BIOCATALYTIC APPROACH TO ENANTIOMERICALLY PURE BETA-AMINO ACIDS

Citation
Va. Soloshonok et al., BIOCATALYTIC APPROACH TO ENANTIOMERICALLY PURE BETA-AMINO ACIDS, Tetrahedron : asymmetry, 6(7), 1995, pp. 1601-1610
Citations number
133
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
ISSN journal
09574166
Volume
6
Issue
7
Year of publication
1995
Pages
1601 - 1610
Database
ISI
SICI code
0957-4166(1995)6:7<1601:BATEPB>2.0.ZU;2-X
Abstract
beta-Aryl-beta-amino acids were prepared in good chemical yield and hi gh enantiomeric purity (> 95% eel via penicillin acylase-catalyzed hyd rolysis of the corresponding N-phenylacetyl derivatives. The (R)-enant iomers were the fast-reacting isomers in all cases studied. The biocat alytic procedure described employs very simple set or reactions using inexpensive commercially available chemicals and enzyme, and could be easily scaled up.