The coupling of aryl halides with catalytically activated aryl C–H bondsprovides a desirable
and atom-economical alternative to standard cross-coupling reactions for the construction of …

Visible light along with 1 mol% eosin Y catalyzes the direct C–H bond arylation of
heteroarenes with aryl diazonium salts by a photoredox process. We have investigated the …

For synthesis of π-conjugated polymers, polycondensation via direct arylation reactions of C–
H bonds in aromatic monomers with dibromo-arylenes has attracted increasing attention as …

A PANI (polyaniline)-g-C3N4-TiO2 composite was prepared and found to be efficient for
radical C–H arylation reactions. The arylation process involved coupling of in situ generated …

Sequence-specific C-arylation strategies have important applications in medicinal and
material research. These strategies allow C–C bond formations in a regioselective manner …

An efficient C–H heteroarylation of heteroarenes is achieved through visible‐light
photoredox‐catalyzed diazotization of heteroarylamines in situ by tBuONO at room …

Dihydro-10-methylacridine (AcrH 2), a NADH coenzyme model compound, as an organo-
photoredox catalyst is demonstrated for the cross-coupling of aryl diazonium salts with …

Abstract A solvent‐controlled C2/C5‐selective alkenylation of 3, 4‐disubstituted pyrroles has
been developed. The C3 substituent of pyrroles proved crucial to the regioselectivity …

A palladium-catalyzed direct arylation of (3-thiophene) S (O) Me derivatives has been
developed. This protocol is effective for the selective synthesis of 2-arylated and 2, 5 …

Efficient and practically attractive stepwise ruthenium-and palladium-catalyzed
regioselective C–H bond functionalizations were achieved to produce 4-substituted …