Issue 17, 2000
From the journal:

Chemical Communications

Direct formation of 1-vinyl-1H-isochromene derivatives via a palladium-catalysed coupling reaction

Roger Mutter,a   Eva M. Martin de la Neva†a  and  Martin Wills*a  

* Corresponding authors

a Department of Chemistry, University of Warwick, Coventry, UK
E-mail: m.wills@warwick.ac.uk

Abstract

The palladium-catalysed reaction of the tert-butyldimethylsilyl ether of a 3-(o-bromophenyl)allylic alcohol with a methyl ketone leads directly to a 1-vinyl-1H-isochromene via a tandem ketone arylation–allylic cyclisation reaction.

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Article information

DOI
https://doi.org/10.1039/B005519K
Article type
Communication
Submitted
06 Jul 2000
Accepted
26 Jul 2000
First published
16 Aug 2000

Chem. Commun., 2000, 1675-1676

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Direct formation of 1-vinyl-1H-isochromene derivatives via a palladium-catalysed coupling reaction

R. Mutter, E. M. Martin de la Neva and M. Wills, Chem. Commun., 2000, 1675 DOI: 10.1039/B005519K

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