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7184

O=C(O)CCNC(=O)C(CS)Cc1ccccc1
Reaction #3851
(±)-3-[[2-(Mercaptomethyl)-1-oxo-3-phenylpropyl]amino]propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
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
O=C(O)CCCCNC(=O)C(CS)Cc1ccccc1
Reaction #3853
(±)-5-[[2-(mercaptomethyl)-1-oxo-3-phenylpropyl]amino] pentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCCNC(=O)C(CS)Cc1ccccc1
Reaction #3854
(±)-7-[[2-(mercaptomethyl)-1-oxo-3-phenylpropyl]amino]heptanoic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccc(NC(=O)C(CSC(C)=O)Cc2ccccc2)c1
Reaction #175900
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cccc(NC(=O)C(CS)Cc2ccccc2)c1
Reaction #222058
DOI: 10.1039/C8SC04228D
COC(=O)C(CSC(C)(C)C)NC(=O)C(CSC(C)=O)Cc1ccccc1
Reaction #244048
DOI: 10.1039/C8SC04228D
CC(=O)SCC(Cc1ccccc1)C(=O)NCc1ccc(C(=O)O)cc1
Reaction #251704
DOI: 10.1039/C8SC04228D
COC(=O)CC(NC(=O)C(CSC(C)=O)Cc1ccccc1)c1ccc2ccccc2c1
Reaction #265330
DOI: 10.1039/C8SC04228D
CC(=O)SCC(Cc1ccccc1)C(=O)Nc1cc(C)cc(C(=O)O)c1
Reaction #273093
DOI: 10.1039/C8SC04228D
O=C(O)C(CS)Cc1ccccc1
Reaction #277969
DOI: 10.1039/C8SC04228D
CC(=O)SCC(Cc1ccccc1)C(=O)NC1CCCNC(=O)C1
Reaction #282410
DOI: 10.1039/C8SC04228D
CC(=O)SCC(Cc1ccccc1)C(=O)Cl
Reaction #302139
DOI: 10.1039/C8SC04228D
CC(=O)SCC(Cc1ccccc1)C(=O)Nc1cc(C)cc(C(=O)O)c1
Reaction #335850
title compound
Ausbeute 51.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SCC(Cc1ccccc1)C(=O)Nc1cc(C(=O)O)ccc1C
Reaction #335857
title compound
Ausbeute 52.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(NC(=O)C(CSC(C)=O)Cc2ccccc2)cc(C(=O)O)c1
Reaction #335872
title compound
Ausbeute 62.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccc(NC(=O)C(CSC(C)=O)Cc2ccccc2)c1
Reaction #335874
title compound
Ausbeute 67.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cccc(NC(=O)C(CS)Cc2ccccc2)c1
Reaction #335875
title compound
Ausbeute 76.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SCC(Cc1ccccc1)C(=O)Nc1cccc(C(=O)O)c1
Reaction #335876
title compound
Ausbeute 41.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SCC(Cc1ccccc1)C(=O)NCc1ccc(C(=O)O)cc1
Reaction #335878
title compound
Ausbeute 32.6%DOI: 10.6084/m9.figshare.5104873.v1
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