Triterpenoid Chemistry. VI. Lycopodium Triterpenoid. (5). The Structures and Stereochemistry of Serratriol, 21-Episerratriol, and Lycoclavanol

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概要

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• The structures of triterpenoid-triols, serratriol, 21-episerratriol, and lycoclavanol, isolated from Lycopodium plants, were established as serrat-14-en-3β, 21α, 24-triol (3), serrat-14-en-3β, 21β, 24-triol (36), and serrat-14-en-3α, 21β, 24-triol (22), respectively. The fourth possible stereoisomeric triol, serrat-14-en-3α, 21α, 24-triol (43), was prepared from lycoclavanol. New method of acetonide formation of 1,3-glycol was reported.

• 社団法人日本薬学会の論文
• 1974-10-25

著者

• 津田 喜典

  Faculty of Pharmaceutical Sciences, Kanazawa University

• 犬伏 康夫

  Faculty of Pharmaceutical Sciences, Kyoto University

• 津田 喜典

  Faculty Of Pharmaceutical Sciences Kanazawa University

• 畠中 稔

  The Institute of Scientific and Industrial Research, Osaka University

• 森本 明

  Showa College Of Pharmaceutical Sciences

• 佐野 武弘

  Faculty of Pharmaceutical Sciences, Osaka University

• 森本 明

  Faculty of Pharmaceutical Sciences, Osaka University

• 畠中 稔

  Faculty of Pharmaceutical Sciences, Osaka University

• 犬伏 康夫

  Faculty Of Pharmaceutical Sciences Kyoto University

• 犬伏 康夫

  Faculty Of Pharmaceutical Sciences Osaka University

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