FIRST SYNTHESIS OF THE ENANTIOMERICALLY PURE ALPHA-HYDROXY ANALOG OF S-TERT-BUTYL CYSTEINE

Authors
CAVELIER F
Citation
F. Cavelier, FIRST SYNTHESIS OF THE ENANTIOMERICALLY PURE ALPHA-HYDROXY ANALOG OF S-TERT-BUTYL CYSTEINE, Tetrahedron : asymmetry, 8(1), 1997, pp. 41-43
Citations number
13
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
8
Issue
1
Year of publication
1997
Pages
41 - 43
Database
ISI
SICI code
0957-4166(1997)8:1<41:FSOTEP>2.0.ZU;2-I
Abstract
The first synthesis of enantiomerically pure 2-hydroxy 3-tert-butylthi o propionic acid in a one-pot reaction from chiral glycidate has been achieved with total conservation of stereochemistry. (C) 1997, Elsevie r Science Ltd.