A general approach for the enantioselective synthesis of anti-β- hydroxy-α-amino acids: Preparation of an oxazolidine-functionalized chiral glycine equivalent

Article abstract of DOI:10.1080/00397919808004918

The preparation of 2,4-disubstituted oxazolidine-functionalized glycine ester 3a derived from phenylglycinol is described.

Full text of DOI:10.1080/00397919808004918

Synthetic Communications
ISSN: 0039-7911 (Print) 1532-2432 (Online) Journal homepage: http://www.tandfonline.com/loi/lsyc20
A General Approach for the Enantioselective
Synthesis of anti-β-Hydroxy-α-Amino Acids:
Preparation of an Oxazolidine-Functionalized
Chiral Glycine Equivalent
Edwin J. Iwanowicz , Mary F. Malley & Kennith Smith
To cite this article: Edwin J. Iwanowicz , Mary F. Malley & Kennith Smith (1998) A General
Approach for the Enantioselective Synthesis of anti-β-Hydroxy-α-Amino Acids: Preparation of
an Oxazolidine-Functionalized Chiral Glycine Equivalent, Synthetic Communications, 28:19,
3711-3714, DOI: 10.1080/00397919808004918
To link to this article: http://dx.doi.org/10.1080/00397919808004918
Published online: 22 Aug 2006.
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Date: 25 January 2016, At: 06:28