A NEW SYNTHETIC APPROACH TO (+)-GALANTINIC ACID, DEGRADATION PRODUCT FROM THE PEPTIDE ANTIBIOTIC GALANTIN I, VIA 4-AMINO-3-HYDROXYPYRANOSE

DOI: 10.3987/COM-89-5207

Source and publish data:

Heterocycles p. 13 - 16 (1990)

Update date:2022-08-03

Topics:

Authors:

Kano, Shinzo

Yokomatsu, Tsutomu

Shibuya, Shiroshi

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Article abstract of DOI:10.3987/COM-89-5207

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.

Full text of DOI:10.3987/COM-89-5207

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