Issue 1, 2011
From the journal:

Chemical Communications

Highly regio- and enantioselective catalytic asymmetric hydroboration of α-substituted styrenyl derivatives†‡

Clément Mazet*a  and  David Gérarda  

* Corresponding authors

a University of Geneva, Organic Chemistry Department, Quai Ernest Ansermet 30, 1211-Geneva, Switzerland
E-mail: clement.mazet@unige.ch
Fax: +41 (0)22 3793215
Tel: +41 (0)22 3796288

Abstract

The catalytic asymmetric hydroboration of a variety of 1,1-disubstituted olefins has been achieved with excellent yields, perfect regioselectivity and in some cases, high levels of enantioselectivity using readily accessible iridium catalyst.

Graphical abstract: Highly regio- and enantioselective catalytic asymmetric hydroboration of α-substituted styrenyl derivatives

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Article information

DOI
https://doi.org/10.1039/C0CC01547D
Article type
Communication
Submitted
24 May 2010
Accepted
07 Jul 2010
First published
14 Oct 2010

Chem. Commun., 2011,47, 298-300

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Highly regio- and enantioselective catalytic asymmetric hydroboration of α-substituted styrenyl derivatives

C. Mazet and D. Gérard, Chem. Commun., 2011, 47, 298 DOI: 10.1039/C0CC01547D

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