Chemoselective Reduction of β-Keto esters to β-Keto-alcohols

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概要

• 論文の詳細を見る

• Chemoselective reduction of the ester group in keto-esters was studied. Treatment of potassium (or lithium) enolate anions of β-keto-esters with aluminum hydride reduced the ester group chemoselectively to give β-keto-alcohols in moderate yield. Similar reactions of γ-and δ-keto-esters were not chemoselective, yielding a mixture of the diol and the keto-alcohol.

• 社団法人日本薬学会の論文
• 1986-07-25

著者

• 津田 喜典

  Faculty of Pharmaceutical Sciences, Kanazawa University

• 毛利 邦彦

  Showa College Of Pharmaceutical Sciences

• 毛利 邦彦

  Showa College Of Pharmaceutical Sciences:kanazawa University

• 磯部 公明

  昭和薬大

• 津田 喜典

  Faculty Of Pharmaceutical Sciences Kanazawa University

• 多賀 淳一

  Showa College of Pharmaceutical Sciences

• 津田 喜典

  金沢大薬

• 磯部 公明

  Showa Collefe of Pharmaceutical Sciences

• 佐野 博充

  Showa College of Pharmaceutical Sciences

• 磯部 公明

  Showa College Of Pharmaceutical Sciences

• 多賀 淳一

  Showa College Of Pharmaceutical Sciences:kanazawa University

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