4","1","","Zhu, Lixiang; Ren, Xiaoyu; Du, Juan; Wu, Jia-Hong; Tan, Jian-Ping; Che, Jixing; Pan, Jianke; Wang, Tianli","A transition-metal-free multicomponent reaction towards constructing chiral 2H-1,4-benzoxazine scaffolds","Green Chemistry","2020","22","21","7506","7512","10.1039/D0GC02134B","","x-ray","1.54184","CuKα","","0.0748","0.0726","","","0.1591","0.164","","","","","","1.115","","","","has coordinates","258882","2020-11-06","12:34:04",""
"7241225","8.4921","0.0002","13.5753","0.0004","15.0981","0.0005","90","","90","","90","","1740.55","0.09","295.88","0.16","295.88","0.16","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C23 H19 N O2 -","- C23 H19 N O2 -","- C92 H76 N4 O8 -","4","1","","Zhu, Lixiang; Ren, Xiaoyu; Du, Juan; Wu, Jia-Hong; Tan, Jian-Ping; Che, Jixing; Pan, Jianke; Wang, Tianli","A transition-metal-free multicomponent reaction towards constructing chiral 2H-1,4-benzoxazine scaffolds","Green Chemistry","2020","22","21","7506","7512","10.1039/D0GC02134B","","x-ray","1.54184","CuKα","","0.069","0.0666","","","0.1623","0.1667","","","","","","1.116","","","","has coordinates","258882","2020-11-06","12:34:05",""
"7241226","8.352","0.0009","5.7066","0.0006","22.623","0.002","90","","91.45","0.003","90","","1077.9","0.19","293","2","293","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C44 H48 O20 -","- C44 H48 O20 -","- C44 H48 O20 -","1","0.5","","Wang, Pei-Long; Shen, Hui-Zhi; Cheng, Hui-Hui; Gao, Hui; Li, Pin-Hua","Electrochemical esterification reaction of alkynes with diols via cleavage of carbon‒carbon triple bonds without catalyst and oxidant","Green Chemistry","2020","22","20","6783","6791","10.1039/D0GC02193H","","","0.71073","MoKα","","0.0594","0.045","","","0.135","0.1507","","","","","","0.961","","","","has coordinates","258876","2020-11-06","12:32:51",""
"7241227","8.7517","0.0001","11.7055","0.0001","19.7505","0.0002","90","","101.925","0.001","90","","1979.64","0.04","293","2","293","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","111","","- C22 H21 N O4 S -","- C22 H21 N O4 S -","- C88 H84 N4 O16 S4 -","4","1","","Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai","Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study","Green Chemistry","2020","22","20","6798","6803","10.1039/D0GC01860K","","x-ray","1.54184","CuKα","","0.0399","0.0355","","","0.0997","0.1028","","","","","","1.067","","","","has coordinates","258878","2020-11-06","12:33:20",""
"7241228","13.9122","0.001","12.1203","0.0009","14.5292","0.0011","90","","103.724","0.008","90","","2380","0.3","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C23 H25 Cl2 N O5 S -","- C23 H25 Cl2 N O5 S -","- C92 H100 Cl8 N4 O20 S4 -","4","1","","Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai","Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study","Green Chemistry","2020","22","20","6798","6803","10.1039/D0GC01860K","","x-ray","0.71073","MoKα","","0.0739","0.0436","","","0.1083","0.1263","","","","","","1.035","","","","has coordinates","258878","2020-11-06","12:33:21",""
"7241229","10.7314","0.0018","10.99","0.002","12.275","0.003","71.712","0.017","69.196","0.017","68.46","0.016","1230.5","0.5","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C24 H25 Cl2 N O4 S -","- C24 H25 Cl2 N O4 S -","- C48 H50 Cl4 N2 O8 S2 -","2","1","","Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai","Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study","Green Chemistry","2020","22","20","6798","6803","10.1039/D0GC01860K","","x-ray","0.71073","MoKα","","0.1394","0.0668","","","0.1672","0.2251","","","","","","1.017","","","","has coordinates","258878","2020-11-06","12:33:21",""
"7241230","9.5153","0.001","17.8775","0.0017","24.2427","0.0018","90","","90","","90","","4123.9","0.7","296","","296","","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C22 H21 N O6 S -","- C22 H21 N O6 S -","- C176 H168 N8 O48 S8 -","8","1","","Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai","Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study","Green Chemistry","2020","22","20","6798","6803","10.1039/D0GC01860K","","x-ray","0.71073","MoKα","","0.095","0.0491","","","0.1199","0.1584","","","","","","1.025","","","","has coordinates","258878","2020-11-06","12:33:21",""
"7241231","12.239","0.005","19.008","0.007","20.975","0.008","90","","100.52","0.006","90","","4798","3","296","2","296.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H19 N O2 S -","- C16 H19 N O2 S -","- C192 H228 N12 O24 S12 -","12","3","","Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai","Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study","Green Chemistry","2020","22","20","6798","6803","10.1039/D0GC01860K","","","0.71073","MoKα","","0.231","0.1242","","","0.3124","0.3852","","","","","","1.103","","","","has coordinates,has disorder","258878","2020-11-06","12:33:21",""
"7241232","12.0121","0.0017","9.9422","0.0014","15.9636","0.0019","90","","99.105","0.013","90","","1882.5","0.4","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C22 H19 N O3 S -","- C22 H19 N O3 S -","- C88 H76 N4 O12 S4 -","4","1","","Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai","Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study","Green Chemistry","2020","22","20","6798","6803","10.1039/D0GC01860K","","x-ray","0.71073","MoKα","","0.1209","0.0608","","","0.1178","0.1489","","","","","","0.926","","","","has coordinates","258878","2020-11-06","12:33:21",""
"7241233","11.9374","0.0002","18.7941","0.0002","16.6525","0.0002","90","","95.525","0.001","90","","3718.68","0.09","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C21 H19 N O4 S -","- C21 H19 N O4 S -","- C168 H152 N8 O32 S8 -","8","1","","Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai","Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study","Green Chemistry","2020","22","20","6798","6803","10.1039/D0GC01860K","","x-ray","1.54184","CuKα","","0.0626","0.0567","","","0.1762","0.1827","","","","","","1.099","","","","has coordinates","258878","2020-11-06","12:33:21",""
"7241234","9.0842","0.0012","11.168","0.0014","11.3556","0.0013","108.185","0.011","106.055","0.011","109.685","0.012","932","0.3","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C19 H23 N O4 S -","- C19 H23 N O4 S -","- C38 H46 N2 O8 S2 -","2","1","","Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai","Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study","Green Chemistry","2020","22","20","6798","6803","10.1039/D0GC01860K","","x-ray","0.71073","MoKα","","0.1322","0.0743","","","0.2022","0.2594","","","","","","1.036","","","","has coordinates","258878","2020-11-06","12:33:21",""
"7241235","9.489","0.002","10.341","0.002","12.078","0.003","75.859","0.003","82.328","0.003","69.425","0.003","1074.5","0.4","296.15","","296.15","","","","","","","","","5","P -1","-P 1","2","","qq","","- C20 H23 N O4 S -","- C20 H23 N O4 S -","- C40 H46 N2 O8 S2 -","2","1","","Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai","Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study","Green Chemistry","2020","22","20","6798","6803","10.1039/D0GC01860K","","","0.71073","MoKα","","0.0843","0.0513","","","0.1276","0.1449","","","","","","1.032","","","","has coordinates","258878","2020-11-06","12:33:21",""
"7241236","4.9632","0.0001","9.9037","0.0003","33.603","0.0009","90","","90","","90","","1651.72","0.07","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C19 H17 N O2 S -","- C19 H17 N O2 S -","- C76 H68 N4 O8 S4 -","4","1","","Shen, Jinhui; Yu, Aimin; Zhang, Lei; Meng, Xiangtai","Construction of benzothiophene fused pyrrolidone in water via a catalyst-free process and a mechanism study","Green Chemistry","2020","22","20","6798","6803","10.1039/D0GC01860K","","x-ray","1.54184","CuKα","","0.058","0.0466","","","0.1096","0.119","","","","","","1.061","","","","has coordinates","258878","2020-11-06","12:33:21",""
"7241295","9.1121","0.0018","9.4374","0.0019","10.647","0.002","95.85","0.03","104.17","0.03","111.98","0.03","803.9","0.4","295","2","295","2","","","","","","","","3","P -1","-P 1","2","","","","- C18 H16 O6 -","- C18 H16 O6 -","- C36 H32 O12 -","2","1","","Hu, Deqing; Yang, Lu; Wan, Jie-Ping","Biaryl and atropisomeric biaryl aldehyde synthesis by one-step, metal-free benzannulation of aryl enals and propiolates","Green Chemistry","2020","22","20","6773","6777","10.1039/D0GC02806A","","","0.71073","MoKα","","0.0573","0.0412","","","0.1138","0.1337","","","","","","1.132","","","","has coordinates","258877","2020-11-06","12:33:04",""
"7241315","11.6196","0.0004","12.0604","0.0005","12.2162","0.0004","63.651","0.002","75.955","0.002","61.239","0.002","1343.91","0.09","293","2","293","","","","","","","","","6","P -1","-P 1","2","","","","- C24 H20 Cu2 N8 O6 V2 -","- C24 H20 Cu2 N8 O6 V2 -","- C48 H40 Cu4 N16 O12 V4 -","2","1","","Tian, Hong-Rui; Zhang, Zhong; Liu, Shu-Mei; Dang, Tian-Yi; Li, Zhuo; Lu, Ying; Liu, Shu-Xia","A highly stable polyoxovanadate-based Cu(i)‒MOF for the carboxylative cyclization of CO2 with propargylic alcohols at room temperature","Green Chemistry","2020","22","21","7513","7520","10.1039/D0GC02812F","","","0.71073","MoKα","","0.0458","0.0292","","","0.0606","0.0681","","","","","","1.072","","","","has coordinates","258881","2020-11-06","12:33:57",""
"7241334","10.3539","0.0005","10.9951","0.0006","11.059","0.0007","90","","90","","90","","1258.98","0.12","293","2","293","2","","","","","","","","6","P n a 21","P 2c -2n","33","","","","- C13 H11 B F4 N2 O -","- C13 H11 B F4 N2 O -","- C52 H44 B4 F16 N8 O4 -","4","1","","Gao, Wenjing; Wan, Yameng; Zhang, Zhiguo; Wu, Hao; Liu, Tongxin; Zhang, Guisheng","The Hofmann reaction involving annulation of o-(pyridin-2-yl)aryl amides selectively and rapidly leads to potential photocatalytically active 6H-pyrido[1,2-c]quinazolin-6-one derivatives","Green Chemistry","2020","22","22","7955","7961","10.1039/D0GC02777D","","x-ray","0.71073","MoKα","","0.0505","0.0443","","","0.1253","0.1345","","","","","","0.87","","","","has coordinates","259605","2020-12-06","14:25:50",""
"7241345","8.1303","0.0009","8.5936","0.0011","9.2306","0.0012","88.833","0.011","68.333","0.011","89.254","0.01","599.23","0.14","173.15","","173.15","","","","","","","","","5","P -1","-P 1","2","","lithiumdimethylamide","","- C20 H44 Li2 N2 O4 -","- C20 H44 Li2 N2 O4 -","- C20 H44 Li2 N2 O4 -","1","0.5","","Yang, Hongzhi; Zeng, Tianying; Xi, Shuang; Hu, Shengkun; Wu, Yunfei; Tang, Yefeng","Photoinduced, strain-promoted cycloadditions of trans-cycloheptenones and azides","Green Chemistry","2020","22","20","7023","7030","10.1039/D0GC02347G","","x-ray","0.71073","MoKα","","0.0926","0.0589","","","0.1658","0.1789","","","","","","0.92","","","","has coordinates,has disorder","258875","2020-11-06","12:32:29",""
"7241346","13.1208","0.0003","7.6644","0.0001","15.2725","0.0004","90","","111.229","0.003","90","","1431.63","0.06","173","0.1","173","0.1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C17 H21 N O2 -","- C17 H21 N O2 -","- C68 H84 N4 O8 -","4","1","","Yang, Hongzhi; Zeng, Tianying; Xi, Shuang; Hu, Shengkun; Wu, Yunfei; Tang, Yefeng","Photoinduced, strain-promoted cycloadditions of trans-cycloheptenones and azides","Green Chemistry","2020","22","20","7023","7030","10.1039/D0GC02347G","","x-ray","1.54184","CuKα","","0.0406","0.0376","","","0.0948","0.0972","","","","","","1.02","","","","has coordinates","258875","2020-11-06","12:32:36",""
"7241383","8.4738","0.0005","9.6099","0.0006","12.106","0.0009","88.37","0.002","69.823","0.002","84.352","0.002","920.81","0.11","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C21 H16 Cl N3 S -","- C21 H16 Cl N3 S -","- C42 H32 Cl2 N6 S2 -","2","1","","Wang, Guanjie; Wei, Chenlong; Hong, Xianfang; Fu, Zhenqian; Huang, Wei","Sodium pyruvate as a peroxide scavenger in aerobic oxidation under carbene catalysis","Green Chemistry","2020","22","20","6819","6826","10.1039/D0GC02555K","","","0.71073","MoKα","","0.0515","0.0395","","","0.0908","0.0991","","","","","","1.024","","","","has coordinates","258880","2020-11-06","12:33:36",""
"7241409","12.863","0.004","7.173","0.002","16.464","0.005","90","","90","","90","","1519.1","0.8","296.15","","296.15","","","","","","","","","4","P n m a","-P 2ac 2n","62","","","","- C16 H20 N2 O2 -","- C16 H20 N2 O2 -","- C64 H80 N8 O8 -","4","0.5","","Zhou, Hui; Chen, Wei; Liu, Ji-Hong; Zhang, Wen-Zhen; Lu, Xiao-Bing","Highly effective capture and subsequent catalytic transformation of low-concentration CO2 by superbasic guanidines","Green Chemistry","2020","22","22","7832","7838","10.1039/D0GC03009K","","","0.71073","MoKα","","0.0994","0.0472","","","0.1207","0.1486","","","","","","1.024","","","","has coordinates,has disorder","259604","2020-12-06","14:25:42",""
"7241410","20.029","0.003","20.029","0.003","9.929","0.003","90","","90","","90","","3983.1","1.5","296","2","296","2","","","","","","","","4","P 42 b c","P 4c -2ab","106","","","","- C22 H28 N2 O2 -","- C22 H28 N2 O2 -","- C176 H224 N16 O16 -","8","1","","Zhou, Hui; Chen, Wei; Liu, Ji-Hong; Zhang, Wen-Zhen; Lu, Xiao-Bing","Highly effective capture and subsequent catalytic transformation of low-concentration CO2 by superbasic guanidines","Green Chemistry","2020","22","22","7832","7838","10.1039/D0GC03009K","","","0.71073","MoKα","","0.1293","0.0577","","","0.1304","0.1664","","","","","","1.001","","","","has coordinates","259604","2020-12-06","14:25:43",""
"7241411","11.9503","0.0006","12.9375","0.0006","19.6351","0.001","90","","90","","90","","3035.7","0.3","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C27 H47 N7 S2 -","- C27 H47 N7 S2 -","- C108 H188 N28 S8 -","4","1","","Zhou, Hui; Chen, Wei; Liu, Ji-Hong; Zhang, Wen-Zhen; Lu, Xiao-Bing","Highly effective capture and subsequent catalytic transformation of low-concentration CO2 by superbasic guanidines","Green Chemistry","2020","22","22","7832","7838","10.1039/D0GC03009K","","","0.71073","MoKα","","0.0518","0.0407","","","0.0952","0.1016","","","","","","1.048","","","","has coordinates","259604","2020-12-06","14:25:43",""
"7241412","12.003","0.007","19.823","0.011","16.309","0.009","90","","111.59","","90","","3608","4","296","2","296.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C28 H49 N7 O2 -","- C28 H49 N7 O2 -","- C112 H196 N28 O8 -","4","1","","Zhou, Hui; Chen, Wei; Liu, Ji-Hong; Zhang, Wen-Zhen; Lu, Xiao-Bing","Highly effective capture and subsequent catalytic transformation of low-concentration CO2 by superbasic guanidines","Green Chemistry","2020","22","22","7832","7838","10.1039/D0GC03009K","","","0.71073","MoKα","","0.1252","0.0574","","","0.1321","0.1506","","","","","","0.787","","","","has coordinates","259604","2020-12-06","14:25:43",""
"7241413","12.8442","0.0007","17.5019","0.0009","18.6407","0.0009","63.996","0.001","70.836","0.001","69.475","0.001","3450.4","0.3","200","2","200","","","","","","","","","4","P -1","-P 1","2","","","","- C62 H115 N14 O9 -","- C62 H115 N14 O9 -","- C124 H230 N28 O18 -","2","1","","Zhou, Hui; Chen, Wei; Liu, Ji-Hong; Zhang, Wen-Zhen; Lu, Xiao-Bing","Highly effective capture and subsequent catalytic transformation of low-concentration CO2 by superbasic guanidines","Green Chemistry","2020","22","22","7832","7838","10.1039/D0GC03009K","","","0.71073","MoKα","","0.1006","0.0793","","","0.228","0.2485","","","","","","1.041","","","","has coordinates,has disorder","259604","2020-12-06","14:25:43",""
"7241648","7.2328","0.0014","19.384","0.004","25.55","0.005","90","","90","","90","","3582.1","1.2","133.15","","133.15","","","","","","","","","6","P n m a","-P 2ac 2n","62","","","","- C45 H24 Cl N2 O3 Re -","- C45 H24 Cl N2 O3 Re -","- C180 H96 Cl4 N8 O12 Re4 -","4","0.5","","Qiu, Li-Qi; Chen, Kai-Hong; Yang, Zhi-Wen; He, Liang-Nian","A rhenium catalyst with bifunctional pyrene groups boosts natural light-driven CO2 reduction","Green Chemistry","2020","22","24","8614","8622","10.1039/D0GC03111A","","","0.71073","MoKα","","0.0573","0.0529","","","0.1233","0.1251","","","","","","1.244","","","","has coordinates","260797","2021-01-07","06:41:30",""
"7241649","7.1176","0.0002","16.5556","0.0005","14.6211","0.0004","90","","98.965","0.001","90","","1701.85","0.08","150","2","150","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C17 H17 N3 O5 S -","- C17 H17 N3 O5 S -","- C68 H68 N12 O20 S4 -","4","1","","Cioc, Răzvan C.; Lutz, Martin; Pidko, Evgeny A.; Crockatt, Marc; van der Waal, Jan C.; Bruijnincx, Pieter C. A.","Direct Diels‒Alder reactions of furfural derivatives with maleimides","Green Chemistry","2021","23","1","367","373","10.1039/D0GC03558K","","","0.71073","MoKα","","0.0443","0.0333","","","0.0866","0.0927","","","","","","1.033","","","","has coordinates","261712","2021-02-04","23:23:05",""
"7241699","16.2484","0.0001","11.3597","0.0001","8.2456","0.0001","90","","100.148","0.001","90","","1498.14","0.02","100.01","0.1","100.01","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C13 H11 Na O6 S -","- C13 H11 Na O6 S -","- C52 H44 Na4 O24 S4 -","4","1","","Zhang, Hui; Wang, Ming; Jiang, Xuefeng","Sustainable access to sulfonic acids from halides and thiourea dioxide with air","Green Chemistry","2020","22","23","8238","8242","10.1039/D0GC03135F","","x-ray","1.54184","CuKα","","0.0733","0.0725","","","0.1605","0.1609","","","","","","1.166","","","","has coordinates,has disorder","260798","2021-01-07","06:41:50",""
"7241700","16.8614","0.0016","19.0598","0.0014","8.8881","0.0006","90","","103.357","0.008","90","","2779.1","0.4","100","0.3","100","0.3","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C32 H30 Cl2 N2 O5 -","- C32 H30 Cl2 N2 O5 -","- C128 H120 Cl8 N8 O20 -","4","0.5","","Zhang, Ming-Zhong; Liu, Long; Gou, Quan; Wang, Qi; Li, Yi; Li, Wan-Ting; Luo, Fei; Yuan, Min; Chen, Tieqiao; He, Wei-Min","Synthesis of hydroxyl-containing oxindoles and 3,4-dihydroquinolin-2-ones through oxone-mediated cascade arylhydroxylation of activated alkenes","Green Chemistry","2020","22","23","8369","8374","10.1039/D0GC02205E","","x-ray","0.71073","MoKα","","0.116","0.0873","","","0.2041","0.2387","","","","","","1.015","","","","has coordinates","260799","2021-01-07","06:41:56",""
"7241884","7.7399","0.0002","13.3332","0.0003","10.8147","0.0002","90","","95.823","0.002","90","","1110.29","0.04","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C10 H7 I N2 O S -","- C10 H7 I N2 O S -","- C40 H28 I4 N8 O4 S4 -","4","1","","Lu, Fangling; Zhang, Kan; Yao, Yanxiu; Yin, Ying; Chen, Jiafu; Zhang, Xinwei; Wang, Yin; Lu, Lijun; Gao, Ziwei; Lei, Aiwen","Electrochemical oxidative thiocyanation and amination of enaminones towards the synthesis of multi-substituted alkenes","Green Chemistry","2021","23","2","763","766","10.1039/D0GC03590D","","","1.54178","CuKα","","0.0639","0.0623","","","0.1647","0.1679","","","","","","1.043","","","","has coordinates","261714","2021-02-04","23:23:14",""
"7241885","10.7742","0.0005","7.035","0.0003","12.0329","0.0006","90","","101.619","0.0017","90","","893.36","0.07","150","2","150","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C9 H12 O5 -","- C9 H12 O5 -","- C36 H48 O20 -","4","1","","Kirchhecker, Sarah; Dell'Acqua, Andrea; Angenvoort, Astrid; Spannenberg, Anke; Ito, Kenji; Tin, Sergey; Taden, Andreas; de Vries, Johannes G.","HMF‒glycerol acetals as additives for the debonding of polyurethane adhesives","Green Chemistry","2021","23","2","957","965","10.1039/D0GC04093B","","","0.71073","MoKα","","0.0355","0.0331","","","0.0888","0.092","","","","","","1.048","","","","has coordinates","261717","2021-02-04","23:23:30",""
"7241886","7.7476","0.0007","18.5104","0.0019","23.642","0.002","72.297","0.003","85.352","0.003","85.778","0.003","3215.1","0.5","296.15","","296.15","","","","","","","","","5","P -1","-P 1","2","","","","- C20 H11 F5 O5 S4 -","- C20 H11 F5 O5 S4 -","- C120 H66 F30 O30 S24 -","6","3","","Cai, Song-Zhou; Ge, Danhua; Sun, Li-Wen; Rao, Weidong; Wang, Xin; Shen, Zhi-Liang; Chu, Xue-Qiang","Three-component heteroannulation for tetrasubstituted furan construction enabled by successive defluorination and dual sulfonylation relay","Green Chemistry","2021","23","2","935","941","10.1039/D0GC03922E","","","0.71073","MoKα","","0.1628","0.0603","","","0.0998","0.1238","","","","","","1.003","","","","has coordinates,has disorder","261716","2021-02-04","23:23:25",""
"7241887","9.8524","0.0001","12.043","0.0001","12.4397","0.0001","90","","112.982","0.001","90","","1358.85","0.02","294.15","","294.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H16 F2 N2 O -","- C15 H16 F2 N2 O -","- C60 H64 F8 N8 O4 -","4","1","","Niu, Kaikai; Hao, Yanke; Song, Lingyun; Liu, Yuxiu; Wang, Qingmin","Electro-oxidative C‒H alkylation of quinoxalin-2(1H)-ones with organoboron compounds","Green Chemistry","2021","23","1","302","306","10.1039/D0GC03892J","","x-ray","1.54184","CuKα","","0.0403","0.0379","","","0.1144","0.1169","","","","","","1.092","","","","has coordinates","261713","2021-02-04","23:23:10",""
"7241930","10.624","0.0012","23.227","0.003","17.226","0.002","90","","97.34","0.003","90","","4215.9","0.9","200","2","200","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","DPrCuCl in manuscript","","","- C41 H49 Cl6 Cu N2 -","- C41 H49 Cl6 Cu N2 -","- C164 H196 Cl24 Cu4 N8 -","4","1","","Cervantes-Reyes, Alejandro; Farshadfar, Kaveh; Rudolph, Matthias; Rominger, Frank; Schaub, Thomas; Ariafard, Alireza; Hashmi, A. Stephen K.","Copper-catalysed synthesis of α-alkylidene cyclic carbonates from propargylic alcohols and CO2","Green Chemistry","2021","23","2","889","897","10.1039/D0GC03990J","","","0.71073","MoKα","","0.1245","0.0755","","","0.1998","0.232","","","","","","1.029","","","","has coordinates","261715","2021-02-04","23:23:20",""
"7241931","33.614","0.006","6.0727","0.001","14.459","0.003","90","","93.236","0.003","90","","2946.8","0.9","200","2","200","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","A8 in manuscript","","","- C18 H16 O4 -","- C18 H16 O4 -","- C144 H128 O32 -","8","1","","Cervantes-Reyes, Alejandro; Farshadfar, Kaveh; Rudolph, Matthias; Rominger, Frank; Schaub, Thomas; Ariafard, Alireza; Hashmi, A. Stephen K.","Copper-catalysed synthesis of α-alkylidene cyclic carbonates from propargylic alcohols and CO2","Green Chemistry","2021","23","2","889","897","10.1039/D0GC03990J","","","0.71073","MoKα","","0.1147","0.0593","","","0.1334","0.1601","","","","","","1.04","","","","has coordinates","261715","2021-02-04","23:23:20",""
"7242054","9.099","0.0006","12.6543","0.0009","17.4953","0.0014","69.761","0.007","87.356","0.006","78.198","0.006","1849.4","0.3","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C24 H19 N O3 -","- C24 H19 N O3 -","- C96 H76 N4 O12 -","4","2","","Kong, Yanyan; Kim, Jung Keun; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Wu, Yangjie","An oxidant- and catalyst-free electrooxidative cross-coupling approach to 3-tetrahydroisoquinoline substituted coumarins","Green Chemistry","2021","23","3","1274","1279","10.1039/D0GC03930F","","x-ray","1.54184","CuKα","","0.071","0.0512","","","0.1315","0.1504","","","","","","1.022","","","","has coordinates","262666","2021-03-05","02:12:45",""
"7242055","8.6666","0.0005","23.4805","0.0011","9.5853","0.0004","90","","102.461","0.006","90","","1904.62","0.17","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C24 H20 N2 O2 -","- C24 H20 N2 O2 -","- C96 H80 N8 O8 -","4","1","","Kong, Yanyan; Kim, Jung Keun; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Wu, Yangjie","An oxidant- and catalyst-free electrooxidative cross-coupling approach to 3-tetrahydroisoquinoline substituted coumarins","Green Chemistry","2021","23","3","1274","1279","10.1039/D0GC03930F","","x-ray","1.54184","CuKα","","0.069","0.0517","","","0.1347","0.1502","","","","","","1.032","","","","has coordinates","262666","2021-03-05","02:12:45",""
"7242064","16.647","0.003","16.647","0.003","7.749","0.003","90","","90","","120","","1859.7","0.9","293","2","293","2","","","","","","","","4","R 3 m :H","R 3 -2""","160","","","","- C24 H27 Br3 N6 -","- C24 H27 Br3 N6 -","- C72 H81 Br9 N18 -","3","0.166667","","Ma, Shuai; Cui, Jing-Wang; Rao, Cai-Hui; Jia, Meng-Ze; Chen, Yun-Rui; Zhang, Jie","Boosting activity of molecular oxygen by pyridinium-based photocatalysts for metal-free alcohol oxidation","Green Chemistry","2021","23","3","1337","1343","10.1039/D0GC03730C","","","0.71073","MoKα","","0.0752","0.0518","","","0.147","0.2245","","","","","","0.886","","","","has coordinates","262669","2021-03-05","02:13:30",""
"7242065","4.7015","0.0006","7.5668","0.0009","13.7164","0.0015","100.964","0.01","91.553","0.01","102.63","0.01","466.26","0.1","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C12 H6 F N O3 -","- C12 H6 F N O3 -","- C24 H12 F2 N2 O6 -","2","1","","Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu","Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water","Green Chemistry","2021","23","3","1136","1139","10.1039/D0GC03861J","","x-ray","1.54184","CuKα","","0.0691","0.0462","","","0.1245","0.143","","","","","","1.037","","","","has coordinates","262667","2021-03-05","02:12:58",""
"7242066","6.182","0.0007","7.343","0.0007","15.4344","0.0009","97.694","0.006","93.323","0.007","97.422","0.009","686.49","0.11","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C14 H12 F N O4 S -","- C14 H12 F N O4 S -","- C28 H24 F2 N2 O8 S2 -","2","1","","Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu","Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water","Green Chemistry","2021","23","3","1136","1139","10.1039/D0GC03861J","","x-ray","1.54184","CuKα","","0.062","0.0456","","","0.1115","0.1235","","","","","","1.044","","","","has coordinates","262667","2021-03-05","02:12:58",""
"7242067","28.1572","0.0005","11.7989","0.0002","6.8522","0.00014","90","","107.682","0.002","90","","2168.92","0.07","293","2","293","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C13 H9 N O4 -","- C13 H9 N O4 -","- C104 H72 N8 O32 -","8","1","","Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu","Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water","Green Chemistry","2021","23","3","1136","1139","10.1039/D0GC03861J","","x-ray","1.54184","CuKα","","0.054","0.0398","","","0.1113","0.1211","","","","","","1.072","","","","has coordinates","262667","2021-03-05","02:12:58",""
"7242068","7.7844","0.0015","7.8633","0.0012","9.9225","0.0018","71.839","0.015","82.19","0.016","67.855","0.016","534.42","0.18","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C13 H8 F N O3 -","- C13 H8 F N O3 -","- C26 H16 F2 N2 O6 -","2","1","","Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu","Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water","Green Chemistry","2021","23","3","1136","1139","10.1039/D0GC03861J","","x-ray","1.54184","CuKα","","0.0759","0.0509","","","0.135","0.1615","","","","","","1.037","","","","has coordinates","262667","2021-03-05","02:12:58",""
"7242069","4.6906","0.0003","14.7537","0.0009","16.5416","0.0011","90","","97.187","0.006","90","","1135.75","0.13","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C14 H11 N O3 -","- C14 H11 N O3 -","- C56 H44 N4 O12 -","4","1","","Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu","Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water","Green Chemistry","2021","23","3","1136","1139","10.1039/D0GC03861J","","x-ray","1.54184","CuKα","","0.1001","0.059","","","0.1356","0.1657","","","","","","1.014","","","","has coordinates","262667","2021-03-05","02:12:58",""
"7242070","4.70525","0.00016","13.1424","0.0004","18.3356","0.0005","90","","96.343","0.003","90","","1126.9","0.06","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C13 H8 Br N O3 -","- C13 H8 Br N O3 -","- C52 H32 Br4 N4 O12 -","4","1","","Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu","Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water","Green Chemistry","2021","23","3","1136","1139","10.1039/D0GC03861J","","x-ray","1.54184","CuKα","","0.0584","0.0495","","","0.1296","0.142","","","","","","1.03","","","","has coordinates","262667","2021-03-05","02:12:58",""
"7242071","7.6718","0.0015","7.8925","0.0013","10.0037","0.0014","71.388","0.014","80.879","0.014","66.502","0.017","526.1","0.17","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C13 H9 N O3 -","- C13 H9 N O3 -","- C26 H18 N2 O6 -","2","1","","Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu","Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water","Green Chemistry","2021","23","3","1136","1139","10.1039/D0GC03861J","","x-ray","1.54184","CuKα","","0.0732","0.0472","","","0.1264","0.1481","","","","","","1.025","","","","has coordinates","262667","2021-03-05","02:12:58",""
"7242072","14.4314","0.0008","4.4645","0.0003","18.5538","0.0011","90","","90.744","0.005","90","","1195.3","0.13","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C14 H11 N O5 -","- C14 H11 N O5 -","- C56 H44 N4 O20 -","4","1","","Li, Wenhao; Duan, Wenxue; Tang, Qingxuan; Li, Zhan-Ting; Yang, Guanyu","Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water","Green Chemistry","2021","23","3","1136","1139","10.1039/D0GC03861J","","x-ray","1.54184","CuKα","","0.0786","0.0493","","","0.1205","0.1454","","","","","","1.017","","","","has coordinates","262667","2021-03-05","02:12:58",""
"7242118","13.2958","0.0007","10.0194","0.0007","16.6456","0.0007","90","","106.404","0.005","90","","2127.2","0.2","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C36 H46 Mn3 N10 O16 -","- C36 H46 Mn3 N10 O16 -","- C72 H92 Mn6 N20 O32 -","2","0.5","","Asghar, Aisha; Iqbal, Naseem; Noor, Tayyaba; Kariuki, Benson M.; Kidwell, Luke; Easun, Timothy L.","Efficient electrochemical synthesis of a manganese-based metal‒organic framework for H2 and CO2 uptake","Green Chemistry","2021","23","3","1220","1227","10.1039/D0GC03292A","","","1.54184","CuKα","","0.1136","0.0772","","","0.2024","0.2381","","","","","","1.043","","","","has coordinates,has disorder","262668","2021-03-05","02:13:07",""
"7242119","13.4484","0.0004","10.1799","0.0003","17.656","0.0005","90","","90.271","0.003","90","","2417.14","0.12","150","2","150","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C11 H11 Mn N O5 -","- C11 H11 Mn N O5 -","- C88 H88 Mn8 N8 O40 -","8","2","","Asghar, Aisha; Iqbal, Naseem; Noor, Tayyaba; Kariuki, Benson M.; Kidwell, Luke; Easun, Timothy L.","Efficient electrochemical synthesis of a manganese-based metal‒organic framework for H2 and CO2 uptake","Green Chemistry","2021","23","3","1220","1227","10.1039/D0GC03292A","","","0.71073","MoKα","","0.0401","0.0315","","","0.0711","0.0772","","","","","","1.056","","","","has coordinates","262668","2021-03-05","02:13:17",""
"7242163","9.448","0.007","11.423","0.009","30.49","0.02","90","","90","","90","","3291","4","296","","296","","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C15 H22 N2 O4 -","- C15 H22 N2 O4 -","- C120 H176 N16 O32 -","8","1","","Morita, Shunya; Yoshimura, Tomoyuki; Matsuo, Jun-ichi","Catalytic intermolecular aldol reactions of transient amide enolates in domino Michael/aldol reactions of nitroalkanes, acrylamides, and aldehydes","Green Chemistry","2021","23","3","1160","1164","10.1039/D0GC04111D","","","0.71075","MoKα","","0.2338","0.1122","","","0.233","0.2951","","","","","","1.107","","","","has coordinates","262665","2021-03-05","02:12:38",""
"7242201","14.7118","0.0006","9.3818","0.0004","14.7793","0.0007","90","","91.266","0.002","90","","2039.39","0.15","100","","100","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C21 H32 Cl N O2 Ru -","- C21 H32 Cl N O2 Ru -","- C84 H128 Cl4 N4 O8 Ru4 -","4","1","","Phearman, Alexander S.; Moore, Jewelianna M.; Bhagwandin, Dayanni D.; Goldberg, Jonathan M.; Heinekey, D. Michael; Goldberg, Karen I.","(Hexamethylbenzene)Ru catalysts for the Aldehyde-Water Shift reaction","Green Chemistry","2021","23","4","1609","1615","10.1039/D0GC03809A","","","0.71073","MoKα","","0.0168","0.0161","","","0.0418","0.0423","","","","","","1.063","","","","has coordinates","262663","2021-03-05","02:12:24",""
"7242202","6.5462","0.0006","27.28","0.002","14.4106","0.0012","90","","90.549","0.003","90","","2573.3","0.4","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C25 H36 B2 O4 -","- C25 H36 B2 O4 -","- C100 H144 B8 O16 -","4","1","","Zhang, Yahui; Zhao, Xiangyu; Bi, Ce; Lu, Wenqi; Song, Mengyuan; Wang, Dongdong; Qing, Guangyan","Selective electrocatalytic hydroboration of aryl alkenes","Green Chemistry","2021","23","4","1691","1699","10.1039/D0GC03890C","","","0.71073","MoKα","","0.1952","0.1499","","","0.3733","0.3965","","","","","","1.001","","","","has coordinates,has disorder","262664","2021-03-05","02:12:30",""
"7242218","5.6416","0.0002","5.8788","0.0002","18.0049","0.0008","95.374","0.003","95.693","0.004","96.475","0.003","587.08","0.04","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C10 H11 Cl F3 N O2 -","- C10 H11 Cl F3 N O2 -","- C20 H22 Cl2 F6 N2 O4 -","2","1","","Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.","A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones","Green Chemistry","2021","23","6","2336","2351","10.1039/D0GC04395H","","x-ray","1.54184","CuKα","","0.0855","0.0724","","","0.1829","0.1917","","","","","","1.037","","","","has coordinates","263797","2021-04-05","15:05:22",""
"7242219","6.099","0.0001","7.7041","0.0001","25.2722","0.0004","90","","94.075","0.002","90","","1184.47","0.03","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C12 H16 Cl N O2 -","- C12 H16 Cl N O2 -","- C48 H64 Cl4 N4 O8 -","4","1","","Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.","A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones","Green Chemistry","2021","23","6","2336","2351","10.1039/D0GC04395H","","x-ray","0.71073","MoKα","","0.0418","0.0341","","","0.0835","0.0884","","","","","","1.071","","","","has coordinates,has disorder","263797","2021-04-05","15:05:23",""
"7242220","5.7769","0.0003","7.6286","0.0005","21.5338","0.001","90","","96.167","0.005","90","","943.5","0.09","100","1","100","1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C10 H13 N O2 -","- C10 H13 N O2 -","- C40 H52 N4 O8 -","4","1","","Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.","A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones","Green Chemistry","2021","23","6","2336","2351","10.1039/D0GC04395H","","x-ray","1.54184","CuKα","","0.0577","0.0432","","","0.1094","0.1245","","","","","","1.056","","","","has coordinates","263797","2021-04-05","15:05:23",""
"7242221","18.9356","0.0003","3.81317","0.0001","21.672","0.0005","90","","101.702","0.0019","90","","1532.29","0.06","100","0.1","100","0.1","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C8 H8 N2 O2 -","- C8 H8 N2 O2 -","- C64 H64 N16 O16 -","8","1","","Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.","A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones","Green Chemistry","2021","23","6","2336","2351","10.1039/D0GC04395H","","x-ray","1.54184","CuKα","","0.044","0.0378","","","0.099","0.105","","","","","","1.043","","","","has coordinates","263797","2021-04-05","15:05:23",""
"7242222","5.7548","0.0003","10.5744","0.0005","10.5916","0.0006","110.243","0.005","102.912","0.005","100.879","0.005","563.94","0.06","100","0.1","100","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C12 H14 Cl N O2 -","- C12 H14 Cl N O2 -","- C24 H28 Cl2 N2 O4 -","2","1","","Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.","A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones","Green Chemistry","2021","23","6","2336","2351","10.1039/D0GC04395H","","x-ray","1.54184","CuKα","","0.0425","0.0377","","","0.0973","0.1015","","","","","","1.051","","","","has coordinates,has disorder","263797","2021-04-05","15:05:23",""
"7242223","9.0379","0.0003","10.044","0.0003","11.0835","0.0003","90","","99.123","0.003","90","","993.4","0.05","100","","100","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C11 H13 N O2 -","- C11 H13 N O2 -","- C44 H52 N4 O8 -","4","1","","Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.","A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones","Green Chemistry","2021","23","6","2336","2351","10.1039/D0GC04395H","","x-ray","1.54184","CuKα","","0.0604","0.0447","","","0.1086","0.122","","","","","","1.054","","","","has coordinates","263797","2021-04-05","15:05:23",""
"7242224","7.6334","0.0002","8.7609","0.0003","14.2366","0.0003","81.705","0.002","88.677","0.002","73.562","0.003","903.45","0.05","100","0.1","100","0.1","","","","","","","","3","P -1","-P 1","2","","","","- C7 H12 O6 -","- C7 H12 O6 -","- C28 H48 O24 -","4","2","","Kassin, Victor-Emmanuel H.; Morodo, Romain; Toupy, Thomas; Jacquemin, Isaline; Van Hecke, Kristof; Robiette, Raphaël; Monbaliu, Jean-Christophe M.","A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones","Green Chemistry","2021","23","6","2336","2351","10.1039/D0GC04395H","","x-ray","1.54184","CuKα","","0.047","0.0419","","","0.113","0.1176","","","","","","1.046","","","","has coordinates","263797","2021-04-05","15:05:23",""
"7242249","6.7011","0.0011","9.1071","0.0011","28.951","0.003","90","","92.176","0.01","90","","1765.5","0.4","295","2","295","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H19 N5 O -","- C20 H19 N5 O -","- C80 H76 N20 O4 -","4","1","","Akulov, Alexey A.; Varaksin, Mikhail V.; Tsmokalyuk, Anton N.; Charushin, Valery N.; Chupakhin, Oleg N.","Blue-light-promoted radical C‒H azolation of cyclic nitrones enabled by Selectfluor®","Green Chemistry","2021","23","5","2049","2057","10.1039/D1GC00175B","","","0.71073","MoKα","","0.1457","0.0638","","","0.1434","0.1986","","","","","","1.002","","","","has coordinates","263796","2021-04-05","15:05:12",""
"7242297","15.5231","0.0005","3.8267","0.0001","23.9744","0.0008","90","","93.432","0.001","90","","1421.58","0.08","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C7 H6 Cl N O2 -","- C7 H6 Cl N O2 -","- C56 H48 Cl8 N8 O16 -","8","1","","Li, Yiming; Wang, Yuhong; Yang, Tilong; Lin, Zhenyang; Jiang, Xuefeng","Selenium-catalyzed intramolecular atom- and redox-economical transformation of o-nitrotoluenes into anthranilic acids","Green Chemistry","2021","23","8","2986","2991","10.1039/D0GC04407E","","","0.71073","MoKα","","0.0345","0.0305","","","0.0815","0.0861","","","","","","1.064","","","","has coordinates","264909","2021-05-05","08:48:30",""
"7242298","7.9048","0.0001","11.2276","0.0001","19.3205","0.0002","90","","90","","90","","1714.73","0.03","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C17 H26 N2 O4 -","- C17 H26 N2 O4 -","- C68 H104 N8 O16 -","4","1","","Li, Yiming; Wang, Yuhong; Yang, Tilong; Lin, Zhenyang; Jiang, Xuefeng","Selenium-catalyzed intramolecular atom- and redox-economical transformation of o-nitrotoluenes into anthranilic acids","Green Chemistry","2021","23","8","2986","2991","10.1039/D0GC04407E","","x-ray","1.54184","CuKα","","0.0277","0.0273","","","0.071","0.0712","","","","","","1.037","","","","has coordinates","264909","2021-05-05","08:48:33",""
"7242323","10.6894","0.0013","10.6948","0.0014","13.7194","0.0017","90","","91.046","0.002","90","","1568.2","0.3","296","2","296.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C19 H18 N2 O2 -","- C19 H18 N2 O2 -","- C76 H72 N8 O8 -","4","1","","Xu, Jun; Huang, Lin; He, Lei; Ni, Zhigang; Shen, Jiabin; Li, Xiaoling; Chen, Kaixian; Li, Wanmei; Zhang, Pengfei","A combination of heterogeneous catalysis and photocatalysis for the olefination of quinoxalin-2(1H)-ones with ketones in water: a green and efficient route to (Z)-enaminones","Green Chemistry","2021","23","5","2123","2129","10.1039/D0GC04235H","","","0.71073","MoKα","","0.0533","0.0397","","","0.101","0.1121","","","","","","1.038","","","","has coordinates","263795","2021-04-05","15:05:07",""
"7242329","15.40316","0.00012","7.20606","0.00003","15.43887","0.00009","90","","116.871","0.0009","90","","1528.62","0.02","170","0.15","170","0.15","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C17 H18 O3 S -","- C17 H18 O3 S -","- C68 H72 O12 S4 -","4","1","","Du, Wu-Bo; Wang, Ning-Ning; Pan, Chao; Ni, Shao-Fei; Wen, Li-Rong; Li, Ming; Zhang, Lin-Bao","Regio- and stereoselective electrochemical synthesis of sulfonylated enethers from alkynes and sulfonyl hydrazides","Green Chemistry","2021","23","6","2420","2426","10.1039/D1GC00027F","","x-ray","1.54184","CuKα","","0.0328","0.0326","","","0.0873","0.0874","","","","","","1.066","","","","has coordinates","263798","2021-04-05","15:05:29",""
"7242330","8.5976","0.0008","10.8141","0.0009","15.2294","0.0014","90","","90","","90","","1416","0.2","298","2","298","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C16 H14 O2 S -","- C16 H14 O2 S -","- C64 H56 O8 S4 -","4","1","","Du, Wu-Bo; Wang, Ning-Ning; Pan, Chao; Ni, Shao-Fei; Wen, Li-Rong; Li, Ming; Zhang, Lin-Bao","Regio- and stereoselective electrochemical synthesis of sulfonylated enethers from alkynes and sulfonyl hydrazides","Green Chemistry","2021","23","6","2420","2426","10.1039/D1GC00027F","","","0.71073","MoKα","","0.085","0.0577","","","0.1067","0.1143","","","","","","1.022","","","","has coordinates","263798","2021-04-05","15:05:32",""
"7242405","15.138","0.003","10.099","0.002","22.516","0.007","90","","90","","90","","3442.2","1.4","296","2","296","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C36 H32 Br2 N6 O4 S2 -","- C36 H32 Br2 N6 O4 S2 -","- C144 H128 Br8 N24 O16 S8 -","4","0.5","","Jiang, Shuai; Cao, Wen-Bin; Li, Hai-Yan; Xu, Xiao-Ping; Ji, Shun-Jun","Convenient synthesis of spiroindolenines from tryptamine-derived isocyanides and organic azides by cobalt catalysis in pure water","Green Chemistry","2021","23","7","2619","2623","10.1039/D1GC00270H","","","0.71073","MoKα","","0.1204","0.0555","","","0.1415","0.1881","","","","","","1.061","","","","has coordinates","264912","2021-05-05","08:49:25",""
"7242512","12.3598","0.0005","12.8606","0.0005","15.4574","0.0006","81.976","0.001","75.455","0.001","70.669","0.001","2239.9","0.15","296","2","296","2","","","","","","","","6","P -1","-P 1","2","","","","- C25 H22 Cl N O4 S -","- C25 H22 Cl N O4 S -","- C100 H88 Cl4 N4 O16 S4 -","4","2","","Liu, Chengkou; Lin, Yang; Cai, Chen; Yuan, Chengcheng; Fang, Zheng; Guo, Kai","Continuous-flow electro-oxidative coupling of sulfides with activated methylene compounds leading to sulfur ylides","Green Chemistry","2021","23","8","2956","2961","10.1039/D1GC00226K","","","0.71073","MoKα","","0.0884","0.0691","","","0.1813","0.203","","","","","","1","","","","has coordinates","264911","2021-05-05","08:49:14",""
"7242526","12.5878","0.0006","12.6544","0.0006","13.1098","0.0006","106.319","0.003","105.558","0.002","107.521","0.003","1763.44","0.16","100","","100","","","","","","","","","4","P -1","-P 1","2","","Bismuth 2-phenylisobutyrate","","- C38 H49 Bi O8 -","- C38 H49 Bi O8 -","- C76 H98 Bi2 O16 -","2","1","","Levent, Emre; Sala, Oliver; Wilm, Lukas F. B.; Löwe, Pawel; Dielmann, Fabian","Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts ‒ alternatives to organotin compounds","Green Chemistry","2021","23","7","2747","2755","10.1039/D1GC00446H","","","0.71073","MoKα","","0.0501","0.0412","","","0.0944","0.0986","","","","","","1.079","","","","has coordinates","264913","2021-05-05","08:49:44",""
"7242527","13.3571","0.0003","14.0806","0.0003","18.593","0.0003","90","","95.0534","0.0009","90","","3483.3","0.12","100","2","100","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C54 H96 Bi2 Li4 N2 O20 -","- C54 H96 Bi2 Li4 N2 O20 -","- C108 H192 Bi4 Li8 N4 O40 -","2","0.5","","Levent, Emre; Sala, Oliver; Wilm, Lukas F. B.; Löwe, Pawel; Dielmann, Fabian","Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts ‒ alternatives to organotin compounds","Green Chemistry","2021","23","7","2747","2755","10.1039/D1GC00446H","","","0.71073","MoKα","","0.0268","0.0227","","","0.0548","0.0562","","","","","","1.054","","","","has coordinates","264913","2021-05-05","08:49:46",""
"7242528","16.1427","0.0002","13.2582","0.0002","18.584","0.0002","90","","110.087","0.0006","90","","3735.47","0.08","100","2","100","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C58 H102 Bi2 Li4 N4 O20 -","- C58 H102 Bi2 Li4 N4 O20 -","- C116 H204 Bi4 Li8 N8 O40 -","2","0.5","","Levent, Emre; Sala, Oliver; Wilm, Lukas F. B.; Löwe, Pawel; Dielmann, Fabian","Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts ‒ alternatives to organotin compounds","Green Chemistry","2021","23","7","2747","2755","10.1039/D1GC00446H","","","0.71073","MoKα","","0.0215","0.0183","","","0.0409","0.0418","","","","","","1.079","","","","has coordinates","264913","2021-05-05","08:49:46",""
