A Stereoselective Synthesis of the A, B, C-Ring System of a Triterpene, Pollinastanol

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概要

• 論文の詳細を見る

• The A, B, C-ring system of a triterpene, pollinastanol, was stereoselectively constructed by intramolecular γ-alkylation of the β, γ-unsaturated ketone prepared from the thermal cycloaddition product of a benzocyclobutene derivative as a key reaction.

• 社団法人日本薬学会の論文
• 1986-08-25

著者

• 本多 利雄

  Institute Of Medicinal Chemistry Hoshi University

• 亀谷 哲治

  Institute of Medicinal Chemistry, Hoshi University

• 河合 賢一

  Faculty Of Pharmaceutical Sciences Hoshi University

• 戸谷 哲也

  Institute of Medicinal Chemistry, Hoshi University

• 津吹 政可

  Institute of Medicinal Chemistry, Hoshi University

• 河合 賢一

  Institute of Medicinal Chemistry, Hoshi University

• 亀谷 哲治

  Institute Of Medicinal Chemistry Hoshi University

• 津吹 政可

  星薬科大学薬品製造化学教室

• 戸谷 哲也

  Institute Of Medicinal Chemistry Hoshi University

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