# Search results of SQL query from the Crystallography Open Database
# Date and time performed: 2025-04-23T08:13:26+02:00
# Query:
# SELECT data.*
# FROM
#  data JOIN jaltnames
#  ON altname = journal
# WHERE
#  (status is null or status != 'retracted') and
#  (journal_id IN (SELECT DISTINCT(journal_id) FROM jaltnames WHERE altname LIKE 'Organic Chemistry Frontiers') AND volume = 5 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
"1553856","12.0438","0.0011","14.5042","0.0014","22.049","0.003","72.623","0.005","76.291","0.005","77.888","0.005","3530.8","0.7","150","2","150","2","","","","","","","","3","P -1","-P 1","2","Benzoxymethoxy Pillerene","","","- C81 H82 O10 -","- C81 H82 O10 -","- C162 H164 O20 -","2","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","0.2028","0.1038","","","0.2834","0.3483","","","","","","1.001","","","","has coordinates,has disorder","236101","2020-10-21","18:00:00",""
"1553857","12.791","0.004","20.978","0.007","14.779","0.004","90","","98.582","0.007","90","","3921","2","150","","150","","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C44 H48 O12 -","- C44 H48 O12 -","- C176 H192 O48 -","4","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","","0.0801","","","","0.232","","","","","","0.967","","","","has coordinates","236101","2020-10-21","18:00:00",""
"1553858","13.633","0.004","15.357","0.004","20.965","0.005","91.591","0.007","94.087","0.007","111.251","0.008","4073.6","1.9","150","","150","","","","","","","","","4","P -1","-P 1","2","","","","- C90 H125 N3 O10 -","- C90 H125 N3 O10 -","- C180 H250 N6 O20 -","2","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","","0.0506","","","","0.1486","","","","","","1.07","","","","has coordinates","236101","2020-10-21","18:00:00",""
"1553859","14.289","0.003","23.102","0.006","20.977","0.006","90","","108.428","0.008","90","","6570","3","150","2","150","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C42 H46 O11 -","- C42 H46 O11 -","- C252 H276 O66 -","6","3","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","0.158","0.0925","","","0.2471","0.2924","","","","","","0.855","","","","has coordinates","236101","2020-10-21","18:00:00",""
"1553860","14.89","0.008","18.123","0.008","21.671","0.01","81.371","0.006","82.134","0.009","87.707","0.013","5726","5","150","2","150","2","","","","","","","","4","P -1","-P 1","2","OctoxyBenzoxyPillerene_3","","","- C119 H158 Cl9 O10 -","- C119 H158 Cl9 O10 -","- C238 H316 Cl18 O20 -","2","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","0.1761","0.111","","","0.3038","0.3479","","","","","","1.042","","","","has coordinates","236101","2020-10-21","18:00:00",""
"1553861","43.045","0.01","21.347","0.005","23.043","0.005","90","","104.773","0.007","90","","20474","8","150","2","150","","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C110 H140 O10 -","- C110 H140 O10 -","- C880 H1120 O80 -","8","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","0.2489","0.148","","","0.3802","0.4289","","","","","","1.094","","","","has coordinates","236101","2020-10-21","18:00:00",""
"1553862","16.77","0.04","21.69","0.05","18.89","0.04","90","","93.48","0.04","90","","6858","3","150","","150","","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C82 H85 O12 -","- C82 H85 O12 -","- C328 H340 O48 -","4","2","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","","0.0751","","","","0.2118","","","","","","1.013","","","","has coordinates","273808","2022-03-18","10:32:15",""
"1553863","16.619","0.003","16.686","0.003","16.858","0.003","95.191","0.007","117.822","0.009","114.325","0.008","3527.9","1.3","150","","150","","","","","","","","","3","P -1","-P 1","2","","","","- C75 H110 O10 -","- C75 H110 O10 -","- C150 H220 O20 -","2","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","","0.1159","","","","0.3888","","","","","","0.799","","","","has coordinates","236101","2020-10-21","18:00:00",""
"1553864","12.31","0.03","16.48","0.04","18.98","0.04","83.427","0.016","80.887","0.014","69.254","0.017","3548","14","150","","150","","","","","","","","","3","P -1","-P 1","2","","","","- C81 H84 O10 -","- C81 H84 O10 -","- C162 H168 O20 -","2","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","","0.0892","","","","0.3047","","","","","","1.018","","","","has coordinates","236101","2020-10-21","18:00:00",""
"1553865","12.2178","0.001","15.0675","0.0014","20.9593","0.0017","78.186","0.006","85.869","0.006","67.284","0.005","3483.6","0.5","150","","150","","","","","","","","","4","P -1","-P 1","2","","","","- C82 H86 Cl2 O10 -","- C82 H86 Cl2 O10 -","- C164 H172 Cl4 O20 -","2","1","","Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.","A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state","Organic Chemistry Frontiers","2018","5","1","10","","10.1039/C7QO00641A","","","0.71075","MoKα","","","0.1051","","","","0.3493","","","","","","1.293","","","","has coordinates","236101","2020-10-21","18:00:00",""
"1553872","12.1518","0.0014","12.3848","0.0015","19.412","0.002","90","","90","","90","","2921.5","0.6","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C30 H30 I N3 O5 -","- C30 H30 I N3 O5 -","- C120 H120 I4 N12 O20 -","4","1","","Zhu, Jing-Yan; Yang, Wu-Lin; Liu, Yang-Zi; Shang, Shao-Jing; Deng, Wei-Ping","A copper(i)-catalyzed asymmetric Mannich reaction of glycine Schiff bases with isatin-derived ketimines: enantioselective synthesis of 3-substituted 3-aminooxindoles","Organic Chemistry Frontiers","2018","5","1","70","","10.1039/C7QO00691H","","","0.71073","MoKα","","0.0383","0.0336","","","0.0775","0.0799","","","","","","1.038","","","","has coordinates","236109","2020-10-21","18:00:00",""
"1553873","6.1598","0.0003","8.133","0.0004","31.1006","0.0015","90","","90","","90","","1558.07","0.13","293","2","293.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C13 H23 N O4 S -","- C13 H23 N O4 S -","- C52 H92 N4 O16 S4 -","4","1","","Wang, Zhi-Peng; Wu, Qi; Jiang, Jia; Li, Zi-Rui; Peng, Xiao-Jiao; Shao, Pan-Lin; He, Yun","Catalytic asymmetric synthesis of pyrrolidine derivatives bearing heteroatom-substituted quaternary stereocenters","Organic Chemistry Frontiers","2018","5","1","36","","10.1039/C7QO00692F","","x-ray","0.71073","MoKα","","0.0588","0.0466","","","0.0947","0.1025","","","","","","1.058","","","","has coordinates","236111","2020-10-21","18:00:00",""
"1553874","7.9925","0.0003","13.9906","0.0004","19.0487","0.0006","90","","90","","90","","2130.02","0.12","292","2","292","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C21 H24 N2 O6 S -","- C21 H24 N2 O6 S -","- C84 H96 N8 O24 S4 -","4","1","","Wang, Zhi-Peng; Wu, Qi; Jiang, Jia; Li, Zi-Rui; Peng, Xiao-Jiao; Shao, Pan-Lin; He, Yun","Catalytic asymmetric synthesis of pyrrolidine derivatives bearing heteroatom-substituted quaternary stereocenters","Organic Chemistry Frontiers","2018","5","1","36","","10.1039/C7QO00692F","","","0.71073","MoKα","","0.0451","0.0389","","","0.0939","0.098","","","","","","1.113","","","","has coordinates","236111","2020-10-21","18:00:00",""
"1553880","3.8516","0.0002","11.2844","0.0004","21.4208","0.0008","90","","89.074","0.003","90","","930.89","0.07","","","","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C10 H8 Cl N O2 -","- C10 H8 Cl N O2 -","- C40 H32 Cl4 N4 O8 -","4","1","","Ledovskaya, Maria S.; Rodygin, Konstantin S.; Ananikov, Valentine P.","Calcium-mediated one-pot preparation of isoxazoles with deuterium incorporation","Organic Chemistry Frontiers","2018","5","2","226","","10.1039/C7QO00705A","","","","","","0.058","","","","","","","","","","","","","","","has coordinates","236116","2020-10-21","18:00:00",""
"1553883","10.8597","0.0007","13.0923","0.0008","18.0508","0.0012","75.984","0.002","74.865","0.002","66.722","0.002","2247.6","0.3","273","2","273","2","","","","","","","","6","P -1","-P 1","2","","","","- C43 H60 N2 P Sc Si2 -","- C43 H60 N2 P Sc Si2 -","- C86 H120 N4 P2 Sc2 Si4 -","2","1","","Gao, Hongjie; Su, Jianhong; Xu, Pengfei; Xu, Xin","Scandium-catalyzed C(sp3)‒H alkylation of N,N-dimethyl anilines with alkenes","Organic Chemistry Frontiers","2018","5","1","59","","10.1039/C7QO00718C","","","0.71073","MoKα","","0.09","0.0474","","","0.1213","0.1448","","","","","","1.07","","","","has coordinates","236120","2020-10-21","18:00:00",""
"1553884","8.859","0.0015","21.377","0.004","8.0979","0.0014","90","","106.44","0.004","90","","1470.9","0.5","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C19 H20 O -","- C19 H20 O -","- C76 H80 O4 -","4","1","","Zang, Wenqing; Wei, Yin; Shi, Min","Gold(i) catalyzed cascade cyclization: intramolecular two-fold nucleophilic addition to vinylidenecyclopropanes (VDCPs)","Organic Chemistry Frontiers","2018","5","2","197","","10.1039/C7QO00722A","","","0.71073","MoKα","","0.0664","0.0449","","","0.115","0.1272","","","","","","1.034","","","","has coordinates","236121","2020-10-21","18:00:00",""
"1553885","6.059","0.0012","8.893","0.0018","13.346","0.003","91.59","0.03","93.75","0.03","108.42","0.03","679.9","0.3","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C15 H12 Cl2 O2 -","- C15 H12 Cl2 O2 -","- C30 H24 Cl4 O4 -","2","1","","Dai, Jie; Ren, Wenlong; Li, Jingfu; Shi, Yian","An effective approach to aryl-substituted propanoic acids via the Pd-catalyzed hydrocarboxylation of stilbenes","Organic Chemistry Frontiers","2018","5","4","561","","10.1039/C7QO00726D","","","0.71073","MoKα","","0.0734","0.0514","","","0.1484","0.166","","","","","","1.004","","","","has coordinates","236123","2020-10-21","18:00:00",""
"1553886","8.26","0.0017","10.221","0.002","10.602","0.002","102.5","0.03","107.52","0.03","109.03","0.03","756.2","0.4","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C18 H20 O2 -","- C18 H20 O2 -","- C36 H40 O4 -","2","1","","Dai, Jie; Ren, Wenlong; Li, Jingfu; Shi, Yian","An effective approach to aryl-substituted propanoic acids via the Pd-catalyzed hydrocarboxylation of stilbenes","Organic Chemistry Frontiers","2018","5","4","561","","10.1039/C7QO00726D","","","0.71073","MoKα","","0.0901","0.0617","","","0.168","0.1912","","","","","","1.001","","","","has coordinates","236123","2020-10-21","18:00:00",""
"1553887","17.558","0.0012","9.331","0.0006","9.8891","0.0006","90","","91.367","0.002","90","","1619.71","0.18","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C18 H17 N O3 S -","- C18 H17 N O3 S -","- C72 H68 N4 O12 S4 -","4","1","","Sun, Deli; Zhang, Ronghua","Transition-metal-free, visible-light-induced oxidative cross-coupling for constructing β-acetylamino acrylosulfones from sodium sulfinates and enamides","Organic Chemistry Frontiers","2018","5","1","92","","10.1039/C7QO00729A","","","0.71073","MoKα","","0.067","0.0466","","","0.1158","0.1264","","","","","","1.048","","","","has coordinates","236125","2020-10-21","18:00:00",""
"1553888","15.8995","0.0014","8.3725","0.0008","9.9537","0.0009","90","","100.406","0.003","90","","1303.2","0.2","295","2","295","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C13 H15 N O3 S -","- C13 H15 N O3 S -","- C52 H60 N4 O12 S4 -","4","1","","Sun, Deli; Zhang, Ronghua","Transition-metal-free, visible-light-induced oxidative cross-coupling for constructing β-acetylamino acrylosulfones from sodium sulfinates and enamides","Organic Chemistry Frontiers","2018","5","1","92","","10.1039/C7QO00729A","","","0.71073","MoKα","","0.0959","0.0708","","","0.1171","0.1261","","","","","","1.155","","","","has coordinates","236125","2020-10-21","18:00:00",""
"1553889","13.2285","0.0011","9.3407","0.0008","14.9536","0.0012","90","","95.087","0.001","90","","1840.4","0.3","298","2","298","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C18 H17 Cl N2 O3 S -","- C18 H17 Cl N2 O3 S -","- C72 H68 Cl4 N8 O12 S4 -","4","1","","Jiang, Dong-Fang; Hu, Jie-Yu; Hao, Wen-Juan; Wang, Shu-Liang; Tu, Shu-Jiang; Jiang, Bo","Tunable Cu(i)-catalyzed site-selective dehydrogenative amination of β,γ-unsaturated hydrazones for divergent synthesis of pyrazol-4-ones and 1,6-dihydropyradazines","Organic Chemistry Frontiers","2018","5","2","189","","10.1039/C7QO00743D","","","0.71073","MoKα","","0.1116","0.0511","","","0.15","0.2046","","","","","","0.943","","","","has coordinates","236127","2020-10-21","18:00:00",""
"1553890","11.6687","0.0009","8.7574","0.0006","17.8369","0.0015","90","","96.512","0.001","90","","1810.9","0.2","298","2","298","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C17 H14 Cl2 N2 O2 S -","- C17 H14 Cl2 N2 O2 S -","- C68 H56 Cl8 N8 O8 S4 -","4","1","","Jiang, Dong-Fang; Hu, Jie-Yu; Hao, Wen-Juan; Wang, Shu-Liang; Tu, Shu-Jiang; Jiang, Bo","Tunable Cu(i)-catalyzed site-selective dehydrogenative amination of β,γ-unsaturated hydrazones for divergent synthesis of pyrazol-4-ones and 1,6-dihydropyradazines","Organic Chemistry Frontiers","2018","5","2","189","","10.1039/C7QO00743D","","","0.71073","MoKα","","0.1131","0.0508","","","0.0895","0.1018","","","","","","0.996","","","","has coordinates","236127","2020-10-21","18:00:00",""
"1553891","10.5217","0.0013","14.8118","0.0018","29.451","0.003","90","","94.42","0.003","90","","4576.1","0.9","128","2","128","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C27 H35 N O1.5 P -","- C27 H35 N O1.5 P -","- C216 H280 N8 O12 P8 -","8","1","","Wang, Huanan; Li, Shuaiqi; Wang, Baiquan; Li, Bin","The regioselective synthesis of 2-phosphinoylindoles via Rh(iii)-catalyzed C‒H activation","Organic Chemistry Frontiers","2018","5","1","88","","10.1039/C7QO00746A","","","0.71073","MoKα","","0.0427","0.0357","","","0.0934","0.0968","","","","","","1.057","","","","has coordinates","236129","2020-10-21","18:00:00",""
"1553892","24.609","0.006","9.508","0.002","21.415","0.005","90","","115.972","0.004","90","","4504.7","1.8","213","2","213.15","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C28 H24 N O2 P -","- C28 H24 N O2 P -","- C224 H192 N8 O16 P8 -","8","1","","Wang, Huanan; Li, Shuaiqi; Wang, Baiquan; Li, Bin","The regioselective synthesis of 2-phosphinoylindoles via Rh(iii)-catalyzed C‒H activation","Organic Chemistry Frontiers","2018","5","1","88","","10.1039/C7QO00746A","","","0.71073","MoKα","","0.0569","0.0471","","","0.132","0.1488","","","","","","1.029","","","","has coordinates","236129","2020-10-21","18:00:00",""
"1553893","11.707","0.005","16.717","0.007","15.157","0.007","90","","96.39","0.007","90","","2948","2","296","2","296","2","","","","","","","","8","P 1 21/c 1","-P 2ybc","14","","","","- C30 H23 Au F3 N4 O3 P S -","- C30 H23 Au F3 N4 O3 P S -","- C120 H92 Au4 F12 N16 O12 P4 S4 -","4","1","","Huang, Ronghui; Yang, Yongchun; Wang, Duo-Sheng; Zhang, Liang; Wang, Dawei","Where does Au coordinate to N-(2-pyridiyl)benzotriazole: gold-catalyzed chemoselective dehydrogenation and borrowing hydrogen reactions","Organic Chemistry Frontiers","2018","5","2","203","","10.1039/C7QO00756F","","","0.71073","MoKα","","0.0791","0.046","","","0.1132","0.1336","","","","","","1.027","","","","has coordinates","236131","2020-10-21","18:00:00",""
"1553894","10.31419","0.00017","19.2062","0.0003","11.0205","0.0002","90","","109.532","0.002","90","","2057.49","0.07","135","","135","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C24 H20 N2 O5 -","- C24 H20 N2 O5 -","- C96 H80 N8 O20 -","4","2","","Ruan, Sai; Lin, Xiaobin; Xie, Lihua; Lin, Lili; Feng, Xiaoming; Liu, Xiaohua","Asymmetric synthesis of 3-aminodihydrocoumarins via the chiral guanidine catalyzed cascade reaction of azlactones","Organic Chemistry Frontiers","2018","5","1","32","","10.1039/C7QO00768J","","x-ray","1.54184","CuKα","","0.0427","0.0414","","","0.1079","0.1097","","","","","","1.061","","","","has coordinates","275856","2022-06-07","07:08:27",""
"1553895","8.7889","0.0018","8.9182","0.0018","22.444","0.005","90","","91.02","0.03","90","","1758.9","0.6","293","2","","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","9b-(2-bromobenzyl)-5-methyl-5,9b-dihydropyrrolizino[3,2-b]indol-10(4aH)-one","","- C21 H17 Br N2 O -","- C10.5 H8.5 Br0.5 N O0.5 -","- C84 H68 Br4 N8 O4 -","8","2","","Zhang, Qianqian; Song, Chuanjun; Huang, He; Zhang, Kun; Chang, Junbiao","Cesium carbonate promoted cascade reaction involving DMF as a reactant for the synthesis of dihydropyrrolizino[3,2-b]indol-10-ones","Organic Chemistry Frontiers","2018","5","1","80","","10.1039/C7QO00771J","","","0.71073","MoKα","","0.119","0.0742","","","0.2136","0.2675","","","","","","1.095","","","","has coordinates","236135","2020-10-21","18:00:00",""
"1553896","9.8465","0.0005","26.3558","0.0014","9.9725","0.0005","90","","104.267","0.002","90","","2508.2","0.2","292","2","292","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H14 N2 O -","- C15 H14 N2 O -","- C120 H112 N16 O8 -","8","2","","Zhang, Qianqian; Song, Chuanjun; Huang, He; Zhang, Kun; Chang, Junbiao","Cesium carbonate promoted cascade reaction involving DMF as a reactant for the synthesis of dihydropyrrolizino[3,2-b]indol-10-ones","Organic Chemistry Frontiers","2018","5","1","80","","10.1039/C7QO00771J","","","1.54178","CuKα","","0.0474","0.042","","","0.1109","0.1155","","","","","","1.033","","","","has coordinates","275434","2022-05-16","05:31:57",""
"1553897","18.1727","0.0015","10.5743","0.0009","23.813","0.0019","90","","90","","90","","4576","0.7","293","2","293","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C23 H20 Cl F3 N2 O3 -","- C23 H20 Cl F3 N2 O3 -","- C184 H160 Cl8 F24 N16 O24 -","8","1","","Sun, Yao-Liang; Wei, Yin; Shi, Min","Phosphine catalyzed δ-carbon addition and isomerization of alkynones to ketimines: the preparation of 1,3-diene substituted dihydroquinazolinones and 3-aminooxindoles","Organic Chemistry Frontiers","2018","5","2","210","","10.1039/C7QO00772H","","","0.71073","MoKα","","0.1089","0.0596","","","0.1255","0.1478","","","","","","1.032","","","","has coordinates","236137","2020-10-21","18:00:00",""
"1553898","18.416","0.005","11.31","0.003","9.759","0.003","90","","93.907","0.007","90","","2027.9","1","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H24 N2 O4 -","- C20 H24 N2 O4 -","- C80 H96 N8 O16 -","4","1","","Sun, Yao-Liang; Wei, Yin; Shi, Min","Phosphine catalyzed δ-carbon addition and isomerization of alkynones to ketimines: the preparation of 1,3-diene substituted dihydroquinazolinones and 3-aminooxindoles","Organic Chemistry Frontiers","2018","5","2","210","","10.1039/C7QO00772H","","","0.71073","MoKα","","0.0672","0.0457","","","0.1271","0.1398","","","","","","1.027","","","","has coordinates","236137","2020-10-21","18:00:00",""
"1553899","5.36821","0.00006","11.71337","0.00015","21.6232","0.0003","90","","90","","90","","1359.66","0.03","100","0.1","100","0.1","","","","","","","synthesis as described","5","P 21 21 21","P 2ac 2ab","19","","(2R,4S,5R)-3-(Hydroxymethyl)-8,8-dimethyl-2-(thiophen-2-yl)-7-oxa-1-azaspiro[4.4]nonan-6-one","","- C14 H19 N O3 S -","- C14 H19 N O3 S -","- C56 H76 N4 O12 S4 -","4","1","","Reboredo, Silvia; García-Marijuan, Ainara; Uria, Uxue; Reyes, Efraím; Carrillo, Luisa; Ugarriza, Iratxe; Vicario, Jose L.","Highly diastereoselective C →N acyl rearrangement in polysubstituted pyrrolidine 2,2-dicarboxylates. Stereocontrolled synthesis of densely functionalized prolines","Organic Chemistry Frontiers","2018","5","6","933","","10.1039/C7QO00793K","","x-ray","1.54184","CuKα","","0.0263","0.0254","","","0.0615","0.062","","","","","","1.079","","","","has coordinates,has disorder","236139","2020-10-21","18:00:00",""
"1553900","9.673","0.0007","11.975","0.0008","10.6305","0.0008","90","","96.144","0.002","90","","1224.3","0.15","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C13 H13 Br N2 O -","- C13 H13 Br N2 O -","- C52 H52 Br4 N8 O4 -","4","1","","Zhao, He; Chen, Xiuwen; Jiang, Huanfeng; Zhang, Min","Copper-catalysed dehydrogenative α-C(sp3)‒H amination of tetrahydroquinolines with O-benzoyl hydroxylamines","Organic Chemistry Frontiers","2018","5","4","539","","10.1039/C7QO00794A","","","0.71073","MoKα","","0.0725","0.0383","","","0.0891","0.1042","","","","","","1.001","","","","has coordinates","236142","2020-10-21","18:00:00",""
"1553901","6.5337","0.0001","8.4509","0.0001","26.0879","0.0003","90","","90","","90","","1440.46","0.03","289","2","289","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","2-((1R,5R)-1-hydroxy-3-oxo-5-phenylcyclohexyl)pyridine 1-oxide","","- C17 H17 N O3 -","- C17 H17 N O3 -","- C68 H68 N4 O12 -","4","1","","Xu, Youguo; Zhang, Sheng; Li, Lijun; Wang, Yukang; Zha, Zhenggen; Wang, Zhiyong","l-Phenylalanine potassium catalyzed asymmetric formal [3 + 3] annulation of 2-enoyl-pyridine N-oxides with acetone","Organic Chemistry Frontiers","2018","5","3","376","","10.1039/C7QO00796E","","","1.54184","CuKα","","0.0349","0.0324","","","0.0876","0.0987","","","","","","1.068","","","","has coordinates","295937","2024-11-15","14:43:14",""
"1553902","18.4928","0.0016","11.5835","0.0008","11.4759","0.0008","90","","90","","90","","2458.3","0.3","293","2","293","2","","","","","","","","6","P n n a","-P 2a 2bc","52","","","","- C16 H36 Br Cl3 Fe N -","- C16 H36 Br Cl3 Fe N -","- C64 H144 Br4 Cl12 Fe4 N4 -","4","0.5","","Li, Sanliang; Zhu, Bo; Lee, Richmond; Qiao, Baokun; Jiang, Zhiyong","Visible light-induced selective aerobic oxidative transposition of vinyl halides using a tetrahalogenoferrate(iii) complex catalyst","Organic Chemistry Frontiers","2018","5","3","380","","10.1039/C7QO00798A","","x-ray","1.54184","CuKα","","0.0724","0.0426","","","0.1123","0.1363","","","","","","1.026","","","","has coordinates,has disorder","236146","2020-10-21","18:00:00",""
"1553903","10.4684","0.0007","7.428","0.0004","18.7773","0.0011","90","","90.086","0.003","90","","1460.11","0.15","150","","150","","","","","","","","synthesis as described","3","P 1 21/n 1","-P 2yn","14","","","","- C24 H13 F -","- C24 H13 F -","- C96 H52 F4 -","4","1","","Shi, Xinzhe; Roisnel, Thierry; Soulé, Jean-François; Doucet, Henri","Synthesis of mono- and di-arylated acenaphthylenes and programmed access to dibenzo[j,l]fluoranthenes via palladium-catalysed C‒H bond functionalisation","Organic Chemistry Frontiers","2018","5","3","398","","10.1039/C7QO00799J","","x-ray","0.71073","MoKα","","0.0962","0.0647","","","0.1592","0.1789","","","","","","1.047","","","","has coordinates,has disorder","236148","2020-10-21","18:00:00",""
"1553904","16.8237","0.0012","11.333","0.0007","10.2994","0.0008","90","","114.382","0.003","90","","1788.6","0.2","150","","150","","","","","","","","synthesis as described","3","C 1 2/c 1","-C 2yc","15","","","","- C24 H14 Cl2 -","- C24 H14 Cl2 -","- C96 H56 Cl8 -","4","0.5","","Shi, Xinzhe; Roisnel, Thierry; Soulé, Jean-François; Doucet, Henri","Synthesis of mono- and di-arylated acenaphthylenes and programmed access to dibenzo[j,l]fluoranthenes via palladium-catalysed C‒H bond functionalisation","Organic Chemistry Frontiers","2018","5","3","398","","10.1039/C7QO00799J","","x-ray","0.71073","MoKα","","0.0404","0.0331","","","0.0828","0.0889","","","","","","1.039","","","","has coordinates","236148","2020-10-21","18:00:00",""
"1553905","17.47","0.004","5.702","0.0013","20.396","0.005","90","","114.211","0.004","90","","1853","0.8","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","1-(4-julolidylidene)-4-phenylthiosemicarbazide","","","- C20 H22 N4 S -","- C20 H22 N4 S -","- C80 H88 N16 S4 -","4","1","","Amendola, Valeria; Boiocchi, Massimo; Fabbrizzi, Luigi; La Cognata, Sonia; Legnani, Laura; Lo Presti, Eliana; Mangano, Carlo; Miljkovic, Ana","Anion-induced isomerization of fluorescent semi(thio)carbazones","Organic Chemistry Frontiers","2018","5","3","391","","10.1039/C7QO00805H","","","0.7107","MoKα","","0.1167","0.0691","","","0.1993","0.2389","","","","","","1.004","","","","has coordinates","236150","2020-10-21","18:00:00",""
"1553906","17.0278","0.0009","8.4534","0.0005","14.668","0.0008","90","","110.034","0.002","90","","1983.59","0.19","301","2","301.2","","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C23 H25 N O2 -","- C23 H25 N O2 -","- C92 H100 N4 O8 -","4","1","","Shen, Hong-Qiang; Liu, Cong; Zhou, Ji; Zhou, Yong-Gui","Enantioselective palladium-catalyzed C‒H functionalization of pyrroles using an axially chiral 2,2′-bipyridine ligand","Organic Chemistry Frontiers","2018","5","4","611","","10.1039/C7QO00815E","","","1.54178","CuKα","","0.0703","0.064","","","0.1766","0.1844","","","","","","1.048","","","","has coordinates","236152","2020-10-21","18:00:00",""
"1553907","16.1979","0.0011","9.8887","0.0007","17.2384","0.0015","90","","100.854","0.002","90","","2711.8","0.4","296","2","296","2","","","","","","","","6","P 1 21 1","P 2yb","4","","FeCl2-OIP-iPr","","- C25.5 H35 Cl2 Fe N3 O1.5 -","- C25.5 H35 Cl2 Fe N3 O1.5 -","- C102 H140 Cl8 Fe4 N12 O6 -","4","2","","Chen, Jianhui; Xi, Tuo; Lu, Zhan","10 gram-scale synthesis of a chiral oxazoline iminopyridine ligand and its applications","Organic Chemistry Frontiers","2018","5","2","247","","10.1039/C7QO00816C","","","0.71073","MoKα","","0.1689","0.0788","","","0.1317","0.1638","","","","","","1","","","","has coordinates","275434","2022-05-16","05:31:57",""
"1553908","8.277","0.002","19.206","0.006","11.294","0.004","90","","93.738","0.006","90","","1791.6","1","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C21 H19 Br O2 -","- C21 H19 Br O2 -","- C84 H76 Br4 O8 -","4","1","","Qi, Jifeng; Zheng, Jing; Cui, Sunliang","Facile synthesis of carbo- and heterocycles via Fe(iii)-catalyzed alkene hydrofunctionalization","Organic Chemistry Frontiers","2018","5","2","222","","10.1039/C7QO00817A","","","0.71073","MoKα","","0.1121","0.05","","","0.0829","0.1024","","","","","","1.003","","","","has coordinates","236155","2020-10-21","18:00:00",""
"1553909","8.914","0.01","9.542","0.011","13.652","0.015","86.106","0.014","80.322","0.012","67.976","0.012","1061","2","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C26 H28 O2 -","- C26 H28 O2 -","- C52 H56 O4 -","2","1","","Qi, Jifeng; Zheng, Jing; Cui, Sunliang","Facile synthesis of carbo- and heterocycles via Fe(iii)-catalyzed alkene hydrofunctionalization","Organic Chemistry Frontiers","2018","5","2","222","","10.1039/C7QO00817A","","","0.71073","MoKα","","0.1976","0.1187","","","0.312","0.3561","","","","","","1.049","","","","has coordinates","236155","2020-10-21","18:00:00",""
"1553910","21.1618","0.0016","11.9414","0.0011","23.2097","0.0017","90","","90","","90","","5865.1","0.8","291","","291","","","","","","","","","4","P b c n","-P 2n 2ab","60","","7,16-[2,2'-(hexano-2,4-diyne-1,6-dioxy)-dibenzoylo]-5,14-dihydrodibenzo[b,i][1,4,8,11]tetraazacyclotetradecine","","- C38 H26 N4 O4 -","- C38 H26 N4 O4 -","- C304 H208 N32 O32 -","8","1","","Zwoliński, K. M.; Sieroń, L.; Eilmes, J.","One-flask synthesis of dibenzotetraaza[14]annulene cyclic congeners bearing buta-1,3-diyne bridges","Organic Chemistry Frontiers","2018","5","2","171","","10.1039/C7QO00821J","","","0.71073","MoKα","","0.0954","0.0404","","","0.0583","0.0619","","","","","","0.954","","","","has coordinates","236157","2020-10-21","18:00:00",""
"1553911","11.2639","0.0012","15.6341","0.0017","13.7495","0.0015","90","","110.204","0.002","90","","2272.3","0.4","90","2","90","2","","","","","","","","6","P 1 21 1","P 2yb","4","","{7,16-bis[2-(prop-2-yn-1-yloxy)benzoyl]-5,14-dihydrodibenzo[b,i][1,4,8,11]tetraazacyclotetradecinato(2-)k^4^N} zinc(II)","","- C46 H50 N4 O8 S4 Zn -","- C46 H50 N4 O8 S4 Zn -","- C92 H100 N8 O16 S8 Zn2 -","2","1","","Zwoliński, K. M.; Sieroń, L.; Eilmes, J.","One-flask synthesis of dibenzotetraaza[14]annulene cyclic congeners bearing buta-1,3-diyne bridges","Organic Chemistry Frontiers","2018","5","2","171","","10.1039/C7QO00821J","","","0.71073","MoKα","","0.0275","0.0269","","","0.0703","0.0708","","","","","","1.011","","","","has coordinates,has disorder","236157","2020-10-21","18:00:00",""
