Fischer Indolization of N^α-Alkyl-2-allylphenylhydrazones
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概要
- 論文の詳細を見る
Fischer indolization of the hydrazones of 8-allyl-1-amino-, 1,2,3,4-tetrahydroquinoline and related compounds was investigated. Fischer indolization induced Cope rearrangement of the allyl group and acid-catalyzed intramolecular cycloaddition between the hydrazonyl group and the vinyl group. The base treatment of the latter reaction product caused eliminative ring-opening of the adduct and led to the formation of an indoline skeleton bearing a 2-ketoalkyl group at the C-2 position.
- 社団法人日本薬学会の論文
- 1993-05-15
著者
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片山 肇
Niigata College Of Pharmacy
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片山 肇
新潟薬科大学薬化学教室
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高津 徳行
Niigata College of Pharmacy
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竹内 庸子
Niigata College of Pharmacy
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山際 道代
Niigata College of Pharmacy
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