# Search results of SQL query from the Crystallography Open Database
# Date and time performed: 2024-10-05T23:13:06+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 letters') AND volume = 17 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
"1518403","8.2167","0.0008","16.3939","0.0017","25.795","0.003","90","","86.989","0.009","90","","3469.9","0.6","153","","153","","","","","","","","","4","P -1","-P 1","2","","","","- C25 H17 N O -","- C25 H17 N O -","- C200 H136 N8 O8 -","8","4","","Wang, Zhen; Li, Ting","Facile Synthesis of 6-Acylated Pyrido[2,1-a]isoindoles from 2-Arylpyridines and γ-Substituted tert-Propargyl Alcohols via Rhodium-Catalyzed C-H Bond Activation and β-Carbon Elimination.","Organic letters","2015","17","5","1348","","10.1021/ol503157k","","","0.71073","MoKα","","0.2551","0.1039","","","0.1608","0.2302","","","","","","0.923","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518421","10.543","0.002","9.344","0.002","22.465","0.005","90","","92.128","0.003","90","","2211.6","0.8","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C23 H28 N2 O4 S -","- C23 H28 N2 O4 S -","- C92 H112 N8 O16 S4 -","4","1","","Xu, Hua-Dong; Jia, Zhi-Hong; Xu, Ke; Zhou, Hao; Shen, Mei-Hua","One-Pot Protocol to Functionalized Benzopyrrolizidine Catalyzed Successively by Rh2(OAc)4 and Cu(OTf)2: A Transition Metal-Lewis Acid Catalysis Relay.","Organic letters","2015","17","1","66","69","10.1021/ol503247t","","","0.71073","MoKα","","0.1189","0.1127","","","0.2855","0.288","","","","","","1.126","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518422","26.688","0.006","18.145","0.005","9.062","0.002","90","","90","","90","","4388.3","1.8","296","2","296","2","","","","","","","","5","P n a 21","P 2c -2n","33","","N-(9a-allyl-6,8-dimethoxy-2,3,9,9a-tetrahydro-1H-pyrrolo[1,2-a]indol-9-yl)-4-methylbenzenesulfonamide","","- C23 H28 N2 O4 S -","- C23 H28 N2 O4 S -","- C184 H224 N16 O32 S8 -","8","2","","Xu, Hua-Dong; Jia, Zhi-Hong; Xu, Ke; Zhou, Hao; Shen, Mei-Hua","One-Pot Protocol to Functionalized Benzopyrrolizidine Catalyzed Successively by Rh2(OAc)4 and Cu(OTf)2: A Transition Metal-Lewis Acid Catalysis Relay.","Organic letters","2015","17","1","66","69","10.1021/ol503247t","","","0.71073","MoKα","","0.136","0.0785","","","0.1259","0.1555","","","","","","1.187","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518427","16.6085","0.001","7.853","0.0006","20.7239","0.0015","90","","103.721","0.003","90","","2625.8","0.3","300","2","300","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C15 H9 F3 N2 O2 -","- C15 H9 F3 N2 O2 -","- C120 H72 F24 N16 O16 -","8","2","","Kumar, Shailesh; Rathore, Vandana; Verma, Ajay; Prasad, Ch Durga; Kumar, Amit; Yadav, Abhimanyu; Jana, Sadhan; Sattar, Moh; Meenakshi, ?; Kumar, Sangit","KO(t)Bu-Mediated Aerobic Transition-Metal-Free Regioselective β-Arylation of Indoles: Synthesis of β-(2-/4-Nitroaryl)-indoles.","Organic letters","2015","17","1","82","85","10.1021/ol503274z","","x-ray","0.71073","MoKα","","0.1472","0.0989","","","0.278","0.3228","","","","","","1.055","","","","has coordinates","182022","2020-10-21","18:00:00",""
"1518428","19.16","0.002","11.3942","0.0014","15.345","0.003","90","","126.612","0.002","90","","2689","0.7","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C15 H11 Cl N2 O2 -","- C15 H11 Cl N2 O2 -","- C120 H88 Cl8 N16 O16 -","8","1","","Kumar, Shailesh; Rathore, Vandana; Verma, Ajay; Prasad, Ch Durga; Kumar, Amit; Yadav, Abhimanyu; Jana, Sadhan; Sattar, Moh; Meenakshi, ?; Kumar, Sangit","KO(t)Bu-Mediated Aerobic Transition-Metal-Free Regioselective β-Arylation of Indoles: Synthesis of β-(2-/4-Nitroaryl)-indoles.","Organic letters","2015","17","1","82","85","10.1021/ol503274z","","x-ray","0.71073","MoKα","","0.0743","0.0555","","","0.157","0.1695","","","","","","1.041","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518455","7.788","0.0004","16.0615","0.001","20.7023","0.0012","90","","90","","90","","2589.6","0.3","103","2","103","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","tert-butyl 3-((E)-(((S)-2-(methoxymethyl)pyrrolidin-1-yl)imino)methyl) -2-((R)-1-phenylethyl)-1H-indole-1-carboxylate","","- C29 H37 N3 O4 -","- C29 H37 N3 O4 -","- C116 H148 N12 O16 -","4","1","","Lee, Pin-Sheng; Yoshikai, Naohiko","Cobalt-catalyzed enantioselective directed C-h alkylation of indole with styrenes.","Organic letters","2015","17","1","22","25","10.1021/ol503119z","","","0.71073","MoKα","","0.0971","0.059","","","0.1014","0.1162","","","","","","0.971","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518456","19.3925","0.0007","6.0017","0.0001","17.9993","0.0006","90","","107.635","0.004","90","","1996.45","0.11","150","","150","","","","","","","","local","4","C 1 2 1","C 2y","5","","","","- C21 H28 O4 S -","- C21 H28 O4 S -","- C84 H112 O16 S4 -","4","1","","Lan, Ping; Banwell, Martin G.; Willis, Anthony C.","Chemoenzymatic Synthesis of the Enantiomer of 4,12-Dihydroxysterpurene, the Structure Assigned to a Metabolite Isolated from the Culture Broth of Stereum purpureum.","Organic letters","2015","17","1","166","169","10.1021/ol5034817","","","1.5418","CuKα","","0.0443","0.0435","","0.1216","0.1212","0.1216","","","","","","1.0367","","","","has coordinates","176432","2020-10-21","18:00:00",""
"1518457","6.2688","0.0001","16.308","0.0001","18.2849","0.0002","90","","90","","90","","1869.29","0.04","150","","150","","","","","","","","local","3","P 21 21 21","P 2ac 2ab","19","","","","- C21 H28 O4 -","- C21 H28 O4 -","- C84 H112 O16 -","4","1","","Lan, Ping; Banwell, Martin G.; Willis, Anthony C.","Chemoenzymatic Synthesis of the Enantiomer of 4,12-Dihydroxysterpurene, the Structure Assigned to a Metabolite Isolated from the Culture Broth of Stereum purpureum.","Organic letters","2015","17","1","166","169","10.1021/ol5034817","","","1.5418","CuKα","","0.0257","0.0252","","0.0656","0.0651","0.0656","","","","","","1.005","","","","has coordinates","176432","2020-10-21","18:00:00",""
"1518458","9.0419","0.0001","12.2803","0.0002","19.0748","0.0002","90","","90","","90","","2118.01","0.05","291","2","291","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C24 H25 N O5 -","- C24 H25 N O5 -","- C96 H100 N4 O20 -","4","1","","Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong","Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.","Organic letters","2015","17","1","150","153","10.1021/ol503383x","","","1.54184","CuKα","","0.0303","0.0298","","","0.0823","0.0829","","","","","","1.096","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518459","9.6257","0.0001","24.6776","0.0002","9.1983","0.0001","90","","108.936","0.001","90","","2066.71","0.04","290","2","290","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H23 N O4 -","- C24 H23 N O4 -","- C96 H92 N4 O16 -","4","1","","Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong","Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.","Organic letters","2015","17","1","150","153","10.1021/ol503383x","","","1.54184","CuKα","","0.0403","0.0384","","","0.1062","0.1081","","","","","","1.057","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518460","10.1067","0.0002","11.5787","0.0003","19.2079","0.0005","83.811","0.002","82.159","0.002","76.354","0.002","2157.2","0.09","291","2","291","2","","","","","","","","4","P -1","-P 1","2","","","","- C25 H25 N O4 -","- C25 H25 N O4 -","- C100 H100 N4 O16 -","4","2","","Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong","Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.","Organic letters","2015","17","1","150","153","10.1021/ol503383x","","","1.54184","CuKα","","0.0436","0.0412","","","0.1115","0.114","","","","","","1.038","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518461","21.3083","0.0015","16.6395","0.0006","17.8923","0.0007","90","","118.967","0.004","90","","5550.3","0.5","291","2","291","2","","","","","","","","5","C 1 2 1","C 2y","5","","","","- C24 H21 Cl2 N O4 -","- C24 H21 Cl2 N O4 -","- C192 H168 Cl16 N8 O32 -","8","2","","Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong","Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.","Organic letters","2015","17","1","150","153","10.1021/ol503383x","","","0.71073","MoKα","","0.0845","0.054","","","0.1342","0.1464","","","","","","1.043","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518462","24.0183","0.0013","11.2598","0.0006","7.4174","0.0004","90","","90","","90","","2005.97","0.19","123","","123","","","","","","","","","6","P c a 21","P 2c -2ac","29","","","","- C21 H21 Br N2 O3 S -","- C21 H21 Br N2 O3 S -","- C84 H84 Br4 N8 O12 S4 -","4","1","","Arai, Noriyoshi; Mizota, Moe; Ohkuma, Takeshi","Stereoselective preparation of spiro[4.4] cyclic compounds by the photochemical activation of oxazoles.","Organic letters","2015","17","1","86","89","10.1021/ol5032848","","","0.71075","MoKα","","","0.0395","","","","0.097","","","","","","1.106","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518463","8.12","0.0006","11.101","0.0008","21.7055","0.0013","90","","94.955","0.003","90","","1949.2","0.2","123","","123","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C21 H21 Br N2 O3 S -","- C21 H21 Br N2 O3 S -","- C84 H84 Br4 N8 O12 S4 -","4","1","","Arai, Noriyoshi; Mizota, Moe; Ohkuma, Takeshi","Stereoselective preparation of spiro[4.4] cyclic compounds by the photochemical activation of oxazoles.","Organic letters","2015","17","1","86","89","10.1021/ol5032848","","","0.71075","MoKα","","","0.0615","","","","0.1925","","","","","","1.274","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518464","9.1452","0.0001","12.5627","0.0002","16.2841","0.0002","90","","90","","90","","1870.85","0.04","291","2","291","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C19 H26 O7 -","- C19 H26 O7 -","- C76 H104 O28 -","4","1","","Xu, Jin-Fang; Zhao, Hui-Jun; Wang, Xiao-Bing; Li, Zhong-Rui; Luo, Jun; Yang, Ming-Hua; Yang, Lei; Yu, Wen-Ying; Yao, He-Quan; Luo, Jian-Guang; Kong, Ling-Yi","(±)-Melicolones A and B, Rearranged Prenylated Acetophenone Stereoisomers with an Unusual 9-Oxatricyclo[3.2.1.1(3,8)]nonane Core from the Leaves of Melicope ptelefolia.","Organic letters","2015","17","1","146","149","10.1021/ol5033738","","","1.54184","CuKα","","0.0315","0.0304","","","0.0855","0.0868","","","","","","1.042","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518465","9.2683","0.0001","9.2683","0.0001","18.5901","0.0003","90","","90","","120","","1382.97","0.03","291","2","291","2","","","","","","","","3","P 32","P 32","145","","","","- C19 H26 O7 -","- C19 H26 O7 -","- C57 H78 O21 -","3","1","","Xu, Jin-Fang; Zhao, Hui-Jun; Wang, Xiao-Bing; Li, Zhong-Rui; Luo, Jun; Yang, Ming-Hua; Yang, Lei; Yu, Wen-Ying; Yao, He-Quan; Luo, Jian-Guang; Kong, Ling-Yi","(±)-Melicolones A and B, Rearranged Prenylated Acetophenone Stereoisomers with an Unusual 9-Oxatricyclo[3.2.1.1(3,8)]nonane Core from the Leaves of Melicope ptelefolia.","Organic letters","2015","17","1","146","149","10.1021/ol5033738","","","1.54184","CuKα","","0.0241","0.024","","","0.0643","0.0644","","","","","","1.061","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518466","43.491","0.004","5.5109","0.0005","18.3225","0.0015","90","","95.331","0.007","90","","4372.4","0.7","100","2","100.09","","","","","","","","","3","C 1 2 1","C 2y","5","","","","- C24.5 H26.52 O7 -","- C24.5 H26.518 O7 -","- C196 H212.144 O56 -","8","2","","McDonald, Benjamin R.; Nibbs, Antoinette E.; Scheidt, Karl A.","A biomimetic strategy to access the silybins: total synthesis of (-)-isosilybin a.","Organic letters","2015","17","1","98","101","10.1021/ol503303w","","","1.54178","CuKα","","0.1121","0.0768","","","0.2036","0.2394","","","","","","1.053","","","","has coordinates,has disorder","176435","2020-10-21","18:00:00",""
"1518467","7.1391","0.0015","7.5445","0.0014","15.455","0.004","88.709","0.007","83.268","0.005","76.661","0.006","804.4","0.3","103","","103","","","","","","","","synthesis as described","3","P -1","-P 1","2","","","","- C18 H26 O4 -","- C18 H26 O4 -","- C36 H52 O8 -","2","1","","Suizu, Hiroshi; Shigeoka, Daisuke; Aoyama, Hiroshi; Yoshimitsu, Takehiko","Total synthesis of clavilactone B: a radical cyclization-fragmentation strategy.","Organic letters","2015","17","1","126","129","10.1021/ol503356m","","x-ray","0.71073","MoKα","","0.0446","0.0412","","","0.1201","0.1255","","","","","","0.687","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518468","16.194","0.003","6.597","0.0012","18.175","0.004","90","","102.603","0.002","90","","1894.9","0.6","123","2","123","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C19 H24 O7 S -","- C19 H24 O7 S -","- C76 H96 O28 S4 -","4","1","","Suizu, Hiroshi; Shigeoka, Daisuke; Aoyama, Hiroshi; Yoshimitsu, Takehiko","Total synthesis of clavilactone B: a radical cyclization-fragmentation strategy.","Organic letters","2015","17","1","126","129","10.1021/ol503356m","","","0.71073","MoKα","","0.0566","0.0488","","","","0.1635","","","","","","0.632","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518482","8.8127","0.001","13.2298","0.0012","32.5","0.003","90","","90","","90","","3789.2","0.7","296","2","296","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","20120034","","","- C24 H20 N2 O -","- C24 H20 N2 O -","- C192 H160 N16 O8 -","8","1","","Fan, Zhoulong; Song, Shanshan; Li, Wei; Geng, Kaijun; Xu, Youjun; Miao, Ze-Hong; Zhang, Ao","Rh(III)-Catalyzed Redox-Neutral C-H Activation of Pyrazolones: An Economical Approach for the Synthesis of N-Substituted Indoles.","Organic letters","2015","17","2","310","313","10.1021/ol503404p","","","0.71073","MoKα","","0.0945","0.058","","","0.1122","0.1267","","","","","","1.084","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518483","10.0098","0.0005","10.1777","0.0007","12.0505","0.0007","67.347","0.006","70.617","0.005","79.738","0.005","1066.95","0.12","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","5-(2-chloroethyl)-2,2-diphenyl-3-(methylcarbonyloxyethyl)-6-methyl- 1,3-oxazinen-4-one","","- C23 H24 Cl N O4 -","- C23 H24 Cl N O4 -","- C46 H48 Cl2 N2 O8 -","2","1","","Craig, Alexander J.; van der Salm, Louise; Stevens-Cullinane, Lars; Lucas, Nigel T.; Tan, Eng Wui; Hawkins, Bill C.","Expedient Metal-Free Synthesis of 1,3-Oxazinen-4-ones.","Organic letters","2015","17","2","234","237","10.1021/ol503350h","","","1.54184","CuKα","","0.0383","0.0341","","","0.0848","0.089","","","","","","1.043","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518484","9.1948","0.0011","12.5947","0.0014","13.668","0.0016","79.379","0.003","77.83","0.003","78.547","0.003","1499.6","0.3","100","2","100","2","","","","","","","synthesis","5","P 1","P 1","1","Ac-UgF(D)A-(S,S)gTS-UgFU-CONH2","Ac-UgF(D)A-(S,S)gTS-UgFU-CONH2","","- C54 H75 N8 O16 S -","- C54 H75 N8 O16 S -","- C54 H75 N8 O16 S -","1","1","","Ganesh Kumar, Mothukuri; Mali, Sachitanand M.; Raja, K. Muruga Poopathi; Gopi, Hosahudya N.","Design of Stable β-Hairpin Mimetics through Backbone Disulfide Bonds.","Organic letters","2015","17","2","230","233","10.1021/ol503310r","","","0.71073","MoKα","","0.0586","0.0492","","","0.1307","0.1388","","","","","","0.967","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518485","8.0428","0.0005","19.587","0.0008","12.8121","0.0007","90","","104.921","0.006","90","","1950.29","0.19","293","2","293.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C22 H16 I N O2 S -","- C22 H16 I N O2 S -","- C88 H64 I4 N4 O8 S4 -","4","1","","Sun, Lang; Zhu, Yuanxun; Wang, Jing; Lu, Ping; Wang, Yanguang","Lewis Acid Catalyzed Cascade Reaction of 3-(2-Benzenesulfonamide)propargylic Alcohols to Spiro[indene-benzosultam]s.","Organic letters","2015","17","2","242","245","10.1021/ol503316e","","","0.71073","MoKα","","0.0459","0.0354","","","0.0753","0.0818","","","","","","1.042","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518486","8.195","0.0005","10.1773","0.0006","11.9407","0.0008","86.942","0.005","83.912","0.005","76.661","0.005","963.13","0.11","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C21 H14 I N O2 S -","- C21 H14 I N O2 S -","- C42 H28 I2 N2 O4 S2 -","2","1","","Sun, Lang; Zhu, Yuanxun; Wang, Jing; Lu, Ping; Wang, Yanguang","Lewis Acid Catalyzed Cascade Reaction of 3-(2-Benzenesulfonamide)propargylic Alcohols to Spiro[indene-benzosultam]s.","Organic letters","2015","17","2","242","245","10.1021/ol503316e","","","0.71073","MoKα","","0.042","0.0323","","","0.0707","0.076","","","","","","1.055","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518487","17.142","0.003","9.0363","0.0018","12.653","0.003","90","","90.03","0.03","90","","1960","0.7","113","2","113","2","","","","","","","","3","C 1 c 1","C -2yc","9","","","","- C24 H24 O6 -","- C24 H24 O6 -","- C96 H96 O24 -","4","1","","Zhang, Junhui; Xing, Siyang; Ren, Jun; Jiang, Shende; Wang, Zhongwen","Lewis Acid catalyzed intramolecular [3 + 2] cross cycloadditions of cobalt-alkynylcyclopropane 1,1-diesters with carbonyls for construction of medium-sized and polycyclic skeletons.","Organic letters","2015","17","2","218","221","10.1021/ol503285u","","","0.71073","MoKα","","0.0477","0.0318","","","0.0698","0.0802","","","","","","1.014","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518488","14.969","0.008","7.307","0.004","12.761","0.007","90","","90","","90","","1395.8","1.3","113","2","113","2","","","","","","","","3","P n a 21","P 2c -2n","33","","","","- C16 H16 O5 -","- C16 H16 O5 -","- C64 H64 O20 -","4","1","","Zhang, Junhui; Xing, Siyang; Ren, Jun; Jiang, Shende; Wang, Zhongwen","Lewis Acid catalyzed intramolecular [3 + 2] cross cycloadditions of cobalt-alkynylcyclopropane 1,1-diesters with carbonyls for construction of medium-sized and polycyclic skeletons.","Organic letters","2015","17","2","218","221","10.1021/ol503285u","","","0.71073","MoKα","","0.0386","0.0342","","","0.0664","0.0684","","","","","","0.999","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518489","8.0572","0.0016","8.3258","0.0017","17.63","0.004","88.79","0.03","84.64","0.03","75.45","0.03","1139.7","0.4","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H14 Co2 O11 -","- C22 H14 Co2 O11 -","- C44 H28 Co4 O22 -","2","1","","Zhang, Junhui; Xing, Siyang; Ren, Jun; Jiang, Shende; Wang, Zhongwen","Lewis Acid catalyzed intramolecular [3 + 2] cross cycloadditions of cobalt-alkynylcyclopropane 1,1-diesters with carbonyls for construction of medium-sized and polycyclic skeletons.","Organic letters","2015","17","2","218","221","10.1021/ol503285u","","","0.71073","MoKα","","0.0819","0.0379","","","0.0723","0.0893","","","","","","1","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518490","15.8829","0.0006","19.5684","0.0009","11.5831","0.0005","90","","90","","90","","3600.1","0.3","100","2","100","2","","","","","","","","7","P 21 21 2","P 2 2ab","18","","","","- C36 H34 Co2 F6 N O5 P2 -","- C36 H34 Co2 F6 N O5 P2 -","- C144 H136 Co8 F24 N4 O20 P8 -","4","1","","Orgué, Sílvia; León, Thierry; Riera, Antoni; Verdaguer, Xavier","Asymmetric Intermolecular Cobalt-Catalyzed Pauson-Khand Reaction Using a P-Stereogenic Bis-phosphane.","Organic letters","2015","17","2","250","253","10.1021/ol503329g","","","0.71073","MoKα","","0.0475","0.035","","","0.0861","0.0937","","","","","","1.046","","","","has coordinates,has disorder","176729","2020-10-21","18:00:00",""
"1518491","8.8649","0.0008","20.8055","0.0019","9.1083","0.0008","90","","101.487","0.003","90","","1646.3","0.3","100","2","100","2","","","","","","","","7","P 1 21 1","P 2yb","4","","","","- C30 H37 Co2 N3 O5 P2 Si -","- C29.97 H34.91 Co2 N3 O5 P2 Si -","- C59.94 H69.82 Co4 N6 O10 P4 Si2 -","2","1","","Orgué, Sílvia; León, Thierry; Riera, Antoni; Verdaguer, Xavier","Asymmetric Intermolecular Cobalt-Catalyzed Pauson-Khand Reaction Using a P-Stereogenic Bis-phosphane.","Organic letters","2015","17","2","250","253","10.1021/ol503329g","","","0.71073","MoKα","","0.0234","0.0225","","","0.0584","0.0591","","","","","","1.013","","","","has coordinates,has disorder","176729","2020-10-21","18:00:00",""
"1518492","30.8526","0.0005","11.997","0.0002","18.7562","0.0003","90","","113.744","0.001","90","","6354.75","0.19","100","2","100","2","","","","","","","","7","C 1 2/c 1","-C 2yc","15","","","","- C32 H22 B Cl3 F4 N2 O2 -","- C32 H22 B Cl3 F4 N2 O2 -","- C256 H176 B8 Cl24 F32 N16 O16 -","8","1","","Greulich, Tobias W.; Daniliuc, Constantin G.; Studer, Armido","N-aminopyridinium salts as precursors for N-centered radicals - direct amidation of arenes and heteroarenes.","Organic letters","2015","17","2","254","257","10.1021/ol503338b","","","1.54178","CuKα","","0.0665","0.0491","","","0.1259","0.1329","","","","","","1.119","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518493","8.5347","0.0002","14.9824","0.0004","10.2813","0.0002","90","","96.632","0.0009","90","","1305.88","0.05","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","TOG579B","","","- C15 H10 Cl N O3 -","- C15 H10 Cl N O3 -","- C60 H40 Cl4 N4 O12 -","4","1","","Greulich, Tobias W.; Daniliuc, Constantin G.; Studer, Armido","N-aminopyridinium salts as precursors for N-centered radicals - direct amidation of arenes and heteroarenes.","Organic letters","2015","17","2","254","257","10.1021/ol503338b","","","1.54178","CuKα","","0.0364","0.0316","","","0.0763","0.0793","","","","","","1.055","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518494","12.7796","0.0003","13.8018","0.0004","18.4448","0.0005","90","","90","","90","","3253.32","0.15","100","2","100","2","","","","","","","","5","P c a 21","P 2c -2ac","29","","","","- C18 H20 N2 O2 S -","- C18 H20 N2 O2 S -","- C144 H160 N16 O16 S8 -","8","2","","Greulich, Tobias W.; Daniliuc, Constantin G.; Studer, Armido","N-aminopyridinium salts as precursors for N-centered radicals - direct amidation of arenes and heteroarenes.","Organic letters","2015","17","2","254","257","10.1021/ol503338b","","","1.54178","CuKα","","0.0317","0.0283","","","0.0711","0.0731","","","","","","1.033","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518495","10.18","0.0012","10.18","0.0012","10.954","0.003","90","","90","","120","","983.1","0.3","173","2","173","2","","","","","","","","4","P 32","P 32","145","","","","- C16 H12 Br N3 -","- C16 H12 Br N3 -","- C48 H36 Br3 N9 -","3","1","","Tang, Hai-Tao; Xiong, Kai; Li, Ren-Hao; Ding, Zong-Cang; Zhan, Zhuang-Ping","Synthesis of 5,6-Dihydropyrazolo[1,5-c]quinazolines through Gold-Catalyzed Chemoselective Bicyclization of N-Propargylic Sulfonylhydrazones.","Organic letters","2015","17","2","326","329","10.1021/ol503437n","","","0.71073","MoKα","","0.0431","0.0413","","","0.1031","0.1042","","","","","","1.026","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518565","12.483","0.0003","12.4917","0.0003","14.6608","0.0004","71.195","0.001","68.259","0.001","69.138","0.001","1935.93","0.09","193","2","193","2","","","","","","","","4","P -1","-P 1","2","","","","- C24 H23 N O3 -","- C24 H23 N O3 -","- C96 H92 N4 O12 -","4","2","","Oka, Junko; Okamoto, Ryuichi; Noguchi, Keiichi; Tanaka, Ken","Asymmetric dearomatization of 1-aminonaphthalene derivatives by gold-catalyzed intramolecular double C-C bond formation.","Organic letters","2015","17","3","676","679","10.1021/ol503698s","","","1.54187","CuKα","","0.0832","0.0561","","","0.1498","0.1852","","","","","","1.058","","","","has coordinates,has disorder","176729","2020-10-21","18:00:00",""
"1518566","13.1285","0.0008","8.9817","0.0005","17.2111","0.001","90","","107.754","0.003","90","","1932.8","0.2","193","2","193","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C24 H27 N O3 -","- C24 H27 N O3 -","- C96 H108 N4 O12 -","4","1","","Oka, Junko; Okamoto, Ryuichi; Noguchi, Keiichi; Tanaka, Ken","Asymmetric dearomatization of 1-aminonaphthalene derivatives by gold-catalyzed intramolecular double C-C bond formation.","Organic letters","2015","17","3","676","679","10.1021/ol503698s","","","1.54187","CuKα","","0.1013","0.0704","","","0.1967","0.2382","","","","","","1.005","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518567","8.9945","0.0002","12.4644","0.0002","17.7143","0.0003","90","","90","","90","","1985.97","0.06","193","2","193","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C24 H22 Br N O3 -","- C24 H22 Br N O3 -","- C96 H88 Br4 N4 O12 -","4","1","","Oka, Junko; Okamoto, Ryuichi; Noguchi, Keiichi; Tanaka, Ken","Asymmetric dearomatization of 1-aminonaphthalene derivatives by gold-catalyzed intramolecular double C-C bond formation.","Organic letters","2015","17","3","676","679","10.1021/ol503698s","","","1.54187","CuKα","","0.027","0.0257","","","0.0686","0.0696","","","","","","1.045","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518568","10.9519","0.0005","18.6953","0.0007","14.864","0.0006","90","","100.907","0.003","90","","2988.4","0.2","100","2","100","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C31 H37 N5 O8 S -","- C31 H37 N5 O8 S -","- C124 H148 N20 O32 S4 -","4","2","","Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.","Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.","Organic letters","2015","17","3","418","421","10.1021/ol503273v","","","1.54178","CuKα","","0.0692","0.0591","","","0.1409","0.1474","","","","","","1.023","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518569","6.6977","0.0007","8.9166","0.001","11.8671","0.0013","97.4234","0.0016","102.013","0.0016","108.163","0.0015","644.13","0.12","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C15 H19 N O2 -","- C15 H19 N O2 -","- C30 H38 N2 O4 -","2","1","","Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.","Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.","Organic letters","2015","17","3","418","421","10.1021/ol503273v","","","0.71073","MoKα","","0.0485","0.038","","","0.0969","0.1017","","","","","","1.055","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518570","9.0807","0.0002","9.5935","0.0002","12.844","0.0002","90","","90","","90","","1118.91","0.04","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C13 H15 N O2 -","- C13 H15 N O2 -","- C52 H60 N4 O8 -","4","1","","Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.","Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.","Organic letters","2015","17","3","418","421","10.1021/ol503273v","","","1.54178","CuKα","","0.0242","0.0241","","","0.0629","0.063","","","","","","1.052","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518571","7.0255","0.0007","8.3274","0.0008","8.5054","0.0008","64.8193","0.0014","75.8585","0.0015","86.3999","0.0015","436.19","0.07","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C8 H13 N O3 -","- C8 H13 N O3 -","- C16 H26 N2 O6 -","2","1","","Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.","Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.","Organic letters","2015","17","3","418","421","10.1021/ol503273v","","","0.71073","MoKα","","0.0375","0.0335","","","0.0852","0.0879","","","","","","1.066","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518572","16.694","0.0011","9.6688","0.0007","18.2592","0.0013","90","","101.972","0.0011","90","","2883.1","0.3","100","2","100","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C18 H17 N O2 -","- C18 H17 N O2 -","- C144 H136 N8 O16 -","8","1","","Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.","Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.","Organic letters","2015","17","3","418","421","10.1021/ol503273v","","","0.71073","MoKα","","0.0437","0.0365","","","0.0925","0.0956","","","","","","1.093","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518573","10.359","0.003","8.616","0.002","22.998","0.005","90","","98.931","0.014","90","","2027.8","0.9","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C25 H20 N2 O4 -","- C25 H20 N2 O4 -","- C100 H80 N8 O16 -","4","1","","Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.","Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.","Organic letters","2015","17","3","438","441","10.1021/ol5033909","","","0.71073","MoKα","","0.0836","0.0545","","","0.133","0.1563","","","","","","1.018","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518574","8.5149","0.0001","11.4869","0.0002","11.4981","0.0002","90.53","0.001","111.599","0.001","91.352","0.001","1045.17","0.03","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C26 H22 N2 O4 -","- C26 H22 N2 O4 -","- C52 H44 N4 O8 -","2","1","","Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.","Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.","Organic letters","2015","17","3","438","441","10.1021/ol5033909","","","0.71073","MoKα","","0.0432","0.04","","","0.1093","0.1133","","","","","","1.035","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518575","8.1999","0.0005","23.636","0.0014","10.7112","0.0006","90","","97.847","0.003","90","","2056.5","0.2","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C26 H22 N2 O4 -","- C26 H22 N2 O4 -","- C104 H88 N8 O16 -","4","1","","Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.","Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.","Organic letters","2015","17","3","438","441","10.1021/ol5033909","","","0.71073","MoKα","","0.0422","0.0389","","","0.1026","0.1056","","","","","","1.034","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518576","15.0058","0.0002","16.0652","0.0002","9.235","0.0001","90","","90","","90","","2226.29","0.05","296","2","296","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C25 H21 N5 O4 -","- C25 H21 N5 O4 -","- C100 H84 N20 O16 -","4","1","","Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.","Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.","Organic letters","2015","17","3","438","441","10.1021/ol5033909","","","0.71073","MoKα","","0.0424","0.0393","","","0.1126","0.1165","","","","","","1.045","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518577","13.7112","0.0003","7.9341","0.0002","22.1644","0.0005","90","","101.626","0.001","90","","2361.71","0.1","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C26 H21 N3 O4 S -","- C26 H21 N3 O4 S -","- C104 H84 N12 O16 S4 -","4","1","","Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.","Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.","Organic letters","2015","17","3","438","441","10.1021/ol5033909","","","0.71073","MoKα","","0.0411","0.038","","","0.1046","0.1089","","","","","","1.029","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518578","12.2086","0.0002","8.2983","0.0001","20.1576","0.0004","90","","94.952","0.001","90","","2034.56","0.06","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C25 H22 N2 O5 -","- C25 H22 N2 O5 -","- C100 H88 N8 O20 -","4","1","","Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.","Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.","Organic letters","2015","17","3","438","441","10.1021/ol5033909","","","0.71073","MoKα","","0.0403","0.0358","","","0.1031","0.111","","","","","","0.844","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518579","25.4401","0.0006","25.4401","0.0006","14.9071","0.0004","90","","90","","90","","9647.9","0.4","296","2","296","2","","","","","","","","4","I 41/a :2","-I 4ad","88","","","","- C25 H19 N3 O4 -","- C25 H19 N3 O4 -","- C400 H304 N48 O64 -","16","1","","Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.","Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.","Organic letters","2015","17","3","438","441","10.1021/ol5033909","","","0.71073","MoKα","","0.0738","0.0448","","","0.1433","0.1747","","","","","","0.638","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518580","8.2122","0.0001","14.1107","0.0003","17.9598","0.0003","100.563","0.001","95.565","0.001","90.101","0.001","2035.86","0.06","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C25 H19 N3 O4 -","- C25 H19 N3 O4 -","- C100 H76 N12 O16 -","4","2","","Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.","Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.","Organic letters","2015","17","3","438","441","10.1021/ol5033909","","","0.71073","MoKα","","0.055","0.0444","","","0.1134","0.1207","","","","","","1.078","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518581","10.68","0.002","10.806","0.002","12.352","0.003","90","","107.01","0.03","90","","1363.2","0.5","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C14 H16 F N O3 -","- C14 H16 F N O3 -","- C56 H64 F4 N4 O12 -","4","2","","Xu, Yan-Shuang; Tang, Yu; Feng, He-Jing; Liu, Ji-Tian; Hsung, Richard P.","A Highly Regio- and Stereoselective Synthesis of α-Fluorinated Imides via Fluorination of Chiral Enamides.","Organic letters","2015","17","3","572","575","10.1021/ol503591d","","","0.71073","MoKα","","0.1563","0.0782","","","0.1602","0.1916","","","","","","0.997","","","","has coordinates","182022","2020-10-21","18:00:00",""
"1518582","6.5754","0.0013","10.311","0.002","11.071","0.002","90","","95.19","0.03","90","","747.5","0.2","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C17 H14 F N O3 -","- C17 H14 F N O3 -","- C34 H28 F2 N2 O6 -","2","1","","Xu, Yan-Shuang; Tang, Yu; Feng, He-Jing; Liu, Ji-Tian; Hsung, Richard P.","A Highly Regio- and Stereoselective Synthesis of α-Fluorinated Imides via Fluorination of Chiral Enamides.","Organic letters","2015","17","3","572","575","10.1021/ol503591d","","","0.71073","MoKα","","0.0874","0.0513","","","0.1237","0.1395","","","","","","1.017","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518583","8.0591","0.0004","9.6081","0.0005","15.5767","0.0008","90","","90","","90","","1206.14","0.11","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C14 H18 O2 -","- C14 H18 O2 -","- C56 H72 O8 -","4","1","","Homs, Anna; Muratore, Michael E.; Echavarren, Antonio M.","Enantioselective Total Synthesis of (-)-Nardoaristolone B via a Gold(I)-Catalyzed Oxidative Cyclization.","Organic letters","2015","17","3","461","463","10.1021/ol503531n","","","0.71073","MoKα","","0.0355","0.0331","","","0.0893","0.0915","","","","","","1.102","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518584","8.4438","0.0002","10.9189","0.0003","32.745","0.002","90","","95.201","0.007","90","","3006.6","0.2","93","","93","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C32 H33 Br N O2 P -","- C32 H33 Br N O2 P -","- C128 H132 Br4 N4 O8 P4 -","4","1","","Barrett, Kimberly T.; Miller, Scott J.","Regioselective derivatizations of a tribrominated atropisomeric benzamide scaffold.","Organic letters","2015","17","3","580","583","10.1021/ol503593y","","","1.54187","CuKα","","0.0821","0.0532","","","0.1115","0.1185","","","","","","1.034","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518585","9.848","0.0004","24.3169","0.0011","15.0477","0.001","90","","104.667","0.007","90","","3486.1","0.3","223","","223","","","","","","","","","8","P 1 21/n 1","-P 2yn","14","","","","- C33 H35 Au Br Cl3 N O2 P -","- C33 H35 Au Br Cl3 N O2 P -","- C132 H140 Au4 Br4 Cl12 N4 O8 P4 -","4","1","","Barrett, Kimberly T.; Miller, Scott J.","Regioselective derivatizations of a tribrominated atropisomeric benzamide scaffold.","Organic letters","2015","17","3","580","583","10.1021/ol503593y","","","0.71075","MoKα","","0.0754","0.0571","","","0.1116","0.1171","","","","","","1.241","","","","has coordinates,has disorder","176729","2020-10-21","18:00:00",""
"1518586","16.1723","0.0013","24.7158","0.0017","24.1251","0.0018","90","","90.474","0.003","90","","9642.7","1.2","100","1","100","1","","","","","","","","4","C 1 c 1","C -2yc","9","","","","- C60.5 H56 N4 O6 -","- C60.5 H56 N4 O6 -","- C484 H448 N32 O48 -","8","2","","Liu, Lei; Carroll, Patrick J.; Kozlowski, Marisa C.","Vanadium-catalyzed regioselective oxidative coupling of 2-hydroxycarbazoles.","Organic letters","2015","17","3","508","511","10.1021/ol503521b","","","0.71073","MoKα","","0.0863","0.0735","","","0.1673","0.1763","","","","","","1.052","","","","has coordinates","182022","2020-10-21","18:00:00",""
"1518613","8.8912","0.0013","16.859","0.003","11.238","0.0011","90","","108.555","0.008","90","","1597","0.4","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H17 N O -","- C22 H17 N O -","- C88 H68 N4 O4 -","4","1","","Bunescu, Ala; Piou, Tiffany; Wang, Qian; Zhu, Jieping","Pd-Catalyzed Dehydrogenative Aryl-Aryl Bond Formation via Double C(sp(2))-H Bond Activation: Efficient Synthesis of [3,4]-Fused Oxindoles.","Organic letters","2015","17","2","334","337","10.1021/ol503442n","","","0.71073","MoKα","","0.0618","0.0459","","","0.1036","0.1152","","","","","","1.116","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518614","8.922","0.0005","16.7585","0.0007","11.2263","0.0006","90","","108.038","0.006","90","","1596.05","0.15","140","2","140","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C22 H16 F N O -","- C22 H16 F N O -","- C88 H64 F4 N4 O4 -","4","1","","Bunescu, Ala; Piou, Tiffany; Wang, Qian; Zhu, Jieping","Pd-Catalyzed Dehydrogenative Aryl-Aryl Bond Formation via Double C(sp(2))-H Bond Activation: Efficient Synthesis of [3,4]-Fused Oxindoles.","Organic letters","2015","17","2","334","337","10.1021/ol503442n","","","1.54178","CuKα","","0.0432","0.0393","","","0.1017","0.1115","","","","","","1.095","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518615","18.2078","0.0017","16.5273","0.0017","14.8317","0.0014","90","","98.447","0.003","90","","4414.8","0.7","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C52 H50 N4 Ni O2 -","- C52 H50 N4 Ni O2 -","- C208 H200 N16 Ni4 O8 -","4","1","","Gehrold, Andreas C.; Bruhn, Torsten; Schneider, Heidi; Radius, Udo; Bringmann, Gerhard","Chiral and achiral basket-handle porphyrins: short synthesis and stereostructures of these versatile building blocks.","Organic letters","2015","17","2","210","213","10.1021/ol503286s","","","0.71073","MoKα","","0.0795","0.0489","","","0.1191","0.1293","","","","","","1.092","","","","has coordinates,has disorder","176729","2020-10-21","18:00:00",""
"1518616","17.719","0.004","6.475","0.0014","22.501","0.005","90","","100.868","0.003","90","","2535.2","1","296","2","296","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C15 H13 N3 -","- C15 H13 N3 -","- C120 H104 N24 -","8","1","","Quan, Xue-Jing; Ren, Zhi-Hui; Wang, Yao-Yu; Guan, Zheng-Hui","Correction to p-Toluenesulfonic Acid Mediated 1,3-Dipolar Cycloaddition of Nitroolefins with NaN3 for Synthesis of 4-Aryl-NH-1,2,3-triazoles.","Organic letters","2015","17","2","393","","10.1021/ol503621y","","","0.71073","MoKα","","0.0471","0.0385","","","0.1088","0.1157","","","","","","1.087","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518617","12.9116","0.0006","15.1292","0.0007","18.7417","0.0009","90","","90","","90","","3661","0.3","100","2","100","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C37 H36 Cl2 N4 O8 S2 -","- C37 H36 Cl2 N4 O8 S2 -","- C148 H144 Cl8 N16 O32 S8 -","4","1","","Liang, Kangjiang; Deng, Xu; Tong, Xiaogang; Li, Dashan; Ding, Ming; Zhou, Ankun; Xia, Chengfeng","Copper-Mediated Dimerization to Access 3a,3a'-Bispyrrolidinoindoline: Diastereoselective Synthesis of (+)-WIN 64821 and (-)-Ditryptophenaline.","Organic letters","2015","17","2","206","209","10.1021/ol5032365","","","0.71073","MoKα","","0.0411","0.0339","","","0.0918","0.0969","","","","","","1.019","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518618","9.8359","0.0019","10.161","0.002","10.307","0.002","76.557","0.012","73.136","0.013","64.754","0.01","884.6","0.3","173.15","","173.15","","","","","","","","","5","P 1","P 1","1","","","","- C20 H17 Br N2 O -","- C20 H17 Br N2 O -","- C40 H34 Br2 N4 O2 -","2","2","","Fu, Niankai; Zhang, Long; Luo, Sanzhong","Chiral Primary Amine Catalyzed Asymmetric Michael Addition of Malononitrile to α-Substituted Vinyl Ketone.","Organic letters","2015","17","2","382","385","10.1021/ol503566a","","","0.71073","MoKα","","0.0349","0.032","","","0.0718","0.0739","","","","","","1.066","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518619","10.5861","0.0003","10.618","0.0003","17.0439","0.0004","90","","90","","90","","1915.79","0.09","173","2","173.15","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C24 H20 N2 O -","- C24 H20 N2 O -","- C96 H80 N8 O4 -","4","1","","Fu, Niankai; Zhang, Long; Luo, Sanzhong","Chiral Primary Amine Catalyzed Asymmetric Michael Addition of Malononitrile to α-Substituted Vinyl Ketone.","Organic letters","2015","17","2","382","385","10.1021/ol503566a","","","1.54178","CuKα","","0.0295","0.029","","","0.0751","0.0757","","","","","","1.047","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518620","9.559","0.0013","9.3155","0.0013","15.051","0.002","90","","102.64","0.002","90","","1307.8","0.3","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C16 H10 B F2 N3 -","- C16 H10 B F2 N3 -","- C64 H40 B4 F8 N12 -","4","1","","Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan","Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.","Organic letters","2015","17","2","278","281","10.1021/ol503379c","","","0.71073","MoKα","","0.0456","0.0382","","","0.1001","0.1079","","","","","","1.051","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518621","7.7337","0.0007","19.0699","0.0017","9.655","0.0008","90","","105.059","0.001","90","","1375","0.2","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C16 H9 B Cl F2 N3 -","- C16 H9 B Cl F2 N3 -","- C64 H36 B4 Cl4 F8 N12 -","4","1","","Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan","Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.","Organic letters","2015","17","2","278","281","10.1021/ol503379c","","","0.71073","MoKα","","0.0455","0.037","","","0.1006","0.106","","","","","","1.055","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518622","7.9215","0.0009","14.0077","0.0015","25.071","0.003","90","","102.609","0.003","90","","2714.8","0.5","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C15 H10 B F2 N3 S -","- C15 H10 B F2 N3 S -","- C120 H80 B8 F16 N24 S8 -","8","2","","Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan","Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.","Organic letters","2015","17","2","278","281","10.1021/ol503379c","","","0.71073","MoKα","","0.0845","0.0505","","","0.1314","0.1497","","","","","","1.052","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518623","10.092","0.004","10.383","0.004","10.434","0.004","65.025","0.004","82.642","0.004","75.499","0.004","959.2","0.6","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C22 H18 B F2 N3 S -","- C22 H18 B F2 N3 S -","- C44 H36 B2 F4 N6 S2 -","2","1","","Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan","Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.","Organic letters","2015","17","2","278","281","10.1021/ol503379c","","","0.71073","MoKα","","0.1237","0.1159","","","0.418","0.4223","","","","","","1.067","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518624","7.4838","0.0008","9.1552","0.001","11.5629","0.0012","79.781","0.001","71.778","0.001","67.825","0.001","695.26","0.13","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C18 H10 B F2 N3 -","- C18 H10 B F2 N3 -","- C36 H20 B2 F4 N6 -","2","1","","Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan","Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.","Organic letters","2015","17","2","278","281","10.1021/ol503379c","","","0.71073","MoKα","","0.0506","0.0423","","","0.119","0.1289","","","","","","1.053","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518625","9.1788","0.0011","9.5551","0.0011","9.9844","0.0012","87.602","0.002","71.441","0.002","65.179","0.001","749.15","0.15","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C18 H9 B Br F2 N3 -","- C18 H9 B Br F2 N3 -","- C36 H18 B2 Br2 F4 N6 -","2","1","","Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan","Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.","Organic letters","2015","17","2","278","281","10.1021/ol503379c","","","0.71073","MoKα","","0.0507","0.0368","","","0.1003","0.1068","","","","","","1.059","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518626","11.3331","0.0009","34.017","0.003","12.736","0.001","90","","109.159","0.001","90","","4638","0.7","293","2","293","2","","","","","","","","7","C 1 2/c 1","-C 2yc","15","","","","- C24 H17 B Br F2 N3 S -","- C24 H17 B Br F2 N3 S -","- C192 H136 B8 Br8 F16 N24 S8 -","8","1","","Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan","Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.","Organic letters","2015","17","2","278","281","10.1021/ol503379c","","","0.71073","MoKα","","0.1374","0.073","","","0.208","0.2366","","","","","","1.001","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518627","15.6314","0.0015","21.884","0.002","11.7948","0.0012","90","","108.565","0.002","90","","3824.8","0.6","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C21 H20 Cl N O3 -","- C21 H20 Cl N O3 -","- C168 H160 Cl8 N8 O24 -","8","2","","Li, Lei; Zhao, Yu-Long; Wang, Qian; Lin, Tao; Liu, Qun","Base-Promoted Oxidative C-H Functionalization of α-Amino Carbonyl Compounds under Mild Metal-Free Conditions: Using Molecular Oxygen as the Oxidant.","Organic letters","2015","17","2","370","373","10.1021/ol503495h","","","0.71073","MoKα","","0.0722","0.0448","","","0.1044","0.1182","","","","","","1.012","","","","has coordinates","176435","2020-10-21","18:00:00",""
"1518633","9.5489","0.0005","9.6991","0.0005","19.1473","0.001","90","","97.465","0.002","90","","1758.31","0.16","173","2","173","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C24 H17 N O -","- C24 H17 N O -","- C96 H68 N4 O4 -","4","1","","Li, Ziyuan; Huang, Xiaoqiang; Chen, Feng; Zhang, Chun; Wang, Xiaoyang; Jiao, Ning","Cu-Catalyzed Concise Synthesis of Pyridines and 2-(1H)-Pyridones from Acetaldehydes and Simple Nitrogen Donors.","Organic letters","2015","17","3","584","587","10.1021/ol5035996","","","0.71073","MoKα","","0.0433","0.0333","","","0.0784","0.0854","","","","","","1.014","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518634","6.3906","0.0003","7.7434","0.0003","38.9797","0.0017","90","","90","","90","","1928.91","0.14","100","2","100","2","","","","","","","","7","P 21 21 21","P 2ac 2ab","19","","","","- C20 H22 B F3 K N O -","- C20 H22 B F3 K N O -","- C80 H88 B4 F12 K4 N4 O4 -","4","1","","Hoang, Gia L.; Yang, Zhao-Di; Smith, Sean M.; Pal, Rhitankar; Miska, Judy L.; Pérez, Damaris E; Pelter, Libbie S. W.; Zeng, Xiao Cheng; Takacs, James M.","Enantioselective Desymmetrization via Carbonyl-Directed Catalytic Asymmetric Hydroboration and Suzuki-Miyaura Cross-Coupling.","Organic letters","2015","17","4","940","943","10.1021/ol503764d","","","1.54178","CuKα","","0.0252","0.024","","","0.0592","0.0596","","","","","","1.044","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518635","8.447","0.0004","16.3195","0.0008","17.2927","0.0008","90","","90","","90","","2383.8","0.2","100","2","100","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C26 H29 B F4 N2 O2 -","- C26 H29 B F4 N2 O2 -","- C104 H116 B4 F16 N8 O8 -","4","1","","Hoang, Gia L.; Yang, Zhao-Di; Smith, Sean M.; Pal, Rhitankar; Miska, Judy L.; Pérez, Damaris E; Pelter, Libbie S. W.; Zeng, Xiao Cheng; Takacs, James M.","Enantioselective Desymmetrization via Carbonyl-Directed Catalytic Asymmetric Hydroboration and Suzuki-Miyaura Cross-Coupling.","Organic letters","2015","17","4","940","943","10.1021/ol503764d","","","1.54178","CuKα","","0.0412","0.041","","","0.1083","0.1085","","","","","","1.051","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518636","16.559","0.003","16.774","0.003","15.989","0.003","90","","115.658","0.008","90","","4003.2","1.3","103","2","103","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C46 H44 B3 N3 O7 -","- C46 H44 B3 N3 O7 -","- C184 H176 B12 N12 O28 -","4","1","","Li, Gang; Xiong, Wei-Wei; Gu, Pei-Yang; Cao, Jun; Zhu, Jia; Ganguly, Rakesh; Li, Yongxin; Grimsdale, Andrew C.; Zhang, Qichun","1,5,9-Triaza-2,6,10-triphenylboracoronene: BN-Embedded Analogue of Coronene.","Organic letters","2015","17","3","560","563","10.1021/ol503575t","","","0.71073","MoKα","","0.2341","0.0956","","","0.2482","0.3405","","","","","","0.996","","","","has coordinates,has disorder","176729","2020-10-21","18:00:00",""
"1518637","19.9798","0.0003","19.9798","0.0003","12.6217","0.0003","90","","90","","120","","4363.46","0.14","293","2","293","2","","","","","","","","5","R -3 :H","-R 3","148","","","","- C27 H24 B3 N3 O12 -","- C27 H24 B3 N3 O12 -","- C162 H144 B18 N18 O72 -","6","0.333333","","Li, Gang; Xiong, Wei-Wei; Gu, Pei-Yang; Cao, Jun; Zhu, Jia; Ganguly, Rakesh; Li, Yongxin; Grimsdale, Andrew C.; Zhang, Qichun","1,5,9-Triaza-2,6,10-triphenylboracoronene: BN-Embedded Analogue of Coronene.","Organic letters","2015","17","3","560","563","10.1021/ol503575t","","","1.54178","CuKα","","0.0742","0.0663","","","0.2386","0.2557","","","","","","1.067","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518638","13.0661","0.0011","12.1247","0.0009","22.3242","0.0017","90","","98.251","0.006","90","","3500","0.5","103","2","103","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C37 H33 B3 Cl3 N3 O7 -","- C37 H33 B3 Cl3 N3 O7 -","- C148 H132 B12 Cl12 N12 O28 -","4","1","","Li, Gang; Xiong, Wei-Wei; Gu, Pei-Yang; Cao, Jun; Zhu, Jia; Ganguly, Rakesh; Li, Yongxin; Grimsdale, Andrew C.; Zhang, Qichun","1,5,9-Triaza-2,6,10-triphenylboracoronene: BN-Embedded Analogue of Coronene.","Organic letters","2015","17","3","560","563","10.1021/ol503575t","","","0.71073","MoKα","","0.3037","0.1742","","","0.3497","0.4257","","","","","","1.124","","","","has coordinates,has disorder","176729","2020-10-21","18:00:00",""
"1518639","13.3949","0.001","14.3478","0.0012","15.283","0.0012","90","","92.281","0.003","90","","2934.9","0.4","123","","123","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C33 H40 B N O4 Si -","- C33 H40 B N O4 Si -","- C132 H160 B4 N4 O16 Si4 -","4","1","","Kubota, Koji; Iwamoto, Hiroaki; Yamamoto, Eiji; Ito, Hajime","Silicon-tethered strategy for copper(i)-catalyzed stereo- and regioselective alkylboration of alkynes.","Organic letters","2015","17","3","620","623","10.1021/ol503620n","","","0.71075","MoKα","","","0.097","","","","0.3491","","","","","","1.16","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518640","9.272","0.005","15.087","0.008","26.669","0.014","75.828","0.011","88.836","0.013","88.885","0.012","3616","3","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C20 H22 N2 O5 -","- C20 H22.25 N2 O5 -","- C160 H178 N16 O40 -","8","4","","Zhong, Xue; Li, You; Zhang, Jing; Han, Fu-She","Synthetic Study toward the Misassigned (±)-Tronoharine.","Organic letters","2015","17","3","720","723","10.1021/ol503734x","","","0.71073","MoKα","","0.3073","0.074","","","0.0831","0.1209","","","","","","0.781","","","","has coordinates","182022","2020-10-21","18:00:00",""
"1518641","8.2569","0.0007","11.5402","0.001","15.727","0.0014","90","","102.251","0.001","90","","1464.4","0.2","185","2","185","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C18 H18 N2 O3 -","- C18 H18 N2 O3 -","- C72 H72 N8 O12 -","4","1","","Zhong, Xue; Li, You; Zhang, Jing; Han, Fu-She","Synthetic Study toward the Misassigned (±)-Tronoharine.","Organic letters","2015","17","3","720","723","10.1021/ol503734x","","","0.71073","MoKα","","0.0507","0.0414","","","0.0915","0.0964","","","","","","1.033","","","","has coordinates","201370","2020-10-21","18:00:00",""
"1518642","9.562","0.0005","10.2591","0.0006","10.618","0.0003","87.713","0.004","85.512","0.004","88.206","0.005","1037.16","0.09","150","1","150","1","","","","","","","","3","P -1","-P 1","2","","","","- C13 H12 O3 -","- C13 H12 O3 -","- C52 H48 O12 -","4","2","","Kratochvíl, Jiří; Novák, Zdeněk; Ghavre, Mukund; Nováková, Lucie; Růžička, Aleš; Kuneš, Jiří; Pour, Milan","Fully Substituted Pyranones via Quasi-Heterogeneous Genuinely Ligand-Free Migita-Stille Coupling of Iodoacrylates.","Organic letters","2015","17","3","520","523","10.1021/ol5035113","","","0.71073","MoKα","","0.0658","0.0465","","","0.1018","0.1154","","","","","","1.067","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518643","8.964","0.004","12.046","0.004","16.315","0.007","90","","90","","90","","1761.7","1.2","296","2","296.15","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C21 H18 N2 O -","- C21 H18 N2 O -","- C84 H72 N8 O4 -","4","1","","Manna, Manash Kumar; Hossian, Asik; Jana, Ranjan","Merging C-h activation and alkene difunctionalization at room temperature: a palladium-catalyzed divergent synthesis of indoles and indolines.","Organic letters","2015","17","3","672","675","10.1021/ol5036968","","","0.71073","MoKα","","0.1216","0.0486","","","0.1067","0.1361","","","","","","0.916","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518644","6.345","0.0014","11.725","0.003","13.3","0.003","67.812","0.003","80.532","0.003","84.005","0.003","902.7","0.4","296","2","296.15","","","","","","","","","4","P -1","-P 1","2","","","","- C23 H20 N2 O -","- C23 H20 N2 O -","- C46 H40 N4 O2 -","2","1","","Manna, Manash Kumar; Hossian, Asik; Jana, Ranjan","Merging C-h activation and alkene difunctionalization at room temperature: a palladium-catalyzed divergent synthesis of indoles and indolines.","Organic letters","2015","17","3","672","675","10.1021/ol5036968","","","0.71073","MoKα","","0.0663","0.0468","","","0.1351","0.1589","","","","","","1.027","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518645","12.8948","0.0011","9.7854","0.0008","18.3889","0.0016","90","","94.667","0.006","90","","2312.6","0.3","110","","110","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C24 H35 N3 O2 -","- C24 H35 N3 O2 -","- C96 H140 N12 O8 -","4","2","","Li, Xun; Taechalertpaisarn, Jaru; Xin, Dongyue; Burgess, Kevin","Protein-Protein Interface Mimicry by an Oxazoline Piperidine-2,4-dione.","Organic letters","2015","17","3","632","635","10.1021/ol5036547","","x-ray","1.54178","CuKα","","0.1065","0.0694","","","0.1565","0.1819","","","","","","1.041","","","","has coordinates","214153","2020-10-21","18:00:00",""
"1518646","9.052","0.0001","19.871","0.0003","22.2031","0.0003","90","","90","","90","","3993.72","0.09","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C34 H56 N2 O7 Si2 -","- C34 H57 N2 O7 Si2 -","- C136 H228 N8 O28 Si8 -","4","1","","Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez","Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.","Organic letters","2015","17","3","512","515","10.1021/ol503523h","","","1.54184","CuKα","","0.0614","0.0565","","","0.163","0.1692","","","","","","1.053","","","","has coordinates,has disorder","176729","2020-10-21","18:00:00",""
"1518647","18.0919","0.0007","10.7097","0.0004","18.935","0.0007","90","","107.979","0.002","90","","3489.7","0.2","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C33 H44 N2 O7 Si -","- C33 H44 N2 O7 Si -","- C132 H176 N8 O28 Si4 -","4","2","","Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez","Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.","Organic letters","2015","17","3","512","515","10.1021/ol503523h","","","0.71073","MoKα","","0.1851","0.0874","","","0.1825","0.2369","","","","","","1.021","","","","has coordinates,has disorder","176729","2020-10-21","18:00:00",""
"1518648","11.0538","0.0002","12.5835","0.0002","15.8359","0.0002","90","","90","","90","","2202.7","0.06","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C22 H28 N2 O7 -","- C22 H28 N2 O7 -","- C88 H112 N8 O28 -","4","1","","Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez","Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.","Organic letters","2015","17","3","512","515","10.1021/ol503523h","","","1.54184","CuKα","","0.0403","0.0378","","","0.1068","0.1102","","","","","","1.038","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518649","8.9854","0.0003","18.5028","0.0005","9.4678","0.0003","90","","109.249","0.002","90","","1486.07","0.08","223","2","223","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H17 N O3 -","- C17 H17 N O3 -","- C68 H68 N4 O12 -","4","1","","Ramella, Vincenzo; He, Zhiheng; Daniliuc, Constantin G.; Studer, Armido","Palladium-catalyzed diastereoselective oxyarylation of 2-alkylindoles.","Organic letters","2015","17","3","664","667","10.1021/ol503689r","","","1.54178","CuKα","","0.041","0.0398","","","0.1035","0.1048","","","","","","1.045","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518650","8.5929","0.0002","9.9207","0.0003","13.6227","0.0006","73.585","0.001","78.745","0.001","86.593","0.001","1092.53","0.06","223","2","223","2","","","","","","","","5","P -1","-P 1","2","","","","- C25 H22 Cl N O4 -","- C25 H22 Cl N O4 -","- C50 H44 Cl2 N2 O8 -","2","1","","Ramella, Vincenzo; He, Zhiheng; Daniliuc, Constantin G.; Studer, Armido","Palladium-catalyzed diastereoselective oxyarylation of 2-alkylindoles.","Organic letters","2015","17","3","664","667","10.1021/ol503689r","","","0.71073","MoKα","","0.0834","0.0635","","","0.1189","0.1326","","","","","","1.079","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518651","7.6192","0.0007","12.0803","0.0011","14.0233","0.0012","90","","102.158","0.001","90","","1261.8","0.2","298","2","298","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C31 H27 N3 O2 -","- C31 H27 N3 O2 -","- C62 H54 N6 O4 -","2","1","","Pertejo, Pablo; Corres, Nazaret; Torroba, Tomás; García-Valverde, María","Reversal of Diastereoselectivity in the Synthesis of Peptidomimetic 3-Carboxamide-1,4-benzodiazepin-5-ones.","Organic letters","2015","17","3","612","615","10.1021/ol503628r","","","0.71073","MoKα","","0.0392","0.0381","","","0.1007","0.102","","","","","","1.065","","","","has coordinates","176432","2020-10-21","18:00:00",""
"1518652","11.3323","0.0004","8.5548","0.0003","14.1288","0.0005","90","","92.453","0.001","90","","1368.47","0.08","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C30 H38 N2 O7 -","- C30 H38 N2 O7 -","- C60 H76 N4 O14 -","2","1","","Chen, Chunmei; Zhu, Hucheng; Li, Xiao-Nian; Yang, Jing; Wang, Jianping; Li, Gentao; Li, Yan; Tong, Qingyi; Yao, Guangmin; Luo, Zengwei; Xue, Yongbo; Zhang, Yonghui","Armochaeglobines A and B, Two New Indole-Based Alkaloids from the Arthropod-Derived Fungus Chaetomium globosum.","Organic letters","2015","17","3","644","647","10.1021/ol503666b","","","1.54178","CuKα","","0.056","0.0552","","","0.1521","0.1529","","","","","","1.143","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518653","13.4499","0.0006","7.46","0.0004","14.9726","0.0007","90","","104.948","0.002","90","","1451.46","0.12","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C32 H40 N2 O7 -","- C32 H36 N2 O7 -","- C64 H72 N4 O14 -","2","1","","Chen, Chunmei; Zhu, Hucheng; Li, Xiao-Nian; Yang, Jing; Wang, Jianping; Li, Gentao; Li, Yan; Tong, Qingyi; Yao, Guangmin; Luo, Zengwei; Xue, Yongbo; Zhang, Yonghui","Armochaeglobines A and B, Two New Indole-Based Alkaloids from the Arthropod-Derived Fungus Chaetomium globosum.","Organic letters","2015","17","3","644","647","10.1021/ol503666b","","","1.54178","CuKα","","0.1064","0.0907","","","0.2211","0.2412","","","","","","1.134","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518654","13.4566","0.0003","8.18811","0.00015","19.1862","0.0004","90","","100.629","0.0007","90","","2077.74","0.07","93","","93","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C42 H59 F3 O10 -","- C42 H59 F3 O10 -","- C84 H118 F6 O20 -","2","1","","Inahashi, Yuki; Iwatsuki, Masato; Ishiyama, Aki; Matsumoto, Atsuko; Hirose, Tomoyasu; Oshita, Jun; Sunazuka, Toshiaki; Panbangred, Watanalai; Takahashi, Yoko; Kaiser, Marcel; Otoguro, Kazuhiko; O̅mura, Satoshi","Actinoallolides A-E, New Anti-trypanosomal Macrolides, Produced by an Endophytic Actinomycete, Actinoallomurus fulvus MK10-036.","Organic letters","2015","17","4","864","867","10.1021/ol5037216","","","1.54187","CuKα","","","0.0279","","","","0.0702","","","","","","1.018","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518655","11.9124","0.0016","7.5041","0.001","14.67","0.002","90","","111.533","0.005","90","","1219.9","0.3","120","2","120","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C13 H10 N2 O2 S -","- C13 H10 N2 O2 S -","- C52 H40 N8 O8 S4 -","4","1","","Pawar, Amit B.; Chang, Sukbok","Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.","Organic letters","2015","17","3","660","663","10.1021/ol503680d","","","0.71073","MoKα","","0.117","0.0543","","","0.1187","0.1399","","","","","","1.033","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518656","6.9373","0.0006","8.2261","0.0007","9.7516","0.0008","85.814","0.004","78.171","0.004","89.197","0.004","543.22","0.08","120","2","120","2","","","","","","","","4","P -1","-P 1","2","","","","- C13 H10 N4 O -","- C13 H10 N4 O -","- C26 H20 N8 O2 -","2","1","","Pawar, Amit B.; Chang, Sukbok","Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.","Organic letters","2015","17","3","660","663","10.1021/ol503680d","","","0.71073","MoKα","","0.0378","0.0359","","","0.1014","0.1033","","","","","","1.093","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518657","7.9667","0.0003","8.6666","0.0004","9.6847","0.0004","109.198","0.002","107.554","0.002","92.006","0.002","595.36","0.04","120","2","120","2","","","","","","","","3","P -1","-P 1","2","","","","- C14 H11 N5 -","- C14 H11 N5 -","- C28 H22 N10 -","2","1","","Pawar, Amit B.; Chang, Sukbok","Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.","Organic letters","2015","17","3","660","663","10.1021/ol503680d","","","0.71073","MoKα","","0.1012","0.0557","","","0.1267","0.1462","","","","","","1.045","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518658","8.2102","0.0016","6.2167","0.0012","14.102","0.003","90","","90.69","0.03","90","","719.7","0.2","296","2","296","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C16 H19 N O4 -","- C16 H19 N O4 -","- C32 H38 N2 O8 -","2","1","","Lou, Yan-Peng; Zheng, Chang-Wu; Pan, Ren-Ming; Jin, Qiao-Wen; Zhao, Gang; Li, Zhong","Enantioselective Direct Mannich Reactions of Cyclic β-Ketoesters Catalyzed by Chiral Phosphine via a Novel Dual-Reagent Catalysis.","Organic letters","2015","17","3","688","691","10.1021/ol503712m","","","1.54178","CuKα","","0.0374","0.0373","","","0.0975","0.0976","","","","","","1.143","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518659","9.5704","0.0013","11.7332","0.0016","21.056","0.003","90","","97.692","0.003","90","","2343.1","0.6","173","2","173","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C25 H23 Br O S2 Se -","- C25 H23 Br O S2 Se -","- C100 H92 Br4 O4 S8 Se4 -","4","1","","Wu, Ping; Wang, Liandi; Wu, Kaikai; Yu, Zhengkun","Brønsted Acid Catalyzed PhSe Transfer versus Radical Aryl Transfer: Linear Codimerization of Styrenes and Internal Olefins.","Organic letters","2015","17","4","868","871","10.1021/ol503731s","","","0.71073","MoKα","","0.0589","0.0349","","","0.0716","0.0799","","","","","","1.016","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518660","10.5963","0.0005","16.7072","0.0009","10.9555","0.0006","90","","95.184","0.005","90","","1931.57","0.17","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C20 H21 F O2 S2 -","- C20 H21 F O2 S2 -","- C80 H84 F4 O8 S8 -","4","1","","Wu, Ping; Wang, Liandi; Wu, Kaikai; Yu, Zhengkun","Brønsted Acid Catalyzed PhSe Transfer versus Radical Aryl Transfer: Linear Codimerization of Styrenes and Internal Olefins.","Organic letters","2015","17","4","868","871","10.1021/ol503731s","","","0.71073","MoKα","","0.0622","0.0422","","","0.1018","0.1156","","","","","","1.018","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518685","18.809","0.01","10.08","0.005","20.725","0.011","90","","90","","90","","3929","4","100","","100","","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C52 H48 N4 O4 -","- C52 H48 N4 O4 -","- C208 H192 N16 O16 -","4","1","","Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu","Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.","Organic letters","2015","17","4","786","789","10.1021/ol503466e","","","0.71073","MoKα","","0.0366","0.0309","","","0.071","0.0741","","","","","","1.037","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518686","9.8315","0.0017","14.743","0.003","21.249","0.004","101.193","0.002","91.334","0.002","94.028","0.002","3011.8","1","100","","100","","","","","","","","","5","P -1","-P 1","2","","","","- C62 H66 Cl6 N4 O12 -","- C62 H66 Cl6 N4 O12 -","- C124 H132 Cl12 N8 O24 -","2","1","","Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu","Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.","Organic letters","2015","17","4","786","789","10.1021/ol503466e","","","0.71073","MoKα","","0.0592","0.0427","","","0.1042","0.1135","","","","","","1.068","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518687","11.12","0.003","14.029","0.004","20.02","0.006","108.726","0.004","98.537","0.004","94.981","0.004","2894.8","1.4","100","","100","","","","","","","","","4","P -1","-P 1","2","","","","- C63 H70 N4 O16 -","- C63 H70 N4 O16 -","- C126 H140 N8 O32 -","2","1","","Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu","Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.","Organic letters","2015","17","4","786","789","10.1021/ol503466e","","","0.71073","MoKα","","0.1056","0.0618","","","0.1532","0.1783","","","","","","1.049","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518712","6.0078","0.0002","15.1366","0.0005","20.0221","0.0007","90","","90","","90","","1820.76","0.11","173","2","173","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C21 H28 O3 -","- C21 H28 O3 -","- C84 H112 O12 -","4","1","","Parr, Brendan T.; Davies, Huw M. L.","Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence.","Organic letters","2015","17","4","794","797","10.1021/ol503508k","","","1.54178","CuKα","","0.0366","0.0358","","","0.0964","0.0974","","","","","","1.084","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518713","6.2097","0.0001","14.9142","0.0002","23.193","0.0003","90","","90","","90","","2147.97","0.05","173","2","173","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C23 H27 F3 O3 -","- C23 H27 F3 O3 -","- C92 H108 F12 O12 -","4","1","","Parr, Brendan T.; Davies, Huw M. L.","Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence.","Organic letters","2015","17","4","794","797","10.1021/ol503508k","","","1.54178","CuKα","","0.0416","0.0407","","","0.1058","0.1067","","","","","","1.038","","","","has coordinates,has disorder","176729","2020-10-21","18:00:00",""
"1518718","16.759","0.004","7.4334","0.0018","30.141","0.007","90","","90","","90","","3754.9","1.5","250","2","250","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","Organics","Organics","","- C18 H26 O4 Si -","- C18 H26 O4 Si -","- C144 H208 O32 Si8 -","8","1","","Xu, Xinfang; Wang, Xiangbo; Zavalij, Peter Y.; Doyle, Michael P.","Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade.","Organic letters","2015","17","4","790","793","10.1021/ol503498n","","","0.71073","MoKα","","0.0479","0.0388","","","0.0719","0.0773","","","","","","1","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518719","6.1239","0.0005","16.8945","0.0012","17.8873","0.0013","91.468","0.0009","95.3024","0.001","90.184","0.0011","1842.1","0.2","150","2","150","2","","","","","","","","4","P -1","-P 1","2","Organics","Organics","","- C18 H26 O4 Si -","- C18 H26 O4 Si -","- C72 H104 O16 Si4 -","4","2","","Xu, Xinfang; Wang, Xiangbo; Zavalij, Peter Y.; Doyle, Michael P.","Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade.","Organic letters","2015","17","4","790","793","10.1021/ol503498n","","","0.71073","MoKα","","0.0494","0.038","","","0.072","0.0761","","","","","","1","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518723","7.0418","0.0005","10.4998","0.0008","17.4226","0.0012","93.591","0.005","96.204","0.005","103.663","0.005","1239.21","0.16","123","2","123","2","","","","","","","","4","P -1","-P 1","2","","14214b","","- C32 H28 O4 Si -","- C32 H28 O4 Si -","- C64 H56 O8 Si2 -","2","1","","Pogula, Vedamayee D.; Wang, Tao; Hoye, Thomas R.","Intramolecular [4 + 2] Trapping of a Hexadehydro-Diels-Alder (HDDA) Benzyne by Tethered Arenes.","Organic letters","2015","17","4","856","859","10.1021/ol5037024","","","1.54178","CuKα","","0.0874","0.0653","","","0.1476","0.158","","","","","","1.118","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518724","14.0146","0.0007","10.5314","0.0005","16.6752","0.0008","90","","100.775","0.003","90","","2417.8","0.2","123","2","123","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","14239b","","","- C31 H28 O4 Si -","- C31 H28 O4 Si -","- C124 H112 O16 Si4 -","4","1","","Pogula, Vedamayee D.; Wang, Tao; Hoye, Thomas R.","Intramolecular [4 + 2] Trapping of a Hexadehydro-Diels-Alder (HDDA) Benzyne by Tethered Arenes.","Organic letters","2015","17","4","856","859","10.1021/ol5037024","","","1.54178","CuKα","","0.0649","0.0484","","","0.1154","0.1273","","","","","","1.035","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518725","3.798","0.006","11.416","0.015","31.2","0.04","90","","90.82","0.02","90","","1353","3","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C18 H12 F N O3 -","- C18 H12 F N O3 -","- C72 H48 F4 N4 O12 -","4","1","","Qian, Jinlong; Yi, Wenbin; Huang, Xin; Miao, Yongbo; Zhang, Junkai; Cai, Chun; Zhang, Wei","One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors.","Organic letters","2015","17","5","1090","1093","10.1021/ol503615n","","","0.71073","MoKα","","0.1059","0.0868","","","0.1799","0.1937","","","","","","1.163","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518726","7.668","0.003","11.45","0.004","11.497","0.004","97.96","0.006","98.584","0.006","103.944","0.006","952.6","0.6","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H16 F4 O3 -","- C22 H16 F4 O3 -","- C44 H32 F8 O6 -","2","1","","Qian, Jinlong; Yi, Wenbin; Huang, Xin; Miao, Yongbo; Zhang, Junkai; Cai, Chun; Zhang, Wei","One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors.","Organic letters","2015","17","5","1090","1093","10.1021/ol503615n","","","0.71073","MoKα","","0.0502","0.04","","","0.1015","0.1122","","","","","","1.022","","","","has coordinates,has disorder","176729","2020-10-21","18:00:00",""
"1518747","11.31","0.003","13.792","0.003","13.982","0.003","93.902","0.003","90.56","0.003","112.233","0.003","2012.7","0.8","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C14 H9 Cl N4 O2 -","- C14 H9 Cl N4 O2 -","- C84 H54 Cl6 N24 O12 -","6","3","","Chen, Yunfeng; Nie, Gang; Zhang, Qi; Ma, Shan; Li, Huan; Hu, Qinquan","Copper-Catalyzed [3 + 2] Cycloaddition/Oxidation Reactions between Nitro-olefins and Organic Azides: Highly Regioselective Synthesis of NO2-Substituted 1,2,3-Triazoles.","Organic letters","2015","17","5","1118","1121","10.1021/ol503687w","","","0.71073","MoKα","","0.0828","0.0745","","","0.2121","0.2337","","","","","","1.06","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518748","10.784","0.0017","9.6655","0.0016","28.858","0.005","90","","90","","90","","3007.9","0.9","296","2","296","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C15 H11 Br N4 O2 -","- C15 H11 Br N4 O2 -","- C120 H88 Br8 N32 O16 -","8","1","","Chen, Yunfeng; Nie, Gang; Zhang, Qi; Ma, Shan; Li, Huan; Hu, Qinquan","Copper-Catalyzed [3 + 2] Cycloaddition/Oxidation Reactions between Nitro-olefins and Organic Azides: Highly Regioselective Synthesis of NO2-Substituted 1,2,3-Triazoles.","Organic letters","2015","17","5","1118","1121","10.1021/ol503687w","","","0.71073","MoKα","","0.0987","0.0498","","","0.1184","0.1363","","","","","","1.02","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518770","11.2813","0.0006","14.1148","0.0007","24.5832","0.0014","90","","90","","90","","3914.5","0.4","180.01","0.1","180.01","0.1","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C20 H16 Cl4 N2 -","- C20 H16 Cl4 N2 -","- C160 H128 Cl32 N16 -","8","1","","Zhan, Ming; Zhang, Shaoguang; Huang, Zhe; Xi, Zhenfeng","Synthesis of α,α,α',α'-Tetrachloro-Δ(1)-bipyrrolines and 4,8-Dichloro-2,6-diazasemibuvallenes.","Organic letters","2015","17","4","1026","1029","10.1021/acs.orglett.5b00136","","","0.7107","MoKα","","0.0582","0.0361","","","0.0726","0.0821","","","","","","1.046","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518771","9.3474","0.0007","9.8657","0.0007","12.3923","0.0009","66.695","0.007","69.579","0.007","62.115","0.007","908.59","0.13","180","0.1","180","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C18 H26 Cl2 N2 -","- C18 H26 Cl2 N2 -","- C36 H52 Cl4 N4 -","2","1","","Zhan, Ming; Zhang, Shaoguang; Huang, Zhe; Xi, Zhenfeng","Synthesis of α,α,α',α'-Tetrachloro-Δ(1)-bipyrrolines and 4,8-Dichloro-2,6-diazasemibuvallenes.","Organic letters","2015","17","4","1026","1029","10.1021/acs.orglett.5b00136","","","0.71073","MoKα","","0.08","0.0548","","","0.1337","0.1527","","","","","","1.033","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518772","9.6557","0.0002","10.7366","0.0003","25.0366","0.0004","90","","90","","90","","2595.53","0.1","130","2","130","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C28 H23 Br Cl3 N O2 -","- C28 H23 Br Cl3 N O2 -","- C112 H92 Br4 Cl12 N4 O8 -","4","1","","Saha, Satyajit; Schneider, Christoph","Directing Group Assisted Nucleophilic Substitution of Propargylic Alcohols via o-Quinone Methide Intermediates: Brønsted Acid Catalyzed, Highly Enantio- and Diastereoselective Synthesis of 7-Alkynyl-12a-acetamido-Substituted Benzoxanthenes.","Organic letters","2015","17","3","648","651","10.1021/ol503662g","","x-ray","0.71073","MoKα","","0.0425","0.034","","","0.0628","0.0662","","","","","","1.024","","","","has coordinates,has disorder","176729","2020-10-21","18:00:00",""