"7242529","14.3713","0.0002","17.9791","0.0002","15.3608","0.0002","90","","92.508","0.001","90","","3965.17","0.09","100","2","100","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C64 H116 Bi2 Li4 N2 O20 -","- C64 H116 Bi2 Li4 N2 O20 -","- C128 H232 Bi4 Li8 N4 O40 -","2","0.5","","Levent, Emre; Sala, Oliver; Wilm, Lukas F. B.; Löwe, Pawel; Dielmann, Fabian","Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts ‒ alternatives to organotin compounds","Green Chemistry","2021","23","7","2747","2755","10.1039/D1GC00446H","","","0.71073","MoKα","","0.0224","0.0182","","","0.0413","0.0429","","","","","","1.012","","","","has coordinates,has disorder","264913","2021-05-05","08:49:46",""
"7242530","24.0601","0.0012","18.8535","0.0009","22.3563","0.0012","90","","92.989","0.003","90","","10127.4","0.9","100","2","100","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C106 H119 Bi2 Li4 N3 O20 -","- C106 H119 Bi2 Li4 N3 O20 -","- C424 H476 Bi8 Li16 N12 O80 -","4","1","","Levent, Emre; Sala, Oliver; Wilm, Lukas F. B.; Löwe, Pawel; Dielmann, Fabian","Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts ‒ alternatives to organotin compounds","Green Chemistry","2021","23","7","2747","2755","10.1039/D1GC00446H","","","0.71073","MoKα","","0.0385","0.0298","","","0.0669","0.07","","","","","","1.031","","","","has coordinates","264913","2021-05-05","08:49:46",""
"7242531","24.7978","0.0008","16.4792","0.0005","24.6871","0.0008","90","","103.624","0.001","90","","9804.5","0.5","100","2","100","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C104 H116 Bi2 Li4 N2 O20 -","- C104 H116 Bi2 Li4 N2 O20 -","- C416 H464 Bi8 Li16 N8 O80 -","4","1","","Levent, Emre; Sala, Oliver; Wilm, Lukas F. B.; Löwe, Pawel; Dielmann, Fabian","Heterobimetallic complexes composed of bismuth and lithium carboxylates as polyurethane catalysts ‒ alternatives to organotin compounds","Green Chemistry","2021","23","7","2747","2755","10.1039/D1GC00446H","","","0.71073","MoKα","","0.0335","0.0235","","","0.0501","0.053","","","","","","1.015","","","","has coordinates,has disorder","264913","2021-05-05","08:49:46",""
"7242532","24.437","0.003","24.437","0.003","7.3579","0.0008","90","","90","","90","","4393.9","0.9","296.15","","296.15","","","","","","","","","5","P 4/n :2","-P 4a","85","","","","- C24 H18 F3 N3 O2 -","- C24 H18 F3 N3 O2 -","- C192 H144 F24 N24 O16 -","8","1","","Pan, Zhentao; Shi, Shuaijun; Yang, Xuancheng; Xiao, Xuqiong; Zhang, Wangqin; Wang, Shiliang; Ma, Yongmin","Eco-friendly construction of spiroquinazolin-2-(thi)ones and quinolin-(thio)ureas via Fe(iii)-catalyzed multi-component domino double [4 + 2] annulations","Green Chemistry","2021","23","8","2944","2949","10.1039/D1GC00889G","","","0.71073","MoKα","","0.1369","0.0753","","","0.2175","0.245","","","","","","1.109","","","","has coordinates,has disorder","264910","2021-05-05","08:48:44",""
"7242533","8.754","0.005","18.911","0.01","11.952","0.005","90","","104.763","0.013","90","","1913.3","1.7","296.15","","296.15","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C23 H19 N3 O S -","- C23 H19 N3 O S -","- C92 H76 N12 O4 S4 -","4","1","","Pan, Zhentao; Shi, Shuaijun; Yang, Xuancheng; Xiao, Xuqiong; Zhang, Wangqin; Wang, Shiliang; Ma, Yongmin","Eco-friendly construction of spiroquinazolin-2-(thi)ones and quinolin-(thio)ureas via Fe(iii)-catalyzed multi-component domino double [4 + 2] annulations","Green Chemistry","2021","23","8","2944","2949","10.1039/D1GC00889G","","","0.71073","MoKα","","0.0989","0.0501","","","0.1163","0.1386","","","","","","1.025","","","","has coordinates","264910","2021-05-05","08:48:47",""
"7242534","13.632","0.018","13.694","0.018","22.48","0.03","98.57","0.03","95.81","0.03","92.8","0.03","4120","9","296.15","","296.15","","","","","","","","","5","P -1","-P 1","2","","","","- C23 H14 N3 O S -","- C23 H14 N3 O S -","- C184 H112 N24 O8 S8 -","8","4","","Pan, Zhentao; Shi, Shuaijun; Yang, Xuancheng; Xiao, Xuqiong; Zhang, Wangqin; Wang, Shiliang; Ma, Yongmin","Eco-friendly construction of spiroquinazolin-2-(thi)ones and quinolin-(thio)ureas via Fe(iii)-catalyzed multi-component domino double [4 + 2] annulations","Green Chemistry","2021","23","8","2944","2949","10.1039/D1GC00889G","","","0.71073","MoKα","","0.2273","0.0746","","","0.1651","0.2275","","","","","","0.921","","","","has coordinates","264910","2021-05-05","08:48:57",""
"7242571","12.5419","0.0005","22.4521","0.0009","11.6246","0.0005","90","","109.951","0.001","90","","3076.9","0.2","296","2","296","2","","","","","","","","7","C 1 m 1","C -2y","8","","","","- C32 H46 Cu2 Ge N12 O48 W12 -","- C32 H26.94 Cu2 Ge N12 O43.4 W12 -","- C64 H53.88 Cu4 Ge2 N24 O86.8 W24 -","2","0.5","","Shen, Qingbo; Gómez-García, Carlos J.; Sun, Wenlong; Lai, Xiaoyong; Pang, Haijun; Ma, Huiyuan","Improving the photocatalytic H2 evolution activity of Keggin polyoxometalates anchoring copper-azole complexes","Green Chemistry","2021","23","8","3104","3114","10.1039/D1GC00692D","","","0.71073","MoKα","","0.0774","0.0579","","","0.1378","0.1487","","","","","","1.046","","","","has coordinates","264908","2021-05-05","08:48:19",""
"7242572","12.203","0.005","13.495","0.005","14.262","0.005","104.873","0.005","111.48","0.005","105.681","0.005","1931.3","1.3","296","2","296","2","","","","","","","","7","P -1","-P 1","2","","","","- C36 H32 Cu5 Ge N30 O44 W12 -","- C36 H24 Cu5 Ge N30 O46 W12 -","- C36 H24 Cu5 Ge N30 O46 W12 -","1","0.5","","Shen, Qingbo; Gómez-García, Carlos J.; Sun, Wenlong; Lai, Xiaoyong; Pang, Haijun; Ma, Huiyuan","Improving the photocatalytic H2 evolution activity of Keggin polyoxometalates anchoring copper-azole complexes","Green Chemistry","2021","23","8","3104","3114","10.1039/D1GC00692D","","","0.71069","MoKα","","0.1124","0.0934","","","0.1908","0.2006","","","","","","1.094","","","","has coordinates","264908","2021-05-05","08:48:19",""
"7242614","7.1154","0.0007","9.6387","0.0008","10.8333","0.0009","93.473","0.007","98.583","0.007","109.416","0.008","688.03","0.11","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C18 H13 N O -","- C18 H13 N O -","- C36 H26 N2 O2 -","2","1","","Li, Wenjing; Li, Shun; Luo, Lihua; Ge, Yicen; Xu, Jiaqi; Zheng, Xueli; Yuan, Maolin; Li, Ruixiang; Chen, Hua; Fu, Haiyan","Visible-light-initiated catalyst-free oxidative cleavage of (Z)-triaryl-substituted alkenes containing pyridyl motif under ambient conditions","Green Chemistry","2021","23","10","3649","3655","10.1039/D1GC00716E","","","0.71073","MoKα","","0.0737","0.0502","","","0.1137","0.1315","","","","","","1.033","","","","has coordinates","266112","2021-06-05","19:11:38",""
"7242618","17.7729","0.0017","19.2994","0.0018","7.3793","0.0008","90","","95.972","0.001","90","","2517.4","0.4","298","2","298","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C26 H21 Cl4 N2 O4 -","- C26 H21 Cl4 N2 O4 -","- C104 H84 Cl16 N8 O16 -","4","1","","Liu, Xu; Liu, Chang; Cheng, Xu","Ring-contraction of hantzsch esters and their derivatives to pyrroles via electrochemical extrusion of ethyl acetate out of aromatic rings","Green Chemistry","2021","23","9","3468","3473","10.1039/D1GC00487E","","","0.71073","MoKα","","0.1707","0.0782","","","0.1561","0.175","","","","","","1.031","","","","has coordinates","266115","2021-06-05","19:12:04",""
"7242639","15.0319","0.0003","11.2984","0.0002","16.0579","0.0003","90","","107.022","0.002","90","","2607.74","0.09","173.15","","173.15","","","","","","","","","6","I 1 2/a 1","-I 2ya","15","","","","- C22 H20 Cl6 N4 Ni O2 -","- C22 H20 Cl6 N4 Ni O2 -","- C88 H80 Cl24 N16 Ni4 O8 -","4","0.5","","Bertini, Simone; Rahaman, Motiar; Dutta, Abhijit; Schollhammer, Philippe; Rudnev, Alexander V.; Gloaguen, Fredric; Broekmann, Peter; Albrecht, Martin","Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO2 to formate","Green Chemistry","2021","23","9","3365","3373","10.1039/D1GC00388G","","","0.71073","MoKα","","0.0462","0.043","","","0.1041","0.1064","","","","","","1.065","","","","has coordinates,has disorder","266116","2021-06-05","19:12:16",""
"7242640","12.7952","0.0001","18.3813","0.0001","18.9751","0.0001","90","","109.067","0.001","90","","4217.96","0.05","173.01","0.1","173.01","0.1","","","","","","","","5","I 1 2/a 1","-I 2ya","15","","","","- C42 H64 N6 Ni O2 -","- C42 H64 N6 Ni O2 -","- C168 H256 N24 Ni4 O8 -","4","0.5","","Bertini, Simone; Rahaman, Motiar; Dutta, Abhijit; Schollhammer, Philippe; Rudnev, Alexander V.; Gloaguen, Fredric; Broekmann, Peter; Albrecht, Martin","Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO2 to formate","Green Chemistry","2021","23","9","3365","3373","10.1039/D1GC00388G","","x-ray","1.54184","CuKα","","0.0405","0.0398","","","0.1104","0.111","","","","","","1.041","","","","has coordinates,has disorder","266116","2021-06-05","19:12:17",""
"7242641","12.0724","0.0002","10.2682","0.0002","24.5315","0.0004","90","","102.057","0.001","90","","2973.89","0.09","173.01","0.1","173.01","0.1","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C30 H40 N6 Ni O2 -","- C30 H40 N6 Ni O2 -","- C120 H160 N24 Ni4 O8 -","4","0.5","","Bertini, Simone; Rahaman, Motiar; Dutta, Abhijit; Schollhammer, Philippe; Rudnev, Alexander V.; Gloaguen, Fredric; Broekmann, Peter; Albrecht, Martin","Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO2 to formate","Green Chemistry","2021","23","9","3365","3373","10.1039/D1GC00388G","","x-ray","1.54184","CuKα","","0.0518","0.0448","","","0.1225","0.1289","","","","","","1.026","","","","has coordinates","266116","2021-06-05","19:12:17",""
"7242642","7.7855","0.0001","14.7244","0.0002","22.189","0.0003","90","","98.032","0.001","90","","2518.72","0.06","173","2","173","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C30 H24 N6 Ni O2 -","- C30 H24 N6 Ni O2 -","- C120 H96 N24 Ni4 O8 -","4","1","","Bertini, Simone; Rahaman, Motiar; Dutta, Abhijit; Schollhammer, Philippe; Rudnev, Alexander V.; Gloaguen, Fredric; Broekmann, Peter; Albrecht, Martin","Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO2 to formate","Green Chemistry","2021","23","9","3365","3373","10.1039/D1GC00388G","","x-ray","0.71073","MoKα","","0.0461","0.0346","","","0.0765","0.0817","","","","","","1.028","","","","has coordinates","266116","2021-06-05","19:12:17",""
"7242643","12.8828","0.0001","18.5259","0.0002","22.3137","0.0003","90","","98.798","0.001","90","","5262.85","0.1","173","2","173","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C26 H34 N6 Ni O3 -","- C26 H34 N6 Ni O3 -","- C208 H272 N48 Ni8 O24 -","8","2","","Bertini, Simone; Rahaman, Motiar; Dutta, Abhijit; Schollhammer, Philippe; Rudnev, Alexander V.; Gloaguen, Fredric; Broekmann, Peter; Albrecht, Martin","Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO2 to formate","Green Chemistry","2021","23","9","3365","3373","10.1039/D1GC00388G","","x-ray","0.71073","MoKα","","0.0623","0.0455","","","0.0971","0.1047","","","","","","1.095","","","","has coordinates","266116","2021-06-05","19:12:17",""
"7242644","11.1131","0.0001","10.3896","0.0001","14.6952","0.0001","90","","109.634","0.001","90","","1598.07","0.03","173","0.1","173","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C36 H36 N6 Ni O2 -","- C36 H36 N6 Ni O2 -","- C72 H72 N12 Ni2 O4 -","2","0.5","","Bertini, Simone; Rahaman, Motiar; Dutta, Abhijit; Schollhammer, Philippe; Rudnev, Alexander V.; Gloaguen, Fredric; Broekmann, Peter; Albrecht, Martin","Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO2 to formate","Green Chemistry","2021","23","9","3365","3373","10.1039/D1GC00388G","","x-ray","0.71073","MoKα","","0.0346","0.0298","","","0.0817","0.0844","","","","","","1.073","","","","has coordinates","266116","2021-06-05","19:12:17",""
"7242664","18.0472","0.0007","7.044","0.0003","16.9293","0.0008","90","","96.096","0.004","90","","2139.96","0.16","113.15","","113.15","","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C12 H11 N4 O1.5 -","- C12 H11 N4 O1.5 -","- C96 H88 N32 O12 -","8","1","","Niu, Kaikai; Ding, Ling; Zhou, Pan; Hao, Yanke; Liu, Yuxiu; Song, Hongjian; Wang, Qingmin","Electro-oxidative C‒H azolation of quinoxalin-2(1H)-ones","Green Chemistry","2021","23","9","3246","3249","10.1039/D1GC00861G","","x-ray","0.71073","MoKα","","0.0568","0.0471","","","0.1138","0.1226","","","","","","1.052","","","","has coordinates,has disorder","266114","2021-06-05","19:11:55",""
"7242675","5.5069","0.0006","13.3044","0.0016","35.296","0.004","84.488","0.005","88.558","0.005","89.975","0.005","2573.2","0.5","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C13 H12 O3 S2 -","- C13 H12 O3 S2 -","- C104 H96 O24 S16 -","8","4","","Pampana, V. Kishore Kumar; Charpe, Vaibhav Pramod; Sagadevan, Arunachalam; Das, Deb Kumar; Lin, Chun-Cheng; Hwu, Jih Ru; Hwang, Kuo Chu","Oxy-sulfonylation of terminal alkynes via C‒S coupling enabled by copper photoredox catalysis","Green Chemistry","2021","23","10","3569","3574","10.1039/D1GC00736J","","","0.71073","MoKα","","0.1488","0.1323","","","0.301","0.3075","","","","","","1.214","","","","has coordinates","266113","2021-06-05","19:11:45",""
"7242676","13.3682","0.0005","7.2588","0.0003","26.6061","0.001","90","","90","","90","","2581.78","0.17","100","2","100","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C14 H11 Cl O3 S -","- C14 H11 Cl O3 S -","- C112 H88 Cl8 O24 S8 -","8","1","","Pampana, V. Kishore Kumar; Charpe, Vaibhav Pramod; Sagadevan, Arunachalam; Das, Deb Kumar; Lin, Chun-Cheng; Hwu, Jih Ru; Hwang, Kuo Chu","Oxy-sulfonylation of terminal alkynes via C‒S coupling enabled by copper photoredox catalysis","Green Chemistry","2021","23","10","3569","3574","10.1039/D1GC00736J","","","0.71073","MoKα","","0.0335","0.0295","","","0.0744","0.0771","","","","","","1.043","","","","has coordinates","266113","2021-06-05","19:11:45",""
"7242866","23.4643","0.0005","11.4906","0.0002","16.2903","0.0004","90","","122.775","0.001","90","","3692.95","0.14","105","","105","","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C32 H36 Ca3 O24 -","- C32 H36 Ca3 O24 -","- C128 H144 Ca12 O96 -","4","0.5","","Pan, Yanxiong; Li, Hui; Lenertz, Mary; Han, Yulun; Ugrinov, Angel; Kilin, Dmitri; Chen, Bingcan; Yang, Zhongyu","One-pot synthesis of enzyme@metal‒organic material (MOM) biocomposites for enzyme biocatalysis","Green Chemistry","2021","23","12","4466","4476","10.1039/D1GC00775K","","","1.54178","CuKα","","0.0374","0.0345","","","0.0891","0.0909","","","","","","1.09","","","","has coordinates,has disorder","267206","2021-07-05","17:57:17",""
"7242945","31.1491","0.0011","7.2268","0.0004","13.9772","0.0007","90","","92.13","0.004","90","","3144.2","0.3","150.01","0.11","150.01","0.11","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C17 H8 F6 N2 O3 -","- C17 H8 F6 N2 O3 -","- C136 H64 F48 N16 O24 -","8","1","","Brahmachari, Goutam; Karmakar, Indrajit; Karmakar, Pintu","Catalyst- and solvent-free Csp2‒H functionalization of 4-hydroxycoumarins via C-3 dehydrogenative aza-coupling under ball-milling","Green Chemistry","2021","23","13","4762","4770","10.1039/D1GC01341F","","","0.71073","MoKα","","0.1339","0.1088","","","0.2891","0.3394","","","","","","1.174","","","","has coordinates,has disorder","268821","2021-09-06","11:47:19",""
"7243033","10.249","0.003","11.657","0.004","14.822","0.004","104.005","0.008","92.306","0.008","109.243","0.007","1608.2","0.9","223","2","223","2","","","","","","","","4","P -1","-P 1","2","","3-Methoxy-10,10-dimethyl-6,9,10,11-tetrahydrobenzo[c]acridin-8(5H)-one","","- C20 H21 N O2 -","- C20 H21 N O2 -","- C80 H84 N4 O8 -","4","2","","Jamshaid, Sana; Mohandoss, Sonaimuthu; Lee, Yong Rok","Indium(iii)-catalyzed solvent-free multicomponent [2 + 2 + 1 + 1]-annulation to polycyclic functionalized fused pyridines as potential optical chemosensors","Green Chemistry","2021","23","14","5113","5119","10.1039/D1GC01332G","","","0.71073","MoKα","","0.1518","0.0755","","","0.1895","0.2295","","","","","","1.042","","","","has coordinates","268823","2021-09-06","11:47:39",""
"7243034","5.8897","0.0012","19.96","0.004","11.987","0.003","90","","103.094","0.007","90","","1372.5","0.5","223","2","223","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","8,8-Dimethyl-6,7,8,11-tetrahydro-9H-indeno[1,2-b]quinolin-9-one","","- C18 H17 N O -","- C18 H17 N O -","- C72 H68 N4 O4 -","4","1","","Jamshaid, Sana; Mohandoss, Sonaimuthu; Lee, Yong Rok","Indium(iii)-catalyzed solvent-free multicomponent [2 + 2 + 1 + 1]-annulation to polycyclic functionalized fused pyridines as potential optical chemosensors","Green Chemistry","2021","23","14","5113","5119","10.1039/D1GC01332G","","","0.71073","MoKα","","0.0915","0.0567","","","0.1367","0.1594","","","","","","1.042","","","","has coordinates,has disorder","268823","2021-09-06","11:47:40",""
"7243035","11.1052","0.001","16.1802","0.0015","9.2208","0.0009","90","","90","","90","","1656.8","0.3","223","2","223","2","","","","","","","","3","P b c n","-P 2n 2ab","60","","5,6,7,9,10,11-Hexahydrobenzo[6,7]cyclohepta[1,2-b]benzo[6,7]cyclohepta[2,1-e]pyridine","","- C23 H21 N -","- C23 H21 N -","- C92 H84 N4 -","4","0.5","","Jamshaid, Sana; Mohandoss, Sonaimuthu; Lee, Yong Rok","Indium(iii)-catalyzed solvent-free multicomponent [2 + 2 + 1 + 1]-annulation to polycyclic functionalized fused pyridines as potential optical chemosensors","Green Chemistry","2021","23","14","5113","5119","10.1039/D1GC01332G","","","0.71073","MoKα","","0.0577","0.0412","","","0.1","0.1118","","","","","","1.061","","","","has coordinates","268823","2021-09-06","11:47:40",""
"7243062","3.8618","0.0003","33.708","0.003","11.8039","0.0012","90","","98.934","0.003","90","","1517.9","0.2","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H14 N2 O S -","- C20 H14 N2 O S -","- C80 H56 N8 O4 S4 -","4","1","","Charpe, Vaibhav Pramod; Ragupathi, Ayyakkannu; Sagadevan, Arunachalam; Hwang, Kuo Chu","Photoredox synthesis of functionalized quinazolines via copper-catalyzed aerobic oxidative Csp2‒H annulation of amidines with terminal alkynes","Green Chemistry","2021","23","14","5024","5030","10.1039/D1GC01493E","","","0.71073","MoKα","","0.044","0.0346","","","0.0802","0.0856","","","","","","1.034","","","","has coordinates,has disorder","268822","2021-09-06","11:47:30",""
"7243063","9.3403","0.0006","17.0872","0.0009","10.882","0.0007","90","","106.207","0.003","90","","1667.74","0.18","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C21 H18 N2 O2 S -","- C21 H18 N2 O2 S -","- C84 H72 N8 O8 S4 -","4","1","","Charpe, Vaibhav Pramod; Ragupathi, Ayyakkannu; Sagadevan, Arunachalam; Hwang, Kuo Chu","Photoredox synthesis of functionalized quinazolines via copper-catalyzed aerobic oxidative Csp2‒H annulation of amidines with terminal alkynes","Green Chemistry","2021","23","14","5024","5030","10.1039/D1GC01493E","","","0.71073","MoKα","","0.0428","0.0359","","","0.0878","0.0924","","","","","","1.04","","","","has coordinates,has disorder","268822","2021-09-06","11:47:30",""
"7243064","14.02","0.004","8.187","0.002","15.972","0.004","90","","104.692","0.008","90","","1773.4","0.8","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C22 H15 Cl N2 O2 -","- C22 H15 Cl N2 O2 -","- C88 H60 Cl4 N8 O8 -","4","1","","Charpe, Vaibhav Pramod; Ragupathi, Ayyakkannu; Sagadevan, Arunachalam; Hwang, Kuo Chu","Photoredox synthesis of functionalized quinazolines via copper-catalyzed aerobic oxidative Csp2‒H annulation of amidines with terminal alkynes","Green Chemistry","2021","23","14","5024","5030","10.1039/D1GC01493E","","","0.71073","MoKα","","0.0553","0.0354","","","0.0811","0.0907","","","","","","1.008","","","","has coordinates","268822","2021-09-06","11:47:30",""
"7243065","18.517","0.0002","6.9182","0.0001","38.2895","0.0004","90","","90","","90","","4905.05","0.1","100","0.1","100","0.1","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C16 H11 N O4 -","- C16 H11 N O4 -","- C256 H176 N16 O64 -","16","2","","Bashir, Muhammad Adnan; Zhang, Yulong; Yu, Huaibin; Wang, Bofei; Zhao, Weining; Zhong, Fangrui","Bimetallic copper/cobalt-cocatalyzed double aerobic phenol oxidation/cyclization toward π-extended benzofuro[2,3-b]indoles as electron donors for electroluminescence","Green Chemistry","2021","23","14","5031","5036","10.1039/D1GC01658J","","x-ray","1.54184","CuKα","","0.039","0.037","","","0.095","0.0966","","","","","","1.046","","","","has coordinates","268825","2021-09-06","11:48:00",""
"7243079","15.6432","0.0003","13.2799","0.0002","17.6411","0.0004","90","","114.078","0.002","90","","3345.9","0.12","272","1","272","1","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C42 H36 N4 -","- C42 H36 N4 -","- C168 H144 N16 -","4","1","","Luo, Zhenli; Pan, Yixiao; Yao, Zhen; Yang, Ji; Zhang, Xin; Liu, Xintong; Xu, Lijin; Fan, Qing-Hua","BF3·Et2O as a metal-free catalyst for direct reductive amination of aldehydes with amines using formic acid as a reductant","Green Chemistry","2021","23","14","5205","5211","10.1039/D1GC01468D","","x-ray","1.54184","","","0.0559","0.0447","","","0.1198","0.1279","","","","","","1.027","","","","has coordinates","268824","2021-09-06","11:47:52",""
"7243088","11.9297","0.001","12.924","0.0009","13.666","0.002","75.136","0.009","78.644","0.01","89.902","0.006","1994","0.4","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C48 H55 N4 O2 -","- C48 H55 N4 O2 -","- C96 H110 N8 O4 -","2","1","","Hu, Fangzhi; Wang, Liang; Ge, Chunyan; Li, Xinyao; Ding, Zhanshuai; Xu, Lubin; Li, Shuai-Shuai","Divergent α-functionalization of cyclic amines via ring construction by molecular O2 oxidized dearomatization and ring deconstruction by aromatization-driven C‒C σ-bond cleavage","Green Chemistry","2021","23","15","5535","5541","10.1039/D1GC00941A","","","1.54184","CuKα","","0.1753","0.1157","","","0.2884","0.3647","","","","","","1.071","","","","has coordinates","268826","2021-09-06","11:48:12",""
"7243089","34.3408","0.0011","34.3408","0.0011","10.4316","0.0003","90","","90","","120","","10653.7","0.6","293","2","293","2","","","","","","","","4","R -3 :H","-R 3","148","","","","- C25 H34 N2 O2 -","- C25 H34 N2 O2 -","- C450 H612 N36 O36 -","18","1","","Hu, Fangzhi; Wang, Liang; Ge, Chunyan; Li, Xinyao; Ding, Zhanshuai; Xu, Lubin; Li, Shuai-Shuai","Divergent α-functionalization of cyclic amines via ring construction by molecular O2 oxidized dearomatization and ring deconstruction by aromatization-driven C‒C σ-bond cleavage","Green Chemistry","2021","23","15","5535","5541","10.1039/D1GC00941A","","","1.54184","CuKα","","0.1047","0.0732","","","0.2217","0.2539","","","","","","1.048","","","","has coordinates,has disorder","268826","2021-09-06","11:48:12",""
"7243090","15.3242","0.0006","13.8242","0.0005","9.0303","0.0004","90","","104.165","0.004","90","","1854.86","0.13","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C21 H25 Cl N2 O -","- C21 H25 Cl N2 O -","- C84 H100 Cl4 N8 O4 -","4","1","","Hu, Fangzhi; Wang, Liang; Ge, Chunyan; Li, Xinyao; Ding, Zhanshuai; Xu, Lubin; Li, Shuai-Shuai","Divergent α-functionalization of cyclic amines via ring construction by molecular O2 oxidized dearomatization and ring deconstruction by aromatization-driven C‒C σ-bond cleavage","Green Chemistry","2021","23","15","5535","5541","10.1039/D1GC00941A","","","1.54184","CuKα","","0.0502","0.0407","","","0.1046","0.1108","","","","","","1.057","","","","has coordinates","268826","2021-09-06","11:48:12",""
"7243091","11.3246","0.0003","11.0147","0.0003","9.1513","0.0003","90","","90","","90","","1141.51","0.06","100","0.1","100","0.1","","","","","","","","4","A e a 2","A 2 -2ab","41","","Ammonium pentaborate","","- B5 H12 N O12 -","- B5 H12 N O12 -","- B20 H48 N4 O48 -","4","0.5","","Kusy, Rafał; Grela, Karol","Ligand-free (Z)-selective transfer semihydrogenation of alkynes catalyzed by in situ generated oxidizable copper nanoparticles","Green Chemistry","2021","23","15","5494","5502","10.1039/D1GC01206A","","","0.71073","MoKα","","0.0314","0.0297","","","0.0748","0.0764","","","","","","1.092","","","","has coordinates","268827","2021-09-06","11:48:18",""
"7243119","5.4771","0.0002","9.0324","0.0004","31.6646","0.0014","90","","90","","90","","1566.49","0.11","150","2","150","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C16 H15 I O2 S -","- C16 H15 I O2 S -","- C64 H60 I4 O8 S4 -","4","1","","Lin, Li; Yang, Zhonglie; Liu, Jianchen; Wang, Jingxia; Zheng, Jiale; Li, Jun-Long; Zhang, Xiaobin; Liu, Xiang-Wei; Jiang, Hezhong; Li, Jiahong","Visible-light-induced surfactant-promoted sulfonylation of alkenes and alkynes with sulfonyl chloride by the formation of an EDA-complex with NaI in water at room temperature","Green Chemistry","2021","23","15","5467","5473","10.1039/D1GC00956G","","","0.71073","MoKα","","0.0152","0.0149","","","0.0346","0.0348","","","","","","1.088","","","","has coordinates","268828","2021-09-06","11:48:23",""
"7243124","11.6106","0.0003","16.0508","0.0003","7.5624","0.0002","90","","104.79","0.002","90","","1362.63","0.06","123","0.1","123","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H14 O2 S -","- C17 H14 O2 S -","- C68 H56 O8 S4 -","4","1","","Klöpfer, Viktor; Eckl, Robert; Floß, Johannes; Roth, Philippe M. C.; Reiser, Oliver; Barham, Joshua P.","Catalyst-free, scalable heterocyclic flow photocyclopropanation","Green Chemistry","2021","23","17","6366","6372","10.1039/D1GC01624E","","x-ray","1.54184","CuKα","","0.0489","0.0461","","","0.1254","0.1274","","","","","","1.077","","","","has coordinates","268818","2021-09-06","11:46:57",""
"7243270","14.62006","0.00016","5.80584","0.00006","22.6165","0.0002","90","","104.199","0.0011","90","","1861.08","0.03","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H17 Br2 N3 -","- C20 H17 Br2 N3 -","- C80 H68 Br8 N12 -","4","1","","Yang, Jingya; Song, Menghui; Zhou, Hongyan; Qi, Yanfang; Ma, Ben; Wang, Xi-Cun","Visible-light-promoted decarboxylative addition cyclization of N-aryl glycines and azobenzenes to access 1,2,4-triazolidines","Green Chemistry","2021","23","16","5806","5811","10.1039/D1GC02272E","","","1.54184","CuKα","","0.0481","0.0458","","","0.1208","0.1229","","","","","","1.037","","","","has coordinates","268820","2021-09-06","11:47:12",""
"7243271","14.62006","0.00016","5.80584","0.00006","22.6165","0.0002","90","","104.199","0.0011","90","","1861.08","0.03","294.65","0.1","294.65","0.1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H17 Br2 N3 -","- C20 H17 Br2 N3 -","- C80 H68 Br8 N12 -","4","1","","Yang, Jingya; Song, Menghui; Zhou, Hongyan; Qi, Yanfang; Ma, Ben; Wang, Xi-Cun","Visible-light-promoted decarboxylative addition cyclization of N-aryl glycines and azobenzenes to access 1,2,4-triazolidines","Green Chemistry","2021","23","16","5806","5811","10.1039/D1GC02272E","","x-ray","1.54184","CuKα","","0.0481","0.0458","","","0.1208","0.1229","","","","","","1.037","","","","has coordinates","268820","2021-09-06","11:47:13",""
"7243278","8.0894","0.0008","8.6805","0.0009","16.3072","0.0015","80.083","0.002","79.077","0.001","79.493","0.001","1094.2","0.19","298","2","298","2","","","","","","","","5","P -1","-P 1","2","","","","- C22 H17 F3 O3 S2 -","- C22 H17 F3 O3 S2 -","- C44 H34 F6 O6 S4 -","2","1","","Qin, Long-Zhou; Yuan, Xin; Liu, Jie; Wu, Meng-Yu; Sun, Qi; Duan, Xiu; Zhang, Xin-Peng; Qiu, Jiang-Kai; Guo, Kai","Continuous-flow processes for the S-alkynylation of cysteine-containing peptides and thioglycosides under catalyst-free, oxidant-free and mild conditions","Green Chemistry","2021","23","17","6598","6603","10.1039/D1GC01937F","","","0.71073","MoKα","","0.131","0.0911","","","0.2679","0.3079","","","","","","1.114","","","","has coordinates","268817","2021-09-06","11:46:50",""
"7243303","8.4879","0.001","9.8238","0.0014","10.6092","0.0011","110.924","0.012","95.681","0.009","108.558","0.012","760.4","0.2","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C18 H18 N2 O3 -","- C18 H18 N2 O3 -","- C36 H36 N4 O6 -","2","1","","Han, Zhi-Peng; Xu, Meng-Meng; Zhang, Rui-Ying; Xu, Xiao-Ping; Ji, Shun-Jun","Rh(iii)-Catalyzed C(sp2)‒H functionalization/cyclization cascade of N-carboxamide indole and iodonium reagents for access to indoloquinazolinone derivatives","Green Chemistry","2021","23","17","6337","6340","10.1039/D1GC01820E","","","1.54184","CuKα","","0.1197","0.084","","","0.2306","0.308","","","","","","1.095","","","","has coordinates","268819","2021-09-06","11:47:05",""
"7243507","8.4671","0.0005","10.5451","0.0006","14.4131","0.0007","88.379","0.004","80.098","0.004","73.608","0.005","1215.92","0.12","113","2","113.15","","","","","","","","","4","P -1","-P 1","2","","","","- C27 H26 P4 Pd -","- C27 H26 P4 Pd -","- C54 H52 P8 Pd2 -","2","1","","Xia, Shu-Mei; Yang, Zhi-Wen; Yao, Xiang-Yang; Chen, Kai-Hong; Qiu, Li-Qi; He, Liang-Nian","The synergistic copper/ppm Pd-catalyzed hydrocarboxylation of alkynes with formic acid as a CO surrogate as well as a hydrogen source: an alternative indirect utilization of CO2","Green Chemistry","2021","23","20","8089","8095","10.1039/D1GC02735B","","x-ray","0.71073","MoKα","","0.0536","0.0439","","","0.1112","0.1177","","","","","","1.057","","","","has coordinates","270457","2021-11-06","20:13:19",""
"7243508","5.5094","0.0003","15.212","0.0008","18.2863","0.0009","90","","96.429","0.006","90","","1522.92","0.14","100","0.1","100","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H10 F6 O2 -","- C17 H10 F6 O2 -","- C68 H40 F24 O8 -","4","1","","Xia, Shu-Mei; Yang, Zhi-Wen; Yao, Xiang-Yang; Chen, Kai-Hong; Qiu, Li-Qi; He, Liang-Nian","The synergistic copper/ppm Pd-catalyzed hydrocarboxylation of alkynes with formic acid as a CO surrogate as well as a hydrogen source: an alternative indirect utilization of CO2","Green Chemistry","2021","23","20","8089","8095","10.1039/D1GC02735B","","x-ray","0.71073","MoKα","","0.0524","0.0404","","","0.0977","0.1026","","","","","","1.073","","","","has coordinates","270457","2021-11-06","20:13:19",""
"7243522","7.5329","0.001","10.6912","0.0014","34.1","0.008","90","","95.908","0.017","90","","2731.7","0.8","297","2","297","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C26 H47 N O2 S -","- C26 H47 N O2 S -","- C104 H188 N4 O8 S4 -","4","1","","Bisz, Elwira; Koston, Martina; Szostak, Michal","N-Butylpyrrolidone (NBP) as a non-toxic substitute for NMP in iron-catalyzed C(sp2)‒C(sp3) cross-coupling of aryl chlorides","Green Chemistry","2021","","","","","10.1039/D1GC02377B","","","1.54184","CuKα","","0.0849","0.0523","","","0.1403","0.1696","","","","","","1.039","","","","has coordinates","269142","2021-09-14","23:27:26",""
"7243545","8.3414","0.0008","10.8615","0.0011","11.6407","0.0012","69.332","0.003","87.543","0.003","76.539","0.003","958.77","0.17","273.15","","273.15","","","","","","","","","6","P -1","-P 1","2","","","","- C21 H16 Cl N3 O3 S -","- C21 H16 Cl N3 O3 S -","- C42 H32 Cl2 N6 O6 S2 -","2","1","","Kumar, Navaneet; Bhadoria, Deepak; Kumar, Atul","Visible-light-promoted three-component cycloaddition reaction: synthesis of 4-functionalized 1,5-disubstituted 1,2,3-triazoles","Green Chemistry","2021","23","20","7987","7995","10.1039/D1GC02328D","","","0.71073","synchrotron","","0.0411","0.0346","","","0.0836","0.0887","","","","","","1.085","","","","has coordinates","270459","2021-11-06","20:13:49",""
"7243613","11.1446","0.0013","6.5924","0.0009","29.135","0.004","90","","93.968","0.01","90","","2135.4","0.5","293","2","293","2","","","","","","","","5","C 1 2 1","C 2y","5","","","","- C19 H17 F8 N5 O3 -","- C19 H17 F8 N5 O3 -","- C76 H68 F32 N20 O12 -","4","1","","Ning, Yongquan; Wang, Hongwei; Sivaguru, Paramasivam; Li, Shuang; Zanoni, Giuseppe; Nolan, Steven P.; Bi, Xihe","Defluorinative [4 + 1] annulation of perfluoroalkyl N-mesylhydrazones with primary amines provides 5-fluoroalkyl 1,2,3-triazoles","Green Chemistry","2021","23","20","7976","7981","10.1039/D1GC02749B","","x-ray","0.71073","MoKα","","0.097","0.0646","","","0.1551","0.1818","","","","","","1.015","","","","has coordinates","270460","2021-11-06","20:13:57",""
"7243618","3.8635","0.0001","26.708","0.001","12.5375","0.0003","90","","90.609","0.003","90","","1293.63","0.07","150","2","150","2","","","","","","","","4","C 1 c 1","C -2yc","9","","","","- C19 H11 F2 N -","- C19 H11 F2 N -","- C76 H44 F8 N4 -","4","1","","Xiang, Shiqun; Fan, Weibin; Zhang, Wei; Li, Yinghua; Guo, Shiwei; Huang, Deguang","Aqueous CO2 fixation: construction of pyridine skeletons in cooperation with ammonium cations","Green Chemistry","2021","23","20","7950","7955","10.1039/D1GC02303A","","","1.54184","CuKα","","0.0465","0.0459","","","0.1169","0.1172","","","","","","1.176","","","","has coordinates","270461","2021-11-06","20:14:15",""
"7243619","11.0913","0.0014","16.1163","0.0018","9.1839","0.0009","90","","90","","90","","1641.6","0.3","150","2","150","2","","","","","","","","3","P b c n","-P 2n 2ab","60","","","","- C23 H21 N -","- C23 H21 N -","- C92 H84 N4 -","4","0.5","","Xiang, Shiqun; Fan, Weibin; Zhang, Wei; Li, Yinghua; Guo, Shiwei; Huang, Deguang","Aqueous CO2 fixation: construction of pyridine skeletons in cooperation with ammonium cations","Green Chemistry","2021","23","20","7950","7955","10.1039/D1GC02303A","","","1.54184","CuKα","","0.067","0.0498","","","0.1344","0.1468","","","","","","1.091","","","","has coordinates","270461","2021-11-06","20:14:17",""
"7243620","7.1916","0.0003","8.2658","0.0004","13.5299","0.0005","87.021","0.004","75.797","0.004","68.795","0.005","726.3","0.06","150","2","150","2","","","","","","","","4","P -1","-P 1","2","","","","- C19 H11 Cl2 N -","- C19 H11 Cl2 N -","- C38 H22 Cl4 N2 -","2","1","","Xiang, Shiqun; Fan, Weibin; Zhang, Wei; Li, Yinghua; Guo, Shiwei; Huang, Deguang","Aqueous CO2 fixation: construction of pyridine skeletons in cooperation with ammonium cations","Green Chemistry","2021","23","20","7950","7955","10.1039/D1GC02303A","","","1.54184","CuKα","","0.0496","0.0432","","","0.1269","0.1327","","","","","","1.087","","","","has coordinates","270461","2021-11-06","20:14:18",""
"7243621","12.6441","0.0002","17.5664","0.0003","15.456","0.0003","90","","114.037","0.002","90","","3135.26","0.11","150","2","150","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H17 N O2 -","- C21 H17 N O2 -","- C168 H136 N8 O16 -","8","2","","Xiang, Shiqun; Fan, Weibin; Zhang, Wei; Li, Yinghua; Guo, Shiwei; Huang, Deguang","Aqueous CO2 fixation: construction of pyridine skeletons in cooperation with ammonium cations","Green Chemistry","2021","23","20","7950","7955","10.1039/D1GC02303A","","","1.54184","CuKα","","0.0466","0.0402","","","0.103","0.1074","","","","","","1.05","","","","has coordinates","270461","2021-11-06","20:14:18",""
"7243648","14.8126","0.0013","11.5893","0.0009","18.701","0.0015","90","","91.746","0.002","90","","3208.9","0.5","200","2","200","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","Boscalid","","","- C18 H12 Cl2 N2 O -","- C18 H12 Cl2 N2 O -","- C144 H96 Cl16 N16 O8 -","8","2","","Orecchia, Patrizio; Petkova, Desislava Slavcheva; Goetz, Roland; Rominger, Frank; Hashmi, A. Stephen K.; Schaub, Thomas","Pd-Catalysed Suzuki‒Miyaura cross-coupling of aryl chlorides at low catalyst loadings in water for the synthesis of industrially important fungicides","Green Chemistry","2021","","","","","10.1039/D1GC02602J","","","0.71073","MoKα","","0.1146","0.0537","","","0.1205","0.1473","","","","","","1.032","","","","has coordinates","269414","2021-09-30","23:48:58",""
"7243649","12.8826","0.0006","9.2515","0.0005","28.4963","0.0012","90","","90","","90","","3396.3","0.3","200","2","200","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","Fluxapyroxad","","","- C18 H12 F5 N3 O -","- C18 H12 F5 N3 O -","- C144 H96 F40 N24 O8 -","8","1","","Orecchia, Patrizio; Petkova, Desislava Slavcheva; Goetz, Roland; Rominger, Frank; Hashmi, A. Stephen K.; Schaub, Thomas","Pd-Catalysed Suzuki‒Miyaura cross-coupling of aryl chlorides at low catalyst loadings in water for the synthesis of industrially important fungicides","Green Chemistry","2021","","","","","10.1039/D1GC02602J","","","1.54178","CuKα","","0.1054","0.051","","","0.0997","0.1203","","","","","","1.021","","","","has coordinates,has disorder","269414","2021-09-30","23:48:58",""
"7243650","11.8929","0.0007","18.0476","0.0011","8.6239","0.0005","90","","110.092","0.0015","90","","1738.37","0.18","200","2","200","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","Bixafen","","","- C18 H12 Cl2 F3 N3 O -","- C18 H12 Cl2 F3 N3 O -","- C72 H48 Cl8 F12 N12 O4 -","4","1","","Orecchia, Patrizio; Petkova, Desislava Slavcheva; Goetz, Roland; Rominger, Frank; Hashmi, A. Stephen K.; Schaub, Thomas","Pd-Catalysed Suzuki‒Miyaura cross-coupling of aryl chlorides at low catalyst loadings in water for the synthesis of industrially important fungicides","Green Chemistry","2021","","","","","10.1039/D1GC02602J","","","0.71073","MoKα","","0.0968","0.0523","","","0.1039","0.1227","","","","","","1.019","","","","has coordinates","269414","2021-09-30","23:48:58",""
"7243651","15.4459","0.0006","7.45856","0.00017","16.2431","0.0006","90","","118.081","0.005","90","","1650.99","0.12","293","2","293","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C21 H23 N3 -","- C21 H23 N3 -","- C84 H92 N12 -","4","1","","Wang, Lin-Xuan; Qiu, Bin; An, Xiao-De; Dong, Pei-Zhen; Liu, Rui-Bin; Xiao, Jian","Organocatalytic cascade aldimine condensation/[1,6]-hydride transfer/Mannich-type cyclization: sustainable access to indole-2,3-fused diazocanes","Green Chemistry","2021","23","20","8181","8186","10.1039/D1GC02570H","","","1.54184","CuKα","","0.0518","0.045","","","0.1197","0.1254","","","","","","1.06","","","","has coordinates","270458","2021-11-06","20:13:30",""
"7243704","7.2246","0.0008","11.8631","0.0011","20.815","0.002","90","","90","","90","","1784","0.3","298","2","298","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C21 H19 N3 O S -","- C21 H19 N3 O S -","- C84 H76 N12 O4 S4 -","4","1","","Duan, Xiu; Sun, Qi; Yuan, Xin; Qin, Long-Zhou; Zhang, Xin-Peng; Liu, Jie; Wu, Meng-Yu; Zhu, Shan-Shan; Ma, Can-Liang; Qiu, Jiang-Kai; Guo, Kai","Photoinduced remote heteroaryl migration accompanied by cyanoalkylacylation in continuous flow","Green Chemistry","2021","23","22","8916","8921","10.1039/D1GC03060D","","","0.71073","MoKα","","0.0825","0.0549","","","0.1279","0.139","","","","","","1.031","","","","has coordinates","271850","2022-01-06","21:30:41",""
"7243738","12.35","0.03","13.16","0.03","8.567","0.018","90","","93","0.03","90","","1390","5","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H13 F N2 O3 -","- C15 H13 F N2 O3 -","- C60 H52 F4 N8 O12 -","4","1","","Luo, Mu-Jia; Ouyang, Xuan-Hui; Zhu, Yan-Ping; Li, Yang; Li, Jin-Heng","Metal-free electrochemical [3 + 2] heteroannulation of anilines with pyridines enabled by dual C–H radical aminations","Green Chemistry","2021","23","22","9024","9029","10.1039/D1GC02922C","","","0.71073","MoKα","","0.2881","0.1215","","","0.1976","0.2314","","","","","","1.16","","","","has coordinates","271849","2022-01-06","21:30:36",""
"7243739","35.1668","0.0009","35.1668","0.0009","20.227","0.0006","90","","90","","120","","21663.5","1","190","2","190","2","","","","","","","","8","R -3 :H","-R 3","148","","BWCu","","- C18 H48 B Cu3 K3 N24 O66 W12 -","- C18 H18 B Cu3 K3 N24 O66 W12 -","- C162 H162 B9 Cu27 K27 N216 O594 W108 -","9","0.5","","Chang, Shenzhen; Chen, Yanhong; An, Haiyan; Zhu, Qingshan; Luo, Huiyun; Huang, Yaohui","Polyoxometalate-based supramolecular porous frameworks with dual-active centers towards highly efficient synthesis of functionalized p-benzoquinones","Green Chemistry","2021","23","21","8591","8603","10.1039/D1GC03061B","","","0.71073","MoKα","","0.0808","0.0775","","","0.1653","0.1667","","","","","","1.35","","","","has coordinates,has disorder","270462","2021-11-06","20:14:41",""
"7243740","15.57","0.003","15.57","0.003","10.337","0.003","90","","90","","120","","2170.2","0.9","296","2","296","2","","","","","","","","8","P -3","-P 3","147","","SiWCu","","- C18 H67 Cu3 K3 N24 O76 Si W12 -","- C18 H18 Cu3 K3 N24 O76 Si W12 -","- C18 H18 Cu3 K3 N24 O76 Si W12 -","1","0.166667","","Chang, Shenzhen; Chen, Yanhong; An, Haiyan; Zhu, Qingshan; Luo, Huiyun; Huang, Yaohui","Polyoxometalate-based supramolecular porous frameworks with dual-active centers towards highly efficient synthesis of functionalized p-benzoquinones","Green Chemistry","2021","23","21","8591","8603","10.1039/D1GC03061B","","","0.71073","MoKα","","0.0475","0.0445","","","0.1258","0.1284","","","","","","1.075","","","","has coordinates,has disorder","270462","2021-11-06","20:14:41",""
"7243782","9.52643","0.00009","14.88162","0.00013","12.71774","0.00011","90","","90.7242","0.0008","90","","1802.83","0.03","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C21 H18 N O3 P -","- C21 H18 N O3 P -","- C84 H72 N4 O12 P4 -","4","1","","Zhu, Yuan-Yuan; Zhang, Tao; Zhou, Linlin; Yang, Shang-Dong","Concise synthesis of N-phosphorylated amides through three-component reactions","Green Chemistry","2021","23","23","9417","9421","10.1039/D1GC03065E","","x-ray","1.54184","CuKα","","0.0387","0.0365","","","0.1057","0.1077","","","","","","1.025","","","","has coordinates","271853","2022-01-06","21:31:17",""
"7243783","15.6285","0.0003","9.3057","0.0002","14.6152","0.0002","90","","95.164","0.002","90","","2116.92","0.07","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C26 H22 N O2 P -","- C26 H22 N O2 P -","- C104 H88 N4 O8 P4 -","4","1","","Zhu, Yuan-Yuan; Zhang, Tao; Zhou, Linlin; Yang, Shang-Dong","Concise synthesis of N-phosphorylated amides through three-component reactions","Green Chemistry","2021","23","23","9417","9421","10.1039/D1GC03065E","","x-ray","1.54184","CuKα","","0.0486","0.0408","","","0.106","0.1137","","","","","","1.034","","","","has coordinates","271853","2022-01-06","21:31:17",""
"7243784","9.87","0.04","20.34","0.08","8.95","0.04","90","0.07","108.57","0.07","90","0.08","1703","12","296","2","296.15","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C22 H18 N2 -","- C22 H18 N2 -","- C88 H72 N8 -","4","1","","Chen, Wei-Li; Li, Kun; Liao, Wei-Cong; Liang, Wang-Fu; Qiu, Pei-Wen; Liang, Cui; Su, Gui-Fa; Mo, Dong-Liang","An iron(iii)-catalyzed dehydrogenative cross-coupling reaction of indoles with benzylamines to prepare 3-aminoindole derivatives","Green Chemistry","2021","23","23","9610","9616","10.1039/D1GC02849A","","","0.71073","MoKα","","0.1015","0.0701","","","0.187","0.2176","","","","","","1.012","","","","has coordinates","271852","2022-01-06","21:31:10",""
"7243785","7.9106","0.0003","10.4113","0.0004","18.0346","0.0009","90","","98.689","0.004","90","","1468.28","0.11","293","2","293","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C20 H14 N2 -","- C20 H14 N2 -","- C80 H56 N8 -","4","1","","Chen, Wei-Li; Li, Kun; Liao, Wei-Cong; Liang, Wang-Fu; Qiu, Pei-Wen; Liang, Cui; Su, Gui-Fa; Mo, Dong-Liang","An iron(iii)-catalyzed dehydrogenative cross-coupling reaction of indoles with benzylamines to prepare 3-aminoindole derivatives","Green Chemistry","2021","23","23","9610","9616","10.1039/D1GC02849A","","x-ray","0.71073","MoKα","","0.1247","0.0639","","","0.1251","0.1526","","","","","","1.034","","","","has coordinates","271852","2022-01-06","21:31:10",""
"7243842","15.4121","0.0006","8.5604","0.0003","15.8404","0.0006","90","","98.365","0.001","90","","2067.65","0.13","100","","100","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C23 H22 I N O4 -","- C23 H22 I N O4 -","- C92 H88 I4 N4 O16 -","4","1","","Wei, Xiaohui; Liang, Xuewu; Li, Yazhou; Liu, Qi; Liu, Xuyi; Zhou, Yu; Liu, Hong","I2-induced cascade cyclization and dearomatization of indoles for the highly efficient synthesis of iodinated and vinylic spiroindolenines","Green Chemistry","2021","23","22","9165","9171","10.1039/D1GC02713A","","","0.71073","MoKα","","0.0244","0.0219","","","0.0504","0.0524","","","","","","1.064","","","","has coordinates","271848","2022-01-06","21:30:29",""
"7243843","9.216","0.005","21.035","0.01","10.878","0.006","90","","98.207","0.019","90","","2087.2","1.9","170","","170","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C25 H25 N O4 -","- C25 H25 N O4 -","- C100 H100 N4 O16 -","4","1","","Wei, Xiaohui; Liang, Xuewu; Li, Yazhou; Liu, Qi; Liu, Xuyi; Zhou, Yu; Liu, Hong","I2-induced cascade cyclization and dearomatization of indoles for the highly efficient synthesis of iodinated and vinylic spiroindolenines","Green Chemistry","2021","23","22","9165","9171","10.1039/D1GC02713A","","","0.71073","MoKα","","0.1381","0.0664","","","0.1388","0.1799","","","","","","1.007","","","","has coordinates","271848","2022-01-06","21:30:30",""
"7243844","8.0055","0.0002","15.3728","0.0005","17.6184","0.0004","90","","101.571","0.001","90","","2124.18","0.1","100","","100","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C23 H22 I N O4 -","- C23 H22 I N O4 -","- C92 H88 I4 N4 O16 -","4","1","","Wei, Xiaohui; Liang, Xuewu; Li, Yazhou; Liu, Qi; Liu, Xuyi; Zhou, Yu; Liu, Hong","I2-induced cascade cyclization and dearomatization of indoles for the highly efficient synthesis of iodinated and vinylic spiroindolenines","Green Chemistry","2021","23","22","9165","9171","10.1039/D1GC02713A","","","0.71073","MoKα","","0.0534","0.0434","","","0.1082","0.1176","","","","","","1.04","","","","has coordinates,has disorder","271848","2022-01-06","21:30:30",""
