# Search results of SQL query from the Crystallography Open Database
# Date and time performed: 2025-12-07T23:37:10+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 Chem.') 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
"1540034","8.8018","0.0015","9.2775","0.0016","11.3673","0.0019","82.433","0.002","68.031","0.002","67.635","0.002","796","0.2","296","","296","","","","","","","","","6","P -1","-P 1","2","","","","- C32 H28 F6 N8 O4 Zn -","- C32 H28 F6 N8 O4 Zn -","- C32 H28 F6 N8 O4 Zn -","1","0.5","","Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi","A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand","Green Chem.","2016","18","6","1524","","10.1039/C5GC02056E","","","0.71075","MoKα","","0.0265","0.0264","","","0.0723","0.0726","","","","","","0.966","","","","has coordinates","181749","2020-10-21","18:00:00",""
"1540035","14.5768","0.0012","8.9341","0.0007","15.9047","0.0013","90","","103.294","0.001","90","","2015.8","0.3","296","","296","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C40 H44 F6 N8 O4 Zn -","- C40 H44 F6 N8 O4 Zn -","- C80 H88 F12 N16 O8 Zn2 -","2","0.5","","Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi","A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand","Green Chem.","2016","18","6","1524","","10.1039/C5GC02056E","","","0.71075","MoKα","","0.0386","0.037","","","0.1","0.102","","","","","","1.06","","","","has coordinates","181749","2020-10-21","18:00:00",""
"1540036","9.7675","0.0012","11.262","0.0014","11.576","0.0014","98.815","0.001","107.953","0.001","112.944","0.001","1059.8","0.2","296","","296","","","","","","","","","6","P -1","-P 1","2","","","","- C18 H14 F6 N4 O4 Zn -","- C18 H14 F6 N4 O4 Zn -","- C36 H28 F12 N8 O8 Zn2 -","2","1","","Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi","A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand","Green Chem.","2016","18","6","1524","","10.1039/C5GC02056E","","","0.71075","MoKα","","0.0269","0.0256","","","0.0663","0.0681","","","","","","1.066","","","","has coordinates","181749","2020-10-21","18:00:00",""
"7204165","11.2391","0.0002","12.889","0.0002","14.478","0.0004","90.734","0.001","110.956","0.001","112.21","0.001","1786.49","0.07","","","123","2","","","","","","","","4","P -1","-P 1","2","2,8,14,20-tetra(p-butoxy-phenyl)resorcinarene DMF/acetone solvate","2,8,14,20-tetra(p-butoxy-phenyl)pentacyclo-[19.3.1.13,7.19,13.115,19]octacosa- 1-(25),3,5,7(28),9,11,13(27),15,17,19(26),21,23-dodecaene- 4,6,10,12,16,18,22,24-octaol","","- C80 H98 N2 O16 -","- C80.02 H98.06 N2 O16 -","- C80.02 H98.06 N2 O16 -","1","0.5","","Brett A. Roberts; Gareth W. V. Cave; Colin L. Raston; Janet L. Scott","Solvent-free synthesis of calix[4]resorcinarenes","Green Chem.","","3","6","280","284","10.1039/b104430n","","","0.71073","MoKα","","0.2155","0.0979","","","0.2273","0.2877","","","","","","0.938","","","","has coordinates,has disorder","213973","2020-10-21","18:00:00",""
"7204653","5.912","0.001","8.043","0.001","25.07","0.002","90","","90","","90","","1192.1","0.3","293","2","293","2","","","","","","","","3","P b c 21","P 2c -2b","29","cis-2-benzoyl-3-hydroxy-2,3-dihydrobenzofuran (8a)","cis-2-benzoyl-3-hydroxy-2,3-dihydrobenzofuran (8a)","","- C15 H12 O3 -","- C15 H12 O3 -","- C60 H48 O12 -","4","1","","Kazuhiro Yoshizawa; Shinji Toyota; Fumio Toda; Ingeborg Csöregh","Preparative and mechanistic studies of solvent-free Rap–Stoermer reactions","Green Chem.","2003","5","3","353","356","10.1039/b303802p","","","0.71073","MoKa","","0.0532","0.0411","","0.1043","0.102","","","","1.06","1.092","1.092","","","","","has coordinates","301863","2025-08-22","13:06:55",""
"7217280","27.1582","0.0014","28.5362","0.0013","24.0085","0.0011","90","","113.869","0.001","90","","17015","1.4","200","2","200","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","PPh4-Aletbat","","","- C86.5 H113 Al Cl5 O4 P -","- C86.5 H113 Al Cl5 O4 P -","- C692 H904 Al8 Cl40 O32 P8 -","8","1","","Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F.","Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions","Green Chem.","2014","16","11","4696","","10.1039/C4GC00928B","","","0.71073","MoKα","","0.1435","0.0843","","","0.2228","0.2696","","","","","","1.013","","","","has coordinates,has disorder","176453","2020-10-21","18:00:00",""
"7217281","16.4252","0.001","16.4896","0.001","29.6929","0.0018","90","","102.666","0.001","90","","7846.5","0.8","200","2","200","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","Li(thf)4-Aletbat","","","- C77 H122 Al Cl2 Li O8 -","- C77 H122 Al Cl2 Li O8 -","- C308 H488 Al4 Cl8 Li4 O32 -","4","1","","Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F.","Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions","Green Chem.","2014","16","11","4696","","10.1039/C4GC00928B","","","0.71073","MoKα","","0.1094","0.0789","","","0.2113","0.2375","","","","","","1.013","","","","has coordinates,has disorder","180503","2020-10-21","18:00:00",""
"7217282","14.1898","0.0002","14.7188","0.0003","19.354","0.0004","83.112","0.001","89.299","0.001","71.328","0.001","3800.35","0.13","200","2","200","2","","","","","","","","5","P -1","-P 1","2","Na(thf)4 Aletbat","","","- C76 H120 Al Na O8 -","- C76 H120 Al Na O8 -","- C152 H240 Al2 Na2 O16 -","2","1","","Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F.","Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions","Green Chem.","2014","16","11","4696","","10.1039/C4GC00928B","","","0.71073","MoKα","","0.1158","0.07","","","0.1787","0.2055","","","","","","1.039","","","","has coordinates,has disorder","180503","2020-10-21","18:00:00",""
"7217283","24.3711","0.0015","24.6465","0.0015","25.3492","0.0015","90","","90","","90","","15226.3","1.6","200","2","200","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","NBu4-Aletbat","","","- C77 H126 Al Cl2 N O4 -","- C77 H126 Al Cl2 N O4 -","- C616 H1008 Al8 Cl16 N8 O32 -","8","1","","Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F.","Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions","Green Chem.","2014","16","11","4696","","10.1039/C4GC00928B","","","0.71073","MoKα","","0.1351","0.0788","","","0.1755","0.2123","","","","","","1.019","","","","has coordinates,has disorder","180503","2020-10-21","18:00:00",""
"7217284","5.9662","0.0013","10.201","0.002","14.27","0.003","101.025","0.005","93.011","0.005","104.712","0.005","819.8","0.3","200","2","200","2","","","","","","","","4","P -1","-P 1","2","Aletbat Bisphenol","","","- C34 H52 N2 O2 -","- C34 H52 N2 O2 -","- C34 H52 N2 O2 -","1","0.5","","Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F.","Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions","Green Chem.","2014","16","11","4696","","10.1039/C4GC00928B","","","0.71073","MoKα","","0.1321","0.07","","","0.1515","0.1785","","","","","","1.06","","","","has coordinates,has disorder","301864","2025-08-22","15:14:36",""
"7217285","24.5162","0.0013","14.2702","0.0007","27.0151","0.0013","90","","90","","90","","9451.3","0.8","200","2","200","2","","","","","","","","7","P c a 21","P 2c -2ac","29","IPrAuSMe2-Aletbat","","","- C94 H142 Al Au N2 O4 S -","- C94 H142 Al Au N2 O4 S -","- C376 H568 Al4 Au4 N8 O16 S4 -","4","1","","Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F.","Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions","Green Chem.","2014","16","11","4696","","10.1039/C4GC00928B","","","0.71073","MoKα","","0.0908","0.0586","","","0.1074","0.1213","","","","","","1.023","","","","has coordinates,has disorder","180503","2020-10-21","18:00:00",""
"7217286","11.081","0.002","23.961","0.006","24.439","0.006","90","","101.533","0.007","90","","6358","3","200","2","200","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","Na(thf)2-Aletbat","","","- C68 H104 Al Na O6 -","- C68 H104 Al Na O6 -","- C272 H416 Al4 Na4 O24 -","4","0.5","","Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F.","Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions","Green Chem.","2014","16","11","4696","","10.1039/C4GC00928B","","","0.71073","MoKα","","0.1865","0.1312","","","0.3141","0.3504","","","","","","1.085","","","","has coordinates,has disorder","180503","2020-10-21","18:00:00",""
"7217287","9.971","0.004","11.013","0.004","19.557","0.008","90","","94.091","0.014","90","","2142.1","1.5","200","2","200","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","Alphetbat Brommmethyphenol","","","- C25 H27 Br O -","- C25 H27 Br O -","- C100 H108 Br4 O4 -","4","1","","Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F.","Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions","Green Chem.","2014","16","11","4696","","10.1039/C4GC00928B","","","0.71073","MoKα","","0.094","0.052","","","0.1142","0.1336","","","","","","1.037","","","","has coordinates","301864","2025-08-22","15:14:36",""
"7217288","23.87","0.02","23.87","0.02","10.781","0.009","90","","90","","90","","6143","9","200","2","200","2","","","","","","","","3","I 41/a","-I 4ad","88","Aletpat Bisphenol","","","- C34 H54 O2 -","- C34 H54 O2 -","- C272 H432 O16 -","8","","","Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F.","Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions","Green Chem.","2014","16","11","4696","","10.1039/C4GC00928B","","","0.71073","MoKα","","0.1811","0.1123","","","0.2622","0.3016","","","","","","1.089","","","","has coordinates,has disorder","301864","2025-08-22","15:14:36",""
"7217289","23.163","0.002","27.127","0.003","30.989","0.003","115.645","0.002","99.092","0.003","100.786","0.003","16604","3","200","2","200","2","","","","","","","","5","P -1","-P 1","2","PPh4-Aletpat","","","- C92 H124 Al O4 P -","- C92 H124 Al O4 P -","- C736 H992 Al8 O32 P8 -","8","4","","Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F.","Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions","Green Chem.","2014","16","11","4696","","10.1039/C4GC00928B","","","0.71073","MoKα","","0.1781","0.0947","","","0.2477","0.303","","","","","","1.035","","","","has coordinates","180503","2020-10-21","18:00:00",""
"7217290","11.466","0.003","11.745","0.003","11.838","0.003","71.639","0.007","75.918","0.007","72.993","0.007","1426.7","0.6","200","2","200","2","","","","","","","","3","P -1","-P 1","2","Alphetbat Bisphenol","","","- C66 H86 O6 -","- C66 H86 O6 -","- C66 H86 O6 -","1","0.5","","Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F.","Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions","Green Chem.","2014","16","11","4696","","10.1039/C4GC00928B","","","0.71073","MoKα","","0.0888","0.0593","","","0.1473","0.1689","","","","","","1.031","","","","has coordinates,has disorder","301864","2025-08-22","15:14:36",""
"7217291","14.8662","0.0015","33.789","0.004","27.09","0.003","90","","94.019","0.004","90","","13574","3","200","2","200","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","PPh4-Alphetbat","","","- C136 H152 Al Cl4 O4 P -","- C136 H152 Al Cl4 O4 P -","- C544 H608 Al4 Cl16 O16 P4 -","4","1","","Söhner, T.; Braun, F.; Over, L. C.; Mehlhose, S.; Rominger, F.; Straub, B. F.","Halogen-free water-stable aluminates as replacement for persistent fluorinated weakly-coordinating anions","Green Chem.","2014","16","11","4696","","10.1039/C4GC00928B","","","0.71073","MoKα","","0.1585","0.1064","","","0.3107","0.3518","","","","","","1.227","","","","has coordinates","180503","2020-10-21","18:00:00",""
"7218262","12.2796","0.0006","11.7459","0.0004","15.808","0.0009","90","","102.781","0.005","90","","2223.57","0.19","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C25 H25 N O4 S -","- C25 H25 N O4 S -","- C100 H100 N4 O16 S4 -","4","1","","Nagaraju, Anugula; Ramulu, B. Janaki; Shukla, Gaurav; Srivastava, Abhijeet; Verma, Girijesh Kumar; Raghuvanshi, Keshav; Singh, Maya Shankar","Catalyst-free one-pot four-component domino reactions in water‒PEG-400: highly efficient and convergent approach to thiazoloquinoline scaffolds","Green Chem.","2015","17","2","950","","10.1039/C4GC01431F","","","0.71073","MoKα","","0.1229","0.0597","","","0.1079","0.1339","","","","","","1.023","","","","has coordinates","180513","2020-10-21","18:00:00",""
"7218263","16.581","0.005","11.236","0.005","14.597","0.005","90","0.005","90","0.005","90","0.005","2719.5","1.7","293","2","293","2","","","","","","","","5","P n a 21","P 2c -2n","33","","","","- C31 H29 N O2 S -","- C31 H29 N O2 S -","- C124 H116 N4 O8 S4 -","4","1","","Nagaraju, Anugula; Ramulu, B. Janaki; Shukla, Gaurav; Srivastava, Abhijeet; Verma, Girijesh Kumar; Raghuvanshi, Keshav; Singh, Maya Shankar","Catalyst-free one-pot four-component domino reactions in water–PEG-400: highly efficient and convergent approach to thiazoloquinoline scaffolds","Green Chem.","2015","17","2","950","","10.1039/C4GC01431F","","","0.71073","MoKα","","0.1184","0.0975","","","0.2822","0.3089","","","","","","1.199","","","","has coordinates","301864","2025-08-22","15:14:37",""
"7218264","6.4263","0.0003","12.9536","0.0005","23.9037","0.0011","90","","97.062","0.005","90","","1974.74","0.15","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C22 H25 N O2 S -","- C22 H25 N O2 S -","- C88 H100 N4 O8 S4 -","4","1","","Nagaraju, Anugula; Ramulu, B. Janaki; Shukla, Gaurav; Srivastava, Abhijeet; Verma, Girijesh Kumar; Raghuvanshi, Keshav; Singh, Maya Shankar","Catalyst-free one-pot four-component domino reactions in water–PEG-400: highly efficient and convergent approach to thiazoloquinoline scaffolds","Green Chem.","2015","17","2","950","","10.1039/C4GC01431F","","","0.71073","MoKα","","0.095","0.0586","","","0.1367","0.1621","","","","","","1.025","","","","has coordinates","301864","2025-08-22","15:14:37",""
"7218288","29.745","0.011","5.802","0.002","19.967","0.008","90","","112.103","0.004","90","","3193","2","173.15","","173.15","","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C17 H24 N2 O -","- C17 H24 N2 O -","- C136 H192 N16 O8 -","8","1","","Xie, Yanjun; Cheng, Xiufang; Liu, Saiwen; Chen, Hui; Zhou, Wang; Yang, Luo; Deng, Guo-Jun","Efficient 4,5-dihydro-1H-imidazol-5-one formation from amidines and ketones under transition-metal free conditions","Green Chem.","2015","17","1","209","","10.1039/C4GC01515K","","","0.71073","MoKα","","0.0593","0.0525","","","0.1152","0.119","","","","","","1.118","","","","has coordinates","301864","2025-08-22","15:14:37",""
"7218373","12.771","0.003","14.579","0.003","16.377","0.003","106.53","0.03","105.21","0.03","91.3","0.03","2805.1","1.2","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C30 H26 I N O5 S -","- C30 I N O5 S -","- C60 I2 N2 O10 S2 -","2","1","","Xu, Shijie; Liu, Jianquan; Hu, Donghua; Bi, Xihe","Metal-free hydroacyloxylation and hydration reactions of ynamides: synthesis of α-acyloxyenamides and N-acylsulfonamides","Green Chem.","2015","17","1","184","","10.1039/C4GC01328J","","","0.71073","MoKα","","0.5924","0.5622","","","0.8534","0.8781","","","","","","5.814","","","","has coordinates","206489","2020-10-21","18:00:00",""
"7218396","7.5759","0.0006","11.0478","0.001","23.488","0.002","90","","90","","90","","1965.9","0.3","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C22 H22 Cl N O2 -","- C22 H22 Cl N O2 -","- C88 H88 Cl4 N4 O8 -","4","1","","Ye, Weijian; Li, Yan; Zhou, Lanxiang; Liu, Juanjuan; Wang, Cunde","Three-component reaction between substituted β-nitrostyrenes, β-dicarbonyl compounds and amines: diversity-oriented synthesis of novel β-enaminones","Green Chem.","2015","17","1","188","","10.1039/C4GC01234H","","","0.71073","MoKα","","0.0956","0.0577","","","0.1418","0.1606","","","","","","0.997","","","","has coordinates","301864","2025-08-22","15:14:37",""
"7218397","10.0101","0.001","10.7765","0.001","15.5711","0.0014","90","","93.9","0.003","90","","1675.8","0.3","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C18 H21 N O4 -","- C18 H21 N O4 -","- C72 H84 N4 O16 -","4","1","","Ye, Weijian; Li, Yan; Zhou, Lanxiang; Liu, Juanjuan; Wang, Cunde","Three-component reaction between substituted β-nitrostyrenes, β-dicarbonyl compounds and amines: diversity-oriented synthesis of novel β-enaminones","Green Chem.","2015","17","1","188","","10.1039/C4GC01234H","","","0.71073","MoKα","","0.0771","0.0551","","","0.132","0.1459","","","","","","1.047","","","","has coordinates","301864","2025-08-22","15:14:37",""
"7218398","10.6004","0.0018","13.375","0.002","16.069","0.002","82.836","0.004","71.805","0.005","89.343","0.005","2146.5","0.6","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C24 H18 Cl N O4 -","- C24 H18 Cl N O4 -","- C96 H72 Cl4 N4 O16 -","4","2","","Ye, Weijian; Li, Yan; Zhou, Lanxiang; Liu, Juanjuan; Wang, Cunde","Three-component reaction between substituted β-nitrostyrenes, β-dicarbonyl compounds and amines: diversity-oriented synthesis of novel β-enaminones","Green Chem.","2015","17","1","188","","10.1039/C4GC01234H","","","0.71073","MoKα","","0.1751","0.0778","","","0.1928","0.2233","","","","","","0.964","","","","has coordinates","301864","2025-08-22","15:14:37",""
"7218562","11.4437","0.0004","22.5577","0.0008","8.1293","0.0003","90","","90","","90","","2098.53","0.13","100","2","100","2","","","","","","","","5","P c c n","-P 2ab 2ac","56","","","","- C10 H8 Br N3 O2 -","- C10 H8 Br N3 O2 -","- C80 H64 Br8 N24 O16 -","8","1","","Li, Wenjun; Du, Zhiyun; Zhang, Kun; Wang, Jian","Organocatalytic 1,3-dipolar cycloaddition reaction of α,β-unsaturated ketones with azides through iminium catalysis","Green Chem.","2015","17","2","781","","10.1039/C4GC01929F","","","0.71073","MoKα","","0.0282","0.0219","","","0.0576","0.0597","","","","","","1.079","","","","has coordinates","301864","2025-08-22","15:14:37",""
"7218563","16.4264","0.0014","10.8002","0.0009","17.5844","0.0015","90","","96.397","0.001","90","","3100.2","0.5","273","2","273","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C40 H0 Mo8 N8 O26 -","- C40 Mo8 N8 O26 -","- C80 Mo16 N16 O52 -","2","0.5","","Zhou, Ming-Dong; Liu, Mei-Ju; Huang, Liang-Liang; Zhang, Jian; Wang, Jing-Yun; Li, Xue-Bing; Kühn, Fritz E.; Zang, Shu-Liang","Olefin epoxidation with hydrogen peroxide using octamolybdate-based self-separating catalysts","Green Chem.","2015","17","2","1186","","10.1039/C4GC01411A","","","0.71073","MoKα","","0.0701","0.052","","","0.1348","0.1489","","","","","","1.046","","","","has coordinates","180516","2020-10-21","18:00:00",""
"7218564","15.6345","0.0009","12.1211","0.0007","16.5893","0.001","90","","94.603","0.001","90","","3133.7","0.3","188","2","188","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C44 H0 Mo8 N4 O27 -","- C44 Mo8 N4 O27 -","- C88 Mo16 N8 O54 -","2","0.5","","Zhou, Ming-Dong; Liu, Mei-Ju; Huang, Liang-Liang; Zhang, Jian; Wang, Jing-Yun; Li, Xue-Bing; Kühn, Fritz E.; Zang, Shu-Liang","Olefin epoxidation with hydrogen peroxide using octamolybdate-based self-separating catalysts","Green Chem.","2015","17","2","1186","","10.1039/C4GC01411A","","","0.71073","MoKα","","0.053","0.0415","","","0.1042","0.1109","","","","","","1.046","","","","has coordinates","180516","2020-10-21","18:00:00",""
"7218747","10.1442","0.0016","11.7709","0.0018","15.044","0.002","109.125","0.008","97.344","0.007","109.259","0.008","1545.2","0.4","223","2","223","2","","","","","","","","7","P -1","-P 1","2","","","","- C24 H40 B F4 Ir N4 O2 -","- C24 H40 B F4 Ir N4 O2 -","- C48 H80 B2 F8 Ir2 N8 O4 -","2","1","","Manas, Michael G.; Campos, Jesús; Sharninghausen, Liam S.; Lin, Elisa; Crabtree, Robert H.","Selective catalytic oxidation of sugar alcohols to lactic acid","Green Chem.","2015","17","1","594","","10.1039/C4GC01694G","","","0.71073","MoKα","","0.0775","0.0502","","","0.1043","0.1168","","","","","","1.033","","","","has coordinates,has disorder","180518","2020-10-21","18:00:00",""
