Diastereospecific tandem Prins cyclisation/rearrangement reactions for the desymmetrisation of cyclohexa-1,4-dienes

Elliott, Mark Christopher ORCID: https://orcid.org/0000-0003-0132-0818, El Sayed, Nahed N. E. and Paine, James S. 2007. Diastereospecific tandem Prins cyclisation/rearrangement reactions for the desymmetrisation of cyclohexa-1,4-dienes. European Journal of Organic Chemistry 2007 (5) , pp. 792-803. 10.1002/ejoc.200600928

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Abstract

The Prins cyclisation has been used for the first time to desymmetrise a 1,4-diene. Products derived from both normal Prins and rearrangement pathways were obtained, all with complete stereocontrol.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Chemistry
Uncontrolled Keywords:	Cyclohexadiene ; Prins reaction ; Wagner-Meerwein rearrangement ; Desymmetrisation ; Stereoselective
Publisher:	Wiley
ISSN:	1434-193X
Last Modified:	17 Oct 2022 08:54
URI:	https://orca.cardiff.ac.uk/id/eprint/1427

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