As two coexisting and fast-growing research fields in modern synthetic chemistry, the
merging of organocatalysis and C–H bond functionalization is well foreseeable, and the joint …

Conspectus Introducing aryl-and heteroaryl moieties into molecular scaffolds are often key
steps in the syntheses of natural products, drugs, or functional materials. A variety of cross …

Over the past few decades, photocatalysis has been established as a rapidly escalating
research area to catalyse the chemical reactions induced by visible light through single …

Direct C–H bond arylation of (hetero) arenes is a very convenient approach for the synthesis
of a wide variety of molecular targets, including compounds of pharmaceutical interest and π …

The rich legacy of arenediazonium salts in the synthesis of unsymmetrical biaryls, built
around the seminal works of Pschorr, Gomberg and Bachmann more than a century ago …

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 …

Functionalization of arenes is a topic of central importance in diverse fields ranging from
medicinal chemistry to materials science. Metal-catalyzed cross-coupling and nucleophilic …

Polysulfide anions are endowed with unique redox properties, attracting considerable
attentions for their applications in alkali metals–sulfur batteries. However, the employment of …

A transition metal‐free iodosobenzene‐promoted direct oxidative 3‐arylation of quinoxalin‐
2 (H)‐ones was developed using various arylhydrazines under air. The protocol affords a …

Abstract Imidazo [1, 2-a] pyridines are unique nitrogen-containing organic compounds with
wide applications in pharmaceuticals, natural products, material science and …