2(3H)- and 2(5H)-Furanones. IV. The Di-π-methane Rearrangement of 3,4-Bis(phenymethyl)-2(5H)-furanone

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概要

• 論文の詳細を見る

• The photo-irradiation of 3,4-bis(phenylmethyl)-2(5H)-furanone (5) in acetone or in methanol resulted in selective rearrangement of the 4-phenymethyl moiety and gave 5-phenyl-1-(phenylmethyl)-3-oxabocyclo[3.1.0]hexan-2-one (9)along with cis- and trans-3,4-bis(phenylmethyl)dihydro-2(3H)-furanone (10a and 10b). The difference in photochemical behavior from that of β-apolignan (1) is discussed.

• 社団法人日本薬学会の論文
• 1992-09-25

著者

• 田辺 元三

  近畿大学薬学部

• 村岡 修

  Faculty of Pharmaceutical Sciences, Kinki University

• 田辺 元三

  Faculty of Pharmaceutical Sciences, Kinki University

• 村岡 修

  Faculty Of Pharmaceutical Sciences Kinki University

• 田邉 元三

  近畿大薬

• 百瀬 雄章

  富山医薬大・薬

• 百瀬 雄章

  (present Address)faculty Of Pharmaceutical Sciences Toyama Medical And Pharmaceutical University

• 百瀬 雄章

  Faculty Of Pharmaceutical Sciences Osaka University

• 辻森 久元

  Faculty of Pharmaceutical Sciences, kinki University

• 辻森 久元

  Faculty Of Pharmaceutical Sciences Kinki University

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