複素環化合物の開環反応の研究(第4報) : N置換IminopyridiniumおよびN置換Iminoisoquinolinium Betaine類の合成
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概要
- 論文の詳細を見る
Ring opening of N-(2,4-dinitrophenyl)pyridinium chloride (1) with acylhydrazine or arylhydrazine derivatives followed by cyclization of the resulting 5-(2,4-dinitroanilino)-2,4-pentadienal hydrazone (2a-l) gave N-acylimino or N-aryliminopyridinium betaines (3a-l) (Table I). N-Substituted imino-3-picolinium (3m-o), N-substituted imino-3,5-lutidinium (3p-r), and N-substituted iminoisoquinolinium betaines (9a-l) were also prepared from 3-picoline, 3,5-lutidine, and isoquinoline, respectively, by a similar procedure (Table II and III).
- 公益社団法人日本薬学会の論文
- 1971-01-25
著者
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田村 恭光
Faculty Of Pharmaceutical Sciences Osaka University
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田村 恭光
大阪大学薬学部
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辻本 信子
大阪大学薬学部
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内村 美智子
大阪大学薬学部
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内村 美智子
Faculty of Pharmaceutical Sciences, Osaka University
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内村 美智子
Faculty Of Pharmaceutical Sciences Osaka University
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