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Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/4364

Title: An alkylation route to carbo- and heteroaromatic amino acids
Authors: Jones, Raymond C.F.
Berthelot, Didier J.C.
Iley, James N.
Keywords: Amino acid
Ephedrine glycinamide
Glycine enolate
Issue Date: 2007
Publisher: © ARKAT USA, Inc.
Citation: JONES, R.C.F., BERTHELOT, D.J.C. and ILEY, J.N., 2007. An alkylation route to carbo- and heteroaromatic amino acids. ARKIVOC, 2007 (xi), pp. 73-84
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.
Description: This is an article that was published in the journal, ARKIVOC [© ARKAT USA]. It is also available at; http://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/
Version: Published
URI: https://dspace.lboro.ac.uk/2134/4364
ISSN: 1424-6376
Appears in Collections:Published Articles (Chemistry)

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