"1518773","7.3516","0.0002","9.5635","0.0002","29.4896","0.0005","90","","90","","90","","2073.33","0.08","130","2","130","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C26 H21 N O2 S -","- C26 H21 N O2 S -","- C104 H84 N4 O8 S4 -","4","1","","Saha, Satyajit; Schneider, Christoph","Directing Group Assisted Nucleophilic Substitution of Propargylic Alcohols via o-Quinone Methide Intermediates: Brønsted Acid Catalyzed, Highly Enantio- and Diastereoselective Synthesis of 7-Alkynyl-12a-acetamido-Substituted Benzoxanthenes.","Organic letters","2015","17","3","648","651","10.1021/ol503662g","","x-ray","0.71073","MoKα","","0.0354","0.0311","","","0.069","0.0711","","","","","","1.076","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518783","14.9264","0.0006","8.5389","0.0003","13.3223","0.0006","90","","96.518","0.004","90","","1687.02","0.12","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C23 H16 N2 -","- C23 H16 N2 -","- C92 H64 N8 -","4","1","","Zhang, Wei; Wei, Jun; Fu, Shaomin; Lin, Dongen; Jiang, Huanfeng; Zeng, Wei","Highly Stereoselective Ruthenium(II)-Catalyzed Direct C2-syn-Alkenylation of Indoles with Alkynes.","Organic letters","2015","17","6","1349","1352","10.1021/ol503618m","","","1.54178","CuKα","","0.0583","0.0425","","","0.1006","0.1126","","","","","","1.035","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518820","9.9575","0.0004","10.7208","0.0005","16.4862","0.0008","91.531","0.002","105.749","0.003","104.208","0.003","1633.82","0.13","103","2","103","2","","","","","","","","4","P 1","P 1","1","","","","- C23 H17 N O -","- C23 H17 N O -","- C92 H68 N4 O4 -","4","4","","Yang, Xiao-Fei; Hu, Xu-Hong; Loh, Teck-Peng","Expedient Synthesis of Pyrroloquinolinones by Rh-Catalyzed Annulation of N-Carbamoyl Indolines with Alkynes through a Directed C-H Functionalization/C-N Cleavage Sequence.","Organic letters","2015","17","6","1481","1484","10.1021/acs.orglett.5b00355","","","0.71073","MoKα","","0.0722","0.0518","","","0.1226","0.1427","","","","","","1.06","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518842","5.9536","0.0018","7.269","0.002","31.978","0.011","90","","90","","90","","1383.9","0.7","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C15 H13 F O2 S -","- C15 H13 F O2 S -","- C60 H52 F4 O8 S4 -","4","1","","Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang","Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones.","Organic letters","2015","17","7","1692","1695","10.1021/acs.orglett.5b00461","","","0.71073","MoKα","","0.1027","0.0552","","","0.1143","0.1533","","","","","","1.098","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518936","9.8882","0.0006","17.552","0.001","11.4151","0.0008","90","","103.067","0.006","90","","1929.9","0.2","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C18 H24 F N O4 S -","- C18 H24 F N O4 S -","- C72 H96 F4 N4 O16 S4 -","4","1","","Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.","Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.","Organic letters","2015","17","8","1922","1925","10.1021/acs.orglett.5b00608","","","0.71073","MoKα","","0.0742","0.0467","","","0.112","0.1239","","","","","","0.981","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518937","6.7205","0.0008","8.781","0.0011","11.3856","0.0016","103.22","0.012","104.242","0.011","92.033","0.01","630.98","0.15","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C13 H15 N O4 S -","- C13 H15 N O4 S -","- C26 H30 N2 O8 S2 -","2","1","","Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.","Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.","Organic letters","2015","17","8","1922","1925","10.1021/acs.orglett.5b00608","","","0.71073","MoKα","","0.1355","0.0664","","","0.1302","0.1563","","","","","","0.936","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518938","10.0063","0.0009","10.3287","0.0012","10.8385","0.0012","65.843","0.011","70.701","0.009","84.706","0.008","963.4","0.2","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C19 H28 N2 O4 S -","- C19 H28 N2 O4 S -","- C38 H56 N4 O8 S2 -","2","1","","Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.","Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.","Organic letters","2015","17","8","1922","1925","10.1021/acs.orglett.5b00608","","","0.71073","MoKα","","0.064","0.0445","","","0.1068","0.1172","","","","","","1.059","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518939","10.8363","0.0017","14.406","0.002","9.9733","0.0018","90","","117.4","","90","","1382.2","0.4","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C15 H18 N2 S -","- C15 H18 N2 S -","- C60 H72 N8 S4 -","4","1","","Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.","Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.","Organic letters","2015","17","8","1922","1925","10.1021/acs.orglett.5b00608","","","0.71073","MoKα","","0.1243","0.0513","","","0.1139","0.1403","","","","","","0.884","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518940","7.3226","0.0003","10.563","0.0006","18.9019","0.0011","90","","92.929","0.004","90","","1460.13","0.13","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H21 N O3 S -","- C15 H21 N O3 S -","- C60 H84 N4 O12 S4 -","4","1","","Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.","Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.","Organic letters","2015","17","8","1922","1925","10.1021/acs.orglett.5b00608","","","0.71073","MoKα","","0.0937","0.0502","","","0.1083","0.1238","","","","","","1.038","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518941","8.4818","0.0005","10.9461","0.0008","30.035","0.002","90","","90","","90","","2788.5","0.3","293","2","293","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C14 H19 N O3 S -","- C14 H19 N O3 S -","- C112 H152 N8 O24 S8 -","8","1","","Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K.","Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery.","Organic letters","2015","17","8","1922","1925","10.1021/acs.orglett.5b00608","","","0.71073","MoKα","","0.1063","0.0524","","","0.1226","0.1421","","","","","","0.968","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518989","12.7382","0.0007","11.0562","0.0007","12.4976","0.0008","90","","112.701","0.002","90","","1623.76","0.17","296","","296","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H12 Cl2 N2 -","- C19 H12 Cl2 N2 -","- C76 H48 Cl8 N8 -","4","1","","Tiwari, Virendra Kumar; Kamal, Neha; Kapur, Manmohan","Ruthenium-catalyzed heteroatom-directed regioselective C-h arylation of indoles using a removable tether.","Organic letters","2015","17","7","1766","1769","10.1021/acs.orglett.5b00535","","","0.71073","MoKα","","0.0945","0.0472","","","0.1075","0.1293","","","","","","1.01","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518990","14.4427","0.0008","6.5207","0.0004","16.6673","0.0008","90","","90","","90","","1569.67","0.15","291","2","291.15","","","","","","","","","5","P c a 21","P 2c -2ac","29","","","","- C17 H17 O P Si -","- C17 H17 O P Si -","- C68 H68 O4 P4 Si4 -","4","1","","Xu, Youzhi; Wang, Zhihua; Gan, Zhenjie; Xi, Qiuzhen; Duan, Zheng; Mathey, François","Versatile synthesis of phospholides from open-chain precursors. Application to annelated pyrrole- and silole-phosphole rings.","Organic letters","2015","17","7","1732","1734","10.1021/acs.orglett.5b00598","","","1.54184","CuKα","","0.044","0.0388","","","0.0996","0.1053","","","","","","1.054","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518991","12.402","0.003","5.782","0.0011","24.377","0.005","90","","100.253","0.003","90","","1720.1","0.6","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C21 H17 F O2 S -","- C21 H17 F O2 S -","- C84 H68 F4 O8 S4 -","4","1","","Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang","Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones.","Organic letters","2015","17","7","1692","1695","10.1021/acs.orglett.5b00461","","","0.71073","MoKα","","0.0804","0.048","","","0.1125","0.1302","","","","","","1.027","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518992","5.7471","0.0008","8.0541","0.0011","31.351","0.004","90","","90","","90","","1451.2","0.3","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C16 H16 O2 S -","- C16 H16 O2 S -","- C64 H64 O8 S4 -","4","1","","Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang","Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones.","Organic letters","2015","17","7","1692","1695","10.1021/acs.orglett.5b00461","","","0.71073","MoKα","","0.0772","0.0517","","","0.1038","0.1162","","","","","","1.044","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518993","12.3084","0.0018","5.8277","0.0009","24.345","0.004","90","","100.373","0.002","90","","1717.7","0.5","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C21 H18 O2 S -","- C21 H18 O2 S -","- C84 H72 O8 S4 -","4","1","","Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang","Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones.","Organic letters","2015","17","7","1692","1695","10.1021/acs.orglett.5b00461","","","0.71073","MoKα","","0.0562","0.0429","","","0.1155","0.1336","","","","","","1.086","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518994","25.7457","0.001","5.8011","0.0002","19.0494","0.0007","90","","98.23","0.003","90","","2815.79","0.18","296","2","296","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C14 H17 N O3 S -","- C14 H17 N O3 S -","- C112 H136 N8 O24 S8 -","8","1","","Cheng, Cungui; Liu, Shuiyou; Zhu, Gangguo","Palladium-catalyzed cycloisomerization and aerobic oxidative cycloisomerization of homoallenyl amides: a facile and divergent approach to 2-aminofurans.","Organic letters","2015","17","6","1581","1584","10.1021/acs.orglett.5b00464","","","0.71073","MoKα","","0.0672","0.0538","","","0.1309","0.1393","","","","","","1.075","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518995","16.428","0.006","13.329","0.005","14.387","0.005","90","","90","","90","","3150","2","293","2","293","2","","","","","","","","5","P b c n","-P 2n 2ab","60","","","","- C15 H21 N O4 S -","- C15 H21 N O4 S -","- C120 H168 N8 O32 S8 -","8","1","","Zhu, Haitao; Chen, Pinhong; Liu, Guosheng","Palladium-catalyzed intramolecular aminoacetoxylation of unactivated alkenes with hydrogen peroxide as oxidant.","Organic letters","2015","17","6","1485","1488","10.1021/acs.orglett.5b00373","","","0.71073","MoKα","","0.0951","0.0525","","","0.1259","0.1452","","","","","","0.996","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518996","9.8991","0.0011","10.1513","0.0011","17.5003","0.0019","90","","90","","90","","1758.6","0.3","150","2","150","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C20 H20 N2 O3 -","- C20 H20 N2 O3 -","- C80 H80 N8 O12 -","4","1","","Yetra, Santhivardhana Reddy; Mondal, Santigopal; Suresh, Eringathodi; Biju, Akkattu T.","Enantioselective Synthesis of Functionalized Pyrazoles by NHC-Catalyzed Reaction of Pyrazolones with α,β-Unsaturated Aldehydes.","Organic letters","2015","17","6","1417","1420","10.1021/acs.orglett.5b00293","","","0.71073","MoKα","","0.0683","0.0612","","","0.1235","0.1261","","","","","","1.21","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518997","14.5121","0.0011","5.9558","0.0003","24.1332","0.0017","90","","90","","90","","2085.9","0.2","173.15","","173.15","","","","","","","","","3","P n a 21","P 2c -2n","33","","","","- C11 H14 O3 -","- C11 H14 O3 -","- C88 H112 O24 -","8","2","","Qin, Yan; Zhang, Long; Lv, Jian; Luo, Sanzhong; Cheng, Jin-Pei","Bioinspired Organocatalytic Aerobic C-H Oxidation of Amines with an ortho-Quinone Catalyst.","Organic letters","2015","17","6","1469","1472","10.1021/acs.orglett.5b00351","","","0.71073","MoKα","","0.0477","0.0439","","","0.1068","0.1097","","","","","","1.084","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518998","8.477","0.0004","8.5847","0.0005","17.547","0.0005","90","","90","","90","","1276.94","0.1","294.39","0.1","294.39","0.1","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C16 H14 O2 -","- C16 H14 O2 -","- C64 H56 O8 -","4","1","","Jiang, Liyin; Jia, Tao; Wang, Min; Liao, Jian; Cao, Peng","Pd-catalyzed enantioselective hydroalkoxylation of alkoxyallenes with phenol for construction of acyclic o,o-acetals.","Organic letters","2015","17","5","1070","1073","10.1021/acs.orglett.5b00146","","","1.54184","CuKα","","0.0469","0.044","","","0.1064","0.1086","","","","","","1.141","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1518999","9.2698","0.0004","11.0134","0.0005","15.0573","0.0007","90","","105.111","0.002","90","","1484.08","0.12","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C17 H13 F O3 S -","- C17 H13 F O3 S -","- C68 H52 F4 O12 S4 -","4","1","","Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju","Bi(OTf)3-Mediated Cycloisomerization of γ-Alkynyl Arylketones: Application to the Synthesis of Substituted Furans.","Organic letters","2015","17","5","1264","1267","10.1021/acs.orglett.5b00246","","","0.71073","MoKα","","0.0426","0.0345","","","0.1035","0.1286","","","","","","1.245","","","","has coordinates","176729","2020-10-21","18:00:00",""
"1519496","6.134","0.003","7.123","0.004","10.777","0.006","102.328","0.008","106.299","0.008","90.659","0.007","440.2","0.4","173.15","","173.15","","","","","","","","","4","P 1","P 1","1","","","","- C22 H20 Br N -","- C22 H20 Br N -","- C22 H20 Br N -","1","1","","Zhang, Zhenhua; Du, Haifeng","Cis-selective and highly enantioselective hydrogenation of 2,3,4-trisubstituted quinolines.","Organic letters","2015","17","11","2816","2819","10.1021/acs.orglett.5b01240","","","0.71073","MoKα","","0.0418","0.0404","","","0.0902","0.0911","","","","","","1.093","","","","has coordinates","140285","2020-10-21","18:00:00",""
"1519622","19.306","0.008","4.5687","0.0019","22.128","0.009","90","","103.674","0.008","90","","1896.4","1.4","100","2","100","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C22 H18 Cl N O3 Pd -","- C22 H18 Cl N O3 Pd -","- C88 H72 Cl4 N4 O12 Pd4 -","4","1","","Ren, Zhi; Schulz, Jonathan E.; Dong, Guangbin","Catalytic Ortho-Acetoxylation of Masked Benzyl Alcohols via an Exo-Directing Mode.","Organic letters","2015","17","11","2696","2699","10.1021/acs.orglett.5b01098","","","0.71073","MoKα","","0.1351","0.0771","","","0.1476","0.1706","","","","","","1.017","","","","has coordinates","141409","2020-10-21","18:00:00",""
"1519623","24.877","0.01","7.087","0.003","7.92","0.003","90","","90.593","0.006","90","","1396.2","1","296","2","296","2","","","","","","","","5","C 1 c 1","C -2yc","9","","","","- C15 H10 I N O2 -","- C15 H10 I N O2 -","- C60 H40 I4 N4 O8 -","4","1","","Huang, Hai; Zhu, Xiaolin; He, Guangke; Liu, Qi; Fan, Junzhen; Zhu, Hongjun","Controlled Synthesis of 1,3,5-Oxadiazin-2-ones and Oxazolones through Regioselective Iodocyclization of Ynamides.","Organic letters","2015","17","10","2510","2513","10.1021/acs.orglett.5b01045","","","0.71073","MoKα","","0.0822","0.0773","","","0.2091","0.2199","","","","","","1.107","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1519625","10.2671","0.0002","10.1236","0.0002","23.3329","0.0006","90","","98.876","0.002","90","","2396.18","0.09","180","2","180","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C32 H30 B N -","- C32 H30 B N -","- C128 H120 B4 N4 -","4","1","","Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning","One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions.","Organic letters","2015","17","10","2486","2489","10.1021/acs.orglett.5b00994","","","0.71073","MoKα","","0.1202","0.055","","","0.1212","0.1506","","","","","","1.024","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1519626","10.0993","0.0002","10.2609","0.0002","23.8794","0.0005","90","","97.3582","0.0011","90","","2454.19","0.09","180","2","180","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C32 H32 B N -","- C32 H32 B N -","- C128 H128 B4 N4 -","4","1","","Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning","One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions.","Organic letters","2015","17","10","2486","2489","10.1021/acs.orglett.5b00994","","","0.71073","MoKα","","0.1085","0.0783","","","0.1621","0.1772","","","","","","1.154","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1519627","8.8087","0.0005","11.1753","0.0006","16.1219","0.0009","72.148","0.004","78.052","0.004","74.662","0.004","1443.04","0.14","180","2","180","2","","","","","","","","4","P -1","-P 1","2","","","","- C38 H34 B N -","- C38 H34 B N -","- C76 H68 B2 N2 -","2","1","","Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning","One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions.","Organic letters","2015","17","10","2486","2489","10.1021/acs.orglett.5b00994","","","0.71073","MoKα","","0.1254","0.0575","","","0.1344","0.1636","","","","","","1.053","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1519628","30.624","0.013","56.38","0.02","22.177","0.009","90","","93.399","0.011","90","","38223","3","93","2","93","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C102 H70 B4 O20 -","- C102 H70 B4 O20 -","- C816 H560 B32 O160 -","8","1","","Danjo, Hiroshi; Kidena, Yuki; Kawahata, Masatoshi; Sato, Hiroyasu; Katagiri, Kosuke; Miyazawa, Toshifumi; Yamaguchi, Kentaro","Multilayered inclusion nanocycles of anionic spiroborates.","Organic letters","2015","17","10","2466","2469","10.1021/acs.orglett.5b00974","","","0.7107","MoKα","","0.3251","0.1864","","","0.4594","0.5366","","","","","","1.108","","","","has coordinates","140264","2020-10-21","18:00:00",""
"1519629","7.3915","0.0012","13.779","0.002","19.135","0.003","90","","93.863","0.003","90","","1944.4","0.5","294","2","294","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C21 H26 N2 O2 S -","- C21 H26 N2 O2 S -","- C84 H104 N8 O8 S4 -","4","1","","Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar","Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion.","Organic letters","2015","17","9","2226","2229","10.1021/acs.orglett.5b00832","","","0.71073","MoKα","","0.0769","0.0695","","","0.1907","0.1983","","","","","","0.962","","","","has coordinates,has disorder","138312","2020-10-21","18:00:00",""
"1519630","11.225","0.0018","13.361","0.002","11.0143","0.0018","90","","118.102","0.002","90","","1457.2","0.4","294","2","294","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H14 N2 O2 S -","- C16 H14 N2 O2 S -","- C64 H56 N8 O8 S4 -","4","1","","Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar","Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion.","Organic letters","2015","17","9","2226","2229","10.1021/acs.orglett.5b00832","","","0.71073","MoKα","","0.0598","0.0526","","","0.1324","0.1378","","","","","","1.087","","","","has coordinates","138312","2020-10-21","18:00:00",""
"1519631","8.9148","0.0006","16.7339","0.0011","10.5655","0.0007","90","","95.855","0.001","90","","1567.93","0.18","294","2","294","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C17 H16 N2 O2 S -","- C17 H16 N2 O2 S -","- C68 H64 N8 O8 S4 -","4","1","","Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar","Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion.","Organic letters","2015","17","9","2226","2229","10.1021/acs.orglett.5b00832","","","0.71073","MoKα","","0.0436","0.0399","","","0.1154","0.1199","","","","","","1.058","","","","has coordinates","138312","2020-10-21","18:00:00",""
"1519651","5.4571","0.0005","34.89","0.003","7.6271","0.0007","90","","96.378","0.002","90","","1443.2","0.2","130","","130","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C14 H15 F3 O4 S -","- C14 H15 F3 O4 S -","- C56 H60 F12 O16 S4 -","4","1","","Liu, Yafei; Shao, Xinxin; Zhang, Panpan; Lu, Long; Shen, Qilong","Trifluoromethyl-substituted sulfonium ylide: rh-catalyzed carbenoid addition to trifluoromethylthioether.","Organic letters","2015","17","11","2752","2755","10.1021/acs.orglett.5b01170","","","0.71073","MoKα","","0.053","0.0446","","","0.121","0.1316","","","","","","1.184","","","","has coordinates","152909","2020-10-21","18:00:00",""
"1519652","18.4589","0.0002","58.006","0.0009","11.59672","0.00017","90","","90","","90","","12416.9","0.3","180","","180","","","","101","","","","","4","P n 21 a","P -2ac -2n","33","","","","- C47 H59 N O5 -","- C47 H59 N O5 -","- C564 H708 N12 O60 -","12","3","","Slavík, Petr; Eigner, Václav; Lhoták, Pavel","Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds.","Organic letters","2015","17","11","2788","2791","10.1021/acs.orglett.5b01200","","","1.5418","CuKα","","0.0526","0.0507","","0.1289","0.1271","0.1288","","","","","","0.8818","","","","has coordinates,has disorder","176429","2020-10-21","18:00:00",""
"1519653","34.9361","0.0016","10.48642","0.00015","26.842","0.0012","90","","135.583","0.008","90","","6882.4","1.1","120","","120","","","","101","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C41 H46 O5 -","- C41 H46 O5 -","- C328 H368 O40 -","8","1","","Slavík, Petr; Eigner, Václav; Lhoták, Pavel","Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds.","Organic letters","2015","17","11","2788","2791","10.1021/acs.orglett.5b01200","","","1.54184","CuKα","","0.038","0.0332","","0.0776","0.0736","0.0776","","","","","","0.8837","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1519654","20.7243","0.0006","10.45113","0.00017","21.5504","0.0005","90","","113.543","0.003","90","","4279.1","0.2","180","","180","","","","101","","","","","3","P 1 21 1","P 2yb","4","","","","- C48.5 H58 O6.5 -","- C48.5 H58 O6.5 -","- C194 H232 O26 -","4","2","","Slavík, Petr; Eigner, Václav; Lhoták, Pavel","Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds.","Organic letters","2015","17","11","2788","2791","10.1021/acs.orglett.5b01200","","","1.54184","CuKα","","0.091","0.0855","","0.2214","0.2127","0.2213","","","","","","0.9818","","","","has coordinates,has disorder","217275","2020-10-21","18:00:00",""
"1519655","14.0307","0.0016","8.5721","0.001","15.203","0.003","90","","109.89","0.001","90","","1719.4","0.4","123","2","123","2","","","","","","","","5","C 1 c 1","C -2yc","9","","","","- C20 H16 Br N O4 -","- C20 H16 Br N O4 -","- C80 H64 Br4 N4 O16 -","4","1","","Lin, Chao; Zhen, Le; Cheng, Yong; Du, Hong-Jin; Zhao, Hui; Wen, Xiaoan; Kong, Ling-Yi; Xu, Qing-Long; Sun, Hongbin","Visible-light induced isoindoles formation to trigger intermolecular diels-alder reactions in the presence of air.","Organic letters","2015","17","11","2684","2687","10.1021/acs.orglett.5b01078","","","0.71073","MoKα","","0.029","0.0273","","","0.0583","0.0588","","","","","","1.056","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1519656","13.373","0.002","16.581","0.003","8.8083","0.0016","90","","93.638","0.003","90","","1949.2","0.6","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C25 H20 N2 O2 -","- C25 H20 N2 O2 -","- C100 H80 N8 O8 -","4","1","","Lin, Chao; Zhen, Le; Cheng, Yong; Du, Hong-Jin; Zhao, Hui; Wen, Xiaoan; Kong, Ling-Yi; Xu, Qing-Long; Sun, Hongbin","Visible-light induced isoindoles formation to trigger intermolecular diels-alder reactions in the presence of air.","Organic letters","2015","17","11","2684","2687","10.1021/acs.orglett.5b01078","","","0.71073","MoKα","","0.0463","0.0364","","","0.1043","0.1201","","","","","","1.069","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1519657","10.5446","0.0012","9.5462","0.001","24.575","0.003","90","","91.778","0.002","90","","2472.5","0.5","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C24 H28 Cl N O7 -","- C24 H28 Cl N O7 -","- C96 H112 Cl4 N4 O28 -","4","1","","Hu, Jiang-Lin; Wang, Lijia; Xu, Hao; Xie, Zuowei; Tang, Yong","Highly diastereoselective and enantioselective formal [4 + 3] cycloaddition of donor-acceptor cyclobutanes with nitrones.","Organic letters","2015","17","11","2680","2683","10.1021/acs.orglett.5b01077","","","0.71073","MoKα","","0.0743","0.0556","","","0.1354","0.1496","","","","","","1.03","","","","has coordinates,has disorder","176428","2020-10-21","18:00:00",""
"1519658","10.409","0.0007","15.4718","0.0011","16.588","0.0011","90","","90","","90","","2671.4","0.3","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C28 H28 Br N O6 -","- C28 H28 Br N O6 -","- C112 H112 Br4 N4 O24 -","4","1","","Hu, Jiang-Lin; Wang, Lijia; Xu, Hao; Xie, Zuowei; Tang, Yong","Highly diastereoselective and enantioselective formal [4 + 3] cycloaddition of donor-acceptor cyclobutanes with nitrones.","Organic letters","2015","17","11","2680","2683","10.1021/acs.orglett.5b01077","","","0.71073","MoKα","","0.0661","0.0414","","","0.093","0.1023","","","","","","1.02","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1519694","5.7372","0.0005","21.0648","0.0018","10.9631","0.0011","90","","94.428","0.007","90","","1321","0.2","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C14 H11 N O4 S -","- C14 H11 N O4 S -","- C56 H44 N4 O16 S4 -","4","1","","Singh, Rahul; Allam, Bharat Kumar; Singh, Neetu; Kumari, Kumkum; Singh, Satish Kumar; Singh, Krishna Nand","A Direct Metal-Free Decarboxylative Sulfono Functionalization (DSF) of Cinnamic Acids to α,β-Unsaturated Phenyl Sulfones.","Organic letters","2015","17","11","2656","2659","10.1021/acs.orglett.5b01037","","","0.71073","MoKα","","0.1744","0.0911","","","0.2394","0.3092","","","","","","1.058","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1519695","8.099","0.003","13.445","0.004","16.407","0.005","90","","90","","90","","1786.6","1","180","2","180","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C23 H22 O2 -","- C23 H22 O2 -","- C92 H88 O8 -","4","1","","Mitra, Nirmal K.; Meudom, Rolande; Gorden, John D.; Merner, Bradley L.","A non-cross-coupling approach to arene-bridged macrocycles: synthesis, structure, and direct, regioselective functionalization of a cycloparaphenylene fragment.","Organic letters","2015","17","11","2700","2703","10.1021/acs.orglett.5b01102","","","0.71073","","","0.0587","0.0404","","","0.068","0.0721","","","","","","0.973","","","","has coordinates","140287","2020-10-21","18:00:00",""
"1519696","6.1061","0.0002","18.8064","0.0005","27.8827","0.0007","90","","90","","90","","3201.88","0.16","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C13 H13 F O -","- C13 H13 F O -","- C156 H156 F12 O12 -","12","3","","Witten, Michael R.; Jacobsen, Eric N.","A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes.","Organic letters","2015","17","11","2772","2775","10.1021/acs.orglett.5b01193","","","1.54178","CuKα","","0.0484","0.0418","","","0.1078","0.1114","","","","","","1.065","","","","has coordinates,has disorder","217633","2020-10-21","18:00:00",""
"1519697","8.013","0.003","5.1662","0.0018","10.972","0.004","90","","93.376","0.005","90","","453.4","0.3","100","2","100","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C9 H10 Br F O -","- C9 H10 Br F O -","- C18 H20 Br2 F2 O2 -","2","1","","Witten, Michael R.; Jacobsen, Eric N.","A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes.","Organic letters","2015","17","11","2772","2775","10.1021/acs.orglett.5b01193","","","0.71073","MoKα","","0.0207","0.0187","","","0.0456","0.0465","","","","","","1.044","","","","has coordinates","140290","2020-10-21","18:00:00",""
"1519698","5.5342","0.0002","11.1421","0.0004","14.6505","0.0006","90","","90","","90","","903.39","0.06","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C10 H13 F O -","- C10 H13 F O -","- C40 H52 F4 O4 -","4","1","","Witten, Michael R.; Jacobsen, Eric N.","A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes.","Organic letters","2015","17","11","2772","2775","10.1021/acs.orglett.5b01193","","","1.54178","CuKα","","0.0271","0.0258","","","0.067","0.0682","","","","","","1.056","","","","has coordinates","140290","2020-10-21","18:00:00",""
"1519755","7.4665","0.0008","21.583","0.002","8.4033","0.0009","90","","107.586","0.002","90","","1290.9","0.2","130","","130","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C15 H16 O4 -","- C15 H16 O4 -","- C60 H64 O16 -","4","1","","Zhang, Xuxue; Dai, Wenpeng; Wu, Wei; Cao, Song","Copper-Catalyzed Coupling Cyclization of gem-Difluoroalkenes with Activated Methylene Carbonyl Compounds: Facile Domino Access to Polysubstituted Furans.","Organic letters","2015","17","11","2708","2711","10.1021/acs.orglett.5b01123","","","0.71073","MoKα","","0.0567","0.0458","","","0.1222","0.1308","","","","","","1.022","","","","has coordinates","141407","2020-10-21","18:00:00",""
"1519756","7.3312","0.0004","12.6193","0.0006","14.4778","0.0008","90","","98.847","0.005","90","","1323.47","0.12","293","2","293","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C30 H42 O5 -","- C30 H42 O5 -","- C60 H84 O10 -","2","1","","Zhao, Qian-Qian; Song, Qiu-Yan; Jiang, Kan; Li, Guang-Da; Wei, Wen-Jun; Li, Ya; Gao, Kun","Spirochensilides A and B, Two New Rearranged Triterpenoids from Abies chensiensis.","Organic letters","2015","17","11","2760","2763","10.1021/acs.orglett.5b01166","","","1.54184","CuKα","","0.0838","0.0629","","","0.1423","0.1788","","","","","","1.124","","","","has coordinates","152911","2020-10-21","18:00:00",""
"1519757","12.6226","0.0008","12.3709","0.0009","14.1124","0.001","90","","90","","90","","2203.7","0.3","298.2","0.1","298.2","0.1","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C10 H7 Br Cl2 N2 O -","- C10 H7 Br Cl2 N2 O -","- C80 H56 Br8 Cl16 N16 O8 -","8","1","","Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz","One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.","Organic letters","2015","17","11","2856","2859","10.1021/acs.orglett.5b01317","","","0.71073","MoKα","","0.07","0.0412","","","0.1007","0.1141","","","","","","1.03","","","","has coordinates","154781","2020-10-21","18:00:00",""
"1519758","7.3945","0.0009","20.124","0.003","17.43","0.002","90","","91.44","0.012","90","","2592.9","0.6","293","0.2","293","0.2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C12 H12 Br2 N2 O -","- C12 H12 Br2.025 N2 O -","- C96 H96 Br16.2 N16 O8 -","8","2","","Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz","One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.","Organic letters","2015","17","11","2856","2859","10.1021/acs.orglett.5b01317","","","0.71073","MoKα","","0.204","0.0595","","","0.105","0.1559","","","","","","0.822","","","","has coordinates,has disorder","154781","2020-10-21","18:00:00",""
"1519759","14.9133","0.0011","10.5056","0.0007","7.3297","0.0008","90","","103.561","0.009","90","","1116.35","0.17","299.5","0.4","299.5","0.4","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C11 H10 Br2 N2 -","- C11 H10 Br2 N2 -","- C44 H40 Br8 N8 -","4","1","","Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz","One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.","Organic letters","2015","17","11","2856","2859","10.1021/acs.orglett.5b01317","","","0.71073","MoKα","","0.0889","0.0511","","","0.1127","0.13","","","","","","1.023","","","","has coordinates","154781","2020-10-21","18:00:00",""
"1519760","7.501","0.0007","40.025","0.005","16.7795","0.0017","90","","94.664","0.009","90","","5021","0.9","293","0.2","293","0.2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C11 H7 Cl2 F3 N2 O1.5 -","- C11 H7 Cl2 F3 N2 O1.5 -","- C176 H112 Cl32 F48 N32 O24 -","16","4","","Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz","One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.","Organic letters","2015","17","11","2856","2859","10.1021/acs.orglett.5b01317","","","0.71073","MoKα","","0.3006","0.1284","","","0.3051","0.4112","","","","","","1.012","","","","has coordinates,has disorder","176429","2020-10-21","18:00:00",""
"1519761","14.443","0.002","7.5861","0.0012","21.306","0.003","90","","90","","90","","2334.4","0.6","293","0.2","293","0.2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C11 H9 Br2 F N2 -","- C11 H9 Br2 F N2 -","- C88 H72 Br16 F8 N16 -","8","1","","Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz","One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.","Organic letters","2015","17","11","2856","2859","10.1021/acs.orglett.5b01317","","","0.71073","MoKα","","0.2105","0.0649","","","0.1359","0.1945","","","","","","0.993","","","","has coordinates,has disorder","154781","2020-10-21","18:00:00",""
"1519848","8.8887","0.0009","18.4179","0.0018","6.9957","0.0007","90","","115.638","0.002","90","","1032.52","0.18","293","","293","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C12 H14 O3 -","- C12 H14 O3 -","- C48 H56 O12 -","4","1","","Hassan, Ahmed H. E.; Lee, Jae Kyun; Pae, Ae Nim; Min, Sun-Joon; Cho, Yong Seo","Synthesis of the Tricyclic Ring Structure of Daphnanes via Intramolecular [4 + 3] Cycloaddition/SmI2-Pinacol Coupling.","Organic letters","2015","17","11","2672","2675","10.1021/acs.orglett.5b01054","","","0.71075","MoKα","","","0.0612","","","","0.2168","","","","","","1.128","","","","has coordinates","140288","2020-10-21","18:00:00",""
"1519849","10.7308","0.001","8.7467","0.0007","12.089","0.0014","90","","109.485","0.003","90","","1069.68","0.18","296","","296","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C12 H14 O3 -","- C12 H14 O3 -","- C48 H56 O12 -","4","1","","Hassan, Ahmed H. E.; Lee, Jae Kyun; Pae, Ae Nim; Min, Sun-Joon; Cho, Yong Seo","Synthesis of the Tricyclic Ring Structure of Daphnanes via Intramolecular [4 + 3] Cycloaddition/SmI2-Pinacol Coupling.","Organic letters","2015","17","11","2672","2675","10.1021/acs.orglett.5b01054","","","0.71075","MoKα","","","0.0425","","","","0.1277","","","","","","1.052","","","","has coordinates","140288","2020-10-21","18:00:00",""
"1519850","5.7399","0.0011","15.532","0.003","20.365","0.004","90","","96.93","0.011","90","","1802.3","0.6","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C22 H16 Br N O2 -","- C22 H16 Br N O2 -","- C88 H64 Br4 N4 O8 -","4","1","","Dhanasekaran, Sivasankaran; Kayet, Anirban; Suneja, Arun; Bisai, Vishnumaya; Singh, Vinod K.","Unified Approach to Isoindolinones and THIQs via Lewis Acid Catalyzed Domino Mukaiyama-Mannich Lactamization/Alkylations: Application in the Synthesis of (±)-Homolaudanosine.","Organic letters","2015","17","11","2780","2783","10.1021/acs.orglett.5b01197","","","0.71073","MoKα","","0.0939","0.0487","","","0.1384","0.1582","","","","","","0.991","","","","has coordinates","152910","2020-10-21","18:00:00",""
"1519851","4.8624","0.0019","11.167","0.004","23.437","0.009","90","","94.33","0.006","90","","1269","0.8","298","2","298","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C16 H12 N4 -","- C16 H12 N4 -","- C64 H48 N16 -","4","1","","Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Li, Deng-Kui; Wu, An-Xin","Consecutive Cycloaddition/SNAr/Reduction/Cyclization/Oxidation Sequences: A Copper-Catalyzed Multicomponent Synthesis of Fused N-Heterocycles.","Organic letters","2015","17","11","2820","2823","10.1021/acs.orglett.5b01242","","","0.71073","MoKα","","0.0783","0.0631","","","0.1712","0.1812","","","","","","1.083","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1519923","6.1791","0.0002","23.0423","0.0006","6.9392","0.0002","90","","110.037","0.001","90","","928.21","0.05","100","2","100","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C21 H34 O3 -","- C21 H34 O3 -","- C42 H68 O6 -","2","1","","Hosseini, Abolfazl; Seidel, Daniel; Miska, Andreas; Schreiner, Peter R.","Fluoride-assisted activation of calcium carbide: a simple method for the ethynylation of aldehydes and ketones.","Organic letters","2015","17","11","2808","2811","10.1021/acs.orglett.5b01219","","","1.54178","CuKα","","0.0283","0.0279","","","0.0746","0.0747","","","","","","1.125","","","","has coordinates","140289","2020-10-21","18:00:00",""
"1519924","10.9392","0.0004","8.3314","0.0003","22.5089","0.0008","90","","102.759","0.003","90","","2000.78","0.13","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C25 H21 Fe N3 -","- C25 H21 Fe N3 -","- C100 H84 Fe4 N12 -","4","1","","Wei, Fang; Li, Haoyu; Song, Chuanling; Ma, Yudao; Zhou, Ling; Tung, Chen-Ho; Xu, Zhenghu","Cu/Pd-Catalyzed, Three-Component Click Reaction of Azide, Alkyne, and Aryl Halide: One-Pot Strategy toward Trisubstituted Triazoles.","Organic letters","2015","17","11","2860","2863","10.1021/acs.orglett.5b01342","","","1.54178","CuKα","","0.0433","0.0361","","","0.0981","0.1034","","","","","","1.029","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1519998","7.0685","0.0016","15.143","0.003","17.388","0.004","90","","90","","90","","1861.2","0.7","298","2","298","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C20 H30 N0 O5 -","- C20 H30 O5 -","- C80 H120 O20 -","4","1","","Annam, S Ch V Appa Rao; Ankireddy, Madhu; Sura, Madhu Babu; Ponnapalli, Mangala Gowri; Sarma, Akella V. S.; S, Jeelani Basha","Epimeric Excolides from the Stems of Excoecaria agallocha and Structural Revision of Rhizophorin A.","Organic letters","2015","17","11","2840","2843","10.1021/acs.orglett.5b01257","","","0.71073","MoKα","","0.0455","0.0395","","","0.0925","0.0961","","","","","","1.062","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1519999","9.4777","0.0006","7.3392","0.0003","13.4089","0.0006","90","","91.432","0.005","90","","932.41","0.08","298","2","298","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C20 H28 O5 -","- C20 H28 O5 -","- C40 H56 O10 -","2","1","","Annam, S Ch V Appa Rao; Ankireddy, Madhu; Sura, Madhu Babu; Ponnapalli, Mangala Gowri; Sarma, Akella V. S.; S, Jeelani Basha","Epimeric Excolides from the Stems of Excoecaria agallocha and Structural Revision of Rhizophorin A.","Organic letters","2015","17","11","2840","2843","10.1021/acs.orglett.5b01257","","","0.71073","MoKα","","0.0595","0.044","","","0.0866","0.0961","","","","","","1.052","","","","has coordinates","141408","2020-10-21","18:00:00",""
"1520000","13.2416","0.0008","13.1779","0.0008","15.2428","0.0008","90","","109.387","0.002","90","","2509","0.3","90","","90","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","(±)-(1SR,5SR,6SR,7SR,10SR,11SR,14SR)-3,13-dioxo-7-methoxymethoxy-11,15,18,18-tetramethyl-2,4-dioxatetracyclo[12.3.1.0^1,5^.0^6,11^]octadec-15-ene-10-yl benzoate","","- C29 H36 O8 -","- C29 H36 O8 -","- C116 H144 O32 -","4","1","","Fukaya, Keisuke; Kodama, Keisuke; Tanaka, Yuta; Yamazaki, Hirohisa; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka","Synthesis of Paclitaxel. 2. Construction of the ABCD Ring and Formal Synthesis.","Organic letters","2015","17","11","2574","2577","10.1021/acs.orglett.5b01174","","","0.71073","MoKα","","0.0832","0.0439","","","0.0884","0.105","","","","","","0.962","","","","has coordinates","140280","2020-10-21","18:00:00",""
"1520001","14.376","0.0006","14.699","0.0006","21.34","0.0008","90","","107.79","0.001","90","","4293.8","0.3","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C54 H46 Co N2 P3 -","- C54 H46 Co N2 P3 -","- C216 H184 Co4 N8 P12 -","4","1","","Scheuermann, Margaret L.; Johnson, Elizabeth J.; Chirik, Paul J.","Alkene isomerization-hydroboration promoted by phosphine-ligated cobalt catalysts.","Organic letters","2015","17","11","2716","2719","10.1021/acs.orglett.5b01135","","","1.54178","CuKα","","0.0269","0.0266","","","0.0696","0.0698","","","","","","1.042","","","","has coordinates","140282","2020-10-21","18:00:00",""
"1520002","9.3612","0.0006","19.6336","0.0015","14.1965","0.0009","90","","101.762","0.002","90","","2554.4","0.3","90","","90","","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","(±)-(1SR,5SR,6SR,7SR,10SR,11SR,13SR,14SR)-13-hydroxy-7-methoxymethoxy-3-oxo-11,15,18,18-tetramethyl-2,4-dioxatetracyclo[12.3.1.0^1,5^.0^6,11^]octadec-15-ene-10-yl benzoate","","- C29 H38 O8 -","- C29 H38 O8 -","- C116 H152 O32 -","4","1","","Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka","Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.","Organic letters","2015","17","11","2570","2573","10.1021/acs.orglett.5b01173","","","0.71073","MoKα","","0.0733","0.0428","","","0.0978","0.1111","","","","","","1.02","","","","has coordinates","140286","2020-10-21","18:00:00",""
"1520003","9.6397","0.0006","13.6008","0.0008","15.0461","0.001","83.6966","0.0019","77.488","0.002","77.9768","0.0018","1879.2","0.2","90","","90","","","","","","","","","3","P -1","-P 1","2","","(±)-(4RS,5RS,7SR)-4-[(1RS,2RS,3RS,6RS)-3-Benzoyloxy-2-(2-hydroxyethyl)-6-methoxymethoxy-2-methylcyclohexyl]-8,10,10-trimethyl-2-oxo-1,3-dioxaspiro[4.5]dec-8-en-7-yl benzoate benzene monosolvate","","- C42 H50 O10 -","- C42 H50 O10 -","- C84 H100 O20 -","2","1","IS5382","Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka","Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.","Organic letters","2015","17","11","2570","2573","10.1021/acs.orglett.5b01173","","","0.71073","MoKα","","0.059","0.0419","","","0.1224","0.1506","","","","","","0.932","","","","has coordinates","140286","2020-10-21","18:00:00",""
"1520004","11.3343","0.0005","15.4666","0.0007","16.487","0.0008","85.1124","0.0014","78.3773","0.0014","78.5231","0.0015","2771.3","0.2","90","","90","","","","","","","","","3","P -1","-P 1","2","","(±)-(1SR,5SR,6SR,7SR,10SR,11SR,13RS,14SR)-13-Hydroxy-7-methoxymethoxy-3-oxo-11,15,18,18-tetramethyl-2,4-dioxatetracyclo[12.3.1.0^1,5^.0^6,11^]octadec-15-en-10-yl benzoate","","- C30.25 H41 O8 -","- C30.25 H41 O8 -","- C121 H164 O32 -","4","2","","Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka","Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.","Organic letters","2015","17","11","2570","2573","10.1021/acs.orglett.5b01173","","","0.71073","MoKα","","0.0636","0.04","","","0.0869","0.0989","","","","","","1.023","","","","has coordinates,has disorder","140286","2020-10-21","18:00:00",""
"1520005","8.5353","0.0012","10.6984","0.0015","15.609","0.002","90","","104.429","0.002","90","","1380.4","0.3","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C15 H21 N O2 -","- C15 H21 N O2 -","- C60 H84 N4 O8 -","4","1","","Zhou, Wei; Ni, Shengyang; Mei, Haibo; Han, Jianlin; Pan, Yi","Hydroxyalkylation-initiated radical cyclization of N-allylbenzamide for direct construction of isoquinolinone.","Organic letters","2015","17","11","2724","2727","10.1021/acs.orglett.5b01140","","","0.71073","MoKα","","0.0675","0.0464","","","0.1233","0.1379","","","","","","1.021","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520068","10.037","0.002","8.2451","0.0018","18.991","0.005","90","","101.279","0.002","90","","1541.3","0.6","173.15","","173.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C32 H36 Br2 N4 O2 -","- C32 H36 Br2 N4 O2 -","- C64 H72 Br4 N8 O4 -","2","0.5","","Zhu, Xiaxia; Du, Haifeng","A Highly Stereoselective Metal-Free Hydrogenation of Diimines for the Synthesis of Cis-Vicinal Diamines.","Organic letters","2015","17","12","3106","3109","10.1021/acs.orglett.5b01380","","","0.71073","MoKα","","0.0448","0.0403","","","0.094","0.0966","","","","","","1.145","","","","has coordinates","140277","2020-10-21","18:00:00",""
"1520116","9.0455","0.0019","9.563","0.002","11.529","0.002","103.716","0.018","98.763","0.017","98.986","0.019","938.1","0.3","100","2","100","2","","","","","","","","3","P -1","-P 1","2","","","","- C28 H19 N -","- C28 H19 N -","- C56 H38 N2 -","2","1","","Liu, Xingyan; Li, Xiaoyu; Liu, Hu; Guo, Qiang; Lan, Jingbo; Wang, Ruilin; You, Jingsong","Aldehyde as a Traceless Directing Group for Rh(III)-Catalyzed C-H Activation: A Facile Access to Diverse Indolo[1,2-a]quinolines.","Organic letters","2015","17","12","2936","2939","10.1021/acs.orglett.5b01171","","","1.54184","CuKα","","0.1332","0.0809","","","0.1909","0.233","","","","","","0.979","","","","has coordinates","140266","2020-10-21","18:00:00",""
"1520117","8.9435","0.0002","12.1892","0.0003","12.2642","0.0003","63.163","0.001","87.526","0.001","77.6","0.001","1162.92","0.05","173","","173","","","","","","","","","6","P -1","-P 1","2","","","","- C17.5 H18 F8 I O3.5 S2 -","- C17.5 H18 F8 I O3.5 S2 -","- C35 H36 F16 I2 O7 S4 -","2","1","","Matsuzaki, Kohei; Okuyama, Kenta; Tokunaga, Etsuko; Saito, Norimichi; Shiro, Motoo; Shibata, Norio","Synthesis of Diaryliodonium Salts Having Pentafluorosulfanylarenes and Their Application to Electrophilic Pentafluorosulfanylarylation of C-, O-, N-, and S-Nucleophiles.","Organic letters","2015","17","12","3038","3041","10.1021/acs.orglett.5b01323","","","0.71075","MoKα","","0.0292","0.0275","","","0.0879","0.0929","","","","","","1.194","","","","has coordinates,has disorder","141406","2020-10-21","18:00:00",""
"1520220","42.784","0.004","6.0454","0.0006","31.552","0.003","90","","119.951","0.002","90","","7071","1.2","293","2","293","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C24 H19 N -","- C24 H19 N -","- C384 H304 N16 -","16","2","","Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong","Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.","Organic letters","2015","17","12","2984","2987","10.1021/acs.orglett.5b01281","","","0.71073","MoKα","","0.0862","0.0594","","","0.1526","0.1703","","","","","","1.054","","","","has coordinates,has disorder","140265","2020-10-21","18:00:00",""
"1520221","12.0216","0.0013","6.2012","0.0007","30.083","0.003","90","","101.315","0.003","90","","2199","0.4","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C30 H23 N -","- C30 H23 N -","- C120 H92 N4 -","4","1","","Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong","Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.","Organic letters","2015","17","12","2984","2987","10.1021/acs.orglett.5b01281","","","0.71073","MoKα","","0.1184","0.0638","","","0.136","0.1576","","","","","","1.026","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520222","29.558","0.003","6.041","0.0006","19.696","0.002","90","","104.661","0.002","90","","3402.4","0.6","293","2","293","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C23 H19 N -","- C23 H19 N -","- C184 H152 N8 -","8","1","","Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong","Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.","Organic letters","2015","17","12","2984","2987","10.1021/acs.orglett.5b01281","","","0.71073","MoKα","","0.0597","0.0476","","","0.1165","0.1247","","","","","","1.037","","","","has coordinates","140265","2020-10-21","18:00:00",""
"1520223","16.1172","0.0012","16.1172","0.0012","5.6393","0.0004","90","","90","","120","","1268.63","0.16","173","2","173","2","","","","","","","","5","P 32","P 32","145","","","","- C14 H16 Cl3 N O3 -","- C14 H16 Cl3 N O3 -","- C42 H48 Cl9 N3 O9 -","3","1","","Skvorcova, Marija; Grigorjeva, Liene; Jirgensons, Aigars","Tetrahydro-1,3-oxazepines via Intramolecular Amination of Cyclopropylmethyl Cation.","Organic letters","2015","17","12","2902","2904","10.1021/acs.orglett.5b01014","","","0.71073","MoKα","","0.2304","0.0888","","","0.1849","0.2421","","","","","","1.007","","","","has coordinates","141403","2020-10-21","18:00:00",""
"1520224","10.363","0.003","9.318","0.002","11.453","0.004","90","","112.7","0.04","90","","1020.3","0.6","291.89","0.1","291.89","0.1","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C22 H22 N4 O2 S -","- C22 H22 N4 O2 S -","- C44 H44 N8 O4 S2 -","2","1","","Wang, Linqing; Yang, Dongxu; Li, Dan; Wang, Rui","Catalytic Enantioselective Ring-Opening and Ring-Closing Reactions of 3-Isothiocyanato Oxindoles and N-(2-Picolinoyl)aziridines.","Organic letters","2015","17","12","3004","3007","10.1021/acs.orglett.5b01291","","","0.71073","MoKα","","0.1","0.0598","","","0.125","0.1618","","","","","","0.994","","","","has coordinates","140271","2020-10-21","18:00:00",""
"1520225","4.5905","0.0005","23.474","0.003","13.2529","0.0015","90","","91.746","0.004","90","","1427.4","0.3","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C13 H21 N3 O3 -","- C13 H21 N3 O3 -","- C52 H84 N12 O12 -","4","1","","Martínez, Luís; Martorell, Gabriel; Sampedro, Ángel; Ballester, Pablo; Costa, Antoni; Rotger, Carmen","Hydrogen Bonded Squaramide-Based Foldable Module Induces Both β- and α-Turns in Hairpin Structures of α-Peptides in Water.","Organic letters","2015","17","12","2980","2983","10.1021/acs.orglett.5b01268","","","0.71073","MoKα","","0.0919","0.0562","","","0.1281","0.145","","","","","","1.031","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520297","26.6011","0.001","19.037","0.0009","14.4208","0.0005","90","","114.731","0.002","90","","6633","0.5","173","2","173","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","Pseudorotaxane of propionic acid","","","- C52 H60 Br N4 O18 S2 -","- C52 H60 Br N4 O18 S2 -","- C208 H240 Br4 N16 O72 S8 -","4","0.5","","Carrasco-Ruiz, Anayeli; Tiburcio, Jorge","Electrostatic Kinetic Barriers in the Threading/Dethreading Motion of a Rotaxane-like Complex.","Organic letters","2015","17","8","1858","1861","10.1021/acs.orglett.5b00530","","","0.71073","MoKα","","0.1888","0.1353","","","0.3612","0.3904","","","","","","1.302","","","","has coordinates","138023","2020-10-21","18:00:00",""
"1520298","11.8381","0.0003","23.4128","0.0006","11.8991","0.0004","90","","107.339","0.001","90","","3148.12","0.16","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","Pseudorotaxane propionate","","","- C52 H86 N4 O32 S2 -","- C52 H86 N4 O32 S2 -","- C104 H172 N8 O64 S4 -","2","0.5","","Carrasco-Ruiz, Anayeli; Tiburcio, Jorge","Electrostatic Kinetic Barriers in the Threading/Dethreading Motion of a Rotaxane-like Complex.","Organic letters","2015","17","8","1858","1861","10.1021/acs.orglett.5b00530","","","0.71073","MoKα","","0.2381","0.1216","","","0.3136","0.3745","","","","","","1.076","","","","has coordinates,has disorder","176428","2020-10-21","18:00:00",""
"1520299","5.7232","0.0004","10.8546","0.001","32.913","0.002","90","","90","","90","","2044.7","0.3","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C22 H23 I O3 -","- C22 H23 I O3 -","- C88 H92 I4 O12 -","4","1","","Merad, Jérémy; Borkar, Prashant; Bouyon Yenda, Tracy; Roux, Christèle; Pons, Jean-Marc; Parrain, Jean-Luc; Chuzel, Olivier; Bressy, Cyril","Highly Enantioselective Acylation of Acyclic Meso 1,3-Diols through Synergistic Isothiourea-Catalyzed Desymmetrization/Chiroablative Kinetic Resolution.","Organic letters","2015","17","9","2118","2121","10.1021/acs.orglett.5b00707","","x-ray","1.54184","CuKα","","0.0749","0.0594","","","0.1674","0.1916","","","","","","1.125","","","","has coordinates","204128","2020-10-21","18:00:00",""
"1520300","7.1052","0.0003","14.1156","0.0006","16.3735","0.0008","105.153","0.002","91.858","0.003","102.309","0.002","1541.85","0.12","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C36 H46 N4 O2 -","- C36 H46 N4 O2 -","- C72 H92 N8 O4 -","2","1","","Meehan, Eileen; Li, Ruoshi; Zeller, Matthias; Brückner, Christian","Octaethyl-1,3-oxazinochlorin: A β-Octaethylchlorin Analogue Made by Pyrrole Expansion.","Organic letters","2015","17","9","2210","2213","10.1021/acs.orglett.5b00800","","","1.54178","CuKα","","0.0721","0.0576","","","0.1555","0.1717","","","","","","1.042","","","","has coordinates,has disorder","138027","2020-10-21","18:00:00",""
"1520301","26.0651","0.0012","15.2582","0.0007","9.5468","0.0005","90","","96.584","0.002","90","","3771.8","0.3","200","2","200","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C41 H58.333 N5 O -","- C40.9994 H58.3322 N4.99998 O -","- C163.998 H233.329 N19.9999 O4 -","4","1","","Meehan, Eileen; Li, Ruoshi; Zeller, Matthias; Brückner, Christian","Octaethyl-1,3-oxazinochlorin: A β-Octaethylchlorin Analogue Made by Pyrrole Expansion.","Organic letters","2015","17","9","2210","2213","10.1021/acs.orglett.5b00800","","","1.54178","CuKα","","0.0578","0.0465","","","0.1324","0.1438","","","","","","1.035","","","","has coordinates,has disorder","138028","2020-10-21","18:00:00",""
"1520302","18.4779","0.0014","9.1189","0.0007","19.3437","0.0015","90","","109.352","0.001","90","","3075.2","0.4","153","2","153","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","syn-1,2-bis(5-bromo-2-hydroxyphenyl)-2-((diphenylmethylene)amino)ethyl acetate","","- C33 H31 Br2 N O6 -","- C33 H31 Br2 N O6 -","- C132 H124 Br8 N4 O24 -","4","1","","Tang, Shaojian; Park, Jong Yeun; Yeagley, Andrew A.; Sabat, Michal; Chruma, Jason J.","Decarboxylative Generation of 2-Azaallyl Anions: 2-Iminoalcohols via a Decarboxylative Erlenmeyer Reaction.","Organic letters","2015","17","9","2042","2045","10.1021/acs.orglett.5b00107","","","0.71073","MoKα","","0.1235","0.0674","","","0.1479","0.1704","","","","","","1.023","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520303","11.1164","0.0006","12.6843","0.0007","11.5897","0.0007","90","","118.363","0.002","90","","1438.02","0.14","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C13 H23 Cl N2 Ni -","- C13 H23 Cl N2 Ni -","- C52 H92 Cl4 N8 Ni4 -","4","1","","Shields, Jason D.; Gray, Erin E.; Doyle, Abigail G.","A modular, air-stable nickel precatalyst.","Organic letters","2015","17","9","2166","2169","10.1021/acs.orglett.5b00766","","","0.71073","MoKα","","0.0583","0.0502","","","0.1216","0.1258","","","","","","1.394","","","","has coordinates","138030","2020-10-21","18:00:00",""
"1520304","15.592","0.0006","20.5827","0.0003","60.065","0.0012","90","","90","","90","","19276.4","0.9","295","2","295","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C66.33 H81.67 N2 O4 Yb -","- C66.3333 H81.6667 N2 O4 Yb -","- C796 H980 N24 O48 Yb12 -","12","3","","Zeng, Chao; Yuan, Dan; Zhao, Bei; Yao, Yingming","Highly Enantioselective Epoxidation of α,β-Unsaturated Ketones Catalyzed by Rare-Earth Amides [(Me3Si)2N]3RE(μ-Cl)Li(THF)3 with Phenoxy-Functionalized Chiral Prolinols.","Organic letters","2015","17","9","2242","2245","10.1021/acs.orglett.5b00833","","","1.54184","CuKα","","0.0944","0.071","","","0.1658","0.1855","","","","","","1.002","","","","has coordinates,has disorder","138031","2020-10-21","18:00:00",""
"1520305","16.4651","0.0013","6.6186","0.0004","14.9686","0.0012","90","","109.033","0.006","90","","1542","0.2","100","2","100","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C6 H9 N O4 -","- C6 H9 N O4 -","- C48 H72 N8 O32 -","8","1","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.0458","0.0329","","","0.0817","0.0845","","","","","","1.005","","","","has coordinates,has disorder","141402","2020-10-21","18:00:00",""
"1520306","11.0623","0.0004","9.4884","0.0004","11.6015","0.0005","90","","90.961","0.004","90","","1217.56","0.09","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","JR2068S3M","","","- C12 H19 N O3 -","- C12 H19 N O3 -","- C48 H76 N4 O12 -","4","1","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.0511","0.0359","","","0.0723","0.0782","","","","","","1.063","","","","has coordinates","141402","2020-10-21","18:00:00",""
"1520307","9.5474","0.0005","11.4938","0.0006","11.5223","0.0006","92.227","0.004","96.964","0.004","91.605","0.004","1253.45","0.11","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C10 H16 B F2 N O3 -","- C10 H16 B F2 N O3 -","- C40 H64 B4 F8 N4 O12 -","4","2","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.0387","0.0296","","","0.0776","0.0796","","","","","","1.056","","","","has coordinates,has disorder","141402","2020-10-21","18:00:00",""
"1520308","7.8638","0.0003","14.0418","0.0005","12.6427","0.0005","90","","91.6599","0.0014","90","","1395.45","0.09","115","2","115","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C12 H20 B F2 N O3 -","- C12 H20 B F2 N O3 -","- C48 H80 B4 F8 N4 O12 -","4","1","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.0353","0.0316","","","0.0768","0.0794","","","","","","1.076","","","","has coordinates","141402","2020-10-21","18:00:00",""
"1520309","14.7772","0.0013","11.1085","0.001","16.6848","0.0013","90","","92.405","0.004","90","","2736.4","0.4","100","2","100","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C12 H18 B F2 N O3 -","- C12 H18 B F2 N O3 -","- C96 H144 B8 F16 N8 O24 -","8","4","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.0954","0.0794","","","0.1921","0.2043","","","","","","1.123","","","","has coordinates","141402","2020-10-21","18:00:00",""
"1520310","10.6399","0.0007","11.8723","0.0007","11.9174","0.0007","90","","107.028","0.002","90","","1439.41","0.15","100","2","100","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C13 H20 B F2 N O3 -","- C13 H20 B F2 N O3 -","- C52 H80 B4 F8 N4 O12 -","4","1","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.0604","0.053","","","0.1483","0.1563","","","","","","1.056","","","","has coordinates","141402","2020-10-21","18:00:00",""
"1520311","11.3963","0.0005","11.7254","0.0005","12.5468","0.0006","74.986","0.004","64.116","0.003","64.237","0.003","1353.47","0.11","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C12 H18 B F2 N O4 -","- C12 H18 B F2 N O4 -","- C48 H72 B4 F8 N4 O16 -","4","2","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.0427","0.0325","","","0.0912","0.0941","","","","","","1.049","","","","has coordinates","141402","2020-10-21","18:00:00",""
"1520312","12.1721","0.0008","49.556","0.003","8.341","0.0006","90","","90","","90","","5031.3","0.6","100","2","100","2","","","","","","","","6","I b a 2","I 2 -2c","45","JR2102A3","","","- C10 H16 B F2 N O4 -","- C10 H16 B F2 N O4 -","- C160 H256 B16 F32 N16 O64 -","16","2","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.0721","0.042","","","0.0643","0.0721","","","","","","1.029","","","","has coordinates","141402","2020-10-21","18:00:00",""
"1520313","7.0022","0.0003","7.7079","0.0004","12.3657","0.0006","83.232","0.002","83.476","0.002","76.265","0.002","641.26","0.05","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C10 H16 B F2 N O4 -","- C10 H16 B F2 N O4 -","- C20 H32 B2 F4 N2 O8 -","2","1","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.0333","0.0297","","","0.0739","0.0763","","","","","","1.063","","","","has coordinates,has disorder","141402","2020-10-21","18:00:00",""
"1520314","7.8792","0.001","8.1476","0.0011","10.2749","0.0013","106.191","0.004","106.585","0.004","104.538","0.004","566.58","0.13","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C10 H17 N O4 -","- C10 H17 N O4 -","- C20 H34 N2 O8 -","2","1","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.0649","0.0492","","","0.1247","0.1358","","","","","","1.059","","","","has coordinates","141402","2020-10-21","18:00:00",""
"1520315","16.8311","0.0007","9.1985","0.0003","18.0999","0.0008","90","","90","","90","","2802.24","0.19","100","2","100","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C12 H20 B F2 N O4 -","- C12 H20 B F2 N O4 -","- C96 H160 B8 F16 N8 O32 -","8","1","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.049","0.0374","","","0.0829","0.0885","","","","","","1.026","","","","has coordinates,has disorder","141402","2020-10-21","18:00:00",""
"1520316","10.3517","0.0006","15.7916","0.0011","9.5485","0.0006","90","","99.476","0.002","90","","1539.59","0.17","100","2","100","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","JR2136","","","- C12 H18 B Br2 F2 N O4 -","- C12 H18 B Br2 F2 N O4 -","- C48 H72 B4 Br8 F8 N4 O16 -","4","1","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.0353","0.0288","","","0.0754","0.0794","","","","","","1.037","","","","has coordinates","141402","2020-10-21","18:00:00",""
"1520317","8.8688","0.0004","18.0772","0.0008","6.0396","0.0003","90","","94.753","0.003","90","","964.96","0.08","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C8 H11 Br O4 -","- C8 H11 Br O4 -","- C32 H44 Br4 O16 -","4","1","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.031","0.0236","","","0.051","0.0538","","","","","","1.052","","","","has coordinates","141402","2020-10-21","18:00:00",""
"1520318","12.2584","0.0005","10.1061","0.0004","31.0115","0.0013","90","","90","","90","","3841.8","0.3","100","2","100","2","","","","","","","","6","P b c n","-P 2n 2ab","60","JR21673","","","- C19 H23.6 B F2 N2 O5.3 -","- C19 H23.603 B F2 N2 O5.3015 -","- C152 H188.824 B8 F16 N16 O42.412 -","8","1","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.0541","0.0383","","","0.0822","0.0887","","","","","","1.072","","","","has coordinates","176429","2020-10-21","18:00:00",""
"1520319","15.4609","0.0006","8.0727","0.0002","15.6576","0.0005","90","","103.611","0.002","90","","1899.36","0.11","100","2","100","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","JR2192","","","- C19 H23 B F2 N2 O5 -","- C19 H23 B F2 N2 O5 -","- C76 H92 B4 F8 N8 O20 -","4","1","","Roßbach, Jan; Harms, Klaus; Koert, Ulrich","α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.","Organic letters","2015","17","12","3122","3125","10.1021/acs.orglett.5b01427","","","0.71073","MoKα","","0.0462","0.04","","","0.0958","0.0994","","","","","","1.054","","","","has coordinates","141402","2020-10-21","18:00:00",""
"1520320","12.5638","0.0015","14.8917","0.0018","13.7164","0.0017","90","","104.477","0.001","90","","2484.8","0.5","120","2","120","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C30 H25 N2 O4 P -","- C30 H25 N2 O4 P -","- C120 H100 N8 O16 P4 -","4","1","","Yamamura, Masaki; Takizawa, Hiroyuki; Nabeshima, Tatsuya","Zwitterionic N2O2-Type Protonated Dipyrrin Bearing a Phosphate Anionic Moiety as a pH-Responsive Fluorescence Indicator.","Organic letters","2015","17","12","3114","3117","10.1021/acs.orglett.5b01414","","","0.71073","MoKα","","0.0424","0.0346","","","0.0867","0.0917","","","","","","1.02","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520385","18.718","0.0014","20.1801","0.0014","21.555","0.002","63.466","0.008","65.8","0.008","82.646","0.006","6629.1","1.1","293","2","293","2","","","","","","","","5","P -1","-P 1","2","sapphyrin","","","- C41 H45 Cl2 N5 O18 -","- C41 H45 Cl2 N5 O18 -","- C246 H270 Cl12 N30 O108 -","6","3","","Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.","β-Decamethoxysapphyrin and Its N-Benzyl Analogue.","Organic letters","2015","17","12","3030","3033","10.1021/acs.orglett.5b01306","","","0.71073","MoKα","","0.2907","0.1035","","","0.2355","0.3555","","","","","","0.957","","","","has coordinates","140270","2020-10-21","18:00:00",""
"1520386","9.5948","0.0003","11.7166","0.0003","43.6295","0.0016","90","","91.392","0.004","90","","4903.3","0.3","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","sapphyrin","decamethoxysapphyrin","","- C48 H53 N5 O16 S2 -","- C48 H53 N5 O16 S2 -","- C192 H212 N20 O64 S8 -","4","1","","Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.","β-Decamethoxysapphyrin and Its N-Benzyl Analogue.","Organic letters","2015","17","12","3030","3033","10.1021/acs.orglett.5b01306","","","1.54184","CuKα","","0.1103","0.0921","","","0.2555","0.2745","","","","","","1.115","","","","has coordinates","140270","2020-10-21","18:00:00",""
"1520387","10.656","0.003","38.925","0.009","11.435","0.003","90","","111.21","0.03","90","","4422","2","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C48 H51 N5 O13 S -","- C48 H51 N5 O13 S -","- C192 H204 N20 O52 S4 -","4","1","","Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.","β-Decamethoxysapphyrin and Its N-Benzyl Analogue.","Organic letters","2015","17","12","3030","3033","10.1021/acs.orglett.5b01306","","","0.71073","MoKα","","0.2418","0.0854","","","0.1505","0.2325","","","","","","0.98","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520388","8.6008","0.0011","10.6881","0.0012","18.1","0.003","90","","90","","90","","1663.9","0.4","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C22 H19 N O2 -","- C22 H19 N O2 -","- C88 H76 N4 O8 -","4","1","","Battini, Narsaiah; Battula, Satyanarayana; Kumar, Raju Ranjith; Ahmed, Qazi Naveed","2-Oxo Driven Unconventional reactions: Microwave Assisted Approaches to Tetrahydrofuro[3,2-d]oxazoles and Furanones.","Organic letters","2015","17","12","2992","2995","10.1021/acs.orglett.5b01271","","","0.71073","MoKα","","0.0697","0.0468","","","0.1004","0.1151","","","","","","1.036","","","","has coordinates","154780","2020-10-21","18:00:00",""
"1520439","7.923","0.003","11.039","0.004","27.77","0.012","90","","96.981","0.014","90","","2410.8","1.6","93","2","93","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C26 H18 B Cl2 F8 N3 -","- C26 H18 B Cl2 F8 N3 -","- C104 H72 B4 Cl8 F32 N12 -","4","1","","Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi","Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.","Organic letters","2015","17","12","3090","3093","10.1021/acs.orglett.5b01363","","","1.54187","CuKα","","0.0569","0.0549","","","0.1471","0.1491","","","","","","1.019","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520440","13.159","0.005","12.065","0.004","15.082","0.006","90","","98.075","0.014","90","","2370.7","1.5","93","2","93","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C26.14 H22.79 B Cl0.79 F2 N3 O3.24 -","- C26.14 H22.794 B Cl0.794 F2 N3 O3.241 -","- C104.56 H91.176 B4 Cl3.176 F8 N12 O12.964 -","4","1","","Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi","Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.","Organic letters","2015","17","12","3090","3093","10.1021/acs.orglett.5b01363","","","1.54187","CuKα","","0.068","0.0577","","","0.154","0.1681","","","","","","1.049","","","","has coordinates,has disorder","176428","2020-10-21","18:00:00",""
"1520441","15.429","0.002","41.602","0.007","24.49","0.004","90","","91.209","0.006","90","","15716","4","93","2","93","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C707 H656 B16 F32 N48 O9 -","- C706.992 H656 B16 F32 N48 O9 -","- C706.992 H656 B16 F32 N48 O9 -","1","0.25","","Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi","Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.","Organic letters","2015","17","12","3090","3093","10.1021/acs.orglett.5b01363","","","1.54187","CuKα","","0.171","0.1213","","","0.2993","0.3481","","","","","","1.104","","","","has coordinates,has disorder","176428","2020-10-21","18:00:00",""
"1520442","33.021","0.012","10.588","0.004","23.034","0.008","90","","132.89","0.005","90","","5900","4","93","2","93","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C35.79 H27.57 B Cl1.57 F2 N3 -","- C35.7854 H27.5708 B Cl1.5708 F2 N3 -","- C286.283 H220.566 B8 Cl12.5664 F16 N24 -","8","1","","Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi","Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.","Organic letters","2015","17","12","3090","3093","10.1021/acs.orglett.5b01363","","","1.54187","CuKα","","0.0714","0.061","","","0.1708","0.185","","","","","","1.039","","","","has coordinates,has disorder","176428","2020-10-21","18:00:00",""
"1520443","7.3425","0.0014","11.0127","0.0016","15.884","0.003","94.772","0.004","97.467","0.007","91.375","0.01","1268.3","0.4","93","2","93","2","","","","","","","","6","P -1","-P 1","2","","","","- C32 H24 B Cl2 F2 N3 -","- C32 H24 B Cl2 F2 N3 -","- C64 H48 B2 Cl4 F4 N6 -","2","1","","Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi","Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.","Organic letters","2015","17","12","3090","3093","10.1021/acs.orglett.5b01363","","","1.54187","CuKα","","0.0314","0.0294","","","0.0856","0.0868","","","","","","1.093","","","","has coordinates","140268","2020-10-21","18:00:00",""
"1520444","8.0911","0.0018","21.853","0.005","25.007","0.006","90","","97.291","0.006","90","","4385.9","1.8","93","2","93","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C50.45 H44.9 B Cl2.9 F2 N3 -","- C50.45 H44.9 B Cl2.9 F2 N3 -","- C201.8 H179.6 B4 Cl11.6 F8 N12 -","4","1","","Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi","Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.","Organic letters","2015","17","12","3090","3093","10.1021/acs.orglett.5b01363","","","1.54187","CuKα","","0.1108","0.0935","","","0.2579","0.2764","","","","","","1.026","","","","has coordinates,has disorder","176429","2020-10-21","18:00:00",""
"1520445","9.594","0.002","8.7428","0.0017","21.526","0.006","90","","100.795","0.008","90","","1773.6","0.7","93","2","93","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C23 H18 B F2 N3 -","- C23 H18 B F2 N3 -","- C92 H72 B4 F8 N12 -","4","1","","Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi","Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.","Organic letters","2015","17","12","3090","3093","10.1021/acs.orglett.5b01363","","","1.54187","CuKα","","0.0329","0.0314","","","0.0858","0.0876","","","","","","1","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520446","18.773","0.002","7.8448","0.0005","20.3148","0.0019","90","","90","","90","","2991.8","0.5","293","2","293","2","","","","","","","","5","P c a 21","P 2c -2ac","29","","","","- C16 H15 N O2 S2 -","- C16 H15 N O2 S2 -","- C128 H120 N8 O16 S16 -","8","2","","Siva Reddy, Alla; Kumara Swamy, K. C.","Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.","Organic letters","2015","17","12","2996","2999","10.1021/acs.orglett.5b01287","","","0.71073","MoKα","","0.1094","0.0928","","","0.2179","0.2402","","","","","","1.086","","","","has coordinates","141405","2020-10-21","18:00:00",""
"1520447","15.7817","0.0019","13.0488","0.0012","7.2719","0.0007","90","","92.391","0.009","90","","1496.2","0.3","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C16 H14 F N O2 S2 -","- C16 H14 F N O2 S2 -","- C64 H56 F4 N4 O8 S8 -","4","1","","Siva Reddy, Alla; Kumara Swamy, K. C.","Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.","Organic letters","2015","17","12","2996","2999","10.1021/acs.orglett.5b01287","","","0.71073","MoKα","","0.1406","0.1243","","","0.3279","0.3357","","","","","","1.172","","","","has coordinates","141405","2020-10-21","18:00:00",""
"1520448","9.7686","0.0008","10.4236","0.001","16.0412","0.0015","90.974","0.008","91.846","0.007","107.681","0.008","1554.8","0.3","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C16 H15 N O3 S2 -","- C16 H15 N O3 S2 -","- C64 H60 N4 O12 S8 -","4","2","","Siva Reddy, Alla; Kumara Swamy, K. C.","Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.","Organic letters","2015","17","12","2996","2999","10.1021/acs.orglett.5b01287","","","0.71073","MoKα","","0.0745","0.0465","","","0.0916","0.104","","","","","","1.031","","","","has coordinates","141405","2020-10-21","18:00:00",""
"1520449","7.38023","0.00019","12.875","0.0003","31.8273","0.0008","90","","90","","90","","3024.24","0.13","298","2","298","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C16 H15 N O2 S Se -","- C16 H15 N O2 S Se -","- C128 H120 N8 O16 S8 Se8 -","8","1","","Siva Reddy, Alla; Kumara Swamy, K. C.","Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.","Organic letters","2015","17","12","2996","2999","10.1021/acs.orglett.5b01287","","","1.54184","CuKα","","0.0425","0.0404","","","0.1104","0.1125","","","","","","1.092","","","","has coordinates","141405","2020-10-21","18:00:00",""
"1520450","6.63588","0.00015","12.9255","0.0003","19.0476","0.0004","90","","93.665","0.002","90","","1630.41","0.06","298","2","298","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C17 H17 N O2 S2 -","- C17 H17 N O2 S2 -","- C68 H68 N4 O8 S8 -","4","1","","Siva Reddy, Alla; Kumara Swamy, K. C.","Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.","Organic letters","2015","17","12","2996","2999","10.1021/acs.orglett.5b01287","","","1.54184","CuKα","","0.0415","0.0391","","","0.1054","0.1076","","","","","","1.046","","","","has coordinates","141405","2020-10-21","18:00:00",""
"1520451","12.149","0.004","7.34","0.003","16.53","0.006","90","","101.456","0.004","90","","1444.7","0.9","93","","93","","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C40 H32 N2 -","- C40 H32 N2 -","- C80 H64 N4 -","2","0.5","","Xu, Feng; Peng, Lifen; Shinohara, Kenta; Nishida, Takanori; Wakamatsu, Kan; Uejima, Motoyuki; Sato, Tohru; Tanaka, Kazuyoshi; Machida, Norihiko; Akashi, Haruo; Orita, Akihiro; Otera, Junzo","One-Shot Double Amination of Sondheimer-Wong Diynes: Synthesis of Photoluminescent Dinaphthopentalenes.","Organic letters","2015","17","12","3014","3017","10.1021/acs.orglett.5b01293","","","0.71075","MoKα","","","0.0458","","","","0.1068","","","","","","0.935","","","","has coordinates","140274","2020-10-21","18:00:00",""
"1520491","11.2497","0.0008","12.373","0.0009","20.0241","0.0015","95.185","0.002","106.067","0.002","94.622","0.002","2651.1","0.3","173","2","173","2","","","","","","","","4","P -1","-P 1","2","","","","- C60 H74 N4 O4 -","- C60 H74 N4 O4 -","- C120 H148 N8 O8 -","2","1","","Xia, Debin; Marszalek, Tomasz; Li, Mengmeng; Guo, Xin; Baumgarten, Martin; Pisula, Wojciech; Müllen, Klaus","Solution-Processable n-Type Organic Semiconductors Based on Angular-Shaped 2-(12H-Dibenzofluoren-12-ylidene)malononitrilediimide.","Organic letters","2015","17","12","3074","3077","10.1021/acs.orglett.5b01343","","","0.71073","MoKα","","0.3286","0.1263","","","0.3364","0.4384","","","","","","1.018","","","","has coordinates","140279","2020-10-21","18:00:00",""
