An efficient synthesis of chiral homophenylalanine derivatives via enantioselective hydrogenation

Citation
Xs. Li et al., An efficient synthesis of chiral homophenylalanine derivatives via enantioselective hydrogenation, TETRAHEDR-A, 10(20), 1999, pp. 3863-3867
Citations number
16
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON-ASYMMETRY
ISSN journal
09574166 → ACNP
Volume
10
Issue
20
Year of publication
1999
Pages
3863 - 3867
Database
ISI
SICI code
0957-4166(19991015)10:20<3863:AESOCH>2.0.ZU;2-4
Abstract
Chiral homophenylalanine derivatives were synthesized via enantioselective hydrogenation of 5a and 5b catalyzed by rhodium complexes bearing chiral ph osphine and phosphinite legands. Enantiomeric excesses up to 96.2% were ach ieved when S-spiroOP(S-1) was used as a chiral ligand under 500 psi of H-2 pressure in acetone. (C) 1999 Elsevier Science Ltd. All rights reserved.