Issue 24, 2016
From the journal:

Organic & Biomolecular Chemistry

Enantioselective oxidative boron Heck reactions

A.-L. Lee*a  

* Corresponding authors

a Institute of Chemical Sciences, School of Engineering and Physical Sciences, Heriot-Watt University, Riccarton, Edinburgh EH14 4AS, Scotland, UK
E-mail: A.Lee@hw.ac.uk
Tel: +44 (0)131 4518030

Abstract

This review highlights the use of the oxidative boron Heck reaction in enantioselective Heck-type couplings. The enantioselective oxidative boron Heck reaction overcomes several limitations of the traditional Pd(0)-catalysed Heck coupling and has subsequently allowed for intermolecular couplings of challenging systems such as cyclic enones, acyclic alkenes, and even site selectively on remote alkenes.

Graphical abstract: Enantioselective oxidative boron Heck reactions

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

DOI
https://doi.org/10.1039/C5OB01984B
Article type
Review Article
Submitted
23 Sep 2015
Accepted
29 Oct 2015
First published
29 Oct 2015
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2016,14, 5357-5366

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Enantioselective oxidative boron Heck reactions

A.-L. Lee, Org. Biomol. Chem., 2016, 14, 5357 DOI: 10.1039/C5OB01984B

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