"1553912","17.1209","0.001","6.8257","0.0005","14.2218","0.001","90","","100.2","0.003","90","","1635.72","0.19","150","2","150","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C3.8 H2.8 Br0.2 N0.2 O0.4 -","- C3.8 H2.8 Br0.2 N0.2 O0.4 -","- C76 H56 Br4 N4 O8 -","20","5","","Chen, Changjun; Pan, Yixiao; Zhao, Haoqiang; Xu, Xin; Xu, Jianbin; Zhang, Zongyao; Xi, Siqi; Xu, Lijin; Li, Huanrong","A versatile rhodium(iii) catalyst for direct acyloxylation of aryl and alkenyl C‒H bonds with carboxylic acids","Organic Chemistry Frontiers","2018","5","3","415","","10.1039/C7QO00844A","","","0.71073","MoKα","","0.048","0.0357","","","0.0917","0.0987","","","","","","1.016","","","","has coordinates","236159","2020-10-21","18:00:00",""
"1553913","8.581","0.0017","10.888","0.002","11.352","0.002","93.19","0.03","106.92","0.03","90.49","0.03","1012.8","0.4","194","2","194","2","","","","","","","","5","P -1","-P 1","2","","","","- C24 H28 N O2 Rh -","- C24 H28 N O2 Rh -","- C48 H56 N2 O4 Rh2 -","2","1","","Chen, Changjun; Pan, Yixiao; Zhao, Haoqiang; Xu, Xin; Xu, Jianbin; Zhang, Zongyao; Xi, Siqi; Xu, Lijin; Li, Huanrong","A versatile rhodium(iii) catalyst for direct acyloxylation of aryl and alkenyl C‒H bonds with carboxylic acids","Organic Chemistry Frontiers","2018","5","3","415","","10.1039/C7QO00844A","","","0.7201","","","0.0697","0.0601","","","0.1666","0.1888","","","","","","1.105","","","","has coordinates","236159","2020-10-21","18:00:00",""
"1553914","7.1832","0.001","10.3531","0.0016","12.7041","0.0018","99.499","0.006","102.356","0.006","98.881","0.005","892.4","0.2","150","2","150","2","","","","","","","","4","P -1","-P 1","2","","","","- C2.44 H1.78 N0.22 O0.22 -","- C2.44444 H1.77778 N0.222222 O0.222222 -","- C44 H32 N4 O4 -","18","9","","Chen, Changjun; Pan, Yixiao; Zhao, Haoqiang; Xu, Xin; Xu, Jianbin; Zhang, Zongyao; Xi, Siqi; Xu, Lijin; Li, Huanrong","A versatile rhodium(iii) catalyst for direct acyloxylation of aryl and alkenyl C‒H bonds with carboxylic acids","Organic Chemistry Frontiers","2018","5","3","415","","10.1039/C7QO00844A","","","0.71073","MoKα","","0.0429","0.0369","","","0.0949","0.0987","","","","","","1.052","","","","has coordinates","236159","2020-10-21","18:00:00",""
"1553915","30.962","0.005","10.076","0.0018","20.18","0.004","90","","121.016","0.004","90","","5395.5","1.7","205","","205","","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C29 H32 O3 -","- C29 H32 O3 -","- C232 H256 O24 -","8","1","","Liu, Lina; Yuan, Zhenbo; Pan, Rui; Zeng, Yuye; Lin, Aijun; Yao, Hequan; Huang, Yue","1,6-Conjugated addition-mediated [4 + 1] annulation: an approach to 2,3-dihydrobenzofurans","Organic Chemistry Frontiers","2018","5","4","623","","10.1039/C7QO00846E","","","0.71073","MoKα","","0.11","0.0602","","","0.1559","0.1836","","","","","","0.962","","","","has coordinates","236161","2020-10-21","18:00:00",""
"1553916","10.1754","0.0007","13.7004","0.0008","13.8309","0.001","119.49","0.007","102.929","0.006","92.342","0.005","1609.7","0.2","150","","150","","","","","","","","","5","P -1","-P 1","2","","","","- C17 H13 Cl N2 O4 -","- C17 H13 Cl N2 O4 -","- C68 H52 Cl4 N8 O16 -","4","2","","Daggupati, Ramana V.; Malapaka, Chandrasekharam","Cu(i)-Catalyzed amidation/imidation of N-arylglycine ester derivatives via C‒N coupling under mild conditions","Organic Chemistry Frontiers","2018","5","5","788","","10.1039/C7QO00851A","","x-ray","1.54184","CuKα","","0.057","0.0468","","","0.1497","0.1676","","","","","","1.1456","","","","has coordinates","236163","2020-10-21","18:00:00",""
"1553917","6.0881","0.0002","7.8709","0.0004","14.5993","0.0007","86.207","0.004","88.891","0.003","76.774","0.004","679.53","0.05","100.01","0.1","100.01","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C16 H15 N3 O2 -","- C16 H15 N3 O2 -","- C32 H30 N6 O4 -","2","1","","Zhu, Chuanle; Zeng, Hao; Chen, Fulin; Liu, Chi; Zhu, Rui; Wu, Wanqing; Jiang, Huanfeng","Copper-catalyzed coupling of oxime acetates and aryldiazonium salts: an azide-free strategy toward N-2-aryl-1,2,3-triazoles","Organic Chemistry Frontiers","2018","5","4","571","","10.1039/C7QO00874K","","x-ray","1.54184","CuKα","","0.0414","0.0396","","","0.1061","0.1077","","","","","","1.069","","","","has coordinates","236165","2020-10-21","18:00:00",""
"1553918","6.4301","0.0002","13.8923","0.0003","12.2241","0.0003","90","","103.031","0.002","90","","1063.85","0.05","150","2","150","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C28 H26 N2 -","- C28 H26 N2 -","- C56 H52 N4 -","2","0.5","","Grandl, Markus; Sun, Yu; Pammer, Frank","Electronic and structural properties of N →B-ladder boranes with high electron affinity","Organic Chemistry Frontiers","2018","5","3","336","","10.1039/C7QO00876G","","","1.54184","CuKα","","0.0444","0.0391","","","0.0983","0.1024","","","","","","1.063","","","","has coordinates","236167","2020-10-21","18:00:00",""
"1553919","9.0141","0.0007","12.9277","0.001","15.5179","0.0009","111.75","0.006","98.849","0.006","99.031","0.007","1613.9","0.2","150","2","150","2","","","","","","","","4","P -1","-P 1","2","","","","- C40 H54 B2 N2 -","- C40 H54 B2 N2 -","- C80 H108 B4 N4 -","2","1","","Grandl, Markus; Sun, Yu; Pammer, Frank","Electronic and structural properties of N →B-ladder boranes with high electron affinity","Organic Chemistry Frontiers","2018","5","3","336","","10.1039/C7QO00876G","","","0.71073","MoKα","","0.0891","0.0665","","","0.1693","0.1931","","","","","","1.05","","","","has coordinates","236167","2020-10-21","18:00:00",""
"1553920","17.2519","0.0002","10.4002","0.0001","18.7527","0.0002","90","","94.829","0.001","90","","3352.73","0.06","150","2","150","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C40 H54 B2 N2 -","- C40 H54 B2 N2 -","- C160 H216 B8 N8 -","4","1","","Grandl, Markus; Sun, Yu; Pammer, Frank","Electronic and structural properties of N →B-ladder boranes with high electron affinity","Organic Chemistry Frontiers","2018","5","3","336","","10.1039/C7QO00876G","","","1.54184","CuKα","","0.0727","0.0611","","","0.1623","0.17","","","","","","1.025","","","","has coordinates","236167","2020-10-21","18:00:00",""
"1553921","10.7137","0.0003","14.9388","0.0004","11.2075","0.0004","90","","101.824","0.003","90","","1755.7","0.09","150","2","150","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C44 H56 B2 N2 -","- C44 H56 B2 N2 -","- C88 H112 B4 N4 -","2","1","","Grandl, Markus; Sun, Yu; Pammer, Frank","Electronic and structural properties of N →B-ladder boranes with high electron affinity","Organic Chemistry Frontiers","2018","5","3","336","","10.1039/C7QO00876G","","","0.71073","MoKα","","0.0572","0.0464","","","0.096","0.1036","","","","","","1.039","","","","has coordinates","236167","2020-10-21","18:00:00",""
"1553922","13.3636","0.0003","12.765","0.0002","15.0491","0.0003","90","","111.844","0.002","90","","2382.85","0.09","150","2","150","2","","","","","","","","5","P 1 2/n 1","-P 2yac","13","","","","- C50 H29 B2 F20 N3 -","- C50 H29 B2 F20 N3 -","- C100 H58 B4 F40 N6 -","2","0.5","","Grandl, Markus; Sun, Yu; Pammer, Frank","Electronic and structural properties of N →B-ladder boranes with high electron affinity","Organic Chemistry Frontiers","2018","5","3","336","","10.1039/C7QO00876G","","","1.54184","CuKα","","0.0579","0.051","","","0.1688","0.1791","","","","","","1.094","","","","has coordinates","236167","2020-10-21","18:00:00",""
"1553923","11.196","0.005","13.488","0.007","19.102","0.011","102.11","0.02","104.06","0.02","108.18","0.02","2528","2","150","2","150","2","","","","","","","","5","P -1","-P 1","2","","","","- C60 H38 B2 F20 N2 -","- C60 H38 B2 F20 N2 -","- C120 H76 B4 F40 N4 -","2","1","","Grandl, Markus; Sun, Yu; Pammer, Frank","Electronic and structural properties of N →B-ladder boranes with high electron affinity","Organic Chemistry Frontiers","2018","5","3","336","","10.1039/C7QO00876G","","","0.71073","MoKα","","0.0487","0.041","","","0.0998","0.1044","","","","","","1.079","","","","has coordinates","236167","2020-10-21","18:00:00",""
"1553924","8.616","0.004","21.777","0.009","18.552","0.008","90","","100.259","0.009","90","","3425","3","296","2","296","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C35 H37 Cl2 N3 O4 S2 -","- C35 H37 Cl2 N3 O4 S2 -","- C140 H148 Cl8 N12 O16 S8 -","4","1","","Cao, Bo; Wei, Yin; Shi, Min","Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons","Organic Chemistry Frontiers","2018","5","3","423","","10.1039/C7QO00882A","","","0.71073","MoKα","","0.1275","0.054","","","0.1211","0.1549","","","","","","1.01","","","","has coordinates","236169","2020-10-21","18:00:00",""
"1553925","24.106","0.003","8.4201","0.001","20.584","0.002","90","","90","","90","","4178","0.8","293","2","293","2","","","","","","","","6","P n a 21","P 2c -2n","33","","","","- C8 H12 Cl Cu N4 O4 -","- C8 H12 Cl Cu N4 O4 -","- C96 H144 Cl12 Cu12 N48 O48 -","12","3","","Cao, Bo; Wei, Yin; Shi, Min","Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons","Organic Chemistry Frontiers","2018","5","3","423","","10.1039/C7QO00882A","","","0.71073","MoKα","","0.1417","0.0743","","","0.1769","0.2014","","","","","","0.846","","","","has coordinates","274176","2022-03-31","10:10:26",""
"1553926","33.342","0.003","14.1163","0.0013","13.8882","0.0014","90","","113.533","0.002","90","","5993","1","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C33 H33 N3 O4 S2 -","- C33 H33 N3 O4 S2 -","- C264 H264 N24 O32 S16 -","8","1","","Cao, Bo; Wei, Yin; Shi, Min","Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons","Organic Chemistry Frontiers","2018","5","3","423","","10.1039/C7QO00882A","","","0.71073","MoKα","","0.0784","0.0524","","","0.1319","0.1466","","","","","","1.046","","","","has coordinates","236169","2020-10-21","18:00:00",""
"1553927","20.618","0.002","12.7286","0.0014","11.5829","0.0013","90","","96.577","0.002","90","","3019.8","0.6","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C33 H33 N3 O4 S2 -","- C33 H33 N3 O4 S2 -","- C132 H132 N12 O16 S8 -","4","1","","Cao, Bo; Wei, Yin; Shi, Min","Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons","Organic Chemistry Frontiers","2018","5","3","423","","10.1039/C7QO00882A","","","0.71073","MoKα","","0.0574","0.0436","","","0.1133","0.1233","","","","","","1.027","","","","has coordinates","236169","2020-10-21","18:00:00",""
"1553928","16.4746","0.0007","9.1306","0.0003","19.2167","0.0008","90","","113.764","0.005","90","","2645.5","0.2","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C36 H29 N3 -","- C36 H29 N3 -","- C144 H116 N12 -","4","1","","Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.","A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones","Organic Chemistry Frontiers","2018","5","4","595","","10.1039/C7QO00888K","","","0.71073","MoKα","","0.0512","0.0406","","","0.0952","0.1024","","","","","","1.021","","","","has coordinates","236172","2020-10-21","18:00:00",""
"1553929","9.0006","0.0003","13.4106","0.0007","13.9272","0.0004","73.859","0.004","78.251","0.003","71.617","0.004","1519.94","0.11","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C40.35 H35.05 N3 O1.67 -","- C40.3506 H35.053 N3 O1.675 -","- C80.7012 H70.106 N6 O3.35 -","2","1","","Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.","A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones","Organic Chemistry Frontiers","2018","5","4","595","","10.1039/C7QO00888K","","x-ray","1.54184","CuKα","","0.06","0.0478","","","0.1249","0.1337","","","","","","1.04","","","","has coordinates,has disorder","236172","2020-10-21","18:00:00",""
"1553930","9.8591","0.0003","17.6789","0.0006","16.9614","0.0006","90","","96.753","0.003","90","","2935.83","0.17","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C39 H29 N3 O2 -","- C39 H29 N3 O2 -","- C156 H116 N12 O8 -","4","1","","Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.","A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones","Organic Chemistry Frontiers","2018","5","4","595","","10.1039/C7QO00888K","","","0.71073","MoKα","","0.0712","0.052","","","0.1152","0.1249","","","","","","1.021","","","","has coordinates,has disorder","236172","2020-10-21","18:00:00",""
"1553931","9.7752","0.0005","18.4617","0.0008","18.0848","0.0009","90","","102.389","0.005","90","","3187.7","0.3","100","2","100","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C43 H29 N3 -","- C43 H29 N3 -","- C172 H116 N12 -","4","1","","Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.","A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones","Organic Chemistry Frontiers","2018","5","4","595","","10.1039/C7QO00888K","","","0.71073","MoKα","","0.0534","0.0427","","","0.0926","0.0987","","","","","","1.017","","","","has coordinates","236172","2020-10-21","18:00:00",""
"1553932","9.9057","0.0003","18.2185","0.0005","17.9256","0.0005","90","","94.694","0.003","90","","3224.13","0.16","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C44 H31 N3 O -","- C44 H31 N3 O -","- C176 H124 N12 O4 -","4","1","","Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.","A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones","Organic Chemistry Frontiers","2018","5","4","595","","10.1039/C7QO00888K","","","0.71073","MoKα","","0.0596","0.0442","","","0.0951","0.1036","","","","","","1.014","","","","has coordinates","236172","2020-10-21","18:00:00",""
"1553933","9.9528","0.001","5.6608","0.0006","10.1737","0.0008","90","","119.444","0.007","90","","499.16","0.09","173","2","173","2","","","","","","","","4","P 1 c 1","P -2yc","7","","","","- C10 H15 N O3 -","- C10 H15 N O3 -","- C20 H30 N2 O6 -","2","1","","Peter, Clovis; Geoffroy, Philippe; Miesch, Michel","Highly diastereoselective access to polyfunctionalized 1,3-oxazines promoted by Brønsted/Lewis acids","Organic Chemistry Frontiers","2018","5","4","566","","10.1039/C7QO00891K","","","0.71073","MoKα","","0.0356","0.0326","","","0.0793","0.0816","","","","","","1.044","","","","has coordinates","236174","2020-10-21","18:00:00",""
"1553934","6.934","0.0005","9.4461","0.0008","12.5549","0.0011","77.759","0.001","76.1","0.001","88.981","0.002","779.63","0.11","298","2","298","2","","","","","","","","3","P -1","-P 1","2","","","","- C16 H14 O7 -","- C16 H14 O7 -","- C32 H28 O14 -","2","1","","Xu, Li-Chen; Zhou, Peng; Li, Jia-Zhuo; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo","Thiazolium salt-catalyzed [3 + 2 + 1] cyclization for the synthesis of trisubstituted 2-pyrones using arylglyoxals as a carbonyl source","Organic Chemistry Frontiers","2018","5","5","753","","10.1039/C7QO00899F","","","0.71073","MoKα","","0.1689","0.1071","","","0.2366","0.2612","","","","","","1.071","","","","has coordinates","236176","2020-10-21","18:00:00",""
"1553935","14.18","0.002","16.43","0.003","16.973","0.002","65.7","0.012","71.841","0.016","79.491","0.018","3417.8","1","173","2","173","2","","","","","","","","7","P -1","-P 1","2","","","","- C65 H63 F6 N8 O12 P S6 -","- C65 H63 F6 N8 O12 P S6 -","- C130 H126 F12 N16 O24 P2 S12 -","2","1","","Zhao, Meng-Yao; Guo, Qing-Hui; Wang, Mei-Xiang","Understanding the driving force for the molecular recognition of S6-corona[3]arene[3]pyridazine toward organic ammonium cations","Organic Chemistry Frontiers","2018","5","5","760","","10.1039/C7QO00900C","","","0.71073","MoKα","","0.1783","0.1451","","","0.32","0.3417","","","","","","1.207","","","","has coordinates,has disorder","236178","2020-10-21","18:00:00",""
"1553936","8.4287","0.0001","10.7538","0.0001","30.9419","0.0004","90","","90","","90","","2804.59","0.06","293","2","293","2","","","","","","","synthesis","7","P 21 21 21","P 2ac 2ab","19","","","","- C26 H28 Cl2 N3 O5 P Ru -","- C26 H28 Cl2 N3 O5 P Ru -","- C104 H112 Cl8 N12 O20 P4 Ru4 -","4","1","","de Julián, E.; Menéndez-Pedregal, E.; Claros, M.; Vaquero, M.; Díez, J.; Lastra, E.; Gamasa, P.; Pizzano, A.","Practical synthesis of enantiopure benzylamines by catalytic hydrogenation or transfer hydrogenation reactions in isopropanol using a Ru-pybox catalyst","Organic Chemistry Frontiers","2018","5","5","841","","10.1039/C7QO00908A","","","1.5418","CuKα","","0.053","0.0512","","","0.1296","0.1311","","","","","","1.069","","","","has coordinates","236180","2020-10-21","18:00:00",""
"1553937","28.3195","0.0004","28.3195","0.0004","8.539","0.0002","90","","90","","90","","6848.2","0.2","150","2","150","2","","","","","","","","7","P 4","P 4","75","","","","- C33 H30 Cl2 N3 O4 P Ru -","- C33 H30 Cl2 N3 O4 P Ru -","- C264 H240 Cl16 N24 O32 P8 Ru8 -","8","2","","de Julián, E.; Menéndez-Pedregal, E.; Claros, M.; Vaquero, M.; Díez, J.; Lastra, E.; Gamasa, P.; Pizzano, A.","Practical synthesis of enantiopure benzylamines by catalytic hydrogenation or transfer hydrogenation reactions in isopropanol using a Ru-pybox catalyst","Organic Chemistry Frontiers","2018","5","5","841","","10.1039/C7QO00908A","","x-ray","1.5418","CuKα","","0.0515","0.0432","","","0.1131","0.1184","","","","","","1.062","","","","has coordinates","236180","2020-10-21","18:00:00",""
"1553938","31.825","0.009","31.825","0.009","8.303","0.002","90","","90","","90","","8410","4","296","2","296.15","","","","","","","","","4","I 41 c d","I 4bw -2c","110","","","","- C27 H23 N3 O -","- C27 H23 N3 O -","- C432 H368 N48 O16 -","16","1","","Zhang, Chen; Pi, Junxia; Chen, Shu; Liu, Ping; Sun, Peipei","Construction of a 4H-pyrido[4,3,2-gh]phenanthridin-5(6H)-one skeleton via a catalyst-free radical cascade addition/cyclization using azo compounds as radical sources","Organic Chemistry Frontiers","2018","5","5","793","","10.1039/C7QO00926G","","","0.71073","MoKα","","0.0381","0.0329","","","0.0924","0.0969","","","","","","1.126","","","","has coordinates","236182","2020-10-21","18:00:00",""
"1553939","8.8464","0.0004","13.6195","0.0006","30.1026","0.0012","90","","90","","90","","3626.9","0.3","180","0.1","180","0.1","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C22 H22 Si -","- C22 H22 Si -","- C176 H176 Si8 -","8","1","","Yang, Qi; Liu, Liang; Chi, Yue; Hao, Wei; Zhang, Wen-Xiong; Xi, Zhenfeng","Rhodium-catalyzed intramolecular carbosilylation of alkynes via C(sp3)‒Si bond cleavage","Organic Chemistry Frontiers","2018","5","5","860","","10.1039/C7QO00927E","","x-ray","0.71073","MoKα","","0.04","0.0365","","","0.0977","0.1005","","","","","","1.034","","","","has coordinates","236184","2020-10-21","18:00:00",""
"1553940","12.2864","0.0007","9.5206","0.0006","14.4288","0.0008","90","","96.731","0.006","90","","1676.16","0.17","180","0.1","180","0.1","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C21 H20 Si -","- C21 H20 Si -","- C84 H80 Si4 -","4","1","","Yang, Qi; Liu, Liang; Chi, Yue; Hao, Wei; Zhang, Wen-Xiong; Xi, Zhenfeng","Rhodium-catalyzed intramolecular carbosilylation of alkynes via C(sp3)‒Si bond cleavage","Organic Chemistry Frontiers","2018","5","5","860","","10.1039/C7QO00927E","","","0.71073","MoKα","","0.0575","0.0407","","","0.0958","0.1069","","","","","","1.074","","","","has coordinates","236184","2020-10-21","18:00:00",""
"1553941","9.297","0.007","11.515","0.009","11.957","0.009","61.974","0.007","80.333","0.011","67.602","0.01","1044.6","1.4","296","2","296","2","","","","","","","","4","P 1","P 1","1","","","","- C23 H22 N2 O7 -","- C23 H22 N2 O7 -","- C46 H44 N4 O14 -","2","2","","Han, Jianxin; Niu, Sheng-Tong; Liu, Yushuang; Gan, Lishe; Wang, Tianfu; Lu, Chong-Dao; Yuan, Tao","Robustanoids A and B, two novel pyrrolo[2,3-b]indole alkaloids from Coffea canephora: isolation and total synthesis","Organic Chemistry Frontiers","2018","5","4","586","","10.1039/C7QO00931C","","","0.71073","MoKα","","0.0863","0.0699","","","0.1773","0.2","","","","","","1.028","","","","has coordinates","236186","2020-10-21","18:00:00",""
"1553942","7.483","0.002","12.28","0.004","13.156","0.004","73.055","0.004","75.131","0.005","76.779","0.005","1102.1","0.6","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C28 H21 N5 O -","- C28 H21 N5 O -","- C56 H42 N10 O2 -","2","1","","Gao, Qinghe; He, Shuang; Wu, Xia; Zhang, Jingjing; Bai, Suping; Wu, Yandong; Wu, Anxin","Selective access to dipyrazolo-fused pyridines via formal [3 + 2 + 1] heteroannulation of methyl ketones with pyrazol-5-amines","Organic Chemistry Frontiers","2018","5","5","765","","10.1039/C7QO00941K","","","0.71073","MoKα","","0.1131","0.0584","","","0.1352","0.1763","","","","","","0.885","","","","has coordinates","236188","2020-10-21","18:00:00",""
"1553943","9.6948","0.0002","10.6078","0.0003","14.8224","0.0004","105.266","0.001","103.77","0.002","93.623","0.002","1415.35","0.07","100","1","100","1","","","","","","","","5","P -1","-P 1","2","","","","- C83 H54 Cl2 N2 O2 -","- C83 H54 Cl2 N2 O2 -","- C83 H54 Cl2 N2 O2 -","1","0.5","","Marin, L.; Guillot, R.; Gandon, V.; Schulz, E.; Lebœuf, D.","A diversity-oriented synthesis of cyclopenta[b]pyrroles and related compounds through a calcium(ii)/copper(ii) catalytic sequence","Organic Chemistry Frontiers","2018","5","4","640","","10.1039/C7QO00948H","","","0.71073","MoKα","","0.0984","0.085","","","0.2379","0.2508","","","","","","1.043","","","","has coordinates","236189","2020-10-21","18:00:00",""
"1553944","14.1223","0.0005","10.4359","0.0003","19.4476","0.0006","90","","97.282","0.002","90","","2843.05","0.16","100","1","100","1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C34 H29 Cl2 N O3 -","- C34 H29 Cl2 N O3 -","- C136 H116 Cl8 N4 O12 -","4","1","","Marin, L.; Guillot, R.; Gandon, V.; Schulz, E.; Lebœuf, D.","A diversity-oriented synthesis of cyclopenta[b]pyrroles and related compounds through a calcium(ii)/copper(ii) catalytic sequence","Organic Chemistry Frontiers","2018","5","4","640","","10.1039/C7QO00948H","","","0.71073","MoKα","","0.1094","0.0556","","","0.1196","0.1434","","","","","","1.022","","","","has coordinates,has disorder","236189","2020-10-21","18:00:00",""
"1553945","6.18585","0.00012","19.014","0.0005","13.0299","0.0003","90","","104.086","0.0007","90","","1486.46","0.06","173","","173","","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C13 H9 Br Cl F4 N S -","- C13 H9 Br Cl F4 N S -","- C52 H36 Br4 Cl4 F16 N4 S4 -","4","1","","Das, Prajwalita; Takada, Masahiro; Tokunaga, Etsuko; Saito, Norimichi; Shibata, Norio","Synthesis of pyridine trans-tetrafluoro-λ6-sulfane derivatives via radical addition","Organic Chemistry Frontiers","2018","5","5","719","","10.1039/C7QO00994A","","","0.71075","MoKα","","","0.0243","","","","0.0607","","","","","","1.095","","","","has coordinates","236191","2020-10-21","18:00:00",""
"1553946","24.908","0.003","13.4385","0.0017","8.7528","0.0013","90","","93.042","0.006","90","","2925.7","0.7","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C16 H12 Cl N O2 S -","- C16 H12 Cl N O2 S -","- C128 H96 Cl8 N8 O16 S8 -","8","1","","Zhao, Lang; Liao, Wei-Wei","Pd-Catalyzed intramolecular C‒H addition to the cyano-group: construction of functionalized 2,3-fused thiophene scaffolds","Organic Chemistry Frontiers","2018","5","5","801","","10.1039/C7QO01000A","","","0.71073","MoKα","","0.0507","0.0406","","","0.0937","0.1023","","","","","","1.021","","","","has coordinates","236193","2020-10-21","18:00:00",""
"1553947","9.5527","0.0003","12.362","0.0005","12.0679","0.0005","90","","92.577","0.003","90","","1423.66","0.09","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","N-(8-quinolyl)-N-(2-tetrahydrofuranyl)propionamide","","- C16 H18 N2 O2 -","- C16 H18 N2 O2 -","- C64 H72 N8 O8 -","4","1","","Yue, Qiang; Xiao, Zhen; Ran, Ziyao; Yuan, Songdong; Zhang, Qian; Li, Dong","Copper-catalyzed α-C‒H amidation of simple ethers through C(sp3)‒H/N‒H cross dehydrogenative coupling","Organic Chemistry Frontiers","2018","5","6","967","","10.1039/C7QO01003F","","x-ray","1.54184","CuKα","","0.0642","0.048","","","0.1289","0.1442","","","","","","1.04","","","","has coordinates,has disorder","236195","2020-10-21","18:00:00",""
"1553948","13.1217","0.0007","8.2301","0.0004","15.9865","0.0009","90","","109.525","0.006","90","","1627.15","0.16","298","2","298","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C17 H15.5 N2 O3.5 S -","- C17 H15.5 N2 O3.5 S -","- C68 H62 N8 O14 S4 -","4","2","","Huang, Bing-Bing; Wu, Liang; Liu, Ren-Rong; Xing, Ling-Ling; Liang, Ren-Xiao; Jia, Yi-Xia","Enantioselective Friedel–Crafts C2-alkylation of 3-substituted indoles with trifluoropyruvates and cyclic N-sulfonyl α-ketiminoesters","Organic Chemistry Frontiers","2018","5","6","929","","10.1039/C7QO01014A","","","0.71073","MoKα","","0.0764","0.0593","","","0.1473","0.1627","","","","","","1.015","","","","has coordinates","274567","2022-04-19","14:22:36",""
"1553949","8.0275","0.0005","13.876","0.0008","31.686","0.003","90","","90","","90","","3529.5","0.4","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C19 H17 F3 N O3.5 -","- C19 H17 F3 N O3.5 -","- C152 H136 F24 N8 O28 -","8","2","","Huang, Bing-Bing; Wu, Liang; Liu, Ren-Rong; Xing, Ling-Ling; Liang, Ren-Xiao; Jia, Yi-Xia","Enantioselective Friedel–Crafts C2-alkylation of 3-substituted indoles with trifluoropyruvates and cyclic N-sulfonyl α-ketiminoesters","Organic Chemistry Frontiers","2018","5","6","929","","10.1039/C7QO01014A","","","0.71073","MoKα","","0.0494","0.0384","","","0.1104","0.1192","","","","","","0.853","","","","has coordinates","275434","2022-05-16","05:31:57",""
"1553950","10.4482","0.0002","7.41078","0.00018","13.6312","0.0004","90","","105.538","0.003","90","","1016.88","0.05","172.95","0.1","172.95","0.1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C28 H20 N4 -","- C28 H20 N4 -","- C56 H40 N8 -","2","0.5","","Qin, Wen-Bing; Li, Wei-Wei; Zhu, Peng-Fei; Mo, Xiao-Gang; Zhang, Hui-Jun; Wen, Ting-Bin","Rh(iii)-Catalyzed regio- and stereoselective bisindolylation of vinyl acetate: an efficient approach toward (E)-1,2-bis(2-indolyl)ethenes","Organic Chemistry Frontiers","2018","5","7","1096","","10.1039/C7QO01041A","","","1.54184","CuKα","","0.0309","0.03","","","0.0768","0.0778","","","","","","1.07","","","","has coordinates","236199","2020-10-21","18:00:00",""
"1553951","8.5997","0.0003","11.3141","0.0005","23.5957","0.0009","89.88","0.003","86.923","0.003","89.086","0.003","2292.21","0.16","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C25 H30 N2 O3.5 Rh -","- C25 H30 N2 O3.5 Rh -","- C100 H120 N8 O14 Rh4 -","4","2","","Qin, Wen-Bing; Li, Wei-Wei; Zhu, Peng-Fei; Mo, Xiao-Gang; Zhang, Hui-Jun; Wen, Ting-Bin","Rh(iii)-Catalyzed regio- and stereoselective bisindolylation of vinyl acetate: an efficient approach toward (E)-1,2-bis(2-indolyl)ethenes","Organic Chemistry Frontiers","2018","5","7","1096","","10.1039/C7QO01041A","","","1.54184","CuKα","","0.0587","0.056","","","0.1369","0.1411","","","","","","1.052","","","","has coordinates","236199","2020-10-21","18:00:00",""
"1553952","31.277","0.009","16.691","0.005","10.668","0.003","90","","93.503","0.006","90","","5559","3","296","2","296","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C24 H22 S6 Si2 -","- C24 H22 S6 Si2 -","- C192 H176 S48 Si16 -","8","1","","Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua","Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene","Organic Chemistry Frontiers","2018","5","8","1257","","10.1039/C7QO01049D","","","0.71073","MoKα","","0.1099","0.0642","","","0.1494","0.1644","","","","","","1.046","","","","has coordinates","236200","2020-10-21","18:00:00",""
"1553953","19.71","0.004","13.215","0.003","10.489","0.002","90","","103.753","0.003","90","","2653.7","1","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H20 S7 Si2 -","- C22 H20 S7 Si2 -","- C88 H80 S28 Si8 -","4","1","","Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua","Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene","Organic Chemistry Frontiers","2018","5","8","1257","","10.1039/C7QO01049D","","","0.71073","MoKα","","0.0446","0.0356","","","0.0985","0.1037","","","","","","1.087","","","","has coordinates","236200","2020-10-21","18:00:00",""
