The 3d metallaelectro-catalyzed C–H activation has been identified as an increasingly
viable strategy to access valuable organic molecules in a resource-economic fashion under …

A variety of biologically active molecules, pharmaceuticals, and natural products consist of a
nitrogen-containing heterocyclic backbone. The majority of them are isoquinolones, indoles …

Carboamination of readily available feedstock-like alkenes, alkynes, and allenes has proven
to be an efficient and powerful tool for the synthesis of diverse and valuable amine …

Annulations of unsaturated systems through C–H activation represent a powerful tool for
producing multicyclic scaffolds. Having coordinating centers in both annulation partners (a …

This review focuses on recent results with respect to the use of varied ionic palladium
preparations in the synthesis of tetra-and polycyclic heterocycles bearing a five-membered …

In recent years, transition metal-catalyzed strong C–C bond activation has significantly
attracted the attention of synthetic chemists. This protocol enables simultaneous and direct …

Herein, we report the first palladium/MPAA catalyzed enantioselective C–H activation/[4+ 1]
annulation of diarylmethyltriflamide and olefins to construct chiral cis-1, 3-disubstituted …

The palladium‐catalyzed reaction of aromatic amides with maleimides results in the
formation of a double C− H bond activation product, which occurs at both the benzylic and …

Reported herein is a practical and selective assembly of novel isoquinolone-containing
spirocyclic and oxepine-fused polycyclic skeletons through a rhodium (III)-catalyzed …

Herein, we report an efficient [3+ 2] annulation of ortho-substituted iodoarenes with
maleimides via a palladium-catalyzed consecutive double Heck-type strategy, leading to …