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Amino acid synthesis via ring opening of N-sulphonyl aziridine-2-carboxylate esters with organometallic reagents.

Baldwin, Jack E., Spivey, Alan C., Schofield, Christopher J. and Sweeney, Joseph B. (1993) Amino acid synthesis via ring opening of N-sulphonyl aziridine-2-carboxylate esters with organometallic reagents. Tetrahedron, 49 (28). pp. 6309-6330. ISSN 0040-4020
Abstract

Nucleophilic ring opening of optically active N-sulphonyl aziridine-2-carboxylate esters with organometallic reagents has been investigated as a method of preparation of optically active amino acids

Information
URI:
https://eprints.hud.ac.uk/id/eprint/15415
Title:
Amino acid synthesis via ring opening of N-sulphonyl aziridine-2-carboxylate esters with organometallic reagents.
Creators:
Baldwin, Jack E., Spivey, Alan C., Schofield, Christopher J. and Sweeney, Joseph B.
Identification Number:
10.1016/S0040-4020(01)87968-0
Official URL:
http://dx.doi.org/10.1016/S0040-4020(01)87968-0
Date:
January 1993
Subjects:
Q Science > QD Chemistry
Schools:
School of Applied Sciences
Library
Item Type:
Article
Depositing User:
Joseph Sweeney
Date Deposited:
09 Oct 2012 10:19
Revision:
10
Last Modified:
28 Aug 2021 11:22
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