The Reactions of Activated Amides. I. The Reactions of Iminoethers derived from the Secondary Amides with the Nucleophiles
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概要
- 論文の詳細を見る
The reactions of the iminoether (VII) derived from α-piperidone with alkyl cyanoacetate, ethyl acetoacetate, and acetylacetone were investigated. The highly conjugated condensation products were then converted to the saturated compounds. Thus, isopelletierine (XVIII) was synthesized by the reduction of XIII, followed by reoxidation of the secondary alcohol (XVII) into the corresponding ketone. Then, condensation of the oxindole iminoethers with ethyl cyanoacetate was carried out and their reactivity was found to be considerably less than that of simple iminoethers.
- 公益社団法人日本薬学会の論文
- 1969-11-25
著者
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大沼 毅
北大・薬:(現)ブリストル・マイヤーズ研究所(株)
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伴 義雄
Faculty of Pharmaceutical Sciences, School of Medicine, Hokkaido University
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永井 雅子
Faculty of Pharmaceutical Sciences, School of Medicine, Hokkaido University
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大石 武
Faculty Of Engineering Yokohama National University:(present Address)meiji College Of Pharmacy
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伴 義雄
東邦大・薬
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伴 義雄
Faculty Of Pharmaceutical Sciences Hokkaido University
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大石 武
北大・薬:(現)理化学研究所
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落合 美和子
Faculty Of Pharmaceutical Sciences Hokkaido University
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伝 浩一
Faculty Of Pharmaceutical Sciences Hokkaido University
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大沼 毅
Faculty of Pharmaceutical Sciences, Hokkaido University
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森山 等
Faculty of Pharmaceutical Sciences, Hokkaido University
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永井 雅子
北大・薬
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森山 等
Faculty Of Pharmaceutical Sciences Hokkaido University
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