Boron: A key element in radical reactions

Author:

Renaud Philippe1,Beauseigneur Alice1,Brecht-Forster Andrea1,Becattini Barbara1,Darmency Vincent1,Kandhasamy Sarkunam1,Montermini Florian1,Ollivier Cyril1,Panchaud Philippe1,Pozzi Davide1,Scanlan Eoin Martin1,Schaffner Arnaud-Pierre1,Weber Valéry1

Affiliation:

1. 1Department of Chemistry and Biochemistry, University of Berne, Freiestrasse 3, CH-3000 Berne 9, Switzerland

Abstract

Boron derivatives are becoming key reagents in radical chemistry. Here, we describe reactions where an organoboron derivative is used as a radical initiator, a chain-transfer reagent, and a radical precursor. For instance, B-alkylcatecholboranes, easily prepared by hydroboration of alkenes, represent a very efficient source of primary, secondary, and tertiary alkyl radicals. Their very high sensitivity toward oxygen- and heteroatom-centered radicals makes them particularly attractive for the development of radical chain processes such as conjugate addition, allylation, alkenylation, and alkynylation. Boron derivatives have also been used to develop an attractive new procedure for the reduction of radicals with alcohols and water. The selected examples presented here demonstrate that boron-containing reagents can efficiently replace tin derivatives in a wide range of radical reactions.

Publisher

Walter de Gruyter GmbH

Subject

General Chemical Engineering,General Chemistry

Reference34 articles.

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