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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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Publication details

The article was received on 24 Apr 2014, accepted on 19 May 2014 and first published on 19 May 2014


Article type: Communication
DOI: 10.1039/C4CC03032J
Citation: Chem. Commun., 2014,50, 8886-8888
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    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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