The development of convenient and mild chalcogenylation reactions for the preparation of
unsymmetrical diaryl sulfides and diaryl selenides has received significant attention in …

Diaryl sulfides are a highly valuable class of sulfur‐containing compounds presented in
numerous drugs with a broad range of therapeutic activities and are also employed as …

Herein, we disclosed a sustainable electrochemical approach for site-selective C–H mono
and bis-chalcogenation (sulfenylation or selenylation) of indolizine frameworks. Diversely …

Herein, for the first time, we report the transition metal-free electrochemical site-selective
direct C–H sulfenylation/selenylation of chromone-fused indolizine compounds (CFIs) to …

A novel and sustainable procedure was developed for the synthesis of 3-selenylindoles
employing diorganyl diselenides and indoles or electron-rich arenes as starting materials …

Perfluoroaryl groups are a recurring motif in materials and pharmaceutical chemistry. Here,
we report a method to couple perfluoroarenes and thiols to yield perfluoroaryl sulfides via a …

The synthesis of organochalcogenides remains a valuable area of research due to their
widespread biological applications, particularly in pharmaceuticals. Herein, our study details …

A novel hydroiodic acid-promoted metal-free C (sp2)-H sulfenylation of electron-rich arenes
was developed using stable and easy-to-handle sodium sulfinates as sulfur sources …

Engineering active sites of metal nanoparticle‐based heterogeneous catalysts is one of the
most prerequisite approaches for the efficient production of chemicals, but the limited active …

A metal‐free method for the synthesis of 3‐sulfanyl indolizines from thiols and 2‐
arylindolizines, is reported. The reaction is mediated by eosin Y under blue LED light …