# Search results of SQL query from the Crystallography Open Database
# Date and time performed: 2026-02-02T04:01:32+01:00
# Query:
# SELECT data.*
# FROM
#  data JOIN jaltnames
#  ON altname = journal
# WHERE
#  (status is null or status != 'retracted') and
#  (journal_id IN (SELECT DISTINCT(journal_id) FROM jaltnames WHERE altname LIKE 'Organic Chemistry Frontiers') AND volume = 4 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
"1553497","8.125","0.0016","9.328","0.0019","11.408","0.002","90.91","0.03","96.19","0.03","107.69","0.03","817.8","0.3","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C19 H17 N O4 -","- C19 H17 N O4 -","- C38 H34 N2 O8 -","2","1","","Dai, Jie; Ren, Wenlong; Chang, Wenju; Zhang, Ping; Shi, Yian","An effective route to β2-amino acid derivatives via Pd-catalyzed regioselective hydrocarboxylation of 1,2-disubstituted enimides","Organic Chemistry Frontiers","2017","4","2","297","","10.1039/C6QO00353B","","","0.71073","MoKα","","0.1599","0.0691","","","0.1238","0.1481","","","","","","1.001","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553519","11.5593","0.0003","14.0068","0.0003","17.8914","0.0004","90","","90","","90","","2896.78","0.12","130","","130","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C36 H32 F2 N2 O2 -","- C36 H32 F2 N2 O2 -","- C144 H128 F8 N8 O8 -","4","1","","Zhu, Zi-Qi; Yin, Lei; Wang, Yang; Shen, Yang; Li, Can; Mei, Guang-Jian; Shi, Feng","Diastereo- and enantioselective construction of biologically important pyrrolo[1,2-a]indole scaffolds via catalytic asymmetric [3 + 2] cyclodimerizations of 3-alkyl-2-vinylindoles","Organic Chemistry Frontiers","2017","4","1","57","","10.1039/C6QO00446F","","","1.54178","CuKα","","0.0409","0.0361","","","0.1029","0.1084","","","","","","0.821","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553520","19.661","0.013","10.71","0.007","17.118","0.011","90","","97.306","0.011","90","","3575","4","130","","130","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C44 H50 N2 -","- C44 H50 N2 -","- C176 H200 N8 -","4","1","","Zhu, Zi-Qi; Yin, Lei; Wang, Yang; Shen, Yang; Li, Can; Mei, Guang-Jian; Shi, Feng","Diastereo- and enantioselective construction of biologically important pyrrolo[1,2-a]indole scaffolds via catalytic asymmetric [3 + 2] cyclodimerizations of 3-alkyl-2-vinylindoles","Organic Chemistry Frontiers","2017","4","1","57","","10.1039/C6QO00446F","","","0.71073","MoKα","","0.1483","0.0877","","","0.1849","0.221","","","","","","1.07","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553521","6.9478","0.0005","9.1969","0.0005","11.8012","0.001","82.206","0.006","81.643","0.007","75.22","0.006","717.55","0.09","100","2","100","2","","","","","","","","4","P -1","-P 1","2","(Ph-CH3)-S-[Ph(OCH3)3]","","","- C16 H18 O3 S -","- C16 H18 O3 S -","- C32 H36 O6 S2 -","2","1","","Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang","Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent","Organic Chemistry Frontiers","2017","4","1","31","","10.1039/C6QO00451B","","","1.54184","CuKα","","0.0488","0.0374","","","0.0923","0.0976","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553522","7.68603","0.00016","23.9176","0.0004","7.76261","0.00017","90","","111.053","0.003","90","","1331.76","0.05","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","(Ph-CH3)-S-(Ph-(OCH3)2)","","","- C15 H16 O2 S -","- C15 H16 O2 S -","- C60 H64 O8 S4 -","4","1","","Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang","Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent","Organic Chemistry Frontiers","2017","4","1","31","","10.1039/C6QO00451B","","","1.54184","CuKα","","0.0309","0.0287","","","0.0772","0.0786","","","","","","1.07","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553523","5.7042","0.0003","25.743","0.002","7.8069","0.0004","90","","94.59","0.005","90","","1142.71","0.12","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","(Ph-CH3)-S-(Ph-CN)","","","- C14 H11 N S -","- C14 H11 N S -","- C56 H44 N4 S4 -","4","1","","Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang","Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent","Organic Chemistry Frontiers","2017","4","1","31","","10.1039/C6QO00451B","","","0.71073","MoKα","","0.049","0.0426","","","0.0937","0.0967","","","","","","1.066","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553524","5.7958","0.0003","25.4544","0.0012","8.3123","0.0004","90","","93.626","0.004","90","","1223.85","0.1","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","(Ph-CH3)-S-(PhCOCH3)","","","- C15 H14 O S -","- C15 H14 O S -","- C60 H56 O4 S4 -","4","1","","Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang","Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent","Organic Chemistry Frontiers","2017","4","1","31","","10.1039/C6QO00451B","","","0.71073","MoKα","","0.0442","0.0359","","","0.0856","0.0903","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553525","5.611","0.0003","25.6833","0.0013","8.991","0.0004","90","","98.982","0.004","90","","1279.8","0.11","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","(Ph-CH3)-S-(PhCOOCH3)","","","- C15 H14 O2 S -","- C15 H14 O2 S -","- C60 H56 O8 S4 -","4","1","","Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang","Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent","Organic Chemistry Frontiers","2017","4","1","31","","10.1039/C6QO00451B","","","1.54184","CuKα","","0.0725","0.0551","","","0.1475","0.1531","","","","","","1.18","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553526","5.67633","0.00018","26.8781","0.0008","7.7875","0.0002","90","","95.042","0.003","90","","1183.53","0.06","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","(Ph-CN)-S-(PhOCH3)","","","- C14 H11 N O S -","- C14 H11 N O S -","- C56 H44 N4 O4 S4 -","4","1","","Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang","Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent","Organic Chemistry Frontiers","2017","4","1","31","","10.1039/C6QO00451B","","","1.54184","CuKα","","0.0356","0.0332","","","0.0883","0.0899","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553527","7.8232","0.0004","11.6428","0.0005","14.5818","0.0007","84.863","0.004","83.654","0.004","73.557","0.004","1263.68","0.11","100","2","100","2","","","","","","","","4","P -1","-P 1","2","(Ph-CN)-S-S-(Ph-CN)","","","- C14 H8 N2 S2 -","- C14 H8 N2 S2 -","- C56 H32 N8 S8 -","4","2","","Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang","Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent","Organic Chemistry Frontiers","2017","4","1","31","","10.1039/C6QO00451B","","","1.54184","CuKα","","0.0784","0.0691","","","0.2121","0.2166","","","","","","1.119","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553530","7.455","0.0005","11.3624","0.0007","18.4877","0.0013","90","","92.585","0.006","90","","1564.44","0.18","273.77","0.1","273.77","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C35 H53 N O3 -","- C35 H53 N O3 -","- C70 H106 N2 O6 -","2","1","","Li, Zheng-Yu; Qi, Feng-Ming; Zhi, De-Juan; Hu, Qiao-Ling; Liu, Ying-Hong; Zhang, Zhan-Xin; Fei, Dong-Qing","A novel spirocyclic triterpenoid and a new taraxerane triterpenoid from Teucrium viscidum","Organic Chemistry Frontiers","2017","4","1","42","","10.1039/C6QO00460A","","x-ray","1.54184","CuKα","","0.0628","0.0567","","","0.1539","0.1616","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553531","6.52391","0.0001","12.9427","0.0002","31.7963","0.0006","90","","90","","90","","2684.78","0.08","154.89","0.1","293","","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C30 H50 O3 -","- C30 H50 O3 -","- C120 H200 O12 -","4","1","","Li, Zheng-Yu; Qi, Feng-Ming; Zhi, De-Juan; Hu, Qiao-Ling; Liu, Ying-Hong; Zhang, Zhan-Xin; Fei, Dong-Qing","A novel spirocyclic triterpenoid and a new taraxerane triterpenoid from Teucrium viscidum","Organic Chemistry Frontiers","2017","4","1","42","","10.1039/C6QO00460A","","x-ray","1.54184","CuKα","","0.0436","0.0381","","","0.0965","0.1006","","","","","","1.023","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553543","7.348","0.0009","22.781","0.003","11.236","0.0015","90","","101.092","0.013","90","","1845.7","0.4","293","2","293.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H21 N O2 -","- C22 H21 N O2 -","- C88 H84 N4 O8 -","4","1","","Yu, Wenlong; Zhang, Wei; Liu, Yue; Liu, Zhanxiang; Zhang, Yuhong","Cobalt(iii)-catalyzed cross-coupling of enamides with allyl acetates/maleimides","Organic Chemistry Frontiers","2017","4","1","77","","10.1039/C6QO00479B","","","0.71073","MoKα","","0.1248","0.0677","","","0.1801","0.2255","","","","","","1.024","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553544","9.3103","0.0008","4.8793","0.0005","30.741","0.003","90","","96.596","0.008","90","","1387.3","0.2","293","2","293.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H16 N2 O3 -","- C15 H16 N2 O3 -","- C60 H64 N8 O12 -","4","1","","Yu, Wenlong; Zhang, Wei; Liu, Yue; Liu, Zhanxiang; Zhang, Yuhong","Cobalt(iii)-catalyzed cross-coupling of enamides with allyl acetates/maleimides","Organic Chemistry Frontiers","2017","4","1","77","","10.1039/C6QO00479B","","","0.71073","MoKα","","0.0875","0.0562","","","0.1248","0.1436","","","","","","1.043","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553545","33.922","0.006","33.922","0.006","11.008","0.002","90","","90","","120","","10970","3","173","2","173","2","","","","","","","","5","R 3 c :H","R 3 -2""c","161","","","","- C25 H21 N O2 S -","- C25 H21 N O2 S -","- C450 H378 N18 O36 S18 -","18","1","","Gong, Xinxing; Li, Guangming; Wu, Jie","Synthesis of polycyclic sultams via a palladium-catalyzed reaction of 1-bromo-2-(cyclopropylidenemethyl)benzenes with 2-alkynylbenzenesulfonamides","Organic Chemistry Frontiers","2017","4","1","14","","10.1039/C6QO00480F","","","0.71073","MoKα","","0.0953","0.062","","","0.1336","0.1442","","","","","","0.925","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553547","5.3248","0.0004","17.2473","0.001","7.6729","0.0006","90","","96.167","0.006","90","","700.59","0.09","123","","123","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C18 H12 Br2 -","- C18 H12 Br2 -","- C36 H24 Br4 -","2","0.5","","Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.","Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap","Organic Chemistry Frontiers","2017","4","5","658","","10.1039/C6QO00487C","","","0.71073","MoKα","","0.0461","0.0231","","","0.0494","0.0525","","","","","","0.84","","","","has coordinates","235123","2020-10-21","18:00:00",""
"1553548","6.6723","0.0015","8.653","0.002","15.099","0.003","90","","111.66","0.01","90","","810.2","0.3","123","","123.15","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C20 H16 Br2 -","- C20 H16 Br2 -","- C40 H32 Br4 -","2","0.5","","Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.","Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap","Organic Chemistry Frontiers","2017","4","5","658","","10.1039/C6QO00487C","","","0.71073","MoKα","","0.0845","0.0628","","","0.1605","0.1831","","","","","","1.076","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553549","21.802","0.003","4.9336","0.0005","18.875","0.003","90","","90.188","0.013","90","","2030.2","0.5","123","","123","","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C28 H16 Br2 -","- C28 H16 Br2 -","- C112 H64 Br8 -","4","0.5","","Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.","Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap","Organic Chemistry Frontiers","2017","4","5","658","","10.1039/C6QO00487C","","","0.71073","MoKα","","0.1474","0.0681","","","0.157","0.1785","","","","","","0.831","","","","has coordinates,has disorder","235123","2020-10-21","18:00:00",""
"1553550","10.0648","0.0005","11.6684","0.0006","12.2462","0.0006","77.981","0.002","86.017","0.002","79.287","0.002","1381.44","0.12","100","","100","","","","","","","","","3","P -1","-P 1","2","","jm192.1","","- C36 H32 Br2 -","- C36 H32 Br2 -","- C72 H64 Br4 -","2","1","","Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.","Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap","Organic Chemistry Frontiers","2017","4","5","658","","10.1039/C6QO00487C","","","0.71073","MoKα","","0.0695","0.0508","","","0.1308","0.1396","","","","","","1.07","","","","has coordinates,has disorder","235123","2020-10-21","18:00:00",""
"1553551","11.131","0.0004","10.249","0.0003","11.763","0.0004","90","","101.301","0.002","90","","1315.92","0.08","100","2","100","","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C34 H28 Br2 -","- C34 H28 Br2 -","- C68 H56 Br4 -","2","0.5","","Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.","Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap","Organic Chemistry Frontiers","2017","4","5","658","","10.1039/C6QO00487C","","x-ray","1.54178","CuKα","","0.1028","0.0691","","","0.1474","0.1648","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553552","10.8252","0.0008","13.5794","0.001","14.2122","0.001","114.377","0.004","91.316","0.005","95.604","0.004","1889.2","0.2","100","","100","","","","","","","","","2","P -1","-P 1","2","","jm245.3b","","- C50 H38 -","- C50 H38 -","- C100 H76 -","2","1","","Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.","Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap","Organic Chemistry Frontiers","2017","4","5","658","","10.1039/C6QO00487C","","x-ray","1.54178","CuKα","","0.1377","0.1086","","","0.259","0.2735","","","","","","1.09","","","","has coordinates","235123","2020-10-21","18:00:00",""
"1553554","20.3","0.005","5.882","0.005","27.651","0.005","90","0.002","94.075","0.003","90","0.001","3293","3","100","2","100","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","iodo methoxy phenyl methyl phenylselenophene","3-iodo-5-(methoxy(phenyl)methyl)-2-phenylselenophene","","- C18 H15 I O Se -","- C18 H15 I O Se -","- C144 H120 I8 O8 Se8 -","8","1","","Pistoia, Renan P.; Roehrs, Juliano A.; Back, Davi F.; Zeni, Gilson","Iodine-mediated regioselective 5-endo-dig electrophilic cyclization reaction of selenoenynes: synthesis of selenophene derivatives","Organic Chemistry Frontiers","2017","4","2","277","","10.1039/C6QO00491A","","","0.71073","MoKα","","0.0854","0.046","","","0.0627","0.0699","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553555","19.0809","0.0007","5.7136","0.0002","17.2112","0.0006","90","","100.175","0.001","90","","1846.87","0.11","100","2","100","2","","","","","","","","5","P 1 2/c 1","-P 2yc","13","3-iodo-5-isopropoxy-2,4-diphenylselenophene","3-iodo-5-isopropoxy-2,4-diphenylselenophene","","- C20 H19 I O Se -","- C20 H19 I O Se -","- C80 H76 I4 O4 Se4 -","4","1","","Pistoia, Renan P.; Roehrs, Juliano A.; Back, Davi F.; Zeni, Gilson","Iodine-mediated regioselective 5-endo-dig electrophilic cyclization reaction of selenoenynes: synthesis of selenophene derivatives","Organic Chemistry Frontiers","2017","4","2","277","","10.1039/C6QO00491A","","","0.71073","MoKα","","0.0243","0.0207","","","0.0482","0.0495","","","","","","1.07","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553556","11.4186","0.0019","9.7011","0.0017","13.152","0.002","90","","92.473","0.004","90","","1455.5","0.4","293","2","293","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C29 H25 Cl N2 O8 S -","- C29 H25 Cl N2 O8 S -","- C58 H50 Cl2 N4 O16 S2 -","2","1","","He, Fu-Sheng; Li, Cong-Shan; Deng, Hua; Zheng, Xing; Yang, Zhong-Tao; Deng, Wei-Ping","The facile and stereoselective synthesis of pyrrolidine β-amino acids via copper(i)-catalyzed asymmetric 1,3-dipolar cycloaddition","Organic Chemistry Frontiers","2017","4","1","52","","10.1039/C6QO00512H","","","0.71073","MoKα","","0.0552","0.0461","","","0.1112","0.1179","","","","","","1","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553557","14.3717","0.0006","5.917","0.0002","21.4597","0.0009","90","","90","","90","","1824.88","0.12","300","","300","","","","","","","","","3","P n 21 a","P -2ac -2n","33","","","","- C25 H18 O2 -","- C25 H18 O2 -","- C100 H72 O8 -","4","1","","Sreenivasulu, Chinnabattigalla; Gopi Krishna Reddy, A.; Satyanarayana, G.","Oxidative annulations triggered by a simple Lewis acid: facile synthesis of benzofurans","Organic Chemistry Frontiers","2017","4","6","972","","10.1039/C6QO00531D","","","1.54184","CuKα","","0.1073","0.0671","","","0.1467","0.1967","","","","","","1.0503","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553558","7.9447","0.0003","10.3826","0.0004","17.0108","0.0007","90","","90","","90","","1403.16","0.1","300","","300","","","","","","","","Synthesized compound","3","P 21 21 21","P 2ac 2ab","19","","2,3-diphenylbenzofuran","","- C20 H14 O -","- C20 H14 O -","- C80 H56 O4 -","4","1","","Sreenivasulu, Chinnabattigalla; Gopi Krishna Reddy, A.; Satyanarayana, G.","Oxidative annulations triggered by a simple Lewis acid: facile synthesis of benzofurans","Organic Chemistry Frontiers","2017","4","6","972","","10.1039/C6QO00531D","","","1.54184","CuKα","","0.0579","0.0502","","","0.1222","0.1338","","","","","","1.0451","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553559","21.226","0.003","8.2493","0.0007","16.985","0.002","90","","109.61","0.014","90","","2801.6","0.6","294.74","0.1","294.74","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C27 H31 N O7 S3 -","- C27 H31 N O7 S3 -","- C108 H124 N4 O28 S12 -","4","1","","Chen, Fei; Zhou, Neng-Neng; Zhan, Jun-Long; Han, Bing; Yu, Wei","tert-Butyl nitrite-mediated vicinal sulfoximation of alkenes with sulfinic acids: a highly efficient approach toward α-sulfonyl ketoximes","Organic Chemistry Frontiers","2017","4","1","135","","10.1039/C6QO00535G","","","0.71073","MoKα","","0.1316","0.0909","","","0.2444","0.2645","","","","","","1.073","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553560","25.961","0.0017","5.793","0.0003","22.2512","0.0017","90","","114.088","0.009","90","","3055","0.4","293.64","0.1","293.64","0.1","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C15 H21 N O3 S -","- C15 H21 N O3 S -","- C120 H168 N8 O24 S8 -","8","1","","Chen, Fei; Zhou, Neng-Neng; Zhan, Jun-Long; Han, Bing; Yu, Wei","tert-Butyl nitrite-mediated vicinal sulfoximation of alkenes with sulfinic acids: a highly efficient approach toward α-sulfonyl ketoximes","Organic Chemistry Frontiers","2017","4","1","135","","10.1039/C6QO00535G","","x-ray","0.71073","MoKα","","0.1117","0.0626","","","0.1415","0.1744","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553561","6.52","0.006","8.149","0.007","18.175","0.015","102.278","0.014","95.21","0.015","97.731","0.016","927.9","1.4","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C18 H16 F3 N O2 S2 -","- C18 H16 F3 N O2 S2 -","- C36 H32 F6 N2 O4 S4 -","2","1","","Chen, Min-Tao; Tang, Xiang-Ying; Shi, Min","A facile approach for the trifluoromethylthiolation of methylenecyclopropanes","Organic Chemistry Frontiers","2017","4","1","86","","10.1039/C6QO00536E","","","0.71073","MoKα","","0.1295","0.0942","","","0.2386","0.2635","","","","","","1.05","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553562","13.451","0.004","14.313","0.004","15.248","0.004","86.714","0.004","63.827","0.003","90.014","0.004","2629.2","1.3","110","","110","","","","","","","","","4","P -1","-P 1","2","","","","- C17 H15 N O2 -","- C17 H15 N O2 -","- C136 H120 N8 O16 -","8","4","","Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai","Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles","Organic Chemistry Frontiers","2017","4","1","124","","10.1039/C6QO00541A","","","0.71073","MoKα","","0.0847","0.0536","","","0.1215","0.1378","","","","","","1.039","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553563","7.3875","0.0004","11.6702","0.0006","13.4944","0.0007","64.647","0.001","82.911","0.001","77.69","0.001","1026.5","0.09","100.01","","100.01","","","","","","","","","5","P -1","-P 1","2","","","","- C26 H20 Cl N O3 -","- C26 H20 Cl N O3 -","- C52 H40 Cl2 N2 O6 -","2","1","","Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai","Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles","Organic Chemistry Frontiers","2017","4","1","124","","10.1039/C6QO00541A","","","0.71073","MoKα","","0.0347","0.0314","","","0.0892","0.0913","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553564","8.5455","0.0004","12.047","0.0006","12.1501","0.0006","60.733","0.001","81.883","0.002","87.112","0.002","1079.97","0.09","100.01","","100.01","","","","","","","","","5","P -1","-P 1","2","","","","- C23 H24 N2 O6 S -","- C23 H24 N2 O6 S -","- C46 H48 N4 O12 S2 -","2","1","","Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai","Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles","Organic Chemistry Frontiers","2017","4","1","124","","10.1039/C6QO00541A","","","0.71073","MoKα","","0.0552","0.0474","","","0.1229","0.1296","","","","","","1.069","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553565","9.3265","0.001","9.7095","0.0009","23.593","0.002","78.225","0.008","84.998","0.008","75.52","0.008","2023.6","0.3","193","2","193","2","","","","","","","","4","P -1","-P 1","2","","","","- C44 H52 N4 S4 -","- C44 H52 N4 S4 -","- C88 H104 N8 S8 -","2","1","","Xia, Debin; Keerthi, Ashok; An, Cunbin; Baumgarten, Martin","Synthesis of a quinoidal dithieno[2,3-d;2′,3′-d]benzo[2,1-b;3,4-b′]-dithiophene based open-shell singlet biradicaloid","Organic Chemistry Frontiers","2017","4","1","18","","10.1039/C6QO00543H","","","1.54178","CuKα","","0.1924","0.0676","","","0.1475","0.2042","","","","","","0.802","","","","has coordinates","235142","2020-10-21","18:00:00",""