"7243855","9.4942","0.0008","18.7603","0.001","11.8071","0.0008","90","","112.137","0.009","90","","1948","0.3","100.01","0.1","100.01","0.1","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C22 H19 N O3 S Se -","- C22 H19 N O3 S Se -","- C88 H76 N4 O12 S4 Se4 -","4","1","","Liu, Gong-Qing; Zhou, Chen-Fan; Zhang, Yun-Qian; Yi, Wei; Wang, Peng-Fei; Liu, Ji; Ling, Yong","Visible-light-induced intermolecular aminoselenation of alkenes","Green Chemistry","2021","23","24","9968","9973","10.1039/D1GC03195C","","x-ray","0.71073","MoKα","","0.054","0.0395","","","0.0801","0.0874","","","","","","1.052","","","","has coordinates","271845","2022-01-06","21:29:56",""
"7243856","14.6984","0.0011","11.124","0.0005","14.3493","0.0011","90","","117.396","0.01","90","","2083.1","0.3","149.99","0.1","149.99","0.1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C24 H21 N O3 S Se -","- C24 H21 N O3 S Se -","- C96 H84 N4 O12 S4 Se4 -","4","1","","Liu, Gong-Qing; Zhou, Chen-Fan; Zhang, Yun-Qian; Yi, Wei; Wang, Peng-Fei; Liu, Ji; Ling, Yong","Visible-light-induced intermolecular aminoselenation of alkenes","Green Chemistry","2021","23","24","9968","9973","10.1039/D1GC03195C","","x-ray","0.71073","MoKα","","0.0429","0.0336","","","0.0735","0.0773","","","","","","1.035","","","","has coordinates","271845","2022-01-06","21:29:57",""
"7243857","9.8465","0.0007","23.1935","0.0015","10.1145","0.0008","90","","108.968","0.008","90","","2184.5","0.3","150","0.1","150","0.1","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C24 H29 N O2 S Se -","- C24 H29 N O2 S Se -","- C96 H116 N4 O8 S4 Se4 -","4","2","","Liu, Gong-Qing; Zhou, Chen-Fan; Zhang, Yun-Qian; Yi, Wei; Wang, Peng-Fei; Liu, Ji; Ling, Yong","Visible-light-induced intermolecular aminoselenation of alkenes","Green Chemistry","2021","23","24","9968","9973","10.1039/D1GC03195C","","x-ray","0.71073","MoKα","","0.0471","0.0383","","","0.0703","0.0747","","","","","","1.038","","","","has coordinates","271845","2022-01-06","21:29:57",""
"7243874","12.8766","0.0003","6.3085","0.0001","16.9497","0.0004","90","","90","","90","","1376.86","0.05","169.99","0.1","169.99","0.1","","","","","","","","5","P n a 21","P 2c -2n","33","","","","- C10 H13 N O4 S3 -","- C10 H13 N O4 S3 -","- C40 H52 N4 O16 S12 -","4","1","","Gong, Kai; Zhou, Yilin; Jiang, Xuefeng","From symmetrical tetrasulfides to trisulfide dioxides via photocatalysis","Green Chemistry","2021","23","24","9865","9869","10.1039/D1GC03242A","","x-ray","1.54184","CuKα","","0.033","0.031","","","0.0688","0.0696","","","","","","1.049","","","","has coordinates","271846","2022-01-06","21:30:02",""
"7243893","7.17026","0.00019","21.7971","0.0005","13.6848","0.0004","90","","98.637","0.003","90","","2114.55","0.1","293.1","0.2","293.1","0.2","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C22 H19 Cl F N4 O2 S -","- C22 H18 Cl F N4 O2 S -","- C88 H72 Cl4 F4 N16 O8 S4 -","4","1","","Guo, Sheng-Qiang; Yang, Hui-Qing; Wang, Ai-Lian; Jiang, Yu-Zhen; Xu, Guo-Qiang; Luo, Yong-Chun; Chen, Zhao-Xu; Xu, Peng-Fei","Divergent Ritter-type amination via photoredox catalytic four-component radical-polar crossover reactions","Green Chemistry","2021","23","23","9571","9576","10.1039/D1GC03048E","","x-ray","1.54184","CuKα","","0.0629","0.0545","","","0.1452","0.1552","","","","","","1.04","","","","has coordinates","271851","2022-01-06","21:31:03",""
"7243894","12.7213","0.0003","10.0584","0.0003","17.2909","0.0005","90","","106.273","0.003","90","","2123.84","0.11","292.4","0.4","292.4","0.4","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C23 H20 Cl N O4 S -","- C23 H20 Cl N O4 S -","- C92 H80 Cl4 N4 O16 S4 -","4","1","","Guo, Sheng-Qiang; Yang, Hui-Qing; Wang, Ai-Lian; Jiang, Yu-Zhen; Xu, Guo-Qiang; Luo, Yong-Chun; Chen, Zhao-Xu; Xu, Peng-Fei","Divergent Ritter-type amination via photoredox catalytic four-component radical-polar crossover reactions","Green Chemistry","2021","23","23","9571","9576","10.1039/D1GC03048E","","x-ray","1.54184","CuKα","","0.0474","0.0397","","","0.106","0.1139","","","","","","1.048","","","","has coordinates","271851","2022-01-06","21:31:04",""
"7243895","19.8661","0.0003","9.09317","0.00015","25.7813","0.0004","90","","109.671","0.0018","90","","4385.48","0.13","150","0.2","150","0.2","","","","","","","","5","I 1 2/a 1","-I 2ya","15","","","","- C25 H25 N O4 S -","- C25 H25 N O4 S -","- C200 H200 N8 O32 S8 -","8","1","","Guo, Sheng-Qiang; Yang, Hui-Qing; Wang, Ai-Lian; Jiang, Yu-Zhen; Xu, Guo-Qiang; Luo, Yong-Chun; Chen, Zhao-Xu; Xu, Peng-Fei","Divergent Ritter-type amination via photoredox catalytic four-component radical-polar crossover reactions","Green Chemistry","2021","23","23","9571","9576","10.1039/D1GC03048E","","x-ray","1.54184","CuKα","","0.0481","0.0446","","","0.1253","0.1279","","","","","","1.063","","","","has coordinates","271851","2022-01-06","21:31:04",""
"7243896","8.65981","0.00014","17.7339","0.0002","27.7046","0.0004","90","","90","","90","","4254.66","0.1","293.41","0.1","293.41","0.1","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C23 H22 N4 O2 S -","- C23 H22 N4 O2 S -","- C184 H176 N32 O16 S8 -","8","1","","Guo, Sheng-Qiang; Yang, Hui-Qing; Wang, Ai-Lian; Jiang, Yu-Zhen; Xu, Guo-Qiang; Luo, Yong-Chun; Chen, Zhao-Xu; Xu, Peng-Fei","Divergent Ritter-type amination via photoredox catalytic four-component radical-polar crossover reactions","Green Chemistry","2021","23","23","9571","9576","10.1039/D1GC03048E","","x-ray","1.54184","CuKα","","0.0509","0.0411","","","0.1066","0.1142","","","","","","1.037","","","","has coordinates","271851","2022-01-06","21:31:04",""
"7243979","7.78804","0.00005","10.18953","0.00007","19.93923","0.00014","90","","90","","90","","1582.31","0.019","100","0.1","100","0.1","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C16 H19 Cl N2 O -","- C16 H19 Cl N2 O -","- C64 H76 Cl4 N8 O4 -","4","1","","Fauziev, Ruslan V.; Ivanov, Roman E.; Kuchurov, Ilya V.; Zlotin, Sergei G.","A carbon dioxide-promoted three-component Strecker reaction","Green Chemistry","2021","23","24","10137","10144","10.1039/D1GC03161A","","x-ray","1.54184","CuKα","","0.0249","0.0246","","","0.0639","0.0642","","","","","","1.072","","","","has coordinates","271847","2022-01-06","21:30:08",""
"7244045","10.9525","0.0003","12.9657","0.0004","20.7069","0.0007","90","","103.542","0.003","90","","2858.77","0.16","293","2","293","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C18 H13 N3 -","- C18 H13 N3 -","- C144 H104 N24 -","8","1","","Gong, Ming; Huang, Mengmeng; Li, Yabo; Zhang, Jianye; Kim, Jung Keun; Kim, Jong Seung; Wu, Yangjie","Harnessing visible-light energy for unbiased organic photoelectrocatalysis: synthesis of N-bearing fused rings","Green Chemistry","2022","24","2","837","845","10.1039/D1GC03587H","","x-ray","1.54184","CuKα","","0.0544","0.0439","","","0.1125","0.123","","","","","","1.043","","","","has coordinates","272704","2022-02-04","19:51:00",""
"7244046","8.5331","0.0006","9.1322","0.0006","11.9513","0.001","77.749","0.006","79.907","0.007","65.413","0.007","823.62","0.12","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C19 H15 Br N2 O2 -","- C19 H15 Br N2 O2 -","- C38 H30 Br2 N4 O4 -","2","1","","Gong, Ming; Huang, Mengmeng; Li, Yabo; Zhang, Jianye; Kim, Jung Keun; Kim, Jong Seung; Wu, Yangjie","Harnessing visible-light energy for unbiased organic photoelectrocatalysis: synthesis of N-bearing fused rings","Green Chemistry","2022","24","2","837","845","10.1039/D1GC03587H","","x-ray","1.54184","CuKα","","0.0491","0.0372","","","0.0835","0.0907","","","","","","1.041","","","","has coordinates","272704","2022-02-04","19:51:00",""
"7244047","7.5372","0.0007","7.833","0.0005","13.1572","0.0011","81.704","0.006","86.697","0.007","83.076","0.006","762.41","0.11","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C19 H15 N3 O -","- C19 H15 N3 O -","- C38 H30 N6 O2 -","2","1","","Gong, Ming; Huang, Mengmeng; Li, Yabo; Zhang, Jianye; Kim, Jung Keun; Kim, Jong Seung; Wu, Yangjie","Harnessing visible-light energy for unbiased organic photoelectrocatalysis: synthesis of N-bearing fused rings","Green Chemistry","2022","24","2","837","845","10.1039/D1GC03587H","","x-ray","1.54184","CuKα","","0.066","0.0466","","","0.1078","0.122","","","","","","1.061","","","","has coordinates","272704","2022-02-04","19:51:00",""
"7244048","17.7291","0.0006","7.5614","0.0002","8.1518","0.0002","90","","102.867","0.003","90","","1065.36","0.05","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C12 H14 O3 -","- C12 H14 O3 -","- C48 H56 O12 -","4","1","","Hu, Deqing; Jiang, Xuefeng","Stepwise benzylic oxygenation via uranyl-photocatalysis","Green Chemistry","2022","24","1","124","129","10.1039/D1GC04042A","","x-ray","1.54184","CuKα","","0.0559","0.0499","","","0.1432","0.1488","","","","","","1.075","","","","has coordinates","272702","2022-02-04","19:50:48",""
"7244160","4.8673","0.0012","11.348","0.003","27.751","0.006","90","","90","","90","","1532.8","0.6","174","2","174.29","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C15 H12 Br N3 O2 S -","- C15 H12 Br N3 O2 S -","- C60 H48 Br4 N12 O8 S4 -","4","1","","Prasanth, Thumpati; Chakraborti, Gargi; Mandal, Tirtha; Ravichandiran, Velayutham; Dash, Jyotirmayee","Cycloaddition of N-sulfonyl and N-sulfamoyl azides with alkynes in aqueous media for the selective synthesis of 1,2,3-triazoles","Green Chemistry","2022","24","2","911","915","10.1039/D1GC03340A","","","0.71073","MoKα","","0.0392","0.0317","","","0.0641","0.0665","","","","","","1.06","","","","has coordinates","272703","2022-02-04","19:50:53",""
"7244161","5.3437","0.0005","14.4207","0.0016","16.6141","0.0016","90","","90","","90","","1280.3","0.2","100","2","99.83","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C11 H14 N4 O3 S -","- C11 H14 N4 O3 S -","- C44 H56 N16 O12 S4 -","4","1","","Prasanth, Thumpati; Chakraborti, Gargi; Mandal, Tirtha; Ravichandiran, Velayutham; Dash, Jyotirmayee","Cycloaddition of N-sulfonyl and N-sulfamoyl azides with alkynes in aqueous media for the selective synthesis of 1,2,3-triazoles","Green Chemistry","2022","24","2","911","915","10.1039/D1GC03340A","","","0.71073","MoKα","","0.045","0.0424","","","0.0905","0.0923","","","","","","1.07","","","","has coordinates","272703","2022-02-04","19:50:53",""
"7244265","8.7824","0.0002","8.8235","0.0001","22.0837","0.0004","90","","95.202","0.002","90","","1704.25","0.05","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","diisopropylammonium sulfate","","- C12 H32 N2 O4 S -","- C12 H32 N2 O4 S -","- C48 H128 N8 O16 S4 -","4","1","","Turek, Marika; Biczak, Robert; Pawłowska, Barbara; Różycka-Sokołowska, Ewa; Owsianik, Krzysztof; Marciniak, Bernard; Bałczewski, Piotr","The need to change the approach to the safe use of herbicides by developing chiral and environmentally friendly formulations: a series of enantioselective (R)- and (S)-phenylethylammonium chloroacetates","Green Chemistry","2022","24","4","1693","1703","10.1039/D1GC03970A","","","1.54184","CuKα","","0.0366","0.0349","","","0.096","0.0979","","","","","","1.035","","","","has coordinates,has disorder","273377","2022-03-04","22:16:54",""
"7244297","11.353","0.008","13.367","0.008","12.835","0.007","90","","100.25","0.02","90","","1917","2","293","2","293.15","","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C23 H26 O3 -","- C23 H26 O3 -","- C92 H104 O12 -","4","1","","Sharapov, Ainur D.; Fatykhov, Ramil F.; Khalymbadzha, Igor A.; Sharutin, Vladimir V.; Santra, Sougata; Zyryanov, Grigory V.; Chupakhin, Oleg N.; Ranu, Brindaban C.","Mechanochemical synthesis of coumarins via Pechmann condensation under solvent-free conditions: an easy access to coumarins and annulated pyrano[2,3-f] and [3,2-f]indoles","Green Chemistry","2022","24","6","2429","2437","10.1039/D1GC04564D","","","0.71073","MoKα","","0.0986","0.0705","","","0.212","0.2405","","","","","","1.036","","","","has coordinates","274990","2022-05-05","20:37:33",""
"7244371","10.5639","0.0001","21.9239","0.0002","10.4796","0.0001","90","","111.989","0.001","90","","2250.54","0.04","123","0.1","123","0.1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C26 H32 O4 -","- C26 H32 O4 -","- C104 H128 O16 -","4","1","","Zhao, Quan-Qing; Rehbein, Julia; Reiser, Oliver","Thermoneutral synthesis of spiro-1,4-cyclohexadienes by visible-light-driven dearomatization of benzylmalonates","Green Chemistry","2022","24","7","2772","2776","10.1039/D1GC04686A","","x-ray","1.54184","CuKα","","0.0452","0.0403","","","0.1024","0.1059","","","","","","1.039","","","","has coordinates,has disorder","274998","2022-05-05","20:38:53",""
"7244381","10.1132","0.0013","5.7769","0.0007","20.392","0.003","90","","90","","90","","1191.4","0.3","296","2","296","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C13 H17 N O2 -","- C13 H17 N O2 -","- C52 H68 N4 O8 -","4","1","","Liu, Xiao-Dong; Wang, Qiu-An; Zhu, Yan-Ping; Peng, Zhi-Hong; Li, Jin-Heng","Copper-catalyzed aerobic hydroxyamination of alkenes of unsaturated keto oximes in EtOH toward cyclic nitrones","Green Chemistry","2022","24","6","2476","2482","10.1039/D2GC00017B","","","0.71073","MoKα","","0.0321","0.0284","","","0.0738","0.0772","","","","","","1.04","","","","has coordinates","274989","2022-05-05","20:37:24",""
"7244382","12.0038","0.0006","12.5724","0.0006","8.96","0.0004","90","","100.273","0.002","90","","1330.54","0.11","150","","150","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H12 N2 O -","- C17 H12 N2 O -","- C68 H48 N8 O4 -","4","1","","Li, Jianxiao; He, Dan; Lin, Zidong; Cen, Liying; Wu, Wanqing; Jiang, Huanfeng","NHC–palladium-catalyzed ionic liquid-accelerated regioselective oxyarylation of alkynes with diaryl ethers","Green Chemistry","2022","24","5","1983","1988","10.1039/D1GC04556C","","","0.71073","MoKα","","0.0601","0.0399","","","0.0875","0.1011","","","","","","1.065","","","","has coordinates","274988","2022-05-05","20:37:13",""
"7244383","12.7847","0.0002","19.6339","0.0003","14.688","0.0002","90","","91.112","0.001","90","","3686.19","0.09","100","0.1","100","0.1","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C46 H39 N O P2 Ru -","- C46 H39 N O P2 Ru -","- C184 H156 N4 O4 P8 Ru4 -","4","1","","Kar, Sayan; Luo, Jie; Rauch, Michael; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David","Dehydrogenative ester synthesis from enol ethers and water with a ruthenium complex catalyzing two reactions in synergy","Green Chemistry","2022","24","4","1481","1487","10.1039/D1GC04574A","","x-ray","0.71073","MoKα","","0.0414","0.0322","","","0.0742","0.0775","","","","","","1.053","","","","has coordinates","273376","2022-03-04","22:16:47",""
"7244424","21.1362","0.0006","11.2833","0.0002","38.192","0.002","90","","104.463","0.004","90","","8819.6","0.6","297","2","297","2","","","","","","","","7","I 1 2/a 1","-I 2ya","15","","","","- C336 H312 Cl16 Cu8 N32 O68 S16 -","- C336 H312 Cl16 Cu8 N32 O68 S16 -","- C336 H312 Cl16 Cu8 N32 O68 S16 -","1","0.125","","Jana, Narayan Ch.; Sethi, Subrat; Saha, Ratnakar; Bagh, Bidraha","Aerobic oxidation of vanillyl alcohol to vanillin catalyzed by air-stable and recyclable copper complex and TEMPO under base-free conditions","Green Chemistry","2022","24","6","2542","2556","10.1039/D1GC04690J","","x-ray","1.54184","CuKα","","0.1247","0.1106","","","0.2839","0.2952","","","","","","1.063","","","","has coordinates","274993","2022-05-05","20:38:18",""
"7244425","17.0171","0.0003","9.2223","0.0001","13.3042","0.0002","90","","96.124","0.002","90","","2076","0.05","100.01","0.1","100.01","0.1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C21 H22 Cl2 Cu N2 S -","- C21 H22 Cl2 Cu N2 S -","- C84 H88 Cl8 Cu4 N8 S4 -","4","1","","Jana, Narayan Ch.; Sethi, Subrat; Saha, Ratnakar; Bagh, Bidraha","Aerobic oxidation of vanillyl alcohol to vanillin catalyzed by air-stable and recyclable copper complex and TEMPO under base-free conditions","Green Chemistry","2022","24","6","2542","2556","10.1039/D1GC04690J","","x-ray","1.54184","CuKα","","0.0423","0.0406","","","0.1082","0.1098","","","","","","1.042","","","","has coordinates","274993","2022-05-05","20:38:18",""
"7244426","8.7543","0.0002","8.91433","0.00017","14.2328","0.0006","92.973","0.003","97.234","0.003","113.73","0.002","1002.26","0.06","100","0.1","100","0.1","","","","","","","","6","P -1","-P 1","2","","","","- C21 H20 Cl2 Cu N2 S -","- C21 H20 Cl2 Cu N2 S -","- C42 H40 Cl4 Cu2 N4 S2 -","2","1","","Jana, Narayan Ch.; Sethi, Subrat; Saha, Ratnakar; Bagh, Bidraha","Aerobic oxidation of vanillyl alcohol to vanillin catalyzed by air-stable and recyclable copper complex and TEMPO under base-free conditions","Green Chemistry","2022","24","6","2542","2556","10.1039/D1GC04690J","","","1.54184","CuKα","","0.0873","0.0853","","","0.2628","0.2633","","","","","","1.194","","","","has coordinates","274993","2022-05-05","20:38:18",""
"7244427","19.10688","0.00011","9.75754","0.00006","26.37158","0.00016","90","","90","","90","","4916.62","0.05","100","0.1","100","0.1","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C22 H23 Cl5 Cu N2 S -","- C22 H23 Cl5 Cu N2 S -","- C176 H184 Cl40 Cu8 N16 S8 -","8","1","","Jana, Narayan Ch.; Sethi, Subrat; Saha, Ratnakar; Bagh, Bidraha","Aerobic oxidation of vanillyl alcohol to vanillin catalyzed by air-stable and recyclable copper complex and TEMPO under base-free conditions","Green Chemistry","2022","24","6","2542","2556","10.1039/D1GC04690J","","","1.54184","CuKα","","0.0539","0.0513","","","0.0988","0.1001","","","","","","1.098","","","","has coordinates","274993","2022-05-05","20:38:18",""
"7244428","15.4634","0.0001","16.5496","0.0001","18.8584","0.0001","90","","111.195","0.001","90","","4499.65","0.06","293","2","293","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C43 H48 Cl2 Cu N4 O9 S2 -","- C43 H48 Cl2 Cu N4 O9 S2 -","- C172 H192 Cl8 Cu4 N16 O36 S8 -","4","1","","Jana, Narayan Ch.; Sethi, Subrat; Saha, Ratnakar; Bagh, Bidraha","Aerobic oxidation of vanillyl alcohol to vanillin catalyzed by air-stable and recyclable copper complex and TEMPO under base-free conditions","Green Chemistry","2022","24","6","2542","2556","10.1039/D1GC04690J","","","1.54184","CuKα","","0.0765","0.0736","","","0.2109","0.2138","","","","","","1.083","","","","has coordinates","274993","2022-05-05","20:38:18",""
"7244481","13.5207","0.0004","11.759","0.0003","7.7352","0.0002","90","","97.6","0.002","90","","1219.02","0.06","229.99","0.1","229.99","0.1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C14 H10 O6 -","- C14 H10 O6 -","- C56 H40 O24 -","4","1","","Gan, Shaoyan; Yin, Jingru; Yu, Zhiyou; Song, Lijuan; Shi, Lei","A one-pot and two-stage Baeyer–Villiger reaction using 2,2′-diperoxyphenic acid under biomolecule-compatible conditions","Green Chemistry","2022","24","5","2232","2239","10.1039/D1GC04478H","","x-ray","1.54184","CuKα","","0.0556","0.0522","","","0.1475","0.1525","","","","","","1.052","","","","has coordinates","274987","2022-05-05","20:37:07",""
"7244482","26.979","0.004","9.2286","0.0012","14.3392","0.0019","90","","102.602","0.002","90","","3484.1","0.8","296","1","296","1","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C20 H19 N O2 S -","- C20 H19 N O2 S -","- C160 H152 N8 O16 S8 -","8","1","","He, Jin-Yu; Qian, Wei-Feng; Wang, Yan-Zhao; Yao, Chaochao; Wang, Nana; Liu, Huilin; Zhong, Bing; Zhu, Cuiju; Xu, Hao","Sustainable electrochemical dehydrogenative C(sp3)–H mono/di-alkylations","Green Chemistry","2022","24","6","2483","2491","10.1039/D1GC04479F","","","0.71073","MoKα","","0.0609","0.0439","","","0.1228","0.1375","","","","","","1.026","","","","has coordinates","274991","2022-05-05","20:37:42",""
"7244483","8.224","0.004","14.043","0.007","21.164","0.01","90","","90","","90","","2444","2","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C30 H31 N O3 -","- C30 H31 N O3 -","- C120 H124 N4 O12 -","4","1","","He, Jin-Yu; Qian, Wei-Feng; Wang, Yan-Zhao; Yao, Chaochao; Wang, Nana; Liu, Huilin; Zhong, Bing; Zhu, Cuiju; Xu, Hao","Sustainable electrochemical dehydrogenative C(sp3)–H mono/di-alkylations","Green Chemistry","2022","24","6","2483","2491","10.1039/D1GC04479F","","","1.34139","GaKα","","0.1001","0.0694","","","0.1734","0.207","","","","","","1.099","","","","has coordinates","274991","2022-05-05","20:37:42",""
"7244484","8.0026","0.0011","15.666","0.002","8.8626","0.0012","90","","93.268","0.003","90","","1109.3","0.3","296","2","296","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C26 H29 N O3 -","- C26 H29 N O3 -","- C52 H58 N2 O6 -","2","1","","He, Jin-Yu; Qian, Wei-Feng; Wang, Yan-Zhao; Yao, Chaochao; Wang, Nana; Liu, Huilin; Zhong, Bing; Zhu, Cuiju; Xu, Hao","Sustainable electrochemical dehydrogenative C(sp3)–H mono/di-alkylations","Green Chemistry","2022","24","6","2483","2491","10.1039/D1GC04479F","","","0.71073","MoKα","","0.1044","0.0555","","","0.0955","0.1114","","","","","","1.004","","","","has coordinates","274991","2022-05-05","20:37:42",""
"7244523","12.6825","0.0003","14.325","0.0004","26.5675","0.0006","90","","90","","90","","4826.7","0.2","297","2","297","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C26 H25 N3 O6 -","- C26 H25 N3 O6 -","- C208 H200 N24 O48 -","8","1","","Maiti, Debajit; Das, Ranajit; Prabakar, Tejas; Sen, Subhabrata","Blue LED induced solvent-free multicomponent reactions among aryl diazoacetates, pyridine derivatives and maleimides: direct eco-friendly synthesis of densely functionalized itaconimides","Green Chemistry","2022","24","7","3001","3008","10.1039/D1GC03546K","","","0.71073","MoKα","","0.1499","0.1071","","","0.288","0.3348","","","","","","1.068","","","","has coordinates","274995","2022-05-05","20:38:32",""
"7244542","16.3085","0.0004","7.9252","0.0002","21.384","0.0006","90","","90","","90","","2763.84","0.12","110","","110","","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C15 H20 O4 -","- C15 H20 O4 -","- C120 H160 O32 -","8","1","","Sengoden, Mani; Bhat, Gulzar A.; Darensbourg, Donald J.","Explorations into the sustainable synthesis of cyclic and polymeric carbonates and thiocarbonates from eugenol-derived monomers and their reactions with CO2, COS, or CS2","Green Chemistry","2022","24","6","2535","2541","10.1039/D2GC00327A","","","1.54178","CuKα","","0.074","0.0719","","","0.1937","0.1962","","","","","","1.073","","","","has coordinates","274992","2022-05-05","20:37:57",""
"7244543","13.9329","0.0005","6.1434","0.0002","19.2618","0.0007","90","","96.736","0.0015","90","","1637.34","0.1","110","","110","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C16 H20 O5 S -","- C16 H20 O5 S -","- C64 H80 O20 S4 -","4","1","","Sengoden, Mani; Bhat, Gulzar A.; Darensbourg, Donald J.","Explorations into the sustainable synthesis of cyclic and polymeric carbonates and thiocarbonates from eugenol-derived monomers and their reactions with CO2, COS, or CS2","Green Chemistry","2022","24","6","2535","2541","10.1039/D2GC00327A","","","1.54178","CuKα","","0.037","0.0353","","","0.0949","0.0962","","","","","","1.055","","","","has coordinates","274992","2022-05-05","20:37:58",""
"7244544","10.8206","0.0005","6.2424","0.0003","12.0066","0.0005","90","","109.921","0.001","90","","762.48","0.06","110","","110","","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C16 H20 O6 -","- C16 H20 O6 -","- C32 H40 O12 -","2","1","","Sengoden, Mani; Bhat, Gulzar A.; Darensbourg, Donald J.","Explorations into the sustainable synthesis of cyclic and polymeric carbonates and thiocarbonates from eugenol-derived monomers and their reactions with CO2, COS, or CS2","Green Chemistry","2022","24","6","2535","2541","10.1039/D2GC00327A","","","1.54178","CuKα","","0.0322","0.0308","","","0.0793","0.0802","","","","","","1.057","","","","has coordinates","274992","2022-05-05","20:37:58",""
"7244545","21.6035","0.0006","7.9904","0.0002","16.8357","0.0005","90","","90","","90","","2906.19","0.14","110","","110","","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C15 H20 O3 S -","- C15 H20 O3 S -","- C120 H160 O24 S8 -","8","2","","Sengoden, Mani; Bhat, Gulzar A.; Darensbourg, Donald J.","Explorations into the sustainable synthesis of cyclic and polymeric carbonates and thiocarbonates from eugenol-derived monomers and their reactions with CO2, COS, or CS2","Green Chemistry","2022","24","6","2535","2541","10.1039/D2GC00327A","","","0.71073","MoKα","","0.0599","0.0555","","","0.1589","0.1629","","","","","","1.07","","","","has coordinates,has disorder","274992","2022-05-05","20:37:58",""
"7244580","16.392","0.0006","7.1332","0.0004","20.1084","0.0008","90","","95.662","0.004","90","","2339.75","0.18","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H12 N2 O -","- C15 H12 N2 O -","- C120 H96 N16 O8 -","8","2","","Ren, Jie; Pi, Chao; Cui, Xiuling; Wu, Yangjie","Divergent C(sp2)–H arylation of heterocycles via organic photoredox catalysis","Green Chemistry","2022","24","7","3017","3022","10.1039/D1GC04825B","","x-ray","1.54184","CuKα","","0.0687","0.0497","","","0.1265","0.1434","","","","","","1.045","","","","has coordinates","274997","2022-05-05","20:38:47",""
"7244581","8.9535","0.0003","14.0575","0.0005","9.4542","0.0003","90","","90.799","0.002","90","","1189.83","0.07","149.44","","149.44","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C15 H12 O3 -","- C15 H12 O3 -","- C60 H48 O12 -","4","1","","Zhou, Bei; He, Yu-Juan; Tao, Yun-Feng; Liu, Lan-Xiang; Hu, Min; Chang, Zu-Hui; Lei, Hong; Lin, Jun; Lin, Tong; Du, Guan-Ben","Electrocatalytic synthesis of α,α-gem-dihalide ketones from α-mono-halide ketones and unexpected dimer condensation","Green Chemistry","2022","24","7","2859","2870","10.1039/D1GC04584A","","","1.54178","CuKα","","0.0826","0.0669","","","0.1616","0.1745","","","","","","1.097","","","","has coordinates","274999","2022-05-05","20:38:59",""
"7244591","7.9813","0.0006","11.4019","0.001","17.8408","0.0008","92.73","0.005","90.852","0.005","108.525","0.007","1536.9","0.2","100","0.1","100","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C19 H19 N O2 -","- C19 H19 N O2 -","- C76 H76 N4 O8 -","4","2","","Chen, Zhiyan; Huang, Wenbo; Yi, Liqi; Dong, Xiaohan; Sheng, Keyan; Li, Minghao; Bai, Rongxian; Sidorenko, A. Yu.; Huang, Jiang; Gu, Yanlong","Synthesis of indoles and carbazoles from a lignin model compound α-hydroxyacetophenone","Green Chemistry","2022","24","7","2919","2926","10.1039/D1GC04892A","","x-ray","1.54184","CuKα","","0.1128","0.1046","","","0.3058","0.313","","","","","","1.039","","","","has coordinates","274996","2022-05-05","20:38:40",""
"7244592","8.21","0.0004","9.4039","0.0006","10.1909","0.0008","111.938","0.007","99.562","0.005","97.455","0.005","703.68","0.09","293.75","0.1","293.75","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C18 H17 N O2 -","- C18 H17 N O2 -","- C36 H34 N2 O4 -","2","1","","Chen, Zhiyan; Huang, Wenbo; Yi, Liqi; Dong, Xiaohan; Sheng, Keyan; Li, Minghao; Bai, Rongxian; Sidorenko, A. Yu.; Huang, Jiang; Gu, Yanlong","Synthesis of indoles and carbazoles from a lignin model compound α-hydroxyacetophenone","Green Chemistry","2022","24","7","2919","2926","10.1039/D1GC04892A","","x-ray","0.71073","MoKα","","0.0469","0.0407","","","0.1009","0.1065","","","","","","1.043","","","","has coordinates","274996","2022-05-05","20:38:41",""
"7244593","11.7113","0.0006","9.8511","0.0005","25.285","0.0014","90","","97.144","0.005","90","","2894.5","0.3","293.75","0.1","293.75","0.1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C18 H17 N O2 -","- C18 H17 N O2 -","- C144 H136 N8 O16 -","8","2","","Chen, Zhiyan; Huang, Wenbo; Yi, Liqi; Dong, Xiaohan; Sheng, Keyan; Li, Minghao; Bai, Rongxian; Sidorenko, A. Yu.; Huang, Jiang; Gu, Yanlong","Synthesis of indoles and carbazoles from a lignin model compound α-hydroxyacetophenone","Green Chemistry","2022","24","7","2919","2926","10.1039/D1GC04892A","","x-ray","0.71073","MoKα","","0.0595","0.0479","","","0.1163","0.125","","","","","","1.013","","","","has coordinates","274996","2022-05-05","20:38:41",""
"7244594","12.6474","0.0009","7.3679","0.0005","17.5437","0.0013","90","","110.655","0.009","90","","1529.7","0.2","99.99","0.1","99.99","0.1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C19 H19 N O2 -","- C19 H19 N O2 -","- C76 H76 N4 O8 -","4","1","","Chen, Zhiyan; Huang, Wenbo; Yi, Liqi; Dong, Xiaohan; Sheng, Keyan; Li, Minghao; Bai, Rongxian; Sidorenko, A. Yu.; Huang, Jiang; Gu, Yanlong","Synthesis of indoles and carbazoles from a lignin model compound α-hydroxyacetophenone","Green Chemistry","2022","24","7","2919","2926","10.1039/D1GC04892A","","x-ray","1.54184","CuKα","","0.0589","0.0474","","","0.1173","0.1276","","","","","","1.036","","","","has coordinates","274996","2022-05-05","20:38:41",""
"7244625","11.9441","0.0016","12.2012","0.0017","13.45","0.0019","76.259","0.002","72.322","0.002","79.906","0.002","1802.8","0.4","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C42 H36 N4 O2 S2 -","- C42 H36 N4 O2 S2 -","- C84 H72 N8 O4 S4 -","2","1","","Chen, Ziren; Xue, Fei; Liu, Tianxiang; Wang, Bin; Zhang, Yonghong; Jin, Weiwei; Xia, Yu; Liu, Chenjiang","Synthesis of β-hydroxysulfides via visible-light-driven and EDA complex-promoted hydroxysulfenylation of styrenes with heterocyclic thiols in EtOH under photocatalyst-free conditions","Green Chemistry","2022","24","8","3250","3256","10.1039/D2GC00121G","","","0.71073","MoKα","","0.0628","0.0417","","","0.1007","0.1137","","","","","","1.024","","","","has coordinates","274985","2022-05-05","20:36:44",""
"7244626","24.764","0.005","12.538","0.003","13.43","0.003","90","","91.148","0.003","90","","4169.1","1.6","296.15","","296.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C87 H71 Cl8 N8 O4 S4 -","- C87 H71 Cl8 N8 O4 S4 -","- C174 H142 Cl16 N16 O8 S8 -","2","0.5","","Chen, Ziren; Xue, Fei; Liu, Tianxiang; Wang, Bin; Zhang, Yonghong; Jin, Weiwei; Xia, Yu; Liu, Chenjiang","Synthesis of β-hydroxysulfides via visible-light-driven and EDA complex-promoted hydroxysulfenylation of styrenes with heterocyclic thiols in EtOH under photocatalyst-free conditions","Green Chemistry","2022","24","8","3250","3256","10.1039/D2GC00121G","","","0.71073","MoKα","","0.0807","0.0494","","","0.1375","0.1564","","","","","","1.038","","","","has coordinates","274985","2022-05-05","20:36:55",""
"7244644","4.998","0.0005","19.0007","0.0014","18.7257","0.0019","90","","96.275","0.011","90","","1767.6","0.3","150","0.7","150","0.7","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C24 H16 O5 -","- C24 H16 O5 -","- C96 H64 O20 -","4","1","","Karmakar, Indrajit; Brahmachari, Goutam","Electrochemical and mechanochemical synthesis of dihydrofuro[3,2-c]chromenones via intramolecular Csp3–H cross-dehydrogenative oxygenation within warfarin frameworks: an efficient and straightforward dual approach","Green Chemistry","2022","24","7","2825","2838","10.1039/D2GC00146B","","x-ray","0.71073","MoKα","","0.1489","0.0982","","","0.2102","0.2541","","","","","","0.934","","","","has coordinates","274994","2022-05-05","20:38:25",""
"7244664","9.1359","0.0003","10.8744","0.0003","12.1839","0.0002","83.076","0.002","88.393","0.002","84.055","0.002","1195","0.06","149.98","0.1","149.98","0.1","","","","","","","","3","P -1","-P 1","2","","","","- C29 H24 O5 -","- C29 H24 O5 -","- C58 H48 O10 -","2","1","","Chen, Li; Niu, Shengtong; Lan, Shouang; Liu, Wenjun; Yang, Shuang; Fang, Xinqiang","Organocatalyzed trifunctionalization of alkynyl 1,2-diones for the concise synthesis of acyloxy allylidene malonates and γ-alkylidenebutenolides","Green Chemistry","2022","24","9","3623","3628","10.1039/D2GC00061J","","x-ray","1.54184","CuKα","","0.0558","0.051","","","0.1428","0.1498","","","","","","1.0271","","","","has coordinates","275786","2022-06-06","01:47:51",""
"7244665","12.0593","0.0007","16.1161","0.001","20.7106","0.0009","90","","90","","90","","4025.1","0.4","293","2","293","2","","","","","","","","3","P c c n","-P 2ab 2ac","56","","","","- C23 H20 O6 -","- C23 H20 O6 -","- C184 H160 O48 -","8","1","","Chen, Li; Niu, Shengtong; Lan, Shouang; Liu, Wenjun; Yang, Shuang; Fang, Xinqiang","Organocatalyzed trifunctionalization of alkynyl 1,2-diones for the concise synthesis of acyloxy allylidene malonates and γ-alkylidenebutenolides","Green Chemistry","2022","24","9","3623","3628","10.1039/D2GC00061J","","","1.3414","GaKα","","0.0804","0.067","","","0.1843","0.2027","","","","","","1.07","","","","has coordinates","275786","2022-06-06","01:47:51",""
"7244666","16.277","0.003","14.959","0.003","19.366","0.004","90","","90","","90","","4715.4","1.6","293","2","293","2","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C28 H24 O5 -","- C28 H24 O5 -","- C224 H192 O40 -","8","1","","Chen, Li; Niu, Shengtong; Lan, Shouang; Liu, Wenjun; Yang, Shuang; Fang, Xinqiang","Organocatalyzed trifunctionalization of alkynyl 1,2-diones for the concise synthesis of acyloxy allylidene malonates and γ-alkylidenebutenolides","Green Chemistry","2022","24","9","3623","3628","10.1039/D2GC00061J","","","0.71073","MoKα","","0.1053","0.0931","","","0.1925","0.2006","","","","","","1.004","","","","has coordinates","275786","2022-06-06","01:47:51",""
"7244667","20.333","0.004","6.4811","0.0013","35.365","0.007","90","","90","","90","","4660.4","1.6","293","2","293","2","","","","","","","","3","P n a 21","P 2c -2n","33","","","","- C28 H24 O5 -","- C28 H24 O5 -","- C224 H192 O40 -","8","2","","Chen, Li; Niu, Shengtong; Lan, Shouang; Liu, Wenjun; Yang, Shuang; Fang, Xinqiang","Organocatalyzed trifunctionalization of alkynyl 1,2-diones for the concise synthesis of acyloxy allylidene malonates and γ-alkylidenebutenolides","Green Chemistry","2022","24","9","3623","3628","10.1039/D2GC00061J","","","0.71073","MoKα","","0.0738","0.0592","","","0.1427","0.1542","","","","","","1.119","","","","has coordinates","275786","2022-06-06","01:47:51",""
"7244670","6.3843","0.0011","7.1053","0.0012","15.724","0.003","90","","100.963","0.007","90","","700.3","0.2","100","2","100","2","","","","","","","","5","P 1 21/m 1","-P 2yb","11","","(Z)-3-((4-bromophenyl)amino)-1-phenylbut-2-en-1-one","","- C16 H14 Br N O -","- C16 H14 Br0.5 N O -","- C32 H28 Br N2 O2 -","2","0.5","","Goh, Jeffrey; Ong, Seng Kheong; Tan, Yan Sheng; Loh, Teck-Peng","Catalyst-free C–N bond formation under biocompatible reaction conditions","Green Chemistry","2022","24","8","3321","3325","10.1039/D2GC00027J","","x-ray","0.71073","MoKα","","0.0415","0.0298","","","0.0621","0.066","","","","","","1.042","","","","has coordinates,has disorder","274982","2022-05-05","20:36:23",""
"7244678","20.3983","0.0008","8.668","0.0003","14.0946","0.0006","90","","125.998","0.002","90","","2016.2","0.15","301","2","301","2","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C17 H22 N2 O6 -","- C17 H22 N2 O6 -","- C68 H88 N8 O24 -","4","1","","Yuan, Zhenbo; Lu, Liushen; Liu, Meiling; Liu, Xuanzhong; Liu, Changmei; Yin, Dejing; Zhang, Yan; Rao, Yijian","Natural product cercosporin as a bioinspired photocatalyst for the synthesis of peptides containing kynurenine via an energy transfer mechanism","Green Chemistry","2022","24","8","3277","3283","10.1039/D2GC00116K","","","1.54178","CuKα","","0.062","0.0596","","","0.1787","0.1829","","","","","","1.179","","","","has coordinates","274986","2022-05-05","20:37:02",""
"7244714","6.5529","0.0001","7.7286","0.0001","27.9324","0.0002","90","","93.449","0.001","90","","1412.07","0.03","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","2-(Benzylsulfonyl)-1-(4-nitrophenyl)ethan-1-one","","- C15 H13 N O5 S -","- C15 H13 N O5 S -","- C60 H52 N4 O20 S4 -","4","1","","Chikunova, Elena I.; Kukushkin, Vadim Yu.; Dubovtsev, Alexey Yu.","Atom-economic synthesis of β-ketosulfones based on gold-catalyzed highly regioselective hydration of alkynylsulfones","Green Chemistry","2022","24","8","3314","3320","10.1039/D2GC00541G","","","1.54184","CuKα","","0.0331","0.0319","","","0.0867","0.0878","","","","","","1.088","","","","has coordinates","274984","2022-05-05","20:36:36",""
"7244715","11.1683","0.0005","9.4026","0.0004","16.7625","0.0009","90","","95.079","0.005","90","","1753.34","0.14","303.84","0.1","303.84","0.1","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C17 H18 Br N O3 S -","- C17 H18 Br N O3 S -","- C68 H72 Br4 N4 O12 S4 -","4","1","","Guo, Sheng-Qiang; Yang, Hui-Qing; Jiang, Yu-Zhen; Wang, Ai-Lian; Xu, Guo-Qiang; Luo, Yong-Chun; Chen, Zhao-Xu; Zheng, Haixue; Xu, Peng-Fei","Organophotoredox catalytic four-component radical-polar crossover cascade reactions for the stereoselective synthesis of β-amido sulfones","Green Chemistry","2022","24","8","3120","3124","10.1039/D2GC00224H","","x-ray","0.71073","MoKα","","0.097","0.0563","","","0.1118","0.1262","","","","","","1.025","","","","has coordinates","274983","2022-05-05","20:36:30",""
"7244749","24.355","0.002","6.4076","0.0007","13.2555","0.0016","90","","90","","90","","2068.6","0.4","293","2","293","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C27 H25 N O3 -","- C27 H25 N O3 -","- C108 H100 N4 O12 -","4","1","","Dong, Pei-Zhen; Qiu, Bin; An, Xiao-De; Xiao, Jian","Cascade dearomative [4 + 2] cycloaddition of indoles with in situ generated ortho-quinone methides: practical access to divergent indoline-fused polycycles","Green Chemistry","2022","24","9","3772","3777","10.1039/D2GC00387B","","","1.54184","CuKα","","0.1635","0.0842","","","0.1873","0.2664","","","","","","0.994","","","","has coordinates","275785","2022-06-06","01:47:37",""
"7244750","9.2685","0.0008","18.7779","0.0014","10.9806","0.001","90","","101.311","0.009","90","","1874","0.3","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C25 H20 N2 O -","- C25 H20 N2 O -","- C100 H80 N8 O4 -","4","1","","Dong, Pei-Zhen; Qiu, Bin; An, Xiao-De; Xiao, Jian","Cascade dearomative [4 + 2] cycloaddition of indoles with in situ generated ortho-quinone methides: practical access to divergent indoline-fused polycycles","Green Chemistry","2022","24","9","3772","3777","10.1039/D2GC00387B","","","1.54184","CuKα","","0.1214","0.0572","","","0.1032","0.1399","","","","","","0.983","","","","has coordinates","275785","2022-06-06","01:47:37",""
"7244751","11.9483","0.0006","17.9325","0.0013","16.013","0.0011","90","","90.01","0.006","90","","3431","0.4","293","2","293","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C23 H17 N O3 -","- C23 H17 N O3 -","- C184 H136 N8 O24 -","8","1","","Dong, Pei-Zhen; Qiu, Bin; An, Xiao-De; Xiao, Jian","Cascade dearomative [4 + 2] cycloaddition of indoles with in situ generated ortho-quinone methides: practical access to divergent indoline-fused polycycles","Green Chemistry","2022","24","9","3772","3777","10.1039/D2GC00387B","","","1.54178","CuKα","","0.1454","0.0951","","","0.2612","0.3137","","","","","","1.015","","","","has coordinates","275785","2022-06-06","01:47:37",""
"7244752","23.861","0.0008","6.1612","0.0002","10.0136","0.0003","90","","95.846","0.002","90","","1464.47","0.08","100","2","100","2","","","","","","","","3","C 1 2 1","C 2y","5","","","","- C32 H44 O6 -","- C32 H44 O6 -","- C64 H88 O12 -","2","0.5","","Freese, Thomas; Fridrich, Bálint; Crespi, Stefano; Lubbe, Anouk S.; Barta, Katalin; Feringa, Ben L.","A molecular motor from lignocellulose","Green Chemistry","2022","24","9","3689","3696","10.1039/D2GC00291D","","","1.54178","CuKα","","0.0386","0.0353","","","0.0823","0.0842","","","","","","1.16","","","","has coordinates","275787","2022-06-06","01:48:05",""
"7244753","11.0534","0.0016","11.594","0.0017","12.4153","0.0018","75.979","0.005","86.095","0.005","73.276","0.004","1478.4","0.4","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C16 H20 O4 -","- C16 H20 O4 -","- C64 H80 O16 -","4","2","","Freese, Thomas; Fridrich, Bálint; Crespi, Stefano; Lubbe, Anouk S.; Barta, Katalin; Feringa, Ben L.","A molecular motor from lignocellulose","Green Chemistry","2022","24","9","3689","3696","10.1039/D2GC00291D","","","0.71073","MoKα","","0.1187","0.0666","","","0.1478","0.177","","","","","","1.029","","","","has coordinates","275787","2022-06-06","01:48:08",""
"7244843","20.4311","0.0008","10.9478","0.0004","17.313","0.0007","90","","109.488","0.002","90","","3650.6","0.2","170","2","169.97","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H25 N O4 -","- C19 H25 N O4 -","- C152 H200 N8 O32 -","8","2","","Tao, Ji-Yu; Wang, Ying-Xue; Zhang, Qing-Hong; Ni, Kun; Zhu, Tong-Hao; Zhao, Kai","Transition-metal-free regioselective and stereoselective C(sp2)–C(sp3) coupling of enamides with ethers or alkanes via photoredox-catalyzed cross-dehydrogenative coupling reactions","Green Chemistry","2022","24","10","4004","4011","10.1039/D2GC00472K","","","1.34139","GaKα","","0.0563","0.0431","","","0.1048","0.1137","","","","","","1.042","","","","has coordinates,has disorder","275783","2022-06-06","01:47:15",""
"7244844","12.313","0.003","13.516","0.003","15.514","0.003","90","","129.048","0.012","90","","2005.1","0.8","299","2","299","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H17 F3 O3 -","- C24 H17 F3 O3 -","- C96 H68 F12 O12 -","4","1","","Zhang, Yan; Ma, Chanchan; Cai, Zhenzhi; Struwe, Julia; Chen, Shengjie; Xu, Jinming; Li, Shiyin; Zeng, Wangyu; Ackermann, Lutz","Electrooxidative tricyclic 6–7–6 fused-system domino assembly to allocolchicines by a removable radical strategy","Green Chemistry","2022","24","9","3697","3703","10.1039/D2GC00684G","","","0.71073","MoKα","","0.1581","0.0822","","","0.2011","0.261","","","","","","1.03","","","","has coordinates","275788","2022-06-06","01:48:17",""
"7244845","34.743","0.002","7.6413","0.0003","19.9522","0.0011","90","","100.316","0.002","90","","5211.3","0.5","299","2","299","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C31 H26 O6 S -","- C31 H26 O6 S -","- C248 H208 O48 S8 -","8","1","","Zhang, Yan; Ma, Chanchan; Cai, Zhenzhi; Struwe, Julia; Chen, Shengjie; Xu, Jinming; Li, Shiyin; Zeng, Wangyu; Ackermann, Lutz","Electrooxidative tricyclic 6–7–6 fused-system domino assembly to allocolchicines by a removable radical strategy","Green Chemistry","2022","24","9","3697","3703","10.1039/D2GC00684G","","","0.71073","MoKα","","0.075","0.055","","","0.1407","0.1597","","","","","","1.035","","","","has coordinates","275788","2022-06-06","01:48:17",""
"7244855","9.7488","0.0001","9.7803","0.0001","14.7582","0.0001","90","","90","","90","","1407.14","0.02","99.99","0.1","99.99","0.1","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C17 H19 N O -","- C17 H19 N O -","- C68 H76 N4 O4 -","4","1","","Lu, Hui-Rong; Geng, Hui; Ding, Guan-Tian; Huang, Pei-Qiang","Catalyst- and solvent-free aminolysis of the asymmetric derivatives of Evans’ chiral N-acyloxazolidinones: enantioselective synthesis of chiral amides and its applications","Green Chemistry","2022","24","11","4405","4413","10.1039/D2GC00662F","","x-ray","1.54184","CuKα","","0.0259","0.0257","","","0.0652","0.0654","","","","","","1.061","","","","has coordinates","276627","2022-07-06","08:13:12",""
"7244869","12.403","0.0005","7.2153","0.0002","29.2429","0.0012","90","","90","","90","","2616.99","0.17","170","2","170","","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C16 H14 N2 O2 -","- C16 H14 N2 O2 -","- C128 H112 N16 O16 -","8","1","","Yang, Xinjie; Wang, Hao; Zhang, Yanhua; Su, Weike; Yu, Jingbo","Generation of aryl radicals from in situ activated homolytic scission: driving radical reactions by ball milling","Green Chemistry","2022","24","11","4557","4565","10.1039/D2GC00910B","","","0.71073","MoKα","","0.0498","0.0415","","","0.1042","0.1113","","","","","","1.084","","","","has coordinates","276626","2022-07-06","08:13:07",""
"7244879","5.6","0.02","14.98","0.05","9.85","0.04","90","","105.15","0.04","90","","798","5","273","2","273","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C23 H15 N O -","- C23 H15 N O -","- C46 H30 N2 O2 -","2","1","","Bae, Jaehan; Iqbal, Naeem; Hwang, Ho Seong; Cho, Eun Jin","Sustainable preparation of photoactive indole-fused tetracyclic molecules: a new class of organophotocatalysts","Green Chemistry","2022","24","10","3985","3992","10.1039/D2GC00542E","","","0.71073","MoKα","","0.1539","0.0707","","","0.2264","0.2623","","","","","","0.993","","","","has coordinates","275784","2022-06-06","01:47:21",""
"7244947","12.72729","0.00008","5.5688","0.00005","25.1187","0.0002","90","","92.836","0.0007","90","","1778.13","0.02","169.99","0.11","169.99","0.11","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C22 H15 F2 N O2 S -","- C22 H15 F2 N O2 S -","- C88 H60 F8 N4 O8 S4 -","4","1","","Ma, Qiang; Li, Ming; Chen, Zhuo; Ni, Shao-Fei; Wright, James S.; Wen, Li-Rong; Zhang, Lin-Bao","An approach for the synthesis of 2-aryl-3-sulfonyl substituted quinolines through an electrochemical cascade annulation pathway","Green Chemistry","2022","24","11","4425","4431","10.1039/D2GC00151A","","x-ray","1.54184","CuKα","","0.0342","0.0336","","","0.0894","0.0899","","","","","","1.033","","","","has coordinates","276628","2022-07-06","08:13:21",""
