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CS(=O)(=O)NC1Cc2ccccc2C1

CC(C)S(=O)(=O)NC1Cc2ccccc2C1
Reaction #46695
oil
المردود 164.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)NC1Cc2ccc(I)cc2C1
Reaction #46696
title compound
المردود 437.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)NC1Cc2ccc(-c3cccc([N+](=O)[O-])c3)cc2C1
Reaction #46697
oil
المردود 109.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)NC1Cc2ccc(-c3cccc(N)c3)cc2C1
Reaction #46698
title compound
المردود 81.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cccc(-c2ccc3c(c2)CC(NS(=O)(=O)C(C)C)C3)c1
Reaction #46701
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1cccc(-c2ccc3c(c2)CC(NS(=O)(=O)C(C)C)C3)c1
Reaction #46702
title compound
المردود 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1cccc(-c2ccc3c(c2)CC(NS(=O)(=O)C(C)C)C3)c1
Reaction #46703
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Cc1cccc(-c2ccc3c(c2)CC(NS(=O)(=O)C(C)C)C3)c1
Reaction #46704
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)NC1Cc2ccc(-c3cccc(C#N)c3)cc2C1
Reaction #46705
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)NC1Cc2ccc(-c3cccc(CN)c3)cc2C1
Reaction #46706
title compound
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)NC1Cc2ccc(-c3cccc(CNS(C)(=O)=O)c3)cc2C1
Reaction #46707
title compound
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCc1cccc(-c2ccc3c(c2)CC(NS(=O)(=O)C(C)C)C3)c1
Reaction #46708
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)NC1Cc2ccc(-c3cccc(CN4CCCC4=O)c3)cc2C1
Reaction #46709
title compound
المردود 19.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)NC1Cc2ccc(-c3cccc(N4CCCS4(=O)=O)c3)cc2C1
Reaction #46710
title compound
المردود 9.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)NC1Cc2ccc(-c3cccc(CS(C)(=O)=O)c3)cc2C1
Reaction #46711
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(O)(O)NC1Cc2ccc(-c3cccc(S(=O)(=O)N(C)C)c3)cc2C1
Reaction #46712
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(O)(O)NC1Cc2ccc(-c3cccc(S(N)(=O)=O)c3)cc2C1
Reaction #46713
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC2Cc3ccc(-c4ncccc4C(=O)c4cccnc4-c4ccc5c(c4)CC(NS(=O)(=O)c4ccc(C)cc4)C5)cc3C2)cc1
Reaction #50389
2-(4-Toluenesulphonylamino)indan-5-yl-3-pyridyl ketone
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCC=C(c1cccnc1)c1ccc2c(c1)CC(NS(=O)(=O)c1ccc(Br)cc1)C2
Reaction #50391
Methyl 6-(2-(4-bromobenzenesulphonylamino)indan-5-yl)-6-(3-pyridyl)hex-5-enoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCC=C(c1cccnc1)c1ccc2c(c1)CC(NS(=O)(=O)c1ccc(Br)cc1)C2
Reaction #50392
6-(2-(4-Bromobenzenesulphonylamino)indan-5-yl)-6-(3-pyridyl)hex-5-enoic acid
DOI: 10.6084/m9.figshare.5104873.v1
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