Issue 36, 2008
From the journal:

Chemical Communications

Hydrous zinc halide-catalyzed aminosulfonation of hydrocarbons†

Biswajit Kalita,a   Angus A. Lamara  and  Kenneth M. Nicholas*a  

* Corresponding authors

a Department of Chemistry and Biochemistry, University of Oklahoma, Norman, USA
E-mail: knicholas@ou.edu
Fax: +1 405 325 6111
Tel: +1 405 325 3696

Abstract

Benzylic and allylic hydrocarbons are selectively converted to the corresponding sulfonamides by a ZnBr2–H2O-catalyzed reaction with PhI[double bond, length as m-dash]NTs; saturated adamantane is aminosulfonated at the tertiary C–H bond.

Graphical abstract: Hydrous zinc halide-catalyzed aminosulfonation of hydrocarbons

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Article information

DOI
https://doi.org/10.1039/B805783D
Article type
Communication
Submitted
08 Apr 2008
Accepted
16 Jun 2008
First published
05 Aug 2008

Chem. Commun., 2008, 4291-4293

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Hydrous zinc halide-catalyzed aminosulfonation of hydrocarbons

B. Kalita, A. A. Lamar and K. M. Nicholas, Chem. Commun., 2008, 4291 DOI: 10.1039/B805783D

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