Synthesis of the Aglycones of Poriolide and Isoporiolide, New Biphenyl-type Flavanones

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概要

• 論文の詳細を見る

• A key point of the synthesis of aglycones (12 and 33) derived from poriolide (1) and isoporiolide (2), the toxic constituents of Leucothoe keiskei, is the construction of the unsymmetric biphenyl compounds, this point was effected by application of the rearrangement reaction of suitable phenyltropone derivatives to biphenyl compounds.

• 公益社団法人日本薬学会の論文
• 1974-01-25

著者

• 小木曽 彰

  Central Research Laboratories Sankyo Co. Ltd.

• 杉村 征夫

  Central Research Laboratories, Sankyo Co., Ltd.

• 杉村 征夫

  Central Research Laboratories Sankyo Co. Ltd.

• 佐藤 藹也

  Central Research Laboratories Sankyo Co. Ltd.

• 樫田 育子

  Central Research Laboratories, Sankyo Co., Ltd.

• 樫田 育子

  Central Research Laboratories Sankyo Co. Ltd.

関連論文

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• Isolation and Structure of Antipeptic Ulcer Diterpene from Thai Medicinal Plant
• The Structure of Toxic Components from Leucothoe Keiskei
• The Structure and Total Synthesis of Futoenone, a Constituent of Piper futokadzura SIEB. et ZUCC.
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• Novel Diterpenelactones with Anti-peptic Ulcer Activity from Croton sublyratus
• Total Synthesis of (±)-Ligantrol, a Linear Polyoxygenated Diterpene
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