Difluoromethylation Reactions of Ethyl Pyruvate with the TDAE - A MildApproach to the Synthesis of 3,3-Difluoro-2-hydroxy-2-methyl-4-oxo-butyric Ethyl Esters Derivatives

Difluoromethylation Reactions of Ethyl Pyruvate with the TDAE - A MildApproach to the Synthesis of 3,3-Difluoro-2-hydroxy-2-methyl-4-oxo-butyric Ethyl Esters Derivatives
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丙酮酸乙酯与 TDAE 的二氟甲基化反应 - 合成 3,3-二氟-2-羟基-2-甲基-4-氧代-丁酸乙酯衍生物的温和方法

DOI:
10.1055/s-2002-33517
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发表时间:
2002
期刊:
影响因子:
2
通讯作者:
W. Dolbier
W. Dolbier
中科院分区:
化学4区
文献类型:
--
作者:
M. Médebielle;Katsuya Kato;W. Dolbier

文献摘要

被引文献

相似文献

在丙酮酸乙酯存在下,通过四(二甲氨基)乙烯(TDAE)介导的一系列 RCF 2 X(X = Cl 或Br)起始材料的还原,可以轻松以中等至良好的收率轻松获得新的 3,3-二氟-2-羟基-2-甲基-4-氧代-丁酸乙酯衍生物。
New 3,3-difluoro-2-hydroxy-2-methyl-4-oxo-butyric ethyl esters derivatives are easily obtained in moderate to good yields from the tetrakis(dimethylamino)ethylene (TDAE) mediated reduction of a series of RCF 2 X (X = Cl orBr) starting materials in the presence of ethyl pyruvate.