Issue 44, 2012

A highly efficient catalyst-free protocol for C–H bond activation: sulfamidation of alkyl aromatics and aldehydes

Abstract

A catalyst-free protocol has been developed for amidation of alkyl aromatics and aldehydes using TsNBr2via a nitrene transfer process in the presence of a base in excellent yield within a short time. The reaction was found to be selective for secondary and tertiary benzylic C–H bonds and C–H bonds of aldehydic groups.

Graphical abstract: A highly efficient catalyst-free protocol for C–H bond activation: sulfamidation of alkyl aromatics and aldehydes

Supplementary files

Article information

Article type
Communication
Submitted
20 Feb 2012
Accepted
11 Apr 2012
First published
12 Apr 2012

Chem. Commun., 2012,48, 5491-5493

A highly efficient catalyst-free protocol for C–H bond activation: sulfamidation of alkyl aromatics and aldehydes

A. J. Borah and P. Phukan, Chem. Commun., 2012, 48, 5491 DOI: 10.1039/C2CC31258A

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