Dioxopyrrolines. XLIII. : Diels-Alder Reaction of 4,5-Diethoxycarbonyl-1H-pyrrole-2,3-dione with Butadienes : Synthesis of Polyfunctionalized Hydroindoles

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概要

• 論文の詳細を見る

• A new dioxopyrroline, 4,5-diethoxycarbonyl-1H-pyrrole-2,3-dione (3), was proved to be a strong dienophile in the Diels-Alder reaction with various butadienes. This cycloaddition reaction proceeded in a regio- and stereo-selective manner to give the polyfunctionalized hydroindoles (4-8,10) which may be potential synthetic intermediates of Erythrina alkaloids.

• 社団法人日本薬学会の論文
• 1989-12-25

著者

• 津田 喜典

  Faculty of Pharmaceutical Sciences, Kanazawa University

• 毛利 邦彦

  Showa College Of Pharmaceutical Sciences

• 毛利 邦彦

  Showa College Of Pharmaceutical Sciences:kanazawa University

• 榎本 浩

  Showa College Of Pharmaceutical Sciences Kanazawa University

• 磯部 公明

  昭和薬大

• 津田 喜典

  Faculty Of Pharmaceutical Sciences Kanazawa University

• 佐野 武弘

  Showa College of Pharmaceutical Sciences.

• 津田 喜典

  金沢大薬

• 磯部 公明

  Showa Collefe of Pharmaceutical Sciences

• 毛利 智恵

  Showa College of Pharmaceutical Sciences

• 佐野 博充

  Showa College of Pharmaceutical Sciences

• 佐野 武弘

  Showa Pharmaceutical Univ. Tokyo Jpn

• 佐野 武弘

  Showa College Of Pharmaceutical Sciences

• 磯部 公明

  Showa College Of Pharmaceutical Sciences

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