Synthesis of (±)-β-Cuparenone Based on a Lewis Acid-Promoted [4^++2] Polar Cycloaddition of m-Tolylthiomethyl Chloride

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概要

• 論文の詳細を見る

• In the presence of AlCl_3,m-tolylthiomethyl chloride (1) reaceted with methyl 3,4-dimetylcyclopent-3-ene-1-carboxylate (4) to give the [4^++2] polar cycloadditino product 6,which was transformed into (±)-β-cuparenone (11) in 4 steps.

• 社団法人日本薬学会の論文
• 1990-06-25

著者

• 中谷 浩

  Kyoto Pharmaceutical University

• 池田 正澄

  Kyoto Pharmaceutical University

• 池田 正澄

  京都薬科大学

• 石橋 弘行

  Kyoto Pharmaceutical University

• 石橋 弘行

  金沢大学薬学部

• 石橋 弘行

  京都薬科大学

• 崔 徳載

  Kyoto Pharmaceutical University, Misasagi

• 田口 満美

  Kyoto Pharmaceutical University, Misasagi

• 田口 満美

  Kyoto Pharmaceutical University Misasagi

• 崔 徳載

  Kyoto Pharmaceutical University Misasagi

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