Synthetic Studies on Spirovetivane Phytoalexins. III. : A Total Synthesis of (±)-Lubiminol

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概要

• 論文の詳細を見る

• A total synthesis of (±)-lubiminol (2) from the allylic alcohol (3) was achieved through the introduction of a bis(ethoxycarbonyl)methyl group with inversion at C_2 followed by hydrogenation of the C_6-C_7 double bond and transformation of the bis(ethoxycarbonyl)methyl group into isopropenyl. On the other hand, the alcohol (1) was an inefficient starting material for the synthesis.

• 公益社団法人日本薬学会の論文
• 1989-04-25

著者

• 山田 稔

  Faculty Of Pharmaceutical Sciences Osaka University

• 今西 武

  Faculty Of Pharmaceutical Sciences Osaka University

• 竹本 佳司

  Faculty Of Pharmaceutical Sciences Osaka University

• 田中 徹明

  Faculty of Pharmaceutical Sciences, Osaka University

• 岩田 宙造

  Faculty of Pharmaceutical Sciences, Osaka University

• 内田 秀治

  Faculty of Pharmaceutical Sciences, Osaka University

• 岩田 宙造

  阪大院薬

• 田中 徹明

  阪大院薬

• 田中 徹明

  Faculty Of Pharmaceutical Sciences Osaka University

• Tanaka T

  Kvushu Univ. Fukuoka Jpn

• Tanaka T

  Osaka Univ. Osaka Jpn

• Takemoto Yoshiji

  Faculty Of Pharmaceutical Sciences Osaka University

• Takemoto Y

  Graduate School Of Pharmaceutical Sciences Kyoto University

• 岩田 宙造

  Faculty Of Pharmaceutical Sciences Osaka University

• 窪田 均

  Faculty Of Pharmaceutical Sciences Osaka University

• 内田 秀治

  Faculty Of Pharmaceutical Sciences Osaka University

• Imamura T

  Faculty Of Pharmaceutical Sciences Osaka University

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• ジヒドロピリジノンを共通出発原料としたアルカロイド類の合成

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