Date of Publication
3-1997
Document Type
Master's Thesis
Degree Name
Master of Science in Chemistry
Subject Categories
Chemistry
College
College of Science
Department/Unit
Chemistry
Thesis Adviser
Gerardo C. Janairo
Defense Panel Chair
Martin C. Ilao
Defense Panel Member
Consolacion Y. Ragasa
Angelica R. Martinez
Abstract/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.
Abstract Format
html
Language
English
Format
Electronic
Accession Number
TG02624
Shelf Location
Archives, The Learning Commons, 12F Henry Sy Sr. Hall
Physical Description
76 leaves
Keywords
Organic compounds—Synthesis; Organic semiconductors; Galactose; Infrared spectra; Spectrum analysis
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Recommended Citation
Quibilan, J. d. (1997). Synthesis of D-galactose modified 1,3-dithiole-2-thione derivative. Retrieved from https://animorepository.dlsu.edu.ph/etd_masteral/1812