"1553954","12.594","0.005","7.353","0.003","15.175","0.006","90","","90","","90","","1405.3","1","296","2","296","2","","","","","","","","5","P n m a","-P 2ac 2n","62","","","","- C11 H11 Br S3 Si -","- C11 H11 Br S3 Si -","- C44 H44 Br4 S12 Si4 -","4","0.5","","Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua","Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene","Organic Chemistry Frontiers","2018","5","8","1257","","10.1039/C7QO01049D","","","0.71073","MoKα","","0.0414","0.0314","","","0.0795","0.0832","","","","","","1.018","","","","has coordinates","236200","2020-10-21","18:00:00",""
"1553955","11.5286","0.001","15.8164","0.0013","8.4588","0.0007","90","","110.19","0.001","90","","1447.6","0.2","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C11 H11 Br S3 Si -","- C11 H11 Br S3 Si -","- C44 H44 Br4 S12 Si4 -","4","1","","Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua","Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene","Organic Chemistry Frontiers","2018","5","8","1257","","10.1039/C7QO01049D","","","0.71073","MoKα","","0.0442","0.0296","","","0.0691","0.0751","","","","","","1.024","","","","has coordinates","236200","2020-10-21","18:00:00",""
"1553956","11.566","0.001","31.513","0.003","12.0437","0.001","90","","92.279","0.002","90","","4386.2","0.7","150","2","150","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C53 H49 Cl2 N3 O3 -","- C53 H49 Cl2 N3 O3 -","- C212 H196 Cl8 N12 O12 -","4","1","","Krishnan, Jagadeesh; Jose, Anu; Sasidhar, B. S.; Suresh, E.; Menon, Rajeev S.; Nair, Vijay","An uncommon multicomponent reaction involving nucleophilic heterocyclic carbenes: facile synthesis of fully substituted cyclopentanones","Organic Chemistry Frontiers","2018","5","7","1202","","10.1039/C7QO01051F","","","0.71073","MoKα","","0.1575","0.1192","","","0.199","0.2111","","","","","","1.286","","","","has coordinates","236202","2020-10-21","18:00:00",""
"1553957","29.069","0.003","16.647","0.0018","23.834","0.003","90","","124.203","0.002","90","","9538.8","1.9","150","2","150","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C50.5 H49 Cl I N3 O5 -","- C50.5 H49 Cl I N3 O5 -","- C404 H392 Cl8 I8 N24 O40 -","8","1","","Krishnan, Jagadeesh; Jose, Anu; Sasidhar, B. S.; Suresh, E.; Menon, Rajeev S.; Nair, Vijay","An uncommon multicomponent reaction involving nucleophilic heterocyclic carbenes: facile synthesis of fully substituted cyclopentanones","Organic Chemistry Frontiers","2018","5","7","1202","","10.1039/C7QO01051F","","","0.71073","MoKα","","0.0456","0.0367","","","0.0878","0.0913","","","","","","1.016","","","","has coordinates","236202","2020-10-21","18:00:00",""
"1553958","13.605","0.003","13.333","0.003","23.507","0.006","90","","101.393","0.006","90","","4180","1.7","150","2","150","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C52 H47 N3 O3 -","- C52 H47 N3 O3 -","- C208 H188 N12 O12 -","4","1","","Krishnan, Jagadeesh; Jose, Anu; Sasidhar, B. S.; Suresh, E.; Menon, Rajeev S.; Nair, Vijay","An uncommon multicomponent reaction involving nucleophilic heterocyclic carbenes: facile synthesis of fully substituted cyclopentanones","Organic Chemistry Frontiers","2018","5","7","1202","","10.1039/C7QO01051F","","","0.71073","MoKα","","0.165","0.0784","","","0.1391","0.1724","","","","","","0.999","","","","has coordinates","236202","2020-10-21","18:00:00",""
"1553959","7.6879","0.0003","13.3936","0.0005","15.696","0.0006","90","","103.359","0.001","90","","1572.46","0.1","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H19 N O2 -","- C20 H19 N O2 -","- C80 H76 N4 O8 -","4","1","","Chen, Wei; Zhang, Yicheng; Li, Pinhua; Wang, Lei","tert-Butyl peroxybenzoate mediated formation of 3-alkylated quinolines from N-propargylamines via a cascade radical addition/cyclization reaction","Organic Chemistry Frontiers","2018","5","5","855","","10.1039/C7QO01052D","","","0.71073","MoKα","","0.0535","0.0399","","","0.0985","0.1099","","","","","","1.034","","","","has coordinates","236204","2020-10-21","18:00:00",""
"1553960","12.074","0.003","22.964","0.006","17.711","0.005","90","","93.931","0.005","90","","4899","2","100","","100","","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C51 H51 Cl5 N4 O2 P2 Ru -","- C51 H51 Cl5 N4 O2 P2 Ru -","- C204 H204 Cl20 N16 O8 P8 Ru4 -","4","1","","Roy, Bivas Chandra; Debnath, Subhankar; Chakrabarti, Kaushik; Paul, Bhaskar; Maji, Milan; Kundu, Sabuj","ortho-Amino group functionalized 2,2′-bipyridine based Ru(ii) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols","Organic Chemistry Frontiers","2018","5","6","1008","","10.1039/C7QO01061C","","","0.71073","MoKα","","0.1545","0.0865","","","0.1957","0.2339","","","","","","1.137","","","","has coordinates","236206","2020-10-21","18:00:00",""
"1553961","24.447","0.006","12.95","0.003","7.9","0.0019","90","","90","","90","","2501.1","1","100","","100","","","","","","","","","7","P n a 21","P 2c -2n","33","","","","- C22 H28 Cl F6 N4 P Ru -","- C22 H28 Cl F6 N4 P Ru -","- C88 H112 Cl4 F24 N16 P4 Ru4 -","4","1","","Roy, Bivas Chandra; Debnath, Subhankar; Chakrabarti, Kaushik; Paul, Bhaskar; Maji, Milan; Kundu, Sabuj","ortho-Amino group functionalized 2,2′-bipyridine based Ru(ii) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols","Organic Chemistry Frontiers","2018","5","6","1008","","10.1039/C7QO01061C","","","0.71073","MoKα","","0.0411","0.0357","","","0.082","0.0865","","","","","","1.041","","","","has coordinates","236206","2020-10-21","18:00:00",""
"1553962","9.679","0.003","19.168","0.006","21.719","0.007","90","","91.489","0.006","90","","4028","2","100","","100","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C48 H44 Cl2 N4 P2 Ru -","- C48 H44 Cl2 N4 P2 Ru -","- C192 H176 Cl8 N16 P8 Ru4 -","4","1","","Roy, Bivas Chandra; Debnath, Subhankar; Chakrabarti, Kaushik; Paul, Bhaskar; Maji, Milan; Kundu, Sabuj","ortho-Amino group functionalized 2,2′-bipyridine based Ru(ii) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols","Organic Chemistry Frontiers","2018","5","6","1008","","10.1039/C7QO01061C","","","0.71073","MoKα","","0.1188","0.0606","","","0.1423","0.1855","","","","","","0.952","","","","has coordinates","236206","2020-10-21","18:00:00",""
"1553963","8.0484","0.0007","10.6055","0.0009","21.9053","0.0018","90","","90","","90","","1869.8","0.3","100","2","100","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C23 H21 N O2 S -","- C23 H21 N O2 S -","- C92 H84 N4 O8 S4 -","4","1","","Li, Yun; Chen, Jingchao; He, Zhenxiu; Qin, Hongyu; Zhou, Yongyun; Khan, Ruhima; Fan, Baomin","Cobalt-catalyzed asymmetric reactions of heterobicyclic alkenes with in situ generated organozinc halides","Organic Chemistry Frontiers","2018","5","7","1108","","10.1039/C7QO01064H","","","0.71073","MoKα","","0.0286","0.0274","","","0.0727","0.0736","","","","","","1.086","","","","has coordinates","236208","2020-10-21","18:00:00",""
"1553964","14.839","0.004","17.596","0.004","8.652","0.002","90","","90","","90","","2259.1","1","173","2","173.15","","","","","","","","","4","P 21 21 2","P 2 2ab","18","","","","- C26 H27 Br O3 -","- C26 H27 Br O3 -","- C104 H108 Br4 O12 -","4","1","","Li, Shoulei; Liu, Bin; Chen, Li; Li, Xin; Cheng, Jin-Pei","N-Heterocyclic carbene promoted enantioselective desymmetrization reaction of diarylalkane-bisphenols","Organic Chemistry Frontiers","2018","5","7","1101","","10.1039/C7QO01083D","","","0.71073","MoKα","","0.055","0.048","","","0.0846","0.0877","","","","","","1.101","","","","has coordinates","236210","2020-10-21","18:00:00",""
"1553965","4.3504","0.0004","24.437","0.002","8.5476","0.0007","90","","102.442","0.002","90","","887.36","0.13","153","2","153","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C10 H8 N4 -","- C10 H8 N4 -","- C40 H32 N16 -","4","1","","Qiao, Kai; Zhang, Dong; Zhang, Kai; Yuan, Xin; Zheng, Ming-Wei; Guo, Tian-Fo; Fang, Zheng; Wan, Li; Guo, Kai","Iron(ii)-catalyzed C-2 cyanomethylation of indoles and pyrroles via direct oxidative cross-dehydrogenative coupling with acetonitrile derivatives","Organic Chemistry Frontiers","2018","5","7","1129","","10.1039/C7QO01086A","","","0.71073","MoKα","","0.0481","0.0449","","","0.1151","0.1186","","","","","","1.058","","","","has coordinates","236212","2020-10-21","18:00:00",""
"1553966","9.4077","0.0015","9.9254","0.0016","17.562","0.003","90","","90","","90","","1639.9","0.5","293","","293.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","3-n-Butyl-4-phenyl-3,4-dihydro-2H-benzo[e][1,2]thiazine 1,1-dioxide","","- C18 H21 N O2 S -","- C18 H21 N O2 S -","- C72 H84 N4 O8 S4 -","4","1","","Song, Bo; Chen, Mu-Wang; Zhou, Yong-Gui","Synthesis of chiral sultams with two adjacent stereocenters via palladium-catalyzed dynamic kinetic resolution","Organic Chemistry Frontiers","2018","5","7","1113","","10.1039/C7QO01098B","","","0.71073","MoKα","","0.0932","0.0553","","","0.12","0.1375","","","","","","1.014","","","","has coordinates","236214","2020-10-21","18:00:00",""
"1553967","8.9388","0.0002","9.7832","0.0002","13.5584","0.0003","90","","107.86","0.003","90","","1128.54","0.05","294.5","0.7","294.5","0.7","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C15 H7 Cl F N O -","- C15 H7 Cl F N O -","- C60 H28 Cl4 F4 N4 O4 -","4","1","","Liu, Jianming; Yan, Xuyang; Liu, Na; Zhang, Yanyan; Zhao, Shufang; Wang, Xiaopei; Zhuo, Kelei; Yue, Yuanyuan","Elemental sulfur accelerated the reactivity of the 3-position of indole for the construction of chromeno[2,3-b]indoles","Organic Chemistry Frontiers","2018","5","6","1034","","10.1039/C7QO01114H","","x-ray","1.54184","CuKα","","0.0585","0.0567","","","0.141","0.1433","","","","","","1.047","","","","has coordinates","236215","2020-10-21","18:00:00",""
"1553968","9.2089","0.0003","10.5763","0.0004","10.9769","0.0004","100.503","0.003","95.221","0.003","91.16","0.003","1046.09","0.07","100","0.1","100","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C26 H27 N O3 -","- C26 H27 N O3 -","- C52 H54 N2 O6 -","2","1","","Luo, Hejiang; Liang, Renxiao; Chen, Lianfen; Jiang, Huanfeng; Zhu, Shifa","A silver-catalyzed three-component reaction via stabilized cation: synthesis of polysubstituted tetrahydronaphthols and tetrahydronaphthylamines","Organic Chemistry Frontiers","2018","5","7","1160","","10.1039/C7QO01122A","","x-ray","1.54184","CuKα","","0.0418","0.0398","","","0.102","0.1039","","","","","","1.044","","","","has coordinates","236218","2020-10-21","18:00:00",""
"1553969","8.9683","0.0005","9.8217","0.0005","11.353","0.0007","75.074","0.005","77.458","0.005","63.345","0.005","857.59","0.09","100","0.1","100","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C23 H19 F O2 -","- C23 H19 F O2 -","- C46 H38 F2 O4 -","2","1","","Luo, Hejiang; Liang, Renxiao; Chen, Lianfen; Jiang, Huanfeng; Zhu, Shifa","A silver-catalyzed three-component reaction via stabilized cation: synthesis of polysubstituted tetrahydronaphthols and tetrahydronaphthylamines","Organic Chemistry Frontiers","2018","5","7","1160","","10.1039/C7QO01122A","","x-ray","0.71073","MoKα","","0.0681","0.0489","","","0.1073","0.1198","","","","","","1.034","","","","has coordinates","236218","2020-10-21","18:00:00",""
"1553970","29.1539","0.0005","14.0671","0.0003","24.2333","0.0007","90","","126.156","0.001","90","","8024.4","0.3","190","2","190","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C64 H100 N4 Na4 O46 -","- C64 H84 N4 Na4 O46 -","- C256 H336 N16 Na16 O184 -","4","0.5","","Zhang, Yao; Yu, Shang-Bo; Yang, Bo; Wang, Hui; Zhang, Dan-Wei; Li, Zhan-Ting","Ion-pair electrostatic attraction-enhanced donor‒acceptor interactions between the prototypic 1,4-dialkoxybenzene-viologen binding mode in water","Organic Chemistry Frontiers","2018","5","6","1039","","10.1039/C7QO01126A","","","1.54178","CuKα","","0.1207","0.1053","","","0.2954","0.3094","","","","","","1.041","","","","has coordinates","236220","2020-10-21","18:00:00",""
"1553971","8.7382","0.0006","5.8569","0.0004","23.8346","0.0018","90","","91.141","0.001","90","","1219.58","0.15","298","2","298","2","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C10 H9 Br F N O4 S -","- C10 H9 Br F N O4 S -","- C40 H36 Br4 F4 N4 O16 S4 -","4","1","","Wang, Shi-Meng; Li, Chen; Leng, Jing; Bukhari, Syed Nasir Abbas; Qin, Hua-Li","Rhodium(iii)-catalyzed Oxidative Coupling of N-Methoxybenzamides and Ethenesulfonyl fluoride: a C‒H Bond Activation Strategy for the Preparation of 2-Aryl ethenesulfonyl fluorides and Sulfonyl fluoride Substituted γ-Lactams","Organic Chemistry Frontiers","2018","5","9","1411","","10.1039/C7QO01128H","","","0.71073","MoKα","","0.0627","0.0397","","","0.0926","0.0996","","","","","","1.043","","","","has coordinates","236222","2020-10-21","18:00:00",""
"1553972","8.6492","0.0009","6.7929","0.0008","25.645","0.003","90","","98.112","0.002","90","","1491.6","0.3","298","2","298","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C15 H11 F O5 S -","- C15 H11 F O5 S -","- C60 H44 F4 O20 S4 -","4","1","","Wang, Shi-Meng; Li, Chen; Leng, Jing; Bukhari, Syed Nasir Abbas; Qin, Hua-Li","Rhodium(iii)-catalyzed Oxidative Coupling of N-Methoxybenzamides and Ethenesulfonyl fluoride: a C‒H Bond Activation Strategy for the Preparation of 2-Aryl ethenesulfonyl fluorides and Sulfonyl fluoride Substituted γ-Lactams","Organic Chemistry Frontiers","2018","5","9","1411","","10.1039/C7QO01128H","","","0.71073","MoKα","","0.1039","0.0813","","","0.216","0.2291","","","","","","1.053","","","","has coordinates","236222","2020-10-21","18:00:00",""
"1553973","12.062","0.003","4.0452","0.0009","21.707","0.005","90","","90.12","0.02","90","","1059.2","0.4","294","2","294","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C12 H10 Br N O -","- C12 H10 Br N O -","- C48 H40 Br4 N4 O4 -","4","1","","Reddy, Ganapam Manohar; Rao, Naidu Sambasiva; Maheswaran, H.","Highly meta-selective halogenation of 2-phenylpyridine with a ruthenium(i) catalyst","Organic Chemistry Frontiers","2018","5","7","1118","","10.1039/C7QO01133D","","","0.71073","MoKα","","0.1009","0.0419","","","0.076","0.0864","","","","","","0.776","","","","has coordinates","236224","2020-10-21","18:00:00",""
"1553974","8.799","0.0004","14.7395","0.0006","16.0279","0.0006","90","","90","","90","","2078.7","0.15","200","2","200","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C24 H25 Cl2 N O -","- C24 H25 Cl2 N O -","- C96 H100 Cl8 N4 O4 -","4","1","","Zheng, Long-Sheng; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie","Ruthenium-catalyzed dynamic kinetic asymmetric transfer hydrogenation: stereoselective access to syn 2-(1,2,3,4-tetrahydro-1-isoquinolyl)ethanol derivatives","Organic Chemistry Frontiers","2018","5","8","1366","","10.1039/C7QO01142C","","","1.54178","CuKα","","0.0259","0.0253","","","0.0677","0.0683","","","","","","1.026","","","","has coordinates","236225","2020-10-21","18:00:00",""
"1553975","5.6782","0.0002","8.5568","0.0003","38.5091","0.001","90","","90","","90","","1871.05","0.1","200","1","200","1","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C22 H23 N O S -","- C22 H23 N O S -","- C88 H92 N4 O4 S4 -","4","1","","Zheng, Long-Sheng; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie","Ruthenium-catalyzed dynamic kinetic asymmetric transfer hydrogenation: stereoselective access to syn 2-(1,2,3,4-tetrahydro-1-isoquinolyl)ethanol derivatives","Organic Chemistry Frontiers","2018","5","8","1366","","10.1039/C7QO01142C","","","1.54178","CuKα","","0.042","0.0371","","","0.0905","0.0934","","","","","","1.047","","","","has coordinates","236225","2020-10-21","18:00:00",""
"1553976","10.5329","0.0009","10.3187","0.0008","18.4305","0.0016","90","","97.847","0.002","90","","1984.4","0.3","120","2","120","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H20 N4 O4 -","- C21 H20 N4 O4 -","- C84 H80 N16 O16 -","4","1","","Cao, Wen-Bin; Liu, Bei-Bei; Xu, Xiao-Ping; Ji, Shun-Jun","Cooperation of copper and dioxygen for the site-selective construction of benzo[1,5]diazocin-6(5H)-ones from indoles and enaminone analogues","Organic Chemistry Frontiers","2018","5","7","1194","","10.1039/C7QO01154G","","","0.71073","MoKα","","0.126","0.065","","","0.1819","0.2811","","","","","","1.003","","","","has coordinates","236227","2020-10-21","18:00:00",""
"1553977","11.9446","0.0012","13.7058","0.0014","19.238","0.002","90","","90","","90","","3149.5","0.6","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C34 H28 N O6 P S -","- C34 H28 N O6 P S -","- C136 H112 N4 O24 P4 S4 -","4","1","","Gu, Zheng; Zhou, Ji; Jiang, Guo-Fang; Zhou, Yong-Gui","Synthesis of chiral γ-aminophosphonates through the organocatalytic hydrophosphonylation of azadienes with phosphites","Organic Chemistry Frontiers","2018","5","7","1148","","10.1039/C7QO01158J","","","0.71073","MoKα","","0.0462","0.0322","","","0.0789","0.0874","","","","","","1.038","","","","has coordinates","236229","2020-10-21","18:00:00",""
"1553978","7.9384","0.0009","9.9744","0.0012","17.126","0.002","90","","90","","90","","1356","0.3","294","2","294","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C18 H18 O2 -","- C18 H18 O2 -","- C72 H72 O8 -","4","1","","Someswarao, B.; P., Rasvan Khan; Reddy, B. Jagan Mohan; B., Sridhar; B., V. Subba Reddy","Tandem Prins-type cyclization for the stereoselective construction of fused polycyclic ring systems","Organic Chemistry Frontiers","2018","5","8","1320","","10.1039/C7QO01164D","","","0.71073","MoKα","","0.0732","0.0717","","","0.1684","0.1693","","","","","","1.246","","","","has coordinates","236231","2020-10-21","18:00:00",""
"1553979","12.6396","0.001","9.6186","0.0008","11.8318","0.0009","90","","103.394","0.001","90","","1399.33","0.19","294","2","294","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C18 H18 O3 -","- C18 H18 O3 -","- C72 H72 O12 -","4","1","","Someswarao, B.; P., Rasvan Khan; Reddy, B. Jagan Mohan; B., Sridhar; B., V. Subba Reddy","Tandem Prins-type cyclization for the stereoselective construction of fused polycyclic ring systems","Organic Chemistry Frontiers","2018","5","8","1320","","10.1039/C7QO01164D","","","0.71073","MoKα","","0.0521","0.0445","","","0.1237","0.1298","","","","","","1.034","","","","has coordinates","236231","2020-10-21","18:00:00",""
"1553980","13.13","0.04","12.87","0.04","7.8","0.02","90","","105.51","0.02","90","","1270","6","294","2","294","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C14 H15 N O4 -","- C14 H15 N O4 -","- C56 H60 N4 O16 -","4","1","","Someswarao, B.; P., Rasvan Khan; Reddy, B. Jagan Mohan; B., Sridhar; B., V. Subba Reddy","Tandem Prins-type cyclization for the stereoselective construction of fused polycyclic ring systems","Organic Chemistry Frontiers","2018","5","8","1320","","10.1039/C7QO01164D","","","0.71073","MoKα","","0.1204","0.067","","","0.1725","0.2015","","","","","","1.032","","","","has coordinates","236231","2020-10-21","18:00:00",""
"1554253","8.8119","0.0001","10.4134","0.0001","27.1396","0.0003","90","","90","","90","","2490.38","0.05","293","2","293","2","","","","","","","","7","P 21 21 21","P 2ac 2ab","19","","","","- C25 H21 Br F3 N3 O4 S -","- C25 H21 Br F3 N3 O4 S -","- C100 H84 Br4 F12 N12 O16 S4 -","4","1","","Zhu, Wen-Run; Chen, Qing; Lin, Ning; Chen, Kai-Bin; Zhang, Zhen-Wei; Fang, Gang; Weng, Jiang; Lu, Gui","Organocatalytic Michael/cyclization cascade reactions of 3-isothiocyanato oxindoles with 3-trifluoroethylidene oxindoles: an approach for the synthesis of 3′-trifluoromethyl substituted 3,2′-pyrrolidinyl-bispirooxindoles","Organic Chemistry Frontiers","2018","5","8","1375","","10.1039/C8QO00044A","","","1.54178","CuKα","","0.0329","0.0312","","","0.0763","0.0774","","","","","","1.031","","","","has coordinates","237067","2020-10-21","18:00:00",""
"1554254","13.986","0.0008","14.019","0.0008","28.0285","0.0013","98.119","0.003","91.053","0.003","90.157","0.003","5439.5","0.5","273","2","273","2","","","","","","","","3","P 1","P 1","1","","","","- C28 H36 O8 -","- C28 H36 O8 -","- C224 H288 O64 -","8","8","","Yin, Guo-Ping; Wu, Ya-Rong; Han, Chao; Wang, Xiao-Bing; Gao, Hong-Liang; Yin, Yong; Kong, Ling-Yi; Yang, Ming-Hua","Asperones A‒E, five dimeric polyketides with new carbon skeletons from the fungus Aspergillus sp. AWG 1‒15","Organic Chemistry Frontiers","2018","5","16","2432","","10.1039/C8QO00070K","","","1.54178","CuKα","","0.1592","0.1102","","","0.2928","0.3537","","","","","","1.147","","","","has coordinates","237068","2020-10-21","18:00:00",""
"1554255","8.3949","0.0009","15.0525","0.0016","22.267","0.002","90","","90","","90","","2813.8","0.5","173","","173","","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","15-13","","- C28 H38 O9 -","- C28 H38 O9 -","- C112 H152 O36 -","4","1","","Yin, Guo-Ping; Wu, Ya-Rong; Han, Chao; Wang, Xiao-Bing; Gao, Hong-Liang; Yin, Yong; Kong, Ling-Yi; Yang, Ming-Hua","Asperones A‒E, five dimeric polyketides with new carbon skeletons from the fungus Aspergillus sp. AWG 1‒15","Organic Chemistry Frontiers","2018","5","16","2432","","10.1039/C8QO00070K","","","1.54178","CuKα","","0.0338","0.0326","","","0.0864","0.0873","","","","","","1.052","","","","has coordinates","237068","2020-10-21","18:00:00",""
"1554256","9.34542","0.00007","14.58845","0.00013","24.65138","0.00016","90","","90","","90","","3360.85","0.04","100.01","0.1","100.01","0.1","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","Lithocarpin C","W-55","","- C37 H42 O11 -","- C37 H42 O11 -","- C148 H168 O44 -","4","1","","Xu, Jianlin; Tan, Haibo; Chen, Yuchan; Li, Saini; Huang, Zilei; Guo, Heng; Li, Haohua; Gao, Xiaoxia; Liu, Hongxin; Zhang, Weimin","Lithocarpins A‒D: four tenellone-macrolide conjugated [4 + 2] hetero-adducts from the deep-sea derived fungus Phomopsis lithocarpus FS508","Organic Chemistry Frontiers","2018","5","11","1792","","10.1039/C8QO00095F","","x-ray","1.54184","CuKα","","0.0349","0.034","","","0.0889","0.0897","","","","","","1.047","","","","has coordinates","237071","2020-10-21","18:00:00",""
"1554257","12.0999","0.0003","8.9388","0.0002","17.0397","0.0004","90","","90.378","0.002","90","","1842.95","0.08","100","0.1","100","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","Lithocarpin A","w-36","","- C38 H43 Cl3 O11 -","- C38 H43 Cl3 O11 -","- C76 H86 Cl6 O22 -","2","1","","Xu, Jianlin; Tan, Haibo; Chen, Yuchan; Li, Saini; Huang, Zilei; Guo, Heng; Li, Haohua; Gao, Xiaoxia; Liu, Hongxin; Zhang, Weimin","Lithocarpins A‒D: four tenellone-macrolide conjugated [4 + 2] hetero-adducts from the deep-sea derived fungus Phomopsis lithocarpus FS508","Organic Chemistry Frontiers","2018","5","11","1792","","10.1039/C8QO00095F","","x-ray","1.54184","CuKα","","0.094","0.0906","","","0.2611","0.265","","","","","","1.036","","","","has coordinates,has disorder","237071","2020-10-21","18:00:00",""
"1554258","8.8203","0.0001","9.95","0.0002","11.3663","0.0002","90","","104.882","0.002","90","","964.07","0.03","100","0.1","100","0.1","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C21 H28 O4 -","- C21 H28 O4 -","- C42 H56 O8 -","2","1","","Hu, Li-Jun; Cheng, Min-Jing; Cao, Jia-Qing; Zhong, Li-Ping; Hu, Ya-Jian; Wang, Ying; Wang, Lei; Ye, Wen-Cai; Li, Chuang-Chuang","Asymmetric total syntheses of callistrilones B, G and J","Organic Chemistry Frontiers","2018","5","9","1506","","10.1039/C8QO00130H","","x-ray","1.54178","CuKα","","0.03","0.0298","","","0.0801","0.0804","","","","","","1.046","","","","has coordinates","237073","2020-10-21","18:00:00",""
"1554259","9.56","0.001","10.76","0.003","11.542","0.003","89.84","0.03","78.84","0.02","80.4","0.02","1148","0.5","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","{2-[3-Ethoxy-2-(methoxymethoxy)phenyl]cyclopropane-1,1-diyl}bis(phenylmethanone)","","- C27 H26 O5 -","- C27 H26 O5 -","- C54 H52 O10 -","2","1","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","1.54178","CuKα","","0.0904","0.0459","","","0.1151","0.1363","","","","","","1.04","","","","has coordinates","237075","2020-10-21","18:00:00",""
"1554260","5.565","0.001","17.417","0.006","19.97","0.005","90","","90","","90","","1935.6","0.9","293","2","293","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","9-Methyl-8,10-dioxatricyclo[7.2.1.02,7]dodeca-2,4,6-trien-4-amine","","- C11 H13 N O2 -","- C11 H13 N O2 -","- C88 H104 N8 O16 -","8","1","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","1.54178","CuKα","","0.0728","0.0429","","","0.102","0.1167","","","","","","1.1","","","","has coordinates","237075","2020-10-21","18:00:00",""
"1554261","10.139","0.003","10.399","0.006","14.357","0.005","80.36","0.04","69.86","0.03","89.98","0.04","1398.4","1.1","298","2","298","2","","","","","","","","4","P -1","-P 1","2","","","","- C15 H21 N O2 -","- C15 H21 N O2 -","- C60 H84 N4 O8 -","4","2","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","0.71073","MoKα","","0.141","0.056","","","0.1299","0.1632","","","","","","1.01","","","","has coordinates,has disorder","237075","2020-10-21","18:00:00",""
"1554262","9.9233","0.0007","15.1382","0.001","8.9089","0.0006","90","","105.815","0.001","90","","1287.64","0.15","120","2","120","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","4-Bromo-6-ethoxy-9-methyl-8,10-dioxatricyclo[7.2.1.02,7]dodeca-2,4,6-triene","","- C13 H15 Br O3 -","- C13 H15 Br O3 -","- C52 H60 Br4 O12 -","4","1","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","0.71073","MoKα","","0.0323","0.0251","","","0.0596","0.0618","","","","","","1.052","","","","has coordinates","237075","2020-10-21","18:00:00",""
"1554263","8.638","0.003","15.409","0.007","8.594","0.002","90","","111.43","0.02","90","","1064.8","0.7","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","6-Methoxy-9-methyl-8,10-dioxatricyclo[7.2.1.02,7]dodeca-2,4,6-triene","","- C12 H14 O3 -","- C12 H14 O3 -","- C48 H56 O12 -","4","1","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","0.71073","MoKα","","0.072","0.0393","","","0.0928","0.1071","","","","","","1.02","","","","has coordinates","237075","2020-10-21","18:00:00",""
"1554264","9.944","0.005","16.675","0.008","15.179","0.007","90","","108.38","0.04","90","","2389","2","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","1-[4-(2-Hydroxyphenyl)-2-methyl-4,5-dihydrofuran-3-yl]ethanone","","- C13 H14 O3 -","- C13 H14 O3 -","- C104 H112 O24 -","8","2","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","1.54178","CuKα","","0.1516","0.0589","","","0.1474","0.1892","","","","","","0.995","","","","has coordinates","237075","2020-10-21","18:00:00",""
"1554265","7.1922","0.0006","9.9323","0.0008","16.0391","0.0013","78.066","0.001","84.732","0.001","86.302","0.001","1115.04","0.16","120","2","120","2","","","","","","","","3","P -1","-P 1","2","","{4-[3-Ethoxy-2-(methoxymethoxy)phenyl]-2-phenyl-4,5-dihydrofuran-3-yl}(phenyl)methanone","","- C27 H26 O5 -","- C27 H26 O5 -","- C54 H52 O10 -","2","1","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","0.71073","MoKα","","0.0562","0.0423","","","0.1006","0.109","","","","","","1.029","","","","has coordinates","237075","2020-10-21","18:00:00",""
"1554266","9.9599","0.0006","6.7335","0.0004","20.4059","0.0012","90","","93.522","0.001","90","","1365.94","0.14","120","2","120","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","Methyl 4-[2-(methoxymethoxy)phenyl]-2-methyl-4,5-dihydrofuran-3-carboxylate","","- C15 H18 O5 -","- C15 H18 O5 -","- C60 H72 O20 -","4","1","","Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.","Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans","Organic Chemistry Frontiers","2018","5","10","1655","","10.1039/C8QO00132D","","","0.71073","MoKα","","0.0419","0.0365","","","0.0952","0.0994","","","","","","1.032","","","","has coordinates","237075","2020-10-21","18:00:00",""