"7218933","7.1861","0.0014","7.5759","0.0014","7.6549","0.0014","89.212","0.004","63.414","0.003","64.027","0.003","326.31","0.11","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C6 H8 Cl0 Cu N14 O2 -","- C6 H8 Cu N14 O2 -","- C6 H8 Cu N14 O2 -","1","0.5","","Liu, Xiangyu; Gao, Wenjuan; Sun, Panpan; Su, Zhiyong; Chen, Sanping; Wei, Qing; Xie, Gang; Gao, Shengli","Environmentally-friendly high-energy MOFs: crystal structure, thermostability, insensitivity and remarkable detonation performance","Green Chem.","2015","17","2","831","836","10.1039/C4GC02184C","","","0.71073","MoKα","","0.0815","0.0586","","","0.1434","0.1641","","","","","","0.953","","","","has coordinates","180520","2020-10-21","18:00:00",""
"7218934","7.404","0.003","9.672","0.003","9.341","0.003","90","","113.02","0.004","90","","615.7","0.4","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C3 H Cu N7 O -","- C3 H Cu N7 O -","- C12 H4 Cu4 N28 O4 -","4","1","","Liu, Xiangyu; Gao, Wenjuan; Sun, Panpan; Su, Zhiyong; Chen, Sanping; Wei, Qing; Xie, Gang; Gao, Shengli","Environmentally-friendly high-energy MOFs: crystal structure, thermostability, insensitivity and remarkable detonation performance","Green Chem.","2015","17","2","831","836","10.1039/C4GC02184C","","","0.71073","MoKα","","0.1053","0.0837","","","0.2197","0.2321","","","","","","1.104","","","","has coordinates","180520","2020-10-21","18:00:00",""
"7218935","8.63","0.003","9.867","0.003","6.736","0.002","90","","108.297","0.006","90","","544.6","0.3","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C3 H2 Cu N7 -","- C3 H2 Cu N7 -","- C12 H8 Cu4 N28 -","4","1","","Liu, Xiangyu; Gao, Wenjuan; Sun, Panpan; Su, Zhiyong; Chen, Sanping; Wei, Qing; Xie, Gang; Gao, Shengli","Environmentally-friendly high-energy MOFs: crystal structure, thermostability, insensitivity and remarkable detonation performance","Green Chem.","2015","17","2","831","836","10.1039/C4GC02184C","","","0.71073","MoKα","","0.1081","0.0775","","","0.1842","0.1993","","","","","","1.008","","","","has coordinates","180520","2020-10-21","18:00:00",""
"7218936","4.401","0.0003","12.3035","0.0009","14.8314","0.0011","90","","97.593","0.001","90","","796.04","0.1","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","1,2-bis(4-cyanato-3-methoxyphenyl)ethane","","- C18 H16 N2 O4 -","- C18 H16 N2 O4 -","- C36 H32 N4 O8 -","2","0.5","","Harvey, Benjamin G.; Guenthner, Andrew J.; Meylemans, Heather A.; Haines, Shannon R. L.; Lamison, Kevin R.; Groshens, Thomas J.; Cambrea, Lee R.; Davis, Matthew C.; Lai, William W.","Renewable thermosetting resins and thermoplastics from vanillin","Green Chem.","2015","17","2","1249","","10.1039/C4GC01825G","","","0.71073","","","0.0474","0.035","","","0.0863","0.0962","","","","","","1.038","","","","has coordinates","301864","2025-08-22","15:14:38",""
"7218937","3.8765","0.0004","12.2303","0.0013","16.1995","0.0018","90","","95.906","0.0017","90","","763.95","0.14","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","1,2-bis(4-cyanato-3-methoxyphenyl)ethene","","- C18 H14 N2 O4 -","- C18 H14 N2 O4 -","- C36 H28 N4 O8 -","2","0.5","","Harvey, Benjamin G.; Guenthner, Andrew J.; Meylemans, Heather A.; Haines, Shannon R. L.; Lamison, Kevin R.; Groshens, Thomas J.; Cambrea, Lee R.; Davis, Matthew C.; Lai, William W.","Renewable thermosetting resins and thermoplastics from vanillin","Green Chem.","2015","17","2","1249","","10.1039/C4GC01825G","","","0.71073","MoKα","","0.0635","0.0406","","","0.0764","0.0892","","","","","","1.03","","","","has coordinates","301864","2025-08-22","15:14:38",""
"7218993","7.4354","0.0015","15.648","0.003","21.424","0.004","90","","90","","90","","2492.7","0.8","173","2","173","2","","","","","","","","5","P c c n","-P 2ab 2ac","56","","","","- C14 H8 Cl N3 S -","- C14 H8 Cl N3 S -","- C112 H64 Cl8 N24 S8 -","8","1","","Wen, Li-Rong; Li, Shou-Lei; Zhang, Jian; Li, Ming","Convenient synthesis of benzo[4,5]thiazolo[2,3-c][1,2,4]triazoles with 1 mol% CuCl2·2H2O as catalyst in water","Green Chem.","2015","17","3","1581","","10.1039/C4GC02156H","","","0.71073","MoKα","","0.0446","0.0439","","","0.0959","0.0962","","","","","","1.22","","","","has coordinates","301864","2025-08-22","15:14:38",""
"7219006","11.0519","0.0008","13.5682","0.0009","19.4863","0.0016","107.546","0.002","96.181","0.001","109.124","0.002","2562.3","0.3","298","2","298","2","","","","","","","","4","P -1","-P 1","2","","","","- C30 H31 N5 O2 -","- C30 H31 N5 O2 -","- C120 H124 N20 O8 -","4","2","","Fu, Lei; Feng, Xian; Zhang, Juan-Juan; Hu, Jun-Die; Xun, Zhan; Wang, Jian-Jun; Huang, Zhi-Bin; Shi, Da-Qing","Highly efficient construction of a bridged pentacyclic skeleton via a six-component domino reaction under microwave irradiation","Green Chem.","2015","17","3","1535","","10.1039/C4GC01832J","","","0.71073","MoKα","","0.1291","0.0528","","","0.1003","0.1313","","","","","","1.022","","","","has coordinates","301864","2025-08-22","15:14:38",""
"7219007","18.6242","0.0019","10.3311","0.0007","29.295","0.003","90","","106.496","0.002","90","","5404.6","0.9","298","2","298","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C31 H33 N5 O2 -","- C31 H33 N5 O2 -","- C248 H264 N40 O16 -","8","2","","Fu, Lei; Feng, Xian; Zhang, Juan-Juan; Hu, Jun-Die; Xun, Zhan; Wang, Jian-Jun; Huang, Zhi-Bin; Shi, Da-Qing","Highly efficient construction of a bridged pentacyclic skeleton via a six-component domino reaction under microwave irradiation","Green Chem.","2015","17","3","1535","","10.1039/C4GC01832J","","","0.71073","MoKα","","0.1669","0.0641","","","0.1687","0.2661","","","","","","1.064","","","","has coordinates","301864","2025-08-22","15:14:38",""
"7219041","14.5192","0.0008","4.971","0.0002","16.4551","0.0007","90","","106.074","0.005","90","","1141.21","0.1","294","2","294","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","Ethyl 5-(4-fluorophenyl)-1H-pyrazole-3-carboxylate","","- C12 H11 F N2 O2 -","- C12 H11 F N2 O2 -","- C48 H44 F4 N8 O8 -","4","1","","Marković, Violeta; Joksović, Milan D.","“On water” synthesis of N-unsubstituted pyrazoles: semicarbazide hydrochloride as an alternative to hydrazine for preparation of pyrazole-3-carboxylate derivatives and 3,5-disubstituted pyrazoles","Green Chem.","2015","17","2","842","","10.1039/C4GC02028F","","x-ray","0.71073","MoKα","","0.0685","0.0483","","","0.1277","0.1422","","","","","","1.04","","","","has coordinates","301864","2025-08-22","15:14:38",""
"7219093","13.883","0.003","14.024","0.003","15.361","0.004","109.019","0.003","106.371","0.002","98.531","0.004","2616","1.1","223","2","223","2","","","","","","","","6","P -1","-P 1","2","","","","- C88 H148 N6 Nd2 O9 Si4 -","- C88 H124 N6 Nd2 O9 Si4 -","- C88 H124 N6 Nd2 O9 Si4 -","1","0.5","","Cheng, Hao; Zhao, Bei; Yao, Yingming; Lu, Chengrong","Carboxylation of terminal alkynes with CO2catalyzed by bis(amidate) rare-earth metal amides","Green Chem.","2015","17","3","1675","","10.1039/C4GC02200A","","","0.71075","MoKα","","0.0957","0.0737","","","0.1654","0.1846","","","","","","1.105","","","","has coordinates,has disorder","180521","2020-10-21","18:00:00",""
"7219094","13.963","0.002","14.045","0.002","15.374","0.003","108.936","0.002","106.425","0.002","98.499","0.002","2638.4","0.7","223","2","223","2","","","","","","","","6","P -1","-P 1","2","","","","- C88 H148 La2 N6 O9 Si4 -","- C88 H124 La2 N6 O9 Si4 -","- C88 H124 La2 N6 O9 Si4 -","1","0.5","","Cheng, Hao; Zhao, Bei; Yao, Yingming; Lu, Chengrong","Carboxylation of terminal alkynes with CO2catalyzed by bis(amidate) rare-earth metal amides","Green Chem.","2015","17","3","1675","","10.1039/C4GC02200A","","","0.71075","MoKα","","0.0675","0.0564","","","0.1586","0.1682","","","","","","1.053","","","","has coordinates,has disorder","180521","2020-10-21","18:00:00",""
"7219095","13.74","0.02","14","0.04","15.31","0.03","109.27","0.07","106.002","0.004","98.57","0.02","2577","10","223","2","223","2","","","","","","","","6","P -1","-P 1","2","","","","- C88 H148 N6 O9 Si4 Y2 -","- C88 H148 N6 O9 Si4 Y2 -","- C88 H148 N6 O9 Si4 Y2 -","1","0.5","","Cheng, Hao; Zhao, Bei; Yao, Yingming; Lu, Chengrong","Carboxylation of terminal alkynes with CO2catalyzed by bis(amidate) rare-earth metal amides","Green Chem.","2015","17","3","1675","","10.1039/C4GC02200A","","","0.71075","MoKα","","0.1288","0.0897","","","0.2305","0.2559","","","","","","1.06","","","","has coordinates,has disorder","180521","2020-10-21","18:00:00",""
"7219176","12.291","0.003","7.4147","0.0015","34.667","0.007","90","","90","","90","","3159.3","1.2","296","2","296","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C18 H15 N O5 -","- C18 H15 N O5 -","- C144 H120 N8 O40 -","8","1","","Sharma, Siddharth; Singh, Ajay K.; Singh, Devendra; Kim, Dong-Pyo","Chemical fixation of carbon dioxide by copper catalyzed multicomponent reactions for oxazolidinedione syntheses","Green Chem.","2015","17","3","1404","","10.1039/C4GC02089H","","","0.71073","MoKα","","0.1129","0.0506","","","0.1125","0.1372","","","","","","1.016","","","","has coordinates","301864","2025-08-22","15:14:38",""
"7219241","15.4965","0.0007","16.8579","0.0007","12.6159","0.0006","90","","90","","90","","3295.8","0.3","153","2","153","1","","","","","","","","7","P c a 21","P 2c -2ac","29","","","","- C20 H62 Al3 Fe2 Li N4 O2 -","- C20 H62 Al3 Fe2 Li N4 O2 -","- C80 H248 Al12 Fe8 Li4 N16 O8 -","4","1","","Gieshoff, Tim N.; Villa, Matteo; Welther, Alice; Plois, Markus; Chakraborty, Uttam; Wolf, Robert; Jacobi von Wangelin, Axel","Iron-catalyzed olefin hydrogenation at 1 bar H2with a FeCl3‒LiAlH4catalyst","Green Chem.","2015","17","3","1408","","10.1039/C4GC02368D","","","0.71073","MoKα","","0.0489","0.0329","","","0.0678","0.0741","","","","","","1.019","","","","has coordinates","180523","2020-10-21","18:00:00",""
"7219331","11.9187","0.0017","9.8408","0.0015","24.353","0.004","90","","102.942","0.006","90","","2783.8","0.7","150","2","150","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C33 H33 N5 O -","- C33 H33 N5 O -","- C132 H132 N20 O4 -","4","1","","Sousa, Ana Catarina; Piedade, M. Fátima M. M.; Martins, Lígia O.; Robalo, M. Paula","An enzymatic route to a benzocarbazole framework using bacterial CotA laccase","Green Chem.","2015","17","3","1429","","10.1039/C4GC02511C","","","0.71073","MoKα","","0.1543","0.0646","","","0.1185","0.1455","","","","","","0.889","","","","has coordinates","180524","2020-10-21","18:00:00",""
"7219518","9.1187","0.0009","10.839","0.001","12.4287","0.0011","66.309","0.001","88.214","0.002","81.725","0.002","1112.7","0.18","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C26 H21 N5 O2 -","- C26 H21 N5 O2 -","- C52 H42 N10 O4 -","2","1","","Feng, Xian; Wang, Jian-Jun; Zhang, Juan-Juan; Cao, Cheng-Pao; Huang, Zhi-Bin; Shi, Da-Qing","Regioselective synthesis of functionalized [1,8]naphthyridine derivatives via three-component domino reaction under catalyst-free conditions","Green Chem.","2015","17","2","973","","10.1039/C4GC01469C","","","0.71073","MoKα","","0.1342","0.0595","","","0.0957","0.1339","","","","","","1.032","","","","has coordinates","301864","2025-08-22","15:14:39",""
"7219519","8.5318","0.001","10.724","0.002","13.1003","0.0018","74.306","0.014","87.632","0.01","81.193","0.012","1140.3","0.3","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C27 H23 N5 O2 -","- C27 H23 N5 O2 -","- C54 H46 N10 O4 -","2","1","","Feng, Xian; Wang, Jian-Jun; Zhang, Juan-Juan; Cao, Cheng-Pao; Huang, Zhi-Bin; Shi, Da-Qing","Regioselective synthesis of functionalized [1,8]naphthyridine derivatives via three-component domino reaction under catalyst-free conditions","Green Chem.","2015","17","2","973","","10.1039/C4GC01469C","","","1.54178","CuKα","","0.2516","0.1399","","","0.2392","0.2855","","","","","","1.19","","","","has coordinates","301864","2025-08-22","15:14:39",""
"7219548","7.5044","0.0013","11.9291","0.0019","14.8473","0.0019","90","","90","","90","","1329.1","0.4","293","2","293","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C8 H7 N O -","- C8 H7 N O -","- C64 H56 N8 O8 -","8","1","","Ren, Lanhui; Wang, Lianyue; Lv, Ying; Shang, Sensen; Chen, Bo; Gao, Shuang","Synthesis of 6,7-dihydro-5H-cyclopenta[b]pyridin-5-one analogues through manganese-catalyzed oxidation of the CH2adjacent to pyridine moiety in water","Green Chem.","2015","17","4","2369","","10.1039/C4GC02471K","","","0.71073","MoKα","","0.0693","0.0552","","","0.1269","0.1383","","","","","","1.085","","","","has coordinates","301864","2025-08-22","15:14:39",""
"7219929","6.1459","0.0004","10.5542","0.0006","9.5004","0.0005","90","","93.777","0.002","90","","614.91","0.06","120","","120","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","dimethyl fluoromalonate","","- C5 H7 F O4 -","- C5 H7 F O4 -","- C20 H28 F4 O16 -","4","1","","Harsanyi, Antal; Sandford, Graham","Fluorine gas for life science syntheses: green metrics to assess selective direct fluorination for the synthesis of 2-fluoromalonate esters","Green Chem.","2015","17","5","3000","","10.1039/C5GC00402K","","x-ray","0.71073","MoKα","","0.0704","0.0568","","","0.1547","0.1716","","","","","","1.045","","","","has coordinates","301864","2025-08-22","15:14:40",""
"7220061","6.6676","0.0007","7.3731","0.0007","21.962","0.003","98.895","0.009","91.912","0.009","99.057","0.008","1051.5","0.2","100.01","0.1","100.01","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C24 H26 N4 O3 -","- C24 H26 N4 O3 -","- C48 H52 N8 O6 -","2","1","","Schröder, Felix; Ojeda, Manuel; Erdmann, Nico; Jacobs, Jeroen; Luque, Rafael; Noël, Timothy; Van Meervelt, Luc; Van der Eycken, Johan; Van der Eycken, Erik V.","Supported gold nanoparticles as efficient and reusable heterogeneous catalyst for cycloisomerization reactions","Green Chem.","2015","17","6","3314","","10.1039/C5GC00430F","","","0.7107","MoKα","","0.0632","0.0563","","","0.1475","0.1519","","","","","","1.076","","","","has coordinates","301865","2025-08-22","16:16:38",""
"7220062","13.3119","0.0005","10.7033","0.0004","13.8141","0.0004","90","","91.8261","0.0012","90","","1967.25","0.12","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","quinoline fused isoxazole","quinoline","","- C22 H16 F N5 O3 -","- C22 H16 F N5 O3 -","- C88 H64 F4 N20 O12 -","4","1","","Poomathi, Nataraj; Mayakrishnan, Sivakalai; Muralidharan, Doraiswamy; Srinivasan, Rajagopal; Perumal, Paramasivan T.","Reaction of isatins with 6-amino uracils and isoxazoles: isatin ring-opening vs. annulations and regioselective synthesis of isoxazole fused quinoline scaffolds in water","Green Chem.","2015","17","6","3362","","10.1039/C5GC00006H","","","0.71073","MoKα","","0.0512","0.0373","","","0.0934","0.1036","","","","","","1.032","","","","has coordinates","301865","2025-08-22","16:16:38",""
"7220063","24.9048","0.0006","9.498","0.0002","22.2694","0.0006","90","","110.723","0.001","90","","4926.9","0.2","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","spiro","","- C30 H22 N4 O4.5 S0.5 -","- C30 H22 N4 O4.5 S0.5 -","- C240 H176 N32 O36 S4 -","8","2","","Poomathi, Nataraj; Mayakrishnan, Sivakalai; Muralidharan, Doraiswamy; Srinivasan, Rajagopal; Perumal, Paramasivan T.","Reaction of isatins with 6-amino uracils and isoxazoles: isatin ring-opening vs. annulations and regioselective synthesis of isoxazole fused quinoline scaffolds in water","Green Chem.","2015","17","6","3362","","10.1039/C5GC00006H","","","0.71073","MoKα","","0.2374","0.0662","","","0.1511","0.2177","","","","","","0.942","","","","has coordinates,has disorder","176453","2020-10-21","18:00:00",""
"7220409","11.88","0.007","16.051","0.008","26.14","0.013","90","","90","","90","","4985","5","296","2","296.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C29 H25 Cl N2 O3 -","- C29 H24.5 Cl N2 O3 -","- C232 H196 Cl8 N16 O24 -","8","2","","Vivekanand, Thavaraj; Vinoth, Perumal; Agieshkumar, B.; Sampath, Natarajan; Sudalai, Arumugam; Menéndez, J. Carlos; Sridharan, Vellaisamy","Highly efficient regioselective synthesis of pyrroles via a tandem enamine formation‒Michael addition‒cyclization sequence under catalyst- and solvent-free conditions","Green Chem.","2015","17","6","3415","","10.1039/C5GC00365B","","","0.71073","MoKα","","0.2031","0.0466","","","0.0971","0.1327","","","","","","0.869","","","","has coordinates","192220","2020-10-21","18:00:00",""
"7220410","8.6065","0.0001","7.1858","0.0001","11.184","0.0002","90","","110.985","0.001","90","","645.794","0.017","296","2","296","2","","","","","","","","4","P 1 21 1","P 2yb","4","","3-hydroxy-3-((3-methyl-4-nitroisoxazol-5-yl)methyl)indolin-2-one","","- C13 H11 N3 O5 -","- C13 H11 N3 O5 -","- C26 H22 N6 O10 -","2","1","","Zhang, Yong; Wei, Biao-Wen; Lin, Hui; Zhang, Ling; Liu, Jin-Xiang; Luo, Hai-Qing; Fan, Xiao-Lin","“On water” direct catalytic vinylogous Henry (nitroaldol) reactions of isatins for the efficient synthesis of isoxazole substituted 3-hydroxyindolin-2-ones","Green Chem.","2015","17","6","3266","","10.1039/C5GC00503E","","","0.71073","MoKα","","0.0318","0.0308","","","0.0829","0.084","","","","","","0.992","","","","has coordinates","301865","2025-08-22","16:16:39",""
"7220411","13.5271","0.0006","7.4112","0.0003","16.501","0.0008","90","","94.763","0.001","90","","1648.55","0.13","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","3-(1-(3-ethyl-4-nitroisoxazol-5-yl)ethyl)-3-hydroxy-5-methoxyindolin-2-one","","- C16 H17 N3 O6 -","- C16 H17 N3 O6 -","- C64 H68 N12 O24 -","4","1","","Zhang, Yong; Wei, Biao-Wen; Lin, Hui; Zhang, Ling; Liu, Jin-Xiang; Luo, Hai-Qing; Fan, Xiao-Lin","“On water” direct catalytic vinylogous Henry (nitroaldol) reactions of isatins for the efficient synthesis of isoxazole substituted 3-hydroxyindolin-2-ones","Green Chem.","2015","17","6","3266","","10.1039/C5GC00503E","","","0.71073","MoKα","","0.119","0.0601","","","0.1505","0.183","","","","","","1.02","","","","has coordinates","301865","2025-08-22","16:16:39",""
"7220412","6.3186","0.0004","11.7574","0.0008","16.3886","0.0012","90","","95.537","0.007","90","","1211.83","0.14","294.68","0.1","294.68","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","3-((4-amino-3-methylisoxazol-5-yl)methyl)-3-hydroxyindolin-2-one","","- C13 H13 N3 O3 -","- C13 H13 N3 O3 -","- C52 H52 N12 O12 -","4","1","","Zhang, Yong; Wei, Biao-Wen; Lin, Hui; Zhang, Ling; Liu, Jin-Xiang; Luo, Hai-Qing; Fan, Xiao-Lin","“On water” direct catalytic vinylogous Henry (nitroaldol) reactions of isatins for the efficient synthesis of isoxazole substituted 3-hydroxyindolin-2-ones","Green Chem.","2015","17","6","3266","","10.1039/C5GC00503E","","","0.71073","MoKα","","0.1323","0.0673","","","0.1278","0.1623","","","","","","1.041","","","","has coordinates","301865","2025-08-22","16:16:39",""
"7220413","8.1437","0.0016","11.826","0.002","12.4","0.003","73.31","0.03","88.33","0.03","79.7","0.03","1125.2","0.5","298","2","298","2","","","","","","","","5","P -1","-P 1","2","","N1,N1-dimethyl-N4,2-ditosylbenzene-1,4-diamine","","- C22 H24 N2 O4 S2 -","- C22 H24 N2 O4 S2 -","- C44 H48 N4 O8 S4 -","2","1","","Khazalpour, Sadegh; Nematollahi, Davood","Electrochemical and chemical synthesis of different types of sulfonamide derivatives of N,N-dimethyl-1,4-benzenediamine using 4-nitroso-N,N-dimethylaniline","Green Chem.","2015","17","6","3508","","10.1039/C5GC00438A","","","0.71073","MoKα","","0.0698","0.0526","","","0.1283","0.1333","","","","","","0.816","","","","has coordinates","301865","2025-08-22","16:16:39",""
"7220414","9.441","0.005","10.287","0.005","13.246","0.005","100.627","0.005","94.498","0.005","108.144","0.005","1188.7","1","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C29 H24 N2 O5 -","- C29 H24 N2 O5 -","- C58 H48 N4 O10 -","2","1","","Sarkar, Piyali; Mukhopadhyay, Chhanda","Single step incorporation of carboxylic acid groups in the lower rim of calix[4]arenes: a recyclable catalyst towards assembly of diverse five ring fused acridines","Green Chem.","2015","17","6","3452","","10.1039/C5GC00156K","","","0.71073","MoKα","","0.0525","0.0473","","","0.1212","0.1281","","","","","","1.03","","","","has coordinates","301865","2025-08-22","16:16:39",""
