European Journal of Organic Chemistry · 2012 · 32 citations · 34 references
Life SciencesBiochemistryChemistryBiocatalysisCarbohydrate ChemistryCatalysisCarbohydrate SynthesisGlycan BiosynthesisGlycosidic Bond FormationGlycosylation PathwaysN-linked GlycosylationProtein GlycosylationCatalytic FunctionalizationDisaccharide SynthesisGlycan SynthesisGlycoconjugate SynthesisGlycosylation BiocatalysisGlycosylation Cascade ReactionsGlycosylation MechanismsGlycosylation Method Development
Abstract Efficient and highly selective glycosylation reactions of peracetylated β‐ D ‐ N ‐acetylglucosamine are described using catalytic iron(III) triflate and 2,4,6‐tri‐ tert ‐butylpyrimidine (TTBP) under microwave conditions. We have demonstrated that the formation of β‐(1→6) and β‐(1→3) linked disaccharides are obtained in high yields in the presence ofvarious protecting groups.
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