Concise Synthesis of dl-Febrifugine

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概要

• 論文の詳細を見る

• Racemic compound (1) of the antimalarial agents febrifugine (d-1) was synthesized using an stereoselective Michael reaction of an ω-amidoenone (5) which was prepared by the Wittig reaction of piperidinediol (7).

• 社団法人日本薬学会の論文
• 2005-07-01

著者

• 原山 尚

  Faculty Of Pharmaceutical Sciences Kyoto University

• 竹内 義雄

  富山大院医薬

• Azuma K

  Okayama Univ. Okayama Jpn

• TAKEUCHI Yasuo

  Faculty of Pharmaceutical Sciences, Okayama University

• OSHIGE Miyo

  Faculty of Pharmaceutical Sciences, Okayama University

• AZUMA Kumiko

  Faculty of Pharmaceutical Sciences, Okayama University

• ABE Hitoshi

  Faculty of Pharmaceutical Sciences, Okayama University

• HARAYAMA Takashi

  Faculty of Pharmaceutical Sciences, Okayama University

• Azuma Kumiko

  Faculty Of Pharmaceutical Sciences Okayama University

• Oshige Miyo

  Faculty Of Pharmaceutical Sciences Okayama University

• Abe H

  Graduate School Of Sci. And Engineering Univ. Of Toyama

• Harayama Takashi

  Faculty Of Pharmaceutical Sciences Okayama University

• Abe Hitoshi

  Univ. Toyama Toyama Jpn

• Abe Hitoshi

  Faculty Of Pharmaceutical Sciences Okayama University:advanced Science Research Center Okayama Unive

• Abe Hitoshi

  Faculty Of Pharmaceutical Sciences Okayama University

• Takeuchi Yasuo

  Faculty Of Pharmaceutical Sciences Okayama University

• Harayama Takashi

  Faculty of Pharmaceutical Sciences at Kagawa Campus, Tokushima Bunri University

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