The Schmidt Reaction with Some Tetralone and Indanone Derivatives
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概要
- 論文の詳細を見る
While the Schmidt reaction on indanones or tetralones containing no substituents on the benzene moiety of the respective molecules are reported to yield carbostyrils or homocarbostyrils as the sole isolable product, it has been shown that when these compounds contain an electron releasing substituent (e.g. methoxyl group) in the benzene ring, the Schmidt reaction gives both isocarbostyrils and carbostyrils or homoisocarbosyrils and homocarbostyrils in a variable ratio depending upon the structure of the starting materials.
- 公益社団法人日本薬学会の論文
- 1965-09-25
著者
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高松 秀二
Research Laboratory, Dainippon Pharmaceutical Co., Ltd.
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南 新作
Research Laboratories, Dainippon Pharmaceutical Co., Ltd.
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上尾 庄次郎
Faculty Of Pharmaceutical Sciences Kobe Gakuin University
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南 新作
大日本製薬株式会社
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高松 秀二
大日本製薬株式会社
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富田 真次
Research Laboratory, Dainippon Pharmaceutical Co., Ltd.
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高松 秀二
Research Laboratory Dainippon Pharmaceutical Co. Ltd.
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富田 真次
Research Laboratories Dainippon Pharmaceutical Co. Ltd.
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