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

Mazet, Clement; Gerard, David

doi:10.1039/C0CC01547D

Scientific article

English

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

ContributorsMazet, Clement

; Gerard, David

Published inChemical communications, vol. 47, no. 1, p. 298-300

Publication date2011

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.

Affiliation entities

Faculté des sciences / Section de chimie et biochimie / Département de chimie organique

Citation (ISO format)

MAZET, Clement, GERARD, David. Highly regio- and enantioselective catalytic asymmetric hydroboration of α-substituted styrenyl derivatives. In: Chemical communications, 2011, vol. 47, n° 1, p. 298–300. doi: 10.1039/C0CC01547D

Article (Published version)

Identifiers

PID : unige:12843
DOI : 10.1039/C0CC01547D

Journal ISSN1359-7345

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Creation08/12/2010 10:32:00

First validation08/12/2010 10:32:00

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

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.

Technical informations