"1520504","10.699","0.001","11.726","0.0011","22.2683","0.0012","94.284","0.006","101.795","0.006","109.369","0.008","2549","0.4","291.64","0.1","291.64","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C20 H16 I N O -","- C20 H16 I N O -","- C120 H96 I6 N6 O6 -","6","3","","Wang, Jia; Zhu, Hai-Tao; Qiu, Yi-Feng; Niu, Yuan; Chen, Si; Li, Ying-Xiu; Liu, Xue-Yuan; Liang, Yong-Min","Facile Synthesis of Carbazoles via a Tandem Iodocyclization with 1,2-Alkyl Migration and Aromatization.","Organic letters","2015","17","12","3186","3189","10.1021/acs.orglett.5b01590","","","0.71073","MoKα","","0.1024","0.0555","","","0.1157","0.1481","","","","","","1.032","","","","has coordinates","140275","2020-10-21","18:00:00",""
"1520505","7.2355","0.0005","20.9295","0.0019","23.0167","0.0015","90","","90","","90","","3485.5","0.5","293.1","0.12","293.1","0.12","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C20 H16 I N O -","- C20 H16 I N O -","- C160 H128 I8 N8 O8 -","8","1","","Wang, Jia; Zhu, Hai-Tao; Qiu, Yi-Feng; Niu, Yuan; Chen, Si; Li, Ying-Xiu; Liu, Xue-Yuan; Liang, Yong-Min","Facile Synthesis of Carbazoles via a Tandem Iodocyclization with 1,2-Alkyl Migration and Aromatization.","Organic letters","2015","17","12","3186","3189","10.1021/acs.orglett.5b01590","","x-ray","0.71073","MoKα","","0.1076","0.0639","","","0.1407","0.1839","","","","","","1.032","","","","has coordinates","140275","2020-10-21","18:00:00",""
"1520513","7.4014","0.0009","30.606","0.004","7.739","0.001","90","","100.806","0.003","90","","1722","0.4","100","2","100","2","","","","","","","","2","P 1 21/n 1","-P 2yn","14","","","","- C24 H24 -","- C24 H24 -","- C96 H96 -","4","1","","Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju","Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.","Organic letters","2015","17","12","3142","3145","10.1021/acs.orglett.5b01461","","","0.71073","MoKα","","0.0751","0.0478","","","0.1081","0.12","","","","","","1.04","","","","has coordinates","140267","2020-10-21","18:00:00",""
"1520514","11.2988","0.0018","5.7063","0.0009","14.045","0.002","90","","102.129","0.004","90","","885.3","0.2","100","2","100","2","","","","","","","","4","P 1 n 1","P -2yac","7","","","","- C20 H24 O4 S -","- C20 H24 O4 S -","- C40 H48 O8 S2 -","2","1","","Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju","Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.","Organic letters","2015","17","12","3142","3145","10.1021/acs.orglett.5b01461","","","0.71073","MoKα","","0.0292","0.0275","","","0.0662","0.067","","","","","","1.042","","","","has coordinates","140267","2020-10-21","18:00:00",""
"1520515","22.419","0.008","52.094","0.018","7.523","0.003","90","","90","","90","","8786","6","100","2","100","2","","","","","","","","5","F d d 2","F 2 -2d","43","","","","- C25 H29 N O5 S -","- C25 H29 N O5 S -","- C400 H464 N16 O80 S16 -","16","1","","Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju","Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.","Organic letters","2015","17","12","3142","3145","10.1021/acs.orglett.5b01461","","","0.71073","MoKα","","0.0948","0.0663","","","0.1327","0.1413","","","","","","1.099","","","","has coordinates","140267","2020-10-21","18:00:00",""
"1520516","30.166","0.004","11.6914","0.0015","14.2065","0.0018","90","","113.297","0.003","90","","4601.9","1","100","2","100","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C25 H29 N O5 S -","- C25 H29 N O5 S -","- C200 H232 N8 O40 S8 -","8","1","","Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju","Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.","Organic letters","2015","17","12","3142","3145","10.1021/acs.orglett.5b01461","","","0.71073","MoKα","","0.0591","0.039","","","0.0971","0.1075","","","","","","1.022","","","","has coordinates","140267","2020-10-21","18:00:00",""
"1520517","8.4903","0.001","9.6656","0.0011","18.663","0.002","90","","90","","90","","1531.6","0.3","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C19 H19 F O -","- C19 H19 F O -","- C76 H76 F4 O4 -","4","1","","Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju","Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.","Organic letters","2015","17","12","3142","3145","10.1021/acs.orglett.5b01461","","","0.71073","MoKα","","0.0455","0.0346","","","0.0738","0.0781","","","","","","1.034","","","","has coordinates","140267","2020-10-21","18:00:00",""
"1520518","31.617","0.014","15.428","0.007","14.478","0.006","90","","101.899","0.005","90","","6910","5","103","2","103","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C43 H41 N3 O4 -","- C43 H41 N3 O4 -","- C344 H328 N24 O32 -","8","2","","Zhang, Feng-Lian; Zhu, Xu; Chiba, Shunsuke","Tf~2~NH-Catalyzed Amide Synthesis from Vinyl Azides and Alcohols","Organic Letters","2015","17","12","3138","3141","10.1021/acs.orglett.5b01458","","","0.71073","MoKα","","0.1227","0.0834","","","0.2157","0.2538","","","","","","1.045","","","","has coordinates","180537","2020-10-21","18:00:00",""
"1520519","7.9023","0.0018","12.49","0.003","12.9","0.003","90","","90","","90","","1273.2","0.5","200","2","200","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C13 H12 Cl N O4 -","- C13 H12 Cl N O4 -","- C52 H48 Cl4 N4 O16 -","4","1","","Sekikawa, Tohru; Kitaguchi, Takayuki; Kitaura, Hayato; Minami, Tatsuya; Hatanaka, Yasuo","Catalytic Activity of epi-Quinine-Derived 3,5-Bis(trifluoromethyl)benzamide in Asymmetric Nitro-Michael Reaction of Furanones.","Organic letters","2015","17","12","3026","3029","10.1021/acs.orglett.5b01224","","","0.7107","MoKα","","0.0474","0.0431","","","0.0847","0.0865","","","","","","1.146","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520520","8.745","0.003","10.225","0.003","20.19","0.008","89.48","0.02","86.38","0.02","65.669","0.014","1641.4","1","93","","93","","","","","","","","","6","P -1","-P 1","2","","","","- C39 H40 B F2 N3 O4 -","- C39 H40 B F2 N3 O4 -","- C78 H80 B2 F4 N6 O8 -","2","1","","Hiruta, Yuki; Koiso, Hikaru; Ozawa, Hitoshi; Sato, Hiroyasu; Hamada, Kensaku; Yabushita, Satoshi; Citterio, Daniel; Suzuki, Koji","Near IR Emitting Red-Shifting Ratiometric Fluorophores Based on Borondipyrromethene.","Organic letters","2015","17","12","3022","3025","10.1021/acs.orglett.5b01299","","","0.71075","MoKα","","0.1093","0.049","","","0.1009","0.1242","","","","","","0.984","","","","has coordinates","140273","2020-10-21","18:00:00",""
"1520521","8.776","0.002","10.567","0.003","19.225","0.006","84.193","0.008","82.204","0.007","69.585","0.006","1652.6","0.8","293","","293","","","","","","","","","7","P -1","-P 1","2","","","","- C37.5 H36.5 B Cl1.5 F2 N3 O4 -","- C37.5 H36.5 B Cl1.5 F2 N3 O4 -","- C75 H73 B2 Cl3 F4 N6 O8 -","2","1","","Hiruta, Yuki; Koiso, Hikaru; Ozawa, Hitoshi; Sato, Hiroyasu; Hamada, Kensaku; Yabushita, Satoshi; Citterio, Daniel; Suzuki, Koji","Near IR Emitting Red-Shifting Ratiometric Fluorophores Based on Borondipyrromethene.","Organic letters","2015","17","12","3022","3025","10.1021/acs.orglett.5b01299","","","0.71075","MoKα","","0.0875","0.0551","","","0.1257","0.149","","","","","","1.044","","","","has coordinates","140273","2020-10-21","18:00:00",""
"1520522","7.274","0.003","17.864","0.006","15.322","0.007","90","","100.332","0.016","90","","1958.7","1.4","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C46 H44 B2 N2 O2 -","- C46 H44 B2 N2 O2 -","- C92 H88 B4 N4 O4 -","2","0.5","","Kubota, Yasuhiro; Niwa, Takahiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki","Synthesis, Absorption, and Electrochemical Properties of Quinoid-Type Bisboron Complexes with Highly Symmetrical Structures.","Organic letters","2015","17","12","3174","3177","10.1021/acs.orglett.5b01547","","","0.71075","MoKα","","0.1184","0.0679","","","0.1562","0.1889","","","","","","1.028","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520523","7.054","0.0013","17.672","0.004","13.751","0.003","90","","96.406","0.009","90","","1703.5","0.6","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C42 H36 B2 N2 O2 -","- C42 H36 B2 N2 O2 -","- C84 H72 B4 N4 O4 -","2","0.5","","Kubota, Yasuhiro; Niwa, Takahiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki","Synthesis, Absorption, and Electrochemical Properties of Quinoid-Type Bisboron Complexes with Highly Symmetrical Structures.","Organic letters","2015","17","12","3174","3177","10.1021/acs.orglett.5b01547","","","0.71075","MoKα","","0.0807","0.0553","","","0.1381","0.1572","","","","","","1.028","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520542","6.62144","0.00014","20.1343","0.0004","9.362","0.0002","90","","100.915","0.002","90","","1225.54","0.04","293.69","0.1","293.69","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C32 H25 N O4 -","- C32 H25 N O4 -","- C64 H50 N2 O8 -","2","1","","Zhao, Shuai; Zhao, Yuan-Yuan; Lin, Jun-Bing; Xie, Ting; Liang, Yong-Min; Xu, Peng-Fei","Organocatalyzed Asymmetric Vinylogous Allylic-Allylic Alkylation of Morita-Baylis-Hillman Carbonates with Olefinic Azlactones: Facile Access to Chiral Multifunctional α-Amino Acid Derivatives.","Organic letters","2015","17","13","3206","3209","10.1021/acs.orglett.5b01066","","x-ray","1.54184","CuKα","","0.0336","0.0312","","","0.0776","0.0796","","","","","","1.026","","","","has coordinates","140259","2020-10-21","18:00:00",""
"1520547","9.4128","0.0007","9.6074","0.0008","12.0794","0.0009","97.999","0.007","97.992","0.006","108.357","0.007","1007.08","0.15","180.01","0.1","180.01","0.1","","","","","","","","3","P -1","-P 1","2","","","","- C25 H24 S -","- C25 H24 S -","- C50 H48 S2 -","2","1","","Zhang, Hang; Wang, Bo; Yi, Heng; Zhang, Yan; Wang, Jianbo","Rh(II)-Catalyzed [2,3]-Sigmatropic Rearrangement of Sulfur Ylides Derived from Cyclopropenes and Sulfides.","Organic letters","2015","17","13","3322","3325","10.1021/acs.orglett.5b01542","","","0.7107","MoKα","","0.0659","0.0483","","","0.1219","0.1383","","","","","","1.067","","","","has coordinates","140256","2020-10-21","18:00:00",""
"1520552","15.3809","0.0006","11.5149","0.0006","17.7975","0.0008","90","","90.677","0.002","90","","3151.9","0.2","110","2","110","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C36 H22 N12 -","- C36 H22 N12 -","- C144 H88 N48 -","4","1","","Saltsman, Irena; Goldberg, Israel; Gross, Zeev","Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.","Organic letters","2015","17","13","3214","3217","10.1021/acs.orglett.5b01297","","","0.71073","MoKα","","0.0574","0.0451","","","0.1177","0.1231","","","","","","1.038","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520553","21.689","0.004","29.869","0.005","10.7143","0.0019","90","","90","","90","","6941","2","110","2","110","2","","","","","","","","6","I b a 2","I 2 -2c","45","","","","- C35 H19 F4 N6 O2 P -","- C35 H19 F4 N6 O2 P -","- C280 H152 F32 N48 O16 P8 -","8","1","","Saltsman, Irena; Goldberg, Israel; Gross, Zeev","Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.","Organic letters","2015","17","13","3214","3217","10.1021/acs.orglett.5b01297","","","0.71073","MoKα","","0.0984","0.063","","","0.1414","0.1542","","","","","","0.974","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520554","12.3996","0.0011","15.4999","0.0013","21.5037","0.0019","90","","97.248","0.004","90","","4099.8","0.6","110","2","110","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C51 H33 Co F4 N8 -","- C51 H33 Co F4 N8 -","- C204 H132 Co4 F16 N32 -","4","1","","Saltsman, Irena; Goldberg, Israel; Gross, Zeev","Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.","Organic letters","2015","17","13","3214","3217","10.1021/acs.orglett.5b01297","","","0.71073","MoKα","","0.0442","0.033","","","0.0734","0.0783","","","","","","1.027","","","","has coordinates","211332","2020-10-21","18:00:00",""
"1520555","16.3504","0.0016","14.9527","0.0015","9.2389","0.0009","90","","92.387","0.005","90","","2256.8","0.4","150","2","150","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","cis-di(4-pyridyl)naphthocyclobutane hydrobromide","cis-di(4-pyridyl)naphthocyclobutane hydrobromide","","- C24 H20 Br2 N2 -","- C24 H20 Br2 N2 -","- C96 H80 Br8 N8 -","4","0.5","","Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.","Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.","Organic letters","2015","17","13","3233","3235","10.1021/acs.orglett.5b00527","","","0.71073","MoKα","","0.0698","0.0606","","","0.1346","0.1375","","","","","","1.22","","","","has coordinates,has disorder","176428","2020-10-21","18:00:00",""
"1520556","9.4274","0.0009","12.3411","0.0012","15.5934","0.0016","83.302","0.005","82.714","0.005","79.24","0.005","1759.9","0.3","150","2","150","2","","","","","","","","3","P -1","-P 1","2","DEPN","1,8-bis[(E)-2-(4-pyridyl)ethenyl] naphthalene","","- C24 H18 N2 -","- C24 H18 N2 -","- C96 H72 N8 -","4","2","","Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.","Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.","Organic letters","2015","17","13","3233","3235","10.1021/acs.orglett.5b00527","","","0.71073","MoKα","","0.2015","0.1283","","","0.3784","0.4149","","","","","","1.105","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520557","14.33","0.0015","10.8862","0.0011","17.8919","0.0018","90","","110.048","0.005","90","","2622","0.5","190","","190","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","Ag tosylate DEPN","Silver p-toluenesulfonate 1,8-bis[(E)-2-(4-pyridyl)ethenyl] naphthalene","","- C62 H50 Ag2 N4 O6 S2 -","- C62 H50 Ag2 N4 O6 S2 -","- C124 H100 Ag4 N8 O12 S4 -","2","0.5","","Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.","Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.","Organic letters","2015","17","13","3233","3235","10.1021/acs.orglett.5b00527","","","0.71073","MoKα","","0.0803","0.04","","","0.0898","0.1085","","","","","","0.93","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520558","10.3809","0.0011","10.9748","0.0011","11.0438","0.0012","109.43","0.005","98.185","0.005","97.328","0.005","1153.7","0.2","210","2","210","2","","","","","","","","7","P -1","-P 1","2","Ag triflate DEPN","Silver trifluoromethanesulfonate 1,8-bis[(E)-2-(4-pyridyl)ethenyl] naphthalene","","- C50 H36 Ag2 F6 N4 O6 S2 -","- C50 H36 Ag2 F6 N4 O6 S2 -","- C50 H36 Ag2 F6 N4 O6 S2 -","1","0.5","","Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.","Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.","Organic letters","2015","17","13","3233","3235","10.1021/acs.orglett.5b00527","","","0.71073","MoKα","","0.0377","0.0296","","","0.0818","0.0884","","","","","","0.988","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520559","10.4495","0.001","11.0503","0.0011","11.0576","0.0011","109.671","0.005","96.586","0.005","97.962","0.005","1172.8","0.2","293","2","293","2","","","","","","","","7","P -1","-P 1","2","Ag triflate DEPN","Silver trifluoromethanesulfonate 1,8-bis[(E)-2-(4-pyridyl)ethenyl] naphthalene","","- C50 H36 Ag2 F6 N4 O6 S2 -","- C50 H36 Ag2 F6 N4 O6 S2 -","- C50 H36 Ag2 F6 N4 O6 S2 -","1","0.5","","Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.","Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.","Organic letters","2015","17","13","3233","3235","10.1021/acs.orglett.5b00527","","","0.71073","MoKα","","0.0432","0.0323","","","0.0762","0.0822","","","","","","1.129","","","","has coordinates,has disorder","152906","2020-10-21","18:00:00",""
"1520560","14.369","0.003","10.925","0.002","18.106","0.004","90","","110.574","0.005","90","","2661","0.9","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","Ag tosylate DEPN","Silver p-toluenesulfonate 1,8-bis[(E)-2-(4-pyridyl)ethenyl] naphthalene","","- C62 H50 Ag2 N4 O6 S2 -","- C62 H50 Ag2 N4 O6 S2 -","- C124 H100 Ag4 N8 O12 S4 -","2","0.5","","Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.","Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.","Organic letters","2015","17","13","3233","3235","10.1021/acs.orglett.5b00527","","","0.71073","MoKα","","0.1674","0.0657","","","0.1428","0.196","","","","","","0.903","","","","has coordinates","152906","2020-10-21","18:00:00",""
"1520561","11.2709","0.0006","11.7647","0.0006","20.1194","0.0009","88.271","0.004","83.035","0.003","86.352","0.004","2642.1","0.2","100","2","100.01","","","","","","","","","5","P -1","-P 1","2","","","","- C51 H58 F6 O14 S2 -","- C51 H58 F6 O14 S2 -","- C102 H116 F12 O28 S4 -","2","1","","Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser","Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.","Organic letters","2015","17","13","3260","3263","10.1021/acs.orglett.5b01418","","","1.54178","CuKα","","0.1483","0.096","","","0.2518","0.2897","","","","","","1.075","","","","has coordinates,has disorder","140261","2020-10-21","18:00:00",""
"1520562","11.616","0.0003","18.2419","0.0005","11.617","0.0003","90","","94.1589","0.0015","90","","2455.14","0.11","100","2","99.98","","","","","","","","","6","P 1 n 1","P -2yac","7","","","","- C46 H46 Cl2 F6 O14 S2 -","- C46 H46 Cl2 F6 O14 S2 -","- C92 H92 Cl4 F12 O28 S4 -","2","1","","Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser","Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.","Organic letters","2015","17","13","3260","3263","10.1021/acs.orglett.5b01418","","","1.54178","CuKα","","0.0484","0.0471","","","0.1249","0.1264","","","","","","1.041","","","","has coordinates,has disorder","140261","2020-10-21","18:00:00",""
"1520563","35.9931","0.0011","12.0648","0.0004","11.369","0.0004","90","","90","","90","","4937","0.3","100","2","100","2","","","","","","","","6","P n a 21","P 2c -2n","33","","","","- C48.75 H55.04 Cl2.25 F3 O12 S -","- C48.747 H54.93 Cl2.252 F3 O12 S -","- C194.988 H219.72 Cl9.008 F12 O48 S4 -","4","1","","Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser","Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.","Organic letters","2015","17","13","3260","3263","10.1021/acs.orglett.5b01418","","","1.54178","CuKα","","0.0752","0.075","","","0.2026","0.2029","","","","","","1.156","","","","has coordinates,has disorder","140261","2020-10-21","18:00:00",""
"1520564","11.3045","0.0007","12.1357","0.0007","37.187","0.002","90","","90","","90","","5101.6","0.5","100","2","100.02","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C51 H58 F6 O14 S2 -","- C51 H58 F6 O14 S2 -","- C204 H232 F24 O56 S8 -","4","1","","Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser","Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.","Organic letters","2015","17","13","3260","3263","10.1021/acs.orglett.5b01418","","","0.71073","MoKα","","0.0713","0.0536","","","0.123","0.1318","","","","","","1.047","","","","has coordinates","140261","2020-10-21","18:00:00",""
"1520565","22.0373","0.001","11.9982","0.0005","22.7155","0.001","90","","110.288","0.003","90","","5633.5","0.4","100","2","100.08","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C51 H55 F9 O16 S3 -","- C51 H55 F9 O16 S3 -","- C204 H220 F36 O64 S12 -","4","1","","Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser","Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.","Organic letters","2015","17","13","3260","3263","10.1021/acs.orglett.5b01418","","","1.54178","CuKα","","0.1054","0.0854","","","0.2322","0.2482","","","","","","1.041","","","","has coordinates","140261","2020-10-21","18:00:00",""
"1520566","20.6289","0.0011","22.2856","0.0013","24.1696","0.0014","90","","90","","90","","11111.4","1.1","100","2","99.96","","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C51 H55 F9 O16 S3 -","- C51 H55 F9 O16 S3 -","- C408 H440 F72 O128 S24 -","8","1","","Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser","Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.","Organic letters","2015","17","13","3260","3263","10.1021/acs.orglett.5b01418","","","0.71073","MoKα","","0.1801","0.1169","","","0.3006","0.3487","","","","","","1.093","","","","has coordinates,has disorder","140261","2020-10-21","18:00:00",""
"1520573","6.1669","0.0002","12.182","0.0003","17.8605","0.0006","90","","90","","90","","1341.77","0.07","150","","150","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","3,5-dimethyl-2-phenyl-4-(thiophen-2-yl)pyridine","","- C17 H15 N S -","- C17 H15 N S -","- C68 H60 N4 S4 -","4","1","","Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J.","Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation.","Organic letters","2015","17","13","3222","3225","10.1021/acs.orglett.5b01312","","","1.5418","CuKα","","0.0368","0.0339","","0.088","0.0854","0.088","","","","","","0.9323","","","","has coordinates,has disorder","176429","2020-10-21","18:00:00",""
"1520574","7.4565","0.0001","18.3137","0.0002","20.6855","0.0003","90","","90","","90","","2824.73","0.06","150","","150","","","","","","","","","4","P b c a","-P 2ac 2ab","61","","4-(4-methoxyphenyl)-3-methyl-2-phenylpyridine","","- C19 H17 N O -","- C19 H17 N O -","- C152 H136 N8 O8 -","8","1","","Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J.","Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation.","Organic letters","2015","17","13","3222","3225","10.1021/acs.orglett.5b01312","","","0.71073","MoKα","","0.0604","0.0421","","0.1211","0.102","0.1211","","","","","","0.9741","","","","has coordinates","176429","2020-10-21","18:00:00",""
"1520575","9.7773","0.0002","6.90436","0.00013","9.79548","0.00019","90","","98.985","0.002","90","","653.14","0.02","293","2","293","2","","","","","","","","3","P 1 21/m 1","-P 2yb","11","","","","- C16 H15 N3 -","- C16 H15 N3 -","- C32 H30 N6 -","2","0.5","","Castillo, Juan-Carlos; Quiroga, Jairo; Abonia, Rodrigo; Rodriguez, Jean; Coquerel, Yoann","The Aryne aza-Diels-Alder Reaction: Flexible Syntheses of Isoquinolines.","Organic letters","2015","17","13","3374","3377","10.1021/acs.orglett.5b01704","","x-ray","1.54184","CuKα","","0.0563","0.0555","","","0.1358","0.1373","","","","","","1.123","","","","has coordinates,has disorder","204128","2020-10-21","18:00:00",""
"1520576","14.0946","0.0002","11.4421","0.0002","9.74761","0.00017","90","","99.2056","0.0017","90","","1551.77","0.04","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C21 H15 N3 -","- C21 H15 N3 -","- C84 H60 N12 -","4","1","","Castillo, Juan-Carlos; Quiroga, Jairo; Abonia, Rodrigo; Rodriguez, Jean; Coquerel, Yoann","The Aryne aza-Diels-Alder Reaction: Flexible Syntheses of Isoquinolines.","Organic letters","2015","17","13","3374","3377","10.1021/acs.orglett.5b01704","","x-ray","1.54184","CuKα","","0.0479","0.0421","","","0.1084","0.1158","","","","","","1.018","","","","has coordinates","204128","2020-10-21","18:00:00",""
"1520577","10.1756","0.0004","12.2477","0.0005","13.4918","0.0006","90","","90","","90","","1681.45","0.12","298","2","298","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","Teotihuacanin","","","- C20 H20 O6 -","- C20 H20 O6 -","- C80 H80 O24 -","4","1","","Bautista, Elihú; Fragoso-Serrano, Mabel; Toscano, Rubén A; García-Peña, María Del Rosario; Ortega, Alfredo","Teotihuacanin, a Diterpene with an Unusual Spiro-10/6 System from Salvia amarissima with Potent Modulatory Activity of Multidrug Resistance in Cancer Cells.","Organic letters","2015","17","13","3280","3282","10.1021/acs.orglett.5b01320","","","1.54178","CuKα","","0.0525","0.0421","","","0.1006","0.1066","","","","","","1.062","","","","has coordinates","141399","2020-10-21","18:00:00",""
"1520614","9.4141","0.0007","23.293","0.0014","9.0609","0.0006","90","","92.942","0.003","90","","1984.3","0.2","100","0.2","100","0.2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","2-(benzyl(3-((4-methoxyphenyl)ethynyl)oxetan-3-yl)amino)phenol","","- C25 H23 N O3 -","- C25 H23 N O3 -","- C100 H92 N4 O12 -","4","1","","Brady, Patrick B.; Carreira, Erick M.","Addition of Trifluoroborates to Oxetanyl N,O-Acetals: Entry into Spiro and Fused Saturated Heterocycles.","Organic letters","2015","17","13","3350","3353","10.1021/acs.orglett.5b01607","","x-ray","0.71073","MoKα","","0.0479","0.0388","","","0.0926","0.0987","","","","","","1.029","","","","has coordinates,has disorder","140260","2020-10-21","18:00:00",""
"1520615","8.0166","0.0006","15.8594","0.0012","11.2674","0.0009","90","","98.788","0.002","90","","1415.7","0.19","100","0.2","100","0.2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C18 H17 N O2 -","- C18 H17 N O2 -","- C72 H68 N4 O8 -","4","1","","Brady, Patrick B.; Carreira, Erick M.","Addition of Trifluoroborates to Oxetanyl N,O-Acetals: Entry into Spiro and Fused Saturated Heterocycles.","Organic letters","2015","17","13","3350","3353","10.1021/acs.orglett.5b01607","","x-ray","0.71073","MoKα","","0.0523","0.0434","","","0.1039","0.109","","","","","","1.035","","","","has coordinates,has disorder","140260","2020-10-21","18:00:00",""
"1520616","11.364","0.005","10.93","0.005","24.447","0.005","90","0.005","96.564","0.005","90","0.005","3017","2","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C37 H31 N O5 -","- C37 H31 N O5 -","- C148 H124 N4 O20 -","4","1","","Mo, Lei; Wu, Lin-Lin; Wang, Shaozhong; Yao, Zhu-Jun","Efficient Synthesis of Octahydrophenanthrene Derivatives with Mild Cascade Reactions of Isochromenylium Tetrafluoroborates and Bifunctional Styrenes.","Organic letters","2015","17","13","3314","3317","10.1021/acs.orglett.5b01532","","","0.71069","MoKα","","0.0763","0.0453","","","0.1321","0.1617","","","","","","0.928","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520633","11.7745","0.0002","15.3391","0.0003","24.3582","0.0004","90","","90","","90","","4399.34","0.13","296","2","296","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","CWS-621","","","- C22 H21 Br N2 O3 S2 -","- C22 H21 Br N2 O3 S2 -","- C176 H168 Br8 N16 O24 S16 -","8","1","","Choi, Wonseok; Kim, Jaeeun; Ryu, Taekyu; Kim, Ki-Bbeum; Lee, Phil Ho","Synthesis of N-Imidoyl and N-Oxoimidoyl Sulfoximines from 1-Alkynes, N-Sulfonyl Azides, and Sulfoximines.","Organic letters","2015","17","13","3330","3333","10.1021/acs.orglett.5b01553","","","0.71073","","","0.055","0.0357","","","0.079","0.0874","","","","","","1.033","","","","has coordinates","140262","2020-10-21","18:00:00",""
"1520634","9.0038","0.0002","10.66","0.0002","11.8108","0.0003","75.2664","0.0011","76.0323","0.0011","75.5364","0.0011","1042.26","0.04","296","2","296","2","","","","","","","","5","P -1","-P 1","2","KJE-831","","","- C22 H20 N2 O4 S2 -","- C22 H20 N2 O4 S2 -","- C44 H40 N4 O8 S4 -","2","1","","Choi, Wonseok; Kim, Jaeeun; Ryu, Taekyu; Kim, Ki-Bbeum; Lee, Phil Ho","Synthesis of N-Imidoyl and N-Oxoimidoyl Sulfoximines from 1-Alkynes, N-Sulfonyl Azides, and Sulfoximines.","Organic letters","2015","17","13","3330","3333","10.1021/acs.orglett.5b01553","","","0.71073","","","0.1794","0.128","","","0.3275","0.3916","","","","","","1.344","","","","has coordinates","140262","2020-10-21","18:00:00",""
"1520635","7.37176","0.00017","14.7771","0.0003","21.8173","0.0005","90","","90","","90","","2376.63","0.09","93","","93","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C30 H29 N O3 -","- C30 H29 N O3 -","- C120 H116 N4 O12 -","4","1","","Majumdar, Nilanjana; Saito, Akira; Yin, Liang; Kumagai, Naoya; Shibasaki, Masakatsu","Direct Catalytic Asymmetric Conjugate Addition of Saturated and Unsaturated Thioamides.","Organic letters","2015","17","13","3362","3365","10.1021/acs.orglett.5b01644","","","1.54187","CuKα","","0.0411","0.0358","","","0.0821","0.0848","","","","","","1.081","","","","has coordinates","140263","2020-10-21","18:00:00",""
"1520636","10.39896","0.00019","9.11807","0.00017","13.7409","0.0003","90","","108.291","0.008","90","","1237.06","0.07","93","","93","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C29 H32 N2 S2 -","- C29 H32 N2 S2 -","- C58 H64 N4 S4 -","2","1","","Majumdar, Nilanjana; Saito, Akira; Yin, Liang; Kumagai, Naoya; Shibasaki, Masakatsu","Direct Catalytic Asymmetric Conjugate Addition of Saturated and Unsaturated Thioamides.","Organic letters","2015","17","13","3362","3365","10.1021/acs.orglett.5b01644","","","1.54187","CuKα","","0.0334","0.0313","","","0.0839","0.0911","","","","","","1.11","","","","has coordinates","140263","2020-10-21","18:00:00",""
"1520637","12.0845","0.0012","5.9453","0.0006","22.597","0.002","90","","103.246","0.0016","90","","1580.3","0.3","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H15 F O2 -","- C21 H15 F O2 -","- C84 H60 F4 O8 -","4","1","","Du, Xiang-Wei; Stanley, Levi M.","Tandem Alkyne Hydroacylation and Oxo-Michael Addition: Diastereoselective Synthesis of 2,3-Disubstituted Chroman-4-ones and Fluorinated Derivatives.","Organic letters","2015","17","13","3276","3279","10.1021/acs.orglett.5b01447","","","0.71073","MoKα","","0.0597","0.0446","","","0.1187","0.1309","","","","","","1.001","","","","has coordinates","141400","2020-10-21","18:00:00",""
"1520655","9.2692","0.0007","9.7098","0.0007","34.752","0.003","90","","92.266","0.001","90","","3125.3","0.4","173","","173","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C32 H38 O5 Si2 -","- C32 H38 O5 Si2 -","- C128 H152 O20 Si8 -","4","1","","Zimmerman, Jake R.; Johntony, Olivia; Steigerwald, Daniel; Criss, Cody; Myers, Brian J.; Kinder, David H.","The Synthesis of a New Class of Highly Fluorescent Chromones via an Inverse-Demand Hetero-Diels-Alder Reaction.","Organic letters","2015","17","13","3256","3259","10.1021/acs.orglett.5b01417","","","0.71073","MoKα","","0.0631","0.0429","","","0.0984","0.1091","","","","","","1.028","","","","has coordinates","154764","2020-10-21","18:00:00",""
"1520656","6.9648","0.001","7.7685","0.0011","14.728","0.002","76.228","0.002","76.658","0.002","84.002","0.002","752.04","0.18","173","2","173.15","","","","","","","","","4","P -1","-P 1","2","","","","- C16 H17 Cl O5 -","- C16 H17 Cl O5 -","- C32 H34 Cl2 O10 -","2","1","","Zimmerman, Jake R.; Johntony, Olivia; Steigerwald, Daniel; Criss, Cody; Myers, Brian J.; Kinder, David H.","The Synthesis of a New Class of Highly Fluorescent Chromones via an Inverse-Demand Hetero-Diels-Alder Reaction.","Organic letters","2015","17","13","3256","3259","10.1021/acs.orglett.5b01417","","x-ray","0.71073","MoKα","","0.0551","0.0399","","","0.095","0.1039","","","","","","1.096","","","","has coordinates","154764","2020-10-21","18:00:00",""
"1520657","5.6762","0.0006","10.5443","0.0011","14.1611","0.0014","90","","100.294","0.004","90","","833.92","0.15","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C18 H17 Br O5 -","- C18 H17 Br O5 -","- C36 H34 Br2 O10 -","2","1","","Sinha, Debarshi; Biswas, Arnab; Singh, Vinod K.","Chiral Phosphine-Silver(I) Complex Catalyzed Enantioselective Interrupted Feist-Bénary Reaction with Ynones: The Aldol-Cycloisomerization Cascade.","Organic letters","2015","17","13","3302","3305","10.1021/acs.orglett.5b01468","","","0.71073","MoKα","","0.0872","0.0518","","","0.1107","0.1256","","","","","","0.904","","","","has coordinates","140257","2020-10-21","18:00:00",""
"1520658","5.8624","0.0001","9.6327","0.0002","31.868","0.0006","90","","90","","90","","1799.61","0.06","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C19 H20 N2 O6 -","- C19 H20 N2 O6 -","- C76 H80 N8 O24 -","4","1","","Chen, Shi; Ibrahim, Ahmad A.; Mondal, Mukulesh; Magee, Anthony J.; Cruz, Adam J.; Wheeler, Kraig A.; Kerrigan, Nessan J.","Asymmetric Synthesis of Deoxypropionate Derivatives via Catalytic Hydrogenolysis of Enantioenriched Z-Ketene Heterodimers.","Organic letters","2015","17","13","3248","3251","10.1021/acs.orglett.5b01391","","","1.54178","CuKα","","0.0476","0.04","","","0.0965","0.1003","","","","","","1.056","","","","has coordinates","152907","2020-10-21","18:00:00",""
"1520659","13.1915","0.0004","9.4009","0.0003","22.0383","0.0006","90","","106.275","0.001","90","","2623.49","0.14","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C22 H32 Cl2 I2 Si2 -","- C22 H26 Cl2 I2 Si2 -","- C88 H104 Cl8 I8 Si8 -","4","1","","Sproul, Kyle C.; Chalifoux, Wesley A.","Highly Regio- and Diastereoselective Formation of Tetrasubstituted (Z)-1,2-Dihaloalkenes from the Halogenation of Trimethylsilyl Alkynes with ICl.","Organic letters","2015","17","13","3334","3337","10.1021/acs.orglett.5b01558","","","0.71073","MoKα","","0.0198","0.0183","","","0.044","0.0446","","","","","","1.087","","","","has coordinates","152908","2020-10-21","18:00:00",""
"1520660","9.0806","0.0004","15.5457","0.0006","23.2185","0.0009","90","","90","","90","","3277.6","0.2","100","2","100","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","5","","","- C16 H10 Cl2 I2 -","- C16 H10 Cl2 I2 -","- C128 H80 Cl16 I16 -","8","1","","Sproul, Kyle C.; Chalifoux, Wesley A.","Highly Regio- and Diastereoselective Formation of Tetrasubstituted (Z)-1,2-Dihaloalkenes from the Halogenation of Trimethylsilyl Alkynes with ICl.","Organic letters","2015","17","13","3334","3337","10.1021/acs.orglett.5b01558","","","0.71073","MoKα","","0.0277","0.0255","","","0.0608","0.0617","","","","","","1.174","","","","has coordinates","152908","2020-10-21","18:00:00",""
"1520682","10.4761","0.0005","10.8361","0.0002","11.3358","0.0006","76.911","0.001","61.867","0.001","86.563","0.002","1103.68","0.08","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C26 H19 N3 O5 S -","- C26 H19 N3 O5 S -","- C52 H38 N6 O10 S2 -","2","1","","Rao, Wei-Hao; Zhan, Bei-Bei; Chen, Kai; Ling, Peng-Xiang; Zhang, Zhuo-Zhuo; Shi, Bing-Feng","Pd(II)-Catalyzed Direct Sulfonylation of Unactivated C(sp(3))-H Bonds with Sodium Sulfinates.","Organic letters","2015","17","14","3552","3555","10.1021/acs.orglett.5b01634","","","0.71073","MoKα","","0.0544","0.041","","","0.0998","0.1077","","","","","","1.002","","","","has coordinates","154782","2020-10-21","18:00:00",""
"1520683","10.868","0.0008","6.8325","0.0006","12.6102","0.001","90","","103.793","0.005","90","","909.38","0.13","100","2","100","2","","","","","","","","5","P 1 21 1","P 2yb","4","REJIII-035E2","sarpong111","","- C20 H24 Cl N3 O -","- C20 H24 Cl N3 O -","- C40 H48 Cl2 N6 O2 -","2","1","","Johnson, Rebecca E.; de Rond, Tristan; Lindsay, Vincent N. G.; Keasling, Jay D.; Sarpong, Richmond","Synthesis of Cycloprodigiosin Identifies the Natural Isolate as a Scalemic Mixture.","Organic letters","2015","17","14","3474","3477","10.1021/acs.orglett.5b01527","","","1.54178","CuKα","","0.0562","0.0467","","","0.1104","0.1169","","","","","","1.047","","","","has coordinates","204147","2020-10-21","18:00:00",""
"1520684","28.508","0.002","5.4891","0.0004","8.1976","0.0007","90","","90","","90","","1282.79","0.17","147","2","147","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C13 H17 Cl O3 -","- C13 H17 Cl O3 -","- C52 H68 Cl4 O12 -","4","1","","Tanveer, Kashif; Jarrah, Kareem; Taylor, Mark S.","Borinic Acid Catalyzed, Regioselective Chloroacylations and Chlorosulfonylations of 2,3-Epoxy Alcohols.","Organic letters","2015","17","14","3482","3485","10.1021/acs.orglett.5b01541","","","0.71073","MoKα","","0.0594","0.0445","","","0.0831","0.0885","","","","","","1.039","","","","has coordinates","154783","2020-10-21","18:00:00",""
"1520685","15.5081","0.0014","11.7102","0.0009","20.245","0.002","90","","90","","90","","3676.6","0.6","147","2","147","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C21 H21 Cl O4 -","- C21 H21 Cl O4 -","- C168 H168 Cl8 O32 -","8","1","","Tanveer, Kashif; Jarrah, Kareem; Taylor, Mark S.","Borinic Acid Catalyzed, Regioselective Chloroacylations and Chlorosulfonylations of 2,3-Epoxy Alcohols.","Organic letters","2015","17","14","3482","3485","10.1021/acs.orglett.5b01541","","","0.71073","MoKα","","0.1068","0.0502","","","0.0832","0.0996","","","","","","0.999","","","","has coordinates","154783","2020-10-21","18:00:00",""
"1520686","10.7946","0.0006","12.4093","0.0006","13.1553","0.0007","76.627","0.005","68.739","0.005","81.216","0.004","1593.12","0.16","170","2","170","2","","","","","","","","5","P -1","-P 1","2","","","","- C33 H30 N2 O6 S2 -","- C33 H30 N2 O6 S2 -","- C66 H60 N4 O12 S4 -","2","1","","Yan, Xiaonan; Ling, Fei; Zhang, Yuchen; Ma, Cheng","Three-Component Functionalized Dihydropyridine Synthesis via a Formal Inverse Electron-Demand Hetero-Diels-Alder Reaction.","Organic letters","2015","17","14","3536","3539","10.1021/acs.orglett.5b01622","","","0.71073","MoKα","","0.0532","0.042","","","0.1168","0.1237","","","","","","1.055","","","","has coordinates","152917","2020-10-21","18:00:00",""
"1520694","11.319","0.003","12.665","0.003","14.597","0.003","86.284","0.004","86.306","0.004","68.207","0.003","1937.1","0.8","133","","133","","","","","","","","","4","P -1","-P 1","2","","","","- C33 H27 N3 O13 -","- C33 H27 N3 O13 -","- C66 H54 N6 O26 -","2","1","","Chen, Ji-Peng; He, Wei; Yang, Zhen-Yu; Yao, Zhu-Jun","Synthesis of Tricyclo[4,3,1,0(1,5)]decane Core of Plumisclerin A Using Pauson-Khand Annulation and SmI2-Mediated Radical Cyclization.","Organic letters","2015","17","14","3379","3381","10.1021/acs.orglett.5b01563","","","0.71073","MoKα","","0.0917","0.0739","","","0.2084","0.2246","","","","","","1.053","","","","has coordinates,has disorder","152916","2020-10-21","18:00:00",""
"1520702","19.8643","0.0006","9.0349","0.0002","24.8875","0.0007","90","","106.793","0.002","90","","4276.1","0.2","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C41 H60 N8 O3 Ti2 -","- C41 H60 N8 O3 Ti2 -","- C164 H240 N32 O12 Ti8 -","4","1","","Chen, Zhou; Liu, Jinna; Pei, Hao; Liu, Wei; Chen, Yanmei; Wu, Jian; Li, Wu; Li, Yahong","Directed Amination of Aryl Methyl Ethers Mediated by Ti(NMe2)4 at Room Temperature.","Organic letters","2015","17","14","3406","3409","10.1021/acs.orglett.5b01229","","","0.71073","MoKα","","0.1046","0.0552","","","0.1262","0.1492","","","","","","1.016","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520703","19.976","0.004","20.518","0.004","21.236","0.004","89.583","0.005","78.919","0.005","76.303","0.005","8292","3","203","2","203","2","","","","","","","","5","P -1","-P 1","2","","","","- C163 H221 N28 O13 Ti4 -","- C163 H221 N28 O13 Ti4 -","- C326 H442 N56 O26 Ti8 -","2","1","","Chen, Zhou; Liu, Jinna; Pei, Hao; Liu, Wei; Chen, Yanmei; Wu, Jian; Li, Wu; Li, Yahong","Directed Amination of Aryl Methyl Ethers Mediated by Ti(NMe2)4 at Room Temperature.","Organic letters","2015","17","14","3406","3409","10.1021/acs.orglett.5b01229","","","0.71073","MoKα","","0.1963","0.1169","","","0.3106","0.3742","","","","","","1.024","","","","has coordinates","152914","2020-10-21","18:00:00",""
"1520704","11.7148","0.0005","11.8534","0.0005","14.1205","0.0006","110","0.003","95.83","0.003","100.677","0.003","1781.51","0.14","105","","105","","","","","","","","","4","P -1","-P 1","2","","","","- C22 H20 N2 O3 -","- C22 H20 N2 O3 -","- C88 H80 N8 O12 -","4","2","","Dörr, Aurélie A; Lubell, William D.","γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.","Organic letters","2015","17","14","3592","3595","10.1021/acs.orglett.5b01679","","x-ray","1.34139","GaKα","","0.1461","0.0847","","","0.2272","0.2672","","","","","","1.031","","","","has coordinates,has disorder","154784","2020-10-21","18:00:00",""
"1520705","17.651","0.0003","15.5231","0.0003","13.7865","0.0003","90","","90","","90","","3777.48","0.13","100","","100","","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C22 H22 N2 O3 -","- C22 H22 N2 O3 -","- C176 H176 N16 O24 -","8","2","","Dörr, Aurélie A; Lubell, William D.","γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.","Organic letters","2015","17","14","3592","3595","10.1021/acs.orglett.5b01679","","x-ray","1.54178","CuKα","","0.0345","0.0342","","","0.0932","0.0936","","","","","","1.042","","","","has coordinates,has disorder","154784","2020-10-21","18:00:00",""
"1520706","15.2406","0.0006","5.6664","0.0002","20.6863","0.0009","90","","94.254","0.002","90","","1781.53","0.12","150","","150","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C22 H20 N2 O3 -","- C22 H20 N2 O3 -","- C88 H80 N8 O12 -","4","1","","Dörr, Aurélie A; Lubell, William D.","γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.","Organic letters","2015","17","14","3592","3595","10.1021/acs.orglett.5b01679","","x-ray","1.54178","CuKα","","0.0455","0.0377","","","0.1006","0.1064","","","","","","1.042","","","","has coordinates","154784","2020-10-21","18:00:00",""
"1520707","8.7215","0.0006","11.3257","0.0008","19.217","0.001","90","","90","","90","","1898.2","0.2","90","0.1","90","0.1","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C20 H23 N O8 -","- C20 H23 N O8 -","- C80 H92 N4 O32 -","4","1","","Paladino, Marco; Zaifman, Joshua; Ciufolini, Marco A.","Total Synthesis of (+)-3-Demethoxyerythratidinone and (+)-Erysotramidine via the Oxidative Amidation of a Phenol.","Organic letters","2015","17","14","3422","3425","10.1021/acs.orglett.5b01423","","","1.54178","CuKα","","0.0277","0.0269","","","0.0672","0.068","","","","","","1.072","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520708","11.4762","0.0003","7.95324","0.00015","16.5869","0.0005","90","","107.894","0.003","90","","1440.7","0.07","294.39","0.1","294.39","0.1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H15 N3 O4 -","- C15 H15 N3 O4 -","- C60 H60 N12 O16 -","4","1","","Wang, Qi; Tang, Xuli; Luo, Xiangchao; de Voogd, Nicole J.; Li, Pinglin; Li, Guoqiang","(+)- and (-)-Spiroreticulatine, A Pair of Unusual Spiro Bisheterocyclic Quinoline-imidazole Alkaloids from the South China Sea Sponge Fascaplysinopsis reticulata.","Organic letters","2015","17","14","3458","3461","10.1021/acs.orglett.5b01503","","","1.54184","CuKα","","0.0495","0.0473","","","0.129","0.1317","","","","","","1.065","","","","has coordinates","152919","2020-10-21","18:00:00",""
"1520726","21.512","0.01","10.424","0.005","40.881","0.018","90","","90","","90","","9167","7","294","2","294","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C44 H42 F6 N6 O7 S2 -","- C44 H42 F6 N6 O7 S2 -","- C352 H336 F48 N48 O56 S16 -","8","1","","Zhu, Chuan-Le; Yang, Li-Jun; Li, Shen; Zheng, Yan; Ma, Jun-An","Brine-Stabilized 2,2,2-Trifluorodiazoethane and Its Application in the Synthesis of CF3-Substituted Cyclopropane α-Amino Acids.","Organic letters","2015","17","14","3442","3445","10.1021/acs.orglett.5b01450","","","0.71073","MoKα","","0.243","0.1095","","","0.231","0.2997","","","","","","1.071","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520727","8.882","0.006","10.743","0.009","14.629","0.013","87","0.03","76.43","0.03","65.66","0.02","1234.8","1.7","294","2","294","2","","","","","","","","5","P -1","-P 1","2","","","","- C28 H23 F3 N2 O3 -","- C28 H23 F3 N2 O3 -","- C56 H46 F6 N4 O6 -","2","1","","Zhu, Chuan-Le; Yang, Li-Jun; Li, Shen; Zheng, Yan; Ma, Jun-An","Brine-Stabilized 2,2,2-Trifluorodiazoethane and Its Application in the Synthesis of CF3-Substituted Cyclopropane α-Amino Acids.","Organic letters","2015","17","14","3442","3445","10.1021/acs.orglett.5b01450","","","0.71073","MoKα","","0.1119","0.0622","","","0.1536","0.1916","","","","","","1.05","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520728","10.3059","0.0007","20.6482","0.0013","25.5756","0.0017","90","","90","","90","","5442.4","0.6","150","2","150","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","QY614","Doyle-Quian QY614","","- C25 H34 N2 O9 Si -","- C25 H34 N2 O9 Si -","- C200 H272 N16 O72 Si8 -","8","1","","Cheng, Qing-Qing; Qian, Yu; Zavalij, Peter Y.; Doyle, Michael P.","Lewis Acid/Rhodium-Catalyzed Formal [3 + 3]-Cycloaddition of Enoldiazoacetates with Donor-Acceptor Cyclopropanes.","Organic letters","2015","17","14","3568","3571","10.1021/acs.orglett.5b01674","","","0.71073","MoKα","","0.0387","0.0329","","","0.0648","0.0666","","","","","","1","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520729","6.6067","0.0003","19.709","0.001","9.7407","0.0005","90","","109.22","0.002","90","","1197.65","0.1","100","2","100","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C25 H31 N O3 S2 -","- C25 H31 N O3 S2 -","- C50 H62 N2 O6 S4 -","2","1","","Fernández-Valparís, Javier; Romo, Juan Manuel; Romea, Pedro; Urpí, Fèlix; Kowalski, Hubert; Font-Bardia, Mercè","Stereoselective Alkylation of (S)-N-Acyl-4-isopropyl-1,3-thiazolidine-2-thiones Catalyzed by (Me3P)2NiCl2.","Organic letters","2015","17","14","3540","3543","10.1021/acs.orglett.5b01626","","","0.71073","MoKα","","0.0321","0.0293","","","0.0742","0.0762","","","","","","1.108","","","","has coordinates","154786","2020-10-21","18:00:00",""
"1520753","15.767","0.003","5.759","0.0012","15.721","0.003","90","","112.32","0.03","90","","1320.5","0.5","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C13 H13 Cl N2 O2 S -","- C13 H13 Cl N2 O2 S -","- C52 H52 Cl4 N8 O8 S4 -","4","1","","Lu, Lei; Ma, Juan; Qu, Panpan; Li, Feng","Effective Recognition of Different Types of Amino Groups: From Aminobenzenesulfonamides to Amino-(N-alkyl)benzenesulfonamides via Iridium-Catalyzed N-Alkylation with Alcohols.","Organic letters","2015","17","10","2350","2353","10.1021/acs.orglett.5b00824","","","0.71073","MoKα","","0.0905","0.054","","","0.1473","0.168","","","","","","1.002","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520754","7.667","0.0006","8.7269","0.0006","17.0497","0.0013","88.1161","0.0018","89.15","0.002","62.1966","0.0018","1008.54","0.13","108","2","108","2","","","","","","","","5","P -1","-P 1","2","","","","- C23 H21 N O3 S2 -","- C23 H21 N O3 S2 -","- C46 H42 N2 O6 S4 -","2","1","","Miura, Tomoya; Funakoshi, Yuuta; Fujimoto, Yoshikazu; Nakahashi, Junki; Murakami, Masahiro","Facile synthesis of 2,5-disubstituted thiazoles from terminal alkynes, sulfonyl azides, and thionoesters.","Organic letters","2015","17","10","2454","2457","10.1021/acs.orglett.5b00960","","","0.71075","MoKα","","0.0862","0.0681","","","0.1743","0.1959","","","","","","1.129","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520755","52.579","0.011","21.835","0.004","29.598","0.006","90","","117.54","0.03","90","","30130","13","100","","100","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C270 H372 B6 N8 O30 -","- C270 H372 B6 N8 O30 -","- C1080 H1488 B24 N32 O120 -","4","0.5","","Danjo, Hiroshi; Kidena, Yuki; Kawahata, Masatoshi; Sato, Hiroyasu; Katagiri, Kosuke; Miyazawa, Toshifumi; Yamaguchi, Kentaro","Multilayered inclusion nanocycles of anionic spiroborates.","Organic letters","2015","17","10","2466","2469","10.1021/acs.orglett.5b00974","","","0.8","synchrotron","","0.2913","0.1493","","","0.3772","0.4696","","","","","","1.179","","","","has coordinates,has disorder","140043","2020-10-21","18:00:00",""
"1520756","7.702","0.0001","13.1321","0.0002","27.4999","0.0019","90","","90","","90","","2781.4","0.2","113","2","113","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C28 H44 O4 Si2 -","- C28 H44 O4 Si2 -","- C112 H176 O16 Si8 -","4","1","","Shi, Hang; Tan, Ceheng; Zhang, Weibin; Zhang, Zichun; Long, Rong; Luo, Tuoping; Yang, Zhen","Synthetic Progress toward Azadirachtins. 1. Enantio- and Diastereoselective Synthesis of the Left-Wing Fragment of 11-epi-Azadirachtin I.","Organic letters","2015","17","10","2342","2345","10.1021/acs.orglett.5b00829","","","1.54178","CuKα","","0.0375","0.0326","","","0.0727","0.0861","","","","","","1.143","","","","has coordinates","140044","2020-10-21","18:00:00",""
"1520757","17.7328","0.0009","8.7774","0.0004","13.0228","0.0007","90","","110.419","0.006","90","","1899.61","0.18","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C24 H20 O3 -","- C24 H20 O3 -","- C96 H80 O12 -","4","1","","Li, Mingliang; Yang, Yudong; Zhou, Danni; Wan, Danyang; You, Jingsong","Nickel-Catalyzed Addition-Type Alkenylation of Unactivated, Aliphatic C-H Bonds with Alkynes: A Concise Route to Polysubstituted γ-Butyrolactones.","Organic letters","2015","17","10","2546","2549","10.1021/acs.orglett.5b01128","","x-ray","0.71","MoKα","","0.0622","0.0571","","","0.1554","0.1641","","","","","","1.018","","","","has coordinates","140045","2020-10-21","18:00:00",""
"1520758","9.9044","0.001","11.8847","0.0011","11.9608","0.0011","60.57","0.005","81.21","0.006","75.803","0.005","1187.9","0.2","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H33 N O9 -","- C22 H33 N O9 -","- C44 H66 N2 O18 -","2","1","","Xu, Sanjia; Ciufolini, Marco A.","Formal Synthesis of (±)-Tetrodotoxin via the Oxidative Amidation of a Phenol: On the Structure of the Sato Lactone.","Organic letters","2015","17","10","2424","2427","10.1021/acs.orglett.5b00935","","x-ray","0.71073","MoKα","","0.0504","0.0383","","","0.0963","0.1033","","","","","","1.025","","","","has coordinates","140046","2020-10-21","18:00:00",""
"1520759","10.5221","0.0019","10.6666","0.0019","10.7161","0.0019","74.105","0.004","73.746","0.004","61.845","0.004","1003.6","0.3","90","2","90","2","","","","","","","","4","P -1","-P 1","2","","","","- C19 H27 N O10 -","- C19 H27 N O10 -","- C38 H54 N2 O20 -","2","1","","Xu, Sanjia; Ciufolini, Marco A.","Formal Synthesis of (±)-Tetrodotoxin via the Oxidative Amidation of a Phenol: On the Structure of the Sato Lactone.","Organic letters","2015","17","10","2424","2427","10.1021/acs.orglett.5b00935","","x-ray","0.71073","MoKα","","0.0642","0.0432","","","0.1043","0.1145","","","","","","1.014","","","","has coordinates","140047","2020-10-21","18:00:00",""
"1520760","8.1087","0.0006","11.9482","0.0009","20.232","0.0015","90","","90","","90","","1960.2","0.3","293","2","293","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C22 H36 O3 -","- C22 H36 O3 -","- C88 H144 O12 -","4","1","","Cheng, Shou-Ling; Jiang, Xiao-Ling; Shi, Yong; Tian, Wei-Sheng","Concise synthesis of the core structures of saundersiosides.","Organic letters","2015","17","10","2346","2349","10.1021/acs.orglett.5b00821","","","0.71073","MoKα","","0.0451","0.0412","","","0.102","0.1047","","","","","","1.05","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520761","7.3909","0.0007","12.9276","0.0012","25.254","0.002","90","","90","","90","","2412.9","0.4","293","2","293","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C26 H40 O5 -","- C26 H40 O5 -","- C104 H160 O20 -","4","1","","Cheng, Shou-Ling; Jiang, Xiao-Ling; Shi, Yong; Tian, Wei-Sheng","Concise synthesis of the core structures of saundersiosides.","Organic letters","2015","17","10","2346","2349","10.1021/acs.orglett.5b00821","","","0.71073","MoKα","","0.0435","0.0405","","","0.1091","0.1126","","","","","","1.03","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1520762","5.2667","0.0002","15.2534","0.0006","20.3019","0.0008","90","","90","","90","","1630.95","0.11","150","2","150","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C18 H23 N O4 -","- C18 H23 N O4 -","- C72 H92 N4 O16 -","4","1","","Lin, Cheng-Wei; Hong, Bor-Cherng; Chang, Wan-Chen; Lee, Gene-Hsiang","A New Approach to Nitrones through Cascade Reaction of Nitro Compounds Enabled by Visible Light Photoredox Catalysis.","Organic letters","2015","17","10","2314","2317","10.1021/acs.orglett.5b00684","","","0.71073","MoKα","","0.0698","0.0415","","","0.1009","0.108","","","","","","1.003","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1523614","24.4884","0.0013","7.9625","0.0004","18.5286","0.0011","90","","131.954","0.003","90","","2686.8","0.3","298","2","298","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C16 H13 N O4 -","- C16 H13 N O4 -","- C128 H104 N8 O32 -","8","1","","Verma, Akhilesh K.; Danodia, Abhinandan K.; Saunthwal, Rakesh K.; Patel, Monika; Choudhary, Deepak","Palladium-Catalyzed Triple Successive C-H Functionalization: Direct Synthesis of Functionalized Carbazoles from Indoles.","Organic letters","2015","17","15","3658","3661","10.1021/acs.orglett.5b01476","","","0.71073","MoKα","","0.046","0.0425","","","0.1039","0.1062","","","","","","1.108","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529193","9.823","0.002","10.177","0.002","11.186","0.002","92.48","0.03","113.89","0.03","100.8","0.03","995.5","0.4","298","","298","","","","","","","","","5","P -1","-P 1","2","","","","- C23 H20 Br N O2 -","- C23 H20 Br N O2 -","- C46 H40 Br2 N2 O4 -","2","1","","Sha, Qiang; Arman, Hadi; Doyle, Michael P.","Three-Component Cascade Reactions with 2,3-Diketoesters: A Novel Metal-Free Synthesis of 5-Vinyl-pyrrole and 4-Hydroxy-indole Derivatives.","Organic letters","2015","17","15","3876","3879","10.1021/acs.orglett.5b01855","","","0.71073","MoKα","","0.0547","0.0492","","","0.1299","0.1363","","","","","","1.04","","","","has coordinates","154768","2020-10-21","18:00:00",""
"1529249","9.4119","0.0002","7.6136","0.0002","18.3824","0.0005","90","","104.166","0.001","90","","1277.2","0.06","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C13 H18 N2 O4 -","- C13 H18 N2 O4 -","- C52 H72 N8 O16 -","4","1","","Diaba, Faïza; Montiel, Juan A.; Serban, Georgeta; Bonjoch, Josep","Synthesis of Normorphans through an Efficient Intramolecular Carbamoylation of Ketones.","Organic letters","2015","17","15","3860","3863","10.1021/acs.orglett.5b01832","","","0.71073","MoKα","","0.0905","0.0568","","","0.122","0.1328","","","","","","0.895","","","","has coordinates","154771","2020-10-21","18:00:00",""
"1529250","7.9657","0.0002","14.5166","0.0003","12.0126","0.0003","90","","90","","90","","1389.08","0.06","100","2","100","2","","","","","","","","5","P n a 21","P 2c -2n","33","","","","- C16 H16 Cl N O2 -","- C16 H16 Cl N O2 -","- C64 H64 Cl4 N4 O8 -","4","1","","Diaba, Faïza; Montiel, Juan A.; Serban, Georgeta; Bonjoch, Josep","Synthesis of Normorphans through an Efficient Intramolecular Carbamoylation of Ketones.","Organic letters","2015","17","15","3860","3863","10.1021/acs.orglett.5b01832","","","0.71073","MoKα","","0.0493","0.0467","","","0.1283","0.137","","","","","","1.098","","","","has coordinates","154771","2020-10-21","18:00:00",""
"1529257","11.1369","0.0006","12.7954","0.0006","13.7775","0.0006","90","","105.869","0.005","90","","1888.49","0.16","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C19 H20 N2 O5 S -","- C19 H20 N2 O5 S -","- C76 H80 N8 O20 S4 -","4","2","","Feng, Huan-Xi; Tan, Rui; Liu, Yan-Kai","An Efficient One-Pot Approach to the Construction of Chiral Nitrogen-Containing Heterocycles under Mild Conditions.","Organic letters","2015","17","15","3794","3797","10.1021/acs.orglett.5b01772","","","1.54184","CuKα","","0.07","0.0534","","","0.1288","0.1436","","","","","","1.048","","","","has coordinates","182022","2020-10-21","18:00:00",""
"1529280","8.8383","0.0014","21.101","0.002","6.6024","0.0008","90","","91.311","0.011","90","","1231","0.3","298","2","298","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C17 H13 N -","- C17 H13 N -","- C68 H52 N4 -","4","1","","Mandal, Sumana; Mahato, Sujit; Jana, Chandan K.","Direct β-C(sp(3))-H Functionalization of Aliphatic Amines to α,β-Unsaturated Imines, Aldehydes, and Chromenes.","Organic letters","2015","17","15","3762","3765","10.1021/acs.orglett.5b01744","","","0.71073","MoKα","","0.1363","0.0699","","","0.1329","0.1756","","","","","","1.062","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529281","17.7457","0.0008","5.8725","0.0003","20.1502","0.0009","90","","103.189","0.001","90","","2044.5","0.17","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C24 H21 N O4 S -","- C24 H21 N O4 S -","- C96 H84 N4 O16 S4 -","4","1","","Kuppusamy, Ramajayam; Gandeepan, Parthasarathy; Cheng, Chien-Hong","Rh(III)-Catalyzed [4 + 1] Annulations of 2-Hydroxy- and 2-Aminobenzaldehydes with Allenes: A Simple Method toward 3-Coumaranones and 3-Indolinones.","Organic letters","2015","17","15","3846","3849","10.1021/acs.orglett.5b01825","","","0.71073","MoKα","","0.0505","0.036","","","0.0841","0.0929","","","","","","1.028","","","","has coordinates","154765","2020-10-21","18:00:00",""
"1529282","29.2958","0.0017","6.1415","0.0003","15.5413","0.0009","90","","90","","90","","2796.2","0.3","100","2","100","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C17 H13 Br O2 -","- C17 H13 Br O2 -","- C136 H104 Br8 O16 -","8","2","","Kuppusamy, Ramajayam; Gandeepan, Parthasarathy; Cheng, Chien-Hong","Rh(III)-Catalyzed [4 + 1] Annulations of 2-Hydroxy- and 2-Aminobenzaldehydes with Allenes: A Simple Method toward 3-Coumaranones and 3-Indolinones.","Organic letters","2015","17","15","3846","3849","10.1021/acs.orglett.5b01825","","","0.71073","MoKα","","0.0492","0.0384","","","0.091","0.1152","","","","","","1.086","","","","has coordinates","214153","2020-10-21","18:00:00",""
"1529283","10.1466","0.0003","10.1835","0.0003","16.6612","0.0004","90","","90","","90","","1721.57","0.08","297","2","297","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C18 H27 N O4 -","- C18 H27 N O4 -","- C72 H108 N4 O16 -","4","1","","Lin, Kuo-Wei; Ananthan, Bakthavachalam; Tseng, Sheng-Fang; Yan, Tu-Hsin","Exceedingly Concise and Elegant Synthesis of (+)-Paniculatine, (-)-Magellanine, and (+)-Magellaninone.","Organic letters","2015","17","15","3938","3940","10.1021/acs.orglett.5b01975","","x-ray","0.71073","MoKα","","0.0684","0.0486","","","0.0997","0.1084","","","","","","1.019","","","","has coordinates","154770","2020-10-21","18:00:00",""
"1529284","8.2578","0.0003","7.6701","0.0003","12.4589","0.0005","90","","99.389","0.003","90","","778.55","0.05","110","2","110","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C17 H27 N O2 -","- C17 H27 N O2 -","- C34 H54 N2 O4 -","2","1","","Lin, Kuo-Wei; Ananthan, Bakthavachalam; Tseng, Sheng-Fang; Yan, Tu-Hsin","Exceedingly Concise and Elegant Synthesis of (+)-Paniculatine, (-)-Magellanine, and (+)-Magellaninone.","Organic letters","2015","17","15","3938","3940","10.1021/acs.orglett.5b01975","","","1.54178","CuKα","","0.0423","0.0389","","","0.1047","0.1103","","","","","","1.028","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529285","8.5383","0.0005","7.6057","0.0004","12.8523","0.0008","90","","104.589","0.007","90","","807.71","0.09","297","2","297","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C18 H25 N O4 -","- C18 H25 N O4 -","- C36 H50 N2 O8 -","2","1","","Lin, Kuo-Wei; Ananthan, Bakthavachalam; Tseng, Sheng-Fang; Yan, Tu-Hsin","Exceedingly Concise and Elegant Synthesis of (+)-Paniculatine, (-)-Magellanine, and (+)-Magellaninone.","Organic letters","2015","17","15","3938","3940","10.1021/acs.orglett.5b01975","","x-ray","0.71073","MoKα","","0.0517","0.0377","","","0.0666","0.0686","","","","","","0.986","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529293","8.8494","0.0015","10.974","0.002","17.557","0.004","90","","90","","90","","1705","0.6","93","","93","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C21 H22 N2 O2 -","- C21 H22 N2 O2 -","- C84 H88 N8 O8 -","4","1","","Komine, Keita; Nomura, Yusuke; Ishihara, Jun; Hatakeyama, Susumi","Total Synthesis of (-)-N-Methylwelwitindolinone C Isothiocyanate Based on a Pd-Catalyzed Tandem Enolate Coupling Strategy.","Organic letters","2015","17","15","3918","3921","10.1021/acs.orglett.5b01952","","","0.71075","MoKα","","","0.0317","","","","0.0791","","","","","","1.041","","","","has coordinates","154766","2020-10-21","18:00:00",""
"1529294","10.3796","0.0014","12.9633","0.0017","14.3864","0.0019","71.474","0.011","71.763","0.012","68.137","0.01","1661.2","0.4","93","","93","","","","","","","","","4","P -1","-P 1","2","","","","- C22 H20 N2 O -","- C22 H20 N2 O -","- C88 H80 N8 O4 -","4","2","","Komine, Keita; Nomura, Yusuke; Ishihara, Jun; Hatakeyama, Susumi","Total Synthesis of (-)-N-Methylwelwitindolinone C Isothiocyanate Based on a Pd-Catalyzed Tandem Enolate Coupling Strategy.","Organic letters","2015","17","15","3918","3921","10.1021/acs.orglett.5b01952","","","0.71075","MoKα","","","0.0565","","","","0.1773","","","","","","1.123","","","","has coordinates","154766","2020-10-21","18:00:00",""
"1529307","14.1631","0.0005","11.4869","0.0004","16.4977","0.0005","90","","94.808","0.001","90","","2674.57","0.16","176","2","176","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C29 H36 O7 Si -","- C29 H36 O7 Si -","- C116 H144 O28 Si4 -","4","1","","Sakata, Juri; Ando, Yoshio; Ohmori, Ken; Suzuki, Keisuke","Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle.","Organic letters","2015","17","15","3746","3749","10.1021/acs.orglett.5b01732","","","0.71075","MoKα","","0.0585","0.0498","","","0.1254","0.1311","","","","","","1.068","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529349","10.6416","0.0003","13.3076","0.0006","17.3445","0.0005","90","","92.328","0.002","90","","2454.2","0.15","293","2","293.15","","","","","","","","","7","P 1 21 1","P 2yb","4","","","","- C36 H62 Cl2 Cu2 O6 P2 S2 -","- C36 H62 Cl2 Cu2 O6 P2 S2 -","- C72 H124 Cl4 Cu4 O12 P4 S4 -","2","1","","Wang, Ding; Cao, Peng; Wang, Bing; Jia, Tao; Lou, Yazhou; Wang, Min; Liao, Jian","Copper(I)-Catalyzed Asymmetric Pinacolboryl Addition of N-Boc-imines Using a Chiral Sulfoxide-Phosphine Ligand.","Organic letters","2015","17","10","2420","2423","10.1021/acs.orglett.5b00934","","","0.71073","MoKα","","0.0651","0.0471","","","0.1096","0.1219","","","","","","1.023","","","","has coordinates","214153","2020-10-21","18:00:00",""
"1529350","11.4371","0.0003","13.3473","0.0003","22.4306","0.0007","90","","101.301","0.001","90","","3357.74","0.16","293","2","293","2","","","","","","","","7","I 1 2/a 1","-I 2ya","15","","","","- C16 H10 Br F3 N2 O2 S -","- C16 H10 Br F3 N2 O2 S -","- C128 H80 Br8 F24 N16 O16 S8 -","8","1","","Lee, Eunsook; Ryu, Taekyu; Shin, Eunji; Son, Jeong-Yu; Choi, Wonseok; Lee, Phil Ho","Synthesis of 2-bromoimidazoles from alkynes, N-sulfonylazides, and bromocyanides.","Organic letters","2015","17","10","2470","2473","10.1021/acs.orglett.5b00977","","","0.71073","MoKα","","0.0926","0.0665","","","0.1674","0.1872","","","","","","1.043","","","","has coordinates","152782","2020-10-21","18:00:00",""
"1529362","15.6612","0.0013","9.6881","0.0008","16.3377","0.001","90","","96.112","0.007","90","","2464.8","0.3","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C32 H22 N6 -","- C32 H22 N6 -","- C128 H88 N24 -","4","1","","Constantinides, Christos P.; Zissimou, Georgia A.; Berezin, Andrey A.; Ioannou, Theodosia A.; Manoli, Maria; Tsokkou, Demetra; Theodorou, Eleni; Hayes, Sophia C.; Koutentis, Panayiotis A.","Tetraphenylhexaazaanthracenes: 16π Weakly Antiaromatic Species with Singlet Ground States.","Organic letters","2015","17","16","4026","4029","10.1021/acs.orglett.5b01923","","","1.54184","CuKα","","0.055","0.0423","","","0.111","0.1202","","","","","","1.043","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529363","8.8511","0.0005","9.8863","0.0004","16.5742","0.0006","107.267","0.003","92.876","0.004","90.368","0.004","1382.87","0.11","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C34 H26 Cl2 N6 -","- C34 H26 Cl2 N6 -","- C68 H52 Cl4 N12 -","2","1","","Constantinides, Christos P.; Zissimou, Georgia A.; Berezin, Andrey A.; Ioannou, Theodosia A.; Manoli, Maria; Tsokkou, Demetra; Theodorou, Eleni; Hayes, Sophia C.; Koutentis, Panayiotis A.","Tetraphenylhexaazaanthracenes: 16π Weakly Antiaromatic Species with Singlet Ground States.","Organic letters","2015","17","16","4026","4029","10.1021/acs.orglett.5b01923","","","0.71073","MoKα","","0.0464","0.0412","","","0.1154","0.1206","","","","","","1.088","","","","has coordinates","154774","2020-10-21","18:00:00",""
"1529370","15.9","0.002","21.601","0.003","19.802","0.003","90","","110.332","0.003","90","","6377.4","1.5","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C22 H18 F3 N O4 S -","- C22 H18 F3 N O4 S -","- C264 H216 F36 N12 O48 S12 -","12","3","","Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun","Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.","Organic letters","2015","17","16","3944","3947","10.1021/acs.orglett.5b01474","","","0.71073","MoKα","","0.215","0.0809","","","0.1456","0.1928","","","","","","0.962","","","","has coordinates","154775","2020-10-21","18:00:00",""
"1529371","12.978","0.004","13.576","0.004","16.636","0.005","84.126","0.006","79.909","0.007","65.828","0.007","2631.2","1.4","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C28 H24 F3 N O5 S -","- C28 H24 F3 N O5 S -","- C112 H96 F12 N4 O20 S4 -","4","2","","Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun","Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.","Organic letters","2015","17","16","3944","3947","10.1021/acs.orglett.5b01474","","","0.71073","MoKα","","0.1123","0.0691","","","0.1698","0.1931","","","","","","1.032","","","","has coordinates","154775","2020-10-21","18:00:00",""
"1529372","15.6589","0.0011","9.9834","0.0007","16.2519","0.0012","90","","92.274","0.002","90","","2538.6","0.3","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C28 H24 F3 N O4 S -","- C28 H24 F3 N O4 S -","- C112 H96 F12 N4 O16 S4 -","4","1","","Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun","Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.","Organic letters","2015","17","16","3944","3947","10.1021/acs.orglett.5b01474","","","0.71073","MoKα","","0.1005","0.0489","","","0.106","0.1263","","","","","","0.961","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529373","10.562","0.0012","11.1083","0.0013","11.2554","0.0013","85.47","0.003","66.868","0.003","84.789","0.003","1208","0.2","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C24 H24 F3 N O4 S -","- C24 H24 F3 N O4 S -","- C48 H48 F6 N2 O8 S2 -","2","1","","Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun","Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.","Organic letters","2015","17","16","3944","3947","10.1021/acs.orglett.5b01474","","","0.71073","MoKα","","0.0786","0.0523","","","0.142","0.1614","","","","","","0.986","","","","has coordinates,has disorder","176428","2020-10-21","18:00:00",""
"1529374","11.5958","0.0016","12.0999","0.0017","14.031","0.002","90","","97.891","0.002","90","","1950","0.5","297","2","297","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C22 H20 N2 O2 S -","- C22 H20 N2 O2 S -","- C88 H80 N8 O8 S4 -","4","1","","Zeng, Ting-Ting; Xuan, Jun; Ding, Wei; Wang, Kuan; Lu, Liang-Qiu; Xiao, Wen-Jing","[3 + 2] Cycloaddition/Oxidative Aromatization Sequence via Photoredox Catalysis: One-Pot Synthesis of Oxazoles from 2H-Azirines and Aldehydes.","Organic letters","2015","17","16","4070","4073","10.1021/acs.orglett.5b01994","","","0.71073","MoKα","","0.0693","0.0529","","","0.1371","0.1551","","","","","","1.04","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529381","29.3719","0.0016","14.1615","0.0008","33.703","0.0018","90","","101.172","0.0008","90","","13753.1","1.3","150","2","150","2","","","","","","","","7","C 1 2/c 1","-C 2yc","15","","Potassium CB4(acetone) chloride hydrate","","- C114 H172 Cl K Li0 N47 O38 -","- C114 H146 K N32 O37.884 -","- C456 H584 K4 N128 O151.536 -","4","0.5","","Lu, Xiaoyong; Isaacs, Lyle","Synthesis and Recognition Properties of Enantiomerically Pure Acyclic Cucurbit[n]uril-Type Molecular Containers.","Organic letters","2015","17","16","4038","4041","10.1021/acs.orglett.5b01948","","","0.71073","MoKα","","0.1194","0.0984","","","0.1979","0.2062","","","","","","1.272","","","","has coordinates,has disorder","176428","2020-10-21","18:00:00",""
"1529393","6.9051","0.0007","18.0332","0.0019","18.2794","0.0019","90","","90","","90","","2276.2","0.4","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C25 H24 Cl N O5 -","- C25 H24 Cl N O5 -","- C100 H96 Cl4 N4 O20 -","4","1","","Liu, Qiong-Jie; Yan, Wen-Guang; Wang, Lijia; Zhang, X. Peter; Tang, Yong","One-Pot Catalytic Asymmetric Synthesis of Tetrahydrocarbazoles.","Organic letters","2015","17","16","4014","4017","10.1021/acs.orglett.5b01909","","","0.71073","MoKα","","0.0504","0.0376","","","0.0909","0.0989","","","","","","1.019","","","","has coordinates","154777","2020-10-21","18:00:00",""
"1529398","31.5153","0.0016","8.7548","0.0005","18.0436","0.001","90","","123.435","0.001","90","","4154.5","0.4","296","2","296","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C25 H23 N O6 -","- C25 H23 N O6 -","- C200 H184 N8 O48 -","8","1","","Huang, Jing-Kai; Yang Lauderdale, Tsai-Ling; Shia, Kak-Shan","Studies on Antibiotics Active against Resistant Bacteria. Total Synthesis of MRSA-Active Tetarimycin A and Its Analogues.","Organic letters","2015","17","17","4248","4251","10.1021/acs.orglett.5b02039","","","0.71073","MoKα","","0.0737","0.0434","","","0.0996","0.112","","","","","","1.012","","","","has coordinates","154790","2020-10-21","18:00:00",""
"1529399","16.4511","0.0005","17.491","0.0005","13.5624","0.0004","90","","98.856","0.0013","90","","3856","0.2","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C55 H35 B F2 N2 -","- C55 H35 B F2 N2 -","- C220 H140 B4 F8 N8 -","4","1","","Chua, Ming Hui; Huang, Kuo-Wei; Xu, Jianwei; Wu, Jishan","Unusual Intramolecular Hydrogen Transfer in 3,5-Di(triphenylethylenyl) BODIPY Synthesis and 1,2-Migratory Shift in Subsequent Scholl Type Reaction.","Organic letters","2015","17","17","4168","4171","10.1021/acs.orglett.5b01916","","","1.54178","CuKα","","0.0682","0.0506","","","0.1206","0.1292","","","","","","1.064","","","","has coordinates","154792","2020-10-21","18:00:00",""
"1529400","13.1321","0.0003","10.7218","0.0003","30.2961","0.0008","90","","96.85","0.001","90","","4235.23","0.19","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C55 H36 B F7 N2 -","- C55 H36 B F7 N2 -","- C220 H144 B4 F28 N8 -","4","1","","Chua, Ming Hui; Huang, Kuo-Wei; Xu, Jianwei; Wu, Jishan","Unusual Intramolecular Hydrogen Transfer in 3,5-Di(triphenylethylenyl) BODIPY Synthesis and 1,2-Migratory Shift in Subsequent Scholl Type Reaction.","Organic letters","2015","17","17","4168","4171","10.1021/acs.orglett.5b01916","","","1.54178","CuKα","","0.0584","0.0475","","","0.1353","0.1618","","","","","","1.097","","","","has coordinates","154792","2020-10-21","18:00:00",""
"1529401","21.491","0.0004","13.7296","0.0003","29.3488","0.0006","90","","106.144","0.002","90","","8318.3","0.3","173","2","173","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C55 H41 B F2 N2 -","- C55 H40.52 B F2 N2 -","- C440 H324.16 B8 F16 N16 -","8","1","","Chua, Ming Hui; Huang, Kuo-Wei; Xu, Jianwei; Wu, Jishan","Unusual Intramolecular Hydrogen Transfer in 3,5-Di(triphenylethylenyl) BODIPY Synthesis and 1,2-Migratory Shift in Subsequent Scholl Type Reaction.","Organic letters","2015","17","17","4168","4171","10.1021/acs.orglett.5b01916","","","0.71073","MoKα","","0.0626","0.0604","","","0.1551","0.1582","","","","","","1.082","","","","has coordinates,has disorder","154792","2020-10-21","18:00:00",""
"1529402","5.225","0.0004","13.44","0.0011","11.8487","0.001","90","","90.133","0.002","90","","832.06","0.12","200","2","200","2","","","","","","","","5","P 1 21 1","P 2yb","4","wd154","","","- C19 H20 Br N O -","- C19 H20 Br N O -","- C38 H40 Br2 N2 O2 -","2","1","","Dziechciejewski, Wojciech J.; Weber, Regina; Sowada, Oliver; Boysen, Mike M. K.","Cycloalkene Carbonitriles in Rhodium-Catalyzed 1,4-Addition and Formal Synthesis of Vabicaserin.","Organic letters","2015","17","17","4132","4135","10.1021/acs.orglett.5b01849","","","0.71073","MoKα","","0.0485","0.0464","","","0.1197","0.1215","","","","","","1.087","","","","has coordinates","154795","2020-10-21","18:00:00",""
"1529420","13.1195","0.0009","25.1207","0.0017","6.0786","0.0004","90","","103.299","0.007","90","","1949.6","0.2","173","","173","","","","","","","","","6","C 1 c 1","C -2yc","9","","","","- C21 H23 Cl F2 N2 O -","- C21 H23 Cl F2 N2 O -","- C84 H92 Cl4 F8 N8 O4 -","4","1","","Chen, Qiao; Zhou, Jiawei; Wang, Yanan; Wang, Chao; Liu, Xihong; Xu, Zhaoqing; Lin, Li; Wang, Rui","Transition-Metal-Free Dehydrosilylative Difluoroamidation of Tetrahydroisoquinolines under Mild Conditions.","Organic letters","2015","17","17","4212","4215","10.1021/acs.orglett.5b01997","","x-ray","0.71073","MoKα","","0.0519","0.0412","","","0.0815","0.0889","","","","","","1.044","","","","has coordinates","154789","2020-10-21","18:00:00",""
"1529421","5.917","0.0015","7.864","0.002","13.651","0.003","90","","101.24","0.003","90","","623","0.3","193","2","193","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C13 H18 O4 -","- C13 H18 O4 -","- C26 H36 O8 -","2","1","","Rybak, Taras; Hall, Dennis G.","Stereoselective and Regiodivergent Allylic Suzuki-Miyaura Cross-Coupling of 2-Ethoxydihydropyranyl Boronates: Synthesis and Confirmation of Absolute Stereochemistry of Diospongin B.","Organic letters","2015","17","17","4156","4159","10.1021/acs.orglett.5b01906","","","0.71073","MoKα","","0.0521","0.0407","","","0.0949","0.0997","","","","","","1.035","","","","has coordinates","154793","2020-10-21","18:00:00",""
"1529422","9.7101","0.0004","10.6909","0.0005","23.0359","0.001","90","","92.6548","0.0019","90","","2388.78","0.18","173","2","173","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","ethyl 2,3-dideoxy-3-phenylpentopyranoside","","- C13 H18 O3 -","- C13 H18 O3 -","- C104 H144 O24 -","8","2","","Rybak, Taras; Hall, Dennis G.","Stereoselective and Regiodivergent Allylic Suzuki-Miyaura Cross-Coupling of 2-Ethoxydihydropyranyl Boronates: Synthesis and Confirmation of Absolute Stereochemistry of Diospongin B.","Organic letters","2015","17","17","4156","4159","10.1021/acs.orglett.5b01906","","","1.54178","CuKα","","0.0369","0.0358","","","0.0962","0.0971","","","","","","1.036","","","","has coordinates","154793","2020-10-21","18:00:00",""