"1554267","8.2403","0.0004","11.2635","0.0005","11.6154","0.0007","80.692","0.004","75.701","0.005","83.849","0.004","1028.38","0.1","293","2","293.15","","","","","","","","","3","P -1","-P 1","2","","","","- C23 H32 O6 -","- C23 H32 O6 -","- C46 H64 O12 -","2","1","","Liu, Mengchen; Cheng, Chuanxu; Xiong, Weiyan; Cheng, Hang; Wang, Jian-Li; Xu, Liang","Total synthesis of C19-diterpenoid alkaloid: construction of a functionalized ABCDE-ring system","Organic Chemistry Frontiers","2018","5","9","1502","","10.1039/C8QO00143J","","x-ray","0.71073","MoKα","","0.0702","0.0474","","","0.1041","0.1173","","","","","","1.029","","","","has coordinates","237078","2020-10-21","18:00:00",""
"1554268","10.8545","0.0006","11.1988","0.0004","10.9655","0.0006","90","","117.846","0.007","90","","1178.59","0.13","293","2","293.15","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C13 H20 O4 -","- C13 H20 O4 -","- C52 H80 O16 -","4","1","","Liu, Mengchen; Cheng, Chuanxu; Xiong, Weiyan; Cheng, Hang; Wang, Jian-Li; Xu, Liang","Total synthesis of C19-diterpenoid alkaloid: construction of a functionalized ABCDE-ring system","Organic Chemistry Frontiers","2018","5","9","1502","","10.1039/C8QO00143J","","","0.7107","MoKα","","0.0516","0.0402","","","0.0916","0.1002","","","","","","1.025","","","","has coordinates","237078","2020-10-21","18:00:00",""
"1554269","13.7347","0.0009","21.989","0.0014","13.7372","0.0011","90","","110.63","0.007","90","","3882.8","0.5","150","2","150","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C76 H104 O26 S3 -","- C76 H84 O26 S3 -","- C152 H168 O52 S6 -","2","1","","Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun","Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity","Organic Chemistry Frontiers","2018","5","7","1079","","10.1039/C8QO00154E","","","1.54178","CuKα","","0.1566","0.1161","","","0.2152","0.2368","","","","","","1.02","","","","has coordinates,has disorder","237081","2020-10-21","18:00:00",""
"1554270","10.70154","0.00011","27.4281","0.0003","26.4591","0.0003","90","","90","","90","","7766.35","0.15","150","2","150.15","","","","","","","","","4","C 2 2 21","C 2c 2","20","","","","- C78 H96 N4 O22 -","- C78 H96 N4 O22 -","- C312 H384 N16 O88 -","4","0.5","","Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun","Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity","Organic Chemistry Frontiers","2018","5","7","1079","","10.1039/C8QO00154E","","x-ray","1.54178","CuKα","","0.0776","0.0757","","","0.2014","0.204","","","","","","1.05","","","","has coordinates,has disorder","237081","2020-10-21","18:00:00",""
"1554271","9.18292","0.00014","12.4621","0.0002","28.4369","0.0005","90","","90","","90","","3254.28","0.09","150","2","150","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C35 H44 O12 -","- C35 H44 O12 -","- C140 H176 O48 -","4","1","","Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun","Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity","Organic Chemistry Frontiers","2018","5","7","1079","","10.1039/C8QO00154E","","x-ray","1.54184","CuKα","","0.0272","0.0268","","","0.0674","0.0677","","","","","","1.076","","","","has coordinates","237081","2020-10-21","18:00:00",""
"1554272","15.8696","0.0006","16.1185","0.0005","32.0556","0.0007","90","","90","","90","","8199.6","0.4","123","2","123","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C74 H90 Cl12 O24 -","- C74 H90 Cl12 O24 -","- C296 H360 Cl48 O96 -","4","1","","Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun","Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity","Organic Chemistry Frontiers","2018","5","7","1079","","10.1039/C8QO00154E","","","1.54178","CuKα","","0.0957","0.0812","","","0.1738","0.1837","","","","","","1.003","","","","has coordinates,has disorder","237081","2020-10-21","18:00:00",""
"1554273","10.54064","0.00016","14.6009","0.0003","14.9312","0.0002","62.0192","0.0018","84.9082","0.0013","68.8864","0.0016","1884.1","0.07","293","2","293","2","","","","","","","","4","P 1","P 1","1","","","","- C77.37 H93.1 N4 O24 -","- C77.364 H93.132 N4 O24 -","- C77.364 H93.132 N4 O24 -","1","1","","Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun","Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity","Organic Chemistry Frontiers","2018","5","7","1079","","10.1039/C8QO00154E","","","1.54184","CuKα","","0.051","0.0506","","","0.1346","0.135","","","","","","1.02","","","","has coordinates,has disorder","237081","2020-10-21","18:00:00",""
"1554274","15.2487","0.0011","16.1229","0.0011","29.1352","0.0019","90","","90","","90","","7163","0.9","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C74 H91 N2 O24 -","- C74 H91 N2 O24 -","- C296 H364 N8 O96 -","4","1","","Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun","Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity","Organic Chemistry Frontiers","2018","5","7","1079","","10.1039/C8QO00154E","","","0.71073","MoKα","","0.0842","0.0548","","","0.1445","0.1638","","","","","","1.026","","","","has coordinates,has disorder","237081","2020-10-21","18:00:00",""
"1554275","14.7018","0.0001","14.7018","0.0001","53.2893","0.0002","90","","90","","120","","9974.97","0.1","293","2","293","2","","","","","","","","3","P 65","P 65","170","","","","- C70 H84 O24 -","- C70 H84 O24 -","- C420 H504 O144 -","6","1","","Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun","Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity","Organic Chemistry Frontiers","2018","5","7","1079","","10.1039/C8QO00154E","","","1.54178","CuKα","","0.0736","0.0724","","","0.2119","0.2145","","","","","","1.026","","","","has coordinates,has disorder","237081","2020-10-21","18:00:00",""
"1554276","13.3662","0.0008","19.3514","0.0012","18.2778","0.0011","90","","107.451","0.002","90","","4510","0.5","300","2","300.15","","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C42 H49 Cl2 N3 O3 Ru S -","- C42 H49 Cl2 N3 O3 Ru S -","- C168 H196 Cl8 N12 O12 Ru4 S4 -","4","1","","Sabbasani, Venkata R.; Gupta, Saswata; Young Yun, Sang; Lee, Daesung","A general approach for the formation of oxygen-chelated ruthenium alkylidene complexes relying on the Thorpe‒Ingold effect","Organic Chemistry Frontiers","2018","5","9","1532","","10.1039/C8QO00160J","","","0.71073","MoKα","","0.0556","0.0425","","","0.1139","0.1226","","","","","","1.0356","","","","has coordinates","237085","2020-10-21","18:00:00",""
"1554277","14.573","0.01","14.783","0.01","16.116","0.01","90","","104.49","0.02","90","","3361","4","300","2","300.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C33 H46 Cl2 N2 O Ru -","- C33 H46 Cl2 N2 O Ru -","- C132 H184 Cl8 N8 O4 Ru4 -","4","1","","Sabbasani, Venkata R.; Gupta, Saswata; Young Yun, Sang; Lee, Daesung","A general approach for the formation of oxygen-chelated ruthenium alkylidene complexes relying on the Thorpe‒Ingold effect","Organic Chemistry Frontiers","2018","5","9","1532","","10.1039/C8QO00160J","","","0.71073","MoKα","","0.1839","0.1163","","","0.279","0.3651","","","","","","1.281","","","","has coordinates","237088","2020-10-21","18:00:00",""
"1554278","26.317","0.004","17.57","0.002","17.431","0.002","90","","110.1","0.004","90","","7569","1.7","200","2","200.15","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C36 H44 Cl2 N2 O Ru -","- C36 H44 Cl2 N2 O Ru -","- C288 H352 Cl16 N16 O8 Ru8 -","8","1","","Sabbasani, Venkata R.; Gupta, Saswata; Young Yun, Sang; Lee, Daesung","A general approach for the formation of oxygen-chelated ruthenium alkylidene complexes relying on the Thorpe‒Ingold effect","Organic Chemistry Frontiers","2018","5","9","1532","","10.1039/C8QO00160J","","","0.71073","MoKα","","0.0528","0.0417","","","0.1117","0.124","","","","","","1.08","","","","has coordinates","237088","2020-10-21","18:00:00",""
"1554279","17.5111","0.0007","18.0998","0.0006","8.8623","0.0003","90","","98.023","0.004","90","","2781.39","0.17","291.74","0.1","291.74","0.1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C16 H9 N5 -","- C16 H9 N5 -","- C128 H72 N40 -","8","2","","Xin, Jing-Rui; He, Yan-Hong; Guan, Zhi","Metal-free aerobic oxidative direct C‒H amination of electron-deficient alkenes via photoredox catalysis","Organic Chemistry Frontiers","2018","5","10","1684","","10.1039/C8QO00161H","","x-ray","1.54184","CuKα","","0.0739","0.0585","","","0.2017","0.2344","","","","","","1.092","","","","has coordinates","237090","2020-10-21","18:00:00",""
"1554280","16.9028","0.0008","16.5253","0.0007","9.9901","0.0004","90","","90","","90","","2790.5","0.2","100","2","100","2","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C20 H14 N2 O2 -","- C20 H14 N2 O2 -","- C160 H112 N16 O16 -","8","2","","Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian","Photo-induced C‒H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives","Organic Chemistry Frontiers","2018","5","10","1679","","10.1039/C8QO00183A","","","0.71073","MoKα","","0.0688","0.0592","","","0.1431","0.1482","","","","","","1.597","","","","has coordinates,has disorder","237093","2020-10-21","18:00:00",""
"1554281","13.3145","0.0004","13.4792","0.0004","7.0709","0.0002","90","","93.942","0.001","90","","1266","0.06","100","2","100","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C9 H6 N O -","- C9 H6 N O -","- C72 H48 N8 O8 -","8","1","","Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian","Photo-induced C‒H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives","Organic Chemistry Frontiers","2018","5","10","1679","","10.1039/C8QO00183A","","","1.54178","CuKα","","0.0413","0.0383","","","0.1095","0.1143","","","","","","1.092","","","","has coordinates","237093","2020-10-21","18:00:00",""
"1554282","17.23","0.003","8.7235","0.0016","9.6499","0.0018","90","","90","","90","","1450.4","0.5","100","2","100","2","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C20 H16 N2 O2 -","- C20 H16 N2 O2 -","- C80 H64 N8 O8 -","4","1","","Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian","Photo-induced C‒H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives","Organic Chemistry Frontiers","2018","5","10","1679","","10.1039/C8QO00183A","","","0.71073","MoKα","","0.0518","0.0476","","","0.1125","0.1155","","","","","","1.062","","","","has coordinates","237093","2020-10-21","18:00:00",""
"1554283","8.0334","0.0012","24.561","0.004","9.1052","0.0013","90","","105.603","0.002","90","","1730.3","0.5","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C24 H20 N2 O2 -","- C24 H20 N2 O2 -","- C96 H80 N8 O8 -","4","1","","Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian","Photo-induced C‒H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives","Organic Chemistry Frontiers","2018","5","10","1679","","10.1039/C8QO00183A","","","0.71073","MoKα","","0.0655","0.0516","","","0.1345","0.1443","","","","","","1.059","","","","has coordinates","237093","2020-10-21","18:00:00",""
"1554284","5.3397","0.0005","12.5882","0.001","17.165","0.0013","95.56","0.003","94.461","0.003","101.447","0.003","1119.93","0.16","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C32 H22 N2 O2 -","- C32 H22 N2 O2 -","- C64 H44 N4 O4 -","2","1","","Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian","Photo-induced C‒H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives","Organic Chemistry Frontiers","2018","5","10","1679","","10.1039/C8QO00183A","","","0.71073","MoKα","","0.1775","0.1105","","","0.2431","0.2798","","","","","","1.056","","","","has coordinates,has disorder","237093","2020-10-21","18:00:00",""
"1554285","9.533","0.006","17.215","0.01","11.031","0.005","90","","122.95","0.04","90","","1519.1","1.6","294","2","294","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C21 H14 O -","- C21 H14 O -","- C84 H56 O4 -","4","1","","Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo","Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C‒C bond activation: divergent synthesis of indenones and quinones","Organic Chemistry Frontiers","2018","5","10","1613","","10.1039/C8QO00186C","","","0.71073","MoKα","","0.081","0.0524","","","0.1141","0.1281","","","","","","1.084","","","","has coordinates","237095","2020-10-21","18:00:00",""
"1554286","8.166","0.004","9.066","0.005","9.404","0.006","85.402","0.019","75.824","0.017","71.601","0.017","640.5","0.6","294","2","294","2","","","","","","","","3","P -1","-P 1","2","","","","- C17 H14 O -","- C17 H14 O -","- C34 H28 O2 -","2","1","","Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo","Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C‒C bond activation: divergent synthesis of indenones and quinones","Organic Chemistry Frontiers","2018","5","10","1613","","10.1039/C8QO00186C","","","0.71073","MoKα","","0.0621","0.0469","","","0.1187","0.1288","","","","","","1.044","","","","has coordinates","237095","2020-10-21","18:00:00",""
"1554287","9.603","0.003","10.694","0.004","10.7294","0.0016","70.55","0.05","64.18","0.05","81.02","0.06","935.2","0.7","128","2","128","2","","","","","","","","3","P -1","-P 1","2","","","","- C27 H18 O -","- C27 H18 O -","- C54 H36 O2 -","2","1","","Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo","Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C‒C bond activation: divergent synthesis of indenones and quinones","Organic Chemistry Frontiers","2018","5","10","1613","","10.1039/C8QO00186C","","","0.71073","MoKα","","0.0818","0.0595","","","0.1441","0.1523","","","","","","0.995","","","","has coordinates","237095","2020-10-21","18:00:00",""
"1554288","8.4085","0.0015","9.35","0.0016","14.153","0.003","105.907","0.01","95.411","0.018","97.753","0.013","1050.2","0.4","128","2","128","2","","","","","","","","3","P -1","-P 1","2","","","","- C31 H20 O -","- C31 H20 O -","- C62 H40 O2 -","2","1","","Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo","Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C‒C bond activation: divergent synthesis of indenones and quinones","Organic Chemistry Frontiers","2018","5","10","1613","","10.1039/C8QO00186C","","","0.71073","MoKα","","0.0583","0.0427","","","0.1172","0.1221","","","","","","1.063","","","","has coordinates","237095","2020-10-21","18:00:00",""
"1554289","23.315","0.0015","11.3915","0.0007","18.4957","0.0012","90","","93.135","0.003","90","","4905","0.5","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C3.93 H3.28 Br0.13 N0.26 O0.26 -","- C3.93443 H3.27869 Br0.131148 N0.262295 O0.262295 -","- C240 H200 Br8 N16 O16 -","61","15.25","","Wang, Chao-Ming; Song, Dan; Xia, Peng-Ju; Ye, Zhi-Peng; Xiao, Jun-An; Xiang, Hao-Yue; Chen, Xiao-Qing; Yang, Hua","Photoredox-catalyzed direct aminoalkylation of isatins: diastereoselective access to 3-hydroxy-3-aminoalkylindolin-2-ones analogues","Organic Chemistry Frontiers","2018","5","10","1608","","10.1039/C8QO00201K","","","0.71073","MoKα","","0.0723","0.0513","","","0.1258","0.1394","","","","","","1.029","","","","has coordinates","237097","2020-10-21","18:00:00",""
"1554290","7.6842","0.0009","19.978","0.002","13.7517","0.0018","90","","98.473","0.012","90","","2088","0.4","173","0.1","173","0.1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C26 H21 N3 O2 -","- C26 H21 N3 O2 -","- C104 H84 N12 O8 -","4","1","","Chen, Wei; Ji, Dong-Sheng; Luo, Yong-Chun; Wang, Zhu-Yin; Xu, Peng-Fei","Directing group assisted ZnI2-catalyzed cyclopropanation of indoles via 2-furylcarbenoids","Organic Chemistry Frontiers","2018","5","11","1768","","10.1039/C8QO00232K","","","0.7107","MoKα","","0.1502","0.0669","","","0.1133","0.1605","","","","","","1.028","","","","has coordinates","237098","2020-10-21","18:00:00",""
"1554291","27.4221","0.0008","5.1994","0.0002","19.0212","0.0006","90","","121.717","0.001","90","","2306.99","0.14","298","2","298","2","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C11 H14 O2 S2 -","- C11 H14 O2 S2 -","- C88 H112 O16 S16 -","8","2","","Liu, Yan; Zeng, Jing; Sun, Jiuchang; Cai, Lei; Zhao, Yueqi; Fang, Jing; Hu, Bo; Shu, Penghua; Meng, Lingkui; Wan, Qian","1,4-Dithiothreitol mediated cleavage of the acetal and ketal type of diol protecting groups","Organic Chemistry Frontiers","2018","5","16","2427","","10.1039/C8QO00247A","","","1.54178","CuKα","","0.0409","0.04","","","0.105","0.1096","","","","","","1.094","","","","has coordinates","237099","2020-10-21","18:00:00",""
"1554292","9.0455","0.0008","9.948","0.0009","11.7172","0.0017","94.495","0.01","95.25","0.01","98.331","0.007","1034.4","0.2","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C25 H20 N2 O3 -","- C25 H20 N2 O3 -","- C50 H40 N4 O6 -","2","1","","Li, Bingnan; Mai, Shaoyu; Song, Qiuling","Synthesis of fused benzimidazoles via successive nucleophilic additions of benzimidazole derivatives to arynes under transition metal-free conditions","Organic Chemistry Frontiers","2018","5","10","1639","","10.1039/C8QO00251G","","x-ray","0.71073","MoKα","","0.1661","0.1274","","","0.3304","0.3582","","","","","","1.059","","","","has coordinates","237100","2020-10-21","18:00:00",""
"1554293","10.3357","0.0005","23.6593","0.0011","11.6006","0.0005","90","","104.704","0.002","90","","2743.9","0.2","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C34 H31 N O5 -","- C34 H31 N O5 -","- C136 H124 N4 O20 -","4","1","","Alajarin, Mateo; Bañon, Daniel; Egea, Adrian; Marín-Luna, Marta; Orenes, Raul-Angel; Vidal, Angel","Accessing polysubstituted oxazolidines, pyrrolidines and imidazolidines by regioselective [3 + 2] annulations of ketenimines with donor‒acceptor oxiranes and aziridines","Organic Chemistry Frontiers","2018","5","13","2020","","10.1039/C8QO00255J","","","0.71073","MoKα","","0.0635","0.0477","","","0.1065","0.1145","","","","","","1.043","","","","has coordinates","237103","2020-10-21","18:00:00",""
"1554294","10.9629","0.0005","9.8209","0.0004","27.4846","0.0012","90","","91.397","0.001","90","","2958.3","0.2","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C36 H36 N2 O4 -","- C36 H36 N2 O4 -","- C144 H144 N8 O16 -","4","1","","Alajarin, Mateo; Bañon, Daniel; Egea, Adrian; Marín-Luna, Marta; Orenes, Raul-Angel; Vidal, Angel","Accessing polysubstituted oxazolidines, pyrrolidines and imidazolidines by regioselective [3 + 2] annulations of ketenimines with donor‒acceptor oxiranes and aziridines","Organic Chemistry Frontiers","2018","5","13","2020","","10.1039/C8QO00255J","","","1.54178","CuKα","","0.0398","0.0366","","","0.0937","0.0965","","","","","","1.017","","","","has coordinates","237103","2020-10-21","18:00:00",""
"1554295","18.1688","0.0009","18.3501","0.001","11.8464","0.0007","90","","90","","90","","3949.6","0.4","100","2","100","2","","","","","","","","6","P c a 21","P 2c -2ac","29","","","","- C44 H44 Cl2 N2 O6 S -","- C44 H44 Cl2 N2 O6 S -","- C176 H176 Cl8 N8 O24 S4 -","4","1","","Alajarin, Mateo; Bañon, Daniel; Egea, Adrian; Marín-Luna, Marta; Orenes, Raul-Angel; Vidal, Angel","Accessing polysubstituted oxazolidines, pyrrolidines and imidazolidines by regioselective [3 + 2] annulations of ketenimines with donor‒acceptor oxiranes and aziridines","Organic Chemistry Frontiers","2018","5","13","2020","","10.1039/C8QO00255J","","","0.71073","MoKα","","0.0631","0.0463","","","0.1027","0.1119","","","","","","0.918","","","","has coordinates,has disorder","237103","2020-10-21","18:00:00",""
"1554296","12.143","0.003","10.204","0.002","18.499","0.004","90","","94.972","0.012","90","","2283.5","0.9","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C23 H24 N2 O4 S2 -","- C23 H24 N2 O4 S2 -","- C92 H96 N8 O16 S8 -","4","1","","Luo, Fan; Lu, Yu; Hu, Mengjie; Tian, Junsong; Zhang, Lei; Bao, Wangzhen; Yan, Chao; Huang, Xin; Wang, Zhi-Xiang; Peng, Bo","Reductive ortho C‒H cyanoalkylation of aryl(heteroaryl) sulfoxides: a general approach to α-aryl(heteroaryl) nitriles","Organic Chemistry Frontiers","2018","5","11","1756","","10.1039/C8QO00268A","","","0.71073","MoKα","","","0.0564","","","0.1209","0.1367","","","","","","1.052","","","","has coordinates","237105","2020-10-21","18:00:00",""
"1554297","9.0286","0.0006","24.083","0.0016","10.3285","0.0007","90","","114.965","0.003","90","","2036","0.2","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C21 H22 N2 O2 S2 -","- C21 H22 N2 O2 S2 -","- C84 H88 N8 O8 S8 -","4","1","","Luo, Fan; Lu, Yu; Hu, Mengjie; Tian, Junsong; Zhang, Lei; Bao, Wangzhen; Yan, Chao; Huang, Xin; Wang, Zhi-Xiang; Peng, Bo","Reductive ortho C‒H cyanoalkylation of aryl(heteroaryl) sulfoxides: a general approach to α-aryl(heteroaryl) nitriles","Organic Chemistry Frontiers","2018","5","11","1756","","10.1039/C8QO00268A","","","0.71073","MoKα","","","0.0439","","","0.1166","0.1287","","","","","","1.065","","","","has coordinates","237105","2020-10-21","18:00:00",""
"1554298","10.4066","0.0014","26.417","0.004","12.0692","0.0014","90","","90","","90","","3318","0.8","293","2","293.15","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","ZHY7009","","- C26 H39 Cl2 Co N3 O12 -","- C26 H39 Cl2 Co N3 O12 -","- C104 H156 Cl8 Co4 N12 O48 -","4","1","","Zhang, Heyi; Lu, Zhan","Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation","Organic Chemistry Frontiers","2018","5","11","1763","","10.1039/C8QO00279G","","","0.71073","MoKα","","0.1363","0.0755","","","0.1596","0.1969","","","","","","1.003","","","","has coordinates","237107","2020-10-21","18:00:00",""
"1554299","10.3907","0.0009","11.9429","0.0011","26.537","0.003","90","","90","","90","","3293.1","0.6","293","2","293.15","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","ZHY7163","","- C26 H39 Cl2 N3 Ni O12 -","- C26 H39 Cl2 N3 Ni O12 -","- C104 H156 Cl8 N12 Ni4 O48 -","4","1","","Zhang, Heyi; Lu, Zhan","Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation","Organic Chemistry Frontiers","2018","5","11","1763","","10.1039/C8QO00279G","","","0.71073","MoKα","","0.128","0.0735","","","0.1546","0.1907","","","","","","1.011","","","","has coordinates","237107","2020-10-21","18:00:00",""
"1554300","6.96436","0.00013","7.91974","0.00013","15.2392","0.0003","90","","92.2266","0.0016","90","","839.9","0.03","293","2","293.15","","","","","","","","","3","P 1 21 1","P 2yb","4","","ZHY8126","","- C22 H18 O -","- C22 H18 O -","- C44 H36 O2 -","2","1","","Zhang, Heyi; Lu, Zhan","Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation","Organic Chemistry Frontiers","2018","5","11","1763","","10.1039/C8QO00279G","","","1.54184","CuKα","","0.041","0.0395","","","0.1052","0.1077","","","","","","1.029","","","","has coordinates","237107","2020-10-21","18:00:00",""
"1554301","10.3081","0.0003","11.98","0.0002","26.1548","0.0005","90","","90","","90","","3229.88","0.12","100.01","0.1","100.01","0.1","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","zhy8105","","- C26 H41 Cl2 Fe N3 O12 -","- C26 H41 Cl2 Fe N3 O12 -","- C104 H164 Cl8 Fe4 N12 O48 -","4","1","","Zhang, Heyi; Lu, Zhan","Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation","Organic Chemistry Frontiers","2018","5","11","1763","","10.1039/C8QO00279G","","x-ray","1.54184","CuKα","","0.0535","0.0491","","","0.1266","0.1292","","","","","","1.066","","","","has coordinates","237107","2020-10-21","18:00:00",""
"1554302","10.0093","0.0002","14.3918","0.0003","10.7208","0.0002","90","","104.176","0.002","90","","1497.32","0.05","100","","100","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H19 N O3 S -","- C15 H19 N O3 S -","- C60 H76 N4 O12 S4 -","4","1","","Yu, Ji-cong; Yu, Le-mao; Zhao, Xiao-yun; Gan, Lu; Zhu, Wei-wei; Wang, Ze-chen; Wang, Rui; Jiang, Xianxing","Organocatalytic asymmetric [3 + 2] annulation of 1,4-dithiane-2,5-diol with azlactones: access to chiral dihydrothiophen-2(3H)-one derivatives","Organic Chemistry Frontiers","2018","5","13","2040","","10.1039/C8QO00305J","","x-ray","1.54184","CuKα","","0.031","0.0297","","","0.0746","0.0756","","","","","","1.037","","","","has coordinates","237108","2020-10-21","18:00:00",""
"1554303","6.54242","0.00011","22.4359","0.0003","10.03319","0.00017","90","","102.165","0.0017","90","","1439.65","0.04","100","","100","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H19 N O3 S -","- C15 H19 N O3 S -","- C60 H76 N4 O12 S4 -","4","1","","Yu, Ji-cong; Yu, Le-mao; Zhao, Xiao-yun; Gan, Lu; Zhu, Wei-wei; Wang, Ze-chen; Wang, Rui; Jiang, Xianxing","Organocatalytic asymmetric [3 + 2] annulation of 1,4-dithiane-2,5-diol with azlactones: access to chiral dihydrothiophen-2(3H)-one derivatives","Organic Chemistry Frontiers","2018","5","13","2040","","10.1039/C8QO00305J","","x-ray","1.54184","CuKα","","0.0359","0.0348","","","0.0929","0.094","","","","","","1.057","","","","has coordinates","237108","2020-10-21","18:00:00",""
"1554304","5.9758","0.0003","8.5937","0.0004","15.7695","0.0007","90","","93.352","0.002","90","","808.45","0.07","296","2","296","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C17 H18 Cl N O2 -","- C17 H18 Cl N O2 -","- C34 H36 Cl2 N2 O4 -","2","1","","Hu, Yang; Yin, Xuguang; Chen, Ziyi; Dong, Xiu-Qin; Zhang, Xumu","Highly enantioselective Ir/f-amphox-catalyzed hydrogenation of ketoamides: efficient access to chiral hydroxy amides","Organic Chemistry Frontiers","2018","5","12","2000","","10.1039/C8QO00307F","","","1.54178","CuKα","","0.0426","0.0371","","","0.1144","0.1175","","","","","","1.131","","","","has coordinates","237110","2020-10-21","18:00:00",""
"1554305","6.4792","0.0004","25.1943","0.0014","10.1094","0.0006","90","","106.673","0.006","90","","1580.87","0.17","180","0.1","180","0.1","","","","","","","","6","P 1 21/m 1","-P 2yb","11","","","","- C32 H7 Cl4 F10 N3 O2 -","- C32 H7 Cl4 F10 N3 O2 -","- C64 H14 Cl8 F20 N6 O4 -","2","0.5","","Wang, Jun-Fei; Yao, Yuhang; Ning, Yingying; Meng, Yin-Shan; Hou, Chun-Liang; Zhang, Jing; Zhang, Jun-Long","The design of rigid cyclic tripyrrins: the importance of intermolecular interactions on aggregation and luminescence","Organic Chemistry Frontiers","2018","5","12","1877","","10.1039/C8QO00313K","","x-ray","0.71073","MoKα","","0.0694","0.0441","","","0.0889","0.1004","","","","","","1.025","","","","has coordinates","237111","2020-10-21","18:00:00",""
"1554306","6.3689","0.0005","19.2075","0.001","14.4005","0.0009","90","","96.153","0.007","90","","1751.5","0.2","180.01","0.1","180.01","0.1","","","","","","","","6","P 1 21/m 1","-P 2yb","11","","","","- C36 H11 Cl2 F10 N5 O2.5 -","- C36 H11 Cl2 F10 N5 O2.5 -","- C72 H22 Cl4 F20 N10 O5 -","2","0.5","","Wang, Jun-Fei; Yao, Yuhang; Ning, Yingying; Meng, Yin-Shan; Hou, Chun-Liang; Zhang, Jing; Zhang, Jun-Long","The design of rigid cyclic tripyrrins: the importance of intermolecular interactions on aggregation and luminescence","Organic Chemistry Frontiers","2018","5","12","1877","","10.1039/C8QO00313K","","x-ray","0.71073","MoKα","","0.0931","0.0683","","","0.2181","0.2414","","","","","","1.117","","","","has coordinates","237111","2020-10-21","18:00:00",""
"1554307","18.5573","0.001","18.3335","0.0013","14.8419","0.001","90","","90","","90","","5049.5","0.6","180","0.1","180","0.1","","","","","","","","6","P n m a","-P 2ac 2n","62","","","","- C38 H7 Br2 F10 N5 O3 -","- C38 H7 Br2 F10 N5 O3 -","- C152 H28 Br8 F40 N20 O12 -","4","0.5","","Wang, Jun-Fei; Yao, Yuhang; Ning, Yingying; Meng, Yin-Shan; Hou, Chun-Liang; Zhang, Jing; Zhang, Jun-Long","The design of rigid cyclic tripyrrins: the importance of intermolecular interactions on aggregation and luminescence","Organic Chemistry Frontiers","2018","5","12","1877","","10.1039/C8QO00313K","","x-ray","0.71073","MoKα","","0.0938","0.0702","","","0.1845","0.2056","","","","","","1.065","","","","has coordinates,has disorder","237111","2020-10-21","18:00:00",""
