Publication | Closed Access
NAP Ether Mediated Intramolecular Aglycon Delivery: A Unified Strategy for 1,2‐<i>cis</i>‐Glycosylation
100
Citations
67
References
2008
Year
Man 1Bioorganic ChemistryUnified StrategyGlycobiologyOrganic ChemistryPolysaccharideChemistryStereoselective SynthesisGlycosylationBiochemistryDiversity-oriented SynthesisGlcnac 2BioconjugationNatural Product SynthesisBio-orthogonal ChemistryBiomolecular EngineeringHost-guest ChemistryNatural SciencesDrug Delivery SystemsGlc 3MedicineCarbohydrate-protein Interaction
Abstract A methodology directed towards the stereoselective construction of 1,2‐ cis ‐glycosides through naphthylmethyl (NAP) ether mediated intramolecular aglycon derivery (IAD) has been developed. Stereospecific constructions of various 1,2‐ cis linkages, as in β‐mannopyrano‐, β‐arabinofurano‐, and α‐glucopyranosides, were achieved through NAP‐IAD. This methodology was successfully applied to the synthesis of Glcα(1→2)‐Glcα(1→3)‐Glcα(1→3)Man (Glc 3 Man 1 ), the nonreducing terminal structure of the tetradecasaccharide Glc 3 Man 9 GlcNAc 2 , a common precursor of all N ‐linked glycans.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)
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