Institut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Gottingen, Germany.
Angew Chem Int Ed Engl. 2017 Nov 20;56(47):15063-15067. doi: 10.1002/anie.201708271. Epub 2017 Oct 24.
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.
通过一种新颖的协同 Brønsted 酸/锰(I)催化的 C-H 活化模式,实现了化学选择性的芳基化反应。因此,首次可以使用带有 O-离去基团的炔烃进行 C-H 烯基化反应,而不会发生同时的β-O 消除,从而为多功能的后期多样化奠定了基础。本文还描述了首次在连续流中进行的锰催化的 C-H 活化,从而能够在仅 20 分钟内实现高效的芳基化反应。