"7220488","10.4883","0.0007","11.9211","0.0007","20.6101","0.0014","93.874","0.004","92.989","0.004","115.747","0.003","2306.2","0.3","103","2","103","2","","","","","","","","5","P -1","-P 1","2","","","","- C19 H35 I O4 S -","- C19 H35 I O4 S -","- C76 H140 I4 O16 S4 -","4","2","","Koh, Peng-Fei; Loh, Teck Peng","Synthesis of Biologically Active Natural Products, Aspergillides A and B, Entirely from Biomass Derived Platform Chemicals","Green Chem.","2015","","","","","10.1039/C5GC00900F","","","0.71073","MoKα","","0.1032","0.0584","","","0.1277","0.1466","","","","","","1.087","","","","has coordinates","301865","2025-08-22","16:16:40",""
"7220569","12.645","0.0003","15.1066","0.0004","13.214","0.0002","90","","93.207","0.002","90","","2520.22","0.1","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C11 H18 N2 O S -","- C11 H18 N2 O S -","- C88 H144 N16 O8 S8 -","8","2","","Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing","CO2, COS and CS2 Adducts of N-Heterocyclic Olefin and Their Application as Organocatalysts for Carbon Dioxide Fixation","Green Chem.","2015","","","","","10.1039/C5GC00948K","","","0.71073","MoKα","","0.1071","0.0546","","","0.1051","0.1286","","","","","","1.027","","","","has coordinates","198633","2020-10-21","18:00:00",""
"7220570","10.4317","0.0003","15.4783","0.0005","11.9638","0.0004","90","","102.189","0.002","90","","1888.19","0.1","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C20 H28 N2 O S -","- C20 H28 N2 O S -","- C80 H112 N8 O4 S4 -","4","1","","Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing","CO2, COS and CS2 Adducts of N-Heterocyclic Olefin and Their Application as Organocatalysts for Carbon Dioxide Fixation","Green Chem.","2015","","","","","10.1039/C5GC00948K","","","0.71073","MoKα","","0.0885","0.051","","","0.1149","0.1336","","","","","","1.054","","","","has coordinates","301865","2025-08-22","16:16:40",""
"7220571","7.9953","0.0012","15.115","0.002","11.4875","0.0017","90","","107.186","0.005","90","","1326.3","0.3","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C11 H18 N2 S2 -","- C11 H18 N2 S2 -","- C44 H72 N8 S8 -","4","1","","Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing","CO2, COS and CS2 Adducts of N-Heterocyclic Olefin and Their Application as Organocatalysts for Carbon Dioxide Fixation","Green Chem.","2015","","","","","10.1039/C5GC00948K","","","0.71073","MoKα","","0.0695","0.0464","","","0.1201","0.1329","","","","","","1.074","","","","has coordinates","301865","2025-08-22","16:16:40",""
"7220572","10.1668","0.0011","16.0775","0.0016","12.9862","0.0012","90","","103.802","0.005","90","","2061.4","0.4","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H28 N2 S2 -","- C20 H28 N2 S2 -","- C80 H112 N8 S8 -","4","1","","Wang, Yan-Bo; Sun, Dong-Sheng; Zhou, Hui; Zhang, Wen-Zhen; Lu, Xiao-Bing","CO2, COS and CS2 Adducts of N-Heterocyclic Olefin and Their Application as Organocatalysts for Carbon Dioxide Fixation","Green Chem.","2015","","","","","10.1039/C5GC00948K","","","0.71073","MoKα","","0.0707","0.0441","","","0.1059","0.1202","","","","","","1.037","","","","has coordinates","301865","2025-08-22","16:16:40",""
"7220590","8.686","0.006","10.371","0.008","11.293","0.008","109.138","0.007","111.662","0.009","92.379","0.009","877.8","1.1","293","","293","","","","","","","","see text","5","P -1","-P 1","2","","","","- C23 H14 Cl N O2 -","- C23 H14 Cl N O2 -","- C46 H28 Cl2 N2 O4 -","2","1","","Koneni, Venkata Sashidhara; Palnati, Gopala Reddy; Singh, L. Ravithej; Upadhyay, Amit; Avula, Srinivasa Rao; kumar, Abdhesh; Kant, Ruchir","Molecular Iodine Catalysed One-Pot Synthesis of Chromeno[4,3-b]quinolin-6-ones under Microwave Irradiation","Green Chem.","2015","","","","","10.1039/C5GC00756A","","","0.71075","MoKα","","0.0775","0.0505","","","0.1228","0.1463","","","","","","0.914","","","","has coordinates","301865","2025-08-22","16:16:40",""
"7220686","7.534","0.003","10.682","0.004","16.411","0.005","90","","102.32","0.03","90","","1290.3","0.8","295","2","295","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C12 H12 N4 O2 -","- C12 H12 N4 O2 -","- C48 H48 N16 O8 -","4","1","","Ershov, O. V.; Ievlev, M. Yu.; Tafeenko, V. A.; Nasakin, O. E.","Glycine catalyzed diastereoselective domino-synthesis of 6-imino-2,7-dioxabicyclo[3.2.1]octane-4,4,5-tricarbonitriles in water","Green Chem.","2015","17","8","4234","","10.1039/C5GC00909J","","","1.54184","CuKα","","0.0494","0.0438","","","0.1216","0.1269","","","","","","1.045","","","","has coordinates","301865","2025-08-22","16:16:41",""
"7220692","7.8241","0.0016","24.301","0.005","9.1574","0.0018","90","","93.76","0.03","90","","1737.4","0.6","113","2","113","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H17 N O6 -","- C20 H17 N O6 -","- C80 H68 N4 O24 -","4","1","","Xia, JIa-Ning; Yu, Bing; Guo, Chun-Xiang; He, Liang-Nian","Copper(I)/phosphine-catalyzed tandem carboxylation/annulation of terminal alkynes with ambient pressure of CO2: one-pot access to 3a-hydroxyisoxazolo[3,2-a]isoindol-8(3aH)-ones","Green Chem.","2015","","","","","10.1039/C5GC00926J","","","0.71073","MoKα","","0.066","0.0499","","","0.12","0.1305","","","","","","0.979","","","","has coordinates","301865","2025-08-22","16:16:41",""
"7220977","9.6788","0.0003","9.6941","0.0003","12.4864","0.0004","86.025","0.002","86.707","0.002","89.675","0.002","1166.81","0.06","150","2","150","2","","","","","","","","4","P -1","-P 1","2","[P4444][H(OAc)2]","tetrabutylphosphonium hydrogendiethanoate","","- C20 H43 O4 P -","- C20 H43 O4 P -","- C40 H86 O8 P2 -","2","1","","Anderson, Kris; Atkins, Martin P.; Estager, Julien; Kuah, Yongcheun; Ng, Shieling; Oliferenko, Alexander A.; Plechkova, Natalia V.; Puga, Alberto V.; Seddon, Kenneth R.; Wassell, David F.","Carbon dioxide uptake from natural gas by binary ionic liquid‒water mixtures","Green Chem.","2015","17","8","4340","","10.1039/C5GC00720H","","","0.71073","MoKα","","0.0435","0.0372","","","0.0956","0.0994","","","","","","1.026","","","","has coordinates","176428","2020-10-21","18:00:00",""
"7220978","10.569","0.005","11.627","0.005","31.826","0.005","90","0.005","90.812","0.005","90","0.005","3911","3","150","2","150","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","[P4444][HCO3]","tetrabutylphosphonium hydrogencarbonate","","- C34 H74 O6 P2 -","- C34 H74 O6 P2 -","- C136 H296 O24 P8 -","4","1","","Anderson, Kris; Atkins, Martin P.; Estager, Julien; Kuah, Yongcheun; Ng, Shieling; Oliferenko, Alexander A.; Plechkova, Natalia V.; Puga, Alberto V.; Seddon, Kenneth R.; Wassell, David F.","Carbon dioxide uptake from natural gas by binary ionic liquid–water mixtures","Green Chem.","2015","17","8","4340","","10.1039/C5GC00720H","","","0.71073","MoKα","","0.135","0.0567","","","0.117","0.1331","","","","","","0.88","","","","has coordinates,has disorder","301865","2025-08-22","16:16:42",""
"7220979","11.5582","0.0007","12.3717","0.0007","23.8099","0.0018","90","","90","","90","","3404.7","0.4","115","","115","","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C20 H15 B F4 N2 -","- C20 H15 B F4 N2 -","- C160 H120 B8 F32 N16 -","8","1","","de Robillard, Guillaume; Makni, Oumayma; Cattey, Hélène; Andrieu, Jacques; Devillers, Charles H.","Towards sustainable synthesis of pyren-1-yl azoliums via electrochemical oxidative C–N coupling","Green Chem.","2015","17","9","4669","","10.1039/C5GC01142F","","","0.71073","MoKα","","0.0714","0.0499","","","0.1221","0.1362","","","","","","1.026","","","","has coordinates,has disorder","301865","2025-08-22","16:16:42",""
"7220980","8.5758","0.0006","10.4878","0.0007","12.8368","0.0008","75.32","0.002","78.092","0.002","74.019","0.002","1062.06","0.12","100","","100","","","","","","","","","5","P -1","-P 1","2","","","","- C26 H20 B F4 N3 -","- C26 H20 B F4 N3 -","- C52 H40 B2 F8 N6 -","2","1","","de Robillard, Guillaume; Makni, Oumayma; Cattey, Hélène; Andrieu, Jacques; Devillers, Charles H.","Towards sustainable synthesis of pyren-1-yl azoliums via electrochemical oxidative C–N coupling","Green Chem.","2015","17","9","4669","","10.1039/C5GC01142F","","","0.71073","MoKα","","0.0506","0.0379","","","0.0934","0.1019","","","","","","1.033","","","","has coordinates","301865","2025-08-22","16:16:42",""
"7221692","7.668","0.0005","8.3022","0.0006","13.5405","0.0006","83.606","0.005","81.922","0.005","70.403","0.006","802.11","0.09","150","2","150","2","","","","","","","","6","P -1","-P 1","2","","","","- C15 H14 Cl2 N2 O2 Ru -","- C15 H14 Cl2 N2 O2 Ru -","- C30 H28 Cl4 N4 O4 Ru2 -","2","1","","Gupta, Kavita; Tyagi, Deepika; Dwivedi, Ambikesh D.; Mobin, Shaikh M.; Singh, Sanjay K.","Catalytic transformation of bio-derived furans to valuable ketoacids and diketones by water-soluble ruthenium catalysts","Green Chem.","2015","17","9","4618","","10.1039/C5GC01376C","","","1.5418","CuKα","","0.0493","0.0489","","","0.1363","0.1368","","","","","","1.093","","","","has coordinates","162006","2020-10-21","18:00:00",""
"7221693","17.072","0.0002","12.3086","0.0001","9.1013","0.0001","90","","100.9","0.001","90","","1877.97","0.03","150","2","150","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H22 Cl2 N2 Ru -","- C19 H22 Cl2 N2 Ru -","- C76 H88 Cl8 N8 Ru4 -","4","1","","Gupta, Kavita; Tyagi, Deepika; Dwivedi, Ambikesh D.; Mobin, Shaikh M.; Singh, Sanjay K.","Catalytic transformation of bio-derived furans to valuable ketoacids and diketones by water-soluble ruthenium catalysts","Green Chem.","2015","17","9","4618","","10.1039/C5GC01376C","","","1.5418","CuKα","","0.0271","0.0267","","","0.0705","0.0709","","","","","","1.057","","","","has coordinates","176428","2020-10-21","18:00:00",""
"7221876","12.242","0.002","11.566","0.002","10.526","0.002","90","","93.08","0.03","90","","1488.2","0.5","295","2","295","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H11 N O2 S -","- C19 H11 N O2 S -","- C76 H44 N4 O8 S4 -","4","1","","Wan, Jie-Ping; Zhou, Youyi; Liu, Yunyun; Sheng, Shouri","Metal-free oxidative carbonylation on enaminone CC bond for the cascade synthesis of benzothiazole-containing vicinal diketones","Green Chem.","2016","18","2","402","","10.1039/C5GC01821H","","","0.71073","MoKα","","0.0543","0.0389","","","0.0961","0.1126","","","","","","1.138","","","","has coordinates","301865","2025-08-22","16:16:44",""
"7221978","10.6016","0.0004","9.5305","0.0004","10.7702","0.0005","90","","119.312","0.004","90","","948.88","0.08","110","2","110","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","5-hydroxy-1,3-dioxan-2-one","","- C4 H6 O4 -","- C4 H6 O4 -","- C32 H48 O32 -","8","2","","Tryznowski, M.; Żołek-Tryznowska, Z.; Świderska, A.; Parzuchowski, P. G.","Synthesis, characterization and reactivity of a six-membered cyclic glycerol carbonate bearing a free hydroxyl group","Green Chem.","2016","18","3","802","","10.1039/C5GC01688F","","","0.71073","MoKα","","0.0294","0.027","","","0.0747","0.0756","","","","","","1.07","","","","has coordinates","301865","2025-08-22","16:16:45",""
"7222111","9.384","0.002","10.484","0.002","11.281","0.002","102.829","0.017","94.191","0.018","113.456","0.018","976.4","0.4","298","2","298","2","","","","","","","","4","P -1","-P 1","2","","","","- C18 H31 N O4 -","- C18 H31 N O4 -","- C36 H62 N2 O8 -","2","1","","Maleki, Abbas; Nematollahi, Davood; Rasouli, Fereshteh; Zeinodini-Meimand, Azam","Electrode instead of catalyst and enzyme. A greener protocol for the synthesis of new 2-hydroxyacetamide derivatives containing a γ-lactone ring","Green Chem.","2016","18","3","672","","10.1039/C5GC01863C","","","0.71073","MoKα","","0.1106","0.0744","","","0.188","0.2092","","","","","","1.127","","","","has coordinates","301865","2025-08-22","16:16:45",""
"7222112","23.0884","0.0007","10.4956","0.0004","7.3329","0.0002","90","","90","","90","","1776.96","0.1","100","2","100","","","","","","","","","3","P n a 21","P 2c -2n","33","","","","- C19 H20 O6 -","- C19 H20 O6 -","- C76 H80 O24 -","4","1","","Wang, Zhihan; Kastern, Brent; Randazzo, Katelyn; Ugrinov, Angel; Butz, Jonathan; Seals, David W.; Sibi, Mukund P.; Chu, Qianli R.","Linear polyester synthesized from furfural-based monomer by photoreaction in sunlight","Green Chem.","2015","17","10","4720","","10.1039/C5GC01783A","","","1.54178","CuKα","","0.0366","0.0315","","","0.0791","0.0818","","","","","","1.029","","","","has coordinates","301865","2025-08-22","16:16:45",""
"7222113","22.9356","0.0009","10.4908","0.0004","7.3765","0.0003","90","","90","","90","","1774.88","0.12","100","2","100","2","","","","","","","","3","P n a 21","P 2c -2n","33","","","","- C19 H20 O6 -","- C19 H20 O6 -","- C76 H80 O24 -","4","1","","Wang, Zhihan; Kastern, Brent; Randazzo, Katelyn; Ugrinov, Angel; Butz, Jonathan; Seals, David W.; Sibi, Mukund P.; Chu, Qianli R.","Linear polyester synthesized from furfural-based monomer by photoreaction in sunlight","Green Chem.","2015","17","10","4720","","10.1039/C5GC01783A","","","0.71073","MoKα","","0.0718","0.0535","","","0.1151","0.1229","","","","","","1.092","","","","has coordinates,has disorder","161996","2020-10-21","18:00:00",""
"7222916","8.5224","0.0004","10.305","0.0005","9.1442","0.0004","90","","90.3404","0.0011","90","","803.06","0.06","120","2","120","","","","","","","","","5","P 1 21 1","P 2yb","4","","(S)-methyl 3-fluoro-2-oxopiperidine-3-carboxylate","","- C7 H10 F N O3 -","- C7 H10 F N O3 -","- C28 H40 F4 N4 O12 -","4","2","","Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham","Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy","Green Chem.","2016","18","5","1313","","10.1039/C5GC02209F","","x-ray","1.54178","CuKα","","0.0547","0.0547","","","0.152","0.152","","","","","","1.005","","","","has coordinates","301865","2025-08-22","16:16:47",""
"7222917","8.5211","0.0003","10.3039","0.0003","9.1547","0.0003","90","","90.365","0.0008","90","","803.77","0.05","120","0.2","120","","","","","","","","","5","P 1 21 1","P 2yb","4","","(R)-methyl 3-fluoro-2-oxopiperidine-3-carboxylate","","- C7 H10 F N O3 -","- C7 H10 F N O3 -","- C28 H40 F4 N4 O12 -","4","2","","Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham","Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy","Green Chem.","2016","18","5","1313","","10.1039/C5GC02209F","","x-ray","1.54178","CuKα","","0.0515","0.0513","","","0.1451","0.1455","","","","","","1.103","","","","has coordinates","301865","2025-08-22","16:16:47",""
"7222918","5.821","0.0004","6.4875","0.0005","15.7485","0.0012","100.738","0.007","96.625","0.006","94.612","0.006","577.23","0.08","120","","120","","","","","","","","","6","P -1","-P 1","2","","dimethyl (2-aminopropyl)fluoromalonate hydrochloride","","- C8 H15 Cl F N O4 -","- C8 H15 Cl F N O4 -","- C16 H30 Cl2 F2 N2 O8 -","2","1","","Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham","Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy","Green Chem.","2016","18","5","1313","","10.1039/C5GC02209F","","x-ray","0.71073","MoKα","","0.0626","0.0521","","","0.124","0.1289","","","","","","1.165","","","","has coordinates","301865","2025-08-22","16:16:47",""
"7222919","12.256","0.0004","6.72544","0.00017","10.4787","0.0004","90","","113.193","0.004","90","","793.92","0.05","120","","120","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","(rac)-methyl 3-fluoro-2-oxopiperidine-3-carboxylate","","- C7 H10 F N O3 -","- C7 H10 F N O3 -","- C28 H40 F4 N4 O12 -","4","1","","Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham","Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy","Green Chem.","2016","18","5","1313","","10.1039/C5GC02209F","","","0.71073","MoKα","","0.041","0.0346","","","0.0902","0.0942","","","","","","1.028","","","","has coordinates","301865","2025-08-22","16:16:47",""
"7222920","12.235","0.0007","11.3068","0.0007","7.6415","0.0004","90","","100.289","0.0017","90","","1040.12","0.1","120","","120","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C7 H13 Cl F N O4 -","- C7 H13 Cl F N O4 -","- C28 H52 Cl4 F4 N4 O16 -","4","1","","Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham","Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy","Green Chem.","2016","18","5","1313","","10.1039/C5GC02209F","","x-ray","0.71073","MoKα","","0.0384","0.0341","","","0.0846","0.0873","","","","","","1.097","","","","has coordinates","301865","2025-08-22","16:16:47",""
"7222921","6.5648","0.0007","6.6759","0.0007","9.6206","0.001","98.163","0.003","100.929","0.003","101.047","0.003","399.3","0.07","120","","120","","","","","","","","","5","P -1","-P 1","2","","methyl 3-fluoro-2-oxo-3-pyrrolidinecarboxylate","","- C6 H10 F N O4 -","- C6 H10 F N O4 -","- C12 H20 F2 N2 O8 -","2","1","","Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham","Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy","Green Chem.","2016","18","5","1313","","10.1039/C5GC02209F","","x-ray","0.71073","MoKα","","0.0671","0.0548","","","0.1404","0.1501","","","","","","1.012","","","","has coordinates","301865","2025-08-22","16:16:47",""
"7223202","14.6261","0.0006","23.2526","0.0009","15.7357","0.0007","90","","107.099","0.002","90","","5115.1","0.4","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","Cd-TCA-DMF","","","- C88 H72 Cd5 N6 O28 -","- C88 H72 Cd5 N6 O28 -","- C176 H144 Cd10 N12 O56 -","2","0.5","","Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo","Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry","Green Chem.","2016","18","4","951","","10.1039/C5GC02393A","","","0.71073","MoKα","","0.0598","0.0487","","","0.1587","0.1717","","","","","","1.074","","","","has coordinates","177879","2020-10-21","18:00:00",""
"7223203","14.5196","0.0009","23.367","0.0014","15.6042","0.0009","90","","107.475","0.001","90","","5049.8","0.5","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","Cd-TCA-DEF","","","- C96 H82 Cd5 N8 O28 -","- C96 H82 Cd5 N8 O28 -","- C192 H164 Cd10 N16 O56 -","2","0.5","","Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo","Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry","Green Chem.","2016","18","4","951","","10.1039/C5GC02393A","","","0.71073","MoKα","","0.0587","0.0455","","","0.1473","0.1603","","","","","","1.083","","","","has coordinates","177879","2020-10-21","18:00:00",""
"7223204","14.3997","0.0019","23.362","0.003","15.543","0.003","90","","106.309","0.009","90","","5018.4","1.4","296","2","296","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","CuCd-TCA-DMF","","","- C88 H72 Cd3 Cu2 N6 O27 -","- C88 H64 Cd3 Cu2 N6 O27 -","- C176 H128 Cd6 Cu4 N12 O54 -","2","0.5","","Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo","Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry","Green Chem.","2016","18","4","951","","10.1039/C5GC02393A","","","0.71073","MoKα","","0.2185","0.1079","","","0.2595","0.2908","","","","","","1.318","","","","has coordinates","177879","2020-10-21","18:00:00",""
"7223205","14.583","0.0013","23.241","0.002","15.6338","0.0014","90","","106.99","0.002","90","","5067.4","0.8","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","1-CH3OH","","- C90 H76 Cd5 N6 O28 -","- C90 H76 Cd5 N6 O28 -","- C180 H152 Cd10 N12 O56 -","2","0.5","","Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo","Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry","Green Chem.","2016","18","4","951","","10.1039/C5GC02393A","","","0.71073","MoKα","","0.0801","0.0563","","","0.1619","0.1818","","","","","","1.071","","","","has coordinates","177879","2020-10-21","18:00:00",""
"7223248","19.13","0.03","26.34","0.04","11.628","0.017","90","","90.671","0.018","90","","5859","15","113","2","113","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C26 H16 N4 O8 Zn -","- C26 H16 N4 O8 Zn -","- C104 H64 N16 O32 Zn4 -","4","1","","Gong, Le Le; Feng, Xue Feng; Luo, Feng; Yi, Xian Feng; Zheng, An Min","Removal and safe reuse of highly toxic allyl alcohol using a highly selective photo-sensitive metal‒organic framework","Green Chem.","2016","18","7","2047","","10.1039/C5GC02182K","","","0.71073","MoKα","","0.1668","0.1219","","","0.3075","0.3337","","","","","","1.021","","","","has coordinates","181748","2020-10-21","18:00:00",""
