Recherche de Sous-structure

1029716

O=C1C2CCC(C2)C(=O)N1CCCCN1CCN(c2ncccn2)CC1
Reaction #5014
title compound
Rendement 34.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)C2CCC1C2
Reaction #5020
anhydride
Rendement 79.0%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
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
COC(=O)C1(CI)CCCC1
Reaction #44866
title compound
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(C(=O)O)CCCC3)CC2)c2ccccc21
Reaction #44868
title compound
Rendement 87.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(NC(=O)C1(c2ccccn2)CCCC1)C(Cc1ccc(Cl)cc1)c1ccccc1
Reaction #58672
N-[3-(4-chlorophenyl)-2-phenyl-1-methylpropyl]-1-(2-pyridyl)cyclopentanecarboxamide
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
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 #59201
(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 #59203
title compound
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CCCCC(C)C)CCCC1
Reaction #79343
oil
Rendement 21.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #86068
oil
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CCBr)CCCC1
Reaction #91990
1-[2-bromoethyl]cyclopentanecarboxylic acid methyl ester
Rendement 80.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #92010
oil
Rendement 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)C1CCCC1
Reaction #93009
above-identified compound
Rendement 106.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)N(C(=O)OC(C)(C)C)C1CC2CC(C(=O)OC)C1C2
Reaction #162228
methyl 6-(N-(tert-butoxycarbonyl)-2-ethoxy-2-oxoacetamido)bicyclo[2.2.1]heptane-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(=O)C1CCCC1)c1ccc(Oc2ccccc2)cc1
Reaction #168193
1-cycloperityl-3-(4-phenoxyphenyl)propane-1,3-dione
Rendement 63.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)CC(=O)C2CCCC2)cc1
Reaction #168194
1-cyclopentyl-3-(4-methoxyphenyl)propane-1,3-dione
Rendement 56.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)OCc3ccccc3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172729
title compound
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
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