Stereoselective alpha-alkylation of new chiral auxiliaries: An access to enantiomerically pure alpha- and alpha,beta-substituted beta-amino acids

Citation
C. Agami et al., Stereoselective alpha-alkylation of new chiral auxiliaries: An access to enantiomerically pure alpha- and alpha,beta-substituted beta-amino acids, SYNLETT, (11), 1999, pp. 1838-1840
Citations number
13
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNLETT
ISSN journal
09365214 → ACNP
Issue
11
Year of publication
1999
Pages
1838 - 1840
Database
ISI
SICI code
0936-5214(199911):11<1838:SAONCA>2.0.ZU;2-V
Abstract
New bicyclic heterocycles 5, which are potentially useful for the enantiose lective synthesis of substituted beta-amino acids, have been synthesized. A study on the alpha-alkylation of these chiral auxiliaries is presented. An optically pure beta-amino acid was obtained in excellent yield from its ma sked chiral derivative 6a.