"7223249","8.8542","0.0003","12.9976","0.0004","14.0901","0.0005","100.076","0.001","90.969","0.001","92.406","0.001","1594.63","0.09","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","1, 3-Bis(2-diphenylphosphino-3-methylimidazolyl)benzene","","- C36 H28 N4 P2 -","- C36 H28 N4 P2 -","- C72 H56 N8 P4 -","2","1","","Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye","Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation–acetalization of olefins","Green Chem.","2016","18","6","1798","","10.1039/C5GC02127H","","","0.71073","MoKα","","0.0629","0.0478","","","0.1334","0.1432","","","","","","1.063","","","","has coordinates","301865","2025-08-22","16:16:48",""
"7223250","14.0858","0.0011","14.4866","0.0011","15.7112","0.0012","67.615","0.002","78.55","0.002","62.44","0.002","2627","0.4","173","2","173","2","","","","","","","","7","P -1","-P 1","2","","1,3-Bis(1-methyl-2-diphenylphosphino-3-methylimidazolium)benzene triflate","","- C40 H34 F6 N4 O6 P2 S2 -","- C40 H34 F6 N4 O6 P2 S2 -","- C80 H68 F12 N8 O12 P4 S4 -","2","1","","Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye","Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation–acetalization of olefins","Green Chem.","2016","18","6","1798","","10.1039/C5GC02127H","","","0.71073","MoKα","","0.0763","0.0615","","","0.1803","0.1903","","","","","","1.109","","","","has coordinates","301865","2025-08-22","16:16:48",""
"7223251","9.5438","0.0007","39.836","0.003","10.6814","0.0011","90","","116.464","0.003","90","","3635.4","0.5","173","2","173","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C38 H33 Cl2 I N4 P2 -","- C38 H33 Cl2 I N4 P2 -","- C152 H132 Cl8 I4 N16 P8 -","4","1","","Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye","Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation–acetalization of olefins","Green Chem.","2016","18","6","1798","","10.1039/C5GC02127H","","","0.71073","MoKα","","0.1053","0.0564","","","0.1048","0.1233","","","","","","1.049","","","","has coordinates","301865","2025-08-22","16:16:48",""
"7223441","9.0471","0.0006","17.5709","0.0011","12.943","0.0008","90","","109.25","0.001","90","","1942.5","0.2","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C23 H26 N2 O2 -","- C23 H26 N2 O2 -","- C92 H104 N8 O8 -","4","1","","Harvey, Benjamin G.; Guenthner, Andrew J.; Koontz, Thomas A.; Storch, Perrin J.; Reams, Josiah T.; Groshens, Thomas J.","Sustainable hydrophobic thermosetting resins and polycarbonates from turpentine","Green Chem.","2016","18","8","2416","","10.1039/C5GC02893K","","","0.71073","","","0.0643","0.0495","","","0.1262","0.1367","","","","","","1.035","","","","has coordinates","301865","2025-08-22","16:16:49",""
"7223442","9.0258","0.0009","11.0099","0.001","12.4506","0.0012","79.449","0.004","76.11","0.004","80.803","0.003","1172","0.2","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C28 H24 N2 O3 S -","- C28 H24 N2 O3 S -","- C56 H48 N4 O6 S2 -","2","1","","Dandia, Anshu; Parewa, Vijay; Kumari, Sukhbeer; Bansal, Sarika; Sharma, Amit","Imposed hydrophobic interactions by NaCl: accountable attribute for the synthesis of spiro[acenaphthylene-1,5′-pyrrolo[1,2-c]thiazole] derivatives via 1,3-dipolar cycloaddition reaction in aqueous medium","Green Chem.","2016","18","8","2488","","10.1039/C5GC02816G","","","0.71073","MoKα","","0.0756","0.0496","","","0.14","0.1625","","","","","","1.068","","","","has coordinates","301865","2025-08-22","16:16:49",""
"7223600","11.443","0.002","12.452","0.003","15.01","0.003","71.585","0.01","84.083","0.01","68.386","0.01","1886.3","0.7","100","","100","","","","","","","","","7","P -1","-P 1","2","","","","- C38 H48 Cl Cu N4 O S2 -","- C38 H48 Cl Cu N4 O S2 -","- C76 H96 Cl2 Cu2 N8 O2 S4 -","2","1","","Barman, Milan Kr.; Sinha, Ashish Kumar; Nembenna, Sharanappa","An efficient and recyclable thiourea-supported copper(i) chloride catalyst for azide‒alkyne cycloaddition reactions","Green Chem.","2016","18","8","2534","","10.1039/C5GC02545A","","","0.71069","MoKα","","0.0516","0.037","","","0.0919","0.1012","","","","","","1.018","","","","has coordinates","182761","2020-10-21","18:00:00",""
"7223770","28.525","","29.966","","14.784","","90","","109.02","","90","","11947.1","","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C75 H47 N5 O9 Zn2 -","- C75 H47 N5 O9 Zn2 -","- C600 H376 N40 O72 Zn16 -","8","1","","Liu, Yue; Chen, Dashu; Li, Xingyu; Yu, Ziyang; Xia, Qiansu; Liang, Desheng; Xing, Hongzhu","Visible-light-induced controlled radical polymerization of methacrylates mediated by a pillared-layer metal‒organic framework","Green Chem.","2016","18","6","1475","","10.1039/C5GC02620B","","","0.71073","MoKα","","0.226","0.1421","","","0.3663","0.4121","","","","","","1.085","","","","has coordinates","181751","2020-10-21","18:00:00",""
"7223872","9.7748","0.001","36.406","0.003","6.5704","0.0006","90","","90","","90","","2338.2","0.4","293","2","293","2","","","","","","","","4","P 21 21 2","P 2 2ab","18","","","","- C26 H34 O3 S -","- C26 H34 O3 S -","- C104 H136 O12 S4 -","4","1","","Huang, Mingming; Hu, Liangzhen; Shen, Hang; Liu, Qing; Hussain, Muhammad Ijaz; Pan, Jing; Xiong, Yan","Sulfination of alcohols with sodium sulfinates promoted by BF3·OEt2: an unexpected access","Green Chem.","2016","18","7","1874","","10.1039/C5GC02846A","","","0.71073","MoKα","","0.0657","0.0566","","","0.1607","0.1695","","","","","","1.097","","","","has coordinates","301865","2025-08-22","16:16:50",""
"7224061","8.4061","0.0012","8.6026","0.0012","12.582","0.002","91.647","0.005","102.618","0.005","112.149","0.004","816.1","0.2","0","2","0","2","","","","","","","","3","P -1","-P 1","2","","","","- C20 H22 O -","- C20 H22 O -","- C40 H44 O2 -","2","1","","Wang, Kuai; Meng, Ling-Guo; Zhang, Qi; Wang, Lei","Direct construction of 4-aryl tetralones via visible-light-induced cyclization of styrenes with molecular oxygen","Green Chem.","2016","18","9","2864","","10.1039/C5GC02550H","","","0.71073","MoKα","","0.0642","0.0568","","","0.1689","0.182","","","","","","0.999","","","","has coordinates","301865","2025-08-22","16:16:50",""
"7224113","7.5292","0.0005","5.7936","0.0003","13.9668","0.0009","90","","93.766","0.004","90","","607.93","0.06","293","2","293","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C14 H14 N2 O2 -","- C14 H14 N2 O2 -","- C28 H28 N4 O4 -","2","1","","Chaudhary, Priyanka; Gupta, Surabhi; Muniyappan, Nalluchamy; Sabiah, Shahulhameed; Kandasamy, Jeyakumar","An efficient synthesis of N-nitrosamines under solvent, metal and acid free conditions using tert-butyl nitrite","Green Chem.","2016","18","8","2323","","10.1039/C5GC02880A","","","0.71073","MoKα","","0.0381","0.0299","","","0.0652","0.0712","","","","","","1.046","","","","has coordinates","301865","2025-08-22","16:16:51",""
"7224294","13.0361","0.0007","12.7404","0.0008","20.0773","0.0016","90","","94.398","0.002","90","","3324.7","0.4","130","2","130","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","pdbpn","pdbpn","","- C18 H13 Cl N4 O Pd -","- C18 H13 Cl N4 O Pd -","- C144 H104 Cl8 N32 O8 Pd8 -","8","2","","Arumugam, Vignesh; Kaminsky, Werner; Nallasamy, Dharmaraj","Pd(ii) pincer type complex catalyzed tandem C‒H and N‒H activation of acetanilide in aqueous media: a concise access to functionalized carbazoles in a single step","Green Chem.","2016","18","11","3295","","10.1039/C5GC02937F","","","0.71073","MoKα","","0.1934","0.0553","","","0.0944","0.1258","","","","","","0.846","","","","has coordinates,has disorder","183714","2020-10-21","18:00:00",""
"7224295","18.2644","0.0011","9.0854","0.0006","19.045","0.0011","90","","90","","90","","3160.3","0.3","296","2","296","2","","","","","","","","6","P n a 21","P 2c -2n","33","pdsnah","pdsnah","","- C17 H12 Cl N3 O2 Pd -","- C17 H12 Cl N3 O2 Pd -","- C136 H96 Cl8 N24 O16 Pd8 -","8","2","","Arumugam, Vignesh; Kaminsky, Werner; Nallasamy, Dharmaraj","Pd(ii) pincer type complex catalyzed tandem C‒H and N‒H activation of acetanilide in aqueous media: a concise access to functionalized carbazoles in a single step","Green Chem.","2016","18","11","3295","","10.1039/C5GC02937F","","","0.71073","MoKα","","0.0322","0.0271","","","0.0575","0.0595","","","","","","1.024","","","","has coordinates","183714","2020-10-21","18:00:00",""
"7224493","12.247","0.009","13.34","0.02","8.315","0.008","90","","77.29","0.05","90","","1325","3","","","","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","1-pyrenyl thiourea","","- C17 H12 N2 S -","- C17 H12 N2 S -","- C68 H48 N8 S4 -","4","1","","Đud, Mateja; Magdysyuk, Oxana V.; Margetić, Davor; Štrukil, Vjekoslav","Synthesis of monosubstituted thioureas by vapour digestion and mechanochemical amination of thiocarbamoyl benzotriazoles","Green Chem.","2016","18","9","2666","","10.1039/C6GC00089D","","","0.23307","","","","","","","","","","","","","","","","","","has coordinates","301865","2025-08-22","16:16:52",""
"7224494","5.873","0.004","9.367","0.004","22.93","0.009","91.31","0.03","90","","90","","1261.1","1.1","25","2","","","","","","","","","","4","P 21/c 1 1","-P 2xac","14","","1-anthracenyl thiourea","","- C15 H12 N2 S -","- C15 H12 N2 S -","- C60 H48 N8 S4 -","4","1","","Đud, Mateja; Magdysyuk, Oxana V.; Margetić, Davor; Štrukil, Vjekoslav","Synthesis of monosubstituted thioureas by vapour digestion and mechanochemical amination of thiocarbamoyl benzotriazoles","Green Chem.","2016","18","9","2666","","10.1039/C6GC00089D","","","0.23307","","","","","","","","","","","","","","","","","","has coordinates","301865","2025-08-22","16:16:52",""
"7224566","9.9263","0.0003","15.4568","0.0005","12.4445","0.0004","90","","96.737","0.003","90","","1896.16","0.1","173","2","173","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H21 N5 O4 -","- C20 H21 N5 O4 -","- C80 H84 N20 O16 -","4","1","","Zhang, Xiaofeng; Zhi, Sanjun; Wang, Wei; Liu, Shuai; Jasinski, Jerry P.; Zhang, Wei","A pot-economical and diastereoselective synthesis involving catalyst-free click reaction for fused-triazolobenzodiazepines","Green Chem.","2016","18","9","2642","","10.1039/C6GC00497K","","","1.54184","CuKα","","0.0457","0.0416","","","0.1093","0.1141","","","","","","1.043","","","","has coordinates","301865","2025-08-22","16:16:52",""
"7224593","8.747","0.004","11.406","0.005","16.58","0.006","80.72","0.03","85.21","0.03","85.46","0.04","1623.2","1.2","150","2","150","2","","","","","","","","5","P -1","-P 1","2","","","","- C19 H16 F N O4 -","- C19 H16 F N O4 -","- C76 H64 F4 N4 O16 -","4","2","","Ahankar, Hamideh; Ramazani, Ali; Ślepokura, Katarzyna; Lis, Tadeusz; Joo, Sang Woo","Synthesis of pyrrolidinone derivatives from aniline, an aldehyde and diethyl acetylenedicarboxylate in an ethanolic citric acid solution under ultrasound irradiation","Green Chem.","2016","18","12","3582","","10.1039/C6GC00157B","","","0.71073","MoKα","","0.1212","0.0678","","","0.1539","0.1707","","","","","","1.004","","","","has coordinates","301865","2025-08-22","16:16:52",""
"7224743","23.7419","0.0009","8.0217","0.0003","31.6881","0.0009","90","","127.152","0.002","90","","4810.1","0.3","298","2","298","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C25 H25 N O9 -","- C25 H25 N O9 -","- C200 H200 N8 O72 -","8","2","","Samai, Subhasis; Ghosh, Debasish; Das, Uttam K.; Atta, Sanghamitra; Manna, Saikat K.; Maiti, Dilip K.","Water – the best solvent for DMAP-mediated dual cyclization towards metal-free first synthesis of fully substituted phthalimides","Green Chem.","2016","18","10","2961","","10.1039/C6GC00367B","","","0.71073","MoKα","","0.0671","0.0506","","","0.1259","0.1408","","","","","","1.024","","","","has coordinates","301865","2025-08-22","16:16:52",""
"7224744","8.133","0.003","11.671","0.004","11.708","0.003","63.061","0.014","84.432","0.014","75.914","0.014","960.8","0.6","298","2","298","2","","","","","","","","4","P -1","-P 1","2","","","","- C21 H17 N O8 -","- C21 H17 N O8 -","- C42 H34 N2 O16 -","2","1","","Samai, Subhasis; Ghosh, Debasish; Das, Uttam K.; Atta, Sanghamitra; Manna, Saikat K.; Maiti, Dilip K.","Water – the best solvent for DMAP-mediated dual cyclization towards metal-free first synthesis of fully substituted phthalimides","Green Chem.","2016","18","10","2961","","10.1039/C6GC00367B","","","0.71073","MoKα","","0.0498","0.0405","","","0.1108","0.12","","","","","","1.026","","","","has coordinates","301865","2025-08-22","16:16:52",""
"7225073","10.815","0.002","19.201","0.004","7.858","0.0016","90","","104.8","0.03","90","","1577.6","0.6","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C20 H22 N2 -","- C20 H22 N2 -","- C80 H88 N8 -","4","1","","Cai, Jinhui; Li, Feifei; Deng, Guo-Jun; Ji, Xiaochen; Huang, Huawen","The cyclopropylimine rearrangement/Povarov reaction cascade for the assembly of pyrrolo[3,2-c]quinoline derivatives","Green Chem.","2016","18","12","3503","","10.1039/C6GC00779A","","","0.71073","MoKα","","0.1286","0.076","","","0.2097","0.2812","","","","","","1.149","","","","has coordinates","301865","2025-08-22","16:16:53",""
"7225077","15.4558","0.0007","18.7716","0.001","26.327","0.0012","90","","90","","90","","7638.3","0.6","294.3","0.5","294.3","0.5","","","","","","","","4","P b c n","-P 2n 2ab","60","","","","- C20 H21 N4 O2.5 -","- C20 H21 N4 O2.5 -","- C320 H336 N64 O40 -","16","2","","Singh, Nongthombam Geetmani; Lily, Makroni; Devi, Shougaijam Premila; Rahman, Noimur; Ahmed, Aziz; Chandra, Asit K.; Nongkhlaw, Rishanlang","Synthetic, mechanistic and kinetic studies on the organo-nanocatalyzed synthesis of oxygen and nitrogen containing spiro compounds under ultrasonic conditions","Green Chem.","2016","18","15","4216","","10.1039/C6GC00724D","","","0.71073","MoKα","","0.0955","0.0561","","","0.1147","0.1366","","","","","","1.0392","","","","has coordinates","301865","2025-08-22","16:16:53",""
"7225078","10.3603","0.0015","13.054","0.002","14.655","0.003","75.239","0.015","84.652","0.014","69.915","0.014","1800","0.6","291.6","0.2","291.6","0.2","","","","","","","","4","P -1","-P 1","2","Spirooxindole","2'-amino-2,5'-dioxo-5'H-spiro[indoline-3,4'-pyrano[3,2-c]chromene]-3'-carbonitrile","","- C20 H11 N3 O4 -","- C20 H11 N3 O4 -","- C80 H44 N12 O16 -","4","2","","Singh, Nongthombam Geetmani; Lily, Makroni; Devi, Shougaijam Premila; Rahman, Noimur; Ahmed, Aziz; Chandra, Asit K.; Nongkhlaw, Rishanlang","Synthetic, mechanistic and kinetic studies on the organo-nanocatalyzed synthesis of oxygen and nitrogen containing spiro compounds under ultrasonic conditions","Green Chem.","2016","18","15","4216","","10.1039/C6GC00724D","","x-ray","0.71073","MoKα","","0.1796","0.0942","","","0.2287","0.2954","","","","","","0.9953","","","","has coordinates","301865","2025-08-22","16:16:53",""
"7225170","28.6573","0.0003","28.6573","0.0003","28.6573","0.0003","90","","90","","90","","23534.5","0.4","293","2","293","2","","","","","","","","5","I m -3","-I 2 2 3","204","","","","- C50 H68 N14 O16 Zn2 -","- C35 H28 N9 O9 Zn2 -","- C420 H336 N108 O108 Zn24 -","12","0.25","","Han, Yun-Hu; Zhou, Zhong-Yuan; Tian, Chong-Bin; Du, Shao-Wu","A dual-walled cage MOF as an efficient heterogeneous catalyst for the conversion of CO2under mild and co-catalyst free conditions","Green Chem.","2016","18","14","4086","","10.1039/C6GC00413J","","","0.71073","MoKα","","0.0738","0.0726","","","0.2318","0.2349","","","","","","1.302","","","","has coordinates","185559","2020-10-21","18:00:00",""
"7225274","11.725","0.002","17.259","0.003","16.041","0.003","90","","90.789","0.009","90","","3245.8","1","293","2","293","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C19 H21 N3 O -","- C19 H21 N3 O -","- C152 H168 N24 O8 -","8","1","","Lezana, Nicolás; Matus-Pérez, Massiel; Galdámez, Antonio; Lühr, Susan; Vilches-Herrera, Marcelo","Highly stereoselective and catalyst-free synthesis of annulated tetrahydropyridines by intramolecular imino-Diels–Alder reaction under microwave irradiation in water","Green Chem.","2016","18","13","3712","","10.1039/C6GC00912C","","","0.71073","MoKα","","0.106","0.0982","","","0.2434","0.2486","","","","","","1.123","","","","has coordinates","301865","2025-08-22","16:16:53",""
"7225275","13.61","0.003","15.446","0.003","15.506","0.003","98.661","0.003","107.06","0.002","112.68","0.003","2743.8","1","223","2","223","2","","","","","","","","5","P -1","-P 1","2","","","","- C55 H81 N2 Nd O5 -","- C55 H81 N2 Nd O5 -","- C110 H162 N4 Nd2 O10 -","2","1","","Qin, Jie; Xu, Bin; Zhang, Yong; Yuan, Dan; Yao, Yingming","Cooperative rare earth metal–zinc based heterometallic catalysts for copolymerization of CO2and cyclohexene oxide","Green Chem.","2016","18","15","4270","","10.1039/C6GC00511J","","","0.71075","MoKα","","0.0811","0.0672","","","0.1283","0.1376","","","","","","1.121","","","","has coordinates,has disorder","301865","2025-08-22","16:16:54",""
"7225276","15.2272","0.0013","14.1936","0.0011","24.434","0.002","90","","99.252","0.002","90","","5212.2","0.7","223","2","223","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C55 H79 N2 O4 Y -","- C55 H79 N2 O4 Y -","- C220 H316 N8 O16 Y4 -","4","1","","Qin, Jie; Xu, Bin; Zhang, Yong; Yuan, Dan; Yao, Yingming","Cooperative rare earth metal–zinc based heterometallic catalysts for copolymerization of CO2and cyclohexene oxide","Green Chem.","2016","18","15","4270","","10.1039/C6GC00511J","","","0.71075","MoKα","","0.1297","0.0851","","","0.1648","0.189","","","","","","1.056","","","","has coordinates,has disorder","301865","2025-08-22","16:16:54",""
"7225277","25.713","0.003","25.211","0.003","25.54","0.003","90","","115.838","0.003","90","","14901","3","223","2","223","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C142 H214 N4 Nd2 O10 Zn -","- C142 H124 N4 Nd2 O10 Zn -","- C568 H496 N16 Nd8 O40 Zn4 -","4","0.5","","Qin, Jie; Xu, Bin; Zhang, Yong; Yuan, Dan; Yao, Yingming","Cooperative rare earth metal‒zinc based heterometallic catalysts for copolymerization of CO2and cyclohexene oxide","Green Chem.","2016","18","15","4270","","10.1039/C6GC00511J","","","0.71075","MoKα","","0.099","0.0813","","","0.2179","0.2378","","","","","","1.069","","","","has coordinates,has disorder","185556","2020-10-21","18:00:00",""
"7225288","8.6729","0.0015","11.3034","0.0019","13.751","0.002","85.039","0.003","74.421","0.003","78.507","0.003","1271.7","0.4","293","","293","","","","","","","","","7","P -1","-P 1","2","","","","- C18 H33 B2 F8 Ir N4 O2 -","- C18 H33 B2 F8 Ir N4 O2 -","- C36 H66 B4 F16 Ir2 N8 O4 -","2","1","","Lu, Sheng-Mei; Wang, Zhijun; Li, Jun; Xiao, Jianliang; Li, Can","Base-free hydrogenation of CO2to formic acid in water with an iridium complex bearing a N,N′-diimine ligand","Green Chem.","2016","18","16","4553","","10.1039/C6GC00856A","","","0.71073","MoKα","","0.068","0.0486","","","0.1202","0.1312","","","","","","1.021","","","","has coordinates,has disorder","186446","2020-10-21","18:00:00",""
"7225401","10.6927","0.0002","7.81215","0.00015","10.6458","0.0002","90","","95.5149","0.0018","90","","885.16","0.03","110.05","0.1","110.05","0.1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C10 H10 O5 -","- C10 H10 O5 -","- C40 H40 O20 -","4","1","","Bai, Yinjuan; De bruyn, Mario; Clark, James H.; Dodson, Jennifer R.; Farmer, Thomas J.; Honoré, Mathilde; Ingram, Ian D. V.; Naguib, Mohamed; Whitwood, Adrian C.; North, Michael","Ring opening metathesis polymerisation of a new bio-derived monomer from itaconic anhydride and furfuryl alcohol","Green Chem.","2016","18","14","3945","","10.1039/C6GC00623J","","x-ray","1.54184","CuKα","","0.0354","0.0328","","","0.0809","0.0832","","","","","","1.038","","","","has coordinates","301865","2025-08-22","16:16:54",""
