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622498

CN(C(=O)Oc1ccc(Cl)cc1)[C@H]1CC[C@H](C#CCOS(C)(=O)=O)CC1
Reaction #53911
trans-Methanesulfonic acid 3-{4-[(4-chloro-phenoxycarbonyl)-methyl-amino]-cyclohexyl}-prop-2-ynyl ester
Rendimiento 117.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Nc1ccc(Cl)cc1)[C@H]1CC[C@H](C#CCOS(C)(=O)=O)CC1
Reaction #53912
trans-Methanesulfonic acid 3-{4-[3-(4-chloro-phenyl)-1-methyl-ureido]-cyclohexyl}-prop-2-ynyl ester
Rendimiento 101.9%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])OC[C@H]1O[C@@](COS(=O)(=O)[O-])(O[C@H]2O[C@H](COS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@H](OS(=O)(=O)[O-])[C@H]2OS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@@H]1OS(=O)(=O)[O-].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+]
Reaction #81383
Potassium sucrose octasulfate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CN1C(=O)C(CC(=O)Nc2ccc(N(C)C)cc2)(NC(=O)Nc2ccc(C)cc2)c2ccccc21)OCC.O=S(=O)([O-])O.[K+]
Reaction #453199
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CN1C(=O)C(CC(=O)Nc2ccc(N(C)C)cc2)(NC(=O)Nc2ccc(C)cc2)c2ccccc21)OCC.O=S(=O)([O-])O.[K+]
Reaction #465910
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CN1C(=O)C(CC(=O)Nc2ccc(N(C)C)cc2)(NC(=O)Nc2ccc(C)cc2)c2ccccc21)OCC.O=S(=O)([O-])O.[K+]
Reaction #705745
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Oc1ccc(CNC(=O)CCC#Cc2ccc(OC(F)(F)F)cc2)cc1
Reaction #939578
title compound
Rendimiento 47.3%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])OC[C@H]1O[C@@](COS(=O)(=O)[O-])(O[C@H]2O[C@H](COS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@H](OS(=O)(=O)[O-])[C@H]2OS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@@H]1OS(=O)(=O)[O-].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+]
Reaction #1051149
Potassium Sucrose Octasulfate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](SC(c2ccccc2)(c2ccccc2)c2ccccc2)C[C@H]1C(=O)O
Reaction #1351557
(2S,4R)-4-Tritylsulfanyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester
Rendimiento 103.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@@H]2C[C@@H](C(=O)O)N(S(=O)(=O)CCc3ccccc3)C2)cc1
Reaction #1351586
(2S,4R)-4-(4-Methoxy-benzylsulfanyl)-1-(2-phenyl-ethanesulfonyl)-pyrrolidine-2-carboxylic acid
Rendimiento 138.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@@H]2C[C@@H](C(=O)N(C)Cc3ccccc3)N(S(=O)(=O)CCc3ccccc3)C2)cc1
Reaction #1351587
(2S,4R)-4-(4-Methoxy-benzylsulfanyl)-1-(2-phenyl-ethanesulfonyl)-pyrrolidine-2-carboxylic acid benzyl-methyl-amide
Rendimiento 10.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1COCCN1c1ccc(NC[C@H](CCl)OS(=O)(=O)[O-])cc1.[K+]
Reaction #1594006
crystalline title compound
Rendimiento 126.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CN1C(=O)C(CC(=O)Nc2ccc(N(C)C)cc2)(NC(=O)Nc2ccc(C)cc2)c2ccccc21)OCC.O=S(=O)([O-])O.[K+]
Reaction #1620920
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC1CC=CCC1
Reaction #1915511
4-propyl-1-cyclohexene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1CC=CCC1
Reaction #1915512
4-t-butyl-1-cyclohexene
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CN1C(=O)C(CC(=O)Nc2ccc(N(C)C)cc2)(NC(=O)Nc2ccc(C)cc2)c2ccccc21)OCC.O=S(=O)([O-])O.[K+]
Reaction #2040519
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(Cl)cc1)[C@H]1CC[C@H](C#CCOS(C)(=O)=O)CC1
Reaction #2144490
trans-Methanesulfonic acid 3-{4-[(4-chloro-phenoxycarbonyl)-methyl-amino]-cyclohexyl}-prop-2-ynyl ester
Rendimiento 117.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Nc1ccc(Cl)cc1)[C@H]1CC[C@H](C#CCOS(C)(=O)=O)CC1
Reaction #2144491
trans-Methanesulfonic acid 3-{4-[3-(4-chloro-phenyl)-1-methyl-ureido]-cyclohexyl}-prop-2-ynyl ester
Rendimiento 101.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@H](O)CN(CC(OC)OC)C(=O)[C@H](C)Nc1ccc(C(F)(F)F)c(Cl)c1
Reaction #2182707
titled compound
Rendimiento 122.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@H](O)CN1CCN(c2ccc(C(F)(F)F)c(Cl)c2)[C@@H](C)C1=O
Reaction #2182708
titled compound
Rendimiento 7.2%DOI: 10.6084/m9.figshare.5104873.v1
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