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CCCC(NS(=O)(=O)c1ccc(Cl)cc1)C(=O)O

CCOC(=O)C1CC(=O)C=CN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44018
compound 103
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C(=CN(C)C)C(=O)C=CN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44019
compound 104
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1c2cn[nH]c2C=CN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44020
compound 105
Ausbeute 30.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(=O)CC(CC)N1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44021
oil
Ausbeute 88.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC2(CC(CC)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #44022
mixture
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC2(CC(CO)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #44023
mixture
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC2(CC(CC)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #226296
DOI: 10.1039/C8SC04228D
CCCC(NS(=O)(=O)c1ccc(Cl)cc1)C(=O)Nc1ccc(CC(=O)OCC)cc1
Reaction #231620
DOI: 10.1039/C8SC04228D
O=C(O)C(CC1CCCCC1)NS(=O)(=O)c1ccc(Cl)cc1
Reaction #254252
DOI: 10.1039/C8SC04228D
O=C(NCCCCC(NS(=O)(=O)c1ccc(Cl)cc1)C(=O)O)OCC1c2ccccc2-c2ccccc21
Reaction #255046
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(NC(=O)C(CC2CCCCC2)NS(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #289248
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(NC(=O)C(CCc2ccccc2)NS(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #299280
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(NC(=O)C(CCc2ccccc2)NS(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #353537
(RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)-4-phenylbutanamide
Ausbeute 46.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1ccc(NC(=O)C(CCc2ccccc2)NS(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #353538
(RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(2-methoxycarbonylethyl)phenyl)-4-phenylbutanamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(NS(=O)(=O)c1ccc(Cl)cc1)C(=O)Nc1ccc(CC(=O)OCC)cc1
Reaction #353541
(RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)pentanamide
Ausbeute 27.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[C@H](NS(=O)(=O)c1ccc(Cl)cc1)C(=O)Nc1ccc(CC(=O)OCC)cc1
Reaction #353542
(S)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)hexanamide
Ausbeute 32.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[C@@H](NS(=O)(=O)c1ccc(Cl)cc1)C(=O)Nc1ccc(CC(=O)OCC)cc1
Reaction #353543
(R)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)hexanamide
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(NS(=O)(=O)c1ccc(Cl)cc1)C(=O)Nc1ccc(CC(=O)OCC)cc1
Reaction #353547
(RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)octanamide
Ausbeute 26.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(NC(=O)C(CC(C)C)NS(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #353549
(RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl) phenyl)-4-methylpentanamide
Ausbeute 33.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(CC1CCCCC1)NS(=O)(=O)c1ccc(Cl)cc1
Reaction #353569
(RS)-2-(4-chlorobenzenesulfonylamino)-3-cyclohexylpropanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
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