"1554308","8.2423","0.0002","18.2962","0.0006","34.5544","0.0012","90","","90","","90","","5210.9","0.3","117.5","0.3","117.5","0.3","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C28 H26 F N O8 S -","- C28 H26 F N O8 S -","- C224 H208 F8 N8 O64 S8 -","8","1","","Xing, Siyang; Cui, Hong; Qin, Jiajing; Gu, Nan; Zhang, Bowei; Wang, Kui; Wang, Ying; Xia, Li; Wang, Yumeng","Diastereoselective synthesis of cis-1,3-disubstituted isoindolines via a highly site-selective tandem cyclization reaction","Organic Chemistry Frontiers","2018","5","12","1950","","10.1039/C8QO00316E","","x-ray","1.54184","CuKα","","0.0828","0.0624","","","0.1503","0.167","","","","","","1.01","","","","has coordinates","237113","2020-10-21","18:00:00",""
"1554309","21.4204","0.0015","21.5628","0.0012","14.5587","0.0008","90","","97.091","0.006","90","","6673","0.7","135","0.1","135","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C28.8 H27.6 N2 O10 S -","- C28.8 H27.6 N2 O10 S -","- C230.4 H220.8 N16 O80 S8 -","8","2","","Xing, Siyang; Cui, Hong; Qin, Jiajing; Gu, Nan; Zhang, Bowei; Wang, Kui; Wang, Ying; Xia, Li; Wang, Yumeng","Diastereoselective synthesis of cis-1,3-disubstituted isoindolines via a highly site-selective tandem cyclization reaction","Organic Chemistry Frontiers","2018","5","12","1950","","10.1039/C8QO00316E","","x-ray","0.71073","MoKα","","0.1508","0.0971","","","0.2658","0.32","","","","","","1.057","","","","has coordinates,has disorder","237113","2020-10-21","18:00:00",""
"1554310","10.5915","0.0002","15.1258","0.0002","9.0257","0.0002","90","","109.468","0.002","90","","1363.29","0.05","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C17 H14 O2 -","- C17 H14 O2 -","- C68 H56 O8 -","4","1","","Zheng, Wei-Feng; Zhang, Wanli; Huang, Jianhao; Yu, Yibo; Qian, Hui; Ma, Shengming","2,3-Allenoic acids via palladium-catalyzed carboxylation of propargylic alcohols","Organic Chemistry Frontiers","2018","5","12","1900","","10.1039/C8QO00318A","","x-ray","1.54184","CuKα","","0.0407","0.0369","","","0.0989","0.1021","","","","","","1.014","","","","has coordinates","237115","2020-10-21","18:00:00",""
"1554311","5.6491","0.0004","11.5037","0.0011","11.5175","0.0007","111.795","0.007","99.48","0.006","90.087","0.007","683.87","0.1","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C15 H18 O2 -","- C15 H18 O2 -","- C30 H36 O4 -","2","1","","Zheng, Wei-Feng; Zhang, Wanli; Huang, Jianhao; Yu, Yibo; Qian, Hui; Ma, Shengming","2,3-Allenoic acids via palladium-catalyzed carboxylation of propargylic alcohols","Organic Chemistry Frontiers","2018","5","12","1900","","10.1039/C8QO00318A","","x-ray","1.54184","CuKα","","0.0879","0.068","","","0.2031","0.2213","","","","","","1.06","","","","has coordinates","237116","2020-10-21","18:00:00",""
"1554312","10.573","0.004","7.311","0.002","11.35","0.004","90","","115.216","0.005","90","","793.7","0.5","173","2","173.15","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C16 H17 Br O4 -","- C16 H17 Br O4 -","- C32 H34 Br2 O8 -","2","1","","Li, Sujia; Lv, Jian; Luo, Sanzhong","Enantioselective indium(i)-catalyzed [4 + 2] annulation of alkoxyallenes and β,γ-unsaturated α-keto esters","Organic Chemistry Frontiers","2018","5","11","1787","","10.1039/C8QO00319J","","","0.71073","MoKα","","0.0388","0.0359","","","0.077","0.0793","","","","","","1.076","","","","has coordinates","237118","2020-10-21","18:00:00",""
"1554313","8.46","0.02","9.59","0.02","11.8","0.03","97.55","0.09","104.24","0.19","108.51","0.13","857","4","293","2","293","2","","","","","","","","4","P -1","-P 1","2","Q3","","","- C20 H18 N4 O2 -","- C20 H18 N4 O2 -","- C40 H36 N8 O4 -","2","1","","Toonchue, Saowanee; Sumunnee, Ladawan; Phomphrai, Khamphee; Yotphan, Sirilata","Metal-free direct oxidative C‒C bond coupling of pyrazolones and quinoxalinones","Organic Chemistry Frontiers","2018","5","12","1928","","10.1039/C8QO00328A","","","0.71073","","","0.0784","0.0461","","","0.1022","0.1147","","","","","","1.049","","","","has coordinates","237120","2020-10-21","18:00:00",""
"1554314","9.998","0.005","9.281","0.004","14.416","0.006","90","","95.77","0.02","90","","1330.9","1","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","Q5","","","- C15 H16 N4 O2 -","- C15 H16 N4 O2 -","- C60 H64 N16 O8 -","4","1","","Toonchue, Saowanee; Sumunnee, Ladawan; Phomphrai, Khamphee; Yotphan, Sirilata","Metal-free direct oxidative C‒C bond coupling of pyrazolones and quinoxalinones","Organic Chemistry Frontiers","2018","5","12","1928","","10.1039/C8QO00328A","","","0.71073","","","0.0416","0.037","","","0.0957","0.0993","","","","","","1.066","","","","has coordinates","237120","2020-10-21","18:00:00",""
"1554315","7.3563","0.0012","46.699","0.007","12.909","0.002","90","","92.798","0.004","90","","4429.4","1.2","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C20 H40.5 O3.25 Si -","- C20 H40.5 O3.25 Si -","- C160 H324 O26 Si8 -","8","4","","Santalla, Hugo; Garrido, Fátima; Gómez, Generosa; Fall, Yagamare","A more reliable synthesis of a Gemini vitamin D analog, a potentially effective chemotherapeutic agent for the treatment of colorectal carcinomas","Organic Chemistry Frontiers","2018","5","13","2016","","10.1039/C8QO00338F","","","0.71073","MoKα","","0.2634","0.1846","","","0.3663","0.4018","","","","","","1.088","","","","has coordinates","237122","2020-10-21","18:00:00",""
"1554316","10.1535","0.0002","10.5316","0.0002","25.565","0.0006","90","","90","","90","","2733.73","0.1","297.6","0.8","297.6","0.8","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C32 H31 N O5 -","- C32 H31 N O5 -","- C128 H124 N4 O20 -","4","1","","Duan, Chuan-Qi; He, Xiao-Long; Du, Wei; Chen, Ying-Chun","Asymmetric [4 + 2] cycloadditions with 3-furfural derivatives and α-cyano-α,β-unsaturated ketones","Organic Chemistry Frontiers","2018","5","13","2057","","10.1039/C8QO00351C","","x-ray","1.54184","CuKα","","0.0447","0.0432","","","0.1184","0.1208","","","","","","1.0435","","","","has coordinates","237124","2020-10-21","18:00:00",""
"1554317","10.0726","0.0019","10.735","0.002","19.604","0.004","82.045","0.004","86.428","0.005","81.212","0.005","2072.9","0.7","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C23 H20 Br N O2 S -","- C23 H20 Br N O2 S -","- C92 H80 Br4 N4 O8 S4 -","4","2","","Jiang, Bo; Wei, Yin; Shi, Min","Gold- and silver-catalyzed intramolecular annulation and rearrangement of aniline-linked 1,6-enynes containing methylenecyclopropanes","Organic Chemistry Frontiers","2018","5","13","2091","","10.1039/C8QO00358K","","","0.71073","MoKα","","0.1374","0.0618","","","0.1248","0.1556","","","","","","0.968","","","","has coordinates","237126","2020-10-21","18:00:00",""
"1554318","9.447","0.004","10.559","0.005","12.512","0.006","76.431","0.008","77.755","0.009","64.585","0.007","1087","0.9","296","2","296","","","","","","","","","5","P -1","-P 1","2","","","","- C26 H23 N O2 S -","- C26 H23 N O2 S -","- C52 H46 N2 O4 S2 -","2","1","","Jiang, Bo; Wei, Yin; Shi, Min","Gold- and silver-catalyzed intramolecular annulation and rearrangement of aniline-linked 1,6-enynes containing methylenecyclopropanes","Organic Chemistry Frontiers","2018","5","13","2091","","10.1039/C8QO00358K","","","0.71073","MoKα","","0.1889","0.0964","","","0.2442","0.3157","","","","","","1.014","","","","has coordinates","237126","2020-10-21","18:00:00",""
"1554319","11.7526","0.0016","13.4984","0.0019","13.5265","0.0019","90","","92.44","0.004","90","","2143.9","0.5","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C26 H23 N O2 S -","- C26 H23 N O2 S -","- C104 H92 N4 O8 S4 -","4","1","","Jiang, Bo; Wei, Yin; Shi, Min","Gold- and silver-catalyzed intramolecular annulation and rearrangement of aniline-linked 1,6-enynes containing methylenecyclopropanes","Organic Chemistry Frontiers","2018","5","13","2091","","10.1039/C8QO00358K","","","0.71073","MoKα","","0.1633","0.0757","","","0.1824","0.2426","","","","","","1.047","","","","has coordinates","237126","2020-10-21","18:00:00",""
"1554320","9.00774","0.00012","11.44511","0.00014","29.0288","0.0003","90","","90","","90","","2992.71","0.06","293.8","0.5","293.8","0.5","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","((1R,2R,3R,3aS)-1'-benzyl-2'-oxo-1,2-dihydro-3aH-spiro[benzo[d]pyrrolo[2,1-b]thiazole-3,3'-indoline]-1,2-diyl)bis(phenylmethanone)","","- C38 H28 N2 O3 S -","- C38 H28 N2 O3 S -","- C152 H112 N8 O12 S4 -","4","1","","Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming","Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives","Organic Chemistry Frontiers","2018","5","13","2126","","10.1039/C8QO00370J","","x-ray","1.54184","CuKα","","0.0518","0.0487","","","0.1321","0.1365","","","","","","1.037","","","","has coordinates","237128","2020-10-21","18:00:00",""
"1554321","14.8962","0.0011","11.3205","0.0008","20.153","0.002","90","","102.279","0.009","90","","3320.7","0.5","293","2","293.15","","","","","","","","","5","C 1 2 1","C 2y","5","","","","- C38 H28 N2 O4 S -","- C38 H28 N2 O4 S -","- C152 H112 N8 O16 S4 -","4","1","","Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming","Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives","Organic Chemistry Frontiers","2018","5","13","2126","","10.1039/C8QO00370J","","x-ray","0.71073","MoKα","","0.0546","0.0441","","","0.1095","0.1153","","","","","","1.052","","","","has coordinates","237128","2020-10-21","18:00:00",""
"1554322","6.3467","0.00018","16.1435","0.0004","10.7987","0.0003","90","","96.301","0.003","90","","1099.73","0.05","295.97","0.11","295.97","0.11","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C26 H21 N O4 S -","- C26 H21 N O4 S -","- C52 H42 N2 O8 S2 -","2","1","","Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming","Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives","Organic Chemistry Frontiers","2018","5","13","2126","","10.1039/C8QO00370J","","x-ray","1.54184","CuKα","","0.0639","0.0618","","","0.1519","0.1572","","","","","","1.077","","","","has coordinates","237128","2020-10-21","18:00:00",""
"1554323","10.4185","0.0009","15.4927","0.0012","15.8277","0.0018","90","","95.756","0.008","90","","2541.9","0.4","293","2","293.15","","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C30 H22 Cl N O2 S -","- C30 H22 Cl N O2 S -","- C120 H88 Cl4 N4 O8 S4 -","4","2","","Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming","Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives","Organic Chemistry Frontiers","2018","5","13","2126","","10.1039/C8QO00370J","","x-ray","0.71073","MoKα","","0.1377","0.1004","","","0.2762","0.3105","","","","","","1.026","","","","has coordinates","275856","2022-06-07","07:08:27",""
"1554324","9.2007","0.0002","9.2791","0.0004","14.237","0.0005","97.598","0.003","91.193","0.003","97.349","0.003","1194.02","0.07","139","","139","","","","","","","","","7","P 1","P 1","1","","","","- C31 H56 F6 Mg N4 O14 S2 -","- C31 H56 F6 Mg N4 O14 S2 -","- C31 H56 F6 Mg N4 O14 S2 -","1","1","","Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming","Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives","Organic Chemistry Frontiers","2018","5","13","2126","","10.1039/C8QO00370J","","x-ray","1.54184","CuKα","","0.0653","0.061","","","0.1662","0.1745","","","","","","1.023","","","","has coordinates","237128","2020-10-21","18:00:00",""
"1554325","8.2339","0.0002","14.7918","0.0004","17.1794","0.0005","101.33","0.002","95.203","0.002","106.126","0.002","1947.28","0.1","100.01","0.1","100.01","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C25 H19 N3 O -","- C25 H19 N3 O -","- C100 H76 N12 O4 -","4","2","","Liu, Yun-Lin; Mao, Xiang-Yu; Lin, Xiao-Tong; Chen, Guo-Shu","A Zn(OTf)2 catalyzed Ugi-type reaction of 3-(2-isocyanoethyl)indoles with indole-derived ketimines: rapid access to hexacyclic spiroindolines","Organic Chemistry Frontiers","2018","5","15","2303","","10.1039/C8QO00382C","","x-ray","1.54184","CuKα","","0.0445","0.0407","","","0.0982","0.1005","","","","","","1.03","","","","has coordinates","275434","2022-05-16","05:31:57",""
"1554326","19.5242","0.0003","8.4475","0.0001","25.582","0.0004","90","","107.178","0.002","90","","4031.04","0.11","100","10","100","10","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C25 H16 F3 N3 O2 -","- C25 H16 F3 N3 O2 -","- C200 H128 F24 N24 O16 -","8","2","","Liu, Yun-Lin; Mao, Xiang-Yu; Lin, Xiao-Tong; Chen, Guo-Shu","A Zn(OTf)2 catalyzed Ugi-type reaction of 3-(2-isocyanoethyl)indoles with indole-derived ketimines: rapid access to hexacyclic spiroindolines","Organic Chemistry Frontiers","2018","5","15","2303","","10.1039/C8QO00382C","","","1.54178","CuKα","","0.0536","0.0494","","","0.141","0.1456","","","","","","1.057","","","","has coordinates","237130","2020-10-21","18:00:00",""
"1554327","18.7671","0.0001","18.7671","0.0001","24.2076","0.0003","90","","90","","90","","8526.01","0.12","100","0.1","100","0.1","","","","","","","","4","I 41/a :2","-I 4ad","88","","","","- C26 H21 F2 N3 -","- C26 H21 F2 N3 -","- C416 H336 F32 N48 -","16","1","","Liu, Yun-Lin; Mao, Xiang-Yu; Lin, Xiao-Tong; Chen, Guo-Shu","A Zn(OTf)2 catalyzed Ugi-type reaction of 3-(2-isocyanoethyl)indoles with indole-derived ketimines: rapid access to hexacyclic spiroindolines","Organic Chemistry Frontiers","2018","5","15","2303","","10.1039/C8QO00382C","","x-ray","1.54184","CuKα","","0.0426","0.0395","","","0.098","0.1","","","","","","1.041","","","","has coordinates","237130","2020-10-21","18:00:00",""
"1554328","57.5837","0.0019","5.8021","0.0002","8.0527","0.0003","90","","90","","90","","2690.46","0.16","296","2","296","2","","","","","","","","4","P b c n","-P 2n 2ab","60","","","","- C16 H15 Cl O -","- C16 H15 Cl O -","- C128 H120 Cl8 O8 -","8","1","","Chen, Mintao; Wei, Yin; Shi, Min","A facile method for the synthesis of trifluoromethylthio-/chloro-homoallylic alcohols from methylenecyclopropanes","Organic Chemistry Frontiers","2018","5","13","2030","","10.1039/C8QO00386F","","","0.71073","MoKα","","0.0589","0.0509","","","0.123","0.1297","","","","","","1.067","","","","has coordinates","237132","2020-10-21","18:00:00",""
"1554329","10.0641","0.0003","10.4692","0.0002","12.4244","0.0003","90.033","0.001","93.737","0.001","96.649","0.001","1297.46","0.06","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C12 H13 F3 O2 S -","- C12 H13 F3 O2 S -","- C48 H52 F12 O8 S4 -","4","2","","Chen, Mintao; Wei, Yin; Shi, Min","A facile method for the synthesis of trifluoromethylthio-/chloro-homoallylic alcohols from methylenecyclopropanes","Organic Chemistry Frontiers","2018","5","13","2030","","10.1039/C8QO00386F","","","0.71073","MoKα","","0.0544","0.0413","","","0.1119","0.1252","","","","","","1.026","","","","has coordinates","237132","2020-10-21","18:00:00",""
"1554330","12.134","0.003","13.857","0.004","17.116","0.004","70.214","0.005","75.507","0.005","73.496","0.005","2558.3","1.1","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C66 H78 O2 -","- C66 H78 O2 -","- C132 H156 O4 -","2","1","","Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A.","Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation","Organic Chemistry Frontiers","2018","5","15","2288","","10.1039/C8QO00389K","","","0.71073","MoKα","","0.1305","0.0604","","","0.1323","0.1658","","","","","","1.006","","","","has coordinates,has disorder","237134","2020-10-21","18:00:00",""
"1554331","9.3311","0.0006","9.8219","0.0006","16.1042","0.001","103.794","0.001","94.992","0.001","112.566","0.001","1297.14","0.14","100","2","100","2","","","","","","","","2","P -1","-P 1","2","","","","- C68 H74 -","- C68 H74 -","- C68 H74 -","1","0.5","","Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A.","Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation","Organic Chemistry Frontiers","2018","5","15","2288","","10.1039/C8QO00389K","","","0.71073","MoKα","","0.0998","0.064","","","0.1856","0.203","","","","","","1.1","","","","has coordinates,has disorder","237134","2020-10-21","18:00:00",""
"1554332","15.3329","0.0008","18.3488","0.001","15.6332","0.0008","90","","99.6319","0.001","90","","4336.2","0.4","293","2","293","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C95.5 H118 Cl4.5 O4.93 -","- C95.5 H118 Cl4.497 O4.855 -","- C191 H236 Cl8.994 O9.71 -","2","1","","Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A.","Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation","Organic Chemistry Frontiers","2018","5","15","2288","","10.1039/C8QO00389K","","","0.71073","MoKα","","0.1041","0.0787","","","0.2132","0.2326","","","","","","1.061","","","","has coordinates,has disorder","237134","2020-10-21","18:00:00",""
"1554333","32.048","0.0019","25.4121","0.0015","26.3829","0.0015","90","","102.865","0.0011","90","","20947","2","100","2","100","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C127.75 H123 O1.75 -","- C127.75 H123 O1.75 -","- C1022 H984 O14 -","8","1","","Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A.","Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation","Organic Chemistry Frontiers","2018","5","15","2288","","10.1039/C8QO00389K","","","0.71073","MoKα","","0.1598","0.0833","","","0.2135","0.244","","","","","","1.025","","","","has coordinates,has disorder","237134","2020-10-21","18:00:00",""
"1554334","9.5467","0.0009","13.5703","0.0018","26.06","0.002","90","","90","","90","","3376.1","0.6","294.24","0.1","294.24","0.1","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C11 H10 Cl0.07 Fe N O -","- C9.06667 H9.06667 Cl0.8 Fe0.266667 N0.8 O1.06667 -","- C136 H136 Cl12 Fe4 N12 O16 -","15","3.75","","Zhang, Yuehua; Wang, Chunting; Huang, Wei; Haruehanroengra, Phensinee; Peng, Cheng; Sheng, Jia; Han, Bo; He, Gu","Application of organocatalysis in bioorganometallic chemistry: asymmetric synthesis of multifunctionalized spirocyclic pyrazolone‒ferrocene hybrids as novel RalA inhibitors","Organic Chemistry Frontiers","2018","5","14","2229","","10.1039/C8QO00422F","","x-ray","1.54184","CuKα","","0.079","0.0679","","","0.1643","0.1774","","","","","","1.082","","","","has coordinates","237136","2020-10-21","18:00:00",""
"1554335","12.0535","0.0003","12.0535","0.0003","43.8649","0.0013","90","","90","","90","","6373","0.3","139.05","0.1","139.05","0.1","","","","","","","","6","P 41 21 2","P 4abw 2nw","92","","","","- C34 H35 Cl2 Fe N3 O4 -","- C34 H35 Cl2 Fe N3 O4 -","- C272 H280 Cl16 Fe8 N24 O32 -","8","1","","Zhang, Yuehua; Wang, Chunting; Huang, Wei; Haruehanroengra, Phensinee; Peng, Cheng; Sheng, Jia; Han, Bo; He, Gu","Application of organocatalysis in bioorganometallic chemistry: asymmetric synthesis of multifunctionalized spirocyclic pyrazolone‒ferrocene hybrids as novel RalA inhibitors","Organic Chemistry Frontiers","2018","5","14","2229","","10.1039/C8QO00422F","","x-ray","1.54184","CuKα","","0.0745","0.063","","","0.1467","0.1552","","","","","","1.07","","","","has coordinates","237136","2020-10-21","18:00:00",""
"1554336","18.4603","0.0003","16.6736","0.0003","13.8087","0.001","90","","103.239","0.007","90","","4137.4","0.3","293","2","293","2","","","","","","","","5","C 1 2 1","C 2y","5","","(1R,2R,4aS,12bS)-1-chloro-2-hydroxy-2,5,5,7-tetramethyl-1,2,3,4,4a,5,7,12b-octahydro-12H-isochromeno[3,4-b]quinolin-12-one","","- C20.57 H26.27 Cl N O3.57 -","- C20 H24 Cl N O3 -","- C160 H192 Cl8 N8 O24 -","8","2","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","","1.54187","CuKα","","0.1415","0.0783","","","0.2","0.2755","","","","","","1.043","","","","has coordinates","237138","2020-10-21","18:00:00",""
"1554337","11.4568","0.0005","11.4834","0.0003","14.2866","0.0007","94.508","0.003","106.183","0.004","90.764","0.002","1798.31","0.13","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C20 H24 Cl N O3 -","- C20 H24 Cl N O3 -","- C80 H96 Cl4 N4 O12 -","4","2","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","","0.71073","MoKα","","0.0761","0.0637","","","0.1833","0.1899","","","","","","1.062","","","","has coordinates","237138","2020-10-21","18:00:00",""
"1554338","17.0841","0.0012","18.7193","0.0011","11.1858","0.0007","90","","100.62","0.007","90","","3516","0.4","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C20 H25 N O4 -","- C20 H25 N O4 -","- C160 H200 N8 O32 -","8","2","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","","1.54187","CuKα","","0.054","0.0402","","","0.105","0.1242","","","","","","1.135","","","","has coordinates","237138","2020-10-21","18:00:00",""
"1554339","11.3027","0.0005","7.2512","0.0002","23.102","0.0016","90","","98.784","0.007","90","","1871.19","0.17","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H24 Cl N O5 -","- C20 H24 Cl N O5 -","- C80 H96 Cl4 N4 O20 -","4","1","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","","1.54187","CuKα","","0.0596","0.0463","","","0.1156","0.1277","","","","","","1.084","","","","has coordinates","237138","2020-10-21","18:00:00",""
"1554340","7.508","0.0002","11.2397","0.0003","21.9828","0.0015","90","","90","","90","","1855.08","0.14","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","(6aS,9R,10R,10aS)-10-chloro-9-hydroxy-6,6,9,12-tetramethyl-6,6a,7,8,9,10,10a,12-octahydro-11H-isochromeno[4,3-c]quinolin-11-one)","","- C20 H24 Cl N O3 -","- C20 H24 Cl N O3 -","- C80 H96 Cl4 N4 O12 -","4","1","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","","1.54187","CuKα","","0.1108","0.0543","","","0.0941","0.141","","","","","","1.14","","","","has coordinates","237138","2020-10-21","18:00:00",""
"1554341","17.278","0.002","12.6989","0.001","17.255","0.002","90","","102.191","0.013","90","","3700.6","0.7","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H22 Cl N O4 -","- C20 H22 Cl N O4 -","- C160 H176 Cl8 N8 O32 -","8","2","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","","0.71073","MoKα","","0.1125","0.0613","","","0.1331","0.1521","","","","","","1.026","","","","has coordinates","237138","2020-10-21","18:00:00",""
"1554342","16.127","0.0008","7.209","0.0004","16.3705","0.0009","90","","91.08","0.005","90","","1902.89","0.18","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H26 Cl N O4 -","- C20 H26 Cl N O4 -","- C80 H104 Cl4 N4 O16 -","4","1","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","x-ray","0.71073","MoKα","","0.0917","0.0692","","","0.1793","0.1929","","","","","","1.066","","","","has coordinates","237138","2020-10-21","18:00:00",""
"1554343","10.2096","0.0003","12.8487","0.0004","12.9425","0.0004","90","","107.01","0.004","90","","1623.53","0.09","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H23 N O2 -","- C20 H23 N O2 -","- C80 H92 N4 O8 -","4","1","","Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.","Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines","Organic Chemistry Frontiers","2018","5","14","2171","","10.1039/C8QO00429C","","","0.71073","MoKα","","0.0431","0.0379","","","0.1059","0.1095","","","","","","1.069","","","","has coordinates","237138","2020-10-21","18:00:00",""
"1554344","5.5872","0.0007","13.9109","0.0013","14.4106","0.0018","112.533","0.01","98.978","0.011","94.422","0.009","1010.3","0.2","100","0.1","100","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C24 H24 O5 S -","- C24 H24 O5 S -","- C48 H48 O10 S2 -","2","1","","Cui, Zhiming; Zhu, Baofu; Li, Xuechen; Cao, Hua","Access to sulfonylated furans or imidazo[1,2-a]pyridines via a metal-free three-component, domino reaction","Organic Chemistry Frontiers","2018","5","14","2219","","10.1039/C8QO00443A","","x-ray","0.71073","MoKα","","0.0762","0.0633","","","0.1555","0.1681","","","","","","1.061","","","","has coordinates","237140","2020-10-21","18:00:00",""
"1554345","10.194","0.002","14.232","0.003","12.523","0.003","90","","106.045","0.006","90","","1746.1","0.7","273","2","273.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","3c","","- C20 H19 N O4 -","- C20 H19 N O4 -","- C80 H76 N4 O16 -","4","1","","Jia, Xiaodong; Hou, Wentao; Chen, Qian; Yuan, Yu; Sun, Jing; He, Kaixuan","Oxidation of active sp3C‒H bonds initiated consecutive intermolecular/intramolecular cyclization between glycine derivatives ando-vinylphenols: construction of a polycyclic benzofuroquinoline skeleton","Organic Chemistry Frontiers","2018","5","16","2479","","10.1039/C8QO00444G","","","0.71073","MoKα","","0.1014","0.0609","","","0.1599","0.1822","","","","","","1.067","","","","has coordinates,has disorder","237143","2020-10-21","18:00:00",""
"1554346","9.1376","0.0008","9.5813","0.0009","10.8392","0.001","105.957","0.003","95.789","0.003","98.506","0.003","892.32","0.14","273","2","273.15","","","","","","","","","4","P -1","-P 1","2","","","","- C20 H20 N2 O5 -","- C20 H20 N2 O5 -","- C40 H40 N4 O10 -","2","1","","Jia, Xiaodong; Hou, Wentao; Chen, Qian; Yuan, Yu; Sun, Jing; He, Kaixuan","Oxidation of active sp3C‒H bonds initiated consecutive intermolecular/intramolecular cyclization between glycine derivatives ando-vinylphenols: construction of a polycyclic benzofuroquinoline skeleton","Organic Chemistry Frontiers","2018","5","16","2479","","10.1039/C8QO00444G","","","0.71073","MoKα","","0.0596","0.0459","","","0.1257","0.1347","","","","","","1.04","","","","has coordinates","237143","2020-10-21","18:00:00",""
"1554347","21.194","0.005","8.4619","0.0012","27.57","0.01","90","","109.98","0.03","90","","4647","2","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C11 H10 N O -","- C11.6 H8.6 N0.8 O1.6 -","- C232 H172 N16 O32 -","20","5","","Gong, Hai-Xian; Cao, Zhu; Li, Meng-Hua; Liao, Sai-Hu; Lin, Mei-Jin","Photoexcited perylene diimide radical anions for the reduction of aryl halides: a bay-substituent effect","Organic Chemistry Frontiers","2018","5","15","2296","","10.1039/C8QO00445E","","","0.71073","MoKα","","0.3157","0.1526","","","0.3538","0.4478","","","","","","1.025","","","","has coordinates","237146","2020-10-21","18:00:00",""
"1554348","10.9697","0.0018","16.013","0.003","13.031","0.002","90","","105.898","0.018","90","","2201.4","0.7","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C24 H21 N O2 -","- C24 H21 N O2 -","- C96 H84 N4 O8 -","4","1","","Gong, Hai-Xian; Cao, Zhu; Li, Meng-Hua; Liao, Sai-Hu; Lin, Mei-Jin","Photoexcited perylene diimide radical anions for the reduction of aryl halides: a bay-substituent effect","Organic Chemistry Frontiers","2018","5","15","2296","","10.1039/C8QO00445E","","x-ray","0.71073","MoKα","","0.21","0.1166","","","0.3294","0.3693","","","","","","0.991","","","","has coordinates","237146","2020-10-21","18:00:00",""
"1554349","24.1341","0.0014","25.4123","0.0013","26.638","0.0017","90","","90","","90","","16337.2","1.6","173","2","173.15","","","","","","","","","4","F d d d :2","-F 2uv 2vw","70","","","","- C5.5 H5.62 N0.12 O0.5 -","- C5.5 H5.625 N0.125 O0.5 -","- C704 H720 N16 O64 -","128","4","","Gong, Hai-Xian; Cao, Zhu; Li, Meng-Hua; Liao, Sai-Hu; Lin, Mei-Jin","Photoexcited perylene diimide radical anions for the reduction of aryl halides: a bay-substituent effect","Organic Chemistry Frontiers","2018","5","15","2296","","10.1039/C8QO00445E","","","0.71073","MoKα","","0.0942","0.0766","","","0.2293","0.244","","","","","","1.068","","","","has coordinates","237146","2020-10-21","18:00:00",""
"1554350","9.4355","0.0005","10.2231","0.0006","17.9161","0.0011","87.132","0.005","84.213","0.005","68.822","0.005","1603.09","0.17","173","2","173.15","","","","","","","","","4","P -1","-P 1","2","","","","- C34 H33 N O3 -","- C34 H33 N O3 -","- C68 H66 N2 O6 -","2","1","","Gong, Hai-Xian; Cao, Zhu; Li, Meng-Hua; Liao, Sai-Hu; Lin, Mei-Jin","Photoexcited perylene diimide radical anions for the reduction of aryl halides: a bay-substituent effect","Organic Chemistry Frontiers","2018","5","15","2296","","10.1039/C8QO00445E","","","0.71073","MoKα","","0.1162","0.0845","","","0.2197","0.2349","","","","","","1.068","","","","has coordinates","237146","2020-10-21","18:00:00",""
