NEW SYNTHESIS OF ENANTIOMERICALLY PURE (S)-3-AMINO-2-PHENYL PROPANOICACID VIA THE ASYMMETRIC TRANSFORMATION OF ITS RACEMIC N-PHTHALOYL DERIVATIVE

Authors
CALMES M ESCALE F
Citation
M. Calmes et F. Escale, NEW SYNTHESIS OF ENANTIOMERICALLY PURE (S)-3-AMINO-2-PHENYL PROPANOICACID VIA THE ASYMMETRIC TRANSFORMATION OF ITS RACEMIC N-PHTHALOYL DERIVATIVE, Tetrahedron : asymmetry, 9(16), 1998, pp. 2845-2850
Citations number
20
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
9
Issue
16
Year of publication
1998
Pages
2845 - 2850
Database
ISI
SICI code
0957-4166(1998)9:16<2845:NSOEP(>2.0.ZU;2-Z
Abstract
The synthesis of racemic N-phthalyl 3-amino-2-phenyl propanoic acid an d its asymmetric transformation via the corresponding prochiral ketene have been investigated allowing the preparation of enantiomerically p ure (S)3-amino-2-phenyl propanoic acid. (C) 1998 Elsevier Science Ltd. All rights reserved.