(+)-Camphor-mediated kinetic resolution of allylalanes: a strategy towards enantio-enriched cyclohex-2-en-1-ylalane-Reference-Cited by-同舟云学术

(+)-Camphor-mediated kinetic resolution of allylalanes: a strategy towards enantio-enriched cyclohex-2-en-1-ylalane

Published:2017 Issue:1 Volume:53 Page:111-114
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Coffinet Michaël¹²³⁴,Massicot Fabien¹²³⁴,Joseph Jomy¹²³⁴,Behr Jean-Bernard¹²³⁴,Jaroschik Florian¹²³⁴,Vasse Jean-Luc¹²³⁴

Affiliation:

1. Institut de Chimie Moléculaire

2. CNRS (UMR 7312) and Université de Reims

3. 51687 Reims Cedex 2

4. France

Abstract

The (+)-camphor-mediated kinetic resolution of cyclohex-2-en-1-ylalane is presented.

Funder

Ministère de l'Enseignement Supérieur et de la Recherche Scientifique, Gouvernement de la République Algérienne

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2017/CC/C6CC08649G

Reference72 articles.

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4. Enantioselective Conjugate Silyl Additions to α,β-Unsaturated Aldehydes Catalyzed by Combination of Transition Metal and Chiral Amine Catalysts

5. NHC–Cu(i) catalysed asymmetric conjugate silyl transfer to unsaturated lactones: application in kinetic resolution

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