Recherche de Sous-structure

500189

Cc1c(Cl)cc(C(=O)CCC(=O)O)cc1Cl
Reaction #1591
3-(3,5-dichloro-4-methylbenzoyl)propionic acid
Rendement 44.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cl)cc(C(=O)CCC(=O)O)cc1Cl
Reaction #1658
3-(3,5-dichloro-4-methylbenzoyl)propionic acid
Rendement 44.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cc2c(c(OCCC)c1C)CCC(Cc1cccnc1)C2=O
Reaction #1708
Compound 26
Rendement 68.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cl)cc(C(=O)CCC(=O)O)cc1Cl
Reaction #2163
3-(3,5-dichloro-4-methylbenzoyl)propionic acid
Rendement 44.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cl)cc(C(=O)CCC(=O)O)cc1Cl
Reaction #2204
3-(3,5-dichloro-4-methylbenzoyl)propionic acid
Rendement 44.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #9621
ethyl 4-(4′-nitro-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
Rendement 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc(N)cc2)cc1
Reaction #9622
ethyl 4-(4′-amino-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
Rendement 95.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])c(OC)c2)cc1
Reaction #9652
methyl 4-(3′-methoxy4′-nitro-1,1′-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoate
Rendement 48.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)CC(=O)c1ccc(-c2ccc(N)c(OC)c2)cc1
Reaction #9653
methyl 4-(4′-amino-3′-methoxy-1,1′-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoate
Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CC(=O)c1ccc(-c2ccc(Nc3nccs3)cc2)cc1)C(=O)O
Reaction #9688
desired product
Rendement 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CC(=O)c1ccc(-c2ccc(Nc3ncc([N+](=O)[O-])s3)cc2)cc1)C(=O)O
Reaction #9695
desired product
Rendement 10.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CCCC1C(=O)c1ccc(-c2ccc(Nc3nc4cc(F)ccc4o3)cc2)cc1
Reaction #9700
2-({4′-[(5-fluoro-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid
Rendement 31.7%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
Rendement 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
Rendement 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4cc(F)ccc4s3)cc2)cc1
Reaction #9704
title compound
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2oc(Nc3ccc(-c4ccc(C(=O)[C@@H]5CCC[C@H]5C(=O)O)cc4)cc3)nc2c1
Reaction #9712
(1R,2R)-2-({4′-[(5-methyl-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid
Rendement 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #59115
ethyl 4-(4′-nitro-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
Rendement 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc(N)cc2)cc1
Reaction #59116
ethyl 4-(4′-amino-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
Rendement 95.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)CC(=O)c1ccc(-c2ccc([N+](=O)[O-])c(OC)c2)cc1
Reaction #59149
methyl 4-(3′-methoxy-4′-nitro-1,1′-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoate
Rendement 48.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)CC(=O)c1ccc(-c2ccc(N)c(OC)c2)cc1
Reaction #59150
methyl 4-(4′-amino-3′-methoxy-1,1′-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoate
Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Page 1Suivant