Reaction of 1-Pyrrolidino-1-cyclohexene with Imidoyl Chlorides and a Route to Producing Phenanthridines
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概要
- 論文の詳細を見る
Reaction of 1-pyrrolidino-1-cyclohexene with N-arylbenzimidoyl chlorides has been successfully performed to result in introduction of benzimidoyl groupings at β-carbon of the enamine. Easy hydrolysis of enamine moiety of these products provides an effective means of preparation of mono-anils of 2-benzoylcyclohexanone, from which several phenanthridine derivatives have been newly obtained by action of polyphosphoric acid.
- 公益社団法人日本薬学会の論文
- 1975-06-25
著者
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関屋 実
School Of Pharmaceutical Sciences University Of Shizuoka
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関屋 実
Shizuoka College of Pharmacy
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森本 俊明
Shizuoka College of Pharmacy
関連論文
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