"1529423","18.021","0.004","10.891","0.002","18.559","0.004","90","","103.69","0.03","90","","3539","1.4","113","2","113","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C42 H33 Cl2 Ir N2 O5 -","- C42 H33 Cl2 Ir N2 O5 -","- C168 H132 Cl8 Ir4 N8 O20 -","4","1","","Zhou, Tao; Li, Liubo; Li, Bin; Song, Haibin; Wang, Baiquan","Ir(III)-Catalyzed Oxidative Coupling of NH Isoquinolones with Benzoquinone.","Organic letters","2015","17","17","4204","4207","10.1021/acs.orglett.5b01974","","","0.71073","MoKα","","0.0409","0.0344","","","0.0922","0.0964","","","","","","1.11","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529424","10.069","0.002","10.87","0.002","12.021","0.002","71.67","0.03","82.11","0.03","82.87","0.03","1232.5","0.5","113","2","113","2","","","","","","","","5","P -1","-P 1","2","","","","- C28 H18 Cl2 N2 O5 -","- C28 H18 Cl2 N2 O5 -","- C56 H36 Cl4 N4 O10 -","2","1","","Zhou, Tao; Li, Liubo; Li, Bin; Song, Haibin; Wang, Baiquan","Ir(III)-Catalyzed Oxidative Coupling of NH Isoquinolones with Benzoquinone.","Organic letters","2015","17","17","4204","4207","10.1021/acs.orglett.5b01974","","","0.71073","MoKα","","0.1183","0.0617","","","0.1778","0.2113","","","","","","1.06","","","","has coordinates","154794","2020-10-21","18:00:00",""
"1529448","11.1941","0.0017","11.9877","0.0018","12.3151","0.0019","117.921","0.002","101.02","0.002","90.422","0.002","1424.3","0.4","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","Organics","","- C15 H18 Cl N O2 -","- C15 H18 Cl N O2 -","- C60 H72 Cl4 N4 O8 -","4","2","","Deng, Yongming; Jing, Changcheng; Zavalij, Peter Y.; Doyle, Michael P.","Hg(OTf)2 Catalyzed Intramolecular 1,4-Addition of Donor-Acceptor Cyclopropenes to Arenes.","Organic letters","2015","17","17","4312","4315","10.1021/acs.orglett.5b02129","","","0.71073","MoKα","","0.0641","0.0467","","","0.0928","0.1019","","","","","","1.005","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529469","6.212","0.002","12.231","0.003","28.133","0.007","90","","90","","90","","2137.5","1","295","2","295","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C22 H35 N O3 -","- C22 H35 N O3 -","- C88 H140 N4 O12 -","4","1","","Zhang, Dewu; Tao, Xiaoyu; Chen, Ridao; Liu, Jimei; Li, Li; Fang, Xiaomei; Yu, Liyan; Dai, Jungui","Pericoannosin A, a Polyketide Synthase-Nonribosomal Peptide Synthetase Hybrid Metabolite with New Carbon Skeleton from the Endophytic Fungus Periconia sp.","Organic letters","2015","17","17","4304","4307","10.1021/acs.orglett.5b02123","","","1.54187","CuKα","","0.0404","0.0391","","","0.1037","0.1049","","","","","","1.044","","","","has coordinates","154787","2020-10-21","18:00:00",""
"1529470","12.515","0.003","14.907","0.002","45.898","0.006","90","","90","","90","","8563","3","293","2","295","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C22 H33 N O3.5 -","- C22 H33 N O3.5 -","- C352 H528 N16 O56 -","16","4","","Zhang, Dewu; Tao, Xiaoyu; Chen, Ridao; Liu, Jimei; Li, Li; Fang, Xiaomei; Yu, Liyan; Dai, Jungui","Pericoannosin A, a Polyketide Synthase-Nonribosomal Peptide Synthetase Hybrid Metabolite with New Carbon Skeleton from the Endophytic Fungus Periconia sp.","Organic letters","2015","17","17","4304","4307","10.1021/acs.orglett.5b02123","","","1.54178","CuKα","","0.0719","0.06","","","0.1566","0.1713","","","","","","1.083","","","","has coordinates","176429","2020-10-21","18:00:00",""
"1529473","7.7823","0.0008","10.8987","0.0012","15.2414","0.0018","72.781","0.01","83.016","0.009","85.094","0.009","1224","0.2","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C28 H29 N5 O4 -","- C28 H29 N5 O4 -","- C56 H58 N10 O8 -","2","1","","Samanta, Ritwik; Kumar, B. Sathish; Panda, Pradeepta K.","Calix[4]pyrroles with Shortest Possible Strap: Exclusively Selective toward Fluoride Ion.","Organic letters","2015","17","17","4140","4143","10.1021/acs.orglett.5b01866","","","0.71073","MoKα","","0.1535","0.0722","","","0.1383","0.1848","","","","","","1.039","","","","has coordinates","154791","2020-10-21","18:00:00",""
"1529503","8.374","0.003","10.228","0.004","16.064","0.007","99.954","0.007","98.372","0.007","101.416","0.007","1305.1","0.9","298","2","298","2","","","","","","","","7","P -1","-P 1","2","","","","- C25 H22 Cl3 F3 N2 O2 S -","- C25 H22 Cl3 F3 N2 O2 S -","- C50 H44 Cl6 F6 N4 O4 S2 -","2","1","","Wei, Qiang; Chen, Jia-Rong; Hu, Xiao-Qiang; Yang, Xiao-Chen; Lu, Bin; Xiao, Wen-Jing","Photocatalytic Radical Trifluoromethylation/Cyclization Cascade: Synthesis of CF3-Containing Pyrazolines and Isoxazolines.","Organic letters","2015","17","18","4464","4467","10.1021/acs.orglett.5b02118","","","0.71073","MoKα","","0.0983","0.0618","","","0.1519","0.1806","","","","","","1.016","","","","has coordinates,has disorder","176428","2020-10-21","18:00:00",""
"1529847","9.702","0.003","7.4213","0.0019","12.862","0.004","90","","103.265","0.005","90","","901.4","0.5","93","","93","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C21 H22 N2 O2 -","- C21 H22 N2 O2 -","- C42 H44 N4 O4 -","2","1","","Komine, Keita; Nomura, Yusuke; Ishihara, Jun; Hatakeyama, Susumi","Total Synthesis of (-)-N-Methylwelwitindolinone C Isothiocyanate Based on a Pd-Catalyzed Tandem Enolate Coupling Strategy.","Organic letters","2015","17","15","3918","3921","10.1021/acs.orglett.5b01952","","","0.71075","MoKα","","","0.0396","","","","0.0959","","","","","","1.05","","","","has coordinates","154506","2020-10-21","18:00:00",""
"1529848","13.5566","0.0009","9.9192","0.0006","12.1878","0.0009","90","","114.983","0.001","90","","1485.55","0.17","173","2","173","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C17 H20 O6 -","- C17 H20 O6 -","- C68 H80 O24 -","4","1","","Sakata, Juri; Ando, Yoshio; Ohmori, Ken; Suzuki, Keisuke","Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle.","Organic letters","2015","17","15","3746","3749","10.1021/acs.orglett.5b01732","","","0.71075","MoKα","","0.0654","0.0618","","","0.1477","0.1519","","","","","","1.113","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529849","9.8958","0.0004","32.0974","0.0012","20.6189","0.0009","90","","92.873","0.002","90","","6540.9","0.5","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C37 H54 O6 Si -","- C34 H47 O6 Si -","- C272 H376 O48 Si8 -","8","2","","Sakata, Juri; Ando, Yoshio; Ohmori, Ken; Suzuki, Keisuke","Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle.","Organic letters","2015","17","15","3746","3749","10.1021/acs.orglett.5b01732","","","0.71075","MoKα","","0.0934","0.0642","","","0.1518","0.1698","","","","","","1.05","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529850","15.027","0.003","8.8571","0.0017","11.123","0.003","90","","96.542","0.002","90","","1470.8","0.6","153","","153","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H12 Br F2 N3 -","- C16 H12 Br F2 N3 -","- C64 H48 Br4 F8 N12 -","4","1","","Okusu, Satoshi; Tokunaga, Etsuko; Shibata, Norio","Difluoromethylation of Terminal Alkynes by Fluoroform.","Organic letters","2015","17","15","3802","3805","10.1021/acs.orglett.5b01778","","","0.71075","MoKα","","","0.0732","","","","0.2197","","","","","","1.134","","","","has coordinates","154509","2020-10-21","18:00:00",""
"1529851","17.957","0.004","6.8848","0.0014","22.81","0.005","90","","99.781","0.003","90","","2779","1","153","","153","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C16 H10 Br F2 N O -","- C16 H10 Br F2 N O -","- C128 H80 Br8 F16 N8 O8 -","8","2","","Okusu, Satoshi; Tokunaga, Etsuko; Shibata, Norio","Difluoromethylation of Terminal Alkynes by Fluoroform.","Organic letters","2015","17","15","3802","3805","10.1021/acs.orglett.5b01778","","","0.71075","MoKα","","","0.0681","","","","0.2071","","","","","","1.105","","","","has coordinates","154510","2020-10-21","18:00:00",""
"1529852","19.3661","0.0007","14.8237","0.0006","28.5913","0.0013","90","","90","","90","","8207.9","0.6","150","2","150","2","","","","","","","","8","P n a 21","P 2c -2n","33","","","","- C43 H37 Br2 Cl Cu N3 O4 P2 -","- C43 H37 Br2 Cl Cu N3 O4 P2 -","- C344 H296 Br16 Cl8 Cu8 N24 O32 P16 -","8","2","","Ramakrishna, Kankanala; Murali, Mani; Sivasankar, Chinnappan","Chemoselective Carbene insertion into the N-H Bond over O-H Bond Using a Well-Defined Single Site (P-P)Cu(I) Catalyst.","Organic letters","2015","17","15","3814","3817","10.1021/acs.orglett.5b01776","","","0.7107","MoKα","","0.1201","0.0728","","","0.1676","0.1992","","","","","","1.021","","","","has coordinates","154511","2020-10-21","18:00:00",""
"1529853","5.7487","0.0005","9.5873","0.0008","13.7161","0.0011","85.932","0.007","86.522","0.007","90.042","0.007","752.65","0.11","200","2","200","2","","","","","","","","4","P -1","-P 1","2","","","","- C17 H19 N O3 -","- C17 H19 N O3 -","- C34 H38 N2 O6 -","2","1","","Ramakrishna, Kankanala; Murali, Mani; Sivasankar, Chinnappan","Chemoselective Carbene insertion into the N-H Bond over O-H Bond Using a Well-Defined Single Site (P-P)Cu(I) Catalyst.","Organic letters","2015","17","15","3814","3817","10.1021/acs.orglett.5b01776","","","0.71073","MoKα","","0.1299","0.0635","","","0.1427","0.178","","","","","","1.025","","","","has coordinates","154511","2020-10-21","18:00:00",""
"1529854","7.9153","0.0009","11.4655","0.0013","18.152","0.002","90","","90","","90","","1647.3","0.3","130","","130","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C18 H16 Br N O3 S -","- C18 H16 Br N O3 S -","- C72 H64 Br4 N4 O12 S4 -","4","1","","Xiao, Yonglong; Wang, Jinxin; Xia, Wenjing; Shu, Shuangjie; Jiao, Shenchao; Zhou, Yu; Liu, Hong","γ-Carbon Activation through N-Heterocyclic Carbene/Brønsted Acids Cooperative Catalysis: A Highly Enantioselective Route to δ-Lactams.","Organic letters","2015","17","15","3850","3853","10.1021/acs.orglett.5b01827","","","0.71073","MoKα","","0.0505","0.0354","","","0.0679","0.0718","","","","","","0.989","","","","has coordinates","154512","2020-10-21","18:00:00",""
"1529855","9.919","0.002","19.032","0.004","11.221","0.002","90","","102.942","0.005","90","","2064.5","0.7","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C26 H18 N2 O S -","- C26 H18 N2 O S -","- C104 H72 N8 O4 S4 -","4","1","","Zhu, Yuelu; Li, Cheng; Zhang, Jidong; She, Mengyao; Sun, Wei; Wan, Kerou; Wang, Yaqi; Yin, Bin; Liu, Ping; Li, Jianli","A Facile FeCl3/I2-Catalyzed Aerobic Oxidative Coupling Reaction: Synthesis of Tetrasubstituted Imidazoles from Amidines and Chalcones.","Organic letters","2015","17","15","3872","3875","10.1021/acs.orglett.5b01854","","","0.71073","MoKα","","0.0993","0.051","","","0.089","0.1055","","","","","","1.008","","","","has coordinates,has disorder","154513","2020-10-21","18:00:00",""
"1529856","9.724","0.003","11.142","0.003","12.91","0.004","98.826","0.005","103.604","0.005","112.844","0.005","1205.2","0.6","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C29 H21 Br N2 O -","- C29 H21 Br N2 O -","- C58 H42 Br2 N4 O2 -","2","1","","Zhu, Yuelu; Li, Cheng; Zhang, Jidong; She, Mengyao; Sun, Wei; Wan, Kerou; Wang, Yaqi; Yin, Bin; Liu, Ping; Li, Jianli","A Facile FeCl3/I2-Catalyzed Aerobic Oxidative Coupling Reaction: Synthesis of Tetrasubstituted Imidazoles from Amidines and Chalcones.","Organic letters","2015","17","15","3872","3875","10.1021/acs.orglett.5b01854","","","0.71073","MoKα","","0.1502","0.0613","","","0.1531","0.2146","","","","","","0.997","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529857","6.8305","0.0002","13.7709","0.0006","21.5589","0.0008","90","","90","","90","","2027.88","0.13","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C20 H22 N2 O5 S -","- C20 H22 N2 O5 S -","- C80 H88 N8 O20 S4 -","4","1","","Rao, Wei-Hao; Yin, Xue-Song; Shi, Bing-Feng","Catalyst-Controlled Amino- versus Oxy-Acetoxylation of Urea-Tethered Alkenes: Efficient Synthesis of Cyclic Ureas and Isoureas.","Organic letters","2015","17","15","3758","3761","10.1021/acs.orglett.5b01741","","","0.71073","MoKα","","0.0532","0.0361","","","0.0772","0.0915","","","","","","1.005","","","","has coordinates","154515","2020-10-21","18:00:00",""
"1529858","5.9849","0.0003","8.35","0.0004","21.2894","0.001","90.789","0.002","92.849","0.002","107.436","0.006","1013.32","0.09","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C20 H22 N2 O5 S -","- C20 H22 N2 O5 S -","- C40 H44 N4 O10 S2 -","2","1","","Rao, Wei-Hao; Yin, Xue-Song; Shi, Bing-Feng","Catalyst-Controlled Amino- versus Oxy-Acetoxylation of Urea-Tethered Alkenes: Efficient Synthesis of Cyclic Ureas and Isoureas.","Organic letters","2015","17","15","3758","3761","10.1021/acs.orglett.5b01741","","","0.71073","MoKα","","0.0989","0.0519","","","0.1305","0.1808","","","","","","1.001","","","","has coordinates","154516","2020-10-21","18:00:00",""
"1529859","12.075","0.0014","12.075","0.0014","26.601","0.003","90","","90","","120","","3358.9","0.7","296","2","296","2","","","","","","","","6","P 32 2 1","P 32 2""","154","","","","- C24 H17 Br F3 N O4 -","- C24 H17 Br F3 N O4 -","- C144 H102 Br6 F18 N6 O24 -","6","1","","Zhu, Yuanyuan; Li, Xiaoyuan; Chen, Qiao; Su, Jinhuan; Jia, Fengjing; Qiu, Shuai; Ma, Mingxia; Sun, Quantao; Yan, Wenjin; Wang, Kairong; Wang, Rui","Highly Enantioselective Cascade Reaction Catalyzed by Squaramides: the Synthesis of CF3-Containing Chromanes.","Organic letters","2015","17","15","3826","3829","10.1021/acs.orglett.5b01799","","","0.71073","MoKα","","0.098","0.0566","","","0.1192","0.1357","","","","","","1.008","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529860","10.916","0.002","12.171","0.002","27.176","0.005","90","","90","","90","","3610.6","1.1","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C18 H13 Cl F3 N O4 -","- C18 H13 Cl F3 N O4 -","- C144 H104 Cl8 F24 N8 O32 -","8","2","","Zhu, Yuanyuan; Li, Xiaoyuan; Chen, Qiao; Su, Jinhuan; Jia, Fengjing; Qiu, Shuai; Ma, Mingxia; Sun, Quantao; Yan, Wenjin; Wang, Kairong; Wang, Rui","Highly Enantioselective Cascade Reaction Catalyzed by Squaramides: the Synthesis of CF3-Containing Chromanes.","Organic letters","2015","17","15","3826","3829","10.1021/acs.orglett.5b01799","","","0.71073","MoKα","","0.088","0.0589","","","0.1249","0.1409","","","","","","1.004","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529861","8.3159","0.0007","9.4678","0.0007","23.6499","0.0018","90","","90","","90","","1862","0.3","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C19 H15 Br F3 N O4 -","- C19 H15 Br F3 N O4 -","- C76 H60 Br4 F12 N4 O16 -","4","1","","Zhu, Yuanyuan; Li, Xiaoyuan; Chen, Qiao; Su, Jinhuan; Jia, Fengjing; Qiu, Shuai; Ma, Mingxia; Sun, Quantao; Yan, Wenjin; Wang, Kairong; Wang, Rui","Highly Enantioselective Cascade Reaction Catalyzed by Squaramides: the Synthesis of CF3-Containing Chromanes.","Organic letters","2015","17","15","3826","3829","10.1021/acs.orglett.5b01799","","","0.71073","MoKα","","0.0373","0.0307","","","0.0764","0.0799","","","","","","1.004","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529862","11.943","0.002","12.618","0.003","14.512","0.003","90","","90.2","0.03","90","","2186.9","0.8","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C25 H22 F N3 O3 -","- C25 H22 F N3 O3 -","- C100 H88 F4 N12 O12 -","4","1","","Miao, Jinmin; Yang, Ke; Kurek, Martin; Ge, Haibo","Palladium-Catalyzed Site-Selective Fluorination of Unactivated C(sp(3))-H Bonds.","Organic letters","2015","17","15","3738","3741","10.1021/acs.orglett.5b01710","","","0.71073","MoKα","","0.1521","0.0676","","","0.1345","0.1626","","","","","","1.006","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529863","12.3364","0.0006","8.7782","0.0004","36.9717","0.0014","90","","90","","90","","4003.7","0.3","100","2","100","2","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C25 H26 O2 -","- C25 H26 O2 -","- C200 H208 O16 -","8","1","","Ackrill, Thomas D.; Sparkes, Hazel A.; Willis, Christine L.","Synthesis of Diarylheptanoid Scaffolds Inspired by Calyxins I and J.","Organic letters","2015","17","15","3884","3887","10.1021/acs.orglett.5b01848","","","0.71073","MoKα","","0.1412","0.0598","","","0.117","0.15","","","","","","0.999","","","","has coordinates","154521","2020-10-21","18:00:00",""
"1529864","7.0588","0.0002","11.869","0.0003","15.6316","0.0004","105.145","0.002","101.933","0.002","100.657","0.002","1196.58","0.06","100","","100","","","","","","","","","3","P -1","-P 1","2","","","","- C32 H30 O2 -","- C32 H30 O2 -","- C64 H60 O4 -","2","1","","Ackrill, Thomas D.; Sparkes, Hazel A.; Willis, Christine L.","Synthesis of Diarylheptanoid Scaffolds Inspired by Calyxins I and J.","Organic letters","2015","17","15","3884","3887","10.1021/acs.orglett.5b01848","","","0.71073","MoKα","","0.0937","0.0521","","","0.105","0.1235","","","","","","1.03","","","","has coordinates","154521","2020-10-21","18:00:00",""
"1529865","14.7165","0.0004","5.7937","0.0001","33.4045","0.0008","90","","101.755","0.001","90","","2788.43","0.11","100","2","100","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C35 H36 O5 -","- C35 H36 O5 -","- C140 H144 O20 -","4","1","","Ackrill, Thomas D.; Sparkes, Hazel A.; Willis, Christine L.","Synthesis of Diarylheptanoid Scaffolds Inspired by Calyxins I and J.","Organic letters","2015","17","15","3884","3887","10.1021/acs.orglett.5b01848","","","0.71073","MoKα","","0.0659","0.0416","","","0.0865","0.097","","","","","","1.011","","","","has coordinates","154521","2020-10-21","18:00:00",""
"1529866","9.2832","0.0019","10.302","0.002","12.39","0.002","76.387","0.004","83.994","0.005","64.267","0.004","1037.4","0.3","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C24 H23 N O3 S -","- C24 H23 N O3 S -","- C48 H46 N2 O6 S2 -","2","1","","Zhang, Xiaojuan; Han, Xiuling; Lu, Xiyan","Cationic Pd(II)-Catalyzed Cyclization of N-Tosyl-aniline Tethered Allenyl Aldehydes with Arylboronic Acids: Diastereo- and Enantioselective Synthesis of Tetrahydroquinoline Derivatives.","Organic letters","2015","17","15","3910","3913","10.1021/acs.orglett.5b01894","","","0.71073","MoKα","","0.0793","0.0515","","","0.1285","0.148","","","","","","1.026","","","","has coordinates","154522","2020-10-21","18:00:00",""
"1529867","17.622","0.005","17.622","0.005","37.634","0.011","90","","90","","120","","10121","5","150","","150","","","","","","","","","6","R -3 :H","-R 3","148","","","","- C66 H60 Cl9 N6 O6 P3 -","- C66 H60 Cl9 N6 O6 P3 -","- C396 H360 Cl54 N36 O36 P18 -","6","0.333333","","Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao","Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution.","Organic letters","2015","17","15","3650","3653","10.1021/acs.orglett.5b01455","","","0.71073","MoKα","","0.088","0.0459","","","0.1168","0.1465","","","","","","1.042","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529868","13.721","0.005","14.84","0.006","15.073","0.006","94.518","0.005","91.104","0.005","100.582","0.005","3006","2","100","","100","","","","","","","","","5","P -1","-P 1","2","","","","- C67 H65 N6 O8 P3 -","- C67 H65 N6 O8 P3 -","- C134 H130 N12 O16 P6 -","2","1","","Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao","Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution.","Organic letters","2015","17","15","3650","3653","10.1021/acs.orglett.5b01455","","","0.71073","MoKα","","0.085","0.0455","","","0.1078","0.1235","","","","","","0.985","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529869","13.731","0.003","14.962","0.003","15.117","0.003","94.572","0.003","91.24","0.003","101.538","0.003","3031","1.1","100","","100","","","","","","","","","5","P -1","-P 1","2","","","","- C67 H63 N8 O6 P3 -","- C67 H63 N8 O6 P3 -","- C134 H126 N16 O12 P6 -","2","1","","Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao","Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution.","Organic letters","2015","17","15","3650","3653","10.1021/acs.orglett.5b01455","","","0.71073","MoKα","","0.0903","0.0539","","","0.1387","0.1572","","","","","","1.046","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529870","12.58","0.004","13.197","0.004","19.419","0.006","80.816","0.005","80.935","0.004","69.837","0.004","2969.2","1.6","100","","100","","","","","","","","","5","P -1","-P 1","2","","","","- C66 H65 N6 O7 P3 -","- C66 H65 N6 O7 P3 -","- C132 H130 N12 O14 P6 -","2","1","","Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao","Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution.","Organic letters","2015","17","15","3650","3653","10.1021/acs.orglett.5b01455","","","0.71073","MoKα","","0.0931","0.0593","","","0.1702","0.2191","","","","","","0.786","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529871","13.914","0.003","13.914","0.003","28.339","0.007","90","","90","","120","","4751.4","1.9","100","","100","","","","","","","","","5","P 31","P 31","144","","","","- C63 H57 N6 O9 P3 -","- C63 H57 N6 O9 P3 -","- C189 H171 N18 O27 P9 -","3","1","","Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao","Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution.","Organic letters","2015","17","15","3650","3653","10.1021/acs.orglett.5b01455","","","0.71073","MoKα","","0.1493","0.1137","","","0.2886","0.3204","","","","","","1.196","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529872","13.123","0.002","13.188","0.002","19.257","0.003","73.751","0.002","79.26","0.002","66.588","0.002","2925.5","0.8","100","","100","","","","","","","","","6","P -1","-P 1","2","","","","- C65 H63 N6 O7 P3 S -","- C65 H63 N6 O7 P3 S -","- C130 H126 N12 O14 P6 S2 -","2","1","","Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao","Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution.","Organic letters","2015","17","15","3650","3653","10.1021/acs.orglett.5b01455","","","0.71073","MoKα","","0.0531","0.0378","","","0.0914","0.1017","","","","","","1.04","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529873","11.5233","0.0013","7.6374","0.0008","11.6452","0.0013","90","","110.244","0.002","90","","961.56","0.18","294","2","294","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C20 H24 N2 O4 -","- C20 H24 N2 O4 -","- C40 H48 N4 O8 -","2","1","","Reddy, B. V. Subba; Reddy, C. Ravikumar; Reddy, M. Rajashekhar; Yarlagadda, Suresh; Sridhar, B.","Substrate Directed C-H Activation for the Synthesis of Benzo[c]cinnolines through a Sequential C-C and C-N Bond Formation.","Organic letters","2015","17","15","3730","3733","10.1021/acs.orglett.5b01717","","","0.71073","MoKα","","0.0621","0.0601","","","0.1826","0.1846","","","","","","1.152","","","","has coordinates","154524","2020-10-21","18:00:00",""
"1529874","5.968","0.0009","10.51","0.001","25.663","0.002","90","","90","","90","","1609.7","0.3","100","0.2","100","0.2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","Icacina9","","","- C20 H18 O7 -","- C20 H18 O7 -","- C80 H72 O28 -","4","1","","Zhao, Ming; Onakpa, Monday M.; Santarsiero, Bernard D.; Huang, Xiao-Jun; Zhang, Xiao-Qi; Chen, Jia; Cheng, Jian-Jun; Longnecker, Richard; Che, Chun-Tao","Icacinlactone H and Icacintrichantholide from the Tuber of Icacina trichantha.","Organic letters","2015","17","15","3834","3837","10.1021/acs.orglett.5b01806","","","0.72925","Synchrotron","","0.0494","0.0491","","","0.1243","0.1247","","","","","","1.065","","","","has coordinates","154525","2020-10-21","18:00:00",""
"1529875","6.8018","0.0003","20.5957","0.0009","12.4023","0.0005","90","","90","","90","","1737.41","0.13","100","0.1","100","0.1","","","","","","","","3","P 21 21 2","P 2 2ab","18","Icacinlactone","","","- C20 H20 O7 -","- C20 H20 O7 -","- C80 H80 O28 -","4","1","","Zhao, Ming; Onakpa, Monday M.; Santarsiero, Bernard D.; Huang, Xiao-Jun; Zhang, Xiao-Qi; Chen, Jia; Cheng, Jian-Jun; Longnecker, Richard; Che, Chun-Tao","Icacinlactone H and Icacintrichantholide from the Tuber of Icacina trichantha.","Organic letters","2015","17","15","3834","3837","10.1021/acs.orglett.5b01806","","","1.54178","CuKα","","0.0721","0.0721","","","0.1924","0.1924","","","","","","1.221","","","","has coordinates","154526","2020-10-21","18:00:00",""
"1529876","9.578","0.002","10.805","0.003","12.575","0.002","102.754","0.018","97.366","0.015","93.699","0.019","1253","0.5","293.18","0.1","293.18","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C23 H27 F3 O7 S -","- C23 H27 F3 O7 S -","- C46 H54 F6 O14 S2 -","2","1","","Qiu, Yi-Feng; Zhu, Xin-Yu; Li, Ying-Xiu; He, Yu-Tao; Yang, Fang; Wang, Jia; Hua, Hui-Liang; Zheng, Lan; Wang, Li-Chen; Liu, Xue-Yuan; Liang, Yong-Min","AgSCF3-Mediated Trifluoromethylthiolation/Radical Cascade Cyclization of 1,6-Enynes.","Organic letters","2015","17","15","3694","3697","10.1021/acs.orglett.5b01657","","x-ray","0.71073","MoKα","","0.1711","0.0766","","","0.1432","0.2088","","","","","","1.015","","","","has coordinates","154527","2020-10-21","18:00:00",""
"1529877","5.4961","0.0005","23.714","0.0019","17.6522","0.0013","90","","96.871","0.007","90","","2284.2","0.3","295.35","0.1","295.35","0.1","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C22 H21 Cl F3 N O2 S2 -","- C22 H21 Cl F3 N O2 S2 -","- C88 H84 Cl4 F12 N4 O8 S8 -","4","1","","Qiu, Yi-Feng; Zhu, Xin-Yu; Li, Ying-Xiu; He, Yu-Tao; Yang, Fang; Wang, Jia; Hua, Hui-Liang; Zheng, Lan; Wang, Li-Chen; Liu, Xue-Yuan; Liang, Yong-Min","AgSCF3-Mediated Trifluoromethylthiolation/Radical Cascade Cyclization of 1,6-Enynes.","Organic letters","2015","17","15","3694","3697","10.1021/acs.orglett.5b01657","","x-ray","0.71073","MoKα","","0.2562","0.082","","","0.1621","0.2684","","","","","","0.992","","","","has coordinates","154528","2020-10-21","18:00:00",""
"1529878","9.9242","0.0004","15.9342","0.0006","10.0614","0.0004","90","","106.109","0.004","90","","1528.58","0.11","173","","173","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H15 F3 O3 S -","- C16 H15 F3 O3 S -","- C64 H60 F12 O12 S4 -","4","1","","Qiu, Yi-Feng; Zhu, Xin-Yu; Li, Ying-Xiu; He, Yu-Tao; Yang, Fang; Wang, Jia; Hua, Hui-Liang; Zheng, Lan; Wang, Li-Chen; Liu, Xue-Yuan; Liang, Yong-Min","AgSCF3-Mediated Trifluoromethylthiolation/Radical Cascade Cyclization of 1,6-Enynes.","Organic letters","2015","17","15","3694","3697","10.1021/acs.orglett.5b01657","","x-ray","0.71073","MoKα","","0.0611","0.0433","","","0.0943","0.1049","","","","","","1.022","","","","has coordinates","154529","2020-10-21","18:00:00",""
"1529879","6.1858","0.001","17.934","0.003","11.7423","0.0019","90","","101.212","0.003","90","","1277.8","0.4","200","2","200","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C14 H12 Br N O -","- C14 H12 Br N O -","- C56 H48 Br4 N4 O4 -","4","1","","Haidzinskaya, Tatsiana; Kerchner, Hilary A.; Liu, Jixin; Watson, Mary P.","Diastereoselective, Zinc-Catalyzed Alkynylation of α-Bromo Oxocarbenium Ions.","Organic letters","2015","17","15","3857","3859","10.1021/acs.orglett.5b01838","","","0.71073","MoKα","","0.0711","0.0502","","","0.11","0.1193","","","","","","1.043","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529880","5.7983","0.0001","8.1321","0.0002","24.8527","0.0006","90","","90.153","0.001","90","","1171.86","0.05","200","2","200","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C12 H13 Br O3 -","- C12 H13 Br O3 -","- C48 H52 Br4 O12 -","4","1","","Haidzinskaya, Tatsiana; Kerchner, Hilary A.; Liu, Jixin; Watson, Mary P.","Diastereoselective, Zinc-Catalyzed Alkynylation of α-Bromo Oxocarbenium Ions.","Organic letters","2015","17","15","3857","3859","10.1021/acs.orglett.5b01838","","","0.71073","MoKα","","0.027","0.023","","","0.0575","0.0593","","","","","","1.029","","","","has coordinates","154531","2020-10-21","18:00:00",""
"1529881","6.6041","0.0009","7.3454","0.001","25.445","0.003","90","","90.254","0.003","90","","1234.3","0.3","120","2","120","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C14 H15 N3 O2 -","- C14 H15 N3 O2 -","- C56 H60 N12 O8 -","4","1","","Komkov, Alexander V.; Komendantova, Anna S.; Menchikov, Leonid G.; Chernoburova, Elena I.; Volkova, Yulia A.; Zavarzin, Igor V.","A Straightforward Approach toward Multifunctionalized Pyridazines via Imination/Electrocyclization.","Organic letters","2015","17","15","3734","3737","10.1021/acs.orglett.5b01718","","","0.71073","MoKα","","0.0675","0.0491","","","0.13","0.1415","","","","","","1.011","","","","has coordinates","154532","2020-10-21","18:00:00",""
"1529882","7.4962","0.0003","17.6328","0.0008","16.4671","0.0007","90","","93.865","0.004","90","","2171.65","0.16","291","2","291.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C27 H19 F3 N2 -","- C27 H19 F3 N2 -","- C108 H76 F12 N8 -","4","1","","Cheng, Guolin; Weng, Yunxiang; Yang, Xifa; Cui, Xiuling","Base-Promoted N-Pyridylation of Heteroarenes Using N-Propargyl Enaminones as Equivalents of Pyridine Scaffolds.","Organic letters","2015","17","15","3790","3793","10.1021/acs.orglett.5b01733","","","1.54184","CuKα","","0.0664","0.0517","","","0.1453","0.1602","","","","","","1.039","","","","has coordinates,has disorder","154533","2020-10-21","18:00:00",""
"1529883","7.3862","0.0003","11.9598","0.0005","17.2782","0.0007","90","","90","","90","","1526.31","0.11","291","2","291.15","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C19 H17 N O2 -","- C19 H17 N O2 -","- C76 H68 N4 O8 -","4","1","","Cheng, Guolin; Weng, Yunxiang; Yang, Xifa; Cui, Xiuling","Base-Promoted N-Pyridylation of Heteroarenes Using N-Propargyl Enaminones as Equivalents of Pyridine Scaffolds.","Organic letters","2015","17","15","3790","3793","10.1021/acs.orglett.5b01733","","","1.54184","CuKα","","0.0374","0.0348","","","0.0941","0.0973","","","","","","1.026","","","","has coordinates","154534","2020-10-21","18:00:00",""
"1529884","21.3348","0.0007","10.673","0.0002","18.3612","0.0006","90","","110.777","0.004","90","","3909.1","0.2","291","2","291.15","","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C26 H20 N2 -","- C26 H20 N2 -","- C208 H160 N16 -","8","1","","Cheng, Guolin; Weng, Yunxiang; Yang, Xifa; Cui, Xiuling","Base-Promoted N-Pyridylation of Heteroarenes Using N-Propargyl Enaminones as Equivalents of Pyridine Scaffolds.","Organic letters","2015","17","15","3790","3793","10.1021/acs.orglett.5b01733","","","1.54184","CuKα","","0.0512","0.0406","","","0.1105","0.119","","","","","","1.045","","","","has coordinates","154535","2020-10-21","18:00:00",""
"1529885","13.4407","0.0011","21.762","0.002","8.4346","0.0008","90","","99.174","0.009","90","","2435.5","0.4","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C32 H22 N6 -","- C32 H22 N6 -","- C128 H88 N24 -","4","1","","Constantinides, Christos P.; Zissimou, Georgia A.; Berezin, Andrey A.; Ioannou, Theodosia A.; Manoli, Maria; Tsokkou, Demetra; Theodorou, Eleni; Hayes, Sophia C.; Koutentis, Panayiotis A.","Tetraphenylhexaazaanthracenes: 16π Weakly Antiaromatic Species with Singlet Ground States.","Organic letters","2015","17","16","4026","4029","10.1021/acs.orglett.5b01923","","","1.54184","CuKα","","0.1282","0.0622","","","0.1594","0.2166","","","","","","0.919","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1529886","10.2147","0.0013","11.39","0.0014","12.1881","0.0015","68.285","0.002","71.067","0.002","83.51","0.003","1246.1","0.3","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C28 H24 F3 N O4 S -","- C28 H24 F3 N O4 S -","- C56 H48 F6 N2 O8 S2 -","2","1","","Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun","Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.","Organic letters","2015","17","16","3944","3947","10.1021/acs.orglett.5b01474","","","0.71073","MoKα","","0.0613","0.0468","","","0.1282","0.1401","","","","","","1.036","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1530387","16.472","0.002","18.563","0.0004","11.996","0.002","90","","92.581","0.01","90","","3664.3","0.8","100","2","100","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C32 H59 N O4 Si2 -","- C32 H59 N O4 Si2 -","- C128 H236 N4 O16 Si8 -","4","2","","Fanelli, Roberto; Salah, Khoubaib Ben Haj; Inguimbert, Nicolas; Didierjean, Claude; Martinez, Jean; Cavelier, Florine","Access to α,α-Disubstituted Disilylated Amino Acids and Their Use in Solid-Phase Peptide Synthesis.","Organic letters","2015","17","18","4498","4501","10.1021/acs.orglett.5b02175","","","1.54184","CuKα","","0.091","0.0711","","","0.1853","0.2092","","","","","","1.033","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1530388","13.4257","0.0011","10.9838","0.0007","14.5635","0.0011","90","","109.954","0.009","90","","2018.7","0.3","293","2","293.15","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C22 H22 N2 O3 S -","- C22 H22 N2 O3 S -","- C88 H88 N8 O12 S4 -","4","1","","Wang, Chen; Zhang, Haojie; Lang, Bo; Ren, Anni; Lu, Ping; Wang, Yanguang","Rh-Catalyzed Reactions of 3-Diazoindolin-2-imines: Synthesis of Pyridoindoles and Tetrahydrofuropyrroloindoles.","Organic letters","2015","17","18","4412","4415","10.1021/acs.orglett.5b01943","","","0.71073","MoKα","","0.0772","0.0506","","","0.1324","0.1543","","","","","","1.037","","","","has coordinates","160561","2020-10-21","18:00:00",""
"1530389","7.6543","0.0009","11.1582","0.0012","16.8881","0.0016","90","","101.198","0.011","90","","1414.9","0.3","293","2","293.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C17 H16 N2 O -","- C17 H16 N2 O -","- C68 H64 N8 O4 -","4","1","","Wang, Chen; Zhang, Haojie; Lang, Bo; Ren, Anni; Lu, Ping; Wang, Yanguang","Rh-Catalyzed Reactions of 3-Diazoindolin-2-imines: Synthesis of Pyridoindoles and Tetrahydrofuropyrroloindoles.","Organic letters","2015","17","18","4412","4415","10.1021/acs.orglett.5b01943","","","0.71073","MoKα","","0.0671","0.0467","","","0.1126","0.1297","","","","","","1.032","","","","has coordinates","160561","2020-10-21","18:00:00",""
"1530390","7.3491","0.0002","11.3041","0.0004","30.6417","0.0011","90","","90","","90","","2545.56","0.15","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C29 H44 O4 -","- C29 H44 O4 -","- C116 H176 O16 -","4","1","","Hu, Zheng-Xi; Shi, Yi-Ming; Wang, Wei-Guang; Li, Xiao-Nian; Du, Xue; Liu, Miao; Li, Yan; Xue, Yong-Bo; Zhang, Yong-Hui; Pu, Jian-Xin; Sun, Han-Dong","Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea.","Organic letters","2015","17","18","4616","4619","10.1021/acs.orglett.5b02360","","","1.54178","CuKα","","0.0421","0.0409","","","0.1073","0.1084","","","","","","1.032","","","","has coordinates","160562","2020-10-21","18:00:00",""
"1530391","7.3331","0.0001","10.1624","0.0002","19.3573","0.0003","90","","97.23","","90","","1431.07","0.04","100","2","100","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C32 H48 O5 -","- C32 H48 O5 -","- C64 H96 O10 -","2","1","","Hu, Zheng-Xi; Shi, Yi-Ming; Wang, Wei-Guang; Li, Xiao-Nian; Du, Xue; Liu, Miao; Li, Yan; Xue, Yong-Bo; Zhang, Yong-Hui; Pu, Jian-Xin; Sun, Han-Dong","Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea.","Organic letters","2015","17","18","4616","4619","10.1021/acs.orglett.5b02360","","","1.54178","CuKα","","0.1036","0.1026","","","0.2723","0.2762","","","","","","1.366","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1530392","7.357","0.0003","11.5004","0.0005","15.8083","0.0006","101.789","0.002","102.383","0.002","90.228","0.001","1277.24","0.09","100","2","100","2","","","","","","","","3","P 1","P 1","1","","","","- C29 H44 O4 -","- C29 H44 O4 -","- C58 H88 O8 -","2","2","","Hu, Zheng-Xi; Shi, Yi-Ming; Wang, Wei-Guang; Li, Xiao-Nian; Du, Xue; Liu, Miao; Li, Yan; Xue, Yong-Bo; Zhang, Yong-Hui; Pu, Jian-Xin; Sun, Han-Dong","Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea.","Organic letters","2015","17","18","4616","4619","10.1021/acs.orglett.5b02360","","","1.54178","CuKα","","0.0967","0.0954","","","0.2396","0.2429","","","","","","1.183","","","","has coordinates","160562","2020-10-21","18:00:00",""
"1530393","7.9562","0.0003","33.6801","0.0014","12.617","0.0005","90","","107.429","0.002","90","","3225.7","0.2","100","2","100","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C34 H54 O6 -","- C34 H54 O6 -","- C136 H216 O24 -","4","2","","Hu, Zheng-Xi; Shi, Yi-Ming; Wang, Wei-Guang; Li, Xiao-Nian; Du, Xue; Liu, Miao; Li, Yan; Xue, Yong-Bo; Zhang, Yong-Hui; Pu, Jian-Xin; Sun, Han-Dong","Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea.","Organic letters","2015","17","18","4616","4619","10.1021/acs.orglett.5b02360","","","1.54178","CuKα","","0.0701","0.0663","","","0.1867","0.1902","","","","","","1.058","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1531034","10.82123","0.00016","22.8438","0.0003","8.59627","0.00014","90","","108.437","0.0016","90","","2015.91","0.05","290.23","0.1","290.23","0.1","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C23 H22 N2 O5 -","- C23 H22 N2 O5 -","- C92 H88 N8 O20 -","4","1","","Zhan, Gu; Shi, Ming-Lin; He, Qing; Du, Wei; Chen, Ying-Chun","[4 + 3] Cycloadditions with Bromo-Substituted Morita-Baylis-Hillman Adducts of Isatins and N-(ortho-Chloromethyl)aryl Amides.","Organic letters","2015","17","19","4750","4753","10.1021/acs.orglett.5b02279","","x-ray","1.54184","CuKα","","0.0445","0.0422","","","0.1096","0.1122","","","","","","1.06","","","","has coordinates","160565","2020-10-21","18:00:00",""
"1531035","16.017","0.003","18.231","0.003","18.359","0.003","115.519","0.003","101.669","0.003","92.884","0.003","4680.3","1.4","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C93 H37 Cu F35 N14 -","- C93 H37 Cu F35 N14 -","- C186 H74 Cu2 F70 N28 -","2","1","","Zhang, Kai; Zhang, Junda; Li, Xin; Guo, Rui; Ågren, Hans; Ou, Zhongping; Ishida, Masatoshi; Furuta, Hiroyuki; Xie, Yongshu","Synthesis of a Neo-Confused Octaphyrin and the Formation of Its Mononuclear Complexes.","Organic letters","2015","17","19","4806","4809","10.1021/acs.orglett.5b02363","","","0.71073","MoKα","","0.0996","0.0693","","","0.205","0.2318","","","","","","0.982","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1531036","16.045","0.003","18.292","0.004","18.495","0.004","115.633","0.004","101.728","0.004","93.013","0.004","4730.7","1.7","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C89 H31 F35 N12 Zn -","- C89 H31 F35 N12 Zn -","- C178 H62 F70 N24 Zn2 -","2","1","","Zhang, Kai; Zhang, Junda; Li, Xin; Guo, Rui; Ågren, Hans; Ou, Zhongping; Ishida, Masatoshi; Furuta, Hiroyuki; Xie, Yongshu","Synthesis of a Neo-Confused Octaphyrin and the Formation of Its Mononuclear Complexes.","Organic letters","2015","17","19","4806","4809","10.1021/acs.orglett.5b02363","","","0.71073","MoKα","","0.1569","0.1107","","","0.2933","0.3206","","","","","","1.009","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1531166","9.2332","0.0003","11.8033","0.0005","13.4383","0.0006","78.564","0.004","74.091","0.004","80.538","0.003","1371.04","0.1","289.2","0.4","289.2","0.4","","","","","","","","5","P -1","-P 1","2","","","","- C28 H26 N2 O4 S2 -","- C28 H26 N2 O4 S2 -","- C56 H52 N4 O8 S4 -","2","1","","Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui","Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines.","Organic letters","2015","17","19","4870","4873","10.1021/acs.orglett.5b02423","","x-ray","1.54184","CuKα","","0.0481","0.0427","","","0.1227","0.1283","","","","","","1.038","","","","has coordinates","160567","2020-10-21","18:00:00",""
"1531170","7.8395","0.00006","12.02537","0.00011","26.9644","0.0002","90","","90","","90","","2542.01","0.04","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C28 H26 N2 O4 S2 -","- C28 H26 N2 O4 S2 -","- C112 H104 N8 O16 S8 -","4","1","","Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui","Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines.","Organic letters","2015","17","19","4870","4873","10.1021/acs.orglett.5b02423","","","1.54184","CuKα","","0.0259","0.0255","","","0.0683","0.0689","","","","","","0.925","","","","has coordinates","160567","2020-10-21","18:00:00",""
"1531174","5.35547","0.00005","17.35361","0.00013","27.184","0.0002","90","","90","","90","","2526.39","0.04","284.46","0.1","284.46","0.1","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C28 H26 N2 O4 S2 -","- C28 H26 N2 O4 S2 -","- C112 H104 N8 O16 S8 -","4","1","","Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui","Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines.","Organic letters","2015","17","19","4870","4873","10.1021/acs.orglett.5b02423","","x-ray","1.54184","CuKα","","0.0265","0.0263","","","0.0696","0.0698","","","","","","1.035","","","","has coordinates","160567","2020-10-21","18:00:00",""
"1532457","9.799","0.004","11.932","0.007","13.735","0.007","84.22","0.03","72.85","0.03","66.98","0.02","1412.1","1.3","110","","110","2","","","","","","","","3","P -1","-P 1","2","","","","- C32 H40 S3 -","- C32 H40 S3 -","- C64 H80 S6 -","2","1","","Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji","Synthesis and Properties of Ethene-Bridged Terthiophenes.","Organic letters","2015","17","19","4858","4861","10.1021/acs.orglett.5b02417","","","0.71075","MoKα","","0.0666","0.0545","","","0.1303","0.1388","","","","","","1.011","","","","has coordinates,has disorder","160564","2020-10-21","18:00:00",""
"1532458","10.274","0.013","10.828","0.013","13.62","0.015","73.61","0.04","83.52","0.06","85.57","0.05","1443","3","110","","110","2","","","","","","","","3","P -1","-P 1","2","EBTT-C8-2","","","- C32 H40 S3 -","- C32 H40 S3 -","- C64 H80 S6 -","2","1","","Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji","Synthesis and Properties of Ethene-Bridged Terthiophenes.","Organic letters","2015","17","19","4858","4861","10.1021/acs.orglett.5b02417","","","0.71075","MoKα","","0.09","0.0654","","","0.1536","0.1683","","","","","","1.048","","","","has coordinates","160564","2020-10-21","18:00:00",""
"1532459","7.769","0.003","12.591","0.004","12.753","0.004","93.524","0.003","98.169","0.006","101.228","0.006","1206.1","0.7","110","2","110","2","","","","","","","","3","P -1","-P 1","2","EBTT-C6","","","- C28 H32 S3 -","- C28 H32 S3 -","- C56 H64 S6 -","2","1","","Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji","Synthesis and Properties of Ethene-Bridged Terthiophenes.","Organic letters","2015","17","19","4858","4861","10.1021/acs.orglett.5b02417","","","0.71075","MoKα","","0.0324","0.0283","","","0.0823","0.0837","","","","","","1.073","","","","has coordinates","160564","2020-10-21","18:00:00",""
"1532460","11.959","0.011","22.114","0.019","7.632","0.006","90","","97.436","0.014","90","","2001","3","100.15","","100.15","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C24 H24 S3 -","- C24 H24 S3 -","- C96 H96 S12 -","4","1","","Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji","Synthesis and Properties of Ethene-Bridged Terthiophenes.","Organic letters","2015","17","19","4858","4861","10.1021/acs.orglett.5b02417","","","0.71075","MoKα","","0.0687","0.0595","","","0.1166","0.122","","","","","","1.162","","","","has coordinates","160564","2020-10-21","18:00:00",""
"1532461","13.033","0.007","3.916","0.002","24.464","0.013","90","","103.214","0.008","90","","1215.5","1.1","113","","113","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","EBTT","","","- C16 H8 S3 -","- C16 H8 S3 -","- C64 H32 S12 -","4","1","","Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji","Synthesis and Properties of Ethene-Bridged Terthiophenes.","Organic letters","2015","17","19","4858","4861","10.1021/acs.orglett.5b02417","","","0.71075","MoKα","","0.0422","0.0347","","","0.0738","0.0779","","","","","","1.063","","","","has coordinates","160564","2020-10-21","18:00:00",""
"1534096","5.1904","0.0007","9.7263","0.0012","29.581","0.003","90","","90","","90","","1493.3","0.3","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C16 H16 Br N O2 -","- C16 H16 Br N O2 -","- C64 H64 Br4 N4 O8 -","4","1","","Pathipati, Stalin R.; Singh, Vipender; Eriksson, Lars; Selander, Nicklas","Lewis Acid Catalyzed Annulation of Nitrones with Oxiranes, Aziridines, and Thiiranes.","Organic letters","2015","17","18","4506","4509","10.1021/acs.orglett.5b02195","","","0.71073","MoKα","","0.0579","0.0421","","","0.0765","0.0822","","","","","","1.099","","","","has coordinates","160449","2020-10-21","18:00:00",""
"1534097","11.7836","0.0012","8.1908","0.0007","21.1196","0.0019","90","","92.216","0.004","90","","2036.9","0.3","99.9","","99.9","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C27 H21 N O4 -","- C27 H21 N O4 -","- C108 H84 N4 O16 -","4","1","","Jung, Youngeun; Kim, Ikyon","Deformylative Intramolecular Hydroarylation: Synthesis of Benzo[e]pyrido[1,2-a]indoles.","Organic letters","2015","17","18","4600","4603","10.1021/acs.orglett.5b02331","","","0.71073","MoKα","","0.0479","0.0366","","","0.0843","0.0961","","","","","","1.072","","","","has coordinates","160450","2020-10-21","18:00:00",""
"1534098","11.5406","0.0012","9.3427","0.001","18.9135","0.0016","90","","96.804","0.003","90","","2024.9","0.3","303.7","","303.7","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C26 H21 N O3 -","- C26 H21 N O3 -","- C104 H84 N4 O12 -","4","1","","Jung, Youngeun; Kim, Ikyon","Deformylative Intramolecular Hydroarylation: Synthesis of Benzo[e]pyrido[1,2-a]indoles.","Organic letters","2015","17","18","4600","4603","10.1021/acs.orglett.5b02331","","","0.71073","MoKα","","0.1088","0.0511","","","0.1001","0.1187","","","","","","1.032","","","","has coordinates,has disorder","160451","2020-10-21","18:00:00",""
"1534099","13.9954","0.0019","19.389","0.003","14.02","0.002","90","","115.309","0.002","90","","3439.3","0.9","140","2","140","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C62 H60 Cl N4 O4 P -","- C62 H60 Cl N4 O4 P -","- C124 H120 Cl2 N8 O8 P2 -","2","1","","Gao, Xing; Han, Jianwei; Wang, Limin","Design of Highly Stable Iminophosphoranes as Recyclable Organocatalysts: Application to Asymmetric Chlorinations of Oxindoles.","Organic letters","2015","17","18","4596","4599","10.1021/acs.orglett.5b02323","","","0.71073","MoKα","","0.1028","0.0861","","","0.2341","0.2495","","","","","","1.029","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1534100","12.0658","0.001","17.7295","0.0013","13.2309","0.001","90","","104.155","0.002","90","","2744.4","0.4","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C65 H65 N4 O5 P -","- C65 H65 N4 O5 P -","- C130 H130 N8 O10 P2 -","2","1","","Gao, Xing; Han, Jianwei; Wang, Limin","Design of Highly Stable Iminophosphoranes as Recyclable Organocatalysts: Application to Asymmetric Chlorinations of Oxindoles.","Organic letters","2015","17","18","4596","4599","10.1021/acs.orglett.5b02323","","","0.71073","MoKα","","0.1192","0.06","","","0.1167","0.1386","","","","","","0.94","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1534101","31.82","0.005","31.82","0.005","6.203","0.0012","90","","90","","120","","5439.2","1.6","294","2","294","2","","","","","","","","5","R 3 :H","R 3","146","","","","- C24 H29 F N2 O5 -","- C24 H29 F N2 O5 -","- C216 H261 F9 N18 O45 -","9","1","","Bonetti, Andrea; Pellegrino, Sara; Das, Priyadip; Yuran, Sivan; Bucci, Raffaella; Ferri, Nicola; Meneghetti, Fiorella; Castellano, Carlo; Reches, Meital; Gelmi, Maria Luisa","Dipeptide Nanotubes Containing Unnatural Fluorine-Substituted β(2,3)-Diarylamino Acid and l-Alanine as Candidates for Biomedical Applications.","Organic letters","2015","17","18","4468","4471","10.1021/acs.orglett.5b02132","","","0.71073","MoKα","","0.0712","0.0497","","","0.127","0.1434","","","","","","1.053","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1534102","9.507","0.002","9.4923","0.0013","14.387","0.002","90","","90.344","0.013","90","","1298.3","0.4","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C15 H17 N3 -","- C15 H17 N3 -","- C60 H68 N12 -","4","1","","Hassan, Haitham; Mohammed, Shireen; Robert, Frédéric; Landais, Yannick","Total Synthesis of (±)-Eucophylline. A Free-Radical Approach to the Synthesis of the Azabicyclo[3.3.1]nonane Skeleton.","Organic letters","2015","17","18","4518","4521","10.1021/acs.orglett.5b02218","","","1.54187","CuKα","","0.0441","0.0379","","","0.0994","0.1067","","","","","","1.016","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1534103","7.4677","0.0011","18.793","0.003","24.102","0.004","90","","94.988","0.006","90","","3369.7","0.9","133","2","133","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C24 H21 N -","- C24 H21 N -","- C192 H168 N8 -","8","2","","Hassan, Haitham; Mohammed, Shireen; Robert, Frédéric; Landais, Yannick","Total Synthesis of (±)-Eucophylline. A Free-Radical Approach to the Synthesis of the Azabicyclo[3.3.1]nonane Skeleton.","Organic letters","2015","17","18","4518","4521","10.1021/acs.orglett.5b02218","","","1.54187","CuKα","","0.0734","0.0507","","","0.1377","0.1448","","","","","","1.013","","","","has coordinates","182022","2020-10-21","18:00:00",""
"1534104","25.108","0.0017","25.108","0.0017","8.6289","0.0008","90","","90","","90","","5439.8","0.7","293","2","293","2","","","","","","","","6","I 41/a :2","-I 4ad","88","","","","- C13 H14 B Cl F2 N2 -","- C13 H14 B Cl F2 N2 -","- C208 H224 B16 Cl16 F32 N32 -","16","1","","Zhou, Xin; Yu, Changjiang; Feng, Zeya; Yu, Yang; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan","Highly Regioselective α-Chlorination of the BODIPY Chromophore with Copper(II) Chloride.","Organic letters","2015","17","18","4632","4635","10.1021/acs.orglett.5b02383","","","0.71073","MoKα","","0.0707","0.0579","","","0.1733","0.1872","","","","","","1.034","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1534105","15.6318","0.0017","13.1816","0.0014","15.4701","0.0017","90","","96.971","0.001","90","","3164.1","0.6","293","2","293","2","","","","","","","","7","C 1 2/c 1","-C 2yc","15","","","","- C16 H11 B Cl2 F2 N2 O -","- C16 H11 B Cl2 F2 N2 O -","- C128 H88 B8 Cl16 F16 N16 O8 -","8","1","","Zhou, Xin; Yu, Changjiang; Feng, Zeya; Yu, Yang; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan","Highly Regioselective α-Chlorination of the BODIPY Chromophore with Copper(II) Chloride.","Organic letters","2015","17","18","4632","4635","10.1021/acs.orglett.5b02383","","","0.71073","MoKα","","0.0433","0.0374","","","0.1032","0.1086","","","","","","1.039","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1534106","10.1284","0.0011","11.8356","0.0013","12.656","0.0013","91.216","0.001","110.273","0.001","107.739","0.001","1341.8","0.2","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C12 H11 B Cl2 F2 N2 -","- C12 H11 B Cl2 F2 N2 -","- C48 H44 B4 Cl8 F8 N8 -","4","2","","Zhou, Xin; Yu, Changjiang; Feng, Zeya; Yu, Yang; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan","Highly Regioselective α-Chlorination of the BODIPY Chromophore with Copper(II) Chloride.","Organic letters","2015","17","18","4632","4635","10.1021/acs.orglett.5b02383","","","0.71073","MoKα","","0.0427","0.0358","","","0.0953","0.102","","","","","","1.045","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1534107","7.4471","0.0009","9.4405","0.0011","12.781","0.0016","79.059","0.003","79.842","0.003","75.136","0.003","844.95","0.18","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C20 H13 F3 O2 S -","- C20 H13 F3 O2 S -","- C40 H26 F6 O4 S2 -","2","1","","Xu, Chunfa; Shen, Qilong","Lewis Acid Mediated Trifluoromethylthio Lactonization/Lactamization.","Organic letters","2015","17","18","4561","4563","10.1021/acs.orglett.5b02315","","","0.71073","MoKα","","0.0926","0.067","","","0.146","0.1591","","","","","","1.051","","","","has coordinates,has disorder","160459","2020-10-21","18:00:00",""
"1534108","8.2556","0.0017","14.406","0.003","17.938","0.004","90","","93.63","0.03","90","","2129.1","0.8","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","141208b","","","- C24 H21 N O4 S -","- C24 H21 N O4 S -","- C96 H84 N4 O16 S4 -","4","1","","Liu, Hongxu; Yang, Yanyan; Wang, Shen; Wu, Jie; Wang, Xiao-Na; Chang, Junbiao","Synthesis of 3-Substituted 2-Aminochromones via Sn(IV)-Promoted Annulation of Ynamides with 2-Methoxyaroyl Chlorides.","Organic letters","2015","17","18","4472","4475","10.1021/acs.orglett.5b02137","","","0.71073","MoKα","","0.1084","0.0941","","","0.2494","0.2603","","","","","","1.5","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1534109","5.9946","0.0002","7.961","0.0002","12.7201","0.0004","85.167","0.002","84.614","0.002","73.532","0.002","578.51","0.03","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C14 H11 N O S -","- C14 H11 N O S -","- C28 H22 N2 O2 S2 -","2","1","","Lemercier, Bérénice C; Pierce, Joshua G.","Synthesis of 1,4,2-Oxathiazoles via Oxidative Cyclization of Thiohydroximic Acids.","Organic letters","2015","17","18","4542","4545","10.1021/acs.orglett.5b02256","","","0.71073","MoKα","","0.0564","0.0433","","","0.1057","0.114","","","","","","1.067","","","","has coordinates,has disorder","160461","2020-10-21","18:00:00",""
"1534110","10.469","0.003","11.122","0.003","11.473","0.004","90","","92.129","0.015","90","","1335","0.7","100","","100","","","","","","","","","7","P 1 21 1","P 2yb","4","","","","- C25 H22 Cl2 I N3 O4 S -","- C25 H22 Cl2 I N3 O4 S -","- C50 H44 Cl4 I2 N6 O8 S2 -","2","1","","Tripathi, Chandra Bhushan; Mukherjee, Santanu","Catalytic Enantioselective 1,4-Iodofunctionalizations of Conjugated Dienes.","Organic letters","2015","17","18","4424","4427","10.1021/acs.orglett.5b02026","","x-ray","0.71073","MoKα","","0.072","0.0503","","","0.1055","0.1149","","","","","","0.999","","","","has coordinates","160462","2020-10-21","18:00:00",""
"1534111","9.9179","0.0015","5.7432","0.0007","14.186","0.002","90","","95.817","0.009","90","","803.88","0.19","298","","298","","","","","","","","","5","P 1 21 1","P 2yb","4","","CBT-V-255-01","","- C18 H16 I N O -","- C18 H16 I N O -","- C36 H32 I2 N2 O2 -","2","1","","Tripathi, Chandra Bhushan; Mukherjee, Santanu","Catalytic Enantioselective 1,4-Iodofunctionalizations of Conjugated Dienes.","Organic letters","2015","17","18","4424","4427","10.1021/acs.orglett.5b02026","","x-ray","0.71073","MoKα","","0.1043","0.0448","","","0.0803","0.096","","","","","","1","","","","has coordinates,has disorder","160463","2020-10-21","18:00:00",""
"1534112","11.3632","0.0014","11.802","0.0015","15.831","0.002","90","","109.817","0.002","90","","1997.3","0.4","296","2","296","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C21 H21 N O5 S -","- C21 H21 N O5 S -","- C84 H84 N4 O20 S4 -","4","2","","Qiao, Baokun; Huang, Yin-Jun; Nie, Jing; Ma, Jun-An","Highly Regio-, Diastereo-, and Enantioselective Mannich Reaction of Allylic Ketones and Cyclic Ketimines: Access to Chiral Benzosultam.","Organic letters","2015","17","18","4608","4611","10.1021/acs.orglett.5b02351","","","0.71073","MoKα","","0.0436","0.0376","","","0.0993","0.1041","","","","","","1.03","","","","has coordinates","182022","2020-10-21","18:00:00",""
"1534113","11.7071","0.001","15.8544","0.0013","9.4636","0.0007","90","","113.637","0.01","90","","1609.2","0.3","293","2","293.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H18 N2 O2 -","- C19 H18 N2 O2 -","- C76 H72 N8 O8 -","4","1","","Shao, Jiaan; Liu, Xingyu; Shu, Ke; Tang, Pai; Luo, Jing; Chen, Wenteng; Yu, Yongping","Tuning the Annulation Reactivity of Vinyl Azides and Carbazates: A Divergent Synthesis of Aza-pyrimidinones and Imidazoles.","Organic letters","2015","17","18","4502","4505","10.1021/acs.orglett.5b02180","","","0.71073","MoKα","","0.0673","0.0462","","","0.114","0.1275","","","","","","1.023","","","","has coordinates","160465","2020-10-21","18:00:00",""
"1534114","6.9191","0.0002","16.135","0.0005","14.3518","0.0006","90","","104.515","0.003","90","","1551.09","0.09","293","2","293.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C14 H17 N3 O4 -","- C14 H17 N3 O4 -","- C56 H68 N12 O16 -","4","1","","Shao, Jiaan; Liu, Xingyu; Shu, Ke; Tang, Pai; Luo, Jing; Chen, Wenteng; Yu, Yongping","Tuning the Annulation Reactivity of Vinyl Azides and Carbazates: A Divergent Synthesis of Aza-pyrimidinones and Imidazoles.","Organic letters","2015","17","18","4502","4505","10.1021/acs.orglett.5b02180","","","1.54184","CuKα","","0.0632","0.0503","","","0.1418","0.1554","","","","","","1.049","","","","has coordinates","160466","2020-10-21","18:00:00",""
"1534115","16.9438","0.0002","7.2054","0.0001","21.3218","0.0003","90","","95.864","0.001","90","","2589.49","0.06","290","2","290","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C33 H25 N3 O2 -","- C33 H25 N3 O2 -","- C132 H100 N12 O8 -","4","1","","Peng, Jing; Ran, Guang-Yao; Du, Wei; Chen, Ying-Chun","Divergent Cyclization Reactions of Morita-Baylis-Hillman Carbonates of 2-Cyclohexenone and Isatylidene Malononitriles.","Organic letters","2015","17","18","4490","4493","10.1021/acs.orglett.5b02157","","","1.54184","CuKα","","0.0435","0.0403","","","0.1058","0.1084","","","","","","1.039","","","","has coordinates","160467","2020-10-21","18:00:00",""
"1534116","7.3218","0.0003","32.2827","0.0012","11.6678","0.0004","90","","91.975","0.003","90","","2756.25","0.18","290","2","291","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C27 H20 N4 O4 -","- C27 H20 N4 O4 -","- C108 H80 N16 O16 -","4","1","","Peng, Jing; Ran, Guang-Yao; Du, Wei; Chen, Ying-Chun","Divergent Cyclization Reactions of Morita-Baylis-Hillman Carbonates of 2-Cyclohexenone and Isatylidene Malononitriles.","Organic letters","2015","17","18","4490","4493","10.1021/acs.orglett.5b02157","","","1.54184","CuKα","","0.082","0.0589","","","0.1524","0.1687","","","","","","1.072","","","","has coordinates","160468","2020-10-21","18:00:00",""
"1534117","22.1268","0.0006","5.3611","0.0001","16.7753","0.0004","90","","101.52","0.0009","90","","1949.86","0.08","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C21 H19 F3 N4 O2 -","- C21 H19 F3 N4 O2 -","- C84 H76 F12 N16 O8 -","4","1","","Chung, Tim S.; Lopez, Steven A.; Houk, K. N.; Garcia-Garibay, Miguel A","Stereospecific Synthesis of Substituted Aziridines by a Crystal-to-Crystal Photodenitrogenation of Δ(2)-1,2,3-Triazolines.","Organic letters","2015","17","18","4568","4571","10.1021/acs.orglett.5b02290","","","1.54178","CuKα","","0.0385","0.0376","","","0.1011","0.1023","","","","","","1.027","","","","has coordinates","160469","2020-10-21","18:00:00",""
"1534118","16.6564","0.0006","5.4719","0.0002","39.3699","0.0015","90","","90","","90","","3588.3","0.2","100","2","100","2","","","","","","","","5","P c a 21","P 2c -2ac","29","","","","- C20 H18 F3 N3 O2 -","- C20 H18 F3 N3 O2 -","- C160 H144 F24 N24 O16 -","8","2","","Chung, Tim S.; Lopez, Steven A.; Houk, K. N.; Garcia-Garibay, Miguel A","Stereospecific Synthesis of Substituted Aziridines by a Crystal-to-Crystal Photodenitrogenation of Δ(2)-1,2,3-Triazolines.","Organic letters","2015","17","18","4568","4571","10.1021/acs.orglett.5b02290","","","1.54178","CuKα","","0.0867","0.0719","","","0.1785","0.1912","","","","","","1.039","","","","has coordinates","160470","2020-10-21","18:00:00",""
"1534119","11.4428","0.0007","15.4354","0.0009","24.3994","0.0015","90","","90","","90","","4309.5","0.5","296","2","296.15","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C53 H45 N2 O8 -","- C53 H45 N2 O8 -","- C212 H180 N8 O32 -","4","1","","Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.","Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.","Organic letters","2015","17","18","4440","4443","10.1021/acs.orglett.5b02085","","","0.71073","MoKα","","0.1268","0.056","","","0.121","0.1458","","","","","","0.986","","","","has coordinates","160471","2020-10-21","18:00:00",""
"1534120","14.958","0.002","25.526","0.004","11.093","0.002","90","","90","","90","","4235.5","1.2","296","2","296.15","","","","","","","","","4","P 21 21 2","P 2 2ab","18","","","","- C48 H52 N4 O9 -","- C48 H52 N4 O9 -","- C192 H208 N16 O36 -","4","1","","Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.","Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.","Organic letters","2015","17","18","4440","4443","10.1021/acs.orglett.5b02085","","","0.71073","MoKα","","0.2581","0.0681","","","0.1272","0.1914","","","","","","0.898","","","","has coordinates","160472","2020-10-21","18:00:00",""
"1534121","35.02","0.004","16.0741","0.0018","20.002","0.003","90","","111.769","0.007","90","","10456","2","296","2","296.15","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C45 H42 I2 N4 O8 -","- C45 H42 I2 N4 O8 -","- C360 H336 I16 N32 O64 -","8","1","","Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.","Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.","Organic letters","2015","17","18","4440","4443","10.1021/acs.orglett.5b02085","","","0.71073","MoKα","","0.2643","0.0822","","","0.2268","0.3508","","","","","","0.835","","","","has coordinates","160473","2020-10-21","18:00:00",""
"1534122","20.0623","0.0018","15.4284","0.0014","19.2848","0.0017","90","","120.843","0.005","90","","5125","0.8","296","2","296.15","","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C59 H63 N6 O8 -","- C59 H62 N6 O8 -","- C236 H248 N24 O32 -","4","0.5","","Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.","Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.","Organic letters","2015","17","18","4440","4443","10.1021/acs.orglett.5b02085","","","0.71073","MoKα","","0.1188","0.0507","","","0.1179","0.1471","","","","","","0.966","","","","has coordinates","160474","2020-10-21","18:00:00",""
"1534123","13.787","0.002","14.6","0.003","24.867","0.004","90","","105.219","0.011","90","","4829.9","1.5","296","2","296.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C47 H48 N4 O8 -","- C47 H48 N4 O8 -","- C188 H192 N16 O32 -","4","1","","Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.","Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.","Organic letters","2015","17","18","4440","4443","10.1021/acs.orglett.5b02085","","","0.71073","MoKα","","0.2199","0.0708","","","0.1777","0.2478","","","","","","0.898","","","","has coordinates","160475","2020-10-21","18:00:00",""
"1534124","13.203","0.003","13.977","0.003","14.658","0.003","90.494","0.013","100.476","0.013","113.249","0.013","2434.2","1","296","2","296.15","","","","","","","","","5","P -1","-P 1","2","","","","- C49 H50 Cl6 N4 O8 -","- C49 H50 Cl6 N4 O8 -","- C98 H100 Cl12 N8 O16 -","2","1","","Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.","Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.","Organic letters","2015","17","18","4440","4443","10.1021/acs.orglett.5b02085","","","0.71073","MoKα","","0.2899","0.0974","","","0.2499","0.3544","","","","","","0.934","","","","has coordinates,has disorder","160476","2020-10-21","18:00:00",""
"1534125","12.2439","0.0017","13.8398","0.0016","14.5323","0.0018","91.544","0.009","97.532","0.009","110.103","0.009","2285.7","0.5","296","2","296.15","","","","","","","","","4","P -1","-P 1","2","","","","- C45 H44 N4 O8 -","- C45 H44 N4 O8 -","- C90 H88 N8 O16 -","2","1","","Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.","Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.","Organic letters","2015","17","18","4440","4443","10.1021/acs.orglett.5b02085","","","0.71073","MoKα","","0.1801","0.0676","","","0.1804","0.2348","","","","","","0.922","","","","has coordinates","160477","2020-10-21","18:00:00",""
"1539135","16.571","0.0018","5.5448","0.0005","20.45","0.002","90","","111.604","0.013","90","","1747","0.3","293","2","293.15","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H15 Cl N2 O3 -","- C20 H15 Cl N2 O3 -","- C80 H60 Cl4 N8 O12 -","4","1","","Li, Danyang; Yu, Ming; Zhang, Jitan; Liu, Zhanxiang; Zhang, Yuhong","Synthesis of Benzyl Esters via Functionalization of Multiple C-H Bonds by Palladium Catalysis.","Organic letters","2015","17","21","5300","5303","10.1021/acs.orglett.5b02518","","","0.71073","MoKα","","0.0731","0.0432","","","0.1047","0.1251","","","","","","1.002","","","","has coordinates","170829","2020-10-21","18:00:00",""
"1540373","20.4242","0.0004","25.5132","0.0004","32.3262","0.0007","90","","105.672","0.001","90","","16218.5","0.5","90","0.5","90","0.5","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C135 H42 Cl3 O2 -","- C126 H36 O2 -","- C1008 H288 O16 -","8","1","","Abeyratne Kuragama, Peumie L.; Fronczek, Frank R.; Sygula, Andrzej","Bis-corannulene Receptors for Fullerenes Based on Klärner's Tethers: Reaching the Affinity Limits.","Organic letters","2015","17","21","5292","5295","10.1021/acs.orglett.5b02666","","","1.54184","CuKα","","0.0692","0.0589","","","0.1515","0.1574","","","","","","1.023","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1540374","6.2372","0.0009","11.1508","0.0016","28.596","0.004","90","","90","","90","","1988.8","0.5","293","2","293","2","","","","","","","synthesis as described","5","P 21 21 21","P 2ac 2ab","19","","","","- C16 H26 N2 O6 S -","- C16 H26 N2 O6 S -","- C64 H104 N8 O24 S4 -","4","1","","Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François","Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.","Organic letters","2015","17","21","5408","5411","10.1021/acs.orglett.5b02755","","x-ray","0.71073","MoKα","","0.1194","0.0509","","","0.1157","0.1467","","","","","","0.976","","","","has coordinates","170828","2020-10-21","18:00:00",""
"1540375","6.282","0.002","9.924","0.004","24.859","0.01","90","","90","","90","","1549.8","1","293","2","293","2","","","","","","","synthesis as described","4","P 21 21 21","P 2ac 2ab","19","","","","- C13 H21 N O6 -","- C13 H21 N O6 -","- C52 H84 N4 O24 -","4","1","","Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François","Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.","Organic letters","2015","17","21","5408","5411","10.1021/acs.orglett.5b02755","","x-ray","0.71073","MoKα","","0.1392","0.0587","","","0.1363","0.1637","","","","","","0.958","","","","has coordinates","170828","2020-10-21","18:00:00",""
"1540376","10.248","0.002","9.553","0.002","11.932","0.003","90","","99.477","0.004","90","","1152.2","0.4","293","2","293","2","","","","","","","synthesis as described","4","P 1 21 1","P 2yb","4","","","","- C16 H27 N O8 -","- C16 H27 N O8 -","- C32 H54 N2 O16 -","2","1","","Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François","Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.","Organic letters","2015","17","21","5408","5411","10.1021/acs.orglett.5b02755","","x-ray","0.71073","MoKα","","0.0776","0.0524","","","0.1165","0.1261","","","","","","0.956","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1540377","10.375","0.0011","17.5559","0.0019","10.8576","0.0012","90","","95.023","0.002","90","","1970","0.4","293","2","293","2","","","","","","","synthesis as described","4","P 1 21 1","P 2yb","4","","","","- C17 H28 N2 O6 -","- C17 H28 N2 O6 -","- C68 H112 N8 O24 -","4","2","","Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François","Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.","Organic letters","2015","17","21","5408","5411","10.1021/acs.orglett.5b02755","","x-ray","0.71073","MoKα","","0.0564","0.0411","","","0.1002","0.1085","","","","","","1.02","","","","has coordinates","170828","2020-10-21","18:00:00",""
"1540378","11.0948","0.0013","6.112","0.0007","15.1863","0.0018","90","","92.704","0.002","90","","1028.7","0.2","293","2","293","2","","","","","","","synthesis as described","5","P 1 21 1","P 2yb","4","","","","- C19 H24 N2 O6 S -","- C19 H24 N2 O6 S -","- C38 H48 N4 O12 S2 -","2","1","","Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François","Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.","Organic letters","2015","17","21","5408","5411","10.1021/acs.orglett.5b02755","","x-ray","0.71073","MoKα","","0.048","0.0459","","","0.1208","0.1229","","","","","","1.112","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1540379","9.6081","0.0009","10.7346","0.001","20.0544","0.0018","90","","91.493","0.001","90","","2067.7","0.3","293","2","293","2","","","","","","","synthesis as described","4","P 1 21 1","P 2yb","4","","","","- C20 H26 N2 O6 -","- C20 H26 N2 O6 -","- C80 H104 N8 O24 -","4","2","","Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François","Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.","Organic letters","2015","17","21","5408","5411","10.1021/acs.orglett.5b02755","","x-ray","0.71073","MoKα","","0.0462","0.0396","","","0.1067","0.1113","","","","","","1.021","","","","has coordinates","176428","2020-10-21","18:00:00",""
"1540534","12.452","0.002","9.3523","0.0016","11.841","0.002","90","","98.748","0.004","90","","1362.9","0.4","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H15 N O2 -","- C17 H15 N O2 -","- C68 H60 N4 O8 -","4","1","","Zhou, Zhi; Liu, Guixia; Chen, Yan; Lu, Xiyan","Cascade Synthesis of 3-Alkylidene Dihydrobenzofuran Derivatives via Rhodium(III)-Catalyzed Redox-Neutral C-H Functionalization/Cyclization.","Organic letters","2015","17","23","5874","5877","10.1021/acs.orglett.5b03060","","","0.71073","MoKα","","0.0894","0.0641","","","0.1315","0.1392","","","","","","1.077","","","","has coordinates","170830","2020-10-21","18:00:00",""
"1540535","11.3831","0.0003","11.7165","0.0003","12.5092","0.0003","77.777","0.002","83.9","0.002","89.052","0.002","1621.27","0.07","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C44 H28 Cl4 O -","- C44 H28 Cl4 O -","- C88 H56 Cl8 O2 -","2","1","","Das, Soumyajit; Wu, Jishan","Toward Singlet-Triplet Bistable Nonalternant Kekulé Hydrocarbons: Azulene-to-Naphthalene Rearrangement.","Organic letters","2015","17","23","5854","5857","10.1021/acs.orglett.5b03028","","","1.54178","CuKα","","0.0997","0.0583","","","0.12","0.1372","","","","","","1.018","","","","has coordinates","170831","2020-10-21","18:00:00",""
"1540536","6.359","0.002","22.998","0.005","32.023","0.007","90","","90.01","0.001","90","","4683","2","173","2","173","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C15 H21 N3 O5 -","- C15 H21 N3 O5 -","- C180 H252 N36 O60 -","12","6","","Zhang, Xiaofei; Yang, Haodong; Tang, Pingping","Transition-Metal-Free Oxidative Aliphatic C-H Azidation.","Organic letters","2015","17","23","5828","5831","10.1021/acs.orglett.5b03001","","","1.54187","CuKα","","0.0806","0.0682","","","0.1499","0.1575","","","","","","1.099","","","","has coordinates","170834","2020-10-21","18:00:00",""
"1540537","10.9076","0.0008","6.7702","0.0004","21.2437","0.0015","90","","103.38","0.002","90","","1526.19","0.18","120","2","120","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H24 N2 O2 S -","- C15 H24 N2 O2 S -","- C60 H96 N8 O8 S4 -","4","1","","Kröger, Denis; Franz, Max; Schmidtmann, Marc; Martens, Jürgen","Sequential Multicomponent Reactions and a Cu-Mediated Rearrangement: Diastereoselective Synthesis of Tricyclic Ketones.","Organic letters","2015","17","23","5866","5869","10.1021/acs.orglett.5b03057","","","0.71073","MoKα","","0.0535","0.0367","","","0.0845","0.0924","","","","","","1.029","","","","has coordinates","170835","2020-10-21","18:00:00",""
"1540559","6.8195","0.0012","8.3525","0.0014","20.053","0.003","90","","90","","90","","1142.2","0.3","298","2","298","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C15 H13 N -","- C15 H13 N -","- C60 H52 N4 -","4","1","","Kanchupalli, Vinaykumar; Joseph, Desna; Katukojvala, Sreenivas","Pyridazine N-Oxides as Precursors of Metallocarbenes: Rhodium-Catalyzed Transannulation with Pyrroles.","Organic letters","2015","17","23","5878","5881","10.1021/acs.orglett.5b03064","","","0.71073","MoKα","","0.0858","0.0449","","","0.1181","0.1538","","","","","","0.943","","","","has coordinates","170832","2020-10-21","18:00:00",""
"1540569","13.835","0.003","14.066","0.002","7.7299","0.0013","90","","97.446","0.008","90","","1491.6","0.5","125","","125","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C17 H11 F3 N2 O3 -","- C17 H11 F3 N2 O3 -","- C68 H44 F12 N8 O12 -","4","1","","Fugard, Alison J.; Thompson, Bethany K.; Slawin, Alexandra M. Z.; Taylor, James E.; Smith, Andrew D.","Organocatalytic Synthesis of Fused Bicyclic 2,3-Dihydro-1,3,4-oxadiazoles through an Intramolecular Cascade Cyclization.","Organic letters","2015","17","23","5824","5827","10.1021/acs.orglett.5b02997","","","1.54187","CuKα","","","0.0359","","","","0.0993","","","","","","1.024","","","","has coordinates","170833","2020-10-21","18:00:00",""
"1540574","12.134","0.0003","7.418","0.0002","26.1516","0.0007","90","","91.845","0.001","90","","2352.69","0.11","200","2","200","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H11 N O3 -","- C15 H11 N O3 -","- C120 H88 N8 O24 -","8","2","","Tomás-Mendivil, Eder; Starck, Jérôme; Ortuno, Jean-Claude; Michelet, Véronique","Synthesis of Functionalized 1H-Isochromene Derivatives via a Au-Catalyzed Domino Cycloisomerization/Reduction Approach.","Organic letters","2015","17","24","6126","6129","10.1021/acs.orglett.5b03146","","","1.54178","CuKα","","0.0629","0.0563","","","0.1508","0.1566","","","","","","1.085","","","","has coordinates","173606","2020-10-21","18:00:00",""
"1540580","26.2091","0.0005","26.2091","0.0005","6.7076","0.0005","90","","90","","120","","3990.3","0.3","123","2","123","2","","","","","","","","3","P 65","P 65","170","","","","- C34 H30 O2 -","- C34 H30 O2 -","- C204 H180 O12 -","6","1","","Kumar, Ravindra; Tokura, Hiromu; Nishimura, Akira; Mori, Tadashi; Hoshimoto, Yoichi; Ohashi, Masato; Ogoshi, Sensuke","Nickel(0)/N-Heterocyclic Carbene-Catalyzed Asymmetric [2 + 2 + 2] Cycloaddition of Two Enones and an Alkyne: Access to Cyclohexenes with Four Contiguous Stereogenic Centers.","Organic letters","2015","17","24","6018","6021","10.1021/acs.orglett.5b02983","","","1.54187","CuKα","","0.0568","0.0451","","","0.0852","0.0892","","","","","","1.041","","","","has coordinates","173604","2020-10-21","18:00:00",""
