Issue 20, 2004
From the journal:

Chemical Communications

An active ferrocenyl triarylphosphine for palladium-catalyzed Suzuki–Miyaura cross-coupling of aryl halides†

Fuk Yee Kwong,*a   Kin Shing Chan,b   Chi Hung Yeunga  and  Albert S. C. Chan*a  

* Corresponding authors

a Open Laboratory of Chirotechnology of the Institute of Molecular Technology for Drug Discovery and Synthesis, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Hong Kong
E-mail: bcfyk@inet.polyu.edu.hk, bcachan@polyu.edu.hk

b Department of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong

Abstract

Pd-catalyzed Suzuki–Miyaura reaction of aryl chlorides was accomplished through the use of an active ferrocene-based triarylphosphine ligand. This air- and moisture-stable ligand was found to be effective for the cross-coupling of aryl halides at room temperature to 115 °C.

Graphical abstract: An active ferrocenyl triarylphosphine for palladium-catalyzed Suzuki–Miyaura cross-coupling of aryl halides

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Article information

DOI
https://doi.org/10.1039/B407661C
Article type
Communication
Submitted
24 May 2004
Accepted
29 Jul 2004
First published
21 Sep 2004

Chem. Commun., 2004, 2336-2337

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An active ferrocenyl triarylphosphine for palladium-catalyzed Suzuki–Miyaura cross-coupling of aryl halides

F. Y. Kwong, K. S. Chan, C. H. Yeung and A. S. C. Chan, Chem. Commun., 2004, 2336 DOI: 10.1039/B407661C

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