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1,2-cis-β-Mannopyranoside Formation by the Dimethylphosphinothioate Method
12
Citations
7
References
1993
Year
Enantioselective SynthesisBioorganic ChemistryDerivativesBiochemistryEngineeringNatural Sciences1,2-Cis-β-mannopyranoside FormationAbstract 1,2-Cis-β-mannopyranosidesSeveral AlcoholsOrganic ChemistryStereoselective SynthesisChemistryAsymmetric CatalysisSynthetic ChemistryMannopyranosyl Dimethylphosphinothioate DerivativesBiomolecular Engineering
Abstract 1,2-cis-β-Mannopyranosides were obtained predominantly by reactions of mannopyranosyl dimethylphosphinothioate derivatives with several alcohols in the presence of iodine and a catalytic amount of triphenylmethyl perchlorate as the activator in benzene.
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