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Magnetically Separable CuFe 2 O 4 Nanoparticles Catalyzed Ligand‐Free CS Coupling in Water: Access to ( E )‐ and ( Z )‐Styrenyl‐, Heteroaryl and Sterically Hindered Aryl Sulfides
Author(s) -
Kundu Debasish,
Chatterjee Tanmay,
Ranu Brindaban C.
Publication year - 2013
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.201300261
Subject(s) - chemistry , steric effects , aryl , bimetallic strip , catalysis , ligand (biochemistry) , bromide , combinatorial chemistry , medicinal chemistry , organic chemistry , biochemistry , alkyl , receptor
An efficient coupling of styrenyl, heteroaryl and sterically hindered aryl halides with aryl‐ and heteroarylthiols catalyzed by the bimetallic Cu and Fe nanomaterial, CuFe 2 O 4 , in water in the presence of tetrabutylammonium bromide and potassium phosphate (K 3 PO 4 ) 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.

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