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 Dit 2016
Accepted
23 Kax 2016
First published
23 Kax 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

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements