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An alkylation route to carbo- and heteroaromatic amino acids
journal contribution
posted on 2009-03-20, 14:55 authored by Ray Jones, Didier J.C. Berthelot, James N. IleyAmino 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.
History
School
- Science
Department
- Chemistry
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. 73-84Publisher
© ARKAT USA, Inc.Version
- VoR (Version of Record)
Publication date
2007Notes
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/ISSN
1424-6376Language
- en