"1554351","40.9015","0.0014","40.9015","0.0014","9.3338","0.0005","90","","90","","90","","15614.8","1.1","100","","100","","","","","","","","","4","I 41/a :2","-I 4ad","88","","","","- C45 H68 N2 O2 -","- C45 H68 N2 O2 -","- C720 H1088 N32 O32 -","16","1","","Mahoney, Janell K.; Regnier, Vianney; Romero, Erik A.; Molton, Florian; Royal, Guy; Jazzar, Rodolphe; Martin, David; Bertrand, Guy","The serendipitous discovery of a readily available redox-bistable molecule derived from cyclic(alkyl)(amino)carbenes","Organic Chemistry Frontiers","2018","5","13","2073","","10.1039/C8QO00447A","","x-ray","1.54178","CuKα","","0.053","0.039","","","0.0921","0.1006","","","","","","1.038","","","","has coordinates","237149","2020-10-21","18:00:00",""
"1554352","21.6194","0.0008","10.6383","0.0004","26.8304","0.001","90","","95.299","0.002","90","","6144.4","0.4","100","","100","","","","","","","","","7","C 1 2/c 1","-C 2yc","15","","","","- C56 H78 B2 F8 Fe N2 O2 -","- C56 H78 B2 F8 Fe N2 O2 -","- C224 H312 B8 F32 Fe4 N8 O8 -","4","0.5","","Mahoney, Janell K.; Regnier, Vianney; Romero, Erik A.; Molton, Florian; Royal, Guy; Jazzar, Rodolphe; Martin, David; Bertrand, Guy","The serendipitous discovery of a readily available redox-bistable molecule derived from cyclic(alkyl)(amino)carbenes","Organic Chemistry Frontiers","2018","5","13","2073","","10.1039/C8QO00447A","","","0.71073","MoKα","","0.068","0.0546","","","0.1126","0.1185","","","","","","1.039","","","","has coordinates,has disorder","237149","2020-10-21","18:00:00",""
"1554353","21.3381","0.0005","10.2919","0.0003","24.6126","0.0006","90","","111.615","0.001","90","","5025.1","0.2","100","","100","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C47 H71 B2 F8 N3 O2 -","- C47 H71 B2 F8 N3 O2 -","- C188 H284 B8 F32 N12 O8 -","4","1","","Mahoney, Janell K.; Regnier, Vianney; Romero, Erik A.; Molton, Florian; Royal, Guy; Jazzar, Rodolphe; Martin, David; Bertrand, Guy","The serendipitous discovery of a readily available redox-bistable molecule derived from cyclic(alkyl)(amino)carbenes","Organic Chemistry Frontiers","2018","5","13","2073","","10.1039/C8QO00447A","","x-ray","1.54178","CuKα","","0.0641","0.0515","","","0.1361","0.1447","","","","","","1.03","","","","has coordinates,has disorder","237149","2020-10-21","18:00:00",""
"1554354","6.4711","0.0006","15.6577","0.0015","9.2786","0.0009","90","","90.334","0.007","90","","940.12","0.16","100","2","100","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C19 H28 O7 -","- C19 H26 O7 -","- C38 H52 O14 -","2","1","","Hu, Zheng-Xi; Xu, Hou-Chao; Hu, Kun; Liu, Miao; Li, Xiao-Nian; Li, Xing-Ren; Du, Xue; Zhang, Yong-Hui; Puno, Pema-Tenzin; Sun, Han-Dong","Structurally diverse diterpenoids from Isodon pharicus","Organic Chemistry Frontiers","2018","5","15","2379","","10.1039/C8QO00477C","","","1.54178","CuKα","","0.1943","0.1909","","","0.4189","0.4274","","","","","","1.932","","","","has coordinates","237151","2020-10-21","18:00:00",""
"1554355","6.6084","0.0001","11.8396","0.0002","22.9114","0.0004","90","","90","","90","","1792.61","0.05","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C20 H32 O5 -","- C20 H32 O5 -","- C80 H128 O20 -","4","1","","Hu, Zheng-Xi; Xu, Hou-Chao; Hu, Kun; Liu, Miao; Li, Xiao-Nian; Li, Xing-Ren; Du, Xue; Zhang, Yong-Hui; Puno, Pema-Tenzin; Sun, Han-Dong","Structurally diverse diterpenoids from Isodon pharicus","Organic Chemistry Frontiers","2018","5","15","2379","","10.1039/C8QO00477C","","","1.54178","CuKα","","0.0305","0.0305","","","0.0772","0.0772","","","","","","1.131","","","","has coordinates","237151","2020-10-21","18:00:00",""
"1554356","7.2615","0.0001","11.8328","0.0002","14.2292","0.0003","90","","94.546","0.002","90","","1218.78","0.04","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C14 H11 N S2 -","- C14 H11 N S2 -","- C56 H44 N4 S8 -","4","1","","Tan, Wei; Wang, Cuihong; Jiang, Xuefeng","Green carbon disulfide surrogateviaa combination of potassium sulfide and chloroform for benzothiazine-thione and benzothiazole-thione construction","Organic Chemistry Frontiers","2018","5","15","2390","","10.1039/C8QO00481A","","x-ray","1.54184","CuKα","","0.0363","0.0343","","","0.094","0.0954","","","","","","1.071","","","","has coordinates","237153","2020-10-21","18:00:00",""
"1554357","8.3766","0.0002","6.2895","0.0001","25.7206","0.0006","90","","95.618","0.002","90","","1348.57","0.05","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C15 H13 N S2 -","- C15 H13 N S2 -","- C60 H52 N4 S8 -","4","1","","Tan, Wei; Wang, Cuihong; Jiang, Xuefeng","Green carbon disulfide surrogateviaa combination of potassium sulfide and chloroform for benzothiazine-thione and benzothiazole-thione construction","Organic Chemistry Frontiers","2018","5","15","2390","","10.1039/C8QO00481A","","x-ray","1.54184","CuKα","","0.0488","0.042","","","0.1073","0.1121","","","","","","1.043","","","","has coordinates","237153","2020-10-21","18:00:00",""
"1554358","12.874","0.0005","4.9","0.0002","13.9299","0.0006","90","","93.36","0.003","90","","877.22","0.06","100","","100","","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C20 H22 O5 -","- C20 H22 O5 -","- C40 H44 O10 -","2","1","","Cheng, Yuyu; Fang, Zhiqiang; Li, Wenjun; Li, Pengfei","Phosphine-mediated enantioselective [4 + 1] annulations between ortho-quinone methides and Morita‒Baylis‒Hillman carbonates","Organic Chemistry Frontiers","2018","5","18","2728","","10.1039/C8QO00487K","","x-ray","1.54178","CuKα","","0.079","0.0699","","","0.1821","0.1928","","","","","","1.048","","","","has coordinates,has disorder","237154","2020-10-21","18:00:00",""
"1554359","9.6906","0.0009","10.9669","0.0011","11.5436","0.0013","70.045","0.01","86.183","0.008","84.832","0.008","1147.6","0.2","295.1","0.2","295.1","0.2","","","","","","","","5","P -1","-P 1","2","","","","- C21 H31 B2 N O4 -","- C21 H31 B2 N O4 -","- C42 H62 B4 N2 O8 -","2","1","","Gao, Guoliang; Kuang, Zhijie; Song, Qiuling","Functionalized geminal-diborylalkanes from various electron-deficient alkynes and B2pin2","Organic Chemistry Frontiers","2018","5","14","2249","","10.1039/C8QO00513C","","x-ray","0.71073","MoKα","","0.1265","0.0724","","","0.1726","0.2056","","","","","","1.032","","","","has coordinates","237156","2020-10-21","18:00:00",""
"1554360","10.0513","0.0014","15.5408","0.0016","19.0622","0.0018","88.904","0.008","83.3","0.01","87.795","0.01","2954.8","0.6","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C30 H42 B2 O5 -","- C30 H42 B2 O5 -","- C120 H168 B8 O20 -","4","2","","Gao, Guoliang; Kuang, Zhijie; Song, Qiuling","Functionalized geminal-diborylalkanes from various electron-deficient alkynes and B2pin2","Organic Chemistry Frontiers","2018","5","14","2249","","10.1039/C8QO00513C","","","0.71073","MoKα","","0.1816","0.0933","","","0.2566","0.3251","","","","","","1.012","","","","has coordinates","274567","2022-04-19","14:22:36",""
"1554361","10.3174","0.0005","12.4692","0.0006","20.4932","0.001","90","","96.89","0.001","90","","2617.4","0.2","153","2","153","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C28 H31 Cl3 N2 Pd -","- C28 H31 Cl3 N2 Pd -","- C112 H124 Cl12 N8 Pd4 -","4","1","","Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan","Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides","Organic Chemistry Frontiers","2018","5","16","2484","","10.1039/C8QO00517F","","","0.71073","MoKα","","0.0291","0.0258","","","0.0618","0.0636","","","","","","1.023","","","","has coordinates","237157","2020-10-21","18:00:00",""
"1554362","10.0241","0.0006","11.2921","0.0007","11.727","0.0007","92.4","0.002","105.358","0.001","106.802","0.001","1215.24","0.13","296","2","296","2","","","","","","","","6","P -1","-P 1","2","","","","- C28 H31 Cl N2 O Pd -","- C28 H31 Cl N2 O Pd -","- C56 H62 Cl2 N4 O2 Pd2 -","2","1","","Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan","Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides","Organic Chemistry Frontiers","2018","5","16","2484","","10.1039/C8QO00517F","","","0.71073","MoKα","","0.0232","0.0216","","","0.057","0.058","","","","","","1.063","","","","has coordinates","237157","2020-10-21","18:00:00",""
"1554363","18.6245","0.0007","13.7023","0.0006","22.6048","0.0011","90","","90","","90","","5768.7","0.4","153","2","153","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C28 H28 Cl F3 N2 Pd -","- C28 H28 Cl F3 N2 Pd -","- C224 H224 Cl8 F24 N16 Pd8 -","8","1","","Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan","Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides","Organic Chemistry Frontiers","2018","5","16","2484","","10.1039/C8QO00517F","","","0.71073","MoKα","","0.0752","0.0525","","","0.1484","0.1683","","","","","","1.052","","","","has coordinates,has disorder","237157","2020-10-21","18:00:00",""
"1554364","18.9753","0.0007","19.6328","0.0008","20.1865","0.0008","90","","90","","90","","7520.2","0.5","153","2","153","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C48 H39 Cl N2 Pd -","- C48 H39 Cl N2 Pd -","- C384 H312 Cl8 N16 Pd8 -","8","1","","Jin, Liqun; Wei, Wei; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan","Unsymmetrical CNN-palladacycles with geometry-constrained iminopyridyl ligands: an efficient precatalyst in Suzuki coupling for accessing 1,1-diarylalkanes from secondary benzylic bromides","Organic Chemistry Frontiers","2018","5","16","2484","","10.1039/C8QO00517F","","","0.71073","MoKα","","0.0436","0.0295","","","0.0645","0.0701","","","","","","1.041","","","","has coordinates","237157","2020-10-21","18:00:00",""
"1554365","12.6497","0.0005","9.0221","0.0002","14.1532","0.0005","90","","113.568","0.004","90","","1480.53","0.1","294.46","0.1","294.46","0.1","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C35 H32 Br N3 O3 -","- C35 H32 Br N3 O3 -","- C70 H64 Br2 N6 O6 -","2","1","","Mei, Hongjiang; Lin, Lili; Shen, Bin; Liu, Xiaohua; Feng, Xiaoming","Highly enantioselective desymmetrization of prochiral cyclic α,α-dicyanoalkenes via the direct vinylogous Michael/cyclization domino reaction","Organic Chemistry Frontiers","2018","5","16","2505","","10.1039/C8QO00545A","","x-ray","1.54184","CuKα","","0.0462","0.0455","","","0.1144","0.1157","","","","","","1.072","","","","has coordinates","237159","2020-10-21","18:00:00",""
"1554366","18.6922","0.0009","5.447","0.0003","14.5323","0.0007","90","","92.936","0.004","90","","1477.68","0.13","99.9","0.2","99.9","0.2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","2-(methylsulfonyl)-8-phenyl-2,8-dihydroindeno[1,2-c]pyrrole","","- C18 H15 N O2 S -","- C18 H15 N O2 S -","- C72 H60 N4 O8 S4 -","4","1","","Shen, Wen-Bo; Zhou, Bo; Zhang, Zhi-Xin; Yuan, Han; Fang, Wei; Ye, Long-Wu","Gold-catalyzed cascade cyclization of N-propargyl ynamides: rapid access to functionalized indeno[1,2-c]pyrroles","Organic Chemistry Frontiers","2018","5","16","2468","","10.1039/C8QO00552D","","x-ray","1.54184","CuKα","","0.0473","0.0457","","","0.1183","0.1198","","","","","","1.081","","","","has coordinates","237160","2020-10-21","18:00:00",""
"1554367","7.5235","0.0007","5.5446","0.0008","10.2976","0.001","90","","99.85","0.01","90","","423.23","0.08","293","2","293","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C10 H9 N O -","- C10 H9 N O -","- C20 H18 N2 O2 -","2","1","","Wu, Qi; Li, Yabo; Wang, Chenyang; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie","1,4-Refunctionalization of β-diketones to γ-keto nitriles via C‒C single bond cleavage","Organic Chemistry Frontiers","2018","5","16","2496","","10.1039/C8QO00556G","","x-ray","1.54184","CuKα","","0.0863","0.0682","","","0.1904","0.2218","","","","","","1.054","","","","has coordinates","237161","2020-10-21","18:00:00",""
"1554368","7.933","0.0006","11.1848","0.0007","13.1762","0.001","72.919","0.006","73.841","0.006","84.499","0.005","1073.26","0.14","100","2","100.15","","","","","","","","Synthesis","5","P -1","-P 1","2","5,6-Diphenyl-3-(trifluoromethoxy)indazolo[2,3-a]quinoline","5,6-Diphenyl-3-(trifluoromethoxy)indazolo[2,3-a]quinoline","","- C28 H17 F3 N2 O1.01 -","- C28 H17 F3 N2 O -","- C56 H34 F6 N4 O2 -","2","1","","Vivek Kumar, Sundaravel; Ellairaja, Sundaram; Satheesh, Vanaparthi; Sivasamy Vasantha, Vairathevar; Punniyamurthy, Tharmalingam","Rh-Catalyzed regioselective C‒H activation and C‒C bond formation: synthesis and photophysical studies of indazolo[2,3-a]quinolines","Organic Chemistry Frontiers","2018","5","18","2630","","10.1039/C8QO00557E","","x-ray","0.71073","MoKα","","0.1282","0.0827","","","0.1973","0.2309","","","","","","1.051","","","","has coordinates,has disorder","237163","2020-10-21","18:00:00",""
"1554369","10.757","0.009","12.558","0.01","14.389","0.012","90","","99.306","0.01","90","","1918","3","296","2","296.15","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C43 H37 Cl3 N2 O2 -","- C43 H37 Cl3 N2 O2 -","- C86 H74 Cl6 N4 O4 -","2","1","","Lu, Yi-Nan; Ma, Chun; Lan, Jin-Ping; Zhu, Caiqiang; Mao, Yu-Jia; Mei, Guang-Jian; Zhang, Shu; Shi, Feng","Catalytic enantioselective and regioselective substitution of 2,3-indolyldimethanols with enaminones","Organic Chemistry Frontiers","2018","5","18","2657","","10.1039/C8QO00565F","","","0.71073","MoKα","","0.1189","0.0663","","","0.1372","0.1587","","","","","","0.988","","","","has coordinates","237164","2020-10-21","18:00:00",""
"1554370","22.7223","0.0019","5.7888","0.0004","25.159","0.002","90","","95.416","0.008","90","","3294.5","0.4","293","2","293.15","","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C20 H18 O4 -","- C20 H18 O4 -","- C160 H144 O32 -","8","1","","Ma, Dengke; Song, Yulong; Fu, Chunling; Zhang, Fang; Guo, Yinlong; Huang, Xin; Ma, Shengming","E-Selective N-heterocyclic carbene-catalyzed reaction of aldehydes and butadienoates: effect of water and chloroform as the proton shuttle","Organic Chemistry Frontiers","2018","5","17","2560","","10.1039/C8QO00579F","","","0.71073","MoKα","","0.0817","0.0554","","","0.1329","0.1558","","","","","","1.045","","","","has coordinates","237166","2020-10-21","18:00:00",""
"1554371","10.2719","0.0007","10.4262","0.0007","11.7012","0.0008","69.168","0.002","73.012","0.002","86.849","0.002","1118.45","0.13","153","2","153","2","","","","","","","","6","P -1","-P 1","2","","","","- C25 H22 Cl N O3 S -","- C25 H22 Cl N O3 S -","- C50 H44 Cl2 N2 O6 S2 -","2","1","","Wang, Hepan; Wang, Bingbing; Sun, Song; Cheng, Jiang","Copper-catalyzed radical Heck type cyclization: a three-component reaction of DABCO·(SO2)2, aryldiazonium tetrafluoroborates and dienes toward sulfonated benzo- seven-membered nitrogen heterocycles","Organic Chemistry Frontiers","2018","5","17","2547","","10.1039/C8QO00615F","","","0.71073","MoKα","","0.0482","0.0415","","","0.1106","0.1153","","","","","","1.021","","","","has coordinates","237167","2020-10-21","18:00:00",""
"1554372","9.5372","0.0007","10.0615","0.0008","11.5029","0.0009","74.116","0.002","83.655","0.002","71.87","0.002","1008.56","0.14","120","2","120","2","","","","","","","","6","P -1","-P 1","2","","","","- C21 H19 Cl F N O6 -","- C21 H19 Cl F N O6 -","- C42 H38 Cl2 F2 N2 O12 -","2","1","","Motornov, Vladimir A.; Tabolin, Andrey A.; Novikov, Roman A.; Nelyubina, Yulia V.; Nenajdenko, Valentine G.; Ioffe, Sema L.","Fluoronitroalkenes in tandem [4 + 1]/[3 + 2]-cycloaddition: one-pot three-component assembly of fluorinated bicyclic nitroso acetals","Organic Chemistry Frontiers","2018","5","17","2588","","10.1039/C8QO00623G","","","0.71073","MoKα","","0.0519","0.0403","","","0.0957","0.1035","","","","","","1.033","","","","has coordinates","237169","2020-10-21","18:00:00",""
"1554373","16.4649","0.0014","6.9417","0.0006","15.0372","0.0013","90","","93.483","0.002","90","","1715.5","0.3","120","2","120","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C16 H14 Cl F N2 O6 -","- C16 H14 Cl F N2 O6 -","- C64 H56 Cl4 F4 N8 O24 -","4","1","","Motornov, Vladimir A.; Tabolin, Andrey A.; Novikov, Roman A.; Nelyubina, Yulia V.; Nenajdenko, Valentine G.; Ioffe, Sema L.","Fluoronitroalkenes in tandem [4 + 1]/[3 + 2]-cycloaddition: one-pot three-component assembly of fluorinated bicyclic nitroso acetals","Organic Chemistry Frontiers","2018","5","17","2588","","10.1039/C8QO00623G","","","0.71073","MoKα","","0.0624","0.0423","","","0.1111","0.1236","","","","","","1.036","","","","has coordinates","237169","2020-10-21","18:00:00",""
"1554374","6.812","0.005","11.371","0.008","13.441","0.009","80.287","0.013","84.84","0.013","77.986","0.012","1002.1","1.2","130","","130","","","","","","","","","5","P -1","-P 1","2","","","","- C23 H31 N O2 S -","- C23 H31 N O2 S -","- C46 H62 N2 O4 S2 -","2","1","","Han, Yulin; Ma, Shengming","Rhodium-catalyzed highly diastereoselective intramolecular [4 + 2] cycloaddition of 1,3-disubstituted allene-1,3-dienes","Organic Chemistry Frontiers","2018","5","18","2680","","10.1039/C8QO00650D","","","0.71073","MoKα","","0.0764","0.055","","","0.1307","0.1388","","","","","","1.071","","","","has coordinates","237171","2020-10-21","18:00:00",""
"1554375","10.6868","0.0014","20.2","0.003","8.0112","0.001","90","","101.747","0.003","90","","1693.2","0.4","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C18 H23 N O2 S -","- C18 H23 N O2 S -","- C72 H92 N4 O8 S4 -","4","1","","Han, Yulin; Ma, Shengming","Rhodium-catalyzed highly diastereoselective intramolecular [4 + 2] cycloaddition of 1,3-disubstituted allene-1,3-dienes","Organic Chemistry Frontiers","2018","5","18","2680","","10.1039/C8QO00650D","","","0.71073","MoKα","","0.0611","0.0486","","","0.1232","0.1316","","","","","","1.029","","","","has coordinates","237171","2020-10-21","18:00:00",""
"1554376","8.9632","0.001","26.894","0.003","9.2793","0.001","90","","110.151","0.002","90","","2099.9","0.4","130","","130","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C24 H30 O4 -","- C24 H30 O4 -","- C96 H120 O16 -","4","1","","Han, Yulin; Ma, Shengming","Rhodium-catalyzed highly diastereoselective intramolecular [4 + 2] cycloaddition of 1,3-disubstituted allene-1,3-dienes","Organic Chemistry Frontiers","2018","5","18","2680","","10.1039/C8QO00650D","","","0.71073","MoKα","","0.0781","0.0453","","","0.106","0.1227","","","","","","1.013","","","","has coordinates","237171","2020-10-21","18:00:00",""
"1554377","11.0672","0.0002","24.0508","0.0005","11.3892","0.0002","90","","91.3083","0.0019","90","","3030.73","0.1","296.31","0.1","296.31","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C36 H34 N O6 -","- C36 H34 N O6 -","- C144 H136 N4 O24 -","4","2","","Yue, Jing-Fei; Ran, Guang-Yao; Yang, Xing-Xing; Du, Wei; Chen, Ying-Chun","Asymmetric Diels–Alder cycloadditions of benzofulvene-based 2,4-dienals via trienamine activation","Organic Chemistry Frontiers","2018","5","18","2676","","10.1039/C8QO00653A","","x-ray","1.54184","CuKα","","0.0565","0.0538","","","0.14","0.145","","","","","","1.02","","","","has coordinates","274567","2022-04-19","14:22:36",""
"1554378","10.2146","0.0004","11.7243","0.0005","10.2644","0.0004","90","","119.315","0.002","90","","1071.84","0.08","170","2","170","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C24 H26 N2 O3 -","- C24 H26 N2 O3 -","- C48 H52 N4 O6 -","2","1","","Zhang, Zi-Jing; Song, Jin","An isothiourea-catalyzed asymmetric formal [4 + 2] cycloaddition of in situ generated azoalkenes with C1 ammonium enolates","Organic Chemistry Frontiers","2018","5","17","2578","","10.1039/C8QO00657A","","","1.34139","GaKα","","0.0428","0.0399","","","0.0983","0.101","","","","","","1.041","","","","has coordinates","237175","2020-10-21","18:00:00",""
"1554379","10.276","0.0012","12.5669","0.0014","13.0463","0.0013","66.455","0.01","73.203","0.009","66.317","0.011","1397.8","0.3","268","40","268","40","","","","","","","","5","P -1","-P 1","2","","6o","","- C32 H27 N O5 S -","- C32 H27 N O5 S -","- C64 H54 N2 O10 S2 -","2","1","","Zhang, Changyuan; Chen, Lianfen; Chen, Kai; Wang, Chuntao; Xu, Zurong; Jiang, Huanfeng; Zhu, Shifa","Cu(i)-Catalyzed stereoselective synthesis of trisubstituted Z-enol esters via interrupting the 1,3-O-transposition reaction","Organic Chemistry Frontiers","2018","5","16","2510","","10.1039/C8QO00664D","","x-ray","0.71073","MoKα","","0.1099","0.0613","","","0.1333","0.1707","","","","","","1.064","","","","has coordinates","237176","2020-10-21","18:00:00",""
"1554380","8.611","0.0012","11.3415","0.0015","28.819","0.004","90","","90","","90","","2814.5","0.7","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C29 H28 Cl N3 O7 -","- C29 H28 Cl N3 O7 -","- C116 H112 Cl4 N12 O28 -","4","1","","Wei, Qinghua; Ma, Xiaochu; Chen, Jianghui; Niu, Li; Yang, Xi; Xia, Fei; Liu, Shunying","A triple-functionalised metal centre-catalyzed enantioselective multicomponent reaction","Organic Chemistry Frontiers","2018","5","19","2799","","10.1039/C8QO00703A","","","0.71073","MoKα","","0.1382","0.0564","","","0.1135","0.1486","","","","","","1.002","","","","has coordinates","237178","2020-10-21","18:00:00",""
"1554381","8.4477","0.0015","11.883","0.002","15.889","0.003","97.79","0.004","90.12","0.004","96.968","0.004","1568.3","0.5","298","2","298","2","","","","","","","","6","P -1","-P 1","2","","","","- C29 H43 I Mg N2 O -","- C29 H43 I Mg N2 O -","- C58 H86 I2 Mg2 N4 O2 -","2","1","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.0749","0.0511","","","0.1217","0.1345","","","","","","1.02","","","","has coordinates","237180","2020-10-21","18:00:00",""
"1554382","12.5799","0.0011","19.2069","0.0016","20.3357","0.0017","90","","102.473","0.002","90","","4797.6","0.7","140","2","140","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C25 H33 Mg N2 -","- C25 H33 Mg N2 -","- C200 H264 Mg8 N16 -","8","2","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.0853","0.0641","","","0.181","0.1988","","","","","","1.024","","","","has coordinates","237180","2020-10-21","18:00:00",""
"1554383","21.9804","0.0013","19.3508","0.0011","11.283","0.0007","90","","90","","90","","4799.1","0.5","140","2","140","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C25 H33 Mg N2 -","- C25 H33 Mg N2 -","- C200 H264 Mg8 N16 -","8","2","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.1069","0.0662","","","0.0993","0.1125","","","","","","1.157","","","","has coordinates","237180","2020-10-21","18:00:00",""
"1554384","11.0139","0.0012","11.3202","0.0012","18.565","0.002","75.316","0.003","83.401","0.003","62.905","0.003","1993.3","0.4","140","2","140","2","","","","","","","","4","P -1","-P 1","2","","","","- C46 H58 Mg N4 -","- C46 H58 Mg N4 -","- C92 H116 Mg2 N8 -","2","1","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.1505","0.0747","","","0.1632","0.1991","","","","","","1.028","","","","has coordinates","237180","2020-10-21","18:00:00",""
"1554385","11.4271","0.0014","17.954","0.002","20.908","0.003","90","","93.495","0.003","90","","4281.6","0.9","130","2","130","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C54 H53 Mg N2 -","- C54 H53 Mg N2 -","- C216 H212 Mg4 N8 -","4","1","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.0857","0.0559","","","0.1467","0.1664","","","","","","1.023","","","","has coordinates","237180","2020-10-21","18:00:00",""
"1554386","21.607","0.002","13.2782","0.0012","14.0261","0.0013","90","","90","","90","","4024.1","0.6","130","2","130","2","","","","","","","","4","P c c n","-P 2ab 2ac","56","","","","- C48 H49 Cl2 N2 -","- C48 H49 Cl2 N2 -","- C192 H196 Cl8 N8 -","4","0.5","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.0855","0.0641","","","0.1752","0.1939","","","","","","1.033","","","","has coordinates","237180","2020-10-21","18:00:00",""
"1554387","25.689","0.003","11.0511","0.0014","32.698","0.004","90","","105.996","0.003","90","","8923.3","1.9","298","2","298","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C51 H55 I Mg N2 O -","- C51 H55 I Mg N2 O -","- C408 H440 I8 Mg8 N16 O8 -","8","1","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.0857","0.0517","","","0.1234","0.1396","","","","","","1.015","","","","has coordinates","237180","2020-10-21","18:00:00",""
"1554388","11.9804","0.0006","15.2444","0.0007","15.0882","0.0007","90","","95.298","0.001","90","","2743.8","0.2","135","2","135","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C58 H76 Cl2 Mg2 N4 -","- C58 H76 Cl2 Mg2 N4 -","- C116 H152 Cl4 Mg4 N8 -","2","0.5","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.0573","0.0406","","","0.0939","0.1047","","","","","","1.033","","","","has coordinates","237180","2020-10-21","18:00:00",""
"1554389","13.2295","0.0008","13.2295","0.0008","19.2267","0.0013","90","","90","","90","","3365.1","0.4","140","2","140","2","","","","","","","","6","P -4","P -4","81","","","","- C68 H96 B2 Mg2 N4 O6 -","- C68 H96 B2 Mg2 N4 O6 -","- C136 H192 B4 Mg4 N8 O12 -","2","0.5","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.1547","0.0647","","","0.1293","0.1641","","","","","","0.886","","","","has coordinates","237180","2020-10-21","18:00:00",""
"1554390","10.58","0.0007","10.4047","0.0007","10.785","0.0007","90","","118.687","0.002","90","","1041.5","0.12","140","2","140","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C18 H36 B2 O6 -","- C18 H36 B2 O6 -","- C36 H72 B4 O12 -","2","0.5","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.0877","0.0677","","","0.1435","0.1529","","","","","","1.103","","","","has coordinates","237180","2020-10-21","18:00:00",""
"1554391","17.7085","0.0009","33.2898","0.0016","17.0054","0.0009","90","","90","","90","","10024.9","0.9","135","2","135","2","","","","","","","","4","P c c n","-P 2ab 2ac","56","","","","- C26 H35 Mg N2 -","- C26 H35 Mg N2 -","- C416 H560 Mg16 N32 -","16","2","","Li, Jia; Luo, Man; Sheng, Xingchao; Hua, Haiming; Yao, Weiwei; Pullarkat, Sumod A.; Xu, Li; Ma, Mengtao","Unsymmetrical β-diketiminate magnesium(i) complexes: syntheses and application in catalytic hydroboration of alkyne, nitrile and carbonyl compounds","Organic Chemistry Frontiers","2018","5","24","3538","","10.1039/C8QO00720A","","","0.71073","MoKα","","0.1431","0.1024","","","0.1999","0.2137","","","","","","1.236","","","","has coordinates","237180","2020-10-21","18:00:00",""
"1554392","8.5511","0.0003","10.4286","0.0003","14.3935","0.0004","88.875","0.002","87.601","0.002","68.209","0.003","1190.78","0.07","291","2","291","2","","","","","","","","5","P -1","-P 1","2","","","","- C30 H21 Cl N2 O2 -","- C30 H21 Cl N2 O2 -","- C60 H42 Cl2 N4 O4 -","2","1","","Xu, Hui; Chen, Kuan; Liu, Hong-Wei; Wang, Guan-Wu","Solvent-free N-iodosuccinimide-promoted synthesis of spiroimidazolines from alkenes and amidines under ball-milling conditions","Organic Chemistry Frontiers","2018","5","19","2864","","10.1039/C8QO00723C","","","1.54184","CuKα","","0.0501","0.0464","","","0.127","0.1306","","","","","","1.04","","","","has coordinates","237183","2020-10-21","18:00:00",""
"1554393","8.1716","0.0004","30.1115","0.0013","10.9853","0.0005","90","","95.159","0.002","90","","2692.1","0.2","100","","100","","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C22 H24 Cl3 F6 N4 P Ru -","- C22 H24 Cl3 F6 N4 P Ru -","- C88 H96 Cl12 F24 N16 P4 Ru4 -","4","1","","Wu, Qiang; Pan, Le; Du, Guangming; Zhang, Chi; Wang, Dawei","Preparation of pyridyltriazole ruthenium complexes as effective catalysts for the selective alkylation and one-pot C‒H hydroxylation of 2-oxindole with alcohols and mechanism exploration","Organic Chemistry Frontiers","2018","5","18","2668","","10.1039/C8QO00725J","","","0.71075","MoKα","","0.049","0.0457","","","0.0973","0.0986","","","","","","1.266","","","","has coordinates,has disorder","237185","2020-10-21","18:00:00",""
