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Aldol–Tishchenko reaction
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Aldol–Tishchenko reaction : ウィキペディア英語版
Aldol–Tishchenko reaction
The Aldol–Tishchenko reaction is a tandem reaction involving an aldol reaction and a Tishchenko reaction. In organic synthesis it is a method to convert aldehydes and ketones into 1,3-hydroxyl compounds. The reaction sequence in many examples starts from conversion of a ketone into an enolate by action of lithium diisopropylamide (LDA). The mono-ester diol is then converted into the diol by a hydrolysis step. With both the acetyl trimethylsilane〔 and propiophenone〔 as reactants, the diol is obtained as a pure diastereoisomer.

== References ==


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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