Synthetic Approach to the Quassinoid Klaineanone : The Synthesis of a Potential Intermediate by Intramolecular Cycloaddition

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概要

• 論文の詳細を見る

• Thermolysis of 4-acetoxymethylene-2-[2-benzyloxy-2-(5-methoxy-3-methylbenzo-cyclobuten-1-yl] ethyl-2-methylcyclopentan-1,3-dione 1-ethylene ketal (21) gave the stachane-type tetracyclic compound (24), whose deketalization afforded 26,a potential synthetic intermediate to the quassinoid klaineanone (1).

• 公益社団法人日本薬学会の論文
• 1980-08-25

著者

• 本多 利雄

  Institute Of Medicinal Chemistry Hoshi University

• 亀谷 哲治

  Institute of Medicinal Chemistry, Hoshi University

• 亀谷 哲治

  Pharmaceutical Institute, Tohoku University School of Medicine

• 福本 圭一郎

  東北大・薬

• 福本 圭一郎

  Pharmaceutical Institute, Tohoku University

• 千尋 正利

  Pharmaceutical Institute, Tohoku University

• 千尋 正利

  東北大薬

• 本多 利雄

  Pharmaceutical Institute, Tohoku University

• 千尋 正利

  Tokushima Research Institute, Otsuka Pharmaceutical Co., Ltd.,

• 亀谷 哲治

  Pharmaceutical Institute Medical Faculty University Of Osaka

• 福本 圭一郎

  Pharmaceutical Institute Tohoku University School Of Medicine

• 千壽 正利

  Tokushima Research Institute Otsuka Pharmaceutical Co. Ltd.

• 千尋 正利

  Tokushima Research Institute Otsuka Pharmaceutical Co. Ltd.

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