"1554394","8.3324","0.0007","18.0049","0.0015","18.9382","0.0019","90","","90","","90","","2841.2","0.4","296.32","0.1","296.32","0.1","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C17 H13 F2 N O2 -","- C17 H13 F2 N O2 -","- C136 H104 F16 N8 O16 -","8","1","","Ma, Xingxing; Deng, Shuilin; Song, Qiuling","Halodifluoroacetates as formylation reagents for various amines via unprecedented quadruple cleavage","Organic Chemistry Frontiers","2018","5","24","3505","","10.1039/C8QO00727F","","x-ray","0.71073","MoKα","","0.0657","0.0445","","","0.1082","0.1237","","","","","","1.0611","","","","has coordinates","237187","2020-10-21","18:00:00",""
"1554395","6.32","0.002","11.047","0.004","16.999","0.006","90.548","0.009","95.825","0.009","90.542","0.009","1180.6","0.7","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C14 H17 N O -","- C14 H17 N O -","- C56 H68 N4 O4 -","4","2","","Liu, Yang; Cerveri, Alessandro; De Nisi, Assunta; Monari, Magda; Nieto Faza, Olalla; Lopez, Carlos Silva; Bandini, Marco","Nickel catalyzed regio- and stereoselective arylation and methylation of allenamides via coupling reactions. An experimental and computational study","Organic Chemistry Frontiers","2018","5","22","3231","","10.1039/C8QO00729B","","","0.71073","MoKα","","0.1543","0.0971","","","0.2356","0.268","","","","","","1.137","","","","has coordinates","237189","2020-10-21","18:00:00",""
"1554396","6.9966","0.001","12.0579","0.0017","12.9998","0.0018","63.724","0.003","88.61","0.003","86.344","0.003","981.4","0.2","296","2","296","2","","","","","","","","6","P -1","-P 1","2","","","","- C12 H26 Cl2 N2 Ni O7 -","- C12 H26 Cl2 N2 Ni O7 -","- C24 H52 Cl4 N4 Ni2 O14 -","2","1","","Liu, Yang; Cerveri, Alessandro; De Nisi, Assunta; Monari, Magda; Nieto Faza, Olalla; Lopez, Carlos Silva; Bandini, Marco","Nickel catalyzed regio- and stereoselective arylation and methylation of allenamides via coupling reactions. An experimental and computational study","Organic Chemistry Frontiers","2018","5","22","3231","","10.1039/C8QO00729B","","","0.71073","MoKα","","0.0746","0.0594","","","0.1628","0.1738","","","","","","1.029","","","","has coordinates","237189","2020-10-21","18:00:00",""
"1554397","10.9821","0.0005","9.771","0.0003","21.137","0.0009","90","","119.629","0.003","90","","1971.56","0.15","295","2","295","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","7,8,9,11,12-pentamethoxy-1,2,5,13b-tetrahydrodibenzo[c,e]pyrrolo[1,2-a]azepin-3-one","","- C22 H25 N O6 -","- C22 H25 N O6 -","- C88 H100 N4 O24 -","4","1","","Boichenko, Maksim A.; Ivanova, Olga A.; Andreev, Ivan A.; Chagarovskiy, Alexey O.; Levina, Irina I.; Rybakov, Victor B.; Skvortsov, Dmitriy A.; Trushkov, Igor V.","Convenient approach to polyoxygenated dibenzo[c,e]pyrrolo[1,2-a]azepines from donor‒acceptor cyclopropanes","Organic Chemistry Frontiers","2018","5","19","2829","","10.1039/C8QO00742J","","","1.5418","CuKα","","0.0595","0.0486","","","0.1264","0.1338","","","","","","1.004","","","","has coordinates","237191","2020-10-21","18:00:00",""
"1554398","7.0556","0.0003","15.3824","0.0005","10.7866","0.0005","90","","108.471","0.003","90","","1110.38","0.08","295","2","295","2","","","","","","","","4","P 1 c 1","P -2yc","7","","1-(3,4,5-trimethoxybenzyl)-5-(3,4,5-trimethoxyphenyl)pyrrolidin-2-one","","- C23 H29 N O7 -","- C23 H29 N O7 -","- C46 H58 N2 O14 -","2","1","","Boichenko, Maksim A.; Ivanova, Olga A.; Andreev, Ivan A.; Chagarovskiy, Alexey O.; Levina, Irina I.; Rybakov, Victor B.; Skvortsov, Dmitriy A.; Trushkov, Igor V.","Convenient approach to polyoxygenated dibenzo[c,e]pyrrolo[1,2-a]azepines from donor‒acceptor cyclopropanes","Organic Chemistry Frontiers","2018","5","19","2829","","10.1039/C8QO00742J","","","1.54186","CuKα","","0.0433","0.0421","","","0.1117","0.1128","","","","","","1.043","","","","has coordinates","237191","2020-10-21","18:00:00",""
"1554399","15.7969","0.0003","8.7827","0.0002","14.6012","0.0004","90","","103.801","0.002","90","","1967.28","0.08","295","2","295","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","7,8,10,11,12-Pentamethoxy-1,2,5,13b-tetrahydrodibenzo[c,e]pyrrolo[1,2-a]azepin-3-one","","- C22 H25 N O6 -","- C22 H25 N O6 -","- C88 H100 N4 O24 -","4","1","","Boichenko, Maksim A.; Ivanova, Olga A.; Andreev, Ivan A.; Chagarovskiy, Alexey O.; Levina, Irina I.; Rybakov, Victor B.; Skvortsov, Dmitriy A.; Trushkov, Igor V.","Convenient approach to polyoxygenated dibenzo[c,e]pyrrolo[1,2-a]azepines from donor‒acceptor cyclopropanes","Organic Chemistry Frontiers","2018","5","19","2829","","10.1039/C8QO00742J","","","1.5418","CuKα","","0.0475","0.0414","","","0.1116","0.1156","","","","","","1.061","","","","has coordinates","237191","2020-10-21","18:00:00",""
"1554400","9.516","0.003","11.551","0.006","13.616","0.007","91.24","0.04","106.05","0.04","99.94","0.03","1412.9","1.2","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","5,6-dioxophenanthriporphyrin","","- C43 H26 N2 O2 -","- C43 H26 N2 O2 -","- C86 H52 N4 O4 -","2","1","","Kupietz, Kamil; Białek, Michał J.; Białońska, Agata; Szyszko, Bartosz; Latos-Grażyński, Lechosław","Aromaticity control via modifications of a macrocyclic frame: 5,6-dimethoxyphenanthriporphyrin and 5,6-dioxophenanthriporphyrin","Organic Chemistry Frontiers","2018","5","21","3068","","10.1039/C8QO00751A","","","1.54184","CuKα","","0.3027","0.1221","","","0.2214","0.3452","","","","","","0.895","","","","has coordinates","237194","2020-10-21","18:00:00",""
"1554401","14.154","0.003","17.553","0.003","19.832","0.003","90","","106.78","0.03","90","","4717.4","1.6","100","2","100","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","monocation of 5,6-dioxophenanthriporphyrin","","- C61 H45 B F4 N2 O2 -","- C61 H45 B F4 N2 O2 -","- C244 H180 B4 F16 N8 O8 -","4","1","","Kupietz, Kamil; Białek, Michał J.; Białońska, Agata; Szyszko, Bartosz; Latos-Grażyński, Lechosław","Aromaticity control via modifications of a macrocyclic frame: 5,6-dimethoxyphenanthriporphyrin and 5,6-dioxophenanthriporphyrin","Organic Chemistry Frontiers","2018","5","21","3068","","10.1039/C8QO00751A","","","1.54175","CuKα","","0.0708","0.0564","","","0.1492","0.16","","","","","","0.947","","","","has coordinates","237194","2020-10-21","18:00:00",""
"1554402","8.09","0.002","12.074","0.003","24.254","0.003","82.58","0.02","89.11","0.02","70.85","0.03","2218.3","0.9","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C86 H54 B8 F22 N4 O7 -","- C86 H54 B8 F22 N4 O7 -","- C86 H54 B8 F22 N4 O7 -","1","0.5","","Kupietz, Kamil; Białek, Michał J.; Białońska, Agata; Szyszko, Bartosz; Latos-Grażyński, Lechosław","Aromaticity control via modifications of a macrocyclic frame: 5,6-dimethoxyphenanthriporphyrin and 5,6-dioxophenanthriporphyrin","Organic Chemistry Frontiers","2018","5","21","3068","","10.1039/C8QO00751A","","","1.54175","CuKα","","0.2001","0.081","","","0.1883","0.2196","","","","","","0.664","","","","has coordinates,has disorder","237194","2020-10-21","18:00:00",""
"1554404","12.2892","0.0006","11.6999","0.0005","19.3795","0.0009","90","","103.521","0.005","90","","2709.2","0.2","293","2","293","2","","","","","","","","4","P 1 21 1","P 2yb","4","","zwm-132","","- C29 H37 N O7 -","- C29 H37 N O7 -","- C116 H148 N4 O28 -","4","2","","Fan, Yaqin; Wang, Yi; Fu, Peng; Chairoungdua, Arthit; Piyachaturawat, Pawinee; Zhu, Weiming","Secopaxilline A, an indole-diterpenoid derivative from an aciduric Penicillium fungus, its identification and semisynthesis","Organic Chemistry Frontiers","2018","5","19","2835","","10.1039/C8QO00756J","","","1.54178","CuKα","","0.0676","0.0491","","","0.1065","0.1205","","","","","","1.033","","","","has coordinates","237198","2020-10-21","18:00:00",""
"1554405","9.5523","0.0004","9.8572","0.0003","23.9209","0.0009","90","","99.141","0.004","90","","2223.76","0.14","296.83","0.1","296.83","0.1","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C28 H24 O5 -","- C28 H24 O5 -","- C112 H96 O20 -","4","1","","Zhao, Yinsong; Zheng, Qinze; Yu, Chuangui; Liu, Zheng; Wang, Deping; You, Jingsong; Gao, Ge","Rh(iii)-Catalyzed regioselective C‒H [4 + 2] C-annulation of vinyl enaminones with alkynes to form polysubstituted salicylaldehydes","Organic Chemistry Frontiers","2018","5","19","2875","","10.1039/C8QO00759D","","x-ray","1.54184","CuKα","","0.0773","0.0673","","","0.2147","0.2311","","","","","","1.124","","","","has coordinates","237200","2020-10-21","18:00:00",""
"1554406","13.248","0.002","7.6262","0.0012","27.213","0.004","90","","97.298","0.003","90","","2727.1","0.7","296.15","","296.15","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C30 H31 Br N2 O3 -","- C30 H31 Br N2 O3 -","- C120 H124 Br4 N8 O12 -","4","2","","Yuan, Yang; Zheng, Zhan-Jiang; Ye, Fei; Ma, Jun-Han; Xu, Zheng; Bai, Xing-Feng; Li, Li; Xu, Li-Wen","Highly efficient desymmetrization of cyclopropenes to azabicyclo[3.1.0]hexanes with five continuous stereogenic centers by copper-catalyzed [3 + 2] cycloadditions","Organic Chemistry Frontiers","2018","5","18","2759","","10.1039/C8QO00761F","","","0.71073","MoKα","","0.1405","0.0694","","","0.179","0.2167","","","","","","1.026","","","","has coordinates","237202","2020-10-21","18:00:00",""
"1554407","7.3005","0.0004","12.1224","0.0005","11.9121","0.0006","90","","105.259","0.006","90","","1017.05","0.09","293","2","293","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C23 H28 O6 -","- C23 H28 O6 -","- C46 H56 O12 -","2","1","","Zhang, Xun; Li, Zhongle; Yong, Huaya; Xie, Zhixiang","Biomimetic syntheses of C23 terpenoids: structural revision of salyunnanin A and confirmation of hassanane","Organic Chemistry Frontiers","2018","5","23","3469","","10.1039/C8QO00772A","","","1.54184","CuKα","","0.0514","0.0506","","","0.1379","0.1395","","","","","","1.04","","","","has coordinates","237204","2020-10-21","18:00:00",""
"1554408","7.5983","0.0003","16.424","0.0007","20.8458","0.0008","90","","90","","90","","2601.44","0.18","223","2","223","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","Methyl 5-(5-bromo-2-hydroxybenzoyl) nicotinate","","- C14 H10 Br N O4 -","- C14 H10 Br N O4 -","- C112 H80 Br8 N8 O32 -","8","1","","Maezono, Shizuka Mei Bautista; Kim, Sung Hong; Lee, Yong Rok","Copper-catalyzed [3 + 2 + 1] annulation for functionalized pyridines as potent and dynamic UV absorbers","Organic Chemistry Frontiers","2018","5","23","3368","","10.1039/C8QO00782A","","","0.71073","MoKα","","0.0345","0.0252","","","0.0607","0.0658","","","","","","1.055","","","","has coordinates","237206","2020-10-21","18:00:00",""
"1554409","9.0575","0.0017","12.288","0.002","12.993","0.003","90","","94.793","0.002","90","","1441","0.5","293","2","293","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C18 H18 O2 -","- C18 H18 O2 -","- C72 H72 O8 -","4","1","","Yang, Binmiao; Zhai, Xuejie; Feng, Shubo; Shao, Zhihui","Dearomatization of naphthols using oxy-allyl cations: efficient construction of α-all-carbon quaternary center-containing 2-(2-oxocycloalkyl)cycloalkyl diketones","Organic Chemistry Frontiers","2018","5","19","2794","","10.1039/C8QO00783G","","","0.71073","MoKα","","0.0735","0.0518","","","0.1412","0.155","","","","","","1.095","","","","has coordinates","237208","2020-10-21","18:00:00",""
"1554410","17.135","0.003","17.343","0.003","20.802","0.003","106.696","0.004","98.131","0.004","118.106","0.003","4934.7","1.4","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C44 H42 Cl N5 O8 -","- C44 H42 Cl N5 O8 -","- C176 H168 Cl4 N20 O32 -","4","2","","Yang, Wen-Juan; Sun, Qiu; Sun, Jing; Yan, Chao-Guo","Domino aza/oxa-hetero-Diels‒Alder reaction for construction of novel spiro[pyrido[3′,2′:5,6]pyrano[2,3-d]pyrimidine-7,5′-pyrimidine]","Organic Chemistry Frontiers","2018","5","18","2754","","10.1039/C8QO00784E","","","0.71073","MoKα","","0.1882","0.0908","","","0.2191","0.2653","","","","","","1.017","","","","has coordinates","237209","2020-10-21","18:00:00",""
"1554411","12.086","0.003","12.455","0.003","17.13","0.004","96.558","0.009","109.996","0.008","107.812","0.009","2236.9","1","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C42 H38 Cl N5 O6 -","- C42 H38 Cl N5 O6 -","- C84 H76 Cl2 N10 O12 -","2","1","","Yang, Wen-Juan; Sun, Qiu; Sun, Jing; Yan, Chao-Guo","Domino aza/oxa-hetero-Diels‒Alder reaction for construction of novel spiro[pyrido[3′,2′:5,6]pyrano[2,3-d]pyrimidine-7,5′-pyrimidine]","Organic Chemistry Frontiers","2018","5","18","2754","","10.1039/C8QO00784E","","","0.71073","MoKα","","0.2438","0.1197","","","0.2511","0.3034","","","","","","1.01","","","","has coordinates","237209","2020-10-21","18:00:00",""
"1554412","9.7638","0.0005","10.0633","0.0005","10.6246","0.0005","100.341","0.004","103.17","0.004","95.285","0.004","990.28","0.09","122.98","0.13","122.98","0.13","","","","","","","","2","P -1","-P 1","2","tetraarylethene","tetraarylethene","","- C28 H22 -","- C28 H22 -","- C56 H44 -","2","1","","Chuskit, Deachen; Chaudhary, Renu; Venugopalan, Paloth; König, Burkhard; Natarajan, Palani","Oxidative homodimerization of substituted olefins by DDQ visible light photocatalysis","Organic Chemistry Frontiers","2018","5","24","3553","","10.1039/C8QO00792F","","x-ray","1.54184","CuKα","","0.0434","0.0358","","","0.0881","0.0934","","","","","","1.036","","","","has coordinates","237211","2020-10-21","18:00:00",""
"1554413","10","0.002","14.827","0.003","13.344","0.003","90","","101.939","0.003","90","","1935.7","0.7","173","2","173","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C18 H25 N O7 S -","- C18 H25 N O7 S -","- C72 H100 N4 O28 S4 -","4","1","","Lei, Meng; Li, Yanjun; Cao, Shi; Hou, Xinyi; Gong, Lei","Alkylation‒peroxidation of α-carbonyl imines or ketones catalyzed by a copper salt via radical-mediated Csp3‒H functionalization","Organic Chemistry Frontiers","2018","5","21","3083","","10.1039/C8QO00797G","","","0.71073","MoKα","","0.0888","0.0813","","","0.2211","0.2292","","","","","","1.011","","","","has coordinates","237213","2020-10-21","18:00:00",""
"1554414","12.1127","0.001","13.1333","0.0012","13.1505","0.0011","76.939","0.007","79.228","0.007","63.194","0.009","1810.2","0.3","173","","173","","","","","","","","","5","P -1","-P 1","2","","7-endo","","- C19 H24 F3 N O2 -","- C19 H24 F3 N O2 -","- C76 H96 F12 N4 O8 -","4","2","","Long, Hao; Song, Jinshuai; Xu, Hai-Chao","Electrochemical synthesis of 7-membered carbocycles through cascade 5-exo-trig/7-endo-trig radical cyclization","Organic Chemistry Frontiers","2018","5","21","3129","","10.1039/C8QO00803E","","x-ray","1.54184","CuKα","","0.0851","0.0762","","","0.2009","0.2149","","","","","","1.035","","","","has coordinates,has disorder","237214","2020-10-21","18:00:00",""
"1554415","8.6306","0.0004","10.9636","0.0006","14.5139","0.0007","90","","90.644","0.002","90","","1373.25","0.12","100","2","100","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C30 H29 N3 O4 S -","- C30 H29 N3 O4 S -","- C60 H58 N6 O8 S2 -","2","1","","Huang, Qiuhong; Cheng, Yuyu; Yuan, Huijun; Chang, Xiaoyong; Li, Pengfei; Li, Wenjun","Organocatalytic enantioselective Mannich-type addition of 5H-thiazol-4-ones to isatin-derived imines: access to 3-substituted 3-amino-2-oxindoles featured by vicinal sulfur-containing tetrasubstituted stereocenters","Organic Chemistry Frontiers","2018","5","22","3226","","10.1039/C8QO00814K","","x-ray","0.71073","MoKα","","0.0375","0.0331","","","0.0767","0.0786","","","","","","1.049","","","","has coordinates","237217","2020-10-21","18:00:00",""
"1554416","18.2546","0.0006","9.1982","0.0003","13.3199","0.0004","90","","108.231","0.001","90","","2124.27","0.12","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H22 N4 O4 -","- C24 H22 N4 O4 -","- C96 H88 N16 O16 -","4","1","","Qiu, Shaobing; Guo, Chunlei; Wang, Mingkang; Sun, Zhenglong; Li, Hui; Qian, Xuhong; Yang, Youjun","Mild dealkylative N-nitrosation of N,N-dialkylaniline derivatives for convenient preparation of photo-triggered and photo-calibrated NO donors","Organic Chemistry Frontiers","2018","5","22","3206","","10.1039/C8QO00818C","","","0.71073","MoKα","","0.0736","0.0494","","","0.1184","0.1352","","","","","","1.038","","","","has coordinates","237219","2020-10-21","18:00:00",""
"1554417","11.2278","0.0005","13.7389","0.0006","7.4364","0.0003","90","","107.173","0.001","90","","1095.98","0.08","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C12 H12 N2 O3 -","- C12 H12 N2 O3 -","- C48 H48 N8 O12 -","4","1","","Qiu, Shaobing; Guo, Chunlei; Wang, Mingkang; Sun, Zhenglong; Li, Hui; Qian, Xuhong; Yang, Youjun","Mild dealkylative N-nitrosation of N,N-dialkylaniline derivatives for convenient preparation of photo-triggered and photo-calibrated NO donors","Organic Chemistry Frontiers","2018","5","22","3206","","10.1039/C8QO00818C","","","0.71073","MoKα","","0.05","0.0387","","","0.0914","0.0998","","","","","","1.042","","","","has coordinates","237219","2020-10-21","18:00:00",""
"1554418","13.145","0.0005","14.0218","0.0006","12.9264","0.0005","90","","114.416","0.001","90","","2169.47","0.15","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H20 N4 O5 -","- C24 H20 N4 O5 -","- C96 H80 N16 O20 -","4","1","","Qiu, Shaobing; Guo, Chunlei; Wang, Mingkang; Sun, Zhenglong; Li, Hui; Qian, Xuhong; Yang, Youjun","Mild dealkylative N-nitrosation of N,N-dialkylaniline derivatives for convenient preparation of photo-triggered and photo-calibrated NO donors","Organic Chemistry Frontiers","2018","5","22","3206","","10.1039/C8QO00818C","","","0.71073","MoKα","","0.0592","0.0411","","","0.0889","0.1004","","","","","","1.028","","","","has coordinates","237219","2020-10-21","18:00:00",""
"1554421","5.628","0.002","19.385","0.004","17.569","0.004","90","0.03","91.36","0.03","90","0.03","1916.2","0.9","173","2","173","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C24 H19 Cl N2 O -","- C24 H19 Cl N2 O -","- C96 H76 Cl4 N8 O4 -","4","1","","Tong, Mengchao; Zhang, Yong; Qin, Cong; Fu, Yiwei; Liu, Yonghai; Li, Hao; Wang, Wei","Alkenylazaarenes as dipolarophiles in 1,3-dipolar cycloaddition of nitrones: regioselectivity-switchable and highly diastereoselective synthesis of multisubstituted isoxazolidines","Organic Chemistry Frontiers","2018","5","20","2945","","10.1039/C8QO00826D","","","1.54178","CuKα","","0.0357","0.03","","","0.0779","0.0819","","","","","","1.015","","","","has coordinates","237223","2020-10-21","18:00:00",""
"1554422","5.7976","0.0009","9.4263","0.0014","17.097","0.003","87.715","0.003","87.737","0.003","86.465","0.003","931.2","0.3","130","","130","","","","","","","","","5","P -1","-P 1","2","","","","- C24 H19 Cl N2 O -","- C24 H19 Cl N2 O -","- C48 H38 Cl2 N4 O2 -","2","1","","Tong, Mengchao; Zhang, Yong; Qin, Cong; Fu, Yiwei; Liu, Yonghai; Li, Hao; Wang, Wei","Alkenylazaarenes as dipolarophiles in 1,3-dipolar cycloaddition of nitrones: regioselectivity-switchable and highly diastereoselective synthesis of multisubstituted isoxazolidines","Organic Chemistry Frontiers","2018","5","20","2945","","10.1039/C8QO00826D","","","0.71073","MoKα","","0.1002","0.0533","","","0.107","0.1273","","","","","","1.005","","","","has coordinates","237223","2020-10-21","18:00:00",""
"1554423","6.229","0.0001","13.6065","0.0002","14.6177","0.0003","90","","90","","90","","1238.92","0.04","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C17 H0.25 N O -","- C17 H11 N O -","- C68 H44 N4 O4 -","4","1","","Xu, Xin-Ming; Lei, Chuan-Hu; Tong, Shuo; Zhu, Jieping; Wang, Mei-Xiang","Lewis acid catalyst-steered divergent synthesis of functionalized vicinal amino alcohols and pyrroles from tertiary enamides","Organic Chemistry Frontiers","2018","5","21","3138","","10.1039/C8QO00839F","","","1.54184","CuKα","","0.0369","0.0343","","","0.0834","0.0862","","","","","","1.11","","","","has coordinates","237224","2020-10-21","18:00:00",""
"1554424","13.42","0.002","5.3749","0.0008","17.821","0.003","90","","105.381","0.005","90","","1239.4","0.3","296","2","296","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C27 H25 F N2 O5 S -","- C27 H25 F N2 O5 S -","- C54 H50 F2 N4 O10 S2 -","2","1","","Cao, Zhong-Yan; Wang, Wenmin; Liao, Kui; Wang, Xiaoming; Zhou, Jian; Ma, Jing","Catalytic enantioselective synthesis of cyclopropanes featuring vicinal all-carbon quaternary stereocenters with a CH2F group; study of the influence of C‒F⋯H‒N interactions on reactivity","Organic Chemistry Frontiers","2018","5","20","2960","","10.1039/C8QO00842F","","","0.71073","MoKα","","0.1349","0.0661","","","0.1551","0.1967","","","","","","1.024","","","","has coordinates","237226","2020-10-21","18:00:00",""
"1554425","6.6841","0.0006","8.7074","0.0008","14.4482","0.0013","87.391","0.003","81.591","0.002","78.532","0.003","815.14","0.13","296","2","296","2","","","","","","","","5","P 1","P 1","1","","","","- C18 H16 Br F O2 -","- C18 H16 Br F O2 -","- C36 H32 Br2 F2 O4 -","2","2","","Cao, Zhong-Yan; Wang, Wenmin; Liao, Kui; Wang, Xiaoming; Zhou, Jian; Ma, Jing","Catalytic enantioselective synthesis of cyclopropanes featuring vicinal all-carbon quaternary stereocenters with a CH2F group; study of the influence of C‒F⋯H‒N interactions on reactivity","Organic Chemistry Frontiers","2018","5","20","2960","","10.1039/C8QO00842F","","","0.71073","MoKα","","0.0577","0.0518","","","0.1409","0.1463","","","","","","1.065","","","","has coordinates","237226","2020-10-21","18:00:00",""
"1554426","10.0137","0.0006","10.3706","0.0006","11.987","0.0007","90","","109.801","0.002","90","","1171.23","0.12","150","2","150","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C14 H13 N O3 -","- C14 H13 N O3 -","- C56 H52 N4 O12 -","4","2","","Kim, Simon J.; Batey, Robert A.","Enantioselective isoquinuclidine synthesis via sequential Diels‒Alder/visible-light photoredox C‒C bond cleavage: a formal synthesis of the indole alkaloid catharanthine","Organic Chemistry Frontiers","2018","5","20","2934","","10.1039/C8QO00849C","","","1.54178","CuKα","","0.0278","0.0276","","","0.0695","0.0697","","","","","","1.09","","","","has coordinates","237227","2020-10-21","18:00:00",""
"1554427","7.6019","0.0006","7.7795","0.0007","17.7908","0.0015","94.036","0.005","92.577","0.005","114.867","0.004","948.98","0.14","296","2","296","2","","","","","","","","4","P -1","-P 1","2","Organic Compound","","","- C42 H50 O2 Si2 -","- C42 H50 O2 Si2 -","- C42 H50 O2 Si2 -","1","0.5","","Ozdemir, Resul; Park, Sangyun; Deneme, İbrahim; Park, Yonghan; Zorlu, Yunus; Alidagi, Husniye Ardic; Harmandar, Kevser; Kim, Choongik; Usta, Hakan","Triisopropylsilylethynyl-substituted indenofluorenes: carbonyl versus dicyanovinylene functionalization in one-dimensional molecular crystals and solution-processed n-channel OFETs","Organic Chemistry Frontiers","2018","5","20","2912","","10.1039/C8QO00856F","","","0.71073","MoKα","","0.0982","0.086","","","0.2596","0.2746","","","","","","1.078","","","","has coordinates","237229","2020-10-21","18:00:00",""
"1554428","39.755","0.005","10.0294","0.0012","11.4351","0.0014","90","","102.874","0.008","90","","4444.8","1","296","2","296","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","Organic Compound","","","- C48 H50 N4 Si2 -","- C48 H50 N4 Si2 -","- C192 H200 N16 Si8 -","4","0.5","","Ozdemir, Resul; Park, Sangyun; Deneme, İbrahim; Park, Yonghan; Zorlu, Yunus; Alidagi, Husniye Ardic; Harmandar, Kevser; Kim, Choongik; Usta, Hakan","Triisopropylsilylethynyl-substituted indenofluorenes: carbonyl versus dicyanovinylene functionalization in one-dimensional molecular crystals and solution-processed n-channel OFETs","Organic Chemistry Frontiers","2018","5","20","2912","","10.1039/C8QO00856F","","","0.71073","MoKα","","0.202","0.1097","","","0.3031","0.373","","","","","","1.016","","","","has coordinates","237229","2020-10-21","18:00:00",""
"1554429","17.45405","0.00014","8.11896","0.00007","19.929","0.00015","90","","91.5647","0.0007","90","","2823.06","0.04","100","","100","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C33 H35 N O6 -","- C33 H35 N O6 -","- C132 H140 N4 O24 -","4","1","","Yi, Xiao; Tang, Hongxia; Chen, Jing; Xu, Xiuling; Ma, Yongmin","Facile one-pot synthesis of a 3-azabicyclo[3.3.1]nonane scaffold by a tandem Mannich reaction","Organic Chemistry Frontiers","2018","5","20","3003","","10.1039/C8QO00870A","","","1.54184","CuKα","","0.042","0.0402","","0.1087","0.1047","0.101","","","","","","1.021","","","","has coordinates","237230","2020-10-21","18:00:00",""
"1554430","11.083","0.007","21.629","0.013","12.241","0.007","90","","116.92","","90","","2616","3","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C30 H26 Cl3 N O3 -","- C30 H26 Cl3 N O3 -","- C120 H104 Cl12 N4 O12 -","4","1","","Yi, Xiao; Tang, Hongxia; Chen, Jing; Xu, Xiuling; Ma, Yongmin","Facile one-pot synthesis of a 3-azabicyclo[3.3.1]nonane scaffold by a tandem Mannich reaction","Organic Chemistry Frontiers","2018","5","20","3003","","10.1039/C8QO00870A","","","0.71073","MoKα","","0.1545","0.0998","","","0.2507","0.2824","","","","","","0.952","","","","has coordinates","237230","2020-10-21","18:00:00",""
"1554431","8.7333","0.001","32.515","0.005","11.3552","0.0017","90","","92.555","0.004","90","","3221.3","0.8","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","(E)-(1-(2-cyclopropyl-3-tosylprop-1-en-1-yl)-2-(4-methoxyphenyl)-2-methylcyclopropyl)diphenylphosphine oxide","","- C36 H37 O4 P S -","- C36 H37 O4 P S -","- C144 H148 O16 P4 S4 -","4","1","","Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei","Transition-metal-free radical cleavage of a hydrazonyl N‒S bond: tosyl radical-initiated cascade C(sp3)‒OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation","Organic Chemistry Frontiers","2018","5","24","3567","","10.1039/C8QO00873F","","","0.71073","MoKα","","0.1292","0.0566","","","0.1176","0.1417","","","","","","1.015","","","","has coordinates,has disorder","237232","2020-10-21","18:00:00",""
"1554432","10.244","0.0003","13.1272","0.0005","15.4443","0.0005","85.216","0.001","77.319","0.001","69.981","0.001","1903.71","0.11","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","(E)-(1-(2-([1,1'-biphenyl]-4-yl)-3-tosylprop-1-en-1-yl)-2-(4-methoxyphenyl)-2-methylcyclopropyl)diphenylphosphine oxide","","- C45 H41 O4 P S -","- C45 H41 O4 P S -","- C90 H82 O8 P2 S2 -","2","1","","Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei","Transition-metal-free radical cleavage of a hydrazonyl N‒S bond: tosyl radical-initiated cascade C(sp3)‒OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation","Organic Chemistry Frontiers","2018","5","24","3567","","10.1039/C8QO00873F","","","0.71073","MoKα","","0.0945","0.0539","","","0.1232","0.1402","","","","","","1.024","","","","has coordinates","237232","2020-10-21","18:00:00",""
"1554433","10.9576","0.0005","24.0001","0.0011","13.0509","0.0006","90","","94.036","0.002","90","","3423.7","0.3","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","(E)-(2,2-dibenzyl-1-(2-methyl-3-tosylprop-1-en-1-yl)cyclopropyl)diphenylphosphine oxide","","- C40 H39 O3 P S -","- C40 H39 O3 P S -","- C160 H156 O12 P4 S4 -","4","1","","Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei","Transition-metal-free radical cleavage of a hydrazonyl N‒S bond: tosyl radical-initiated cascade C(sp3)‒OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation","Organic Chemistry Frontiers","2018","5","24","3567","","10.1039/C8QO00873F","","","0.71073","MoKα","","0.0969","0.0501","","","0.1136","0.1315","","","","","","1.018","","","","has coordinates","237232","2020-10-21","18:00:00",""
