Chemical Modification of Lactose. VII. Synthesis of 4-0-β-D-Idopyranosyl-D-glucopyranose

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概要

• 論文の詳細を見る

• The title new reducing disaccharide (10) was synthesized starting from 1,6-anhydro-4', 6'-O-benzylidene-β-lactose (1) via selective benzoylation, epoxide formation, alkaline cleavage of the epoxide, and removal of the blocking groups. This is the first reported example of isomerization of the secondary hydroxyl groups in the D-galactopyranosyl moiety of lactose.

• 公益社団法人日本薬学会の論文
• 1976-07-25

著者

• 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

• 千葉 拓

  Faculty of Pharmaceutical Sciences, Nagoya City University

• 手島 節三

  Faculty Of Pharmaceutical Sciences Nagoya City University

• 千葉 拓

  名古屋市立大学薬学部

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