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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
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

Information
URI:
https://eprints.hud.ac.uk/id/eprint/15291
URI:
https://eprints.hud.ac.uk/id/eprint/15291
Title:
Diastereoselective preparation of cis-2-substituted 3-ethenyl prolines via [3,2]-sigmatropic rearrangements of didehydropiperidinium ylids
Creators:
Hayes, Jerome, Tavassoli, Ali and Sweeney, Joseph B.
Identification Number:
10.1055/s-2000-6742
Official URL:
http://dx.doi.org/10.1055/s-2000-6742
Date:
August 2000
Subjects:
Q Science > QD Chemistry
Schools:
School of Applied Sciences
Library
Item Type:
Article
Depositing User:
Joseph Sweeney
Date Deposited:
18 Oct 2012 10:28
Revision:
8
Last Modified:
28 Aug 2021 11:22
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