"1540584","6.1386","0.0002","8.845","0.0003","20.0476","0.0007","100.943","0.003","95.193","0.003","92.11","0.003","1062.7","0.06","130","0.1","130","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C21 H29 N O7 -","- C21 H29 N O7 -","- C42 H58 N2 O14 -","2","1","","Cameron, Alex; Fisher, Brendan; Fisk, Nicholas; Hummel, Jessica; White, Jonathan M.; Krenske, Elizabeth H.; Rizzacasa, Mark A.","Towards the Synthesis of Dihydrooxepino[4,3-b]pyrrole-Containing Natural Products via Cope Rearrangement of Vinyl Pyrrole Epoxides.","Organic letters","2015","17","24","5998","6001","10.1021/acs.orglett.5b02965","","x-ray","1.54184","CuKα","","0.0408","0.0366","","","0.0952","0.0993","","","","","","1.051","","","","has coordinates","173605","2020-10-21","18:00:00",""
"1540590","7.2431","0.0002","9.1369","0.0003","9.4709","0.0003","67.245","0.001","89.096","0.001","67.767","0.001","528.73","0.03","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C15 H7 F O2 -","- C15 H7 F O2 -","- C30 H14 F2 O4 -","2","1","","Wu, Xunshen; Yang, Yang; Han, Jianwei; Wang, Limin","Palladium Catalyzed C-I and Vicinal C-H Dual Activation of Diaryliodonium Salts for Diarylation: Synthesis of 4,5-Benzocoumarins.","Organic letters","2015","17","22","5654","5657","10.1021/acs.orglett.5b02938","","","0.71073","MoKα","","0.0411","0.0366","","","0.1035","0.1091","","","","","","1.068","","","","has coordinates","170739","2020-10-21","18:00:00",""
"1540591","12.335","0.003","13.08","0.003","12.657","0.003","90","","102.79","0.03","90","","1991.4","0.8","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C23 H31 N O2 -","- C23 H26 N O2 -","- C92 H104 N4 O8 -","4","1","","Wang, Xinbo; Pan, Yupeng; Huang, Kuo-Wei; Lai, Zhiping","One-Pot Synthesis of N-(α-Peroxy)Indole/Carbazole via Chemoselective Three-Component Condensation Reaction in Open Atmosphere.","Organic letters","2015","17","22","5630","5633","10.1021/acs.orglett.5b02881","","","0.71073","MoKα","","0.1484","0.1446","","","0.4974","0.5083","","","","","","2.694","","","","has coordinates","170740","2020-10-21","18:00:00",""
"1540592","11.418","0.006","10.794","0.006","17.585","0.01","90","","102.207","0.019","90","","2118","2","296","2","296","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C12 H12 O2 -","- C12 H12 O2 -","- C96 H96 O16 -","8","2","","Mao, Wenbin; Zhu, Chen","Synergistic Acid-Promoted Synthesis of Highly Substituted Butenolides via the Annulation of Keto Acids and Tertiary Alcohols.","Organic letters","2015","17","22","5710","5713","10.1021/acs.orglett.5b03026","","","0.71073","MoKα","","0.1199","0.0502","","","0.1259","0.1584","","","","","","0.971","","","","has coordinates","170741","2020-10-21","18:00:00",""
"1540593","14.2696","0.0019","14.853","0.002","14.948","0.003","67.375","0.018","72.768","0.015","89.623","0.012","2772.3","0.9","298","2","298","2","","","","","","","","6","P -1","-P 1","2","","","","- C33 H24 F3 N O4 S -","- C33 H24 F3 N O4 S -","- C132 H96 F12 N4 O16 S4 -","4","2","","Nayak, Sanatan; Ghosh, Nayan; Prabagar, B.; Sahoo, Akhila K.","p-TsOH Promoted Au(I)-Catalyzed Consecutive Endo Cyclization of Yne-Tethered Ynamide: Access to Benzofused Dihydroisoquinolones.","Organic letters","2015","17","22","5662","5665","10.1021/acs.orglett.5b02946","","","0.71073","MoKα","","0.29","0.0755","","","0.0821","0.1429","","","","","","0.896","","","","has coordinates","170742","2020-10-21","18:00:00",""
"1540594","11.3289","0.0006","14.3997","0.0007","19.8404","0.001","90","","90","","90","","3236.6","0.3","223","2","223","2","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C21 H16 O4 -","- C21 H16 O4 -","- C168 H128 O32 -","8","1","","Zheng, Yang; Mao, Jincheng; Weng, Yuecheng; Zhang, Xiaolu; Xu, Xinfang","Cyclopentadiene Construction via Rh-Catalyzed Carbene/Alkyne Metathesis Terminated with Intramolecular Formal [3 + 2] Cycloaddition.","Organic letters","2015","17","22","5638","5641","10.1021/acs.orglett.5b02912","","","0.71073","MoKα","","0.0564","0.0395","","","0.0925","0.0994","","","","","","1.029","","","","has coordinates","170743","2020-10-21","18:00:00",""
"1540595","8.1024","0.0011","11.3536","0.0015","14.828","0.002","90","","90","","90","","1364","0.3","100","","100","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","(S)-4-(4-methoxyphenyl)-4-phenyl-1,2,3-oxathiazolidine 2,2-dioxide","","- C15 H15 N O4 S -","- C15 H15 N O4 S -","- C60 H60 N4 O16 S4 -","4","1","","Kong, Jongrock; McLaughlin, Mark; Belyk, Kevin; Mondschein, Ryan","Enantioselective Rh(I)-Catalyzed Addition of Arylboronic Acids to Cyclic Ketimines.","Organic letters","2015","17","22","5520","5523","10.1021/acs.orglett.5b02032","","x-ray","1.54184","CuKα","","0.022","0.0218","","","0.0582","0.0588","","","","","","1.032","","","","has coordinates","170744","2020-10-21","18:00:00",""
"1540596","8.1709","0.0002","8.6771","0.0002","25.4706","0.0006","90","","90","","90","","1805.86","0.07","100","2","100","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","(6R,7S)-5-(3-Nitro-1-(3-bromophenyl)2-phenylpropyl)-2-furfural","","- C20 H16 Br N O4 -","- C20 H16 Br N O4 -","- C80 H64 Br4 N4 O16 -","4","1","","Skrzyńska, Anna; Przydacz, Artur; Albrecht, Łukasz","Organocatalytic Nonclassical Trienamine Activation in the Remote Alkylation of Furan Derivatives.","Organic letters","2015","17","22","5682","5685","10.1021/acs.orglett.5b02979","","","1.54178","CuKα","","0.0206","0.0201","","","0.0532","0.0536","","","","","","1.051","","","","has coordinates","170745","2020-10-21","18:00:00",""
"1540597","10.3902","0.0005","11.1304","0.0004","17.5579","0.0007","90","","95.9749","0.0016","90","","2019.49","0.15","173","","173","","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C22 H15 Cl F3 N O3 S -","- C22 H15 Cl F3 N O3 S -","- C88 H60 Cl4 F12 N4 O12 S4 -","4","1","","Huang, Zhongyan; Wang, Chen; Tokunaga, Etsuko; Sumii, Yuji; Shibata, Norio","Stereoselective Synthesis of β-Lactam-triflones under Catalyst-Free Conditions.","Organic letters","2015","17","22","5610","5613","10.1021/acs.orglett.5b02827","","","0.71075","MoKα","","","0.0421","","","","0.1109","","","","","","1.217","","","","has coordinates","170746","2020-10-21","18:00:00",""
"1540598","10.2204","0.0005","10.3756","0.0007","18.4485","0.0012","95.235","0.005","105.12","0.005","108.782","0.005","1754.9","0.2","180","0.1","180","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C21 H21 N Si -","- C21 H21 N Si -","- C84 H84 N4 Si4 -","4","2","","Hao, Wei; Wang, Han; Ye, Qingyu; Zhang, Wen-Xiong; Xi, Zhenfeng","Cyclopentadiene-Phosphine/Palladium-Catalyzed Synthesis of Indolizines from Pyrrole and 1,4-Dibromo-1,3-butadienes.","Organic letters","2015","17","22","5674","5677","10.1021/acs.orglett.5b02959","","","0.71073","MoKα","","0.0984","0.0662","","","0.1487","0.1689","","","","","","1.046","","","","has coordinates","170747","2020-10-21","18:00:00",""
"1540599","7.2793","0.0007","12.9826","0.0013","18.8537","0.0019","90","","90","","90","","1781.8","0.3","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C23 H17 N O3 -","- C23 H17 N O3 -","- C92 H68 N4 O12 -","4","1","","Banerjee, Arghya; Santra, Sourav Kumar; Mohanta, Prakash Ranjan; Patel, Bhisma K.","Ruthenium(II) Catalyzed Regiospecific C-H/O-H Annulations of Directing Arenes via Weak Coordination.","Organic letters","2015","17","22","5678","5681","10.1021/acs.orglett.5b02967","","","0.71073","MoKα","","0.0674","0.0418","","","0.0816","0.0893","","","","","","1.012","","","","has coordinates","170748","2020-10-21","18:00:00",""
"1540600","9.6188","0.0004","10.5071","0.0004","11.1216","0.0004","94.256","0.002","104.939","0.002","102.615","0.002","1049.6","0.07","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C29 H18 Cl N O -","- C29 H18 Cl N O -","- C58 H36 Cl2 N2 O2 -","2","1","","Banerjee, Arghya; Santra, Sourav Kumar; Mohanta, Prakash Ranjan; Patel, Bhisma K.","Ruthenium(II) Catalyzed Regiospecific C-H/O-H Annulations of Directing Arenes via Weak Coordination.","Organic letters","2015","17","22","5678","5681","10.1021/acs.orglett.5b02967","","","0.71073","MoKα","","0.0454","0.0355","","","0.0998","0.111","","","","","","1.094","","","","has coordinates","170750","2020-10-21","18:00:00",""
"1540601","7.5747","0.0003","10.8659","0.0005","20.7341","0.0009","90","","90","","90","","1706.54","0.13","300","2","300","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C20 H21 N O2 -","- C20 H21 N O2 -","- C80 H84 N4 O8 -","4","1","","Karmakar, Raju; Suneja, Arun; Bisai, Vishnumaya; Singh, Vinod K.","Ni(II)-Catalyzed Highly Stereo- and Regioselective Syntheses of Isoindolinones and Isoquinolinones from in Situ Prepared Aldimines Triggered by Homoallylation/Lactamization Cascade.","Organic letters","2015","17","22","5650","5653","10.1021/acs.orglett.5b02932","","","0.71073","MoKα","","0.0734","0.0464","","","0.1273","0.1463","","","","","","1.039","","","","has coordinates","170751","2020-10-21","18:00:00",""
"1540602","8.1069","0.0011","8.3799","0.0011","8.9188","0.0011","102.823","0.004","100.864","0.004","113.21","0.004","516.59","0.12","173","2","173","2","","","","","","","","3","P -1","-P 1","2","","","","- C13 H12 O2 -","- C13 H12 O2 -","- C26 H24 O4 -","2","1","","Sekine, Kohei; Sadamitsu, Yuta; Yamada, Tohru","SilverCatalyzed Cascade Carboxylation and Cyclization of Trimethyl(2-methylenebut-3-yn-1-yl)silane Derivatives.","Organic letters","2015","17","22","5706","5709","10.1021/acs.orglett.5b03023","","","0.71073","(MoKα)","","0.0535","0.0411","","","0.1202","0.1439","","","","","","1.167","","","","has coordinates","170752","2020-10-21","18:00:00",""
"1540603","7.6982","0.0002","5.5273","0.0002","29.041","0.0008","90","","90","","90","","1235.7","0.06","147","2","147","2","","","","","","","","5","P c a 21","P 2c -2ac","29","","","","- C15 H12 B N3 O -","- C15 H12 B N3 O -","- C60 H48 B4 N12 O4 -","4","1","","Adachi, Shinya; Liew, Sean K.; Lee, C. Frank; Lough, Alan; He, Zhi; Denis, Jeffrey D St; Poda, Gennady; Yudin, Andrei K.","Condensation-Driven Assembly of Boron-Containing Bis(Heteroaryl) Motifs Using a Linchpin Approach.","Organic letters","2015","17","22","5594","5597","10.1021/acs.orglett.5b02741","","","1.54178","CuKα","","0.0399","0.0384","","","0.0961","0.0968","","","","","","1.196","","","","has coordinates","170753","2020-10-21","18:00:00",""
"1540604","10.6778","0.0003","8.9179","0.0002","27.039","0.0007","90","","90","","90","","2574.75","0.11","147","2","147","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C15 H13 B N4 -","- C15 H13 B N4 -","- C120 H104 B8 N32 -","8","1","","Adachi, Shinya; Liew, Sean K.; Lee, C. Frank; Lough, Alan; He, Zhi; Denis, Jeffrey D St; Poda, Gennady; Yudin, Andrei K.","Condensation-Driven Assembly of Boron-Containing Bis(Heteroaryl) Motifs Using a Linchpin Approach.","Organic letters","2015","17","22","5594","5597","10.1021/acs.orglett.5b02741","","","1.54178","CuKα","","0.036","0.0319","","","0.0769","0.0794","","","","","","1.074","","","","has coordinates","170754","2020-10-21","18:00:00",""
"1540605","10.332","0.002","10.435","0.002","13.632","0.003","67.996","0.005","82.773","0.006","76.624","0.006","1324.5","0.5","103","2","103","2","","","","","","","","4","P -1","-P 1","2","","10,11,12-Triphenyl-10H-phenanthro[9,10-f]phosphindole 10-oxide","","- C38 H25 O P -","- C38 H25 O P -","- C76 H50 O2 P2 -","2","1","","Wu, Bin; Chopra, Rena; Yoshikai, Naohiko","One-Pot Benzo[b]phosphole Synthesis through Sequential Alkyne Arylmagnesiation, Electrophilic Trapping, and Intramolecular Phospha-Friedel-Crafts Cyclization.","Organic letters","2015","17","22","5666","5669","10.1021/acs.orglett.5b02950","","","0.71073","MoKα","","0.1224","0.0585","","","0.1177","0.1468","","","","","","0.997","","","","has coordinates","170755","2020-10-21","18:00:00",""
"1540606","8.7469","0.0002","13.4624","0.0003","24.6866","0.0005","90","","90","","90","","2906.95","0.11","100","2","100","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C12 H17 N O3 S2 -","- C12 H17 N O3 S2 -","- C96 H136 N8 O24 S16 -","8","2","","Marsini, Maurice A.; Reeves, Jonathan T.; Desrosiers, Jean-Nicolas; Herbage, Melissa A.; Savoie, Jolaine; Li, Zhibin; Fandrick, Keith R.; Sader, C. Avery; McKibben, Bryan; Gao, Donghong A.; Cui, Jianwen; Gonnella, Nina C.; Lee, Heewon; Wei, Xudong; Roschangar, Frank; Lu, Bruce Z.; Senanayake, Chris H.","Diastereoselective Synthesis of α-Quaternary Aziridine-2-carboxylates via Aza-Corey-Chaykovsky Aziridination of N-tert-Butanesulfinyl Ketimino Esters.","Organic letters","2015","17","22","5614","5617","10.1021/acs.orglett.5b02838","","","1.54178","CuKα","","0.0237","0.0231","","","0.0606","0.061","","","","","","1.08","","","","has coordinates","214153","2020-10-21","18:00:00",""
"1540607","5.9251","0.0001","14.3949","0.0003","17.8151","0.0004","90","","90","","90","","1519.47","0.05","100","2","100","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C15 H21 N O3 S -","- C15 H21 N O3 S -","- C60 H84 N4 O12 S4 -","4","1","","Marsini, Maurice A.; Reeves, Jonathan T.; Desrosiers, Jean-Nicolas; Herbage, Melissa A.; Savoie, Jolaine; Li, Zhibin; Fandrick, Keith R.; Sader, C. Avery; McKibben, Bryan; Gao, Donghong A.; Cui, Jianwen; Gonnella, Nina C.; Lee, Heewon; Wei, Xudong; Roschangar, Frank; Lu, Bruce Z.; Senanayake, Chris H.","Diastereoselective Synthesis of α-Quaternary Aziridine-2-carboxylates via Aza-Corey-Chaykovsky Aziridination of N-tert-Butanesulfinyl Ketimino Esters.","Organic letters","2015","17","22","5614","5617","10.1021/acs.orglett.5b02838","","","1.54178","CuKα","","0.0257","0.0253","","","0.0637","0.0641","","","","","","1.097","","","","has coordinates","170757","2020-10-21","18:00:00",""
"1540608","9.9554","0.0003","13.0776","0.0004","14.9103","0.0004","75.045","0.001","78.893","0.001","69.659","0.001","1747.12","0.09","100","2","100","","","","","","","","","7","P 1","P 1","1","","","","- C32 H37 Br Cl N3 O6 S2 -","- C32 H37 Br Cl N3 O6 S2 -","- C64 H74 Br2 Cl2 N6 O12 S4 -","2","2","","Marsini, Maurice A.; Reeves, Jonathan T.; Desrosiers, Jean-Nicolas; Herbage, Melissa A.; Savoie, Jolaine; Li, Zhibin; Fandrick, Keith R.; Sader, C. Avery; McKibben, Bryan; Gao, Donghong A.; Cui, Jianwen; Gonnella, Nina C.; Lee, Heewon; Wei, Xudong; Roschangar, Frank; Lu, Bruce Z.; Senanayake, Chris H.","Diastereoselective Synthesis of α-Quaternary Aziridine-2-carboxylates via Aza-Corey-Chaykovsky Aziridination of N-tert-Butanesulfinyl Ketimino Esters.","Organic letters","2015","17","22","5614","5617","10.1021/acs.orglett.5b02838","","","1.54178","CuKα","","0.0409","0.0404","","","0.1053","0.1058","","","","","","1.052","","","","has coordinates,has disorder","170758","2020-10-21","18:00:00",""
"1540609","10.5944","0.0018","5.6765","0.001","27.958","0.005","90","","94.681","0.003","90","","1675.8","0.5","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C20 H20 N2 O S -","- C20 H20 N2 O S -","- C80 H80 N8 O4 S4 -","4","1","","Zhu, Longzhi; Qiu, Renhua; Cao, Xin; Xiao, Song; Xu, Xinhua; Au, Chak-Tong; Yin, Shuang-Feng","Copper-Mediated Remote C-H Bond Chalcogenation of Quinolines on the C5 Position.","Organic letters","2015","17","22","5528","5531","10.1021/acs.orglett.5b02511","","","0.71073","MoKα","","0.0953","0.0913","","","0.2157","0.2174","","","","","","1.179","","","","has coordinates","170759","2020-10-21","18:00:00",""
"1540610","7.7796","0.0013","34.171","0.006","8.2694","0.0014","90","","93.715","0.005","90","","2193.7","0.6","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C23 H30 N2 O4 S -","- C22 H30 N2 O4 S -","- C88 H120 N8 O16 S4 -","4","1","","Shen, Mei-Hua; Xu, Ke; Sun, Chu-Han; Xua, Hua-Dong","Stereoselective Construction of Bridged trans-aza-Bicyclo[7/6,3/2,1]alkenyl Imines through Ring Expansion aza-Cope Rearrangement.","Organic letters","2015","17","22","5598","5601","10.1021/acs.orglett.5b02798","","","0.71073","MoKα","","0.2189","0.1536","","","0.2663","0.2998","","","","","","1.16","","","","has coordinates","170760","2020-10-21","18:00:00",""
"1540611","16.685","0.004","16.536","0.004","37.285","0.008","90","","90","","90","","10287","4","173.15","","173.15","","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C60 H56 Si4 -","- C60 H56 Si4 -","- C480 H448 Si32 -","8","1","","Fu, Xiangyu; Zhao, Dahui","Cyclo-oligomerization of 6,12-Diethynyl Indeno[1,2-b]fluorenes via Diradical Intermediates.","Organic letters","2015","17","22","5694","5697","10.1021/acs.orglett.5b03000","","","0.71073","MoKα","","0.0923","0.0829","","","0.1789","0.1845","","","","","","1.32","","","","has coordinates","170761","2020-10-21","18:00:00",""
"1540612","8.1446","0.0001","8.8894","0.0002","22.8882","0.0004","90","","97.4066","0.0012","90","","1643.29","0.05","200","","200","","","","","","","","local","3","P 1 21/n 1","-P 2yn","14","","","","- C20 H22 O4 -","- C20 H22 O4 -","- C80 H88 O16 -","4","1","","Mackay, Emily G.; Nörret, Marck; Wong, Leon S.-M.; Louis, Ignace; Lawrence, Andrew L.; Willis, Anthony C.; Sherburn, Michael S.","A Domino Diels-Alder Approach toward the Tetracyclic Nicandrenone Framework.","Organic letters","2015","17","22","5517","5519","10.1021/acs.orglett.5b02412","","","0.71073","MoKα","","0.067","0.0338","","0.1157","0.0805","0.1157","","","","","","0.997","","","","has coordinates","170762","2020-10-21","18:00:00",""
"1540613","14.271","0.002","7.3032","0.001","15.87","0.002","90","","97.862","0.007","90","","1638.5","0.4","200","","200","","","","","","","","local","3","P 1 21/c 1","-P 2ybc","14","","","","- C20 H22 O4 -","- C20 H22 O4 -","- C80 H88 O16 -","4","1","","Mackay, Emily G.; Nörret, Marck; Wong, Leon S.-M.; Louis, Ignace; Lawrence, Andrew L.; Willis, Anthony C.; Sherburn, Michael S.","A Domino Diels-Alder Approach toward the Tetracyclic Nicandrenone Framework.","Organic letters","2015","17","22","5517","5519","10.1021/acs.orglett.5b02412","","","0.71073","MoKα","","0.1808","0.0751","","0.2255","0.1758","0.2255","","","","","","0.9869","","","","has coordinates","170763","2020-10-21","18:00:00",""
"1540614","6.8857","0.0011","7.8782","0.0012","14.23","0.002","73.669","0.005","85.904","0.005","80.621","0.005","730.62","0.19","100","2","100","2","","","","","","","","4","P -1","-P 1","2","FW155","","","- C15 H14 N2 O7 -","- C15 H14 N2 O7 -","- C30 H28 N4 O14 -","2","1","","Wagner, Frederic; Harms, Klaus; Koert, Ulrich","Hauser-Heck: Efficient Synthesis of γ-Aryl-β-ketoesters en Route to Substituted Naphthalenes.","Organic letters","2015","17","22","5670","5673","10.1021/acs.orglett.5b02952","","","0.71073","MoKα","","0.0637","0.0397","","","0.0895","0.0987","","","","","","1.052","","","","has coordinates","170764","2020-10-21","18:00:00",""
"1540615","6.4851","0.0006","8.2205","0.0008","12.0587","0.001","92.463","0.003","91.458","0.003","99.303","0.003","633.47","0.1","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C13 H10 N2 O7 -","- C13 H10 N2 O7 -","- C26 H20 N4 O14 -","2","1","","Wagner, Frederic; Harms, Klaus; Koert, Ulrich","Hauser-Heck: Efficient Synthesis of γ-Aryl-β-ketoesters en Route to Substituted Naphthalenes.","Organic letters","2015","17","22","5670","5673","10.1021/acs.orglett.5b02952","","","0.71073","MoKα","","0.0395","0.0328","","","0.087","0.0914","","","","","","1.076","","","","has coordinates","170764","2020-10-21","18:00:00",""
"1540616","7.9292","0.0004","8.4053","0.0004","10.7094","0.0005","93.039","0.002","104.73","0.002","106.745","0.002","654.85","0.06","100","2","100","2","","","","","","","","3","P -1","-P 1","2","FWHA041b","","","- C15 H16 O5 -","- C15 H16 O5 -","- C30 H32 O10 -","2","1","","Wagner, Frederic; Harms, Klaus; Koert, Ulrich","Hauser-Heck: Efficient Synthesis of γ-Aryl-β-ketoesters en Route to Substituted Naphthalenes.","Organic letters","2015","17","22","5670","5673","10.1021/acs.orglett.5b02952","","","0.71073","MoKα","","0.0442","0.0353","","","0.0954","0.1016","","","","","","1.038","","","","has coordinates","170764","2020-10-21","18:00:00",""
"1540617","14.188","0.0006","5.8892","0.0003","15.3276","0.0006","90","","103.795","0.002","90","","1243.77","0.1","296","2","296","2","","","","","","","","4","P 1 n 1","P -2yac","7","","","","- C30 H26 O3 S -","- C30 H26 O3 S -","- C60 H52 O6 S2 -","2","1","","Chang, Meng-Yang; Cheng, Yu-Chieh","Bi(OTf)3 Mediated exo-Olefin Isomerization of α-Benzoyl β-Styrylsulfones.","Organic letters","2015","17","22","5702","5705","10.1021/acs.orglett.5b03020","","","0.71073","MoKα","","0.0509","0.0369","","","0.102","0.1294","","","","","","1.158","","","","has coordinates","170765","2020-10-21","18:00:00",""
"1540618","7.1637","0.0004","11.4472","0.0005","11.9023","0.0005","79.27","0.002","77.811","0.002","87.147","0.002","937.3","0.08","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C24 H20 O2 -","- C24 H20 O2 -","- C48 H40 O4 -","2","1","","Chang, Meng-Yang; Cheng, Yu-Chieh","Bi(OTf)3 Mediated exo-Olefin Isomerization of α-Benzoyl β-Styrylsulfones.","Organic letters","2015","17","22","5702","5705","10.1021/acs.orglett.5b03020","","","0.71073","MoKα","","0.057","0.0393","","","0.1184","0.1402","","","","","","1.147","","","","has coordinates","170766","2020-10-21","18:00:00",""
"1540619","15.3544","0.0007","5.9154","0.0003","21.8657","0.0011","90","","90.554","0.002","90","","1985.91","0.17","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C24 H21 F O3 S -","- C24 H21 F O3 S -","- C96 H84 F4 O12 S4 -","4","1","","Chang, Meng-Yang; Cheng, Yu-Chieh","Bi(OTf)3 Mediated exo-Olefin Isomerization of α-Benzoyl β-Styrylsulfones.","Organic letters","2015","17","22","5702","5705","10.1021/acs.orglett.5b03020","","","0.71073","MoKα","","0.0537","0.0371","","","0.1035","0.1264","","","","","","1.152","","","","has coordinates","170767","2020-10-21","18:00:00",""
"1540620","16.1272","0.0015","8.2497","0.0008","17.782","0.0016","90","","90","","90","","2365.8","0.4","100","2","100","2","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C30 H26 O3 S -","- C30 H26 O3 S -","- C120 H104 O12 S4 -","4","1","","Chang, Meng-Yang; Cheng, Yu-Chieh","Bi(OTf)3 Mediated exo-Olefin Isomerization of α-Benzoyl β-Styrylsulfones.","Organic letters","2015","17","22","5702","5705","10.1021/acs.orglett.5b03020","","","0.71073","MoKα","","0.0475","0.0371","","","0.0808","0.0863","","","","","","1.026","","","","has coordinates","170768","2020-10-21","18:00:00",""
"1540621","14.7522","0.0008","13.9738","0.0008","6.7673","0.0004","90","","100.152","0.004","90","","1373.2","0.14","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C14 H11 Br N4 O -","- C14 H11 Br N4 O -","- C56 H44 Br4 N16 O4 -","4","1","","Rajamanickam, Suresh; Majji, Ganesh; Santra, Sourav Kumar; Patel, Bhisma K.","Bu4NI Catalyzed C-N Bond Formation via Cross-Dehydrogenative Coupling of Aryl Ethers (Csp3-H) and Tetrazoles (N-H).","Organic letters","2015","17","22","5586","5589","10.1021/acs.orglett.5b02749","","","0.71073","MoKα","","0.0678","0.0341","","","0.0841","0.1042","","","","","","1.002","","","","has coordinates","170769","2020-10-21","18:00:00",""
"1540622","19.9301","0.0018","11.6169","0.001","12.0116","0.0011","90","","106.035","0.002","90","","2672.8","0.4","130","","130","","","","","","","","","6","C 1 2 1","C 2y","5","","","","- C27 H20 Cl F3 N2 O3 -","- C27 H20 Cl F3 N2 O3 -","- C108 H80 Cl4 F12 N8 O12 -","4","1","","Zhou, Ding; Huang, Zheng; Yu, Xueting; Wang, Youxin; Li, Jian; Wang, Wei; Xie, Hexin","A Quinine-Squaramide Catalyzed Enantioselective Aza-Friedel-Crafts Reaction of Cyclic Trifluoromethyl Ketimines with Naphthols and Electron-Rich Phenols.","Organic letters","2015","17","22","5554","5557","10.1021/acs.orglett.5b02668","","","0.71073","MoKα","","0.051","0.0413","","","0.099","0.1038","","","","","","1.035","","","","has coordinates","170770","2020-10-21","18:00:00",""
"1540623","17.598","0.006","6.875","0.002","10.631","0.004","90","","90","","90","","1286.2","0.8","100","2","100","2","","","","","","","","4","P n m a","-P 2ac 2n","62","t-butyl pyridine indenone","1-(t-butyl)-3-methyl-9H-indeno[2,1-c]pyridin-9-one","","- C17 H17 N O -","- C17 H17 N O -","- C68 H68 N4 O4 -","4","0.5","","Das, Sajal; Hong, Dongsub; Chen, Zhiwei; She, Zhigang; Hersh, William H.; Subramaniam, Gopal; Chen, Yu","Auto-Tandem Palladium Catalysis: From Isoxazole to 2-Azafluorenone.","Organic letters","2015","17","22","5578","5581","10.1021/acs.orglett.5b02731","","","0.71073","MoKα","","0.0401","0.039","","","0.1077","0.1094","","","","","","1.041","","","","has coordinates","170771","2020-10-21","18:00:00",""
"1540624","9.5944","0.0018","19.75","0.004","7.917","0.0015","90","","90.554","0.002","90","","1500.1","0.5","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","o-(t-Bu isoxazole) MVK benzene","(E)-4-(2-(3-(tert-butyl)isoxazol-5-yl)phenyl)but-3-en-2-one","","- C17 H19 N O2 -","- C17 H19 N O2 -","- C68 H76 N4 O8 -","4","1","","Das, Sajal; Hong, Dongsub; Chen, Zhiwei; She, Zhigang; Hersh, William H.; Subramaniam, Gopal; Chen, Yu","Auto-Tandem Palladium Catalysis: From Isoxazole to 2-Azafluorenone.","Organic letters","2015","17","22","5578","5581","10.1021/acs.orglett.5b02731","","","0.71073","MoKα","","0.0463","0.0378","","","0.0897","0.0957","","","","","","1.05","","","","has coordinates","170772","2020-10-21","18:00:00",""
"1540625","11.521","0.0004","11.9824","0.0004","20.383","0.0006","90","","98.02","0.003","90","","2786.34","0.16","291","2","291.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C32 H21 O5 P W -","- C32 H21 O5 P W -","- C128 H84 O20 P4 W4 -","4","1","","Zhou, Yang; Gan, Zhenjie; Su, Bo; Li, Jun; Duan, Zheng; Mathey, François","Intramolecular, Pd/Cu-Co-catalyzed P-C Bond Cleavage and Addition onto an Alkyne: A Route to Benzophospholes.","Organic letters","2015","17","22","5722","5724","10.1021/acs.orglett.5b02926","","","0.71073","MoKα","","0.046","0.0318","","","0.0562","0.061","","","","","","1.038","","","","has coordinates","170773","2020-10-21","18:00:00",""
"1540649","7.687","0.0012","5.6405","0.0009","26.624","0.004","90","","97.533","0.002","90","","1144.4","0.3","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C11 H10 Br N2 S -","- C10 H10 Br N3 S -","- C40 H40 Br4 N12 S4 -","4","1","","Shen, Tao; Huang, Xiaoqiang; Liang, Yu-Feng; Jiao, Ning","Cu-Catalyzed Transformation of Alkynes and Alkenes with Azide and Dimethyl Sulfoxide Reagents.","Organic letters","2015","17","24","6186","6189","10.1021/acs.orglett.5b03179","","","0.71073","MoKα","","0.0435","0.0312","","","0.0719","0.0768","","","","","","1.043","","","","has coordinates","173607","2020-10-21","18:00:00",""
"1554753","7.9152","0.0009","11.4088","0.0014","28.388","0.003","90","","90","","90","","2563.5","0.5","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C31 H26 Cl N O4 -","- C31 H26 Cl N O4 -","- C124 H104 Cl4 N4 O16 -","4","1","","He, Zhao-Lin; Sheong, Fu Kit; Li, Qing-Hua; Lin, Zhenyang; Wang, Chun-Jiang","Exoselective 1,3-dipolar [3 + 6] cycloaddition of azomethine ylides with 2-acylcycloheptatrienes: stereoselectivity and mechanistic insight.","Organic letters","2015","17","6","1365","1368","10.1021/acs.orglett.5b00011","","","0.71073","MoKα","","0.0692","0.0397","","","0.0708","0.0821","","","","","","0.993","","","","has coordinates","238101","2020-10-21","18:00:00",""
"1554755","7.8931","0.0002","9.4542","0.0002","14.3399","0.0004","89.1605","0.0015","82.9814","0.0016","69.4905","0.0014","994.29","0.04","296","2","296","2","","","","","","","","4","P -1","-P 1","2","KCE2","","","- C22 H25 O5 P -","- C22 H25 O5 P -","- C44 H50 O10 P2 -","2","1","","Kim, Cheol-Eui; Son, Jeong-Yu; Shin, Seohyun; Seo, Boram; Lee, Phil Ho","Alkenylation of phosphacoumarins via aerobic oxidative Heck reactions and their synthetic application to fluorescent benzophosphacoumarins.","Organic letters","2015","17","4","908","911","10.1021/acs.orglett.5b00020","","","0.71073","MoKα","","0.1165","0.0635","","","0.1755","0.2068","","","","","","1.048","","","","has coordinates","238103","2020-10-21","18:00:00",""
"1554756","12.2068","0.0019","13.731","0.002","14.626","0.002","90","","99.027","0.003","90","","2421.1","0.6","200","2","200","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C26 H23 B F4 N2 O2 -","- C26 H23 B F4 N2 O2 -","- C104 H92 B4 F16 N8 O8 -","4","1","","Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong","Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.","Organic letters","2015","17","4","924","927","10.1021/acs.orglett.5b00028","","","0.71073","MoKα","","0.1044","0.0605","","","0.1551","0.1851","","","","","","1.057","","","","has coordinates","238104","2020-10-21","18:00:00",""
"1554764","10.72","0.003","18.331","0.004","12.174","0.003","90","","110.527","0.006","90","","2240.4","1","200","2","200","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C25 H20 B F4 N O -","- C25 H20 B F4 N O -","- C100 H80 B4 F16 N4 O4 -","4","1","","Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong","Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.","Organic letters","2015","17","4","924","927","10.1021/acs.orglett.5b00028","","","0.71073","MoKα","","0.098","0.073","","","0.2044","0.2217","","","","","","1.091","","","","has coordinates,has disorder","238106","2020-10-21","18:00:00",""
"1554765","12.3471","0.0004","13.3272","0.0004","13.9786","0.0005","90","","98.588","0.002","90","","2274.42","0.13","100","2","100","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C25 H21 B F4 N2 O2 -","- C25 H21 B F4 N2 O2 -","- C100 H84 B4 F16 N8 O8 -","4","1","","Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong","Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.","Organic letters","2015","17","4","924","927","10.1021/acs.orglett.5b00028","","","0.71073","MoKα","","0.0607","0.0426","","","0.1293","0.1557","","","","","","1.087","","","","has coordinates","238107","2020-10-21","18:00:00",""
"1554767","7.081","0.0004","19.406","0.0012","9.491","0.0006","90","","98.161","0.002","90","","1290.99","0.14","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C31 H24 Cl N O3 -","- C31 H24 Cl N O3 -","- C62 H48 Cl2 N2 O6 -","2","1","","Jayakumar, Samydurai; Kumarswamyreddy, Nandarapu; Prakash, Muthuraj; Kesavan, Venkitasamy","Palladium catalyzed asymmetric allylation of 3-OBoc-oxindoles: an efficient synthesis of 3-allyl-3-hydroxyoxindoles.","Organic letters","2015","17","5","1066","1069","10.1021/acs.orglett.5b00034","","","0.71073","MoKα","","0.0981","0.0425","","","0.1003","0.1228","","","","","","0.977","","","","has coordinates","238109","2020-10-21","18:00:00",""
"1554773","10.3083","0.0006","14.3567","0.0007","19.2355","0.001","75.287","0.003","74.747","0.003","84.913","0.003","2655.7","0.2","100","2","100","2","","","","","","","","7","P -1","-P 1","2","","","","- C49.05 H59.38 Cl5.87 Li0.15 N3 P3 Ti2 -","- C49.0508 H59.377 Cl5.8696 Li0.145 N3 P3 Ti2 -","- C98.1016 H118.754 Cl11.7392 Li0.29 N6 P6 Ti4 -","2","1","","Walker, Whitney K.; Anderson, Diana L.; Stokes, Ryjul W.; Smith, Stacey J.; Michaelis, David J.","Allylic aminations with hindered secondary amine nucleophiles catalyzed by heterobimetallic Pd-Ti complexes.","Organic letters","2015","17","3","752","755","10.1021/acs.orglett.5b00058","","","1.54178","CuKα","","0.0484","0.043","","","0.1133","0.1166","","","","","","1.084","","","","has coordinates,has disorder","238111","2020-10-21","18:00:00",""
"1554774","8.8951","0.0003","9.2936","0.0003","13.0036","0.0004","79.226","0.0012","76.069","0.0013","64.74","0.0011","939.24","0.05","173","2","173","2","","","","","","","","6","P -1","-P 1","2","","","","- C16 H19 Cl3 N P Ti -","- C16 H19 Cl3 N P Ti -","- C32 H38 Cl6 N2 P2 Ti2 -","2","1","","Walker, Whitney K.; Anderson, Diana L.; Stokes, Ryjul W.; Smith, Stacey J.; Michaelis, David J.","Allylic aminations with hindered secondary amine nucleophiles catalyzed by heterobimetallic Pd-Ti complexes.","Organic letters","2015","17","3","752","755","10.1021/acs.orglett.5b00058","","","1.54178","CuKα","","0.0295","0.028","","","0.0747","0.0763","","","","","","1.036","","","","has coordinates,has disorder","238112","2020-10-21","18:00:00",""
"1554776","13.871","0.0009","15.1622","0.0009","64.627","0.004","90","","90","","90","","13592","1.5","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C35 H26 N1.6 O10 -","- C33 H26 N1.6 O10 -","- C660 H520 N32 O200 -","20","5","","Cao, Pei; Yang, Jing; Miao, Cui-Ping; Yan, Yijun; Ma, Ya-Tuan; Li, Xiao-Nian; Zhao, Li-Xing; Huang, Sheng-Xiong","New duclauxamide from Penicillium manginii YIM PH30375 and structure revision of the duclauxin family.","Organic letters","2015","17","5","1146","1149","10.1021/acs.orglett.5b00081","","","1.54178","CuKα","","0.2965","0.1368","","","0.2977","0.3783","","","","","","1.082","","","","has coordinates","274567","2022-04-19","14:22:36",""
"1554782","9.7972","0.0007","10.509","0.0008","15.4371","0.0011","72.931","0.007","74.564","0.006","84.268","0.006","1464.2","0.2","170","","170","","","","","","","","","5","P -1","-P 1","2","","","","- C34 H29 N5 O4 S -","- C34 H29 N5 O4 S -","- C68 H58 N10 O8 S2 -","2","1","","Du, Zao; Xing, Yanpeng; Lu, Ping; Wang, Yanguang","Copper-catalyzed cascade double C3-indolations of 3-diazoindolin-2-imines with indoles: convenient access to 3,3-diaryl-2-iminoindoles.","Organic letters","2015","17","5","1192","1195","10.1021/acs.orglett.5b00089","","","0.71073","MoKα","","0.0625","0.043","","","0.0952","0.1066","","","","","","1.027","","","","has coordinates","238116","2020-10-21","18:00:00",""
"1554783","17.5333","0.0008","9.245","0.0004","13.3467","0.0006","90","","107.946","0.002","90","","2058.18","0.16","130","","130","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H27 N3 O2 -","- C24 H27 N3 O2 -","- C96 H108 N12 O8 -","4","1","","Bechara, William S.; Khazhieva, Inna S.; Rodriguez, Elsa; Charette, André B","One-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles via the addition of hydrazides to activated secondary amides.","Organic letters","2015","17","5","1184","1187","10.1021/acs.orglett.5b00128","","x-ray","1.34139","GaKα","","0.0386","0.036","","","0.0925","0.0947","","","","","","1.033","","","","has coordinates","238117","2020-10-21","18:00:00",""
"1554791","10.5706","0.0011","17.3802","0.0016","10.1316","0.001","90","","96.996","0.007","90","","1847.5","0.3","150","","150","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H15 N3 O -","- C21 H15 N3 O -","- C84 H60 N12 O4 -","4","1","","Bechara, William S.; Khazhieva, Inna S.; Rodriguez, Elsa; Charette, André B","One-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles via the addition of hydrazides to activated secondary amides.","Organic letters","2015","17","5","1184","1187","10.1021/acs.orglett.5b00128","","x-ray","1.34139","GaKα","","0.1117","0.0595","","","0.1454","0.1626","","","","","","0.985","","","","has coordinates","238119","2020-10-21","18:00:00",""
"1554793","10.7482","0.0003","12.7229","0.0005","16.152","0.0007","90","","90","","90","","2208.76","0.14","293","","293","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C24 H21 I N2 O3 S -","- C24 H21 I N2 O3 S -","- C96 H84 I4 N8 O12 S4 -","4","1","","Fu, Shaomin; Yang, Honghao; Li, Guoqiang; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei","Copper(II)-catalyzed enantioselective intramolecular cyclization of N-alkenylureas.","Organic letters","2015","17","4","1018","1021","10.1021/acs.orglett.5b00131","","","0.71073","MoKα","","0.0649","0.0416","","","0.0732","0.0828","","","","","","1.021","","","","has coordinates","238121","2020-10-21","18:00:00",""
"1554794","12.8993","0.0014","10.853","0.0011","11.6466","0.0011","90","","90","","90","","1630.5","0.3","293","2","293.15","","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C19 H24 N2 O -","- C19 H24 N2 O -","- C76 H96 N8 O4 -","4","1","","Li, Bo; Wang, Si-Qing; Liu, Bin; Shi, Bing-Feng","Synthesis of oxazolines from amides via palladium-catalyzed functionalization of unactivated C(sp(3))-H bond.","Organic letters","2015","17","5","1200","1203","10.1021/acs.orglett.5b00151","","","0.71073","MoKα","","0.0566","0.0396","","","0.0889","0.0969","","","","","","1.073","","","","has coordinates","238122","2020-10-21","18:00:00",""
"1554796","12.939","0.003","13.093","0.003","15.573","0.004","90","","90","","90","","2638.2","1.1","193","2","193","2","","","","","","","","5","P b a m","-P 2 2ab","55","","","","- C24 H44 B2 N2 O4 -","- C24 H44 B2 N2 O4 -","- C96 H176 B8 N8 O16 -","4","0.5","","Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto","Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.","Organic letters","2015","17","5","1212","1215","10.1021/acs.orglett.5b00163","","","0.71075","MoKα","","0.1042","0.0729","","","0.1696","0.1916","","","","","","1.09","","","","has coordinates,has disorder","238124","2020-10-21","18:00:00",""
"1554797","18.923","0.011","58.36","0.03","11.127","0.006","90","","90","","90","","12288","12","93","2","93","2","","","","","","","","6","F d d 2","F 2 -2d","43","","","","- C29 H49 B2 Co N2 O4 -","- C29 H49 B2 Co N2 O4 -","- C464 H784 B32 Co16 N32 O64 -","16","1","","Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto","Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.","Organic letters","2015","17","5","1212","1215","10.1021/acs.orglett.5b00163","","","0.71075","MoKα","","0.0539","0.0487","","","0.1098","0.1144","","","","","","1.076","","","","has coordinates,has disorder","238124","2020-10-21","18:00:00",""
"1554798","10.74","0.003","19.626","0.006","13.066","0.004","90","","93.197","0.005","90","","2749.8","1.4","93","","93","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C24 H46 B2 N2 O5 -","- C24 H46 B2 N2 O5 -","- C96 H184 B8 N8 O20 -","4","1","","Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto","Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.","Organic letters","2015","17","5","1212","1215","10.1021/acs.orglett.5b00163","","","0.71075","MoKα","","0.1097","0.0813","","","0.1827","0.1992","","","","","","1.144","","","","has coordinates","238124","2020-10-21","18:00:00",""
"1554802","8.6014","0.0001","17.6656","0.0003","16.4517","0.0003","90","","107.162","0.001","90","","2388.51","0.07","115","","115","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C24 H41 B2 O2 P -","- C24 H41 B2 O2 P -","- C96 H164 B8 O8 P4 -","4","1","","Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain","Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes.","Organic letters","2015","17","5","1216","1219","10.1021/acs.orglett.5b00167","","x-ray","0.71073","MoKα","","0.067","0.0417","","","0.0987","0.1084","","","","","","1.042","","","","has coordinates","238127","2020-10-21","18:00:00",""
"1554803","12.674","0.002","9.2986","0.0014","12.919","0.002","90","","113.497","0.006","90","","1396.3","0.4","296","","296","","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C28 H33 B2 Fe O2 P -","- C28 H33 B2 Fe O2 P -","- C56 H66 B4 Fe2 O4 P2 -","2","1","","Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain","Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes.","Organic letters","2015","17","5","1216","1219","10.1021/acs.orglett.5b00167","","x-ray","0.71073","MoKα","","0.0613","0.0394","","","0.1001","0.1114","","","","","","1.019","","","","has coordinates,has disorder","238127","2020-10-21","18:00:00",""
"1554804","10.3874","0.0006","17.4963","0.001","18.3521","0.0009","90","","90","","90","","3335.3","0.3","115","","115","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C40 H43 B2 Fe P -","- C40 H43 B2 Fe P -","- C160 H172 B8 Fe4 P4 -","4","1","","Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain","Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes.","Organic letters","2015","17","5","1216","1219","10.1021/acs.orglett.5b00167","","x-ray","0.71073","MoKα~1~","K-L~3~","0.0293","0.0265","","","0.0669","0.0688","","","","","","1.063","","","","has coordinates,has disorder","238127","2020-10-21","18:00:00",""
"1554806","10.5408","0.0012","14.0223","0.0015","15.567","0.0017","90","","95.216","0.002","90","","2291.4","0.4","293","2","293","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C13 H12 O4 -","- C13 H12 O4 -","- C104 H96 O32 -","8","2","","Wang, Hong-Li; Shang, Ming; Sun, Shang-Zheng; Zhou, Zeng-Le; Laforteza, Brian N.; Dai, Hui-Xiong; Yu, Jin-Quan","Cu(II)-catalyzed coupling of aromatic C-H bonds with malonates.","Organic letters","2015","17","5","1228","1231","10.1021/acs.orglett.5b00193","","","0.71073","MoKα","","0.0837","0.0625","","","0.164","0.182","","","","","","1.029","","","","has coordinates","238129","2020-10-21","18:00:00",""
"1554809","7.9459","0.0004","8.3713","0.0005","15.0845","0.0006","98.477","0.004","91.135","0.004","97.754","0.005","982.54","0.09","293.35","0.1","293.35","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C19 H18 N O5 S2 -","- C19 H18 N O5 S2 -","- C38 H36 N2 O10 S4 -","2","1","","Deng, Zhimin; Wei, Jialiang; Liao, Lihao; Huang, Haiyan; Zhao, Xiaodan","Organoselenium-catalyzed, hydroxy-controlled regio- and stereoselective amination of terminal alkenes: efficient synthesis of 3-amino allylic alcohols.","Organic letters","2015","17","8","1834","1837","10.1021/acs.orglett.5b00213","","","0.71073","MoKα","","0.0703","0.056","","","0.1359","0.1442","","","","","","1.071","","","","has coordinates,has disorder","238131","2020-10-21","18:00:00",""
"1554810","14.8194","0.0008","23.1341","0.0013","17.3079","0.001","90","","104.994","0.002","90","","5731.7","0.6","100","2","100","2","","","","","","","","3","C 1 c 1","C -2yc","9","","","","- C24 H22 O3 -","- C24 H22 O3 -","- C288 H264 O36 -","12","3","","Gelat, Fabien; Richard, Vincent; Berger, Olivier; Montchamp, Jean-Luc","Development of a new family of chiral auxiliaries.","Organic letters","2015","17","8","1819","1821","10.1021/acs.orglett.5b00278","","","0.71073","","","0.0767","0.0598","","","0.1421","0.1543","","","","","","1.083","","","","has coordinates","238132","2020-10-21","18:00:00",""
"1554813","8.6811","0.0005","13.1015","0.0008","15.2298","0.0009","66.74","0.006","82.416","0.005","77.876","0.005","1553.57","0.18","171.6","","171.6","","","","","","","","","5","P -1","-P 1","2","","","","- C17 H16 Cl N3 O -","- C17 H16 Cl N3 O -","- C68 H64 Cl4 N12 O4 -","4","2","","Guo, Xiao; Chen, Wenteng; Chen, Binhui; Huang, Wei; Qi, Weixing; Zhang, Guolin; Yu, Yongping","One-pot three-component strategy for functionalized 2-aminoimidazoles via ring opening of α-nitro epoxides.","Organic letters","2015","17","5","1157","1159","10.1021/acs.orglett.5b00289","","","0.71073","MoKα","","0.0699","0.0475","","","0.1077","0.124","","","","","","1.037","","","","has coordinates","238134","2020-10-21","18:00:00",""
"1554814","9.4387","0.001","22.551","0.002","28.131","0.004","90","","90","","90","","5987.7","1.2","100","2","100","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C34 H35 N O6 S -","- C34 H35 N O6 S -","- C272 H280 N8 O48 S8 -","8","2","","Peng, Peng; Geng, Yiqun; Göttker-Schnetmann, Inigo; Schmidt, Richard R.","2-Nitro-thioglycosides: α- and β-selective generation and their potential as β-selective glycosyl donors.","Organic letters","2015","17","6","1421","1424","10.1021/acs.orglett.5b00295","","","0.71073","MoKα","","0.087","0.0428","","","0.0557","0.0645","","","","","","0.751","","","","has coordinates,has disorder","238136","2020-10-21","18:00:00",""
"1554815","9.9286","0.0007","17.0093","0.0013","10.0841","0.0008","90","","90.259","0.004","90","","1703","0.2","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H21 F2 N O -","- C19 H21 F2 N O -","- C76 H84 F8 N4 O4 -","4","1","","He, Zhengbiao; Tan, Ping; Ni, Chuanfa; Hu, Jinbo","Fluoroalkylative aryl migration of conjugated N-arylsulfonylated amides using easily accessible sodium di- and monofluoroalkanesulfinates.","Organic letters","2015","17","8","1838","1841","10.1021/acs.orglett.5b00308","","","1.54178","CuKα","","0.0581","0.0534","","","0.1608","0.1673","","","","","","1.015","","","","has coordinates","238137","2020-10-21","18:00:00",""
"1554822","6.4176","0.0003","20.0965","0.001","9.335","0.0005","90","","98.274","0.005","90","","1191.42","0.1","291","2","291.15","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C16 H10 N2 O -","- C16 H10 N2 O -","- C64 H40 N8 O4 -","4","1","","Chen, Xiaopei; Cui, Xiuling; Yang, Fangfang; Wu, Yangjie","Base-promoted cross-dehydrogenative coupling of quinoline N-oxides with 1,3-azoles.","Organic letters","2015","17","6","1445","1448","10.1021/acs.orglett.5b00330","","","0.71073","MoKα","","0.0788","0.0487","","","0.1001","0.117","","","","","","1.049","","","","has coordinates","238139","2020-10-21","18:00:00",""
"1554824","9.0391","0.0003","9.7069","0.0003","17.2285","0.0005","90","","102.573","0.002","90","","1475.41","0.08","296","2","296","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C20 H14 O5 -","- C20 H14 O5 -","- C80 H56 O20 -","4","1","","Tian, Yuan; Jiang, Nan; Zhang, Ai Hua; Chen, Chao Jun; Deng, Xin Zhao; Zhang, Wen Jing; Tan, Ren Xiang","Muta-mycosynthesis of naphthalene analogs.","Organic letters","2015","17","6","1457","1460","10.1021/acs.orglett.5b00335","","","1.54178","CuKα","","0.0408","0.0379","","","0.1013","0.1042","","","","","","1.033","","","","has coordinates","238141","2020-10-21","18:00:00",""
"1554830","8.128","0.001","15.344","0.003","16.979","0.002","90","","102.44","0.01","90","","2067.8","0.5","123","2","123","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","(Z)-1-(1-(mesitylimino)-2,2-dimethylpropyl)pyridin-1-ium triflate","","- C20 H25 F3 N2 O3 S -","- C20 H25 F3 N2 O3 S -","- C80 H100 F12 N8 O12 S4 -","4","1","","van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop","Base-stabilized nitrilium ions as convenient imine synthons.","Organic letters","2015","17","6","1461","1464","10.1021/acs.orglett.5b00339","","","0.71073","MoKα","","0.0583","0.0445","","","0.1067","0.1152","","","","","","1.077","","","","has coordinates,has disorder","238143","2020-10-21","18:00:00",""
"1554831","15.441","0.002","10.924","0.001","27.769","0.006","90","","90.9","0.02","90","","4683.4","1.3","123","2","123","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","(Z)-4-(dimethylamino)-1-(1-(mesitylamino)-2,2-dimethylpropyl)pyridin-1-ium trifluoromethanesulfonate","","- C22 H30 F3 N3 O3 S -","- C22 H30 F3 N3 O3 S -","- C176 H240 F24 N24 O24 S8 -","8","1","","van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop","Base-stabilized nitrilium ions as convenient imine synthons.","Organic letters","2015","17","6","1461","1464","10.1021/acs.orglett.5b00339","","","0.71073","MoKα","","0.0994","0.0754","","","0.1711","0.1826","","","","","","1.138","","","","has coordinates","238143","2020-10-21","18:00:00",""
"1554832","8.4815","0.0002","11.074","0.0003","21.3223","0.0006","90","","93.426","0.001","90","","1999.1","0.09","120","2","120","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","4-(dimethylamino)-1-((isopropylimino)(phenyl)methyl)pyridin- 1-ium trifluoromethanesulfonate","","- C18 H22 F3 N3 O3 S -","- C18 H22 F3 N3 O3 S -","- C72 H88 F12 N12 O12 S4 -","4","1","","van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop","Base-stabilized nitrilium ions as convenient imine synthons.","Organic letters","2015","17","6","1461","1464","10.1021/acs.orglett.5b00339","","","0.71073","MoKα","","0.0388","0.033","","","0.0842","0.0881","","","","","","1.026","","","","has coordinates","238143","2020-10-21","18:00:00",""
"1554833","8.61","0.001","9.179","0.001","11.835","0.001","93.38","0.01","95.73","0.01","105.2","0.01","894.57","0.17","123","2","123","2","","","","","","","","3","P -1","-P 1","2","","(Z)-N-(1-(1H-benzo[d]imidazol-1-yl)-2,2-dimethylpropylidene)aniline","","- C21 H25 N3 -","- C21 H25 N3 -","- C42 H50 N6 -","2","1","","van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop","Base-stabilized nitrilium ions as convenient imine synthons.","Organic letters","2015","17","6","1461","1464","10.1021/acs.orglett.5b00339","","","0.71073","MoKα","","0.1082","0.0878","","","0.2187","0.237","","","","","","1.037","","","","has coordinates","238143","2020-10-21","18:00:00",""
"1554834","8.693","0.001","17.464","0.002","11.525","0.001","90","","103.69","0.01","90","","1700","0.3","123","2","123","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","(Z)-N-mesityl-N'-phenylpivalimidamide","","- C20 H26 N2 -","- C20 H26 N2 -","- C80 H104 N8 -","4","1","","van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop","Base-stabilized nitrilium ions as convenient imine synthons.","Organic letters","2015","17","6","1461","1464","10.1021/acs.orglett.5b00339","","","0.71073","MoKα","","0.0515","0.0402","","","0.1012","0.1109","","","","","","1.054","","","","has coordinates","238143","2020-10-21","18:00:00",""
"1554835","26.3163","0.0012","26.3163","0.0012","10.403","0.0005","90","","90","","120","","6239.3","0.5","123","2","123","2","","","","","","","","3","R 3 c :H","R 3 -2""c","161","","(Z)-N'-mesitylpivalimidamide","","- C14 H22 N2 -","- C14 H22 N2 -","- C252 H396 N36 -","18","1","","van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop","Base-stabilized nitrilium ions as convenient imine synthons.","Organic letters","2015","17","6","1461","1464","10.1021/acs.orglett.5b00339","","","0.71073","MoKα","","0.069","0.0638","","","0.1563","0.1614","","","","","","1.035","","","","has coordinates,has disorder","238143","2020-10-21","18:00:00",""
"1554837","12.2787","0.0002","24.2002","0.0004","15.5541","0.0011","90","","101.818","0.007","90","","4523.9","0.4","93","2","93","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C49 H29 B F20 N O2 Rh -","- C49 H29 B F20 N O2 Rh -","- C196 H116 B4 F80 N4 O8 Rh4 -","4","1","","Otley, Kate D.; Ellman, Jonathan A.","An efficient method for the preparation of styrene derivatives via Rh(III)-catalyzed direct C-H vinylation.","Organic letters","2015","17","5","1332","1335","10.1021/acs.orglett.5b00340","","","0.71075","MoKα","","0.0463","0.036","","","0.0742","0.078","","","","","","1.031","","","","has coordinates","238145","2020-10-21","18:00:00",""
"1554838","14.026","0.0015","8.7035","0.0009","12.0599","0.0012","90","","104.008","0.002","90","","1428.4","0.3","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C18 H18 O2 -","- C18 H18 O2 -","- C72 H72 O8 -","4","1","","Liu, Rui; Lu, Ze-Hai; Hu, Xiao-Hui; Li, Jun-Li; Yang, Xian-Jin","Monocarboxylation and intramolecular coupling of butenylated arenes via palladium-catalyzed C-H activation process.","Organic letters","2015","17","6","1489","1492","10.1021/acs.orglett.5b00376","","","0.71073","MoKα","","0.0777","0.05","","","0.133","0.1469","","","","","","1.065","","","","has coordinates","238146","2020-10-21","18:00:00",""
"1554839","6.9078","0.0004","10.3981","0.0006","10.0732","0.0006","90","","95.471","0.0017","90","","720.24","0.07","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C17 H16 O2 Se -","- C17 H16 O2 Se -","- C34 H32 O4 Se2 -","2","1","","Niu, Wenxue; Yeung, Ying-Yeung","Catalytic and highly enantioselective selenolactonization.","Organic letters","2015","17","7","1660","1663","10.1021/acs.orglett.5b00377","","","0.71073","MoKα","","0.0141","0.0139","","","0.0372","0.0373","","","","","","1.07","","","","has coordinates","238147","2020-10-21","18:00:00",""
"1554840","13.594","0.0003","13.594","0.0003","5.7493","0.0004","90","","90","","120","","920.11","0.07","85","2","85","2","","","","","","","","3","P 32","P 32","145","","","","- C12 H20 O4 -","- C12 H20 O4 -","- C36 H60 O12 -","3","1","","Wang, Hengbin; Negretti, Solymar; Knauff, Allison R.; Montgomery, John","Exo-selective reductive macrocyclization of ynals.","Organic letters","2015","17","6","1493","1496","10.1021/acs.orglett.5b00381","","","1.54178","CuKα","","0.0269","0.0265","","","0.0645","0.0648","","","","","","1.084","","","","has coordinates","238148","2020-10-21","18:00:00",""
"1554841","9.2455","0.0012","10.1411","0.0013","14.412","0.0018","90","","90","","90","","1351.3","0.3","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C14 H15 Br N2 O2 -","- C14 H15 Br N2 O2 -","- C56 H60 Br4 N8 O8 -","4","1","","Gu, Xiaodong; Dai, Yuanyuan; Guo, Tingting; Franchino, Allegra; Dixon, Darren J.; Ye, Jinxing","A general, scalable, organocatalytic nitro-Michael addition to enones: enantioselective access to all-carbon quaternary stereocenters.","Organic letters","2015","17","6","1505","1508","10.1021/acs.orglett.5b00387","","","0.71073","MoKα","","0.0414","0.0334","","","0.0811","0.0843","","","","","","1.006","","","","has coordinates","238149","2020-10-21","18:00:00",""
"1554842","15.7629","0.0008","11.6907","0.0005","10.7408","0.0007","90","","100.958","0.005","90","","1943.22","0.18","297","2","297","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C22 H18 F N3 O2 S -","- C22 H18 F N3 O2 S -","- C88 H72 F4 N12 O8 S4 -","4","1","","Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng","I₂-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles.","Organic letters","2015","17","6","1521","1524","10.1021/acs.orglett.5b00398","","x-ray","0.71073","MoKα","","0.0797","0.0536","","","0.1244","0.1418","","","","","","1.019","","","","has coordinates","238150","2020-10-21","18:00:00",""
"1554855","10.0095","0.0004","11.563","0.0004","16.5773","0.0006","90","","99.859","0.004","90","","1890.32","0.12","297","2","297","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C18 H21 N3 O2 S2 -","- C18 H21 N3 O2 S2 -","- C72 H84 N12 O8 S8 -","4","1","","Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng","I₂-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles.","Organic letters","2015","17","6","1521","1524","10.1021/acs.orglett.5b00398","","x-ray","0.71073","MoKα","","0.094","0.0627","","","0.166","0.1923","","","","","","1.029","","","","has coordinates","238152","2020-10-21","18:00:00",""
"1554856","18.687","0.007","6.709","0.002","37.603","0.013","90","","90.534","0.004","90","","4714","3","296","2","296.15","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C20 H26 N2 O8 Si -","- C20 H26 N2 O8 Si -","- C160 H208 N16 O64 Si8 -","8","1","","Yin, Zhiping; Liu, Zengjin; Huang, Zhenggang; Chu, Yang; Chu, Zhiwen; Hu, Jia; Gao, Lu; Song, Zhenlei","Synthesis of functionalized γ-lactone via Sakurai exo-cyclization/rearrangement of 3,3-bis(silyl) enol ester with a tethered acetal.","Organic letters","2015","17","6","1553","1556","10.1021/acs.orglett.5b00437","","","0.71073","MoKα","","0.1503","0.0814","","","0.2045","0.2506","","","","","","1.019","","","","has coordinates,has disorder","238153","2020-10-21","18:00:00",""
"1554858","14.2686","0.0006","14.6629","0.0006","17.0163","0.0007","80.443","0.001","70.781","0.001","82.037","0.001","3301.6","0.2","150","2","150","2","","","","","","","","5","P -1","-P 1","2","","","","- C60 H85 I3 N10 O12 -","- C60 H85 I3 N10 O12 -","- C120 H170 I6 N20 O24 -","2","1","","Saha, Subrata; Santra, Saikat; Ghosh, Pradyut","[2]Pseudorotaxane composed of heteroditopic macrobicycle and pyridine N-oxide based axle: recognition site dependent axle orientation.","Organic letters","2015","17","8","1854","1857","10.1021/acs.orglett.5b00470","","","0.71073","MoKα","","0.0348","0.0311","","","0.0924","0.1039","","","","","","1.037","","","","has coordinates","238155","2020-10-21","18:00:00",""
"1554860","22.9779","0.0017","30.564","0.002","22.926","0.002","90","","114.207","0.0019","90","","14685.1","1.9","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C60 H78 Cl6 N10 O10 -","- C60 H78 Cl6 N10 O10 -","- C480 H624 Cl48 N80 O80 -","8","1","","Saha, Subrata; Santra, Saikat; Ghosh, Pradyut","[2]Pseudorotaxane composed of heteroditopic macrobicycle and pyridine N-oxide based axle: recognition site dependent axle orientation.","Organic letters","2015","17","8","1854","1857","10.1021/acs.orglett.5b00470","","","0.71073","MoKα","","0.189","0.1709","","","0.4969","0.5109","","","","","","2.263","","","","has coordinates,has disorder","238157","2020-10-21","18:00:00",""
"1554862","8.5362","0.0003","11.0883","0.0005","14.8339","0.001","89.337","0.006","75.808","0.005","89.011","0.006","1360.96","0.12","295","2","295","2","","","","","","","","5","P -1","-P 1","2","","","","- C27 H27 F3 N2 O8 -","- C27 H27 F3 N2 O8 -","- C54 H54 F6 N4 O16 -","2","1","","Huang, Lin; Zheng, Sheng-Cai; Tan, Bin; Liu, Xin-Yuan","Metal-free direct 1,6- and 1,2-difunctionalization triggered by radical trifluoromethylation of alkenes.","Organic letters","2015","17","6","1589","1592","10.1021/acs.orglett.5b00479","","","1.54178","CuKα","","0.1057","0.0873","","","0.2181","0.2574","","","","","","1.457","","","","has coordinates","238159","2020-10-21","18:00:00",""
"1554864","8.6933","0.0005","19.9383","0.0012","7.6281","0.0004","90","","90","","90","","1322.18","0.13","100","1","100","1","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C14 H11 N O7 -","- C14 H11 N O7 -","- C56 H44 N4 O28 -","4","1","","Dorfner, Walter L.; Carroll, Patrick J.; Schelter, Eric J.","Substituted quinoline quinones as surrogates for the PQQ cofactor: an electrochemical and computational study.","Organic letters","2015","17","8","1850","1853","10.1021/acs.orglett.5b00486","","","0.71073","MoKα","","0.0229","0.0222","","","0.0602","0.0607","","","","","","1.039","","","","has coordinates","238161","2020-10-21","18:00:00",""
"1554867","9.8067","0.0014","9.9678","0.0014","11.8916","0.0017","90","","104.237","0.007","90","","1126.7","0.3","200","2","200","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C23 H26 Br N O4 S -","- C23 H26 Br N O4 S -","- C46 H52 Br2 N2 O8 S2 -","2","1","","Serpier, Fabien; Flamme, Benjamin; Brayer, Jean-Louis; Folléas, Benoît; Darses, Sylvain","Chiral pyrrolidines and piperidines from enantioselective rhodium-catalyzed cascade arylative cyclization.","Organic letters","2015","17","7","1720","1723","10.1021/acs.orglett.5b00493","","","0.71073","MoKα","","0.0256","0.0234","","","0.0609","0.062","","","","","","1.019","","","","has coordinates","238163","2020-10-21","18:00:00",""
"1554869","10.443","0.0011","11.228","0.0011","11.795","0.0011","70.186","0.002","87.728","0.002","65.484","0.002","1175.6","0.2","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C28 H19 N O3 S2 -","- C28 H19 N O3 S2 -","- C56 H38 N2 O6 S4 -","2","1","","Ming, Wenbo; Liu, Xiaocui; Wang, Lianjie; Liu, Jun; Wang, Mang","Tandem Thien- and benzannulations of α-alkenoyl-α-alkynyl ketene dithioacetals with cyanoacetates: synthesis of functionalized benzo[b]thiophenes.","Organic letters","2015","17","7","1746","1749","10.1021/acs.orglett.5b00523","","","0.71069","MoKα","","0.1137","0.0537","","","0.1078","0.1355","","","","","","1.006","","","","has coordinates","238165","2020-10-21","18:00:00",""
"1554871","5.1627","0.0004","14.8595","0.0012","17.7219","0.0014","90","","96.198","0.001","90","","1351.59","0.19","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H21 N O3 -","- C15 H21 N O3 -","- C60 H84 N4 O12 -","4","1","","Borrero, Nicholas V.; DeRatt, Lindsey G.; Ferreira Barbosa, Lais; Abboud, Khalil A.; Aponick, Aaron","Tandem gold-catalyzed dehydrative cyclization/diels-alder reactions: facile access to indolocarbazole alkaloids.","Organic letters","2015","17","7","1754","1757","10.1021/acs.orglett.5b00528","","","0.71073","MoKα","","0.042","0.0381","","","0.1042","0.1072","","","","","","1.076","","","","has coordinates","238167","2020-10-21","18:00:00",""
"1554873","5.9724","0.0004","14.8969","0.001","16.4863","0.0011","90","","90","","90","","1466.79","0.17","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C20 H16 O2 -","- C20 H16 O2 -","- C80 H64 O8 -","4","1","","Peraino, Nicholas J.; Wheeler, Kraig A.; Kerrigan, Nessan J.","Diastereoselective synthesis of γ-lactones through reaction of enediolates with α,β-unsaturated sulfoxonium salts.","Organic letters","2015","17","7","1735","1737","10.1021/acs.orglett.5b00545","","","1.54178","CuKα","","0.0441","0.0392","","","0.0962","0.1003","","","","","","1.051","","","","has coordinates","238169","2020-10-21","18:00:00",""
"1554875","6.0066","0.0008","11.7969","0.0015","16.772","0.002","90","","97.594","0.003","90","","1178","0.3","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C12 H13 Br O2 -","- C12 H13 Br O2 -","- C48 H52 Br4 O8 -","4","1","","Che, Chao; Zheng, Hanliang; Zhu, Gangguo","Copper-catalyzed trans-carbohalogenation of terminal alkynes with functionalized tertiary alkyl halides.","Organic letters","2015","17","6","1617","1620","10.1021/acs.orglett.5b00546","","","0.71073","MoKα","","0.0433","0.0332","","","0.0804","0.0846","","","","","","1.038","","","","has coordinates","238171","2020-10-21","18:00:00",""
"1554877","10.4176","0.0004","11.9596","0.0004","16.0413","0.0006","90","","114.231","0.002","90","","1822.51","0.12","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C23 H21 N -","- C23 H21 N -","- C92 H84 N4 -","4","1","","Che, Chao; Zheng, Hanliang; Zhu, Gangguo","Copper-catalyzed trans-carbohalogenation of terminal alkynes with functionalized tertiary alkyl halides.","Organic letters","2015","17","6","1617","1620","10.1021/acs.orglett.5b00546","","","0.71073","MoKα","","0.2233","0.1153","","","0.2096","0.24","","","","","","1.295","","","","has coordinates","288245","2023-12-12","10:28:21",""
"1554878","8.527","0.0004","16.7982","0.0007","9.3056","0.0004","90","","102.717","0.003","90","","1300.22","0.1","100","2","100","2","","","","","","","synthesis as described","4","P 1 21 1","P 2yb","4","JSGP952CRIS","((1S,5S,6Z,8Z)-cyclonona-6,8-diene-1,5-diyl)bis(methylene) bis(((S)-1-phenylethyl)carbamate)","","- C29 H36 N2 O4 -","- C29 H36 N2 O4 -","- C58 H72 N4 O8 -","2","1","","Prado, Gustavo; Veiga, Alberte X.; Fernández-Nieto, Fernando; Paleo, M. Rita; Sardina, F. Javier","A two-step, stereoselective synthesis of nine- and ten-membered carbocycles from phthalates.","Organic letters","2015","17","9","2054","2057","10.1021/acs.orglett.5b00552","","x-ray","0.71073","MoKα","","0.0594","0.042","","","0.0901","0.0972","","","","","","1.061","","","","has coordinates","238174","2020-10-21","18:00:00",""
"1554880","14.0887","0.0005","10.5929","0.0004","9.0247","0.0003","90","","114.771","0.002","90","","1222.92","0.08","100","2","100","2","","","","","","","","3","C 1 c 1","C -2yc","9","JSGP1059","trans-(6Z,8Z)-1,5-Dimethylcyclonona-6,8-diene-1,5-diyl)dimethanol","","- C13 H22 O2 -","- C13 H22 O2 -","- C52 H88 O8 -","4","1","","Prado, Gustavo; Veiga, Alberte X.; Fernández-Nieto, Fernando; Paleo, M. Rita; Sardina, F. Javier","A two-step, stereoselective synthesis of nine- and ten-membered carbocycles from phthalates.","Organic letters","2015","17","9","2054","2057","10.1021/acs.orglett.5b00552","","x-ray","0.71073","MoKα","","0.0604","0.0455","","","0.0925","0.099","","","","","","0.995","","","","has coordinates","238176","2020-10-21","18:00:00",""
"1554885","5.0746","0.0009","14.828","0.003","16.699","0.003","65.191","0.003","89.579","0.004","80.838","0.003","1123.5","0.4","100","2","100","","","","","","","","","6","P 1","P 1","1","","","","- C20 H20 Br2 Cl2 N2 O4 -","- C20 H20 Br2 Cl2 N2 O4 -","- C40 H40 Br4 Cl4 N4 O8 -","2","2","","Shemet, Andrej; Sarlah, David; Carreira, Erick M.","Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.","Organic letters","2015","17","8","1878","1881","10.1021/acs.orglett.5b00558","","x-ray","0.71073","MoKα","","0.1174","0.0611","","","0.1252","0.1461","","","","","","0.988","","","","has coordinates","238178","2020-10-21","18:00:00",""
"1554887","4.8035","0.0006","8.2644","0.001","18.363","0.002","90","","94.441","0.003","90","","726.79","0.15","100","","99.99","","","","","","","","","6","P 1 21 1","P 2yb","4","","ca180213","","- C13 H15 Br Cl N O3 -","- C13 H15 Br Cl N O3 -","- C26 H30 Br2 Cl2 N2 O6 -","2","1","","Shemet, Andrej; Sarlah, David; Carreira, Erick M.","Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.","Organic letters","2015","17","8","1878","1881","10.1021/acs.orglett.5b00558","","","0.71073","MoKα","","0.0354","0.0267","","","0.0424","0.044","","","","","","0.948","","","","has coordinates","238180","2020-10-21","18:00:00",""
"1554890","10.669","0.003","4.7706","0.0014","15.964","0.005","90","","107.952","0.004","90","","773","0.4","100","","100","","","","","","","","","6","P 1 21 1","P 2yb","4","","(2R,4R,5R)-2,5-dichlorohexane-1,3-diyl bis((4-bromophenyl)carbamate)","","- C13 H16 Br Cl2 N O3 -","- C13 H16 Br Cl2 N O3 -","- C26 H32 Br2 Cl4 N2 O6 -","2","1","","Shemet, Andrej; Sarlah, David; Carreira, Erick M.","Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.","Organic letters","2015","17","8","1878","1881","10.1021/acs.orglett.5b00558","","x-ray","0.71073","MoKα","K-L~3~","0.0266","0.0214","","","0.039","0.0399","","","","","","0.899","","","","has coordinates","238182","2020-10-21","18:00:00",""
"1554894","4.9886","0.0007","19.578","0.003","9.0155","0.0013","90","","92.03","0.003","90","","880","0.2","100","2","100","","","","","","","","","4","P 1 21 1","P 2yb","4","","(5R)-2,5-dichlorohexane-1,3-diol","","- C6 H12 Cl2 O2 -","- C6 H12 Cl2 O2 -","- C24 H48 Cl8 O8 -","4","2","","Shemet, Andrej; Sarlah, David; Carreira, Erick M.","Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.","Organic letters","2015","17","8","1878","1881","10.1021/acs.orglett.5b00558","","","0.71073","MoKα","","0.0203","0.019","","","0.0479","0.0484","","","","","","1.071","","","","has coordinates","238184","2020-10-21","18:00:00",""
"1554896","12.2792","0.0011","4.9357","0.0003","13.4763","0.0012","90","","115.38","0.002","90","","737.92","0.1","100","","100","","","","","","","","","6","P 1 21 1","P 2yb","4","","((2S,3S)-3-((R)-1-chloropropyl)oxiran-2-yl)methyl (4-bromophenyl)carbamate","","- C13 H15 Br Cl N O3 -","- C13 H15 Br Cl N O3 -","- C26 H30 Br2 Cl2 N2 O6 -","2","1","","Shemet, Andrej; Sarlah, David; Carreira, Erick M.","Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.","Organic letters","2015","17","8","1878","1881","10.1021/acs.orglett.5b00558","","x-ray","0.71073","MoKα","K-L~3~","0.072","0.0486","","","0.0994","0.1074","","","","","","1.062","","","","has coordinates","238186","2020-10-21","18:00:00",""
"1554898","16.929","0.008","4.841","0.002","36.446","0.016","90","","101.211","0.009","90","","2930","2","100","","100","","","","","","","","","6","C 1 2 1","C 2y","5","","","","- C13 H15 Br Cl N O3 -","- C13 H15 Br Cl N O3 -","- C104 H120 Br8 Cl8 N8 O24 -","8","2","","Shemet, Andrej; Sarlah, David; Carreira, Erick M.","Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.","Organic letters","2015","17","8","1878","1881","10.1021/acs.orglett.5b00558","","","0.71073","MoKα","","0.144","0.0989","","","0.2008","0.2163","","","","","","1.098","","","","has coordinates","238188","2020-10-21","18:00:00",""
"1554900","6.1403","0.001","13.657","0.003","20.719","0.004","90","","90","","90","","1737.5","0.6","100","2","100.04","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","(2S,3R,5R)-ethyl 5-chloro-3-hydroxy-2-(((4-nitrophenyl)sulfonyl)oxy)hexanoate","","- C14 H18 Cl N O8 S -","- C14 H18 Cl N O8 S -","- C56 H72 Cl4 N4 O32 S4 -","4","1","","Shemet, Andrej; Sarlah, David; Carreira, Erick M.","Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.","Organic letters","2015","17","8","1878","1881","10.1021/acs.orglett.5b00558","","","0.71073","MoKα","","0.0649","0.0403","","","0.0738","0.0828","","","","","","1.022","","","","has coordinates","238191","2020-10-21","18:00:00",""
"1554902","5.8932","0.0006","9.8358","0.001","14.7998","0.0015","90","","90","","90","","857.86","0.15","100","","99.98","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","(3S,4R)-2,4-dichlorohexane-1,3-diol","","- C6 H12 Cl2 O2 -","- C6 H12 Cl2 O2 -","- C24 H48 Cl8 O8 -","4","1","","Shemet, Andrej; Sarlah, David; Carreira, Erick M.","Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.","Organic letters","2015","17","8","1878","1881","10.1021/acs.orglett.5b00558","","x-ray","0.71073","MoKα","K-L~3~","0.0179","0.0172","","","0.0441","0.0445","","","","","","1.1","","","","has coordinates","238193","2020-10-21","18:00:00",""
"1554904","17.283","0.002","5.72","0.0004","16.0086","0.0018","90","","115.367","0.008","90","","1430","0.3","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C18 H14 N2 O -","- C18 H14 N2 O -","- C72 H56 N8 O4 -","4","1","","Bunescu, Ala; Wang, Qian; Zhu, Jieping","Synthesis of functionalized epoxides by copper-catalyzed alkylative epoxidation of allylic alcohols with alkyl nitriles.","Organic letters","2015","17","8","1890","1893","10.1021/acs.orglett.5b00571","","","0.71073","MoKα","","0.0871","0.0545","","","0.1082","0.1246","","","","","","1.082","","","","has coordinates","238195","2020-10-21","18:00:00",""
"1554907","8.2684","0.0004","13.1049","0.0005","14.9823","0.0006","90","","98.209","0.004","90","","1606.8","0.12","223","0.1","223","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C28 H36 N2 O10 Pd3 -","- C28 H36 N2 O10 Pd3 -","- C56 H72 N4 O20 Pd6 -","2","0.5","","Guo, Kun; Chen, Xiaolan; Guan, Mingyu; Zhao, Yingsheng","Direct ortho-C-H functionalization of aromatic alcohols masked by acetone oxime ether via exo-palladacycle.","Organic letters","2015","17","7","1802","1805","10.1021/acs.orglett.5b00594","","","0.71073","MoKα","","0.0367","0.0288","","","0.0694","0.0733","","","","","","1.085","","","","has coordinates","238197","2020-10-21","18:00:00",""
"1554909","9.82013","0.00019","15.1033","0.0003","12.9881","0.0002","90","","93.8267","0.0017","90","","1922.05","0.06","150","2","150","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C21 H24 B N O2 -","- C21 H24 B N O2 -","- C84 H96 B4 N4 O8 -","4","1","","Pareek, Manish; Fallon, Thomas; Oestreich, Martin","Platinum(0)-Catalyzed Indolyne Insertion into Bis(pinacolato)diboron Followed by Site-Selective Suzuki-Miyaura Cross-Coupling.","Organic letters","2015","17","9","2082","2085","10.1021/acs.orglett.5b00604","","x-ray","1.54184","CuKα","","0.0464","0.0402","","","0.0988","0.104","","","","","","1.03","","","","has coordinates","238199","2020-10-21","18:00:00",""
"1554912","9.9728","0.0013","10.8425","0.0014","25.575","0.003","90","","90","","90","","2765.4","0.6","173","2","173","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C20 H41 B2 F8 N5 O -","- C20 H41 B2 F8 N5 O -","- C80 H164 B8 F32 N20 O4 -","4","1","","Mirabdolbaghi, Roya; Dudding, Travis","Expanding the forefront of strong organic Brønsted acids: proton-catalyzed hydroamination of unactivated alkenes and activation of Au(I) for alkyne hydroamination.","Organic letters","2015","17","8","1930","1933","10.1021/acs.orglett.5b00617","","","0.71073","MoKα","","0.0584","0.0481","","","0.1346","0.1405","","","","","","1.071","","","","has coordinates","238202","2020-10-21","18:00:00",""
"1554914","7.9555","0.0007","12.7291","0.0011","14.1773","0.0012","101.894","0.002","105.578","0.002","101.34","0.002","1304","0.2","100","0.2","100","0.2","","","","","","","","5","P -1","-P 1","2","","","","- C25 H36 F3 N3 O4 -","- C25 H36 F3 N3 O4 -","- C50 H72 F6 N6 O8 -","2","1","","Geoghegan, Kimberly; Bode, Jeffrey W.","Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.","Organic letters","2015","17","8","1934","1937","10.1021/acs.orglett.5b00618","","x-ray","0.71073","MoKα","","0.0713","0.0557","","","0.1451","0.1567","","","","","","1.035","","","","has coordinates,has disorder","238204","2020-10-21","18:00:00",""
"1554915","9.676","0.002","6.0187","0.0014","35.338","0.008","90","","90.313","0.003","90","","2057.9","0.8","100","0.2","100","0.2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C20 H27 F3 N2 O3 -","- C20 H27 F3 N2 O3 -","- C80 H108 F12 N8 O12 -","4","1","","Geoghegan, Kimberly; Bode, Jeffrey W.","Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.","Organic letters","2015","17","8","1934","1937","10.1021/acs.orglett.5b00618","","x-ray","0.71073","MoKα","","0.102","0.061","","","0.1201","0.1345","","","","","","1.059","","","","has coordinates,has disorder","238205","2020-10-21","18:00:00",""
"1554916","8.4082","0.0007","8.9935","0.0007","12.6932","0.001","109.241","0.002","90.111","0.002","102.16","0.002","883.25","0.12","100","0.2","100","0.2","","","","","","","","5","P -1","-P 1","2","","","","- C18 H23 F3 N2 O3 -","- C18 H23 F3 N2 O3 -","- C36 H46 F6 N4 O6 -","2","1","","Geoghegan, Kimberly; Bode, Jeffrey W.","Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.","Organic letters","2015","17","8","1934","1937","10.1021/acs.orglett.5b00618","","x-ray","0.71073","MoKα","","0.0574","0.0392","","","0.0873","0.0978","","","","","","1.016","","","","has coordinates,has disorder","238206","2020-10-21","18:00:00",""
"1554917","5.8836","0.0004","19.2027","0.0012","26.5181","0.0016","90","","90","","90","","2996","0.3","100","0.2","100","0.2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C18 H16 F3 N O -","- C18 H16 F3 N O -","- C144 H128 F24 N8 O8 -","8","2","","Geoghegan, Kimberly; Bode, Jeffrey W.","Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.","Organic letters","2015","17","8","1934","1937","10.1021/acs.orglett.5b00618","","x-ray","1.54178","CuKα","","0.0467","0.0355","","","0.0773","0.0821","","","","","","1.014","","","","has coordinates","238207","2020-10-21","18:00:00",""
