Journal of the Chemical Society Chemical Communications · 1988 · 121 citations · 0 references
Life SciencesBiochemistryChemistryCarbohydrate ChemistryGlycobiologyPost-translational ModificationCarbohydrate SynthesisGlycan BiosynthesisGlycan StructureGlycosidic Bond FormationMonosaccharide ChemistryN-linked GlycosylationDisaccharide AnalysisDisaccharide SynthesisGlycosylation Method DevelopmentOligosaccharide SynthesisProtecting Group Effects On GlycosylationSelective Deprotection
Pent-4-enyl glycosides, on treatment with halonium ions, become chemospecifically activated so that coupling with partially protected monosaccharides can be effected, leading to the in situ formation of disaccharides.