Palladium/norbornene cooperative catalysis has emerged as a distinct approach to
construct polyfunctionalized arenes from readily available starting materials. This Review …

The Catellani reaction is known as a powerful strategy for the expeditious synthesis of highly
substituted arenes and benzo‐fused rings, which are usually difficult to access through …

Methods that can simultaneously install multiple different functional groups to heteroarenes
via C− H functionalizations are valuable for complex molecule synthesis, which, however …

Palladium/norbornene (Pd/NBE) cooperative catalysis has received enormous attention and
found numerous synthetic applications in the past two decades. Considering the critical …

The Catellani reaction is a palladium-catalyzed hydrocarbon-activated multicomponent
tandem reaction involving an aryl halide, an electrophilic coupling reagent and a terminating …

Herein, we report a modular and convergent strategy for the assembly of atropisomeric o-
terphenyls with 1, 2-diaxes via palladium/chiral norbornene cooperative catalysis and axial …

C–H functionalization chemistry is one of the most vibrant research areas within synthetic
organic chemistry. While most researchers focus on the development of small-scale batch …

We report a dual-tasked methylation that is based on cooperative palladium/norbornene
catalysis. Readily available (hetero) aryl halides (39 iodides and 4 bromides) and …

Herein, we present a novel Catellani-type reaction that employed aryl-thianthrenium salts as
aryl substrates to trigger the subsequent palladium/norbornene cooperatively catalyzed …

Carbazole alkaloids hold great potential in pharmaceutical and material sciences. However,
the current approaches for C1 functionalization of carbazoles rely on the use of a pre …