Electrochemical Oxidation of Olefins Using N-Hydroxyphthalimide as a Mediator
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概要
- 論文の詳細を見る
Electrochemical oxidation of olefins using N-hydroxyphthalimide as a mediator was studied. Allylic methylene and allylic methine groups were oxidized to give the corresponding enones, while allylic methyl groups were not readily oxidized except for those of 2,3-dimethyl-2-butene. The product distribution was similar to that observed in free radical autoxidation of olefins. A possible mechanism of the oxidation is proposed.
- 公益社団法人日本薬学会の論文
- 1985-11-25
著者
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土田 圭一
Faculty Of Pharmaceutical Sciences Osaka University
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枡井 雅一郎
Faculty Of Pharmaceutical Sciences Osaka University
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尾崎 茂子
Faculty of Pharmaceutical Sciences, Osaka University
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細見 克子
Faculty of Pharmaceutical Sciences, Osaka University
-
尾崎 茂子
Faculty Of Pharmaceutical Sciences Osaka University
-
細見 克子
Faculty Of Pharmaceutical Sciences Osaka University
-
枡井 雅一郎
大阪大学薬学部
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