An alkylation route to carbo- and heteroaromatic amino acids

Jones, Raymond C.F.; Berthelot, Didier J.C. and Iley, James N. (2007). An alkylation route to carbo- and heteroaromatic amino acids. Arkivoc(11) pp. 73–84.

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URL:	http://www.arkat-usa.org/get-file/23153/
DOI (Digital Object Identifier) Link:	https://doi.org/10.3998/ark.5550190.0008.b07
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Abstract

Amino acids carrying aromatic carbo- and heterocycles in the side chain, such as naphthyl-, biphenyl- and pyridylalanines, have been prepared by alkylation of a glycine enolate with a haloalkyl carbocycle or heterocycle, with enantiomeric excess up to 87% using the ephedrine amide protocol.

Item Type:	Journal Item
Copyright Holders:	2007 ARKAT USA, Inc.
ISSN:	1551-7012
Extra Information:	for the Heterocyclic Group on their 40th Anniversary
Keywords:	amino acid; non-proteinogenic; ephedrine glycinamide; glycine enolate; pyridylalanine
Academic Unit/School:	Faculty of Science, Technology, Engineering and Mathematics (STEM) > Life, Health and Chemical Sciences Faculty of Science, Technology, Engineering and Mathematics (STEM)
Item ID:	5974
Depositing User:	James Iley
Date Deposited:	04 Dec 2006
Last Modified:	05 Sep 2017 18:55
URI:	http://oro.open.ac.uk/id/eprint/5974
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