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首页> 外文期刊>Angewandte Chemie >Rhodium Catalyzed Regioselective C-H Allylation of Simple Arenes via C-C Bond Activation of Gem-difluorinated Cyclopropanes
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Rhodium Catalyzed Regioselective C-H Allylation of Simple Arenes via C-C Bond Activation of Gem-difluorinated Cyclopropanes

机译:通过C-C键的泡氟环丙烷的C-C键活化,铑催化的细节C-H allylation简单芳烃

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摘要

Herein, we report a rhodium catalyzed directing-group free regioselective C-H allylation of simple arenes. Readily available gem-difluorinated cyclopropanes can be employed as highly reactive allyl surrogates via a sequence of C-C and C-F bond activation, providing allyl arene derivatives in good yields with high regioselectivity under mild conditions. The robust methodology enables facile late-stage functionalization of complex bioactive molecules. The high efficiency of this reaction is also demonstrated by the high turnover number (TON, up to 1700) of the rhodium catalyst on gram-scale experiments. Preliminary success on kinetic resolution of this transformation is achieved, providing a promising access to enantio-enriched gem-difluorinated cyclopropanes.
机译:在此,我们报道了铑催化的简单芳烃的无基团区域选择性C-H烯丙基化反应。可通过一系列C-C和C-F键活化将现成的gem二氟环丙烷用作高反应性烯丙基替代物,在温和条件下以良好产率提供具有高区域选择性的烯丙基芳烃衍生物。稳健的方法使复杂生物活性分子的后期功能化变得容易。在克级实验中,铑催化剂的高周转数(吨,高达1700)也证明了该反应的高效性。这种转化在动力学拆分方面取得了初步成功,为获得富含对映体的gem二氟环丙烷提供了一条有希望的途径。

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