# Search results of SQL query from the Crystallography Open Database # Date and time performed: 2024-12-01T04:10:25+01:00 # Query: # SELECT data.* # FROM # data JOIN jaltnames # ON altname = journal # WHERE # (status is null or status != 'retracted') and # (journal_id IN (SELECT DISTINCT(journal_id) FROM jaltnames WHERE altname LIKE 'Green Chemistry') AND volume = 23 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 "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","" "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","","","","- C21 H18 N2 -","- C21 H18 N2 -","- C168 H144 N16 -","8","2","","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","292638","2024-06-28","09:33:37","" "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","","","","- C24 H27.5 N2 O -","- C24 H27.5 N2 O -","- C96 H110 N8 O4 -","4","2","","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","295543","2024-10-18","15:17:09","" "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","" "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","" "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",""