Selective Reduction of Conjugated Enones and Dienones with Trialkylsilane and Titanium Tetrachloride

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概要

• 論文の詳細を見る

• The reaction of conjugated enones and dienones with trimethyl- or triethyl-silane in the presence of titanium tetrachloride followed aqueous workup produced the corresponding α, β-saturated ketones. This particular Lewis acid catalysis has advantage over Rh (I) complex catalysis which fails for sterically hindered substrates.

• 社団法人日本薬学会の論文
• 1977-06-25

著者

• 小泉 徹

  富山医科薬科大学薬学部薬化学

• 小泉 徹

  Faculty Of Pharmaceutical Sciences Toyama Medical And Pharmaceutical University

• Koizumi T

  Faculty Of Pharmaceutical Sciences Toyama Medical And Pharmaceutical University

• 吉井 英一

  Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University

• 林 市裕

  Faculty of Pharmaceutical Sciences, University of Toyama

• 広井 靖子

  Faculty of Pharmaceutical Sciences, University of Toyama

• 吉井 英一

  Faculty Of Pharmaceutical Sciences Toyama Medical And Pharmaceutical University

• 吉井 英一

  富山医科薬科大学薬学部

• 広井 靖子

  Faculty Of Pharmaceutical Sciences University Of Toyama

• Koizumi Toru

  Faculty Of Pharmaceutical Sciences Toyama Medical And Pharmaceutical University

• 林 市裕

  Faculty Of Pharmaceutical Sciences University Of Toyama

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