"1554920","13.529","0.0011","16.7566","0.0013","8.6938","0.0007","90","","116.175","0.001","90","","1768.8","0.2","200","2","200","2","","","","","","","","5","C 1 c 1","C -2yc","9","","","","- C21 H16 N2 O2 S -","- C21 H16 N2 O2 S -","- C84 H64 N8 O8 S4 -","4","1","","Lee, Dong Jin; Yoo, Eun Jeong","Efficient synthesis of C-N-coupled heterobiaryls by sequential N-H functionalization reactions.","Organic letters","2015","17","8","1830","1833","10.1021/acs.orglett.5b00625","","","0.71073","MoKα","","0.0773","0.045","","","0.0859","0.1431","","","","","","1.28","","","","has coordinates","238209","2020-10-21","18:00:00",""
"1554921","12.5268","0.001","10.8502","0.0008","16.3904","0.0013","90","","103.482","0.002","90","","2166.4","0.3","200","2","200","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C24 H24 N2 O2 S -","- C24 H24 N2 O2 S -","- C96 H96 N8 O8 S4 -","4","1","","Lee, Dong Jin; Yoo, Eun Jeong","Efficient synthesis of C-N-coupled heterobiaryls by sequential N-H functionalization reactions.","Organic letters","2015","17","8","1830","1833","10.1021/acs.orglett.5b00625","","","0.71073","MoKα","","0.1661","0.0968","","","0.2808","0.3388","","","","","","1.089","","","","has coordinates","238210","2020-10-21","18:00:00",""
"1554924","6.42","0.0003","8.0707","0.0003","40.1927","0.0015","90","","90","","90","","2082.54","0.15","173","2","173","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C19 H29 F N2 O5 Si -","- C19 H29 F N2 O5 Si -","- C76 H116 F4 N8 O20 Si4 -","4","1","","Istrate, Alena; Medvecky, Michal; Leumann, Christian J.","2'-Fluorination of tricyclo-DNA controls furanose conformation and increases RNA affinity.","Organic letters","2015","17","8","1950","1953","10.1021/acs.orglett.5b00662","","x-ray","0.71073","MoKα","","0.0472","0.0432","","","0.0973","0.0995","","","","","","1.1","","","","has coordinates","238212","2020-10-21","18:00:00",""
"1554926","7.5248","0.0006","11.7969","0.0011","18.7512","0.0017","90","","98.035","0.002","90","","1648.2","0.3","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C19 H16 N2 O4 -","- C19 H16 N2 O4 -","- C76 H64 N8 O16 -","4","2","","Bisai, Vishnumaya; Unhale, Rajshekhar A.; Suneja, Arun; Dhanasekaran, Sivasankaran; Singh, Vinod K.","An Efficient Entry to syn- and anti-Selective Isoindolinones via an Organocatalytic Direct Mannich/Lactamization Sequence.","Organic letters","2015","17","9","2102","2105","10.1021/acs.orglett.5b00676","","","0.71073","MoKα","","0.0694","0.0382","","","0.0763","0.0858","","","","","","1.058","","","","has coordinates","288505","2023-12-22","15:12:00",""
"1554930","5.36225","0.00005","12.0412","0.0001","27.5363","0.0003","90","","90","","90","","1777.96","0.03","100","2","100","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C16 H25 N O2 S3 -","- C16 H25 N O2 S3 -","- C64 H100 N4 O8 S12 -","4","1","","Das, Manas; O'Shea, Donal F","Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.","Organic letters","2015","17","8","1962","1965","10.1021/acs.orglett.5b00697","","","0.71073","MoKα","","0.0242","0.0226","","","0.0567","0.0576","","","","","","1.063","","","","has coordinates","238216","2020-10-21","18:00:00",""
"1554932","11.7646","0.0004","15.4251","0.0003","12.0356","0.0004","90","","118.452","0.004","90","","1920.3","0.12","100","2","100","2","","","","","","","","7","P 1 21 1","P 2yb","4","","","","- C18 H19 Cl F3 N O S -","- C18 H19 Cl F3 N O S -","- C72 H76 Cl4 F12 N4 O4 S4 -","4","2","","Das, Manas; O'Shea, Donal F","Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.","Organic letters","2015","17","8","1962","1965","10.1021/acs.orglett.5b00697","","","0.71073","MoKα","","0.0356","0.0325","","","0.0677","0.0705","","","","","","1.039","","","","has coordinates","238218","2020-10-21","18:00:00",""
"1554934","5.84461","0.00004","11.3132","0.00006","13.829","0.00008","90","","95.4227","0.0006","90","","910.298","0.01","100","2","100","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C19 H23 Fe N O2 S -","- C19 H23 Fe N O2 S -","- C38 H46 Fe2 N2 O4 S2 -","2","1","","Das, Manas; O'Shea, Donal F","Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.","Organic letters","2015","17","8","1962","1965","10.1021/acs.orglett.5b00697","","","1.54184","CuKα","","0.0205","0.0199","","","0.0497","0.0499","","","","","","1.046","","","","has coordinates","238220","2020-10-21","18:00:00",""
"1554935","9.353","0.004","7.448","0.003","12.251","0.005","90","","93.725","0.008","90","","851.6","0.6","293","2","293","2","","","","","","","","4","P 1 21/m 1","-P 2yb","11","","","","- C23 H17 Cl O2 -","- C23 H17 Cl O2 -","- C46 H34 Cl2 O4 -","2","0.5","","Liu, Yang; Jin, Shiyu; Huang, Liping; Hu, Youhong","Phase transfer reagent promoted tandem ring-opening and ring-closing reactions of unique 3-(1-alkynyl) chromones.","Organic letters","2015","17","9","2134","2137","10.1021/acs.orglett.5b00721","","","0.71073","MoKα","","0.0579","0.0483","","","0.1395","0.1509","","","","","","1.044","","","","has coordinates","238221","2020-10-21","18:00:00",""
"1554937","10.8299","0.0004","17.8426","0.0007","16.7462","0.0006","90","","105.418","0.004","90","","3119.5","0.2","223","2","223","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C133 H116 N8 O21 S4 -","- C133 H112 N8 O21 S4 -","- C133 H112 N8 O21 S4 -","1","0.5","","Xie, Danbo; Yang, Limin; Lin, Youqiang; Zhang, Zhiming; Chen, Dongdong; Zeng, Xiaofei; Zhong, Guofu","Rapid access to spirocylic oxindoles: application of asymmetric N-heterocyclic carbene-catalyzed [3 + 3] cycloaddition of imines to oxindole-derived enals.","Organic letters","2015","17","10","2318","2321","10.1021/acs.orglett.5b00726","","","0.71073","MoKα","","0.0898","0.071","","","0.1937","0.2096","","","","","","1.057","","","","has coordinates","238223","2020-10-21","18:00:00",""
"1554941","14.7817","0.0005","10.4931","0.0003","20.1054","0.0007","90","","110.04","0.0011","90","","2929.66","0.17","160","2","160","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C39 H30 Cl N O -","- C39 H30 Cl N O -","- C156 H120 Cl4 N4 O4 -","4","1","","Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.","Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.","Organic letters","2015","17","8","1986","1989","10.1021/acs.orglett.5b00743","","","0.71073","MoKα","","0.0729","0.053","","","0.136","0.1495","","","","","","1.079","","","","has coordinates","238226","2020-10-21","18:00:00",""
"1554944","12.0241","0.0005","10.8634","0.0004","15.0306","0.0006","90","","92.829","0.002","90","","1960.94","0.13","100","","100","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C24 H24 Cl N O -","- C24 H24 Cl N O -","- C96 H96 Cl4 N4 O4 -","4","1","","Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.","Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.","Organic letters","2015","17","8","1986","1989","10.1021/acs.orglett.5b00743","","","0.71073","MoKα","","0.0526","0.0372","","","0.1016","0.112","","","","","","1.047","","","","has coordinates","238229","2020-10-21","18:00:00",""
"1554948","16.3879","0.0009","7.0026","0.0004","17.8667","0.001","90","","103.718","0.003","90","","1991.86","0.19","100","","100","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C24 H24 Cl N O -","- C24 H24 Cl N O -","- C96 H96 Cl4 N4 O4 -","4","1","","Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.","Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.","Organic letters","2015","17","8","1986","1989","10.1021/acs.orglett.5b00743","","","0.71073","MoKα","","0.0713","0.044","","","0.1046","0.1102","","","","","","1.703","","","","has coordinates","238232","2020-10-21","18:00:00",""
"1554950","11.705","0.002","28.512","0.006","22.406","0.005","90","","98.94","0.03","90","","7387","3","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C152.5 H199 B4 N7 O23 -","- C152.028 H198.732 B4 N6.676 O22.676 -","- C304.056 H397.464 B8 N13.352 O45.352 -","2","0.5","","Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro","Nestable Tetrakis(spiroborate) Nanocycles.","Organic letters","2015","17","9","2154","2157","10.1021/acs.orglett.5b00747","","","0.8","synchrotron","","0.1905","0.1828","","","0.4757","0.5029","","","","","","2.579","","","","has coordinates","238234","2020-10-21","18:00:00",""
"1554955","13.488","0.003","14.281","0.003","14.287","0.003","90","","108.36","0.03","90","","2611.9","1.1","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C50 H44 F24 N4 P4 -","- C50 H44 F24 N4 P4 -","- C100 H88 F48 N8 P8 -","2","0.5","","Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro","Nestable Tetrakis(spiroborate) Nanocycles.","Organic letters","2015","17","9","2154","2157","10.1021/acs.orglett.5b00747","","","0.7","synchrotron","","0.0765","0.0625","","","0.1881","0.2002","","","","","","1.097","","","","has coordinates,has disorder","238236","2020-10-21","18:00:00",""
"1554956","16.134","0.003","16.609","0.003","16.766","0.003","85.82","0.03","65.15","0.03","75.26","0.03","3939.7","1.7","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C186 H168 B4 N14 O31 -","- C186 H168 B4 N14 O31 -","- C186 H168 B4 N14 O31 -","1","0.5","","Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro","Nestable Tetrakis(spiroborate) Nanocycles.","Organic letters","2015","17","9","2154","2157","10.1021/acs.orglett.5b00747","","","0.7","synchrotron","","0.1734","0.0878","","","0.2443","0.2936","","","","","","1.038","","","","has coordinates","238237","2020-10-21","18:00:00",""
"1554959","42.193","0.008","8.356","0.0017","15.63","0.003","90","","90.76","0.03","90","","5510.1","1.9","100","","100","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C117 H171 B4 N4 O20 -","- C117 H171 B4 N4 O20 -","- C234 H342 B8 N8 O40 -","2","0.5","","Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro","Nestable Tetrakis(spiroborate) Nanocycles.","Organic letters","2015","17","9","2154","2157","10.1021/acs.orglett.5b00747","","","0.8","synchrotron","","0.0714","0.0697","","","0.1964","0.1988","","","","","","1.032","","","","has coordinates,has disorder","238239","2020-10-21","18:00:00",""
"1554960","16.67","0.003","17.44","0.004","19.659","0.004","81.21","0.03","74.06","0.03","62.19","0.03","4859","2","100","","100","","","","","","","","","7","P -1","-P 1","2","","","","- C180 H112 B4 D84 N4 O34 S14 -","- C179.868 H112 B4 D83.604 N4 O33.934 S13.934 -","- C179.868 H112 B4 D83.604 N4 O33.934 S13.934 -","1","0.5","","Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro","Nestable Tetrakis(spiroborate) Nanocycles.","Organic letters","2015","17","9","2154","2157","10.1021/acs.orglett.5b00747","","","0.8","synchrotron","","0.2091","0.1643","","","0.4341","0.4745","","","","","","1.787","","","","has coordinates,has disorder","238240","2020-10-21","18:00:00",""
"1554968","11.446","0.002","13.451","0.003","22.036","0.004","98.71","0.03","104.3","0.03","98.36","0.03","3189.9","1.3","123","2","123","2","","","","","","","","4","P -1","-P 1","2","","","","- C70 H56 N8 O8 -","- C70 H56 N8 O8 -","- C140 H112 N16 O16 -","2","1","","Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David","Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.","Organic letters","2015","17","9","2194","2197","10.1021/acs.orglett.5b00767","","","1.54178","CuKα","","0.1175","0.0986","","","0.2998","0.3166","","","","","","1.14","","","","has coordinates","238242","2020-10-21","18:00:00",""
"1554969","16.098","0.003","8.0852","0.0016","19.417","0.004","90","","103.12","0.03","90","","2461.3","0.9","123","2","123","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C32 H26 N4 O2 -","- C32 H26 N4 O2 -","- C128 H104 N16 O8 -","4","0.5","","Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David","Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.","Organic letters","2015","17","9","2194","2197","10.1021/acs.orglett.5b00767","","","1.54178","CuKα","","0.059","0.0527","","","0.1479","0.1506","","","","","","1.119","","","","has coordinates","238243","2020-10-21","18:00:00",""
"1554971","7.3964","0.0015","23.302","0.005","16.073","0.003","90","","94.05","0.03","90","","2763.3","1","123","2","123","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C34 H30 N4 O4 -","- C34 H30 N4 O4 -","- C136 H120 N16 O16 -","4","1","","Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David","Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.","Organic letters","2015","17","9","2194","2197","10.1021/acs.orglett.5b00767","","","1.54178","CuKα","","0.0508","0.049","","","0.1373","0.1391","","","","","","1.032","","","","has coordinates","238245","2020-10-21","18:00:00",""
"1554973","37.78","0.008","8.9173","0.0018","26.953","0.005","90","","133.41","0.03","90","","6596","4","123","2","123","2","","","","","","","","6","C 1 c 1","C -2yc","9","","","","- C70 H58 Cl6 N8 O12 S -","- C70 H58 Cl6 N8 O12 S -","- C280 H232 Cl24 N32 O48 S4 -","4","1","","Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David","Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.","Organic letters","2015","17","9","2194","2197","10.1021/acs.orglett.5b00767","","","1.54178","CuKα","","0.1583","0.1172","","","0.2834","0.3225","","","","","","1.146","","","","has coordinates,has disorder","238247","2020-10-21","18:00:00",""
"1554978","12.4447","0.0011","15.6502","0.0013","7.9646","0.0007","90","","105.739","0.006","90","","1493","0.2","298","2","298","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H10 Br N O4 -","- C16 H10 Br N O4 -","- C64 H40 Br4 N4 O16 -","4","1","","Bag, Raghunath; Sar, Dinabandhu; Punniyamurthy, Tharmalingam","Copper(II)-catalyzed direct dioxygenation of alkenes with air and N-hydroxyphthalimide: synthesis of β-keto-N-alkoxyphthalimides.","Organic letters","2015","17","8","2010","2013","10.1021/acs.orglett.5b00770","","","0.71073","MoKα","","0.1404","0.0738","","","0.1947","0.2308","","","","","","1.052","","","","has coordinates","238249","2020-10-21","18:00:00",""
"1554981","13.0106","0.0005","13.1402","0.0006","14.3888","0.0007","80.344","0.004","63.999","0.004","78.993","0.003","2160.42","0.18","175","","175","","","","","","","","","5","P -1","-P 1","2","","","","- C70 H120 N14 O26 S8 -","- C70 H120 N14 O26 S8 -","- C70 H120 N14 O26 S8 -","1","0.5","","Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail","New ""pyrene box"" cages for adaptive guest conformations.","Organic letters","2015","17","9","2178","2181","10.1021/acs.orglett.5b00779","","","0.71073","MoKα","","0.0605","0.0483","","0.0645","0.055","0.055","","","","","","1.0683","","","","has coordinates","238251","2020-10-21","18:00:00",""
"1554982","13.4741","0.0003","14.6965","0.0003","22.6791","0.0004","90","","92.704","0.0017","90","","4485.96","0.16","175","","175","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C30 H60 N12 O16 S4 -","- C30 H60 N12 O16 S4 -","- C120 H240 N48 O64 S16 -","4","0.5","","Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail","New ""pyrene box"" cages for adaptive guest conformations.","Organic letters","2015","17","9","2178","2181","10.1021/acs.orglett.5b00779","","","0.71073","MoKα","","0.0871","0.0769","","0.0751","0.0684","0.0684","","","","","","1.1565","","","","has coordinates","238252","2020-10-21","18:00:00",""
"1554988","11.2634","0.0018","15.966","0.002","16.009","0.004","111.587","0.016","100.691","0.016","109.004","0.013","2373.6","1","175","","175","","","","","","","","","5","P -1","-P 1","2","","","","- C40 H69.97 N4 O14 S4 -","- C40 H69.973 N4 O14 S4 -","- C80 H139.946 N8 O28 S8 -","2","1","","Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail","New ""pyrene box"" cages for adaptive guest conformations.","Organic letters","2015","17","9","2178","2181","10.1021/acs.orglett.5b00779","","","0.71073","MoKα","","0.0969","0.0729","","0.0545","0.0454","0.0454","","","","","","1.018","","","","has coordinates,has disorder","238254","2020-10-21","18:00:00",""
"1554990","8.1609","0.0013","9.0398","0.0014","19.318","0.003","90","","90","","90","","1425.1","0.4","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C15 H13 N O4 S -","- C15 H13 N O4 S -","- C60 H52 N4 O16 S4 -","4","1","","Liu, Yan-Kai; Li, Zhi-Long; Li, Ji-Yao; Feng, Huan-Xi; Tong, Zhi-Ping","Open-close: an alternative strategy to α-functionalization of lactone via enamine catalysis in one pot under mild conditions.","Organic letters","2015","17","8","2022","2025","10.1021/acs.orglett.5b00794","","","0.71073","MoKα","","0.0846","0.0806","","","0.2376","0.2429","","","","","","1.08","","","","has coordinates","238256","2020-10-21","18:00:00",""
"1554994","12.8623","0.0002","11.3355","0.0002","16.9579","0.0003","90","","94.493","0.001","90","","2464.87","0.07","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","CG0201","","","- C28 H23 N3 O4 S -","- C28 H23 N3 O4 S -","- C112 H92 N12 O16 S4 -","4","1","","Chen, Jing; Li, Jianjun; Wang, Jiazhe; Li, Hao; Wang, Wei; Guo, Yuewei","Phosphine-Catalyzed Aza-MBH Reactions of Vinylpyridines: Efficient and Rapid Access to 2,3,5-Triarylsubstituted 3-Pyrrolines.","Organic letters","2015","17","9","2214","2217","10.1021/acs.orglett.5b00811","","","0.71073","MoKα","","0.0355","0.0306","","","0.0738","0.0771","","","","","","0.998","","","","has coordinates","238258","2020-10-21","18:00:00",""
"1554996","6.0808","0.0001","23.3393","0.0006","12.5225","0.0008","90","","94.028","0.007","90","","1772.82","0.13","293","2","293","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C19 H22 O7 -","- C19 H22 O7 -","- C76 H88 O28 -","4","1","","Tan, Ceheng; Chen, Wei; Mu, Xinpeng; Chen, Qi; Gong, Jianxian; Luo, Tuoping; Yang, Zhen","Synthetic Progress toward Azadirachtins. 2. Enantio- and Diastereoselective Synthesis of the Right-Wing Fragment of 11-epi-Azadirachtin I.","Organic letters","2015","17","10","2338","2341","10.1021/acs.orglett.5b00831","","","1.54187","CuKα","","0.0864","0.0782","","","0.2202","0.2328","","","","","","1.052","","","","has coordinates","238260","2020-10-21","18:00:00",""
"1554998","9.6121","0.0018","11.761","0.002","13.648","0.003","98.331","0.003","109.571","0.003","113.637","0.003","1260.2","0.4","298","2","298","2","","","","","","","","5","P -1","-P 1","2","","","","- C26 H31 Br N2 O3 -","- C26 H31 Br N2 O3 -","- C52 H62 Br2 N4 O6 -","2","1","","Zeng, Xiao-Hua; Wang, Hong-Mei; Ding, Ming-Wu","Unexpected Synthesis of 5,6-Dihydropyridin-2(1H)-ones by a Domino Ugi/Aldol/Hydrolysis Reaction Starting from Baylis-Hillman Phosphonium Salts.","Organic letters","2015","17","9","2234","2237","10.1021/acs.orglett.5b00849","","","0.71073","MoKα","","0.0635","0.0431","","","0.135","0.1492","","","","","","1.033","","","","has coordinates","238262","2020-10-21","18:00:00",""
"1555000","9.7881","0.0002","13.2333","0.0004","16.5195","0.0011","67.596","0.005","77.669","0.006","72.069","0.005","1870.86","0.16","193","2","193","2","","","","","","","","6","P -1","-P 1","2","","","","- C38 H44 B2 F4 N4 O6 -","- C38 H44 B2 F4 N4 O6 -","- C76 H88 B4 F8 N8 O12 -","2","1","","Huaulmé, Quentin; Mirloup, Antoine; Retailleau, Pascal; Ziessel, Raymond","Synthesis of Highly Functionalized BOPHY Chromophores Displaying Large Stokes Shifts.","Organic letters","2015","17","9","2246","2249","10.1021/acs.orglett.5b00858","","","1.54187","CuKα","","0.0875","0.0565","","","0.1427","0.1927","","","","","","1.175","","","","has coordinates,has disorder","238265","2020-10-21","18:00:00",""
"1555003","9.3088","0.0004","9.5092","0.0004","14.5742","0.0007","92.724","0.004","104.673","0.004","110","0.004","1159.92","0.1","150","","150","","","","","","","","","5","P -1","-P 1","2","","","","- C27 H30 F N O2 -","- C27 H30 F N O2 -","- C54 H60 F2 N2 O4 -","2","1","","Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.","Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.","Organic letters","2015","17","9","2254","2257","10.1021/acs.orglett.5b00880","","","1.54184","CuKα","","0.0486","0.0438","","0.1201","0.1143","0.12","","","","","","0.9873","","","","has coordinates","238268","2020-10-21","18:00:00",""
"1555004","8.03153","0.00018","10.686","0.0002","28.3689","0.0007","90","","90","","90","","2434.76","0.09","150","","150","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C28 H32 F N O2 -","- C28 H32 F N O2 -","- C112 H128 F4 N4 O8 -","4","1","","Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.","Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.","Organic letters","2015","17","9","2254","2257","10.1021/acs.orglett.5b00880","","","1.54184","CuKα","","0.0328","0.0318","","0.0801","0.0793","0.0801","","","","","","1.0054","","","","has coordinates","238268","2020-10-21","18:00:00",""
"1555005","11.32263","0.00012","11.32263","0.00012","35.383","0.0004","90","","90","","120","","3928.44","0.07","150","","150","","","","","","","","","4","P 32 2 1","P 32 2""","154","","","","- C28 H32 N4 O2 -","- C28 H32 N4 O2 -","- C168 H192 N24 O12 -","6","1","","Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.","Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.","Organic letters","2015","17","9","2254","2257","10.1021/acs.orglett.5b00880","","","1.54184","CuKα","","0.0529","0.0514","","0.1369","0.1355","0.1369","","","","","","0.9984","","","","has coordinates","238268","2020-10-21","18:00:00",""
"1555006","9.7073","0.0003","10.168","0.0003","14.0374","0.0004","85.597","0.002","85.998","0.002","82.306","0.002","1366.53","0.07","150","","150","","","","","","","","","4","P 1","P 1","1","","","","- C30 H35 N O4 -","- C30 H35 N O4 -","- C60 H70 N2 O8 -","2","2","","Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.","Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.","Organic letters","2015","17","9","2254","2257","10.1021/acs.orglett.5b00880","","","1.54184","CuKα","","0.0522","0.0493","","0.1433","0.1377","0.1431","","","","","","0.9127","","","","has coordinates,has disorder","238268","2020-10-21","18:00:00",""
"1555007","10.4764","0.0005","10.6867","0.0005","12.3768","0.0004","85.757","0.003","70.552","0.003","69.477","0.004","1222.26","0.1","150","","150","","","","","","","","","5","P 1","P 1","1","","","","- C28 H31 F2 N O2 -","- C28 H31 F2 N O2 -","- C56 H62 F4 N2 O4 -","2","2","","Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.","Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.","Organic letters","2015","17","9","2254","2257","10.1021/acs.orglett.5b00880","","","1.54184","CuKα","","0.0561","0.0557","","0.1558","0.1549","0.1558","","","","","","0.9989","","","","has coordinates","238268","2020-10-21","18:00:00",""
"1555008","7.90952","0.00011","16.3522","0.0003","9.53794","0.00013","90","","95.6737","0.0013","90","","1227.58","0.03","150","","150","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C28 H31 F2 N O2 -","- C28 H31 F2 N O2 -","- C56 H62 F4 N2 O4 -","2","1","","Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.","Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.","Organic letters","2015","17","9","2254","2257","10.1021/acs.orglett.5b00880","","","1.54184","CuKα","","0.0282","0.028","","0.0721","0.0718","0.0721","","","","","","1.011","","","","has coordinates","238268","2020-10-21","18:00:00",""
"1555011","8.3956","0.0008","11.6027","0.0011","23.715","0.002","90","","91.1454","0.0011","90","","2309.7","0.4","173","","173","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","arai20150110","","","- C23 H27 Br N2 O5 -","- C23 H27 Br N2 O5 -","- C92 H108 Br4 N8 O20 -","4","1","","Arai, Takayoshi; Tsuchiya, Kento; Matsumura, Eri","PyBidine-NiCl2-Catalyzed Asymmetric Addition of Alcohols and Peroxides to Isatin-Derived Ketimines.","Organic letters","2015","17","10","2416","2419","10.1021/acs.orglett.5b00928","","","0.71073","MoKα","","0.062","0.0382","","","0.0931","0.1109","","","","","","1.068","","","","has coordinates","238270","2020-10-21","18:00:00",""
"1555012","8.4044","0.0011","11.3774","0.0015","11.5451","0.0015","90","","96.16","0.003","90","","1097.6","0.2","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C8 H11 F3 N2 O S -","- C8 H11 F3 N2 O S -","- C32 H44 F12 N8 O4 S4 -","4","1","","Liang, Zhaoli; Wang, Fei; Chen, Pinhong; Liu, Guosheng","Copper-Catalyzed Intermolecular Trifluoromethylthiocyanation of Alkenes: Convenient Access to CF3-Containing Alkyl Thiocyanates.","Organic letters","2015","17","10","2438","2441","10.1021/acs.orglett.5b00939","","","0.71073","MoKα","","0.0661","0.059","","","0.1531","0.1617","","","","","","1.042","","","","has coordinates","238271","2020-10-21","18:00:00",""
"1555018","10.7975","0.0005","11.121","0.0004","17.986","0.0005","82.945","0.002","76.059","0.003","70.925","0.004","1978.74","0.14","115","1","115","1","","","","","","","","5","P -1","-P 1","2","","","","- C76 H112 F14 N4 Sn4 -","- C76 H112 F14 N4 Sn4 -","- C76 H112 F14 N4 Sn4 -","1","0.5","","Hahn, Lena; Wadepohl, Hubert; Gade, Lutz H.","Tetralithiated tetraazaperopyrene as a key intermediate for the synthesis of functionalized derivatives.","Organic letters","2015","17","9","2266","2269","10.1021/acs.orglett.5b00942","","x-ray","1.5418","CuKα","","0.0704","0.0589","","","0.1497","0.1612","","","","","","1.065","","","","has coordinates","238273","2020-10-21","18:00:00",""
"1555019","6.15317","0.00018","9.3804","0.0003","13.8177","0.0004","103.878","0.003","100.265","0.002","98.23","0.003","747.31","0.04","120","1","120","1","","","","","","","","4","P -1","-P 1","2","","","","- C32 H4 F26 N4 -","- C32 H4 F26 N4 -","- C32 H4 F26 N4 -","1","0.5","","Hahn, Lena; Wadepohl, Hubert; Gade, Lutz H.","Tetralithiated tetraazaperopyrene as a key intermediate for the synthesis of functionalized derivatives.","Organic letters","2015","17","9","2266","2269","10.1021/acs.orglett.5b00942","","x-ray","1.54184","CuKα","","0.0314","0.029","","","0.0801","0.0819","","","","","","1.033","","","","has coordinates","238273","2020-10-21","18:00:00",""
"1555021","12.91","0.005","9.664","0.005","12.157","0.006","90","","90","","90","","1516.7","1.2","293","","293","","","","","","","","","3","P n a 21","P 2c -2n","33","","6-((2-hydroxyphenyl)(phenyl)methyl)cyclohex-2-enone","","- C19 H18 O2 -","- C19 H18 O2 -","- C76 H72 O8 -","4","1","","Lewis, Robert S.; Garza, Christopher J.; Dang, Ann T.; Pedro, Te Kie A.; Chain, William J.","Michael Additions of Highly Basic Enolates to ortho-Quinone Methides.","Organic letters","2015","17","9","2278","2281","10.1021/acs.orglett.5b00972","","x-ray","0.71075","MoKα","","","0.0567","","","","0.1731","","","","","","0.845","","","","has coordinates","238275","2020-10-21","18:00:00",""
"1555022","8.6511","0.0017","11.009","0.002","15.784","0.003","90","","90","","90","","1503.3","0.5","273","","273","","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","6-(1-(2-hydroxyphenyl)pentyl)cyclohex-2-enone","","- C17 H22 O2 -","- C17 H22 O2 -","- C68 H88 O8 -","4","1","","Lewis, Robert S.; Garza, Christopher J.; Dang, Ann T.; Pedro, Te Kie A.; Chain, William J.","Michael Additions of Highly Basic Enolates to ortho-Quinone Methides.","Organic letters","2015","17","9","2278","2281","10.1021/acs.orglett.5b00972","","x-ray","0.71075","MoKα","","","0.1289","","","","0.4135","","","","","","1.577","","","","has coordinates","238275","2020-10-21","18:00:00",""
"1555026","9.724","0.004","10.178","0.004","10.676","0.004","62.165","0.007","79.328","0.007","69.089","0.007","872.6","0.6","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H21 N O3 -","- C22 H21 N O3 -","- C44 H42 N2 O6 -","2","1","","Capreti, Naylil M. R.; Jurberg, Igor D.","Michael Addition of Soft Carbon Nucleophiles to Alkylidene Isoxazol-5-ones: A Divergent Entry to β-Branched Carbonyl Compounds.","Organic letters","2015","17","10","2490","2493","10.1021/acs.orglett.5b01004","","","0.71073","MoKα","","0.0692","0.041","","","0.0958","0.1082","","","","","","1.008","","","","has coordinates","238277","2020-10-21","18:00:00",""
"1555028","26.4383","0.0016","26.4383","0.0016","8.6956","0.0005","90","","90","","120","","5263.8","0.5","170","2","170","","","","","","","","","4","R -3 :H","-R 3","148","","","","- C15 H13 N O -","- C15 H13 N O -","- C270 H234 N18 O18 -","18","1","","Zhang, Yan; Wang, Dahai; Cui, Sunliang","Facile Synthesis of Isoindolinones via Rh(III)-Catalyzed One-Pot Reaction of Benzamides, Ketones, and Hydrazines.","Organic letters","2015","17","10","2494","2497","10.1021/acs.orglett.5b01016","","","0.71073","MoKα","","0.0492","0.038","","","0.0861","0.0943","","","","","","1.048","","","","has coordinates","238279","2020-10-21","18:00:00",""
"1555031","14.8225","0.0019","11.0736","0.0013","18.657","0.003","90","","100.056","0.006","90","","3015.3","0.7","100","","100","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C36 H39 N O2 -","- C36 H39 N O2 -","- C144 H156 N4 O8 -","4","1","","Reddy, Virsinha; Vijaya Anand, Ramasamy","Expedient Access to Unsymmetrical Diarylindolylmethanes through Palladium-Catalyzed Domino Electrophilic Cyclization-Extended Conjugate Addition Approach.","Organic letters","2015","17","14","3390","3393","10.1021/acs.orglett.5b01030","","","0.71073","MoKα","","0.2069","0.0971","","","0.1779","0.235","","","","","","1.088","","","","has coordinates","238281","2020-10-21","18:00:00",""
"1555034","15.0789","0.0011","8.6357","0.0007","18.2167","0.0014","90","","106.122","0.001","90","","2278.8","0.3","173","","173","","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C25 H27 Fe N O3 S -","- C25 H27 Fe N O3 S -","- C100 H108 Fe4 N4 O12 S4 -","4","2","","Ogasawara, Masamichi; Wada, Shiro; Isshiki, Erika; Kamimura, Takumi; Yanagisawa, Akira; Takahashi, Tamotsu; Yoshida, Kazuhiro","Enantioselective synthesis of planar-chiral ferrocene-fused 4-pyridones and their application in construction of pyridine-based organocatalyst library.","Organic letters","2015","17","9","2286","2289","10.1021/acs.orglett.5b01044","","","0.71073","MoKα","","0.0452","0.0349","","","0.0656","0.0736","","","","","","1.036","","","","has coordinates,has disorder","279649","2022-11-30","18:17:27",""
"1555037","8.9224","0.0002","9.3813","0.0002","18.2533","0.0004","90","","103.064","0.0012","90","","1488.32","0.06","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","SJY-002","","","- C17 H14 N2 O3 -","- C17 H14 N2 O3 -","- C68 H56 N8 O12 -","4","1","","Son, Jeong-Yu; Kim, Sunghwa; Jeon, Woo Hyung; Lee, Phil Ho","Synthesis of Cinnolin-3(2H)-one Derivatives from Rh-Catalyzed Reaction of Azobenzenes with Diazotized Meldrum's Acid.","Organic letters","2015","17","10","2518","2521","10.1021/acs.orglett.5b01052","","","0.71073","","","0.0899","0.0572","","","0.1118","0.1245","","","","","","1.042","","","","has coordinates","238285","2020-10-21","18:00:00",""
"1555039","10.896","0.004","11.118","0.005","11.442","0.004","109.812","0.005","100.766","0.0013","111.223","0.006","1137.4","0.8","293","2","293","2","","","","","","","see text","3","P -1","-P 1","2","","","","- C26 H28 O5 -","- C26 H28 O5 -","- C52 H56 O10 -","2","1","","Naresh, Gunaganti; Kant, Ruchir; Narender, Tadigoppula","Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products.","Organic letters","2015","17","14","3446","3449","10.1021/acs.orglett.5b01477","","","0.71075","MoKα","","0.1048","0.0663","","","0.1736","0.1906","","","","","","0.856","","","","has coordinates","238287","2020-10-21","18:00:00",""
"1555041","8.428","0.003","11.011","0.003","11.459","0.003","65.415","0.008","87.993","0.015","89.668","0.015","966.4","0.5","293","2","293","2","","","","","","","see text","3","P -1","-P 1","2","","","","- C23 H24 O3 -","- C23 H24 O3 -","- C46 H48 O6 -","2","1","","Naresh, Gunaganti; Kant, Ruchir; Narender, Tadigoppula","Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products.","Organic letters","2015","17","14","3446","3449","10.1021/acs.orglett.5b01477","","","0.71075","MoKα","","0.1148","0.0724","","","0.2165","0.2395","","","","","","1.001","","","","has coordinates","238289","2020-10-21","18:00:00",""
"1555044","22.265","0.003","7.7011","0.001","12.8529","0.0015","90","","102.095","0.003","90","","2154.9","0.5","100","2","100","2","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C21 H36 O4 Si -","- C21 H36 O4 Si -","- C84 H144 O16 Si4 -","4","1","","Peng, Shao-Zheng; Sha, Chin-Kang","Stereoselective Total Syntheses of Guanacastepenes N and O.","Organic letters","2015","17","14","3486","3489","10.1021/acs.orglett.5b01498","","","0.71073","MoKα","","0.0708","0.0584","","","0.153","0.1604","","","","","","1.097","","","","has coordinates","238292","2020-10-21","18:00:00",""
"1555045","12.324","0.001","7.8713","0.0006","10.6532","0.0008","90","","92.217","0.001","90","","1032.65","0.14","295","2","295","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C12 H14 O3 -","- C12 H14 O3 -","- C48 H56 O12 -","4","1","","Peng, Shao-Zheng; Sha, Chin-Kang","Stereoselective Total Syntheses of Guanacastepenes N and O.","Organic letters","2015","17","14","3486","3489","10.1021/acs.orglett.5b01498","","","0.71073","MoKα","","0.0541","0.0451","","","0.1254","0.1336","","","","","","1.058","","","","has coordinates","238293","2020-10-21","18:00:00",""
"1555051","8.9128","0.0003","10.9914","0.0003","20.184","0.0006","91.339","0.001","96.624","0.001","104.357","0.001","1899.99","0.1","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C36 H55 N O7 Si2 -","- C36 H55 N O7 Si2 -","- C72 H110 N2 O14 Si4 -","2","1","","Peng, Shao-Zheng; Sha, Chin-Kang","Stereoselective Total Syntheses of Guanacastepenes N and O.","Organic letters","2015","17","14","3486","3489","10.1021/acs.orglett.5b01498","","","0.71073","MoKα","","0.0401","0.0332","","","0.0911","0.1005","","","","","","1.08","","","","has coordinates","238295","2020-10-21","18:00:00",""
"1555052","7.3936","0.0009","10.5735","0.0012","17.817","0.002","90","","90","","90","","1392.9","0.3","295","2","295","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C15 H20 O5 -","- C15 H20 O5 -","- C60 H80 O20 -","4","1","","Peng, Shao-Zheng; Sha, Chin-Kang","Stereoselective Total Syntheses of Guanacastepenes N and O.","Organic letters","2015","17","14","3486","3489","10.1021/acs.orglett.5b01498","","","0.71073","MoKα","","0.0452","0.04","","","0.0951","0.0993","","","","","","1.084","","","","has coordinates","238296","2020-10-21","18:00:00",""
"1555053","16.4753","0.0003","10.1532","0.0002","13.8282","0.0003","90","","98.669","0.001","90","","2286.71","0.08","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H38 O5 S -","- C21 H38 O5 S -","- C84 H152 O20 S4 -","4","1","","Peng, Shao-Zheng; Sha, Chin-Kang","Stereoselective Total Syntheses of Guanacastepenes N and O.","Organic letters","2015","17","14","3486","3489","10.1021/acs.orglett.5b01498","","","0.71073","MoKα","","0.0667","0.0534","","","0.184","0.2002","","","","","","1.073","","","","has coordinates","238297","2020-10-21","18:00:00",""
"1555059","8.5281","0.0002","18.7862","0.0005","9.5185","0.0003","90","","100.368","0.001","90","","1500.07","0.07","296","2","296","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C15 H22 O6 -","- C15 H22 O6 -","- C60 H88 O24 -","4","1","","Peng, Shao-Zheng; Sha, Chin-Kang","Stereoselective Total Syntheses of Guanacastepenes N and O.","Organic letters","2015","17","14","3486","3489","10.1021/acs.orglett.5b01498","","","0.71073","MoKα","","0.0548","0.0389","","","0.0963","0.11","","","","","","1.051","","","","has coordinates","238299","2020-10-21","18:00:00",""
"1555060","6.9082","0.0001","11.2913","0.0002","19.3834","0.0003","90","","91.357","0.001","90","","1511.53","0.04","296","2","296","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C16 H17 N O4 -","- C16 H17 N O4 -","- C64 H68 N4 O16 -","4","2","","Peng, Shao-Zheng; Sha, Chin-Kang","Stereoselective Total Syntheses of Guanacastepenes N and O.","Organic letters","2015","17","14","3486","3489","10.1021/acs.orglett.5b01498","","","1.54178","CuKα","","0.0501","0.0455","","","0.1313","0.1377","","","","","","1.049","","","","has coordinates","238300","2020-10-21","18:00:00",""
"1555061","10.6177","0.0009","21.038","0.003","26.249","0.002","90","","90","","90","","5863.4","1.1","175","","175","","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C34 H22 Cl2 N4 O4 -","- C34 H22 Cl2 N4 O4 -","- C272 H176 Cl16 N32 O32 -","8","1","","Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion","Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.","Organic letters","2015","17","14","3494","3497","10.1021/acs.orglett.5b01576","","","0.71073","MoKα","","0.188","0.078","","0.0928","0.0458","0.0458","","","","","","1.0968","","","","has coordinates","288248","2023-12-12","12:55:27",""
"1555077","10.6627","0.0003","10.6627","0.0003","29.5381","0.0018","90","","90","","90","","3358.3","0.2","175","","175","","","","","","","","","5","P 43","P 4cw","78","","","","- C30 H22 Cl2 N4 O12 -","- C30 H22 Cl2 N4 O12 -","- C120 H88 Cl8 N16 O48 -","4","1","","Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion","Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.","Organic letters","2015","17","14","3494","3497","10.1021/acs.orglett.5b01576","","","0.71073","MoKα","","0.0899","0.0713","","0.0978","0.0848","0.0848","","","","","","1.1026","","","","has coordinates","288248","2023-12-12","12:55:27",""
"1555078","12.1779","0.0011","21.8512","0.0015","21.9539","0.0015","60.52","0.007","87.603","0.006","86.921","0.007","5077.5","0.8","175","","175","","","","","","","","","4","P -1","-P 1","2","","","","- C29 H20 I4 O4 -","- C28.6667 H18.6667 I4 O4 -","- C172 H112 I24 O24 -","6","3","","Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion","Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.","Organic letters","2015","17","14","3494","3497","10.1021/acs.orglett.5b01576","","","0.71073","MoKα","","0.1383","0.1138","","0.1501","0.1235","0.1235","","","","","","1.1","","","","has coordinates","274567","2022-04-19","14:22:36",""
"1555080","13.2235","0.0013","24.195","0.002","10.2868","0.0012","90","","110.556","0.011","90","","3081.6","0.6","175","","175","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C38 H26 Cl2 O4 -","- C38 H26 Cl2 O4 -","- C152 H104 Cl8 O16 -","4","1","","Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion","Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.","Organic letters","2015","17","14","3494","3497","10.1021/acs.orglett.5b01576","","","0.71073","MoKα","","0.0867","0.0653","","0.0675","0.0613","0.0613","","","","","","1.1873","","","","has coordinates","238306","2020-10-21","18:00:00",""
"1555083","8.2569","0.0002","11.0688","0.0002","20.1396","0.0004","90","","95.9683","0.0011","90","","1830.66","0.07","296","2","296","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","SKL-20150324","","","- C19 H21 N O4 S -","- C19 H21 N O4 S -","- C76 H84 N4 O16 S4 -","4","1","","Jung, Da Jung; Jeon, Hyun Ji; Lee, Joo Hyun; Lee, Sang-gi","Cu(I)/Rh(II)-Catalyzed Tandem Convergent Multicomponent Reaction for the Regio- and Stereocontrolled Synthesis of γ-Oxo-β-amino Esters.","Organic letters","2015","17","14","3498","3501","10.1021/acs.orglett.5b01587","","","0.71073","","","0.0636","0.0461","","","0.1072","0.1168","","","","","","1.037","","","","has coordinates","238308","2020-10-21","18:00:00",""
"1555086","10.98","0.002","21.409","0.004","11.347","0.002","90","","104.07","0.03","90","","2587.3","0.9","295","2","295","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C27 H27 N O5 S -","- C27 H27 N O5 S -","- C108 H108 N4 O20 S4 -","4","1","","Jung, Da Jung; Jeon, Hyun Ji; Lee, Joo Hyun; Lee, Sang-gi","Cu(I)/Rh(II)-Catalyzed Tandem Convergent Multicomponent Reaction for the Regio- and Stereocontrolled Synthesis of γ-Oxo-β-amino Esters.","Organic letters","2015","17","14","3498","3501","10.1021/acs.orglett.5b01587","","","0.71073","MoKα","","0.0544","0.0403","","","0.1108","0.1178","","","","","","1.067","","","","has coordinates","238310","2020-10-21","18:00:00",""
"1555089","8.6263","0.0009","12.097","0.002","16.023","0.006","107.86","0.03","95.73","0.03","104.279","0.013","1514.1","0.7","291","2","291.15","","","","","","","","","3","P -1","-P 1","2","","","","- C38 H34 P2 -","- C38 H34 P2 -","- C76 H68 P4 -","2","1","","Hu, Zhengsong; Li, Zongyang; Zhao, Kang; Tian, Rongqiang; Duan, Zheng; Mathey, François","Reaction of Phospholes with Aldimines: A One-Step Synthesis of Chelating, Alpha-C2-Bridged Biphospholes.","Organic letters","2015","17","14","3518","3520","10.1021/acs.orglett.5b01604","","","1.54184","CuKα","","0.0461","0.0393","","","0.1078","0.1148","","","","","","1.034","","","","has coordinates","238313","2020-10-21","18:00:00",""
"1555090","14.7596","0.0008","10.4392","0.0006","17.7877","0.0005","90","","105.924","0.004","90","","2635.5","0.2","291","2","291.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C32 H32 O P2 -","- C32 H32 O P2 -","- C128 H128 O4 P8 -","4","1","","Hu, Zhengsong; Li, Zongyang; Zhao, Kang; Tian, Rongqiang; Duan, Zheng; Mathey, François","Reaction of Phospholes with Aldimines: A One-Step Synthesis of Chelating, Alpha-C2-Bridged Biphospholes.","Organic letters","2015","17","14","3518","3520","10.1021/acs.orglett.5b01604","","","1.54184","CuKα","","0.0487","0.0409","","","0.1107","0.1173","","","","","","1.049","","","","has coordinates","238314","2020-10-21","18:00:00",""
"1555091","12.58","0.005","15.83","0.005","8.839","0.005","90","0.005","109.551","0.005","90","0.005","1658.7","1.3","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C18 H23 N O2 -","- C18 H23 N O2 -","- C72 H92 N4 O8 -","4","1","","Ren, Wenlong; Chang, Wenju; Wang, Yang; Li, Jingfu; Shi, Yian","Pd-Catalyzed Regiodivergent Hydroesterification of Aryl Olefins with Phenyl Formate.","Organic letters","2015","17","14","3544","3547","10.1021/acs.orglett.5b01630","","","0.71069","MoKα","","0.173","0.0912","","","0.259","0.326","","","","","","0.996","","","","has coordinates","238315","2020-10-21","18:00:00",""
"1555095","17.095","0.003","5.874","0.0012","15.476","0.003","90","","106","0.03","90","","1493.8","0.5","293","2","293","2","","","","","","","","3","C 1 2 1","C 2y","5","","","","- C19 H16 O2 -","- C19 H16 O2 -","- C76 H64 O8 -","4","1","","Ren, Wenlong; Chang, Wenju; Wang, Yang; Li, Jingfu; Shi, Yian","Pd-Catalyzed Regiodivergent Hydroesterification of Aryl Olefins with Phenyl Formate.","Organic letters","2015","17","14","3544","3547","10.1021/acs.orglett.5b01630","","","0.71073","MoKα","","0.0778","0.051","","","0.1258","0.1435","","","","","","1.004","","","","has coordinates","238317","2020-10-21","18:00:00",""
"1555096","8.885","0.0008","11.599","0.001","11.638","0.0011","87.07","0.002","72.279","0.001","76.183","0.002","1109.11","0.17","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C21 H13 Cl I3 N O2 -","- C21 H13 Cl I3 N O2 -","- C42 H26 Cl2 I6 N2 O4 -","2","1","","Zhang, Xue; Feng, Chengjie; Jiang, Tao; Li, Yifei; Pan, Ling; Xu, Xianxiu","Expedient and Divergent Tandem One-Pot Synthesis of Benz[e]indole and Spiro[indene-1,3'-pyrrole] Derivatives from Alkyne-Tethered Chalcones/Cinnamates and TosMIC.","Organic letters","2015","17","14","3576","3579","10.1021/acs.orglett.5b01676","","","0.71069","MoKα","","0.0387","0.0313","","","0.0871","0.0911","","","","","","1.045","","","","has coordinates","238318","2020-10-21","18:00:00",""
"1555100","11.057","0.003","13.631","0.003","13.716","0.003","90","","110.38","0.003","90","","1937.8","0.8","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C21 H15 Cl I N O2 -","- C21 H15 Cl I N O2 -","- C84 H60 Cl4 I4 N4 O8 -","4","1","","Zhang, Xue; Feng, Chengjie; Jiang, Tao; Li, Yifei; Pan, Ling; Xu, Xianxiu","Expedient and Divergent Tandem One-Pot Synthesis of Benz[e]indole and Spiro[indene-1,3'-pyrrole] Derivatives from Alkyne-Tethered Chalcones/Cinnamates and TosMIC.","Organic letters","2015","17","14","3576","3579","10.1021/acs.orglett.5b01676","","","0.71069","MoKα","","0.0906","0.043","","","0.0857","0.1","","","","","","1","","","","has coordinates","238321","2020-10-21","18:00:00",""
"1555102","9.1622","0.0018","9.508","0.002","10.568","0.002","83","0.016","65.519","0.019","78.417","0.018","820","0.3","298","","298","","","","","","","","","3","P -1","-P 1","2","","","","- C22 H22 O -","- C22 H22 O -","- C44 H44 O2 -","2","1","","Manojveer, Seetharaman; Balamurugan, Rengarajan","In Situ Formed Acetal-Facilitated Synthesis of Substituted Indene Derivatives from o-Alkenylbenzaldehydes.","Organic letters","2015","17","14","3600","3603","10.1021/acs.orglett.5b01695","","","0.71073","MoKα","","0.0795","0.0502","","","0.1132","0.1293","","","","","","1.041","","","","has coordinates","238323","2020-10-21","18:00:00",""
"1555105","10.571","0.006","5.838","0.003","12.338","0.007","90","","90","","90","","761.4","0.7","291","2","291","2","","","","","","","see text","3","P c a 21","P 2c -2ac","29","","(3aR,3bR,6aS,7aR)-hexahydrodifuro[2,3-b:3',2'-d]furan-2(3H)-one","","- C8 H10 O4 -","- C8 H10 O4 -","- C32 H40 O16 -","4","1","","Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan","Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.","Organic letters","2015","17","14","3604","3607","10.1021/acs.orglett.5b01707","","","0.71073","MoKa","","0.0623","0.058","","","0.1408","0.144","","","","","","1.122","","","","has coordinates","238325","2020-10-21","18:00:00",""
"1555106","37.2102","0.0015","18.06","0.0005","6.8155","0.0003","90","","90","","90","","4580.1","0.3","291","2","291","2","","","","","","","see text","3","F d d 2","F 2 -2d","43","","(1S,2S,3R,7R,9S,11R,13S,17R)-6,8,10,12,14- pentaoxapentacyclo[9.6.0.0^2,9^.0^3,7^.0^13,17^]heptadecan-5-one","","- C12 H14 O6 -","- C12 H14 O6 -","- C192 H224 O96 -","16","1","","Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan","Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.","Organic letters","2015","17","14","3604","3607","10.1021/acs.orglett.5b01707","","","1.5418","CuKα","","0.0414","0.0391","","","0.1012","0.1035","","","","","","1.06","","","","has coordinates,has disorder","238325","2020-10-21","18:00:00",""
"1555107","8.8394","0.001","8.5924","0.001","23.437","0.003","90","","90","","90","","1780.1","0.4","291","2","291","2","","","","","","","see text","3","P b c a","-P 2ac 2ab","61","","(1R*,5S*,8S*)-4,6-Dioxatricyclo[6.4.0.0^1,5^]dodec-10-en-7-one","","- C10 H12 O3 -","- C10 H12 O3 -","- C80 H96 O24 -","8","1","","Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan","Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.","Organic letters","2015","17","14","3604","3607","10.1021/acs.orglett.5b01707","","","0.71073","MoKa","","0.0796","0.0696","","","0.1582","0.1644","","","","","","1.22","","","","has coordinates","238325","2020-10-21","18:00:00",""
"1555108","6.345","0.001","8.9881","0.0015","15.108","0.003","90","","90","","90","","861.6","0.3","291","2","291","2","","","","","","","see text","3","P 21 21 21","P 2ac 2ab","19","","(1R,2R,6R,8S)-5,7,9-trioxatricyclo[6.4.0.0^2,6^]dodecan-4-one","","- C9 H12 O4 -","- C9 H12 O4 -","- C36 H48 O16 -","4","1","","Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan","Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.","Organic letters","2015","17","14","3604","3607","10.1021/acs.orglett.5b01707","","","0.71073","MoKa","","0.0357","0.0346","","","0.0865","0.0875","","","","","","1.082","","","","has coordinates","238325","2020-10-21","18:00:00",""
"1555109","5.3883","0.0011","12.812","0.002","6.0438","0.0013","90","","114.32","0.03","90","","380.21","0.16","291","2","291","2","","","","","","","see text","3","P 1 21 1","P 2yb","4","","(1S,2R,6R,8R)-5,7,9-trioxatricyclo[6.3.0.0^2,6^]undecan-4-one","","- C8 H10 O4 -","- C8 H10 O4 -","- C16 H20 O8 -","2","1","","Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan","Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.","Organic letters","2015","17","14","3604","3607","10.1021/acs.orglett.5b01707","","","0.7107","MoKα","","0.0459","0.043","","","0.1133","0.1164","","","","","","1.051","","","","has coordinates","238325","2020-10-21","18:00:00",""
"1555112","7.4987","0.0002","12.2482","0.0003","16.8063","0.0003","90","","90","","90","","1543.58","0.06","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","Arboridinine","","","- C19 H22 N2 O -","- C19 H22 N2 O -","- C76 H88 N8 O4 -","4","1","","Wong, Suet-Pick; Gan, Chew-Yan; Lim, Kuan-Hon; Ting, Kang-Nee; Low, Yun-Yee; Kam, Toh-Seok","Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon-Nitrogen Skeleton Derived from a Pericine Precursor.","Organic letters","2015","17","14","3628","3631","10.1021/acs.orglett.5b01757","","","0.71073","MoKα","","0.033","0.0314","","","0.0864","0.088","","","","","","1.09","","","","has coordinates","238327","2020-10-21","18:00:00",""
"1555114","8.6291","0.0003","9.4332","0.0003","12.4474","0.0004","82.659","0.003","70.506","0.003","68.236","0.003","887.04","0.06","150.01","0.1","150.01","0.1","","","","","","","","5","P 1","P 1","1","","","","- C18 H23 N O5 S -","- C18 H23 N O5 S -","- C36 H46 N2 O10 S2 -","2","2","","Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael","Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.","Organic letters","2015","17","14","3632","3635","10.1021/acs.orglett.5b01777","","x-ray","1.54184","CuKα","","0.0445","0.0436","","","0.1158","0.1167","","","","","","1.08","","","","has coordinates","238329","2020-10-21","18:00:00",""
"1555119","6.70613","0.00009","8.92562","0.00011","21.9646","0.0003","90","","91.7362","0.0013","90","","1314.12","0.03","150","2","150","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C12 H15 F N2 O4 S -","- C12 H15 F N2 O4 S -","- C48 H60 F4 N8 O16 S4 -","4","1","","Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael","Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.","Organic letters","2015","17","14","3632","3635","10.1021/acs.orglett.5b01777","","x-ray","1.54184","CuKα","","0.0417","0.0402","","","0.1091","0.1104","","","","","","1.112","","","","has coordinates,has disorder","238331","2020-10-21","18:00:00",""
"1555122","15.2033","0.0005","5.10542","0.00013","15.6074","0.0006","90","","108.006","0.004","90","","1152.1","0.07","150","2","150","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C11 H14 N2 O2 S -","- C11 H14 N2 O2 S -","- C44 H56 N8 O8 S4 -","4","1","","Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael","Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.","Organic letters","2015","17","14","3632","3635","10.1021/acs.orglett.5b01777","","x-ray","1.54184","CuKα","","0.0413","0.0372","","","0.1042","0.1081","","","","","","1.052","","","","has coordinates","238333","2020-10-21","18:00:00",""
"1555124","8.236","0.0002","21.1919","0.0005","8.4904","0.0002","90","","103.856","0.003","90","","1438.76","0.06","200","2","200","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C16 H16 N2 O2 S -","- C16 H16 N2 O2 S -","- C64 H64 N8 O8 S4 -","4","1","","Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael","Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.","Organic letters","2015","17","14","3632","3635","10.1021/acs.orglett.5b01777","","x-ray","1.54184","CuKα","","0.0581","0.0448","","","0.1168","0.1278","","","","","","1.067","","","","has coordinates","238335","2020-10-21","18:00:00",""
"1555126","7.789","0.002","11.669","0.003","15.029","0.004","90","","90","","90","","1366","0.6","173.15","","173.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C13 H19 N O3 S -","- C13 H19 N O3 S -","- C52 H76 N4 O12 S4 -","4","1","","Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian","Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.","Organic letters","2015","17","16","3956","3959","10.1021/acs.orglett.5b01779","","","0.71073","MoKα","","0.0361","0.0357","","","0.0838","0.084","","","","","","1.187","","","","has coordinates","238337","2020-10-21","18:00:00",""
"1555128","9.24","0.005","6.262","0.003","14.504","0.008","90","","91.561","0.009","90","","838.9","0.8","173.15","","173.15","","","","","","","","","7","P 1 21 1","P 2yb","4","","","","- C14 H17 Br Cl N O4 S -","- C14 H17 Br Cl N O4 S -","- C28 H34 Br2 Cl2 N2 O8 S2 -","2","1","","Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian","Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.","Organic letters","2015","17","16","3956","3959","10.1021/acs.orglett.5b01779","","","0.71073","MoKα","","0.0285","0.0276","","","0.0644","0.0647","","","","","","1.105","","","","has coordinates","238339","2020-10-21","18:00:00",""
"1555130","14.656","0.003","10.051","0.002","14.998","0.003","90","","104.87","0.03","90","","2135.3","0.8","173.15","","173.15","","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C20 H24 Br N O4 S -","- C20 H24 Br N O4 S -","- C80 H96 Br4 N4 O16 S4 -","4","2","","Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian","Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.","Organic letters","2015","17","16","3956","3959","10.1021/acs.orglett.5b01779","","","0.71073","MoKα","","0.0703","0.0597","","","0.127","0.1338","","","","","","1.132","","","","has coordinates","238341","2020-10-21","18:00:00",""
"1555133","6.4495","0.0013","15.276","0.003","8.0516","0.0016","90","","96.47","0.03","90","","788.2","0.3","100","2","100","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C14 H18 Br N O4 S -","- C14 H18 Br N O4 S -","- C28 H36 Br2 N2 O8 S2 -","2","1","","Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian","Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.","Organic letters","2015","17","16","3956","3959","10.1021/acs.orglett.5b01779","","","0.71073","MoKα","","0.0253","0.0246","","","0.0605","0.061","","","","","","1.057","","","","has coordinates","238343","2020-10-21","18:00:00",""
"1555134","7.6751","0.0015","12.59","0.003","22.275","0.005","90","","90","","90","","2152.4","0.8","173.15","","173.15","","","","","","","","","7","P 21 21 21","P 2ac 2ab","19","","","","- C20 H23 Br Cl N O4 S -","- C20 H23 Br Cl N O4 S -","- C80 H92 Br4 Cl4 N4 O16 S4 -","4","1","","Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian","Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.","Organic letters","2015","17","16","3956","3959","10.1021/acs.orglett.5b01779","","","0.71073","MoKα","","0.0369","0.034","","","0.0661","0.0674","","","","","","1.109","","","","has coordinates,has disorder","238344","2020-10-21","18:00:00",""
"1555135","11.0456","0.0007","12.0988","0.0008","14.8761","0.001","68.867","0.001","70.725","0.001","86.448","0.001","1746.7","0.2","298","2","298","2","","","","","","","","5","P -1","-P 1","2","","","","- C40 H41 N O4 S2 -","- C40 H41 N O4 S2 -","- C80 H82 N2 O8 S4 -","2","1","","Ding, Ran; Zheng, Bo; Wang, Yan; Peng, Yungui","A Cation-Directed Enantioselective Sulfur-Mediated Michael/Mannich Three-Component Domino Reaction involving Chalcones as Michael Acceptors.","Organic letters","2015","17","17","4128","4131","10.1021/acs.orglett.5b01833","","","0.71073","MoKα","","0.0484","0.0413","","","0.13","0.1559","","","","","","1.062","","","","has coordinates","238345","2020-10-21","18:00:00",""
"1555148","11.13642","0.00007","14.74032","0.00008","46.2616","0.0003","90","","90","","90","","7594.04","0.08","293","2","293","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C43 H48 N O3 S2 -","- C43 H48 N O3 S2 -","- C344 H384 N8 O24 S16 -","8","2","","Ding, Ran; Zheng, Bo; Wang, Yan; Peng, Yungui","A Cation-Directed Enantioselective Sulfur-Mediated Michael/Mannich Three-Component Domino Reaction involving Chalcones as Michael Acceptors.","Organic letters","2015","17","17","4128","4131","10.1021/acs.orglett.5b01833","","","1.54184","CuKα","","0.0459","0.0455","","","0.1247","0.125","","","","","","1.059","","","","has coordinates,has disorder","275856","2022-06-07","07:08:27",""
"1555149","4.888","0.001","9.8","0.002","18.388","0.004","90","","90","","90","","880.8","0.3","298","2","298","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C8 H8 N2 O4 -","- C8 H8 N2 O4 -","- C32 H32 N8 O16 -","4","1","","Salahifar, Eslam; Nematollahi, Davood; Bayat, Mehdi; Mahyari, Amir; Amiri Rudbari, Hadi","Regioselective Green Electrochemical Approach to the Synthesis of Nitroacetaminophen Derivatives.","Organic letters","2015","17","19","4666","4669","10.1021/acs.orglett.5b01837","","","0.71073","MoKα","","0.0506","0.029","","","0.0558","0.06","","","","","","0.808","","","","has coordinates","238348","2020-10-21","18:00:00",""
"1555151","9.1308","0.0009","14.0389","0.0016","14.7904","0.0017","90","","106.943","0.002","90","","1813.6","0.3","294","1","294","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","(E)-2-tert-butyl-5-((4-methylphenyl)(phenyl)methylene) -4,5-dihydrooxazole","","- C21 H23 N O -","- C21 H23 N O -","- C84 H92 N4 O4 -","4","1","","Sinai, Ádám; Vangel, Dóra; Gáti, Tamás; Bombicz, Petra; Novák, Zoltán","Utilization of Copper-Catalyzed Carboarylation-Ring Closure for the Synthesis of New Oxazoline Derivatives.","Organic letters","2015","17","17","4136","4139","10.1021/acs.orglett.5b01860","","","0.71073","MoKα","","0.1242","0.0694","","","0.1791","0.2182","","","","","","0.996","","","","has coordinates","238350","2020-10-21","18:00:00",""
"1555154","15.4081","0.0005","7.7461","0.0003","19.9246","0.0006","90","","98.208","0.003","90","","2353.69","0.14","571","2","571","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C14 H11 Cl N2 -","- C14 H11 Cl N2 -","- C112 H88 Cl8 N16 -","8","2","","Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei","Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.","Organic letters","2015","17","16","3998","4001","10.1021/acs.orglett.5b01868","","","1.54178","CuKα","","0.0577","0.0522","","","0.1478","0.1562","","","","","","1.043","","","","has coordinates","275434","2022-05-16","05:31:57",""
"1555155","11.949","0.002","8.5662","0.0017","17.479","0.003","90","","103.621","0.002","90","","1738.8","0.5","296","2","296","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C19 H14 Cl N2 O P -","- C19 H14 Cl N2 O P -","- C76 H56 Cl4 N8 O4 P4 -","4","1","","Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei","Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.","Organic letters","2015","17","16","3998","4001","10.1021/acs.orglett.5b01868","","","0.71073","MoKα","","0.0374","0.0335","","","0.0895","0.0933","","","","","","1.045","","","","has coordinates","238353","2020-10-21","18:00:00",""
"1555158","11.4945","0.0005","7.5152","0.0004","17.4299","0.0009","90","","90","","90","","1505.66","0.13","293","2","293","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C7 H3 Cl2 N2 -","- C7 H4 Cl2 N2 -","- C56 H32 Cl16 N16 -","8","1","","Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei","Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.","Organic letters","2015","17","16","3998","4001","10.1021/acs.orglett.5b01868","","","1.54178","CuKα","","0.0457","0.0372","","","0.0946","0.1032","","","","","","1.056","","","","has coordinates","238355","2020-10-21","18:00:00",""
"1555161","8.759","0.0018","21.523","0.004","10.067","0.002","90","","104.55","0.03","90","","1837","0.7","113","2","113","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C23 H24 O4 -","- C23 H24 O4 -","- C92 H96 O16 -","4","1","","Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen","Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.","Organic letters","2015","17","17","4180","4183","10.1021/acs.orglett.5b01927","","","0.71073","MoKα","","0.0748","0.0485","","","0.1113","0.1233","","","","","","1.019","","","","has coordinates","238357","2020-10-21","18:00:00",""
"1555162","7.7505","0.0016","21.813","0.004","9.5132","0.0019","90","","94.65","0.03","90","","1603","0.6","113","2","113","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C18 H20 O6 -","- C18 H20 O6 -","- C72 H80 O24 -","4","1","","Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen","Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.","Organic letters","2015","17","17","4180","4183","10.1021/acs.orglett.5b01927","","","0.71073","MoKα","","0.0501","0.04","","","0.1076","0.1153","","","","","","1.082","","","","has coordinates","238358","2020-10-21","18:00:00",""
"1555163","16.298","0.003","11.852","0.002","9.939","0.002","90","","90.99","0.03","90","","1919.6","0.6","293.15","","293.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16.5 H16 Cl1.5 N2 O3 -","- C16.5 H16 Cl1.5 N2 O3 -","- C66 H64 Cl6 N8 O12 -","4","1","","Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen","Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.","Organic letters","2015","17","17","4180","4183","10.1021/acs.orglett.5b01927","","","0.71073","MoKα","","0.1439","0.1147","","","0.3265","0.3439","","","","","","1.12","","","","has coordinates,has disorder","238359","2020-10-21","18:00:00",""
"1555165","11.48","0.002","10.279","0.002","26.181","0.005","90","","90","","90","","3089.4","1","113","2","113","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C17 H17 Br O5 -","- C17 H17 Br O5 -","- C136 H136 Br8 O40 -","8","1","","Wang, Zhenjun; Chen, Shuai; Ren, Jun; Wang, Zhongwen","Cooperative Photo-/Lewis Acid Catalyzed Tandem Intramolecular [3 + 2] Cross-Cycloadditions of Cyclopropane 1,1-Diesters with α,β-Unsaturated Carbonyls for Medium-Sized Carbocycles.","Organic letters","2015","17","17","4184","4187","10.1021/acs.orglett.5b01928","","","0.71073","MoKα","","0.0493","0.0384","","","0.1015","0.1085","","","","","","1.062","","","","has coordinates","238361","2020-10-21","18:00:00",""
"1555167","10.526","0.002","19.394","0.004","7.8119","0.0016","90","","96.58","0.03","90","","1584.2","0.6","113","2","113","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C18 H20 O5 -","- C18 H20 O5 -","- C72 H80 O20 -","4","1","","Wang, Zhenjun; Chen, Shuai; Ren, Jun; Wang, Zhongwen","Cooperative Photo-/Lewis Acid Catalyzed Tandem Intramolecular [3 + 2] Cross-Cycloadditions of Cyclopropane 1,1-Diesters with α,β-Unsaturated Carbonyls for Medium-Sized Carbocycles.","Organic letters","2015","17","17","4184","4187","10.1021/acs.orglett.5b01928","","","0.71073","MoKα","","0.0501","0.0429","","","0.1054","0.1107","","","","","","1.043","","","","has coordinates","238363","2020-10-21","18:00:00",""
"1555170","9.136","0.0003","10.6809","0.0003","42.2825","0.0012","90","","90","","90","","4126","0.2","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C22 H26 O7 -","- C22 H26 O7 -","- C176 H208 O56 -","8","2","","Bera, Srikrishna; Daniliuc, Constantin G.; Studer, Armido","Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis.","Organic letters","2015","17","20","4940","4943","10.1021/acs.orglett.5b01932","","","1.54178","CuKα","","0.0231","0.0227","","","0.0585","0.0589","","","","","","1.04","","","","has coordinates","238365","2020-10-21","18:00:00",""
"1555171","8.5586","0.0003","9.2119","0.0003","27.3349","0.0008","90","","90","","90","","2155.11","0.12","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C23 H28 O7 -","- C23 H28 O7 -","- C92 H112 O28 -","4","1","","Bera, Srikrishna; Daniliuc, Constantin G.; Studer, Armido","Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis.","Organic letters","2015","17","20","4940","4943","10.1021/acs.orglett.5b01932","","","1.54178","CuKα","","0.0631","0.0618","","","0.1241","0.1245","","","","","","1.358","","","","has coordinates","238365","2020-10-21","18:00:00",""
"1555172","11.4637","0.0005","45.4434","0.0019","12.0124","0.0006","90","","116.324","0.002","90","","5608.9","0.5","103","2","103","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C34 H30 N2 O6 -","- C34 H30 N2 O6 -","- C272 H240 N16 O48 -","8","2","","Yan, Jianming; Tay, Guan Liang; Neo, Cuien; Lee, Bo Ra; Chan, Philip Wai Hong","Gold-Catalyzed Cycloisomerization and Diels-Alder Reaction of 1,6-Diyne Esters with Alkenes and Diazenes to Hydronaphthalenes and -cinnolines.","Organic letters","2015","17","17","4176","4179","10.1021/acs.orglett.5b01935","","","0.71073","MoKα","","0.1184","0.0647","","","0.1358","0.1555","","","","","","1.046","","","","has coordinates","238366","2020-10-21","18:00:00",""
"1555175","9.141","0.006","10.706","0.009","12.0986","0.001","73.26","0.03","68.76","0.03","72.31","0.04","1030.1","1.1","173","","173","","","","","","","","","4","P -1","-P 1","2","","","","- C26 H18 N4 O5 -","- C26 H18 N4 O5 -","- C52 H36 N8 O10 -","2","1","","Miura, Wataru; Hirano, Koji; Miura, Masahiro","Copper-Mediated Oxidative Coupling of Benzamides with Maleimides via Directed C-H Cleavage.","Organic letters","2015","17","16","4034","4037","10.1021/acs.orglett.5b01940","","","0.71075","MoKα","","","0.0496","","","","0.1505","","","","","","0.801","","","","has coordinates","238368","2020-10-21","18:00:00",""
"1555177","16.334","0.009","13.572","0.007","7.87","0.005","90","","104.13","0.03","90","","1691.9","1.7","273","","273","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H15 N3 O3 -","- C21 H15 N3 O3 -","- C84 H60 N12 O12 -","4","1","","Miura, Wataru; Hirano, Koji; Miura, Masahiro","Copper-Mediated Oxidative Coupling of Benzamides with Maleimides via Directed C-H Cleavage.","Organic letters","2015","17","16","4034","4037","10.1021/acs.orglett.5b01940","","","0.71075","MoKα","","","0.0435","","","","0.1107","","","","","","1.068","","","","has coordinates","238370","2020-10-21","18:00:00",""
"1555181","8.3103","0.0004","22.0934","0.001","11.8386","0.0006","90","","104.267","0.005","90","","2106.56","0.18","223","2","223","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C24 H19 N2 O2 S2 -","- C24 H19 N2 O2 S2 -","- C96 H76 N8 O8 S8 -","4","1","","Chen, Xiang; Zhang, Jun-Qi; Yin, Shao-Jie; Li, Hai-Yan; Zhou, Wei-Qun; Wang, Xing-Wang","Asymmetric Construction of Spiro[thiopyranoindole-benzoisothiazole] Scaffold via a Formal [3 + 3] Spiroannulation.","Organic letters","2015","17","17","4188","4191","10.1021/acs.orglett.5b01951","","","0.71073","MoKα","","0.0538","0.0406","","","0.1001","0.1064","","","","","","1.05","","","","has coordinates","238372","2020-10-21","18:00:00",""
"1555183","12.652","0.002","19.153","0.004","22.403","0.004","90","","90","","90","","5428.8","1.7","130","","130","","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C48 H38 Cl2 N4 O4 S4 -","- C48 H38 Cl2 N4 O4 S4 -","- C192 H152 Cl8 N16 O16 S16 -","4","1","","Chen, Xiang; Zhang, Jun-Qi; Yin, Shao-Jie; Li, Hai-Yan; Zhou, Wei-Qun; Wang, Xing-Wang","Asymmetric Construction of Spiro[thiopyranoindole-benzoisothiazole] Scaffold via a Formal [3 + 3] Spiroannulation.","Organic letters","2015","17","17","4188","4191","10.1021/acs.orglett.5b01951","","","0.71073","MoKα","","0.1102","0.0573","","","0.1242","0.1396","","","","","","0.868","","","","has coordinates","238374","2020-10-21","18:00:00",""
"1555187","6.1472","0.0015","11.724","0.003","27.834","0.007","90","","90","","90","","2006","0.9","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C19 H21 Cl2 N O2 S -","- C19 H21 Cl2 N O2 S -","- C76 H84 Cl8 N4 O8 S4 -","4","1","","Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun","Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines.","Organic letters","2015","17","16","4042","4045","10.1021/acs.orglett.5b01954","","","0.71073","MoKα","","0.0396","0.0323","","","0.0782","0.0828","","","","","","1.017","","","","has coordinates","238376","2020-10-21","18:00:00",""
"1555188","10.133","0.003","9.753","0.003","19.638","0.005","90","","100.289","0.004","90","","1909.6","0.9","296","2","296","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C19 H20 Cl N O2 S -","- C19 H20 Cl N O2 S -","- C76 H80 Cl4 N4 O8 S4 -","4","2","","Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun","Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines.","Organic letters","2015","17","16","4042","4045","10.1021/acs.orglett.5b01954","","","0.71073","MoKα","","0.126","0.0596","","","0.0957","0.12","","","","","","1","","","","has coordinates","238377","2020-10-21","18:00:00",""
"1555192","8.434","0.006","9.511","0.007","23.843","0.016","90","","90","","90","","1913","2","296","2","296","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C19 H20 Cl N O2 S -","- C19 H20 Cl N O2 S -","- C76 H80 Cl4 N4 O8 S4 -","4","1","","Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun","Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines.","Organic letters","2015","17","16","4042","4045","10.1021/acs.orglett.5b01954","","","0.71073","MoKα","","0.1328","0.0515","","","0.0798","0.1024","","","","","","0.996","","","","has coordinates","238379","2020-10-21","18:00:00",""
"1555194","7.2944","0.0019","14.078","0.004","19.047","0.006","90","","90","","90","","1955.9","1","293","","293","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C25 H19 N3 O -","- C25 H19 N3 O -","- C100 H76 N12 O4 -","4","1","","Takamatsu, Kazutaka; Hirano, Koji; Miura, Masahiro","Copper-Catalyzed Formal [4 + 1] Cycloaddition of Benzamides and Isonitriles via Directed C-H Cleavage.","Organic letters","2015","17","16","4066","4069","10.1021/acs.orglett.5b01986","","","0.71075","MoKα","","","0.0765","","","","0.1834","","","","","","1.037","","","","has coordinates","238381","2020-10-21","18:00:00",""
"1555196","12.7097","0.0009","15.6515","0.0013","17.3613","0.0014","90","","90","","90","","3453.6","0.5","173","","173","","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C21 H19 N3 O -","- C21 H19 N3 O -","- C168 H152 N24 O8 -","8","1","","Takamatsu, Kazutaka; Hirano, Koji; Miura, Masahiro","Copper-Catalyzed Formal [4 + 1] Cycloaddition of Benzamides and Isonitriles via Directed C-H Cleavage.","Organic letters","2015","17","16","4066","4069","10.1021/acs.orglett.5b01986","","","0.71075","MoKα","","","0.0446","","","","0.1156","","","","","","1.076","","","","has coordinates","238383","2020-10-21","18:00:00",""
"1555197","9.7492","0.0019","10.793","0.002","12.316","0.003","106.75","0.03","97.22","0.03","95.45","0.03","1219.3","0.5","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H34 N4 O9 -","- C22 H34 N4 O9 -","- C44 H68 N8 O18 -","2","1","","Jia, Yan-Lai; Wei, Mei-Yan; Chen, Hai-Yan; Guan, Fei-Fei; Wang, Chang-Yun; Shao, Chang-Lun","(+)- and (-)-Pestaloxazine A, a Pair of Antiviral Enantiomeric Alkaloid Dimers with a Symmetric Spiro[oxazinane-piperazinedione] Skeleton from Pestalotiopsis sp.","Organic letters","2015","17","17","4216","4219","10.1021/acs.orglett.5b01995","","","0.71073","MoKα","","0.0756","0.0473","","","0.0894","0.101","","","","","","1.01","","","","has coordinates,has disorder","238384","2020-10-21","18:00:00",""
"1555206","9.0718","0.0018","20.806","0.004","12.975","0.003","90","","107.07","0.03","90","","2341.1","0.9","173.15","","173.15","","","","","","","","","4","C 1 c 1","C -2yc","9","","","","- C26 H24 N4 O4 -","- C26 H24 N4 O4 -","- C104 H96 N16 O16 -","4","1","","Liu, Honglei; Yuan, Chunhao; Wu, Yang; Xiao, Yumei; Guo, Hongchao","Sc(OTf)3-Catalyzed [3 + 3] Cycloaddition of Cyclopropane 1,1-Diesters with Phthalazinium Dicyanomethanides.","Organic letters","2015","17","17","4220","4223","10.1021/acs.orglett.5b02003","","","0.71073","MoKα","","0.0391","0.0363","","","0.0758","0.0776","","","","","","1.103","","","","has coordinates","238387","2020-10-21","18:00:00",""
"1555207","9.9256","0.0003","11.9918","0.0003","12.9082","0.0004","90.335","0.0017","100.557","0.0017","103.488","0.0017","1466.85","0.07","100","","100","","","","","","","","","3","P -1","-P 1","2","","","","- C42 H22 F6 -","- C42 H22 F6 -","- C84 H44 F12 -","2","1","","Rao, M. Rajeswara; Black, Hayden T.; Perepichka, Dmitrii F.","Synthesis and Divergent Electronic Properties of Two Ring-Fused Derivatives of 9,10-Diphenylanthracene.","Organic letters","2015","17","17","4224","4227","10.1021/acs.orglett.5b02009","","x-ray","1.54178","CuKα","","0.0429","0.0387","","","0.1033","0.1075","","","","","","1.041","","","","has coordinates","238388","2020-10-21","18:00:00",""
"1555208","9.5341","0.0002","17.1742","0.0004","34.8068","0.0007","90","","90","","90","","5699.3","0.2","100","","100","","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C42 H22 F6 -","- C42 H22 F6 -","- C336 H176 F48 -","8","1","","Rao, M. Rajeswara; Black, Hayden T.; Perepichka, Dmitrii F.","Synthesis and Divergent Electronic Properties of Two Ring-Fused Derivatives of 9,10-Diphenylanthracene.","Organic letters","2015","17","17","4224","4227","10.1021/acs.orglett.5b02009","","x-ray","1.54178","CuKα","","0.0436","0.0363","","","0.0954","0.1011","","","","","","1.039","","","","has coordinates","238389","2020-10-21","18:00:00",""
"1555211","18.5406","0.0005","18.5406","0.0005","21.1268","0.001","90","","90","","90","","7262.4","0.4","115","3","115","3","","","","","","","","6","P 43","P 4cw","78","","","","- C65 H65 Cl3 N4 O6 Zn -","- C65 H65 Cl3 N4 O6 Zn -","- C260 H260 Cl12 N16 O24 Zn4 -","4","1","","Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin","Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.","Organic letters","2015","17","16","4078","4081","10.1021/acs.orglett.5b02010","","","1.54184","CuKα","","0.1261","0.0929","","","0.2435","0.273","","","","","","0.928","","","","has coordinates","238391","2020-10-21","18:00:00",""
"1555213","39.3331","0.0014","14.7758","0.0005","28.6914","0.0009","90","","131.696","0.002","90","","12450.8","0.8","112.8","0.3","112.8","0.3","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C70 H77 Cl1.5 N4 O5 Zn -","- C70 H77 Cl1.5 N4 O5 Zn -","- C560 H616 Cl12 N32 O40 Zn8 -","8","1","","Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin","Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.","Organic letters","2015","17","16","4078","4081","10.1021/acs.orglett.5b02010","","","1.54184","CuKα","","0.0911","0.0644","","","0.1645","0.1817","","","","","","1.06","","","","has coordinates","238393","2020-10-21","18:00:00",""
