Tan Xuefeng, Massignan Leonardo, Hou Xiaoyan, Frey Johanna, Oliveira João C A, Hussain Masoom Nasiha, Ackermann Lutz
Institut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.
Wöhler Research Institute for Sustainable Chemistry, Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.
Angew Chem Int Ed Engl. 2021 Jun 7;60(24):13264-13270. doi: 10.1002/anie.202017359. Epub 2021 May 7.
Rhodium-electrocatalyzed arene C-H oxygenation by weakly O-coordinating amides and ketones have been established by bimetallic electrocatalysis. Likewise, diverse dihydrooxazinones were selectively accessed by the judicious choice of current, enabling twofold C-H functionalization. Detailed mechanistic studies by experiment, mass spectroscopy and cyclovoltammetric analysis provided support for an unprecedented electrooxidation-induced C-H activation by a bimetallic rhodium catalysis manifold.
通过双金属电催化已实现了铑催化的芳烃C-H与弱氧配位酰胺和酮的氧化反应。同样,通过明智地选择电流,可以选择性地得到多种二氢恶嗪酮,实现双重C-H官能化。通过实验、质谱和循环伏安分析进行的详细机理研究,为双金属铑催化体系中前所未有的电氧化诱导C-H活化提供了支持。