Issue 30, 2006
From the journal:

Chemical Communications

Pallado-catalysed hydrophosphination of alkynes: access to enantio-enriched P-stereogenic vinyl phosphine–boranes†

Benoît Join,a   David Mimeau,b   Olivier Delacroixa  and  Annie-Claude Gaumont*a  

* Corresponding authors

a Laboratoire de Chimie Moléculaire et Thio-organique, UMR CNRS 6507, ENSI-CAEN, and Université de Caen, 6 bd du Maréchal Juin, Caen, France
E-mail: annie-claude.gaumont@ensicaen.fr
Fax: 0033 2 31 45 28 77
Tel: 0033 2 31 45 28 73

b Laboratoire de Synthèse et d'Electrosynthèse Organique, UMR CNRS 6510 Université de Rennes, Campus de Beaulieu, Rennes, France

Abstract

Preliminary results dealing with the synthesis of non-racemic P-stereogenic vinylphosphine–boranes by hydrophosphination of alkynes in the presence of a chiral catalyst are reported.

Graphical abstract: Pallado-catalysed hydrophosphination of alkynes: access to enantio-enriched P-stereogenic vinyl phosphine–boranes

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Article information

DOI
https://doi.org/10.1039/B607434K
Article type
Communication
Submitted
25 May 2006
Accepted
09 Jun 2006
First published
26 Jun 2006

Chem. Commun., 2006, 3249-3251

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Pallado-catalysed hydrophosphination of alkynes: access to enantio-enriched P-stereogenic vinyl phosphine–boranes

B. Join, D. Mimeau, O. Delacroix and A. Gaumont, Chem. Commun., 2006, 3249 DOI: 10.1039/B607434K

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