Enantiospecific Synthesis of Polyoxamic Acid from L-Arabinose
- 1 February 1991
- journal article
- research article
- Published by Georg Thieme Verlag KG in Synthesis
- Vol. 1991 (02) , 150-155
- https://doi.org/10.1055/s-1991-26401
Abstract
An enantiospecific synthesis of polyoxamic acid, 2-amino-2-deoxy-L-xylonic acid, by phenylthiolate opening of a five-carbon chiral hydroxylated aziridine easily derived from L-arabinose is reported. The formation of the carboxyl group resulted from a Pummerer reaction.Keywords
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