Issue 29, 2011

Mechanistic considerations of guanidine-catalyzed reactions

Abstract

This feature article discusses the various mechanistic aspects of guanidine-catalyzed reactions. Guanidines are well known as strong organic bases; however, in the first section, three most common commercially available guanidines, TMG, TBD and MTBD, will be used to illustrate the use of guanidines as nucleophilic catalysts. In the second section, different modes of hydrogen bonding interactions of the conjugate acid of guanidine, the guanidinium, are discussed. Particularly interesting are the possibilities of mono-functional or bifunctional activation of a nucleophile and an electrophile by guanidinium.

Graphical abstract: Mechanistic considerations of guanidine-catalyzed reactions

Article information

Article type
Feature Article
Submitted
07 Sep 2010
Accepted
07 Apr 2011
First published
04 May 2011

Chem. Commun., 2011,47, 8210-8222

Mechanistic considerations of guanidine-catalyzed reactions

X. Fu and C. Tan, Chem. Commun., 2011, 47, 8210 DOI: 10.1039/C0CC03691A

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