Issue 23, 2014

Metal-catalyzed activation of ethers via C–O bond cleavage: a new strategy for molecular diversity

Abstract

In 1979, the seminal work of Wenkert set the standards for the utilization of aryl and vinyl ethers as coupling partners via C–O bond-cleavage. Although the topic remained dormant for almost three decades, the last few years have witnessed a renaissance in this area of expertise, experiencing an exponential growth and becoming a significant discipline within the cross-coupling arena. The means to utilize readily accessible aryl or vinyl ethers as counterparts does not only represent a practical, powerful and straightforward alternative to organic halides, but also constitutes an excellent opportunity to improve our chemical knowledge about a relatively unexplored area of expertise. This review summarizes the most significant developments in the area of C–O bond-cleavage when employing aryl or vinyl ethers, providing a detailed overview of the current state of the art and including future aspects, when applicable.

Graphical abstract: Metal-catalyzed activation of ethers via C–O bond cleavage: a new strategy for molecular diversity

Article information

Article type
Review Article
Submitted
17 Jun 2014
First published
26 Aug 2014

Chem. Soc. Rev., 2014,43, 8081-8097

Author version available

Metal-catalyzed activation of ethers via C–O bond cleavage: a new strategy for molecular diversity

J. Cornella, C. Zarate and R. Martin, Chem. Soc. Rev., 2014, 43, 8081 DOI: 10.1039/C4CS00206G

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