Anodic Pyridination of 2,6-Di-tert-butyl-4-methylphenol
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概要
- 論文の詳細を見る
Anodic pyridination of 2,6-di-tert-butyl-4-methylphenol (1) in acetonitrile gave the corresponding 4-pyridinated cyclohexadienone and the side-chain pyridinated phenol. The yield of the former dienone decreased and that of the latter product increased with increase in the amount of added bases, pyridine and/or 2,6-lutidine. On the other hand, the product distribution in the methoxylation of 1 in methanol or in acetonitrile containing methanol was little affected by the addition of 2,6-lutidine, and 4-methoxylated dienone was the main product.
- 公益社団法人日本薬学会の論文
- 1982-10-25
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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植田 千裕
Faculty of Pharmaceutical Sciences, Osaka University
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植田 千裕
大阪大学薬学部
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徳野 美
Faculty of Pharmaceutical Sciences, Osaka University
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徳野 美
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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