首页> 外文期刊>Journal of the American Chemical Society >Three-Component Ruthenium-Catalyzed Direct Mefa-Selective C-H Activation of Arenes: A New Approach to the Alkylarylation of Alkenes
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Three-Component Ruthenium-Catalyzed Direct Mefa-Selective C-H Activation of Arenes: A New Approach to the Alkylarylation of Alkenes

机译:芳烃的三组分钌催化直接甲基选择性C-H活化:烯烃烷基芳基化的新方法

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摘要

Multicomponent reactions are fundamentally different from two-component reactions, as multicomponent reactions can enable the efficient and step-economical construction of complex molecular scaffolds from simple precursors. Here, an unprecedented three-component direct C-H addition was achieved in the challenging meta-selective fashion. Fluoroalkyl halides and a wide range of alkenes, including vinylarenes, unactivated alkenes, and internal alkenes, were employed as the coupling partners of arenes in this strategy. The detailed mechanism presented is supported by kinetic isotope studies, radical clock experiments, and density functional theory calculations. Moreover, this strategy provided access to various fluoride-containing bioactive 1,1-diarylalkanes and other challenging synthetically potential products.
机译:多组分反应从根本上不同于两组分反应,因为多组分反应可以从简单的前体高效,分步经济地构建复杂的分子支架。在此,以具有挑战性的亚选择性方式实现了前所未有的三组分直接C-H加成。氟代烷基卤化物和各种烯烃(包括乙烯基芳烃,未活化的烯烃和内部烯烃)被用作该策略中芳烃的偶联伙伴。提出的详细机理得到动力学同位素研究,自由基钟实验和密度泛函理论计算的支持。而且,该策略提供了获得各种含氟化物的生物活性1,1-二芳基烷烃和其他具有挑战性的合成潜在产品的途径。

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