Azine‐containing biaryls are ubiquitous scaffolds in many areas of chemistry, and efficient
methods for their synthesis are continually desired. Pyridine rings are prominent amongst …

para-Selective C–H functionalization of pyridines holds a significant value but remains
underdeveloped. Site-switchable C–H functionalization of pyridines under easily tunable …

Pyridine is a crucial heterocyclic scaffold that is widely found in organic chemistry,
medicines, natural products, and functional materials. In spite of the discovery of several …

Herein, a Pd/Cu bimetallic-catalyzed direct C–H heteroarylation of pyridines via the
traceless protecting group strategy is described. A series of N-methyl-activated pyridines …

Diverse C–H functionalizations catalyzed by Pd employ Ag (I) salts added as halide
abstractors or oxidants. Recent reports have shown that Ag can also perform the crucial C–H …

The first Pd/Cu catalyzed selective C2-alkenylation of pyridines with internal alkynes has
been developed via the pyridinium salt activation strategy. Importantly, the configuration of …

A direct pyridinium C–H sulfonylimination has been developed for the synthesis of sulfonyl
iminopyridine derivatives with high efficiency. This transformation features the direct and …

A remarkable metal-oxidant-solvent-and base-free domino route for regioselective access to
a wide range of 2, 4-di-and 2, 3, 4/6-trisubstituted pyridines including carbo-and heterocyclic …

An elegant pre‐activation strategy, based on the formation of N‐methylpyridinium iodide
salts for C6‐selective direct arylation of 2‐phenylpyridines using Pd/Cu cooperative …

This study reports the invention of di‐or trifunctionalization of readily available pyridines
(including all the pyridine substrates utilized in this paper, such as 3‐cyanopyridine and 3 …