异恶唑
化学
芳基
钯
表面改性
催化作用
三氟甲基
反应性(心理学)
羧酸盐
组合化学
溴化物
腈
药物化学
环加成
有机化学
物理化学
病理
替代医学
烷基
医学
作者
Rabeb Ben Romdhane,Linhao Liu,Ridha Ben Salem,Henri Doucet
标识
DOI:10.1002/ejoc.202401036
摘要
Abstract The Pd‐catalyzed C4‐arylation of 3,5‐disubstituted isoxazoles via C−H bond functionalization has been largely described. By contrast, the reactivity of isoxazoles in C−H bond functionalization with both unsubstituted C4 and C5 positions remains largely unexplored. Herein, we report on the reactivity in Pd‐catalyzed double C−H bond arylation of an isoxazole with unsubstituted C4 and C5 positions. Conditions for the palladium‐catalyzed direct C4,C5‐diarylation of ethyl isoxazole‐3‐carboxylate using aryl bromides as the aryl source are reported. This procedure tolerates several useful substituents on the aryl bromide such as nitrile, acetyl, formyl, benzoyl, alkoxycarbonyl, chloro, fluoro, trifluoromethyl, trifluoromethoxy, cyanomethyl, tert butyl and methoxy at para ‐ and meta ‐positions. Conversely, with ortho ‐substituted aryl bromides, mixtures of mono‐ and di‐arylated isoxazoles were generally obtained. This methodology provides a simple one pot access to a wide variety of C4,C5‐diarylated isoxazoles from commercially available substrates allowing to modify easily their biological properties.
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