SYNTHESIS OF UNPROTECTED 2-DEOXYGLYCOSYL DONORS, S-(2-DEOXY-ALPHA-D-ARABINO-HEXOPYRANOSYL)-0,0-DIALKYLPHOSPHORODITHIOATES

被引：0
|
作者：
KUDELSKA, W
CZYZEWSKACHLEBNY, J
MICHALSKA, M
机构：
来源：
POLISH JOURNAL OF CHEMISTRY | 1994年 / 68卷 / 09期
关键词：
2-DEOXYGLYCOSYL PHOSPHORODITHIOATES; SUGAR O-UNPROTECTED GLYCOSYL DONORS;
D O I：
暂无
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Sugar-O-unprotected S-(2-deoxyglycosyl)phosphorodithioates were synthesized by two routes: 1) Addition of O,O-dialkylphosphorodithioic acids to unsubstituted D-glucal 2) Deprotection of the adducts obtained by addition of phosphorodithioic acids to 4,6-O-isopropylidene-D-glucal. These sugar-O-unprotected 2-deoxyglycosyl phosphorodithioates were obtained in high yield and their ability to act as glycosyl donors was demonstrated.
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页码：1767 / 1773
页数：7
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