Поиск подструктуры

254875

CCCCCCC[C@H](C)Oc1c(F)cc(-c2ccc([C@H]3CC[Si@H](CCCCCCC)CC3)cc2)cc1F
Reaction #2738
(S)-4-(4-(trans-4-n-heptyl-4-silacyclohexyl)phenyl)-1-(1-methyloctyloxy)-2,6-difluorobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC[C@@H](F)COc1c(F)cc(-c2ccc([C@H]3CC[Si@H](CCC)CC3)cc2)cc1F
Reaction #2740
(R)-4-(4-(trans-4-n-propyl-4-silacyclohexyl)phenyl)-1-(2-fluorooctyloxy)2,6-difluorobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC[C@@H](F)COc1c(F)cc(-c2ccc([C@H]3CC[Si@H](CCCCC)CC3)cc2)cc1F
Reaction #2741
(R)-4-(4-(trans-4-n-pentyl-4-silacyclohexyl)phenyl)-1-(2-fluorodecyloxy)-2,6-difluorobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCC[Si@H]1CC[C@H](c2cc(F)c(-c3cc(F)c(C(F)=CF)c(F)c3)c(F)c2)CC1
Reaction #2750
4'-(trans-4-n-propyl-4-silacyclohexyl)-2',6',3,5-tetrafluoro-4-(1,2-difluorovinyl)biphenyl
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCCC1C(=O)c1ccc(-c2ccc(N)c(F)c2)cc1
Reaction #9649
methyl 2-[(4′-amino-3′-fluoro-1,1′-biphenyl-4-yl)carbonyl]cyclopentane-carboxylate
Выход 89.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)CC(=O)c1ccc(-c2ccc(NC=O)c(F)c2)cc1
Reaction #9650
methyl 4-[3′-fluoro-4′-(formylamino)-1,1′-biphenyl-4-yl]-2,2-dimethyl-4-oxobutanoate
Выход 46.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)CC(=O)c1ccc(-c2ccc(N)c(F)c2)cc1
Reaction #9651
methyl 4-(4′-amino-3′-fluoro-1,1′-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoate
Выход 89.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(OC)cc4s3)c(F)c2)cc1
Reaction #9693
butyl (1R,2R)-2-({3′-fluoro-4′-[(6-methoxy-1,3-benzothiazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylate
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(C)cc4o3)c(F)c2)cc1
Reaction #9701
methyl (1R,2R)-2-({3′-fluoro-4′-[(6-methyl-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)-cyclopentanecarboxylate
Выход 42.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(Nc3ccc(-c4ccc(C(=O)[C@@H]5CCC[C@H]5C(=O)O)cc4)cc3F)oc2c1
Reaction #9702
(1R,2R)-2-({3′-fluoro-4′-[(6-methyl-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid
Выход 15.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCCC1C(=O)c1ccc(-c2ccc(N)c(F)c2)cc1
Reaction #59146
methyl 2-[(4′-amino-3′-fluoro-1,1′-biphenyl-4-yl)carbonyl]cyclopentane-carboxylate
Выход 89.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)CC(=O)c1ccc(-c2ccc(NC=O)c(F)c2)cc1
Reaction #59147
methyl 4-[3′-fluoro-4′-(formylamino)-1,1′-biphenyl-4-yl]-2,2-dimethyl-4-oxobutanoate
Выход 46.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)CC(=O)c1ccc(-c2ccc(N)c(F)c2)cc1
Reaction #59148
methyl 4-(4′-amino-3′-fluoro-1,1′-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoate
Выход 89.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(OC)cc4s3)c(F)c2)cc1
Reaction #59192
butyl (1R,2R)-2-({3′-fluoro-4′-[(6-methoxy-1,3-benzothiazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylate
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(C)cc4o3)c(F)c2)cc1
Reaction #59200
methyl (1R,2R)-2-({3′-fluoro-4′-[(6-methyl-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)-cyclopentanecarboxylate
Выход 42.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(Nc3ccc(-c4ccc(C(=O)[C@@H]5CCC[C@H]5C(=O)O)cc4)cc3F)oc2c1
Reaction #59201
(1R,2R)-2-({3′-fluoro-4′-[(6-methyl-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid
Выход 15.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@H](Cc1ccc(-c2cc(F)ccc2OC)cc1)NC(=O)CCC(=O)OC(C)(C)C
Reaction #158007
(R)-tert-butyl 4-(4-ethoxy-1-(5′-fluoro-2′-methoxybiphenyl-4-yl)-4-oxobutan-2-ylamino)-4-oxobutanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@H](Cc1ccc(-c2cc(F)ccc2OC)cc1)NC(=O)CCC(=O)O
Reaction #158008
(R)-4-(4-ethoxy-1-(5′-fluoro-2′-methoxybiphenyl-4-yl)-4-oxobutan-2-ylamino)-4-oxobutanoic acid
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(F)cc1-c1ccc(C[C@H](CC(=O)O)NC(=O)CCC(=O)O)cc1
Reaction #158028
(R)-4-(1-carboxy-3-(5′-fluoro-2′-methoxybiphenyl-4-yl)propan-2-ylamino)-4-oxobutanoic acid
Выход 74.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@H](Cc1ccc(-c2cc(F)ccc2OC)cc1)NC(=O)OC(C)(C)C
Reaction #158070
(R)-ethyl 3-(tert-butoxycarbonylamino)-4-(5′-fluoro-2′-methoxybiphenyl-4-yl)butanoate
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее