首页> 外文期刊>Journal of Fluorine Chemistry >Regio- and stereo-specific preparation of (E)-1 -aryl-3,3,3-trifluoro-1 -iodo-propenes and their palladium-catalyzed reaction with terminal alkynes
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Regio- and stereo-specific preparation of (E)-1 -aryl-3,3,3-trifluoro-1 -iodo-propenes and their palladium-catalyzed reaction with terminal alkynes

机译:(E)-1-芳基-3,3,3-三氟-1-碘丙烯的区域和立体特异性制备及其与末端炔烃的钯催化反应

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摘要

A new type of iodo-containing trifluoromethylated building blocks were synthesized. The reaction of 1-aryl-3,3,3-trifluoropropynes 1 with lithium iodide in acetic acid at 75 °C gave (E)-1-aryl-3,3,3-trifiuoro-1-iodo-propenes 2 in high yield, which undergo the palladium-catalyzed Sonogashira reaction with terminal alkynes afforded trifiuoromethyl-containing 1,3-enynes in high yield.
机译:合成了一种新型的含碘三氟甲基化结构单元。 1-芳基-3,3,3-三氟丙炔1与碘化锂在乙酸中在75°C下反应,可得到(E)-1-芳基-3,3,3,3-三氟-1-碘丙烯2通过与末端炔烃进行钯催化的Sonogashira反应,得到高收率的含三氟甲基的1,3-烯炔。

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