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Dispiroketals in Synthesis (Part 3):<sup>1</sup>Selective Protection of Diequatorial Vicinal Diols in Carbohydrates
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1993
Year
Bioorganic ChemistrySelective ProtectionGlycobiologyOrganic ChemistryPolysaccharidePart 3Stereoselective SynthesisBiochemistryBioassay-guided IsolationTrans Vicinal DiolsNatural Product SynthesisPharmacologyEnantioselective SynthesisBiomolecular EngineeringDiequatorial Vicinal DiolsNatural SciencesMedicineSynthetic ChemistryDrug DiscoveryDrug Analysis
The selective protection of trans vicinal diols of a range of monosaccharides by formation of 1,8,13,16-tetraoxadispiro[5.0.5.4]hexadecanes (dispiroketals) is reported.