In recent years, radical C–C bond cleavage reactions have been increasingly understood
and used to perform transformations that complement traditional ionic processes. However …

The direct C3-functionalization of quinoxalin-2 (1H)-ones via C–H bond activation has
recently attracted considerable attention, due to their diverse biological activities and …

Carbon–carbon/carbon–heteroatom bond formation via oxidative transformations is a
heavily explored topic at the frontier of chemistry. Potassium persulfate (K2S2O8) has …

The development of P (O)–heteroatom bond-forming reactions is of vital importance.
However, previous methods all have their own limitations and drawbacks. Herein, we …

The Mn (OAc) 3-promoted oxidative phosphonylation of N, N-dimethylenaminones with H-
phosphonates, involving a chemo-and regioselective Csp2–Csp2 bond cleavage and Csp3 …

C–H phosphorylation was achieved by Earth-abundant nickel catalysts with waste-free
electricity as the redox surrogate. The robust nickela-electrooxidative C–H activation of …

A phosphoryl radical-initiated Atherton–Todd-type reaction using air as the radical initiator
and CHCl3 as the halogenating reagent for the phosphorylation of alcohols, phenols, and …

AgSbF6 has been established as an effective catalyst for the hydroboration of structurally
and electronically diverse isocyanates under ligand-and solvent-free conditions which …

Silver, as one of the most ancient coinage metals, has attracted a plethora of attention from
chemists in recent years due to the easy availability, high catalytic efficiency and multiple …

The first successful example of deacylative annulation of 1, 3-diones with sulfoxonium ylides
was achieved through Ru (II)-catalyzed C–C bond activation. The excellent chemoselectivity …