A New Method for the Preparation of 2-Hydroxymethyl-3-quinolinecarboxylic Acid Lactone Derivatives
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概要
- 論文の詳細を見る
The reaction of 2-acetoxymethyl-3-acetylquinolines (V, VI) with sodium hydride gave 2-hydroxymethyl-3-quinolinecarboxylic acid lactones (IX, X), presumably formed with the migration of acetyl group. On the other hand, the fact that the reaction of 3-acetyl-2-benzoyloxymethylquinoline (VIII) with sodium hydride gave a lactone (IX) and acetophenone would strongly support for the mechanism of the lactone formation with the acyl migration.
- 公益社団法人日本薬学会の論文
- 1975-10-25
著者
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栗原 拓史
Osaka University of Pharmaceutical Sciences
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平野 弘
Osaka College of Pharmacy
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道田 隆
Faculty Of Pharmaceutical Sciences Osaka University
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道田 隆
Osaka College of Pharmacy
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栗原 拓史
Osaka College Of Pharmacy
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