Diastereoselective preparation of cis-2-substituted 3-ethenyl prolines via [3,2]-sigmatropic rearrangements of didehydropiperidinium ylids

Hayes, Jerome, Tavassoli, Ali and Sweeney, Joseph B. (2000) Diastereoselective preparation of cis-2-substituted 3-ethenyl prolines via [3,2]-sigmatropic rearrangements of didehydropiperidinium ylids. Synlett. pp. 1208-1209. ISSN 0936-5214

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Abstract

The [3,2]-sigmatropic rearrangements of N-(methoxycarbonyl)methyl-N-methyl-1,2,3,6-tetrahydropyridinium bromide (1a) has been extrapolated to allow preparation of (±)-cis-2-aryl-3-ethenyl prolines, and certain spiro-prolines

Item Type:	Article
Subjects:	Q Science > QD Chemistry
Schools:	School of Applied Sciences
Related URLs:	Author
Depositing User:	Joseph Sweeney
Date Deposited:	18 Oct 2012 10:28
Last Modified:	05 Apr 2018 12:00
URI:	http://eprints.hud.ac.uk/id/eprint/15291

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