COMPETITIVE REARRANGEMENT AND CYCLOREVERSION REACTIONS OF THE DIMETHOXYSUBSTITUTED COOKSON'S CAGE DIKETONE EFFECTED WITH LEWIS ACID CATALYST
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概要
- 論文の詳細を見る
The dimethoxy-substituted Cookson's cage diketone (1a) underwent competitive rearrangement and cycloreversion reactions under treatment with Lewis acid, where two types of electron push-pull interaction are operative.
- 社団法人日本薬学会の論文
- 1985-07-25
著者
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岡本 康
Institute Of Synthetic Organic Chemistry Faculty Of Pharmaceutical Sciences Kyushu University 62
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兼松 顯
Institute of Synthetic Organic Chemistry, Faculty of Pharmaceutical Sciences, Kyushu University
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瀬ノ口 和彦
Institute of Synthetic Organic Chemistry, Faculty of Pharmaceutical Sciences, Kyushu University 62
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兼松 顯
Institute Of Synthetic Organic Chemistry Faculty Of Pharmaceutical Sciences Kyushu University
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兼松 顕
Institute Of Applied Organic Chemistry Faculty Of Engineering Nagoya University
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瀬ノ口 和彦
Institute Of Synthetic Organic Chemistry Faculty Of Pharmaceutical Sciences Kyushu University 62
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