"7244948","12.5262","0.0004","5.4497","0.0002","25.0014","0.0009","90","","93.991","0.003","90","","1702.56","0.1","170.01","0.1","170.01","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C22 H17 N O2 S -","- C22 H17 N O2 S -","- C88 H68 N4 O8 S4 -","4","1","","Ma, Qiang; Li, Ming; Chen, Zhuo; Ni, Shao-Fei; Wright, James S.; Wen, Li-Rong; Zhang, Lin-Bao","An approach for the synthesis of 2-aryl-3-sulfonyl substituted quinolines through an electrochemical cascade annulation pathway","Green Chemistry","2022","24","11","4425","4431","10.1039/D2GC00151A","","x-ray","0.71073","MoKα","","0.0409","0.0353","","","0.0989","0.102","","","","","","1.081","","","","has coordinates","276628","2022-07-06","08:13:21",""
"7244962","8.5655","0.0003","25.6875","0.0012","7.7171","0.0003","90","","99.014","0.001","90","","1677","0.12","170","","170","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C19 H13 F3 N2 O S -","- C19 H13 F3 N2 O S -","- C76 H52 F12 N8 O4 S4 -","4","1","","Chen, Shiliu; Yan, Qinqin; Fan, Jie; Gao, Yongjun; Yang, Xiulong; Li, Lijun; Liu, Zhongquan; Li, Zejiang","Photoinduced cascade cyclization of alkynes with NH4SCN: access to SCN-containing dibenzazepines or dioxodibenzothiazepines","Green Chemistry","2022","24","12","4742","4747","10.1039/D2GC01276F","","","0.71073","MoKα","","0.0929","0.0504","","","0.093","0.1122","","","","","","1.046","","","","has coordinates","276630","2022-07-06","08:13:34",""
"7244963","5.64","0.02","23.42","0.1","24.97","0.09","90","","90","","90","","3298","2","293","2","293","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C17 H20 O2 S -","- C17 H20 O2 S -","- C136 H160 O16 S8 -","8","1","","Sharma, Deepak; Hussain, Yaseen; Sharma, Manisha; Chauhan, Pankaj","Electrochemical cascade synthesis of α-thio-substituted masked aldehydes","Green Chemistry","2022","24","12","4783","4788","10.1039/D2GC00845A","","","0.71073","MoKα","","0.1141","0.0654","","","0.1669","0.212","","","","","","1.071","","","","has coordinates","276631","2022-07-06","08:13:42",""
"7244969","8.858","0.0002","9.5201","0.0002","9.7104","0.0002","101.608","0.002","109.911","0.002","92.242","0.002","749","0.03","293","2","293","","","","","","","","","3","P -1","-P 1","2","","","","- C18 H18 O2 -","- C18 H18 O2 -","- C36 H36 O4 -","2","1","","Zhou, Chunlin; Wang, Xinchao; Yang, Lei; Fu, Lei; Li, Gang","Visible-light-driven regioselective carbocarboxylation of 1,3-dienes with organic halides and CO2","Green Chemistry","2022","24","16","6100","6107","10.1039/D2GC01256A","","x-ray","1.3405","synchrotron","","0.0556","0.0443","","","0.1139","0.1197","","","","","","1.0649","","","","has coordinates","278424","2022-10-07","00:56:03",""
"7244970","9.5909","0.0004","23.7105","0.0009","10.2921","0.0004","90","","106.352","0.004","90","","2245.8","0.16","293","","293","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C28 H32 O2 -","- C28 H32 O2 -","- C112 H128 O8 -","4","1","","Zhou, Chunlin; Wang, Xinchao; Yang, Lei; Fu, Lei; Li, Gang","Visible-light-driven regioselective carbocarboxylation of 1,3-dienes with organic halides and CO2","Green Chemistry","2022","24","16","6100","6107","10.1039/D2GC01256A","","x-ray","1.3405","GaKα","","0.0572","0.0451","","","0.1212","0.1295","","","","","","1.106","","","","has coordinates","278424","2022-10-07","00:56:04",""
"7244984","9.8859","0.001","9.9067","0.0009","23.766","0.002","89.459","0.007","81.983","0.008","73.84","0.008","2212.7","0.4","150","0.1","150","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C27 H21 N3 O2 S -","- C27 H21 N3 O2 S -","- C108 H84 N12 O8 S4 -","4","2","","Meng, Xiangtai; Xu, Hehua; Liu, Rui; Zheng, Yu; Huang, Shenlin","Electrochemical triamination of alkynes: controllable synthesis of functionalized indolines and indoles","Green Chemistry","2022","24","12","4754","4760","10.1039/D2GC01129H","","x-ray","0.71073","MoKα","","0.1101","0.0888","","","0.1899","0.2028","","","","","","1.068","","","","has coordinates","276629","2022-07-06","08:13:27",""
"7244985","8.5563","0.001","11.6457","0.0013","12.4602","0.0016","75.907","0.011","77.454","0.011","74.029","0.01","1142.6","0.2","149.99","0.1","149.99","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C25 H26 N2 O4 S -","- C25 H26 N2 O4 S -","- C50 H52 N4 O8 S2 -","2","1","","Meng, Xiangtai; Xu, Hehua; Liu, Rui; Zheng, Yu; Huang, Shenlin","Electrochemical triamination of alkynes: controllable synthesis of functionalized indolines and indoles","Green Chemistry","2022","24","12","4754","4760","10.1039/D2GC01129H","","x-ray","0.71073","MoKα","","0.0535","0.0426","","","0.1018","0.1089","","","","","","1.027","","","","has coordinates","276629","2022-07-06","08:13:28",""
"7245027","8.1325","0.0004","9.3708","0.0005","11.6459","0.0007","74.368","0.002","81.158","0.002","83.467","0.002","842.08","0.08","193","","193","","","","","","","","","4","P -1","-P 1","2","","","","- C23 H18 N2 O -","- C23 H18 N2 O -","- C46 H36 N4 O2 -","2","1","","Guan, Wenjing; Ying, Ke; Yuan, Chengcheng; Hang, Jinlin; Liu, Chengkou; Huang, Xiangxing; Fang, Zheng; Guo, Kai","Catalyst- and oxidant-free electrooxidative site-selective [3/4 + 2] annulation to fused polycyclic heteroaromatics","Green Chemistry","2022","24","13","5191","5196","10.1039/D2GC01248K","","","0.71073","MoKα","","0.0772","0.0529","","","0.1291","0.1481","","","","","","1.016","","","","has coordinates","276625","2022-07-06","08:12:57",""
"7245081","12.921","0.003","22.128","0.005","14.966","0.004","90","","113.873","0.007","90","","3912.9","1.7","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C44 H46 N6 O6 -","- C44 H42 N6 O6 -","- C176 H168 N24 O24 -","4","1","","Sarkar, Rajib; Dam, Binoyargha; Kyndiah, Lenida; Sarkar, Fillip Kumar; Gajurel, Sushmita; Pal, Amarta Kumar","Graphite oxide catalyzed one-pot synthesis of highly functionalized spirodibenzo[1,4]diazepine derivatives in aqueous ethanol medium","Green Chemistry","2022","24","14","5579","5591","10.1039/D2GC00194B","","","0.71073","MoKα","","0.1501","0.0838","","","0.222","0.2658","","","","","","1.023","","","","has coordinates","277111","2022-08-06","11:49:23",""
"7245085","8.0016","0.0016","9.3863","0.0019","18.181","0.004","90","","97.48","0.03","90","","1353.9","0.5","295","2","295","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C12 H13 F N2 O3 S -","- C12 H13 F N2 O3 S -","- C48 H52 F4 N8 O12 S4 -","4","1","","Guo, Haijin; Liu, Yunyun; Wen, Chengping; Wan, Jie-Ping","Electrochemical enaminone C–H thiolation/C–N amination cascade for thiazole synthesis and its diastereoselective dearomatization","Green Chemistry","2022","24","13","5058","5063","10.1039/D2GC01644C","","","0.71073","MoKα","","0.0491","0.0378","","","0.0961","0.107","","","","","","1.079","","","","has coordinates","276624","2022-07-06","08:12:51",""
"7245136","15.627","0.003","21.005","0.008","21.972","0.006","90","","78.05","0.03","90","","7056","4","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","PTP-dq-PF6","","- C72 H48 Cl3 F18 N18 P3 -","- C72 H48 Cl3 F18 N18 P3 -","- C288 H192 Cl12 F72 N72 P12 -","4","1","","Rao, Cai-Hui; Ma, Shuai; Cui, Jing-Wang; Jia, Meng-Ze; Yao, Xin-Rong; Zhang, Jie","A bifunctional small molecular photocatalyst with a redox center and a Lewis acid site for one-pot tandem oxidation–acetalization","Green Chemistry","2022","24","15","5862","5868","10.1039/D2GC01321E","","","0.71073","MoKα","","0.2578","0.0957","","","0.2467","0.3531","","","","","","1.017","","","","has coordinates","277112","2022-08-06","11:49:36",""
"7245189","8.8424","0.0009","12.5877","0.0012","26.417","0.004","90","","90","","90","","2940.4","0.6","200","0.1","200","0.1","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C18 H19 N O2 -","- C18 H19 N O2 -","- C144 H152 N8 O16 -","8","1","","Qu, Zhonghua; Tian, Tong; Tan, Yongbo; Ji, Xiaochen; Deng, Guo-Jun; Huang, Huawen","Redox-neutral ketyl radical coupling/cyclization of carbonyls with N-aryl acrylamides through consecutive photoinduced electron transfer","Green Chemistry","2022","24","19","7403","7409","10.1039/D2GC01966C","","x-ray","0.71073","MoKα","","0.0566","0.0443","","","0.1028","0.1108","","","","","","1.077","","","","has coordinates","278421","2022-10-07","00:55:38",""
"7245190","7.8246","0.0006","9.2051","0.0007","10.7849","0.0012","94.614","0.008","101.272","0.008","99.213","0.007","746.96","0.12","200","0.1","200","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C18 H19 N O2 -","- C18 H19 N O2 -","- C36 H38 N2 O4 -","2","1","","Qu, Zhonghua; Tian, Tong; Tan, Yongbo; Ji, Xiaochen; Deng, Guo-Jun; Huang, Huawen","Redox-neutral ketyl radical coupling/cyclization of carbonyls with N-aryl acrylamides through consecutive photoinduced electron transfer","Green Chemistry","2022","24","19","7403","7409","10.1039/D2GC01966C","","x-ray","0.71073","MoKα","","0.0547","0.0469","","","0.1131","0.1209","","","","","","1.054","","","","has coordinates","278421","2022-10-07","00:55:38",""
"7245191","6.7194","0.0006","7.7474","0.0007","12.013","0.0011","88.533","0.007","79.948","0.008","87.813","0.007","615.21","0.1","199.99","0.1","199.99","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C10 H13 Br O4 S -","- C10 H13 Br O4 S -","- C20 H26 Br2 O8 S2 -","2","1","","Liu, Jiang; Xu, Jingcheng; Mei, Haibo; Han, Jianlin","Electrochemical multi-component reaction of potassium metabisulfite with alkenes and alcohols enabling synthesis of sulfonate esters","Green Chemistry","2022","24","16","6113","6118","10.1039/D2GC01909D","","x-ray","0.71073","MoKα","","0.0601","0.0418","","","0.0872","0.096","","","","","","1.005","","","","has coordinates","278426","2022-10-07","00:56:22",""
"7245192","9.3505","0.001","10.5661","0.0014","11.8126","0.0013","79.178","0.004","74.762","0.003","80.249","0.004","1097.1","0.2","296","","296","","","","","","","","","4","P -1","-P 1","2","","","","- C29 H21 N3 O -","- C29 H21 N3 O -","- C58 H42 N6 O2 -","2","1","","Jalani, Hitesh B.; Sivaraman, Aneesh; Min, Kyoung ho; Lee, Hwa Young; Oh, Na Kyoung; Kang, Hyeseul; Keum, Gyochang; Choi, Yongseok; Lee, Kyeong","Metal/catalyst-free sequential C–N bond forming cascades at room temperature: environment-friendly one-pot synthesis of 5-aminoimidazoles from aryl glyoxals, anilines, and amidines","Green Chemistry","2022","24","17","6501","6510","10.1039/D2GC01407F","","","0.71075","MoKα","","0.0593","0.0472","","","0.133","0.1444","","","","","","1.144","","","","has coordinates","278418","2022-10-07","00:55:11",""
"7245193","8.7917","0.00018","10.247","0.0002","19.1126","0.0004","90","","98.05","0.002","90","","1704.86","0.06","149.99","0.1","149.99","0.1","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C19 H17 F3 N2 O S -","- C19 H17 F3 N2 O S -","- C76 H68 F12 N8 O4 S4 -","4","1","","Lan, Jianyong; Lin, Kejun; Zhang, Xing; Zhu, Tingshun","Stereoselective migratory heteroaryltrifluoromethylation of allylic amines via electrosynthesis","Green Chemistry","2022","24","16","6138","6144","10.1039/D2GC00960A","","x-ray","1.54184","CuKα","","0.0447","0.0415","","","0.1047","0.1072","","","","","","1.066","","","","has coordinates","278425","2022-10-07","00:56:11",""
"7245194","15.1633","0.001","5.1388","0.0003","17.4106","0.0011","90","","101.494","0.003","90","","1329.45","0.14","209.99","","209.99","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","LXF-118-nl","","- C14 H16 N2 O3 -","- C14 H16 N2 O3 -","- C56 H64 N8 O12 -","4","1","","Lei, Xiaofang; Angeli, Giasemi K.; Neochoritis, Constantinos G.; Dömling, Alexander","Sustainable multicomponent indole synthesis with broad scope","Green Chemistry","2022","24","16","6168","6171","10.1039/D2GC02060B","","","1.54178","CuKα","","0.0426","0.0384","","","0.1097","0.1248","","","","","","1.142","","","","has coordinates","278423","2022-10-07","00:55:56",""
"7245195","9.4666","0.0003","9.9691","0.0003","16.311","0.0004","100.153","0.001","104.072","0.001","92.751","0.001","1463.08","0.07","199.98","","199.98","","","","","","","","","5","P -1","-P 1","2","","LXF-125nl","","- C17 H15 Cl N2 O -","- C17 H15 Cl N2 O -","- C68 H60 Cl4 N8 O4 -","4","2","","Lei, Xiaofang; Angeli, Giasemi K.; Neochoritis, Constantinos G.; Dömling, Alexander","Sustainable multicomponent indole synthesis with broad scope","Green Chemistry","2022","24","16","6168","6171","10.1039/D2GC02060B","","","1.54178","CuKα","","0.0413","0.0375","","","0.108","0.1122","","","","","","1.065","","","","has coordinates","278423","2022-10-07","00:55:56",""
"7245196","9.4927","0.0005","9.4927","0.0005","47.965","0.005","90","","90","","90","","4322.2","0.6","296","2","296","2","","","","","","","","4","P 41 21 2","P 4abw 2nw","92","","","","- C23 H27 O6 P -","- C23 H27 O6 P -","- C184 H216 O48 P8 -","8","1","","Li, Hai; Yu, Kai-Cheng; Su, Jia-Kun; Ouyang, Wei; Fan, Nai-Li; Hu, Xiang-Guo","Photo-mediated synthesis of 1,2-dideoxy-2-phosphinylated carbohydrates from glycals: the reduction of glycosyl radicals to glycosyl anions","Green Chemistry","2022","24","21","8280","8291","10.1039/D2GC01513G","","","0.71073","MoKα","","0.0505","0.0454","","","0.0966","0.0988","","","","","","1.145","","","","has coordinates","278992","2022-11-07","05:26:47",""
"7245197","11.9882","0.0007","12.7368","0.0008","16.1339","0.0009","90","","90","","90","","2463.5","0.3","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C24 H27 O8 P -","- C24 H27 O8 P -","- C96 H108 O32 P4 -","4","1","","Li, Hai; Yu, Kai-Cheng; Su, Jia-Kun; Ouyang, Wei; Fan, Nai-Li; Hu, Xiang-Guo","Photo-mediated synthesis of 1,2-dideoxy-2-phosphinylated carbohydrates from glycals: the reduction of glycosyl radicals to glycosyl anions","Green Chemistry","2022","24","21","8280","8291","10.1039/D2GC01513G","","","0.71073","MoKα","","0.0476","0.042","","","0.1002","0.1033","","","","","","1.047","","","","has coordinates","278992","2022-11-07","05:26:47",""
"7245256","10.1227","0.0017","19.823","0.002","21.73","0.005","90","","90","","90","","4360.4","1.3","250","2","250","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","MSP-348_250K","","","- C24 H28 F2 N2 O -","- C24 H28 F2 N2 O -","- C192 H224 F16 N16 O8 -","8","1","","Rodríguez, Ricardo I.; Sicignano, Marina; García, Montaña J.; Enríquez, Rodrigo G.; Cabrera, Silvia; Alemán, José","Taming photocatalysis in flow: easy and speedy preparation of α-aminoamide derivatives","Green Chemistry","2022","24","17","6613","6618","10.1039/D2GC02087D","","","0.71073","MoKα","","0.1001","0.0504","","","0.1215","0.1445","","","","","","1.042","","","","has coordinates","278419","2022-10-07","00:55:18",""
"7245271","14.6248","0.0003","11.859","0.0002","11.3672","0.0002","90","","107.271","0.001","90","","1882.58","0.06","193","2","193","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H24 N2 O2 -","- C22 H24 N2 O2 -","- C88 H96 N8 O8 -","4","1","","Guan, Ting; Guo, Jing-Yu; Zhang, Qing-Hong; Xu, Xin-Wen; Yu, Xiao-Yu; Zhang, Yu; Zhao, Kai","Photoredox-catalyzed regio- & stereoselective C(sp2)–H cyanoalkylation of enamides with cycloketone oximes via selective C–C bond cleavage/radical addition cascade","Green Chemistry","2022","24","17","6524","6530","10.1039/D2GC01978G","","","1.34139","GaKα","","0.0508","0.0411","","","0.1011","0.1089","","","","","","1.048","","","","has coordinates","278415","2022-10-07","00:54:49",""
"7245278","10.6469","0.0003","15.8266","0.0004","28.9384","0.0007","90","","90","","90","","4876.2","0.2","120","2","120","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C28 H30 N2 O3 S -","- C28 H30 N2 O3 S -","- C224 H240 N16 O24 S8 -","8","2","","SCHLIMPEN, Fabian; AST, Tun; Benneteau, Valerie; Pale, Patrick; Chassaing, Stefan","From A3/KA2 to AYA/KYA Multicomponent Coupling Reactions with Terminal Ynamides as Alkyne Surrogates - A Direct, Green Route to γ-Amino-Ynamides","Green Chemistry","2022","","","","","10.1039/D2GC00966H","","","1.54178","CuKα","","0.0356","0.0327","","","0.0886","0.0907","","","","","","1.043","","","","has coordinates","277161","2022-08-09","00:15:32",""
"7245304","9.9628","0.0002","10.1107","0.0002","12.9334","0.0002","71.458","0.002","73.161","0.002","63.999","0.002","1092.75","0.04","100","","100","","","","","","","","","3","P -1","-P 1","2","","","","- C29 H24 Se -","- C29 H24 Se -","- C58 H48 Se2 -","2","1","","Mukherjee, Nilanjana; Satyanarayana, Appanapalli N. V.; Singh, Priti; Dixit, Mudit; Chatterjee, Tanmay","Recyclable iodine-catalyzed radical selenylative annulation of 2-alkynyl biaryls with diselenides in water: a green approach to selanyl polycyclic aromatic hydrocarbons and polycyclic heteroaromatics","Green Chemistry","2022","24","18","7029","7038","10.1039/D2GC02256G","","x-ray","1.54184","CuKα","","0.0319","0.0309","","","0.0809","0.0814","","","","","","1.0273","","","","has coordinates","278430","2022-10-07","00:57:09",""
"7245305","15.3921","0.0002","10.1833","0.0001","13.1358","0.0002","90","","107.775","0.001","90","","1960.65","0.05","100","","100","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","NM-730","","- C26 H17 Cl Se -","- C26 H17 Cl Se -","- C104 H68 Cl4 Se4 -","4","1","","Mukherjee, Nilanjana; Satyanarayana, Appanapalli N. V.; Singh, Priti; Dixit, Mudit; Chatterjee, Tanmay","Recyclable iodine-catalyzed radical selenylative annulation of 2-alkynyl biaryls with diselenides in water: a green approach to selanyl polycyclic aromatic hydrocarbons and polycyclic heteroaromatics","Green Chemistry","2022","24","18","7029","7038","10.1039/D2GC02256G","","x-ray","1.54184","CuKα","","0.0317","0.0299","","","0.0869","0.0882","","","","","","1.149","","","","has coordinates","278430","2022-10-07","00:57:09",""
"7245306","11.2182","0.0003","10.3531","0.0003","17.3831","0.0005","90","","100.258","0.003","90","","1986.66","0.1","100","","100","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","NM-731","","- C27 H20 Se -","- C27 H20 Se -","- C108 H80 Se4 -","4","1","","Mukherjee, Nilanjana; Satyanarayana, Appanapalli N. V.; Singh, Priti; Dixit, Mudit; Chatterjee, Tanmay","Recyclable iodine-catalyzed radical selenylative annulation of 2-alkynyl biaryls with diselenides in water: a green approach to selanyl polycyclic aromatic hydrocarbons and polycyclic heteroaromatics","Green Chemistry","2022","24","18","7029","7038","10.1039/D2GC02256G","","x-ray","1.54184","CuKα","","0.0475","0.0435","","","0.1215","0.1256","","","","","","1.0185","","","","has coordinates","278430","2022-10-07","00:57:10",""
"7245307","12.839","0.0012","9.1349","0.0011","13.4055","0.0016","90","","99.269","0.011","90","","1551.7","0.3","249.97","0.1","249.97","0.1","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C17 H11 Br N2 O S -","- C17 H11 Br N2 O S -","- C68 H44 Br4 N8 O4 S4 -","4","1","","Gu, Qingyun; Cheng, Zhenfeng; Xiong, Xing; Xiong, Biao; Zhao, Yu; Xu, Hua-Dong; Zhang, Yanan; Qiu, Xiaodong; Zeng, Xiaobao","Electrochemical oxidative regio- and stereo-selective thio(seleno)cyanation of enamides and mechanistic insights","Green Chemistry","2022","24","17","6556","6561","10.1039/D2GC01932A","","x-ray","0.71073","MoKα","","0.0876","0.0524","","","0.1072","0.126","","","","","","0.991","","","","has coordinates","278416","2022-10-07","00:54:56",""
"7245329","8.2932","0.001","8.8298","0.0011","12.4718","0.0014","95.863","0.01","90.752","0.01","116.824","0.012","808.94","0.19","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C17 H16 Br N O3 S -","- C17 H16 Br N O3 S -","- C34 H32 Br2 N2 O6 S2 -","2","1","","Wu, Ying-Ai; Wang, Rui-An; Jiang, Shu-Yun; Jiang, Tai-Bai; Song, Jun-Rong; Shi, Jun; Wu, Wei; Pan, Wei-Dong; Ren, Hai","Water enables the tunable electrochemical synthesis of heterocyclic 3a- or 5a-bromoindolines","Green Chemistry","2022","24","17","6720","6726","10.1039/D2GC02086F","","x-ray","0.71073","MoKα","","0.0813","0.0572","","","0.1393","0.1524","","","","","","1.074","","","","has coordinates","278417","2022-10-07","00:55:02",""
"7245347","7.8039","0.0002","17.1774","0.0004","14.8916","0.0003","90","","91.57","0.002","90","","1995.48","0.08","100.01","0.1","100.01","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H33 B N2 S -","- C20 H33 B N2 S -","- C80 H132 B4 N8 S4 -","4","1","","Miao, Yu-Qi; Li, Xin-Ying; Pan, Qiao-Jing; Ma, Yubin; Kang, Jia-Xin; Ma, Yan-Na; Liu, Zhenxing; Chen, Xuenian","A general photo-induced wide-scope regioselective hydroboration of alkenes without using a photocatalyst or an external initiator","Green Chemistry","2022","24","18","7113","7121","10.1039/D2GC02313J","","x-ray","1.54184","CuKα","","0.0532","0.0505","","","0.133","0.1347","","","","","","1.135","","","","has coordinates","278428","2022-10-07","00:56:47",""
"7245348","6.2427","0.0005","7.8871","0.0006","29.178","0.002","90","","90","","90","","1436.63","0.19","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C15 H20 B N3 O -","- C15 H20 B N3 O -","- C60 H80 B4 N12 O4 -","4","1","","Miao, Yu-Qi; Li, Xin-Ying; Pan, Qiao-Jing; Ma, Yubin; Kang, Jia-Xin; Ma, Yan-Na; Liu, Zhenxing; Chen, Xuenian","A general photo-induced wide-scope regioselective hydroboration of alkenes without using a photocatalyst or an external initiator","Green Chemistry","2022","24","18","7113","7121","10.1039/D2GC02313J","","x-ray","1.54184","CuKα","","0.065","0.0452","","","0.1025","0.1264","","","","","","1.096","","","","has coordinates","278428","2022-10-07","00:56:48",""
"7245349","9.0836","0.0006","9.1558","0.0008","11.0863","0.0008","114.228","0.008","106.84","0.006","93.503","0.006","787.46","0.13","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C16 H21 B N2 O2 -","- C16 H21 B N2 O2 -","- C32 H42 B2 N4 O4 -","2","1","","Miao, Yu-Qi; Li, Xin-Ying; Pan, Qiao-Jing; Ma, Yubin; Kang, Jia-Xin; Ma, Yan-Na; Liu, Zhenxing; Chen, Xuenian","A general photo-induced wide-scope regioselective hydroboration of alkenes without using a photocatalyst or an external initiator","Green Chemistry","2022","24","18","7113","7121","10.1039/D2GC02313J","","x-ray","1.54184","CuKα","","0.067","0.0514","","","0.1436","0.1538","","","","","","1.058","","","","has coordinates","278428","2022-10-07","00:56:48",""
"7245350","16.3755","0.0011","7.2951","0.0004","23.9248","0.0014","90","","103.152","0.007","90","","2783.1","0.3","100","0.2","100","0.2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C15 H9 Cl2 N O S -","- C15 H9 Cl2 N O S -","- C120 H72 Cl16 N8 O8 S8 -","8","2","","Fu, Yuanyuan; Zhu, Shengzhen; Zhao, Xueyan; Huang, Shenlin","Photoredox-catalyzed coupling of acyl oxime acetates with thiophenols to give arylthioesters in water at room temperature","Green Chemistry","2022","24","18","6849","6853","10.1039/D2GC02438A","","x-ray","0.71073","MoKα","","0.0609","0.047","","","0.107","0.117","","","","","","1.035","","","","has coordinates","278431","2022-10-07","00:57:16",""
"7245376","8.293","0.006","8.812","0.006","19.773","0.014","88.368","0.01","87.164","0.01","67.4","0.01","1332.3","1.6","296","2","296.15","","","","","","","","","5","P -1","-P 1","2","","","","- C27 H28 Cl N3 O3 -","- C27 H28 Cl N3 O3 -","- C54 H56 Cl2 N6 O6 -","2","1","","Zhang, Aijiang; Chen, Changjuan; Zuo, Chunshan; Xu, Xiaobo; Cai, Tao; Li, Xiaotao; Yuan, Ying; Yang, Huanhuan; Meng, Gege","Imidazolium-based ionic liquids containing multipoint hydrogen bond donors as bifunctional organocatalysts for efficient cooperative conversion of CO2 to cyclic carbonates","Green Chemistry","2022","24","18","7194","7207","10.1039/D2GC02517E","","","0.71073","MoKα","","0.1368","0.0938","","","0.2353","0.2639","","","","","","0.965","","","","has coordinates","278433","2022-10-07","00:57:28",""
"7245393","6.9187","0.001","12.6378","0.0019","14.994","0.002","90","","96.541","0.005","90","","1302.5","0.3","150","","150","","","","","","","","","4","P 1 c 1","P -2yc","7","","","","- C17 H15 N O2 -","- C17 H15 N O2 -","- C68 H60 N4 O8 -","4","2","","Meng, Haifang; Xu, Huiying; Zhou, Zhi; Tang, Zhenhao; Li, Yidi; Zhou, Yu; Yi, Wei; Wu, Xiaowei","Recyclable rhodium-catalyzed C–H activation/[4 + 2] annulation with unconventional regioselectivity at ambient temperature: experimental development and mechanistic insight","Green Chemistry","2022","24","18","7012","7021","10.1039/D2GC02347D","","","0.71073","MoKα","","0.1481","0.0692","","","0.1402","0.1807","","","","","","1.008","","","","has coordinates","278434","2022-10-07","00:57:33",""
"7245396","5.6822","0.0004","9.1526","0.0006","14.0751","0.001","108.654","0.002","100.575","0.002","91.47","0.002","678.97","0.08","273","2","273","2","","","","","","","","5","P -1","-P 1","2","","","","- C15 H13 F O3 S -","- C15 H13 F O3 S -","- C30 H26 F2 O6 S2 -","2","1","","Dam, Binoyargha; Sahoo, Ashish Kumar; Patel, Bhisma K.","Visible-light-mediated synthesis of β-keto sulfones using g-C3N4 as a recyclable photocatalyst under sustainable conditions","Green Chemistry","2022","24","18","7122","7130","10.1039/D2GC02254K","","","0.71073","MoKα","","0.1331","0.1031","","","0.233","0.2627","","","","","","1.224","","","","has coordinates","278432","2022-10-07","00:57:22",""
"7245397","11.5468","0.0016","10.2038","0.0011","22.824","0.003","90","","90","","90","","2689.2","0.6","296","2","296","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C15 H14 O3 S -","- C15 H14 O3 S -","- C120 H112 O24 S8 -","8","1","","Dam, Binoyargha; Sahoo, Ashish Kumar; Patel, Bhisma K.","Visible-light-mediated synthesis of β-keto sulfones using g-C3N4 as a recyclable photocatalyst under sustainable conditions","Green Chemistry","2022","24","18","7122","7130","10.1039/D2GC02254K","","","0.71073","MoKα","","0.1411","0.0621","","","0.1496","0.2039","","","","","","1.06","","","","has coordinates","278432","2022-10-07","00:57:22",""
"7245398","6.4061","0.0014","11.99","0.003","12.381","0.003","96.571","0.008","104.937","0.006","105.103","0.005","870.1","0.4","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C19 H20 N2 O6 -","- C19 H20 N2 O6 -","- C38 H40 N4 O12 -","2","1","","Pereira, Juliana G.; Ravasco, João M. J. M.; Vale, João R.; Queda, Fausto; Gomes, Rafael F. A.","A direct Diels–Alder reaction of chitin derived 3-acetamido-5-acetylfuran","Green Chemistry","2022","24","18","7131","7136","10.1039/D2GC00253A","","x-ray","0.71073","MoKα","","0.165","0.0751","","","0.1548","0.1761","","","","","","1.042","","","","has coordinates","278435","2022-10-07","00:57:38",""
"7245399","7.23789","0.00013","12.2345","0.0002","13.6811","0.0003","72.142","0.005","82.584","0.006","80.322","0.006","1132.82","0.05","93","","93","","","","","","","","","5","P -1","-P 1","2","","","","- C23 H19 N3 O9 S -","- C23 H19 N3 O9 S -","- C46 H38 N6 O18 S2 -","2","1","","Yamamoto, Daisuke; Hirano, Issei; Narushima, Yuki; Soga, Masayuki; Ansai, Hiromasa; Makino, Kazuishi","Stereoselective synthesis of the isoxazolidine ring via manganese(iii)-catalysed aminoperoxidation of unactivated alkenes using molecular oxygen in air under ambient conditions","Green Chemistry","2022","24","18","7162","7170","10.1039/D2GC02205B","","","1.54187","CuKα","","0.0462","0.0394","","","0.0929","0.0963","","","","","","1.036","","","","has coordinates","278427","2022-10-07","00:56:38",""
"7245400","15.7934","0.0003","6.97062","0.00013","20.9252","0.0004","90","","106.862","0.008","90","","2204.61","0.12","93","","93","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C23 H19 N3 O9 S -","- C23 H19 N3 O9 S -","- C92 H76 N12 O36 S4 -","4","1","","Yamamoto, Daisuke; Hirano, Issei; Narushima, Yuki; Soga, Masayuki; Ansai, Hiromasa; Makino, Kazuishi","Stereoselective synthesis of the isoxazolidine ring via manganese(iii)-catalysed aminoperoxidation of unactivated alkenes using molecular oxygen in air under ambient conditions","Green Chemistry","2022","24","18","7162","7170","10.1039/D2GC02205B","","","1.54187","CuKα","","0.0385","0.034","","","0.0828","0.0852","","","","","","1.04","","","","has coordinates","278427","2022-10-07","00:56:39",""
"7245401","11.5777","0.0002","23.2895","0.0004","17.4903","0.0003","90","","92.923","0.007","90","","4709.93","0.14","93","","93","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C54 H63 Fe3 Mn O6 -","- C54 H63 Fe3 Mn O6 -","- C216 H252 Fe12 Mn4 O24 -","4","1","","Yamamoto, Daisuke; Hirano, Issei; Narushima, Yuki; Soga, Masayuki; Ansai, Hiromasa; Makino, Kazuishi","Stereoselective synthesis of the isoxazolidine ring via manganese(iii)-catalysed aminoperoxidation of unactivated alkenes using molecular oxygen in air under ambient conditions","Green Chemistry","2022","24","18","7162","7170","10.1039/D2GC02205B","","","1.54187","CuKα","","0.1145","0.0785","","","0.1957","0.2166","","","","","","1.081","","","","has coordinates","278427","2022-10-07","00:56:39",""
"7245456","9.206","0.003","10.087","0.003","13.161","0.004","99.033","0.004","97.884","0.004","107.657","0.004","1127.7","0.6","296","2","296.15","","","","","","","","","4","P -1","-P 1","2","","","","- C2.61 H2.17 N0.09 O0.17 -","- C2.6087 H2.17391 N0.0869565 O0.173913 -","- C60 H50 N2 O4 -","23","11.5","","Nie, Chang-Rui; Zhao, Hong-Ping; Liang, Wang-Fu; Zhong, Xin-Xian; Liang, Cui; Su, Gui-Fa; Mo, Dong-Liang","Base-catalyzed and DMSO-promoted intramolecular hydroalkoxylation to prepare pentacyclic chromeno[4,3-b]indolines","Green Chemistry","2022","24","18","6854","6859","10.1039/D2GC02225G","","","0.71073","MoKα","","0.0537","0.0417","","","0.1158","0.1257","","","","","","1.034","","","","has coordinates","278429","2022-10-07","00:56:54",""
"7245467","17.2287","0.0005","17.2287","0.0005","50.201","0.003","90","","90","","90","","14901.1","1.1","100","0.2","100","0.2","","","","","","","","6","I 41/a c d :2","-I 4bd 2c","142","","","","- C36 H30 Br2 N10 Ni O2 -","- C36 H30 Br2 N10 Ni O2 -","- C576 H480 Br32 N160 Ni16 O32 -","16","0.5","","Zhang, Chunyan; Liang, Qianqian; Yang, Wei; Zhang, Guohui; Hu, Maolin; Zhang, Guoying","Nickel(i)-catalyzed (de)hydrogenative coupling of amines and alkyl heteroarenes with alcohols","Green Chemistry","2022","24","19","7368","7375","10.1039/D2GC02206K","","x-ray","0.71073","MoKα","","0.1034","0.0713","","","0.1898","0.2181","","","","","","1.049","","","","has coordinates","278422","2022-10-07","00:55:47",""
"7245475","5.6133","0.0016","11.125","0.003","23.1","0.006","91.6","0.012","90.153","0.012","90.094","0.013","1442","0.7","273","2","273.15","","","","","","","","","3","P -1","-P 1","2","","9-benzyl-9H-xanthene","","- C20 H16 O -","- C20 H16 O -","- C80 H64 O4 -","4","2","","Li, Chao; Ding, Ran; Guo, Heng-Yi; Xia, Shuang; Shu, Lei; Wang, Pei-Long; Li, Hongji","Catalyst-free benzylic C(sp3)–H cross-coupling with organotrifluoroborates enabled by electrochemistry","Green Chemistry","2022","24","20","7883","7888","10.1039/D2GC02204D","","","0.71073","MoKα","","0.0768","0.0495","","","0.1192","0.1355","","","","","","1.07","","","","has coordinates","278989","2022-11-07","05:26:20",""
"7245495","21.4567","0.0008","11.733","0.0004","15.3116","0.0005","90","","109.708","0.004","90","","3628.9","0.2","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H25 N O3 -","- C19 H25 N O3 -","- C152 H200 N8 O24 -","8","2","","Yao, Zhen; Yang, Ji; Luo, Zhenli; Wang, Heyu; Zhang, Xin; Ye, Jianhan; Xu, Lijin; Shi, Qian","Photo-driven metal-free multicomponent reaction between aldehydes, anilines and 4-substituted-DHPs for the synthesis of secondary amines","Green Chemistry","2022","24","20","7968","7973","10.1039/D2GC02613A","","","1.54178","CuKα","","0.1001","0.0648","","","0.1992","0.246","","","","","","1.08","","","","has coordinates","278990","2022-11-07","05:26:27",""
"7245545","15.828","0.0009","9.9575","0.0004","16.1714","0.0009","90","","116.785","0.007","90","","2275.3","0.2","169.99","0.1","169.99","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C24 H21 Cl4 N O2 -","- C24 H21 Cl4 N O2 -","- C96 H84 Cl16 N4 O8 -","4","1","","Chen, Shaomin; Chen, Zhiyan; Zhang, Tianjian; Zhao, Bo; You, Bo; Li, Minghao; Gu, Yanlong","Brønsted acid-catalyzed cascade cyclization: an efficient strategy for divergent synthesis of cyclohepta[b]indole derivatives","Green Chemistry","2022","24","19","7376","7381","10.1039/D2GC02072F","","x-ray","1.54184","CuKα","","0.1107","0.0866","","","0.2314","0.2709","","","","","","1.035","","","","has coordinates","278420","2022-10-07","00:55:30",""
"7245546","9.1441","0.0002","10.1797","0.0003","10.2607","0.0003","114.406","0.003","94.673","0.002","99.133","0.002","847.17","0.05","170","0.11","170","0.11","","","","","","","","6","P -1","-P 1","2","","","","- C16 H17 Cl F3 N O4 -","- C16 H17 Cl F3 N O4 -","- C32 H34 Cl2 F6 N2 O8 -","2","1","","Yi, Yaping; Fan, Zhengning; Xi, Chanjuan","Photoredox-catalyzed intermolecular dearomative trifluoromethylcarboxylation of indoles and heteroanalogues with CO2 and fluorinated radical precursors","Green Chemistry","2022","24","20","7894","7899","10.1039/D2GC03000D","","x-ray","1.54184","CuKα","","0.0353","0.0334","","","0.0921","0.0934","","","","","","1.093","","","","has coordinates","278988","2022-11-07","05:26:13",""
"7245547","9.5056","0.0005","28.8708","0.0009","13.6219","0.0008","90","","114.812","0.005","90","","3393.2","0.3","293","2","123.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","Metamitron-Cinnamic acid","","- C19 H18 N4 O3 -","- C19 H18 N4 O3 -","- C152 H144 N32 O24 -","8","2","","Xiao, Yuntian; Wu, Chuanhua; Zhou, Ling; Yin, Qiuxiang; Yang, Jingxiang","Cocrystal engineering strategy for sustained release and leaching reduction of herbicides: a case study of metamitron","Green Chemistry","2022","24","20","8088","8099","10.1039/D2GC02949A","","x-ray","0.71073","MoKα","","0.0756","0.0517","","","0.1166","0.1361","","","","","","1.038","","","","has coordinates","278986","2022-11-07","05:25:55",""
"7245548","11.8352","0.0012","14.4349","0.0012","6.7368","0.0008","90","","105.77","0.012","90","","1107.6","0.2","113.15","","123.15","","","","","","","","","4","P 1 c 1","P -2yc","7","","Metamitron-Naringenin","","- C25 H22 N4 O6 -","- C25 H22 N4 O6 -","- C50 H44 N8 O12 -","2","1","","Xiao, Yuntian; Wu, Chuanhua; Zhou, Ling; Yin, Qiuxiang; Yang, Jingxiang","Cocrystal engineering strategy for sustained release and leaching reduction of herbicides: a case study of metamitron","Green Chemistry","2022","24","20","8088","8099","10.1039/D2GC02949A","","x-ray","0.71073","MoKα","","0.0851","0.0574","","","0.1285","0.1459","","","","","","1.046","","","","has coordinates","278986","2022-11-07","05:25:56",""
"7245549","5.2165","0.0002","13.1426","0.0004","31.0132","0.001","90","","89.95","0.003","90","","2126.21","0.12","113.15","","123.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","Metamitron-Baicalein","","- C25 H20 N4 O6 -","- C25 H20 N4 O6 -","- C100 H80 N16 O24 -","4","1","","Xiao, Yuntian; Wu, Chuanhua; Zhou, Ling; Yin, Qiuxiang; Yang, Jingxiang","Cocrystal engineering strategy for sustained release and leaching reduction of herbicides: a case study of metamitron","Green Chemistry","2022","24","20","8088","8099","10.1039/D2GC02949A","","x-ray","0.71073","MoKα","","0.0789","0.0525","","","0.1221","0.1376","","","","","","1.026","","","","has coordinates,has disorder","278986","2022-11-07","05:25:56",""
"7245565","7.6126","0.0001","23.4046","0.0002","11.2824","0.0001","90","","103.859","0.001","90","","1951.66","0.04","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C20 H17 I2 N O2 -","- C20 H17 I2 N O2 -","- C80 H68 I8 N4 O8 -","4","1","","Lu, Yuling; Chen, Chunmei; Zhu, Hucheng; Luo, Zengwei; Zhang, Yonghui","Highly efficient and fast synthesis of di-iodinated succinimide derivatives from 1,6-enyne and I2 under air at room temperature","Green Chemistry","2022","24","20","8021","8028","10.1039/D2GC02058K","","","1.54178","CuKα","","0.0433","0.0432","","","0.1279","0.128","","","","","","1.096","","","","has coordinates","278985","2022-11-07","05:25:34",""
"7245574","5.819","0.0002","9.8242","0.0004","20.3104","0.001","92.796","0.004","92.658","0.003","95.189","0.003","1153.44","0.08","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C24 H23 Cl3 N2 O3 -","- C24 H23 Cl3 N2 O3 -","- C48 H46 Cl6 N4 O6 -","2","1","","Liang, Jiazhi; Huang, Jian; Yang, Qin; Fu, Yang; Ding, Qiuping; Peng, Yiyuan","Synthesis of dihydroindazolo[2,3-f]phenanthridin-5(6H)-ones via Rh(iii)-catalyzed C–H activation of 2-aryl indazoles and annulation with iodonium ylides","Green Chemistry","2022","24","21","8441","8446","10.1039/D2GC03020A","","","0.71073","MoKα","","0.0544","0.0428","","","0.1082","0.1154","","","","","","1.047","","","","has coordinates","278991","2022-11-07","05:26:38",""
"7245575","12.5652","0.0002","14.3595","0.0003","12.2203","0.0002","90","","100.202","0.001","90","","2170.05","0.07","298","2","298","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","6a","","- C24 H25 N3 O5 -","- C24 H25 N3 O5 -","- C96 H100 N12 O20 -","4","1","","González-Saiz, Beatriz; Pertejo, Pablo; Peña-Calleja, Pablo; Mielczarek, Marcin; Hermosilla, Tomás; Carreira-Barral, Israel; de Miguel, Olivia; Rodríguez-Vidal, Francisco; Quesada, Roberto; García-Valverde, María","Base-selective access to highly functionalized heterocycles from multicomponent Ugi adducts","Green Chemistry","2022","24","20","7988","7995","10.1039/D2GC02896D","","","1.54178","CuKα","","0.0511","0.0421","","","0.1003","0.11","","","","","","1.028","","","","has coordinates","278987","2022-11-07","05:26:06",""
"7245576","10.1914","0.0011","10.379","0.0011","11.8123","0.0013","73.566","0.002","67.677","0.002","83.029","0.002","1108.5","0.2","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","7d","","- C25 H27 N3 O5 -","- C25 H27 N3 O5 -","- C50 H54 N6 O10 -","2","1","","González-Saiz, Beatriz; Pertejo, Pablo; Peña-Calleja, Pablo; Mielczarek, Marcin; Hermosilla, Tomás; Carreira-Barral, Israel; de Miguel, Olivia; Rodríguez-Vidal, Francisco; Quesada, Roberto; García-Valverde, María","Base-selective access to highly functionalized heterocycles from multicomponent Ugi adducts","Green Chemistry","2022","24","20","7988","7995","10.1039/D2GC02896D","","","0.71073","MoKα","","0.0843","0.0502","","","0.117","0.1274","","","","","","0.914","","","","has coordinates,has disorder","278987","2022-11-07","05:26:07",""
"7245577","9.94","0.016","10.793","0.01","16.25","0.02","108.53","0.04","96.84","0.07","106.91","0.05","1538","4","230","2","230","2","","","","","","","","6","P -1","-P 1","2","","7jdiast2","","- C31 H29 Cl3 F N3 O5 -","- C31 H29 Cl3 F N3 O5 -","- C62 H58 Cl6 F2 N6 O10 -","2","1","","González-Saiz, Beatriz; Pertejo, Pablo; Peña-Calleja, Pablo; Mielczarek, Marcin; Hermosilla, Tomás; Carreira-Barral, Israel; de Miguel, Olivia; Rodríguez-Vidal, Francisco; Quesada, Roberto; García-Valverde, María","Base-selective access to highly functionalized heterocycles from multicomponent Ugi adducts","Green Chemistry","2022","24","20","7988","7995","10.1039/D2GC02896D","","","1.54184","CuKα","","0.115","0.0657","","","0.1647","0.216","","","","","","1.023","","","","has coordinates","278987","2022-11-07","05:26:07",""
"7245578","8.9559","0.0003","11.0368","0.0004","12.1951","0.0005","90.73","0.001","106.001","0.001","100.401","0.001","1137.18","0.07","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","8m","","- C25 H24 N2 O4 -","- C25 H24 N2 O4 -","- C50 H48 N4 O8 -","2","1","","González-Saiz, Beatriz; Pertejo, Pablo; Peña-Calleja, Pablo; Mielczarek, Marcin; Hermosilla, Tomás; Carreira-Barral, Israel; de Miguel, Olivia; Rodríguez-Vidal, Francisco; Quesada, Roberto; García-Valverde, María","Base-selective access to highly functionalized heterocycles from multicomponent Ugi adducts","Green Chemistry","2022","24","20","7988","7995","10.1039/D2GC02896D","","","1.54178","CuKα","","0.0707","0.0605","","","0.1691","0.1716","","","","","","1.136","","","","has coordinates","278987","2022-11-07","05:26:07",""
"7245579","10.9497","0.0011","10.1546","0.0011","12.5474","0.0019","90","","111.425","0.008","90","","1298.7","0.3","230","2","230","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","9n","","- C13 H18 N2 O3 -","- C13 H18 N2 O3 -","- C52 H72 N8 O12 -","4","1","","González-Saiz, Beatriz; Pertejo, Pablo; Peña-Calleja, Pablo; Mielczarek, Marcin; Hermosilla, Tomás; Carreira-Barral, Israel; de Miguel, Olivia; Rodríguez-Vidal, Francisco; Quesada, Roberto; García-Valverde, María","Base-selective access to highly functionalized heterocycles from multicomponent Ugi adducts","Green Chemistry","2022","24","20","7988","7995","10.1039/D2GC02896D","","","1.54184","CuKα","","0.0506","0.0423","","","0.0995","0.1093","","","","","","1.065","","","","has coordinates","278987","2022-11-07","05:26:07",""
"7245608","9.8007","0.0008","19.457","0.0018","15.5025","0.0012","90","","99.565","0.007","90","","2915.1","0.4","150","0.1","150","0.1","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C28 H27 F7 N4 O4 -","- C28 H27 F7 N4 O4 -","- C112 H108 F28 N16 O16 -","4","2","","Chen, Yu-Lan; Sun, Li-Wen; Chen, Jia-Wei; Zhu, Ming-Quan; Ma, Mengtao; Shen, Zhi-Liang; Chu, Xue-Qiang","Four-component defluorinative reaction of allylic fluorides, amidines, and Cs2CO3 under transition-metal-free conditions","Green Chemistry","2022","24","18","6816","6822","10.1039/D2GC02045A","","x-ray","0.71073","MoKα","","0.1359","0.0926","","","0.2199","0.2673","","","","","","1.005","","","","has coordinates,has disorder","278366","2022-10-05","20:19:13",""
"7245620","8.9547","0.0002","8.4131","0.0001","16.386","0.0003","90","","99.853","0.002","90","","1216.26","0.04","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C11 H14 N2 O3 S -","- C11 H14 N2 O3 S -","- C44 H56 N8 O12 S4 -","4","1","","Wang, Hai-Xia; Li, Zhi-Hao; Li, Wan-Wan; Qu, Gui-Rong; Yang, Qi-Liang; Guo, Hai-Ming","Electrochemically driven oxidative C–H/N–H cross-coupling reactions of cyclic sulfamidate imines with primary anilines and secondary amines","Green Chemistry","2022","24","21","8377","8385","10.1039/D2GC03218J","","x-ray","1.54184","CuKα","","0.0434","0.0398","","","0.1122","0.1169","","","","","","1.051","","","","has coordinates","278993","2022-11-07","05:26:57",""
"7245621","6.9208","0.0009","7.4115","0.0006","11.9359","0.0012","101.965","0.007","90.131","0.009","92.439","0.008","598.35","0.11","169.99","0.1","169.99","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C13 H10 N2 O3 S -","- C13 H10 N2 O3 S -","- C26 H20 N4 O6 S2 -","2","1","","Wang, Hai-Xia; Li, Zhi-Hao; Li, Wan-Wan; Qu, Gui-Rong; Yang, Qi-Liang; Guo, Hai-Ming","Electrochemically driven oxidative C–H/N–H cross-coupling reactions of cyclic sulfamidate imines with primary anilines and secondary amines","Green Chemistry","2022","24","21","8377","8385","10.1039/D2GC03218J","","x-ray","1.54184","CuKα","","0.1294","0.1261","","","0.3218","0.3232","","","","","","1.205","","","","has coordinates,has disorder","278993","2022-11-07","05:26:57",""
"7245622","7.9773","0.0004","8.6323","0.0004","8.8553","0.0004","92.357","0.004","103.812","0.004","111.69","0.004","544.55","0.05","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C11 H12 N2 O3 S -","- C11 H12 N2 O3 S -","- C22 H24 N4 O6 S2 -","2","1","","Wang, Hai-Xia; Li, Zhi-Hao; Li, Wan-Wan; Qu, Gui-Rong; Yang, Qi-Liang; Guo, Hai-Ming","Electrochemically driven oxidative C–H/N–H cross-coupling reactions of cyclic sulfamidate imines with primary anilines and secondary amines","Green Chemistry","2022","24","21","8377","8385","10.1039/D2GC03218J","","x-ray","1.54184","CuKα","","0.044","0.0421","","","0.1115","0.1128","","","","","","1.058","","","","has coordinates","278993","2022-11-07","05:26:57",""
"7245623","8.0147","0.0002","8.1452","0.0002","9.4761","0.0002","94.6","0.002","107.839","0.002","107.022","0.002","553.18","0.03","295.12","0.1","295.12","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C11 H12 N2 O3 S -","- C11 H12 N2 O3 S -","- C22 H24 N4 O6 S2 -","2","1","","Wang, Hai-Xia; Li, Zhi-Hao; Li, Wan-Wan; Qu, Gui-Rong; Yang, Qi-Liang; Guo, Hai-Ming","Electrochemically driven oxidative C–H/N–H cross-coupling reactions of cyclic sulfamidate imines with primary anilines and secondary amines","Green Chemistry","2022","24","21","8377","8385","10.1039/D2GC03218J","","x-ray","1.54184","CuKα","","0.0424","0.0414","","","0.1188","0.1203","","","","","","1.053","","","","has coordinates","278993","2022-11-07","05:26:57",""
"7245624","9.887","0.0002","7.8158","0.0002","18.9459","0.0004","90","","101.306","0.002","90","","1435.63","0.06","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H14 N2 O3 S -","- C15 H14 N2 O3 S -","- C60 H56 N8 O12 S4 -","4","1","","Wang, Hai-Xia; Li, Zhi-Hao; Li, Wan-Wan; Qu, Gui-Rong; Yang, Qi-Liang; Guo, Hai-Ming","Electrochemically driven oxidative C–H/N–H cross-coupling reactions of cyclic sulfamidate imines with primary anilines and secondary amines","Green Chemistry","2022","24","21","8377","8385","10.1039/D2GC03218J","","x-ray","1.54184","CuKα","","0.0606","0.056","","","0.1512","0.1601","","","","","","1.061","","","","has coordinates","278993","2022-11-07","05:26:57",""
