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首页> 外文期刊>Letters in organic chemistry >Efficient One-pot Synthesis of alpha-Alkylated beta-Ketothioesters from H2SO4-Catalyzed Tandem Alkylation/Hydrolysis Reaction of Acyclic alpha-Oxo Ketene Dithioacetals with Alcohols
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Efficient One-pot Synthesis of alpha-Alkylated beta-Ketothioesters from H2SO4-Catalyzed Tandem Alkylation/Hydrolysis Reaction of Acyclic alpha-Oxo Ketene Dithioacetals with Alcohols

机译:从H 2 SO 4催化串联烷基化/水解反应与醇的高效单壶合成α-烷基化β-酮磷酸酯的合成烷基化/水解反应

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摘要

In the paper, we wish to report an efficient one-pot synthesis of alpha-alkylated beta-ketothioesters based on H2SO4-catalyzed tandem alkylation/hydrolysis reaction between acyclic alpha-oxo ketene dithio-acetals and alcohols. It was shown that the tandem reaction could efficiently occur in the presence of 5 mol% H2SO4 at room temperature in CH3CN, affording the desired alpha-alkylated beta-ketothioesters in excellent yields. The use of very small amounts of catalyst, good generality, low cost of the reagents, excellent yield and mild reaction conditions outline the notable features of the reaction.
机译:在本文中,我们希望基于环α-氧代酮二硫代 - 缩醛和醇之间的H 2 SO 4催化串联烷基化/水解反应报告高效的单罐合成α-烷基化β-酮磷酸酯。 结果表明,在CH3CN的室温下,可以在5mol%H 2 SO 4存在下有效地发生串联反应,得到所需的α-烷基化β-酮甾体以优异的产率。 使用非常少量的催化剂,良好的一般性,低成本的试剂,优异的产率和温和的反应条件概述了反应的显着特征。

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