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1404260

COC(=O)CCCNC(=O)C(CSC(C)=O)Cc1ccccc1
Reaction #3852
(±)-4-[[2-[(Acetylthio)methyl]-1 oxo-3-phenylpropyl]amino]butanoic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)S(=O)(=O)CC(Cc1ccccc1)C(=O)O
Reaction #6178
2-benzyl-3-tert.-butylsulfonyl-propionic acid
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@](Cc1ccccc1)(CS(=O)(=O)N1CCN(Cc2ccccc2)CC1)C(=O)O
Reaction #8943
white solid
Ausbeute 36.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CSC(C)(C)C)Cc2ccccc2C1
Reaction #50790
2-carbomethoxy-2-(t-butyl)thiomethylindan
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)SCC1(C(=O)O)Cc2ccccc2C1
Reaction #50791
2-carboxy-2-(t-butyl)thiomethyl-indan
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCSCC(Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #64654
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCS(=O)(=O)CC(Cc1ccccc1)C(=O)O
Reaction #64655
title compound
Ausbeute 91.9%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCSCC(Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #65025
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCS(=O)(=O)CC(Cc1ccccc1)C(=O)O
Reaction #65026
title compound
Ausbeute 91.9%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCSCC(Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #65027
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCS(=O)(=O)CC(Cc1ccccc1)C(=O)O
Reaction #65028
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CSC(C)(C)C)Cc2ccccc2C1
Reaction #65657
2-carbomethoxy-2-(t-butyl)thiomethylindan
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)SCC1(C(=O)O)Cc2ccccc2C1
Reaction #65658
2-carboxy-2-(t-butyl)thiomethyl-indan
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C2c3cc([N+](=O)[O-])ccc3SC1(C)NC(=O)N2C(C)=O
Reaction #92872
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1ccc(C(=O)SCC2C(=O)OCC2c2ccccc2)cc1
Reaction #93538
title compound
Ausbeute 79.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(SCC1C(=O)OCC1c1ccc(Cl)cc1)c1ccccc1
Reaction #93539
title compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(SCC1C(=O)OCC1c1ccccc1)c1ccccc1F
Reaction #93540
title compound
Ausbeute 67.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCC(c2ccccc2)C1CS
Reaction #93541
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2COC(=O)C2CSC2CCCCC2)cc1
Reaction #93542
title compound
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCC(c2ccc(Cl)cc2)C1CSCc1ccccc1
Reaction #93543
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
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