"7225495","13.2486","0.0015","7.0891","0.0009","13.5496","0.0018","90","","114.155","0.004","90","","1161.2","0.3","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H11 N O -","- C15 H11 N O -","- C60 H44 N4 O4 -","4","1","","Shi, Qing; Li, Pinhua; Zhu, Xianjin; Wang, Lei","Decarboxylative/decarbonylative C3-acylation of indoles via photocatalysis: a simple and efficient route to 3-acylindoles","Green Chem.","2016","18","18","4916","","10.1039/C6GC00516K","","","0.71073","MoKα","","0.0744","0.0567","","","0.1437","0.1532","","","","","","1.101","","","","has coordinates","301865","2025-08-22","16:16:54",""
"7225644","9.5598","0.0006","9.6393","0.0007","18.0624","0.0012","75.207","0.006","81.884","0.006","72.871","0.006","1533.97","0.19","290.5","0.9","290.5","0.9","","","","","","","","4","P -1","-P 1","2","","","","- C17 H17 Br O2 -","- C17 H17 Br O2 -","- C68 H68 Br4 O8 -","4","2","","Chen, Dao-Qian; Guo, Chun-Huan; Zhang, Heng-Rui; Jin, Dong-Po; Li, Xue-Song; Gao, Pin; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min","A metal-free transformation of alkynes to carbonyls directed by remote OH group","Green Chem.","2016","18","15","4176","","10.1039/C6GC01141A","","x-ray","0.71","MoKα","","0.0911","0.0673","","","0.1682","0.1845","","","","","","1.05","","","","has coordinates","301865","2025-08-22","16:16:54",""
"7225655","10.392","0.0011","15.7128","0.0016","9.0091","0.001","90","","102.556","0.003","90","","1435.9","0.3","296","2","296","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C16 H8 F3 I N0 O2 -","- C16 H8 F3 I O2 -","- C64 H32 F12 I4 O8 -","4","1","","Ni, Shengyang; Cao, Jia; Mei, Haibo; Han, Jianlin; Li, Shuhua; Pan, Yi","Sunlight-promoted cyclization versus decarboxylation in the reaction of alkynoates with N-iodosuccinimide: easy access to 3-iodocoumarins","Green Chem.","2016","18","14","3935","","10.1039/C6GC01027J","","","0.71073","MoKα","","0.0402","0.0361","","","0.0996","0.1044","","","","","","1.075","","","","has coordinates","185560","2020-10-21","18:00:00",""
"7225779","7.1649","0.0011","7.1976","0.0011","25.276","0.004","92.384","0.003","92.571","0.003","90.05","0.003","1301","0.3","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C17 H12 O2 -","- C17 H12 O2 -","- C68 H48 O8 -","4","2","","Zhang, Wen-Zhen; Yang, Ming-Wang; Lu, Xiao-Bing","Carboxylative cyclization of substituted propenyl ketones using CO2: transition-metal-free synthesis of α-pyrones","Green Chem.","2016","18","15","4181","","10.1039/C6GC01346E","","","0.71073","MoKα","","0.0921","0.0817","","","0.251","0.2593","","","","","","1.059","","","","has coordinates","301865","2025-08-22","16:16:55",""
"7225883","12.9435","0.0017","13.19","0.0016","17.35","0.002","90","","96.085","0.002","90","","2945.4","0.6","93","","93","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C32 H27 Br Cl3 O P -","- C32 H27 Br Cl3 O P -","- C128 H108 Br4 Cl12 O4 P4 -","4","1","","Liu, Shiyao; Suematsu, Naoki; Maruoka, Keiji; Shirakawa, Seiji","Design of bifunctional quaternary phosphonium salt catalysts for CO2fixation reaction with epoxides under mild conditions","Green Chem.","2016","18","17","4611","","10.1039/C6GC01630H","","","0.71075","MoKα","","0.0311","0.0253","","","0.0543","0.0567","","","","","","1.039","","","","has coordinates","301865","2025-08-22","16:17:03",""
"7225884","8.8686","0.0003","6.9699","0.0003","27.0903","0.001","90","","98.69","0.003","90","","1655.32","0.11","294.9","0.3","294.9","0.3","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C22 H18 O2 -","- C22 H18 O2 -","- C88 H72 O8 -","4","1","","Zhang, Zhenbei; Sun, Qiangsheng; Xu, Daqian; Xia, Chungu; Sun, Wei","Direct halogenative dearomatization of 2-naphthols by NXS (X = Cl, Br) in water","Green Chem.","2016","18","20","5485","","10.1039/C6GC01673A","","x-ray","0.71073","MoKα","","0.0868","0.0545","","","0.1229","0.1434","","","","","","1.028","","","","has coordinates","301865","2025-08-22","16:17:03",""
"7225942","22.7475","0.0015","11.3014","0.0007","27.0251","0.0016","90","","104.181","0.006","90","","6735.9","0.7","120.02","0.16","120.02","0.16","","","","","","","","6","I 1 2/a 1","-I 2ya","15","","","","- C16 H13 Br Cl F3 N2 -","- C16 H13 Br Cl F3 N2 -","- C256 H208 Br16 Cl16 F48 N32 -","16","2","","Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N.","Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions","Green Chem.","2016","18","17","4623","","10.1039/C6GC01601D","","x-ray","0.71073","MoKα","","0.1118","0.066","","","0.1191","0.1368","","","","","","1.04","","","","has coordinates,has disorder","186448","2020-10-21","18:00:00",""
"7225943","16.4865","0.0009","10.7791","0.0005","13.0845","0.0008","90","","110.686","0.006","90","","2175.3","0.2","120","0.13","120","0.13","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C9 H10 Br I N2 -","- C9 H10 Br I N2 -","- C72 H80 Br8 I8 N16 -","8","1","","Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N.","Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions","Green Chem.","2016","18","17","4623","","10.1039/C6GC01601D","","x-ray","0.71073","MoKα","","0.0588","0.0432","","","0.0761","0.0819","","","","","","1.072","","","","has coordinates","301865","2025-08-22","16:17:03",""
"7225944","16.7925","0.0007","8.3062","0.0004","15.0809","0.0007","90","","108.294","0.005","90","","1997.2","0.17","120.01","0.1","120.01","0.1","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C9 H11 Br N2 -","- C9 H11 Br N2 -","- C72 H88 Br8 N16 -","8","1","","Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N.","Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions","Green Chem.","2016","18","17","4623","","10.1039/C6GC01601D","","","0.71073","MoKα","","0.0623","0.0442","","","0.0869","0.0961","","","","","","1.071","","","","has coordinates","301865","2025-08-22","16:17:03",""
"7225945","7.4282","0.0007","14.952","0.0014","8.9188","0.0007","90","","94.547","0.009","90","","987.46","0.15","120.01","0.1","120.01","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C9 H11 Br N2 -","- C9 H11 Br N2 -","- C36 H44 Br4 N8 -","4","1","","Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N.","Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions","Green Chem.","2016","18","17","4623","","10.1039/C6GC01601D","","x-ray","1.54184","CuKα","","0.0849","0.0686","","","0.174","0.1896","","","","","","1.086","","","","has coordinates","301865","2025-08-22","16:17:03",""
"7225946","3.9883","0.0006","17.853","0.002","11.2011","0.0012","90","","91.622","0.011","90","","797.23","0.17","120.01","0.16","120.01","0.16","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C8 H7 Br N2 -","- C8 H7 Br N2 -","- C32 H28 Br4 N8 -","4","1","","Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N.","Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions","Green Chem.","2016","18","17","4623","","10.1039/C6GC01601D","","x-ray","1.54184","CuKα","","0.0797","0.0667","","","0.173","0.1847","","","","","","1.06","","","","has coordinates","301865","2025-08-22","16:17:03",""
"7225947","6.0553","0.0004","14.8323","0.001","12.439","0.001","90","","103.295","0.008","90","","1087.25","0.14","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C8 H8 Br I N2 -","- C8 H8 Br I N2 -","- C32 H32 Br4 I4 N8 -","4","1","","Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N.","Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions","Green Chem.","2016","18","17","4623","","10.1039/C6GC01601D","","x-ray","0.71073","MoKα","","0.0602","0.0401","","","0.0692","0.0781","","","","","","1.03","","","","has coordinates","301865","2025-08-22","16:17:03",""
"7225948","11.0563","0.0012","11.1805","0.0012","12.0711","0.0012","98.874","0.009","103.353","0.009","103.781","0.009","1375","0.3","120","0.11","120","0.11","","","","","","","","6","P -1","-P 1","2","","","","- C12 H11 Br Cl F3 N2 -","- C12 H11 Br Cl F3 N2 -","- C48 H44 Br4 Cl4 F12 N8 -","4","2","","Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N.","Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions","Green Chem.","2016","18","17","4623","","10.1039/C6GC01601D","","x-ray","0.71073","MoKα","","0.1488","0.0758","","","0.1163","0.15","","","","","","1.025","","","","has coordinates","301865","2025-08-22","16:17:03",""
"7225949","12.0869","0.0014","8.1608","0.001","19.776","0.003","90","","102.192","0.012","90","","1906.7","0.4","120.01","0.15","120.01","0.15","","","","","","","","5","I 1 2/a 1","-I 2ya","15","","","","- C9 H6 Cl F3 N2 -","- C9 H6 Cl F3 N2 -","- C72 H48 Cl8 F24 N16 -","8","1","","Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N.","Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions","Green Chem.","2016","18","17","4623","","10.1039/C6GC01601D","","x-ray","0.71073","MoKα","","0.1075","0.0707","","","0.1274","0.1426","","","","","","1.091","","","","has coordinates","301865","2025-08-22","16:17:03",""
"7225950","24.304","0.002","24.304","0.002","6.8579","0.0005","90","","90","","120","","3508.1","0.5","119.99","0.14","119.99","0.14","","","","","","","","4","R -3","-R 3","148","","","","- C8 H7 N3 O2 -","- C8 H7 N3 O2 -","- C144 H126 N54 O36 -","18","","","Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; Willans, Charlotte E.; Nguyen, Bao N.","Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions","Green Chem.","2016","18","17","4623","","10.1039/C6GC01601D","","x-ray","0.71073","MoKα","","0.0713","0.052","","","0.1218","0.1324","","","","","","1.074","","","","has coordinates","301865","2025-08-22","16:17:03",""
"7226057","6.6884","0.0005","7.6318","0.0006","12.9438","0.0011","90","","100.414","0.002","90","","649.83","0.09","200","2","200","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","8 in manuscript","","","- C8 H8 O2 -","- C8 H8 O2 -","- C32 H32 O8 -","4","1","","Tšupova, Svetlana; Rominger, Frank; Rudolph, Matthias; Hashmi, A. Stephen K.","Synthesis of phenols from hydroxymethylfurfural (HMF)","Green Chem.","2016","18","21","5800","","10.1039/C6GC01622G","","","0.71073","MoKα","","0.0551","0.0421","","","0.1313","0.1366","","","","","","1.183","","","","has coordinates","301865","2025-08-22","16:17:03",""
"7226058","4.5985","0.0006","20.751","0.003","10.2612","0.0013","90","","91.893","0.003","90","","978.6","0.2","200","2","200","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","9 in manuscript","","","- C11 H14 O3 -","- C11 H14 O3 -","- C44 H56 O12 -","4","1","","Tšupova, Svetlana; Rominger, Frank; Rudolph, Matthias; Hashmi, A. Stephen K.","Synthesis of phenols from hydroxymethylfurfural (HMF)","Green Chem.","2016","18","21","5800","","10.1039/C6GC01622G","","","0.71073","MoKα","","0.0498","0.0417","","","0.1264","0.131","","","","","","1.206","","","","has coordinates","301865","2025-08-22","16:17:03",""
"7226098","7.8642","0.0008","4.0675","0.0003","14.5155","0.0013","90","","96.896","0.008","90","","460.96","0.07","120","2","120","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","dimethyl (2R,5S,E)-2,5-dihydroxyhex-3-enedioate","","- C8 H12 O6 -","- C8 H12 O6 -","- C16 H24 O12 -","2","0.5","","Sølvhøj, Amanda; Taarning, Esben; Madsen, Robert","Methyl vinyl glycolate as a diverse platform molecule","Green Chem.","2016","18","20","5448","","10.1039/C6GC01556E","","x-ray","1.54184","CuKα","","0.06","0.0553","","","0.1654","0.1685","","","","","","1.268","","","","has coordinates","301865","2025-08-22","16:17:03",""
"7226477","13.5515","0.0011","3.9004","0.0003","20.9865","0.0016","90","","94.725","0.004","90","","1105.5","0.15","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C13 H13 N3 O -","- C13 H13 N3 O -","- C52 H52 N12 O4 -","4","1","","Sousa, Ana Catarina; Piedade, M. Fátima M. M.; Martins, Lígia O.; Robalo, M. Paula","Eco-friendly synthesis of indo dyes mediated by a bacterial laccase","Green Chem.","2016","18","22","6063","","10.1039/C6GC02050J","","","0.71073","MoKα","","0.0603","0.0399","","","0.1021","0.1106","","","","","","1.043","","","","has coordinates","301865","2025-08-22","16:17:07",""
"7226516","15.7341","0.0018","19.19","0.002","8.3925","0.001","90","","90","","90","","2534","0.5","296","2","296","2","","","","","","","","5","P 21 21 2","P 2 2ab","18","","","","- C27 H18 N2 O7 Zn -","- C27 H18 N2 O7 Zn -","- C108 H72 N8 O28 Zn4 -","4","1","","Liu, Bo; Zhou, Hui-Fang; Guan, Zheng-Hui; Hou, Lei; Cui, Bin; Wang, Yao-Yu","Cleavage of a C‒C σ bond between two phenyl groups under mild conditions during the construction of Zn(ii) organic frameworks","Green Chem.","2016","18","20","5418","","10.1039/C6GC01686C","","","0.71073","MoKα","","0.1014","0.0702","","","0.1932","0.2214","","","","","","1.079","","","","has coordinates","188252","2020-10-21","18:00:00",""
"7226517","10.8088","0.0015","10.8088","0.0015","16.283","0.005","90","","90","","90","","1902.3","0.7","123","2","123","2","","","","","","","","5","P 4/m m m","-P 4 2","123","","","","- C28 H18 N2 O8 Zn2 -","- C28 H18 N2 O8 Zn2 -","- C28 H18 N2 O8 Zn2 -","1","0.0625","","Liu, Bo; Zhou, Hui-Fang; Guan, Zheng-Hui; Hou, Lei; Cui, Bin; Wang, Yao-Yu","Cleavage of a C‒C σ bond between two phenyl groups under mild conditions during the construction of Zn(ii) organic frameworks","Green Chem.","2016","18","20","5418","","10.1039/C6GC01686C","","","0.71073","MoKα","","0.0968","0.0863","","","0.2481","0.2583","","","","","","1.145","","","","has coordinates,has disorder","188252","2020-10-21","18:00:00",""
"7226602","18.7062","0.0012","8.1149","0.0005","28.815","0.002","90","","106.281","0.007","90","","4198.7","0.5","296","2","296","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C27 H22 N2 O -","- C27 H22 N2 O -","- C216 H176 N16 O8 -","8","1","","Mishra, Pawan K.; Verma, Akhilesh K.","Metal-free regioselective tandem synthesis of diversely substituted benzimidazo-fused polyheterocycles in aqueous medium","Green Chem.","2016","18","23","6367","","10.1039/C6GC02330D","","x-ray","0.71073","MoKα","","0.1113","0.0634","","","0.1215","0.1453","","","","","","1.06","","","","has coordinates","301865","2025-08-22","16:17:08",""
"7226670","9.5392","0.0007","12.9758","0.0009","13.6796","0.0009","95.066","0.006","96.544","0.006","107.057","0.006","1595","0.2","298","","298","2","","","","","","","","5","P -1","-P 1","2","","Ps Ai 1","","- C36.75 H35 Br N2 O -","- C36.75 H35 Br N2 O -","- C73.5 H70 Br2 N4 O2 -","2","1","","Sarkar, Piyali; Mukhopadhyay, Chhanda","The synthesis of new 8-imino-1-one acridine derivatives catalyzed by a calix[4]arene mono-acid core","Green Chem.","2016","18","24","6556","","10.1039/C6GC02144A","","x-ray","1.54184","CuKα","","0.0979","0.0696","","","0.193","0.2061","","","","","","1.149","","","","has coordinates","190220","2020-10-21","18:00:00",""
"7226726","14.697","0.003","6.6112","0.0011","17.826","0.003","90","","96.96","0.004","90","","1719.3","0.5","298","1","298","1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","(Z)-Diphenyl(styryl)phosphine sulfide","","- C20 H17 P S -","- C20 H17 P S -","- C80 H68 P4 S4 -","4","1","","Moglie, Yanina; González-Soria, María José; Martín-García, Iris; Radivoy, Gabriel; Alonso, Francisco","Catalyst- and solvent-free hydrophosphination and multicomponent hydrothiophosphination of alkenes and alkynes","Green Chem.","2016","18","18","4896","","10.1039/C6GC00903D","","","0.71073","MoKα","","0.0538","0.0395","","","0.097","0.1062","","","","","","1.028","","","","has coordinates","301865","2025-08-22","16:17:08",""
"7226727","5.719","0.0003","17.9432","0.001","9.0209","0.0005","90","","99.0333","0.0015","90","","914.22","0.09","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","(S)-[(4-Isopropylcyclohex-1-en-1-yl)methyl]diphenylphosphine oxide","","- C22 H27 O P -","- C22 H27 O P -","- C44 H54 O2 P2 -","2","1","","Moglie, Yanina; González-Soria, María José; Martín-García, Iris; Radivoy, Gabriel; Alonso, Francisco","Catalyst- and solvent-free hydrophosphination and multicomponent hydrothiophosphination of alkenes and alkynes","Green Chem.","2016","18","18","4896","","10.1039/C6GC00903D","","","1.54178","CuKα","","0.0308","0.0305","","","0.0741","0.0744","","","","","","1.123","","","","has coordinates","301865","2025-08-22","16:17:08",""
"7226749","7.3261","0.0005","20.1659","0.0012","13.1676","0.0008","90","","102.555","0.007","90","","1898.8","0.2","100.01","0.1","100.01","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","3-(2-methoxypyridin-3-yl)-1,1-dimethylurea","","- C9 H13 N3 O2 -","- C9 H13 N3 O2 -","- C72 H104 N24 O16 -","8","2","","Rassadin, Valentin A.; Zimin, Dmitry P.; Raskil'dina, Gulnara Z.; Ivanov, Alexander Yu.; Boyarskiy, Vadim P.; Zlotskii, Semen S.; Kukushkin, Vadim Yu.","Solvent- and halide-free synthesis of pyridine-2-yl substituted ureas through facile C–H functionalization of pyridine N-oxides","Green Chem.","2016","18","24","6630","","10.1039/C6GC02556K","","","0.71073","MoKα","","0.0737","0.0542","","","0.1212","0.1325","","","","","","1.05","","","","has coordinates","301865","2025-08-22","16:17:08",""
"7226750","4.18964","0.00013","21.1953","0.0008","10.4364","0.0004","90","","95.814","0.003","90","","921.99","0.06","100.01","0.1","100.01","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","3-(6-bromopyridin-2-yl)-1,1-dimethylurea","","- C8 H10 Br N3 O -","- C8 H10 Br N3 O -","- C32 H40 Br4 N12 O4 -","4","1","","Rassadin, Valentin A.; Zimin, Dmitry P.; Raskil'dina, Gulnara Z.; Ivanov, Alexander Yu.; Boyarskiy, Vadim P.; Zlotskii, Semen S.; Kukushkin, Vadim Yu.","Solvent- and halide-free synthesis of pyridine-2-yl substituted ureas through facile C–H functionalization of pyridine N-oxides","Green Chem.","2016","18","24","6630","","10.1039/C6GC02556K","","","0.71073","MoKα","","0.0657","0.0503","","","0.0946","0.1016","","","","","","1.132","","","","has coordinates","301865","2025-08-22","16:17:08",""
"7226751","4.1274","0.0003","20.8167","0.0012","10.4887","0.0006","90","","95.909","0.005","90","","896.39","0.1","100.01","0.1","100.01","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","3-(6-chloropyridin-2-yl)-1,1-dimethylurea","","- C8 H10 Cl N3 O -","- C8 H10 Cl N3 O -","- C32 H40 Cl4 N12 O4 -","4","1","","Rassadin, Valentin A.; Zimin, Dmitry P.; Raskil'dina, Gulnara Z.; Ivanov, Alexander Yu.; Boyarskiy, Vadim P.; Zlotskii, Semen S.; Kukushkin, Vadim Yu.","Solvent- and halide-free synthesis of pyridine-2-yl substituted ureas through facile C–H functionalization of pyridine N-oxides","Green Chem.","2016","18","24","6630","","10.1039/C6GC02556K","","","0.71073","MoKα","","0.0552","0.0416","","","0.0926","0.1028","","","","","","1.075","","","","has coordinates","301865","2025-08-22","16:17:08",""
"7226790","15.6898","0.0004","10.314","0.0002","13.7275","0.0003","90","","90","","90","","2221.45","0.09","296","2","296","2","","","","","","","","3","P n a 21","P 2c -2n","33","methoxyphenyl phenyl benzo cyclohepta benzofuran","6-(2-methoxyphenyl)-5a-phenyl-5aH-benzo[4,5]cyclohepta[1,2-b]benzofuran","","- C30 H22 O2 -","- C30 H22 O2 -","- C120 H88 O8 -","4","1","","Gai, Rafaela; do Carmo Pinheiro, Roberto; Neto, José S. S.; Iglesias, Bernardo A.; Acunha, Thiago V.; Back, Davi F.; Zeni, Gilson","The intramolecular 5-exo, 7-endo-dig transition metal-free cyclization sequence of (2-alkynylphenyl) benzyl ethers: synthesis of seven-membered fused benzo[b]furans","Green Chem.","2016","18","24","6648","","10.1039/C6GC02423H","","","1.54178","CuKα","","0.0294","0.0291","","","0.0753","0.0757","","","","","","1.083","","","","has coordinates","301865","2025-08-22","16:17:08",""
"7226791","11.309","0.002","12.473","0.003","16.361","0.004","111.827","0.018","92.561","0.018","104.099","0.012","2054.3","0.9","296","2","296","2","","","","","","","","4","P -1","-P 1","2","fluorophenyl phenyl benzo cyclohepta benzofuran","5a-(4- fluorophenyl)-6- phenyl-5aH-benzo[4,5]cyclohepta[1,2-b]benzofuran","","- C29 H19 F O -","- C29 H19 F O -","- C116 H76 F4 O4 -","4","2","","Gai, Rafaela; do Carmo Pinheiro, Roberto; Neto, José S. S.; Iglesias, Bernardo A.; Acunha, Thiago V.; Back, Davi F.; Zeni, Gilson","The intramolecular 5-exo, 7-endo-dig transition metal-free cyclization sequence of (2-alkynylphenyl) benzyl ethers: synthesis of seven-membered fused benzo[b]furans","Green Chem.","2016","18","24","6648","","10.1039/C6GC02423H","","","1.54178","CuKα","","0.1016","0.0508","","","0.1069","0.1292","","","","","","1.013","","","","has coordinates","301865","2025-08-22","16:17:08",""
