Ähnlichkeitssuche

796006

Cn1ccc(S(=O)(=O)N(Cc2ccc(Cl)cc2)c2cccc(C(=O)OC(C)(C)C)c2)n1
Reaction #91090
title compound
Ausbeute 9.6%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(S(=O)(=O)N(Cc2ccc(Cl)cc2)c2cccc(C(=O)O)c2)n1
Reaction #91091
title compound
Ausbeute 16.9%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #91092
solid
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(S(=O)(=O)N(Cc2ccc(Cl)cc2)c2cccc(O)c2)n1
Reaction #473668
solid
Ausbeute 77.6%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(S(=O)(=O)N(Cc2ccc(Cl)cc2)c2cccc(OCC(=O)OC(C)(C)C)c2)n1
Reaction #473669
oil
Ausbeute 82.8%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(S(=O)(=O)N(Cc2ccc(Cl)cc2)c2cccc(O)c2)n1
Reaction #1226439
DOI: 10.1039/C8SC04228D
Cn1ccc(S(=O)(=O)N(Cc2ccc(Cl)cc2)c2cccc(C(=O)OC(C)(C)C)c2)n1
Reaction #1273437
3-[(4-Chloro-benzyl)-(1-methyl-1H-pyrazole-3-sulfonyl)-amino]-benzoic acid tert-butyl ester
Ausbeute 9.6%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(S(=O)(=O)N(Cc2ccc(Cl)cc2)c2cccc(C(=O)O)c2)n1
Reaction #1273438
title compound
Ausbeute 16.9%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(S(=O)(=O)N(Cc2ccc(Cl)cc2)c2cccc(C(=O)NCCO)c2)n1
Reaction #1273439
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(S(=O)(=O)N(Cc2ccc(Cl)cc2)c2cccc(C(=O)OC(C)(C)C)c2)n1
Reaction #1606169
title compound
Ausbeute 9.6%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(S(=O)(=O)N(Cc2ccc(Cl)cc2)c2cccc(C(=O)O)c2)n1
Reaction #1606170
title compound
Ausbeute 16.9%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1606171
solid
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(S(=O)(=O)N(Cc2ccc(Cl)cc2)c2cccc(OCC(=O)OC(C)(C)C)c2)n1
Reaction #1627340
DOI: 10.1039/C8SC04228D