Heterocycles. XVII. Sodium Borohydride Reduction of Flavanonols and Hydrolysis of (±)-Fistacacidin Acetates
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概要
- 論文の詳細を見る
The effects of 5-substituents on sodium borohydride reduction of flavanonols have been examined. The bulk of substituents governs the stereochemistry of reduction, and particularly, the acetoxy group gives an interesting result accompanied by over-reduction. In addition, the 5-acetoxy group plays an improtant role in the stereochemistry of the newly introduced 4-oxygen functions in hydrolysis of (±)-fistacacidin acetates.
- 社団法人日本薬学会の論文
- 1985-08-25
著者
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恩田 政行
School of Pharmaceutical Sciences, Kitasato University
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高橋 洋
School Of Pharmaceutical Sciences Kitasato University
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窪田 由美子
School Of Pharmaceutical Sciences Kitasato University
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恩田 政行
Shenyang Pharmaceutical University
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井口 三恵子
School of Pharmaceutical Sciences, Kitasato University
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井口 三恵子
School Of Pharmaceutical Sciences Kitasato University
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