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1096333

O=C(O)CNS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3cc4ccccc4o3)cc2)cc1
Reaction #57551
N-({4′-[(1-benzofuran-2-ylcarbonyl)amino]-1,1′-biphenyl-4-yl}sulfonyl)glycine
Ausbeute 73.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3cc4c(O)cccc4o3)cc2)cc1)C(C)C
Reaction #57556
4′-[(4-hydroxy-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonyl-L-valine methyl ester
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc([N+](=O)[O-])cc2)cc1)C(C)C
Reaction #57559
methyl N-[(4′-nitro-1,1′-biphenyl-4-yl)sulfonyl]-L-valinate
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](C(C)C)N(C)S(=O)(=O)c1ccc(-c2ccc(N)cc2)cc1
Reaction #57593
methyl N-[(4′-amino-1,1′-biphenyl-4-yl)sulfonyl]-N-methyl-D-valinate
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](C(C)C)N(C)S(=O)(=O)c1ccc(-c2ccc(NC(=O)c3cc4ccccc4o3)cc2)cc1
Reaction #57594
methyl N-({4′-[(1-benzofuran-2-ylcarbonyl)amino]-1,1′-biphenyl-4-yl}sulfonyl)-N-methyl-D-valinate
Ausbeute 86.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](C(=O)O)N(C)S(=O)(=O)c1ccc(-c2ccc(NC(=O)c3cc4ccccc4o3)cc2)cc1
Reaction #57595
N-({4′-[(1-benzofuran-2-ylcarbonyl)amino]-1,1′-biphenyl-4-yl}sulfonyl)-N-methyl-D-valine
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)OC)C(C)C)cc4)cc3)c(C)c2c1O
Reaction #57603
methyl N-[(4′-{[(5-ethyl-4-hydroxy-3-methyl-1-benzofuran-2-yl)carbonyl]amino}-1,1′-biphenyl-4-yl)sulfonyl]-L-valinate
Ausbeute 129.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)Nc2ccc(-c3ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc3)cc2)oc2cccc(C(C)O)c12
Reaction #57610
N-{[4′-({[4-(1-hydroxyethyl)-3-methyl-1-benzofuran-2-yl]carbonyl}amino)-1,1′-biphenyl-4-yl]sulfonyl}-L-valine
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(C(O)CO)c4c3C)cc2)cc1)C(C)C
Reaction #57611
methyl N-{[4′-({[4-(1,2-dihydroxyethyl)-3-methyl-1-benzofuran-2-yl]carbonyl}amino)-1,1′-biphenyl-4-yl]sulfonyl}-L-valinate
Ausbeute 85.2%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N(C)[C@H](C(=O)OC)C(C)C)cc4)cc3)c(C)c12
Reaction #57612
methyl N-methyl-N-[(4′-{[(3-methyl-4-vinyl-1-benzofuran-2-yl)carbonyl]amino}-1,1′-biphenyl-4-yl)sulfonyl]-L-valinate
Ausbeute 63.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(OC)c4c3C)cc2)cc1)C(C)C
Reaction #57620
(S)-2-{4′-[(4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc4)cc3)c(C)c12
Reaction #57621
(S)-2-{4′-[(4-methoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)OC)C(C)C)cc4)cc3)c(C)c12
Reaction #57624
(S)-2-{4′-[(4-ethoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc4)cc3)c(C)c12
Reaction #57625
(S)-2-{4′-[(4-ethoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)OC)C(C)C)cc4)cc3)c(C)c12
Reaction #57628
(S)-2-{4′-[(3-methyl-4-propoxy-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc4)cc3)c(C)c12
Reaction #57629
(S)-3-methyl-2-{4′-[(3-methyl-4-propoxy-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(OC(C)C)c4c3C)cc2)cc1)C(C)C
Reaction #57632
(S)-2-{4′-[(4-Isopropoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid methyl ester
Ausbeute 75.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)Nc2ccc(-c3ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc3)cc2)oc2cccc(OC(C)C)c12
Reaction #57633
(S)-2-{4′-[(4-isopropoxy-3-methyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-3-methyl-butyric acid
Ausbeute 79.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3oc4cccc(-c5ccccc5)c4c3C)cc2)cc1)C(C)C
Reaction #57636
(S)-3-methyl-2-{4′-[(3-methyl-4-phenyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid methyl ester
Ausbeute 29.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)Nc2ccc(-c3ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)C)cc3)cc2)oc2cccc(-c3ccccc3)c12
Reaction #57637
(S)-3-methyl-2-{4′-[(3-methyl-4-phenyl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid
Ausbeute 32.3%DOI: 10.6084/m9.figshare.5104873.v1
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