"1553566","8.101","0.0016","19.041","0.004","13.693","0.003","90","","107.19","0.03","90","","2017.8","0.8","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H21 N O8 -","- C20 H21 N O8 -","- C80 H84 N4 O32 -","4","1","","Zhang, Li; Zhang, Beichen; Jiang, Teng; Lu, Tao; Zhou, Qingfa","Synthesis of tricyclic 3-hydroxyisoindolin-1-ones via triethylamine-catalyzed domino reactions of electron-deficient alkynes with phthalimidomalonate derivatives","Organic Chemistry Frontiers","2017","4","1","119","","10.1039/C6QO00544F","","","0.71073","MoKα","","0.1304","0.0679","","","0.1552","0.1807","","","","","","1.008","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553567","11.366","0.004","11.305","0.004","14.788","0.006","90","","110.536","0.006","90","","1779.4","1.1","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C22 H16 Cl N O2 -","- C22 H16 Cl N O2 -","- C88 H64 Cl4 N4 O8 -","4","1","","Zhu, Chao-Qun; Deng, Zhuo-Fei; Zhang, Yahong; Wang, You-Qing","Synthesis of 4-substituted 3-(2-hydroxyphenyl)-quinolines through an unexpected iron(iii) chloride promoted reaction of cyclic imine dibenzo[b,f][1,4]oxazepines with alkynes","Organic Chemistry Frontiers","2017","4","2","196","","10.1039/C6QO00545D","","","0.71073","MoKα","","0.0485","0.0359","","","0.11","0.1195","","","","","","0.973","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553568","8.902","0.006","13.209","0.009","12.059","0.008","90","","99.65","0.007","90","","1397.9","1.6","296","2","296","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C33 H30 N4 O3 -","- C33 H30 N4 O3 -","- C66 H60 N8 O6 -","2","1","","Cheng, Cang; Lu, Xuehe; Ge, Luo; Chen, Jie; Cao, Weiguo; Wu, Xiaoyu; Zhao, Gang","Effective asymmetric vinylogous Mannich reaction of isatin imines with α,α-dicyanoolefins in the presence of a simple chiral amide phosphonium bifunctional phase transfer catalyst","Organic Chemistry Frontiers","2017","4","1","101","","10.1039/C6QO00546B","","","0.71073","MoKα","","0.0389","0.0335","","","0.0782","0.0823","","","","","","1.051","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553569","9.662","0.004","12.286","0.006","24.441","0.011","90","","90","","90","","2901","2","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C31 H27 Br N4 O3 -","- C31 H27 Br N4 O3 -","- C124 H108 Br4 N16 O12 -","4","1","","Cheng, Cang; Lu, Xuehe; Ge, Luo; Chen, Jie; Cao, Weiguo; Wu, Xiaoyu; Zhao, Gang","Effective asymmetric vinylogous Mannich reaction of isatin imines with α,α-dicyanoolefins in the presence of a simple chiral amide phosphonium bifunctional phase transfer catalyst","Organic Chemistry Frontiers","2017","4","1","101","","10.1039/C6QO00546B","","","0.71073","MoKα","","0.0536","0.0363","","","0.0791","0.0854","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553570","8.4091","0.0001","8.4091","0.0001","29.3175","0.0006","90","","90","","90","","2073.13","0.05","293","2","293","2","","","","","","","","4","P 41","P 4w","76","","","","- C25 H23 N O3 -","- C25 H23 N O3 -","- C100 H92 N4 O12 -","4","1","","Xu, Meng-Meng; Wang, Hai-Qing; Wan, Ying; He, Guofeng; Yan, Jingjing; Zhang, Shu; Wang, Shu-Liang; Shi, Feng","Catalytic asymmetric substitution of ortho-hydroxybenzyl alcohols with tetronic acid-derived enamines: enantioselective synthesis of tetronic acid-derived diarylmethanes","Organic Chemistry Frontiers","2017","4","3","358","","10.1039/C6QO00549G","","","1.54178","CuKα","","0.0591","0.0574","","","0.1527","0.155","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553571","7.2915","0.0005","12.7983","0.001","15.9552","0.0009","90","","90","","90","","1488.92","0.18","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C15 H17 Cl N2 O3 -","- C15 H17 Cl N2 O3 -","- C60 H68 Cl4 N8 O12 -","4","1","","Peng, Xiao-Jiao; Ho, Yee Ann; Wang, Zhi-Peng; Shao, Pan-Lin; Zhao, Yu; He, Yun","Formal [3 + 2] cycloaddition of α-unsubstituted isocyanoacetates and methyleneindolinones: enantioselective synthesis of spirooxindoles","Organic Chemistry Frontiers","2017","4","1","81","","10.1039/C6QO00555A","","","0.71073","MoKα","","0.071","0.0481","","","0.095","0.1103","","","","","","1.052","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553572","7.74798","0.00019","9.1129","0.0002","21.719","0.0005","90","","90","","90","","1533.5","0.06","293","2","293","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C15 H11 Cl F3 N3 O3 -","- C15 H11 Cl F3 N3 O3 -","- C60 H44 Cl4 F12 N12 O12 -","4","1","","Hao, Xin-Qi; Wang, Cong; Liu, Shuang-Liang; Wang, Xiao; Wang, Li; Gong, Jun-Fang; Song, Mao-Ping","Cobalt(ii)/(imidazoline–oxazoline)-catalyzed enantioselective Michael addition of 2-acetyl azaarenes to β-CF3-β-disubstituted nitroalkenes","Organic Chemistry Frontiers","2017","4","2","308","","10.1039/C6QO00562D","","x-ray","1.54184","CuKα","","0.039","0.0367","","","0.0913","0.094","","","","","","1.069","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553573","7.68","0.005","8.494","0.005","11.449","0.007","85.96","0.007","77.314","0.007","66.467","0.007","667.9","0.7","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C14 H13 N3 O S -","- C14 H13 N3 O S -","- C28 H26 N6 O2 S2 -","2","1","","Chen, Jichao; Wang, Tianyu; Wang, Tong; Lin, Aijun; Yao, Hequan; Xu, Jinyi","Copper-catalyzed C5-selective thio/selenocyanation of 8-aminoquinolines","Organic Chemistry Frontiers","2017","4","1","130","","10.1039/C6QO00590J","","","0.71073","MoKα","","0.0618","0.0458","","","0.1472","0.1661","","","","","","0.986","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553574","9.8916","0.0007","26.4389","0.0019","7.7778","0.0006","90","","90","","90","","2034.1","0.3","133","2","133","2","","","","","","","","6","P 21 21 2","P 2 2ab","18","","","","- C19 H23 Br N O3 P -","- C19 H23 Br N O3 P -","- C76 H92 Br4 N4 O12 P4 -","4","1","","Wang, Xubin; Wang, Xiaoming; Han, Zhaobin; Wang, Zheng; Ding, Kuiling","Palladium-catalyzed asymmetric allylic amination: enantioselective synthesis of chiral α-methylene substituted β-aminophosphonates","Organic Chemistry Frontiers","2017","4","2","271","","10.1039/C6QO00597G","","","0.71073","MoKα","","0.0629","0.0454","","","0.1077","0.1145","","","","","","1.092","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553575","21.2715","0.0003","21.2715","0.0003","64.3247","0.0014","90","","90","","90","","29105.4","0.9","293","2","293","2","","","","","","","","5","P 41 21 2","P 4abw 2nw","92","","azahelicene dimer","","- C153.47 H187.47 Cl4.41 N2 Si8 -","- C153.47 H187.479 Cl4.41 N2 Si8 -","- C1227.76 H1499.83 Cl35.28 N16 Si64 -","8","1","","Ushiyama, Ayako; Hiroto, Satoru; Yuasa, Junpei; Kawai, Tsuyoshi; Shinokubo, Hiroshi","Synthesis of a figure-eight azahelicene dimer with high emission and CPL properties","Organic Chemistry Frontiers","2017","4","5","664","","10.1039/C6QO00629A","","","0.71073","MoKα","","0.1947","0.1475","","","0.3637","0.4128","","","","","","1.172","","","","has coordinates,has disorder","235160","2020-10-21","18:00:00",""
"1553576","9.4639","0.0002","21.8249","0.0005","9.3192","0.0002","90","","104.752","0.003","90","","1861.42","0.07","150","0.1","150","0.1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C21 H21 Cl F N O2 -","- C21 H21 Cl F N O2 -","- C84 H84 Cl4 F4 N4 O8 -","4","1","","Li, Jianxiao; Hu, Weigao; Li, Chunsheng; Yang, Shaorong; Wu, Wanqing; Jiang, Huanfeng","Palladium-catalyzed cascade reaction of haloalkynes with unactivated alkenes for assembly of functionalized oxetanes","Organic Chemistry Frontiers","2017","4","3","373","","10.1039/C6QO00633G","","x-ray","1.54184","CuKα","","0.0476","0.0446","","","0.1182","0.1209","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553577","7.813","0.004","5.321","0.003","15.394","0.008","90","","91.594","0.008","90","","639.7","0.6","173.15","","173.15","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C15 H15 Br O2 -","- C15 H15 Br O2 -","- C30 H30 Br2 O4 -","2","1","","Li, Jing; Li, Zequan; Zhang, Xun; Xu, Bing; Shi, Yian","Catalytic enantioselective bromohydroxylation of aryl olefins with flexible functionalities","Organic Chemistry Frontiers","2017","4","6","1084","","10.1039/C6QO00636A","","","0.71073","MoKα","","0.0582","0.0575","","","0.1494","0.1501","","","","","","1.071","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553578","5.651","0.002","16.364","0.007","38.4918","0.0016","90","","90","","90","","3559","2","173.15","","173.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C11 H14 Br F O2 -","- C11 H14 Br F O2 -","- C132 H168 Br12 F12 O24 -","12","3","","Li, Jing; Li, Zequan; Zhang, Xun; Xu, Bing; Shi, Yian","Catalytic enantioselective bromohydroxylation of aryl olefins with flexible functionalities","Organic Chemistry Frontiers","2017","4","6","1084","","10.1039/C6QO00636A","","","0.71073","MoKα","","0.0824","0.0694","","","0.1075","0.1135","","","","","","1.159","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553579","10.248","0.006","14.634","0.007","11.146","0.005","90","","107.352","0.018","90","","1595.5","1.4","110","","110","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C17 H12 B F2 N5 O -","- C17 H12 B F2 N5 O -","- C68 H48 B4 F8 N20 O4 -","4","0.5","","Barbon, Stephanie M.; Novoa, Samantha; Bender, Desiree; Groom, Hilary; Luyt, Leonard G.; Gilroy, Joe B.","Copper-assisted azide‒alkyne cycloaddition chemistry as a tool for the production of emissive boron difluoride 3-cyanoformazanates","Organic Chemistry Frontiers","2017","4","2","178","","10.1039/C6QO00640J","","","0.71073","MoKα","","0.077","0.0428","","","0.0962","0.1107","","","","","","1.037","","","","has coordinates,has disorder","235166","2020-10-21","18:00:00",""
"1553580","7.3184","0.0002","13.4865","0.0003","17.4149","0.0004","101.672","0.002","94.139","0.002","101.918","0.002","1635.33","0.07","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C16 H10 Br2 Cl F3 -","- C16 H10 Br2 Cl F3 -","- C64 H40 Br8 Cl4 F12 -","4","2","","Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.","Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes","Organic Chemistry Frontiers","2017","4","2","255","","10.1039/C6QO00643D","","","1.54184","CuKα","","0.0611","0.0454","","","0.1445","0.1869","","","","","","1.067","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553581","7.8481","0.0005","10.5581","0.0007","12.2042","0.001","75.472","0.006","72.741","0.006","72.301","0.006","905.55","0.12","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C20 H20 Br F3 O -","- C20 H20 Br F3 O -","- C40 H40 Br2 F6 O2 -","2","1","","Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.","Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes","Organic Chemistry Frontiers","2017","4","2","255","","10.1039/C6QO00643D","","","1.54184","CuKα","","0.0414","0.0388","","","0.1066","0.1098","","","","","","1.022","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553582","8.3533","0.0005","9.4941","0.0004","12.1934","0.0007","100.216","0.004","97.306","0.005","100.289","0.004","923.7","0.09","105","8","105","8","","","","","","","","5","P -1","-P 1","2","","","","- C20 H20 Br F3 O2 -","- C20 H20 Br F3 O2 -","- C40 H40 Br2 F6 O4 -","2","1","","Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.","Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes","Organic Chemistry Frontiers","2017","4","2","255","","10.1039/C6QO00643D","","","0.7107","MoKα","","0.0345","0.0286","","","0.0627","0.0651","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553583","16.4974","0.0002","6.84171","0.0001","28.6498","0.0003","90","","90","","90","","3233.72","0.07","100","2","100","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C18 H15 Br2 F3 -","- C18 H15 Br2 F3 -","- C144 H120 Br16 F24 -","8","1","","Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.","Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes","Organic Chemistry Frontiers","2017","4","2","255","","10.1039/C6QO00643D","","","1.5418","CuKα","","0.0263","0.0232","","","0.0596","0.0612","","","","","","1.055","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553584","7.1399","0.0002","9.7404","0.0003","22.8361","0.0006","97.673","0.002","97.146","0.002","106.455","0.003","1487.32","0.08","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C16 H11 Br2 F3 -","- C16 H11 Br2 F3 -","- C64 H44 Br8 F12 -","4","2","","Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.","Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes","Organic Chemistry Frontiers","2017","4","2","255","","10.1039/C6QO00643D","","","1.54184","CuKα","","0.0498","0.0469","","","0.1234","0.1276","","","","","","1.057","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553585","22.8229","0.0015","7.4881","0.0004","16.5828","0.0011","90","","102.102","0.007","90","","2771","0.3","100","2","100","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C17 H12 Br F3 -","- C17 H12 Br F3 -","- C136 H96 Br8 F24 -","8","1","","Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.","Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes","Organic Chemistry Frontiers","2017","4","2","255","","10.1039/C6QO00643D","","","1.54184","CuKα","","0.0498","0.0379","","","0.0933","0.1027","","","","","","1.044","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553586","8.2233","0.0003","22.8182","0.0007","10.0565","0.0003","90","","109.447","0.004","90","","1779.36","0.11","100","2","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H17 Br Cl F3 -","- C19 H17 Br Cl F3 -","- C76 H68 Br4 Cl4 F12 -","4","1","","Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.","Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes","Organic Chemistry Frontiers","2017","4","2","255","","10.1039/C6QO00643D","","","0.7107","MoKα","","0.0347","0.0266","","","0.0598","0.0631","","","","","","1.011","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553587","6.9379","0.0019","19.798","0.006","17.773","0.004","90","","90","","90","","2441.2","1.1","296","2","296","2","","","","","","","","5","C m c e","-C 2ac 2","64","","","","- C12 H11 I N2 O2 -","- C12 H11 I N2 O2 -","- C96 H88 I8 N16 O16 -","8","0.5","","He, Xin; Xu, Yi-zhu; Kong, Ling-xuan; Wu, Huan-huan; Ji, De-zhong; Wang, Zhi-bin; Xu, Yun-gen; Zhu, Qi-hua","Copper(i) and N-fluorobenzenesulfonimide-mediated direct regioselective halogenation of 8-amidoquinolines on the C5 position","Organic Chemistry Frontiers","2017","4","6","1046","","10.1039/C6QO00644B","","","0.71073","MoKα","","0.044","0.0379","","","0.0866","0.0901","","","","","","1.13","","","","has coordinates","235172","2020-10-21","18:00:00",""
"1553588","10.4263","0.0009","10.2668","0.0009","40.789","0.004","90","","90.6212","0.0014","90","","4366","0.7","193","2","193","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","3,3,3-tris(3,5-di-t-butyl)prop-1-yne, dichloromethane solvate","","- C46 H66 Cl2 -","- C45 H64 -","- C180 H256 -","4","1","","Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R.","Polymerization of acetylene: polyynes, but not carbyne","Organic Chemistry Frontiers","2017","4","5","668","","10.1039/C6QO00648E","","","0.71073","MoKα","","0.0826","0.0607","","","0.1479","0.1593","","","","","","1.065","","","","has coordinates,has disorder","235174","2020-10-21","18:00:00",""
"1553589","10.3367","0.0013","10.4631","0.0013","19.275","0.002","88.5549","0.0018","78.0127","0.0018","88.5903","0.0019","2038.2","0.4","193","2","193","2","","","","","","","","2","P -1","-P 1","2","","5,5,5-tris(3,5-di-t-butylphenyl)penta-1,3-diyne","","- C47 H64 -","- C47 H64 -","- C94 H128 -","2","1","","Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R.","Polymerization of acetylene: polyynes, but not carbyne","Organic Chemistry Frontiers","2017","4","5","668","","10.1039/C6QO00648E","","","0.71073","MoKα","","0.0692","0.0523","","","0.1344","0.1467","","","","","","1.031","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553590","14.154","0.003","14.154","0.003","12.123","0.002","90","","90","","120","","2103.3","0.7","173","2","173","2","","","","","","","","2","P 3 1 c","P 3 -2c","159","","1,1,1-tris(3,5-di-t-butylphenyl)hepta-2,4,6-triyne","","- C49 H64 -","- C49 H64 -","- C98 H128 -","2","0.333333","","Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R.","Polymerization of acetylene: polyynes, but not carbyne","Organic Chemistry Frontiers","2017","4","5","668","","10.1039/C6QO00648E","","","0.71073","MoKα","","0.072","0.0411","","","0.0776","0.0882","","","","","","1.035","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553591","7.858","0.003","26.656","0.008","8.984","0.003","90","","90.001","0.001","90","","1881.8","1.1","296.15","","296.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C20 H13 F7 N2 O -","- C20 H13 F7 N2 O -","- C80 H52 F28 N8 O4 -","4","1","","Xu, Jun; Qiao, Li; Ying, Beibei; Zhu, Xiaolei; Shen, Chao; Zhang, Pengfei","Transition-metal-free direct perfluoroalkylation of quinoline amides at C5 position through radical cross-coupling under mild conditions","Organic Chemistry Frontiers","2017","4","6","1116","","10.1039/C6QO00655H","","","0.71073","MoKα","","0.1144","0.0545","","","0.1328","0.1523","","","","","","0.887","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553592","14.2771","0.0002","14.228","0.0002","22.6224","0.0004","90","","99.427","0.001","90","","4533.33","0.12","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C44 H58 N2 Se2 Si4 -","- C44 H58 N2 Se2 Si4 -","- C176 H232 N8 Se8 Si16 -","4","1","","Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C.","Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties","Organic Chemistry Frontiers","2017","4","5","682","","10.1039/C6QO00662K","","","0.71073","MoKα","","0.1114","0.0471","","","0.094","0.1178","","","","","","1.01","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553593","14.2494","0.0006","14.1245","0.0006","22.4876","0.0009","90","","98.8","0.002","90","","4472.7","0.3","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C44 H58 N2 S2 Si4 -","- C44 H58 N2 S2 Si4 -","- C176 H232 N8 S8 Si16 -","4","1","","Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C.","Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties","Organic Chemistry Frontiers","2017","4","5","682","","10.1039/C6QO00662K","","","0.71073","MoKα","","0.0919","0.0569","","","0.148","0.1716","","","","","","1.023","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553594","10.8503","0.0005","12.4427","0.0005","12.9897","0.0005","100.306","0.002","91.28","0.002","108.652","0.002","1628.82","0.12","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C32 H22 Br8 N2 -","- C32 H22 Br8 N2 -","- C64 H44 Br16 N4 -","2","1","","Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C.","Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties","Organic Chemistry Frontiers","2017","4","5","682","","10.1039/C6QO00662K","","","0.71073","MoKα","","0.0558","0.0405","","","0.099","0.1057","","","","","","1.028","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553595","9.842","0.002","21.609","0.004","25.234","0.005","90","","91.32","0.03","90","","5365.2","1.8","173.15","","173.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C50 H52 N14 O4 -","- C50 H52 N14 O4 -","- C200 H208 N56 O16 -","4","1","","Zhang, Qian; Wang, Mei-Xiang","Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule","Organic Chemistry Frontiers","2017","4","2","283","","10.1039/C6QO00669H","","","0.71073","MoKα","","0.1092","0.0942","","","0.2041","0.2128","","","","","","1.208","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553596","28.402","0.006","9.816","0.002","18.722","0.004","90","","90.7","0.03","90","","5219.2","1.9","173.15","","173.15","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C54.83 H62.12 Cl1.76 N16.83 O2 -","- C54.824 H62.12 Cl1.764 N16.824 O2 -","- C219.296 H248.48 Cl7.056 N67.296 O8 -","4","0.5","","Zhang, Qian; Wang, Mei-Xiang","Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule","Organic Chemistry Frontiers","2017","4","2","283","","10.1039/C6QO00669H","","","0.71073","MoKα","","0.087","0.0805","","","0.2196","0.2259","","","","","","1.088","","","","has coordinates,has disorder","235183","2020-10-21","18:00:00",""