"1555214","16.9996","0.0005","24.3355","0.0006","32.7331","0.0008","89.3681","0.0019","83.194","0.002","89.522","0.002","13444.9","0.6","115","4","115","4","","","","","","","","5","P -1","-P 1","2","","","","- C67 H71 N4 O5 Zn -","- C67 H72 N4 O5 Zn -","- C536 H576 N32 O40 Zn8 -","8","4","","Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin","Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.","Organic letters","2015","17","16","4078","4081","10.1021/acs.orglett.5b02010","","","1.54184","CuKα","","0.1144","0.0831","","","0.2249","0.2456","","","","","","1","","","","has coordinates,has disorder","279649","2022-11-30","18:17:27",""
"1555216","14.857","0.004","12.127","0.003","13.289","0.004","90","","106.898","0.003","90","","2290.9","1.1","173","2","173","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C14 H11 N3 -","- C14 H11 N3 -","- C112 H88 N24 -","8","1","","Jia, Feng-Cheng; Zhou, Zhi-Wen; Xu, Cheng; Cai, Qun; Li, Deng-Kui; Wu, An-Xin","Expeditious Synthesis of 2-Phenylquinazolin-4-amines via a Fe/Cu Relay-Catalyzed Domino Strategy.","Organic letters","2015","17","17","4236","4239","10.1021/acs.orglett.5b02020","","","0.71073","MoKα","","0.0443","0.0421","","","0.1175","0.1202","","","","","","1.047","","","","has coordinates","238396","2020-10-21","18:00:00",""
"1555218","9.07268","0.00016","11.9732","0.0002","13.4535","0.0003","90","","106.945","0.0007","90","","1397.99","0.05","165","","165","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C33 H23 Cl3 N2 O2 -","- C33 H23 Cl3 N2 O2 -","- C66 H46 Cl6 N4 O4 -","2","1","","Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro","Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.","Organic letters","2015","17","16","4098","4101","10.1021/acs.orglett.5b02041","","","1.54187","CuKα","","0.0303","0.0271","","","0.0631","0.0669","","","","","","1.066","","","","has coordinates","238398","2020-10-21","18:00:00",""
"1555219","11.4574","0.0002","24.0028","0.0004","9.1294","0.0001","90","","90","","90","","2510.67","0.07","165","","165","","","","","","","","","4","P 21 21 2","P 2 2ab","18","","","","- C32.5 H26 N2 O3.5 -","- C32.5 H26 N2 O3.5 -","- C130 H104 N8 O14 -","4","1","","Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro","Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.","Organic letters","2015","17","16","4098","4101","10.1021/acs.orglett.5b02041","","","1.54187","CuKα","","0.1111","0.0853","","","0.2206","0.2499","","","","","","1.136","","","","has coordinates","238399","2020-10-21","18:00:00",""
"1555220","11.1679","0.0002","24.1852","0.0005","9.1499","0.0002","90","","90","","90","","2471.37","0.09","90","","90","","","","","","","","","3","P 21 21 2","P 2 2ab","18","","","","- C34 H24 O2 -","- C34 H24 O2 -","- C136 H96 O8 -","4","1","","Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro","Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.","Organic letters","2015","17","16","4098","4101","10.1021/acs.orglett.5b02041","","","0.71073","MoKα","","0.0599","0.0461","","","0.0968","0.1038","","","","","","1.075","","","","has coordinates","238400","2020-10-21","18:00:00",""
"1555221","10.41941","0.00001","18.297","0.0002","36.8632","0.0005","90","","90","","90","","7027.75","0.12","90","","90","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C32 H22.67 N2 O2.33 -","- C32 H22.6193 N2 O2.33333 -","- C384 H271.432 N24 O28 -","12","3","","Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro","Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.","Organic letters","2015","17","16","4098","4101","10.1021/acs.orglett.5b02041","","","0.71073","MoKα","","0.0594","0.0406","","","0.0937","0.1041","","","","","","1.044","","","","has coordinates,has disorder","238401","2020-10-21","18:00:00",""
"1555222","7.9491","0.0005","16.7592","0.001","18.1848","0.001","90","","90","","90","","2422.6","0.2","123","","123","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C32 H22 N2 O2 -","- C32 H22 N2 O2 -","- C128 H88 N8 O8 -","4","1","","Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro","Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.","Organic letters","2015","17","16","4098","4101","10.1021/acs.orglett.5b02041","","","0.71073","MoKα","","0.0357","0.0347","","","0.076","0.0766","","","","","","1.095","","","","has coordinates","238402","2020-10-21","18:00:00",""
"1555223","16.057","0.004","18.336","0.005","18.879","0.005","79.909","0.013","74.398","0.012","79.264","0.013","5214","2","152","2","152","2","","","","","","","","7","P -1","-P 1","2","","","","- C245 H138 Cl10 F24 N8 O32 S8 -","- C245 H138 Cl10 F24 N8 O32 S8 -","- C245 H138 Cl10 F24 N8 O32 S8 -","1","0.5","","Węcławski, Marek K; Meiling, Till T.; Leniak, Arkadiusz; Cywiński, Piotr J; Gryko, Daniel T.","Planar, Fluorescent Push-Pull System That Comprises Benzofuran and Iminocoumarin Moieties.","Organic letters","2015","17","17","4252","4255","10.1021/acs.orglett.5b02042","","","1.54178","CuKα","","0.1395","0.0675","","","0.1941","0.2609","","","","","","1.112","","","","has coordinates,has disorder","238403","2020-10-21","18:00:00",""
"1555224","19.0503","0.0004","11.68507","0.00017","14.8134","0.0003","90","","92.939","0.0019","90","","3293.19","0.11","102.3","","102.3","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C41 H36 N2 O9 -","- C41 H36 N2 O9 -","- C164 H144 N8 O36 -","4","1","","Sai, Chun-Mei; Li, Da-Hong; Xue, Chun-Mei; Wang, Kai-Bo; Hu, Ping; Pei, Yue-Hu; Bai, Jiao; Jing, Yong-Kui; Li, Zhan-Lin; Hua, Hui-Ming","Two Pairs of Enantiomeric Alkaloid Dimers from Macleaya cordata.","Organic letters","2015","17","16","4102","4105","10.1021/acs.orglett.5b02044","","","1.5418","CuKα","","0.0476","0.0404","","","0.0982","0.1033","","","","","","1.024","","","","has coordinates","238404","2020-10-21","18:00:00",""
"1555225","13.9815","0.0008","16.6793","0.0006","26.5582","0.0009","90","","90","","90","","6193.4","0.5","217.9","","217.9","","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C40 H32 N2 O9 -","- C40 H32 N2 O9 -","- C320 H256 N16 O72 -","8","1","","Sai, Chun-Mei; Li, Da-Hong; Xue, Chun-Mei; Wang, Kai-Bo; Hu, Ping; Pei, Yue-Hu; Bai, Jiao; Jing, Yong-Kui; Li, Zhan-Lin; Hua, Hui-Ming","Two Pairs of Enantiomeric Alkaloid Dimers from Macleaya cordata.","Organic letters","2015","17","16","4102","4105","10.1021/acs.orglett.5b02044","","","0.7107","MoKα","","0.0667","0.0481","","","0.095","0.1037","","","","","","1.032","","","","has coordinates","238405","2020-10-21","18:00:00",""
"1555226","8.9629","0.0004","14.1297","0.0008","18.6198","0.0009","90","","90","","90","","2358.1","0.2","295.42","0.1","295.42","0.1","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C28 H24 N2 O3 S -","- C28 H24 N2 O3 S -","- C112 H96 N8 O12 S4 -","4","1","","Wang, Linqing; Yang, Dongxu; Li, Dan; Liu, Xihong; Zhao, Qian; Zhu, Ranran; Zhang, Bangzhi; Wang, Rui","Catalytic Asymmetric [3 + 2] Cyclization Reactions of 3-Isothiocyanato Oxindoles and Alkynyl Ketones Via an in Situ Generated Magnesium Catalyst.","Organic letters","2015","17","17","4260","4263","10.1021/acs.orglett.5b02052","","x-ray","0.71073","MoKα","","0.0578","0.0459","","","0.0877","0.0957","","","","","","1.068","","","","has coordinates","238406","2020-10-21","18:00:00",""
"1555227","13.4658","0.0003","20.2837","0.0007","19.439","0.0005","90","","100.921","0.002","90","","5213.3","0.3","293.18","0.1","293.18","0.1","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C24 H25 F3 I N O4 S -","- C24 H25 F3 I N O4 S -","- C192 H200 F24 I8 N8 O32 S8 -","8","2","","Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min","Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.","Organic letters","2015","17","17","4280","4283","10.1021/acs.orglett.5b02068","","x-ray","0.71073","MoKα","","0.1263","0.06","","","0.1152","0.1529","","","","","","1.044","","","","has coordinates","238407","2020-10-21","18:00:00",""
"1555229","12.121","0.0006","15.7186","0.0008","25.7853","0.0011","90","","91.321","0.004","90","","4911.4","0.4","290.92","0.1","290.92","0.1","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C24 H26 F2 I N O4 S -","- C24 H26 F2 I N O4 S -","- C192 H208 F16 I8 N8 O32 S8 -","8","2","","Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min","Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.","Organic letters","2015","17","17","4280","4283","10.1021/acs.orglett.5b02068","","","0.71073","MoKα","","0.0636","0.0438","","","0.0863","0.0994","","","","","","1.078","","","","has coordinates","238409","2020-10-21","18:00:00",""
"1555230","24.1416","0.0007","10.1959","0.0003","20.5376","0.0006","90","","90","","90","","5055.2","0.3","293.78","0.1","293.78","0.1","","","","","","","","7","P n a 21","P 2c -2n","33","","","","- C23 H25 F2 I N2 O4 S -","- C23 H25 F2 I N2 O4 S -","- C184 H200 F16 I8 N16 O32 S8 -","8","2","","Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min","Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.","Organic letters","2015","17","17","4280","4283","10.1021/acs.orglett.5b02068","","x-ray","0.71","MoKα","","0.0663","0.0424","","","0.0717","0.0853","","","","","","1.047","","","","has coordinates","238410","2020-10-21","18:00:00",""
"1555231","6.5502","0.0013","13.639","0.003","9.1291","0.0018","90","","91.21","0.03","90","","815.4","0.3","150","2","150","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C16 H26 O6 -","- C16 H26 O6 -","- C32 H52 O12 -","2","1","","Hwang, In Hyun; Swenson, Dale C.; Gloer, James B.; Wicklow, Donald T.","Pestaloporonins: Caryophyllene-Derived Sesquiterpenoids from a Fungicolous Isolate of Pestalotiopsis sp.","Organic letters","2015","17","17","4284","4287","10.1021/acs.orglett.5b02080","","","1.2399","synchrotron","","0.0529","0.0499","","","0.1342","0.1375","","","","","","1.051","","","","has coordinates","238411","2020-10-21","18:00:00",""
"1555233","6.395","0.0007","46.881","0.006","8.2621","0.001","90","","111.164","0.005","90","","2309.9","0.5","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C22 H36 O6 Si -","- C22 H36 O6 Si -","- C88 H144 O24 Si4 -","4","2","","Clark, J. Stephen; Romiti, Filippo; Sieng, Bora; Paterson, Laura C.; Stewart, Alister; Chaudhury, Subhabrata; Thomas, Lynne H.","Synthesis of the A-D Ring System of the Gambieric Acids.","Organic letters","2015","17","19","4694","4697","10.1021/acs.orglett.5b02093","","","0.71073","MoKα","","0.0857","0.0779","","","0.2029","0.2101","","","","","","1.094","","","","has coordinates","238413","2020-10-21","18:00:00",""
"1555236","5.8616","0.0002","11.0435","0.0004","18.6965","0.0008","90","","90","","90","","1210.27","0.08","100","","100","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C14 H17 F O2 -","- C14 H17 F O2 -","- C56 H68 F4 O8 -","4","1","","Navuluri, Chandrasekhar; Charette, André B","Diastereoselective Fluorocyclopropanation of Chiral Allylic Alcohols Using an α-Fluoroiodomethylzinc Carbenoid.","Organic letters","2015","17","17","4288","4291","10.1021/acs.orglett.5b02097","","x-ray","1.34139","GaKα","","0.0251","0.0241","","","0.0579","0.0586","","","","","","1.048","","","","has coordinates","238415","2020-10-21","18:00:00",""
"1555237","7.9045","0.0005","11.1779","0.0007","11.7527","0.0007","91.21","0.003","92.807","0.003","94","0.004","1034.33","0.11","100","","100","","","","","","","","","5","P -1","-P 1","2","","","","- C23 H23 F N2 O6 -","- C23 H23 F N2 O6 -","- C46 H46 F2 N4 O12 -","2","1","","Navuluri, Chandrasekhar; Charette, André B","Diastereoselective Fluorocyclopropanation of Chiral Allylic Alcohols Using an α-Fluoroiodomethylzinc Carbenoid.","Organic letters","2015","17","17","4288","4291","10.1021/acs.orglett.5b02097","","x-ray","1.54178","CuKα","","0.0384","0.0358","","","0.0955","0.0978","","","","","","1.022","","","","has coordinates","238416","2020-10-21","18:00:00",""
"1555241","9.5716","0.0005","40.233","0.002","14.5609","0.0008","90","","90","","90","","5607.3","0.5","100","2","100","2","","","","","","","","3","C 2 2 21","C 2c 2","20","","","","- C76 H48 O4 -","- C76 H48 O4 -","- C304 H192 O16 -","4","0.5","","Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.","Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.","Organic letters","2015","17","17","4296","4299","10.1021/acs.orglett.5b02102","","","0.71073","MoKα","","0.0375","0.0319","","","0.0901","0.0998","","","","","","1.105","","","","has coordinates","238418","2020-10-21","18:00:00",""
"1555242","9.6233","0.0002","28.1324","0.0004","14.4388","0.0002","90","","90","","90","","3908.97","0.11","100","2","100","2","","","","","","","","3","C 2 2 21","C 2c 2","20","","","","- C26 H18 O2 -","- C26 H18 O2 -","- C208 H144 O16 -","8","1","","Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.","Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.","Organic letters","2015","17","17","4296","4299","10.1021/acs.orglett.5b02102","","","1.54178","CuKα","","0.0318","0.0297","","","0.0749","0.0764","","","","","","1.026","","","","has coordinates","238419","2020-10-21","18:00:00",""
"1555243","9.5385","0.0015","16.362","0.003","14.106","0.002","90","","90","","90","","2201.5","0.6","293","2","293","2","","","","","","","","4","C 2 2 21","C 2c 2","20","","","","- C26 H18 Br2 O2 -","- C26 H18 Br2 O2 -","- C104 H72 Br8 O8 -","4","0.5","","Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.","Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.","Organic letters","2015","17","17","4296","4299","10.1021/acs.orglett.5b02102","","","0.71073","MoKα","","0.0562","0.0455","","","0.1026","0.1057","","","","","","0.928","","","","has coordinates","238420","2020-10-21","18:00:00",""
"1555244","13.3557","0.0007","13.3557","0.0007","44.138","0.003","90","","90","","90","","7873.1","0.8","293","2","293","2","","","","","","","","4","P 43 21 2","P 4nw 2abw","96","","","","- C76 H78 O16 S4 -","- C76 H78 O16 S4 -","- C304 H312 O64 S16 -","4","0.5","","Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.","Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.","Organic letters","2015","17","17","4296","4299","10.1021/acs.orglett.5b02102","","","0.71073","MoKα","","0.0848","0.0679","","","0.1641","0.1731","","","","","","1.08","","","","has coordinates","238421","2020-10-21","18:00:00",""
"1555249","12.8306","0.0006","13.8096","0.0006","19.054","0.0009","90","","90","","90","","3376.1","0.3","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C40 H34 Br N3 O3 -","- C40 H34 Br N3 O3 -","- C160 H136 Br4 N12 O12 -","4","1","","Jing, Changcheng; Xing, Dong; Hu, Wenhao","Catalytic Asymmetric Four-Component Reaction for the Rapid Construction of 3,3-Disubstituted 3-Indol-3'-yloxindoles.","Organic letters","2015","17","17","4336","4339","10.1021/acs.orglett.5b02160","","","0.71073","MoKα","","0.1007","0.0454","","","0.0916","0.1161","","","","","","1.012","","","","has coordinates","238423","2020-10-21","18:00:00",""
"1555251","5.3543","0.0011","15.615","0.003","17.226","0.003","90","","93.57","0.03","90","","1437.4","0.5","173","2","173","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C18 H16 O S -","- C18 H16 O S -","- C72 H64 O4 S4 -","4","1","","Zhao, Peng; Liu, Yu; Xi, Chanjuan","MeOTf-Induced Carboannulation of Isothiocyanates and Aryl Alkynes with C═S Bond Cleavage: Access to Indenones.","Organic letters","2015","17","17","4388","4391","10.1021/acs.orglett.5b02201","","","0.71073","MoKα","","0.0457","0.0442","","","0.1271","0.1287","","","","","","1.052","","","","has coordinates","238425","2020-10-21","18:00:00",""
"1555254","9.1038","0.0018","11.532","0.002","16.523","0.003","90","","101.54","0.03","90","","1699.6","0.6","173","2","173","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H16 O S -","- C24 H16 O S -","- C96 H64 O4 S4 -","4","1","","Zhao, Peng; Liu, Yu; Xi, Chanjuan","MeOTf-Induced Carboannulation of Isothiocyanates and Aryl Alkynes with C═S Bond Cleavage: Access to Indenones.","Organic letters","2015","17","17","4388","4391","10.1021/acs.orglett.5b02201","","","0.71073","MoKα","","0.0571","0.0518","","","0.1064","0.1137","","","","","","1.038","","","","has coordinates","238427","2020-10-21","18:00:00",""
"1555256","15.86","0.003","8.9849","0.0015","32.138","0.004","90","","117.571","0.007","90","","4059.6","1.2","100","2","100.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H30 O4 Si -","- C21 H30 O4 Si -","- C168 H240 O32 Si8 -","8","2","","Khatri, Buddha B.; Sieburth, Scott McN","Enyne-2-pyrone [4 + 4]-Photocycloaddition: Sesquiterpene Synthesis and a Low-Temperature Cope Rearrangement.","Organic letters","2015","17","17","4360","4363","10.1021/acs.orglett.5b02207","","","0.71073","MoKα","","0.0889","0.0651","","","0.1741","0.1884","","","","","","1.072","","","","has coordinates,has disorder","238429","2020-10-21","18:00:00",""
"1555257","34.403","0.003","6.7764","0.0006","16.1333","0.0016","90","","92.333","0.002","90","","3758","0.6","130","2","130","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C20 H28 O3 Si -","- C20 H28 O3 Si -","- C160 H224 O24 Si8 -","8","1","","Khatri, Buddha B.; Sieburth, Scott McN","Enyne-2-pyrone [4 + 4]-Photocycloaddition: Sesquiterpene Synthesis and a Low-Temperature Cope Rearrangement.","Organic letters","2015","17","17","4360","4363","10.1021/acs.orglett.5b02207","","","0.71073","MoKα","","0.0376","0.0326","","","0.0862","0.091","","","","","","1.044","","","","has coordinates","238430","2020-10-21","18:00:00",""
"1555258","6.9189","0.0001","13.8264","0.0003","21.5767","0.0005","90","","90","","90","","2064.1","0.07","100","0.2","100","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C9 H5 Cl2 N3 S -","- C9 H5 Cl2 N3 S -","- C72 H40 Cl16 N24 S8 -","8","1","","Kalogirou, Andreas S.; Manoli, Maria; Koutentis, Panayiotis A.","Synthesis of N-Aryl-3,5-dichloro-4H-1,2,6-thiadiazin-4-imines from 3,4,4,5-Tetrachloro-4H-1,2,6-thiadiazine.","Organic letters","2015","17","16","4118","4121","10.1021/acs.orglett.5b02237","","","1.54184","CuKα","","0.0317","0.0315","","","0.0835","0.0838","","","","","","1.111","","","","has coordinates","238431","2020-10-21","18:00:00",""
"1555276","13.414","0.011","13.414","0.011","13.869","0.011","90","","90","","120","","2161","3","100","2","100","2","","","","","","","synthesis","4","P 32","P 32","145","Boc-gV(NM)-gV(NM)-OEt","Boc-gV(NM)-gV(NM)-OEt","","- C23 H42 N4 O9 -","- C23 H42 N4 O9 -","- C69 H126 N12 O27 -","3","1","","Ganesh Kumar, Mothukuri; Gopi, Hosahudya N.","γ- and β-Peptide Foldamers from Common Multifaceted Building Blocks: Synthesis and Structural Characterization.","Organic letters","2015","17","19","4738","4741","10.1021/acs.orglett.5b02263","","x-ray","0.71073","MoKα","","0.1322","0.0726","","","0.161","0.1902","","","","","","1.013","","","","has coordinates","238433","2020-10-21","18:00:00",""
"1555277","15.4725","0.0013","16.0538","0.0014","16.749","0.003","107.8","0.002","106.461","0.002","106.157","0.002","3482.3","0.8","100","2","100","2","","","","","","","synthesis","4","P 1","P 1","1","Boc-gVNM-gVNM-gVNM-OEt","Boc-gVNM-gVNM-gVNM-OEt","","- C32.33333 H57.66667 N6 O12.66667 -","- C32.3333 H57.6667 N6 O12.6667 -","- C97 H173 N18 O38 -","3","3","","Ganesh Kumar, Mothukuri; Gopi, Hosahudya N.","γ- and β-Peptide Foldamers from Common Multifaceted Building Blocks: Synthesis and Structural Characterization.","Organic letters","2015","17","19","4738","4741","10.1021/acs.orglett.5b02263","","x-ray","0.71073","MoKα","","0.1225","0.0678","","","0.1875","0.2276","","","","","","0.699","","","","has coordinates","274567","2022-04-19","14:22:36",""
"1555278","9.319","0.004","23.446","0.01","11.396","0.005","90","","108.442","0.007","90","","2362.1","1.8","100","2","100","2","","","","","","","synthesis","4","P 1 21 1","P 2yb","4","Boc-gV(NM)-gV(NM)-gV(NM)-gV(NM)-OEt","Boc-gV(NM)-gV(NM)-gV(NM)-gV(NM)-OEt","","- C39 H70 N8 O15 -","- C39 H70 N8 O15 -","- C78 H140 N16 O30 -","2","1","","Ganesh Kumar, Mothukuri; Gopi, Hosahudya N.","γ- and β-Peptide Foldamers from Common Multifaceted Building Blocks: Synthesis and Structural Characterization.","Organic letters","2015","17","19","4738","4741","10.1021/acs.orglett.5b02263","","x-ray","0.71073","MoKα","","0.0531","0.041","","","0.0938","0.1012","","","","","","1.001","","","","has coordinates","238433","2020-10-21","18:00:00",""
"1555279","11.813","0.003","9.272","0.002","19.747","0.004","90","","104.524","0.005","90","","2093.8","0.8","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","Boc-UgFNMUgFNHMe","Boc-UgFNMUgFNHMe","","- C37 H54 N6 O8 -","- C37 H54 N6 O8 -","- C74 H108 N12 O16 -","2","1","","Ganesh Kumar, Mothukuri; Gopi, Hosahudya N.","γ- and β-Peptide Foldamers from Common Multifaceted Building Blocks: Synthesis and Structural Characterization.","Organic letters","2015","17","19","4738","4741","10.1021/acs.orglett.5b02263","","","0.71073","MoKα","","0.0877","0.0559","","","0.1314","0.1528","","","","","","0.758","","","","has coordinates","238433","2020-10-21","18:00:00",""
"1555280","27.637","0.018","27.637","0.018","11.845","0.008","90","","90","","120","","7835","9","100","2","100","2","","","","","","","","4","P 61","P 61","169","Boc-(UgFNM)2-NHMe","Boc-(UgFNM)2-NHMe","","- C44 H71 N7 O12 -","- C44 H71 N7 O12 -","- C264 H426 N42 O72 -","6","1","","Ganesh Kumar, Mothukuri; Gopi, Hosahudya N.","γ- and β-Peptide Foldamers from Common Multifaceted Building Blocks: Synthesis and Structural Characterization.","Organic letters","2015","17","19","4738","4741","10.1021/acs.orglett.5b02263","","","0.71073","MoKα","","0.2669","0.1189","","","0.2095","0.2638","","","","","","0.928","","","","has coordinates","238433","2020-10-21","18:00:00",""
"1555281","11.226","0.002","12.666","0.002","33.431","0.006","90","","90","","90","","4753.5","1.4","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","Boc-bV(CH2COOEt)-bL(CH2COOEt)-bV(CH2COOEt)-OBn","Boc-bV(CH2COOEt)-bL(CH2COOEt)-bV(CH2COOEt)-OBn","","- C43 H69 N3 O12 -","- C43 H69 N3 O12 -","- C172 H276 N12 O48 -","4","1","","Ganesh Kumar, Mothukuri; Gopi, Hosahudya N.","γ- and β-Peptide Foldamers from Common Multifaceted Building Blocks: Synthesis and Structural Characterization.","Organic letters","2015","17","19","4738","4741","10.1021/acs.orglett.5b02263","","","0.71073","MoKα","","0.1533","0.0709","","","0.1583","0.2027","","","","","","0.997","","","","has coordinates,has disorder","238433","2020-10-21","18:00:00",""
"1555283","9.874","0.001","10.305","0.002","18.765","0.003","90","","99.09","0.01","90","","1885.4","0.5","293","2","293","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C18 H28 O7 -","- C18 H28 O7 -","- C72 H112 O28 -","4","2","","Chaudhary, Sandeep; Sharma, Vashundhra; Jaiswal, Pradeep K.; Gaikwad, Anil N.; Sinha, Sudhir K.; Puri, Sunil K.; Sharon, Ashoke; Maulik, Prakas R.; Chaturvedi, Vinita","Stable Tricyclic Antitubercular Ozonides Derived from Artemisinin.","Organic letters","2015","17","20","4948","4951","10.1021/acs.orglett.5b02296","","","0.71073","MoKα","","0.1535","0.0731","","","0.1768","0.2449","","","","","","1.047","","","","has coordinates","238435","2020-10-21","18:00:00",""
"1555284","27.579","0.006","8.3362","0.0017","17.969","0.004","90","","122.94","0.03","90","","3467","1.7","113","2","113","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C19 H29 N O -","- C19 H29 N O -","- C152 H232 N8 O8 -","8","1","","Cheng, Yong-Feng; Rong, Hao-Jie; Yi, Cheng-Bo; Yao, Jun-Jun; Qu, Jin","Redox-Triggered α-C-H Functionalization of Pyrrolidines: Synthesis of Unsymmetrically 2,5-Disubstituted Pyrrolidines.","Organic letters","2015","17","19","4758","4761","10.1021/acs.orglett.5b02298","","","0.71073","MoKα","","0.0982","0.0835","","","0.2453","0.26","","","","","","1.131","","","","has coordinates,has disorder","238436","2020-10-21","18:00:00",""
"1555291","9.87691","0.00018","17.4624","0.0003","14.111","0.0003","90","","101.632","0.007","90","","2383.81","0.1","93","","93","","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C28 H22 Cl N2 O2 P S -","- C28 H22 Cl N2 O2 P S -","- C112 H88 Cl4 N8 O8 P4 S4 -","4","1","","Takada, Hisashi; Kumagai, Naoya; Shibasaki, Masakatsu","Stereoselective Total Synthesis of KAE609 via Direct Catalytic Asymmetric Alkynylation to Ketimine.","Organic letters","2015","17","19","4762","4765","10.1021/acs.orglett.5b02300","","","1.54187","CuKα","","0.0572","0.0474","","","0.1232","0.1292","","","","","","1.146","","","","has coordinates","238438","2020-10-21","18:00:00",""
"1555293","4.4189","0.00005","10.48312","0.00013","16.03096","0.00017","90","","95.3299","0.001","90","","739.405","0.015","100","2","100","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C9 H7 N O2 -","- C9 H7 N O2 -","- C36 H28 N4 O8 -","4","1","","Liu, Wei; Li, Hou-Jin; Xu, Meng-Yang; Ju, Ying-Chen; Wang, Lai-You; Xu, Jun; Yang, De-Po; Lan, Wen-Jian","Pseudellones A-C, Three Alkaloids from the Marine-Derived Fungus Pseudallescheria ellipsoidea F42-3.","Organic letters","2015","17","21","5156","5159","10.1021/acs.orglett.5b02311","","x-ray","1.54184","CuKα","","0.0366","0.0341","","","0.088","0.0909","","","","","","1.027","","","","has coordinates","238440","2020-10-21","18:00:00",""
"1555294","8.9685","0.0001","11.8374","0.0001","12.3725","0.0001","90","","90","","90","","1313.51","0.02","293","2","293","2","","","","","","","","5","P n a 21","P 2c -2n","33","","","","- C14 H13 N3 O3 S -","- C14 H13 N3 O3 S -","- C56 H52 N12 O12 S4 -","4","1","","Liu, Wei; Li, Hou-Jin; Xu, Meng-Yang; Ju, Ying-Chen; Wang, Lai-You; Xu, Jun; Yang, De-Po; Lan, Wen-Jian","Pseudellones A-C, Three Alkaloids from the Marine-Derived Fungus Pseudallescheria ellipsoidea F42-3.","Organic letters","2015","17","21","5156","5159","10.1021/acs.orglett.5b02311","","","0.71073","MoKα","","0.0327","0.0323","","","0.0846","0.0849","","","","","","1.086","","","","has coordinates","238441","2020-10-21","18:00:00",""
"1555296","10.449","0.002","10.564","0.002","10.913","0.002","65.028","0.008","72.368","0.011","76.052","0.011","1031.7","0.3","173.15","","173.15","","","","","","","","","5","P -1","-P 1","2","","","","- C21 H22 N2 O6 S -","- C21 H22 N2 O6 S -","- C42 H44 N4 O12 S2 -","2","1","","Xu, Changming; Zhang, Long; Luo, Sanzhong","Catalytic Asymmetric Oxidative α-C-H N,O-Ketalization of Ketones by Chiral Primary Amine.","Organic letters","2015","17","17","4392","4395","10.1021/acs.orglett.5b02322","","","0.71073","MoKα","","0.047","0.0428","","","0.0939","0.0959","","","","","","1.109","","","","has coordinates","238443","2020-10-21","18:00:00",""
"1555300","8.5759","0.0005","13.69","0.0008","15.1168","0.0009","94.615","0.001","91.322","0.002","103.134","0.002","1721.18","0.18","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C35 H44 N6 O9 S -","- C35 H44 N6 O9 S -","- C70 H88 N12 O18 S2 -","2","1","","Dabrowa, Kajetan; Niedbala, Patryk; Majdecki, Maciej; Duszewski, Piotr; Jurczak, Janusz","A General Method for Synthesis of Unclosed Cryptands via H-Bond Templated Macrocyclization and Subsequent Mild Postfunctionalization.","Organic letters","2015","17","19","4774","4777","10.1021/acs.orglett.5b02324","","","0.71073","MoKα","","0.0479","0.0359","","","0.087","0.0942","","","","","","1.021","","","","has coordinates,has disorder","238446","2020-10-21","18:00:00",""
"1555301","13.5559","0.0002","16.9708","0.0003","16.5586","0.0003","90","","103.987","0.002","90","","3696.43","0.11","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C34 H43 N7 O11 S -","- C34 H43 N7 O11 S -","- C136 H172 N28 O44 S4 -","4","1","","Dabrowa, Kajetan; Niedbala, Patryk; Majdecki, Maciej; Duszewski, Piotr; Jurczak, Janusz","A General Method for Synthesis of Unclosed Cryptands via H-Bond Templated Macrocyclization and Subsequent Mild Postfunctionalization.","Organic letters","2015","17","19","4774","4777","10.1021/acs.orglett.5b02324","","","1.54184","CuKα","","0.0675","0.0483","","","0.1149","0.1275","","","","","","1.027","","","","has coordinates","238446","2020-10-21","18:00:00",""
"1555303","17.897","0.003","4.7536","0.0007","21.443","0.004","90","","105.729","0.004","90","","1756","0.5","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C10 H9 N3 O -","- C10 H9 N3 O -","- C80 H72 N24 O8 -","8","2","","Nguyen, Thanh Binh; Corbin, Mathilde; Retailleau, Pascal; Ermolenko, Ludmila; Al-Mourabit, Ali","Elements as Direct Feedstocks for Organic Synthesis: Fe/I2/O2 for Diamination of 2-Cyclohexenones with 2-Aminopyrimidine and 2-Aminopyridines.","Organic letters","2015","17","20","4956","4959","10.1021/acs.orglett.5b02340","","","0.71075","MoKα","","0.0731","0.0449","","","0.1048","0.122","","","","","","1.015","","","","has coordinates,has disorder","238448","2020-10-21","18:00:00",""
"1555304","10.972","0.0003","11.356","0.0003","12.6933","0.0003","105.75","0.001","96.509","0.001","100.348","0.001","1475.31","0.07","93","2","93","2","","","","","","","","5","P -1","-P 1","2","","","","- C36 H26 N2 O4 S2 -","- C36 H26 N2 O4 S2 -","- C72 H52 N4 O8 S4 -","2","1","","Sumi, Takaki; Kaburagi, Tomohiro; Morimoto, Masakazu; Une, Kanako; Sotome, Hikaru; Ito, Syoji; Miyasaka, Hiroshi; Irie, Masahiro","Fluorescent Photochromic Diarylethene That Turns on with Visible Light.","Organic letters","2015","17","19","4802","4805","10.1021/acs.orglett.5b02361","","","1.54178","CuKα","","0.0408","0.0392","","","0.1073","0.109","","","","","","1.035","","","","has coordinates","238450","2020-10-21","18:00:00",""
"1555305","7.8828","0.0002","13.6596","0.0003","14.9014","0.0003","112.825","0.001","96.4272","0.0011","96.2488","0.0013","1449.13","0.06","93","2","93","2","","","","","","","","5","P -1","-P 1","2","","","","- C36 H26 N2 O4 S2 -","- C36 H26 N2 O4 S2 -","- C72 H52 N4 O8 S4 -","2","1","","Sumi, Takaki; Kaburagi, Tomohiro; Morimoto, Masakazu; Une, Kanako; Sotome, Hikaru; Ito, Syoji; Miyasaka, Hiroshi; Irie, Masahiro","Fluorescent Photochromic Diarylethene That Turns on with Visible Light.","Organic letters","2015","17","19","4802","4805","10.1021/acs.orglett.5b02361","","","1.54178","CuKα","","0.0457","0.0421","","","0.1177","0.1215","","","","","","1.037","","","","has coordinates","238451","2020-10-21","18:00:00",""
"1555306","11.3073","0.0003","12.3863","0.0002","11.762","0.0002","90","","103.475","0.002","90","","1601.99","0.06","293","","293","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C18 H18 N2 O4 -","- C18 H18 N2 O4 -","- C72 H72 N8 O16 -","4","1","","Deng, Guisheng; Wang, Feng; Lu, Shengle; Cheng, Bo","Synthesis of Pyrano[3,2-c]pyrazol-7(1H)-one Derivatives by Tandem Cyclization of 2-Diazo-3,5-dioxo-6-ynoates (Ynones).","Organic letters","2015","17","19","4651","4653","10.1021/acs.orglett.5b02369","","","1.54184","CuKα","","0.0524","0.0487","","","0.1377","0.1433","","","","","","1.051","","","","has coordinates","238453","2020-10-21","18:00:00",""
"1555307","13.19","0.0011","10.5762","0.0009","12.1985","0.001","90","","109.1","0.001","90","","1608","0.2","296","2","296","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C16 H22 O5 -","- C16 H22 O5 -","- C64 H88 O20 -","4","1","","Gao, Bao; Xie, Yinjun; Shen, Zhiqiang; Yang, Lei; Huang, Hanmin","Decarboxylative Alkylcarboxylation of α,β-Unsaturated Acids Enabled by Copper-Catalyzed Oxidative Coupling.","Organic letters","2015","17","20","4968","4971","10.1021/acs.orglett.5b02382","","","0.71073","MoKα","","0.0489","0.0411","","","0.1201","0.1299","","","","","","1.007","","","","has coordinates","238455","2020-10-21","18:00:00",""
"1555308","7.1386","0.0001","8.0009","0.0001","23.6032","0.0004","90","","90","","90","","1348.1","0.03","130","","130","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C17 H13 N O3 -","- C17 H13 N O3 -","- C68 H52 N4 O12 -","4","1","","Cheng, Tanyu; Ye, Qunqun; Zhao, Qiankun; Liu, Guohua","Dynamic Kinetic Resolution of Phthalides via Asymmetric Transfer Hydrogenation: A Strategy Constructs 1,3-Distereocentered 3-(2-Hydroxy-2-arylethyl)isobenzofuran-1(3H)-one.","Organic letters","2015","17","20","4972","4975","10.1021/acs.orglett.5b02394","","","1.54178","CuKα","","0.0322","0.032","","","0.082","0.0822","","","","","","1.086","","","","has coordinates","238457","2020-10-21","18:00:00",""
"1555309","6.9324","0.0002","8.0825","0.0003","12.0884","0.0003","92.847","0.002","95.144","0.002","94.822","0.002","671.09","0.04","147","2","147","2","","","","","","","","4","P -1","-P 1","2","","","","- C17 H12 N2 O -","- C17 H12 N2 O -","- C34 H24 N4 O2 -","2","1","","Petrone, David A.; Yen, Andy; Zeidan, Nicolas; Lautens, Mark","Dearomative Indole Bisfunctionalization via a Diastereoselective Palladium-Catalyzed Arylcyanation.","Organic letters","2015","17","19","4838","4841","10.1021/acs.orglett.5b02403","","","1.54178","CuKα","","0.0441","0.0357","","","0.0843","0.0885","","","","","","1.043","","","","has coordinates","238458","2020-10-21","18:00:00",""
"1555310","14.5086","0.0013","13.0756","0.0009","15.3147","0.001","90","","90","","90","","2905.3","0.4","147","2","147","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C19 H14 N2 O -","- C19 H14 N2 O -","- C152 H112 N16 O8 -","8","1","","Petrone, David A.; Yen, Andy; Zeidan, Nicolas; Lautens, Mark","Dearomative Indole Bisfunctionalization via a Diastereoselective Palladium-Catalyzed Arylcyanation.","Organic letters","2015","17","19","4838","4841","10.1021/acs.orglett.5b02403","","","0.71073","MoKα","","0.0539","0.0398","","","0.0926","0.1022","","","","","","1.038","","","","has coordinates","238459","2020-10-21","18:00:00",""
"1555311","9.9575","0.0004","10.3499","0.0004","34.9584","0.0014","90","","95.625","0.002","90","","3585.4","0.2","147","2","147","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H20 N2 O3 -","- C21 H20 N2 O3 -","- C168 H160 N16 O24 -","8","2","","Petrone, David A.; Yen, Andy; Zeidan, Nicolas; Lautens, Mark","Dearomative Indole Bisfunctionalization via a Diastereoselective Palladium-Catalyzed Arylcyanation.","Organic letters","2015","17","19","4838","4841","10.1021/acs.orglett.5b02403","","","1.54178","CuKα","","0.0339","0.033","","","0.0808","0.0814","","","","","","1.061","","","","has coordinates","238460","2020-10-21","18:00:00",""
"1555312","12.4989","0.0005","10.3089","0.0004","15.2366","0.0005","90","","91.7","0.002","90","","1962.37","0.13","147","2","147","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C23 H22 N2 O3 -","- C23 H22 N2 O3 -","- C92 H88 N8 O12 -","4","1","","Petrone, David A.; Yen, Andy; Zeidan, Nicolas; Lautens, Mark","Dearomative Indole Bisfunctionalization via a Diastereoselective Palladium-Catalyzed Arylcyanation.","Organic letters","2015","17","19","4838","4841","10.1021/acs.orglett.5b02403","","","1.54178","CuKα","","0.0343","0.0327","","","0.0825","0.0844","","","","","","1.035","","","","has coordinates","238461","2020-10-21","18:00:00",""
"1555313","10.027","0.002","5.4598","0.0013","16.953","0.004","90","","106.348","0.004","90","","890.6","0.3","100","2","100","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C25 H17 Cl -","- C25 H17 Cl -","- C50 H34 Cl2 -","2","1","","Mendis, Shehani N.; Tunge, Jon A.","Palladium-Catalyzed Stereospecific Decarboxylative Benzylation of Alkynes.","Organic letters","2015","17","21","5164","5167","10.1021/acs.orglett.5b02410","","","1.54178","CuKα","","0.0255","0.0255","","","0.0661","0.0661","","","","","","1.065","","","","has coordinates","238462","2020-10-21","18:00:00",""
"1555314","8.1216","0.0007","11.5944","0.001","21.1982","0.0018","90","","90","","90","","1996.1","0.3","100","","100","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C20 H18 F3 N3 O5 -","- C20 H18 F3 N3 O5 -","- C80 H72 F12 N12 O20 -","4","1","","Henderson, Alexander S.; Medina, Sandra; Bower, John F.; Galan, M. Carmen","Nucleophilic Aromatic Substitution (SNAr) as an Approach to Challenging Carbohydrate-Aryl Ethers.","Organic letters","2015","17","19","4846","4849","10.1021/acs.orglett.5b02413","","","0.71073","MoKα","","0.0555","0.0368","","","0.0712","0.0791","","","","","","1.044","","","","has coordinates","238464","2020-10-21","18:00:00",""
"1555315","12.1722","0.0005","5.9237","0.0002","12.6791","0.0006","90","","115.892","0.0015","90","","822.45","0.06","296","","296","","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C22 H17 P -","- C22 H17 P -","- C44 H34 P2 -","2","1","","Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke","Practical Synthesis and Properties of 2,5-Diarylarsoles.","Organic letters","2015","17","19","4854","4857","10.1021/acs.orglett.5b02416","","","0.71075","MoKα","","","0.0308","","","","0.0618","","","","","","1.036","","","","has coordinates","238466","2020-10-21","18:00:00",""
"1555316","8.5323","0.0003","19.1547","0.0004","12.0545","0.0004","90","","99.9913","0.0011","90","","1940.23","0.1","296","","296","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C22 H17 As Au Cl -","- C22 H17 As Au Cl -","- C88 H68 As4 Au4 Cl4 -","4","1","","Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke","Practical Synthesis and Properties of 2,5-Diarylarsoles.","Organic letters","2015","17","19","4854","4857","10.1021/acs.orglett.5b02416","","","0.71075","MoKα","","","0.0271","","","","0.0534","","","","","","1.045","","","","has coordinates","238467","2020-10-21","18:00:00",""
"1555317","9.915","0.003","17.298","0.005","22.652","0.006","90","","90","","90","","3885","1.9","273","","273","","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C22 H17 Au Cl P -","- C22 H17 Au Cl P -","- C176 H136 Au8 Cl8 P8 -","8","1","","Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke","Practical Synthesis and Properties of 2,5-Diarylarsoles.","Organic letters","2015","17","19","4854","4857","10.1021/acs.orglett.5b02416","","","0.71075","MoKα","","0.0525","0.0413","","","0.0889","0.0949","","","","","","0.934","","","","has coordinates","238469","2020-10-21","18:00:00",""
"1555318","7.88163","0.00018","16.2823","0.0004","15.3253","0.0003","90","","90","","90","","1966.71","0.08","296","","296","","","","","","","","","4","P n m a","-P 2ac 2n","62","","","","- C24 H21 As O2 -","- C24 H21 As O2 -","- C96 H84 As4 O8 -","4","0.5","","Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke","Practical Synthesis and Properties of 2,5-Diarylarsoles.","Organic letters","2015","17","19","4854","4857","10.1021/acs.orglett.5b02416","","","0.71075","MoKα","","","0.0306","","","","0.0934","","","","","","1.009","","","","has coordinates","238470","2020-10-21","18:00:00",""
"1555319","12.2262","0.0004","6.03311","0.00018","12.5465","0.0005","90","","115.216","0.001","90","","837.26","0.05","296","","296","","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C22 H17 As -","- C22 H17 As -","- C44 H34 As2 -","2","1","","Ishidoshiro, Makoto; Matsumura, Yoshimasa; Imoto, Hiroaki; Irie, Yasuyuki; Kato, Takuji; Watase, Seiji; Matsukawa, Kimihiro; Inagi, Shinsuke; Tomita, Ikuyoshi; Naka, Kensuke","Practical Synthesis and Properties of 2,5-Diarylarsoles.","Organic letters","2015","17","19","4854","4857","10.1021/acs.orglett.5b02416","","","0.71075","MoKα","","","0.0246","","","","0.0409","","","","","","1.205","","","","has coordinates","238472","2020-10-21","18:00:00",""
"1555320","20.9818","0.0003","8.85852","0.0001","8.04013","0.0001","90","","90","","90","","1494.4","0.03","123","","123","","","","","","","","","3","P c a 21","P 2c -2ac","29","","","","- C21 H17 N -","- C21 H17 N -","- C84 H68 N4 -","4","1","","Yamada, Shinji; Yamamoto, Natsuo; Takamori, Eri","A Molecular Seesaw Balance: Evaluation of Solvent and Counteranion Effects on Pyridinium-π Interactions.","Organic letters","2015","17","19","4862","4865","10.1021/acs.orglett.5b02420","","","1.54187","CuKα","","0.0358","0.0328","","","0.0837","0.0868","","","","","","1.076","","","","has coordinates","238475","2020-10-21","18:00:00",""
"1555321","8.30165","0.00015","11.9912","0.0002","19.0328","0.0004","81.1115","0.0007","89.9577","0.0007","75.0852","0.0007","1807.32","0.06","123","","123","","","","","","","","","5","P -1","-P 1","2","","","","- C22 H20 B F4 N -","- C22 H20 B F4 N -","- C88 H80 B4 F16 N4 -","4","2","","Yamada, Shinji; Yamamoto, Natsuo; Takamori, Eri","A Molecular Seesaw Balance: Evaluation of Solvent and Counteranion Effects on Pyridinium-π Interactions.","Organic letters","2015","17","19","4862","4865","10.1021/acs.orglett.5b02420","","","1.54187","CuKα","","0.0684","0.0607","","","0.155","0.164","","","","","","1.042","","","","has coordinates","238476","2020-10-21","18:00:00",""
"1555322","8.35321","0.00019","18.1932","0.0003","12.3367","0.0003","90","","109.572","0.0013","90","","1766.51","0.07","123","","123","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H20 I N -","- C22 H20 I N -","- C88 H80 I4 N4 -","4","1","","Yamada, Shinji; Yamamoto, Natsuo; Takamori, Eri","A Molecular Seesaw Balance: Evaluation of Solvent and Counteranion Effects on Pyridinium-π Interactions.","Organic letters","2015","17","19","4862","4865","10.1021/acs.orglett.5b02420","","","1.54187","CuKα","","0.0456","0.0409","","","0.0977","0.1004","","","","","","1.06","","","","has coordinates","238478","2020-10-21","18:00:00",""
"1555323","6.5669","0.0008","20.611","0.002","7.3177","0.0009","90","","92.8","0.003","90","","989.3","0.2","293","2","293","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C20 H16 Cl N3 O6 -","- C20 H16 Cl N3 O6 -","- C40 H32 Cl2 N6 O12 -","2","1","","He, Fu-Sheng; Zhu, Han; Wang, Zheng; Gao, Ming; Yu, Xingxin; Deng, Wei-Ping","Asymmetric Construction of 3,4-Diamino Pyrrolidines via Chiral N,O-Ligand/Cu(I) Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides with β-Phthalimidonitroethene.","Organic letters","2015","17","20","4988","4991","10.1021/acs.orglett.5b02431","","","0.71073","MoKα","","0.0432","0.036","","","0.0867","0.0908","","","","","","1.022","","","","has coordinates","238480","2020-10-21","18:00:00",""
"1555324","11.813","0.009","18.382","0.014","21.241","0.016","90","","92.944","0.011","90","","4606","6","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C51 H53 Cl2 N5 O3 -","- C51 H53 Cl2 N5 O3 -","- C204 H212 Cl8 N20 O12 -","4","1","","Tian, Yaming; Tian, Lumin; He, Xiang; Li, Chunju; Jia, Xueshun; Li, Jian","Indium(III) Chloride-Catalyzed Isocyanide Insertion Reaction to Construct Complex Spirooxindole.","Organic letters","2015","17","19","4874","4877","10.1021/acs.orglett.5b02432","","","0.71073","MoKα","","0.1909","0.0992","","","0.2468","0.3239","","","","","","0.994","","","","has coordinates","238482","2020-10-21","18:00:00",""
"1555325","6.5951","0.0014","11.238","0.003","12.03","0.003","105.996","0.006","93.545","0.006","94.888","0.006","850.6","0.4","200","2","200","2","","","","","","","","3","P -1","-P 1","2","12mem_dimer","","","- C17 H31 Si -","- C17 H31 Si -","- C34 H62 Si2 -","2","1","","Sabbasani, Venkata R.; Lee, Daesung","Oxidative Dimerization of Silylallenes via Activation of the Allenic C(sp(2))-H Bond Catalyzed by Copper(I) Chloride and N-Hydroxyphthalimide.","Organic letters","2015","17","19","4878","4881","10.1021/acs.orglett.5b02433","","","0.71073","","","0.0807","0.0526","","","0.1526","0.1784","","","","","","1.154","","","","has coordinates","238484","2020-10-21","18:00:00",""
"1555326","6.2702","0.0009","10.955","0.0019","11.088","0.0019","75.965","0.005","74.11","0.005","74.699","0.005","694.6","0.2","200","2","200","2","","","","","","","","3","P -1","-P 1","2","","","","- C13 H23 Si -","- C13 H23 Si -","- C26 H46 Si2 -","2","1","","Sabbasani, Venkata R.; Lee, Daesung","Oxidative Dimerization of Silylallenes via Activation of the Allenic C(sp(2))-H Bond Catalyzed by Copper(I) Chloride and N-Hydroxyphthalimide.","Organic letters","2015","17","19","4878","4881","10.1021/acs.orglett.5b02433","","","0.71073","","","0.1155","0.0964","","","0.3005","0.3182","","","","","","2.442","","","","has coordinates","238486","2020-10-21","18:00:00",""
"1555327","6.5538","0.0005","13.9376","0.001","13.754","0.0011","90","","92.544","0.003","90","","1255.11","0.17","93","2","93","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C15 H10 Cl F2 N -","- C15 H10 Cl F2 N -","- C60 H40 Cl4 F8 N4 -","4","1","","Aikawa, Kohsuke; Maruyama, Kenichi; Honda, Kazuya; Mikami, Koichi","α-Difluoromethylation on sp(3) Carbon of Nitriles Using Fluoroform and Ruppert-Prakash Reagent.","Organic letters","2015","17","19","4882","4885","10.1021/acs.orglett.5b02438","","","0.71073","","","0.0864","0.0462","","","0.0827","0.0955","","","","","","1.027","","","","has coordinates","238488","2020-10-21","18:00:00",""
"1555328","8.4125","0.0004","9.7659","0.0005","11.5692","0.0006","108.577","0.003","95.876","0.003","110.228","0.003","820.9","0.08","296","2","296","2","","","","","","","","6","P 1","P 1","1","","","","- C35 H30 Br F N4 O4 -","- C35 H30 Br F N4 O4 -","- C35 H30 Br F N4 O4 -","1","1","","Bao, Xiaoze; Wang, Baomin; Cui, Longchen; Zhu, Guodong; He, Yuli; Qu, Jingping; Song, Yuming","An Organocatalytic Asymmetric Friedel-Crafts Addition/Fluorination Sequence: Construction of Oxindole-Pyrazolone Conjugates Bearing Vicinal Tetrasubstituted Stereocenters.","Organic letters","2015","17","21","5168","5171","10.1021/acs.orglett.5b02470","","","0.71073","MoKα","","0.043","0.0366","","","0.0948","0.098","","","","","","1.04","","","","has coordinates","238490","2020-10-21","18:00:00",""
"1555329","24.4402","0.0007","52.631","0.004","4.31801","0.00013","90","","90","","90","","5554.3","0.5","293","","293","","","","","","","","","4","F d d 2","F 2 -2d","43","","","","- C17 H13 Cl O2 -","- C17 H13 Cl O2 -","- C272 H208 Cl16 O32 -","16","1","","Suzuki, Takeyuki; Ismiyarto, ?; Ishizaka, Yuka; Zhou, Da-Yang; Asano, Kaori; Sasai, Hiroaki","One-Pot Catalysis Using a Chiral Iridium Complex/Brønsted Base: Catalytic Asymmetric Synthesis of Catalponol.","Organic letters","2015","17","21","5176","5179","10.1021/acs.orglett.5b02480","","","1.54187","CuKα","","","0.0493","","","","0.1249","","","","","","1.044","","","","has coordinates","238492","2020-10-21","18:00:00",""
"1555330","19.794","0.004","11.828","0.002","7.3236","0.0015","90","","91.476","0.005","90","","1714.1","0.6","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H15 F3 N2 -","- C21 H15 F3 N2 -","- C84 H60 F12 N8 -","4","1","","Tang, Mi; Tong, Lingfeng; Ju, Lei; Zhai, Wanwan; Hu, Yang; Yu, Xinhong","Benzoic Acid Catalyzed Annulations of α-Amino Acids and Aromatic Aldehydes Containing an ortho-Michael Acceptor: Access to 2,5-Dihydro-1H-benzo[c]azepines and 10,11-Dihydro-5H-benzo[e]pyrrolo[1,2-a]azepines.","Organic letters","2015","17","21","5180","5183","10.1021/acs.orglett.5b02484","","","0.71073","MoKα","","0.1182","0.0606","","","0.1366","0.1647","","","","","","1.022","","","","has coordinates,has disorder","238494","2020-10-21","18:00:00",""
"1555331","8.34","0.011","25.16","0.03","8.134","0.01","90","","109.63","0.02","90","","1608","3","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C18 H22 N2 O2 -","- C18 H22 N2 O2 -","- C72 H88 N8 O8 -","4","1","","Yuan, Jingwen; Zhang, Qian; Yu, Mangfei; Huang, Peng; Zhang, Rui; Dong, Dewen","Phenyliodine(III) Diacetate Mediated Oxidative Cyclization of 1-Alkenoyl-1-carbamoyl Cycloalkanes: Access to Spiro-Fused Dihydrofuran-3(2H)-ones.","Organic letters","2015","17","20","5012","5015","10.1021/acs.orglett.5b02485","","","0.71073","MoKα","","0.2259","0.0841","","","0.2134","0.3043","","","","","","0.972","","","","has coordinates,has disorder","238496","2020-10-21","18:00:00",""
"1555332","8.126","0.003","9.511","0.003","12.21","0.004","84.646","0.013","78.696","0.012","74.768","0.01","892","0.5","173.15","","173.15","","","","","","","","","5","P -1","-P 1","2","","","","- C24 H15 F2 N O2 -","- C24 H15 F2 N O2 -","- C48 H30 F4 N2 O4 -","2","1","","Chen, Qi; Chen, Hao; Meng, Xiao; Ma, Yuguo","Lewis Acid Assisted Diels-Alder Reaction with Regio- and Stereoselectivity: Anti-1,4-Adducts with Rigid Scaffolds and Their Application in Explosives Sensing.","Organic letters","2015","17","20","5016","5019","10.1021/acs.orglett.5b02487","","","0.71073","MoKα","","0.0505","0.048","","","0.1232","0.1251","","","","","","1.107","","","","has coordinates","238498","2020-10-21","18:00:00",""
"1555333","6.2172","0.0005","11.8634","0.001","29.226","0.002","90","","94.257","0.007","90","","2149.7","0.3","180","0.1","180","0.1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C44 H36 F4 N2 O4 Si2 -","- C44 H36 F4 N2 O4 Si2 -","- C88 H72 F8 N4 O8 Si4 -","2","0.5","","Chen, Qi; Chen, Hao; Meng, Xiao; Ma, Yuguo","Lewis Acid Assisted Diels-Alder Reaction with Regio- and Stereoselectivity: Anti-1,4-Adducts with Rigid Scaffolds and Their Application in Explosives Sensing.","Organic letters","2015","17","20","5016","5019","10.1021/acs.orglett.5b02487","","","0.71073","MoKα","","0.1105","0.0625","","","0.1376","0.1568","","","","","","1.042","","","","has coordinates","238500","2020-10-21","18:00:00",""
"1555334","17.755","0.005","9.629","0.003","15.724","0.006","90","","99.347","0.006","90","","2652.5","1.5","173.15","","173.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C34 H20 F4 N2 O4 -","- C34 H20 F4 N2 O4 -","- C136 H80 F16 N8 O16 -","4","1","","Chen, Qi; Chen, Hao; Meng, Xiao; Ma, Yuguo","Lewis Acid Assisted Diels-Alder Reaction with Regio- and Stereoselectivity: Anti-1,4-Adducts with Rigid Scaffolds and Their Application in Explosives Sensing.","Organic letters","2015","17","20","5016","5019","10.1021/acs.orglett.5b02487","","","0.71073","MoKα","","0.0618","0.0526","","","0.1134","0.118","","","","","","1.105","","","","has coordinates","238502","2020-10-21","18:00:00",""
"1555335","13.6455","0.0003","18.1359","0.0005","24.9551","0.0006","90","","104.465","0.0011","90","","5979.9","0.3","93","","93","","","","","","","","","7","P 1 21 1","P 2yb","4","","","","- C51 H46 F12 N6 Ni O16 S4 -","- C51 H46 F11.735 N6 Ni O15.735 S4 -","- C204 H184 F46.94 N24 Ni4 O62.94 S16 -","4","2","","Takeda, Takuya; Harada, Shinji; Nishida, Atsushi","Catalytic Asymmetric Nazarov Cyclization of Heteroaryl Vinyl Ketones through a Crystallographically Defined Chiral Dinuclear Nickel Complex.","Organic letters","2015","17","21","5184","5187","10.1021/acs.orglett.5b02497","","","1.54187","CuKα","","0.3164","0.1394","","","0.328","0.454","","","","","","0.961","","","","has coordinates,has disorder","238504","2020-10-21","18:00:00",""
"1555336","10.612","0.002","16.848","0.003","23.394","0.005","90","","96.68","0.03","90","","4154.2","1.4","113","2","113","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C26 H18 Br N O2 -","- C26 H18 Br N O2 -","- C208 H144 Br8 N8 O16 -","8","2","","Liang, Ling; Li, Erqing; Dong, Xuelin; Huang, You","DABCO-Mediated [4 + 4]-Domino Annulation: Access to Functionalized Eight-Membered Cyclic Ethers.","Organic letters","2015","17","19","4914","4917","10.1021/acs.orglett.5b02498","","","0.71073","MoKα","","0.1526","0.0745","","","0.1647","0.2052","","","","","","1.019","","","","has coordinates","238506","2020-10-21","18:00:00",""
"1555337","8.3018","0.0001","14.7835","0.0002","12.3636","0.0002","90","","101.126","0.001","90","","1488.86","0.04","140","2","140","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C17 H20 O3 -","- C17 H20 O3 -","- C68 H80 O12 -","4","2","","Liao, Hai-Bing; Lei, Chun; Gao, Li-Xin; Li, Jing-Ya; Li, Jia; Hou, Ai-Jun","Two Enantiomeric Pairs of Meroterpenoids from Rhododendron capitatum.","Organic letters","2015","17","20","5040","5043","10.1021/acs.orglett.5b02515","","","1.54178","CuKα","","0.0326","0.0322","","","0.0895","0.09","","","","","","1.067","","","","has coordinates","238508","2020-10-21","18:00:00",""
"1555338","8.0539","0.0001","9.0826","0.0001","9.9175","0.0001","102.862","0.001","97.071","0.001","96.384","0.001","694.648","0.014","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C17 H20 O3 -","- C17 H20 O3 -","- C34 H40 O6 -","2","1","","Liao, Hai-Bing; Lei, Chun; Gao, Li-Xin; Li, Jing-Ya; Li, Jia; Hou, Ai-Jun","Two Enantiomeric Pairs of Meroterpenoids from Rhododendron capitatum.","Organic letters","2015","17","20","5040","5043","10.1021/acs.orglett.5b02515","","","1.54178","CuKα","","0.0441","0.0426","","","0.1205","0.1234","","","","","","1.063","","","","has coordinates","238509","2020-10-21","18:00:00",""
"1555339","11.3754","0.0001","11.9359","0.0001","14.185","0.0001","90","","90","","90","","1925.98","0.03","140","2","140","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C22 H28 O3 -","- C22 H28 O3 -","- C88 H112 O12 -","4","1","","Liao, Hai-Bing; Lei, Chun; Gao, Li-Xin; Li, Jing-Ya; Li, Jia; Hou, Ai-Jun","Two Enantiomeric Pairs of Meroterpenoids from Rhododendron capitatum.","Organic letters","2015","17","20","5040","5043","10.1021/acs.orglett.5b02515","","","1.54178","CuKα","","0.0363","0.0351","","","0.0942","0.0959","","","","","","1.041","","","","has coordinates","238511","2020-10-21","18:00:00",""
"1555340","45.917","0.004","10.214","0.0009","19.5587","0.0017","90","","104.361","0.002","90","","8886.3","1.3","188","2","188","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C81 H22 O S2 -","- C81 H22 O S2 -","- C648 H176 O8 S16 -","8","1","","Chen, Si; Li, Zong-Jun; Li, Shu-Hui; Gao, Xiang","Base-Promoted Consecutive Enolate Addition Reaction of [60]Fullerene with Ketones.","Organic letters","2015","17","21","5192","5195","10.1021/acs.orglett.5b02528","","","0.71073","MoKα","","0.1478","0.0699","","","0.1228","0.1507","","","","","","1.033","","","","has coordinates","238513","2020-10-21","18:00:00",""
"1555341","9.9134","0.0007","14.8425","0.001","17.0648","0.0012","67.983","0.001","89.643","0.001","77.467","0.001","2264.5","0.3","188","2","188","2","","","","","","","","3","P -1","-P 1","2","","","","- C79 H22 O -","- C79 H22 O -","- C158 H44 O2 -","2","1","","Chen, Si; Li, Zong-Jun; Li, Shu-Hui; Gao, Xiang","Base-Promoted Consecutive Enolate Addition Reaction of [60]Fullerene with Ketones.","Organic letters","2015","17","21","5192","5195","10.1021/acs.orglett.5b02528","","","0.71073","MoKα","","0.1288","0.0702","","","0.1675","0.1969","","","","","","0.968","","","","has coordinates","238515","2020-10-21","18:00:00",""
"1555342","14.971","0.0007","17.4948","0.001","16.7353","0.0009","90","","107.46","0.006","90","","4181.3","0.4","104","2","104","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C80 H24 O -","- C80 H24 O -","- C320 H96 O4 -","4","1","","Chen, Si; Li, Zong-Jun; Li, Shu-Hui; Gao, Xiang","Base-Promoted Consecutive Enolate Addition Reaction of [60]Fullerene with Ketones.","Organic letters","2015","17","21","5192","5195","10.1021/acs.orglett.5b02528","","","0.71073","MoKα","","0.0862","0.0551","","","0.1044","0.1169","","","","","","1.052","","","","has coordinates,has disorder","238517","2020-10-21","18:00:00",""
"1555343","6.0749","0.0007","8.2818","0.0009","25.017","0.003","90","","90","","90","","1258.6","0.3","298","2","298","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C13 H21 N O2 -","- C13 H21 N O2 -","- C52 H84 N4 O8 -","4","1","","Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.","Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.","Organic letters","2015","17","21","5204","5207","10.1021/acs.orglett.5b02533","","","1.54178","CuKα","","0.0533","0.0499","","","0.1302","0.1356","","","","","","1.034","","","","has coordinates","238519","2020-10-21","18:00:00",""
"1555344","10.7069","0.0007","10.8672","0.0006","19.656","0.0012","90","","90","","90","","2287.1","0.2","296","2","296","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C11 H19 N O2 -","- C11 H19 N O2 -","- C88 H152 N8 O16 -","8","2","","Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.","Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.","Organic letters","2015","17","21","5204","5207","10.1021/acs.orglett.5b02533","","","1.54178","CuKα","","0.0492","0.0473","","","0.1307","0.1334","","","","","","0.936","","","","has coordinates","238520","2020-10-21","18:00:00",""
"1555345","5.8171","0.0005","7.1215","0.0007","16.2736","0.0015","90","","94.53","0.005","90","","672.05","0.11","123","2","123","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C15 H19 N O3 -","- C15 H19 N O3 -","- C30 H38 N2 O6 -","2","1","","Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.","Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.","Organic letters","2015","17","21","5204","5207","10.1021/acs.orglett.5b02533","","","1.54178","CuKα","","0.0607","0.0497","","","0.1277","0.1372","","","","","","1.061","","","","has coordinates","238522","2020-10-21","18:00:00",""
"1555346","6.1254","0.0003","6.9441","0.0004","10.8047","0.0006","90","","102.426","0.002","90","","448.82","0.04","123","2","123","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C9 H15 N O2 -","- C9 H15 N O2 -","- C18 H30 N2 O4 -","2","1","","Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.","Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.","Organic letters","2015","17","21","5204","5207","10.1021/acs.orglett.5b02533","","","1.54178","CuKα","","0.0458","0.045","","","0.1053","0.1061","","","","","","1.197","","","","has coordinates","238524","2020-10-21","18:00:00",""
"1555347","6.742","0.0002","7.2944","0.0002","15.8577","0.0004","90","","90","","90","","779.86","0.04","123","2","123","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C8 H11 N O2 -","- C8 H11 N O2 -","- C32 H44 N4 O8 -","4","1","","Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.","Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.","Organic letters","2015","17","21","5204","5207","10.1021/acs.orglett.5b02533","","","1.54178","CuKα","","0.0616","0.0613","","","0.1297","0.131","","","","","","1.339","","","","has coordinates","238526","2020-10-21","18:00:00",""
"1555348","8.236","0.0004","6.3687","0.0003","10.9331","0.0005","90","","92.94","0.001","90","","572.71","0.05","290","2","290","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C13 H13 N O3 -","- C13 H13 N O3 -","- C26 H26 N2 O6 -","2","1","","Wright, Stephen W.; Choi, Chulho; Chung, Seungwon; Boscoe, Brian P.; Drozda, Susan E.; Mousseau, James J.; Trzupek, John D.","Reversal of Diastereoselection in the Conjugate Addition of Cuprates to Unsaturated Lactams.","Organic letters","2015","17","21","5204","5207","10.1021/acs.orglett.5b02533","","","0.71073","MoKα","","0.0447","0.0413","","","0.1097","0.1135","","","","","","1.051","","","","has coordinates","238527","2020-10-21","18:00:00",""
"1555349","7.32024","0.00009","8.9338","0.0001","17.2413","0.0002","90","","91.3123","0.0012","90","","1127.24","0.02","150","2","150","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C24 H40 O8 -","- C24 H40 O8 -","- C48 H80 O16 -","2","1","","Wu, Ping; Xue, Jinghua; Yao, Lei; Xu, Liangxiong; Li, Hanxiang; Wei, Xiaoyi","Bisacremines E-G, Three Polycyclic Dimeric Acremines Produced by Acremonium persicinum SC0105.","Organic letters","2015","17","19","4922","4925","10.1021/acs.orglett.5b02536","","","1.54184","CuKα","","0.0314","0.0293","","","0.0706","0.0727","","","","","","1.073","","","","has coordinates","238529","2020-10-21","18:00:00",""
"1555350","10.925","0.005","10.939","0.005","11.295","0.005","113.793","0.008","97.632","0.008","99.629","0.008","1187.3","0.9","273","2","273","2","","","","","","","","4","P -1","-P 1","2","","","","- C25 H25 N O9 -","- C25 H25 N O9 -","- C50 H50 N2 O18 -","2","1","","Shu, Wen-Ming; Zheng, Kai-Lu; Ma, Jun-Rui; Wu, An-Xin","Transition-Metal-Free Multicomponent Benzannulation Reactions for the Construction of Polysubstituted Benzene Derivatives.","Organic letters","2015","17","21","5216","5219","10.1021/acs.orglett.5b02548","","","0.71073","MoKα","","0.1281","0.0964","","","0.3085","0.3404","","","","","","1.095","","","","has coordinates,has disorder","238531","2020-10-21","18:00:00",""
"1555351","10.167","0.0017","11.5366","0.0019","11.951","0.002","68.165","0.002","67.543","0.002","79.903","0.003","1201.6","0.3","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C25 H22 O6 -","- C25 H22 O6 -","- C50 H44 O12 -","2","1","","Shu, Wen-Ming; Zheng, Kai-Lu; Ma, Jun-Rui; Wu, An-Xin","Transition-Metal-Free Multicomponent Benzannulation Reactions for the Construction of Polysubstituted Benzene Derivatives.","Organic letters","2015","17","21","5216","5219","10.1021/acs.orglett.5b02548","","","0.71073","MoKα","","0.0829","0.068","","","0.1885","0.2095","","","","","","1.049","","","","has coordinates,has disorder","238532","2020-10-21","18:00:00",""
"1555352","10.2764","0.0008","23.0983","0.0019","7.47","0.0006","90","","101.197","0.002","90","","1739.4","0.2","293","2","293","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C24 H20 O2 -","- C24 H20 O2 -","- C96 H80 O8 -","4","1","","Siyang, Hai Xiao; Ji, Xiao Yue; Wu, Xu Rui; Wu, Xin Yan; Liu, Pei Nian","Lewis Acid Catalyzed Tandem Polycyclization of Internal Alkynols and Vinyl Azides.","Organic letters","2015","17","21","5220","5223","10.1021/acs.orglett.5b02556","","","0.71073","MoKα","","0.0487","0.0412","","","0.11","0.1169","","","","","","1.022","","","","has coordinates","238533","2020-10-21","18:00:00",""
"1555353","8.3568","0.0005","9.126","0.0006","13.2967","0.0008","72.212","0.002","72.822","0.002","85.148","0.002","922.49","0.1","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C21 H24 Br N O -","- C21 H24 Br N O -","- C42 H48 Br2 N2 O2 -","2","1","","Wong, Ying-Chieh; Ke, Zhihai; Yeung, Ying-Yeung","Lewis Basic Sulfide Catalyzed Electrophilic Bromocyclization of Cyclopropylmethyl Amide.","Organic letters","2015","17","20","4944","4947","10.1021/acs.orglett.5b02557","","","0.71073","MoKα","","0.0423","0.0347","","","0.0782","0.0814","","","","","","1.051","","","","has coordinates","238535","2020-10-21","18:00:00",""
"1555354","5.287","0.0002","9.4826","0.0003","34.033","0.0012","90","","90","","90","","1706.23","0.1","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C18 H32 N2 O -","- C18 H32 N2 O -","- C72 H128 N8 O4 -","4","1","","Bosch, Caroline; Fiser, Béla; Gómez-Bengoa, Enrique; Bradshaw, Ben; Bonjoch, Josep","Approach to cis-Phlegmarine Alkaloids via Stereodivergent Reduction: Total Synthesis of (+)-Serratezomine E and Putative Structure of (-)-Huperzine N.","Organic letters","2015","17","20","5084","5087","10.1021/acs.orglett.5b02581","","","1.54178","CuKα","","0.0401","0.036","","","0.0915","0.0943","","","","","","1.083","","","","has coordinates","238539","2020-10-21","18:00:00",""
"1555355","6.6742","0.0015","12.874","0.003","25.688","0.005","90","","90","","90","","2207.2","0.8","140","2","140","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C24 H24 Br N O4 -","- C24 H24 Br N O4 -","- C96 H96 Br4 N4 O16 -","4","1","","Das, Tapas; Saha, Prasenjit; Singh, Vinod K.","Silver(I)-Ferrophox Catalyzed Enantioselective Desymmetrization of Cyclopentenedione: Synthesis of Highly Substituted Bicyclic Pyrrolidines.","Organic letters","2015","17","20","5088","5091","10.1021/acs.orglett.5b02582","","","0.71073","MoKα","","0.1257","0.063","","","0.1431","0.1703","","","","","","0.996","","","","has coordinates","238541","2020-10-21","18:00:00",""
"1555356","35.112","0.002","12.3662","0.0005","19.6459","0.001","90","","90","","90","","8530.3","0.7","293","2","293","2","","","","","","","","7","P n m a","-P 2ac 2n","62","ZWX","","","- C98 H156 Cd4 Cl14 Lu2 N56 O62 -","- C98 H98 Cd4 Cl14 Lu2 N56 O37 -","- C196 H196 Cd8 Cl28 Lu4 N112 O74 -","2","0.25","","Zhao, Wen-Xuan; Wang, Chuan-Zeng; Chen, Li-Xia; Cong, Hang; Xiao, Xin; Zhang, Yun-Qian; Xue, Sai-Feng; Huang, Ying; Tao, Zhu; Zhu, Qian-Jiang","A Hemimethyl-Substituted Cucurbit[7]uril Derived from 3α-Methyl-glycoluril.","Organic letters","2015","17","20","5072","5075","10.1021/acs.orglett.5b02588","","","1.54184","CuKα","","0.1815","0.1322","","","0.3694","0.4214","","","","","","1.015","","","","has coordinates,has disorder","238543","2020-10-21","18:00:00",""
"1555357","8.2834","0.0012","10.8217","0.0016","18.382","0.003","78.708","0.014","82.706","0.014","89.789","0.012","1602.4","0.4","293.18","0.1","293.18","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C21 H16 F2 O -","- C21 H16 F2 O -","- C84 H64 F8 O4 -","4","2","","Yang, Chao; Xu, Zheng-Liang; Shao, Hui; Mou, Xue-Qing; Wang, Jie; Wang, Shao-Hua","A Tin(IV) Chloride Promoted Tandem C-O Bond Cleavage/Nazarov Cyclization/Nucleophilic Addition Reaction of 1,1-Disubstituted Allylic Ethers toward the Synthesis of Multisubstituted Indenes.","Organic letters","2015","17","21","5288","5291","10.1021/acs.orglett.5b02610","","x-ray","0.71073","MoKα","","0.1376","0.0748","","","0.1774","0.2409","","","","","","1.004","","","","has coordinates","238545","2020-10-21","18:00:00",""
"1555358","9.6947","0.0012","12.5617","0.0014","21.062","0.003","90","","90","","90","","2565","0.6","213","2","213","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C25 H26 F6 N3 P Pd -","- C25 H26 F6 N3 P Pd -","- C100 H104 F24 N12 P4 Pd4 -","4","1","","Álvarez-Casao, Yolanda; Monge, David; Álvarez, Eleuterio; Fernández, Rosario; Lassaletta, José M","Pyridine-Hydrazones as N,N'-Ligands in Asymmetric Catalysis: Pd(II)-Catalyzed Addition of Boronic Acids to Cyclic Sulfonylketimines.","Organic letters","2015","17","20","5104","5107","10.1021/acs.orglett.5b02613","","","0.71073","MoKα","","0.0327","0.0312","","","0.0845","0.0855","","","","","","1.04","","","","has coordinates,has disorder","238546","2020-10-21","18:00:00",""
"1555359","12.3361","0.0004","6.0532","0.0002","13.2095","0.0004","90","","115.922","0.002","90","","887.15","0.05","93","2","93","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C19 H23 F2 N O3 -","- C19 H23 F2 N O3 -","- C38 H46 F4 N2 O6 -","2","1","","Aikawa, Kohsuke; Yoshida, Seiya; Kondo, Daisuke; Asai, Yuya; Mikami, Koichi","Catalytic Asymmetric Synthesis of Tertiary Alcohols and Oxetenes Bearing a Difluoromethyl Group.","Organic letters","2015","17","20","5108","5111","10.1021/acs.orglett.5b02617","","","1.54178","CuKα","","0.0455","0.0362","","","0.0839","0.0876","","","","","","1.041","","","","has coordinates","238547","2020-10-21","18:00:00",""
"1555360","9.37","0.003","12.582","0.004","14.702","0.004","90.83","0.003","105.888","0.003","110.831","0.003","1546","0.8","296.15","","296.15","","","","","","","","","5","P -1","-P 1","2","","","","- C38 H30 N2 O4 S2 -","- C38 H30 N2 O4 S2 -","- C76 H60 N4 O8 S4 -","2","1","","Dhiman, Seema; Ramasastry, S. S. V.","One-Pot Relay Gold(I) and Brønsted Acid Catalysis: Cyclopenta[b]annulation of Indoles via Hydroamination/Nazarov-Type Cyclization Cascade of Enynols.","Organic letters","2015","17","20","5116","5119","10.1021/acs.orglett.5b02632","","","0.71073","MoKα","","0.0523","0.0391","","","0.0965","0.1058","","","","","","1.027","","","","has coordinates","238549","2020-10-21","18:00:00",""
"1555361","12.0889","0.0008","12.4331","0.0008","18.0531","0.0012","75.323","0.007","86.447","0.007","89.594","0.006","2619.7","0.3","293","","293","","","","","","","","","6","P -1","-P 1","2","","","","- C60 H60 Cl2 N4 O4 Ru -","- C60 H60 Cl2 N4 O4 Ru -","- C120 H120 Cl4 N8 O8 Ru2 -","2","1","","Maeda, Kazuki; Terada, Takuma; Iwamoto, Takahiro; Kurahashi, Takuya; Matsubara, Seijiro","Ruthenium-Porphyrin-Catalyzed [4 + 2] Cycloaddition of α,β-Unsaturated Imines and Aldehydes.","Organic letters","2015","17","21","5284","5287","10.1021/acs.orglett.5b02654","","","0.71075","MoKα","","","0.0407","","","","0.112","","","","","","1.037","","","","has coordinates","238551","2020-10-21","18:00:00",""
"1555362","15.928","0.004","11.573","0.003","11.95","0.003","90","","107.075","0.008","90","","2105.7","0.9","293","","293","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C22 H24 N2 O4 S -","- C22 H24 N2 O4 S -","- C88 H96 N8 O16 S4 -","4","1","","Maeda, Kazuki; Terada, Takuma; Iwamoto, Takahiro; Kurahashi, Takuya; Matsubara, Seijiro","Ruthenium-Porphyrin-Catalyzed [4 + 2] Cycloaddition of α,β-Unsaturated Imines and Aldehydes.","Organic letters","2015","17","21","5284","5287","10.1021/acs.orglett.5b02654","","","0.71075","MoKα","","","0.0502","","","","0.1335","","","","","","1.032","","","","has coordinates","238553","2020-10-21","18:00:00",""
"1555363","16.4534","0.0012","8.1341","0.0006","16.6107","0.0012","90","","116.278","0.009","90","","1993.3","0.3","293","","293","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C24 H23 N O2 S -","- C24 H21 N O2 S -","- C96 H84 N4 O8 S4 -","4","1","","Maeda, Kazuki; Terada, Takuma; Iwamoto, Takahiro; Kurahashi, Takuya; Matsubara, Seijiro","Ruthenium-Porphyrin-Catalyzed [4 + 2] Cycloaddition of α,β-Unsaturated Imines and Aldehydes.","Organic letters","2015","17","21","5284","5287","10.1021/acs.orglett.5b02654","","","0.71075","MoKα","","","0.0476","","","","0.16","","","","","","1.088","","","","has coordinates","238554","2020-10-21","18:00:00",""
"1555364","8.1967","0.0014","9.0717","0.0015","15.216","0.003","87.208","0.006","82.37","0.006","65.005","0.005","1016.4","0.3","293","","293","","","","","","","","","5","P -1","-P 1","2","","","","- C22 H25 N O2 S -","- C22 H25 N O2 S -","- C44 H50 N2 O4 S2 -","2","1","","Maeda, Kazuki; Terada, Takuma; Iwamoto, Takahiro; Kurahashi, Takuya; Matsubara, Seijiro","Ruthenium-Porphyrin-Catalyzed [4 + 2] Cycloaddition of α,β-Unsaturated Imines and Aldehydes.","Organic letters","2015","17","21","5284","5287","10.1021/acs.orglett.5b02654","","","0.71075","MoKα","","","0.0739","","","","0.1786","","","","","","1.038","","","","has coordinates","238556","2020-10-21","18:00:00",""
"1555365","9.512","0.004","19.054","0.007","30.838","0.014","90","","93.81","0.008","90","","5577","4","100","2","100","","","","","","","","","6","C 1 2 1","C 2y","5","","","","- C24 H25 Br N2 O4 S -","- C24 H25 Br N2 O4 S -","- C192 H200 Br8 N16 O32 S8 -","8","2","","Shu, Xing-zhong; Schienebeck, Casi M.; Li, Xiaoxun; Zhou, Xin; Song, Wangze; Chen, Lianqing; Guzei, Ilia A.; Tang, Weiping","Rhodium-Catalyzed Stereoselective Intramolecular [5 + 2] Cycloaddition of 3-Acyloxy 1,4-Enyne and Alkene.","Organic letters","2015","17","20","5128","5131","10.1021/acs.orglett.5b02665","","x-ray","0.71073","MoKα","K-L~3~","0.057","0.0499","","","0.1229","0.1259","","","","","","1.062","","","","has coordinates,has disorder","238558","2020-10-21","18:00:00",""
"1555366","12.4342","0.0007","16.375","0.0011","8.6369","0.0005","90","","106.914","0.004","90","","1682.49","0.18","298","2","298","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C19 H20 N2 O3 -","- C19 H20 N2 O3 -","- C76 H80 N8 O12 -","4","1","","Sar, Dinabandhu; Bag, Raghunath; Yashmeen, Afsana; Bag, Subhendu Sekhar; Punniyamurthy, Tharmalingam","Synthesis of Functionalized Pyrazoles via Vanadium-Catalyzed C-N Dehydrogenative Cross-Coupling and Fluorescence Switch-On Sensing of BSA Protein.","Organic letters","2015","17","21","5308","5311","10.1021/acs.orglett.5b02669","","","0.71073","MoKα","","0.0906","0.0563","","","0.1581","0.1899","","","","","","1.042","","","","has coordinates","238560","2020-10-21","18:00:00",""
"1555367","10.2093","0.0001","10.2093","0.0001","30.4222","0.0003","90","","90","","120","","2746.08","0.05","295","2","295","2","","","","","","","","4","P 65","P 65","170","","","","- C18 H23 N O7 -","- C18 H23 N O7 -","- C108 H138 N6 O42 -","6","1","","N V G, Moorthy; Dyapa, Rajendar; Pansare, Sunil V.","Formal Synthesis of (+)-Lasubine II and (-)-Subcosine II via Organocatalytic Michael Addition of a Ketone to an α-Nitrostyrene.","Organic letters","2015","17","21","5312","5315","10.1021/acs.orglett.5b02677","","","1.54178","CuKα","","0.0321","0.0314","","","0.0911","0.0929","","","","","","1.075","","","","has coordinates,has disorder","238562","2020-10-21","18:00:00",""
"1555368","9.5014","0.001","17.2076","0.0019","9.9401","0.001","90","","90.682","0.002","90","","1625.1","0.3","90","2","90.15","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C19 H21 N2 O2.5 -","- C19 H21 N2 O2.5 -","- C76 H84 N8 O10 -","4","2","","Palazzo, Teresa A.; Patra, Digambara; Yang, Joung S.; El Khoury, Elsy; Appleton, Mackenzie G.; Haddadin, Makhluf J.; Tantillo, Dean J.; Kurth, Mark J.","Dibenzonaphthyridinones: Heterocycle-to-Heterocycle Synthetic Strategies and Photophysical Studies.","Organic letters","2015","17","23","5732","5735","10.1021/acs.orglett.5b02680","","","0.71073","MoKα","","0.0346","0.0335","","","0.0924","0.0935","","","","","","1.033","","","","has coordinates","275434","2022-05-16","05:31:57",""
"1555369","21.8506","0.0005","6.802","0.0001","25.1773","0.0005","90","","113.248","0.001","90","","3438.21","0.12","90","2","90.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C42 H46 N4 O5 -","- C42 H46 N4 O5 -","- C168 H184 N16 O20 -","4","1","","Palazzo, Teresa A.; Patra, Digambara; Yang, Joung S.; El Khoury, Elsy; Appleton, Mackenzie G.; Haddadin, Makhluf J.; Tantillo, Dean J.; Kurth, Mark J.","Dibenzonaphthyridinones: Heterocycle-to-Heterocycle Synthetic Strategies and Photophysical Studies.","Organic letters","2015","17","23","5732","5735","10.1021/acs.orglett.5b02680","","","1.54178","CuKα","","0.0663","0.0599","","","0.1708","0.1775","","","","","","1.039","","","","has coordinates","238565","2020-10-21","18:00:00",""
