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New 1,3,4-thiadiazole thioglycosides linked to substituted arylidine systems were synthesized via glycosylation of the prepared 1,3,4-thiadiazole thiol compounds. Click strategy was also used for the synthesis of new 1,3,4-thiadiazole and 1,2,3-triazole hybrid glycosides by reaction of the acetylenic derivatives with different glycosyl azids followed by deacetylation process. The cytotoxic.
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NOVEL GLYCOSYLATION METHODOLOGY AND THE SYNTHESIS OF HETEROANALOGUES OF DISACCHARIDES Seema Mehta B.Sc.(Hons.), University of Delhi (India), 1988 THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY in the Department of Chemistry O Seema Mehta 1994 Simon Fraser University April 1994.
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Thioglycosides, however, are prepared from thiols, which can be challenging to use because of their pungent and generally unpleasant odors, as well as their tendency to form disulfides through oxidation, and these factors have effectively limited the application of thioglycosides in organic synthesis. Herein, we describe recent efforts towards.
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The synthesis of two protected tetrasaccharide pentenyl glycosides with diarabinan and digalactan branching related to the pectic polysaccharide rhamnogalacturonan I is reported. The strategy relies on the coupling of N-phenyl trifluoroacetimidate disaccharide donors to a common rhamnosyl acceptor. The resulting trisaccharide thioglycosides.
THE SYNTHESIS, IMMUNOLOGICAL CHAFWTERIZATION AND NMR ANALYSIS OF CELL-WALL OLIGOSACCHARIDES OF BACTERIAL ORIGIN Kerry Bruce Reimer M.Sc. Simon Fraser University, 1987 B.Sc. University of British Columbia, 1985 THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY in the Department 0 f.
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These engineered GHs were already successfully applied to the biocatalysed synthesis of thiodi- or -trisaccharides, neo-thioglycoprotein, or even simple thioglycosides with potent inhibitory properties. More complex biomolecules were also obtained like glycans or glycopolymers, or even rarer thiofuranosides.