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首页> 外文期刊>Advanced synthesis & catalysis >Manganese-Catalyzed ortho-C-H Alkenylation of Aromatic N-H Imidates with Alkynes: Versatile Access to Mono-Alkenylated Aromatic Nitriles
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Manganese-Catalyzed ortho-C-H Alkenylation of Aromatic N-H Imidates with Alkynes: Versatile Access to Mono-Alkenylated Aromatic Nitriles

机译:锰催化的含炔烃的芳族N-H酰亚胺的邻位C-H烯基化反应:多途径获得单烯化芳族腈

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摘要

So far, the direct C-H alkenylation of aromatic nitriles with alkynes has not been achieved. Herein, we discribe the first manganese-catalyzed C-H alkenylation of aromatic N-H imidates to access mono-alkenylated aromatic nitriles. The reaction is accelerated by the presence of a catalytic amount of sodium pivalate. This protocol is also highlighted by the simple catalytic system, good compatibility of functional groups, and excellent mono-/dialkenylation selectivity as well as E/Z stereoselectivity.
机译:迄今为止,还没有实现芳族腈与炔的直接C-H烯基化。在这里,我们描述了芳族N-H酰亚胺的锰的第一个锰催化的C-H烯基化以访问单烯基化的芳族腈。通过催化量的新戊酸钠的存在促进反应。该方案还以简单的催化体系,良好的官能团相容性,出色的单/二烯基化选择性以及E / Z立体选择性而著称。

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