Synthetic Studies on Lignans and Related Compounds. VII. : Synthesis of β-Apoplicatitoxin Trimethyl Ether

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概要

• 論文の詳細を見る

• β-Apoplicatitoxin trimethyl ether (8) was synthesized by selective photocyclization of a dibenzylidenebutyrolactone (6). The photocyclization was preliminarily examined in various solvents by use of a model compound (1), and the total yield of resulting isomeric β-apolignans (2a and 2b) and the ratio of 2a/2b were shown to increase with increasing solvent polarity.

• 社団法人日本薬学会の論文
• 1978-10-25

著者

• 百瀬 雄章

  Faculty of Pharmaceutical Sciences, Kinki University

• 金井 健一

  Faculty Of Pharmaceutical Sciences Osaka University

• 百瀬 雄章

  富山医薬大・薬

• 中村 健

  Faculty of Pharmaceutical Sciences, Osaka University

• 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

• 中村 健

  Faculty Of Pharmaceutical Sciences University Of Tokyo

• 百瀬 雄章

  Faculty Of Pharmaceutical Sciences Kanazawa University

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