"7245625","11.2705","0.0001","12.223","0.0002","20.2303","0.0002","90","","90","","90","","2786.91","0.06","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C15 H14 N2 O4 S -","- C15 H14 N2 O4 S -","- C120 H112 N16 O32 S8 -","8","2","","Wang, Hai-Xia; Li, Zhi-Hao; Li, Wan-Wan; Qu, Gui-Rong; Yang, Qi-Liang; Guo, Hai-Ming","Electrochemically driven oxidative C–H/N–H cross-coupling reactions of cyclic sulfamidate imines with primary anilines and secondary amines","Green Chemistry","2022","24","21","8377","8385","10.1039/D2GC03218J","","x-ray","1.54184","CuKα","","0.034","0.0322","","","0.0879","0.0896","","","","","","1.044","","","","has coordinates","278993","2022-11-07","05:26:57",""
"7245630","8.6009","0.0012","21.017","0.003","11.5416","0.0015","90","","94.661","0.003","90","","2079.4","0.5","296","2","296","2","","","","","","","","5","C 1 c 1","C -2yc","9","","","","- C22 H22 F3 N3 O2 -","- C22 H22 F3 N3 O2 -","- C88 H88 F12 N12 O8 -","4","1","","Xuan, Liangming; Du, Ruyang; Lei, Panpan; Zhao, Wei; Tan, Lixiang; Ni, Chuanzhi; Wang, Haifeng; Yan, Qiongjiao; Wang, Wei; Chen, Fener","Remote C(sp3)–H heteroarylation of N-fluorocarboxamides with quinoxalin-2(1H)-ones under visible-light-induced photocatalyst-free conditions","Green Chemistry","2022","24","24","9475","9481","10.1039/D2GC02874C","","","0.71073","MoKα","","0.091","0.052","","","0.106","0.1244","","","","","","1.061","","","","has coordinates","280174","2023-01-06","09:40:59",""
"7245730","17.601","0.002","11.3637","0.0015","24.466","0.003","90","","93.413","0.004","90","","4884.8","1","110","","110","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C40 H36 N8 Ni O2 -","- C40 H36 N8 Ni O2 -","- C160 H144 N32 Ni4 O8 -","4","0.5","","Sekar, Pandiaraj; Vasanthakumar, Punitharaj; Shanmugam, Ramasamy; Senthil Kumar, Shanmugam; Agnoli, Stefano; Deepak, Rajasekharan Jayakumari; Murugan, Karthik; Bhuvanesh, Nattamai; Karvembu, Ramasamy","Green synthesis of a redox-active riboflavin-integrated Ni-MOF and its versatile electrocatalytic applications towards oxygen evolution and reduction, and HMF oxidation reactions","Green Chemistry","2022","24","23","9233","9244","10.1039/D2GC02939A","","","0.71073","MoKα","","0.0985","0.0914","","","0.2182","0.2214","","","","","","1.052","","","","has coordinates","280177","2023-01-06","09:41:39",""
"7245762","8.3612","0.0002","9.7442","0.0002","10.6475","0.0002","65.818","0.001","86.321","0.001","79.417","0.001","777.84","0.03","200","","200","","","","","","","","","4","P -1","-P 1","2","","","","- C19 H17 N3 S -","- C19 H17 N3 S -","- C38 H34 N6 S2 -","2","1","","Li, Sifeng; Wang, Taimin; Li, Xingchen; Fang, Lijing; Zhai, Hongbin; Cheng, Bin","Switchable electrooxidative N-methyl amines: access to C3-aminomethylated and C3-arylmethylated imidazo[1,2-a] pyridines","Green Chemistry","2022","24","24","9482","9488","10.1039/D2GC03464F","","","1.54178","CuKα","","0.0503","0.0466","","","0.1197","0.1229","","","","","","1.099","","","","has coordinates,has disorder","280176","2023-01-06","09:41:17",""
"7245763","6.3317","0.0002","10.0072","0.0003","29.5714","0.0008","90","","92.36","0.002","90","","1872.13","0.1","200","","200","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H20 Br N3 -","- C22 H20 Br N3 -","- C88 H80 Br4 N12 -","4","1","","Li, Sifeng; Wang, Taimin; Li, Xingchen; Fang, Lijing; Zhai, Hongbin; Cheng, Bin","Switchable electrooxidative N-methyl amines: access to C3-aminomethylated and C3-arylmethylated imidazo[1,2-a] pyridines","Green Chemistry","2022","24","24","9482","9488","10.1039/D2GC03464F","","","1.54178","CuKα","","0.0543","0.0417","","","0.1057","0.1127","","","","","","1.044","","","","has coordinates","280176","2023-01-06","09:41:17",""
"7245764","8.365","0.004","10.655","0.005","10.809","0.005","115.055","0.014","99.78","0.014","98.016","0.015","835.6","0.7","298","","298","","","","","","","","","3","P -1","-P 1","2","","","","- C21 H19 N3 -","- C21 H19 N3 -","- C42 H38 N6 -","2","1","","Li, Sifeng; Wang, Taimin; Li, Xingchen; Fang, Lijing; Zhai, Hongbin; Cheng, Bin","Switchable electrooxidative N-methyl amines: access to C3-aminomethylated and C3-arylmethylated imidazo[1,2-a] pyridines","Green Chemistry","2022","24","24","9482","9488","10.1039/D2GC03464F","","","0.71073","MoKα","","0.0676","0.047","","","0.1198","0.1352","","","","","","1.033","","","","has coordinates","280176","2023-01-06","09:41:17",""
"7245794","6.0752","0.0003","9.8777","0.0005","22.1887","0.0013","90","","91.536","0.005","90","","1331.04","0.12","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C16 H16 O S -","- C16 H16 O S -","- C64 H64 O4 S4 -","4","1","","Zhu, Can-Ming; Liang, Rong-Bin; Xiao, Yonghong; Zhou, Wei; Tong, Qing-Xiao; Zhong, Jian-Ji","Metal-free and site-selective α-C–H functionalization of tetrahydrofuran enabled by the photocatalytic generation of bromine radicals","Green Chemistry","2023","25","3","960","965","10.1039/D2GC03347J","","x-ray","1.54184","CuKα","","0.0621","0.0538","","","0.138","0.1429","","","","","","1.069","","","","has coordinates","281484","2023-03-04","18:25:46",""
"7245915","8.6271","0.0004","11.5365","0.0006","12.0186","0.0008","112.233","0.006","90.786","0.005","95.43","0.004","1100.68","0.12","292.8","0.2","292.8","0.2","","","","","","","","4","P -1","-P 1","2","","","","- C23 H26 N2 O6 -","- C23 H26 N2 O6 -","- C46 H52 N4 O12 -","2","1","","Qian, Hang; Wang, Cui-Cui; Shen, Zi-Chen; Sun, Ming-Xue; Zhang, Hong-Chao; Fan, Shiming; Feng, Juan; Liu, Shouxin; Zhang, Zhi-Wei","Catalyst- and additive-free [3 + 3] cyclization–aromatization of β,γ-dioxobutanoate with amines for synthesis of p-aminophenols","Green Chemistry","2022","24","24","9690","9696","10.1039/D2GC03936B","","x-ray","1.54184","CuKα","","0.0843","0.0624","","","0.1739","0.1903","","","","","","1.057","","","","has coordinates","280175","2023-01-06","09:41:08",""
"7245933","15.9403","0.001","15.9403","0.001","31.662","0.002","90","","90","","90","","8045.1","0.9","173","2","173","2","","","","","","","","6","I 41/a c d :2","-I 4bd 2c","142","","","","- C4 H6.22 B0.22 F0.89 N0.89 Rh0.22 -","- C4 H6.22222 B0.222222 F0.888889 N0.888889 Rh0.222222 -","- C288 H448 B16 F64 N64 Rh16 -","72","2.25","","Qian, Chun; Zheng, Qingshu; Chen, Jie; Tu, Bo; Tu, Tao","Coordination assembly enables highly selective catalytic hydroaminomethylation of olefins","Green Chemistry","2023","25","4","1368","1379","10.1039/D2GC04195B","","","1.34138","GaKα","","0.0427","0.0387","","","0.1083","0.1118","","","","","","1.121","","","","has coordinates,has disorder","281473","2023-03-04","18:24:22",""
"7245934","13.617","0.001","17.292","0.0012","13.8897","0.001","90","","116.871","0.002","90","","2917.4","0.4","181","2","181","2","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C13.5 H17 B0.5 Cl F2 N2 Rh0.5 -","- C13.5 H17 B0.5 Cl F2 N2 Rh0.5 -","- C108 H136 B4 Cl8 F16 N16 Rh4 -","8","2","","Qian, Chun; Zheng, Qingshu; Chen, Jie; Tu, Bo; Tu, Tao","Coordination assembly enables highly selective catalytic hydroaminomethylation of olefins","Green Chemistry","2023","25","4","1368","1379","10.1039/D2GC04195B","","","1.34138","GaKα","","0.0428","0.037","","","0.0895","0.0941","","","","","","1.035","","","","has coordinates,has disorder","281473","2023-03-04","18:24:22",""
"7245935","15.1914","0.0009","15.8408","0.0009","55.703","0.003","90","","93.157","0.002","90","","13384.2","1.3","175","2","175","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C127 H147 B2 Cl9 F8 N8 Rh2 -","- C127 H147 B2 Cl9 F8 N8 Rh2 -","- C508 H588 B8 Cl36 F32 N32 Rh8 -","4","1","","Qian, Chun; Zheng, Qingshu; Chen, Jie; Tu, Bo; Tu, Tao","Coordination assembly enables highly selective catalytic hydroaminomethylation of olefins","Green Chemistry","2023","25","4","1368","1379","10.1039/D2GC04195B","","","1.34138","GaKα","","0.1326","0.1248","","","0.3036","0.3069","","","","","","1.087","","","","has coordinates,has disorder","281473","2023-03-04","18:24:22",""
"7245956","9.7566","0.001","23.006","0.002","13.329","0.0013","90","","109.053","0.002","90","","2827.9","0.5","296","2","296.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C38 H29 N O -","- C38 H29 N O -","- C152 H116 N4 O4 -","4","1","","Zhuang, Hongfeng; Hou, Qin; Han, Feng; Lv, Haotian; Miao, Chengxia","Heteropolyacid catalyzed O-alkylation of oximes with alcohols via a carbocation in dimethyl carbonate and mechanism insight","Green Chemistry","2023","25","1","310","317","10.1039/D2GC03214G","","","0.71073","MoKα","","0.0939","0.0487","","","0.1079","0.1339","","","","","","1.0678","","","","has coordinates","281471","2023-03-04","18:24:00",""
"7245973","11.7823","0.0009","17.2564","0.0012","8.5563","0.0005","90","","90","","90","","1739.7","0.2","273","2","273","2","","","","","","","","5","P n a 21","P 2c -2n","33","","","","- C22 H13 N O2 S -","- C22 H13 N O2 S -","- C88 H52 N4 O8 S4 -","4","1","","Chen, Shiliu; Yan, Qinqin; Fan, Jie; Guo, Changyou; Li, Lijun; Liu, Zhong-Quan; Li, Zejiang","Photo-induced spirocyclization of biaryl ynones with ammonium thiocyanate: access to thiocyanate-featured spiro[5,5]trienones","Green Chemistry","2023","25","1","153","160","10.1039/D2GC03710F","","","0.71073","MoKα","","0.0415","0.0339","","","0.0732","0.0788","","","","","","1.049","","","","has coordinates","281472","2023-03-04","18:24:06",""
"7245974","9.705","0.001","16.0805","0.0014","13.7744","0.0013","90","","93.165","0.009","90","","2146.4","0.4","298","","298","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C26 H22 F3 N3 -","- C26 H22 F3 N3 -","- C104 H88 F12 N12 -","4","1","","Sharma, Himanshi; Kumar, Manoj; Sethi, Aaftaab; Poonam,; Rathi, Brijesh","Metal-free construction of aminated isoquinoline frameworks from 2-(2-oxo-2-arylethyl) benzonitrile in an aqueous medium","Green Chemistry","2023","25","1","167","171","10.1039/D2GC04044A","","x-ray","0.71073","MoKα","","0.198","0.0777","","","0.1986","0.2893","","","","","","0.992","","","","has coordinates,has disorder","281470","2023-03-04","18:23:53",""
"7246014","6.8727","0.0009","7.4757","0.001","10.7012","0.0013","75.161","0.012","88.164","0.011","77.878","0.012","519.48","0.12","293","","293","","","","","","","","","5","P 1","P 1","1","","1","","- C20 H19 I O6 S -","- C20 H19 I O6 S -","- C20 H19 I O6 S -","1","1","","Peng, Chuxiong; Gu, Fengyan; Lin, Xiaofeng; Ding, Ning; Zhan, Qichen; Cao, Peng; Cao, Tao","Highly selective catalyst- and additive-free iodosulfonylation of cyclopropenes in water","Green Chemistry","2023","25","2","671","677","10.1039/D2GC04296G","","x-ray","1.54184","CuKα","","0.1093","0.0875","","","0.212","0.2652","","","","","","1.056","","","","has coordinates","281476","2023-03-04","18:24:43",""
"7246049","7.9459","0.0009","13.5525","0.0012","15.5352","0.0009","90","","90","","90","","1672.9","0.3","296","2","296.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C13 H25 N O7 S -","- C13 H25 N O7 S -","- C52 H100 N4 O28 S4 -","4","1","","Kuhl, Nadine; Turnbull, Ben W. H.; Ji, Yining; Larson, Reed T.; Shevlin, Michael; Prier, Christopher K.; Chung, Cheol K.; Desmond, Richard; Guetschow, Erik; He, Cyndi Qixin; Itoh, Tetsuji; Kuethe, Jeffrey T.; Newman, Justin A.; Reibarkh, Mikhail; Rivera, Nelo R.; Shang, Gao; Wang, Zhixun; Zewge, Daniel; Thaisrivongs, David A.","Utilizing biocatalysis and a sulfolane-mediated reductive acetal opening to access nemtabrutinib from cyrene","Green Chemistry","2023","25","2","606","613","10.1039/D2GC04117K","","","1.54184","CuKα","","0.0329","0.0307","","","0.0803","0.0823","","","","","","1.049","","","","has coordinates","281478","2023-03-04","18:24:56",""
"7246050","6.1009","0.0003","12.5179","0.0006","19.3009","0.0011","90","","90","","90","","1474.02","0.13","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C13 H19 N O5 S -","- C13 H19 N O5 S -","- C52 H76 N4 O20 S4 -","4","1","","Kuhl, Nadine; Turnbull, Ben W. H.; Ji, Yining; Larson, Reed T.; Shevlin, Michael; Prier, Christopher K.; Chung, Cheol K.; Desmond, Richard; Guetschow, Erik; He, Cyndi Qixin; Itoh, Tetsuji; Kuethe, Jeffrey T.; Newman, Justin A.; Reibarkh, Mikhail; Rivera, Nelo R.; Shang, Gao; Wang, Zhixun; Zewge, Daniel; Thaisrivongs, David A.","Utilizing biocatalysis and a sulfolane-mediated reductive acetal opening to access nemtabrutinib from cyrene","Green Chemistry","2023","25","2","606","613","10.1039/D2GC04117K","","","1.54178","CuKα","","0.0479","0.0431","","","0.1073","0.111","","","","","","1.074","","","","has coordinates,has disorder","281478","2023-03-04","18:24:56",""
"7246051","6.7731","0.0006","10.9956","0.0011","12.2301","0.0006","72.319","0.007","75.206","0.006","77.254","0.008","828.85","0.12","199.99","0.1","199.99","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C23 H16 Fe O2 -","- C23 H16 Fe O2 -","- C46 H32 Fe2 O4 -","2","1","","Lv, Hong; Wang, Xinchao; Hao, Yanzhao; Ma, Chao; Li, Shangda; Li, Gang; Zhang, Jian","Rhodium(ii)-catalyzed C–H carboxylation of ferrocenes with CO2","Green Chemistry","2023","25","2","554","559","10.1039/D2GC04337H","","x-ray","1.3405","GaKα","","0.0712","0.0563","","","0.139","0.161","","","","","","1.109","","","","has coordinates","281479","2023-03-04","18:25:11",""
"7246052","10.4854","0.0004","11.7036","0.0004","12.3518","0.0004","72.325","0.003","79.087","0.003","75.017","0.003","1384.97","0.09","100","0.2","100","0.2","","","","","","","","4","P -1","-P 1","2","","","","- C36 H28 Fe2 O6 -","- C36 H28 Fe2 O6 -","- C72 H56 Fe4 O12 -","2","1","","Lv, Hong; Wang, Xinchao; Hao, Yanzhao; Ma, Chao; Li, Shangda; Li, Gang; Zhang, Jian","Rhodium(ii)-catalyzed C–H carboxylation of ferrocenes with CO2","Green Chemistry","2023","25","2","554","559","10.1039/D2GC04337H","","x-ray","1.3405","GaKα","","0.0404","0.0373","","","0.0993","0.1011","","","","","","1.024","","","","has coordinates","281479","2023-03-04","18:25:11",""
"7246055","11.9543","0.0002","8.3309","0.0001","24.4205","0.0004","90","","102.103","0.002","90","","2377.98","0.07","293","2","293","2","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C10.8 H8.8 Cl0.4 N0.4 O0.8 S0.4 Se0.4 -","- C10.8 H8.8 Cl0.4 N0.4 O0.8 S0.4 Se0.4 -","- C108 H88 Cl4 N4 O8 S4 Se4 -","10","2.5","","Satyanarayana, Appanapalli N. V.; Mukherjee, Nilanjana; Chatterjee, Tanmay","100% atom-economical and highly regio- and stereoselective iodosulfenylation of alkynes: a reagentless and sustainable approach to access (E)-β-iodoalkenyl sulfides and (Z)-tamoxifen","Green Chemistry","2023","25","2","779","788","10.1039/D2GC04101D","","x-ray","1.54184","CuKα","","0.0403","0.0371","","","0.1043","0.1065","","","","","","1.116","","","","has coordinates","281475","2023-03-04","18:24:37",""
"7246056","17.9022","0.0003","6.0537","0.0001","34.1626","0.0006","90","","91.27","0.002","90","","3701.45","0.11","220","","220","","","","","","","","","5","I 1 2/a 1","-I 2ya","15","","","","- C21 H14 I N S2 -","- C21 H14 I N S2 -","- C168 H112 I8 N8 S16 -","8","1","","Satyanarayana, Appanapalli N. V.; Mukherjee, Nilanjana; Chatterjee, Tanmay","100% atom-economical and highly regio- and stereoselective iodosulfenylation of alkynes: a reagentless and sustainable approach to access (E)-β-iodoalkenyl sulfides and (Z)-tamoxifen","Green Chemistry","2023","25","2","779","788","10.1039/D2GC04101D","","x-ray","1.54184","CuKα","","0.0451","0.0449","","","0.1001","0.1002","","","","","","1.182","","","","has coordinates,has disorder","281475","2023-03-04","18:24:37",""
"7246068","6.7166","0.0012","9.3699","0.0017","12.656","0.002","68.667","0.017","79.026","0.015","72.896","0.016","706","0.2","179.99","0.1","179.99","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C17 H16 Cl N3 -","- C17 H16 Cl N3 -","- C34 H32 Cl2 N6 -","2","1","","Liu, Qingqing; Ci, Chenggang; Zhao, He; Xie, Rong; Jiang, HuanFeng; Zhang, Min","Direct access to functional phenazines via oxidative annulation of anilines and o-phenylenediamines with a reusable cobalt catalyst","Green Chemistry","2023","25","2","678","683","10.1039/D2GC03878A","","x-ray","1.54184","CuKα","","0.0893","0.067","","","0.1771","0.1991","","","","","","1.047","","","","has coordinates","281480","2023-03-04","18:25:18",""
"7246122","25.911","0.004","4.6748","0.0007","23.299","0.004","90","","104.436","0.002","90","","2733.1","0.8","100","2","100","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C13 H15 N O6 -","- C13 H15 N O6 -","- C104 H120 N8 O48 -","8","1","","Das, Tamal Kanti; Rodriguez Treviño, Agustin M.; Pandiri, Sanjay; Irvankoski, Sini; Siitonen, Juha H.; Rodriguez, Sara M.; Yousufuddin, Muhammed; Kürti, László","Catalyst-free transfer hydrogenation of activated alkenes exploiting isopropanol as the sole and traceless reductant","Green Chemistry","2023","25","2","746","754","10.1039/D2GC04315G","","","0.71073","MoKα","","0.0746","0.0504","","","0.1097","0.1221","","","","","","1.035","","","","has coordinates","281477","2023-03-04","18:24:49",""
"7246123","6.5868","0.0015","8.2313","0.0018","11.126","0.003","106.015","0.003","97.159","0.003","95.387","0.003","570.1","0.2","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C13 H12 O4 -","- C13 H12 O4 -","- C26 H24 O8 -","2","1","","Das, Tamal Kanti; Rodriguez Treviño, Agustin M.; Pandiri, Sanjay; Irvankoski, Sini; Siitonen, Juha H.; Rodriguez, Sara M.; Yousufuddin, Muhammed; Kürti, László","Catalyst-free transfer hydrogenation of activated alkenes exploiting isopropanol as the sole and traceless reductant","Green Chemistry","2023","25","2","746","754","10.1039/D2GC04315G","","","0.71073","MoKα","","0.0703","0.0449","","","0.1116","0.1289","","","","","","1.035","","","","has coordinates","281477","2023-03-04","18:24:49",""
"7246138","8.3761","0.0005","8.4007","0.0005","16.0336","0.0009","98.767","0.002","99.704","0.002","91.221","0.002","1097.79","0.11","293","2","293.15","","","","","","","","","4","P -1","-P 1","2","","","","- C24 H20 F5 O4 -","- C24 H21 F5 O4 -","- C48 H42 F10 O8 -","2","1","","Singh, Sanjay; Mondal, Sankalan; Vodnala, Nagaraju; Hazra, Chinmoy Kumar","Hydrogen bonding network-enabled Brønsted acid-catalyzed Friedel–Crafts reactions: a green approach to access unsymmetrical diaryl- and triarylmethanes","Green Chemistry","2023","25","3","1014","1022","10.1039/D2GC04684A","","","0.71073","MoKα","","0.1089","0.0574","","","0.1445","0.1702","","","","","","1.029","","","","has coordinates","281485","2023-03-04","18:26:09",""
"7246139","7.0243","0.0006","20.574","0.0016","11.0931","0.0009","90","","91.591","0.004","90","","1602.5","0.2","273","2","273.15","","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C18 H22 O4 -","- C18 H22 O4 -","- C72 H88 O16 -","4","1","","Singh, Sanjay; Mondal, Sankalan; Vodnala, Nagaraju; Hazra, Chinmoy Kumar","Hydrogen bonding network-enabled Brønsted acid-catalyzed Friedel–Crafts reactions: a green approach to access unsymmetrical diaryl- and triarylmethanes","Green Chemistry","2023","25","3","1014","1022","10.1039/D2GC04684A","","","0.71073","MoKα","","0.0487","0.0428","","","0.1194","0.1244","","","","","","1.0649","","","","has coordinates","281485","2023-03-04","18:26:10",""
"7246144","18.6508","0.0003","5.8796","0.0001","14.7464","0.0003","90","","94.7151","0.0007","90","","1611.61","0.05","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","Dimethyl 1-hydroxy-1,3,3a,3a1,5a,5a1,6,8,8a,10a-decahydro-3a,5a:8a,10adiepoxyisochromeno[ 6,5,4-def]isochromene-4,5-dicarboxylate","","- C18 H18 O9 -","- C18 H18 O9 -","- C72 H72 O36 -","4","1","","Averochkin, Gleb M.; Gordeev, Evgeniy G.; Kucherov, Fedor A.; Ananikov, Valentine P.","Rapid access to molecular complexity from bioderived 5-HMF derivatives via cascade cycloadditions","Green Chemistry","2023","25","3","1045","1055","10.1039/D2GC04197A","","","0.71073","MoKα","","0.0391","0.028","","","0.0647","0.0707","","","","","","1.038","","","","has coordinates","281481","2023-03-04","18:25:27",""
"7246145","10.361","0.0002","13.355","0.0003","13.4649","0.0003","62.271","0.002","70.487","0.002","70.729","0.002","1520.04","0.06","100","0.1","100","0.1","","","","","","","","3","P -1","-P 1","2","","(5-Benzoyl-4-(methoxycarbonyl)-3a1,6a-dihydro-1H,3H,6H,7H-3a,6:7,9adiepoxybenzo[ de]isochromene-6,7-diyl)bis(methylene) dibenzoate","","- C37 H30 O10 -","- C37 H30 O10 -","- C74 H60 O20 -","2","1","","Averochkin, Gleb M.; Gordeev, Evgeniy G.; Kucherov, Fedor A.; Ananikov, Valentine P.","Rapid access to molecular complexity from bioderived 5-HMF derivatives via cascade cycloadditions","Green Chemistry","2023","25","3","1045","1055","10.1039/D2GC04197A","","x-ray","1.54184","CuKα","","0.0585","0.0564","","","0.1665","0.1688","","","","","","1.047","","","","has coordinates","281481","2023-03-04","18:25:27",""
"7246146","10.5648","0.0003","16.247","0.0005","12.4776","0.0004","90","","110.308","0.001","90","","2008.6","0.11","100","2","100","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","Dimethyl 6-(acetoxymethyl)-7-(hydroxy(methoxy)methyl)-3a1,6a-dihydro- 1H,3H,6H,7H-3a,6:7,9a-diepoxybenzo[de]isochromene-4,5-dicarboxylate","","- C21 H24 O11 -","- C21 H24 O11 -","- C84 H96 O44 -","4","1","","Averochkin, Gleb M.; Gordeev, Evgeniy G.; Kucherov, Fedor A.; Ananikov, Valentine P.","Rapid access to molecular complexity from bioderived 5-HMF derivatives via cascade cycloadditions","Green Chemistry","2023","25","3","1045","1055","10.1039/D2GC04197A","","","0.71073","MoKα","","0.0563","0.0372","","","0.0816","0.0912","","","","","","1.049","","","","has coordinates","281481","2023-03-04","18:25:27",""
"7246147","9.1956","0.0001","33.6799","0.0005","10.508","0.0001","90","","97.813","0.001","90","","3224.19","0.07","100","0.1","100","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","Dimethyl 6,7-bis((benzoyloxy)methyl)-2-benzyl-2,3,3a1,6a-tetrahydro-1H,6H,7H- 3a,6:7,9a-diepoxybenzo[de]isoquinoline-4,5-dicarboxylate","","- C39 H35 N O10 -","- C39 H35 N O10 -","- C156 H140 N4 O40 -","4","1","","Averochkin, Gleb M.; Gordeev, Evgeniy G.; Kucherov, Fedor A.; Ananikov, Valentine P.","Rapid access to molecular complexity from bioderived 5-HMF derivatives via cascade cycloadditions","Green Chemistry","2023","25","3","1045","1055","10.1039/D2GC04197A","","x-ray","1.54184","CuKα","","0.0693","0.064","","","0.1588","0.1613","","","","","","1.089","","","","has coordinates","281481","2023-03-04","18:25:27",""
"7246166","18.0732","0.0003","8.28431","0.00018","20.8875","0.0004","90","","90","","90","","3127.36","0.1","169.99","0.1","169.99","0.1","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C19 H19 N O3 -","- C19 H19 N O3 -","- C152 H152 N8 O24 -","8","1","","Wei, Wan-Jie; Zhan, Lei; Jiang, Cai-Na; Tang, Hai-Tao; Pan, Ying-Ming; Ma, Xian-Li; Mo, Zu-Yu","Electrochemical oxidative cascade cyclization of olefinic amides and alcohols leading to the synthesis of alkoxylated 4H-3,1-benzoxazines and indolines","Green Chemistry","2023","25","3","928","933","10.1039/D2GC04645H","","x-ray","1.54184","CuKα","","0.0425","0.04","","","0.1012","0.1034","","","","","","1.05","","","","has coordinates","281482","2023-03-04","18:25:33",""
"7246185","7.7837","0.0001","31.1021","0.0004","8.6447","0.0001","90","","90","","90","","2092.79","0.05","100","0.1","100","0.1","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C27 H27 N O -","- C27 H27 N O -","- C108 H108 N4 O4 -","4","1","","Luo, Yu; Wang, Xilong; Liu, Qianwen; He, Yimiao; Li, Jing; Luo, Shuang; Zhu, Qiang","Palladium-catalyzed alkyne hydrocarbonylation under atmospheric pressure of carbon monoxide in the presence of hydrosilane","Green Chemistry","2023","25","3","1120","1127","10.1039/D2GC04689J","","x-ray","1.54184","CuKα","","0.0484","0.0471","","","0.1222","0.1231","","","","","","1.061","","","","has coordinates","281483","2023-03-04","18:25:39",""
"7246186","11.2","0.0002","7.8745","0.0001","11.8582","0.0002","90","","103.292","0.001","90","","1017.81","0.03","100","0.1","100","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C25 H29 N O -","- C25 H29 N O -","- C50 H58 N2 O2 -","2","1","","Luo, Yu; Wang, Xilong; Liu, Qianwen; He, Yimiao; Li, Jing; Luo, Shuang; Zhu, Qiang","Palladium-catalyzed alkyne hydrocarbonylation under atmospheric pressure of carbon monoxide in the presence of hydrosilane","Green Chemistry","2023","25","3","1120","1127","10.1039/D2GC04689J","","x-ray","1.54184","CuKα","","0.0317","0.0312","","","0.08","0.0804","","","","","","1.083","","","","has coordinates,has disorder","281483","2023-03-04","18:25:40",""
"7246229","3.7252","0.0001","11.5014","0.0004","18.9837","0.0006","90","","91.706","0.003","90","","813","0.04","100","2","100","0.1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C9 H5 N3 O -","- C9 H5 N3 O -","- C36 H20 N12 O4 -","4","1","","Li, Xin; Zarganes-Tzitzikas, Tryfon; Kurpiewska, Katarzyna; Dömling, Alexander","Amenamevir by Ugi-4CR","Green Chemistry","2023","25","4","1322","1325","10.1039/D2GC04869H","","x-ray","1.54184","CuKα","","0.0404","0.0362","","","0.1008","0.104","","","","","","1.083","","","","has coordinates","281474","2023-03-04","18:24:29",""
"7246230","19.6089","0.0003","13.7807","0.0002","17.823","0.0003","90","","101.936","0.002","90","","4712.08","0.13","100","2","100","2","","","","","","","","5","I 1 2/a 1","-I 2ya","15","","","","- C24 H26 N4 O5 S -","- C24 H26 N4 O5 S -","- C192 H208 N32 O40 S8 -","8","1","","Li, Xin; Zarganes-Tzitzikas, Tryfon; Kurpiewska, Katarzyna; Dömling, Alexander","Amenamevir by Ugi-4CR","Green Chemistry","2023","25","4","1322","1325","10.1039/D2GC04869H","","x-ray","1.54184","CuKα","","0.0629","0.0585","","","0.1579","0.1615","","","","","","1.085","","","","has coordinates","281474","2023-03-04","18:24:30",""
"7246286","18.8874","0.0014","6.1813","0.0005","17.2323","0.0011","90","","91.402","0.006","90","","2011.2","0.3","100.01","0.1","100.01","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C24 H16 F5 O2 P -","- C24 H16 F5 O2 P -","- C96 H64 F20 O8 P4 -","4","1","","Chu, Xue-Qiang; Cai, Song-Zhou; Chen, Jia-Wei; Yu, Zi-Lun; Ma, Mengtao; Walsh, Patrick J.; Shen, Zhi-Liang","Defluorophosphorylation of fluoroalkyl peroxides for the synthesis of highly substituted furans","Green Chemistry","2023","25","5","2000","2010","10.1039/D2GC04512E","","x-ray","0.71073","MoKα","","0.0522","0.0413","","","0.0952","0.1029","","","","","","1.053","","","","has coordinates","283364","2023-05-05","02:48:34",""
"7246287","11.345","0.0006","12.0953","0.0006","14.1162","0.0007","89.245","0.004","77.498","0.004","62.787","0.005","1673.55","0.17","100.01","0.1","100.01","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C36 H25 F5 O3 P2 -","- C36 H25 F5 O3 P2 -","- C72 H50 F10 O6 P4 -","2","1","","Chu, Xue-Qiang; Cai, Song-Zhou; Chen, Jia-Wei; Yu, Zi-Lun; Ma, Mengtao; Walsh, Patrick J.; Shen, Zhi-Liang","Defluorophosphorylation of fluoroalkyl peroxides for the synthesis of highly substituted furans","Green Chemistry","2023","25","5","2000","2010","10.1039/D2GC04512E","","x-ray","0.71073","MoKα","","0.0701","0.0556","","","0.1543","0.1719","","","","","","1.068","","","","has coordinates","283364","2023-05-05","02:48:34",""
"7246321","10.3322","0.0002","10.7423","0.0002","14.3583","0.0002","97.245","0.002","100.734","0.002","116.704","0.002","1358.21","0.05","298.06","0.1","298.06","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C10.33 H7.33 N1.33 O1.33 S0.67 -","- C10.3333 H7.33333 N1.33333 O1.33333 S0.666667 -","- C62 H44 N8 O8 S4 -","6","3","","Zhang, Zhicheng; Wen, Linzi; Xu, Shihai; Tang, Yu; Cao, Xiaohui; Feng, Pengju","Consecutive cross-dehydrogenative C–O and C–N construction for the synthesis of polyarene with AIE properties under electrochemical condition involving oxygen radical species","Green Chemistry","2023","25","6","2287","2292","10.1039/D3GC00124E","","x-ray","1.54184","CuKα","","0.0763","0.0683","","","0.1977","0.2069","","","","","","1.049","","","","has coordinates","283366","2023-05-05","02:48:50",""
"7246353","9.877","0.0006","12.1262","0.0009","12.1406","0.0008","66.668","0.006","83.456","0.005","83.448","0.005","1322.68","0.17","150.01","0.1","150","","","","","","","","","6","P -1","-P 1","2","","","","- C25 H30 Fe K N2 O8 -","- C25 H30 Fe K N2 O8 -","- C50 H60 Fe2 K2 N4 O16 -","2","1","","Diment, Wilfred T.; Rosetto, Gloria; Ezaz-Nikpay, Noura; Kerr, Ryan W. F.; Williams, Charlotte K.","A highly active, thermally robust iron(iii)/potassium(i) heterodinuclear catalyst for bio-derived epoxide/anhydride ring-opening copolymerizations","Green Chemistry","2023","25","6","2262","2267","10.1039/D2GC04580J","","x-ray","1.54184","CuKα","","0.0423","0.0358","","","0.0905","0.0969","","","","","","1.035","","","","has coordinates","283367","2023-05-05","02:49:24",""
"7246354","9.0238","0.0002","12.9234","0.0002","19.4802","0.0003","90","","96.797","0.002","90","","2255.78","0.07","150","0.5","150","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C23 H27 Fe N2 O6 -","- C23 H27 Fe N2 O6 -","- C92 H108 Fe4 N8 O24 -","4","1","","Diment, Wilfred T.; Rosetto, Gloria; Ezaz-Nikpay, Noura; Kerr, Ryan W. F.; Williams, Charlotte K.","A highly active, thermally robust iron(iii)/potassium(i) heterodinuclear catalyst for bio-derived epoxide/anhydride ring-opening copolymerizations","Green Chemistry","2023","25","6","2262","2267","10.1039/D2GC04580J","","","1.54184","CuKα","","0.0392","0.0311","","","0.0762","0.0809","","","","","","1.029","","","","has coordinates","283367","2023-05-05","02:49:24",""
"7246413","13.0551","0.0006","7.4021","0.0003","13.9932","0.0006","90","","101.381","0.002","90","","1325.65","0.1","300","","300","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H10 I N O -","- C15 H10 I N O -","- C60 H40 I4 N4 O4 -","4","1","","Wu, Jianglong; Ma, Yinfeng; Wang, Yan; Wang, Chenyu; Luo, Hui; Li, Dianjun; Yang, Jinhui","Copper-catalyzed direct synthesis of 3-methylene-2-arylisoindolin-1-ones with calcium carbide as a surrogate of gaseous acetylene","Green Chemistry","2023","25","9","3425","3430","10.1039/D2GC03572C","","","0.71073","MoKα","","0.033","0.027","","","0.0803","0.0982","","","","","","0.997","","","","has coordinates","284285","2023-06-05","04:36:46",""
"7246418","9.58017","0.00005","9.58017","0.00005","33.7964","0.0003","90","","90","","90","","3101.82","0.04","100.01","0.16","100.01","0.16","","","","","","","","4","P 43","P 4cw","78","","(4R,7aR)-4-methyl-3,7-diphenyl-5,6,7,7a-tetrahydrofuro[2,3-b]pyridin-2(4H)-one","","- C20 H19 N O2 -","- C20 H19 N O2 -","- C160 H152 N8 O16 -","8","2","","Feng, Tian; Zhu, Zile; Zhang, Dongmei; Wang, Siyi; Li, Ruopu; Zhu, Zhaolin; Zhang, Xinxing; Qiu, Youai","Electrochemical dual α,β-C(sp3)–H functionalization of cyclic N-aryl amines","Green Chemistry","2023","25","7","2681","2689","10.1039/D3GC00344B","","x-ray","1.54184","CuKα","","0.0527","0.0518","","","0.1242","0.1247","","","","","","1.142","","","","has coordinates","283368","2023-05-05","02:49:30",""
"7246419","11.6432","0.0002","16.4149","0.0002","9.6857","0.0002","90","","113.866","0.002","90","","1692.87","0.06","294.5","0.3","294.5","0.3","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H19 N O3 S2 -","- C16 H19 N O3 S2 -","- C64 H76 N4 O12 S8 -","4","1","","Wang, Qian; Meng, Xiu-Jin; Tang, Hai-Tao; Pan, Ying-Ming; Duan, Wen-Gui; He, Mu-Xue","Electrochemically driven α-thiocarbamylation via a dehydrocoupling strategy of β-ketoesters with amines and CS2","Green Chemistry","2023","25","7","2572","2576","10.1039/D2GC04544C","","x-ray","1.54184","CuKα","","0.0636","0.0618","","","0.1713","0.1736","","","","","","0.911","","","","has coordinates","283369","2023-05-05","02:49:37",""
"7246425","25.949","0.007","10.787","0.003","11.392","0.003","90","","101.972","0.008","90","","3119.4","1.5","193","","193","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H19 N O -","- C20 H19 N O -","- C160 H152 N8 O8 -","8","2","","Wei, Minghui; Liu, Chengkou; Wang, Chang-Sheng; Li, Yuguang; Qiu, Peng; Dong, Quanxiao; Yang, Zhao; Fang, Zheng; Guo, Kai","Synthesis of pyrido[1,2-a]indol-6(7H)-ones via a visible light-photocatalyzed formal (4 + 2) cycloaddition of indole-derived bromides and alkenes or alkynes","Green Chemistry","2023","25","6","2453","2457","10.1039/D2GC04491A","","","0.71073","MoKα","","0.1969","0.0996","","","0.1989","0.2444","","","","","","1.061","","","","has coordinates","283365","2023-05-05","02:48:43",""
"7246452","4.9594","0.0001","10.7311","0.0001","27.2017","0.0003","90","","90","","90","","1447.67","0.04","294.15","","294.15","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","(S)-N-(3-(2-chlorophenyl)-2-methylpropyl)prop-2-en-1-amine hydrochloride","","- C13 H19 Cl2 N -","- C13 H19 Cl2 N -","- C52 H76 Cl8 N4 -","4","1","","Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming","Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization","Green Chemistry","2023","25","12","4667","4673","10.1039/D3GC00047H","","x-ray","1.54184","CuKα","","0.0306","0.0297","","","0.0858","0.0867","","","","","","1.032","","","","has coordinates","286153","2023-09-05","19:59:18",""
"7246453","4.8988","0.0002","10.7881","0.0003","13.7759","0.0004","90","","98.02","0.003","90","","720.92","0.04","113.15","","113.15","","","","","","","","","6","P 1 21 1","P 2yb","4","","(S)-N-(3-(2-bromo-3-fluorophenyl)-2-methylpropyl)prop-2-en-1-amine hydrochloride","","- C13 H18 Br Cl F N -","- C13 H18 Br Cl F N -","- C26 H36 Br2 Cl2 F2 N2 -","2","1","","Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming","Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization","Green Chemistry","2023","25","12","4667","4673","10.1039/D3GC00047H","","x-ray","0.71073","MoKα","","0.0615","0.0589","","","0.15","0.1517","","","","","","1.122","","","","has coordinates","286153","2023-09-05","19:59:18",""
"7246454","4.9604","0.0002","10.8195","0.0004","29.3754","0.001","90","","90","","90","","1576.55","0.1","113.15","","113.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","(S)-N-(3-(2-bromo-3-methylphenyl)-2-methylpropyl)prop-2-en-1-amine hydrochloride","","- C14 H21 Br Cl N -","- C14 H21 Br Cl N -","- C56 H84 Br4 Cl4 N4 -","4","1","","Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming","Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization","Green Chemistry","2023","25","12","4667","4673","10.1039/D3GC00047H","","x-ray","0.71073","MoKα","","0.0375","0.035","","","0.0842","0.0855","","","","","","1.088","","","","has coordinates","286153","2023-09-05","19:59:18",""
"7246455","9.5543","0.0002","6.5919","0.0002","12.4634","0.0003","90","","98.424","0.002","90","","776.49","0.03","113.15","","113.15","","","","","","","","","5","P 1 21 1","P 2yb","4","","(S)-N-(3-(2-bromo-4-methylphenyl)-2-methylpropyl)prop-2-en-1-amine hydrochloride","","- C14 H21 Br Cl N -","- C14 H21 Br Cl N -","- C28 H42 Br2 Cl2 N2 -","2","1","","Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming","Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization","Green Chemistry","2023","25","12","4667","4673","10.1039/D3GC00047H","","x-ray","0.71073","MoKα","","0.0495","0.038","","","0.082","0.0866","","","","","","1.029","","","","has coordinates","286153","2023-09-05","19:59:18",""
"7246456","7.6197","0.0002","14.1232","0.0003","27.1001","0.0007","90","","90","","90","","2916.36","0.12","113.15","","113.15","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","(S)-N-(3-(2-bromo-4-fluorophenyl)-2-methylpropyl)prop-2-en-1-amine hydrochloride","","- C13 H18 Br Cl F N -","- C13 H18 Br Cl F N -","- C104 H144 Br8 Cl8 F8 N8 -","8","2","","Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming","Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization","Green Chemistry","2023","25","12","4667","4673","10.1039/D3GC00047H","","x-ray","0.71073","MoKα","","0.0529","0.0427","","","0.0909","0.0959","","","","","","0.997","","","","has coordinates","286153","2023-09-05","19:59:18",""
"7246457","4.8335","0.0001","26.095","0.0006","11.3444","0.0003","90","","90.954","0.002","90","","1430.67","0.06","113","2","113.15","","","","","","","","","6","P 1 21 1","P 2yb","4","","(S)-N-(3-(2-bromo-5-fluorophenyl)-2-methylpropyl)prop-2-en-1-amine hydrochloride","","- C13 H18 Br Cl F N -","- C13 H18 Br Cl F N -","- C52 H72 Br4 Cl4 F4 N4 -","4","2","","Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming","Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization","Green Chemistry","2023","25","12","4667","4673","10.1039/D3GC00047H","","x-ray","0.71073","MoKα","","0.0531","0.0491","","","0.1436","0.1472","","","","","","1.018","","","","has coordinates","286153","2023-09-05","19:59:18",""
"7246458","4.7559","0.0002","10.6799","0.0004","28.6366","0.0009","90","","90","","90","","1454.53","0.09","113.15","","113.15","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","(S)-N-(3-(2-bromo-6-fluorophenyl)-2-methylpropyl)prop-2-en-1-amine hydrochloride","","- C13 H18 Br Cl F N -","- C13 H18 Br Cl F N -","- C52 H72 Br4 Cl4 F4 N4 -","4","1","","Xu, Zefei; Feng, Jinhui; Yao, Peiyuan; Wu, Qiaqing; Zhu, Dunming","Chemo-enzymatic synthesis of chiral 3-substituted tetrahydroquinolines by a sequential biocatalytic cascade and Buchwald–Hartwig cyclization","Green Chemistry","2023","25","12","4667","4673","10.1039/D3GC00047H","","x-ray","0.71073","MoKα","","0.0467","0.0394","","","0.0842","0.0879","","","","","","1.06","","","","has coordinates","286153","2023-09-05","19:59:18",""
"7246493","8.6581","0.0015","12.1447","0.0018","22.107","0.003","90","","90","","90","","2324.6","0.6","293","2","293","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C14 H13 N O2 -","- C14 H13 N O2 -","- C112 H104 N8 O16 -","8","1","","Xu, Feng; Li, Zao; Zhang, Li-Long; Liu, Shengqi; Li, Hu; Liao, Yuhe; Yang, Song","Synthesis of renewable isoindolines from bio-based furfurals","Green Chemistry","2023","25","8","3297","3305","10.1039/D2GC04786A","","","1.54178","CuKα","","0.1112","0.0577","","","0.1195","0.1568","","","","","","1","","","","has coordinates","283360","2023-05-05","02:47:40",""
"7246494","13.6538","0.0011","9.0781","0.0008","10.6852","0.0009","90","","108.522","0.004","90","","1255.83","0.19","298","2","298","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C14 H12 Cl N O2 -","- C14 H12 Cl N O2 -","- C56 H48 Cl4 N4 O8 -","4","1","","Xu, Feng; Li, Zao; Zhang, Li-Long; Liu, Shengqi; Li, Hu; Liao, Yuhe; Yang, Song","Synthesis of renewable isoindolines from bio-based furfurals","Green Chemistry","2023","25","8","3297","3305","10.1039/D2GC04786A","","","0.71073","MoKα","","0.0832","0.0481","","","0.0946","0.1024","","","","","","1.079","","","","has coordinates","283360","2023-05-05","02:47:40",""
"7246495","5.9303","0.0007","7.6388","0.0009","23.149","0.003","90","","94.506","0.003","90","","1045.4","0.2","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C14 H11 N O -","- C14 H11 N O -","- C56 H44 N4 O4 -","4","1","","Xu, Feng; Li, Zao; Zhang, Li-Long; Liu, Shengqi; Li, Hu; Liao, Yuhe; Yang, Song","Synthesis of renewable isoindolines from bio-based furfurals","Green Chemistry","2023","25","8","3297","3305","10.1039/D2GC04786A","","","1.54178","CuKα","","0.1104","0.0905","","","0.234","0.2474","","","","","","1.395","","","","has coordinates","283360","2023-05-05","02:47:40",""
"7246496","5.4795","0.0004","11.4206","0.0009","19.3592","0.0016","90","","90","","90","","1211.48","0.16","298","2","298","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C14 H12 Br N O2 -","- C14 H12 Br N O2 -","- C56 H48 Br4 N4 O8 -","4","1","","Xu, Feng; Li, Zao; Zhang, Li-Long; Liu, Shengqi; Li, Hu; Liao, Yuhe; Yang, Song","Synthesis of renewable isoindolines from bio-based furfurals","Green Chemistry","2023","25","8","3297","3305","10.1039/D2GC04786A","","","0.71073","MoKα","","0.0543","0.0413","","","0.0881","0.0922","","","","","","1.013","","","","has coordinates","283360","2023-05-05","02:47:40",""
"7246497","10.7651","0.0005","4.8762","0.0002","13.0778","0.0005","90","","106.91","0.005","90","","656.81","0.05","120.01","0.1","120.01","0.1","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C14 H12 Cl N3 O S -","- C14 H12 Cl N3 O S -","- C28 H24 Cl2 N6 O2 S2 -","2","1","","Hommelsheim, Renè; Bausch, Sandra; van Nahl, Robin; Ward, Jas S.; Rissanen, Kari; Bolm, Carsten","Synthesis of 3-amino-substituted benzothiadiazine oxides by a palladium-catalysed cascade reaction","Green Chemistry","2023","25","8","3021","3026","10.1039/D3GC00442B","","x-ray","1.54184","CuKα","","0.0473","0.0431","","","0.1078","0.1119","","","","","","1.028","","","","has coordinates","283362","2023-05-05","02:48:05",""
"7246540","7.079","0.002","9.363","0.003","11.864","0.003","93.881","0.005","97.142","0.005","100.629","0.004","763.5","0.4","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C15 H20 Br N O2 -","- C15 H20 Br N O2 -","- C30 H40 Br2 N2 O4 -","2","1","","Zhang, Zhongyi; Hou, Zhong-Wei; Chen, Hao; Li, Pinhua; Wang, Lei","Electrochemical electrophilic bromination/spirocyclization of N-benzyl-acrylamides to brominated 2-azaspiro[4.5]decanes","Green Chemistry","2023","25","9","3543","3548","10.1039/D3GC00728F","","","0.71073","MoKα","","0.0643","0.0443","","","0.1089","0.1155","","","","","","0.996","","","","has coordinates","284281","2023-06-05","04:36:13",""
"7246541","6.676","0.0017","23.1","0.006","9.948","0.003","90","","94.562","0.004","90","","1529.3","0.7","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C16 H23 N O3 -","- C16 H23 N O3 -","- C64 H92 N4 O12 -","4","1","","Zhang, Zhongyi; Hou, Zhong-Wei; Chen, Hao; Li, Pinhua; Wang, Lei","Electrochemical electrophilic bromination/spirocyclization of N-benzyl-acrylamides to brominated 2-azaspiro[4.5]decanes","Green Chemistry","2023","25","9","3543","3548","10.1039/D3GC00728F","","","0.71073","MoKα","","0.0492","0.0398","","","0.1031","0.1081","","","","","","1.019","","","","has coordinates","284281","2023-06-05","04:36:13",""
"7246546","8.415","0.001","8.415","0.001","13.689","0.002","90","","90","","120","","839.48","0.19","273","2","273","2","","","","","","","","3","P 32 2 1","P 32 2""","154","","","","- C14 H10 O2 -","- C14 H10 O2 -","- C42 H30 O6 -","3","0.5","","Bhukta, Swadhapriya; Chatterjee, Rana; Dandela, Rambabu","Metal-free, 2-MeTHF mediated C(sp)–H functionalization of alkynes with anilines to access diaryl 1,2-diketones bearing lower E-factors","Green Chemistry","2023","25","8","3034","3039","10.1039/D3GC00267E","","","0.71073","MoKα","","0.1336","0.0494","","","0.1259","0.2289","","","","","","0.771","","","","has coordinates","283361","2023-05-05","02:47:48",""
"7246554","12.54957","0.00013","5.45668","0.00004","21.5051","0.0003","90","","100.046","0.001","90","","1450.07","0.03","100","2","100","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C20 H18 N2 -","- C20 H18 N2 -","- C80 H72 N8 -","4","1","","Everaert, Jonas; Leus, Karen; Rijckaert, Hannes; Debruyne, Maarten; Van Hecke, Kristof; Morent, Rino; De Geyter, Nathalie; Van Speybroeck, Veronique; Van Der Voort, Pascal; Stevens, Christian V.","A recyclable rhodium catalyst anchored onto a bipyridine covalent triazine framework for transfer hydrogenation of N-heteroarenes in water","Green Chemistry","2023","25","8","3267","3277","10.1039/D3GC00167A","","x-ray","1.54184","CuKα","","0.0378","0.0351","","","0.0938","0.0962","","","","","","1.04","","","","has coordinates","283363","2023-05-05","02:48:25",""
"7246560","9.7371","0.0009","10.1536","0.001","12.7652","0.0012","102.012","0.003","94.177","0.002","110.29","0.002","1143.27","0.19","100","","100","","","","","","","","","3","P -1","-P 1","2","","","","- C30 H28 O3 -","- C30 H28 O3 -","- C60 H56 O6 -","2","1","","Nandi, Shantanu; Das, Pritha; Das, Subhodeep; Mondal, Shuvam; Jana, Ranjan","Visible-light-mediated β-acylative divergent alkene difunctionalization with Katritzky salt/CO2","Green Chemistry","2023","25","9","3633","3643","10.1039/D3GC00143A","","","1.54178","CuKα","","0.0689","0.0676","","","0.1901","0.1918","","","","","","1.045","","","","has coordinates","284284","2023-06-05","04:36:39",""
"7246561","8.998","0.0002","11.5521","0.0002","18.5351","0.0004","79.764","0.001","84.293","0.001","67.467","0.001","1750.2","0.06","298","","298","","","","","","","","","3","P -1","-P 1","2","","SNAN-966","","- C44 H36 O6 -","- C44 H36 O6 -","- C88 H72 O12 -","2","1","","Nandi, Shantanu; Das, Pritha; Das, Subhodeep; Mondal, Shuvam; Jana, Ranjan","Visible-light-mediated β-acylative divergent alkene difunctionalization with Katritzky salt/CO2","Green Chemistry","2023","25","9","3633","3643","10.1039/D3GC00143A","","","1.54178","CuKα","","0.0788","0.0684","","","0.1755","0.1871","","","","","","1.098","","","","has coordinates","284284","2023-06-05","04:36:39",""