"7226792","9.5556","0.0017","18.935","0.003","11.627","0.003","90","","96.866","0.008","90","","2088.6","0.7","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","chlorophenyl phenyl benzo cyclohepta benzofuran","5a-(4-chlorophenyl)-6-phenyl-5aH-benzo[4,5]cyclohepta[1,2-b]benzofuran","","- C29 H19 Cl O -","- C29 H19 Cl O -","- C116 H76 Cl4 O4 -","4","1","","Gai, Rafaela; do Carmo Pinheiro, Roberto; Neto, José S. S.; Iglesias, Bernardo A.; Acunha, Thiago V.; Back, Davi F.; Zeni, Gilson","The intramolecular 5-exo, 7-endo-dig transition metal-free cyclization sequence of (2-alkynylphenyl) benzyl ethers: synthesis of seven-membered fused benzo[b]furans","Green Chem.","2016","18","24","6648","","10.1039/C6GC02423H","","","0.71073","MoKα","","0.1013","0.0626","","","0.1381","0.1546","","","","","","1.027","","","","has coordinates","301865","2025-08-22","16:17:08",""
"7226822","17.4184","0.0011","8.2542","0.0005","18.8202","0.0012","90","","104.911","0.007","90","","2614.8","0.3","293.23","0.1","293.23","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C27 H26 N4 O6 S -","- C27 H26 N4 O6 S -","- C108 H104 N16 O24 S4 -","4","1","","Liu, Xihong; Yang, Dongxu; Wang, Kezhou; Zhang, Jinlong; Wang, Rui","A catalyst-free 1,3-dipolar cycloaddition of C,N-cyclic azomethine imines and 3-nitroindoles: an easy access to five-ring-fused tetrahydroisoquinolines","Green Chem.","2017","19","1","82","","10.1039/C6GC02517J","","x-ray","0.71073","MoKα","","0.0979","0.0573","","","0.1216","0.1517","","","","","","1.035","","","","has coordinates","301865","2025-08-22","16:17:08",""
"7226888","4.958","0.002","21.437","0.01","12.165","0.006","90","","98.132","0.007","90","","1280","1","296.15","","296.15","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C16 H11 N3 O -","- C16 H11 N3 O -","- C64 H44 N12 O4 -","4","2","","Xie, Yu-Yang; Wang, Ying-Chun; He, Yan; Hu, Da-Chao; Wang, Heng-Shan; Pan, Ying-Ming","Catalyst-free synthesis of fused 1,2,3-triazole and isoindoline derivatives via an intramolecular azide‒alkene cascade reaction","Green Chem.","2017","19","3","656","","10.1039/C6GC01553K","","","0.71073","MoKα","","0.0494","0.0354","","","0.1048","0.1182","","","","","","0.834","","","","has coordinates","193863","2020-10-21","18:00:00",""
"7226889","8.4892","0.0006","17.7731","0.0015","9.0884","0.0007","90","","107.345","0.008","90","","1308.9","0.18","150","2","150","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C19 H13 N -","- C19 H13 N -","- C76 H52 N4 -","4","1","","Senadi, Gopal Chandru; Dhandabani, Ganesh Kumar; Hu, Wan-Ping; Wang, Jeh-Jeng","Metal-free annulation/aerobic oxidative dehydrogenation of cyclohexanones with o-acylanilines: efficient syntheses of acridines","Green Chem.","2016","18","23","6241","","10.1039/C6GC02396G","","x-ray","0.71073","MoKα","","0.1114","0.0639","","","0.1252","0.1479","","","","","","1.012","","","","has coordinates","301865","2025-08-22","16:17:08",""
"7226890","7.5233","0.0011","9.2661","0.0015","11.5013","0.0015","109.068","0.014","96.475","0.012","105.036","0.013","714.5","0.2","297","2","297","2","","","","","","","","4","P -1","-P 1","2","","","","- C19 H12 Cl N -","- C19 H12 Cl N -","- C38 H24 Cl2 N2 -","2","1","","Senadi, Gopal Chandru; Dhandabani, Ganesh Kumar; Hu, Wan-Ping; Wang, Jeh-Jeng","Metal-free annulation/aerobic oxidative dehydrogenation of cyclohexanones with o-acylanilines: efficient syntheses of acridines","Green Chem.","2016","18","23","6241","","10.1039/C6GC02396G","","x-ray","0.71073","MoKα","","0.2208","0.0807","","","0.1897","0.2825","","","","","","0.984","","","","has coordinates","301865","2025-08-22","16:17:08",""
"7226891","9.0735","0.0009","9.1093","0.001","9.1688","0.0009","71.085","0.003","75.202","0.003","85.168","0.004","693.13","0.12","150","2","150","2","","","","","","","","3","P -1","-P 1","2","","","","- C19 H17 N -","- C19 H17 N -","- C38 H34 N2 -","2","1","","Senadi, Gopal Chandru; Dhandabani, Ganesh Kumar; Hu, Wan-Ping; Wang, Jeh-Jeng","Metal-free annulation/aerobic oxidative dehydrogenation of cyclohexanones with o-acylanilines: efficient syntheses of acridines","Green Chem.","2016","18","23","6241","","10.1039/C6GC02396G","","x-ray","0.71073","MoKα","","0.107","0.0689","","","0.1792","0.209","","","","","","1.029","","","","has coordinates","301865","2025-08-22","16:17:08",""
"7226892","8.2767","0.0007","8.6984","0.0006","11.4987","0.0009","110.318","0.002","90.656","0.003","115.299","0.003","689.29","0.1","150","2","150","2","","","","","","","","4","P -1","-P 1","2","","","","- C19 H15 N O -","- C19 H15 N O -","- C38 H30 N2 O2 -","2","1","","Senadi, Gopal Chandru; Dhandabani, Ganesh Kumar; Hu, Wan-Ping; Wang, Jeh-Jeng","Metal-free annulation/aerobic oxidative dehydrogenation of cyclohexanones with o-acylanilines: efficient syntheses of acridines","Green Chem.","2016","18","23","6241","","10.1039/C6GC02396G","","x-ray","0.71073","MoKα","","0.0619","0.0533","","","0.1515","0.1625","","","","","","1.021","","","","has coordinates","301865","2025-08-22","16:17:08",""
"7226984","14.2255","0.0014","6.0009","0.0006","13.9246","0.0013","90","","114.398","0.001","90","","1082.53","0.18","130","","130","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C13 H13 F O2 -","- C13 H13 F O2 -","- C52 H52 F4 O8 -","4","1","","Tian, Qingshan; Chen, Bin; Zhang, Guozhu","Silver-initiated radical ring expansion/fluorination of ethynyl cyclobutanols: efficient synthesis of monofluoroethenyl cyclopentanones","Green Chem.","2016","18","23","6236","","10.1039/C6GC02656G","","","0.71073","MoKα","","0.066","0.0552","","","0.1464","0.1576","","","","","","1.039","","","","has coordinates","301865","2025-08-22","16:17:09",""
"7226985","14.2032","0.0008","4.6426","0.0003","18.5046","0.001","90","","99.389","0.006","90","","1203.84","0.12","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","3,4-dihydro-(3Z)-(2-oxohex-5-enylidene)-1,4-benzoxazin-2-one","","- C14 H13 N O3 -","- C14 H13 N O3 -","- C56 H52 N4 O12 -","4","1","","Petronijević, Jelena; Bugarčić, Zorica; Bogdanović, Goran A.; Stefanović, Srđan; Janković, Nenad","An enolate ion as a synthon in biocatalytic synthesis of 3,4-dihydro-2(1H)-quinoxalinones and 3,4-dihydro-1,4-benzoxazin-2-ones: lemon juice as an alternative to hazardous solvents and catalysts","Green Chem.","2017","19","3","707","","10.1039/C6GC02893D","","x-ray","0.71073","MoKα","","0.0845","0.0462","","","0.0951","0.1153","","","","","","1.032","","","","has coordinates","301865","2025-08-22","16:17:09",""
"7227222","6.6847","0.0005","8.2593","0.0007","12.7076","0.0012","71.172","0.004","85.353","0.003","72.077","0.003","631.7","0.09","110","2","110","2","","","","","","","","5","P -1","-P 1","2","","5-bromo-2,3-difluorophenyl 4-methoxybenzoate","","- C14 H9 Br F2 O3 -","- C14 H9 Br F2 O3 -","- C28 H18 Br2 F4 O6 -","2","1","","Gautam, Prashant; Kathe, Prasad; Bhanage, Bhalchandra M.","Pd/C catalyzed phenoxycarbonylation using N-formylsaccharin as a CO surrogate in propylene carbonate, a sustainable solvent","Green Chem.","2017","19","3","823","","10.1039/C6GC03027K","","","0.71073","MoKα","","0.0363","0.0282","","","0.0575","0.06","","","","","","1.061","","","","has coordinates","301865","2025-08-22","16:17:10",""
"7227271","12.1733","0.0007","12.9667","0.0007","19.521","0.0011","93.601","0.002","96.085","0.002","111.847","0.002","2826.4","0.3","296","2","296","2","","","","","","","","9","P -1","-P 1","2","","","","- C49 H44 Cl5 F6 Ir N4 O7 P2 S2 -","- C49 H44 Cl5 F6 Ir N4 O7 P2 S2 -","- C98 H88 Cl10 F12 Ir2 N8 O14 P4 S4 -","2","1","","Liu, Huan; Wang, Dong-Liang; Chen, Xia; Lu, Yong; Zhao, Xiao-Li; Liu, Ye","Efficient and recyclable Ir(i)-catalysts with the involvement of π-acceptor phosphines for N-alkylation of aryl amines with alcohols","Green Chem.","2017","19","4","1109","","10.1039/C6GC03096C","","","0.71073","MoKα","","0.0814","0.0582","","","0.1562","0.1798","","","","","","1.018","","","","has coordinates","193860","2020-10-21","18:00:00",""
"7227272","9.0997","0.0003","15.2322","0.0005","13.1977","0.0005","90","","93.109","0.001","90","","1826.62","0.11","296","2","296","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C42 H34 Cl2 Ir N4 P2 -","- C42 H34 Cl2 Ir N4 P2 -","- C84 H68 Cl4 Ir2 N8 P4 -","2","0.5","","Liu, Huan; Wang, Dong-Liang; Chen, Xia; Lu, Yong; Zhao, Xiao-Li; Liu, Ye","Efficient and recyclable Ir(i)-catalysts with the involvement of π-acceptor phosphines for N-alkylation of aryl amines with alcohols","Green Chem.","2017","19","4","1109","","10.1039/C6GC03096C","","","0.71073","MoKα","","0.0271","0.0222","","","0.0495","0.0522","","","","","","1.089","","","","has coordinates","193860","2020-10-21","18:00:00",""
"7227333","25.4682","0.0009","25.4682","0.0009","12.316","0.0005","90","","90","","120","","6918.3","0.4","223","0.1","223","0.1","","","","","","","","6","R -3","-R 3","148","","","","- C14 H18 Cl N3 O Se -","- C14 H16 Cl N3 O Se -","- C252 H288 Cl18 N54 O18 Se18 -","18","","","Fang, Yi; Zhu, Zheng-Lin; Xu, Pei; Wang, Shun-Yi; Ji, Shun-Jun","Aerobic radical-cascade cycloaddition of isocyanides, selenium and imidamides: facile access to 1,2,4-selenadiazoles under metal-free conditions","Green Chem.","2017","19","7","1613","","10.1039/C6GC03521C","","","0.71073","MoKα","","0.0706","0.0475","","","0.109","0.1206","","","","","","1.05","","","","has coordinates,has disorder","195144","2020-10-21","18:00:00",""
"7227453","9.2637","0.0004","10.3529","0.0004","10.4849","0.0005","86.787","0.004","75.671","0.004","82.064","0.004","964.7","0.07","293","","293","","","","","","","","","3","P -1","-P 1","2","","N-((1-(2,6-dimethylphenyl)-1H-tetrazol-5-yl)(phenyl)methyl)aniline","","- C22 H21 N5 -","- C22 H21 N5 -","- C44 H42 N10 -","2","1","","Pharande, Shrikant G.; Corrales Escobosa, Alma Rosa; Gámez-Montaño, Rocío","Endogenous water-triggered and ultrasound accelerated synthesis of 1,5-disubstituted tetrazoles via a solvent and catalyst-free Ugi-azide reaction","Green Chem.","2017","19","5","1259","","10.1039/C6GC03324E","","x-ray","0.71073","MoKα","","0.0699","0.0533","","","0.1293","0.1424","","","","","","1.033","","","","has coordinates","301865","2025-08-22","16:17:11",""
"7227474","44.778","0.005","5.5195","0.0006","8.2452","0.0009","90","","93.029","0.009","90","","2035","0.4","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","3-(4-phenoxyphenyl)-6-(p-tolyl)-1,2,4,5-tetrazine","","- C24 H22 N4 O -","- C24 H22 N4 O -","- C96 H88 N16 O4 -","4","1","","Fang, Zheng; Hu, Wen-Li; Liu, De-Yong; Yu, Chu-Yi; Hu, Xiang-Guo","Synthesis of tetrazines from gem-difluoroalkenes under aerobic conditions at room temperature","Green Chem.","2017","19","5","1299","","10.1039/C6GC03494B","","","0.71073","MoKα","","0.1254","0.0942","","","0.2486","0.2688","","","","","","1.085","","","","has coordinates","301865","2025-08-22","16:17:11",""
"7227475","4.8044","0.0003","34.603","0.003","9.8785","0.0007","90","","100.443","0.007","90","","1615.1","0.2","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","3,6-bis(4-bromophenyl)-1,2,4,5-tetrazine","","- C16 H12 Br2 N4 -","- C16 H12 Br2 N4 -","- C64 H48 Br8 N16 -","4","1","","Fang, Zheng; Hu, Wen-Li; Liu, De-Yong; Yu, Chu-Yi; Hu, Xiang-Guo","Synthesis of tetrazines from gem-difluoroalkenes under aerobic conditions at room temperature","Green Chem.","2017","19","5","1299","","10.1039/C6GC03494B","","","0.71073","MoKα","","0.1105","0.0744","","","0.2029","0.2436","","","","","","1.04","","","","has coordinates","301865","2025-08-22","16:17:11",""
"7227519","11.0928","0.0002","12.4805","0.0002","15.1388","0.0002","81.463","0.001","83.416","0.001","64.133","0.001","1862.06","0.05","150","2","150","2","","","","","","","","7","P -1","-P 1","2","1-Sm","","","- C48 H72 Cu2 I2 N14 O23 Sm2 -","- C48 H72 Cu2 I2 N14 O23 Sm2 -","- C48 H72 Cu2 I2 N14 O23 Sm2 -","1","0.5","","Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen","Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework","Green Chem.","2017","19","5","1250","","10.1039/C6GC02833K","","","0.71073","MoKα","","0.0279","0.0245","","","0.0764","0.0791","","","","","","1.024","","","","has coordinates","195138","2020-10-21","18:00:00",""
"7227520","11.1874","0.0008","12.6","0.0009","15.1798","0.0011","92.528","0.001","96.837","0.001","116.289","0.001","1893.5","0.2","150","2","150","2","","","","","","","","7","P -1","-P 1","2","1-Eu","","","- C48 H72 Cu2 Eu2 I2 N14 O23 -","- C48 H72 Cu2 Eu2 I2 N14 O23 -","- C48 H72 Cu2 Eu2 I2 N14 O23 -","1","0.5","","Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen","Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework","Green Chem.","2017","19","5","1250","","10.1039/C6GC02833K","","","0.71073","MoKα","","0.0326","0.0274","","","0.0894","0.0975","","","","","","1.02","","","","has coordinates","195138","2020-10-21","18:00:00",""
"7227521","11.1994","0.0012","12.5884","0.0014","15.174","0.0017","92.438","0.002","96.979","0.002","116.308","0.001","1892.3","0.4","150","2","150","2","","","","","","","","7","P -1","-P 1","2","1-Gd","","","- C48 H72 Cu2 Gd2 I2 N14 O23 -","- C48 H72 Cu2 Gd2 I2 N14 O23 -","- C48 H72 Cu2 Gd2 I2 N14 O23 -","1","0.5","","Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen","Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework","Green Chem.","2017","19","5","1250","","10.1039/C6GC02833K","","","0.71073","MoKα","","0.0291","0.0261","","","0.0796","0.0821","","","","","","1.024","","","","has coordinates","195138","2020-10-21","18:00:00",""
"7227522","11.2008","0.001","12.5798","0.0011","15.1576","0.0014","92.291","0.001","97.131","0.001","116.347","0.001","1888.2","0.3","150","2","150","2","","","","","","","","7","P -1","-P 1","2","1-Tb","","","- C48 H72 Cu2 I2 N14 O23 Tb2 -","- C48 H72 Cu2 I2 N14 O23 Tb2 -","- C48 H72 Cu2 I2 N14 O23 Tb2 -","1","0.5","","Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen","Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework","Green Chem.","2017","19","5","1250","","10.1039/C6GC02833K","","","0.71073","MoKα","","0.0269","0.0249","","","0.0779","0.0799","","","","","","1.024","","","","has coordinates","195138","2020-10-21","18:00:00",""
"7227523","11.1272","0.0005","12.4509","0.0006","15.132","0.0007","81.365","0.001","82.847","0.001","63.926","0.001","1857.69","0.15","150","2","150","2","","","","","","","","7","P -1","-P 1","2","1-Dy","","","- C48 H72 Cu2 Dy2 I2 N14 O23 -","- C48 H72 Cu2 Dy2 I2 N14 O23 -","- C48 H72 Cu2 Dy2 I2 N14 O23 -","1","0.5","","Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen","Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework","Green Chem.","2017","19","5","1250","","10.1039/C6GC02833K","","","0.71073","MoKα","","0.024","0.0222","","","0.0698","0.0713","","","","","","1.025","","","","has coordinates","195138","2020-10-21","18:00:00",""
"7227524","11.1399","0.0009","12.4564","0.001","15.1237","0.0012","81.32","0.001","82.723","0.001","63.883","0.001","1858.5","0.3","150","2","150","2","","","","","","","","7","P -1","-P 1","2","1-Ho","","","- C48 H72 Cu2 Ho2 I2 N14 O23 -","- C48 H72 Cu2 Ho2 I2 N14 O23 -","- C48 H72 Cu2 Ho2 I2 N14 O23 -","1","0.5","","Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen","Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework","Green Chem.","2017","19","5","1250","","10.1039/C6GC02833K","","","0.71073","MoKα","","0.0232","0.0218","","","0.0705","0.0719","","","","","","1.029","","","","has coordinates","195138","2020-10-21","18:00:00",""
"7227525","11.2006","0.0009","12.5227","0.001","15.113","0.0013","92.084","0.001","97.414","0.001","116.45","0.001","1871.5","0.3","150","2","150","2","","","","","","","","7","P -1","-P 1","2","1-Er","","","- C48 H72 Cu2 Er2 I2 N14 O23 -","- C48 H72 Cu2 Er2 I2 N14 O23 -","- C48 H72 Cu2 Er2 I2 N14 O23 -","1","0.5","","Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen","Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework","Green Chem.","2017","19","5","1250","","10.1039/C6GC02833K","","","0.71073","MoKα","","0.025","0.0228","","","0.0722","0.074","","","","","","1.047","","","","has coordinates","195138","2020-10-21","18:00:00",""
"7227526","11.1943","0.0004","12.4986","0.0004","15.077","0.0005","91.996","0.002","97.522","0.002","116.512","0.002","1861.03","0.11","150","2","150","2","","","","","","","","7","P -1","-P 1","2","1-Yb","","","- C48 H72 Cu2 I2 N14 O23 Yb2 -","- C48 H72 Cu2 I2 N14 O23 Yb2 -","- C48 H72 Cu2 I2 N14 O23 Yb2 -","1","0.5","","Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen","Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework","Green Chem.","2017","19","5","1250","","10.1039/C6GC02833K","","","0.71073","MoKα","","0.0281","0.0248","","","0.078","0.081","","","","","","1.043","","","","has coordinates","195138","2020-10-21","18:00:00",""
"7227527","11.2135","0.0007","12.5387","0.0007","15.1202","0.0009","92.092","0.001","97.415","0.001","116.389","0.001","1877.91","0.19","150","2","150","2","","","","","","","","7","P -1","-P 1","2","1-Y","","","- C48 H72 Cu2 I2 N14 O23 Y2 -","- C48 H72 Cu2 I2 N14 O23 Y2 -","- C48 H72 Cu2 I2 N14 O23 Y2 -","1","0.5","","Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen","Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework","Green Chem.","2017","19","5","1250","","10.1039/C6GC02833K","","","0.71073","MoKα","","0.0379","0.0322","","","0.1095","0.1141","","","","","","1.027","","","","has coordinates","195138","2020-10-21","18:00:00",""
"7227528","17.8961","0.0019","31.932","0.003","25.078","0.003","90","","90","","90","","14331","3","150","2","150","2","","","","","","","","8","C 2 2 21","C 2c 2","20","2-Pr","","","- C48 H40 Cu8 I8 N8 Na2 O25 Pr2 -","- C48 H40 Cu8 I8 N8 Na2 O25 Pr2 -","- C192 H160 Cu32 I32 N32 Na8 O100 Pr8 -","4","0.5","","Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen","Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework","Green Chem.","2017","19","5","1250","","10.1039/C6GC02833K","","","0.71073","MoKα","","0.106","0.0862","","","0.2128","0.229","","","","","","1.06","","","","has coordinates","195138","2020-10-21","18:00:00",""
"7227529","17.889","0.002","31.835","0.004","24.831","0.003","90","","90","","90","","14141","3","150","2","150","2","","","","","","","","9","C 2 2 21","C 2c 2","20","2-Nd","","","- C48 H40 Cl0 Cu8 I8 N8 Na2 Nd2 O25 -","- C48 H40 Cu8 I8 N8 Na2 Nd2 O25 -","- C192 H160 Cu32 I32 N32 Na8 Nd8 O100 -","4","0.5","","Hu, Yue-Qiao; Zhang, Tao; Li, Mu-Qing; Wang, Yanyan; Zheng, Zhiping; Zheng, Yan-Zhen","Copper(i)/(ii)-redox triggered efficient and green rare-earth separation using a heterometallic metal‒organic framework","Green Chem.","2017","19","5","1250","","10.1039/C6GC02833K","","","0.71073","MoKα","","0.1594","0.0853","","","0.2168","0.2635","","","","","","1.071","","","","has coordinates","195138","2020-10-21","18:00:00",""
"7227553","7.1841","0.0014","18.013","0.004","14.832","0.003","90","","95.33","0.03","90","","1911.1","0.7","293","2","293","2","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C21 H17 F N0 O2 S Se -","- C21 H17 F O2 S Se -","- C84 H68 F4 O8 S4 Se4 -","4","1","","Sun, Kai; Wang, Xin; Fu, Fangfang; Zhang, Chong; Chen, Yao; Liu, Lin","Metal-free selenosulfonylation of alkynes: rapid access to β-(seleno)vinyl sulfones via a cationic-species-induced pathway","Green Chem.","2017","19","6","1490","","10.1039/C6GC03420A","","","0.71073","MoKα","","0.0786","0.055","","","0.1703","0.189","","","","","","1.061","","","","has coordinates","195140","2020-10-21","18:00:00",""
