Angewandte Chemie International Edition in English · 1994 · 139 citations · 15 references
Life SciencesBiochemistryMicrobiologyCarbohydrate BiochemistryCarbohydrate ChemistryGlycobiologyCarbohydrate StructureCarbohydrate SynthesisGlycan BiosynthesisMicrobial GlycobiologyMonosaccharide ChemistryPolysaccharide StructureBacterial PolysaccharidesGlycoconjugate SynthesisGlycosylation Method DevelopmentMonosaccharide SynthesisOligosaccharide SynthesisOne-pot Oligosaccharide SynthesisPolysaccharide Antigen ChemistryRegioselective Glycosylation
The reactivity of sugars in glycosylation reactions can be tuned by the cyclohexane-1,2-diacetal (CDA) protecting group. In the efficient synthesis of trisaccharide 1 from three monosaccharide units, no functional group conversions are necessary between glycosylation steps.
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G.H. Veeneman, Steven H. van Leeuwen, Jacques H. van Boom · Tetrahedron Letters · 1990 · 866 citations
<i>n</i>-Pentenyl Glycosides in Organic Chemistry: A Contemporary Example of Serendipity
Bert Fraser‐Reid, Uko E. Udodong, Zufan Wu et al. · Synlett · 1992 · 336 citations