"7246605","6.607","0.002","10.064","0.002","21.6","0.004","90","","90","","90","","1436.2","0.6","296","2","296","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C18 H16 N2 -","- C18 H16 N2 -","- C72 H64 N8 -","4","1","","Devi, Arpita; Bharali, Mrinmoy Manash; Biswas, Subir; Bora, Tonmoy J.; Nath, Jayanta K.; Lee, Seonghwan; Park, Young-Bin; Saikia, Lakshi; Baruah, Manash J.; Bania, Kusum K.","Utilization of methanol and ethanol for 3,3′-bis(indolyl)methane synthesis through activation of peroxymonosulfate over a copper catalyst","Green Chemistry","2023","25","9","3443","3448","10.1039/D3GC00440F","","","0.71073","MoKα","","0.112","0.0627","","","0.1339","0.1528","","","","","","1.015","","","","has coordinates","284283","2023-06-05","04:36:32",""
"7246606","7.817","0.015","18.49","0.03","11.24","0.02","90","","96.61","0.04","90","","1614","5","296","2","296","2","","","","","","","","4","I 1 c 1","I -2yc","9","","","","- C18 H14 Cl2 N2 -","- C18 H14 Cl2 N2 -","- C72 H56 Cl8 N8 -","4","1","","Devi, Arpita; Bharali, Mrinmoy Manash; Biswas, Subir; Bora, Tonmoy J.; Nath, Jayanta K.; Lee, Seonghwan; Park, Young-Bin; Saikia, Lakshi; Baruah, Manash J.; Bania, Kusum K.","Utilization of methanol and ethanol for 3,3′-bis(indolyl)methane synthesis through activation of peroxymonosulfate over a copper catalyst","Green Chemistry","2023","25","9","3443","3448","10.1039/D3GC00440F","","","0.71073","MoKα","","0.061","0.048","","","0.1152","0.1238","","","","","","1.089","","","","has coordinates","284283","2023-06-05","04:36:32",""
"7246607","12.96","0.005","18.557","0.01","7.814","0.003","90","","120.687","0.009","90","","1616.1","1.2","296","2","296","2","","","","","","","","4","C 1 c 1","C -2yc","9","","","","- C18 H14 Br2 N2 -","- C18 H14 Br2 N2 -","- C72 H56 Br8 N8 -","4","1","","Devi, Arpita; Bharali, Mrinmoy Manash; Biswas, Subir; Bora, Tonmoy J.; Nath, Jayanta K.; Lee, Seonghwan; Park, Young-Bin; Saikia, Lakshi; Baruah, Manash J.; Bania, Kusum K.","Utilization of methanol and ethanol for 3,3′-bis(indolyl)methane synthesis through activation of peroxymonosulfate over a copper catalyst","Green Chemistry","2023","25","9","3443","3448","10.1039/D3GC00440F","","","0.71073","MoKα","","0.1275","0.0529","","","0.0992","0.1278","","","","","","0.92","","","","has coordinates","284283","2023-06-05","04:36:32",""
"7246608","14.852","0.003","8.3709","0.0017","15.745","0.003","90","","111.498","0.004","90","","1821.3","0.6","296.15","","296.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C19 H19 N O3 S Se -","- C19 H19 N O3 S Se -","- C76 H76 N4 O12 S4 Se4 -","4","1","","Wang, Renjie; Zhang, Nana; Zhang, Yonghong; Wang, Bin; Xia, Yu; Sun, Kai; Jin, Weiwei; Li, Xinyong; Liu, Chenjiang","Versatile electrooxidative amino- and oxyselenation of alkenes","Green Chemistry","2023","25","10","3925","3930","10.1039/D3GC00837A","","","0.71073","MoKα","","0.0802","0.0406","","","0.0854","0.0967","","","","","","1.033","","","","has coordinates","284279","2023-06-05","04:35:56",""
"7246609","6.042","0.0006","7.1534","0.0007","41.598","0.004","90","","91.97","0.002","90","","1796.8","0.3","296.15","","296.15","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C19 H19 N O4 Se -","- C19 H19 N O4 Se -","- C76 H76 N4 O16 Se4 -","4","1","","Wang, Renjie; Zhang, Nana; Zhang, Yonghong; Wang, Bin; Xia, Yu; Sun, Kai; Jin, Weiwei; Li, Xinyong; Liu, Chenjiang","Versatile electrooxidative amino- and oxyselenation of alkenes","Green Chemistry","2023","25","10","3925","3930","10.1039/D3GC00837A","","","0.71073","MoKα","","0.079","0.0442","","","0.078","0.0873","","","","","","1.036","","","","has coordinates","284279","2023-06-05","04:35:56",""
"7246610","9.9532","0.0009","24.647","0.002","17.5152","0.0015","90","","90","","90","","4296.8","0.6","296.15","","296.15","","","","","","","","","7","P b c a","-P 2ac 2ab","61","","","","- C23 H18 Br N O3 S Se -","- C23 H18 Br N O3 S Se -","- C184 H144 Br8 N8 O24 S8 Se8 -","8","1","","Wang, Renjie; Zhang, Nana; Zhang, Yonghong; Wang, Bin; Xia, Yu; Sun, Kai; Jin, Weiwei; Li, Xinyong; Liu, Chenjiang","Versatile electrooxidative amino- and oxyselenation of alkenes","Green Chemistry","2023","25","10","3925","3930","10.1039/D3GC00837A","","","0.71073","MoKα","","0.0625","0.0333","","","0.0606","0.0691","","","","","","1.006","","","","has coordinates","284279","2023-06-05","04:35:56",""
"7246637","6.1791","0.0001","15.1836","0.0002","14.4771","0.0002","90","","95.557","0.001","90","","1351.87","0.03","170.01","0.1","170.01","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C26 H30 Br2 O6 -","- C26 H30 Br2 O6 -","- C52 H60 Br4 O12 -","2","1","","Qiu, Huixin; Ren, Jiayi; Zhang, Long; Song, Ran; Si, Wen; Yang, Daoshan; Wen, Lirong; Lv, Jian","Enantioselective Meerwein–Ponndorf–Verley reduction of β,γ-unsaturated α-keto esters by asymmetric binary-acid catalysis in the green solvent iPrOH","Green Chemistry","2023","25","10","3948","3955","10.1039/D2GC03441G","","x-ray","1.54184","CuKα","","0.0312","0.0304","","","0.0864","0.0872","","","","","","1.099","","","","has coordinates,has disorder","284277","2023-06-05","04:35:31",""
"7246659","17.1352","0.0004","7.89497","0.00016","14.2824","0.0004","90","","110.302","0.003","90","","1812.12","0.08","293","2","293","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","1","","- C20 H14 F5 N O3 -","- C20 H14 F5 N O3 -","- C80 H56 F20 N4 O12 -","4","1","","Huang, Panyi; Yan, Zhiyang; Ling, Jiaxin; Li, Peixuan; Wang, Jiayang; Li, Jianjun; Sun, Bin; Jin, Can","Catalyst-free intramolecular radical cyclization cascades initiated by the direct homolysis of Csp3–Br under visible light","Green Chemistry","2023","25","10","3989","3994","10.1039/D3GC00304C","","x-ray","1.54184","CuKα","","0.0739","0.0662","","","0.1892","0.1987","","","","","","1.027","","","","has coordinates,has disorder","284280","2023-06-05","04:36:02",""
"7246660","6.4643","0.0002","21.3155","0.0007","11.9798","0.0004","90","","91.899","0.003","90","","1649.79","0.09","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C16 H25 B O4 -","- C16 H25 B O4 -","- C64 H100 B4 O16 -","4","2","","Huninik, Paweł; Szyling, Jakub; Czapik, Agnieszka; Walkowiak, Jędrzej","Organocatalytic hydroboration of olefins in pyrrolidinium ionic liquids","Green Chemistry","2023","25","9","3715","3722","10.1039/D2GC04163D","","","1.54184","CuKα","","0.0696","0.0686","","","0.1812","0.1823","","","","","","1.07","","","","has coordinates","284282","2023-06-05","04:36:21",""
"7246679","9.521","0.0011","12.027","0.003","12.459","0.002","63.128","0.014","82.674","0.012","72.395","0.015","1212.9","0.4","180","","180","","","","","","","","","6","P -1","-P 1","2","","","","- C58 H37.89 Cl0.11 N6 O8 S2 -","- C58 H37.888 Cl0.112 N6 O8 S2 -","- C58 H37.888 Cl0.112 N6 O8 S2 -","1","0.5","","Li, Yao; Zhang, Jun; She, Mengyao; Liu, Lang; Yang, Zheng; Liu, Ping; Zhang, Shengyong; Li, Jianli","Electrochemical single-step N-acylation and S-cyclization synthesis of thiazolimide via radical process","Green Chemistry","2023","25","11","4302","4308","10.1039/D3GC00664F","","","1.34138","GaKα","","0.0361","0.0358","","","0.0904","0.0906","","","","","","1.056","","","","has coordinates,has disorder","286151","2023-09-05","19:59:00",""
"7246680","9.279","0.003","11.406","0.002","13.046","0.005","80.4","0.02","80.8","0.03","69.338","0.016","1266.2","0.7","180","","180","","","","","","","","","6","P -1","-P 1","2","","","","- C31 H23.91 Cl0.09 N2 O2 S -","- C31 H23.915 Cl0.085 N2 O2 S -","- C62 H47.83 Cl0.17 N4 O4 S2 -","2","1","","Li, Yao; Zhang, Jun; She, Mengyao; Liu, Lang; Yang, Zheng; Liu, Ping; Zhang, Shengyong; Li, Jianli","Electrochemical single-step N-acylation and S-cyclization synthesis of thiazolimide via radical process","Green Chemistry","2023","25","11","4302","4308","10.1039/D3GC00664F","","","1.34138","GaKα","","0.046","0.0395","","","0.104","0.1069","","","","","","1.05","","","","has coordinates,has disorder","286151","2023-09-05","19:59:00",""
"7246681","9.907","0.0013","11.5183","0.0016","11.8511","0.001","108.421","0.01","104.16","0.009","99.584","0.012","1199.6","0.3","100","","100","","","","","","","","","5","P -1","-P 1","2","","","","- C30 H22 N2 O2 S -","- C30 H22 N2 O2 S -","- C60 H44 N4 O4 S2 -","2","1","","Li, Yao; Zhang, Jun; She, Mengyao; Liu, Lang; Yang, Zheng; Liu, Ping; Zhang, Shengyong; Li, Jianli","Electrochemical single-step N-acylation and S-cyclization synthesis of thiazolimide via radical process","Green Chemistry","2023","25","11","4302","4308","10.1039/D3GC00664F","","","1.34138","GaKα","","0.0412","0.0355","","","0.095","0.0983","","","","","","1.053","","","","has coordinates","286151","2023-09-05","19:59:00",""
"7246682","11.803","0.003","12.782","0.002","17.329","0.002","89.118","0.01","81.911","0.012","71.924","0.015","2459.5","0.8","180","","180","","","","","","","","","6","P -1","-P 1","2","","","","- C60 H43.54 Cl0.56 N4 O6 S2 -","- C60 H43.54 Cl0.56 N4 O6 S2 -","- C120 H87.08 Cl1.12 N8 O12 S4 -","2","1","","Li, Yao; Zhang, Jun; She, Mengyao; Liu, Lang; Yang, Zheng; Liu, Ping; Zhang, Shengyong; Li, Jianli","Electrochemical single-step N-acylation and S-cyclization synthesis of thiazolimide via radical process","Green Chemistry","2023","25","11","4302","4308","10.1039/D3GC00664F","","","1.34138","GaKα","","0.0587","0.0427","","","0.0997","0.1071","","","","","","1.031","","","","has coordinates,has disorder","286151","2023-09-05","19:59:00",""
"7246708","14.2948","0.0008","8.5708","0.0004","15.3612","0.0008","90","","95.345","0.005","90","","1873.84","0.17","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C21 H19 N2 O3 S -","- C21 H18 N2 O3 S -","- C84 H72 N8 O12 S4 -","4","1","","Zhong, Qiang; Wang, Pei-Long; Gao, Hui; Ma, Fang; Yang, Youqing; Li, Hongji","Electrochemical intramolecular N(sp2)–H/N(sp3)–H coupling for the synthesis of 1H-indazoles","Green Chemistry","2023","25","10","3982","3988","10.1039/D3GC00380A","","","0.71073","MoKα","","0.0838","0.0517","","","0.1545","0.1746","","","","","","1.026","","","","has coordinates","284278","2023-06-05","04:35:43",""
"7246709","11.349","0.008","10.096","0.007","15.893","0.011","90","0.03","97.84","0.04","90","0.03","1804","2","273.15","","273.15","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C19 H19 N3 O2 S -","- C20 H18 N2 O2 S -","- C80 H72 N8 O8 S4 -","4","1","","Zhong, Qiang; Wang, Pei-Long; Gao, Hui; Ma, Fang; Yang, Youqing; Li, Hongji","Electrochemical intramolecular N(sp2)–H/N(sp3)–H coupling for the synthesis of 1H-indazoles","Green Chemistry","2023","25","10","3982","3988","10.1039/D3GC00380A","","","0.71073","MoKα","","0.0501","0.0418","","","0.1142","0.1207","","","","","","1.025","","","","has coordinates","284278","2023-06-05","04:35:46",""
"7246809","7.3092","0.0006","10.4613","0.0009","12.143","0.001","72.439","0.003","87.404","0.003","81.976","0.003","876.56","0.13","296","2","296.15","","","","","","","","","6","P -1","-P 1","2","","","","- C17 H16 Cl N3 O3 Se -","- C17 H16 Cl N3 O3 Se -","- C34 H32 Cl2 N6 O6 Se2 -","2","1","","Liu, Huan; Ye, Zi-Lin; Cai, Zhong-Jian; Ji, Shun-Jun","A multicomponent reaction of isocyanides, selenium powder and 3-aminooxetanes in pure water: green and efficient synthesis of 1,3-selenazolines","Green Chemistry","2023","25","11","4239","4243","10.1039/D3GC00708A","","","0.71073","MoKα","","0.0563","0.0399","","","0.0966","0.1061","","","","","","1.03","","","","has coordinates","286152","2023-09-05","19:59:06",""
"7246811","9.1149","0.0002","7.9249","0.0002","10.3451","0.0002","90","","92.043","0.001","90","","746.8","0.03","298","","298","","","","","","","","","5","P 1 2/n 1","-P 2yac","13","","","","- C8 H20 Au Cl4 N -","- C8 H20 Au Cl4 N -","- C16 H40 Au2 Cl8 N2 -","2","0.5","","Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav","Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts","Green Chemistry","2023","25","15","5899","5906","10.1039/D3GC01150J","","","1.54178","CuKα","","0.0198","0.0188","","","0.044","0.0445","","","","","","1.116","","","","has coordinates","286150","2023-09-05","19:58:50",""
"7246812","9.3812","0.0003","8.2418","0.0003","10.5053","0.0004","90","","90.562","0.002","90","","812.21","0.05","298","","298","","","","","","","","","5","P 1 2/n 1","-P 2yac","13","","","","- C8 H20 Au Br4 N -","- C8 H20 Au Br4 N -","- C16 H40 Au2 Br8 N2 -","2","0.5","","Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav","Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts","Green Chemistry","2023","25","15","5899","5906","10.1039/D3GC01150J","","","1.54178","CuKα","","0.0301","0.028","","","0.0698","0.072","","","","","","1.043","","","","has coordinates","286150","2023-09-05","19:58:50",""
"7246813","14.8787","0.0003","8.931","0.0002","18.277","0.0004","90","","107.259","0.001","90","","2319.32","0.09","298","","298","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C16 H36 Au Cl4 N -","- C16 H36 Au Cl4 N -","- C64 H144 Au4 Cl16 N4 -","4","1","","Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav","Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts","Green Chemistry","2023","25","15","5899","5906","10.1039/D3GC01150J","","","1.54178","CuKα","","0.0684","0.0568","","","0.1422","0.1604","","","","","","1.051","","","","has coordinates","286150","2023-09-05","19:58:50",""
"7246814","12.1431","0.0006","12.1431","0.0006","8.5038","0.0005","90","","90","","90","","1253.93","0.11","298","","298","","","","","","","","","5","P 4/n :2","-P 4a","85","","","","- C16 H36 Au Br4 N -","- C16 H36 Au Br4 N -","- C32 H72 Au2 Br8 N2 -","2","0.25","","Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav","Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts","Green Chemistry","2023","25","15","5899","5906","10.1039/D3GC01150J","","","1.54178","CuKα","","0.0819","0.0759","","","0.1804","0.1886","","","","","","1.168","","","","has coordinates,has disorder","286150","2023-09-05","19:58:51",""
"7246815","8.1965","0.0002","8.7398","0.0002","38.9304","0.001","90","","92.271","0.001","90","","2786.62","0.12","298","","298","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H42 Au Br4 N -","- C19 H42 Au Br4 N -","- C76 H168 Au4 Br16 N4 -","4","1","","Do, Jean-Louis; Auvray, Thomas; Lennox, Cameron B.; Titi, Hatem M.; Cuccia, Louis A.; Friščić, Tomislav","Rapid, room-temperature, solvent-free mechanochemical oxidation of elemental gold into organosoluble gold salts","Green Chemistry","2023","25","15","5899","5906","10.1039/D3GC01150J","","","1.54178","CuKα","","0.1","0.0762","","","0.2057","0.226","","","","","","1.082","","","","has coordinates","286150","2023-09-05","19:58:51",""
"7246829","12.545","0.005","3.9268","0.0016","21.018","0.009","90","","106.758","0.006","90","","991.4","0.7","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C11 H9 N O2 S -","- C11 H9 N O2 S -","- C44 H36 N4 O8 S4 -","4","1","","Li, Dandan; Chen, Long; Jin, Yang; Wang, Xiaochen; Liu, Long; Li, Yilin; Chen, Gongyuan; Wu, Guanhao; Qin, Yujie; Yang, Leilei; Wang, Mengke; Zhao, Lulu; Xu, Zhihong; Wen, Jiangwei","An electrochemical-enabled cascaded cyclization of enaminones with potassium thiocyanate and alcohols to access 2-alkoxythiazoles","Green Chemistry","2023","25","12","4656","4661","10.1039/D3GC01194A","","","0.71073","MoKα","","0.0349","0.0305","","","0.0943","0.0979","","","","","","1.01","","","","has coordinates","286154","2023-09-05","19:59:24",""
"7246830","8.998","0.003","13.804","0.004","14.731","0.004","90","","92.647","0.01","90","","1827.8","0.9","273","2","273.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H19 N O3 -","- C24 H19 N O3 -","- C96 H76 N4 O12 -","4","1","","Yang, Na; Li, Anni; Gao, Hui; Liao, Li-Mei; Yang, Yu-Ping; Wang, Pei-Long; Li, Hongji","Electrochemical oxidation-induced benzylic C(sp3)–H functionalization towards the atom-economic synthesis of oxazole heterocycles","Green Chemistry","2023","25","13","5128","5133","10.1039/D2GC04782A","","","0.71073","MoKα","","0.0523","0.0401","","","0.1013","0.1142","","","","","","1.057","","","","has coordinates","286144","2023-09-05","19:57:42",""
"7246831","22.70389","0.00013","13.29859","0.00007","5.82409","0.00003","90","","90","","90","","1758.47","0.016","100","0.1","100","0.1","","","","","","","","5","P 21 21 2","P 2 2ab","18","","","","- C22 H16 Br N S -","- C22 H16 Br N S -","- C88 H64 Br4 N4 S4 -","4","1","","Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen","Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions","Green Chemistry","2023","25","13","5206","5212","10.1039/D3GC01329D","","x-ray","1.54184","CuKα","","0.0168","0.0167","","","0.043","0.043","","","","","","1.068","","","","has coordinates","286146","2023-09-05","19:58:00",""
"7246832","24.9095","0.0005","5.8669","0.0001","25.8562","0.0006","90","","111.533","0.002","90","","3514.94","0.13","100","0.1","100","0.1","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","(Z)-5-chloro-3-methyl-N,4-diphenyl-1H-isothiochromen-1-imine","","- C22 H16 Cl N S -","- C22 H16 Cl N S -","- C176 H128 Cl8 N8 S8 -","8","1","","Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen","Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions","Green Chemistry","2023","25","13","5206","5212","10.1039/D3GC01329D","","x-ray","1.54184","CuKα","","0.0382","0.0348","","","0.0865","0.0899","","","","","","1.089","","","","has coordinates","286146","2023-09-05","19:58:00",""
"7246833","10.2654","0.0002","7.0454","0.0001","12.4963","0.0003","90","","92.802","0.002","90","","902.7","0.03","100","0.1","100","0.1","","","","","","","","5","P 1 21/m 1","-P 2yb","11","","(Z)-7-bromo-3-methyl-N,4-diphenyl-1H-isothiochromen-1-imine","","- C22 H16 Br N S -","- C22 H16 Br N S -","- C44 H32 Br2 N2 S2 -","2","0.5","","Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen","Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions","Green Chemistry","2023","25","13","5206","5212","10.1039/D3GC01329D","","x-ray","1.54184","CuKα","","0.0303","0.028","","","0.0782","0.0805","","","","","","1.007","","","","has coordinates,has disorder","286146","2023-09-05","19:58:00",""
"7246834","10.1263","0.0003","6.9258","0.0002","12.6138","0.0004","90","","92.516","0.003","90","","883.79","0.05","100","0.1","100","0.1","","","","","","","","5","P 1 21/m 1","-P 2yb","11","","(Z)-7-chloro-3-methyl-N,4-diphenyl-1H-isothiochromen-1-imine","","- C22 H17 Cl N S -","- C22 H16 Cl N S -","- C44 H32 Cl2 N2 S2 -","2","0.5","","Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen","Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions","Green Chemistry","2023","25","13","5206","5212","10.1039/D3GC01329D","","x-ray","1.54184","CuKα","","0.0375","0.0342","","","0.1099","0.1159","","","","","","0.916","","","","has coordinates,has disorder","286146","2023-09-05","19:58:00",""
"7246835","11.3822","0.0002","12.2394","0.0003","16.8294","0.0004","74.05","0.002","80.114","0.002","67.955","0.002","2083.27","0.09","99.99","0.1","99.99","0.1","","","","","","","","4","P -1","-P 1","2","","(Z)-5-(tert-butyl)-3-methyl-N,4-diphenyl-1H-isothiochromen-1-imine","","- C26 H25 N S -","- C26 H25 N S -","- C104 H100 N4 S4 -","4","2","","Guo, Yanmin; Chang, Rong; Fu, Zhen; Zhou, Cong-Ying; Guo, Zhen","Heterogeneous visible-light promoted dehydrogenative [4 + 2] annulation of benzothioamides and alkynes under aerobic conditions","Green Chemistry","2023","25","13","5206","5212","10.1039/D3GC01329D","","x-ray","1.54184","CuKα","","0.0704","0.0658","","","0.1765","0.1816","","","","","","1.046","","","","has coordinates","286146","2023-09-05","19:58:00",""
"7246851","9.3303","0.0017","17.815","0.003","10.836","0.0018","90","","112.207","0.005","90","","1667.6","0.5","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C17 H14 F3 N O2 S -","- C17 H14 F3 N O2 S -","- C68 H56 F12 N4 O8 S4 -","4","1","","Liao, Tian-Ming; Ma, Wen-Jiang; Gao, Yu-Ning; Bian, Ming; Jiang, Min; Liu, Jin-Tao; Chen, Hui-Yu; Liu, Zhen-Jiang","Facile synthesis of (polyfluoro)alkanesulfinyl 4-isoxazolines: a stepwise solvent- and catalyst-free approach or a one-pot process in water","Green Chemistry","2023","25","13","5233","5239","10.1039/D3GC00557G","","","0.71073","MoKα","","0.0759","0.0578","","","0.1455","0.1624","","","","","","1.131","","","","has coordinates","286145","2023-09-05","19:57:50",""
"7246852","9.8704","0.0003","16.865","0.0005","11.3723","0.0004","90","","115.314","0.001","90","","1711.3","0.1","213","2","213","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C18 H16 F3 N O2 S -","- C18 H16 F3 N O2 S -","- C72 H64 F12 N4 O8 S4 -","4","1","","Liao, Tian-Ming; Ma, Wen-Jiang; Gao, Yu-Ning; Bian, Ming; Jiang, Min; Liu, Jin-Tao; Chen, Hui-Yu; Liu, Zhen-Jiang","Facile synthesis of (polyfluoro)alkanesulfinyl 4-isoxazolines: a stepwise solvent- and catalyst-free approach or a one-pot process in water","Green Chemistry","2023","25","13","5233","5239","10.1039/D3GC00557G","","","0.71073","MoKα","","0.0413","0.0375","","","0.0967","0.1008","","","","","","1.027","","","","has coordinates","286145","2023-09-05","19:57:50",""
"7246853","8.9764","0.0005","9.7004","0.0006","10.5392","0.0006","102.617","0.002","92.927","0.002","99.557","0.002","879.46","0.09","213","2","213","2","","","","","","","","6","P -1","-P 1","2","","","","- C18 H16 F3 N O2 S -","- C18 H16 F3 N O2 S -","- C36 H32 F6 N2 O4 S2 -","2","1","","Liao, Tian-Ming; Ma, Wen-Jiang; Gao, Yu-Ning; Bian, Ming; Jiang, Min; Liu, Jin-Tao; Chen, Hui-Yu; Liu, Zhen-Jiang","Facile synthesis of (polyfluoro)alkanesulfinyl 4-isoxazolines: a stepwise solvent- and catalyst-free approach or a one-pot process in water","Green Chemistry","2023","25","13","5233","5239","10.1039/D3GC00557G","","","0.71073","MoKα","","0.0429","0.0399","","","0.1082","0.1116","","","","","","1.027","","","","has coordinates","286145","2023-09-05","19:57:50",""
"7246854","8.8998","0.0002","16.2836","0.0004","10.5436","0.0003","90","","107.423","0.001","90","","1457.88","0.06","213","2","213","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H11 F3 O2 S -","- C16 H11 F3 O2 S -","- C64 H44 F12 O8 S4 -","4","1","","Liao, Tian-Ming; Ma, Wen-Jiang; Gao, Yu-Ning; Bian, Ming; Jiang, Min; Liu, Jin-Tao; Chen, Hui-Yu; Liu, Zhen-Jiang","Facile synthesis of (polyfluoro)alkanesulfinyl 4-isoxazolines: a stepwise solvent- and catalyst-free approach or a one-pot process in water","Green Chemistry","2023","25","13","5233","5239","10.1039/D3GC00557G","","","0.71073","MoKα","","0.0449","0.034","","","0.0692","0.0746","","","","","","1.054","","","","has coordinates","286145","2023-09-05","19:57:51",""
"7246876","7.6105","0.001","12.1722","0.0014","19.257","0.002","90","","90","","90","","1783.9","0.4","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C24 H21 N -","- C24 H21 N -","- C96 H84 N4 -","4","1","","Zárate-Roldán, Stephany; Gimeno, M. Concepción; Herrera, Raquel P.","Alkylation of amines with allylic alcohols and deep eutectic solvents as metal-free and green promoters","Green Chemistry","2023","25","14","5601","5612","10.1039/D3GC01017A","","","0.71073","MoKα","","0.0321","0.0308","","","0.0812","0.0822","","","","","","1.043","","","","has coordinates","286148","2023-09-05","19:58:16",""
"7246877","15.447","0.003","5.6795","0.0011","21.658","0.004","90","","108.34","0.03","90","","1803.6","0.7","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C23 H23 N -","- C23 H23 N -","- C92 H92 N4 -","4","1","","Zárate-Roldán, Stephany; Gimeno, M. Concepción; Herrera, Raquel P.","Alkylation of amines with allylic alcohols and deep eutectic solvents as metal-free and green promoters","Green Chemistry","2023","25","14","5601","5612","10.1039/D3GC01017A","","","0.71073","MoKα","","0.1029","0.0925","","","0.2656","0.2781","","","","","","1.057","","","","has coordinates","286148","2023-09-05","19:58:16",""
"7246939","5.2503","0.0005","16.2082","0.0013","12.1305","0.0019","90","","99.976","0.013","90","","1016.7","0.2","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C11 H12 F N O2 -","- C11 H12 F N O2 -","- C44 H48 F4 N4 O8 -","4","1","","Hu, Fangzhi; Sun, Zhipeng; Pan, Mengzhe; Wang, Liang; Xu, Lubin; Liu, Xiong-Li; Li, Shuai-Shuai","Divergent synthesis of nitrogen heterocycles via H2O-mediated hydride transfer reactions","Green Chemistry","2023","25","13","5134","5141","10.1039/D3GC00166K","","","1.54184","CuKα","","0.1142","0.0665","","","0.1672","0.2021","","","","","","1.031","","","","has coordinates","286143","2023-09-05","19:57:34",""
"7246940","7.6044","0.0005","9.6671","0.0006","31.908","0.002","90","","90","","90","","2345.6","0.3","193","","193","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C26 H25 N O8 -","- C26 H25 N O8 -","- C104 H100 N4 O32 -","4","1","","Fu, Yun-Dong; Gao, Xiang; Jia, Shi-Kun; Xiao, Xiao; Wang, Min-Can; Huang, Lihua; Mei, Guang-Jian","Catalyst-free racemic and H2O/CPA-catalyzed asymmetric regio-reversed domino processes of triketone enones with azlactones","Green Chemistry","2023","25","14","5692","5697","10.1039/D3GC01445B","","x-ray","1.34139","GaKα","","0.0623","0.0521","","","0.1154","0.1214","","","","","","1.091","","","","has coordinates,has disorder","286147","2023-09-05","19:58:08",""
"7246941","24.16","0.0005","14.7868","0.0003","33.2539","0.0011","90","","103.708","0.003","90","","11541.5","0.5","109.3","0.8","109.3","0.8","","","","","","","","6","P 1 21 1","P 2yb","4","","Boc-L-Pro-Mn-Anderson","","- C81 H161.5 Mn Mo6 N9.5 O30 -","- C81 H161.5 Mn Mo6 N9.5 O30 -","- C324 H646 Mn4 Mo24 N38 O120 -","4","2","","Dai, Guoyong; Li, Qi; Zang, Dejin; Wei, Yongge","A bifunctional molecular catalyst built up of l-proline grafted polyoxometalate for one-pot three-component green synthesis of heterocycles","Green Chemistry","2023","25","16","6263","6269","10.1039/D3GC00951C","","x-ray","1.54184","CuKα","","0.1161","0.0872","","","0.2165","0.2342","","","","","","1.042","","","","has coordinates,has disorder","286140","2023-09-05","19:57:05",""
"7246942","33.5555","0.0004","30.4959","0.0004","9.33799","0.00009","90","","90","","90","","9555.61","0.19","293","2","293","2","","","","","","","","7","P 21 21 2","P 2 2ab","18","","L-Pro-Mn-Anderson","","- C46 H106 Mn Mo7.5 N4 O44 S14 -","- C40 H98 Mn Mo7.5 N4 O41 S11 -","- C160 H392 Mn4 Mo30 N16 O164 S44 -","4","1","","Dai, Guoyong; Li, Qi; Zang, Dejin; Wei, Yongge","A bifunctional molecular catalyst built up of l-proline grafted polyoxometalate for one-pot three-component green synthesis of heterocycles","Green Chemistry","2023","25","16","6263","6269","10.1039/D3GC00951C","","x-ray","1.54184","CuKα","","0.0533","0.0482","","","0.1165","0.1195","","","","","","1.043","","","","has coordinates,has disorder","286140","2023-09-05","19:57:05",""
"7246950","12.4459","0.0002","27.609","0.0004","4.7734","0.0001","90","","90","","90","","1640.23","0.05","100","2","100","2","","","","","","","","5","P n a 21","P 2c -2n","33","","","","- C23 H16 F N O -","- C23 H16 F N O -","- C92 H64 F4 N4 O4 -","4","1","","Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.","A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes","Green Chemistry","2023","25","14","5654","5660","10.1039/D3GC01403G","","x-ray","1.54184","CuKα","","0.0313","0.0299","","","0.0786","0.0794","","","","","","1.065","","","","has coordinates","286149","2023-09-05","19:58:36",""
"7246951","4.8075","0.0001","27.2149","0.0004","12.4496","0.0002","90","","92.523","0.001","90","","1627.27","0.05","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C23 H17 N O -","- C23 H17 N O -","- C92 H68 N4 O4 -","4","1","","Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.","A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes","Green Chemistry","2023","25","14","5654","5660","10.1039/D3GC01403G","","x-ray","1.54184","CuKα","","0.0454","0.0402","","","0.0932","0.0957","","","","","","1.062","","","","has coordinates","286149","2023-09-05","19:58:38",""
"7246952","6.3822","0.0004","10.211","0.0008","11.3886","0.0012","84.533","0.007","89.069","0.007","74.931","0.006","713.37","0.11","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C20 H16 O -","- C20 H16 O -","- C40 H32 O2 -","2","1","","Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.","A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes","Green Chemistry","2023","25","14","5654","5660","10.1039/D3GC01403G","","x-ray","1.54184","CuKα","","0.1453","0.1351","","","0.3868","0.3906","","","","","","1.171","","","","has coordinates","286149","2023-09-05","19:58:38",""
"7246953","12.0444","0.0009","5.6218","0.0003","27.7622","0.0017","90","","99.864","0.007","90","","1852","0.2","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C23 H23 N O3 -","- C23 H23 N O3 -","- C92 H92 N4 O12 -","4","1","","Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.","A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes","Green Chemistry","2023","25","14","5654","5660","10.1039/D3GC01403G","","x-ray","0.71073","MoKα","","0.127","0.053","","","0.0972","0.1166","","","","","","0.992","","","","has coordinates","286149","2023-09-05","19:58:38",""
"7246954","13.198","0.0002","5.6188","0.0001","18.6771","0.0003","90","","97.268","0.001","90","","1373.91","0.04","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H15 N O -","- C19 H15 N O -","- C76 H60 N4 O4 -","4","1","","Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.","A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes","Green Chemistry","2023","25","14","5654","5660","10.1039/D3GC01403G","","x-ray","1.54184","CuKα","","0.0607","0.0564","","","0.152","0.1564","","","","","","1.025","","","","has coordinates","286149","2023-09-05","19:58:38",""
"7246955","5.6809","0.0002","13.8095","0.0005","21.8999","0.0009","90","","91.229","0.003","90","","1717.66","0.11","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C24 H18 F N O -","- C24 H18 F N O -","- C96 H72 F4 N4 O4 -","4","1","","Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.","A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes","Green Chemistry","2023","25","14","5654","5660","10.1039/D3GC01403G","","x-ray","1.54184","CuKα","","0.1488","0.1448","","","0.4312","0.4329","","","","","","1.091","","","","has coordinates","286149","2023-09-05","19:58:38",""
"7246956","19.3497","0.0007","7.1784","0.0002","12.8947","0.0005","90","","103.665","0.004","90","","1740.37","0.11","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H21 N O3 -","- C22 H21 N O3 -","- C88 H84 N4 O12 -","4","1","","Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.","A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes","Green Chemistry","2023","25","14","5654","5660","10.1039/D3GC01403G","","x-ray","1.54184","CuKα","","0.0509","0.0446","","","0.1391","0.1443","","","","","","1.096","","","","has coordinates","286149","2023-09-05","19:58:38",""
"7246957","7.6458","0.0002","6.1433","0.0001","66.279","0.002","90","","91.529","0.002","90","","3112.05","0.13","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C21 H18 O2 -","- C21 H18 O2 -","- C168 H144 O16 -","8","2","","Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.","A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes","Green Chemistry","2023","25","14","5654","5660","10.1039/D3GC01403G","","x-ray","1.54184","CuKα","","0.1323","0.1298","","","0.348","0.3493","","","","","","1.09","","","","has coordinates","286149","2023-09-05","19:58:38",""
"7246958","5.4064","0.0001","9.6437","0.0001","36.2282","0.0005","90","","90","","90","","1888.86","0.05","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C23 H23 N O4 -","- C23 H23 N O4 -","- C92 H92 N4 O16 -","4","1","","Kehoe, Roberta A.; Light, Mark E.; Jones, David J.; McGlacken, Gerard P.","A phosphine free, inorganic base free, one-pot tandem Mizoroki–Heck olefination/direct arylation/hydrogenation sequence, to give multicyclic alkylated heteroarenes","Green Chemistry","2023","25","14","5654","5660","10.1039/D3GC01403G","","x-ray","1.54184","CuKα","","0.0311","0.0293","","","0.0739","0.0751","","","","","","1.029","","","","has coordinates","286149","2023-09-05","19:58:38",""
"7246994","13.4433","0.0011","13.4433","0.0011","7.1126","0.0011","90","","90","","90","","1285.4","0.2","300","","300","","","","","","","","","5","P 4/m b m","-P 4 2ab","127","","","","- C8 H6 N4 Ni O2 -","- C8 H6 N4 Ni O2 -","- C32 H24 N16 Ni4 O8 -","4","0.25","","Huang, Hengcong; Gu, Yifan; Wang, Luyao; Jia, Tao; Kitagawa, Susumu; Li, Fengting","A scalable stable porous coordination polymer synthesized from low-cost precursors for efficient C2H2/C2H4 separation","Green Chemistry","2023","25","20","8040","8046","10.1039/D3GC01114C","","x-ray","1.34139","GaKα","","0.0446","0.0371","","","0.1027","0.1057","","","","","","1.107","","","","has coordinates,has disorder","287354","2023-11-06","07:43:28",""
"7247074","16.316","0.0012","5.3605","0.0004","17.8044","0.0015","90","","102.726","0.003","90","","1519","0.2","273","2","273.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H17 N3 O3 S -","- C16 H17 N3 O3 S -","- C64 H68 N12 O12 S4 -","4","1","","Pal, Nilay Kumar; Singh, Kuldeep; Patra, Moumita; Yadav, Suman; Pandey, Prabhakar K.; Bera, Jitendra K.","Ni(ii)-catalyzed oxidative deamination of benzyl amines with water","Green Chemistry","2023","25","16","6212","6217","10.1039/D3GC00672G","","","0.71073","MoKα","","0.0687","0.041","","","0.0868","0.102","","","","","","1.069","","","","has coordinates","286141","2023-09-05","19:57:20",""
"7247075","10.662","0.0004","22.8698","0.0009","14.5817","0.0005","90","","95.618","0.001","90","","3538.5","0.2","273","2","273.15","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C18 H20 N3 Ni O4 S -","- C17 H20 N3 Ni0.5 O4 S -","- C136 H160 N24 Ni4 O32 S8 -","8","1","","Pal, Nilay Kumar; Singh, Kuldeep; Patra, Moumita; Yadav, Suman; Pandey, Prabhakar K.; Bera, Jitendra K.","Ni(ii)-catalyzed oxidative deamination of benzyl amines with water","Green Chemistry","2023","25","16","6212","6217","10.1039/D3GC00672G","","","0.71073","MoKα","","0.0374","0.0318","","","0.0871","0.0914","","","","","","1.068","","","","has coordinates","286141","2023-09-05","19:57:20",""
"7247076","10.0731","0.0002","20.1087","0.0005","10.8313","0.0003","90","","105.39","0.001","90","","2115.28","0.09","273","2","273.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C21 H20 Br Cl2 N3 Ni -","- C21 H20 Br Cl2 N3 Ni -","- C84 H80 Br4 Cl8 N12 Ni4 -","4","1","","Pal, Nilay Kumar; Singh, Kuldeep; Patra, Moumita; Yadav, Suman; Pandey, Prabhakar K.; Bera, Jitendra K.","Ni(ii)-catalyzed oxidative deamination of benzyl amines with water","Green Chemistry","2023","25","16","6212","6217","10.1039/D3GC00672G","","","0.71073","MoKα","","0.0558","0.036","","","0.0719","0.0832","","","","","","1.044","","","","has coordinates,has disorder","286141","2023-09-05","19:57:20",""
"7247077","13.746","0.003","16.148","0.004","16.995","0.004","65.764","0.007","69.468","0.006","74.898","0.005","3191.2","1.3","273","2","273.15","","","","","","","","","6","P -1","-P 1","2","","","","- C31 H28 Br2 Cl2 N6 Ni -","- C31 H28 Br2 Cl2 N6 Ni -","- C124 H112 Br8 Cl8 N24 Ni4 -","4","2","","Pal, Nilay Kumar; Singh, Kuldeep; Patra, Moumita; Yadav, Suman; Pandey, Prabhakar K.; Bera, Jitendra K.","Ni(ii)-catalyzed oxidative deamination of benzyl amines with water","Green Chemistry","2023","25","16","6212","6217","10.1039/D3GC00672G","","","0.71073","MoKα","","0.1094","0.0655","","","0.1726","0.2051","","","","","","1.034","","","","has coordinates,has disorder","286141","2023-09-05","19:57:20",""
"7247092","6.1385","0.0004","11.76","0.0008","17.0258","0.0011","104.208","0.006","96.087","0.005","103.597","0.006","1140.46","0.14","149.99","0.1","149.99","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C28 H21 F2 O2 P -","- C28 H21 F2 O2 P -","- C56 H42 F4 O4 P2 -","2","1","","Chu, Xue-Qiang; Sun, Li-Wen; Ma, Cheng; Chen, Jia-Wei; Chen, Yu-Lan; Ni, Shao-Fei; Zhu, Ming-Quan; Zhou, Jie; Ma, Mengtao; Shen, Zhi-Liang","“On-water” defluorophosphorylation of trifluoromethylated enones with phosphine oxides","Green Chemistry","2023","25","16","6489","6497","10.1039/D3GC01565C","","x-ray","0.71073","MoKα","","0.0559","0.0428","","","0.0947","0.1041","","","","","","1.047","","","","has coordinates","286142","2023-09-05","19:57:28",""
"7247093","13.606","0.0003","16.1758","0.0004","14.0833","0.0003","90","","98.198","0.002","90","","3067.89","0.12","149.99","0.1","149.99","0.1","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C36 H26 F2 N3 O4 P -","- C36 H26 F2 N3 O4 P -","- C144 H104 F8 N12 O16 P4 -","4","1","","Chu, Xue-Qiang; Sun, Li-Wen; Ma, Cheng; Chen, Jia-Wei; Chen, Yu-Lan; Ni, Shao-Fei; Zhu, Ming-Quan; Zhou, Jie; Ma, Mengtao; Shen, Zhi-Liang","“On-water” defluorophosphorylation of trifluoromethylated enones with phosphine oxides","Green Chemistry","2023","25","16","6489","6497","10.1039/D3GC01565C","","x-ray","1.54184","CuKα","","0.0475","0.0417","","","0.1071","0.1131","","","","","","1.025","","","","has coordinates","286142","2023-09-05","19:57:29",""
"7247094","11.5388","0.0005","15.217","0.0007","31.3898","0.0014","88.955","0.002","88.529","0.002","76.813","0.003","5364.1","0.4","173","2","173","","","","","","","","","5","P -1","-P 1","2","","","","- C27 H39 B2 N3 O4 -","- C27 H39 B2 N3 O4 -","- C216 H312 B16 N24 O32 -","8","4","","Tao, Sheng; Wang, Yang; Pan, Qianxiu; Zhao, Jixing; Bu, Qingqing; Chen, Fei; Liu, Jichang; Dai, Bin; Wei, Donghui; Liu, Ning","Aqueous hydroboration of alkynes via nonclassical generation of N-heterocyclic carbenes","Green Chemistry","2023","25","17","6704","6716","10.1039/D3GC01232H","","","1.54178","CuKα","","0.1375","0.0966","","","0.2478","0.2946","","","","","","1.101","","","","has coordinates,has disorder","286137","2023-09-05","19:56:33",""
"7247095","19.9852","0.0004","7.5581","0.0001","20.2911","0.0004","90","","90","","90","","3064.97","0.1","100","","100","","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C20 H15 N3 O -","- C20 H15 N3 O -","- C160 H120 N24 O8 -","8","1","","Titenkova, Kseniia; Shuvaev, Alexander D.; Teslenko, Fedor E.; Zhilin, Egor S.; Fershtat, Leonid L.","Empowering strategies of electrochemical N–N bond forming reactions: direct access to previously neglected 1,2,3-triazole 1-oxides","Green Chemistry","2023","25","17","6686","6693","10.1039/D3GC01601C","","","0.71073","MoKα","","0.0687","0.0497","","","0.1196","0.1353","","","","","","1.026","","","","has coordinates,has disorder","286139","2023-09-05","19:56:49",""
"7247129","11.9068","0.0017","4.8812","0.0007","22.718","0.004","90","","94.231","0.004","90","","1316.8","0.4","293","2","293","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C16 H16 O2 -","- C16 H16 O2 -","- C64 H64 O8 -","4","2","","Su, Yu; Wang, Chengyi; Chen, Qipeng; Zhu, Yuanli; Deng, Shaomin; Yang, Shoujin; Jin, Ronghua; Liu, Guohua","Harmonization of an incompatible aqueous aldol condensation/oxa-Michael addition/reduction cascade process over a core–shell-structured thermoresponsive catalyst","Green Chemistry","2023","25","17","6859","6868","10.1039/D3GC01670F","","","0.71073","MoKα","","0.1491","0.0702","","","0.1558","0.2035","","","","","","1.041","","","","has coordinates,has disorder","286138","2023-09-05","19:56:41",""
"7247197","5.4248","0.0001","30.6105","0.0006","12.8838","0.0002","90","","94.772","0.001","90","","2132.01","0.07","153","2","153","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C24 H27 N O4 S -","- C24 H27 N O4 S -","- C96 H108 N4 O16 S4 -","4","1","","Gao, Yuzhen; Liu, Siqing; Su, Weiping","CO2-facilitated radical sequential (3 + 2) annulation of 1,6-enynes via cooperation of sulfinate catalysis and photocatalysis","Green Chemistry","2023","25","18","7335","7343","10.1039/D3GC02326E","","","1.54178","CuKα","","0.0689","0.0583","","","0.1855","0.2147","","","","","","1.12","","","","has coordinates","286753","2023-10-06","00:19:30",""
"7247198","8.3269","0.0008","11.8421","0.0012","13.6257","0.0014","69.743","0.004","74.537","0.004","81.231","0.004","1212.2","0.2","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C30 H23 N O3 S -","- C30 H23 N O3 S -","- C60 H46 N2 O6 S2 -","2","1","","Gao, Yuzhen; Liu, Siqing; Su, Weiping","CO2-facilitated radical sequential (3 + 2) annulation of 1,6-enynes via cooperation of sulfinate catalysis and photocatalysis","Green Chemistry","2023","25","18","7335","7343","10.1039/D3GC02326E","","","0.71073","MoKα","","0.145","0.0687","","","0.1731","0.2314","","","","","","1.257","","","","has coordinates","286753","2023-10-06","00:19:30",""
"7247199","23.0076","0.0002","7.7676","0.0001","18.0741","0.0002","90","","99.883","0.001","90","","3182.16","0.06","153","2","153","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C19 H22 O4 -","- C19 H22 O4 -","- C152 H176 O32 -","8","1","","Gao, Yuzhen; Liu, Siqing; Su, Weiping","CO2-facilitated radical sequential (3 + 2) annulation of 1,6-enynes via cooperation of sulfinate catalysis and photocatalysis","Green Chemistry","2023","25","18","7335","7343","10.1039/D3GC02326E","","","1.54178","CuKα","","0.0446","0.0421","","","0.1104","0.1145","","","","","","1.104","","","","has coordinates","286753","2023-10-06","00:19:30",""
"7247212","7.804","0.011","10.261","0.014","11.611","0.016","100.605","0.013","102.623","0.013","94.906","0.013","884","2","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C23 H19 N O2 -","- C23 H19 N O2 -","- C46 H38 N2 O4 -","2","1","","Pathak, Debabrat; Kalita, Bikash Kumar; Sarmah, Ashish; Sharma, Himanshu; Bora, Bidisha; Goswami, Tridib K.; Sarma, Bipul","Metal-free reusable hollow-spherical triazine microporous organic polymer supported quinolines synthesis via hydrogen evolution","Green Chemistry","2023","25","19","7642","7652","10.1039/D3GC02172F","","","0.71073","MoKα","","0.1034","0.0569","","","0.1359","0.1647","","","","","","0.982","","","","has coordinates","286752","2023-10-06","00:19:10",""
"7247213","14.183","0.003","12.855","0.003","8.8411","0.0019","90","","98.111","0.006","90","","1595.8","0.6","296","2","296","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C23 H17 N -","- C23 H17 N -","- C92 H68 N4 -","4","1","","Pathak, Debabrat; Kalita, Bikash Kumar; Sarmah, Ashish; Sharma, Himanshu; Bora, Bidisha; Goswami, Tridib K.; Sarma, Bipul","Metal-free reusable hollow-spherical triazine microporous organic polymer supported quinolines synthesis via hydrogen evolution","Green Chemistry","2023","25","19","7642","7652","10.1039/D3GC02172F","","","0.71073","MoKα","","0.0659","0.0425","","","0.1037","0.1161","","","","","","1.037","","","","has coordinates","286752","2023-10-06","00:19:17",""
"7247214","10.699","0.009","24.611","0.019","11.444","0.009","90","","112.405","0.019","90","","2786","4","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H15 N O2 -","- C17 H15 N O2 -","- C136 H120 N8 O16 -","8","2","","Pathak, Debabrat; Kalita, Bikash Kumar; Sarmah, Ashish; Sharma, Himanshu; Bora, Bidisha; Goswami, Tridib K.; Sarma, Bipul","Metal-free reusable hollow-spherical triazine microporous organic polymer supported quinolines synthesis via hydrogen evolution","Green Chemistry","2023","25","19","7642","7652","10.1039/D3GC02172F","","","0.71073","MoKα","","0.1156","0.0693","","","0.1619","0.1997","","","","","","1.05","","","","has coordinates","286752","2023-10-06","00:19:17",""
"7247248","8.2596","0.0007","11.1219","0.0009","11.4922","0.0009","90","","110.896","0.003","90","","986.27","0.14","100","2","100","","","","","","","","","5","P 1 c 1","P -2yc","7","","","","- C10 H9 N3 O S -","- C10 H9 N3 O S -","- C40 H36 N12 O4 S4 -","4","2","","Maity, Rajib; Bankura, Abhijit; Das, Indrajit","Electrochemical cascade sequences for remote C7–H bond thiocyanation of quinoxalin-2(1H)-ones with ammonium thiocyanate","Green Chemistry","2023","25","19","7774","7781","10.1039/D3GC02153J","","x-ray","1.54178","CuKα","","0.0422","0.0408","","","0.1058","0.1073","","","","","","1.074","","","","has coordinates","286751","2023-10-06","00:18:56",""
"7247249","3.9964","0.0003","8.0048","0.0005","17.9743","0.0012","90.426","0.002","90.934","0.002","98.213","0.002","569","0.07","100","","100","","","","","","","","","5","P -1","-P 1","2","","","","- C12 H11 N3 O S -","- C12 H11 N3 O S -","- C24 H22 N6 O2 S2 -","2","1","","Maity, Rajib; Bankura, Abhijit; Das, Indrajit","Electrochemical cascade sequences for remote C7–H bond thiocyanation of quinoxalin-2(1H)-ones with ammonium thiocyanate","Green Chemistry","2023","25","19","7774","7781","10.1039/D3GC02153J","","x-ray","1.54178","CuKα","","0.0351","0.035","","","0.0921","0.0921","","","","","","1.123","","","","has coordinates","286751","2023-10-06","00:18:56",""
"7247250","6.7604","0.0001","16.4043","0.0003","15.8328","0.0003","90","","95.946","0.002","90","","1746.41","0.05","180","0.1","180","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H22 B P -","- C20 H22 B P -","- C80 H88 B4 P4 -","4","1","","Shi, Wei; Zhong, Ping-Fu; Qi, Xu-Kuan; Yang, Chao; Guo, Lin; Xia, Wujiong","Photoinduced ligand-to-iron charge transfer enabled C(sp3)–H phosphorylation of hydrocarbons","Green Chemistry","2023","25","19","7817","7824","10.1039/D3GC02469E","","x-ray","1.54184","CuKα","","0.0582","0.0536","","","0.1468","0.1532","","","","","","1.03","","","","has coordinates","286750","2023-10-06","00:18:47",""
