Поиск подструктуры

14799

CCCCCOCCCCOc1ccc(B(O)O)c(F)c1F
Reaction #6687
2,3-difluoro-4-(4-pentyloxybutoxy)phenylboronic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCOCCCCOc1ccc(-c2ccc(C(=O)OCC)cc2)c(F)c1F
Reaction #6688
2′,3′-difluoro-4′-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid ethyl ester
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCOCCCCOc1ccc(B(O)O)c(F)c1F
Reaction #6693
2,3-difluoro-4-(4-pentyloxybutoxy)phenylboronic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCOCCCCOc1ccc(-c2ccc(C(=O)OCC)cc2)c(F)c1F
Reaction #6694
2′,3′-difluoro-4′-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid ethyl ester
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2nccc3ccccc23)c(F)c1
Reaction #8651
1-(2,4-difluoro-phenyl)-isoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
OCCC1CCC=C1c1ccccc1F
Reaction #9368
2-[2-(2-fluoro-phenyl)-cyclopent-2-enyl]-ethanol
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1-c1ccccc1F
Reaction #41045
title compound
Выход 76.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@H](C[N+](=O)[O-])c1cccc(F)c1F)C(=O)OCc1ccccc1
Reaction #42668
title compound
Выход 87.4%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccccc1-c1cnc2nnn(Cc3ccc4ncccc4c3)c2n1
Reaction #44265
6-((6-(2-fluorophenyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline
Выход 74.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2F)c(F)c2oc(C3CC3)nc2c1C#N
Reaction #45727
2-Cyclopropyl-7-fluoro-6-(2-fluorophenyl)-5-methyl-1,3-benzoxazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2cccc(F)c2F)c(F)c2oc(C3CC3)nc2c1C#N
Reaction #45731
compound
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnn2c(C3CCC3)nc(-c3cccc(OCc4ccccc4)c3F)c12
Reaction #46254
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Oc1cccc(Br)c1F
Reaction #47415
3-bromo-2-fluoro-phenol
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@H](NC(=O)OCc1ccccc1)C(=O)N(CC(=C)c1cccc(F)c1F)Cc1ccc(OC)cc1OC
Reaction #48407
title compound
Выход 69.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@H](C[N+](=O)[O-])c1cccc(F)c1F)C(=O)OCc1ccccc1
Reaction #48412
title compound
Выход 87.4%DOI: 10.6084/m9.figshare.5104873.v1
COCCn1cc(-c2cccc(F)c2F)cc([N+](=O)[O-])c1=O
Reaction #48453
title compound
Выход 59.7%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cccc(F)c1-c1cc2c3c(c1)C1CNCCC1N3CCSC2
Reaction #51540
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(CSCCc2ccccc2)c2cc(-c3ccccc3F)ccc2N1
Reaction #54076
title compound
DOI: 10.6084/m9.figshare.5104873.v1
OCCC1CCC=C1c1ccccc1F
Reaction #57010
2-[2-(2-fluoro-phenyl)-cyclopent-2-enyl]-ethanol
DOI: 10.6084/m9.figshare.5104873.v1
CCCNC(=O)c1nnc2c(-c3cc(C(F)(F)F)ccc3F)cccc2c1N
Reaction #59378
title compound
Выход 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее