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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Reaction of lithium enediolates with perfluoroketene dithioacetals.Synthesis of a-trifluoromethyl y-dicarboxylic acid derivatives
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Reaction of lithium enediolates with perfluoroketene dithioacetals.Synthesis of a-trifluoromethyl y-dicarboxylic acid derivatives

机译:烯二醇锂与全氟乙烯二硫缩醛的反应α-三氟甲基γ-二羧酸衍生物的合成

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摘要

The reaction of perfluoroketene dithioacetals with dianions of carboxylic acids proceeds through the substitution of the vinylic fluoride.The preparative value of this reaction depends strongly on the reaction and work-up conditions,the optimisation of which led to use LDA as a base and multiple extraction techniques.The overall process may be considered as a formal synthesis of a-trifluoromethyl gamma-dicarboxylic acid derivatives.
机译:全氟乙烯二硫缩醛与羧酸的二价阴离子之间的反应是通过氟乙烯的取代进行的。该反应的制备价值在很大程度上取决于反应条件和后处理条件,其优化导致使用LDA作为碱并多次萃取。整个过程可以被认为是α-三氟甲基γ-二羧酸衍生物的正式合成。

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