"1555370","7.0727","0.0002","8.9761","0.0008","11.4306","0.0005","90","","96.806","0.004","90","","720.56","0.07","150","2","150","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C19 H16 O5 -","- C19 H16 O5 -","- C38 H32 O10 -","2","1","","Yang, Chunfang; Huang, Chunshuai; Zhang, Wenjun; Zhu, Yiguang; Zhang, Changsheng","Heterologous Expression of Fluostatin Gene Cluster Leads to a Bioactive Heterodimer.","Organic letters","2015","17","21","5324","5327","10.1021/acs.orglett.5b02683","","","1.54178","CuKα","","0.032","0.0303","","","0.0772","0.0791","","","","","","1.087","","","","has coordinates","238567","2020-10-21","18:00:00",""
"1555371","7.5169","0.0003","10.5263","0.0005","16.5993","0.0008","90","","90","","90","","1313.42","0.1","88","2","88","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C14 H11 N O2 S2 -","- C14.4167 H11 N O2 S1.8438 -","- C57.6668 H44 N4 O8 S7.3752 -","4","1","","Osborne, Charlotte A.; Endean, Thomas B. D.; Jarvo, Elizabeth R.","Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.","Organic letters","2015","17","21","5340","5343","10.1021/acs.orglett.5b02692","","","0.71073","MoKα","","0.0283","0.0275","","","0.0754","0.0762","","","","","","1.076","","","","has coordinates","238569","2020-10-21","18:00:00",""
"1555372","7.7171","0.0005","7.9486","0.0005","23.816","0.0014","90","","90","","90","","1460.88","0.16","133","2","133","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C15 H17 N O4 S -","- C15 H17 N O4 S -","- C60 H68 N4 O16 S4 -","4","1","","Osborne, Charlotte A.; Endean, Thomas B. D.; Jarvo, Elizabeth R.","Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.","Organic letters","2015","17","21","5340","5343","10.1021/acs.orglett.5b02692","","","0.71073","MoKα","","0.0342","0.0294","","","0.0678","0.0706","","","","","","1.04","","","","has coordinates","238571","2020-10-21","18:00:00",""
"1555373","10.7582","0.0006","10.7582","0.0006","11.4283","0.0007","90","","90","","90","","1322.7","0.13","133","2","133","2","","","","","","","","5","P 43","P 4cw","78","","","","- C16 H13 N O2 S -","- C16 H13 N O2 S -","- C64 H52 N4 O8 S4 -","4","1","","Osborne, Charlotte A.; Endean, Thomas B. D.; Jarvo, Elizabeth R.","Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.","Organic letters","2015","17","21","5340","5343","10.1021/acs.orglett.5b02692","","","0.71073","MoKα","","0.0295","0.0269","","","0.0645","0.0661","","","","","","1.065","","","","has coordinates","238573","2020-10-21","18:00:00",""
"1555374","7.5472","0.0005","10.3052","0.0007","16.2327","0.001","90","","90","","90","","1262.5","0.14","133","2","133","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C14 H11 N O3 S -","- C14.1667 H11 N O2.875 S -","- C56.6668 H44 N4 O11.5 S4 -","4","1","","Osborne, Charlotte A.; Endean, Thomas B. D.; Jarvo, Elizabeth R.","Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.","Organic letters","2015","17","21","5340","5343","10.1021/acs.orglett.5b02692","","","0.71073","MoKα","","0.0403","0.0363","","","0.0881","0.0909","","","","","","1.07","","","","has coordinates","238574","2020-10-21","18:00:00",""
"1555375","8.0916","0.0006","9.4218","0.0007","13.8016","0.001","90","","90","","90","","1052.2","0.13","133","2","133","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C11 H11 N O2 S -","- C11 H11 N O2 S -","- C44 H44 N4 O8 S4 -","4","1","","Osborne, Charlotte A.; Endean, Thomas B. D.; Jarvo, Elizabeth R.","Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines.","Organic letters","2015","17","21","5340","5343","10.1021/acs.orglett.5b02692","","","0.71073","MoKα","","0.0265","0.0259","","","0.0672","0.0679","","","","","","1.058","","","","has coordinates","238576","2020-10-21","18:00:00",""
"1555376","6.625","0.003","10.223","0.004","31.029","0.012","90","","90","","90","","2101.5","1.5","173.15","","173.15","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C24 H21 Br O6 -","- C24 H21 Br O6 -","- C96 H84 Br4 O24 -","4","1","","Liang, Zhi-Qin; Wang, Dong-Ling; Zhang, Han-Ming; Ye, Song","Enantioselective Synthesis of Bicyclic δ-Lactones via N-Heterocyclic Carbene-Catalyzed Cascade Reaction.","Organic letters","2015","17","20","5140","5143","10.1021/acs.orglett.5b02695","","","0.71073","MoKα","","0.063","0.057","","","0.1515","0.1592","","","","","","1.137","","","","has coordinates","238577","2020-10-21","18:00:00",""
"1555377","28.0198","0.0017","9.2681","0.0005","17.0333","0.001","90","","104.376","0.002","90","","4284.9","0.4","100","2","100","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C24 H24 F3 N O4 -","- C24 H24 F3 N O4 -","- C192 H192 F24 N8 O32 -","8","1","","Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming","Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.","Organic letters","2015","17","21","5368","5371","10.1021/acs.orglett.5b02705","","","0.71073","MoKα","","0.0777","0.0485","","","0.1357","0.177","","","","","","1.043","","","","has coordinates","238579","2020-10-21","18:00:00",""
"1555378","9.5002","0.0007","9.6957","0.0006","10.3129","0.0007","96.467","0.004","104.739","0.004","98.162","0.004","898.32","0.11","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C21 H21 N2 O4 -","- C21 H21 N2 O4 -","- C42 H42 N4 O8 -","2","1","","Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming","Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.","Organic letters","2015","17","21","5368","5371","10.1021/acs.orglett.5b02705","","","0.71073","MoKα","","0.0764","0.0488","","","0.1464","0.184","","","","","","1.132","","","","has coordinates","238581","2020-10-21","18:00:00",""
"1555379","13.6453","0.0011","9.9432","0.0008","14.4487","0.0011","90","","91.039","0.002","90","","1960","0.3","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C23 H20 F3 N3 O -","- C23 H20 F3 N3 O -","- C92 H80 F12 N12 O4 -","4","1","","Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming","Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.","Organic letters","2015","17","21","5368","5371","10.1021/acs.orglett.5b02705","","","0.71073","MoKα","","0.0744","0.0481","","","0.1081","0.1209","","","","","","1.021","","","","has coordinates","238583","2020-10-21","18:00:00",""
"1555380","32.003","0.003","7.0392","0.0007","19.0154","0.0019","90","","120.399","0.002","90","","3694.8","0.6","100","2","100","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C22 H27 N3 O -","- C22 H27 N3 O -","- C176 H216 N24 O8 -","8","1","","Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming","Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.","Organic letters","2015","17","21","5368","5371","10.1021/acs.orglett.5b02705","","","0.71073","MoKα","","0.0811","0.0482","","","0.1123","0.1283","","","","","","1.01","","","","has coordinates","238585","2020-10-21","18:00:00",""
"1555381","22.182","0.004","22.337","0.005","14.877","0.003","90","","90","","90","","7371","3","100","2","100","2","","","","","","","","4","P c c n","-P 2ab 2ac","56","","","","- C22 H20 N2 O5 -","- C22 H20 N2 O5 -","- C352 H320 N32 O80 -","16","2","","Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming","Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.","Organic letters","2015","17","21","5368","5371","10.1021/acs.orglett.5b02705","","","0.71073","MoKα","","0.1201","0.0679","","","0.1906","0.2788","","","","","","0.987","","","","has coordinates","238586","2020-10-21","18:00:00",""
"1555382","17.6141","0.0008","8.5636","0.0004","12.8104","0.0006","90","","107.202","0.002","90","","1845.89","0.15","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H22 N2 O -","- C24 H22 N2 O -","- C96 H88 N8 O4 -","4","1","","Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming","Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.","Organic letters","2015","17","21","5368","5371","10.1021/acs.orglett.5b02705","","","0.71073","MoKα","","0.0631","0.043","","","0.134","0.1675","","","","","","1.166","","","","has coordinates","238588","2020-10-21","18:00:00",""
"1555383","17.188","0.006","9.172","0.004","13.025","0.005","90","","108.831","0.008","90","","1943.5","1.3","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C25 H24 N2 O2 -","- C25 H24 N2 O2 -","- C100 H96 N8 O8 -","4","1","","Chung, Tsai-Wen; Narhe, Bharat D.; Lin, Chun-Cheng; Sun, Chung-Ming","Multicomponent Synthesis of Functionalized Tetrahydroacridinones: Insights into a Mechanistic Route.","Organic letters","2015","17","21","5368","5371","10.1021/acs.orglett.5b02705","","","0.71073","MoKα","","0.0641","0.0427","","","0.0982","0.1098","","","","","","1.046","","","","has coordinates","238589","2020-10-21","18:00:00",""
"1555384","12.718","0.002","8.6639","0.0016","12.342","0.002","90","","101.101","0.003","90","","1334.5","0.4","293","2","293.15","","","","","","","","","5","P 1 2/c 1","-P 2yc","13","","","","- C30 H32 B2 F4 N4 -","- C30 H32 B2 F4 N4 -","- C60 H64 B4 F8 N8 -","2","0.5","","Wang, Jun; Wu, Qinghua; Wang, Shaowu; Yu, Changjiang; Li, Jin; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan","Conformation-Restricted Partially and Fully Fused BODIPY Dimers as Highly Stable Near-Infrared Fluorescent Dyes.","Organic letters","2015","17","21","5360","5363","10.1021/acs.orglett.5b02717","","","0.71073","MoKα","","0.1728","0.0614","","","0.1313","0.1804","","","","","","0.981","","","","has coordinates,has disorder","238591","2020-10-21","18:00:00",""
"1555385","17.6404","0.0015","8.5702","0.0008","20.1377","0.0017","90","","114.568","0.001","90","","2768.8","0.4","293","2","293.15","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C30 H34 B2 F4 N4 -","- C30 H34 B2 F4 N4 -","- C120 H136 B8 F16 N16 -","4","1","","Wang, Jun; Wu, Qinghua; Wang, Shaowu; Yu, Changjiang; Li, Jin; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan","Conformation-Restricted Partially and Fully Fused BODIPY Dimers as Highly Stable Near-Infrared Fluorescent Dyes.","Organic letters","2015","17","21","5360","5363","10.1021/acs.orglett.5b02717","","","0.71073","MoKα","","0.0864","0.0571","","","0.1591","0.1764","","","","","","1.289","","","","has coordinates","238591","2020-10-21","18:00:00",""
"1555386","8.7914","0.0004","22.2498","0.0011","11.9566","0.0005","90","","90","","90","","2338.79","0.19","105","","105","","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C25 H24 N4 O4 -","- C25 H24 N4 O4 -","- C100 H96 N16 O16 -","4","1","","Chingle, Ramesh; Lubell, William D.","Azopeptides: Synthesis and Pericyclic Chemistry.","Organic letters","2015","17","21","5400","5403","10.1021/acs.orglett.5b02723","","x-ray","1.34139","GaKα","","0.049","0.0388","","","0.0922","0.0979","","","","","","1.05","","","","has coordinates","238593","2020-10-21","18:00:00",""
"1555387","7.8202","0.0005","15.433","0.0009","28.4386","0.0017","90","","90","","90","","3432.2","0.4","100","","100","","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C37 H42 N4 O6 -","- C37 H42 N4 O6 -","- C148 H168 N16 O24 -","4","1","","Chingle, Ramesh; Lubell, William D.","Azopeptides: Synthesis and Pericyclic Chemistry.","Organic letters","2015","17","21","5400","5403","10.1021/acs.orglett.5b02723","","x-ray","1.34139","GaKα","","0.046","0.0437","","","0.1225","0.1248","","","","","","1.022","","","","has coordinates,has disorder","238595","2020-10-21","18:00:00",""
"1555388","10.2983","0.0004","10.6899","0.0005","13.1072","0.0006","90","","94.794","0.003","90","","1437.89","0.11","110","","110","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C34 H34 N4 O4 -","- C34 H34 N4 O4 -","- C68 H68 N8 O8 -","2","1","","Chingle, Ramesh; Lubell, William D.","Azopeptides: Synthesis and Pericyclic Chemistry.","Organic letters","2015","17","21","5400","5403","10.1021/acs.orglett.5b02723","","x-ray","1.34139","GaKα","","0.0576","0.0371","","","0.0778","0.0846","","","","","","1.03","","","","has coordinates,has disorder","238597","2020-10-21","18:00:00",""
"1555389","12.7295","0.0012","15.5318","0.0014","24.571","0.002","90","","90","","90","","4858","0.7","133","2","133","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C29 H25 Br N2 O3 -","- C29 H25 Br N2 O3 -","- C232 H200 Br8 N16 O24 -","8","1","","Li, Falin; Chen, Jiangfei; Hou, Yading; Li, Yujie; Wu, Xin-Yan; Tong, Xiaofeng","1,3-Dipolar Cycloadditions of 4-Acetoxy Allenoates: Access to 2,3-Dihydropyrazoles, 2,3-Dihydroisoxazoles, and Indolizines.","Organic letters","2015","17","21","5376","5379","10.1021/acs.orglett.5b02724","","","0.71073","MoKα","","0.058","0.0371","","","0.0825","0.0917","","","","","","1.017","","","","has coordinates","238599","2020-10-21","18:00:00",""
"1555390","7.4977","0.0014","11.606","0.002","23.037","0.005","90","","91.639","0.003","90","","2003.8","0.7","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C23 H25 N S2 -","- C23 H25 N S2 -","- C92 H100 N4 S8 -","4","1","","Yamauchi, Takayuki; Shibahara, Fumitoshi; Murai, Toshiaki","Direct C-H Bond Arylation of Thienyl Thioamides Catalyzed by Pd-Phenanthroline Complexes.","Organic letters","2015","17","21","5392","5395","10.1021/acs.orglett.5b02742","","","0.71075","MoKα","","0.1112","0.0648","","","0.1384","0.1616","","","","","","1.088","","","","has coordinates","238601","2020-10-21","18:00:00",""
"1555391","11.7863","0.0001","15.6266","0.0002","27.3025","0.0004","90","","90","","90","","5028.57","0.11","133","2","133","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C48 H70 Cl I2 N7 O -","- C48 H70 Cl I2 N7 O -","- C192 H280 Cl4 I8 N28 O4 -","4","1","","Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S.","Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors.","Organic letters","2015","17","23","5740","5743","10.1021/acs.orglett.5b02760","","","0.71073","MoKα","","0.0358","0.0319","","","0.0595","0.061","","","","","","1.082","","","","has coordinates","238603","2020-10-21","18:00:00",""
"1555392","16.4441","0.0003","19.3772","0.0003","19.7044","0.0003","90","","90","","90","","6278.62","0.18","133","2","133","2","","","","","","","","5","P n m a","-P 2ac 2n","62","","","","- C54.5 H73 Cl5 I2 N8 -","- C54.5 H73 Cl5 I2 N8 -","- C218 H292 Cl20 I8 N32 -","4","0.5","","Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S.","Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors.","Organic letters","2015","17","23","5740","5743","10.1021/acs.orglett.5b02760","","","0.71073","MoKα","","0.089","0.0711","","","0.1608","0.1697","","","","","","1.153","","","","has coordinates,has disorder","238603","2020-10-21","18:00:00",""
"1555393","50.2116","0.0013","8.9517","0.0002","25.5239","0.0007","90","","111.754","0.001","90","","10655.4","0.5","133","2","133","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C37 H35 I2 N7 -","- C37 H35 I2 N7 -","- C444 H420 I24 N84 -","12","1.5","","Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S.","Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors.","Organic letters","2015","17","23","5740","5743","10.1021/acs.orglett.5b02760","","","0.71073","MoKα","","0.0534","0.049","","","0.108","0.1107","","","","","","1.145","","","","has coordinates,has disorder","238603","2020-10-21","18:00:00",""
"1555394","20.9995","0.0003","15.2694","0.0002","28.6315","0.0004","90","","90.725","0.004","90","","9179.9","0.2","133","2","133","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C91 H108 Cl3 I4 N15 O4 -","- C91 H108 Cl3 I4 N15 O4 -","- C364 H432 Cl12 I16 N60 O16 -","4","1","","Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S.","Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors.","Organic letters","2015","17","23","5740","5743","10.1021/acs.orglett.5b02760","","","0.71073","MoKα","","0.04","0.0339","","","0.0735","0.0765","","","","","","1.087","","","","has coordinates","238603","2020-10-21","18:00:00",""
"1555395","17.3106","0.0003","15.673","0.0003","15.0038","0.0003","90","","109.469","0.0001","90","","3837.91","0.13","133","2","133","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C37 H35 I2 N7 O2 -","- C37 H35 I2 N7 O2 -","- C148 H140 I8 N28 O8 -","4","1","","Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S.","Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors.","Organic letters","2015","17","23","5740","5743","10.1021/acs.orglett.5b02760","","","0.71073","MoKα","","0.0343","0.0297","","","0.0701","0.072","","","","","","1.055","","","","has coordinates","238603","2020-10-21","18:00:00",""
"1555396","7.5247","0.0004","13.1309","0.0007","15.066","0.0008","90","","90","","90","","1488.61","0.14","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C13 H20 N2 O7 -","- C13 H20 N2 O7 -","- C52 H80 N8 O28 -","4","1","","Habibian, Maryam; Martínez-Montero, Saúl; Portella, Guillem; Chua, Zhijie; Bohle, D. Scott; Orozco, Modesto; Damha, Masad J.","Seven-Membered Ring Nucleoside Analogues: Stereoselective Synthesis and Studies on Their Conformational Properties.","Organic letters","2015","17","21","5416","5419","10.1021/acs.orglett.5b02769","","","0.71073","MoKα","","0.0376","0.0353","","","0.0976","0.0993","","","","","","1.076","","","","has coordinates","238605","2020-10-21","18:00:00",""
"1555397","20.9278","0.0013","20.9278","0.0013","11.7428","0.0016","90","","90","","120","","4454","0.7","100","2","100","2","","","","","","","","4","R -3 :H","-R 3","148","","","","- C62 H73.33 N13 O12 -","- C62 H73.38 N13 O12 -","- C186 H220.14 N39 O36 -","3","0.166667","","Ren, Changliang; Shen, Jie; Zeng, Huaqiang","One-Pot Synthesis of Strained Macrocyclic Pyridone Hexamers and Their High Selectivity toward Cu(2+) Recognition.","Organic letters","2015","17","24","5946","5949","10.1021/acs.orglett.5b02780","","","0.71073","MoKα","","0.0989","0.0838","","","0.2494","0.2672","","","","","","1.108","","","","has coordinates,has disorder","238607","2020-10-21","18:00:00",""
"1555398","7.2207","0.0006","10.6225","0.0008","10.6751","0.0008","90","","101.193","0.004","90","","803.23","0.11","100","2","100","2","","","","","","","","3","P 1 21 1","P 2yb","4","MW5-023","sarpong110","","- C19 H26 O2 -","- C19 H26 O2 -","- C38 H52 O4 -","2","1","","Weber, Manuel; Owens, Kyle; Masarwa, Ahmad; Sarpong, Richmond","Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction.","Organic letters","2015","17","21","5432","5435","10.1021/acs.orglett.5b02797","","","1.54178","CuKα","","0.0266","0.0261","","","0.0663","0.0668","","","","","","1.026","","","","has coordinates","238609","2020-10-21","18:00:00",""
"1555399","7.5988","0.0004","8.4424","0.0004","21.953","0.001","90","","90","","90","","1408.33","0.12","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","MW5128","sarpong118","","- C18 H22 O3 -","- C18 H22 O3 -","- C72 H88 O12 -","4","1","","Weber, Manuel; Owens, Kyle; Masarwa, Ahmad; Sarpong, Richmond","Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction.","Organic letters","2015","17","21","5432","5435","10.1021/acs.orglett.5b02797","","","0.71073","MoKα","","0.032","0.0314","","","0.0817","0.0823","","","","","","1.045","","","","has coordinates","238610","2020-10-21","18:00:00",""
"1555400","7.2672","0.0002","12.3762","0.0004","18.5597","0.0005","90","","90","","90","","1669.27","0.08","100","2","100","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","kro4-035","sarpong115","","- C20 H23 N O3 -","- C20 H23 N O3 -","- C80 H92 N4 O12 -","4","1","","Weber, Manuel; Owens, Kyle; Masarwa, Ahmad; Sarpong, Richmond","Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction.","Organic letters","2015","17","21","5432","5435","10.1021/acs.orglett.5b02797","","","1.54178","CuKα","","0.0296","0.0291","","","0.0748","0.0753","","","","","","1.089","","","","has coordinates","238613","2020-10-21","18:00:00",""
"1555401","7.5354","0.0006","8.5029","0.0008","11.9989","0.0011","90","","90.259","0.006","90","","768.79","0.12","100","2","100","2","","","","","","","","4","P 1 21 1","P 2yb","4","MW5-085","sarpong114","","- C19 H23 N O2 -","- C19 H23 N O2 -","- C38 H46 N2 O4 -","2","1","","Weber, Manuel; Owens, Kyle; Masarwa, Ahmad; Sarpong, Richmond","Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction.","Organic letters","2015","17","21","5432","5435","10.1021/acs.orglett.5b02797","","","1.54178","CuKα","","0.0691","0.0585","","","0.1491","0.1567","","","","","","1.064","","","","has coordinates","238614","2020-10-21","18:00:00",""
"1555402","6.5461","0.0002","8.998","0.0004","14.2101","0.0005","92.224","0.002","101.253","0.0019","92.809","0.002","818.92","0.05","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C22 H15 Cl O -","- C22 H15 Cl O -","- C44 H30 Cl2 O2 -","2","1","","Arunprasath, Dhanarajan; Muthupandi, Pandi; Sekar, Govindasamy","Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones.","Organic letters","2015","17","21","5448","5451","10.1021/acs.orglett.5b02803","","","0.71073","MoKα","","0.0448","0.0354","","","0.0863","0.0924","","","","","","1.049","","","","has coordinates","238616","2020-10-21","18:00:00",""
"1555403","6.253","0.0012","15.418","0.003","17.593","0.004","90","","92.18","0.007","90","","1694.9","0.6","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C22 H15 Br O -","- C22 H15 Br O -","- C88 H60 Br4 O4 -","4","1","","Arunprasath, Dhanarajan; Muthupandi, Pandi; Sekar, Govindasamy","Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones.","Organic letters","2015","17","21","5448","5451","10.1021/acs.orglett.5b02803","","","0.71073","MoKα","","0.0538","0.0307","","","0.0585","0.065","","","","","","1.007","","","","has coordinates","238619","2020-10-21","18:00:00",""
"1555404","16.0902","0.0014","5.6098","0.0005","17.2424","0.0013","90","","94.43","0.003","90","","1551.7","0.2","296","2","296","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C22 H16 O -","- C22 H16 O -","- C88 H64 O4 -","4","1","","Arunprasath, Dhanarajan; Muthupandi, Pandi; Sekar, Govindasamy","Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones.","Organic letters","2015","17","21","5448","5451","10.1021/acs.orglett.5b02803","","","0.71073","MoKα","","0.084","0.0564","","","0.1189","0.1354","","","","","","1.075","","","","has coordinates","238621","2020-10-21","18:00:00",""
"1555405","25.273","0.003","6.4369","0.0009","12.9596","0.0018","90","","90","","90","","2108.3","0.5","296","2","296","2","","","","","","","","5","P 21 21 2","P 2 2ab","18","","","","- C23 H22 Cl N O4 -","- C23 H22 Cl N O4 -","- C92 H88 Cl4 N4 O16 -","4","1","","Liu, Hua-Chao; Liu, Kang; Xue, Zhi-Yong; He, Zhao-Lin; Wang, Chun-Jiang","Silver(I)-Catalyzed Enantioselective Desymmetrization of Cyclopentenediones: Access to Highly Functionalized Bicyclic Pyrrolidines.","Organic letters","2015","17","21","5440","5443","10.1021/acs.orglett.5b02810","","","0.71073","MoKα","","0.0722","0.0535","","","0.1133","0.1238","","","","","","0.987","","","","has coordinates","238622","2020-10-21","18:00:00",""
"1555406","7.5529","0.0015","11.091","0.002","10.123","0.002","90","","104.11","0.03","90","","822.4","0.3","173.15","","173.15","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C17 H15 N O6 S -","- C17 H15 N O6 S -","- C34 H30 N2 O12 S2 -","2","1","","Li, Zequan; Shi, Yian","Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.","Organic letters","2015","17","23","5752","5755","10.1021/acs.orglett.5b02817","","","0.71073","MoKα","","0.0475","0.044","","","0.0883","0.0903","","","","","","1.123","","","","has coordinates","238624","2020-10-21","18:00:00",""
"1555407","7.7963","0.0006","11.5859","0.0007","23.086","0.0017","90","","90","","90","","2085.3","0.3","173.15","","173.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C24 H21 N O6 S -","- C24 H21 N O6 S -","- C96 H84 N4 O24 S4 -","4","1","","Li, Zequan; Shi, Yian","Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.","Organic letters","2015","17","23","5752","5755","10.1021/acs.orglett.5b02817","","","0.71073","MoKα","","0.0465","0.0431","","","0.0905","0.0921","","","","","","1.108","","","","has coordinates","238625","2020-10-21","18:00:00",""
"1555408","11.974","0.002","5.7044","0.0011","15.451","0.003","90","","95.49","0.03","90","","1050.5","0.3","173.15","","173.15","","","","","","","","","7","P 1 21 1","P 2yb","4","","","","- C18 H15 Br2 Cl2 N O5 S -","- C18 H15 Br2 Cl2 N O5 S -","- C36 H30 Br4 Cl4 N2 O10 S2 -","2","1","","Li, Zequan; Shi, Yian","Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.","Organic letters","2015","17","23","5752","5755","10.1021/acs.orglett.5b02817","","","0.71073","MoKα","","0.048","0.0465","","","0.1222","0.1248","","","","","","1.076","","","","has coordinates","238627","2020-10-21","18:00:00",""
"1555409","7.7017","0.0015","8.4118","0.0015","27.288","0.005","90","","90","","90","","1767.9","0.6","173.15","","173.15","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C20 H19 N O5 S -","- C20 H19 N O5 S -","- C80 H76 N4 O20 S4 -","4","1","","Li, Zequan; Shi, Yian","Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.","Organic letters","2015","17","23","5752","5755","10.1021/acs.orglett.5b02817","","","0.71073","MoKα","","0.0418","0.0405","","","0.1247","0.1262","","","","","","1.018","","","","has coordinates","238629","2020-10-21","18:00:00",""
"1555410","8.3457","0.0017","10.924","0.002","9.879","0.002","90","","109.46","0.03","90","","849.2","0.3","173.15","","173.15","","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C17 H14 N4 O5 S -","- C17 H14 N4 O5 S -","- C34 H28 N8 O10 S2 -","2","1","","Li, Zequan; Shi, Yian","Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.","Organic letters","2015","17","23","5752","5755","10.1021/acs.orglett.5b02817","","","0.71073","MoKα","","0.0382","0.0367","","","0.0907","0.0916","","","","","","1.074","","","","has coordinates","238631","2020-10-21","18:00:00",""
"1555411","8.091","0.006","6.973","0.005","15.224","0.011","90","","101.811","0.009","90","","840.7","1.1","173.15","","173.15","","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C17 H14 Br N O5 S -","- C17 H14 Br N O5 S -","- C34 H28 Br2 N2 O10 S2 -","2","1","","Li, Zequan; Shi, Yian","Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.","Organic letters","2015","17","23","5752","5755","10.1021/acs.orglett.5b02817","","","0.71073","MoKα","","0.049","0.0477","","","0.119","0.1206","","","","","","1.137","","","","has coordinates","238633","2020-10-21","18:00:00",""
"1555412","6.8957","0.0019","12.551","0.003","22.629","0.006","90","","90","","90","","1958.5","0.9","173.15","","173.15","","","","","","","","","7","P 21 21 21","P 2ac 2ab","19","","","","- C17 H12 Br F2 N O5 S -","- C17 H12 Br F2 N O5 S -","- C68 H48 Br4 F8 N4 O20 S4 -","4","1","","Li, Zequan; Shi, Yian","Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.","Organic letters","2015","17","23","5752","5755","10.1021/acs.orglett.5b02817","","","0.71073","MoKα","","0.0425","0.0397","","","0.095","0.0976","","","","","","1.104","","","","has coordinates","238635","2020-10-21","18:00:00",""
"1555413","11.289","0.003","10.612","0.003","32.425","0.006","90","","90","","90","","3884.5","1.7","173.15","","173.15","","","","","","","","","5","C 2 2 21","C 2c 2","20","","","","- C21 H17 N O5 S2 -","- C21 H17 N O5 S2 -","- C168 H136 N8 O40 S16 -","8","1","","Li, Zequan; Shi, Yian","Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.","Organic letters","2015","17","23","5752","5755","10.1021/acs.orglett.5b02817","","","0.71073","MoKα","","0.0712","0.0696","","","0.1557","0.1564","","","","","","1.171","","","","has coordinates","238636","2020-10-21","18:00:00",""
"1555414","9.155","0.003","9.47","0.003","23.095","0.007","90","","90","","90","","2002.3","1.1","173.15","","173.15","","","","","","","","","7","P 21 21 21","P 2ac 2ab","19","","","","- C19 H17 Br Cl N O5 S -","- C19 H17 Br Cl N O5 S -","- C76 H68 Br4 Cl4 N4 O20 S4 -","4","1","","Li, Zequan; Shi, Yian","Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds.","Organic letters","2015","17","23","5752","5755","10.1021/acs.orglett.5b02817","","","0.71073","MoKα","","0.0493","0.0459","","","0.1068","0.1102","","","","","","1.097","","","","has coordinates","238638","2020-10-21","18:00:00",""
"1555415","6.5953","0.0015","9.079","0.002","21.403","0.005","90","","90","","90","","1281.6","0.5","173","2","173","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C14 H22 O4 -","- C14 H22 O4 -","- C56 H88 O16 -","4","1","","Shen, Yang; Li, Linbin; Pan, Zhisheng; Wang, Yinglu; Li, Jundong; Wang, Kuangyu; Wang, Xiance; Zhang, Youyu; Hu, Tianhui; Zhang, Yandong","Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans.","Organic letters","2015","17","21","5480","5483","10.1021/acs.orglett.5b02845","","","0.71073","MoKα","","0.0512","0.0505","","","0.1765","0.1778","","","","","","1","","","","has coordinates","238640","2020-10-21","18:00:00",""
"1555416","7.2691","0.0008","11.4811","0.001","21.668","0.002","90","","90","","90","","1808.4","0.3","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C18 H28 O4 Si -","- C18 H28 O4 Si -","- C72 H112 O16 Si4 -","4","1","","Shen, Yang; Li, Linbin; Pan, Zhisheng; Wang, Yinglu; Li, Jundong; Wang, Kuangyu; Wang, Xiance; Zhang, Youyu; Hu, Tianhui; Zhang, Yandong","Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans.","Organic letters","2015","17","21","5480","5483","10.1021/acs.orglett.5b02845","","","0.71073","MoKα","","0.0633","0.0497","","","0.1263","0.1379","","","","","","0.879","","","","has coordinates","238640","2020-10-21","18:00:00",""
"1555417","7.187","0.0004","8.7702","0.0004","11.015","0.0006","90","","98.176","0.005","90","","687.23","0.06","293","2","293","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C15 H18 O7 -","- C15 H18 O7 -","- C30 H36 O14 -","2","1","","Shen, Yang; Li, Linbin; Pan, Zhisheng; Wang, Yinglu; Li, Jundong; Wang, Kuangyu; Wang, Xiance; Zhang, Youyu; Hu, Tianhui; Zhang, Yandong","Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans.","Organic letters","2015","17","21","5480","5483","10.1021/acs.orglett.5b02845","","","0.71073","MoKα","","0.0288","0.0279","","","0.0697","0.0702","","","","","","1.046","","","","has coordinates","238640","2020-10-21","18:00:00",""
"1555418","13.5602","0.0009","8.6298","0.0006","17.3709","0.0012","90","","92.1","0.002","90","","2031.4","0.2","150","2","150","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H16 F6 O9 -","- C17 H16 F6 O9 -","- C68 H64 F24 O36 -","4","1","","Nakhla, Mina C.; Lee, Che-Wah; Wood, John L.","Chemoselective Intramolecular Carbonyl Ylide Formation through Electronically Differentiated Malonate Diesters.","Organic letters","2015","17","23","5760","5763","10.1021/acs.orglett.5b02847","","","0.71073","MoKα","","0.1225","0.0647","","","0.1477","0.1763","","","","","","1.019","","","","has coordinates,has disorder","238642","2020-10-21","18:00:00",""
"1555419","6.4697","0.0006","11.6627","0.0011","16.0124","0.0014","90","","93.278","0.003","90","","1206.23","0.19","150","2","150","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C11 H17 O5 -","- C11 H16 O5 -","- C44 H64 O20 -","4","1","","Nakhla, Mina C.; Lee, Che-Wah; Wood, John L.","Chemoselective Intramolecular Carbonyl Ylide Formation through Electronically Differentiated Malonate Diesters.","Organic letters","2015","17","23","5760","5763","10.1021/acs.orglett.5b02847","","","0.71073","MoKα","","0.1458","0.078","","","0.1823","0.2192","","","","","","1.047","","","","has coordinates","238644","2020-10-21","18:00:00",""
"1555420","13.9325","0.0008","8.4366","0.0005","16.9502","0.0009","90","","92.536","0.002","90","","1990.4","0.2","150","2","150","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H19 F3 O9 -","- C17 H19 F3 O9 -","- C68 H76 F12 O36 -","4","1","","Nakhla, Mina C.; Lee, Che-Wah; Wood, John L.","Chemoselective Intramolecular Carbonyl Ylide Formation through Electronically Differentiated Malonate Diesters.","Organic letters","2015","17","23","5760","5763","10.1021/acs.orglett.5b02847","","","0.71073","MoKα","","0.0516","0.0395","","","0.093","0.1004","","","","","","1.043","","","","has coordinates,has disorder","238646","2020-10-21","18:00:00",""
"1555421","5.8376","0.0002","10.6992","0.0004","37.5454","0.0014","90","","90","","90","","2345","0.15","200","2","200","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C24 H31 N O5 S -","- C24 H31 N O5 S -","- C96 H124 N4 O20 S4 -","4","1","","Serpier, Fabien; Brayer, Jean-Louis; Folléas, Benoît; Darses, Sylvain","Access to Polyfunctionalized Chiral Piperidines through Enantioselective Addition-Carbocyclization Cascade Reaction Catalyzed by a Rhodium(I)-Diene Complex.","Organic letters","2015","17","21","5496","5499","10.1021/acs.orglett.5b02858","","","1.54178","CuKα","","0.0712","0.0447","","","0.0912","0.0994","","","","","","1.035","","","","has coordinates","238648","2020-10-21","18:00:00",""
"1555422","15.9311","0.001","9.7436","0.0006","9.2498","0.0006","90","","90","","90","","1435.81","0.16","100","2","100","2","","","","","","","","5","P b c n","-P 2n 2ab","60","","","","- C16 H18 Li N2 O -","- C16 H18 Li N2 O -","- C64 H72 Li4 N8 O4 -","4","0.5","","Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A.","Interaction of Azobenzene and Benzalaniline with Strong Amido Bases.","Organic letters","2015","17","24","6154","6157","10.1021/acs.orglett.5b02860","","","0.71073","MoKα","","0.0456","0.0415","","","0.1115","0.1142","","","","","","1.048","","","","has coordinates","238650","2020-10-21","18:00:00",""
"1555423","8.4866","0.0004","18.1483","0.0008","16.7017","0.0008","90","","97.928","0.001","90","","2547.8","0.2","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C28 H32 N2 Si2 -","- C28 H32 N2 Si2 -","- C112 H128 N8 Si8 -","4","1","","Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A.","Interaction of Azobenzene and Benzalaniline with Strong Amido Bases.","Organic letters","2015","17","24","6154","6157","10.1021/acs.orglett.5b02860","","","0.71073","MoKα","","0.0358","0.0319","","","0.0856","0.0877","","","","","","1.049","","","","has coordinates","238650","2020-10-21","18:00:00",""
"1555424","26.34","0.003","11.0689","0.0003","18.748","0.004","90","","134.32","0.02","90","","3910.7","1.6","100","2","100","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C44 H62 Li2 N4 O2 -","- C44 H62 Li2 N4 O2 -","- C176 H248 Li8 N16 O8 -","4","0.5","","Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A.","Interaction of Azobenzene and Benzalaniline with Strong Amido Bases.","Organic letters","2015","17","24","6154","6157","10.1021/acs.orglett.5b02860","","","0.71073","MoKα","","0.1008","0.062","","","0.1468","0.1666","","","","","","1.028","","","","has coordinates,has disorder","238650","2020-10-21","18:00:00",""
"1555425","13.9869","0.0011","12.5966","0.0011","19.4789","0.0018","90","","90","","90","","3431.9","0.5","100","2","100","2","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C39 H46 N2 Si2 -","- C39 H46 N2 Si2 -","- C156 H184 N8 Si8 -","4","1","","Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A.","Interaction of Azobenzene and Benzalaniline with Strong Amido Bases.","Organic letters","2015","17","24","6154","6157","10.1021/acs.orglett.5b02860","","","0.71073","MoKα","","0.034","0.0299","","","0.0721","0.074","","","","","","1.035","","","","has coordinates","238650","2020-10-21","18:00:00",""
"1555426","13.4038","0.0013","9.8242","0.0009","11.011","0.0011","90","","110.376","0.002","90","","1359.2","0.2","147","2","147","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C13 H15 B F N O5 -","- C13.001 H15.001 B F N O5 -","- C52.004 H60.004 B4 F4 N4 O20 -","4","1","","St Denis, Jeffrey D.; Lee, C. Frank; Yudin, Andrei K.","Access to Cyclic Amino Boronates via Rhodium-Catalyzed Functionalization of Alkyl MIDA Boronates.","Organic letters","2015","17","23","5764","5767","10.1021/acs.orglett.5b02861","","","0.71073","MoKα","","0.0447","0.039","","","0.1028","0.1065","","","","","","1.055","","","","has coordinates,has disorder","238653","2020-10-21","18:00:00",""
"1555427","10.3226","0.0004","15.7804","0.0007","11.1047","0.0005","90","","107.792","0.001","90","","1722.38","0.13","147","2","147","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C15.5 H20 B N2 O7.5 S -","- C15.5 H20 B N2 O7.5 S -","- C62 H80 B4 N8 O30 S4 -","4","1","","St Denis, Jeffrey D.; Lee, C. Frank; Yudin, Andrei K.","Access to Cyclic Amino Boronates via Rhodium-Catalyzed Functionalization of Alkyl MIDA Boronates.","Organic letters","2015","17","23","5764","5767","10.1021/acs.orglett.5b02861","","","0.71073","MoKα","","0.0325","0.0303","","","0.0819","0.0837","","","","","","1.029","","","","has coordinates,has disorder","238655","2020-10-21","18:00:00",""
"1555428","6.9371","0.0004","9.8082","0.0006","22.3442","0.0012","90","","90","","90","","1520.31","0.15","171.5","","171.5","","","","","","","","","5","P n m a","-P 2ac 2n","62","","","","- C15 H12 Cl2 O S2 -","- C15 H12 Cl2 O S2 -","- C60 H48 Cl8 O4 S8 -","4","0.5","","Huang, Xin; Wang, Jichao; Ni, Zhangqin; Wang, Sichang; Pan, Yuanjiang","Synthesis of α,α-Disulfenylated Aldehydes via Oxidative Transformation of Tertiary Amines.","Organic letters","2015","17","21","5488","5491","10.1021/acs.orglett.5b02876","","","0.71073","MoKα","","0.0339","0.029","","","0.0747","0.0778","","","","","","1.095","","","","has coordinates,has disorder","238656","2020-10-21","18:00:00",""
"1555429","10.1789","0.0004","11.9937","0.0005","13.2135","0.0005","108.6","0.001","95.189","0.001","102.354","0.001","1471.38","0.1","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C82 H54 N4 -","- C82 H54 N4 -","- C82 H54 N4 -","1","0.5","","Liu, Yulong; Shan, Tong; Yao, Liang; Bai, Qing; Guo, Yachen; Li, Jinyu; Han, Xiao; Li, Weijun; Wang, Zhiming; Yang, Bing; Lu, Ping; Ma, Yuguang","Isomers of Pyrene-Imidazole Compounds: Synthesis and Configuration Effect on Optical Properties.","Organic letters","2015","17","24","6138","6141","10.1021/acs.orglett.5b02879","","","0.71073","MoKα","","0.0723","0.048","","","0.1244","0.1416","","","","","","1.018","","","","has coordinates","238658","2020-10-21","18:00:00",""
"1555430","10.0347","0.0008","11.9855","0.001","25.329","0.002","77.339","0.002","87.855","0.002","87.767","0.002","2968.7","0.4","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C82 H54 N4 -","- C82 H54 N4 -","- C164 H108 N8 -","2","1","","Liu, Yulong; Shan, Tong; Yao, Liang; Bai, Qing; Guo, Yachen; Li, Jinyu; Han, Xiao; Li, Weijun; Wang, Zhiming; Yang, Bing; Lu, Ping; Ma, Yuguang","Isomers of Pyrene-Imidazole Compounds: Synthesis and Configuration Effect on Optical Properties.","Organic letters","2015","17","24","6138","6141","10.1021/acs.orglett.5b02879","","","0.71073","MoKα","","0.0835","0.0527","","","0.1406","0.1671","","","","","","1.019","","","","has coordinates","238660","2020-10-21","18:00:00",""
"1555431","12.275","0.003","11.187","0.002","13.371","0.003","90","","104.835","0.004","90","","1774.9","0.7","100","2","100","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C20 H15 Cl N2 O5 -","- C20 H15 Cl N2 O5 -","- C80 H60 Cl4 N8 O20 -","4","2","","Gao, Hang; Luo, Zhenli; Ge, Pingjin; He, Junqian; Zhou, Feng; Zheng, Peipei; Jiang, Jun","Direct Catalytic Asymmetric Synthesis of β-Hydroxy Acids from Malonic Acid.","Organic letters","2015","17","24","5962","5965","10.1021/acs.orglett.5b02891","","","0.71073","MoKα","","0.0273","0.0259","","","0.0739","0.087","","","","","","1.015","","","","has coordinates","238662","2020-10-21","18:00:00",""
"1555432","13.5437","0.0009","13.0346","0.0008","16.0277","0.0011","90","","102.411","0.002","90","","2763.4","0.3","273","2","273","2","","","","","","","","7","P 1 21 1","P 2yb","4","","","","- C25.5 H31 Cl1.5 N2 O5 P S -","- C25.5 H31 Cl1.5 N2 O5 P S -","- C102 H124 Cl6 N8 O20 P4 S4 -","4","2","","Kayal, Satavisha; Mukherjee, Santanu","Catalytic Aldol-Cyclization Cascade of 3-Isothiocyanato Oxindoles with α-Ketophosphonates for the Enantioselective Synthesis of β-Amino-α-hydroxyphosphonates.","Organic letters","2015","17","21","5508","5511","10.1021/acs.orglett.5b02929","","","0.71073","MoKα","","0.0479","0.0445","","","0.1138","0.117","","","","","","1.069","","","","has coordinates","279649","2022-11-30","18:17:27",""
"1555433","8.9711","0.0012","9.9056","0.0012","10.1296","0.0013","90","","94.135","0.003","90","","897.8","0.2","130","","130","","","","","","","","","6","P 1 c 1","P -2yc","7","","","","- C19 H18 F3 N O2 S -","- C19 H18 F3 N O2 S -","- C38 H36 F6 N2 O4 S2 -","2","1","","Zhu, Zi-Zhong; Chen, Kai; Yu, Liu-Zhu; Tang, Xiang-Ying; Shi, Min","Copper(I)-Catalyzed Intramolecular Trifluoromethylation of Methylenecyclopropanes.","Organic letters","2015","17","24","5994","5997","10.1021/acs.orglett.5b02940","","","0.71073","MoKα","","0.0846","0.0743","","","0.1954","0.209","","","","","","1.02","","","","has coordinates","238665","2020-10-21","18:00:00",""
"1555434","7.63737","0.00019","22.5914","0.0007","15.1095","0.0004","90","","99.906","0.003","90","","2568.11","0.12","293","","293","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C40 H20 O3 -","- C40 H20 O3 -","- C160 H80 O12 -","4","1","","Shyam Sundar, M.; Bedekar, Ashutosh V.","Synthesis and Study of 7,12,17-Trioxa[11]helicene.","Organic letters","2015","17","23","5808","5811","10.1021/acs.orglett.5b02948","","","1.54184","CuKα","","0.0522","0.0427","","","0.1124","0.1209","","","","","","1.0523","","","","has coordinates","238667","2020-10-21","18:00:00",""
"1555435","23.0883","0.001","8.2485","0.0004","17.6035","0.0008","90","","90","","90","","3352.5","0.3","293","2","293","2","","","","","","","","3","P n a 21","P 2c -2n","33","","","","- C22 H16 O4 -","- C22 H16 O4 -","- C176 H128 O32 -","8","2","","Shyam Sundar, M.; Bedekar, Ashutosh V.","Synthesis and Study of 7,12,17-Trioxa[11]helicene.","Organic letters","2015","17","23","5808","5811","10.1021/acs.orglett.5b02948","","","0.71073","MoKα","","0.0788","0.0533","","","0.1055","0.1179","","","","","","1.034","","","","has coordinates","238668","2020-10-21","18:00:00",""
"1555436","37.9789","0.001","14.5891","0.0004","21.4715","0.0006","90","","119.848","0.0007","90","","10318.8","0.5","200","2","200","2","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C24 H24 N4 O3 -","- C24 H24 N4 O3 -","- C384 H384 N64 O48 -","16","4","","Yang, Van-Wei; Hong, Bor-Cherng; Kao, Hsin-Kai; Tu, Ting-Hsun; Shen, Jiun-Yi; Chen, Chi-Lin; Lee, Gene-Hsiang; Chou, Pi-Tai","One-Pot Dichotomous Construction of Inside-Azayohimban and Pro-Azayohimban Systems via an Enantioselective Organocatalytic Cascade; Their Use as a Model to Probe the (Aza-)Indole Local Solvent Environment.","Organic letters","2015","17","23","5816","5819","10.1021/acs.orglett.5b02949","","","0.71073","MoKα","","0.0672","0.0528","","","0.1326","0.1398","","","","","","1.059","","","","has coordinates,has disorder","238670","2020-10-21","18:00:00",""
"1555437","8.2785","0.0002","9.2956","0.0002","29.7576","0.0007","90","","90","","90","","2289.96","0.09","200","2","200","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C25 H28 N4 O5 -","- C25 H28 N4 O5 -","- C100 H112 N16 O20 -","4","1","","Yang, Van-Wei; Hong, Bor-Cherng; Kao, Hsin-Kai; Tu, Ting-Hsun; Shen, Jiun-Yi; Chen, Chi-Lin; Lee, Gene-Hsiang; Chou, Pi-Tai","One-Pot Dichotomous Construction of Inside-Azayohimban and Pro-Azayohimban Systems via an Enantioselective Organocatalytic Cascade; Their Use as a Model to Probe the (Aza-)Indole Local Solvent Environment.","Organic letters","2015","17","23","5816","5819","10.1021/acs.orglett.5b02949","","","0.71073","MoKα","","0.0909","0.04","","","0.0785","0.1047","","","","","","1.002","","","","has coordinates","238672","2020-10-21","18:00:00",""
"1555438","19.5349","0.0019","6.5541","0.0007","34.67","0.004","90","","95.943","0.005","90","","4415.1","0.8","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C44 H63 N5 O11 -","- C44 H63 N5 O11 -","- C176 H252 N20 O44 -","4","1","","Tabor, M. Greg; Shenvi, Ryan A.","Synthesis of Lepadiformine Using a Hydroamination Transform.","Organic letters","2015","17","23","5776","5779","10.1021/acs.orglett.5b02992","","","0.71073","MoKα","","0.1006","0.0664","","","0.1364","0.15","","","","","","1.056","","","","has coordinates,has disorder","238674","2020-10-21","18:00:00",""
"1555439","7.0716","0.0005","6.6011","0.0003","13.3983","0.001","90","","92.659","0.006","90","","624.76","0.07","292","","292","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C15 H15 N O -","- C15 H15 N O -","- C30 H30 N2 O2 -","2","1","","Vita, Maria Victoria; Caramenti, Paola; Waser, Jerome","Enantioselective Synthesis of Homoallylic Azides and Nitriles via Palladium-Catalyzed Decarboxylative Allylation.","Organic letters","2015","17","23","5832","5835","10.1021/acs.orglett.5b03002","","","1.54186","CuKα","","0.0409","0.0354","","","0.0918","0.0955","","","","","","1.131","","","","has coordinates","238676","2020-10-21","18:00:00",""
"1555440","8.9762","0.001","9.2143","0.001","15.8055","0.001","91.311","0.007","97.75","0.007","93.388","0.009","1292.4","0.2","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C29 H30 Br N3 O -","- C29 H30 Br N3 O -","- C58 H60 Br2 N6 O2 -","2","1","","Duan, Xiao-Yong; Yang, Xiu-Long; Jia, Pan-Pan; Zhang, Man; Han, Bing","Hydrazonyl Radical-Participated Tandem Reaction: A Strategy for the Synthesis of Pyrazoline-Functionalized Oxindoles.","Organic letters","2015","17","24","6022","6025","10.1021/acs.orglett.5b03003","","","0.71","MoKα","","0.0752","0.0646","","","0.1871","0.2043","","","","","","1.105","","","","has coordinates,has disorder","238678","2020-10-21","18:00:00",""
"1555441","9.2686","0.0015","16.156","0.003","9.4109","0.0016","90","","95.246","0.002","90","","1403.3","0.4","173","","173","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C18 H13 N O3 -","- C18 H13 N O3 -","- C72 H52 N4 O12 -","4","1","","Sengoku, Tetsuya; Murata, Yusuke; Aso, Yuwa; Kawakami, Ai; Inuzuka, Toshiyasu; Sakamoto, Masami; Takahashi, Masaki; Yoda, Hidemi","Indium-Catalyzed Amide Allylation of N-Carbonyl Imides: Formation of Azaspiro-γ-lactones via Ring Opening-Reclosure.","Organic letters","2015","17","23","5846","5849","10.1021/acs.orglett.5b03021","","","0.71073","","","0.0429","0.0379","","","0.0937","0.0969","","","","","","1.061","","","","has coordinates","238680","2020-10-21","18:00:00",""
"1555442","25.299","0.002","19.2324","0.0013","28.254","0.004","90","","91.806","0.009","90","","13740","2","120","10","120","0.1","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C104 H170 Cl8 Cu2 N16 O17 -","- C104 H170 Cl8 Cu2 N16 O17 -","- C416 H680 Cl32 Cu8 N64 O68 -","4","0.5","","Ganss, Alexander; Belda, Raquel; Pitarch, Javier; Goddard, Richard; García-España, Enrique; Kubik, Stefan","Synthesis and Structural Characterization of a Cyclen-Derived Molecular Cage.","Organic letters","2015","17","23","5850","5853","10.1021/acs.orglett.5b03027","","","0.7107","MoKα","","0.1702","0.1148","","","0.2927","0.3454","","","","","","0.95","","","","has coordinates,has disorder","238682","2020-10-21","18:00:00",""
"1555443","16.0245","0.0009","8.5681","0.0005","19.233","0.0011","90","","95.076","0.002","90","","2630.3","0.3","105","","105","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C28 H32 Br N3 O3 -","- C28 H32 Br N3 O3 -","- C112 H128 Br4 N12 O12 -","4","1","","Douchez, Antoine; Lubell, William D.","Chemoselective Alkylation for Diversity-Oriented Synthesis of 1,3,4-Benzotriazepin-2-ones and Pyrrolo[1,2][1,3,4]benzotriazepin-6-ones, Potential Turn Surrogates.","Organic letters","2015","17","24","6046","6049","10.1021/acs.orglett.5b03046","","x-ray","1.34139","GaKα","","0.0292","0.0272","","","0.073","0.0746","","","","","","1.049","","","","has coordinates","238685","2020-10-21","18:00:00",""
"1555444","8.8959","0.0011","13.3302","0.0016","15.9639","0.0019","90","","91.132","0.005","90","","1892.7","0.4","100","","100","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C20 H15 Br Cl N3 O3 -","- C20 H15 Br Cl N3 O3 -","- C80 H60 Br4 Cl4 N12 O12 -","4","1","","Douchez, Antoine; Lubell, William D.","Chemoselective Alkylation for Diversity-Oriented Synthesis of 1,3,4-Benzotriazepin-2-ones and Pyrrolo[1,2][1,3,4]benzotriazepin-6-ones, Potential Turn Surrogates.","Organic letters","2015","17","24","6046","6049","10.1021/acs.orglett.5b03046","","x-ray","1.34139","GaKα","","0.0434","0.0425","","","0.114","0.1149","","","","","","1.071","","","","has coordinates","238685","2020-10-21","18:00:00",""
"1555445","8.7322","0.0007","9.9954","0.0007","12.0561","0.001","78.166","0.007","89.574","0.007","82.698","0.006","1021.37","0.14","150","2","150","2","","","","","","","","4","P -1","-P 1","2","","","","- C24 H21 N5 O2 -","- C24 H21 N5 O2 -","- C48 H42 N10 O4 -","2","1","","Ramanathan, Mani; Wang, Yu-Hao; Liu, Shiuh-Tzung","One-Pot Reactions for Synthesis of 2,5-Substituted Tetrazoles from Aryldiazonium Salts and Amidines.","Organic letters","2015","17","23","5886","5889","10.1021/acs.orglett.5b03068","","","1.54178","CuKα","","0.0809","0.0524","","","0.1163","0.1365","","","","","","1.047","","","","has coordinates","238688","2020-10-21","18:00:00",""
"1555446","9.0068","0.0002","10.478","0.0003","16.4734","0.0004","90","","90","","90","","1554.65","0.07","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C18 H22 O2 -","- C18 H22 O2 -","- C72 H88 O8 -","4","1","","Lai, Zengwei; Wang, Zhaobin; Sun, Jianwei","Organocatalytic Asymmetric Nucleophilic Addition to o-Quinone Methides by Alcohols.","Organic letters","2015","17","24","6058","6061","10.1021/acs.orglett.5b03072","","x-ray","1.54184","CuKα","","0.0424","0.0352","","","0.0835","0.0883","","","","","","1","","","","has coordinates","238689","2020-10-21","18:00:00",""
"1555447","15.108","0.0007","7.54","0.0005","27.9119","0.0014","90","","90","","90","","3179.6","0.3","293","2","293","2","","","","","","","","3","P b c a","-P 2ac 2ab","61","","7-methoxy-1-(4-methoxyphenyl)-9H-fluoren-9-one","","- C21 H16 O3 -","- C21 H16 O3 -","- C168 H128 O24 -","8","1","","Ravi Kumar, Devarapalli; Satyanarayana, Gedu","Domino Oxidative [Pd]-Catalysis: One-Pot Synthesis of Fluorenones Starting from Simple Benzylamines and Iodo Arenes.","Organic letters","2015","17","23","5894","5897","10.1021/acs.orglett.5b03077","","","1.54184","CuKα","","0.0806","0.0622","","","0.1677","0.1986","","","","","","1.052","","","","has coordinates","238690","2020-10-21","18:00:00",""
"1555448","7.8593","0.001","4.0079","0.0005","36.679","0.004","90","","93.567","0.011","90","","1153.1","0.2","293","","293","","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","2,7-dimethoxy-9H-fluoren-9-one","","- C15 H12 O3 -","- C15 H12 O3 -","- C60 H48 O12 -","4","1","","Ravi Kumar, Devarapalli; Satyanarayana, Gedu","Domino Oxidative [Pd]-Catalysis: One-Pot Synthesis of Fluorenones Starting from Simple Benzylamines and Iodo Arenes.","Organic letters","2015","17","23","5894","5897","10.1021/acs.orglett.5b03077","","","1.54184","CuKα","","0.1158","0.0849","","","0.2458","0.2543","","","","","","1.361","","","","has coordinates","238691","2020-10-21","18:00:00",""
"1555449","20.0748","0.0007","6.8584","0.0003","25.9078","0.0009","90","","106.399","0.001","90","","3421.9","0.2","100","2","100","2","","","","","","","","3","C 1 2 1","C 2y","5","","","","- C20 H30 O2 -","- C20 H30 O2 -","- C160 H240 O16 -","8","2","","Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong","Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.","Organic letters","2015","17","24","6062","6065","10.1021/acs.orglett.5b03079","","","1.54178","CuKα","","0.0948","0.0936","","","0.2628","0.2745","","","","","","1.387","","","","has coordinates","238694","2020-10-21","18:00:00",""
"1555450","11.623","0.003","7.3026","0.0016","12.673","0.003","90","","95.271","0.003","90","","1071.1","0.4","100","2","100","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C24 H36 O4 -","- C24 H36 O4 -","- C48 H72 O8 -","2","1","","Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong","Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.","Organic letters","2015","17","24","6062","6065","10.1021/acs.orglett.5b03079","","","0.71073","MoKα","","0.0631","0.0462","","","0.1051","0.1163","","","","","","1.033","","","","has coordinates","238696","2020-10-21","18:00:00",""
"1555451","31.775","0.005","7.261","0.0011","19.184","0.003","90","","104.026","0.002","90","","4294.1","1.2","100","2","100","2","","","","","","","","3","C 1 2 1","C 2y","5","","","","- C24 H36 O4 -","- C24 H36 O4 -","- C192 H288 O32 -","8","2","","Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong","Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.","Organic letters","2015","17","24","6062","6065","10.1021/acs.orglett.5b03079","","","0.71073","MoKα","","0.077","0.0668","","","0.1888","0.1942","","","","","","1.101","","","","has coordinates","238698","2020-10-21","18:00:00",""
"1555452","10.27","0.002","7.257","0.0016","14.424","0.003","90","","92.479","0.003","90","","1074","0.4","100","2","100","2","","","","","","","","3","P 1 21 1","P 2yb","4","","","","- C24 H36 O4 -","- C24 H36 O4 -","- C48 H72 O8 -","2","1","","Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong","Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.","Organic letters","2015","17","24","6062","6065","10.1021/acs.orglett.5b03079","","","0.71073","MoKα","","0.0485","0.0399","","","0.0969","0.1018","","","","","","1.054","","","","has coordinates","238700","2020-10-21","18:00:00",""
"1555453","10.0955","0.0006","13.4185","0.0008","24.927","0.0015","90","","90","","90","","3376.8","0.3","100","2","100","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C38 H54 O5 -","- C38 H54 O5 -","- C152 H216 O20 -","4","1","","Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong","Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization.","Organic letters","2015","17","24","6062","6065","10.1021/acs.orglett.5b03079","","","1.54178","CuKα","","0.0662","0.05","","","0.1464","0.1552","","","","","","1.104","","","","has coordinates","238702","2020-10-21","18:00:00",""
"1555454","8.2413","0.0004","12.7682","0.0006","15.6926","0.0006","80.64","0.003","82.824","0.003","75.922","0.004","1574.06","0.13","100.01","0.1","100.01","0.1","","","","","","","synthesis as described","6","P -1","-P 1","2","","","","- C62 H84 N8 O2 S2 Si4 -","- C62 H84 N8 O2 S2 Si4 -","- C62 H84 N8 O2 S2 Si4 -","1","0.5","","Cortizo-Lacalle, Diego; Gozalvez, Cristian; Olano, Mikel; Sun, Xiangnan; Melle-Franco, Manuel; Hueso, Luis E.; Mateo-Alonso, Aurelio","Bisthiadiazole-Fused Tetraazapentacenequinone: An Air-Stable Solution-Processable n-Type Organic Semiconductor.","Organic letters","2015","17","23","5902","5905","10.1021/acs.orglett.5b03099","","x-ray","1.54184","","","0.0671","0.0424","","","0.0833","0.0929","","","","","","0.982","","","","has coordinates","238705","2020-10-21","18:00:00",""
"1555455","9.8014","0.0013","12.1207","0.0015","13.323","0.003","99.552","0.015","106.402","0.016","111.742","0.012","1343.8","0.5","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C31 H23 Cl2 N O4 S -","- C31 H23 Cl2 N O4 S -","- C62 H46 Cl4 N2 O8 S2 -","2","1","","Zhu, Yi-Long; Jiang, Bo; Hao, Wen-Juan; Qiu, Jiang-Kai; Sun, Jun; Wang, De-Cai; Wei, Ping; Wang, Ai-Fang; Li, Guigen; Tu, Shu-Jiang","Catalytic Arylsulfonyl Radical Triggered 1,7-Enyne Bicyclizations.","Organic letters","2015","17","24","6078","6081","10.1021/acs.orglett.5b03100","","","0.71073","MoKα","","0.1619","0.0891","","","0.2108","0.264","","","","","","1.048","","","","has coordinates","238708","2020-10-21","18:00:00",""
"1555456","7.3264","0.0004","7.7051","0.0006","23.332","0.0014","84.594","0.001","88.837","0.002","82.404","0.001","1299.7","0.15","298","2","298","2","","","","","","","","6","P -1","-P 1","2","","","","- C30 H21 Cl2 N O3 S -","- C30 H21 Cl2 N O3 S -","- C60 H42 Cl4 N2 O6 S2 -","2","1","","Zhu, Yi-Long; Jiang, Bo; Hao, Wen-Juan; Qiu, Jiang-Kai; Sun, Jun; Wang, De-Cai; Wei, Ping; Wang, Ai-Fang; Li, Guigen; Tu, Shu-Jiang","Catalytic Arylsulfonyl Radical Triggered 1,7-Enyne Bicyclizations.","Organic letters","2015","17","24","6078","6081","10.1021/acs.orglett.5b03100","","","0.71073","MoKα","","0.1809","0.1041","","","0.2512","0.2841","","","","","","1.093","","","","has coordinates","238710","2020-10-21","18:00:00",""
"1555457","9.5468","0.0005","10.4076","0.0006","11.3179","0.0007","103.653","0.005","93.612","0.005","114.414","0.006","978.53","0.12","291","2","291.15","","","","","","","","","5","P -1","-P 1","2","","","","- C23 H18 N2 O3 S -","- C23 H18 N2 O3 S -","- C46 H36 N4 O6 S2 -","2","1","","Qiao, Huijie; Sun, Suyan; Yang, Fan; Zhu, Yu; Zhu, Weiguo; Dong, Yaxi; Wu, Yusheng; Kong, Xiangtao; Jiang, Ling; Wu, Yangjie","Copper(I)-Catalyzed Sulfonylation of 8-Aminoquinoline Amides with Sulfonyl Chlorides in Air.","Organic letters","2015","17","24","6086","6089","10.1021/acs.orglett.5b03114","","","1.54184","CuKα","","0.0597","0.0522","","","0.1423","0.1513","","","","","","1.051","","","","has coordinates","238713","2020-10-21","18:00:00",""
"1555458","7.398","0.002","11.831","0.003","25.874","0.007","90","","94.823","0.018","90","","2256.6","1","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C56 H40 F6 N6 -","- C56 H40 F6 N6 -","- C112 H80 F12 N12 -","2","0.5","","Tasior, Mariusz; Chotkowski, Maciej; Gryko, Daniel T.","Extension of Pyrrolopyrrole π-System: Approach to Constructing Hexacyclic Nitrogen-Containing Aromatic Systems.","Organic letters","2015","17","24","6106","6109","10.1021/acs.orglett.5b03129","","","1.54178","CuKα","","0.0862","0.0639","","","0.1661","0.184","","","","","","1.069","","","","has coordinates","238715","2020-10-21","18:00:00",""
"1555459","10.6194","0.0012","15.7603","0.0018","16.3359","0.0018","73.944","0.003","87.761","0.003","73.938","0.003","2522.8","0.5","173","2","173","2","","","","","","","","3","P -1","-P 1","2","","","","- C136 H112 O -","- C136 H112 O -","- C136 H112 O -","1","0.5","","He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong","High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.","Organic letters","2015","17","24","6174","6177","10.1021/acs.orglett.5b03152","","","0.71073","MoKα","","0.1677","0.0637","","","0.1181","0.1517","","","","","","1.01","","","","has coordinates","238717","2020-10-21","18:00:00",""
"1555460","9.9913","0.0007","15.4197","0.0012","15.7043","0.0013","102.428","0.003","92.308","0.003","99.776","0.002","2321","0.3","173","2","173","2","","","","","","","","3","P -1","-P 1","2","","","","- C62.74 H45.48 Cl1.48 -","- C62.743 H45.486 Cl1.486 -","- C125.486 H90.972 Cl2.972 -","2","1","","He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong","High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.","Organic letters","2015","17","24","6174","6177","10.1021/acs.orglett.5b03152","","","0.71073","MoKα","","0.1356","0.0583","","","0.1207","0.148","","","","","","1.01","","","","has coordinates,has disorder","238719","2020-10-21","18:00:00",""
"1555461","10.2023","0.0013","12.2529","0.0014","16.1191","0.0019","98.99","0.03","102.37","0.03","105.55","0.03","1846.7","0.6","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C104 H80 O -","- C104 H80 O -","- C104 H80 O -","1","0.5","","He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong","High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.","Organic letters","2015","17","24","6174","6177","10.1021/acs.orglett.5b03152","","","0.71073","MoKα","","0.1839","0.0722","","","0.1547","0.2176","","","","","","1.073","","","","has coordinates","238721","2020-10-21","18:00:00",""
"1555462","10.11","0.002","10.19","0.002","36.97","0.007","91.2","0.03","94.1","0.03","95.6","0.03","3779.3","1.3","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C52 H40 O0.5 -","- C52 H40 O0.5 -","- C208 H160 O2 -","4","2","","He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong","High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.","Organic letters","2015","17","24","6174","6177","10.1021/acs.orglett.5b03152","","","0.71073","MoKα","","0.2558","0.1127","","","0.273","0.341","","","","","","1.198","","","","has coordinates,has disorder","279649","2022-11-30","18:17:27",""
"1555463","30.72","0.003","17.174","0.0011","16.373","0.0012","90","","97.824","0.003","90","","8557.7","1.2","173","2","173","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C58 H52 O -","- C58 H52 O -","- C464 H416 O8 -","8","1","","He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong","High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes.","Organic letters","2015","17","24","6174","6177","10.1021/acs.orglett.5b03152","","","0.71073","MoKα","","0.1893","0.1061","","","0.2099","0.2442","","","","","","1.188","","","","has coordinates,has disorder","238725","2020-10-21","18:00:00",""
"1555464","13.0804","0.0014","18.104","0.002","15.8995","0.0017","90","","102.512","0.003","90","","3675.7","0.7","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H17 Cl N2 O1.425 -","- C19 H17 Cl N2 O1.42655 -","- C152 H136 Cl8 N16 O11.4124 -","8","2","","Jiang, Pingping; Li, Feng; Xu, Yongbao; Liu, Qingwen; Wang, Jing; Ding, Hong; Yu, Renfu; Wang, Qifeng","Aromaticity-Dependent Regioselectivity in Pd(II)-Catalyzed C-H Direct Arylation of Aryl Ureas.","Organic letters","2015","17","23","5918","5921","10.1021/acs.orglett.5b03153","","x-ray","0.71073","MoKα","","0.2165","0.091","","","0.2799","0.329","","","","","","0.918","","","","has coordinates,has disorder","279649","2022-11-30","18:17:27",""
"1555465","9.2786","0.0015","23.641","0.004","7.5289","0.0011","90","","90","","90","","1651.5","0.5","293","2","293","2","","","","","","","","3","P n a 21","P 2c -2n","33","","","","- C21 H14 O4 -","- C21 H14 O4 -","- C84 H56 O16 -","4","1","","Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong","Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.","Organic letters","2015","17","23","5926","5929","10.1021/acs.orglett.5b03160","","","0.71073","MoKα","","0.067","0.0409","","","0.0893","0.1006","","","","","","0.936","","","","has coordinates","238731","2020-10-21","18:00:00",""
"1555466","13.899","0.003","6.5834","0.0012","14.579","0.003","90","","117.751","0.003","90","","1180.6","0.4","293","2","293","2","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C15 H12 O3 -","- C15 H12 O3 -","- C60 H48 O12 -","4","1","","Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong","Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.","Organic letters","2015","17","23","5926","5929","10.1021/acs.orglett.5b03160","","","0.71073","MoKα","","0.0632","0.0468","","","0.1228","0.1326","","","","","","1.07","","","","has coordinates","238733","2020-10-21","18:00:00",""
"1555467","7.3238","0.0008","9.814","0.0011","19.747","0.002","90","","90","","90","","1419.3","0.3","130","","130","","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C20 H14 O2 -","- C20 H14 O2 -","- C80 H56 O8 -","4","1","","Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong","Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.","Organic letters","2015","17","23","5926","5929","10.1021/acs.orglett.5b03160","","","0.71073","MoKα","","0.0784","0.0491","","","0.0937","0.1054","","","","","","0.998","","","","has coordinates","238735","2020-10-21","18:00:00",""
"1555468","10.271","0.0011","9.1771","0.001","11.2051","0.0012","90","","97.686","0.002","90","","1046.7","0.2","130","","130","","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C14 H10 O3 -","- C14 H10 O3 -","- C56 H40 O12 -","4","1","","Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong","Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.","Organic letters","2015","17","23","5926","5929","10.1021/acs.orglett.5b03160","","","0.71073","MoKα","","0.0542","0.0434","","","0.1155","0.1237","","","","","","1.053","","","","has coordinates","238737","2020-10-21","18:00:00",""
"1555469","12.5409","0.0014","7.8473","0.0008","31.588","0.003","90","","90","","90","","3108.6","0.6","130","","130","","","","","","","","","3","P b c a","-P 2ac 2ab","61","","","","- C22 H14 O3 -","- C22 H14 O3 -","- C176 H112 O24 -","8","1","","Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong","Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.","Organic letters","2015","17","23","5926","5929","10.1021/acs.orglett.5b03160","","","0.71073","MoKα","","0.0739","0.0467","","","0.1095","0.1241","","","","","","1.019","","","","has coordinates","238739","2020-10-21","18:00:00",""
"1555470","6.866","0.005","10.24","0.007","11.188","0.007","69.311","0.011","72.734","0.012","83.093","0.013","702.6","0.8","130","2","130","","","","","","","","","3","P -1","-P 1","2","","","","- C19 H14 O3 -","- C19 H14 O3 -","- C38 H28 O6 -","2","1","","Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong","Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.","Organic letters","2015","17","23","5926","5929","10.1021/acs.orglett.5b03160","","","0.71073","MoKα","","0.1169","0.0767","","","0.1861","0.223","","","","","","0.983","","","","has coordinates","238741","2020-10-21","18:00:00",""
"1555471","4.629","0.002","16.421","0.008","17.474","0.008","90","","91.158","0.01","90","","1328","1.1","130","","130","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H13 N O3 -","- C17 H13 N O3 -","- C68 H52 N4 O12 -","4","1","","Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong","Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.","Organic letters","2015","17","23","5926","5929","10.1021/acs.orglett.5b03160","","","0.71073","MoKα","","0.0896","0.068","","","0.1958","0.2214","","","","","","1.043","","","","has coordinates","238743","2020-10-21","18:00:00",""
"1555472","7.4224","0.0019","7.787","0.002","12.133","0.003","99.775","0.005","91.453","0.005","97.925","0.005","683.6","0.3","293","2","293","2","","","","","","","","3","P -1","-P 1","2","","","","- C18 H12 O3 -","- C18 H12 O3 -","- C36 H24 O6 -","2","1","","Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong","Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols.","Organic letters","2015","17","23","5926","5929","10.1021/acs.orglett.5b03160","","","0.71073","MoKα","","0.0592","0.0485","","","0.1213","0.1295","","","","","","1.029","","","","has coordinates","238745","2020-10-21","18:00:00",""
"1555473","9.3725","0.001","21.712","0.002","9.3146","0.001","90","","106.094","0.002","90","","1821.2","0.3","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C21 H19 N O5 -","- C21 H19 N O5 -","- C84 H76 N4 O20 -","4","1","","Hong, Jung-Ho; Atta, Ananta Kumar; Jung, Kwang-Bok; Kim, Seul-Bi; Heo, Jungseok; Cho, Dong-Gyu","Conformationally Locked Tolans, β-Sheet Structures, and Photophysical Properties.","Organic letters","2015","17","24","6222","6225","10.1021/acs.orglett.5b03205","","","0.71073","MoKα","","0.1887","0.0621","","","0.1486","0.2009","","","","","","0.965","","","","has coordinates","238747","2020-10-21","18:00:00",""
"1555474","8.5345","0.0004","8.8037","0.0004","11.0062","0.0007","90","","90.369","0.005","90","","826.94","0.08","150","0.1","150","0.1","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C17 H22 N O3 S -","- C17 H22 N O3 S -","- C34 H44 N2 O6 S2 -","2","1","","Moynihan, Lorna; Chadda, Rekha; McArdle, Patrick; Murphy, Paul V.","Allylic Azide Rearrangement in Tandem with Huisgen Cycloaddition for Stereoselective Annulation: Synthesis of C-Glycosyl Iminosugars.","Organic letters","2015","17","24","6226","6229","10.1021/acs.orglett.5b03209","","","0.71073","MoKα","","0.0703","0.0527","","","0.1269","0.1409","","","","","","1.025","","","","has coordinates","238749","2020-10-21","18:00:00",""
"1555475","6.1187","0.0002","15.5628","0.0007","7.4298","0.0003","90","","90.617","0.004","90","","707.46","0.05","150","0.1","150","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C13 H18 N3 O4 -","- C13 H18 N3 O4 -","- C26 H36 N6 O8 -","2","1","","Moynihan, Lorna; Chadda, Rekha; McArdle, Patrick; Murphy, Paul V.","Allylic Azide Rearrangement in Tandem with Huisgen Cycloaddition for Stereoselective Annulation: Synthesis of C-Glycosyl Iminosugars.","Organic letters","2015","17","24","6226","6229","10.1021/acs.orglett.5b03209","","","0.71073","MoKα","","0.0365","0.0341","","","0.0887","0.0907","","","","","","1.068","","","","has coordinates","238751","2020-10-21","18:00:00",""
"1555476","6.642","0.0002","14.2879","0.0004","13.6807","0.0004","90","","91.605","0.002","90","","1297.79","0.07","100","2","100","1","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C10 H20 O S2 Si -","- C10 H20 O S2 Si -","- C40 H80 O4 S8 Si4 -","4","2","","Melillo, Bruno; Chen, Ming Z.; Forestieri, Roberto; Smith, 3rd, Amos B","An Effective Bifunctional Aldehyde Linchpin for Type II Anion Relay Chemistry: Development and Application to the Synthesis of a C16-C29 Fragment of Rhizopodin.","Organic letters","2015","17","24","6242","6245","10.1021/acs.orglett.5b03235","","","0.71073","MoKα","","0.0353","0.0307","","","0.0867","0.0999","","","","","","1.146","","","","has coordinates","238753","2020-10-21","18:00:00",""
"1555477","9.7683","0.0006","10.4783","0.0007","12.5293","0.0008","102.548","0.003","99.034","0.002","115.038","0.002","1088.3","0.13","100","1","100","1","","","","","","","","5","P -1","-P 1","2","","","","- C18 H34 O S4 Si -","- C18 H34 O S4 Si -","- C36 H68 O2 S8 Si2 -","2","1","","Melillo, Bruno; Chen, Ming Z.; Forestieri, Roberto; Smith, 3rd, Amos B","An Effective Bifunctional Aldehyde Linchpin for Type II Anion Relay Chemistry: Development and Application to the Synthesis of a C16-C29 Fragment of Rhizopodin.","Organic letters","2015","17","24","6242","6245","10.1021/acs.orglett.5b03235","","","0.71073","MoKα","","0.0198","0.0194","","","0.0502","0.0506","","","","","","1.047","","","","has coordinates","238755","2020-10-21","18:00:00",""
"1555478","12.2975","0.0008","14.2131","0.0009","10.3046","0.0007","90","","107.61","0.005","90","","1716.7","0.2","293","","293","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C23 H21 N O -","- C23 H21 N O -","- C92 H84 N4 O4 -","4","1","","Taguchi, Masamitsu; Tokimizu, Yusuke; Oishi, Shinya; Fujii, Nobutaka; Ohno, Hiroaki","Synthesis of Fused Carbazoles by Gold-Catalyzed Tricyclization of Conjugated Diynes via Rearrangement of an N-Propargyl Group.","Organic letters","2015","17","24","6250","6253","10.1021/acs.orglett.5b03254","","","1.54187","CuKα","","0.0466","0.0437","","","0.1168","0.1187","","","","","","1.082","","","","has coordinates","238758","2020-10-21","18:00:00",""
"1555480","10.094","0.003","14.285","0.004","11.689","0.003","90","","90.952","0.004","90","","1685.2","0.8","173.15","","173.15","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C21 H18 Br N -","- C21 H18 Br N -","- C84 H72 Br4 N4 -","4","2","","Zhang, Zhenhua; Du, Haifeng","Enantioselective Metal-Free Hydrogenations of Disubstituted Quinolines.","Organic letters","2015","17","24","6266","6269","10.1021/acs.orglett.5b03307","","","0.71073","MoKα","","0.0402","0.0362","","","0.0687","0.0708","","","","","","1.083","","","","has coordinates","238762","2020-10-21","18:00:00",""
"1555481","9.0073","0.0002","29.18","0.0007","7.8919","0.0002","90","","104.587","0.001","90","","2007.39","0.08","200","2","200","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H24 N2 O2 -","- C24 H24 N2 O2 -","- C96 H96 N8 O8 -","4","1","","Bhojgude, Sachin Suresh; Baviskar, Dnyaneshwar R.; Gonnade, Rajesh G.; Biju, Akkattu T.","Three-Component Coupling Involving Arynes, Aromatic Tertiary Amines, and Aldehydes via Aryl-Aryl Amino Group Migration.","Organic letters","2015","17","24","6270","6273","10.1021/acs.orglett.5b03319","","","0.71073","MoKα","","0.0677","0.0569","","","0.1243","0.1293","","","","","","1.112","","","","has coordinates","238764","2020-10-21","18:00:00",""
"1555482","10.369","0.003","13.94","0.005","14.494","0.005","83.533","0.004","85.279","0.004","75.051","0.008","2008.1","1.2","200","2","200","2","","","","","","","","4","P -1","-P 1","2","","","","- C24 H24 N2 O -","- C24 H24 N2 O -","- C96 H96 N8 O4 -","4","2","","Bhojgude, Sachin Suresh; Baviskar, Dnyaneshwar R.; Gonnade, Rajesh G.; Biju, Akkattu T.","Three-Component Coupling Involving Arynes, Aromatic Tertiary Amines, and Aldehydes via Aryl-Aryl Amino Group Migration.","Organic letters","2015","17","24","6270","6273","10.1021/acs.orglett.5b03319","","","0.71073","MoKα","","0.1847","0.111","","","0.3108","0.4024","","","","","","1.341","","","","has coordinates","238766","2020-10-21","18:00:00",""
"1555483","8.73","0.0001","13.8357","0.0002","9.1173","0.0001","90","","93.75","0.001","90","","1098.88","0.02","140","2","140.15","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C25 H30 N2 O5 -","- C25 H30 N2 O5 -","- C50 H60 N4 O10 -","2","1","","Zhang, Hua; Zhu, Kong-Kai; Han, Ying-Shan; Luo, Cheng; Wainberg, Mark A.; Yue, Jian-Min","Flueggether A and Virosinine A, Anti-HIV Alkaloids from Flueggea virosa.","Organic letters","2015","17","24","6274","6277","10.1021/acs.orglett.5b03320","","","1.54178","CuKα","","0.0376","0.0372","","","0.098","0.0985","","","","","","1.045","","","","has coordinates,has disorder","238768","2020-10-21","18:00:00",""
"1556257","13.389","0.003","7.794","0.0019","13.881","0.003","90","","90.579","0.004","90","","1448.5","0.6","296","2","296","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C17 H12 N2 O4 -","- C17 H12 N2 O4 -","- C68 H48 N8 O16 -","4","1","","Gao, Qinghe; Zhang, Jingjing; Wu, Xia; Liu, Shan; Wu, Anxin","Direct regioselective oxidative cross-coupling of indoles with methyl ketones: a novel route to C3-dicarbonylation of indoles.","Organic letters","2015","17","1","134","137","10.1021/ol503366r","","","0.71073","MoKα","","0.0567","0.0398","","","0.1124","0.1252","","","","","","1.037","","","","has coordinates","243603","2020-10-21","18:00:00",""