Issue 24, 2016

Trihaloethenes as versatile building blocks for organic synthesis

Abstract

This review highlights the chemistry of trihaloethene building blocks with a special focus on commercially available 1,1,2-trichloroethene. The topics surveyed herein include the use of trihaloethenes as C2-building blocks for transition metal-catalyzed coupling reactions, addition, elimination and cycloaddition reactions as well as natural product syntheses.

Graphical abstract: Trihaloethenes as versatile building blocks for organic synthesis

  • This article is part of the themed collection: New Talent

Article information

Article type
Review Article
Submitted
13 Jan 2016
Accepted
26 Jan 2016
First published
26 Jan 2016
This article is Open Access
Creative Commons BY-NC license

Org. Biomol. Chem., 2016,14, 5377-5389

Trihaloethenes as versatile building blocks for organic synthesis

A. S. Grossmann and T. Magauer, Org. Biomol. Chem., 2016, 14, 5377 DOI: 10.1039/C6OB00091F

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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