Naturally Occurring 5-Lipoxygenase Inhibitors. VII. Practical Synthesis of Ardisiaquinones D, E and F

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概要

• 論文の詳細を見る

• The convergent synthesis of ardisiaquinones D (1), E (3) and F (4), isolated as 5-lipoxygenase inhibitors from Ardisia sieboldii, has been achieved efficiently by a cross-coupling reaction via an acetylene between two benzene units bearing appropriate functional groups readily derived from 2,5-dimethoxy-1,4-benzoquinone.

• 社団法人日本薬学会の論文
• 1998-11-15

著者

• 桐山 優子

  Faculty of Pharmaceutical Sciences, Tokushima Bunri University

• 福山 愛保

  徳島文理大薬

• KODAMA Mitsuaki

  Faculty of Pharmaceutical Sciences, Tokushima Bunri University

• FUKUYAMA Yoshiyasu

  Faculty of Pharmaceutical Sciences, Tokushima Bunri University

• KIRIYAMA Yuuko

  Faculty of Pharmaceutical Sciences, Tokushima Bunri University

• 桐山 優子

  Faculty Of Pharmaceutical Sciences Tokushima Bunri University

• Kiriyama Y

  Faculty Of Pharmaceutical Sciences Tokushima Bunri University

• Kodama Mitsuaki

  Faculty Of Pharmaceutical Sciences Tokushima Bunri University

• Fukuyama Yoshiyasu

  Faculty Of Pharmaceutical Science Tokushima Bunri University

• Kiriyama Yuuko

  Faculty Of Pharmaceutical Sciences Tokushima Bunri University

• Kodama Mitsuaki

  Faculty of Pharmaceutical Science, Tokushima Bunri University

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