STEREOSELECTIVE SYNTHESIS OF ALL INDIVIDUAL ISOMERS OF BETA-METHYL-2',6'-DIMETHYLPHENYLALANINE

Authors
XIANG L WU HW HRUBY VJ
Citation
L. Xiang et al., STEREOSELECTIVE SYNTHESIS OF ALL INDIVIDUAL ISOMERS OF BETA-METHYL-2',6'-DIMETHYLPHENYLALANINE, Tetrahedron : asymmetry, 6(1), 1995, pp. 83-86
Citations number
21
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
6
Issue
1
Year of publication
1995
Pages
83 - 86
Database
ISI
SICI code
0957-4166(1995)6:1<83:SSOAII>2.0.ZU;2-3
Abstract
Asymmetric synthesis of all four isomers of beta-methyl-2',6'-dimethyl phenylalanine was accomplished with complete stereoselectivities and h igh yields by using the Evans-like auxiliary 4-phenyl-oxazolidinone as a chiral auxiliary and as a chiral resolution reagent.