"1553597","9.6636","0.0003","15.1098","0.0006","18.1939","0.0007","69.768","0.004","84.466","0.003","84.513","0.003","2475.53","0.17","150","0.1","150","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C54 H60 N16 O2 -","- C54 H60 N16 O2 -","- C108 H120 N32 O4 -","2","1","","Zhang, Qian; Wang, Mei-Xiang","Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule","Organic Chemistry Frontiers","2017","4","2","283","","10.1039/C6QO00669H","","x-ray","0.71073","MoKα","","0.0858","0.0575","","","0.1283","0.1452","","","","","","1.0409","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553598","7.5051","0.0007","8.6296","0.0007","11.6509","0.0011","73.729","0.005","77.669","0.004","77.532","0.006","697.78","0.11","200","2","200","2","","","","","","","","3","P -1","-P 1","2","","","","- C40 H24 S2 -","- C40 H24 S2 -","- C40 H24 S2 -","1","0.5","","Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung","The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices","Organic Chemistry Frontiers","2017","4","5","675","","10.1039/C6QO00673F","","","0.71073","MoKα","","0.1065","0.0617","","","0.1647","0.1884","","","","","","1.036","","","","has coordinates","235187","2020-10-21","18:00:00",""
"1553599","16.8864","0.0004","7.4906","0.0002","24.7447","0.0007","90","","90","","90","","3129.94","0.14","200","2","200","2","","","","","","","","2","P n a 21","P 2c -2n","33","","","","- C46 H32 -","- C46 H32 -","- C184 H128 -","4","1","","Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung","The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices","Organic Chemistry Frontiers","2017","4","5","675","","10.1039/C6QO00673F","","","0.71073","MoKα","","0.0692","0.0504","","","0.1175","0.1276","","","","","","1.019","","","","has coordinates","235187","2020-10-21","18:00:00",""
"1553600","7.597","0.0004","8.9994","0.0004","11.0344","0.0005","78.931","0.002","75.805","0.002","83.409","0.002","715.94","0.06","200","2","200","2","","","","","","","","2","P -1","-P 1","2","","","","- C44 H28 -","- C44 H28 -","- C44 H28 -","1","0.5","","Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung","The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices","Organic Chemistry Frontiers","2017","4","5","675","","10.1039/C6QO00673F","","","0.71073","MoKα","","0.0955","0.0504","","","0.1131","0.1326","","","","","","0.988","","","","has coordinates","235187","2020-10-21","18:00:00",""
"1553601","26.478","0.002","8.1615","0.0006","23.0582","0.0017","90","","96.411","0.003","90","","4951.7","0.6","296","2","296","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C26 H22 N4 O5 S -","- C26 H22 N4 O5 S -","- C208 H176 N32 O40 S8 -","8","1","","Chen, Dianpeng; Xing, Gangdong; Yao, Jinzhong; Zhou, Hongwei","Applicable β-sulfonium carbanions: facile construction of thiophene derivatives","Organic Chemistry Frontiers","2017","4","6","1042","","10.1039/C6QO00675B","","","0.71073","MoKα","","0.1002","0.055","","","0.1165","0.1398","","","","","","1.003","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553602","7.9629","0.0003","16.9905","0.0006","18.7808","0.0005","90","","90","","90","","2540.92","0.15","294.06","0.1","294.06","0.1","","","","","","","","5","P b c n","-P 2n 2ab","60","","","","- C12 H9 N O S3 -","- C12 H9 N O S3 -","- C96 H72 N8 O8 S24 -","8","1","","Chen, Qiao; Lei, Yingjie; Wang, Yanfang; Wang, Chao; Wang, Yanan; Xu, Zhaoqing; Wang, Huan; Wang, Rui","Direct thiocyanation of ketene dithioacetals under transition-metal-free conditions","Organic Chemistry Frontiers","2017","4","3","369","","10.1039/C6QO00676K","","x-ray","0.71073","MoKα","","0.0697","0.0482","","","0.1129","0.1301","","","","","","1.049","","","","has coordinates","277994","2022-09-20","08:32:41",""
"1553603","12.2302","0.0009","15.3106","0.0011","36.571","0.003","90","","90","","90","","6848","0.9","296","2","296","2","","","","","","","","8","P 21 21 21","P 2ac 2ab","19","","","","- C71 H46 B F24 Ir N O P -","- C71 H46 B F24 Ir N O P -","- C284 H184 B4 F96 Ir4 N4 O4 P4 -","4","1","","Wang, Qian; Zhang, Zongpeng; Chen, Caiyou; Yang, Hailong; Han, Zhengyu; Dong, Xiu-Qin; Zhang, Xumu","Iridium catalysts with modular axial-unfixed biphenyl phosphine‒oxazoline ligands: asymmetric hydrogenation of α,β-unsaturated carboxylic acids","Organic Chemistry Frontiers","2017","4","4","627","","10.1039/C6QO00677A","","","0.71073","MoKα","","0.0652","0.045","","","0.1009","0.1099","","","","","","1.007","","","","has coordinates","235193","2020-10-21","18:00:00",""
"1553604","11.1134","0.0005","21.1702","0.0009","9.8578","0.0004","90","","101.189","0.0013","90","","2275.19","0.17","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C26 H16 Cu N4 O8 -","- C26 H16 Cu N4 O8 -","- C104 H64 Cu4 N16 O32 -","4","1","","Baur, Andreas; Bustin, Katelyn A.; Aguilera, Ellen; Petersen, Jeffrey L.; Hoover, Jessica M.","Copper and silver benzoate and aryl complexes and their implications for oxidative decarboxylative coupling reactions","Organic Chemistry Frontiers","2017","4","4","519","","10.1039/C6QO00678G","","","0.71073","MoKα","","0.0616","0.037","","","0.078","0.0858","","","","","","1.053","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553605","8.269","0.003","9.296","0.004","16.904","0.007","90","","93.281","0.004","90","","1297.3","0.9","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C16 H11 N O3 -","- C16 H11 N O3 -","- C64 H44 N4 O12 -","4","1","","Fang, Xinxin; Gao, Shang; Wu, Zijun; Yao, Hequan; Lin, Aijun","Pd(ii)-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones","Organic Chemistry Frontiers","2017","4","2","292","","10.1039/C6QO00698A","","","0.71073","MoKα","","0.0456","0.0372","","","0.0974","0.1039","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553606","8.874","0.006","13.733","0.009","27.215","0.017","90","","90","","90","","3317","4","296","2","296","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C22 H15 N O2 -","- C22 H15 N O2 -","- C176 H120 N8 O16 -","8","1","","Fang, Xinxin; Gao, Shang; Wu, Zijun; Yao, Hequan; Lin, Aijun","Pd(ii)-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones","Organic Chemistry Frontiers","2017","4","2","292","","10.1039/C6QO00698A","","","0.71073","MoKα","","0.0465","0.0354","","","0.0886","0.0962","","","","","","1.031","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553607","8.066","0.008","8.242","0.008","12.157","0.013","92.727","0.013","102.604","0.012","98.233","0.011","778","1.4","293","2","293","2","","","","","","","","4","P -1","-P 1","2","2-((3-benzoylisoxazol-5-yl)methyl)isoindoline-1,3-dione","","","- C19 H12 N2 O4 -","- C19 H12 N2 O4 -","- C38 H24 N4 O8 -","2","1","","Li, Yingying; Gao, Mingchun; Liu, Bingxin; Xu, Bin","Copper nitrate-mediated chemo- and regioselective annulation from two different alkynes: a direct route to isoxazoles","Organic Chemistry Frontiers","2017","4","3","445","","10.1039/C6QO00704J","","","0.71073","MoKα","","0.0515","0.039","","","0.0985","0.1077","","","","","","1.086","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553608","9.4574","0.0007","9.9936","0.0009","14.0156","0.0013","89.023","0.007","76.071","0.007","71.074","0.008","1213.5","0.2","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C26 H31 F2 N O3 -","- C26 H31 F2 N O3 -","- C52 H62 F4 N2 O6 -","2","1","","Xu, Jian; Song, Qiuling","Synthesis of fully-substituted 1,2,3-triazoles via copper(i)-catalyzed three-component coupling of sulfoximines, alkynes and azides","Organic Chemistry Frontiers","2017","4","6","938","","10.1039/C6QO00725B","","x-ray","0.71073","MoKα","","0.0814","0.0532","","","0.1352","0.156","","","","","","1.031","","","","has coordinates","300101","2025-06-17","17:58:10",""
"1553609","9.7469","0.0007","13.1171","0.0008","17.5212","0.0012","70.806","0.008","75.292","0.008","73.524","0.008","1996.5","0.3","113","2","113","2","","","","","","","","3","P -1","-P 1","2","","","","- C41 H40 O11 -","- C41 H40 O11 -","- C82 H80 O22 -","2","1","","Lu, Kui; Yang, Ke; Jia, Xiaoliang; Gao, Xing; Zhao, Xia; Pan, Guojun; Ma, Yantao; Huang, Qiyao; Yu, Peng","Total synthesis of I3,II8-biapigenin and ridiculuflavone A","Organic Chemistry Frontiers","2017","4","4","578","","10.1039/C6QO00726K","","","0.71073","MoKα","","0.0639","0.0482","","","0.1461","0.1549","","","","","","1.092","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553610","15.1534","0.001","15.8118","0.001","17.7296","0.001","68.774","0.004","76.898","0.005","79.352","0.005","3832","0.4","113","2","113","2","","","","","","","","3","P -1","-P 1","2","","","","- C43 H46 O11 -","- C43 H46 O11 -","- C172 H184 O44 -","4","2","","Lu, Kui; Yang, Ke; Jia, Xiaoliang; Gao, Xing; Zhao, Xia; Pan, Guojun; Ma, Yantao; Huang, Qiyao; Yu, Peng","Total synthesis of I3,II8-biapigenin and ridiculuflavone A","Organic Chemistry Frontiers","2017","4","4","578","","10.1039/C6QO00726K","","","0.71073","MoKα","","0.0567","0.0442","","","0.1178","0.1244","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553611","9.9046","0.0013","10.4946","0.0012","23.736","0.003","90","","90","","90","","2467.2","0.5","297","2","297","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C31 H23 Cl0 N O4 -","- C31 H23 N O4 -","- C124 H92 N4 O16 -","4","1","","Xu, Junyu; Cao, Jing; Fang, Chao; Lu, Tao; Du, Ding","Organocatalytic C‒C bond activation of cyclopropenones for ring-opening formal [3 + 2] cycloaddition with isatins","Organic Chemistry Frontiers","2017","4","4","560","","10.1039/C6QO00734A","","","0.71073","MoKα","","0.1682","0.0492","","","0.0947","0.1414","","","","","","0.943","","","","has coordinates","235205","2020-10-21","18:00:00",""
"1553612","9.263","0.0019","16.211","0.003","15.413","0.003","90","","91.21","0.03","90","","2313.9","0.8","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C30 H21 N O3 -","- C30 H21 N O3 -","- C120 H84 N4 O12 -","4","1","","Xu, Junyu; Cao, Jing; Fang, Chao; Lu, Tao; Du, Ding","Organocatalytic C–C bond activation of cyclopropenones for ring-opening formal [3 + 2] cycloaddition with isatins","Organic Chemistry Frontiers","2017","4","4","560","","10.1039/C6QO00734A","","","0.71073","MoKα","","0.144","0.0673","","","0.155","0.1945","","","","","","1","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553613","12.3342","0.0005","12.422","0.0005","20.4886","0.0009","94.35","0.003","97.642","0.003","100.981","0.003","3037.8","0.2","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C38.5 H33 Cl O3 -","- C38.5 H33 Cl O3 -","- C154 H132 Cl4 O12 -","4","2","","Zhang, Yuexia; Wu, Xingxing; Hao, Lin; Wong, Zeng Rong; Lauw, Sherman J. L.; Yang, Song; Webster, Richard D.; Chi, Yonggui Robin","Trimerization of enones under air enabled by NHC/NaOtBu via a SET radical pathway","Organic Chemistry Frontiers","2017","4","3","467","","10.1039/C6QO00738D","","","0.71073","MoKα","","0.1569","0.0817","","","0.1959","0.2444","","","","","","1.021","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553614","9.077","0.004","10.4","0.004","11.75","0.005","90","","90","","90","","1109.2","0.8","173.15","","173.15","","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C13 H12 N2 O -","- C13 H12 N2 O -","- C52 H48 N8 O4 -","4","1","","Guo, Wei-Si; Wang, Yuan-Chao; Dou, Qian; Wen, Li-Rong; Li, Ming","A copper-catalyzed arylation/nucleophilic addition/fragmentation/C–S bond formation cascade: synthesis of bis(arylthio)imines","Organic Chemistry Frontiers","2017","4","4","510","","10.1039/C6QO00739B","","","0.71073","MoKα","","0.0383","0.0374","","","0.1194","0.1208","","","","","","1.013","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553615","8.189","0.002","14.782","0.004","17.421","0.005","90","","90","","90","","2108.8","1","173.15","","173.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C23 H19 N O2 S2 -","- C23 H19 N O2 S2 -","- C92 H76 N4 O8 S8 -","4","1","","Guo, Wei-Si; Wang, Yuan-Chao; Dou, Qian; Wen, Li-Rong; Li, Ming","A copper-catalyzed arylation/nucleophilic addition/fragmentation/C–S bond formation cascade: synthesis of bis(arylthio)imines","Organic Chemistry Frontiers","2017","4","4","510","","10.1039/C6QO00739B","","","0.71073","MoKα","","0.0577","0.052","","","0.0937","0.0959","","","","","","1.15","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553616","10.5479","0.0013","16.6","0.002","13.9079","0.0017","90","","92.242","0.002","90","","2433.3","0.5","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H24 S4 Si2 -","- C22 H24 S4 Si2 -","- C88 H96 S16 Si8 -","4","1","","Li, Lu; Li, Bingbing; Li, Chunli; Ma, Zhiying; Xu, Li; Wang, Hua","Selective deprotonation of tetra[3,4]thienylene in the presence of n-BuLi","Organic Chemistry Frontiers","2017","4","6","1019","","10.1039/C6QO00754F","","","0.71073","MoKα","","0.0597","0.0447","","","0.1207","0.1333","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553617","20.763","0.003","20.763","0.003","13.7545","0.0018","90","","90","","90","","5929.6","1.4","296","2","296.15","","","","","","","","","6","I 41/a :2","-I 4ad","88","","","","- C44 H72 Li4 O4 S4 Si4 -","- C44 H72 Li4 O4 S4 Si4 -","- C176 H288 Li16 O16 S16 Si16 -","4","0.25","","Li, Lu; Li, Bingbing; Li, Chunli; Ma, Zhiying; Xu, Li; Wang, Hua","Selective deprotonation of tetra[3,4]thienylene in the presence of n-BuLi","Organic Chemistry Frontiers","2017","4","6","1019","","10.1039/C6QO00754F","","","0.71073","MoKα","","0.1222","0.0831","","","0.2424","0.2973","","","","","","1.024","","","","has coordinates","235211","2020-10-21","18:00:00",""
"1553618","5.7832","0.0006","10.4921","0.0011","12.3215","0.0012","90.576","0.003","97.913","0.002","93.157","0.003","739.28","0.13","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C17 H17 N O4 -","- C17 H17 N O4 -","- C34 H34 N2 O8 -","2","1","","Chen, Hui; Lin, Cong; Xiong, Chunhua; Liu, Zhanxiang; Zhang, Yuhong","One-pot synthesis of fluorescent 2,4-dialkenylindoles by rhodium-catalyzed dual C–H functionalization","Organic Chemistry Frontiers","2017","4","3","455","","10.1039/C6QO00755D","","","0.71073","MoKα","","0.1123","0.0541","","","0.1153","0.1708","","","","","","1.002","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553619","13.585","0.004","12.569","0.003","9.741","0.003","90","","106.741","0.006","90","","1592.8","0.8","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H17 F O -","- C21 H17 F O -","- C84 H68 F4 O4 -","4","1","","Cao, Tongxiang; Chen, Kai; Zhu, Shifa","An efficient approach to generate aryl carbenes: gold-catalyzed sequential activation of 1,6-diynes","Organic Chemistry Frontiers","2017","4","3","450","","10.1039/C6QO00769D","","","0.71073","MoKα","","0.1216","0.0562","","","0.1286","0.1552","","","","","","0.984","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553620","12.3103","0.0016","20.299","0.003","6.9248","0.0009","90","","95.884","0.003","90","","1721.3","0.4","130","","130","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C23 H26 O -","- C23 H26 O -","- C92 H104 O4 -","4","1","","Cao, Tongxiang; Chen, Kai; Zhu, Shifa","An efficient approach to generate aryl carbenes: gold-catalyzed sequential activation of 1,6-diynes","Organic Chemistry Frontiers","2017","4","3","450","","10.1039/C6QO00769D","","","0.71073","MoKα","","0.0754","0.0487","","","0.1184","0.133","","","","","","1.023","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553621","12.4994","0.0013","13.1859","0.0014","16.0253","0.0017","102.651","0.005","95.439","0.006","92.29","0.006","2560.5","0.5","180","2","180","2","","","","","","","","5","P -1","-P 1","2","","","","- C60 H28 F20 N6 O2 -","- C60 H28 F20 N6 O2 -","- C120 H56 F40 N12 O4 -","2","1","","Almeida, José; Aguiar, António; Leite, Andreia; Silva, André M. N.; Cunha-Silva, Luís; de Castro, Baltazar; Rangel, Maria; Barone, Giampaolo; Tomé, Augusto C.; Silva, Ana M. G.","1,3-Dipolar cycloadditions with meso-tetraarylchlorins ‒ site selectivity and mixed bisadducts","Organic Chemistry Frontiers","2017","4","4","534","","10.1039/C6QO00771F","","","0.71073","MoKα","","0.1877","0.1387","","","0.4059","0.434","","","","","","1.614","","","","has coordinates","235216","2020-10-21","18:00:00",""
"1553622","15.6516","0.0005","14.7041","0.0004","20.8303","0.0006","90","","90","","90","","4793.9","0.2","180","","180","","","","101","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C23 H30 N4 O2 Si -","- C23 H30 N4 O2 Si -","- C184 H240 N32 O16 Si8 -","8","1","","Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.","Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry","Organic Chemistry Frontiers","2017","4","6","978","","10.1039/C6QO00787B","","","0.71073","MoKα","","0.048","0.0389","","0.1007","0.0942","0.1005","","","","","","1.0233","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553623","9.4684","0.0003","10.4692","0.0004","12.771","0.0004","96.2634","0.0012","95.7478","0.0012","113.644","0.0011","1138.27","0.07","180","","180","","","","101","","","","","5","P -1","-P 1","2","","","","- C20 H21 N5 O2 Si -","- C20 H21 N5 O2 Si -","- C40 H42 N10 O4 Si2 -","2","1","","Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.","Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry","Organic Chemistry Frontiers","2017","4","6","978","","10.1039/C6QO00787B","","","1.54178","CuKα","","0.0524","0.0469","","0.1317","0.1269","0.1317","","","","","","1.0042","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553624","16.2913","0.0007","10.0932","0.0004","19.7897","0.0008","90","","112.895","0.0012","90","","2997.7","0.2","180","","180","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C14 H8 Br3 N3 -","- C14 H8 Br3 N3 -","- C112 H64 Br24 N24 -","8","2","","Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.","Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry","Organic Chemistry Frontiers","2017","4","6","978","","10.1039/C6QO00787B","","","0.71073","MoKα","","0.0659","0.0374","","0.0956","0.0746","0.0956","","","","","","0.9177","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553625","8.9462","0.0005","11.9145","0.0006","43.549","0.002","90","","90","","90","","4641.9","0.4","180","","180","","","","101","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C21 H34 N4 O2 Si -","- C21 H34 N4 O2 Si -","- C168 H272 N32 O16 Si8 -","8","1","","Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.","Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry","Organic Chemistry Frontiers","2017","4","6","978","","10.1039/C6QO00787B","","","1.54178","CuKα","","0.0668","0.0577","","0.1162","0.1136","0.1162","","","","","","0.9617","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553626","11.9761","0.0003","15.4866","0.0004","11.0055","0.0003","90","","106.167","0.001","90","","1960.46","0.09","296","2","296","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C25 H20 O4 -","- C25 H20 O4 -","- C100 H80 O16 -","4","1","","Mao, Wenbin; Zhu, Chen","Efficient synthesis of multiply substituted butenolides from keto acids and terminal alkynes promoted by combined acids","Organic Chemistry Frontiers","2017","4","6","1029","","10.1039/C6QO00820H","","","0.71073","MoKα","","0.0815","0.0435","","","0.1177","0.1338","","","","","","1.066","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553627","8.8576","0.0007","9.515","0.0007","15.8743","0.0012","79.571","0.002","74.479","0.002","86.413","0.002","1267.66","0.17","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C35 H18 Fe O4 -","- C35 H18 Fe O4 -","- C70 H36 Fe2 O8 -","2","1","","Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian","From tetrabenzoheptafulvalene to sp2 carbon nano-rings","Organic Chemistry Frontiers","2017","4","5","699","","10.1039/C6QO00828C","","","0.71073","MoKα","","0.0571","0.0504","","","0.1402","0.1485","","","","","","1.058","","","","has coordinates","235222","2020-10-21","18:00:00",""