"7247251","6.6016","0.0001","17.7257","0.0004","14.5686","0.0003","90","","101.613","0.002","90","","1669.89","0.06","180.3","0.7","180.3","0.7","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H24 B P -","- C19 H24 B P -","- C76 H96 B4 P4 -","4","1","","Shi, Wei; Zhong, Ping-Fu; Qi, Xu-Kuan; Yang, Chao; Guo, Lin; Xia, Wujiong","Photoinduced ligand-to-iron charge transfer enabled C(sp3)–H phosphorylation of hydrocarbons","Green Chemistry","2023","25","19","7817","7824","10.1039/D3GC02469E","","x-ray","1.54184","CuKα","","0.0677","0.0625","","","0.1659","0.1725","","","","","","1.077","","","","has coordinates","286750","2023-10-06","00:18:48",""
"7247297","13.552","0.0014","10.2862","0.001","23.234","0.003","90","","95.963","0.01","90","","3221.3","0.6","292.99","0.1","292.99","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C40 H33 N O5 -","- C40 H33 N O5 -","- C160 H132 N4 O20 -","4","1","","Luo, Jian; Zhong, Ai-Qing; Qiu, Jia-Hao; Liu, Xiong-Wei; Tian, You-Ping; Zhang, Bao-Hua; Chen, Guo-Shu; Shu, Wei; Liu, Yun-Lin","Green and effective synthesis of multisubstituted α-pyrones via K2CO3 catalyzed formal insertion of ketenimines into C(CO)–C bonds of 1,3-diketones","Green Chemistry","2023","25","20","8057","8067","10.1039/D3GC02073H","","x-ray","0.71073","MoKα","","0.1788","0.0724","","","0.1445","0.1931","","","","","","1.024","","","","has coordinates","287352","2023-11-06","07:42:26",""
"7247298","10.4332","0.0005","10.0121","0.0004","27.9684","0.0013","90","","98.05","0.004","90","","2892.7","0.2","150","0.1","150","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C35 H30 Cl N O6 -","- C35 H30 Cl N O6 -","- C140 H120 Cl4 N4 O24 -","4","1","","Luo, Jian; Zhong, Ai-Qing; Qiu, Jia-Hao; Liu, Xiong-Wei; Tian, You-Ping; Zhang, Bao-Hua; Chen, Guo-Shu; Shu, Wei; Liu, Yun-Lin","Green and effective synthesis of multisubstituted α-pyrones via K2CO3 catalyzed formal insertion of ketenimines into C(CO)–C bonds of 1,3-diketones","Green Chemistry","2023","25","20","8057","8067","10.1039/D3GC02073H","","x-ray","1.54184","CuKα","","0.0732","0.053","","","0.1325","0.1478","","","","","","1.046","","","","has coordinates","287352","2023-11-06","07:42:29",""
"7247299","10.3653","0.0009","11.5399","0.0008","12.1483","0.0009","86.936","0.006","75.711","0.007","69.063","0.007","1314.21","0.19","170","0.1","170","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C36 H27 N O -","- C36 H27 N O -","- C72 H54 N2 O2 -","2","1","","Luo, Jian; Zhong, Ai-Qing; Qiu, Jia-Hao; Liu, Xiong-Wei; Tian, You-Ping; Zhang, Bao-Hua; Chen, Guo-Shu; Shu, Wei; Liu, Yun-Lin","Green and effective synthesis of multisubstituted α-pyrones via K2CO3 catalyzed formal insertion of ketenimines into C(CO)–C bonds of 1,3-diketones","Green Chemistry","2023","25","20","8057","8067","10.1039/D3GC02073H","","x-ray","1.54184","CuKα","","0.0652","0.0485","","","0.1269","0.1374","","","","","","1.164","","","","has coordinates","287352","2023-11-06","07:42:32",""
"7247300","5.8318","0.0004","11.6046","0.0008","26.5835","0.0015","86.525","0.005","87.942","0.005","87.181","0.005","1792.6","0.2","170","0.1","170","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C23 H21 N O -","- C23 H21 N O -","- C92 H84 N4 O4 -","4","2","","Luo, Jian; Zhong, Ai-Qing; Qiu, Jia-Hao; Liu, Xiong-Wei; Tian, You-Ping; Zhang, Bao-Hua; Chen, Guo-Shu; Shu, Wei; Liu, Yun-Lin","Green and effective synthesis of multisubstituted α-pyrones via K2CO3 catalyzed formal insertion of ketenimines into C(CO)–C bonds of 1,3-diketones","Green Chemistry","2023","25","20","8057","8067","10.1039/D3GC02073H","","x-ray","1.54184","CuKα","","0.0868","0.0614","","","0.172","0.1892","","","","","","1.097","","","","has coordinates","287352","2023-11-06","07:42:38",""
"7247301","11.0361","0.0005","14.2348","0.0005","16.7656","0.0006","79.529","0.003","88.302","0.003","75.05","0.004","2501.88","0.18","150","0.1","150","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C29 H27 N O5 -","- C29 H27 N O5 -","- C116 H108 N4 O20 -","4","2","","Luo, Jian; Zhong, Ai-Qing; Qiu, Jia-Hao; Liu, Xiong-Wei; Tian, You-Ping; Zhang, Bao-Hua; Chen, Guo-Shu; Shu, Wei; Liu, Yun-Lin","Green and effective synthesis of multisubstituted α-pyrones via K2CO3 catalyzed formal insertion of ketenimines into C(CO)–C bonds of 1,3-diketones","Green Chemistry","2023","25","20","8057","8067","10.1039/D3GC02073H","","x-ray","0.71073","MoKα","","0.0963","0.0603","","","0.1368","0.1608","","","","","","1.023","","","","has coordinates","287352","2023-11-06","07:42:51",""
"7247337","8.791","0.0004","18.1795","0.001","17.9329","0.001","90","","95.505","0.004","90","","2852.7","0.3","113","2","113","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C36 H29 N O3 S -","- C36 H29 N O3 S -","- C144 H116 N4 O12 S4 -","4","1","","Mutra, Mohana Reddy; Chandana, T. L.; Wang, Yun-Jou; Wang, Jeh-Jeng","Green and rapid acid-catalyzed ynamide skeletal rearrangement and stereospecific functionalization with anisole derivatives","Green Chemistry","2023","25","20","8124","8133","10.1039/D3GC02460A","","x-ray","0.71073","MoKα","","0.122","0.0756","","","0.1917","0.2127","","","","","","1.064","","","","has coordinates","287356","2023-11-06","07:44:07",""
"7247338","18.4742","0.0008","5.9923","0.0002","19.2732","0.0009","90","","98.981","0.002","90","","2107.44","0.15","100","2","100","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C15 H10 O2 -","- C15 H10 O2 -","- C120 H80 O16 -","8","1","","Ragupathi, Ayyakkannu; Charpe, Vaibhav Pramod; Hwu, Jih Ru; Hwang, Kuo Chu","Oxidative destruction of chlorinated persistent organic pollutants by hydroxyl radicals via ozone and UV light irradiation","Green Chemistry","2023","25","23","9695","9704","10.1039/D3GC02365F","","","0.71073","MoKα","","0.0495","0.0383","","","0.0945","0.1025","","","","","","1.076","","","","has coordinates","288823","2024-01-06","08:25:00",""
"7247352","10.2545","0.0003","11.784","0.0004","18.9397","0.0006","90","","91.018","0.003","90","","2288.29","0.13","113","2","113","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C30 H26 N2 O3 -","- C30 H26 N2 O3 -","- C120 H104 N8 O12 -","4","1","","Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng","Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light","Green Chemistry","2023","25","20","8074","8081","10.1039/D3GC02364H","","x-ray","0.71073","MoKα","","0.0646","0.0523","","","0.1389","0.1457","","","","","","1.054","","","","has coordinates","287355","2023-11-06","07:43:48",""
"7247353","16.0365","0.0003","8.141","0.0002","19.083","0.0005","90","","93.993","0.002","90","","2485.3","0.1","113","2","113","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C33 H28 N2 O -","- C33 H28 N2 O -","- C132 H112 N8 O4 -","4","1","","Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng","Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light","Green Chemistry","2023","25","20","8074","8081","10.1039/D3GC02364H","","x-ray","0.71073","MoKα","","0.0438","0.0392","","","0.1021","0.1049","","","","","","1.069","","","","has coordinates","287355","2023-11-06","07:43:56",""
"7247354","18.5654","0.0004","11.0141","0.0002","23.246","0.0005","90","","104.797","0.002","90","","4595.73","0.17","113","2","113","2","","","","","","","","4","I 1 2/a 1","-I 2ya","15","","","","- C58 H52 N4 O4 -","- C58 H52 N4 O4 -","- C232 H208 N16 O16 -","4","0.5","","Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng","Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light","Green Chemistry","2023","25","20","8074","8081","10.1039/D3GC02364H","","x-ray","0.71073","MoKα","","0.0498","0.0453","","","0.1069","0.1097","","","","","","1.046","","","","has coordinates","287355","2023-11-06","07:43:56",""
"7247355","18.9264","0.0003","10.15909","0.00017","12.951","0.0002","90","","100.384","0.0015","90","","2449.37","0.07","113","2","113","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C29 H27 Br N2 O2 -","- C29 H27 Br N2 O2 -","- C116 H108 Br4 N8 O8 -","4","1","","Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng","Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light","Green Chemistry","2023","25","20","8074","8081","10.1039/D3GC02364H","","x-ray","0.71073","MoKα","","0.0372","0.0302","","","0.0672","0.0692","","","","","","1.036","","","","has coordinates","287355","2023-11-06","07:43:56",""
"7247356","11.9969","0.0006","12.1767","0.0006","18.3724","0.0011","90","","103.405","0.006","90","","2610.8","0.2","113","2","113","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C35 H32 N2 O -","- C35 H32 N2 O -","- C140 H128 N8 O4 -","4","1","","Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng","Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light","Green Chemistry","2023","25","20","8074","8081","10.1039/D3GC02364H","","x-ray","0.71073","MoKα","","0.0842","0.059","","","0.1574","0.1723","","","","","","1.068","","","","has coordinates","287355","2023-11-06","07:43:56",""
"7247357","10.605","0.0003","11.8204","0.0003","17.9554","0.0005","90","","92.512","0.003","90","","2248.64","0.11","113","2","113","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C29 H26 N2 O2 -","- C29 H26 N2 O2 -","- C116 H104 N8 O8 -","4","1","","Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng","Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light","Green Chemistry","2023","25","20","8074","8081","10.1039/D3GC02364H","","x-ray","0.71073","MoKα","","0.0503","0.04","","","0.1011","0.1057","","","","","","1.082","","","","has coordinates","287355","2023-11-06","07:43:56",""
"7247358","9.1217","0.0002","17.3684","0.0004","23.9176","0.0006","90","","90","","90","","3789.25","0.15","113","2","113","2","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C11.76 H8.47 N0.94 O0.94 -","- C11.7647 H8.47059 N0.941176 O0.941176 -","- C200 H144 N16 O16 -","17","4.25","","Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng","Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light","Green Chemistry","2023","25","20","8074","8081","10.1039/D3GC02364H","","x-ray","0.71073","MoKα","","0.0674","0.0621","","","0.153","0.1582","","","","","","1.018","","","","has coordinates","287355","2023-11-06","07:43:56",""
"7247359","24.6112","0.0004","10.2554","0.0002","36.0411","0.0005","90","","99.385","0.002","90","","8974.9","0.3","113","2","113","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C58 H52 N4 O2 -","- C58 H52 N4 O2 -","- C464 H416 N32 O16 -","8","1","","Gore, Babasaheb Sopan; Kuo, Chiao-Ying; Wang, Jeh-Jeng","Photocatalyst- and transition-metal-free syntheses of furan-fused dihydroazepines by visible light","Green Chemistry","2023","25","20","8074","8081","10.1039/D3GC02364H","","x-ray","0.71073","MoKα","","0.082","0.0689","","","0.1766","0.1844","","","","","","1.088","","","","has coordinates","287355","2023-11-06","07:43:56",""
"7247377","11.3019","0.0004","6.9207","0.0003","16.2735","0.0006","90","","101.713","0.004","90","","1246.36","0.09","299.03","","299.03","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C14 H13 N O4 -","- C14 H13 N O4 -","- C56 H52 N4 O16 -","4","1","","Krishna, Anugam V.; Sanwal, Shyam D.; Rath, Sibani; Lakshmi, P. R.; Ramachary, Dhevalapally B.","Conformation-controlled catalytic asymmetric synthesis of Swaminathan ketones","Green Chemistry","2024","26","2","771","784","10.1039/D3GC02975A","","x-ray","0.71073","MoKα","","0.0909","0.0765","","","0.2144","0.2262","","","","","","1.076","","","","has coordinates","289571","2024-02-04","12:17:26",""
"7247378","8.6941","0.0004","17.9069","0.001","10.1924","0.0005","90","","90","","90","","1586.8","0.14","299","","299","","","","","","","","","3","P n a 21","P 2c -2n","33","","","","- C18 H22 O3 -","- C18 H22 O3 -","- C72 H88 O12 -","4","1","","Krishna, Anugam V.; Sanwal, Shyam D.; Rath, Sibani; Lakshmi, P. R.; Ramachary, Dhevalapally B.","Conformation-controlled catalytic asymmetric synthesis of Swaminathan ketones","Green Chemistry","2024","26","2","771","784","10.1039/D3GC02975A","","x-ray","0.71073","MoKα","","0.0566","0.0434","","","0.0984","0.1091","","","","","","1.04","","","","has coordinates","289571","2024-02-04","12:17:27",""
"7247379","7.97","0.0005","11.1812","0.0006","7.9888","0.0004","90","","110.788","0.007","90","","665.57","0.07","299","0.2","299","0.2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C16 H18 O3 -","- C16 H18 O3 -","- C32 H36 O6 -","2","1","","Krishna, Anugam V.; Sanwal, Shyam D.; Rath, Sibani; Lakshmi, P. R.; Ramachary, Dhevalapally B.","Conformation-controlled catalytic asymmetric synthesis of Swaminathan ketones","Green Chemistry","2024","26","2","771","784","10.1039/D3GC02975A","","x-ray","0.71073","MoKα","","0.0583","0.0433","","","0.0875","0.0974","","","","","","0.978","","","","has coordinates","289571","2024-02-04","12:17:28",""
"7247380","16.4952","0.0007","5.821","0.0003","14.2222","0.0007","90","","112.011","0.005","90","","1266.06","0.11","293","0.1","293","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C14 H15 N O4 -","- C14 H15 N O4 -","- C56 H60 N4 O16 -","4","1","","Krishna, Anugam V.; Sanwal, Shyam D.; Rath, Sibani; Lakshmi, P. R.; Ramachary, Dhevalapally B.","Conformation-controlled catalytic asymmetric synthesis of Swaminathan ketones","Green Chemistry","2024","26","2","771","784","10.1039/D3GC02975A","","x-ray","0.71073","MoKα","","0.1008","0.0692","","","0.1831","0.2185","","","","","","1.06","","","","has coordinates","289571","2024-02-04","12:17:28",""
"7247381","7.3138","0.0004","12.607","0.0006","15.9123","0.001","90","","90","","90","","1467.19","0.14","299.2","0.2","299.2","0.2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C18 H20 O2 -","- C18 H20 O2 -","- C72 H80 O8 -","4","1","","Krishna, Anugam V.; Sanwal, Shyam D.; Rath, Sibani; Lakshmi, P. R.; Ramachary, Dhevalapally B.","Conformation-controlled catalytic asymmetric synthesis of Swaminathan ketones","Green Chemistry","2024","26","2","771","784","10.1039/D3GC02975A","","x-ray","0.71073","MoKα","","0.0518","0.0381","","","0.0938","0.1021","","","","","","1.044","","","","has coordinates","289571","2024-02-04","12:17:28",""
"7247383","8.9531","0.0003","9.9751","0.0003","11.6032","0.0003","81.655","0.003","89.531","0.002","72.972","0.003","979.7","0.05","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C23 H19 N O3 S -","- C23 H19 N O3 S -","- C46 H38 N2 O6 S2 -","2","1","","Xia, Wen; Yang, Yawen; Zhang, Xiaohui; Hu, Liangzhen; Xiong, Yan","Electrochemical synthesis of γ-keto sulfones containing a β-quaternary carbon center via 1,2-migration","Green Chemistry","2023","25","20","8273","8279","10.1039/D3GC02128A","","x-ray","1.54184","CuKα","","0.0455","0.038","","","0.1022","0.1098","","","","","","1.038","","","","has coordinates","287353","2023-11-06","07:43:13",""
"7247384","14.1955","0.0011","11.0133","0.0009","13.4688","0.001","90","","99.284","0.007","90","","2078.1","0.3","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C25 H24 O3 S -","- C25 H24 O3 S -","- C100 H96 O12 S4 -","4","1","","Xia, Wen; Yang, Yawen; Zhang, Xiaohui; Hu, Liangzhen; Xiong, Yan","Electrochemical synthesis of γ-keto sulfones containing a β-quaternary carbon center via 1,2-migration","Green Chemistry","2023","25","20","8273","8279","10.1039/D3GC02128A","","x-ray","0.71073","MoKα","","0.0788","0.0451","","","0.1043","0.1185","","","","","","1.023","","","","has coordinates","287353","2023-11-06","07:43:14",""
"7247432","9.4617","0.0005","11.8672","0.0007","13.219","0.0008","90","","90","","90","","1484.28","0.15","293","2","293","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","NM-1287","","- C17 H18 S -","- C17 H18 S -","- C68 H72 S4 -","4","1","","Mukherjee, Nilanjana; Chatterjee, Tanmay","Recyclable iodine-catalyzed oxidative C–H chalcogenation of 1,1-diarylethenes in water: green synthesis of trisubstituted vinyl sulfides and selenides","Green Chemistry","2023","25","21","8798","8807","10.1039/D3GC02999A","","x-ray","1.54184","CuKα","","0.0484","0.042","","","0.1146","0.1227","","","","","","1.084","","","","has coordinates","287360","2023-11-06","07:45:05",""
"7247433","8.19","0.0003","10.9737","0.0003","16.0251","0.0005","92.841","0.001","98.85","0.001","91.328","0.001","1420.66","0.08","150","","150","","","","","","","","","4","P -1","-P 1","2","","","","- C16 H16 O3 S -","- C16 H16 O3 S -","- C64 H64 O12 S4 -","4","2","","Mei, Lan; Shu, Xiao-Rong; Liu, Fa-Liang; Li, Jiao-Zhe; Zhang, Jian-Feng; Tang, Keqi; Wei, Wen-Ting","Multicomponent hydrosulfonylation of alkynes for the synthesis of vinyl sulfones","Green Chemistry","2023","25","21","8820","8825","10.1039/D3GC02284F","","","0.71073","MoKα","","0.0973","0.0571","","","0.1096","0.1341","","","","","","1.031","","","","has coordinates","287357","2023-11-06","07:44:25",""
"7247437","10.7008","0.0004","13.6759","0.0003","11.2342","0.0005","90","","113.51","0.005","90","","1507.58","0.11","180","0.1","180","0.1","","","","","","","","8","P 1 21 1","P 2yb","4","","","","- C29 H31 Cl2 Co I O3 P S -","- C29 H31 Cl2 Co I O3 P S -","- C58 H62 Cl4 Co2 I2 O6 P2 S2 -","2","1","","Ma, Shuang-Shuang; Sun, Rui; Zhang, Zi-Heng; Guan, Peng-Xin; Lin, Jin-Qing; Li, Chun-Shan; Xu, Bao-Hua","Co(dppbsa)-catalyzed reductive N,N-dimethylation of nitroaromatics with CO2 and hydrosilane","Green Chemistry","2023","25","21","8625","8632","10.1039/D3GC02517A","","x-ray","0.71073","MoKα","","0.049","0.0403","","","0.0837","0.0883","","","","","","1.018","","","","has coordinates,has disorder","287361","2023-11-06","07:45:21",""
"7247479","11.4448","0.0003","8.3202","0.0002","20.9237","0.0006","90","","104.738","0.001","90","","1926.87","0.09","134.68","","134.68","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H23 N5 O4 -","- C20 H23 N5 O4 -","- C80 H92 N20 O16 -","4","1","","Liu, Mengjia; He, Ying; Wojtas, Lukasz; Shi, Xiaodong","Design and synthesis of covalently tethered “isoG-star” as a recyclable host for selective cesium separation","Green Chemistry","2023","25","21","8494","8499","10.1039/D3GC02932H","","x-ray","1.54178","CuKα","","0.0575","0.0491","","","0.1279","0.1358","","","","","","1.046","","","","has coordinates","287359","2023-11-06","07:44:56",""
"7247480","44.243","0.001","19.9018","0.0006","17.7791","0.0006","90","","110.985","0.002","90","","14616.5","0.8","100","","100","","","","","","","","","5","C 1 2 1","C 2y","5","","","","- C32.05 H47.58 N5 O8.68 Si -","- C32.0517 H47.577 N5 O8.67675 Si -","- C512.828 H761.232 N80 O138.828 Si16 -","16","4","","Liu, Mengjia; He, Ying; Wojtas, Lukasz; Shi, Xiaodong","Design and synthesis of covalently tethered “isoG-star” as a recyclable host for selective cesium separation","Green Chemistry","2023","25","21","8494","8499","10.1039/D3GC02932H","","x-ray","1.54178","CuKα","","0.0799","0.0569","","","0.1498","0.1661","","","","","","1.05","","","","has coordinates,has disorder","287359","2023-11-06","07:44:56",""
"7247486","15.093","0.0006","8.0955","0.0003","20.7666","0.0007","90","","105.204","0.002","90","","2448.56","0.16","296","2","296.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C H F O S -","- C3.29412 H2.82353 F0.235294 O0.470588 S0.117647 -","- C112 H96 F8 O16 S4 -","34","8.5","","Li, Jiayu; Guo, Zipeng; Zhang, Xiaofeng; Meng, Xiaoli; Dai, Zhenyang; Gao, Meiyun; Guo, Shuo; Tang, Pingping","Light-induced aryldifluoromethyl-sulfonylation/thioetherification of alkenes using arenethiolates as a photoreductant and sulfur source","Green Chemistry","2023","25","22","9292","9300","10.1039/D3GC03471B","","","0.71073","MoKα","","0.0705","0.0443","","","0.1176","0.1329","","","","","","1.042","","","","has coordinates","288820","2024-01-06","08:24:09",""
"7247510","5.78002","0.00017","18.6163","0.0006","15.854","0.0005","90","","95.564","0.003","90","","1697.89","0.09","300.88","0.1","300.88","0.1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C18 H21 N O5 -","- C18 H21 N O5 -","- C72 H84 N4 O20 -","4","1","","Zhao, Tian-Tian; Zhang, Xu-Gang; He, Wen-Bo; Xu, Peng-Fei","A novel approach for synthesizing α-amino acids via formate mediated hydrogen transfer using a carbon source","Green Chemistry","2023","25","21","8539","8543","10.1039/D3GC02955G","","x-ray","1.54184","CuKα","","0.0544","0.044","","","0.1198","0.1268","","","","","","1.082","","","","has coordinates","287358","2023-11-06","07:44:36",""
"7247511","10.4508","0.0002","12.4654","0.0002","14.1577","0.0003","90","","99.135","0.002","90","","1820.98","0.06","300.88","0.1","300.88","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C21 H18 Cl N O2 -","- C21 H18 Cl N O2 -","- C84 H72 Cl4 N4 O8 -","4","1","","Zhao, Tian-Tian; Zhang, Xu-Gang; He, Wen-Bo; Xu, Peng-Fei","A novel approach for synthesizing α-amino acids via formate mediated hydrogen transfer using a carbon source","Green Chemistry","2023","25","21","8539","8543","10.1039/D3GC02955G","","x-ray","1.54184","CuKα","","0.0414","0.0381","","","0.0988","0.1009","","","","","","1.06","","","","has coordinates","287358","2023-11-06","07:44:37",""
"7247521","7.2763","0.0002","7.6736","0.0003","18.9654","0.0005","83.579","0.002","82.28","0.002","64.68","0.003","946.79","0.06","100.01","0.1","100.01","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C22 H18 O3 S Se -","- C22 H18 O3 S Se -","- C44 H36 O6 S2 Se2 -","2","1","","Xie, Shu-Li; Yan, Jian-Zhong; Xie, Meng-Jun; Li, Xuan; Zhou, Fan; Zheng, Mei-Qiong; Wang, Xue-Lin; Feng, Junhao; Zhang, Yao; Duan, Ya-Nan; Niu, Yong-Dong; Li, Dong; Xia, Hai-Dong","Visible-light-driven graphitic carbon nitride-catalyzed ATRA of alkynes: highly regio- and stereoselective synthesis of (E)-β-functionalized vinylsulfones","Green Chemistry","2024","26","1","323","329","10.1039/D3GC02897F","","x-ray","1.54184","CuKα","","0.0404","0.0389","","","0.1051","0.1061","","","","","","1.076","","","","has coordinates,has disorder","289569","2024-02-04","12:17:09",""
"7247529","13.8459","0.0001","10.3707","0.0001","26.6399","0.0003","90","","90","","90","","3825.27","0.06","293","2","293","2","","","","","","","","4","P b c n","-P 2n 2ab","60","","","","- C20 H20 O6 S -","- C20 H20 O6 S -","- C160 H160 O48 S8 -","8","1","","Chandu, Palasetty; Biswas, Sourabh; Garai, Sumit; Sureshkumar, Devarajulu","Diastereoselective organophotocatalytic hydrosulfonylation of cyclopropenes","Green Chemistry","2023","25","22","9086","9091","10.1039/D3GC03303A","","x-ray","1.54184","CuKα","","0.0432","0.0382","","","0.1069","0.1114","","","","","","1.073","","","","has coordinates","288819","2024-01-06","08:23:34",""
"7247530","9.6633","0.0005","10.4825","0.0005","11.2824","0.0007","84.233","0.004","68.85","0.005","83.784","0.004","1057.28","0.11","100","0.13","100","0.13","","","","","","","","4","P -1","-P 1","2","","","","- C25 H24 O4 S -","- C25 H24 O4 S -","- C50 H48 O8 S2 -","2","1","","Chandu, Palasetty; Biswas, Sourabh; Garai, Sumit; Sureshkumar, Devarajulu","Diastereoselective organophotocatalytic hydrosulfonylation of cyclopropenes","Green Chemistry","2023","25","22","9086","9091","10.1039/D3GC03303A","","x-ray","1.54184","CuKα","","0.0807","0.0784","","","0.2295","0.2302","","","","","","1.104","","","","has coordinates","288819","2024-01-06","08:23:42",""
"7247531","12.5068","0.0001","10.9444","0.0001","15.0198","0.0001","90","","99.867","0.001","90","","2025.49","0.03","100","5","100","5","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C24 H0.25 O4 S -","- C24 H22 O4 S -","- C96 H88 O16 S4 -","4","1","","Chandu, Palasetty; Biswas, Sourabh; Garai, Sumit; Sureshkumar, Devarajulu","Diastereoselective organophotocatalytic hydrosulfonylation of cyclopropenes","Green Chemistry","2023","25","22","9086","9091","10.1039/D3GC03303A","","x-ray","1.54184","CuKα","","0.0344","0.0331","","","0.0907","0.0919","","","","","","1.054","","","","has coordinates","288819","2024-01-06","08:23:45",""
"7247532","5.7239","0.0002","16.0544","0.0004","20.5787","0.0007","94.727","0.002","94.995","0.003","90.152","0.002","1877.37","0.1","100","5","100","5","","","","","","","","4","P -1","-P 1","2","","","","- C40 H44 O12 S2 -","- C40 H44 O12 S2 -","- C80 H88 O24 S4 -","2","1","","Chandu, Palasetty; Biswas, Sourabh; Garai, Sumit; Sureshkumar, Devarajulu","Diastereoselective organophotocatalytic hydrosulfonylation of cyclopropenes","Green Chemistry","2023","25","22","9086","9091","10.1039/D3GC03303A","","x-ray","0.71073","MoKα","","0.1966","0.1794","","","0.4517","0.4613","","","","","","1.103","","","","has coordinates","288819","2024-01-06","08:23:48",""
"7247533","19.6119","0.0002","16.7818","0.0002","10.1615","0.0001","90","","92.942","0.001","90","","3339.98","0.06","100","0.1","100","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C36 H36 O8 S2 -","- C36 H36 O8 S2 -","- C144 H144 O32 S8 -","4","1","","Chandu, Palasetty; Biswas, Sourabh; Garai, Sumit; Sureshkumar, Devarajulu","Diastereoselective organophotocatalytic hydrosulfonylation of cyclopropenes","Green Chemistry","2023","25","22","9086","9091","10.1039/D3GC03303A","","x-ray","1.54184","CuKα","","0.0709","0.0589","","","0.1577","0.1691","","","","","","1.132","","","","has coordinates","288819","2024-01-06","08:23:56",""
"7247573","13.3936","0.0003","27.474","0.0006","9.584","0.0002","90","","90","","90","","3526.68","0.13","170","","170","","","","","","","","","6","P 21 21 2","P 2 2ab","18","","","","- C76 H81 I N4 O10 Si2 -","- C76 H81 I N4 O10 Si2 -","- C152 H162 I2 N8 O20 Si4 -","2","0.5","","Zhou, Hai-Jie; Yao, Yi-Ping; Zhang, Tonghui; Chen, Biao; Wang, Xu; Zhao, Hang; Zeng, Jie; Chen, Jian-Ai; Xiao, Xiao; Chen, Fen-Er","New conformationally flexible and recyclable aryl iodine catalysts from an inexpensive chiral source for asymmetric oxidations","Green Chemistry","2023","25","24","10447","10457","10.1039/D3GC02429F","","","0.71073","MoKα","","0.0285","0.0245","","","0.056","0.0584","","","","","","1.046","","","","has coordinates,has disorder","288816","2024-01-06","08:21:41",""
"7247574","28.216","0.009","13.252","0.002","14.528","0.003","90","","90","","90","","5432","2","170","","170","","","","","","","","","6","P 21 21 2","P 2 2ab","18","","","","- C56 H61 I N4 O8 Si2 -","- C56 H60 I N4 O8 Si2 -","- C224 H240 I4 N16 O32 Si8 -","4","1","","Zhou, Hai-Jie; Yao, Yi-Ping; Zhang, Tonghui; Chen, Biao; Wang, Xu; Zhao, Hang; Zeng, Jie; Chen, Jian-Ai; Xiao, Xiao; Chen, Fen-Er","New conformationally flexible and recyclable aryl iodine catalysts from an inexpensive chiral source for asymmetric oxidations","Green Chemistry","2023","25","24","10447","10457","10.1039/D3GC02429F","","","0.71073","MoKα","","0.0724","0.0439","","","0.1027","0.1185","","","","","","1.035","","","","has coordinates,has disorder","288816","2024-01-06","08:21:49",""
"7247578","7.5418","0.0003","11.3152","0.0004","12.9845","0.0005","90","","96.939","0.001","90","","1099.94","0.07","142","2","142","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C9 H10 N2 O2 S2 -","- C9 H10 N2 O2 S2 -","- C36 H40 N8 O8 S8 -","4","1","","Pal, Satyajit; Sarkar, Subhankar; Mukherjee, Anindita; Kundu, Anupam; Sen, Animesh; Rath, Jnanendra; Santra, Sougata; Zyryanov, Grigory V.; Majee, Adinath","Metal-free, tert-butyl nitrite promoted C(sp2)–S coupling reaction: the synthesis of aryl dithiocarbamates and analysis of antimicrobial activity by ‘in silico’ and ‘in vitro’ methods for drug modification","Green Chemistry","2023","25","23","9847","9856","10.1039/D3GC03153E","","","0.71073","MoKα","","0.0669","0.0475","","","0.1383","0.1668","","","","","","1.023","","","","has coordinates","288822","2024-01-06","08:24:46",""
"7247605","21.1054","0.001","11.235","0.0003","24.6803","0.0012","90","","106.321","0.005","90","","5616.3","0.4","240","0.1","240","0.1","","","","","","","","5","P 1 2/n 1","-P 2yac","13","","","","- C32 H28 Br O4 P -","- C32 H28 Br O4 P -","- C256 H224 Br8 O32 P8 -","8","2","","Li, Chaoyang; Niu, Xinyue; Xu, Wan; Bu, Zhanwei; Zhang, Wenjing; Wang, Qilin","Distinct reactivities of ortho-chalcone-substituted organophosphines with activated alkynes: skeletal editing or periphery modification","Green Chemistry","2023","25","24","10587","10595","10.1039/D3GC03165A","","x-ray","1.54184","CuKα","","0.1087","0.0807","","","0.2286","0.2568","","","","","","1.043","","","","has coordinates,has disorder","288817","2024-01-06","08:22:01",""
"7247606","9.7322","0.0016","10.0029","0.0016","12.561","0.002","89.918","0.004","88.573","0.004","81.09","0.004","1207.7","0.3","296.15","","296.15","","","","","","","","","6","P -1","-P 1","2","","","","- C30 H23 Cl N O2 P -","- C30 H23 Cl N O2 P -","- C60 H46 Cl2 N2 O4 P2 -","2","1","","Li, Chaoyang; Niu, Xinyue; Xu, Wan; Bu, Zhanwei; Zhang, Wenjing; Wang, Qilin","Distinct reactivities of ortho-chalcone-substituted organophosphines with activated alkynes: skeletal editing or periphery modification","Green Chemistry","2023","25","24","10587","10595","10.1039/D3GC03165A","","","0.71073","MoKα","","0.132","0.0581","","","0.0897","0.1155","","","","","","1.04","","","","has coordinates","288817","2024-01-06","08:22:03",""
"7247607","14.9304","0.0002","9.0992","0.0001","21.2031","0.0003","90","","106.572","0.002","90","","2760.89","0.07","170","2","170","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C33 H26 Cl O5 P -","- C33 H26 Cl O5 P -","- C132 H104 Cl4 O20 P4 -","4","1","","Li, Chaoyang; Niu, Xinyue; Xu, Wan; Bu, Zhanwei; Zhang, Wenjing; Wang, Qilin","Distinct reactivities of ortho-chalcone-substituted organophosphines with activated alkynes: skeletal editing or periphery modification","Green Chemistry","2023","25","24","10587","10595","10.1039/D3GC03165A","","x-ray","1.54184","CuKα","","0.0399","0.0367","","","0.0987","0.1008","","","","","","1.053","","","","has coordinates","288817","2024-01-06","08:22:07",""
"7247608","14.38","0.0005","15.4793","0.0007","17.346","0.0006","101.507","0.003","108.532","0.003","108.298","0.004","3278.1","0.3","149.99","0.1","149.99","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C54 H40 Br2 O2 P2 -","- C54 H40 Br2 O2 P2 -","- C162 H120 Br6 O6 P6 -","3","1.5","","Li, Chaoyang; Niu, Xinyue; Xu, Wan; Bu, Zhanwei; Zhang, Wenjing; Wang, Qilin","Distinct reactivities of ortho-chalcone-substituted organophosphines with activated alkynes: skeletal editing or periphery modification","Green Chemistry","2023","25","24","10587","10595","10.1039/D3GC03165A","","x-ray","1.54184","CuKα","","0.0753","0.0534","","","0.1433","0.1573","","","","","","1.038","","","","has coordinates,has disorder","288817","2024-01-06","08:22:14",""
"7247703","11.5372","0.0011","11.7335","0.0009","10.3893","0.0009","90","","104.132","0.009","90","","1363.9","0.2","199.99","0.1","199.99","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C13 H8 F7 N3 -","- C13 H8 F7 N3 -","- C52 H32 F28 N12 -","4","1","","Han, Wei; Chen, Yu-Lan; Tang, Xi; Zhou, Jie; Ma, Mengtao; Shen, Zhi-Liang; Chu, Xue-Qiang","Water-promoted defluorinative synthesis of fluoroalkylated 1,5-diazapentadienes by using (NH4)2CO3 as an NH2 and NH source","Green Chemistry","2023","25","23","9672","9679","10.1039/D3GC03717G","","x-ray","0.71073","MoKα","","0.0479","0.0395","","","0.0986","0.1047","","","","","","1.069","","","","has coordinates","288821","2024-01-06","08:24:32",""
"7247704","6.2755","0.001","8.141","0.0009","19.0094","0.0012","81.051","0.007","85.123","0.009","84.276","0.011","952.2","0.2","150","0.1","150","0.1","","","","","","","","6","P -1","-P 1","2","","","","- C19 H14 F7 N O3 S -","- C19 H14 F7 N O3 S -","- C38 H28 F14 N2 O6 S2 -","2","1","","Han, Wei; Chen, Yu-Lan; Tang, Xi; Zhou, Jie; Ma, Mengtao; Shen, Zhi-Liang; Chu, Xue-Qiang","Water-promoted defluorinative synthesis of fluoroalkylated 1,5-diazapentadienes by using (NH4)2CO3 as an NH2 and NH source","Green Chemistry","2023","25","23","9672","9679","10.1039/D3GC03717G","","x-ray","1.54184","CuKα","","0.106","0.0955","","","0.268","0.2865","","","","","","1.087","","","","has coordinates","288821","2024-01-06","08:24:34",""
"7247725","9.5594","0.0007","19.9216","0.0015","10.3113","0.0008","90","","110.294","0.009","90","","1841.8","0.3","220.03","0.1","220.03","0.1","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C21 H17 Br F2 N2 O -","- C21 H17 Br F2 N2 O -","- C84 H68 Br4 F8 N8 O4 -","4","1","","Pan, Dongping; Liu, Fu-Xiaomin; Zeng, Zhongyi; Ye, Junwei; Cai, Ying; Wang, Shengdong; Zhou, Zhi; Yi, Wei","Practical conversion of gem-difluorocyclopropenes for the chemodivergent assembly of fluorinated heterocyclic frameworks","Green Chemistry","2023","25","24","10630","10637","10.1039/D3GC03203E","","x-ray","0.71073","MoKα","","0.0546","0.0372","","","0.0795","0.0874","","","","","","1.034","","","","has coordinates","288818","2024-01-06","08:22:34",""
"7247726","8.8203","0.0005","9.1068","0.0006","10.6468","0.0006","67.05","0.006","88.22","0.004","71.172","0.005","740.95","0.09","149.99","0.1","149.99","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C17 H15 F N2 O2 -","- C17 H15 F N2 O2 -","- C34 H30 F2 N4 O4 -","2","1","","Pan, Dongping; Liu, Fu-Xiaomin; Zeng, Zhongyi; Ye, Junwei; Cai, Ying; Wang, Shengdong; Zhou, Zhi; Yi, Wei","Practical conversion of gem-difluorocyclopropenes for the chemodivergent assembly of fluorinated heterocyclic frameworks","Green Chemistry","2023","25","24","10630","10637","10.1039/D3GC03203E","","x-ray","1.54184","CuKα","","0.0611","0.0581","","","0.1552","0.1585","","","","","","1.082","","","","has coordinates","288818","2024-01-06","08:22:42",""
"7247727","37.7194","0.0004","16.9142","0.0002","9.49011","0.00012","90","","90","","90","","6054.63","0.12","294.6","0.1","294.6","0.1","","","","","","","","5","F d d 2","F 2 -2d","43","","","","- C17 H16 F2 N2 O -","- C17 H16 F2 N2 O -","- C272 H256 F32 N32 O16 -","16","1","","Pan, Dongping; Liu, Fu-Xiaomin; Zeng, Zhongyi; Ye, Junwei; Cai, Ying; Wang, Shengdong; Zhou, Zhi; Yi, Wei","Practical conversion of gem-difluorocyclopropenes for the chemodivergent assembly of fluorinated heterocyclic frameworks","Green Chemistry","2023","25","24","10630","10637","10.1039/D3GC03203E","","x-ray","1.54184","CuKα","","0.0335","0.0323","","","0.0859","0.0871","","","","","","1.051","","","","has coordinates","288818","2024-01-06","08:22:54",""
"7247728","11.0253","0.0012","19.0234","0.0019","11.08","0.0013","90","","117.375","0.015","90","","2063.7","0.5","150","0.1","150","0.1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C24 H21 F N2 O3 S -","- C24 H21 F N2 O3 S -","- C96 H84 F4 N8 O12 S4 -","4","1","","Pan, Dongping; Liu, Fu-Xiaomin; Zeng, Zhongyi; Ye, Junwei; Cai, Ying; Wang, Shengdong; Zhou, Zhi; Yi, Wei","Practical conversion of gem-difluorocyclopropenes for the chemodivergent assembly of fluorinated heterocyclic frameworks","Green Chemistry","2023","25","24","10630","10637","10.1039/D3GC03203E","","x-ray","0.71073","MoKα","","0.0518","0.0422","","","0.0986","0.1036","","","","","","1.073","","","","has coordinates","288818","2024-01-06","08:23:06",""
"7247742","6.8294","0.0001","14.2435","0.0002","20.7154","0.0002","90","","90","","90","","2015.08","0.05","100.01","0.1","100.01","0.1","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C24 H23 Br O S -","- C24 H23 Br O S -","- C96 H92 Br4 O4 S4 -","4","1","","Fan, Xin-Yang; Li, Jia-Cheng; Zhou, Ji-Jia; Zhou, Bo; Ye, Long-Wu","Chiral Brønsted acid-catalyzed asymmetric dearomative spirocyclization of alkynyl thioethers","Green Chemistry","2023","25","24","10638","10643","10.1039/D3GC03222A","","x-ray","1.54184","CuKα","","0.0275","0.0258","","","0.0648","0.0655","","","","","","1.038","","","","has coordinates","288815","2024-01-06","08:21:21",""
"7247784","6.8883","0.0009","15.522","0.002","16.668","0.002","90","","90","","90","","1782.1","0.4","298","","298","","","","","","","","","5","P c a 21","P 2c -2ac","29","","","","- C22 H16 F3 N O -","- C22 H16 F3 N O -","- C88 H64 F12 N4 O4 -","4","1","","Lamba, Manisha; Singh, Prasoon Raj; Bhatt, Shubham; Goswami, Avijit","Metal- and additive-free TfOH catalyzed chemoselective O- and S-trifluoroethylation of oxindoles, isoindolines and thio-oxindoles","Green Chemistry","2024","26","1","448","455","10.1039/D3GC03702A","","x-ray","0.71073","MoKα","","0.0521","0.0387","","","0.0883","0.0965","","","","","","1.035","","","","has coordinates","289565","2024-02-04","12:16:46",""
"7247785","6.8631","0.0003","16.0474","0.0005","16.9025","0.0006","90","","90","","90","","1861.56","0.12","298","","298","","","","","","","","","5","P c a 21","P 2c -2ac","29","","","","- C22 H15 F4 N S -","- C22 H15 F4 N S -","- C88 H60 F16 N4 S4 -","4","1","","Lamba, Manisha; Singh, Prasoon Raj; Bhatt, Shubham; Goswami, Avijit","Metal- and additive-free TfOH catalyzed chemoselective O- and S-trifluoroethylation of oxindoles, isoindolines and thio-oxindoles","Green Chemistry","2024","26","1","448","455","10.1039/D3GC03702A","","x-ray","0.71073","MoKα","","0.0496","0.0441","","","0.1068","0.1112","","","","","","1.045","","","","has coordinates","289565","2024-02-04","12:16:46",""
"7247786","17.093","0.012","10.057","0.01","6.991","0.004","90","","113.89","0.03","90","","1098.8","1.5","298","","298","","","","","","","","","6","C 1 2 1","C 2y","5","","","","- C10 H6 Br F3 N O -","- C10 H6 Br F3 N O -","- C40 H24 Br4 F12 N4 O4 -","4","1","","Lamba, Manisha; Singh, Prasoon Raj; Bhatt, Shubham; Goswami, Avijit","Metal- and additive-free TfOH catalyzed chemoselective O- and S-trifluoroethylation of oxindoles, isoindolines and thio-oxindoles","Green Chemistry","2024","26","1","448","455","10.1039/D3GC03702A","","","0.71073","MoKα","","0.0497","0.0421","","","0.107","0.1132","","","","","","0.986","","","","has coordinates","289565","2024-02-04","12:16:46",""
"7247787","10.0648","0.0008","11.6308","0.0008","13.8611","0.001","68.976","0.002","87.671","0.003","69.921","0.002","1416.21","0.18","298","","298","","","","","","","","","5","P -1","-P 1","2","","","","- C34 H26 F6 N2 O2 -","- C34 H26 F6 N2 O2 -","- C68 H52 F12 N4 O4 -","2","1","","Lamba, Manisha; Singh, Prasoon Raj; Bhatt, Shubham; Goswami, Avijit","Metal- and additive-free TfOH catalyzed chemoselective O- and S-trifluoroethylation of oxindoles, isoindolines and thio-oxindoles","Green Chemistry","2024","26","1","448","455","10.1039/D3GC03702A","","x-ray","0.71073","MoKα","","0.0737","0.0626","","","0.1794","0.1917","","","","","","1.033","","","","has coordinates","289565","2024-02-04","12:16:46",""
"7247788","7.9716","0.0002","10.9315","0.0003","15.7731","0.0004","75.98","0.001","78.693","0.001","81.338","0.001","1299.96","0.06","298","","298","","","","","","","","","6","P -1","-P 1","2","","","","- C28 H26 Br F3 N O -","- C28 H26 Br F3 N O -","- C56 H52 Br2 F6 N2 O2 -","2","1","","Lamba, Manisha; Singh, Prasoon Raj; Bhatt, Shubham; Goswami, Avijit","Metal- and additive-free TfOH catalyzed chemoselective O- and S-trifluoroethylation of oxindoles, isoindolines and thio-oxindoles","Green Chemistry","2024","26","1","448","455","10.1039/D3GC03702A","","x-ray","0.71073","MoKα","","0.0766","0.0639","","","0.1626","0.1725","","","","","","1.03","","","","has coordinates","289565","2024-02-04","12:16:46",""
"7247789","7.0705","0.0006","16.8461","0.0016","32.575","0.003","90","","90","","90","","3880","0.6","298","","298","","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C23 H18 F3 N S -","- C23 H18 F3 N S -","- C184 H144 F24 N8 S8 -","8","1","","Lamba, Manisha; Singh, Prasoon Raj; Bhatt, Shubham; Goswami, Avijit","Metal- and additive-free TfOH catalyzed chemoselective O- and S-trifluoroethylation of oxindoles, isoindolines and thio-oxindoles","Green Chemistry","2024","26","1","448","455","10.1039/D3GC03702A","","x-ray","0.71073","MoKα","","0.0553","0.0507","","","0.1272","0.1296","","","","","","1.151","","","","has coordinates","289565","2024-02-04","12:16:46",""
"7247827","12.2243","0.0004","10.5039","0.0003","23.3691","0.0008","90","","91.697","0.003","90","","2999.34","0.17","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C29 H40 N2 O4 S Si -","- C29 H40 N2 O4 S Si -","- C116 H160 N8 O16 S4 Si4 -","4","1","","Li, Zengzeng; Lu, Fei; Xu, Qingchun; Liu, Gang; Zhao, Ximei; Wang, Guanghui","Unexpected stereoselective CuBr2-catalyzed cascade reaction of 2-ethynylanilines with silylynamides: facile and atom-economical access to N-vinylsilylindoles","Green Chemistry","2024","26","1","259","263","10.1039/D3GC04244H","","","1.54184","CuKα","","0.0786","0.0615","","","0.1674","0.1835","","","","","","1.036","","","","has coordinates,has disorder","289570","2024-02-04","12:17:16",""
"7247828","22.937","0.004","8.7952","0.0015","11.1318","0.0019","90","","90","","90","","2245.7","0.7","296.15","","296.15","","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C28 H23 O3 P -","- C28 H23 O3 P -","- C112 H92 O12 P4 -","4","1","","Huang, Mingqing; Huang, Haiyang; You, Mengyao; Zhang, Xinxin; Sun, Longgen; Chen, Chao; Mei, Zhichao; Yang, Ruchun; Xiao, Qiang","Direct air-induced arylphosphinoyl radicals for the synthesis of benzo[b]phosphole oxides","Green Chemistry","2024","26","1","295","299","10.1039/D3GC03947A","","","0.71073","MoKα","","0.0562","0.0421","","","0.0963","0.1046","","","","","","1.044","","","","has coordinates","289563","2024-02-04","12:16:13",""
"7247829","13.961","0.002","9.9168","0.0016","21.452","0.003","90","","106.577","0.003","90","","2846.6","0.7","296.15","","296.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C28 H25 O P -","- C28 H25 O P -","- C112 H100 O4 P4 -","4","1","","Huang, Mingqing; Huang, Haiyang; You, Mengyao; Zhang, Xinxin; Sun, Longgen; Chen, Chao; Mei, Zhichao; Yang, Ruchun; Xiao, Qiang","Direct air-induced arylphosphinoyl radicals for the synthesis of benzo[b]phosphole oxides","Green Chemistry","2024","26","1","295","299","10.1039/D3GC03947A","","","0.71073","MoKα","","0.1132","0.0555","","","0.1352","0.1541","","","","","","0.836","","","","has coordinates","289563","2024-02-04","12:16:14",""
"7247831","39.4459","0.0015","39.4459","0.0015","12.5093","0.0008","90","","90","","120","","16856.5","1.4","200","2","200","2","","","","","","","","4","R -3 :H","-R 3","148","","","","- C50 H33 N3 O2 -","- C50 H33 N3 O2 -","- C900 H594 N54 O36 -","18","1","","Amiri, Kamran; Nayebzadeh, Behrouz; Kamangar, Mohammad; Babazadeh, Mohammad; Ariafard, Alireza; Shiri, Farshad; Rominger, Frank; Balalaie, Saeed","Synthesis of a fused N-bridged [3.3.1]nonadiquinoline multicyclic skeleton via a metal-free formal [4 + 2] cycloaddition/Mannich/dearomatization domino reaction","Green Chemistry","2023","25","22","9203","9208","10.1039/D3GC03026A","","","0.71073","MoKα","","0.1113","0.0526","","","0.1126","0.1369","","","","","","1.04","","","","has coordinates","288029","2023-12-05","04:10:14",""
"7247832","6.345","0.0006","7.2323","0.0007","10.5606","0.001","94.218","0.002","100.28","0.002","97.907","0.002","469.9","0.08","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C4 H9 O11 -","- C4 H9 O11 -","- C8 H18 O22 -","2","1","","Ragupathi, Ayyakkannu; Charpe, Vaibhav Pramod; Hwu, Jih Ru; Hwang, Kuo Chu","Oxidative destruction of chlorinated persistent organic pollutants by hydroxyl radicals via ozone and UV light irradiation","Green Chemistry","2023","25","23","9695","9704","10.1039/D3GC02365F","","","0.71073","MoKα","","0.0535","0.0461","","","0.1211","0.1274","","","","","","1.055","","","","has coordinates","288030","2023-12-05","04:12:00",""
"7247835","15.156","0.0003","6.0528","0.0001","20.8658","0.0004","90","","104.934","0.001","90","","1849.5","0.06","297","2","297","","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C23 H24 N2 -","- C23 H24 N2 -","- C92 H96 N8 -","4","2","","Yang, Zhi; Chen, Yu; Wan, Linxi; Li, Yuxiao; Chen, Dan; Tao, Jianlin; Tang, Pei; Chen, Fen-Er","Iridium-catalyzed asymmetric, complete hydrogenation of pyrimidinium salts under batch and flow","Green Chemistry","2024","26","1","317","322","10.1039/D3GC04364A","","","1.54178","CuKα","","0.0513","0.0457","","","0.1214","0.1257","","","","","","1.065","","","","has coordinates","289567","2024-02-04","12:16:59",""
"7247850","7.9414","0.0006","9.2292","0.0007","13.4539","0.0011","71.148","0.003","82.961","0.003","81.232","0.003","919.44","0.13","289","2","289.27","","","","","","","","","4","P -1","-P 1","2","","1,3-benozoxazine","","- C21 H21 N O5 -","- C21 H21 N O5 -","- C42 H42 N2 O10 -","2","1","","Duhan, Vaishaly; Yadav, Shivani; Len, Christophe; Lochab, Bimlesh","The mechanochemical synthesis of environmentally benign fully biobased 4th generation benzoxazines and their polymers: mechanistic insights into the catalytic activity of latent catalysts","Green Chemistry","2024","26","1","483","497","10.1039/D3GC03522K","","","0.71073","MoKα","","0.0614","0.048","","","0.1248","0.1397","","","","","","1.089","","","","has coordinates","289564","2024-02-04","12:16:35",""
