Functional group directed C-H borylation

The direct borylation of hydrocarbons via C-H activation has reached an impressive level of sophistication and efficiency, emerging as a fundamental tool in synthesis because of the versatility offered by organoboron compounds. As a remarkable particularity, the catalytic systems originally develope...

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Veröffentlicht in:Chemical Society reviews 2014-05, Vol.43 (10), p.3229-3243
Hauptverfasser: Ros, A, Fernández, R, Lassaletta, J M
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Lassaletta, J M
description The direct borylation of hydrocarbons via C-H activation has reached an impressive level of sophistication and efficiency, emerging as a fundamental tool in synthesis because of the versatility offered by organoboron compounds. As a remarkable particularity, the catalytic systems originally developed for these reactions are relatively insensitive to directing effects, and the regioselectivity of the borylations is typically governed by steric factors. Likely stimulated by the great synthetic potential of the expected functionalised organoboranes, however, many groups have recently focused on the development of complementary strategies for directed, site-selective borylation reactions where a directing group controls the course of the reaction. In this tutorial review, the different strategies and findings related to the development of these directed borylation reactions via C(sp(2))-H or C(sp(3))-H activation will be summarized and discussed.
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source Royal Society Of Chemistry Journals; Alma/SFX Local Collection
subjects Activation
Functional groups
Hydrocarbons
Organoboron compounds
Strategy
Synthesis
Versatility
title Functional group directed C-H borylation
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