1454680-46-6Relevant academic research and scientific papers
Carbon-sulfur bond formation catalyzed by [Pd(IPr*OMe) (cin)Cl] (cin = cinnamyl)
Bastug, Gulluzar,Nolan, Steven P.
supporting information, p. 9303 - 9308 (2013/10/08)
The newly prepared complex [Pd(IPr*OMe)(cin)(Cl)] provides high catalytic activity for carbon-sulfur cross-coupling reactions. Nonactivated and deactivated aryl halides were successfully coupled with a large variety of aryl- and alkylthiols using this well-defined palladium N-heterocyclic carbene (NHC) complex.
Magnetically separable CuFe2O4 nanoparticles catalyzed ligand-free C-S coupling in water: Access to (E)- and (Z)-styrenyl-, heteroaryl and sterically hindered aryl sulfides
Kundu, Debasish,Chatterjee, Tanmay,Ranu, Brindaban C.
, p. 2285 - 2296 (2013/10/01)
An efficient coupling of styrenyl, heteroaryl and sterically hindered aryl halides with aryl- and heteroarylthiols catalyzed by the bimetallic Cu and Fe nanomaterial, CuFe2O4, in water in the presence of tetrabutylammonium bromide and potassium phosphate (K3PO4) has been achieved without using any ligand. A series of unsymmetrical functionalized (E)- and (Z)-styrenyl aryl, heteroaryl heteroaryl and sterically hindered aryl aryl sulfides has been obtained by this procedure. The compounds are obtained in high yields and excellent stereoselectivity has been observed for styrenyl sulfides. The catalyst can be easily separated by an external magnet and recycled for ten times without any appreciable loss of activity. This procedure provides an easy access to useful and challenging biologically active organosulfides which are difficult to achieve by other methods.