"7247851","7.9467","0.0003","9.2458","0.0004","13.4593","0.0005","71.201","0.001","83.031","0.002","81.265","0.002","922.52","0.06","313","2","313","2","","","","","","","","4","P -1","-P 1","2","","","","- C21 H21 N O5 -","- C21 H21 N O5 -","- C42 H42 N2 O10 -","2","1","","Duhan, Vaishaly; Yadav, Shivani; Len, Christophe; Lochab, Bimlesh","The mechanochemical synthesis of environmentally benign fully biobased 4th generation benzoxazines and their polymers: mechanistic insights into the catalytic activity of latent catalysts","Green Chemistry","2024","26","1","483","497","10.1039/D3GC03522K","","","0.71073","MoKα","","0.1834","0.0747","","","0.2045","0.274","","","","","","1.059","","","","has coordinates","289564","2024-02-04","12:16:35",""
"7247852","7.9501","0.0004","9.2801","0.0006","13.4663","0.0008","71.289","0.002","83.005","0.002","81.107","0.002","926.92","0.09","343","","343","","","","","","","","","4","P -1","-P 1","2","","","","- C21 H21 N O5 -","- C21 H21 N O5 -","- C42 H42 N2 O10 -","2","1","","Duhan, Vaishaly; Yadav, Shivani; Len, Christophe; Lochab, Bimlesh","The mechanochemical synthesis of environmentally benign fully biobased 4th generation benzoxazines and their polymers: mechanistic insights into the catalytic activity of latent catalysts","Green Chemistry","2024","26","1","483","497","10.1039/D3GC03522K","","","0.71073","MoKα","","0.1485","0.0932","","","0.2818","0.3861","","","","","","1.4868","","","","has coordinates","289564","2024-02-04","12:16:35",""
"7247855","7.985","0.002","8.521","0.002","21.601","0.005","90","","96.717","0.009","90","","1459.6","0.6","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C18 H17 N O2 -","- C18 H17 N O2 -","- C72 H68 N4 O8 -","4","1","","Zeng, Kui; Pandit, Neeraj Kumar; Oliveira, João C. A.; Dechert, Sebastian; Ackermann, Lutz; Zhang, Kai","Weak-coordination-auxiliary aminocatalysis enables directed [3+2] cyclization for 2-acylindolizines","Green Chemistry","2024","","","","","10.1039/D3GC03552B","","","0.71073","MoKα","","0.0469","0.0378","","","0.0883","0.0942","","","","","","1.026","","","","has coordinates","288293","2023-12-14","00:38:36",""
"7247856","7.519","0.0013","12.05","0.002","11.678","0.002","90","","100.317","0.006","90","","1041","0.3","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C13 H15 N O -","- C13 H15 N O -","- C52 H60 N4 O4 -","4","1","","Zeng, Kui; Pandit, Neeraj Kumar; Oliveira, João C. A.; Dechert, Sebastian; Ackermann, Lutz; Zhang, Kai","Weak-coordination-auxiliary aminocatalysis enables directed [3+2] cyclization for 2-acylindolizines","Green Chemistry","2024","","","","","10.1039/D3GC03552B","","","0.71073","MoKα","","0.0863","0.0505","","","0.1167","0.1372","","","","","","1.078","","","","has coordinates","288293","2023-12-14","00:38:36",""
"7247857","3.7781","0.0002","7.5804","0.0003","14.7776","0.0006","94.101","0.002","93.691","0.002","96.948","0.002","417.9","0.03","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C9 H6 N2 O2 -","- C9 H6 N2 O2 -","- C18 H12 N4 O4 -","2","1","","Qi, Jing; Wang, Xiyan; Wang, Gan; Dubbaka, Srinivas Reddy; O'Neill, Patrick; Ang, Hwee Ting; Wu, Jie","Sustainable electrocatalytic oxidation of N-alkylamides to acyclic imides using H2O","Green Chemistry","2024","26","1","306","311","10.1039/D3GC04010K","","","0.71073","MoKα","","0.0419","0.0385","","","0.1091","0.1135","","","","","","1.055","","","","has coordinates","289568","2024-02-04","12:17:03",""
"7247858","4.61033","0.00012","11.7809","0.0004","29.1594","0.0012","90","","90","","90","","1583.76","0.09","149.99","0.1","149.99","0.1","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C14 H19 N O10 -","- C14 H19 N O10 -","- C56 H76 N4 O40 -","4","1","","Chen, Shipeng; Wang, Jinping; Feng, Li; Song, Zebin; Wang, Xiaoji; Ke, Yubin; Hua, Lin; Fan, Yange; Li, Zheng; Hou, Yimin; Xue, Baoyu; Liu, Luke","Preparation, characterization and application of d-gluconic acetal-based self-healing supramolecular ionogels for desulphurization of fuels","Green Chemistry","2024","26","2","979","991","10.1039/D3GC04359B","","x-ray","1.54184","CuKα","","0.0515","0.0435","","","0.1022","0.1056","","","","","","1.105","","","","has coordinates","289572","2024-02-04","12:17:34",""
"7247859","10.8293","0.0013","11.2973","0.0014","12.2048","0.0014","82.474","0.004","89.037","0.004","78.85","0.004","1452.3","0.3","150","","150","","","","","","","","","6","P -1","-P 1","2","","","","- C63 H70 Cl2 N2 O5 Ru2 -","- C63 H70 Cl2 N2 O5 Ru2 -","- C63 H70 Cl2 N2 O5 Ru2 -","1","0.5","","Deshmukh, Gopal; Rana, Thakur Rochak Kumar; Yadav, Nikita; Rajaraman, Gopalan; Murugavel, Ramaswamy","A highly active and chemoselective homobimetallic ruthenium catalyst for one-pot reductive amination in water","Green Chemistry","2024","26","3","1610","1626","10.1039/D3GC03374K","","","0.71073","MoKα","","0.0635","0.0555","","","0.1455","0.1523","","","","","","1.119","","","","has coordinates","290224","2024-03-04","20:32:43",""
"7247860","11.3984","0.0001","12.3026","0.0001","18.3366","0.0002","90","","99.351","0.001","90","","2537.17","0.04","104.5","0.7","104.5","0.7","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C29 H36 Cl N O Ru -","- C29 H36 Cl N O Ru -","- C116 H144 Cl4 N4 O4 Ru4 -","4","1","","Deshmukh, Gopal; Rana, Thakur Rochak Kumar; Yadav, Nikita; Rajaraman, Gopalan; Murugavel, Ramaswamy","A highly active and chemoselective homobimetallic ruthenium catalyst for one-pot reductive amination in water","Green Chemistry","2024","26","3","1610","1626","10.1039/D3GC03374K","","x-ray","0.71073","MoKα","","0.0221","0.0212","","","0.0542","0.0549","","","","","","1.033","","","","has coordinates","290224","2024-03-04","20:32:44",""
"7247883","8.95427","0.00016","13.54255","0.00018","9.03971","0.00016","90","","113.787","0.002","90","","1003.07","0.03","100","0.1","100","0.1","","","","","","","","5","P 1 c 1","P -2yc","7","","","","- C23 H26 I N O2 -","- C23 H26 I N O2 -","- C46 H52 I2 N2 O4 -","2","1","","Muskan,; Verma, Akhilesh K.","An environmentally benign and atom-economical protocol for the regioselective synthesis of isoquinolones from o-alkynylaldehydes","Green Chemistry","2024","26","3","1297","1301","10.1039/D3GC04096H","","x-ray","0.71073","MoKα","","0.0217","0.0207","","","0.044","0.0449","","","","","","1.031","","","","has coordinates","290221","2024-03-04","20:32:23",""
"7247899","14.4478","0.0006","17.5319","0.0007","12.9774","0.0004","90","","99.18","0.002","90","","3245","0.2","100","2","100","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C21 H12 F2 N2 -","- C21 H12 F2 N2 -","- C168 H96 F16 N16 -","8","1","","Charpe, Vaibhav Pramod; Gupta, Mahima; Hwang, Kuo Chu","Visible light-mediated copper catalyzed regioselective diamination of terminal alkynes at room temperature: a facile synthesis of substituted imidazo[1,2-α]pyridines","Green Chemistry","2024","26","3","1329","1337","10.1039/D3GC04062C","","","0.71073","MoKα","","0.0681","0.0463","","","0.1156","0.1316","","","","","","1.023","","","","has coordinates","290220","2024-03-04","20:32:16",""
"7247900","9.6958","0.0004","12.8863","0.0005","14.1978","0.0005","95.348","0.002","91.322","0.002","97.198","0.002","1751.19","0.12","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C46 H36 N4 -","- C46 H36 N4 -","- C92 H72 N8 -","2","1","","Charpe, Vaibhav Pramod; Gupta, Mahima; Hwang, Kuo Chu","Visible light-mediated copper catalyzed regioselective diamination of terminal alkynes at room temperature: a facile synthesis of substituted imidazo[1,2-α]pyridines","Green Chemistry","2024","26","3","1329","1337","10.1039/D3GC04062C","","","0.71073","MoKα","","0.0604","0.0447","","","0.1171","0.1344","","","","","","1.08","","","","has coordinates","290220","2024-03-04","20:32:17",""
"7247901","3.8778","0.0005","12.9392","0.0017","16.735","0.002","90","","92.968","0.003","90","","838.56","0.18","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C21 H12 Br2 N2 -","- C21 H12 Br2 N2 -","- C42 H24 Br4 N4 -","2","1","","Charpe, Vaibhav Pramod; Gupta, Mahima; Hwang, Kuo Chu","Visible light-mediated copper catalyzed regioselective diamination of terminal alkynes at room temperature: a facile synthesis of substituted imidazo[1,2-α]pyridines","Green Chemistry","2024","26","3","1329","1337","10.1039/D3GC04062C","","","0.71073","MoKα","","0.0297","0.0255","","","0.054","0.0549","","","","","","0.951","","","","has coordinates","290220","2024-03-04","20:32:17",""
"7247902","7.927","0.0001","11.9867","0.0001","36.2753","0.0004","90","","90","","90","","3446.83","0.06","99.8","0.5","99.8","0.5","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C46 H36 N4 -","- C46 H36 N4 -","- C184 H144 N16 -","4","1","","Charpe, Vaibhav Pramod; Gupta, Mahima; Hwang, Kuo Chu","Visible light-mediated copper catalyzed regioselective diamination of terminal alkynes at room temperature: a facile synthesis of substituted imidazo[1,2-α]pyridines","Green Chemistry","2024","26","3","1329","1337","10.1039/D3GC04062C","","x-ray","1.54184","CuKα","","0.037","0.033","","","0.0805","0.083","","","","","","1.045","","","","has coordinates","290220","2024-03-04","20:32:17",""
"7247903","16.7695","0.0005","8.6997","0.0003","11.0836","0.0003","90","","91.718","0.003","90","","1616.26","0.09","100","0.11","100","0.11","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C44 H32 N4 -","- C44 H32 N4 -","- C88 H64 N8 -","2","0.5","","Charpe, Vaibhav Pramod; Gupta, Mahima; Hwang, Kuo Chu","Visible light-mediated copper catalyzed regioselective diamination of terminal alkynes at room temperature: a facile synthesis of substituted imidazo[1,2-α]pyridines","Green Chemistry","2024","26","3","1329","1337","10.1039/D3GC04062C","","x-ray","1.54184","CuKα","","0.044","0.0341","","","0.0835","0.0877","","","","","","1.062","","","","has coordinates","290220","2024-03-04","20:32:17",""
"7247931","6.343","","9.959","","23.828","","90","","90","","90","","1505.21","","193","","193","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C15 H21 Cl O5 -","- C15 H21 Cl O5 -","- C60 H84 Cl4 O20 -","4","1","","Zhao, Jianyou; Zhang, Jiatai; Fang, Pengkai; Wu, Jintao; Wang, Fan; Liu, Zhong-Quan","Electrochemical chlorination of least hindered tertiary and benzylic C(sp3)–H bonds","Green Chemistry","2024","26","1","507","512","10.1039/D3GC03849A","","","1.34138","GaKα","","0.0458","0.0386","","","0.097","0.1011","","","","","","1.06","","","","has coordinates","289566","2024-02-04","12:16:53",""
"7247966","12.929","0.003","3.949","0.0008","13.092","0.003","90","","103.7","0.03","90","","649.4","0.3","293","2","293","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C20 H12 O -","- C20 H12 O -","- C40 H24 O2 -","2","1","","Bao, Yishu; Ma, Siyuan; Zhu, Jin; Dai, Zonghao; Zhou, Qikun; Yang, Xiuqin; Zhou, Qingfa; Yang, Fulai","TfOH-catalyzed transfer hydrogenation reaction using 1-tetralone as a novel dihydrogen source","Green Chemistry","2024","26","3","1356","1362","10.1039/D3GC04699K","","","0.71073","MoKα","","0.2159","0.0612","","","0.0674","0.1006","","","","","","0.931","","","","has coordinates","290222","2024-03-04","20:32:29",""
"7247999","10.972","0.0005","10.3056","0.0005","29.8407","0.0014","90","","90","","90","","3374.2","0.3","294","2","294","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","2-(4-hydroxyphenyl)-4,4-dimethyl-2-(quinolin-3-yl)oxetan-3-one","","- C20 H17 N O3 -","- C20 H17 N O3 -","- C160 H136 N8 O24 -","8","1","","Venka Reddy, Pammi; Nagireddy, Attunuri; Nanubolu, Jagadeesh Babu; Sridhar Reddy, Maddi","Photoinduced arylative formal 4-endo-dig cyclization of propargyl alcohols/amines to access strained heterocycles","Green Chemistry","2024","26","5","2705","2711","10.1039/D3GC03540A","","","0.71073","MoKα","","0.0836","0.0454","","","0.1073","0.1269","","","","","","1.024","","","","has coordinates,has disorder","290998","2024-04-04","23:54:25",""
"7248000","8.8036","0.0002","21.7067","0.0004","9.8524","0.0002","90","","95.1478","0.0008","90","","1875.17","0.07","294","2","294","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","2-hydroxy-1-(4-hydroxyphenyl)-2-methylpropan-1-one","","- C10 H12 O3 -","- C10 H12 O3 -","- C80 H96 O24 -","8","2","","Venka Reddy, Pammi; Nagireddy, Attunuri; Nanubolu, Jagadeesh Babu; Sridhar Reddy, Maddi","Photoinduced arylative formal 4-endo-dig cyclization of propargyl alcohols/amines to access strained heterocycles","Green Chemistry","2024","26","5","2705","2711","10.1039/D3GC03540A","","","0.71073","MoKα","","0.0827","0.0482","","","0.12","0.1382","","","","","","1.051","","","","has coordinates","290998","2024-04-04","23:54:25",""
"7248007","11.4261","0.0005","9.6846","0.0004","16.4306","0.0007","90","","103.775","0.004","90","","1765.87","0.13","293","2","293.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C17 H16 Cl N3 O3 S -","- C17 H16 Cl N3 O3 S -","- C68 H64 Cl4 N12 O12 S4 -","4","1","","Liu, Ya-Zhou; Chen, Yu; Wang, Amu; Shen, Zhongke; Zhou, Xueting; Zhang, Jichao; Jian, Yinxiang; Ma, Xiaofeng","An electron-donor–acceptor complex between two intermediates enables a N–N bond cleavage cascade process to access 2,3-difunctionalized pyridines","Green Chemistry","2024","26","4","2280","2289","10.1039/D3GC04425D","","x-ray","0.71073","MoKα","","0.0605","0.0444","","","0.1036","0.1133","","","","","","1.048","","","","has coordinates","290218","2024-03-04","20:31:52",""
"7248008","8.1423","0.0008","12.2839","0.0008","12.9853","0.0009","92.802","0.006","98.268","0.007","103.73","0.007","1243.89","0.18","293","2","293.15","","","","","","","","","6","P -1","-P 1","2","","","","- C24 H25 Br N2 O5 S2 -","- C24 H25 Br N2 O5 S2 -","- C48 H50 Br2 N4 O10 S4 -","2","1","","Liu, Ya-Zhou; Chen, Yu; Wang, Amu; Shen, Zhongke; Zhou, Xueting; Zhang, Jichao; Jian, Yinxiang; Ma, Xiaofeng","An electron-donor–acceptor complex between two intermediates enables a N–N bond cleavage cascade process to access 2,3-difunctionalized pyridines","Green Chemistry","2024","26","4","2280","2289","10.1039/D3GC04425D","","x-ray","0.71073","MoKα","","0.1004","0.0543","","","0.113","0.1347","","","","","","1.001","","","","has coordinates","290218","2024-03-04","20:31:52",""
"7248009","21.5028","0.0018","9.2793","0.0006","24.775","0.002","90","","108.353","0.01","90","","4691.9","0.7","293","2","293.15","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C24 H23 Cl N2 O5 S -","- C24 H23 Cl N2 O5 S -","- C192 H184 Cl8 N16 O40 S8 -","8","1","","Liu, Ya-Zhou; Chen, Yu; Wang, Amu; Shen, Zhongke; Zhou, Xueting; Zhang, Jichao; Jian, Yinxiang; Ma, Xiaofeng","An electron-donor–acceptor complex between two intermediates enables a N–N bond cleavage cascade process to access 2,3-difunctionalized pyridines","Green Chemistry","2024","26","4","2280","2289","10.1039/D3GC04425D","","x-ray","0.71073","MoKα","","0.1341","0.0881","","","0.2256","0.2551","","","","","","1.05","","","","has coordinates","290218","2024-03-04","20:31:52",""
"7248010","10.3627","0.0007","10.898","0.0008","14.0931","0.001","90","","99.692","0.001","90","","1568.86","0.19","273","2","273","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C20 H20 N20 O20 S20 -","- C60 H68 N12 O12 S4 -","- C60 H68 N12 O12 S4 -","1","0.25","","Rana, Soumitra; Basu, Soumyadip; Bera, Aswini; Saha, Pinaki; Ghosh, Prasanta; Khatua, Bhanu Bhusan; Mukhopadhyay, Chhanda","“On-water” synthesis of thioxoimidazolidinone-isatin/ninhydrin conjugates, followed by temperature-induced dehydration by a ZnMnO3@Ni(OH)2 nano-catalyst","Green Chemistry","2024","26","5","2750","2762","10.1039/D3GC03730D","","","0.71073","MoKα","","0.0507","0.0419","","","0.1198","0.1289","","","","","","0.779","","","","has coordinates","290999","2024-04-04","23:54:34",""
"7248011","17.0626","0.0012","7.5356","0.0005","21.0257","0.0014","90","","101.637","0.002","90","","2647.9","0.3","293","","293","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C14 H13 N3 O2 S -","- C14 H13 N3 O2 S -","- C112 H104 N24 O16 S8 -","8","1","","Rana, Soumitra; Basu, Soumyadip; Bera, Aswini; Saha, Pinaki; Ghosh, Prasanta; Khatua, Bhanu Bhusan; Mukhopadhyay, Chhanda","“On-water” synthesis of thioxoimidazolidinone-isatin/ninhydrin conjugates, followed by temperature-induced dehydration by a ZnMnO3@Ni(OH)2 nano-catalyst","Green Chemistry","2024","26","5","2750","2762","10.1039/D3GC03730D","","x-ray","0.71073","MoKα","","0.1053","0.0709","","","0.1631","0.1799","","","","","","1.102","","","","has coordinates","290999","2024-04-04","23:54:34",""
"7248012","10.7787","0.0006","10.3552","0.0006","11.3624","0.0007","90","","116.81","0.002","90","","1131.9","0.12","273","2","273","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C21 H18 Cl N2 O5 S2 -","- C21 H16.006 Cl N2 O5 S2 -","- C42 H32.012 Cl2 N4 O10 S4 -","2","1","","Rana, Soumitra; Basu, Soumyadip; Bera, Aswini; Saha, Pinaki; Ghosh, Prasanta; Khatua, Bhanu Bhusan; Mukhopadhyay, Chhanda","“On-water” synthesis of thioxoimidazolidinone-isatin/ninhydrin conjugates, followed by temperature-induced dehydration by a ZnMnO3@Ni(OH)2 nano-catalyst","Green Chemistry","2024","26","5","2750","2762","10.1039/D3GC03730D","","","0.71073","MoKα","","0.0534","0.0416","","","0.1079","0.116","","","","","","0.804","","","","has coordinates,has disorder","290999","2024-04-04","23:54:34",""
"7248015","12.962","0.003","9.7854","0.0017","23.918","0.005","90","","98.354","0.005","90","","3001.5","1.1","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","(E)-5-(3,5-di-tert-butyl-4-hydroxyphenyl)-1-(4-methoxyphenyl)-5-phenylpentan-1-one oxime","","- C32 H41 N O3 -","- C32 H41 N O3 -","- C128 H164 N4 O12 -","4","1","","Zhou, Tongyao; Zeng, Jie; Liu, Yang; Chen, Hang; Wang, Haifeng; Yan, Qiongjiao; Wang, Wei; Chen, Fener","Visible-light-induced tandem ring opening/1,6-conjugate addition of cyclobutanols with p-quinone methides under metal- and additive-free conditions","Green Chemistry","2024","26","3","1375","1380","10.1039/D3GC04286C","","","0.71073","MoKα","","0.1248","0.0635","","","0.1342","0.1642","","","","","","1.018","","","","has coordinates","290223","2024-03-04","20:32:35",""
"7248016","6.3761","0.0008","9.9644","0.0012","22.622","0.003","90","","90","","90","","1437.3","0.3","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C12 H21 N O5 -","- C12 H21 N O5 -","- C48 H84 N4 O20 -","4","1","","Ge, Shuwang; Fu, Mingwei; Gu, Dihai; Wei, Lai; Qian, Kun; Rui, Qi; Ma, Yan; Li, Liang; Wang, Huaiqiu; Li, Lingchao; Ge, Min; Wang, Yihong","Design and process study of chiral separation of (2S,4S)-1-(tert-butoxy carbonyl)-4-(methoxymethyl) pyrrolidine-2-carboxylic acid for green manufacturing","Green Chemistry","2024","26","5","2673","2683","10.1039/D3GC04435A","","","0.71073","MoKα","","0.1084","0.0503","","","0.1033","0.1204","","","","","","1.079","","","","has coordinates,has disorder","290997","2024-04-04","23:54:14",""
"7248017","5.8953","0.0002","7.8109","0.0002","8.5294","0.0002","71.666","0.001","86.269","0.001","86.169","0.001","371.586","0.018","170","","170","","","","","","","","","4","P 1","P 1","1","","","","- C12 H23 N O6 -","- C12 H23 N O6 -","- C12 H23 N O6 -","1","1","","Ge, Shuwang; Fu, Mingwei; Gu, Dihai; Wei, Lai; Qian, Kun; Rui, Qi; Ma, Yan; Li, Liang; Wang, Huaiqiu; Li, Lingchao; Ge, Min; Wang, Yihong","Design and process study of chiral separation of (2S,4S)-1-(tert-butoxy carbonyl)-4-(methoxymethyl) pyrrolidine-2-carboxylic acid for green manufacturing","Green Chemistry","2024","26","5","2673","2683","10.1039/D3GC04435A","","","1.54178","CuKα","","0.0244","0.0243","","","0.0619","0.0619","","","","","","1.089","","","","has coordinates","290997","2024-04-04","23:54:14",""
"7248078","5.4476","0.0004","9.339","0.0008","15.3977","0.0012","75.371","0.003","87.564","0.002","85.468","0.003","755.39","0.1","100","","100","","","","","","","","","4","P 1","P 1","1","","","","- C18 H20 N2 O2 -","- C18 H20 N2 O2 -","- C36 H40 N4 O4 -","2","2","","Wu, Jilai; Zhou, Likai; Xie, Song; Wei, Chao; Li, Xiaoliu; Chen, Hua","Synthesis of 3-arylamino-2-polyhydroxyalkyl-substituted indoles from unprotected saccharides and anilines","Green Chemistry","2024","26","4","1883","1888","10.1039/D3GC04440H","","","0.71073","MoKα","","0.08","0.0546","","","0.112","0.1295","","","","","","1.061","","","","has coordinates","290219","2024-03-04","20:32:01",""
"7248079","6.163","0.002","10.528","0.004","32.488","0.012","90","","90","","90","","2108","1.3","273","","273","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C12 H13 N O2 -","- C12 H13 N O2 -","- C96 H104 N8 O16 -","8","2","","Wu, Jilai; Zhou, Likai; Xie, Song; Wei, Chao; Li, Xiaoliu; Chen, Hua","Synthesis of 3-arylamino-2-polyhydroxyalkyl-substituted indoles from unprotected saccharides and anilines","Green Chemistry","2024","26","4","1883","1888","10.1039/D3GC04440H","","","0.71073","MoKα","","0.1167","0.06","","","0.1327","0.1568","","","","","","1.091","","","","has coordinates","290219","2024-03-04","20:32:02",""
"7248100","9.5606","0.0002","22.0542","0.0004","9.7194","0.0002","90","","108.419","0.002","90","","1944.36","0.07","100","0.1","100","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","3-benzoyl-1-(4-fluorophenyl)-9-methyl-1,5,6,10b-tetrahydro-[1,2,4]triazolo[5,1-a]isoquinolin-2(3H)-one","","- C24 H20 F N3 O2 -","- C24 H20 F N3 O2 -","- C96 H80 F4 N12 O8 -","4","1","","Chen, Lei; Yang, Peiyao; Wang, Qiuying; Zhao, Zhongxiang; Cui, Hui; Zhu, Liping","Transition-metal-free [3 + 2] cycloaddition of C,N-cycloazomethylimines with in situ formed isocyanates from dioxazolones: a facile synthesis of triazolinones","Green Chemistry","2024","26","6","3522","3526","10.1039/D3GC04556K","","x-ray","1.54184","CuKα","","0.0455","0.0403","","","0.1077","0.1118","","","","","","1.061","","","","has coordinates","291001","2024-04-04","23:54:49",""
"7248177","14.088","0.0004","7.8247","0.0002","30.2785","0.0009","90","","102.717","0.001","90","","3255.85","0.16","100","","100","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C37 H12 F10 N5 O2 Sb -","- C37 H12 F10 N5 O2 Sb -","- C148 H48 F40 N20 O8 Sb4 -","4","1","","Yan, Qiao-Wei; Wu, Ling-Wei; Liu, Zhen-Wu; Chen, Feng; Ling, Chen; Liu, Hai-Yang; Xiao, Xin-Yan; Si, Li-Ping","First application of antimony(iii) corrole for electrocatalytic hydrogen evolution","Green Chemistry","2024","26","8","4574","4581","10.1039/D3GC04884E","","","0.71073","MoKα","","0.105","0.0875","","","0.2398","0.2634","","","","","","0.999","","","","has coordinates","291659","2024-05-05","03:36:32",""
"7248178","12.7611","0.0003","18.5038","0.0003","14.1018","0.0003","90","","100.643","0.002","90","","3272.56","0.12","169.99","0.1","169.99","0.1","","","","","","","","5","P 1 21/m 1","-P 2yb","11","","","","- C41.5 H21.5 Cl0.25 N5 O5.5 -","- C40.5 H19.5 N4.5 O3 -","- C162 H78 N18 O12 -","4","1","","Yan, Qiao-Wei; Wu, Ling-Wei; Liu, Zhen-Wu; Chen, Feng; Ling, Chen; Liu, Hai-Yang; Xiao, Xin-Yan; Si, Li-Ping","First application of antimony(iii) corrole for electrocatalytic hydrogen evolution","Green Chemistry","2024","26","8","4574","4581","10.1039/D3GC04884E","","x-ray","1.54184","CuKα","","0.0602","0.0457","","","0.1254","0.1341","","","","","","1.06","","","","has coordinates","291659","2024-05-05","03:36:35",""
"7248181","12.34031","0.00009","7.13358","0.00005","24.66536","0.00018","90","","101.406","0.0003","90","","2128.42","0.03","100","2","100","2","","","","","","","","5","P 1 21 1","P 2yb","4","","(R)-2-cyclohexyl-2-(p-tolylthio)ethyl 3,5-dinitrobenzoate","","- C22 H24 N2 O6 S -","- C22 H24 N2 O6 S -","- C88 H96 N8 O24 S4 -","4","2","","Wang, Zhen; Gausmann, Marcel; Dickoff, Jan-Hendrik; Christmann, Mathias","Iodine-enabled organoelectrocatalysis: enantioselective cross dehydrogenative coupling of sulfides and aldehydes","Green Chemistry","2024","26","5","2546","2551","10.1039/D3GC03828A","","","1.54178","CuKα","","0.0567","0.0552","","","0.1228","0.1244","","","","","","1.124","","","","has coordinates","291000","2024-04-04","23:54:42",""
"7248207","8.2109","0.0002","13.5877","0.0003","15.4845","0.0003","90","","90.659","0.001","90","","1727.45","0.07","303","2","303","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C24 H17 N -","- C24 H17 N -","- C96 H68 N4 -","4","1","","Guo, Tao; Hu, Penghua; Li, Jiaxin; Zhou, Yujia; Zhang, Panke; Zhao, Yunhui; Zhu, Congjun","Synthesis of the dibenzo[b,d]azepine skeleton via a catalyst-free ring expansion domino reaction","Green Chemistry","2024","26","7","3786","3790","10.1039/D3GC04626E","","","1.54178","cukα","","0.0722","0.0416","","","0.1049","0.1161","","","","","","1.039","","","","has coordinates","291003","2024-04-04","23:55:06",""
"7248212","12.6937","0.0006","18.449","0.0008","19.5975","0.0007","75.711","0.004","77.491","0.004","88.11","0.004","4340.9","0.3","293","2","293","2","","","","","","","","8","P -1","-P 1","2","","","","- C120 H163 Ag2 N34 O50 P S16 W12 -","- C112 H145 Ag2 N32 O48 P S16 W12 -","- C112 H145 Ag2 N32 O48 P S16 W12 -","1","0.5","","Song, Yuting; Zhang, Jia-Yi; Yang, Jin; Bo, Tao; Ma, Jian-Fang","Highly efficient photoelectrocatalytic oxidation of arsenic(iii) with a polyoxometalate-thiacalix[4]arene-based metal–organic complex-modified bismuth vanadate photoanode","Green Chemistry","2024","26","7","3874","3883","10.1039/D3GC04755E","","","0.71073","MoKα","","0.0969","0.0556","","","0.1062","0.1277","","","","","","1.055","","","","has coordinates","291002","2024-04-04","23:54:59",""
"7248284","10.476","0.0008","5.0246","0.0005","22.8902","0.0016","90","","97.761","0.007","90","","1193.85","0.17","295","2","295","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H12 N2 O2 -","- C15 H12 N2 O2 -","- C60 H48 N8 O8 -","4","1","","R., Thrilokraj; Małecki, Jan Grzegorz; Budagumpi, Srinivasa; Kshirsagar, Umesh A.; Dateer, Ramesh B.","Biomass derived Cu2O nanoparticles for N-atom insertion reactions: a base-free synthesis of quinazolinones with a green approach","Green Chemistry","2024","26","8","4723","4732","10.1039/D4GC00569D","","x-ray","0.71073","MoKα","","0.0839","0.0538","","","0.1291","0.1467","","","","","","1.046","","","","has coordinates","291658","2024-05-05","03:35:20",""
"7248335","5.71587","0.00008","16.8188","0.0003","20.0111","0.0003","90","","90.7375","0.0013","90","","1923.59","0.05","293.15","","293.15","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C22 H17 Cl N2 O S -","- C22 H17 Cl N2 O S -","- C88 H68 Cl4 N8 O4 S4 -","4","1","","Yang, Beining; Wang, Yatang; Yang, Xiaojuan; Li, Yinyin; Zhang, Zhiying; Hua, Xiaofeng; Ouyang, Lu; Zheng, Lvyin; Guo, Wei","Visible-light-driven three-component annulation for the synthesis of highly functionalized 2-iminothiazolidin-4-ones without photocatalysts","Green Chemistry","2024","26","8","4477","4483","10.1039/D4GC00375F","","x-ray","1.54184","CuKα","","0.0704","0.0685","","","0.1857","0.1876","","","","","","1.008","","","","has coordinates","291661","2024-05-05","03:37:52",""
"7248336","9.6651","0.0006","10.0573","0.0007","18.1252","0.0012","83.474","0.002","89.157","0.002","70.718","0.002","1651.76","0.19","170","","170","","","","","","","","","4","P -1","-P 1","2","","","","- C21 H21 N O2 -","- C21 H21 N O2 -","- C84 H84 N4 O8 -","4","2","","Nie, Guihua; Tu, Ting; Liao, Tianhui; Liu, Donghan; Ye, Wenjun; Ren, Shi-Chao","N-Heterocyclic Carbene and photocatalyst-catalyzed rapid access to indole ketones via radical C(sp3)-H acylation","Green Chemistry","2024","","","","","10.1039/D4GC00653D","","","1.34139","GaKα","","0.091","0.0723","","","0.1966","0.209","","","","","","1.081","","","","has coordinates,has disorder","290621","2024-03-24","00:31:06",""
"7248337","8.746","0.005","14.913","0.009","12.807","0.008","90","","96.41","0.02","90","","1660","1.7","170","","170","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H21 N O2 -","- C21 H21 N O2 -","- C84 H84 N4 O8 -","4","1","","Nie, Guihua; Tu, Ting; Liao, Tianhui; Liu, Donghan; Ye, Wenjun; Ren, Shi-Chao","N-Heterocyclic Carbene and photocatalyst-catalyzed rapid access to indole ketones via radical C(sp3)-H acylation","Green Chemistry","2024","","","","","10.1039/D4GC00653D","","","1.34139","GaKα","","0.1063","0.0632","","","0.1548","0.1759","","","","","","1.061","","","","has coordinates","290621","2024-03-24","00:31:07",""
"7248338","9.9529","0.0005","15.6474","0.0006","10.0527","0.0005","90","","99.83","0.002","90","","1542.59","0.12","170","","170","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H19 N O2 -","- C20 H19 N O2 -","- C80 H76 N4 O8 -","4","1","","Nie, Guihua; Tu, Ting; Liao, Tianhui; Liu, Donghan; Ye, Wenjun; Ren, Shi-Chao","N-Heterocyclic Carbene and photocatalyst-catalyzed rapid access to indole ketones via radical C(sp3)-H acylation","Green Chemistry","2024","","","","","10.1039/D4GC00653D","","","0.71073","MoKα","","0.0895","0.0627","","","0.12","0.1335","","","","","","1.128","","","","has coordinates","290621","2024-03-24","00:31:07",""
"7248360","17.3863","0.0007","8.7024","0.0003","12.251","0.0005","90","","102.256","0.002","90","","1811.36","0.12","150","","150","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C19 H18 N O3 P S -","- C19 H18 N O3 P S -","- C76 H72 N4 O12 P4 S4 -","4","1","","Jiang, Zeqi; Jiang, Shuangfei; Gao, Jin; Xia, Junmei; Yu, Hongwei; Ma, Lixin; Chen, Xi; Chen, Bo; Zhang, Xinghua; Zhu, Wenchao","Inorganic ligand-supported Mo oxide as a hydrogen atom transfer photocatalyst for direct C(sp2)−H phosphorylation","Green Chemistry","2024","","","","","10.1039/D4GC00589A","","","1.54178","CuKα","","0.042","0.037","","","0.0982","0.1023","","","","","","1.06","","","","has coordinates","290705","2024-03-29","00:37:34",""
"7248368","26.013","0.0002","26.013","0.0002","26.013","0.0002","90","","90","","90","","17602.4","0.2","150","","150","","","","","","","","","6","I a -3","-I 2b 2c 3","206","","","","- Fe H30 Mo12 Na3 O55.5 U -","- Fe Mo12 Na3 O55.5 U -","- Fe16 Mo192 Na48 O888 U16 -","16","0.333333","","Li, Ke; Liu, Yufeng; Yang, Guo-Ping; Zheng, Zhijian; Lin, Xiao-Ling; Zhang, Zhibin; Li, Shujun; Liu, Yunhai; Wei, Yongge","Highly-Stable Silverton-Type UIV-Containing Polyoxomolybdates Frameworks for the Heterogeneous Catalytic Synthesis of Quinazolinones","Green Chemistry","2024","","","","","10.1039/D4GC00877D","","","0.71073","MoKα","","0.0235","0.0218","","","0.0506","0.0513","","","","","","1.128","","","","has coordinates,has disorder","290742","2024-04-02","23:50:48",""
"7248369","19.0319","0.0003","19.0319","0.0003","11.446","0.0005","90","","90","","120","","3590.45","0.18","150","","150","","","","","","","","","5","R -3 :H","-R 3","148","","","","- H29.2 Mo12 Na5.8 O55.5 U -","- Mo12 Na5.8 O55.5 U -","- Mo36 Na17.4 O166.5 U3 -","3","0.166667","","Li, Ke; Liu, Yufeng; Yang, Guo-Ping; Zheng, Zhijian; Lin, Xiao-Ling; Zhang, Zhibin; Li, Shujun; Liu, Yunhai; Wei, Yongge","Highly-Stable Silverton-Type UIV-Containing Polyoxomolybdates Frameworks for the Heterogeneous Catalytic Synthesis of Quinazolinones","Green Chemistry","2024","","","","","10.1039/D4GC00877D","","","0.71073","MoKα","","0.0215","0.0201","","","0.0487","0.0494","","","","","","1.093","","","","has coordinates,has disorder","290742","2024-04-02","23:50:49",""
"7248370","25.9609","0.0003","25.9609","0.0003","25.9609","0.0003","90","","90","","90","","17496.8","0.4","150","","150","","","","","","","","","6","I a -3","-I 2b 2c 3","206","","","","- Co H29.4 Mo12 Na3.6 O55.5 U -","- Co Mo12 Na3.6 O55.5 U -","- Co16 Mo192 Na57.6 O888 U16 -","16","0.333333","","Li, Ke; Liu, Yufeng; Yang, Guo-Ping; Zheng, Zhijian; Lin, Xiao-Ling; Zhang, Zhibin; Li, Shujun; Liu, Yunhai; Wei, Yongge","Highly-Stable Silverton-Type UIV-Containing Polyoxomolybdates Frameworks for the Heterogeneous Catalytic Synthesis of Quinazolinones","Green Chemistry","2024","","","","","10.1039/D4GC00877D","","","0.71073","MoKα","","0.0289","0.0235","","","0.053","0.0549","","","","","","1.131","","","","has coordinates,has disorder","290742","2024-04-02","23:50:49",""
"7248371","25.9532","0.0008","25.9532","0.0008","25.9532","0.0008","90","","90","","90","","17481.3","0.9","100","","100","","","","","","","","","6","I a -3","-I 2b 2c 3","206","","","","- H29.7 Mo12 Na3.3 Ni0.58 O55.5 U -","- Mo12 Na3.3 Ni0.576 O55.5 U -","- Mo192 Na52.8 Ni9.216 O888 U16 -","16","0.333333","","Li, Ke; Liu, Yufeng; Yang, Guo-Ping; Zheng, Zhijian; Lin, Xiao-Ling; Zhang, Zhibin; Li, Shujun; Liu, Yunhai; Wei, Yongge","Highly-Stable Silverton-Type UIV-Containing Polyoxomolybdates Frameworks for the Heterogeneous Catalytic Synthesis of Quinazolinones","Green Chemistry","2024","","","","","10.1039/D4GC00877D","","x-ray","0.71073","MoKα","","0.0249","0.0231","","","0.0599","0.0608","","","","","","1.126","","","","has coordinates,has disorder","290742","2024-04-02","23:50:49",""
"7248381","10.2939","0.0004","9.7381","0.0004","25.5602","0.0011","90","","91.73","0.002","90","","2561.06","0.18","170","","170","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C27 H21 F2 N O6 S -","- C27 H21 F2 N O6 S -","- C108 H84 F8 N4 O24 S4 -","4","1","","Sun, Jie; Wang, Chaodong; Wu, Chunlei; Wang, Wenjian; Zeng, Yue; Song, Shengjie; Chen, Zhiwei; Li, Jianjun","Photocatalyst-free H2O-regulated and regiodivergent multicomponent hydrogenation/bifunctional sulfonylation of alkynes","Green Chemistry","2024","26","6","3301","3307","10.1039/D3GC04960D","","","0.71073","MoKα","","0.0662","0.0446","","","0.1016","0.1122","","","","","","1.0574","","","","has coordinates,has disorder","290785","2024-04-04","08:34:19",""
"7248382","6.3919","0.0004","10.6731","0.0006","18.7577","0.0011","73.689","0.002","87.428","0.002","75.023","0.002","1185.92","0.12","170","","170","","","","","","","","","7","P -1","-P 1","2","","","","- C26 H20 Cl F2 N O5 S -","- C26 H20 Cl F2 N O5 S -","- C52 H40 Cl2 F4 N2 O10 S2 -","2","1","","Sun, Jie; Wang, Chaodong; Wu, Chunlei; Wang, Wenjian; Zeng, Yue; Song, Shengjie; Chen, Zhiwei; Li, Jianjun","Photocatalyst-free H2O-regulated and regiodivergent multicomponent hydrogenation/bifunctional sulfonylation of alkynes","Green Chemistry","2024","26","6","3301","3307","10.1039/D3GC04960D","","","1.34139","GaKα","","0.0859","0.0798","","","0.219","0.2236","","","","","","1.125","","","","has coordinates","290785","2024-04-04","08:34:20",""
"7248394","11.5881","0.0001","7.3879","0.0001","14.8464","0.0002","90","","97.522","0.001","90","","1260.09","0.03","126.06","0.1","126.06","0.1","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C16 H16 N2 -","- C16 H16 N2 -","- C64 H64 N8 -","4","1","","Schütte, Jonathan; Corsi, Daria; Haumer, Wolfgang; Schmid, Simon; Zurauskas, Jonas; Barham, Joshua Philip","A Hydrazine Free Photoredox Catalytic Synthesis of Azines by Reductive Activation of Readily Available Oxime Esters","Green Chemistry","2024","","","","","10.1039/D4GC00804A","","x-ray","1.54184","CuKα","","0.0335","0.0324","","","0.0928","0.0938","","","","","","1.08","","","","has coordinates","291167","2024-04-10","23:40:53",""
"7248494","8.9013","0.0001","10.1017","0.0002","15.3407","0.0003","93.41","0.002","99.781","0.002","103.653","0.002","1313.79","0.04","250","0.1","250","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C28 H27 N O5.6 -","- C28 H27 N O5.6 -","- C56 H54 N2 O11.2 -","2","1","","MacLean, Ian; García, Montaña J; Cabrera, Silvia; Marzo, Leyre; Aleman, Jose","Electrochemically Driven Green Synthesis to Unlock Sustainable Routes to β-Keto Spirolactones","Green Chemistry","2024","","","","","10.1039/D4GC01127A","","x-ray","1.54184","CuKα","","0.0827","0.0766","","","0.2364","0.243","","","","","","1.097","","","","has coordinates,has disorder","291301","2024-04-20","00:31:43",""
"7248495","10.438","0.0003","10.4738","0.0003","13.8516","0.0004","105.82","0.001","109.039","0.001","96.807","0.001","1340.97","0.07","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C30 H32 Fe Si3 -","- C30 H32 Fe Si3 -","- C60 H64 Fe2 Si6 -","2","1","","Li, Jia; Ge, Shaozhong","Solvent-free copper-catalyzed trisilylation of alkynes: a practical and atom-economical approach for accessing 1,1,1-trisilylalkanes","Green Chemistry","2024","","","","","10.1039/D4GC00220B","","","0.71073","MoKα","","0.042","0.0306","","","0.0704","0.0744","","","","","","1.036","","","","has coordinates","291302","2024-04-20","00:31:57",""
"7248512","6.8247","0.0001","15.1975","0.0003","20.6745","0.0004","90","","90","","90","","2144.33","0.07","170","","170","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C25 H33 N O4 -","- C25 H33 N O4 -","- C100 H132 N4 O16 -","4","1","","Yu, Jingbo; Chen, Hong; Zhang, Ziwen; Fang, Yuxin; Ying, Tao; Su, Weike","Ethanol-assisted mechanochemical asymmetric cross-dehydrogenative coupling reaction with recoverable chiral amine/NaCl for accessing chiral α-alkyl α-glycine derivatives","Green Chemistry","2024","","","","","10.1039/D4GC00947A","","","1.54178","CuKα","","0.0464","0.0407","","","0.1041","0.1077","","","","","","1.032","","","","has coordinates","291341","2024-04-23","23:31:09",""
"7248591","6.6549","0.0003","12.8056","0.0005","6.6575","0.0003","90","","116.973","0.002","90","","505.64","0.04","200","","200","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C10 H12 N2 O4 -","- C10 H12 N2 O4 -","- C20 H24 N4 O8 -","2","0.5","","Mele, Francesco; Constantin, Ana Maria; Sacchelli, Filippo; Schiroli, Debora; Mazzeo, Paolo Pio; Maestri, Giovanni; Motti, Elena; Maggi, Raimondo; Mancuso, Raffaella; Gabriele, Bartolo; Pancrazzi, francesco; Della Ca', Nicola","Sequential Glaser reaction-diastereoselective cyclocarboxylation of propargylamines with CO2: A green catalytic access to bis-oxazolidinonedienes and their topochemical polymerization","Green Chemistry","2024","","","","","10.1039/D4GC00818A","","","0.71073","MoKα","","0.0347","0.0334","","","0.086","0.0868","","","","","","1.103","","","","has coordinates","291745","2024-05-06","23:38:40",""
"7248592","40.9802","0.0007","5.9856","0.0001","8.7293","0.0002","90","","97.256","0.001","90","","2124.07","0.07","200","","200","","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C24 H24 N2 O6 -","- C24 H24 N2 O6 -","- C96 H96 N8 O24 -","4","0.5","","Mele, Francesco; Constantin, Ana Maria; Sacchelli, Filippo; Schiroli, Debora; Mazzeo, Paolo Pio; Maestri, Giovanni; Motti, Elena; Maggi, Raimondo; Mancuso, Raffaella; Gabriele, Bartolo; Pancrazzi, francesco; Della Ca', Nicola","Sequential Glaser reaction-diastereoselective cyclocarboxylation of propargylamines with CO2: A green catalytic access to bis-oxazolidinonedienes and their topochemical polymerization","Green Chemistry","2024","","","","","10.1039/D4GC00818A","","","1.54178","CuKα","","0.0366","0.0343","","","0.0877","0.0901","","","","","","1.046","","","","has coordinates","291745","2024-05-06","23:38:40",""
"7248593","6.0202","0.0003","13.4077","0.0007","19.4725","0.0012","97.433","0.005","91.503","0.004","92.772","0.004","1555.89","0.15","293","0.1","293.15","","","","","","","","","4","P -1","-P 1","2","","","","- C36 H36 N3 O9 -","- C36 H36 N3 O9 -","- C72 H72 N6 O18 -","2","1","","Mele, Francesco; Constantin, Ana Maria; Sacchelli, Filippo; Schiroli, Debora; Mazzeo, Paolo Pio; Maestri, Giovanni; Motti, Elena; Maggi, Raimondo; Mancuso, Raffaella; Gabriele, Bartolo; Pancrazzi, francesco; Della Ca', Nicola","Sequential Glaser reaction-diastereoselective cyclocarboxylation of propargylamines with CO2: A green catalytic access to bis-oxazolidinonedienes and their topochemical polymerization","Green Chemistry","2024","","","","","10.1039/D4GC00818A","","","1.54184","CuKα","","0.1246","0.0919","","","0.2498","0.2952","","","","","","1.034","","","","has coordinates,has disorder","291745","2024-05-06","23:38:41",""
"7248647","17.0824","0.0002","17.9419","0.0002","30.7631","0.0004","90","","96.314","0.001","90","","9371.4","0.2","148","0.3","148","0.3","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C64 H94 Hf6 O40 -","- C64 H94 Hf6 O40 -","- C256 H376 Hf24 O160 -","4","1","","Wang, Hao-Cheng; Liu, Xiao; Ma, Jian-Gong; Cheng, Peng","Rapid and High-Throughput Synthesis of Diverse MOFs with Centrifuge Tube Grinding Strategy","Green Chemistry","2024","","","","","10.1039/D4GC00865K","","x-ray","0.71073","MoKα","","0.0842","0.0625","","","0.1182","0.1286","","","","","","1.18","","","","has coordinates","291956","2024-05-18","23:26:36",""
"7248670","7.1937","0.0002","9.3874","0.0003","8.8093","0.0003","90","","98.709","0.001","90","","588.03","0.03","294","2","294","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C12 H16 O6 -","- C12 H16 O6 -","- C24 H32 O12 -","2","0.5","","Lebedeva, Daria; Schick, William; Cracco, Daniel; Sangsuwan, Withsakorn; Castiella-Ona, Gonzalo; Silva, Dagoberto; Marson, Alessandro; Grape, Erik; Inge, Andrew Ken; Rossi, Liane Marcia; Subbotina, Elena; Manzardo, Alessandro; Samec, Joseph","Sustainable Aviation Fuel from Prehydrolysis Liquors","Green Chemistry","2024","","","","","10.1039/D4GC01257G","","","1.54178","CuKα","","0.037","0.0336","","","0.0828","0.0855","","","","","","1.075","","","","has coordinates","292011","2024-05-23","23:35:52",""
"7248671","10.5173","0.0006","8.615","0.0005","26.809","0.0015","90","","90","","90","","2429.1","0.2","294","2","294","2","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C12 H16 O6 -","- C12 H16 O6 -","- C96 H128 O48 -","8","1","","Lebedeva, Daria; Schick, William; Cracco, Daniel; Sangsuwan, Withsakorn; Castiella-Ona, Gonzalo; Silva, Dagoberto; Marson, Alessandro; Grape, Erik; Inge, Andrew Ken; Rossi, Liane Marcia; Subbotina, Elena; Manzardo, Alessandro; Samec, Joseph","Sustainable Aviation Fuel from Prehydrolysis Liquors","Green Chemistry","2024","","","","","10.1039/D4GC01257G","","","1.54178","CuKα","","0.0489","0.0431","","","0.1121","0.1172","","","","","","1.048","","","","has coordinates","292011","2024-05-23","23:35:53",""
"7248672","9.4404","0.0003","14.2743","0.0004","9.8596","0.0003","90","","111.083","0.001","90","","1239.69","0.07","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C12 H16 O6 -","- C12 H16 O6 -","- C48 H64 O24 -","4","1","","Lebedeva, Daria; Schick, William; Cracco, Daniel; Sangsuwan, Withsakorn; Castiella-Ona, Gonzalo; Silva, Dagoberto; Marson, Alessandro; Grape, Erik; Inge, Andrew Ken; Rossi, Liane Marcia; Subbotina, Elena; Manzardo, Alessandro; Samec, Joseph","Sustainable Aviation Fuel from Prehydrolysis Liquors","Green Chemistry","2024","","","","","10.1039/D4GC01257G","","","1.54178","CuKα","","0.0465","0.043","","","0.1408","0.1467","","","","","","0.936","","","","has coordinates","292011","2024-05-23","23:35:54",""
"7248756","7.6781","0.0004","27.998","0.0013","9.1512","0.0003","90","","93.736","0.004","90","","1963.07","0.15","","","300","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","GAB","(E)-amino((4-(4-(dimethylamino)styryl)phenyl)amino)methaniminium ethyl carbonate","","- C18 H24 N6 O3 -","- C18 H24 N6 O3 -","- C72 H96 N24 O12 -","4","1","","Murakami, Ryo; Shiota, Keitaro; Uchida, Ayaka; Inagaki, Fuyuhiko","Light-swing CO2 Capture: Photoirradiation-based Chemical CO2 Release Based on Photoisomerization of Azobenzene-Amine/Guanidine Derivatives","Green Chemistry","2024","","","","","10.1039/D4GC00736K","","x-ray","0.71073","MoKα","","0.1458","0.0747","","","0.1742","0.2096","","","","","","1.034","","","","has coordinates","292120","2024-05-30","23:42:30",""
"7248764","9.14","0.002","15.767","0.004","9.982","0.002","90","","101.097","0.005","90","","1411.6","0.6","296","2","296.15","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C17 H10 F N3 S -","- C17 H10 F N3 S -","- C68 H40 F4 N12 S4 -","4","1","","Wen, Changting; Sun, Guojin; Liu, Lang; Zhang, Jun; She, Mengyao; Yang, Zheng; Liu, Ping; Zhang, Shengyong; Li, Jianli","Light-assisted Green and Efficient Construction of Thiadiazole/ Selenadiazole Derivatives","Green Chemistry","2024","","","","","10.1039/D4GC02211D","","","0.71073","MoKα","","0.1314","0.052","","","0.1032","0.1336","","","","","","0.951","","","","has coordinates","292193","2024-06-04","23:54:21",""
"7248765","27.47","0.02","3.862","0.003","32.65","0.03","90","","111.657","0.007","90","","3219","5","220","","220","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C17.3 H10.3 Br Cl0.9 N3 S -","- C17 H10 Br N3 S -","- C136 H80 Br8 N24 S8 -","8","1","","Wen, Changting; Sun, Guojin; Liu, Lang; Zhang, Jun; She, Mengyao; Yang, Zheng; Liu, Ping; Zhang, Shengyong; Li, Jianli","Light-assisted Green and Efficient Construction of Thiadiazole/ Selenadiazole Derivatives","Green Chemistry","2024","","","","","10.1039/D4GC02211D","","","1.34138","GaKα","","0.0426","0.0309","","","0.0778","0.0825","","","","","","1.037","","","","has coordinates","292193","2024-06-04","23:54:22",""
"7248824","25.691","0.002","5.5958","0.0005","19.8517","0.0018","90","","112.73","","90","","2632.3","0.4","122","2","122","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C12 H16 N2 O4 S -","- C12 H16 N2 O4 S -","- C96 H128 N16 O32 S8 -","8","2","","Sang, Ji-Wei; Chen, Hong; Zhang, Yu; Wang, Jinxin; Zhang, Weidong","Photo-mediated radical relay oximinosulfonamidation of alkenes with N-nitrosamines triggered by DABSO","Green Chemistry","2024","","","","","10.1039/D4GC01976H","","","1.54178","CuKα","","0.0409","0.0358","","","0.0986","0.1028","","","","","","1.045","","","","has coordinates","292267","2024-06-07","23:43:00",""