锰
催化作用
化学
连续流动
化学选择性
布朗斯特德-洛瑞酸碱理论
组合化学
药物化学
立体化学
有机化学
物理
机械
作者
Hui Wang,Fabio Pesciaioli,João C. A. Oliveira,Svenja Warratz,Lutz Ackermann
标识
DOI:10.1002/anie.201708271
摘要
Abstract Chemoselective hydroarylations were accomplished by a novel synergistic Brønsted acid/manganese(I)‐catalyzed C−H activation manifold. Thus, alkynes bearing O‐leaving groups could, for the first time, be employed for C−H alkenylations without concurrent β‐O elimination, thereby setting the stage for versatile late‐stage diversifications. Also described is the first manganese‐catalyzed C−H activation in continuous flow, thus enabling efficient hydroarylations within only 20 minutes.
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