Synthesis of Ethyl and Phenyl 1-Thio-1,2-trans-D-Glycopyranosides from the Corresponding Per-O-Acetylated Glycopyranoses having a 1,2-trans-Configuration using Anhydrous Ferric Chloride as a Promoter. - Concepedia

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Synthesis of Ethyl and Phenyl 1-Thio-1,2-trans-D-Glycopyranosides from the Corresponding Per-O-Acetylated Glycopyranoses having a 1,2-trans-Configuration using Anhydrous Ferric Chloride as a Promoter.

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77

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1989

Year

Falguni Dasgupta, Per J. Garegg, Peder Kierkegaard, J. Legendziewicz, Ewa Huskowska, Lija Tekenbergs-Hjelte, Kristina Ohlson, Tomas Alminger, Magnus Erickson, Inger Grundevik,

Acta chemica Scandinavica/Acta chemica Scandinavica. B, Organic chemistry and biochemistry/Acta chemica Scandinavica. A, Physical and inorganic chemistry/Acta chemica Scandinavica. Series B. Organic chemistry and biochemistry/Acta chemica Scandinavica. Series A, Physical and inorganic chemistry

Corresponding Per-o-acetylated GlycopyranosesAsymmetric CatalysisBiosynthesisAnhydrous Ferric ChlorideEngineeringBiochemistryGlycobiologyStereoselective SynthesisNatural Product SynthesisPhenyl 1-Thio-1,2-trans-d-glycopyranosidesEnantioselective SynthesisBiomolecular EngineeringGlycosylation

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