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

Baldwin, Jack E. and Spivey, Alan C. and 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

Full text not available from this repository.

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.

Item Type: Journal Article
Journal or Publication Title: Tetrahedron
Uncontrolled Keywords: /dk/atira/pure/subjectarea/asjc/3000/3002
Subjects:
ID Code: 133274
Deposited By: ep_importer_pure
Deposited On: 30 Apr 2019 11:15
Refereed?: Yes
Published?: Published
Last Modified: 30 Sep 2019 21:55
URI: https://eprints.lancs.ac.uk/id/eprint/133274

Actions (login required)

View Item View Item