A highly stereoselective ether directed palladium catalysed aza-Claisen rearrangement

Jamieson, A. G. and Sutherland, A. (2005) A highly stereoselective ether directed palladium catalysed aza-Claisen rearrangement. Organic and Biomolecular Chemistry, 3, pp. 735-736. (PMID:15731857)

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Abstract

A highly stereoselective rearrangement of allylic trichloroacetimidates to allylic trichloroamides has been achieved using adjacent ether groups to direct facial coordination of the palladium(II) catalyst.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Jamieson, Dr Andrew and Sutherland, Professor Andrew
Authors: Jamieson, A. G., and Sutherland, A.
College/School:College of Science and Engineering > School of Chemistry
Journal Name:Organic and Biomolecular Chemistry
Publisher:Royal Society of Chemistry
ISSN:1477-0520
ISSN (Online):1477-0539
Published Online:07 February 2005

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