Jones, Raymond C.F.; Berthelot, Didier J.C. and Iley, James N.
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|DOI (Digital Object Identifier) Link:||https://doi.org/10.3998/ark.5550190.0008.b07|
|Google Scholar:||Look up in Google Scholar|
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 Article|
|Copyright Holders:||2007 ARKAT USA, Inc.|
|Extra Information:||for the Heterocyclic Group on their 40th Anniversary|
|Keywords:||amino acid; non-proteinogenic; ephedrine glycinamide; glycine enolate; pyridylalanine|
|Academic Unit/Department:||Faculty of Science, Technology, Engineering and Mathematics (STEM) > Life, Health and Chemical Sciences
Faculty of Science, Technology, Engineering and Mathematics (STEM)
|Depositing User:||James Iley|
|Date Deposited:||04 Dec 2006|
|Last Modified:||06 Oct 2016 16:01|
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