Issue 23, 2004
From the journal:

Chemical Communications

A p-phosphinophenolate ligand for the palladium-catalysed arylation of alkenes†

Eiji Shirakawa,*a   Keijiro Ishiib  and  Teruhisa Tsuchimotob  

* Corresponding authors

a Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto, Japan
E-mail: shirakawa@kuchem.kyoto-u.ac.jp
Fax: +81-75-753-3988
Tel: +81-75-753-3985

b Graduate School of Materials Science, Japan Advanced Institute of Science and Technology, Asahidai, Tatsunokuchi, Ishikawa, Japan

Abstract

A triphenylphosphine having a strong electron-donating group, an oxyanion, at the para position of one of the benzene rings was found to show much higher efficiency compared with other structurally related triarylphosphines in the palladium-catalysed arylation of alkenes.

Graphical abstract: A p-phosphinophenolate ligand for the palladium-catalysed arylation of alkenes

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Article information

DOI
https://doi.org/10.1039/B411125G
Article type
Communication
Submitted
22 Jul 2004
Accepted
02 Sep 2004
First published
19 Oct 2004

Chem. Commun., 2004, 2752-2753

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A p-phosphinophenolate ligand for the palladium-catalysed arylation of alkenes

E. Shirakawa, K. Ishii and T. Tsuchimoto, Chem. Commun., 2004, 2752 DOI: 10.1039/B411125G

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