"1553628","12.737","0.003","10.827","0.003","15.738","0.004","90","","105.708","0.006","90","","2089.3","0.9","296","2","296","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C32 H18 O -","- C32 H18 O -","- C128 H72 O4 -","4","1","","Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian","From tetrabenzoheptafulvalene to sp2 carbon nano-rings","Organic Chemistry Frontiers","2017","4","5","699","","10.1039/C6QO00828C","","","0.71073","MoKα","","0.1793","0.0997","","","0.2401","0.2908","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553629","10.5417","0.0004","14.8356","0.0005","24.1274","0.0008","90","","90","","90","","3773.3","0.2","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C51 H29 Cl3 O4 -","- C51 H29 Cl3 O4 -","- C204 H116 Cl12 O16 -","4","1","","Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian","From tetrabenzoheptafulvalene to sp2 carbon nano-rings","Organic Chemistry Frontiers","2017","4","5","699","","10.1039/C6QO00828C","","","1.54178","CuKα","","0.0909","0.0536","","","0.1126","0.131","","","","","","1.023","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553630","12.3541","0.0003","20.5251","0.0006","15.593","0.0004","90","","111.562","0.0016","90","","3677.21","0.17","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C51 H30 Cl2 O -","- C51 H30 Cl2 O -","- C204 H120 Cl8 O4 -","4","1","","Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian","From tetrabenzoheptafulvalene to sp2 carbon nano-rings","Organic Chemistry Frontiers","2017","4","5","699","","10.1039/C6QO00828C","","","0.71073","MoKα","","0.1194","0.0675","","","0.1717","0.2047","","","","","","1.017","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553631","12.2233","0.0002","20.4397","0.0003","15.612","0.0002","90","","111.759","0.0009","90","","3622.59","0.09","296","2","296","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C51 H30 Cl2 -","- C51 H30 Cl2 -","- C204 H120 Cl8 -","4","1","","Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian","From tetrabenzoheptafulvalene to sp2 carbon nano-rings","Organic Chemistry Frontiers","2017","4","5","699","","10.1039/C6QO00828C","","","0.71073","MoKα","","0.0755","0.0569","","","0.1481","0.165","","","","","","1.007","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553632","8.8208","0.0003","12.857","0.0004","18.1141","0.0005","90","","90","","90","","2054.3","0.11","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C20 H19 Br N2 O5 S -","- C20 H19 Br N2 O5 S -","- C80 H76 Br4 N8 O20 S4 -","4","1","","Yu, Lu; Cheng, Yuyu; Qi, Fei; Li, Rou; Li, Pengfei","Organocatalytic regioselective, diastereoselective, and enantioselective annulation of cyclic 1-azadienes with γ-nitro ketones via 3,4-cyclization","Organic Chemistry Frontiers","2017","4","7","1336","","10.1039/C6QO00832A","","","0.71073","MoKα","","0.1259","0.0514","","","0.0608","0.0689","","","","","","0.994","","","","has coordinates","235224","2020-10-21","18:00:00",""
"1553633","5.768","0.002","9.924","0.004","20.463","0.007","100.063","0.004","91.086","0.004","92.46","0.004","1151.8","0.7","298","","298","","","","","","","","","3","P -1","-P 1","2","","","","- C29 H25 N3 -","- C29 H25 N3 -","- C58 H50 N6 -","2","1","","Zhao, Fen; Liu, Yaowen; Yang, Shu; Xie, Kai; Jiang, Yubo","Pd-catalyzed selective N(3)-ortho C–H arylation of 1,4-disubstituted 1,2,3-triazoles","Organic Chemistry Frontiers","2017","4","6","1112","","10.1039/C6QO00834H","","","0.71073","MoKα","","0.0692","0.0457","","","0.1142","0.129","","","","","","1.025","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553634","16.003","0.005","7.036","0.002","16.456","0.005","90","","101.876","0.004","90","","1813.2","0.9","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C21 H15 Br2 N O2 -","- C21 H15 Br2 N O2 -","- C84 H60 Br8 N4 O8 -","4","1","","Qiu, Guanyinsheng; Li, Yuewen; Ma, Lele; Zhou, Hongwei","KBr/K2S2O8-mediated dibromohydration of N-(2-alkynylaryl)acetamide","Organic Chemistry Frontiers","2017","4","6","1069","","10.1039/C6QO00840B","","","0.71073","MoKα","","0.0404","0.0328","","","0.0954","0.0996","","","","","","1.069","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553635","15.552","0.005","9.109","0.003","20","0.006","90","","111.508","0.005","90","","2636","1.5","130","","130","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C33 H31 N O3 -","- C33 H31 N O3 -","- C132 H124 N4 O12 -","4","1","","Liu, Feng; Tian, Jiaxin; Liu, Yong; Tao, Chuangan; Zhu, Hao; Zhang, Aina; Xu, Dongfang; Zhao, Baoguo","Decarboxylative Umpolung of conjugated enals to β-carbanions for intramolecular nucleophilic addition to an aldehyde","Organic Chemistry Frontiers","2017","4","8","1586","","10.1039/C6QO00846A","","","0.71073","MoKα","","0.1011","0.0555","","","0.1276","0.1513","","","","","","0.997","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553636","7.7445","0.0012","13.971","0.002","19.15","0.003","90","","90","","90","","2072","0.5","153","2","153","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","(2'R,3'R,4'R)-4'-benzoyl-1-methyl-3'-phenyl-5'-thioxospiro[indoline-3,2'-pyrrolidin]-2-one","","- C25 H20 N2 O2 S -","- C25 H20 N2 O2 S -","- C100 H80 N8 O8 S4 -","4","1","","Lin, Ye; Liu, Lei; Du, Da-Ming","Squaramide-catalyzed asymmetric Michael/cyclization cascade reaction of 3-isothiocyanato oxindoles with chalcones for synthesis of pyrrolidinyl spirooxindoles","Organic Chemistry Frontiers","2017","4","7","1229","","10.1039/C6QO00852F","","","0.71073","MoKα","","0.0394","0.0361","","","0.0806","0.0827","","","","","","1.001","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553637","8.4855","0.0004","15.887","0.0007","25.5299","0.0013","90","","90","","90","","3441.7","0.3","100","0.2","100","0.2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C16 H21 N3 O5 -","- C16 H21 N3 O5 -","- C128 H168 N24 O40 -","8","2","","Deng, Tao; Thota, Ganesh Kumar; Li, Yi; Kang, Qiang","Enantioselective conjugate addition of hydroxylamines to α,β-unsaturated 2-acyl imidazoles catalyzed by a chiral-at-metal Rh(iii) complex","Organic Chemistry Frontiers","2017","4","4","573","","10.1039/C6QO00865H","","","1.54184","CuKα","","0.0489","0.0384","","","0.0804","0.0857","","","","","","1.003","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553638","11.882","0.002","6.1567","0.0013","22.083","0.004","90","","99.617","0.015","90","","1592.8","0.5","273","2","273","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C36 H40 N2 O4 -","- C36 H40 N2 O4 -","- C72 H80 N4 O8 -","2","0.5","","Purc, Anna; Koszarna, Beata; Iachina, Irina; Friese, Daniel H.; Tasior, Mariusz; Sobczyk, Krzysztof; Pędziński, Tomasz; Brewer, Jonathan; Gryko, Daniel T.","The impact of interplay between electronic and steric effects on the synthesis and the linear and non-linear optical properties of diketopyrrolopyrrole bearing benzofuran moieties","Organic Chemistry Frontiers","2017","4","5","724","","10.1039/C6QO00869K","","","1.54178","CuKα","","0.1821","0.0736","","","0.1614","0.1933","","","","","","0.938","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553639","20.477","0.0009","5.2589","0.0002","28.0402","0.0012","90","","101.007","0.0019","90","","2964","0.2","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C32 H38 N2 O2 S3 -","- C32.4 H37.76 N2 O2 S2.908 -","- C129.6 H151.04 N8 O8 S11.632 -","4","1","","Chen, Wangqiao; Nakano, Masahiro; Takimiya, Kazuo; Zhang, Qichun","Selective thionation of naphtho[2,3-b]thiophene diimide: tuning of the optoelectronic properties and packing structure","Organic Chemistry Frontiers","2017","4","5","704","","10.1039/C6QO00871B","","","1.54187","CuKα","","0.1155","0.0889","","","0.2224","0.2399","","","","","","1.277","","","","has coordinates,has disorder","235238","2020-10-21","18:00:00",""
"1553724","10.445","0.002","14.347","0.003","14.407","0.003","82.53","0.03","85.3","0.03","74.55","0.03","2060.7","0.8","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C22 H23 Cl N2 O0 Ru -","- C22 H23 Cl N2 Ru -","- C88 H92 Cl4 N8 Ru4 -","4","2","","Li, Gang; Lv, Xulu; Guo, Kexiao; Wang, Ya; Yang, Suling; Yu, Liuyang; Yu, Yantang; Wang, Junjie","Ruthenium-catalyzed meta-selective C‒H sulfonation of azoarenes with arylsulfonyl chlorides","Organic Chemistry Frontiers","2017","4","6","1145","","10.1039/C7QO00004A","","","0.71073","MoKα","","0.0817","0.0695","","","0.1802","0.1846","","","","","","1.105","","","","has coordinates","235944","2020-10-21","18:00:00",""
"1553725","34.644","0.007","7.0976","0.0014","13.544","0.003","90","","98.63","0.03","90","","3292.6","1.2","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C18 H13 Cl N2 O2 S -","- C18 H13 Cl N2 O2 S -","- C144 H104 Cl8 N16 O16 S8 -","8","1","","Li, Gang; Lv, Xulu; Guo, Kexiao; Wang, Ya; Yang, Suling; Yu, Liuyang; Yu, Yantang; Wang, Junjie","Ruthenium-catalyzed meta-selective C–H sulfonation of azoarenes with arylsulfonyl chlorides","Organic Chemistry Frontiers","2017","4","6","1145","","10.1039/C7QO00004A","","","0.71073","MoKα","","0.0632","0.0409","","","0.1337","0.1539","","","","","","1.002","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553726","11.4884","0.0005","11.9792","0.0005","20.8251","0.0008","90","","90","","90","","2866","0.2","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C16 H15 N O7 -","- C16 H15 N O7 -","- C128 H120 N8 O56 -","8","2","","Wang, Junliang; Li, Jianneng; Shen, Xianwang; Dong, Cong; Lin, Jun; Wei, Kun","Asymmetric total synthesis of (−)-δ-lycorane","Organic Chemistry Frontiers","2017","4","6","1149","","10.1039/C7QO00021A","","","1.54178","CuKα","","0.0535","0.0527","","","0.1534","0.1545","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553727","13.8813","0.0006","14.4392","0.0007","23.5317","0.0011","95.8618","0.0012","105.365","0.0012","91.4814","0.0011","4517.3","0.4","200","2","200","2","","","","","","","","3","P -1","-P 1","2","","","","- C60 H46 N4.5 -","- C60 H46 N4.5 -","- C240 H184 N18 -","4","2","","Kimura, Yosuke; Kawajiri, Ikumi; Ueki, Masanori; Morimoto, Takayuki; Nishida, Jun-ichi; Ikeda, Hiroshi; Tanaka, Mirai; Kawase, Takeshi","A new fluorophore displaying remarkable solvatofluorochromism and solid-state light emission, and serving as a turn-on fluorescent sensor for cyanide ions","Organic Chemistry Frontiers","2017","4","5","743","","10.1039/C7QO00029D","","","0.71075","MoKα","","0.2091","0.0714","","","0.1685","0.2407","","","","","","0.938","","","","has coordinates,has disorder","274176","2022-03-31","10:10:26",""
"1553728","11.5","0.004","10.46","0.004","11.413","0.005","90","","95.06","0.008","90","","1367.5","0.9","130","","130","","","","","","","","","6","C 1 2 1","C 2y","5","","","","- C11 H16 F3 N O2 S2 -","- C11 H16 F3 N O2 S2 -","- C44 H64 F12 N4 O8 S8 -","4","1","","Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong","(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation","Organic Chemistry Frontiers","2017","4","6","1051","","10.1039/C7QO00042A","","","0.71073","MoKα","","0.0455","0.0404","","","0.0934","0.0982","","","","","","1.108","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553729","6.6977","0.0005","8.1914","0.0006","30.513","0.002","90","","90","","90","","1674.1","0.2","130","","130","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C19 H10 F4 O2 S -","- C19 H10 F4 O2 S -","- C76 H40 F16 O8 S4 -","4","1","","Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong","(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation","Organic Chemistry Frontiers","2017","4","6","1051","","10.1039/C7QO00042A","","","0.71073","MoKα","","0.0353","0.0334","","","0.0865","0.0875","","","","","","1.067","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553730","7.5426","0.0006","13.2312","0.001","15.9887","0.0013","90","","90","","90","","1595.6","0.2","130","2","130","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C15 H15 F3 O5 S -","- C15 H15 F3 O5 S -","- C60 H60 F12 O20 S4 -","4","1","","Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong","(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation","Organic Chemistry Frontiers","2017","4","6","1051","","10.1039/C7QO00042A","","","0.71073","MoKα","","0.0307","0.0273","","","0.07","0.0719","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553731","8.5502","0.0008","11.0835","0.0011","16.8212","0.0016","90","","90","","90","","1594.1","0.3","130","","130","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C17 H11 F3 N2 O S -","- C17 H11 F3 N2 O S -","- C68 H44 F12 N8 O4 S4 -","4","1","","Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong","(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation","Organic Chemistry Frontiers","2017","4","6","1051","","10.1039/C7QO00042A","","","0.71073","MoKα","","0.0471","0.0397","","","0.0975","0.1022","","","","","","1.036","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553732","7.7869","0.0006","10.8732","0.0008","8.8809","0.0007","90","","95.062","0.001","90","","749","0.1","130","","130","","","","","","","","","7","P 1 21 1","P 2yb","4","","","","- C11 H14 Cl2 F3 N O2 S2 -","- C11 H14 Cl2 F3 N O2 S2 -","- C22 H28 Cl4 F6 N2 O4 S4 -","2","1","","Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong","(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation","Organic Chemistry Frontiers","2017","4","6","1051","","10.1039/C7QO00042A","","","0.71073","MoKα","","0.0292","0.0285","","","0.072","0.0725","","","","","","1.035","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553733","12.4266","0.0017","8.8229","0.0012","15.107","0.002","90","","105.7","0.003","90","","1594.5","0.4","130","","130","","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C13 H20 F3 N O4 S2 -","- C13 H20 F3 N O4 S2 -","- C52 H80 F12 N4 O16 S8 -","4","2","","Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong","(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation","Organic Chemistry Frontiers","2017","4","6","1051","","10.1039/C7QO00042A","","","0.71073","MoKα","","0.0445","0.0379","","","0.0862","0.0904","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553734","15.566","0.002","15.831","0.0016","17.7553","0.0019","80.813","0.006","89.907","0.011","88.251","0.009","4317.2","0.8","93","2","93","2","","","","","","","","6","P -1","-P 1","2","","","","- C101 H110 N4 Ni P Pt0.5 -","- C101 H110 N4 Ni P Pt0.5 -","- C202 H220 N8 Ni2 P2 Pt -","2","1","","Fukui, Norihito; Jiang, Hua-Wei; Osuka, Atsuhiro","meso-to-meso PtII-bridged NiII-porphyrin dimers","Organic Chemistry Frontiers","2017","4","5","767","","10.1039/C7QO00093F","","","1.54187","CuKα","","0.0341","0.0313","","","0.0799","0.081","","","","","","1.042","","","","has coordinates,has disorder","235954","2020-10-21","18:00:00",""
"1553735","16.142","0.003","21.227","0.004","22.446","0.004","106.1","0.005","92.132","0.001","93.364","0.006","7365","2","93","2","93","2","","","","","","","","6","P -1","-P 1","2","","","","- C162 H174 Cl10 N8 Ni2 Pt -","- C162 H174 Cl10 N8 Ni2 Pt -","- C324 H348 Cl20 N16 Ni4 Pt2 -","2","1","","Fukui, Norihito; Jiang, Hua-Wei; Osuka, Atsuhiro","meso-to-meso PtII-bridged NiII-porphyrin dimers","Organic Chemistry Frontiers","2017","4","5","767","","10.1039/C7QO00093F","","","1.54187","CuKα","","0.0683","0.0581","","","0.1606","0.1669","","","","","","1.054","","","","has coordinates,has disorder","235954","2020-10-21","18:00:00",""
"1553736","13.8397","0.0009","24.2642","0.0013","16.7166","0.0013","90","","109.444","0.008","90","","5293.4","0.7","180","0.1","180","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C76 H38 Br N O8 -","- C76 H38 Br N O8 -","- C304 H152 Br4 N4 O32 -","4","1","","Xu, Dan; Li, Yanbang; Lou, Ning; Gan, Liangbing","Synthesis of homoazafullerene [C59N(CH2)]R and azahomoazafullerene [C59N(NH)]R","Organic Chemistry Frontiers","2017","4","5","750","","10.1039/C7QO00098G","","","0.71073","MoKα","","0.1521","0.0699","","","0.1429","0.1714","","","","","","0.921","","","","has coordinates","235956","2020-10-21","18:00:00",""
"1553737","21.489","0.004","10.179","0.002","22.215","0.004","90","","90","","90","","4859.2","1.6","100","","100","","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C76 H39 N O9 -","- C76 H39 N O9 -","- C304 H156 N4 O36 -","4","1","","Xu, Dan; Li, Yanbang; Lou, Ning; Gan, Liangbing","Synthesis of homoazafullerene [C59N(CH2)]R and azahomoazafullerene [C59N(NH)]R","Organic Chemistry Frontiers","2017","4","5","750","","10.1039/C7QO00098G","","","0.71073","MoKα","","0.0804","0.0656","","","0.1822","0.1998","","","","","","1.054","","","","has coordinates,has disorder","235956","2020-10-21","18:00:00",""
"1553738","17.5147","0.001","7.024","0.003","15.73","0.009","90","","114.033","0.006","90","","1767.4","1.3","150","","150","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","N-(3-(4-bromophenyl)-5-methylene-2-oxooxazolidin-4-yl)-4-methylbenzenesulfonamide","","- C17 H13 Br N2 O4 S -","- C17 H13 Br N2 O4 S -","- C68 H52 Br4 N8 O16 S4 -","4","1","","Pal, Kuntal; Volla, Chandra M. R.","Rhodium-catalyzed denitrogenative transannulation of 1,2,3-triazolyl-carbamates: efficient access to 4-aminooxazolidinones","Organic Chemistry Frontiers","2017","4","7","1380","","10.1039/C7QO00101K","","","0.7107","MoKα","","0.0547","0.0451","","","0.0991","0.1046","","","","","","1.091","","","","has coordinates","235958","2020-10-21","18:00:00",""
"1553741","28.543","0.006","7.309","0.0015","16.361","0.003","90","","105.04","0.03","90","","3296.3","1.2","293","2","293","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C19 H22 O3 -","- C19 H22 O3 -","- C152 H176 O24 -","8","1","","Chang, Wenju; Dai, Jie; Li, Jingfu; Shi, Yuan; Ren, Wenlong; Shi, Yian","A facile approach to ketones via Pd-catalyzed sequential carbonylation of olefins with formic acid","Organic Chemistry Frontiers","2017","4","6","1074","","10.1039/C7QO00111H","","","0.71073","MoKα","","0.1583","0.0639","","","0.1064","0.1411","","","","","","1.002","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553742","5.69674","0.00011","8.92923","0.00016","19.6982","0.0005","90","","94.927","0.002","90","","998.3","0.04","173","0.1","173","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C11 H8 N O2 S -","- C22 H16 N2 O4 S2 -","- C44 H32 N4 O8 S4 -","2","0.5","","Ammon, Felix; Sauer, Stephanie Theresia; Lippert, Rainer; Lungerich, Dominik; Reger, David; Hampel, Frank; Jux, Norbert","Unexpected formation of [5]helicenes from hexaarylbenzenes containing pyrrole moieties","Organic Chemistry Frontiers","2017","4","5","861","","10.1039/C7QO00112F","","x-ray","1.54184","CuKα","","0.0465","0.043","","","0.1146","0.1186","","","","","","1.054","","","","has coordinates","235964","2020-10-21","18:00:00",""
"1553743","14.0225","0.0007","15.4902","0.001","15.6494","0.0005","109.303","0.004","105.791","0.004","106.459","0.005","2814.2","0.3","152.7","1","152.7","1","","","","","","","","6","P -1","-P 1","2","","","","- C67.5 H66 Cl3 N O2 S -","- C67.5 H66 Cl3 N O2 S -","- C135 H132 Cl6 N2 O4 S2 -","2","1","","Ammon, Felix; Sauer, Stephanie Theresia; Lippert, Rainer; Lungerich, Dominik; Reger, David; Hampel, Frank; Jux, Norbert","Unexpected formation of [5]helicenes from hexaarylbenzenes containing pyrrole moieties","Organic Chemistry Frontiers","2017","4","5","861","","10.1039/C7QO00112F","","x-ray","1.54184","CuKα","","0.0797","0.0729","","","0.1995","0.2094","","","","","","1.021","","","","has coordinates,has disorder","235964","2020-10-21","18:00:00",""
