Carbon–sulfur bond cross-coupling has become more and more attractive as an alternative
protocol to establish carbon–carbon and carbon–heteroatom bonds. Diverse …

As a new transformation of organosulfur compounds, intramolecular desulfitative coupling of
diaryl sulfones to the corresponding biaryls has been developed with the aid of nickel–NHC …

A novel palladium-catalyzed protocol for the synthesis of 2-arylquinolines via tandem
reaction of 2-aminostyryl nitriles with arylboronic acids has been developed with good …

This unprecedented review with 322 references provides a critical up-to-date picture of the
Pd-catalysed intermolecular direct C–H bond arylation of heteroarenes with arylating …

Herein, a novel chelation-assisted C–H arylation reaction of benzo [h] quinoline is
described. This transformation, using [RuCl2 (p-cymene)] 2 as the catalyst and cheap and …

A visible-light-induced difunctionalization of activated alkenes for building alkylsulfonylated
oxindoles and amides through a radical Smiles rearrangement strategy was reported. A …

Sulfonyl chlorides are a class of cheap and readily available basic chemicals, which have
routinely served as electrophilic reagents in their chemical transformations. Herein, we …

A modular approach for the synthesis of planar π-extended selenium containing molecules
from selenophene has been developed. Different combinations of Pd-catalyzed desulfitative …

Biaryls are a key structural motif in compounds with various applications, ranging from
pharmaceuticals to material science, including ligands for organic synthesis. Given the …

Herein, we reported a successful cross coupling of aryl sulfonyl chlorides to forge thioether
skeleton via Pd catalysis. This transformation proceeded in the presence of Xantphos …