水素化リチウムアルミニウムによるVinylogous Esterの還元(第3報)

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概要

• 論文の詳細を見る

• 2-Bromo-5,5-dimethyl-3-methoxy-2-cyclohexenone (V) was reduced in ether to allyl alcohols (VI and VII) with an excess of lithium aluminum hydride, and to VI, VII, and α, β-unsaturated ketone (IX) with a theoretical amount of the hydride. In benzene, V was reduced to VII and IX with an excess hydride. A mechanism is proposed for the random behavior of vinylogous esters (I-V) to lithium aluminum hydride.

• 公益社団法人日本薬学会の論文
• 1970-08-25

著者

• 的場 勝英

  Faculty Of Pharmaceutical Sciences Toyama Medical & Pharmaceutical 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

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