A New Synthetic Approach to (+)-Galantinic Acid, Degradation Product from the Peptide Antibiotic Galantin I, via 4-Amino-3-hydroxypyranose
- 1 January 1990
- journal article
- research article
- Published by The Japan Institute of Heterocyclic Chemistry in HETEROCYCLES
- Vol. 31 (1) , 13-16
- https://doi.org/10.3987/com-89-5207
Abstract
5-Phenylthiooxazolidin-2-ones, derived from L-serine, were subjected to photo-induced radical allylation to give the corresponding 4-substituted 4,5-trans-5-allyloxazolidin-2-ones. 4-Ethoxyethy derivative (13c) was led to N-Boc galantinic acid methyl ester via N-Boc 4-amino-3-hydroxypyranose.Keywords
This publication has 1 reference indexed in Scilit:
- A versatile and stereocontrolled synthesis of hydroxyethylene dipeptide isosteresThe Journal of Organic Chemistry, 1989