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

被引:12
作者
KANO, S
YOKOMATSU, T
SHIBUYA, S
机构
[1] Tokyo College of Pharmacy, Hachioji, Tokyo, 192-03
关键词
D O I
10.3987/COM-89-5207
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
5-Phenylthiooxazolidin-2-ones, derived from L-serine, were subjected to photo-induced radical allylation to give the correspondg 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. © 1990.
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页码:13 / 16
页数:4
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