"1554434","12.3705","0.0006","13.8788","0.0008","19.1238","0.001","90","","106.702","0.001","90","","3144.8","0.3","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","(E)-(2-methyl-1-(2-methyl-3-tosylprop-1-en-1-yl)-2-(naphthalen-2-yl)cyclopropyl)diphenylphosphine oxide","","- C37 H35 O3 P S -","- C37 H35 O3 P S -","- C148 H140 O12 P4 S4 -","4","1","","Chen, Yao-Zhong; Liu, Teng; Zhu, Jie; Zhang, Hui; Wu, Lei","Transition-metal-free radical cleavage of a hydrazonyl N‒S bond: tosyl radical-initiated cascade C(sp3)‒OAr cleavage, sulfonyl rearrangement and atropisomeric cyclopropanation","Organic Chemistry Frontiers","2018","5","24","3567","","10.1039/C8QO00873F","","","0.71073","MoKα","","0.0729","0.0464","","","0.1122","0.1237","","","","","","1.021","","","","has coordinates","237232","2020-10-21","18:00:00",""
"1554435","22.09","0.006","8.574","0.002","9.447","0.003","90","","101.6","0.02","90","","1752.7","0.8","296","2","296","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C22 H24 N2 -","- C22 H24 N2 -","- C88 H96 N8 -","4","1","","Liu, Siyuan; Zhang, Wenzhu; Qu, Jingping; Wang, Baomin","Engaging 2-methyl indolenines in a tandem condensation/1,5-hydride transfer/cyclization process: construction of a novel indolenine‒tetrahydroquinoline assembly","Organic Chemistry Frontiers","2018","5","20","3008","","10.1039/C8QO00875B","","","0.71073","MoKα","","0.0935","0.0493","","","0.1018","0.119","","","","","","1.025","","","","has coordinates","237234","2020-10-21","18:00:00",""
"1554436","8.8385","0.0005","14.3341","0.0009","17.8495","0.0011","90","","90","","90","","2261.4","0.2","100","2","100","2","","","","","","","","7","P 21 21 21","P 2ac 2ab","19","","","","- C21 H21 Br N O7 P S -","- C21 H21 Br N O7 P S -","- C84 H84 Br4 N4 O28 P4 S4 -","4","1","","Sun, Jun; Mou, Chengli; Liu, Changyi; Huang, Ruoyan; Zhang, Shupeng; Zheng, Pengcheng; Chi, Yonggui Robin","Enantioselective access to multi-cyclic α-amino phosphonates via carbene-catalyzed cycloaddition reactions between enals and six-membered cyclic imines","Organic Chemistry Frontiers","2018","5","20","2992","","10.1039/C8QO00877A","","","0.71073","MoKα","","0.0765","0.0451","","","0.0859","0.0981","","","","","","0.948","","","","has coordinates","237236","2020-10-21","18:00:00",""
"1554441","9.0319","0.0004","18.9034","0.0009","14.4632","0.0007","90","","96.64","0.002","90","","2452.8","0.2","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C28 H29 Co P S -","- C28 H29 Co P S -","- C112 H116 Co4 P4 S4 -","4","1","","Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang","Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives","Organic Chemistry Frontiers","2018","5","20","2997","","10.1039/C8QO00887F","","","0.71","MoKα","","0.0352","0.0285","","","0.0704","0.074","","","","","","1.042","","","","has coordinates","237239","2020-10-21","18:00:00",""
"1554442","12.766","0.0003","7.3952","0.0002","18.2702","0.0004","90","","103.067","0.002","90","","1680.17","0.07","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H18 N O2 -","- C22 H18 N O2 -","- C88 H72 N4 O8 -","4","1","","Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang","Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives","Organic Chemistry Frontiers","2018","5","20","2997","","10.1039/C8QO00887F","","x-ray","1.54184","CuKα","","0.0807","0.0707","","","0.1844","0.1974","","","","","","1.187","","","","has coordinates,has disorder","237239","2020-10-21","18:00:00",""
"1554443","7.3192","0.0006","11.4476","0.0007","14.2878","0.0011","109.541","0.006","103.435","0.007","90.85","0.006","1091.7","0.15","173","0.1","173","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C30 H23 N O2 -","- C30 H23 N O2 -","- C60 H46 N2 O4 -","2","1","","Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang","Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives","Organic Chemistry Frontiers","2018","5","20","2997","","10.1039/C8QO00887F","","x-ray","1.54184","CuKα","","0.0655","0.0504","","","0.1343","0.1468","","","","","","1.065","","","","has coordinates","237239","2020-10-21","18:00:00",""
"1554444","7.4718","0.0009","10.17","0.0013","13.6849","0.0015","80.313","0.01","76.092","0.01","74.405","0.011","966.3","0.2","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C26 H21 N O2 -","- C26 H21 N O2 -","- C52 H42 N2 O4 -","2","1","","Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang","Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives","Organic Chemistry Frontiers","2018","5","20","2997","","10.1039/C8QO00887F","","","0.71073","MoKα","","0.0706","0.0523","","","0.1325","0.1454","","","","","","1.079","","","","has coordinates","237239","2020-10-21","18:00:00",""
"1554445","16.6717","0.0015","10.051","0.002","14.516","0.006","90","","90","","90","","2432.4","1.1","172.99","0.1","172.99","0.1","","","","","","","","6","P n a 21","P 2c -2n","33","","","","- C28 H29 Br Co P S -","- C28 H29 Br Co P S -","- C112 H116 Br4 Co4 P4 S4 -","4","1","","Liu, Xiangyu; Wu, Chengjuan; Zhang, Jing; Shi, Yihan; Zhang, Shengnan; Geng, Yan; Tung, Chen-Ho; Wang, Wenguang","Cobalt-catalyzed radical cyclization of isocyanides forming phenanthridine derivatives","Organic Chemistry Frontiers","2018","5","20","2997","","10.1039/C8QO00887F","","x-ray","0.71073","MoKα","","0.0588","0.048","","","0.0977","0.1016","","","","","","1.044","","","","has coordinates","237239","2020-10-21","18:00:00",""
"1554448","26.357","0.0008","7.5712","0.0003","24.9141","0.0008","90","","92.458","0.003","90","","4967.1","0.3","293","2","293","2","","","","","","","","4","I 1 2 1","I 2y","5","","","","- C28 H33 Br O3 -","- C28 H33 Br O3 -","- C224 H264 Br8 O24 -","8","2","","Liu, Lin; Song, Huayue; Chen, Peng; Yuan, Ziyun; Feng, Shangbiao; Zhang, Weiwei; Fang, Bowen; Xie, Xingang; She, Xuegong","Total synthesis of (−)-8-epi-chromazonarol enabled by a unique N2H4·H2O promoted intramolecular oxa-Michael cyclization reaction","Organic Chemistry Frontiers","2018","5","20","3013","","10.1039/C8QO00901E","","","1.54184","CuKα","","0.0497","0.0468","","","0.1352","0.1402","","","","","","0.974","","","","has coordinates","237244","2020-10-21","18:00:00",""
"1554451","12.1152","0.0014","14.1577","0.0018","24.768","0.003","90","","93.519","0.002","90","","4240.3","0.9","296","2","296","2","","","","","","","","5","C 1 c 1","C -2yc","9","","","","- C26 H23 N O2 S -","- C26 H23 N O2 S -","- C208 H184 N8 O16 S8 -","8","2","","Zhang, Jia-hao; Wei, Yin; Shi, Min","Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes","Organic Chemistry Frontiers","2018","5","20","2980","","10.1039/C8QO00907D","","","0.71073","MoKα","","0.0513","0.0373","","","0.0883","0.0965","","","","","","1.031","","","","has coordinates","237247","2020-10-21","18:00:00",""
"1554452","10.875","0.012","11.83","0.014","16.54","0.02","90","","98.8","0.02","90","","2103","4","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C26 H23 N O2 S -","- C26 H23 N O2 S -","- C104 H92 N4 O8 S4 -","4","1","","Zhang, Jia-hao; Wei, Yin; Shi, Min","Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes","Organic Chemistry Frontiers","2018","5","20","2980","","10.1039/C8QO00907D","","","0.71073","MoKα","","0.0859","0.043","","","0.1015","0.1208","","","","","","1.009","","","","has coordinates","237247","2020-10-21","18:00:00",""
"1554453","20.5631","0.0007","27.2351","0.0011","9.3277","0.0003","90","","92.088","0.001","90","","5220.4","0.3","296","2","296","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C26 H23 N O4 S -","- C26 H23 N O4 S -","- C208 H184 N8 O32 S8 -","8","1","","Zhang, Jia-hao; Wei, Yin; Shi, Min","Gold-catalyzed ring enlargement and cycloisomerization of alkynylamide tethered alkylidenecyclopropanes","Organic Chemistry Frontiers","2018","5","20","2980","","10.1039/C8QO00907D","","","0.71073","MoKα","","0.0932","0.0673","","","0.2068","0.2299","","","","","","1.033","","","","has coordinates","237247","2020-10-21","18:00:00",""
"1554454","15.787","0.009","10.811","0.006","13.977","0.008","90","","112.816","0.007","90","","2199","2","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","1,1-phenylenedioxa-5-phenyl-3,3,7,7-tetrakis(trifluoromethyl)-1-phospha-2,6,8-trioxabicyclo[4.3.2(1,5)]octane","","- C20 H11 F12 O5 P -","- C20 H11 F12 O5 P -","- C80 H44 F48 O20 P4 -","4","1","","Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.","Tandem dihetero-Diels‒Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes","Organic Chemistry Frontiers","2018","5","21","3113","","10.1039/C8QO00915E","","x-ray","0.71073","MoKα","","0.0611","0.0444","","","0.1116","0.1226","","","","","","1.028","","","","has coordinates,has disorder","237249","2020-10-21","18:00:00",""
"1554455","7.266","0.003","11.409","0.005","8.573","0.004","90","","96.695","0.006","90","","705.8","0.5","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","triethylammonium oxabenzo-1,3,2-dioxaphosphol-2-oate","","- C12 H20 N O4 P -","- C12 H20 N O4 P -","- C24 H40 N2 O8 P2 -","2","1","","Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.","Tandem dihetero-Diels‒Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes","Organic Chemistry Frontiers","2018","5","21","3113","","10.1039/C8QO00915E","","x-ray","0.71073","MoKα","","0.0589","0.0429","","","0.0846","0.0915","","","","","","1.038","","","","has coordinates,has disorder","237249","2020-10-21","18:00:00",""
"1554456","4.6005","0.0004","10.122","0.0008","16.4334","0.0014","90","","90","","90","","765.24","0.11","150","2","150","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","2-hydroxyphenyl phosphoric acid","","- C6 H7 O5 P -","- C6 H7 O5 P -","- C24 H28 O20 P4 -","4","1","","Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.","Tandem dihetero-Diels‒Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes","Organic Chemistry Frontiers","2018","5","21","3113","","10.1039/C8QO00915E","","x-ray","0.71073","MoKα","","0.044","0.0387","","","0.0831","0.0859","","","","","","1.045","","","","has coordinates","237249","2020-10-21","18:00:00",""
"1554457","10.7892","0.0006","11.1562","0.0006","11.7122","0.0006","101.788","0.003","99.647","0.003","106.558","0.003","1283.93","0.12","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","1,1- phenylenedioxa-5-phenyl-3,7-bis(ethoxycarbonyl)-3,7-bis(trifluoromethyl)-1-phospha-2,6,8-trioxabicyclo[4.3.2(1,5)]octane","","- C24 H21 F6 O9 P -","- C24 H21 F6 O9 P -","- C48 H42 F12 O18 P2 -","2","1","","Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.","Tandem dihetero-Diels‒Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes","Organic Chemistry Frontiers","2018","5","21","3113","","10.1039/C8QO00915E","","x-ray","0.71073","MoKα","","0.0813","0.0442","","","0.1057","0.1222","","","","","","1.027","","","","has coordinates,has disorder","237249","2020-10-21","18:00:00",""
"1554458","27.972","0.006","27.972","0.006","11.844","0.003","90","","90","","90","","9267","4","293","2","293","2","","","","","","","","5","I 41/a :2","-I 4ad","88","","1,1-phenylenedioxa-5-phenyl-3,7-bis(trichloromethyl)-1-phospha-2,6,8-trioxabicyclo[4.3.2(1,5)]octane","","- C18 H13 Cl6 O5 P -","- C18 H13 Cl6 O5 P -","- C288 H208 Cl96 O80 P16 -","16","1","","Khasiyatullina, Nadezhda R.; Baronova, Tamara A.; Mironova, Ekaterina V.; Fayzullin, Robert R.; Litvinov, Igor A.; Efimov, Sergey V.; Musin, Rashid Z.; Klochkov, Vladimir V.; Mironov, Vladimir F.","Tandem dihetero-Diels‒Alder and Huisgen cycloaddition reactions. Synthesis, crystal structure and hydrolysis of the novel cage phosphoranes","Organic Chemistry Frontiers","2018","5","21","3113","","10.1039/C8QO00915E","","x-ray","0.71073","MoKα","","0.05","0.0399","","","0.0929","0.099","","","","","","1.048","","","","has coordinates","237249","2020-10-21","18:00:00",""
"1554459","8.8009","0.0008","12.3786","0.0018","16.3465","0.0019","102.889","0.012","95.068","0.009","108.26","0.011","1624.3","0.4","100","0.2","100","0.2","","","","","","","","5","P -1","-P 1","2","","","","- C40 H40 N O2 S -","- C40 H40 N O2 S -","- C80 H80 N2 O4 S2 -","2","1","","Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang","Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells","Organic Chemistry Frontiers","2018","5","22","3324","","10.1039/C8QO00934A","","x-ray","1.54184","CuKα","","0.1733","0.1048","","","0.2799","0.3361","","","","","","1.039","","","","has coordinates","237251","2020-10-21","18:00:00",""
"1554460","7.1299","0.0011","14.678","0.0013","17.037","0.002","74.911","0.009","81.895","0.013","89.178","0.01","1703.8","0.4","102","4","102","4","","","","","","","","5","P -1","-P 1","2","","","","- C44 H42 N O2 S -","- C44 H42 N O2 S -","- C88 H84 N2 O4 S2 -","2","1","","Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang","Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells","Organic Chemistry Frontiers","2018","5","22","3324","","10.1039/C8QO00934A","","x-ray","1.54184","CuKα","","0.2244","0.0946","","","0.2156","0.2882","","","","","","0.948","","","","has coordinates","237251","2020-10-21","18:00:00",""
"1554461","13.5245","0.0006","24.687","0.003","20.6534","0.0009","90","","102.064","0.004","90","","6743.4","0.9","100","0.13","100","0.13","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C84 H80 N2 O4 S4 -","- C84 H80 N2 O4 S4 -","- C336 H320 N8 O16 S16 -","4","1","","Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang","Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells","Organic Chemistry Frontiers","2018","5","22","3324","","10.1039/C8QO00934A","","x-ray","1.54184","CuKα","","0.21","0.1447","","","0.3854","0.4192","","","","","","1.061","","","","has coordinates","237251","2020-10-21","18:00:00",""
"1554462","14.3142","0.001","16.7266","0.0012","18.5616","0.0011","105.723","0.006","109.469","0.006","90.336","0.006","4010.6","0.5","99.98","0.17","99.98","0.17","","","","","","","","5","P -1","-P 1","2","","","","- C92 H81 N2 O4 S4 -","- C92 H81 N2 O4 S4 -","- C184 H162 N4 O8 S8 -","2","1","","Wu, Minming; Zhou, Jiadong; Luo, Yinqi; Zheng, Nan; Wang, Cong; Liu, Linlin; Xie, Zengqi; Ma, Yuguang","Construction of J-type aggregates as multi-functional interlayers for nonfullerene polymer solar cells","Organic Chemistry Frontiers","2018","5","22","3324","","10.1039/C8QO00934A","","x-ray","1.54184","CuKα","","0.2041","0.1084","","","0.318","0.3849","","","","","","1.051","","","","has coordinates","237251","2020-10-21","18:00:00",""
"1554467","9.7218","0.0008","7.7915","0.0006","24.097","0.002","90","","99.734","0.008","90","","1799","0.3","155.9","","155.9","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H16 N2 O6 S -","- C19 H16 N2 O6 S -","- C76 H64 N8 O24 S4 -","4","1","","Shen, Yangyong; Wang, Chaorong; Chen, Wei; Cui, Sunliang","Cascade reaction involving Diels‒Alder cascade: modular synthesis of amino α-pyrones, indolines and anilines","Organic Chemistry Frontiers","2018","5","24","3574","","10.1039/C8QO00939B","","","0.71073","MoKα","","0.0666","0.0484","","","0.1183","0.1359","","","","","","1.041","","","","has coordinates","237256","2020-10-21","18:00:00",""
"1554468","6.4452","0.0007","11.7323","0.0011","12.5163","0.0012","105.865","0.008","90.612","0.008","93.872","0.008","907.9","0.16","293","2","293.15","","","","","","","","","5","P -1","-P 1","2","","","","- C20 H19 N O4 S -","- C20 H19 N O4 S -","- C40 H38 N2 O8 S2 -","2","1","","Shen, Yangyong; Wang, Chaorong; Chen, Wei; Cui, Sunliang","Cascade reaction involving Diels‒Alder cascade: modular synthesis of amino α-pyrones, indolines and anilines","Organic Chemistry Frontiers","2018","5","24","3574","","10.1039/C8QO00939B","","","0.71073","MoKα","","0.0762","0.0508","","","0.1158","0.1339","","","","","","1.031","","","","has coordinates","237256","2020-10-21","18:00:00",""
"1554469","10.2302","0.0008","24.9417","0.0018","10.532","0.0007","90","","94.66","0.006","90","","2678.4","0.3","293","2","293.15","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C33 H26 Cl N O2 S -","- C33 H26 Cl N O2 S -","- C132 H104 Cl4 N4 O8 S4 -","4","1","","Shen, Yangyong; Wang, Chaorong; Chen, Wei; Cui, Sunliang","Cascade reaction involving Diels‒Alder cascade: modular synthesis of amino α-pyrones, indolines and anilines","Organic Chemistry Frontiers","2018","5","24","3574","","10.1039/C8QO00939B","","","0.71073","MoKα","","0.0692","0.0439","","","0.0958","0.1088","","","","","","1.041","","","","has coordinates","237256","2020-10-21","18:00:00",""
"1554470","9.9349","0.0009","5.4755","0.0005","25.351","0.003","90","","101.162","0.01","90","","1353","0.2","292.9","0.8","292.9","0.8","","","","","","","","4","I 1 2 1","I 2y","5","","","","- C26 H30 N4 O9 -","- C26 H30 N4 O9 -","- C52 H60 N8 O18 -","2","0.5","","Chen, Jinhong; Li, Junfang; Zhu, Longqing; Peng, Xue; Feng, Yiyue; Lu, Yingmei; Hu, Xiaoling; Liang, Jianpin; Zhao, Quanyi; Wang, Zhen","Total synthesis and structure revision of chrysamide B","Organic Chemistry Frontiers","2018","5","23","3402","","10.1039/C8QO00949J","","x-ray","0.71073","MoKα","","0.0558","0.0439","","","0.0971","0.1064","","","","","","1.052","","","","has coordinates","237258","2020-10-21","18:00:00",""
"1554471","11.6963","0.0014","8.9597","0.0008","23.096","0.002","90","","90.67","0.001","90","","2420.2","0.4","293","2","293","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C26 H30 O6 -","- C26 H30 O6 -","- C104 H120 O24 -","4","1","","Xiong, Yan-Jie; Shi, Shao-Qing; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo","A new dehydrogenative [4 + 1] annulation between para-quinone methides (p-QMs) and iodonium ylides for the synthesis of 2,3-dihydrobenzofurans","Organic Chemistry Frontiers","2018","5","23","3483","","10.1039/C8QO00950C","","","1.54178","CuKα","","0.119","0.0723","","","0.1786","0.2119","","","","","","1.081","","","","has coordinates","237259","2020-10-21","18:00:00",""
"1554472","10.805","0.0008","11.7571","0.0009","12.8689","0.0011","106.048","0.002","95.01","0.001","114.103","0.003","1396.3","0.2","298","2","298","2","","","","","","","","6","P -1","-P 1","2","","","","- C27 H28 Cl I N2 O5 -","- C27 H28 Cl I N2 O5 -","- C54 H56 Cl2 I2 N4 O10 -","2","1","","Xiong, Yan-Jie; Shi, Shao-Qing; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo","A new dehydrogenative [4 + 1] annulation between para-quinone methides (p-QMs) and iodonium ylides for the synthesis of 2,3-dihydrobenzofurans","Organic Chemistry Frontiers","2018","5","23","3483","","10.1039/C8QO00950C","","","0.71073","MoKα","","0.0829","0.0495","","","0.1228","0.1373","","","","","","1.039","","","","has coordinates","237259","2020-10-21","18:00:00",""
"1554473","8.4088","0.0005","17.398","0.0011","12.1982","0.0008","90","","101.318","0.001","90","","1749.85","0.19","90","","90","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","2-(3-methyl-1-phenyl-1H-pyrazol-2-ium-4-yl)-1,1-bis((trifluoromethyl)sulfonyl)ethan-1-ide","","- C14 H12 F6 N2 O4 S2 -","- C14 H12 F6 N2 O4 S2 -","- C56 H48 F24 N8 O16 S8 -","4","1","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0469","0.0381","","","0.0886","0.0948","","","","","","1.032","","","","has coordinates","237261","2020-10-21","18:00:00",""
"1554474","12.6441","0.0009","11.3643","0.0008","16.2034","0.0011","90","","111.751","0.001","90","","2162.5","0.3","90","","90","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","2-(2,2-bis((trifluoromethyl)sulfonyl)ethyl)-1-(phenylethynyl)-1,5,6,7-tetrahydro-4H-indol-4-one","","- C20 H15 F6 N O5 S2 -","- C20 H15 F6 N O5 S2 -","- C80 H60 F24 N4 O20 S8 -","4","1","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0363","0.0308","","","0.0755","0.0789","","","","","","1.025","","","","has coordinates","237261","2020-10-21","18:00:00",""
"1554475","13.0371","0.0009","14.5605","0.001","14.0643","0.001","90","","113.617","0.001","90","","2446.2","0.3","90","","90","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","2-(2,4-diphenyloxazol-3-ium-5-yl)-1,1-bis((trifluoromethyl)sulfonyl)ethan-1-ide","","- C21 H19 F6 N O6 S3 -","- C21 H19 F6 N O6 S3 -","- C84 H76 F24 N4 O24 S12 -","4","1","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0493","0.041","","","0.0957","0.1007","","","","","","1.042","","","","has coordinates,has disorder","237261","2020-10-21","18:00:00",""
"1554476","31.442","0.002","7.7594","0.0005","16.3435","0.0011","90","","91.74","0.001","90","","3985.5","0.4","90","","90","","","","","","","","","7","C 1 2/c 1","-C 2yc","15","","2-(1-(4-chlorophenyl)-5-hydroxy-3-methyl-1H-pyrazol-2-ium-4-yl)-1,1-bis((trifluoromethyl)sulfonyl)ethan-1-ide","","- C14 H11 Cl F6 N2 O5 S2 -","- C14 H11 Cl F6 N2 O5 S2 -","- C112 H88 Cl8 F48 N16 O40 S16 -","8","1","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0329","0.029","","","0.0722","0.0748","","","","","","1.03","","","","has coordinates","237261","2020-10-21","18:00:00",""
"1554477","5.7308","0.0005","13.6484","0.0013","21.184","0.002","90","","95.748","0.001","90","","1648.6","0.3","90","","90","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","3-(2,2-Bis((trifluoromethyl)sulfonyl)ethyl)-4-hydroxy-2H-chromen-2-one","","- C13 H8 F6 O7 S2 -","- C13 H8 F6 O7 S2 -","- C52 H32 F24 O28 S8 -","4","1","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0334","0.0292","","","0.071","0.0735","","","","","","1.023","","","","has coordinates","237261","2020-10-21","18:00:00",""
"1554478","14.266","0.002","6.0883","0.0009","18.922","0.003","90","","94.123","0.002","90","","1639.2","0.4","90","","90","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","2-(1-phenyl-1H-pyrazol-2-ium-2-yl)-1,1-bis((trifluoromethyl)sulfonyl)ethan-1-ide","","- C13 H10 F6 N2 O4 S2 -","- C13 H10 F6 N2 O4 S2 -","- C52 H40 F24 N8 O16 S8 -","4","1","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0461","0.0361","","","0.0846","0.0903","","","","","","1.029","","","","has coordinates","237261","2020-10-21","18:00:00",""
"1554479","17.2641","0.001","14.8304","0.0008","23.9088","0.0014","90","","90","","90","","6121.5","0.6","90","","90","","","","","","","","","6","P b c a","-P 2ac 2ab","61","","2-(5-hydroxy-1,3-dimethyl-1H-pyrazol-2-ium-4-yl)- 1,1-bis((trifluoromethyl)sulfonyl)ethan-1-ide","","- C9 H10 F6 N2 O5 S2 -","- C9 H10 F6 N2 O5 S2 -","- C144 H160 F96 N32 O80 S32 -","16","2","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0451","0.0373","","","0.0889","0.0929","","","","","","1.064","","","","has coordinates","237261","2020-10-21","18:00:00",""
"1554480","27.2048","0.0018","18.3507","0.0012","12.2694","0.0008","90","","90","","90","","6125.2","0.7","90","","90","","","","","","","","","6","P n a 21","P 2c -2n","33","","2-(5-hydroxy-2,3-dimethyl-1-phenyl-1H-pyrazol-2-ium-4-yl)- 1,1-bis((trifluoromethyl)sulfonyl)ethan-1-ide","","- C15 H14 F6 N2 O5 S2 -","- C15 H14 F6 N2 O5 S2 -","- C180 H168 F72 N24 O60 S24 -","12","3","","Almendros, Pedro; Yanai, Hikaru; Hoshikawa, Shoki; Aragoncillo, Cristina; Lázaro-Milla, Carlos; Toledano-Pinedo, Mireia; Matsumoto, Takashi; Alcaide, Benito","Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles","Organic Chemistry Frontiers","2018","5","21","3163","","10.1039/C8QO00955D","","","0.71073","MoKα","","0.0291","0.0264","","","0.0653","0.0671","","","","","","1.008","","","","has coordinates","237261","2020-10-21","18:00:00",""
"1554481","17.607","0.0012","5.4871","0.0004","25.7682","0.0017","90","","106.169","0.0015","90","","2391","0.3","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C29 H28 N2 O S2 -","- C29 H28 N2 O S2 -","- C116 H112 N8 O4 S8 -","4","1","","Weldeab, Asmerom O.; Li, Lei; Cekli, Seda; Abboud, Khalil A.; Schanze, Kirk S.; Castellano, Ronald K.","Pyridine-terminated low gap π-conjugated oligomers: design, synthesis, and photophysical response to protonation and metalation","Organic Chemistry Frontiers","2018","5","21","3170","","10.1039/C8QO00963E","","","0.71073","MoKα","","0.0677","0.0456","","","0.1154","0.1232","","","","","","1.008","","","","has coordinates,has disorder","237264","2020-10-21","18:00:00",""
"1554482","11.2685","0.0006","18.6581","0.0007","12.8795","0.0008","90","","111.426","0.007","90","","2520.8","0.3","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C26 H22 Br N O9 -","- C26 H22 Br N O9 -","- C104 H88 Br4 N4 O36 -","4","1","","Agafonova, Anastasiya V.; Smetanin, Ilia A.; Rostovskii, Nikolai V.; Khlebnikov, Alexander F.; Novikov, Mikhail S.","Expedient synthesis of 3-hydroxypyrroles via Bu3SnH-triggered ionic 5-exo-trig-cyclization of 5-chloro-3-azamuconoate derivatives","Organic Chemistry Frontiers","2018","5","23","3396","","10.1039/C8QO00982A","","","0.71073","MoKα","","0.0592","0.0388","","","0.0764","0.0845","","","","","","1.03","","","","has coordinates","237266","2020-10-21","18:00:00",""
"1554483","15.569","0.002","29.973","0.004","7.0564","0.001","90","","90","","90","","3292.9","0.8","293","2","293","2","","","","","","","","7","I b a 2","I 2 -2c","45","","","","- C16 H9 Cl F3 N O3 S -","- C16 H9 Cl F3 N O3 S -","- C128 H72 Cl8 F24 N8 O24 S8 -","8","1","","Yi, Ruxia; Li, Xincheng; Wan, Boshun","Ring-opening and cyclization of aziridines with aryl azides: metal-free synthesis of 6-(triflyloxy)quinolines","Organic Chemistry Frontiers","2018","5","23","3488","","10.1039/C8QO00984H","","","0.71073","MoKα","","0.0547","0.0494","","","0.118","0.1234","","","","","","1.115","","","","has coordinates","237268","2020-10-21","18:00:00",""
"1554484","4.9693","0.0003","5.8579","0.0003","31.3863","0.0017","90","","90","","90","","913.64","0.09","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C11 H9 F O2 -","- C11 H9 F O2 -","- C44 H36 F4 O8 -","4","1","","Han, Sang Hoon; Pandey, Ashok Kumar; Lee, Heeyoung; Kim, Saegun; Kang, Dahye; Jung, Young Hoon; Kim, Hyung Sik; Hong, Sungwoo; Kim, In Su","One-pot synthesis of 2-naphthols from nitrones and MBH adducts via decarboxylative N‒O bond cleavage","Organic Chemistry Frontiers","2018","5","22","3210","","10.1039/C8QO00988K","","","0.71073","MoKα","","0.069","0.0506","","","0.0992","0.106","","","","","","1.064","","","","has coordinates","237270","2020-10-21","18:00:00",""
"1554486","5.7918","0.0006","13.738","0.0014","13.4519","0.0013","90","","101.436","0.004","90","","1049.09","0.18","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C14 H8 N3 O -","- C14 H8 N3 O -","- C56 H32 N12 O4 -","4","1","","Li, Ping-Gui; Yan, Cheng; Zhu, Shuai; Liu, Shu-Hui; Zou, Liang-Hua","Direct construction of benzimidazo[l,2-c]quinazolin-6-ones via metal-free oxidative C‒C bond cleavage","Organic Chemistry Frontiers","2018","5","23","3464","","10.1039/C8QO01039K","","","0.71073","MoKα","","0.0831","0.0547","","","0.1246","0.1389","","","","","","1.042","","","","has coordinates","237273","2020-10-21","18:00:00",""
"1554487","13.6363","0.0006","8.5322","0.0003","15.2209","0.0008","90","","116.205","0.001","90","","1588.9","0.12","296","2","296","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C37 H31 N3 O4 S -","- C37 H31 N3 O4 S -","- C74 H62 N6 O8 S2 -","2","1","","Gu, Bo-Qi; Yang, Wu-Lin; Wu, Shu-Xiao; Wang, Yan-Bing; Deng, Wei-Ping","Organocatalytic asymmetric synthesis of tetrahydrocarbazoles via an inverse-electron-demand Diels‒Alder reaction of 2,3-indole-dienes with enals","Organic Chemistry Frontiers","2018","5","23","3430","","10.1039/C8QO01042K","","","0.71073","MoKα","","0.0513","0.0388","","","0.0783","0.0857","","","","","","1.063","","","","has coordinates","237275","2020-10-21","18:00:00",""
"1554488","9.5039","0.0007","10.0075","0.0008","10.6869","0.0008","64.045","0.002","69.351","0.002","83.294","0.002","854.35","0.11","291","2","291","2","","","","","","","","5","P -1","-P 1","2","","","","- C17 H18 N O5 P -","- C17 H18 N O5 P -","- C34 H36 N2 O10 P2 -","2","1","","Wang, Jie; Li, Jun; Wei, Yuanyuan; Yang, Jingya; Huo, Congde","Copper-catalyzed oxidative phosphonation of 3,4-dihydro-1,4-benzoxazin-2-ones","Organic Chemistry Frontiers","2018","5","24","3534","","10.1039/C8QO01049H","","","1.54178","CuKα","","0.0828","0.082","","","0.1885","0.1899","","","","","","1.081","","","","has coordinates","237276","2020-10-21","18:00:00",""