ASYMMETRIC [2+2] PHOTOCYCLOADDITION REACTION OF A CHIRAL DIOXOPYRROLINE TO 2-(TRIMETHYLSILYLOXY)BUTADIENE : CHIRAL SYNTHESIS OF ERYTHRINA ALKALOIDS

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概要

• 論文の詳細を見る

• The detailed stereochemical pathway of [2+2] photocycloaddition reaction of isoquinolinodioxopyrroline to 2-(rtimethylsilyloxy)butadiene was clarified by using an enantiomerically pure substrate. The photoadducts were converted into the synthetic intermediates of Erythrina alkaloids, providing an efficient synthetic method in optically active forms.

• 社団法人日本薬学会の論文
• 1994-06-15

著者

• 津田 喜典

  金沢大学

• 津田 喜典

  Faculty of Pharmaceutical Sciences, Kanazawa University

• 細井 信造

  Faculty of Pharmaceutical Sciences, Kanazawa University

• 細井 深造

  Faculty of Pharmaceutical Sciences, Kanazawa University

• 細井 深造

  Faculty Of Pharmaceutical Sciences Kanazawa University

• 細井 信造

  金沢大薬

• 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

• 神子 万貴子

  Showa College of Pharmaceutical Sciences

• 戸田 潤

  Showa College of Pharmaceutical Sciences

• 佐野 武弘

  昭和薬科大学

• 佐野 武弘

  Showa Pharmaceutical Univ. Tokyo Jpn

• 佐野 武弘

  Showa College Of Pharmaceutical Sciences

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