"1553744","8.2685","0.0016","13.793","0.003","17.645","0.003","72.588","0.003","88.716","0.003","77.009","0.002","1868.8","0.6","150","","150","","","","","","","","","3","P -1","-P 1","2","","","","- C84 H108 Si4 -","- C84 H108 Si4 -","- C84 H108 Si4 -","1","0.5","","Bettinger, Holger F.; Einholz, Ralf; Göttler, Andreas; Junge, Marc; Sättele, Marie-Sophie; Schnepf, Andreas; Schrenk, Claudio; Schundelmeier, Simon; Speiser, Bernd","6,6′,11,11′-Tetra((triisopropylsilyl)ethynyl)-anti-[2.2](1,4)tetracenophane: a covalently coupled tetracene dimer and its structural, electrochemical, and photophysical characterization","Organic Chemistry Frontiers","2017","4","5","853","","10.1039/C7QO00117G","","","0.8","synchrotron","","0.0904","0.0564","","","0.1314","0.1438","","","","","","1.015","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553745","6.121","0.005","8.835","0.007","13.265","0.012","83.14","0.02","79.6","0.02","72.93","0.02","672.8","1","296","2","296","2","","","","","","","synthesis","5","P -1","-P 1","2","","(E)-6-methyl-N-(1-phenylethylidene)pyridine-2-sulfonamide","","- C14 H14 N2 O2 S -","- C14 H14 N2 O2 S -","- C28 H28 N4 O4 S2 -","2","1","","Wang, Bin; Xu, Tong; Zhu, Lei; Lan, Yu; Wang, Jingdong; Lu, Ning; Wei, Zhonglin; Lin, Yingjie; Duan, Haifeng","Highly enantioselective nitro-Mannich reaction of ketimines under phase-transfer catalysis","Organic Chemistry Frontiers","2017","4","7","1266","","10.1039/C7QO00124J","","","0.71073","MoKα","","0.0942","0.0655","","","0.1851","0.2162","","","","","","0.967","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553746","8.6132","0.0015","7.4744","0.0014","12.867","0.003","90","","109.429","0.005","90","","781.2","0.3","296","2","296","2","","","","","","","synthesis","5","P 1 21 1","P 2yb","4","","(R)-6-methyl-N-(1-nitro-2-phenylpropan-2-yl)pyridine-2-sulfonamide","","- C15 H17 N3 O4 S -","- C15 H17 N3 O4 S -","- C30 H34 N6 O8 S2 -","2","1","","Wang, Bin; Xu, Tong; Zhu, Lei; Lan, Yu; Wang, Jingdong; Lu, Ning; Wei, Zhonglin; Lin, Yingjie; Duan, Haifeng","Highly enantioselective nitro-Mannich reaction of ketimines under phase-transfer catalysis","Organic Chemistry Frontiers","2017","4","7","1266","","10.1039/C7QO00124J","","","0.71073","MoKα","","0.0385","0.0352","","","0.0849","0.0874","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553747","21.7066","0.0008","21.7067","0.0008","20.1949","0.0013","90","","122.509","0.003","90","","8024.4","0.7","213","2","213","2","","","","","","","","2","C 1 c 1","C -2yc","9","","1,4,1',4?-tetramethyl-9,9?-bifluorenylidene","","- C30 H24 -","- C30 H24 -","- C480 H384 -","16","4","","Takai, Atsuro; Freas, Dylan J.; Suzuki, Toshikane; Sugimoto, Manabu; Labuta, Jan; Haruki, Rie; Kumai, Reiji; Adachi, Shin-ichi; Sakai, Hayato; Hasobe, Taku; Matsushita, Yoshitaka; Takeuchi, Masayuki","The effect of a highly twisted CC double bond on the electronic structures of 9,9′-bifluorenylidene derivatives in the ground and excited states","Organic Chemistry Frontiers","2017","4","5","650","","10.1039/C7QO00125H","","","0.71073","MoKα","","0.1838","0.0776","","","0.1578","0.2027","","","","","","0.874","","","","has coordinates","235970","2020-10-21","18:00:00",""
"1553748","7.6834","0.0016","8.0281","0.0017","12.554","0.003","85.471","0.003","73.42","0.003","74.044","0.003","713.6","0.3","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C15 H13 N O4 S2 -","- C15 H13 N O4 S2 -","- C30 H26 N2 O8 S4 -","2","1","","Zhou, Kaida; Xia, Hongguang; Wu, Jie","Generation of benzosultams via a radical process with the insertion of sulfur dioxide","Organic Chemistry Frontiers","2017","4","6","1121","","10.1039/C7QO00127D","","","0.71073","MoKα","","0.0534","0.0396","","","0.1348","0.1787","","","","","","1.22","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553749","8.151","0.01","8.239","0.009","22.94","0.03","90","","100.06","0.02","90","","1517","3","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H13 N O4 S2 -","- C15 H13 N O4 S2 -","- C60 H52 N4 O16 S8 -","4","1","","Zhou, Kaida; Xia, Hongguang; Wu, Jie","Generation of benzosultams via a radical process with the insertion of sulfur dioxide","Organic Chemistry Frontiers","2017","4","6","1121","","10.1039/C7QO00127D","","","0.71073","MoKα","","0.1152","0.0582","","","0.1803","0.2242","","","","","","0.947","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553750","9.0047","0.0003","9.2247","0.0003","9.4826","0.0003","109.875","0.003","108.593","0.003","107.103","0.003","626.45","0.05","100","","100","","","","","","","","","4","P 1","P 1","1","","","","- C26 H31 N3 O6 -","- C26 H31 N3 O6 -","- C26 H31 N3 O6 -","1","1","","Guo, Jing; Lin, Zi-Hui; Chen, Kai-Bin; Xie, Ying; Chan, Albert S. C.; Weng, Jiang; Lu, Gui","Asymmetric amination of 2-substituted indolin-3-ones catalyzed by natural cinchona alkaloids","Organic Chemistry Frontiers","2017","4","7","1400","","10.1039/C7QO00129K","","x-ray","1.54184","CuKα","","0.0421","0.0417","","","0.121","0.122","","","","","","1.0608","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553751","8.9558","0.0013","9.4432","0.0013","13.6247","0.0018","92.926","0.003","95.287","0.004","111","0.003","1066.8","0.3","240","2","240","2","","","","","","","","3","P -1","-P 1","2","10,10""-dioxyl-9,9':10',9""-teranthrylene","","","- C54 H48 O8 -","- C54 H48 O8 -","- C54 H48 O8 -","1","0.5","","Hirao, Yasukazu; Konishi, Akihito; Kubo, Takashi","Anthroxyl-based biradical: toward the construction of highly stable multi-spin systems","Organic Chemistry Frontiers","2017","4","5","828","","10.1039/C7QO00130D","","","0.71075","MoKα","","0.1807","0.076","","","0.1962","0.2698","","","","","","0.968","","","","has coordinates,has disorder","235976","2020-10-21","18:00:00",""
"1553752","11.8673","0.0003","14.8352","0.0003","15.9367","0.0005","90","","102.976","0.0009","90","","2734.08","0.12","120","2","120","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","2,2"",7,7""-tetra-tert-butyl-10,10""-dioxyl-9,9':10',9""-teranthrylene","","","- C66 H72 O6 -","- C66 H68 O6 -","- C132 H136 O12 -","2","0.5","","Hirao, Yasukazu; Konishi, Akihito; Kubo, Takashi","Anthroxyl-based biradical: toward the construction of highly stable multi-spin systems","Organic Chemistry Frontiers","2017","4","5","828","","10.1039/C7QO00130D","","","0.71075","MoKα","","0.0855","0.0637","","","0.1863","0.2067","","","","","","1.103","","","","has coordinates,has disorder","235976","2020-10-21","18:00:00",""
"1553753","23.6823","0.0014","14.1831","0.0008","19.4393","0.001","90","","101.921","0.0017","90","","6388.6","0.6","296","2","296","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C41 H27 O -","- C41 H27 O -","- C328 H216 O8 -","8","1","","Ip, Ho-Wang; Chow, Hak-Fun; Kuck, Dietmar","Electronic and steric effects on the three-fold Scholl-type cycloheptatriene ring formation around a tribenzotriquinacene core","Organic Chemistry Frontiers","2017","4","5","817","","10.1039/C7QO00132K","","","0.71073","MoKα","","0.0864","0.058","","","0.1439","0.1598","","","","","","1.045","","","","has coordinates","235978","2020-10-21","18:00:00",""
"1553754","12.4244","0.0009","8.0614","0.0006","14.7164","0.001","90","","100.607","0.002","90","","1448.78","0.18","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","methyl 2-(3-methyl-11H-benzo[4,5]imidazo[2,1-a]isoindol-11-yl)acetate","","- C18 H16 N2 O2 -","- C18 H16 N2 O2 -","- C72 H64 N8 O8 -","4","1","","Selvaraju, Manikandan; Wang, Ying-Lien; Sun, Chung-Ming","Ruthenium(ii)-catalyzed C–H alkenylation/annulation cascade for the rapid synthesis of benzoimidazoisoindoles","Organic Chemistry Frontiers","2017","4","7","1358","","10.1039/C7QO00136C","","","0.71073","MoKα","","0.0463","0.0376","","","0.0917","0.0982","","","","","","1.03","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553755","8.086","0.005","14.196","0.005","23.304","0.005","90","0.005","90","0.005","90","0.005","2675","2","293","2","293","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C7.75 H7.75 F7.75 N7.75 O7.75 S7.75 -","- C30 H19 F3 N O5 S2 -","- C120 H76 F12 N4 O20 S8 -","4","1","","Pouambeka, Tony Wheellyam; Zhang, Ge; Zheng, Guang-Fan; Xu, Guo-Xing; Zhang, Qian; Xiong, Tao; Zhang, Qian","Copper-catalyzed oxidative amidation of α,β-unsaturated ketones via selective C‒H or C‒C bond cleavage","Organic Chemistry Frontiers","2017","4","7","1420","","10.1039/C7QO00146K","","","0.71069","MoKα","","0.0936","0.064","","","0.1363","0.1534","","","","","","1.03","","","","has coordinates","235982","2020-10-21","18:00:00",""
"1553756","5.9608","0.0004","18.7773","0.0009","20.3817","0.0011","90","","90","","90","","2281.3","0.2","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C27 H21 N O2 S2 -","- C27 H21 N O2 S2 -","- C108 H84 N4 O8 S8 -","4","1","","Shi, Qing; Li, Pinhua; Zhang, Yan; Wang, Lei","Visible light-induced tandem oxidative cyclization of 2-alkynylanilines with disulfides (diselenides) to 3-sulfenyl- and 3-selenylindoles under transition metal-free and photocatalyst-free conditions","Organic Chemistry Frontiers","2017","4","7","1322","","10.1039/C7QO00152E","","","0.71073","MoKα","","0.041","0.0337","","","0.0813","0.0861","","","","","","1.026","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553757","9.0611","0.0006","7.1551","0.0004","20.5051","0.0018","90","","93.684","0.006","90","","1326.66","0.16","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H12 Cl N O -","- C16 H12 Cl N O -","- C64 H48 Cl4 N4 O4 -","4","1","","Zhang, Zhiguo; Zhang, Yongchao; Huang, Guoqing; Zhang, Guisheng","Organoiodine reagent-promoted intermolecular oxidative amination: synthesis of cyclopropyl spirooxindoles","Organic Chemistry Frontiers","2017","4","7","1372","","10.1039/C7QO00156H","","x-ray","1.54184","CuKα","","0.054","0.0443","","","0.1155","0.1246","","","","","","1.039","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553758","8.3955","0.0002","14.09","0.0004","16.7651","0.0005","90","","90","","90","","1983.19","0.09","100","","100","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C17 H18 Br F3 N2 O6 -","- C17 H18 Br F3 N2 O6 -","- C68 H72 Br4 F12 N8 O24 -","4","1","","Liu, Qiang; Zhao, Kun; Zhi, Ying; Raabe, Gerhard; Enders, Dieter","Squaramide-catalyzed domino Michael/aza-Henry [3 + 2] cycloaddition: asymmetric synthesis of functionalized 5-trifluoromethyl and 3-nitro substituted pyrrolidines","Organic Chemistry Frontiers","2017","4","7","1416","","10.1039/C7QO00161D","","","1.54178","CuKα","","0.028","0.028","","0.031","","0.031","","","1.002","","","1.006","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553759","9.593","0.004","15.307","0.007","16.705","0.008","90","","93.785","0.008","90","","2447.6","1.9","100.01","0.1","100.01","0.1","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C23 H22 Br Cl2 N3 O5 -","- C23 H22 Br Cl2 N3 O5 -","- C92 H88 Br4 Cl8 N12 O20 -","4","1","","Chen, Dong-Zhen; Xiao, Wen-Jing; Chen, Jia-Rong","Synthesis of spiropyrazoline oxindoles by a formal [4 + 1] annulation reaction between 3-bromooxindoles and in situ-derived 1,2-diaza-1,3-dienes","Organic Chemistry Frontiers","2017","4","7","1289","","10.1039/C7QO00163K","","","0.71073","MoKα","","0.0598","0.0405","","","0.1088","0.1204","","","","","","1.023","","","","has coordinates,has disorder","235989","2020-10-21","18:00:00",""
"1553760","6.299","0.008","11.774","0.015","14.904","0.019","99.608","0.016","94.163","0.015","96.363","0.016","1078","2","298","2","298.15","","","","","","","","","6","P -1","-P 1","2","","","","- C20 H17 Br Cl3 N3 O3 -","- C20 H17 Br Cl3 N3 O3 -","- C40 H34 Br2 Cl6 N6 O6 -","2","1","","Chen, Dong-Zhen; Xiao, Wen-Jing; Chen, Jia-Rong","Synthesis of spiropyrazoline oxindoles by a formal [4 + 1] annulation reaction between 3-bromooxindoles and in situ-derived 1,2-diaza-1,3-dienes","Organic Chemistry Frontiers","2017","4","7","1289","","10.1039/C7QO00163K","","","0.71073","MoKα","","0.2","0.1125","","","0.2823","0.3492","","","","","","1.051","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553761","7.738","0.0005","11.656","0.0008","14.0895","0.0008","90","","90","","90","","1270.79","0.14","298.84","0.1","298.84","0.1","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","2',3'-dihydrospiro[cyclopentane-1,1'-cyclopenta[a]naphthalen]-2-one","","- C17 H16 O -","- C17 H16 O -","- C68 H64 O4 -","4","1","","Zhang, Bo-Sheng; Hua, Hui-Liang; Gao, Lu-Yao; Liu, Ce; Qiu, Yi-Feng; Zhou, Ping-Xin; Zhou, Zhao-Zhao; Zhao, Jia-Hui; Liang, Yong-Min","Palladium-catalyzed arene C–H activation/ketone C–H functionalization reaction: route to spirodihydroindenones","Organic Chemistry Frontiers","2017","4","7","1376","","10.1039/C7QO00164A","","x-ray","0.71073","MoKα","","0.0845","0.0553","","","0.112","0.1329","","","","","","1.109","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553762","16.382","0.004","18.322","0.004","14.538","0.003","90","","120.472","0.003","90","","3760.9","1.5","","","273.15","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","1-phenyl-2-tosyl-9H-pyrrolo[1,2-a]indole","","- C24 H19 N O2 S -","- C24 H19 N O2 S -","- C192 H152 N8 O16 S8 -","8","1","","Zhang, Pengbo; Gao, Yuzhen; Chen, Su; Tang, Guo; Zhao, Yufen","Direct synthesis of 2-sulfonated 9H-pyrrolo[1,2-a]indoles via NaI-catalyzed cascade radical addition/cyclization/isomerization","Organic Chemistry Frontiers","2017","4","7","1350","","10.1039/C7QO00167C","","","0.71073","MoKα","","0.0751","0.0546","","","0.1568","0.171","","","","","","1.1214","","","","has coordinates","300101","2025-06-17","17:58:10",""
"1553763","7.1026","0.0003","7.8866","0.0003","11.4159","0.0005","92.777","0.002","92.263","0.002","114.968","0.001","577.75","0.04","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C14 H12 N2 O3 -","- C14 H12 N2 O3 -","- C28 H24 N4 O6 -","2","1","","Hong, Longcheng; Ahles, Sebastian; Strauss, Marcel A.; Logemann, Christian; Wegner, Hermann A.","Synthesis of 2,3-diaza-anthraquinones via the bidentate Lewis acid catalysed inverse electron-demand Diels–Alder (IEDDA) reaction","Organic Chemistry Frontiers","2017","4","5","871","","10.1039/C7QO00172J","","","0.71073","MoKα","","0.0557","0.045","","","0.1174","0.1233","","","","","","1.084","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553764","8.7048","0.001","10.5461","0.0013","13.9946","0.0017","82.33","0.002","79.359","0.002","79.1","0.002","1233.4","0.3","293","2","293","2","","","","","","","","7","P -1","-P 1","2","","","","- C25 H22 F I2 N O2 S -","- C25 H22 F I2 N O2 S -","- C50 H44 F2 I4 N2 O4 S2 -","2","1","","Wang, Qiang; Jiang, Bo; Yu, Liu-Zhu; Wei, Yin; Shi, Min","Iron-catalyzed or iodine-induced intramolecular halocyclization of N-vinyl-tethered methylenecyclopropanes: facile access to halogenated 1,2-dihydroquinolines","Organic Chemistry Frontiers","2017","4","7","1294","","10.1039/C7QO00177K","","","0.71073","MoKα","","0.034","0.0293","","","0.0767","0.0796","","","","","","1.045","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553765","13.2671","0.0017","18.296","0.003","19.283","0.003","90","","108.684","0.003","90","","4434","1.2","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C25 H24 Cl N O2 S -","- C25 H24 Cl N O2 S -","- C200 H192 Cl8 N8 O16 S8 -","8","2","","Wang, Qiang; Jiang, Bo; Yu, Liu-Zhu; Wei, Yin; Shi, Min","Iron-catalyzed or iodine-induced intramolecular halocyclization of N-vinyl-tethered methylenecyclopropanes: facile access to halogenated 1,2-dihydroquinolines","Organic Chemistry Frontiers","2017","4","7","1294","","10.1039/C7QO00177K","","","0.71073","MoKα","","0.1036","0.0688","","","0.1689","0.1901","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553766","12.112","0.003","13.064","0.003","13.586","0.003","113.51","0.02","114.37","0.02","96.715","0.018","1690.6","0.9","295","2","295","2","","","","","","","","4","P -1","-P 1","2","","","","- C18 H17 N S3 -","- C18 H17 N S3 -","- C72 H68 N4 S12 -","4","2","","Schneeweis, Arno; Neidlinger, Andreas; Reiss, Guido J.; Frank, Walter; Heinze, Katja; Müller, Thomas J. J.","Radical cation and dication of a 4H-dithieno[2,3-b:3′,2′-e][1,4]-thiazine","Organic Chemistry Frontiers","2017","4","5","839","","10.1039/C7QO00188F","","","0.71073","MoKα","","0.0962","0.0668","","","0.1361","0.1532","","","","","","1.198","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553767","9.3089","0.0019","10.692","0.002","10.826","0.002","98.78","0.004","90.325","0.004","108.111","0.004","1010.5","0.3","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C26 H20 F3 N O -","- C26 H20 F3 N O -","- C52 H40 F6 N2 O2 -","2","1","","An, Yuanyuan; Zhang, Jun; Xia, Hongguang; Wu, Jie","Radical cyclization of benzene-tethered 1,7-enynes with aryldiazonium tetrafluoroborates: a facile route to benzo[j]phenanthridines","Organic Chemistry Frontiers","2017","4","7","1318","","10.1039/C7QO00193B","","","0.71073","MoKα","","0.1156","0.0615","","","0.1912","0.2556","","","","","","0.988","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553768","8.7598","0.0009","25.852","0.003","8.8958","0.0009","90","","96.431","0.002","90","","2001.9","0.4","133","2","133","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C22 H26 F2 N2 O2 -","- C22 H26 F2 N2 O2 -","- C88 H104 F8 N8 O8 -","4","1","","Liu, Kai; Sui, Lin-Chao; Jin, Qiao; Li, Deng-Yuan; Liu, Pei-Nian","CuBr-mediated radical cascade difluoroacetamidation of acrylamides using α,α-difluoro-α-(TMS)-acetamides","Organic Chemistry Frontiers","2017","4","8","1606","","10.1039/C7QO00209B","","","0.71073","MoKα","","0.0599","0.0381","","","0.0827","0.0932","","","","","","1.01","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553769","21.229","0.01","3.919","0.0019","15.628","0.008","90","","105.861","0.011","90","","1250.7","1.1","273","2","273","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H11 F N2 O -","- C16 H11 F N2 O -","- C64 H44 F4 N8 O4 -","4","1","","Ding, Junshuai; Zhang, Yingchao; Li, Jizhen","Nickel-catalyzed selective C-5 fluorination of 8-aminoquinolines with NFSI","Organic Chemistry Frontiers","2017","4","8","1528","","10.1039/C7QO00211D","","","0.71073","MoKα","","0.1172","0.0737","","","0.2007","0.2307","","","","","","0.994","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553770","11.93574","0.00015","7.18231","0.00008","19.3705","0.0002","90","","94.7142","0.0011","90","","1654.94","0.03","150","0.1","150","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H12 Cl3 N O0 -","- C20 H12 Cl3 N -","- C80 H48 Cl12 N4 -","4","1","","Li, Jianxiao; An, Yanni; Li, Jiawei; Yang, Shaorong; Wu, Wanqing; Jiang, Huanfeng","Palladium-catalyzed C‒S bond activation and functionalization of 3-sulfenylindoles and related electron-rich heteroarenes","Organic Chemistry Frontiers","2017","4","8","1590","","10.1039/C7QO00215G","","x-ray","1.54184","CuKα","","0.0414","0.0398","","","0.1081","0.1101","","","","","","1.057","","","","has coordinates","236006","2020-10-21","18:00:00",""
"1553771","9.8942","0.0018","11.644","0.002","20.487","0.004","87.078","0.008","78.302","0.009","68.651","0.006","2152","0.7","173.15","","173.15","","","","","","","","","5","P -1","-P 1","2","","","","- C34 H52 Cl4 N16 O2 -","- C34 H52 Cl4 N16 O2 -","- C68 H104 Cl8 N32 O4 -","2","1","","Liang, Dong-Dong; Wang, Mei-Xiang","Synthesis and conformational structure of hydrazo-bridged homo calix[2]pyridine[2]triazines","Organic Chemistry Frontiers","2017","4","7","1425","","10.1039/C7QO00221A","","","0.71073","MoKα","","0.1208","0.1118","","","0.3058","0.3152","","","","","","1.12","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553772","11.9766","0.0004","19.3355","0.0005","12.7804","0.0004","90","","114.734","0.004","90","","2688.09","0.17","173","0.1","173","0.1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C5.33 H10 Cl0.67 Co0.33 N2.67 O4 -","- C5.33333 H10 Cl0.666667 Co0.333333 N2.66667 O4 -","- C64 H120 Cl8 Co4 N32 O48 -","12","3","","Liang, Dong-Dong; Wang, Mei-Xiang","Synthesis and conformational structure of hydrazo-bridged homo calix[2]pyridine[2]triazines","Organic Chemistry Frontiers","2017","4","7","1425","","10.1039/C7QO00221A","","x-ray","1.54184","CuKα","","0.0713","0.0627","","","0.1679","0.1785","","","","","","1.048","","","","has coordinates","236009","2020-10-21","18:00:00",""
"1553773","13.18","0.003","19.895","0.004","20.59","0.004","108.27","0.03","107.63","0.03","90.48","0.03","4854","2","173.15","","173.15","","","","","","","","","5","P -1","-P 1","2","","","","- C27 H41 N16 O3.5 S1.5 -","- C27 H41 N16 O3.5 S1.5 -","- C108 H164 N64 O14 S6 -","4","2","","Liang, Dong-Dong; Wang, Mei-Xiang","Synthesis and conformational structure of hydrazo-bridged homo calix[2]pyridine[2]triazines","Organic Chemistry Frontiers","2017","4","7","1425","","10.1039/C7QO00221A","","","0.71073","MoKα","","0.1775","0.152","","","0.4104","0.4325","","","","","","1.136","","","","has coordinates","274176","2022-03-31","10:10:26",""
