Issue 17, 2000

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

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.

Article information

Article type
Communication
Submitted
06 Jul 2000
Accepted
26 Jul 2000
First published
16 Aug 2000

Chem. Commun., 2000, 1675-1676

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

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements