1262299-96-6Relevant articles and documents
An efficient protocol for the carbon-sulfur cross-coupling of sulfenyl chlorides with arylboronic acids using a palladium catalyst
Gogoi, Prasanta,Kalita, Mukul,Barman, Pranjit
, p. 866 - 870 (2014)
An efficient protocol for carbon-sulfur bond formation is developed, which involves the cross-coupling of sulfenyl chlorides and arylboronic acids catalyzed by a novel palladium-Schiff base complex. Good to high product yields, short reaction times, and mild reaction conditions are important features of this new method. Georg Thieme Verlag Stuttgart · New York.
Highly regioselective synthesis of aryl chalcogenides through C-H functionalization of arenes
Cheng, Jun-Hao,Yi, Chih-Lun,Liu, Tsung-Jui,Lee, Chin-Fa
supporting information, p. 8440 - 8442 (2012/10/29)
We report here the regioselective synthesis of aryl chalcogenides through the iridium-catalyzed meta C-H borylation followed by copper-catalyzed C-S coupling reaction with chalcogenide sources in one pot, giving the 3,5-disubstituted aryl chalcogenides wi