"1553774","9.003","0.01","10.762","0.012","11.631","0.012","73.19","0.06","69.99","0.05","72.45","0.04","987.6","1.9","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C20 H23 B F2 N2 O2 -","- C20 H23 B F2 N2 O2 -","- C40 H46 B2 F4 N4 O4 -","2","1","","Kubota, Yasuhiro; Tsukamoto, Masahiro; Ohnishi, Katsuhiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki","Synthesis and fluorescence properties of novel squarylium–boron complexes","Organic Chemistry Frontiers","2017","4","8","1522","","10.1039/C7QO00225D","","","0.71075","MoKα","","0.0802","0.0596","","","0.1648","0.1833","","","","","","1.048","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553775","8.6045","0.0006","11.4959","0.0007","10.3691","0.0006","90","","114.544","0.002","90","","933","0.1","296","2","296","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C21 H17 Cl F3 N3 -","- C21 H17 Cl F3 N3 -","- C42 H34 Cl2 F6 N6 -","2","1","","Xie, En; Rahman, Abdul; Lin, Xufeng","Asymmetric synthesis of CF3- and indole-containing tetrahydro-β-carbolines via chiral spirocyclic phosphoric acid-catalyzed aza-Friedel–Crafts reaction","Organic Chemistry Frontiers","2017","4","7","1407","","10.1039/C7QO00229G","","","0.71073","MoKα","","0.0749","0.0341","","","0.0633","0.0903","","","","","","1.003","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553776","10.326","0.002","9.584","0.0019","19.601","0.004","90","","104.43","0.03","90","","1878.6","0.7","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H17 I N2 -","- C22 H17 I N2 -","- C88 H68 I4 N8 -","4","1","","Liu, Cheng-Kou; Yang, Zhao; Zeng, Yu; Guo, Kai; Fang, Zheng; Li, Bo","Sodium nitrite-promoted aerobic oxidative coupling of aryl methyl ketones with ammonium under metal-free conditions: a facile access to polysubstitution imidazoles","Organic Chemistry Frontiers","2017","4","8","1508","","10.1039/C7QO00247E","","","0.71073","MoKα","","0.1106","0.0541","","","0.1168","0.137","","","","","","1","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553777","5.7817","0.0012","8.2558","0.001","19.972","0.002","90","","90","","90","","953.3","0.2","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C10 H12 O2 S -","- C10 H12 O2 S -","- C40 H48 O8 S4 -","4","1","","Meng, Ke; Xia, Jingzhao; Wang, Yanzhao; Zhang, Xinghua; Yang, Guoqiang; Zhang, Wanbin","Ir/BiphPHOX-catalyzed asymmetric hydrogenation of 3-substituted 2,5-dihydropyrroles and 2,5-dihydrothiophene 1,1-dioxides","Organic Chemistry Frontiers","2017","4","8","1601","","10.1039/C7QO00248C","","","1.54178","CuKα","","0.0341","0.034","","","0.0898","0.09","","","","","","1.079","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553778","11.3637","0.0004","6.0455","0.0003","11.3636","0.0004","90","","98.45","","90","","772.2","0.05","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C17 H19 N O2 S -","- C17 H19 N O2 S -","- C34 H38 N2 O4 S2 -","2","1","","Meng, Ke; Xia, Jingzhao; Wang, Yanzhao; Zhang, Xinghua; Yang, Guoqiang; Zhang, Wanbin","Ir/BiphPHOX-catalyzed asymmetric hydrogenation of 3-substituted 2,5-dihydropyrroles and 2,5-dihydrothiophene 1,1-dioxides","Organic Chemistry Frontiers","2017","4","8","1601","","10.1039/C7QO00248C","","","1.54178","CuKα","","0.0426","0.0352","","","0.0792","0.083","","","","","","1.047","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553779","11.0348","0.0007","21.2718","0.0012","7.2221","0.0006","90","","90","","90","","1695.2","0.2","184.3","0.3","184.3","0.3","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C21 H16 N2 O3 -","- C21 H16 N2 O3 -","- C84 H64 N8 O12 -","4","1","","Tang, Hai-Tao; Zeng, Jia-Hao; Chen, Jun-Jia; Zhou, Yun-Bing; Li, Ren-Hao; Zhan, Zhuang-Ping","Synthesis of pyrazolo[5,1-a]isoquinolines through copper-catalyzed regioselective bicyclization of N-propargylic sulfonylhydrazones","Organic Chemistry Frontiers","2017","4","8","1513","","10.1039/C7QO00249A","","","0.71073","MoKα","","0.0713","0.061","","","0.1247","0.1292","","","","","","1.161","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553780","17.5265","0.0008","18.9585","0.0009","11.1154","0.0005","90","","120.995","0.002","90","","3166","0.3","298","2","298","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C19 H11 Cl F3 N O -","- C19 H11 Cl F3 N O -","- C152 H88 Cl8 F24 N8 O8 -","8","1","","Mishra, Kalpana; Singh, Jay Bahadur; Gupta, Tanu; Singh, Radhey M.","TBAB-catalyzed cascade reactions: facile synthesis of 1-trifluoromethyl-3-alkylidene-1,3-dihydrofuro[3,4-b]quinolines via 5-exo-dig cyclization of o-arylalkynylquinoline aldehydes","Organic Chemistry Frontiers","2017","4","10","1926","","10.1039/C7QO00273D","","","0.71073","MoKα","","0.0617","0.0439","","","0.1131","0.1244","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553781","5.0951","0.0004","6.0539","0.0006","14.8931","0.0015","90","","90","","90","","459.38","0.07","273","2","273","2","","","","","","","","4","P n m a","-P 2ac 2n","62","N-Methylcarbamoyl","","","- C2 H4 N4 O -","- C2 H4 N4 O -","- C8 H16 N16 O4 -","4","0.5","","Wan, Huabin; Li, Hongmin; Xu, Jian; Wu, Zhuang; Liu, Qifan; Chu, Xianxu; Abe, Manabu; Bégué, Didier; Zeng, Xiaoqing","N-Methylcarbamoyl azide: spectroscopy, X-ray structure and decomposition via methylcarbamoyl nitrene","Organic Chemistry Frontiers","2017","4","9","1839","","10.1039/C7QO00277G","","","0.71073","MoKα","","0.0512","0.0451","","","0.1313","0.1346","","","","","","2.174","","","","has coordinates","236023","2020-10-21","18:00:00",""
"1553782","12.326","0.004","11.032","0.004","13.445","0.005","90","","90","","90","","1828.3","1.1","293","2","293","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C21 H18 F2 O4 -","- C21 H18 F2 O4 -","- C84 H72 F8 O16 -","4","1","","Li, Yuewen; Lu, Yiye; Mao, Runyu; Li, Zhiming; Wu, Jie","A photoinduced reaction of perfluoroalkyl halides with 1,3-diarylprop-2-yn-1-ones catalyzed by DABSO","Organic Chemistry Frontiers","2017","4","9","1745","","10.1039/C7QO00279C","","","0.71073","MoKα","","0.0343","0.0325","","","0.0913","0.0937","","","","","","1.076","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553783","10.7971","0.0008","15.2395","0.0013","26.1285","0.0019","90","","90","","90","","4299.2","0.6","180","0.1","180","0.1","","","","","","","","4","P b c a","-P 2ac 2ab","61","","Ph-4Br-Pyr","","- C22 H18 Br4 N2 -","- C22 H18 Br4 N2 -","- C176 H144 Br32 N16 -","8","1","","Huang, Zhe; Zhan, Ming; Zhang, Shaoguang; Luo, Qian; Zhang, Wen-Xiong; Xi, Zhenfeng","Synthesis of dibromo- and tetrabromo-bipyrrolines and their corresponding 2,6-diazasemibullvalene derivatives","Organic Chemistry Frontiers","2017","4","9","1785","","10.1039/C7QO00287D","","","0.7107","MoKα","","0.0826","0.0529","","","0.0992","0.1106","","","","","","1.065","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553784","6.6642","0.0004","19.8278","0.0016","14.8224","0.001","90","","101.924","0.007","90","","1916.3","0.2","180.01","0.1","180.01","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","tBu-2Br-NSBV-re","","- C18 H26 Br2 N2 -","- C18 H26 Br2 N2 -","- C72 H104 Br8 N8 -","4","1","","Huang, Zhe; Zhan, Ming; Zhang, Shaoguang; Luo, Qian; Zhang, Wen-Xiong; Xi, Zhenfeng","Synthesis of dibromo- and tetrabromo-bipyrrolines and their corresponding 2,6-diazasemibullvalene derivatives","Organic Chemistry Frontiers","2017","4","9","1785","","10.1039/C7QO00287D","","","0.71073","MoKα","","0.0978","0.0537","","","0.1172","0.132","","","","","","1.028","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553785","23.66","0.002","10.2673","0.001","10.5398","0.001","90","","90","","90","","2560.4","0.4","296","2","296","2","","","","","","","","6","P 21 21 2","P 2 2ab","18","","","","- C26 H25 F3 N O S -","- C26 H25 F3 N O S -","- C104 H100 F12 N4 O4 S4 -","4","1","","Liu, Bing; Zhang, Zhan-Ming; Xu, Bing; Xu, Shan; Wu, Hai-Hong; Liu, Yuanyuan; Zhang, Junliang","Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter","Organic Chemistry Frontiers","2017","4","9","1772","","10.1039/C7QO00291B","","","0.71073","MoKα","","0.0783","0.0617","","","0.1818","0.195","","","","","","1.098","","","","has coordinates","236029","2020-10-21","18:00:00",""
"1553786","8.5817","0.0002","10.4128","0.0003","27.6259","0.0007","90","","90","","90","","2468.64","0.11","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C27 H23 Cl F3 N O3 -","- C27 H23 Cl F3 N O3 -","- C108 H92 Cl4 F12 N4 O12 -","4","1","","Liu, Bing; Zhang, Zhan-Ming; Xu, Bing; Xu, Shan; Wu, Hai-Hong; Liu, Yuanyuan; Zhang, Junliang","Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter","Organic Chemistry Frontiers","2017","4","9","1772","","10.1039/C7QO00291B","","","0.71073","MoKα","","0.0445","0.034","","","0.077","0.0828","","","","","","1.054","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553787","6.2282","0.0002","7.0351","0.0002","36.2461","0.0013","90","","90","","90","","1588.16","0.09","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C15 H16 F3 N O2 S -","- C15 H16 F3 N O2 S -","- C60 H64 F12 N4 O8 S4 -","4","1","","Liu, Bing; Zhang, Zhan-Ming; Xu, Bing; Xu, Shan; Wu, Hai-Hong; Liu, Yuanyuan; Zhang, Junliang","Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter","Organic Chemistry Frontiers","2017","4","9","1772","","10.1039/C7QO00291B","","","0.71073","MoKα","","0.0481","0.0415","","","0.1071","0.1119","","","","","","1.06","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553788","12.9056","0.0003","8.981","0.0002","20.4045","0.0005","90","","106.848","0.003","90","","2263.48","0.1","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C28 H21 N2 O2 P -","- C28 H21 N2 O2 P -","- C112 H84 N8 O8 P4 -","4","1","","Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie","Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides","Organic Chemistry Frontiers","2017","4","10","1981","","10.1039/C7QO00305F","","x-ray","1.54184","CuKα","","0.0506","0.0412","","","0.1062","0.1138","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553789","14.3374","0.0005","9.71","0.0004","18.7718","0.0007","90","","105.341","0.004","90","","2520.22","0.17","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C28 H21 N2 O2 P -","- C28 H21 N2 O2 P -","- C112 H84 N8 O8 P4 -","4","1","","Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie","Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides","Organic Chemistry Frontiers","2017","4","10","1981","","10.1039/C7QO00305F","","x-ray","1.54184","CuKα","","0.0561","0.0467","","","0.1343","0.1436","","","","","","1.049","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553790","9.5853","0.0009","9.8739","0.0008","14.7007","0.0014","103.11","0.008","94.035","0.008","114.371","0.008","1213.1","0.2","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C29 H23 N2 O3 P -","- C29 H23 N2 O3 P -","- C58 H46 N4 O6 P2 -","2","1","","Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie","Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides","Organic Chemistry Frontiers","2017","4","10","1981","","10.1039/C7QO00305F","","x-ray","1.54184","CuKα","","0.0583","0.0467","","","0.1246","0.136","","","","","","1.021","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553791","11.9961","0.0005","8.631","0.0003","21.6563","0.0007","90","","95.014","0.004","90","","2233.68","0.14","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C28 H21 N2 O2 P -","- C28 H21 N2 O2 P -","- C112 H84 N8 O8 P4 -","4","1","","Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie","Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides","Organic Chemistry Frontiers","2017","4","10","1981","","10.1039/C7QO00305F","","x-ray","1.54184","CuKα","","0.0494","0.0406","","","0.1051","0.1133","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553792","9.0757","0.0002","10.4623","0.0002","26.2445","0.0005","90","","90","","90","","2491.99","0.09","290","2","290","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C33 H27 O2 P -","- C33 H27 O2 P -","- C132 H108 O8 P4 -","4","1","","Li, Bin; Zhang, Mingkai; Huang, Xulun; Gu, Zhenhua","Synthesis of 2,3-dihydro-1H-phosphindole-1-oxides via the t-BuLi-mediated rearrangement of vinyl bromides and phosphine oxides","Organic Chemistry Frontiers","2017","4","9","1854","","10.1039/C7QO00310B","","","1.54184","CuKα","","0.0326","0.0313","","","0.0828","0.0843","","","","","","1.046","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553793","12.3885","0.0001","18.8197","0.0002","10.4583","0.0001","90","","103.828","0.001","90","","2367.66","0.04","291","2","291","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C32 H25 O P -","- C32 H25 O P -","- C128 H100 O4 P4 -","4","1","","Li, Bin; Zhang, Mingkai; Huang, Xulun; Gu, Zhenhua","Synthesis of 2,3-dihydro-1H-phosphindole-1-oxides via the t-BuLi-mediated rearrangement of vinyl bromides and phosphine oxides","Organic Chemistry Frontiers","2017","4","9","1854","","10.1039/C7QO00310B","","","1.54184","CuKα","","0.0402","0.0375","","","0.1027","0.1053","","","","","","1.056","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553794","10.0442","0.0004","10.4197","0.0004","11.9542","0.0005","84.471","0.002","84.954","0.002","75.059","0.002","1200.58","0.08","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C28 H33 B O4 -","- C28 H33 B O4 -","- C56 H66 B2 O8 -","2","1","","Hsieh, Jen-Chieh; Hong, Ya-Chun; Yang, Chun-Ming; Mannathan, Subramaniyan; Cheng, Chien-Hong","Nickel-catalyzed highly chemo- and stereoselective borylative cyclization of 1,6-enynes with bis(pinacolato)diboron","Organic Chemistry Frontiers","2017","4","8","1615","","10.1039/C7QO00321H","","","0.71073","MoKα","","0.0726","0.052","","","0.1247","0.1392","","","","","","1.046","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553795","22.0623","0.0004","14.5144","0.0003","5.67392","0.0001","90","","90","","90","","1816.91","0.06","294.08","0.1","294.08","0.1","","","","","","","","4","P 21 21 2","P 2 2ab","18","","","","- C19 H19 Br O6 -","- C19 H19 Br O6 -","- C76 H76 Br4 O24 -","4","1","","Hao, Xiaoyu; Lin, Lili; Tan, Fei; Ge, Shulin; Liu, Xiaohua; Feng, Xiaoming","Asymmetric synthesis of chromans via the Friedel–Crafts alkylation–hemiketalization catalysed by an N,N′-dioxide scandium(iii) complex","Organic Chemistry Frontiers","2017","4","8","1647","","10.1039/C7QO00323D","","x-ray","1.54184","CuKα","","0.0429","0.042","","","0.1027","0.1042","","","","","","1.071","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553796","10.4368","0.0004","6.0294","0.0002","15.7294","0.0005","90","","107.537","0.004","90","","943.81","0.06","200","1","200","1","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C21 H18 Br N O3 -","- C21 H18 Br N O3 -","- C42 H36 Br2 N2 O6 -","2","1","","De Munck, Lode; Sukowski, Verena; Vila, Carlos; Muñoz, M. Carmen; Pedro, José R.","Catalytic enantioselective aza-Reformatsky reaction with seven-membered cyclic imines dibenzo[b,f][1,4]oxazepines","Organic Chemistry Frontiers","2017","4","8","1624","","10.1039/C7QO00329C","","","0.71073","MoKα","","0.0494","0.0362","","","0.0782","0.0855","","","","","","0.969","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553797","9.17425","0.00019","7.88736","0.00013","21.7312","0.0004","90","","99.3556","0.0019","90","","1551.57","0.05","100.01","0.1","100.01","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H13 F N2 O -","- C20 H13 F N2 O -","- C80 H52 F4 N8 O4 -","4","1","","Ren, Xuhong; Wang, Qiyang; Yu, Wenjia; Zhan, Xiaoyu; Yao, Yishan; Qin, Bingjie; Dong, Mingxin; He, Xinhua","Photoredox catalytic intramolecular imine C–H bond functionalization using ligand free Cu(ii) salts","Organic Chemistry Frontiers","2017","4","10","2022","","10.1039/C7QO00348J","","x-ray","1.54184","CuKα","","0.0399","0.0374","","","0.0987","0.1009","","","","","","1.051","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553798","7.6272","0.0007","13.3952","0.0013","11.846","0.0012","90","","90.87","0.003","90","","1210.1","0.2","296","2","296","2","","","","","","","","4","C 1 c 1","C -2yc","9","","2,4,9-trinitro-2,4,9-triazaadamantane-7-yl nitrate","","- C7 H9 N7 O9 -","- C7 H9 N7 O9 -","- C28 H36 N28 O36 -","4","1","","Hou, Tianjiao; Zhang, Jian; Wang, Chenjiao; Luo, Jun","A facile method to construct a 2,4,9-triazaadamantane skeleton and synthesize nitramine derivatives","Organic Chemistry Frontiers","2017","4","9","1819","","10.1039/C7QO00357A","","","0.71073","MoKα","","0.0262","0.0256","","","0.0682","0.0686","","","","","","1.058","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553799","15.7593","0.0003","6.7689","0.0002","21.0839","0.0004","90","","104.622","0.001","90","","2176.24","0.09","200","2","200","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H40 O3 Si -","- C21 H40 O3 Si -","- C84 H160 O12 Si4 -","4","1","","Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis","Gold(i)-catalyzed access to neomerane skeletons","Organic Chemistry Frontiers","2017","4","10","1906","","10.1039/C7QO00360A","","","1.54178","CuKα","","0.0464","0.0372","","","0.0941","0.0995","","","","","","1.04","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553800","8.7959","0.0005","10.4916","0.0006","13.2932","0.0008","70.468","0.002","74.252","0.002","71.371","0.002","1076.8","0.11","200","1","200","1","","","","","","","","4","P -1","-P 1","2","","","","- C22 H26 N4 O6 -","- C22 H26 N4 O6 -","- C44 H52 N8 O12 -","2","1","","Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis","Gold(i)-catalyzed access to neomerane skeletons","Organic Chemistry Frontiers","2017","4","10","1906","","10.1039/C7QO00360A","","","0.71073","MoKα","","0.0542","0.0453","","","0.1248","0.1323","","","","","","1.036","","","","has coordinates,has disorder","236048","2020-10-21","18:00:00",""
"1553801","15.8792","0.0005","7.383","0.0003","18.5839","0.0007","90","","94.011","0.002","90","","2173.37","0.14","200","2","200","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H26 N4 O6 -","- C22 H26 N4 O6 -","- C88 H104 N16 O24 -","4","1","","Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis","Gold(i)-catalyzed access to neomerane skeletons","Organic Chemistry Frontiers","2017","4","10","1906","","10.1039/C7QO00360A","","","1.54178","CuKα","","0.063","0.05","","","0.1208","0.1289","","","","","","1.034","","","","has coordinates","236048","2020-10-21","18:00:00",""
"1553802","19.2372","0.0012","19.7853","0.0013","12.577","0.0007","90","","107.983","0.003","90","","4553.1","0.5","200","1","200","1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H26 N4 O6 -","- C22 H26 N4 O6 -","- C176 H208 N32 O48 -","8","2","","Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis","Gold(i)-catalyzed access to neomerane skeletons","Organic Chemistry Frontiers","2017","4","10","1906","","10.1039/C7QO00360A","","","1.54178","CuKα","","0.0851","0.0689","","","0.2013","0.2182","","","","","","1.066","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553803","15.0743","0.0003","6.8149","0.0001","21.2545","0.0004","90","","92.709","0.001","90","","2181.03","0.07","200","2","200","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C21 H38 O3 Si -","- C21 H38 O3 Si -","- C84 H152 O12 Si4 -","4","1","","Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis","Gold(i)-catalyzed access to neomerane skeletons","Organic Chemistry Frontiers","2017","4","10","1906","","10.1039/C7QO00360A","","","0.71073","MoKα","","0.053","0.0386","","","0.1032","0.1112","","","","","","1.027","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553804","12.0087","0.0006","17.7464","0.0007","12.6045","0.0007","90","","103.892","0.005","90","","2607.6","0.2","293","2","293.15","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C28 H29 I O4 S -","- C28 H29 I O4 S -","- C112 H116 I4 O16 S4 -","4","1","","Miao, Maozhong; Xu, Huaping; Luo, Yi; Jin, Mengchao; Chen, Zhengkai; Xu, Jianfeng; Ren, Hongjun","A modular approach to highly functionalized 3-sulfonylfurans via conjugate addition of 3-cyclopropylideneprop-2-en-1-ones with sodium sulfinates and sequential 5-endo-trig iodocyclization","Organic Chemistry Frontiers","2017","4","9","1824","","10.1039/C7QO00362E","","","0.71073","MoKα","","0.0879","0.0665","","","0.1759","0.1906","","","","","","1.049","","","","has coordinates,has disorder","236050","2020-10-21","18:00:00",""
