Ruthenaelectro-catalyzed C-H phosphorylation: to position-selectivity switch.

The position-selective C-H bond activation of arenes has long been a challenging topic. Herein, we report an expedient ruthenium-electrocatalyzed site-selective -C-H phosphorylation of arenes driven by electrochemical hydrogen evolution reaction (HER), avoiding stoichiometric amounts of chemical redox-waste products. This strategy paved the way to achieve unprecedented ruthenaelectro-catalyzed -C-H phosphorylation with excellent levels of site-selectivity. This electrocatalytic approach was characterized by an ample substrate scope with a broad range of arenes containing N-heterocycles, as well as several aryl/alkylphosphine oxides were well tolerated. Moreover, late-stage C-H phosphorylation of medicinal relevant drugs could also be achieved. DFT mechanistic studies provided support for an unusual ruthenium(iii/iv/ii) regime for the -C-H phosphorylation.