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Cc1noc(NS(=O)(=O)c2ccc(-c3cccc([N+](=O)[O-])c3)s2)c1Br
Reaction #245087
DOI: 10.1039/C8SC04228D
Cc1cc(NS(=O)(=O)c2ccc(-c3cccc([N+](=O)[O-])c3)s2)on1
Reaction #321647
sulfonamide
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(NS(=O)(=O)c2ccc(-c3cccc([N+](=O)[O-])c3)s2)c1Br
Reaction #321648
final product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NS(=O)(=O)c2ccc(-c3cccc([N+](=O)[O-])c3)s2)on1
Reaction #1254161
sulfonamide
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(NS(=O)(=O)c2ccc(-c3cccc([N+](=O)[O-])c3)s2)c1Br
Reaction #1254162
final product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NS(=O)(=O)c2ccc(-c3cccc([N+](=O)[O-])c3)s2)on1
Reaction #1338993
sulfonamide
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(NS(=O)(=O)c2ccc(-c3cccc([N+](=O)[O-])c3)s2)c1Br
Reaction #1338994
final product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NS(=O)(=O)c2ccc(-c3cccc([N+](=O)[O-])c3)s2)on1
Reaction #1825737
sulfonamide
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(NS(=O)(=O)c2ccc(-c3cccc([N+](=O)[O-])c3)s2)c1Br
Reaction #1825738
final product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NS(=O)(=O)c2ccc(-c3cccc([N+](=O)[O-])c3)s2)on1
Reaction #2219309
DOI: 10.1039/C8SC04228D
Cc1noc(NS(=O)(=O)c2ccc(-c3cccc([N+](=O)[O-])c3)s2)c1Br
Reaction #2357922
final product
DOI: 10.6084/m9.figshare.5104873.v1