"1553805","9.8395","0.0017","10.7013","0.0019","10.8636","0.0019","114.335","0.002","94.477","0.002","116.312","0.002","885.4","0.3","296.15","","296.15","","","","","","","","","3","P -1","-P 1","2","","","","- C22 H20 O3 -","- C22 H20 O3 -","- C44 H40 O6 -","2","1","","Shi, Xiaonan; He, Yan; Zhang, Xinying; Fan, Xuesen","Selective syntheses of diversely substituted 2-hydroxy-4′-hydroxybenzophenones through [4 + 2] or [3 + 3] annulation of penta-3,4-dien-2-ones with 3-formylchromones","Organic Chemistry Frontiers","2017","4","10","1967","","10.1039/C7QO00366H","","x-ray","0.71073","MoKα","","0.0628","0.0473","","","0.1274","0.1434","","","","","","1.029","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553806","8.8173","0.0004","14.3926","0.0007","15.3659","0.0007","90","","90","","90","","1949.99","0.16","105.8","","105.8","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C22 H19 N O5 S -","- C22 H19 N O5 S -","- C88 H76 N4 O20 S4 -","4","1","","Xie, Lei; Ma, Hongli; Li, Jiaqi; Yu, Yuan; Qin, Zhaohai; Fu, Bin","Ni(ii)-Catalyzed enantioselective Mukaiyama–Mannich reaction between silyl enol ethers and cyclic N-sulfonyl α-ketiminoesters","Organic Chemistry Frontiers","2017","4","9","1858","","10.1039/C7QO00370F","","","1.5418","CuKα","","0.0275","0.0271","","","0.0686","0.0689","","","","","","1.061","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553807","8.2203","0.0005","9.1263","0.0005","13.0906","0.0007","90","","102.302","0.006","90","","959.52","0.1","106.3","","106.3","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C21 H23 N O5 S -","- C21 H23 N O5 S -","- C42 H46 N2 O10 S2 -","2","1","","Xie, Lei; Ma, Hongli; Li, Jiaqi; Yu, Yuan; Qin, Zhaohai; Fu, Bin","Ni(ii)-Catalyzed enantioselective Mukaiyama–Mannich reaction between silyl enol ethers and cyclic N-sulfonyl α-ketiminoesters","Organic Chemistry Frontiers","2017","4","9","1858","","10.1039/C7QO00370F","","","1.5418","CuKα","","0.0372","0.0366","","","0.0978","0.0986","","","","","","1.032","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553808","29.3492","0.0015","12.5025","0.0006","25.3876","0.0013","90","","113.65","0.003","90","","8533.3","0.8","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C62 H102 Cl8 N26 O21 Zn2 -","- C62 H82 Cl8 N26 O12 Zn2 -","- C248 H328 Cl32 N104 O48 Zn8 -","4","0.5","","Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang","Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril","Organic Chemistry Frontiers","2017","4","9","1799","","10.1039/C7QO00376E","","","0.71073","MoKα","","0.0891","0.077","","","0.2427","0.253","","","","","","1.085","","","","has coordinates","236056","2020-10-21","18:00:00",""
"1553809","27.52","0.003","17.25","0.003","18.358","0.003","90","","94.006","0.007","90","","8694","2","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C60 H68 Cl8 N26 O28 Zn2 -","- C60 H70 Cl8 N26 O12 Zn2 -","- C240 H280 Cl32 N104 O48 Zn8 -","4","0.5","","Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang","Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril","Organic Chemistry Frontiers","2017","4","9","1799","","10.1039/C7QO00376E","","","0.71073","MoKα","","0.1071","0.0703","","","0.2108","0.2315","","","","","","1.079","","","","has coordinates","236056","2020-10-21","18:00:00",""
"1553810","12.2894","0.0018","12.4667","0.0017","14.986","0.002","73.289","0.004","84.747","0.004","62.451","0.004","1947.4","0.5","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C58 H94 Cl6 N26 O22 Zn2 -","- C58 H74 Cl6 N26 O14 Zn2 -","- C58 H74 Cl6 N26 O14 Zn2 -","1","0.5","","Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang","Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril","Organic Chemistry Frontiers","2017","4","9","1799","","10.1039/C7QO00376E","","","0.71073","MoKα","","0.076","0.053","","","0.1377","0.1484","","","","","","1.055","","","","has coordinates","236056","2020-10-21","18:00:00",""
"1553811","12.298","0.003","12.903","0.003","15.662","0.003","75.259","0.003","70.211","0.003","76.684","0.003","2233","0.9","273","2","273","2","","","","","","","","6","P -1","-P 1","2","","","","- C60 H112 Cl10 N26 O28 Zn2 -","- C60 H78 Cl10 N26 O12 Zn2 -","- C60 H78 Cl10 N26 O12 Zn2 -","1","0.5","","Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang","Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril","Organic Chemistry Frontiers","2017","4","9","1799","","10.1039/C7QO00376E","","","0.71073","MoKα","","0.0667","0.0576","","","0.1827","0.1918","","","","","","1.007","","","","has coordinates","236056","2020-10-21","18:00:00",""
"1553812","12.315","0.004","12.875","0.004","15.525","0.006","75.131","0.011","70.361","0.011","77.82","0.01","2219.6","1.3","296","2","296","2","","","","","","","","6","P -1","-P 1","2","","","","- C62 H108 Cl10 N26 O28 Zn2 -","- C62 H74 Cl10 N26 O22 Zn2 -","- C62 H74 Cl10 N26 O22 Zn2 -","1","0.5","","Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang","Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril","Organic Chemistry Frontiers","2017","4","9","1799","","10.1039/C7QO00376E","","","0.71073","MoKα","","0.1104","0.0836","","","0.2457","0.2745","","","","","","1.003","","","","has coordinates","236056","2020-10-21","18:00:00",""
"1553813","5.095","0.008","12.261","0.019","17","0.03","73.395","0.018","81.56","0.02","78.69","0.02","993","3","273","2","273","2","","","","","","","","5","P -1","-P 1","2","","","","- C21 H21 Br N2 O2 -","- C21 H19.5 Br N2 O2 -","- C42 H39 Br2 N4 O4 -","2","1","","Yan, Hao; Li, Xincheng; Wang, Chunxiang; Wan, Boshun","Silver-catalyzed cyclization of nitrones with 2-azetine: a radical approach to 2,3-disubstituted quinolines","Organic Chemistry Frontiers","2017","4","9","1833","","10.1039/C7QO00405B","","","0.71073","MoKα","","0.2545","0.0911","","","0.2098","0.2887","","","","","","0.963","","","","has coordinates,has disorder","236058","2020-10-21","18:00:00",""
"1553814","6.1408","0.0017","10.54","0.003","16.567","0.005","87.399","0.007","81.181","0.006","79.922","0.006","1043.1","0.5","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H26 N2 O4 -","- C22 H26 N2 O4 -","- C44 H52 N4 O8 -","2","1","","Yan, Hao; Li, Xincheng; Wang, Chunxiang; Wan, Boshun","Silver-catalyzed cyclization of nitrones with 2-azetine: a radical approach to 2,3-disubstituted quinolines","Organic Chemistry Frontiers","2017","4","9","1833","","10.1039/C7QO00405B","","","0.71073","MoKα","","0.1062","0.0721","","","0.1651","0.1818","","","","","","1.081","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553815","6.82668","0.00015","9.4989","0.0002","34.5079","0.001","90","","90","","90","","2237.7","0.09","293.49","0.15","293.49","0.15","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C23 H23 Cl O7 -","- C23 H23 Cl O7 -","- C92 H92 Cl4 O28 -","4","1","","Yao, Qian; Lin, Lili; Zhang, Hang; Yu, Han; Xiong, Qian; Liu, Xiaohua; Feng, Xiaoming","The asymmetric synthesis of multisubstituted diquinanes via the domino reaction of electron-deficient enynes","Organic Chemistry Frontiers","2017","4","10","2012","","10.1039/C7QO00408G","","x-ray","1.54184","CuKα","","0.0575","0.0535","","","0.1492","0.1553","","","","","","1.044","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553816","7.8333","0.0001","8.7742","0.0002","23.1441","0.0004","90","","95.475","0.001","90","","1583.46","0.05","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C19 H17 N O3 S -","- C19 H17 N O3 S -","- C76 H68 N4 O12 S4 -","4","1","","De Nisi, A.; Sierra, S.; Ferrara, M.; Monari, M.; Bandini, M.","TBAF catalyzed one-pot synthesis of allenyl-indoles","Organic Chemistry Frontiers","2017","4","9","1849","","10.1039/C7QO00414A","","","0.71073","MoKα","","0.0466","0.0328","","","0.0849","0.0909","","","","","","1.235","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553817","8.5679","0.0012","12.3701","0.0014","18.181","0.003","83.843","0.007","89.595","0.012","80.871","0.009","1891.4","0.5","296","2","296","2","","","","","","","","6","P 1","P 1","1","","","","- C20 H16 F3 N O3 S -","- C20 H15 F3 N O3 S -","- C80 H60 F12 N4 O12 S4 -","4","4","","De Nisi, A.; Sierra, S.; Ferrara, M.; Monari, M.; Bandini, M.","TBAF catalyzed one-pot synthesis of allenyl-indoles","Organic Chemistry Frontiers","2017","4","9","1849","","10.1039/C7QO00414A","","","0.71073","MoKα","","0.2446","0.0738","","","0.1707","0.2621","","","","","","0.892","","","","has coordinates","236062","2020-10-21","18:00:00",""
"1553818","14.884","0.002","4.3831","0.0006","27.39","0.003","90","","117.921","0.006","90","","1578.9","0.4","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C15 H10 I2 O4 -","- C15 H10 I2 O4 -","- C60 H40 I8 O16 -","4","1","","Tang, Yang; Yu, Qiong; Ma, Shengming","Efficient trifluoromethylation via the cyclopropanation of allenes and subsequent C–C bond cleavage","Organic Chemistry Frontiers","2017","4","9","1762","","10.1039/C7QO00419B","","","0.71073","MoKα","","0.1052","0.0835","","","0.1766","0.1859","","","","","","1.14","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553819","14.9433","0.0006","9.3141","0.0004","17.6377","0.0006","90","","102.36","0.001","90","","2397.98","0.16","173","2","173","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C25 H26 F3 N O5 -","- C25 H26 F3 N O5 -","- C100 H104 F12 N4 O20 -","4","1","","Tang, Yang; Yu, Qiong; Ma, Shengming","Efficient trifluoromethylation via the cyclopropanation of allenes and subsequent C–C bond cleavage","Organic Chemistry Frontiers","2017","4","9","1762","","10.1039/C7QO00419B","","","0.71073","MoKα","","0.0948","0.0494","","","0.1183","0.1463","","","","","","1.016","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553820","15.6855","0.0006","9.6366","0.0003","13.4345","0.0005","90","","96.4","0.001","90","","2018.03","0.12","173","2","173","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C21 H24 F3 N O4 -","- C21 H24 F3 N O4 -","- C84 H96 F12 N4 O16 -","4","1","","Tang, Yang; Yu, Qiong; Ma, Shengming","Efficient trifluoromethylation via the cyclopropanation of allenes and subsequent C–C bond cleavage","Organic Chemistry Frontiers","2017","4","9","1762","","10.1039/C7QO00419B","","","0.71073","MoKα","","0.0632","0.0424","","","0.1036","0.1171","","","","","","1.021","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553821","8.577","0.0004","11.253","0.0005","11.3999","0.0005","83.261","0.001","69.715","0.001","68.411","0.001","959.58","0.08","173","2","173","2","","","","","","","","4","P -1","-P 1","2","","","","- C19 H21 F3 O5 -","- C19 H21 F3 O5 -","- C38 H42 F6 O10 -","2","1","","Tang, Yang; Yu, Qiong; Ma, Shengming","Efficient trifluoromethylation via the cyclopropanation of allenes and subsequent C–C bond cleavage","Organic Chemistry Frontiers","2017","4","9","1762","","10.1039/C7QO00419B","","","0.71073","MoKα","","0.074","0.0615","","","0.1764","0.1907","","","","","","1.082","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553822","16.2553","0.0002","8.3116","0.0001","24.8996","0.0004","90","","90","","90","","3364.12","0.08","295","2","295","2","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C19 H15 N3 O4 -","- C19 H15 N3 O4 -","- C152 H120 N24 O32 -","8","2","","Krylov, Igor B.; Paveliev, Stanislav A.; Shelimov, Boris N.; Lokshin, Boris V.; Garbuzova, Irina A.; Tafeenko, Viktor A.; Chernyshev, Vladimir V.; Budnikov, Alexander S.; Nikishin, Gennady I.; Terent'ev, Alexander O.","Selective cross-dehydrogenative C–O coupling of N-hydroxy compounds with pyrazolones. Introduction of the diacetyliminoxyl radical into the practice of organic synthesis","Organic Chemistry Frontiers","2017","4","10","1947","","10.1039/C7QO00447H","","","1.54186","CuKα","","0.078","0.0593","","","0.1415","0.1484","","","","","","0.893","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553823","25.317","0.004","8.8649","0.0015","22.042","0.004","90","","120.571","0.002","90","","4259.3","1.3","100","","100","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C24 H21 F2 O3 P -","- C24 H21 F2 O3 P -","- C192 H168 F16 O24 P8 -","8","1","","Zhang, Pengbo; Ying, Jianxi; Tang, Guo; Zhao, Yufen","Phosphinodifluoroalkylation of alkynes using P(O)H compounds and ethyl difluoroiodoacetate","Organic Chemistry Frontiers","2017","4","10","2054","","10.1039/C7QO00466D","","","0.71073","MoKα","","0.054","0.049","","","0.1296","0.1347","","","","","","1.0601","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553824","7.75","0.001","20.882","0.003","14.5149","0.0019","90","","93.914","0.003","90","","2343.5","0.5","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C26 H28 N2 O5 -","- C26 H28 N2 O5 -","- C104 H112 N8 O20 -","4","1","","Yang, Minghua; Zhang, Shusheng; Zhang, Xiang; Wang, Haoyang; Zhang, Fang; Hou, Yuting; Su, Yue; Guo, Yinlong","An unexpected acid-catalyzed decomposition reaction of cilnidipine and pranidipine to the decarboxylative bridged tricyclic products via cascade rearrangements","Organic Chemistry Frontiers","2017","4","11","2163","","10.1039/C7QO00496F","","","0.71073","MoKα","","0.1081","0.0778","","","0.1691","0.1841","","","","","","1.134","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553825","9.6871","0.0007","14.029","0.0007","23.8866","0.0017","90","","90.258","0.006","90","","3246.2","0.4","289.9","0.3","289.9","0.3","","","","","","","","3","I 1 2/a 1","-I 2ya","15","","","","- C18 H22 O5 -","- C18 H22 O5 -","- C144 H176 O40 -","8","1","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel–Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","","0.7107","MoKα","","0.0806","0.0545","","","0.1326","0.1516","","","","","","1.093","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553826","10.2811","0.0005","28.3515","0.0009","12.9191","0.0005","90","","103.741","0.005","90","","3657.9","0.3","291.08","0.1","291.08","0.1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C20 H26 O6 -","- C20 H26 O6 -","- C160 H208 O48 -","8","2","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel–Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","","0.7107","MoKα","","0.1557","0.0668","","","0.1262","0.1747","","","","","","1.026","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553827","22.151","0.0011","9.8005","0.0004","26.0531","0.0013","90","","117.401","0.006","90","","5021.3","0.5","292.59","0.11","292.59","0.11","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C27 H33 N O7 S -","- C27 H33 N O7 S -","- C216 H264 N8 O56 S8 -","8","1","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel–Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","x-ray","0.71073","MoKα","","0.0815","0.0529","","","0.114","0.1334","","","","","","1.038","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553828","8.9279","0.0006","10.0249","0.0007","10.8557","0.001","115.731","0.008","104.925","0.007","90.322","0.006","838","0.13","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C18 H22 O6 -","- C18 H22 O6 -","- C36 H44 O12 -","2","1","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel–Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","x-ray","0.71073","MoKα","","0.0681","0.0495","","","0.1075","0.1189","","","","","","1.03","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553829","5.9908","0.0005","12.2284","0.001","23.731","0.003","90","","90","","90","","1738.5","0.3","293","2","293","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C19 H23 O6 -","- C19 H24 O6 -","- C76 H96 O24 -","4","1","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel‒Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","","0.71073","MoKα","","0.1199","0.0686","","","0.1491","0.1997","","","","","","0.991","","","","has coordinates","236073","2020-10-21","18:00:00",""
"1553830","13.7047","0.0006","15.4463","0.0007","24.0895","0.001","90","","97.806","0.004","90","","5052.2","0.4","290.74","0.1","290.74","0.1","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C27 H33 N O7 S -","- C27 H33 N O7 S -","- C216 H264 N8 O56 S8 -","8","1","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel–Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","","0.7107","MoKα","","0.1132","0.0598","","","0.1021","0.1244","","","","","","1.062","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553831","8.981","0.002","10.331","0.003","10.885","0.003","66.11","0.03","71.31","0.03","87.32","0.02","870.7","0.5","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C19 H24 O5 -","- C19 H24 O5 -","- C38 H48 O10 -","2","1","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel‒Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","","0.71073","MoKα","","0.1259","0.0673","","","0.1341","0.1744","","","","","","1.034","","","","has coordinates,has disorder","236073","2020-10-21","18:00:00",""
"1553832","9.88","0.002","10.9717","0.0017","12.836","0.002","85.382","0.013","71.391","0.017","65.05","0.019","1193.2","0.4","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C25 H29 N O7 S -","- C25 H29 N O7 S -","- C50 H58 N2 O14 S2 -","2","1","","Sun, Haiyu; Xu, Shiyan; Xing, Zhimin; Liu, Lin; Feng, Shangbiao; Fang, Bowen; Xie, Xingang; She, Xuegong","Rapid construction of complex tetracyclic frameworks via a gold(i)-catalyzed tandem 1,2-acyloxy migration/[3 + 2] cycloaddition/Friedel–Crafts type cyclization reaction of linear enynyl esters","Organic Chemistry Frontiers","2017","4","11","2109","","10.1039/C7QO00511C","","","0.71073","MoKα","","0.095","0.057","","","0.1195","0.1501","","","","","","1.036","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553833","7.3052","0.0011","10.5757","0.0016","14.449","0.002","88.853","0.003","83.694","0.003","77.708","0.003","1084.1","0.3","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C23 H19 Cl F3 N O5 -","- C23 H19 Cl F3 N O5 -","- C46 H38 Cl2 F6 N2 O10 -","2","1","","Sun, Yao-Liang; Wei, Yin; Shi, Min","Tunable regiodivergent phosphine-catalyzed [3 + 2] cycloaddition of alkynones and trifluoroacetyl phenylamides","Organic Chemistry Frontiers","2017","4","12","2392","","10.1039/C7QO00512A","","","0.71073","MoKα","","0.0638","0.0465","","","0.1114","0.1227","","","","","","1.015","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553834","11.287","0.002","12.727","0.002","14.808","0.003","90","","103.68","0.004","90","","2066.8","0.6","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C19 H23 Cl F3 N O4 -","- C19 H23 Cl F3 N O4 -","- C76 H92 Cl4 F12 N4 O16 -","4","1","","Sun, Yao-Liang; Wei, Yin; Shi, Min","Tunable regiodivergent phosphine-catalyzed [3 + 2] cycloaddition of alkynones and trifluoroacetyl phenylamides","Organic Chemistry Frontiers","2017","4","12","2392","","10.1039/C7QO00512A","","","0.71073","MoKα","","0.0781","0.0568","","","0.1427","0.1542","","","","","","1.044","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553835","21.872","0.003","7.604","0.001","24.313","0.003","90","","110.597","0.003","90","","3785.1","0.9","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C21 H17 Cl F3 N O3 -","- C21 H17 Cl F3 N O3 -","- C168 H136 Cl8 F24 N8 O24 -","8","1","","Sun, Yao-Liang; Wei, Yin; Shi, Min","Tunable regiodivergent phosphine-catalyzed [3 + 2] cycloaddition of alkynones and trifluoroacetyl phenylamides","Organic Chemistry Frontiers","2017","4","12","2392","","10.1039/C7QO00512A","","","0.71073","MoKα","","0.0662","0.0487","","","0.1124","0.1212","","","","","","1.037","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553836","6.9086","0.0008","9.5831","0.0007","19.453","0.002","90","","96.737","0.01","90","","1279","0.2","120","","120","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C16 H15 N O -","- C16 H15 N O -","- C64 H60 N4 O4 -","4","2","","Zhang, Wei; Yu, Wenlong; Yan, Qiangqiang; Liu, Zhanxiang; Zhang, Yuhong","Synthesis of substituted oxazoles via Pd-catalyzed tandem oxidative cyclization","Organic Chemistry Frontiers","2017","4","12","2428","","10.1039/C7QO00517B","","","0.71073","MoKα","","0.1472","0.1365","","","0.3471","0.3583","","","","","","1.333","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553837","11.7381","0.0004","13.2058","0.0005","14.4879","0.0006","90","","98.487","0.002","90","","2221.19","0.15","150","2","150","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C25 H29 N O5 S -","- C25 H29 N O5 S -","- C100 H116 N4 O20 S4 -","4","1","","Lv, Leiyang; Lu, Shenglin; Chen, Yuanjin; Li, Zhiping","Diastereoselective building up polycyclic tetrahydrofurans via tandem annulation of 1,n-enynes with aliphatic acids","Organic Chemistry Frontiers","2017","4","11","2147","","10.1039/C7QO00527J","","","0.71073","MoKα","","0.0408","0.0347","","","0.0876","0.0914","","","","","","1.027","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553838","8.0159","0.0011","15.545","0.003","21.174","0.003","90","","90","","90","","2638.4","0.7","133","2","133","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C29 H25 N O7 S -","- C29 H25 N O7 S -","- C116 H100 N4 O28 S4 -","4","1","","Li, Shoulei; Zhang, Enge; Feng, Junjun; Li, Xin","An enantioselective conjugate addition reaction of 3-substituted benzothiophen-2-ones and 2-phthalimidoacrylates","Organic Chemistry Frontiers","2017","4","12","2301","","10.1039/C7QO00531H","","","0.71073","MoKα","","0.0315","0.0276","","","0.07","0.072","","","","","","1.014","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553839","9.5214","0.0008","9.6784","0.0008","9.8861","0.0008","114.205","0.008","92.568","0.007","116.743","0.008","712.04","0.14","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C15 H17 F N2 O2 -","- C15 H17 F N2 O2 -","- C30 H34 F2 N4 O4 -","2","1","","Yang, Zi; Lin, Xing; Wang, Lianhui; Cui, Xiuling","Facile synthesis of 1-aminoindoles via Rh(iii)-catalysed intramolecular three-component annulation","Organic Chemistry Frontiers","2017","4","11","2179","","10.1039/C7QO00541E","","x-ray","1.54184","CuKα","","0.044","0.0376","","","0.1015","0.1075","","","","","","1.042","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553840","10.723","0.016","9.856","0.015","20.94","0.03","90","","100.205","0.017","90","","2178","6","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C23 H22 Br N O4 S -","- C23 H22 Br N O4 S -","- C92 H88 Br4 N4 O16 S4 -","4","1","","Wang, Weiyi; He, Qiuqin; Fan, Renhua","PhI(OAc)2-mediated dialkoxylation of 4-aminostyrenes through a dearomatization process under metal-free conditions","Organic Chemistry Frontiers","2017","4","11","2156","","10.1039/C7QO00545H","","","0.71073","MoKα","","0.1743","0.0976","","","0.2577","0.3288","","","","","","0.996","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553841","13.746","0.002","8.2548","0.0013","15.646","0.003","90","","104.468","0.002","90","","1719.1","0.5","223","2","223","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C17 H21 N O4 S -","- C17 H21 N O4 S -","- C68 H84 N4 O16 S4 -","4","1","","Wang, Weiyi; He, Qiuqin; Fan, Renhua","PhI(OAc)2-mediated dialkoxylation of 4-aminostyrenes through a dearomatization process under metal-free conditions","Organic Chemistry Frontiers","2017","4","11","2156","","10.1039/C7QO00545H","","","0.71073","MoKα","","0.0557","0.0433","","","0.1308","0.1447","","","","","","1.103","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553842","11.7394","0.0011","19.838","0.0019","16.5546","0.0012","90","","94.489","0.007","90","","3843.5","0.6","100","0.1","100","0.1","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C40 H48 Cl2 N2 O2 Pd -","- C40 H48 Cl2 N2 O2 Pd -","- C160 H192 Cl8 N8 O8 Pd4 -","4","1","","Chen, Fu-Min; Huang, Fei-Dong; Yao, Xue-Yi; Li, Tian; Liu, Feng-Shou","Direct C‒H heteroarylation by an acenaphthyl-based α-diimine palladium complex: improvement of the reaction efficiency for bi(hetero)aryls under aerobic conditions","Organic Chemistry Frontiers","2017","4","12","2336","","10.1039/C7QO00562H","","x-ray","0.71073","MoKα","","0.1182","0.0986","","","0.2046","0.2146","","","","","","1.185","","","","has coordinates","236088","2020-10-21","18:00:00",""
