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Issue 64, 2014
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Aminosulfonylation of aromatic amines, sulfur dioxide and hydrazines

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Abstract

A facile route to aryl N-aminosulfonamides under mild conditions is provided. The reaction of aromatic amines (including heteroaromatic amines), sulfur dioxide, and hydrazines proceeds efficiently with good functional group tolerance. The in situ generated diazonium ion is involved in the aminosulfonylation process.

Graphical abstract: Aminosulfonylation of aromatic amines, sulfur dioxide and hydrazines

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Article information


Submitted
24 Apr 2014
Accepted
19 May 2014
First published
19 May 2014

Chem. Commun., 2014,50, 8886-8888
Article type
Communication

Aminosulfonylation of aromatic amines, sulfur dioxide and hydrazines

D. Zheng, Y. Li, Y. An and J. Wu, Chem. Commun., 2014, 50, 8886
DOI: 10.1039/C4CC03032J

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