水素化リチウムアルミニウムによるVinylogous Esterの還元(第1報)

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概要

• 論文の詳細を見る

• Acutumine acetate (I) is reduced to II with an excess of lithium aluminium hydride in ether followed by decomposition of aluminium complex with ammonium chloride and water. It is well known that vinylogous esters of six membered rings are reduced to α, β-unsaturated ketones with lithium aluminium hydride. Our experimentals showed that a vinylogous ester (XIII) of five membered rings is reduced to an allyl alcohol (XIV) in quantitative yield under the conditions described in the reduction of I.

• 公益社団法人日本薬学会の論文
• 1969-04-25

著者

• 佐々木 喜男

  大阪大学薬学部

• 佐々木 喜男

  Faculty Of Pharmaceutical Sciences Osaka University

• 的場 勝英

  Faculty Of Pharmaceutical Sciences Osaka University

• 山崎 高応

  富山医科薬科大学 薬

• 山崎 高応

  富山大学薬学部

• 的場 勝英

  富山大学薬学部

• 吉井 勝美

  富山大学薬学部

• 吉岡 満子

  富山大学薬学部

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