首页> 外文期刊>Journal of the American Chemical Society >Palladium-Catalyzed C-H Funationalization of Pyridine N-Oxides: Highly Selective Alkenylation and Direct Arylation with Unactivated Arenes
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Palladium-Catalyzed C-H Funationalization of Pyridine N-Oxides: Highly Selective Alkenylation and Direct Arylation with Unactivated Arenes

机译:钯催化的吡啶N-氧化物的C-H富氨化:高度选择性的烯化和未活化的芳烃的直接芳基化

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Transition metal-catalyzed C-H bond functionalization for the C-C bond formation has emerged as a promising area in organic synthesis. In particular, reactions involving Pd-catalyzed activation of sp or sp C-H bonds of arenes or alkanes have been extensively investigated. Successful applications of the C-H activation strategy on readily available substrates have been also reported using various metals other than Pd catalysts.rnPyridine moiety is a key component of pharmacophores, natural products, and synthetic building blocks. Substituted pyridines are usually prepared starting from halo- or metallated pyridyl compounds. However, this "prefunctionalization" route is inevitably accompanied with problems such as the need of extra preparation steps for the frequently unstable precursors and the formation of byproducts.
机译:用于C-C键形成的过渡金属催化的C-H键功能化已成为有机合成中有希望的领域。特别是,已经广泛研究了涉及钯催化的芳烃或烷烃的sp或sp C-H键活化的反应。还已经报道了使用Pd催化剂以外的其他金属将C-H活化策略成功应用于容易获得的底物上。吡啶吡啶部分是药效基团,天然产物和合成构件的关键成分。取代的吡啶通常从卤代或金属化吡啶基化合物开始制备。然而,这种“预功能化”途径不可避免地伴随有问题,例如对于经常不稳定的前体需要额外的制备步骤以及副产物的形成。

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