Issue 2, 2001
From the journal:

Chemical Communications

Halide redistribution in Pd-catalysed 1,6-diene cycloisomerisationElectronic supplementary information (ESI) available: general experimental procedure, typical GC analyses and table of regioselectivities obtained with the various catalysts. See http://www.rsc.org/suppdata/cc/b0/b009356o/

Katharine L. Bray,a   Ian J. S. Fairlamba  and  Guy C. Lloyd-Jones*a  

* Corresponding authors

a School of Chemistry, Cantock’s Close, Bristol, UK
E-mail: guy.lloyd-jones@bris.ac.uk

Abstract

[(MeCN)3PdCl]+, generated in situ, reversibly disproportionates to give [(MeCN)2PdCl2] and [(MeCN)4Pd]2+. The neutral species is a reactive and highly regioselective catalyst for 1,6-diene cycloisomerisation.

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Article information

DOI
https://doi.org/10.1039/B009356O
Article type
Communication
Submitted
21 Nov 2000
Accepted
12 Dec 2000
First published
08 Jan 2001

Chem. Commun., 2001, 187-188

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Halide redistribution in Pd-catalysed 1,6-diene cycloisomerisation

K. L. Bray, I. J. S. Fairlamb and G. C. Lloyd-Jones, Chem. Commun., 2001, 187 DOI: 10.1039/B009356O

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