Selective Synthesis of β-D-Glucopyranosyl 1-Triphosphate by Reaction of D-Glucopyranose with Inorganic cyclo-Triphosphate

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概要

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• The stereoselective phosphorylation of D-glucopyranose has been achieved using inorganic sodium cyclo-triphosphate hexahydrate (P_<3m>), Na_3P_3O_9・6H_2O. The reaction product has been confirmed to the β-D-glucopyranosyl 1-triphosphate by multinuclear NMR and HPLC, and its maximum yield was about 47%.

• 公益社団法人日本薬学会の論文
• 1998-04-15

著者

• TSUHAKO Mitsutomo

  Department of Chemistry, Kobe Pharmaceutical University

• NAKAYAMA HIROKAZU

  Department of Biology, Graduate School of Science, Osaka City University

• Watanabe Mitsuo

  School Of Pharmaceutical Sciences Teikyo Univ.

• Watanabe M

  School Of Pharmaceutical Sciences Teikyo Univ.

• Watanabe Mari

  Department Of Obstetrics And Gynecology St Marianna University School Of Medicine

• Watamabe Minae

  Faculty Of Pharmaceutical Sciences Setsunan University

• Nakayama H

  Department Of Functional Molecular Chemistry Kobe Pharmaceutical University

• INOUE Hideko

  Department of Functional Molecular Chemistry, Kobe Pharmaceutical University

• Inoue H

  Department Of Functional Molecular Chemistry Kobe Pharmaceutical University

• Tsuhako M

  Department Of Functional Molecular Chemistry Kobe Pharmaceutical University

• Tsuhako Mitsutomo

  Department Of Chemistry Kobe Pharmaceutical University

• Watanabe Mari

  Department of Internal Medicine, Kitasato Institute Hospital

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