SYNTHESIS OF UNPROTECTED 2-DEOXYGLYCOSYL DONORS, BINO-HEXOPYRANOSYL)-0,0-DIALKYLPHOSPHORODITHIOATES

Citation
W. Kudelska et al., SYNTHESIS OF UNPROTECTED 2-DEOXYGLYCOSYL DONORS, BINO-HEXOPYRANOSYL)-0,0-DIALKYLPHOSPHORODITHIOATES, Polish Journal of Chemistry, 68(9), 1994, pp. 1767-1773
Citations number
14
Categorie Soggetti
Chemistry
Journal title
ISSN journal
01375083
Volume
68
Issue
9
Year of publication
1994
Pages
1767 - 1773
Database
ISI
SICI code
0137-5083(1994)68:9<1767:SOU2DB>2.0.ZU;2-3
Abstract
Sugar-O-unprotected S-(2-deoxyglycosyl)phosphorodithioates were synthe sized 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 obt ained in high yield and their ability to act as glycosyl donors was de monstrated.