"7227554","8.7143","0.0017","10.963","0.002","12.352","0.003","91.21","0.03","95.23","0.03","108.64","0.03","1111.9","0.5","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C24 H24 N0 O2 S Se -","- C24 H24 O2 S Se -","- C48 H48 O4 S2 Se2 -","2","1","","Sun, Kai; Wang, Xin; Fu, Fangfang; Zhang, Chong; Chen, Yao; Liu, Lin","Metal-free selenosulfonylation of alkynes: rapid access to β-(seleno)vinyl sulfones via a cationic-species-induced pathway","Green Chem.","2017","19","6","1490","","10.1039/C6GC03420A","","","0.71073","MoKα","","0.1045","0.0549","","","0.1672","0.2168","","","","","","1.026","","","","has coordinates","195140","2020-10-21","18:00:00",""
"7227555","14.693","0.003","13.577","0.003","17.032","0.003","90","","94.54","0.03","90","","3387","1.2","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C18 H18 N0 O2 S Se -","- C18 H18 O2 S Se -","- C144 H144 O16 S8 Se8 -","8","1","","Sun, Kai; Wang, Xin; Fu, Fangfang; Zhang, Chong; Chen, Yao; Liu, Lin","Metal-free selenosulfonylation of alkynes: rapid access to β-(seleno)vinyl sulfones via a cationic-species-induced pathway","Green Chem.","2017","19","6","1490","","10.1039/C6GC03420A","","","0.71073","MoKα","","0.0375","0.0289","","","0.0737","0.0773","","","","","","1.038","","","","has coordinates","195140","2020-10-21","18:00:00",""
"7227670","6.0657","0.0004","11.6494","0.001","14.2527","0.0012","104.148","0.007","102.007","0.006","92.918","0.006","949.69","0.14","296.9","0.6","296.9","0.6","","","","","","","","4","P -1","-P 1","2","","RJ-17","","- C23 H21 Cl N2 -","- C23 H21 Cl N2 -","- C46 H42 Cl2 N4 -","2","1","","Jamatia, Ramen; Gupta, Ajay; Dam, Binoyargha; Saha, Mithu; Pal, Amarta Kumar","Graphite oxide: a metal free highly efficient carbocatalyst for the synthesis of 1,5-benzodiazepines under room temperature and solvent free heating conditions","Green Chem.","2017","19","6","1576","","10.1039/C6GC03110B","","","0.7107","MoKα","","0.084562","0.056699","","","","0.138382","","","","","","1.04758","","","","has coordinates","301865","2025-08-22","16:17:12",""
"7227708","10.4147","0.0005","10.8221","0.0008","11.4326","0.0007","63.221","0.007","63.896","0.005","74.519","0.005","1029.22","0.13","150","0.1","150","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C27 H23 N O2 -","- C27 H23 N O2 -","- C54 H46 N2 O4 -","2","1","","Xiong, Wenfang; Qi, Chaorong; Guo, Tianzuo; Zhang, Min; Chen, Kai; Jiang, Huanfeng","A copper-catalyzed oxidative coupling reaction of arylboronic acids, amines and carbon dioxide using molecular oxygen as the oxidant","Green Chem.","2017","19","7","1642","","10.1039/C6GC03465A","","x-ray","1.54184","CuKα","","0.0374","0.0353","","","0.091","0.0927","","","","","","1.06","","","","has coordinates","301865","2025-08-22","16:17:12",""
"7227831","10.2857","0.0002","22.5658","0.0004","7.71479","0.00014","90","","97.8249","0.0018","90","","1773.97","0.06","123.01","0.1","123.01","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","methyl (2S*,3R*)-3-(2-ethoxy-2-oxoethyl)-2-(o-tolyl)indoline-1-carboxylate","","- C21 H23 N O4 -","- C21 H23 N O4 -","- C84 H92 N4 O16 -","4","1","","Pagire, Santosh K.; Reiser, Oliver","Tandem cyclisation of vinyl radicals: a sustainable approach to indolines utilizing visible-light photoredox catalysis","Green Chem.","2017","19","7","1721","","10.1039/C7GC00445A","","x-ray","1.54184","CuKα","","0.0487","0.0422","","","0.1101","0.1167","","","","","","1.034","","","","has coordinates,has disorder","301865","2025-08-22","16:17:13",""
"7227985","6.4269","0.0003","8.9443","0.0005","16.3677","0.0009","85.57","0.005","81.795","0.004","86.766","0.005","927.49","0.09","173","2","173","2","","","","","","","","6","P -1","-P 1","2","","","","- C12 H10 F13 I N2 S -","- C12 H10 F13 I N2 S -","- C24 H20 F26 I2 N4 S2 -","2","1","","Hummel, Michael; Markiewicz, Marta; Stolte, Stefan; Noisternig, Michael Franz; Braun, Doris Elfriede; Gelbrich, Thomas; Griesser, Ulrich J.; Partl, Gabriel Julian; Naier, Benjamin Florian; Wurst, Klaus; Krüger, Biljana; Kopacka, Holger; Laus, Gerhard; Huppertz, Hubert; Schottenberger, Herwig","Phase-out-compliant fluorosurfactants: Unique methimazolium derivatives including room temperature ionic liquids","Green Chem.","2017","","","","","10.1039/C7GC00571G","","x-ray","0.71073","MoKα","","0.0359","0.0286","","","0.0522","0.056","","","","","","1.02","","","","has coordinates","301865","2025-08-22","16:17:13",""
"7227986","6.3654","0.0004","9.2363","0.0005","16.0361","0.0012","75.231","0.005","83.709","0.005","76.855","0.005","886.44","0.1","173","2","173","2","","","","","","","","6","P -1","-P 1","2","","","","- C12 H10 Cl F13 N2 S -","- C12 H10 Cl F13 N2 S -","- C24 H20 Cl2 F26 N4 S2 -","2","1","","Hummel, Michael; Markiewicz, Marta; Stolte, Stefan; Noisternig, Michael Franz; Braun, Doris Elfriede; Gelbrich, Thomas; Griesser, Ulrich J.; Partl, Gabriel Julian; Naier, Benjamin Florian; Wurst, Klaus; Krüger, Biljana; Kopacka, Holger; Laus, Gerhard; Huppertz, Hubert; Schottenberger, Herwig","Phase-out-compliant fluorosurfactants: Unique methimazolium derivatives including room temperature ionic liquids","Green Chem.","2017","","","","","10.1039/C7GC00571G","","x-ray","0.71073","MoKα","","0.0621","0.044","","","0.1032","0.114","","","","","","1.029","","","","has coordinates","301865","2025-08-22","16:17:13",""
"7227987","18.463","0.005","8.901","0.003","11.595","0.003","90","","102.185","0.009","90","","1862.6","0.9","173","2","173","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C24 H20 F32 N4 S2 Si -","- C24 H20 F32 N4 S2 Si -","- C48 H40 F64 N8 S4 Si2 -","2","0.5","","Hummel, Michael; Markiewicz, Marta; Stolte, Stefan; Noisternig, Michael Franz; Braun, Doris Elfriede; Gelbrich, Thomas; Griesser, Ulrich J.; Partl, Gabriel Julian; Naier, Benjamin Florian; Wurst, Klaus; Krüger, Biljana; Kopacka, Holger; Laus, Gerhard; Huppertz, Hubert; Schottenberger, Herwig","Phase-out-compliant fluorosurfactants: Unique methimazolium derivatives including room temperature ionic liquids","Green Chem.","2017","","","","","10.1039/C7GC00571G","","","0.71073","MoKα","","0.1554","0.0902","","","0.2128","0.2515","","","","","","1.05","","","","has coordinates","301865","2025-08-22","16:17:13",""
"7227988","6.4954","0.0005","9.2039","0.0008","27.9195","0.0019","94.848","0.006","91.767","0.006","95.367","0.007","1654.6","0.2","173","2","173","2","","","","","","","","6","P -1","-P 1","2","","","","- C20 H10 F30 I2 N2 S -","- C20 H10 F30 I2 N2 S -","- C40 H20 F60 I4 N4 S2 -","2","1","","Hummel, Michael; Markiewicz, Marta; Stolte, Stefan; Noisternig, Michael Franz; Braun, Doris Elfriede; Gelbrich, Thomas; Griesser, Ulrich J.; Partl, Gabriel Julian; Naier, Benjamin Florian; Wurst, Klaus; Krüger, Biljana; Kopacka, Holger; Laus, Gerhard; Huppertz, Hubert; Schottenberger, Herwig","Phase-out-compliant fluorosurfactants: Unique methimazolium derivatives including room temperature ionic liquids","Green Chem.","2017","","","","","10.1039/C7GC00571G","","x-ray","0.71073","MoKα","","0.0686","0.0462","","","0.0977","0.112","","","","","","1.056","","","","has coordinates,has disorder","301865","2025-08-22","16:17:13",""
"7227989","5.8881","0.0003","10.2741","0.0007","25.481","0.001","89.763","0.004","87.419","0.004","77.726","0.003","1504.69","0.14","233","2","233","2","","","","","","","","6","P -1","-P 1","2","","","","- C20 H13 F26 I N2 S -","- C20 H13 F26 I N2 S -","- C40 H26 F52 I2 N4 S2 -","2","1","","Hummel, Michael; Markiewicz, Marta; Stolte, Stefan; Noisternig, Michael Franz; Braun, Doris Elfriede; Gelbrich, Thomas; Griesser, Ulrich J.; Partl, Gabriel Julian; Naier, Benjamin Florian; Wurst, Klaus; Krüger, Biljana; Kopacka, Holger; Laus, Gerhard; Huppertz, Hubert; Schottenberger, Herwig","Phase-out-compliant fluorosurfactants: Unique methimazolium derivatives including room temperature ionic liquids","Green Chem.","2017","","","","","10.1039/C7GC00571G","","","0.71073","MoKα","","0.0917","0.0589","","","0.1519","0.1684","","","","","","1.067","","","","has coordinates","301865","2025-08-22","16:17:13",""
"7227990","8.6657","0.0002","10.1187","0.0004","48.601","0.002","90","","90","","90","","4261.6","0.3","233","2","233","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C15 H15 F13 N2 O3 S2 -","- C15 H15 F13 N2 O3 S2 -","- C120 H120 F104 N16 O24 S16 -","8","1","","Hummel, Michael; Markiewicz, Marta; Stolte, Stefan; Noisternig, Michael Franz; Braun, Doris Elfriede; Gelbrich, Thomas; Griesser, Ulrich J.; Partl, Gabriel Julian; Naier, Benjamin Florian; Wurst, Klaus; Krüger, Biljana; Kopacka, Holger; Laus, Gerhard; Huppertz, Hubert; Schottenberger, Herwig","Phase-out-compliant fluorosurfactants: Unique methimazolium derivatives including room temperature ionic liquids","Green Chem.","2017","","","","","10.1039/C7GC00571G","","","0.71073","MoKα","","0.0942","0.0569","","","0.1283","0.1468","","","","","","0.983","","","","has coordinates,has disorder","301865","2025-08-22","16:17:13",""
"7227991","24.0182","0.0013","26.8445","0.0014","7.914","0.0004","90","","90","","90","","5102.6","0.5","293","2","293","2","","","","","","","","4","F d d 2","F 2 -2d","43","","1-methyl-2-(methylamino)-3-nitro-1H-chromeno[2,3-b]pyridin-5(10aH)-one","","- C14 H13 N3 O4 -","- C14 H13 N3 O4 -","- C224 H208 N48 O64 -","16","1","","Ramakrishna, Seeram; nataraj, poomathi; Perumal, Paramasivan Thirumalai","An efficient and eco-friendly synthesis of 2-pyridones and functionalized azaxanthone frameworks via indium triflate catalyzed domino reaction","Green Chem.","2017","","","","","10.1039/C6GC03440C","","","0.71073","MoKα","","0.0336","0.03","","","0.0733","0.0759","","","","","","1.044","","","","has coordinates","194735","2020-10-21","18:00:00",""
"7227992","14.158","0.003","14.747","0.003","23.048","0.007","90","","90","","90","","4812","2","296","2","296","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","3,3-disubstituted oxindole","","- C27 H22 Br N3 O4 S -","- C27 H22 Br N3 O4 S -","- C216 H176 Br8 N24 O32 S8 -","8","1","","Ramakrishna, Seeram; nataraj, poomathi; Perumal, Paramasivan Thirumalai","An efficient and eco-friendly synthesis of 2-pyridones and functionalized azaxanthone frameworks via indium triflate catalyzed domino reaction","Green Chem.","2017","","","","","10.1039/C6GC03440C","","","0.71073","MoKα","","0.1138","0.0904","","","0.2816","0.3003","","","","","","1.123","","","","has coordinates","301865","2025-08-22","16:17:13",""
"7228109","6.0572","0.0006","12.7385","0.0011","16.2312","0.0015","71.599","0.005","85.516","0.005","80.119","0.005","1170.35","0.19","290","2","290","2","","","","","","","","5","P -1","-P 1","2","(Z)-tert-butyl 3-(4-bromophenyl)-2-((diphenylphosphoryl)methyl)acrylate","xie-3j","","- C26 H26 Br O3 P -","- C26 H26 Br O3 P -","- C52 H52 Br2 O6 P2 -","2","1","","Xie, Peizhong; Wang, Jinyu; Fan, Jiang; Liu, Yanan; Wo, Xiangyang; Loh, Teck Peng","The C-OH/P-H Dehydrative Cross-Coupling for the Construction of P-C Bond under Metal-free Conditions","Green Chem.","2017","","","","","10.1039/C7GC00882A","","","0.71073","MoKα","","0.0993","0.0452","","","0.0842","0.0976","","","","","","1.02","","","","has coordinates","301865","2025-08-22","16:17:13",""
"7228158","10.0024","0.0009","6.9487","0.0007","17.5896","0.0015","90","","98.794","0.009","90","","1208.2","0.2","120","2","120","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C16 H14 N2 -","- C16 H14 N2 -","- C64 H56 N8 -","4","1","","Jin, Jing; Guidi, Sandro; Abada, Zahra; Amara, Zacharias; Selva, Maurizio; George, Michael W.; Poliakoff, Martyn","Continuous niobium phosphate catalysed Skraup reaction for quinoline synthesis from solketal","Green Chem.","2017","","","","","10.1039/C6GC03140D","","x-ray","1.54184","CuKα","","0.0451","0.0395","","","0.1042","0.1091","","","","","","1.026","","","","has coordinates","301865","2025-08-22","16:17:13",""
"7228229","7.1752","0.0011","13.714","0.002","12.346","0.002","90","","91.918","0.005","90","","1214.2","0.3","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","(Z)-2-(aminomethylene)-3-oxo-N-(4-(trifluoromethyl)phenyl)butanamide","(2Z)-2-(aminomethylidene)-3-oxo-N-[4-(trifluoromethyl)phenyl]butanamide","","- C12 H11 F3 N2 O2 -","- C12 H11 F3 N2 O2 -","- C48 H44 F12 N8 O8 -","4","1","","Subramaniam, Palaniraja; Ramasubbu, Chandrasekaran; Athiramu, Selvaraj","Exploiting Intramolecular Hydrogen Bond for Highly (Z)-Selective & Metal Free Synthesis of Amide Substituted β-aminoenones","Green Chem.","2017","","","","","10.1039/C7GC00909G","","","0.71073","MoKα","","0.1254","0.0693","","","0.1557","0.1866","","","","","","1.031","","","","has coordinates","301865","2025-08-22","16:17:13",""
"7228256","9.0731","0.0017","9.3483","0.0017","17.357","0.003","90","","90","","90","","1472.2","0.5","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C14 H13 Br O6 -","- C14 H13 Br O6 -","- C56 H52 Br4 O24 -","4","1","","Guo, Yan-Jun; Xia, Ai-Bao; Meng, Chen-Hong; Xu, Zhen Yuan; Xu, Danqian","Direct Conversion of γ,γ-Dicarbonyl-Substituted Aldehydes into γ- Lactones with a Sodium Chlorite/DBDMH Combination","Green Chem.","2017","","","","","10.1039/C7GC00144D","","","0.71073","MoKα","","0.058","0.0386","","","0.0819","0.0889","","","","","","0.985","","","","has coordinates","301865","2025-08-22","16:17:13",""
"7228288","7.7777","0.0004","13.5678","0.0007","16.7615","0.0009","90","","90","","90","","1768.78","0.16","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C22 H28 O2 -","- C22 H28 O2 -","- C88 H112 O8 -","4","1","","Werner, Georg; Rodygin, Konstantin S.; Kostin, Anton A.; Gordeev, Evgeniy G.; Kashin, Alexey S.; Ananikov, Valentine P.","A solid acetylene reagent with enhanced reactivity: fluoride-mediated functionalization of alcohols and phenols","Green Chem.","2017","","","","","10.1039/C7GC00724H","","","0.71073","MoKα","","0.0475","0.0393","","","0.0911","0.095","","","","","","1.035","","","","has coordinates","301865","2025-08-22","16:17:14",""
"7228289","12.6051","0.0008","8.5936","0.0003","13.0034","0.0008","90","","117.576","0.008","90","","1248.55","0.15","100","2","100","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C29 H48 O -","- C29 H48 O -","- C58 H96 O2 -","2","1","","Werner, Georg; Rodygin, Konstantin S.; Kostin, Anton A.; Gordeev, Evgeniy G.; Kashin, Alexey S.; Ananikov, Valentine P.","A solid acetylene reagent with enhanced reactivity: fluoride-mediated functionalization of alcohols and phenols","Green Chem.","2017","","","","","10.1039/C7GC00724H","","","0.71073","MoKα","","0.0555","0.0426","","","0.0855","0.0929","","","","","","1.008","","","","has coordinates","301865","2025-08-22","16:17:14",""
"7228294","8.1926","0.0011","16.181","0.002","13.1852","0.0018","90","","104.684","0.007","90","","1690.8","0.4","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H14 O3 S -","- C22 H14 O3 S -","- C88 H56 O12 S4 -","4","1","","Majee, Adinath; Mahato, Sachinta; Santra, Sougata; Chatterjee, Rana; Zyryanov, Grigory V.; Hajra, Alakananda","Brønsted acidic ionic liquid-catalyzed tandem reaction: an efficient approach towards regioselective synthesis of pyrano[3,2-c]coumarins under solvent-free conditions bearing lower E-factors","Green Chem.","2017","","","","","10.1039/C7GC01158J","","","0.71073","MoKα","","0.1104","0.0808","","","0.2299","0.2619","","","","","","1.482","","","","has coordinates","206958","2020-10-21","18:00:00",""
"7228330","9.4992","0.0007","12.0176","0.0009","14.7148","0.0011","90","","107.666","0.002","90","","1600.6","0.2","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H17 N O3 -","- C19 H17 N O3 -","- C76 H68 N4 O12 -","4","1","","Upadhyay, Nitinkumar Satyadev; Thorat, Vijaykumar Haridas; Sato, Ryota; Annamalai, Pratheepkumar; Chuang, Shih-Ching; Cheng, Chien Hong","Synthesis of Isoquinolones via Rh-Catalyzed C–H Activation of Substituted Benzamides Using Air as the Sole Oxidant in Water.","Green Chem.","2017","","","","","10.1039/C7GC01221G","","","0.71073","MoKα","","0.1079","0.0588","","","0.1424","0.169","","","","","","1.03","","","","has coordinates","301865","2025-08-22","16:17:14",""
"7228331","10.0712","0.0006","9.0247","0.0005","19.0587","0.0009","90","","99.811","0.003","90","","1706.9","0.16","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H22 N2 O2 -","- C20 H22 N2 O2 -","- C80 H88 N8 O8 -","4","1","","Upadhyay, Nitinkumar Satyadev; Thorat, Vijaykumar Haridas; Sato, Ryota; Annamalai, Pratheepkumar; Chuang, Shih-Ching; Cheng, Chien Hong","Synthesis of Isoquinolones via Rh-Catalyzed C–H Activation of Substituted Benzamides Using Air as the Sole Oxidant in Water.","Green Chem.","2017","","","","","10.1039/C7GC01221G","","","0.71073","MoKα","","0.0539","0.0424","","","0.1059","0.1133","","","","","","1.076","","","","has coordinates","301865","2025-08-22","16:17:14",""
"7228332","9.3178","0.0012","9.5222","0.0012","10.9385","0.0014","68.404","0.003","66.038","0.003","66.642","0.003","789.02","0.18","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H17 N O -","- C22 H17 N O -","- C44 H34 N2 O2 -","2","1","","Upadhyay, Nitinkumar Satyadev; Thorat, Vijaykumar Haridas; Sato, Ryota; Annamalai, Pratheepkumar; Chuang, Shih-Ching; Cheng, Chien Hong","Synthesis of Isoquinolones via Rh-Catalyzed C–H Activation of Substituted Benzamides Using Air as the Sole Oxidant in Water.","Green Chem.","2017","","","","","10.1039/C7GC01221G","","","0.71073","MoKα","","0.0422","0.0354","","","0.0897","0.0944","","","","","","1.043","","","","has coordinates","301865","2025-08-22","16:17:14",""
"7228397","7.4395","0.0002","10.2984","0.0003","10.4052","0.0003","118.125","0.0006","94.6199","0.0007","92.7499","0.0007","697.42","0.03","150","2","150","2","","","","","","","","6","P -1","-P 1","2","","","","- C18 H38 Ca I2 N2 O8 -","- C18 H38 Ca I2 N2 O8 -","- C18 H38 Ca I2 N2 O8 -","1","0.5","","Steinbauer, J.; Spannenberg, A.; Werner, T.","An in situ formed Ca2±-crown ether complex and its use in CO2-fixation reactions with terminal and internal epoxides","Green Chem.","2017","","","","","10.1039/C7GC01114H","","","0.71073","MoKα","","0.0173","0.0158","","","0.0361","0.0369","","","","","","1.088","","","","has coordinates","301865","2025-08-22","16:17:14",""
"7228398","8.6487","0.0002","9.628","0.0002","10.6343","0.0002","90","","90","","90","","885.51","0.03","150","2","150","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C10 H10 O4 -","- C10 H10 O4 -","- C40 H40 O16 -","4","1","","Steinbauer, J.; Spannenberg, A.; Werner, T.","An in situ formed Ca2±-crown ether complex and its use in CO2-fixation reactions with terminal and internal epoxides","Green Chem.","2017","","","","","10.1039/C7GC01114H","","","1.54178","CuKα","","0.0283","0.0282","","","0.0707","0.0708","","","","","","1.113","","","","has coordinates","301865","2025-08-22","16:17:14",""
"7228456","10.7089","0.0007","11.6927","0.0009","13.5483","0.0011","114.506","0.008","99.354","0.006","104.113","0.006","1428.7","0.2","291","2","291","2","","","","","","","","4","P -1","-P 1","2","","","","- C26 H43 B3 O6 -","- C26 H43 B3 O6 -","- C52 H86 B6 O12 -","2","1","","Gao, Guoliang; Yan, Jianxiang; Yang, Kai; Chen, Fen er; Song, Qiuling","Base-Controlled Highly Selective Synthesis of Alkyl 1,2-Bis(boronates) or 1,1,2-Tris(boronates) from Terminal Alkynes","Green Chem.","2017","","","","","10.1039/C7GC01161J","","","0.71073","MoKα","","0.0955","0.0702","","","0.1945","0.2191","","","","","","1.0465","","","","has coordinates","301865","2025-08-22","16:17:14",""
"7228528","12.3686","0.0008","15.9846","0.0011","9.9812","0.0007","90","","113.591","0.001","90","","1808.4","0.2","100","2","100","2","","","","","","","","5","P 1 c 1","P -2yc","7","","","","- C20 H24 F N2 O4.5 -","- C20 H24 F N2 O4.5 -","- C80 H96 F4 N8 O18 -","4","2","","Ma, Yulu; Wang, Kai-Min; Huang, Rong; Lin, Jun; Yan, Sheng-Jiao","An environmentally benign double Michael addition reaction of heterocyclic ketene aminals with quinone monoketals for diastereoselective synthesis of highly functionly morphan derivatives in water","Green Chem.","2017","","","","","10.1039/C7GC01435J","","","0.71073","MoKα","","0.0385","0.0345","","","0.0888","0.0938","","","","","","1.041","","","","has coordinates","301865","2025-08-22","16:17:14",""
