Issue 6, 2017

C–H imidation: a distinct perspective of C–N bond formation

Abstract

The direct imidation strategy proficiently constructs C–N bonds and creates the useful amine functional group in the molecular template. This review briefly discusses the synthetic methods developed for the direct imidation of unactivated C(sp2/sp3/sp)–H bonds. Transition-metal catalysts, metal-free processes, and/or photo-induced methods are invariably employed for accomplishing C–H imidation transformations. The contents summarized herein would benefit the research community to use the C–H imidation reactions for broad synthetic applications and to unravel novel C–N bond forming processes.

Graphical abstract: C–H imidation: a distinct perspective of C–N bond formation

Article information

Article type
Review Article
Submitted
04 oct. 2016
Accepted
23 déc. 2016
First published
23 déc. 2016

Org. Biomol. Chem., 2017,15, 1282-1293

C–H imidation: a distinct perspective of C–N bond formation

R. K. Rit, M. Shankar and A. K. Sahoo, Org. Biomol. Chem., 2017, 15, 1282 DOI: 10.1039/C6OB02162J

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