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CCCCOP(=O)(COS(=O)(=O)c1ccc(Cl)cc1)Cc1ccccc1
Reaction #1640
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@H]1C[C@@H](COS(=O)(=O)c2ccc(Cl)cc2)OC(C)(C)O1
Reaction #6551
product
Ausbeute 130.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@H]1C[C@@H](COS(=O)(=O)c2ccc(Cl)cc2)OC(C)(C)O1
Reaction #6555
product
Ausbeute 130.1%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@H]1CCCC[C@H]1NS(=O)(=O)c1ccc(Cl)cc1
Reaction #7122
(1S,2R)-2-(4-chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide
Ausbeute 53.2%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@@H]1CCCC[C@@H]1NS(=O)(=O)c1ccc(Cl)cc1
Reaction #7123
cis-2-(4-chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide
Ausbeute 45.1%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(Cl)cc1)N1Cc2cnn(S(=O)(=O)c3ccc(Cl)cc3)c2CC1c1ccccc1
Reaction #44002
1,5-bis-(4-chloro-benzenesulfonyl)-6-phenyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCC(NS(=O)(=O)c1ccc(Cl)cc1)C(=O)OC
Reaction #44003
product 57
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CC(=O)C[C@H](C)N1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44015
cis-1-(4-chlorophenylsulfonyl)-2,6-dimethylpiperidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CC(=O)C[C@H](C)N1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44017
product 94
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C1Cc2[nH]ncc2CN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44028
5-(4-Chlorophenylsulfonyl)-6-isopropyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C1Cc2[nH]ncc2CN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44037
5-(4-Chlorophenylsulfonyl)-6-isopropyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(Cl)cc1)c1ccc(-c2ccccc2)cc1
Reaction #44309
4-(4′-chlorobenzenesulphonyl)biphenyl
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(Cl)cc1Cl
Reaction #47149
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(Cl)c(Cl)c1
Reaction #47150
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC[C@@H](COS(=O)(=O)c2ccc(Cl)cc2)O1
Reaction #47278
4-chloro-benzenesulfonic acid (S)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester
Ausbeute 93.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3ccc(Cl)cc3F)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49411
4-(2-fluoro-4-chlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 27.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3ccc(Cl)c(Cl)c3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49419
4-(3,4-dichlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 28.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3ccc(Cl)cc3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49440
4-(4-chlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 41.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3ccc(Cl)cc3Cl)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49455
4-(2,4-dichlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(NCCc1ccccc1)c1ccc(Cl)cc1
Reaction #50384
2-(p-Chlorobenzenesulphonylamino)ethyl-benzene
DOI: 10.6084/m9.figshare.5104873.v1
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