Anodic Acetoxylation of 2-Hydroxy-3-methoxy-5-methylbenzaldehyde and Its Schiff Bases
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概要
- 論文の詳細を見る
Anodic oxidation of 2-hydroxy-3-methoxy-5-methylbenzaldehyde (II) in acetonitrileacetic acid (3 : 1) containing sodium acetate gave an acetoxylated product in which the acetoxyl group is attached to the side-chain methyl group. On the other hand, oxidation of the Schiff bases (I) derived from II under the same conditions gave cyclohexenetriones. The latter products were shown to be formed by further oxidation of the initially formed acetoxylated Schiff bases, in which the acetoxyl group is introduced into the ring meta to the hydroxyl group.
- 公益社団法人日本薬学会の論文
- 1980-06-25
著者
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枡井 雅一郎
Faculty Of Pharmaceutical Sciences Osaka University
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大森 秀信
Faculty of Pharmaceutical Sciences, Osaka University
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大森 秀信
Faculty Of Pharmaceutical Sciences Osaka University
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枡井 雅一郎
大阪大学薬学部
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松本 晃暎
Faculty of Pharmaceutical Sciences, Osaka University
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松本 晃暎
Faculty Of Pharmaceutical Sciences Osaka University
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