Issue 14, 2016

25 years of N-heterocyclic carbenes: activation of both main-group element–element bonds and NHCs themselves

Abstract

N-Heterocyclic carbenes (NHCs) are widely used ligands and reagents in modern inorganic synthesis as well as in homogeneous catalysis and organocatalysis. However, NHCs are not always innocent bystanders. In the last few years, more and more examples were reported of reactions of NHCs with main-group elements which resulted in modification of the NHC. Many of these reactions lead to ring expansion and the formation of six-membered heterocyclic rings involving insertion of the heteroatom into the C–N bond and migration of hydrides, phenyl groups or boron-containing fragments. Furthermore, a few related NHC rearrangements were observed some decades ago. In this Perspective, we summarise the history of NHC ring expansion reactions from the 1960s till the present.

Graphical abstract: 25 years of N-heterocyclic carbenes: activation of both main-group element–element bonds and NHCs themselves

Article information

Article type
Perspective
Submitted
19 okt 2015
Accepted
02 dec 2015
First published
07 dec 2015

Dalton Trans., 2016,45, 5880-5895

25 years of N-heterocyclic carbenes: activation of both main-group element–element bonds and NHCs themselves

S. Würtemberger-Pietsch, U. Radius and T. B. Marder, Dalton Trans., 2016, 45, 5880 DOI: 10.1039/C5DT04106F

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