Synthesis of D-galactose modified 1,3-dithiole-2-thione derivative

A procedure for the synthesis of a D-galactose modified 1,3-dithiole-2-thione derivative is described. D-galactose is converted to 1,2:3,4-di-O-isopropylidene-D-galactopyranose, which is esterified with trifluoromethanesulfonic anhydride. The triflate ester is then treated 2-hydroxyethoxide followed...

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Bibliographic Details
Main Author: Quibilan, Jose Mari dela Cruz
Format: text
Language:English
Published: Animo Repository 1997
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Online Access:https://animorepository.dlsu.edu.ph/etd_masteral/1812
https://animorepository.dlsu.edu.ph/cgi/viewcontent.cgi?article=8650&context=etd_masteral
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Institution: De La Salle University
Language: English
Description
Summary:A procedure for the synthesis of a D-galactose modified 1,3-dithiole-2-thione derivative is described. D-galactose is converted to 1,2:3,4-di-O-isopropylidene-D-galactopyranose, which is esterified with trifluoromethanesulfonic anhydride. The triflate ester is then treated 2-hydroxyethoxide followed by the tosylation of the hydroxyethylene derivative. The target compound is obtained by replacement of the tosylate with the zinc complex of 4,5-dimercapto-1,3-dithiole-2-thione dianion salt.