Studies on Catalytic Hydrogenation of the Exocyclic Double Bond in Reducing Disaccharides

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概要

• 論文の詳細を見る

• Effects of solvents and catalysts in catalytic hydrogenation of the exocyclic double bond in disaccharide-5-ene heptaacetates, synthesized from maltose, lactose, and cellobiose, were investigated. A stereospecific hydrogenation proceeded in such a way that the corresponding 6-deoxy-L-ido isomer was predominant over the 6-deoxy-D-gluco isomer. Preparations of 6-deoxy-maltose, 6-deoxy-α-cellobiose, 4-O-α-D-glucopyranosyl-6-deoxy-L-idopyranose, and 4-O-β-D-glucopyranosyl-6-deoxy-L-idopyranose were also described.

• 社団法人日本薬学会の論文
• 1978-06-25

著者

• 森 雅美

  金城学院大学薬学部

• 森 雅美

  名古屋市立大学看護学部(生化学)

• 森 雅美

  愛知きわみ看護短期大学

• 手島 節三

  名古屋市立大学薬学部

• 手島 節三

  Faculty of Pharmaceutical Sciences, Nagoya City University

• 手島 節三

  Faculty Of Pharmaceutical Sciences Nagoya City University

• 後藤 一

  Department of Biopharmaceutics, Meiji College of Pharmacy

• 森 雅美

  Faculty of Pharmaceutical Sciences, Nagoya City University

• 後藤 一

  Faculty of Pharmaceutical Sciences, Nagoya City University

• 後藤 一

  Department Of Biopharmaceutics Meiji College Of Pharmacy

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