Copper(II)-Catalyzed [2,3]-Sigmatropic Rearrangement ofN-Methyltetrahydropyridinium Ylids

Tools

Heath, Peter, Roberts, Edward, Sweeney, Joseph B., Wessel, Hans Peter and Workman, James A. (2003) Copper(II)-Catalyzed [2,3]-Sigmatropic Rearrangement ofN-Methyltetrahydropyridinium Ylids. The Journal of Organic Chemistry, 68 (10). pp. 4083-4086. ISSN 0022-3263

Metadata only available from this repository.

Official URL: http://dx.doi.org/10.1021/jo034147v

DOI: 10.1021/jo034147v

Abstract

A ring-contractive and highly diastereoselective [2,3]-sigmatropic rearrangement occurs when N-methyl-1,2,3,6-tetrahydropyridine is treated with sub-stoichiometric amounts of copper or rhodium salts, in the presence of ethyl diazoacetate, giving ethyl cis-N-methyl-3-ethenyl proline (4).

Item Type:	Article
Subjects:	Q Science > QD Chemistry
Schools:	School of Applied Sciences > Biomolecular Sciences Research Centre
Related URLs:	Author
Depositing User:	Joseph Sweeney
Date Deposited:	18 Oct 2012 11:46
Last Modified:	18 Oct 2012 11:46
URI:	http://eprints.hud.ac.uk/id/eprint/15277

Item control for Repository Staff only:

View Item