首页> 外文期刊>The Journal of Organic Chemistry >Palladium-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids and Alkenyl Tosylates for the Synthesis of Enynones
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Palladium-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids and Alkenyl Tosylates for the Synthesis of Enynones

机译:钯催化叔羧酸脱羧偶联偶联偶联偶联偶联偶联偶氮酸酯用于合成inynone

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摘要

A palladium-catalyzed decarboxylative coupling reaction was developed for the synthesis of 3-(1-alkynyl)-2-cyclohexen-1-ones. A variety of alkynyl carboxylic acids were coupled with 3-oxocyclohexenyl tosylates to afford the corresponding enynones in good to excellent yields. The developed catalytic system is phosphine free and showed good tolerance toward various functionalities such as chloride, cyano, nitro, ester, aldehyde, and alcohol groups. In addition, phenylpropiolic acid exhibited higher reactivity in the reaction with alkenyl toslyate than phenyl acetylene.
机译:为合成3-(1-炔基)-2-环己酮-1-钯催化脱羧偶羧酸偶联反应。 各种炔基羧酸与3-氧中己烯基甲磺酸盐偶联,得到相应的烯酮,良好至优异的产率。 发育的催化体系是磷酸,并且对各种官能团如氯化物,氰基,硝基,酯,醛和醇组呈现出良好的耐受性。 此外,苯丙吡啶酸在与苯基乙炔的亚己酸酯的反应中表现出更高的反应性。

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