"7228529","23.064","0.002","9.1067","0.0009","19.757","0.002","90","","102.558","0.002","90","","4050.4","0.7","100","2","100","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C21 H28 Cl N2 O5.5 -","- C21 H28 Cl N2 O5.5 -","- C168 H224 Cl8 N16 O44 -","8","1","","Ma, Yulu; Wang, Kai-Min; Huang, Rong; Lin, Jun; Yan, Sheng-Jiao","An environmentally benign double Michael addition reaction of heterocyclic ketene aminals with quinone monoketals for diastereoselective synthesis of highly functionly morphan derivatives in water","Green Chem.","2017","","","","","10.1039/C7GC01435J","","","0.71073","MoKα","","0.0573","0.0528","","","0.1552","0.1596","","","","","","1.08","","","","has coordinates","301865","2025-08-22","16:17:14",""
"7228530","14.6978","0.0015","12.2595","0.0012","21.83","0.002","90","","108.609","0.001","90","","3727.8","0.6","298","2","298","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C21 H26 N2 O4 -","- C21 H26 N2 O4 -","- C168 H208 N16 O32 -","8","1","","Ma, Yulu; Wang, Kai-Min; Huang, Rong; Lin, Jun; Yan, Sheng-Jiao","An environmentally benign double Michael addition reaction of heterocyclic ketene aminals with quinone monoketals for diastereoselective synthesis of highly functionly morphan derivatives in water","Green Chem.","2017","","","","","10.1039/C7GC01435J","","","0.71073","MoKα","","0.0629","0.0426","","","0.1296","0.1494","","","","","","0.981","","","","has coordinates","301865","2025-08-22","16:17:14",""
"7228563","9.7024","0.0003","9.8685","0.0003","12.5819","0.0004","80.421","0.001","70.629","0.001","65.931","0.001","1037.01","0.06","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H19 N5 O5 -","- C22 H19 N5 O5 -","- C44 H38 N10 O10 -","2","1","","m, vadivelu; S, Sugirdha; Pandurangan, Dheenkumar; Arun, Y.; Karthikeyan, K.; Chandrasekar, Praveen","Solvent-free implementation of two dissimilar reactions using recyclable CuO nanoparticle under ball-milling conditions: Synthesis of new oxindole-triazole pharmacophores","Green Chem.","2017","","","","","10.1039/C7GC01284E","","","0.71073","MoKα","","0.049","0.0382","","","0.1014","0.1107","","","","","","1.034","","","","has coordinates","301865","2025-08-22","16:17:14",""
"7228696","7.152","0.0007","8.1484","0.0006","20.7756","0.0009","90.232","0.005","98.462","0.006","113.488","0.009","1095.71","0.16","105","8","105","8","","","","","","","","5","P -1","-P 1","2","","","","- C11 H10 Br0 N O -","- C5.8 H13.6 Br0.8 N0.8 O1.4 -","- C29 H68 Br4 N4 O7 -","5","2.5","","Blesic, Marijana; Gilmore, Brendan F.; Holbrey, John D.; Jacquemin, Johan; Level, Gaelle; Nockemann, Peter; Stella, Lorenzo","An introduction to zwitterionic salts","Green Chem.","2017","","","","","10.1039/C7GC01523B","","x-ray","1.54184","CuKα","","0.0955","0.0907","","","0.3108","0.3187","","","","","","1.44","","","","has coordinates","198818","2020-10-21","18:00:00",""
"7228697","24.0379","0.0003","8.6157","0.0001","16.3926","0.0002","90","","99.7","0.001","90","","3346.43","0.07","293","2","293","2","","","","","","","","7","C 1 2/c 1","-C 2yc","15","","","","- C H Br0 Cl0.02 N O S0.02 -","- C1.41935 H3.85677 Br0.129032 N0.258065 O0.597355 S0.129032 -","- C88 H239.12 Br8 N16 O37.036 S8 -","62","7.75","","Blesic, Marijana; Gilmore, Brendan F.; Holbrey, John D.; Jacquemin, Johan; Level, Gaelle; Nockemann, Peter; Stella, Lorenzo","An introduction to zwitterionic salts","Green Chem.","2017","","","","","10.1039/C7GC01523B","","","1.54184","CuKα","","0.0326","0.0326","","","0.0809","0.0809","","","","","","1.182","","","","has coordinates","198818","2020-10-21","18:00:00",""
"7228815","7.5751","0.0005","10.0045","0.0007","13.9038","0.0009","93.5","0.006","90.41","0.005","104.176","0.006","1019.44","0.12","100.01","0.1","100.01","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C18 H36 B Na O5 -","- C18 H36 B Na O5 -","- C36 H72 B2 Na2 O10 -","2","1","","Wu, Yile; Shan, Changkai; Ying, Jianxi; Su, Jue; Zhu, Jun; Liu, Liu Leo; Zhao, Yufen","Catalytic Hydroboration of Aldehydes, Ketones, Alkynes and Alkenes Initiated by NaOH","Green Chem.","2017","","","","","10.1039/C7GC01632H","","x-ray","1.54184","CuKα","","0.042","0.0394","","","0.1062","0.1096","","","","","","1.024","","","","has coordinates","199426","2020-10-21","18:00:00",""
"7228903","6.3918","0.0005","8.7724","0.0008","33.496","0.003","90","","90.306","0.005","90","","1878.1","0.3","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C26 H21 N O -","- C26 H21 N O -","- C104 H84 N4 O4 -","4","1","","Deb, Mohit L.; Pegu, Choitanya D.; Borpatra, Paran J.; Saikia, Prakash J.; Baruah, Pranjal K.","Catalyst-free multi-component cascade C–H-functionalization in water using molecular oxygen: an approach to 1,3-oxazines","Green Chem.","2017","","","","","10.1039/C7GC01494E","","","0.71073","MoKα","","0.1232","0.0975","","","0.2735","0.2958","","","","","","0.828","","","","has coordinates","301865","2025-08-22","16:17:16",""
"7228924","7.4735","0.0001","11.8551","0.0002","42.384","0.003","90","","90","","90","","3755.2","0.3","293","2","293","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C18 H22 N2 O5 S2 -","- C18 H22 N2 O5 S2 -","- C144 H176 N16 O40 S16 -","8","1","","Nguyen, Le Anh; Ngo, Anh Quoc; Retailleau, Pascal; Nguyen, Thanh Binh","Elemental Sulfur as Polyvalent Reagent in Redox Condensation with o-Chloronitrobenzenes and Benzaldehydes: Three-Component Access to 2-Arylbenzothiazoles","Green Chem.","2017","","","","","10.1039/C7GC01825H","","","1.54187","CuKα","","0.0888","0.0472","","","0.1051","0.1523","","","","","","1.138","","","","has coordinates","301865","2025-08-22","16:17:16",""
"7229020","10.389","0.002","15.957","0.003","8.4911","0.0017","90","","111.16","0.03","90","","1312.7","0.5","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","anti-N-methyl-4,7-bis(methoxymethyl)norcantharimide","anti-4,7-bis(methoxymethyl)-2-methylhexahydro-1H-4,7-epoxyisoindole-1,3(2H)-dione","","- C13 H19 N O5 -","- C13 H19 N O5 -","- C52 H76 N4 O20 -","4","1","","Kucherov, Fedor; Galkin, Konstantin; Gordeev, Evgeniy; Ananikov, Valentine","Efficient route for the construction of polycyclic systems from bioderived HMF","Green Chem.","2017","","","","","10.1039/C7GC02211E","","","0.9699","synchrotron","","0.1043","0.0878","","","0.2002","0.2168","","","","","","1.095","","","","has coordinates","301865","2025-08-22","16:17:17",""
"7229021","11.602","0.002","7.6108","0.0015","11.152","0.002","90","","95.45","0.03","90","","980.3","0.3","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","bis(hydroxymethyl)norcantharimide","endo-4,7-bis(hydroxymethyl)hexahydro-1H-4,7-epoxyisoindole-1,3(2H)-dione","","- C10 H13 N O5 -","- C10 H13 N O5 -","- C40 H52 N4 O20 -","4","1","","Kucherov, Fedor; Galkin, Konstantin; Gordeev, Evgeniy; Ananikov, Valentine","Efficient route for the construction of polycyclic systems from bioderived HMF","Green Chem.","2017","","","","","10.1039/C7GC02211E","","","0.9699","synchrotron","","0.0853","0.0635","","","0.1183","0.1342","","","","","","0.876","","","","has coordinates","301865","2025-08-22","16:17:17",""
"7229055","8.8111","0.0007","8.8406","0.0006","11.0875","0.0008","71.938","0.006","83.952","0.006","85.034","0.006","815.21","0.11","292","2","292","2","","","","","","","","5","P -1","-P 1","2","","","","- C18 H22 N O P -","- C18 H22 N O P -","- C36 H44 N2 O2 P2 -","2","1","","Yukang, Wang; Peng, Qian; Su, Ji-Hu; Li, Yanan; Bi, MeiXiang; Zha, Zhenggen; Wang, Zhiyong","Efficient electrosynthesis of phosphinic amides via oxidative cross-coupling between N−H/P−H","Green Chem.","2017","","","","","10.1039/C7GC01989K","","","1.54184","CuKα","","0.0746","0.0676","","","0.176","0.1887","","","","","","1.082","","","","has coordinates","301865","2025-08-22","16:17:17",""
"7229056","13.49822","0.00011","23.26985","0.00016","27.6329","0.0002","90","","91.6656","0.0008","90","","8675.87","0.11","150","1","150","1","","","","","","","","8","P 1 21/c 1","-P 2ybc","14","Bis(1,1,1-tris(diphenylphosphinomethyl)ethane)-tris(mu2-hydroxo)-di-ruthenium(II) truflate methanol water acetonitrile solvate","","","- C88 H99.54 F3 N O10.77 P6 Ru2 S -","- C88 H81 F3 N O10.77 P6 Ru2 S -","- C352 H324 F12 N4 O43.08 P24 Ru8 S4 -","4","1","","Latifi, Elnaz; Marchese, Austin; Hulls, Margaret; Soldatov, Dmitriy V.; Schlaf, Marcel","[Ru(triphos)(CH3CN)3](OTf)2 as a homogeneous catalyst for the hydrogenation of biomass derived 2,5-hexanedione and 2,5-dimethyl-furan in aqueous acidic medium.","Green Chem.","2017","","","","","10.1039/C7GC01956D","","","0.71073","MoKα","","0.0557","0.05","","","0.1261","0.1284","","","","","","1.208","","","","has coordinates,has disorder","200167","2020-10-21","18:00:00",""
"7229057","16.0271","0.0003","13.2323","0.0003","24.2112","0.0005","90","","91.014","0.002","90","","5133.8","0.18","150","2","150","2","","","","","","","","8","P 1 21 1","P 2yb","4","[Ru(MeCN)3(tripphos)](CF3SO3)2","","","- C49 H48 F6 N3 O6 P3 Ru S2 -","- C49 H48 F6 N3 O6 P3 Ru S2 -","- C196 H192 F24 N12 O24 P12 Ru4 S8 -","4","2","","Latifi, Elnaz; Marchese, Austin; Hulls, Margaret; Soldatov, Dmitriy V.; Schlaf, Marcel","[Ru(triphos)(CH3CN)3](OTf)2 as a homogeneous catalyst for the hydrogenation of biomass derived 2,5-hexanedione and 2,5-dimethyl-furan in aqueous acidic medium.","Green Chem.","2017","","","","","10.1039/C7GC01956D","","","0.71073","MoKα","","0.0822","0.0619","","","0.1605","0.1724","","","","","","1.062","","","","has coordinates,has disorder","301865","2025-08-22","16:17:17",""
"7229225","22.5633","0.0011","10.2111","0.0005","13.1867","0.0005","90","","90","","90","","3038.2","0.2","100","","100","","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C13 H22 N2 O4 -","- C13 H22 N2 O4 -","- C104 H176 N16 O32 -","8","2","","de Robillard, G.; Fournier, A. H.; Cattey, H.; Devillers, C. H.; Andrieu, J.","Bio-based 1,3-diisobutyl imidazolium hydrogen oxalate [iBu2IM](HC2O4) as CO2 shuttle","Green Chem.","2017","","","","","10.1039/C7GC02167D","","","0.71073","MoKα","","0.0581","0.0379","","","0.0744","0.0805","","","","","","1.014","","","","has coordinates,has disorder","301865","2025-08-22","16:17:17",""
"7229226","10.1801","0.0012","12.3007","0.0015","11.6842","0.0015","90","","96.132","0.004","90","","1454.8","0.3","298","","298","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C12 H22 N2 O3 -","- C12 H22 N2 O3 -","- C48 H88 N8 O12 -","4","1","","de Robillard, G.; Fournier, A. H.; Cattey, H.; Devillers, C. H.; Andrieu, J.","Bio-based 1,3-diisobutyl imidazolium hydrogen oxalate [iBu2IM](HC2O4) as CO2 shuttle","Green Chem.","2017","","","","","10.1039/C7GC02167D","","x-ray","0.71073","MoKα","","0.117","0.0679","","","0.1815","0.2294","","","","","","1.017","","","","has coordinates","301865","2025-08-22","16:17:17",""
"7229252","21.6561","0.0006","5.3166","0.0001","22.9403","0.0006","90","","114.074","0.001","90","","2411.53","0.1","150","","150","","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C18 H11 N O -","- C18 H11 N O -","- C144 H88 N8 O8 -","8","1","","Parisien-Collette, Shawn; Cruché, Corentin; Abel-Snape, Xavier; Collins, Shawn K.","Photochemical intramolecular amination for the synthesis of heterocycles","Green Chem.","2017","","","","","10.1039/C7GC02261A","","x-ray","1.34139","GaKα","","0.0428","0.0416","","","0.1042","0.1057","","","","","","1.082","","","","has coordinates","301865","2025-08-22","16:17:17",""
"7229351","10.7579","0.0006","9.2297","0.0005","11.7358","0.0007","90","","92.003","0.005","90","","1164.56","0.11","293","0.1","293","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C12 H13 N O2 S -","- C12 H13 N O2 S -","- C48 H52 N4 O8 S4 -","4","1","","Nguyen, Thanh Binh; Retailleau, Pascal","Methyl ketone break-and-rebuild: a strategy for full α-heterofunctionalization of acetophenones","Green Chem.","2017","","","","","10.1039/C7GC02558K","","x-ray","0.71073","MoKα","","0.0555","0.043","","","0.1159","0.1256","","","","","","1.052","","","","has coordinates","301865","2025-08-22","16:17:17",""
"7229371","14.1736","0.0005","15.6168","0.0007","20.0291","0.0008","90","","90","","90","","4433.4","0.3","99.98","","99.98","","","","","","","","","7","P 21 21 21","P 2ac 2ab","19","","Carbonyl(trihydroborato)(hydruro)[bis(2-diisopropylphosphinoethyl)amido] ruthenium(II)","","- C17 H40 B N O P2 Ru -","- C17 H40 B N O P2 Ru -","- C136 H320 B8 N8 O8 P16 Ru8 -","8","2","","Nguyen, Duc Hanh; Raffa, Guillaume; Morin, Yohann; Desset, Simon Laurent; Capet, Frédéric; nardello-rataj, veronique; Dumeignil, Franck Yves; Gauvin, Régis","Solvent- and Base-Free Synthesis of Wax Esters from Fatty Acid Methyl Esters by Consecutive One-Pot, Two-Step Catalysis.","Green Chem.","2017","","","","","10.1039/C7GC02764H","","","0.71073","MoKα","","0.0416","0.0302","","","0.0493","0.0528","","","","","","1.017","","","","has coordinates","202248","2020-10-21","18:00:00",""
"7229390","8.22","0.0012","8.7275","0.0007","13.0899","0.0009","71.212","0.007","72.443","0.01","79.12","0.01","843.24","0.16","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","8'-bromo-1',2',3',3a'-tetrahydro-5'H-spiro[chromane-3,4'-pyrrolo[1,2-a]quinoline]-2,4-dione","","- C20 H16 Br N O3 -","- C20 H16 Br N O3 -","- C40 H32 Br2 N2 O6 -","2","1","","Zhu, Shuai; chen, Chunqi; Xiao, Mingyan; Yu, Liping; Wang, Liang; Xiao, Jian","Construction of the tetrahydroquinoline spiro skeleton via cascade [1,5]-hydride transfer-involved C(sp3)-H functionalization “on water”","Green Chem.","2017","","","","","10.1039/C7GC02353G","","","1.54184","CuKα","","0.0576","0.052","","","0.1421","0.1484","","","","","","1.069","","","","has coordinates","301865","2025-08-22","16:17:18",""
"7229391","5.4797","0.0004","9.567","0.0007","24.6309","0.0017","90","","90","","90","","1291.26","0.16","173.15","","173.15","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C17 H13 N S -","- C17 H13 N S -","- C68 H52 N4 S4 -","4","1","","Deng, Guo-Jun; Ni, Penghui; Li, Bin; Huang, Huawen; Xiao, Fuhong","Solvent-controlled highly regio-selective thieno[2,3-b]indole formation under metal-free conditions","Green Chem.","2017","","","","","10.1039/C7GC02818K","","","0.71073","MoKα","","0.0417","0.0392","","","0.0857","0.0878","","","","","","1.132","","","","has coordinates","301865","2025-08-22","16:17:18",""
"7229392","6.2817","0.0013","19.73","0.004","23.695","0.005","90","","90","","90","","2936.7","1.1","173","2","173","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C17 H12 I N S -","- C17 H12 I N S -","- C136 H96 I8 N8 S8 -","8","1","","Deng, Guo-Jun; Ni, Penghui; Li, Bin; Huang, Huawen; Xiao, Fuhong","Solvent-controlled highly regio-selective thieno[2,3-b]indole formation under metal-free conditions","Green Chem.","2017","","","","","10.1039/C7GC02818K","","","0.71073","MoKα","","0.0514","0.0469","","","0.09","0.0923","","","","","","1.162","","","","has coordinates","301865","2025-08-22","16:17:18",""
"7229406","7.2077","0.0011","17.214","0.003","18.628","0.003","116.909","0.008","91.456","0.009","101.06","0.009","2006","0.6","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C46 H28 N6 O3 -","- C46 H28 N6 O3 -","- C92 H56 N12 O6 -","2","1","","Patra, Sajal Kumar; Sahu, Kasturi; Patra, Bratati; Sahoo, Dipak Kumar; Mondal, Sruti; Mukherjee, Payel; Biswal, Himansu S.; Kar, Sanjib","Synthesis of urea derivatives via reductive carbon dioxide fixation into contracted porphyrin analogues","Green Chem.","2017","","","","","10.1039/C7GC02798B","","x-ray","0.71073","MoKα","","0.165","0.0695","","","0.1522","0.1763","","","","","","0.989","","","","has coordinates","301865","2025-08-22","16:17:18",""
"7229407","7.7014","0.0005","15.767","0.0009","17.5273","0.001","115.061","0.004","98.474","0.004","93.397","0.004","1889.2","0.2","296.15","0.02","296.15","0.02","","","","","","","","4","P -1","-P 1","2","","","","- C41 H21 N7 O -","- C41 H21 N7 O -","- C82 H42 N14 O2 -","2","1","","Patra, Sajal Kumar; Sahu, Kasturi; Patra, Bratati; Sahoo, Dipak Kumar; Mondal, Sruti; Mukherjee, Payel; Biswal, Himansu S.; Kar, Sanjib","Synthesis of urea derivatives via reductive carbon dioxide fixation into contracted porphyrin analogues","Green Chem.","2017","","","","","10.1039/C7GC02798B","","x-ray","0.71073","MoKα","","0.1474","0.0874","","","0.2467","0.2769","","","","","","0.999","","","","has coordinates","301865","2025-08-22","16:17:18",""
"7229408","16.1335","0.0008","16.7689","0.0008","13.7048","0.0006","90","","111.276","0.002","90","","3455","0.3","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C38 H21 N7 O7 -","- C38 H21 N7 O7 -","- C152 H84 N28 O28 -","4","1","","Patra, Sajal Kumar; Sahu, Kasturi; Patra, Bratati; Sahoo, Dipak Kumar; Mondal, Sruti; Mukherjee, Payel; Biswal, Himansu S.; Kar, Sanjib","Synthesis of urea derivatives via reductive carbon dioxide fixation into contracted porphyrin analogues","Green Chem.","2017","","","","","10.1039/C7GC02798B","","x-ray","0.71073","MoKα","","0.138","0.0641","","","0.1591","0.1831","","","","","","0.959","","","","has coordinates,has disorder","202371","2020-10-21","18:00:00",""
"7229452","9.2362","0.0009","9.2949","0.0008","10.8564","0.0009","89.518","0.007","83.33","0.008","80.219","0.008","912.19","0.14","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C24 H19 N O2 -","- C24 H19 N O2 -","- C48 H38 N2 O4 -","2","1","","Ma, Xiao-Pan; Li, Kun; Wu, Si-Yi; Liang, Cui; SU, Guifa; Mo, Dong-Liang","Construction of 2,3-Quaternary Fused Indolines from Alkynyl tethered Oximes and Diaryliodonium Salts through A Cascade Strategy of N-Arylation/Cycloaddition/[3,3]-Rearrangement","Green Chem.","2017","","","","","10.1039/C7GC02844J","","","0.71073","MoKα","","0.0695","0.0506","","","0.1608","0.1822","","","","","","1.052","","","","has coordinates","301865","2025-08-22","16:17:18",""
"7229453","8.8958","0.0012","18.729","0.002","13.2336","0.0018","90","","108.186","0.002","90","","2094.7","0.5","296","2","296.15","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C24 H17 Br2 N O2 -","- C24 H17 Br2 N O2 -","- C96 H68 Br8 N4 O8 -","4","1","","Ma, Xiao-Pan; Li, Kun; Wu, Si-Yi; Liang, Cui; SU, Guifa; Mo, Dong-Liang","Construction of 2,3-Quaternary Fused Indolines from Alkynyl tethered Oximes and Diaryliodonium Salts through A Cascade Strategy of N-Arylation/Cycloaddition/[3,3]-Rearrangement","Green Chem.","2017","","","","","10.1039/C7GC02844J","","","0.71073","MoKα","","0.1009","0.0597","","","0.1581","0.181","","","","","","1.044","","","","has coordinates","301865","2025-08-22","16:17:18",""
"7229454","9.272","0.003","9.723","0.003","21.851","0.008","90","","90","","90","","1969.9","1.1","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C25 H22 N2 O -","- C25 H22 N2 O -","- C100 H88 N8 O4 -","4","1","","Ma, Xiao-Pan; Li, Kun; Wu, Si-Yi; Liang, Cui; SU, Guifa; Mo, Dong-Liang","Construction of 2,3-Quaternary Fused Indolines from Alkynyl tethered Oximes and Diaryliodonium Salts through A Cascade Strategy of N-Arylation/Cycloaddition/[3,3]-Rearrangement","Green Chem.","2017","","","","","10.1039/C7GC02844J","","","0.71073","MoKα","","0.0738","0.0519","","","0.1485","0.1675","","","","","","1.019","","","","has coordinates","301865","2025-08-22","16:17:18",""
"7229455","11.2923","0.0005","11.1395","0.0005","22.6048","0.0007","90","","90","","90","","2843.5","0.2","292.87","0.1","292.87","0.1","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C16 H13 N O3 Se -","- C16 H13 N O3 Se -","- C128 H104 N8 O24 Se8 -","8","1","","Zhang, Qing-Bao; Ban, Yong-Liang; Yuan, Pan-Feng; Peng, Shoujiao; Fang, Jianguo; Wu, Li-Zhu; Liu, Qiang","Visible-Light-Mediated Aerobic Selenation of (Hetero)Arenes with Diselenides","Green Chem.","2017","","","","","10.1039/C7GC02803B","","","0.71073","MoKα","","0.0705","0.0396","","","0.0726","0.0851","","","","","","1.019","","","","has coordinates","301865","2025-08-22","16:17:18",""