"1553843","7.973","0.0003","12.9128","0.0005","14.3781","0.0008","90","","90","","90","","1480.28","0.11","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","3a","","- C16 H15 N O4 -","- C16 H15 N O4 -","- C64 H60 N4 O16 -","4","1","","Wu, Qiuju; Li, Chengcheng; Wang, Weihong; Wang, Hongling; Pan, Dingwu; Zheng, Pengcheng","NHC-catalyzed enantioselective synthesis of dihydropyran-4-carbonitriles bearing all-carbon quaternary centers","Organic Chemistry Frontiers","2017","4","12","2323","","10.1039/C7QO00571G","","","1.54178","CuKα","","0.0445","0.0406","","","0.106","0.1097","","","","","","1.033","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553844","11.831","0.0008","8.4718","0.0005","16.4581","0.001","90","","90.759","0.006","90","","1649.45","0.18","293","2","293.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H21 N O2 -","- C20 H21 N O2 -","- C80 H84 N4 O8 -","4","1","","Wu, Shangze; Huang, Xin; Fu, Chunling; Ma, Shengming","Asymmetric SN2′-type C–H functionalization of arenes with propargylic alcohols","Organic Chemistry Frontiers","2017","4","10","2002","","10.1039/C7QO00588A","","","0.71073","MoKα","","0.0821","0.0489","","","0.1144","0.1394","","","","","","1.038","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553845","8.316","0.002","10.229","0.002","13.179","0.003","69.905","0.018","82.818","0.018","72.23","0.019","1002.3","0.4","293","2","293.15","","","","","","","","","4","P -1","-P 1","2","","","","- C24 H27 N O -","- C24 H27 N O -","- C48 H54 N2 O2 -","2","1","","Wu, Shangze; Huang, Xin; Fu, Chunling; Ma, Shengming","Asymmetric SN2′-type C–H functionalization of arenes with propargylic alcohols","Organic Chemistry Frontiers","2017","4","10","2002","","10.1039/C7QO00588A","","","0.71073","MoKα","","0.2693","0.0889","","","0.1758","0.2639","","","","","","0.994","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553846","11.781","0.001","12.2621","0.0007","12.7517","0.001","90","","110.261","0.009","90","","1728.1","0.2","293","2","293.15","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C17 H22 I N O2 -","- C17 H22 I N O2 -","- C68 H88 I4 N4 O8 -","4","1","","Wu, Shangze; Huang, Xin; Fu, Chunling; Ma, Shengming","Asymmetric SN2′-type C–H functionalization of arenes with propargylic alcohols","Organic Chemistry Frontiers","2017","4","10","2002","","10.1039/C7QO00588A","","","0.71073","MoKα","","0.0708","0.046","","","0.0999","0.1149","","","","","","1.054","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553847","20.993","0.007","3.9406","0.0012","12.147","0.004","90","","95.906","0.005","90","","999.5","0.6","296","2","296","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C8 H6 Br F3 O S -","- C8 H6 Br F3 O S -","- C32 H24 Br4 F12 O4 S4 -","4","1","","Zhang, Yunxiao; Wu, Dongping; Weng, Zhiqiang","Synthesis of 1,2,2-trifluorovinyl sulphides and selenides from trifluorovinylation of organic thiocyanates and selenocyanates","Organic Chemistry Frontiers","2017","4","11","2226","","10.1039/C7QO00595D","","","0.71073","MoKα","","0.0616","0.0498","","","0.1371","0.1432","","","","","","1.072","","","","has coordinates","236093","2020-10-21","18:00:00",""
"1553848","9.3385","0.0018","11.1134","0.0014","11.912","0.002","69.983","0.007","88.735","0.008","69.443","0.007","1080.8","0.3","113","2","113","2","","","","","","","","6","P -1","-P 1","2","","","","- C26 H20 Br N O4 S -","- C26 H20 Br N O4 S -","- C52 H40 Br2 N2 O8 S2 -","2","1","","Jin, Hongxing; Li, Erqing; Huang, You","Divergent synthesis of hydropyridine derivatives via nitrogen-containing Lewis base mediated regioselective [4 + 2] cyclizations","Organic Chemistry Frontiers","2017","4","11","2216","","10.1039/C7QO00596B","","","0.71073","MoKα","","0.0323","0.0253","","","0.0686","0.0704","","","","","","1.045","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553849","27.96","0.01","10.908","0.003","16.954","0.006","90","","121.023","0.005","90","","4431","3","113","2","113","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C26 H20 Br N O4 S -","- C26 H20 Br N O4 S -","- C208 H160 Br8 N8 O32 S8 -","8","1","","Jin, Hongxing; Li, Erqing; Huang, You","Divergent synthesis of hydropyridine derivatives via nitrogen-containing Lewis base mediated regioselective [4 + 2] cyclizations","Organic Chemistry Frontiers","2017","4","11","2216","","10.1039/C7QO00596B","","","0.71073","MoKα","","0.0333","0.0258","","","0.0619","0.0643","","","","","","1.025","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553850","9.7797","0.001","10.9021","0.0011","14.8619","0.0015","90","","90","","90","","1584.6","0.3","296.15","","296.15","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C18 H16 O4 S -","- C18 H16 O4 S -","- C72 H64 O16 S4 -","4","1","","Zhao, Wei-Wei; Liu, Yan-Kai","Enantio- and diastereoselective synthesis of tetrahydrofuro[2,3-b]furan-2(3H)-one derivatives and related oxygen heterocycles via an asymmetric organocatalytic cascade process","Organic Chemistry Frontiers","2017","4","12","2358","","10.1039/C7QO00621G","","","0.71073","MoKα","","0.0427","0.034","","","0.086","0.0919","","","","","","1.041","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553851","9.8074","0.0005","13.2321","0.0005","17.7176","0.0007","100.836","0.003","99.601","0.004","93.264","0.003","2217.36","0.17","150","","150","","","","","","","","","5","P -1","-P 1","2","","","","- C100 H96 Cl6 N6 O10 -","- C100 H96 Cl6 N6 O10 -","- C100 H96 Cl6 N6 O10 -","1","0.5","","Zhang, Yuehong; Wang, Chiming; Chen, Xin; Pan, Houhe; Qi, Dongdong; Wang, Kang; Jiang, Jianzhuang","Novel, linear oligoisoindole compounds with a conjugated electronic structure","Organic Chemistry Frontiers","2017","4","12","2364","","10.1039/C7QO00631D","","","1.54178","CuKα","","0.0751","0.0658","","","0.183","0.1934","","","","","","1.018","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553852","8.9041","0.0004","14.0916","0.0007","16.2768","0.0008","104.121","0.004","91.824","0.004","94.954","0.004","1970.23","0.17","150","","150","","","","","","","","","5","P 1","P 1","1","","diisoindole","","- C88 H122 N2 O4 S2 -","- C88 H122 N2 O4 S2 -","- C88 H122 N2 O4 S2 -","1","1","","Zhang, Yuehong; Wang, Chiming; Chen, Xin; Pan, Houhe; Qi, Dongdong; Wang, Kang; Jiang, Jianzhuang","Novel, linear oligoisoindole compounds with a conjugated electronic structure","Organic Chemistry Frontiers","2017","4","12","2364","","10.1039/C7QO00631D","","","1.54178","CuKα","","0.0527","0.0466","","","0.1245","0.1314","","","","","","1.024","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553853","18.0089","0.0005","19.4187","0.0005","29.7417","0.0007","90.357","0.002","95.539","0.002","107.328","0.002","9875.8","0.5","150","","150","","","","","","","","","5","P -1","-P 1","2","","hexaisoindole","","- C202 H249 Cl14 N9 O15 -","- C202 H249 Cl14 N9 O15 -","- C404 H498 Cl28 N18 O30 -","2","1","","Zhang, Yuehong; Wang, Chiming; Chen, Xin; Pan, Houhe; Qi, Dongdong; Wang, Kang; Jiang, Jianzhuang","Novel, linear oligoisoindole compounds with a conjugated electronic structure","Organic Chemistry Frontiers","2017","4","12","2364","","10.1039/C7QO00631D","","","1.54178","CuKα","","0.1424","0.1121","","","0.3263","0.3551","","","","","","1.3","","","","has coordinates","236096","2020-10-21","18:00:00",""
"1553854","9.9153","0.0002","27.367","0.0005","23.7531","0.0004","90","","93.29","0.002","90","","6434.8","0.2","249.9","","249.9","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C132 H154 Cl12 N6 O8 -","- C132 H154 Cl12 N6 O8 -","- C264 H308 Cl24 N12 O16 -","2","0.5","","Zhang, Yuehong; Wang, Chiming; Chen, Xin; Pan, Houhe; Qi, Dongdong; Wang, Kang; Jiang, Jianzhuang","Novel, linear oligoisoindole compounds with a conjugated electronic structure","Organic Chemistry Frontiers","2017","4","12","2364","","10.1039/C7QO00631D","","","1.54178","CuKα","","0.095","0.0802","","","0.2411","0.2554","","","","","","1.063","","","","has coordinates,has disorder","301780","2025-08-18","21:43:30",""
"1553855","5.1621","0.0006","16.3247","0.0018","20.251","0.002","90","","90","","90","","1706.5","0.3","293","2","293","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C18 H16 Cl N O4 S -","- C18 H16 Cl N O4 S -","- C72 H64 Cl4 N4 O16 S4 -","4","1","","Deng, Hua; He, Fu-Sheng; Li, Cong-Shan; Yang, Wu-Lin; Deng, Wei-Ping","Enantioselective construction of tricyclic pyrrolidine-fused benzo[b]thiophene 1,1-dioxide derivatives via copper(i)-catalyzed asymmetric 1,3-dipolar cycloaddition","Organic Chemistry Frontiers","2017","4","12","2343","","10.1039/C7QO00640C","","","0.71073","MoKα","","0.0476","0.042","","","0.1066","0.1107","","","","","","1.035","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553866","8.4885","0.0005","10.6796","0.0006","16.8127","0.0009","74.369","0.004","82.265","0.004","75.011","0.005","1414.37","0.14","296","","296.15","","","","","","","","","4","P -1","-P 1","2","","","","- C31 H36 N2 O4 -","- C31 H36 N2 O4 -","- C62 H72 N4 O8 -","2","1","","Wu, Jia-Le; Wang, Jing-Yi; Wu, Ping; Mei, Guang-Jian; Shi, Feng","Catalytic asymmetric C2-nucleophilic substitutions of C3-substituted indoles with ortho-hydroxybenzyl alcohols","Organic Chemistry Frontiers","2017","4","12","2465","","10.1039/C7QO00649G","","","1.54178","CuKα","","0.1161","0.075","","","0.1876","0.2188","","","","","","1.011","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553867","18.5578","0.0009","18.5578","0.0009","9.8682","0.0006","90","","90","","120","","2943.2","0.3","296","","296","","","","","","","","","4","P 61","P 61","169","","","","- C23 H20 N O2 -","- C23 H21 N O2 -","- C138 H126 N6 O12 -","6","1","","Wu, Jia-Le; Wang, Jing-Yi; Wu, Ping; Mei, Guang-Jian; Shi, Feng","Catalytic asymmetric C2-nucleophilic substitutions of C3-substituted indoles with ortho-hydroxybenzyl alcohols","Organic Chemistry Frontiers","2017","4","12","2465","","10.1039/C7QO00649G","","","1.54178","CuKα","","0.0543","0.0434","","","0.1186","0.1284","","","","","","1.015","","","","has coordinates","236104","2020-10-21","18:00:00",""
"1553868","6.0777","0.0007","22.245","0.003","11.8606","0.0015","90","","96.163","0.002","90","","1594.3","0.3","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C17 H22 N2 O2 -","- C17 H22 N2 O2 -","- C68 H88 N8 O8 -","4","1","","Liu, Xueke; Qian, Ping; Wang, Yi; Pan, Yi","Metal-free sequential decarbonylative annulation of N-cyanamides for the construction of 2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-ones","Organic Chemistry Frontiers","2017","4","12","2370","","10.1039/C7QO00677B","","","0.71073","MoKα","","0.1128","0.0778","","","0.2365","0.274","","","","","","1.05","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553869","21.107","0.003","7.3437","0.0011","21.914","0.003","90","","101.993","0.005","90","","3322.6","0.8","296","2","296","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C20 H22 N2 O -","- C20 H22 N2 O -","- C160 H176 N16 O8 -","8","1","","Liu, Xueke; Qian, Ping; Wang, Yi; Pan, Yi","Metal-free sequential decarbonylative annulation of N-cyanamides for the construction of 2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-ones","Organic Chemistry Frontiers","2017","4","12","2370","","10.1039/C7QO00677B","","","0.71073","MoKα","","0.0959","0.0818","","","0.2146","0.2278","","","","","","1.072","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553870","7.9044","0.0001","11.5678","0.0002","15.8146","0.0002","90","","98.267","0.001","90","","1431.01","0.04","290","2","290","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C31 H38 O9 -","- C31 H38 O9 -","- C62 H76 O18 -","2","1","","Luo, Jun; Huang, Wan-Sha; Hu, Sheng-Mou; Zhang, Pan-Pan; Zhou, Xu-Wei; Wang, Xiao-Bing; Yang, Ming-Hua; Luo, Jian-Guang; Wang, Chen; Liu, Chang; Yao, He-Quan; Zhang, Can; Sun, Hong-Bin; Chen, Yi-Jun; Kong, Ling-Yi","Rearranged limonoids with unique 6/5/6/5 tetracarbocyclic skeletons from Toona ciliata and biomimetic structure divergence","Organic Chemistry Frontiers","2017","4","12","2417","","10.1039/C7QO00678K","","","1.54184","CuKα","","0.035","0.0337","","","0.0879","0.0896","","","","","","1.03","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553871","14.6815","0.0001","17.2043","0.0002","23.1115","0.0002","90","","90","","90","","5837.62","0.09","291","2","291","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C31 H38 O9 -","- C31 H38 O9 -","- C248 H304 O72 -","8","2","","Luo, Jun; Huang, Wan-Sha; Hu, Sheng-Mou; Zhang, Pan-Pan; Zhou, Xu-Wei; Wang, Xiao-Bing; Yang, Ming-Hua; Luo, Jian-Guang; Wang, Chen; Liu, Chang; Yao, He-Quan; Zhang, Can; Sun, Hong-Bin; Chen, Yi-Jun; Kong, Ling-Yi","Rearranged limonoids with unique 6/5/6/5 tetracarbocyclic skeletons from Toona ciliata and biomimetic structure divergence","Organic Chemistry Frontiers","2017","4","12","2417","","10.1039/C7QO00678K","","","1.54184","CuKα","","0.0685","0.0635","","","0.1821","0.1891","","","","","","1.034","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553875","8.4549","0.0014","13.872","0.002","14.009","0.002","117.552","0.003","101.368","0.004","92.964","0.004","1408.7","0.4","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C25 H24 Br2 N2 O3 S -","- C25 H24 Br2 N2 O3 S -","- C50 H48 Br4 N4 O6 S2 -","2","1","","Jiang, Bo; Shi, Min","Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene","Organic Chemistry Frontiers","2017","4","12","2459","","10.1039/C7QO00703E","","","0.71073","MoKα","","0.0839","0.0508","","","0.121","0.1326","","","","","","0.919","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553876","13.823","0.002","11.5473","0.0019","30.267","0.005","90","","98.559","0.006","90","","4777.4","1.3","272","2","272.29","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C44 H45 Br2 N3 O6 S2 -","- C44 H45 Br2 N3 O6 S2 -","- C176 H180 Br8 N12 O24 S8 -","4","1","","Jiang, Bo; Shi, Min","Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene","Organic Chemistry Frontiers","2017","4","12","2459","","10.1039/C7QO00703E","","","0.71073","MoKα","","0.154","0.0663","","","0.1613","0.2048","","","","","","0.941","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553877","11.936","0.0015","13.1209","0.0017","13.8558","0.0016","89.702","0.004","84.883","0.003","66.69","0.003","1983.8","0.4","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C43 H38 Br N3 O4 S2 -","- C43 H38 Br N3 O4 S2 -","- C86 H76 Br2 N6 O8 S4 -","2","1","","Jiang, Bo; Shi, Min","Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene","Organic Chemistry Frontiers","2017","4","12","2459","","10.1039/C7QO00703E","","","0.71073","MoKα","","0.1209","0.059","","","0.1505","0.1878","","","","","","0.925","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553878","10.688","0.002","10.745","0.002","11.245","0.002","103.535","0.004","94.412","0.004","96.045","0.004","1241.6","0.4","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C31 H26 N2 O2 S -","- C31 H26 N2 O2 S -","- C62 H52 N4 O4 S2 -","2","1","","Jiang, Bo; Shi, Min","Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene","Organic Chemistry Frontiers","2017","4","12","2459","","10.1039/C7QO00703E","","","0.71073","MoKα","","0.0744","0.0571","","","0.143","0.1554","","","","","","1.015","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553879","24.816","0.003","10.401","0.0011","16.9512","0.0018","90","","96.192","0.002","90","","4349.8","0.8","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C25 H21 Br N2 O2 S -","- C25 H21 Br N2 O2 S -","- C200 H168 Br8 N16 O16 S8 -","8","1","","Jiang, Bo; Shi, Min","Rhodium(ii)-catalyzed intermolecular [3 + 2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene","Organic Chemistry Frontiers","2017","4","12","2459","","10.1039/C7QO00703E","","","0.71073","MoKα","","0.0655","0.0429","","","0.0996","0.1099","","","","","","1.016","","","","has coordinates","301780","2025-08-18","21:43:30",""
"1553881","24.1839","0.0009","31.5567","0.0009","12.6112","0.0003","90","","104.99","0.003","90","","9296.9","0.5","273","2","273","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C72 H112 Cl2 N28 O26 -","- C72 H84 N28 O22 -","- C288 H336 N112 O88 -","4","0.5","","Xiao, Zhi-You; Lin, Rui-Lian; Tao, Zhu; Liu, Qing-Yun; Liu, Jing-Xin; Xiao, Xin","Multiple noncovalent interaction constructed polymeric supramolecular crystals: recognition of butyl viologen by para-dicyclohexanocucurbit[6]uril and α,α′,δ,δ′-tetramethylcucurbit[6]uril","Organic Chemistry Frontiers","2017","4","12","2422","","10.1039/C7QO00708F","","","0.71073","MoKα","","0.1978","0.1121","","","0.2997","0.347","","","","","","1.005","","","","has coordinates,has disorder","236118","2020-10-21","18:00:00",""
"1553882","12.8381","0.0007","15.6916","0.0009","22.2878","0.0013","92.995","0.002","98.521","0.002","106.862","0.002","4227.9","0.4","273","2","273","2","","","","","","","","6","P -1","-P 1","2","","","","- C108 H176 Cl6 N52 O50 Sr2 -","- C108 H124 Cl4 N52 O40 Sr2 -","- C108 H124 Cl4 N52 O40 Sr2 -","1","0.5","","Xiao, Zhi-You; Lin, Rui-Lian; Tao, Zhu; Liu, Qing-Yun; Liu, Jing-Xin; Xiao, Xin","Multiple noncovalent interaction constructed polymeric supramolecular crystals: recognition of butyl viologen by para-dicyclohexanocucurbit[6]uril and α,α′,δ,δ′-tetramethylcucurbit[6]uril","Organic Chemistry Frontiers","2017","4","12","2422","","10.1039/C7QO00708F","","","0.71073","MoKα","","0.081","0.0615","","","0.1789","0.1905","","","","","","1.014","","","","has coordinates,has disorder","236118","2020-10-21","18:00:00",""