Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/2544
Full metadata record
DC FieldValueLanguage
dc.contributor.authorBasu, Basudeb-
dc.contributor.authorDas, Sajal-
dc.contributor.authorMandal, Bablee-
dc.date.accessioned2008-12-05T06:09:48Z-
dc.date.available2008-12-05T06:09:48Z-
dc.date.issued2008-11-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/2544-
dc.description1701-1706en_US
dc.description.abstractFormation of aryl- or heteroaryl-nitrogen (or -oxygen) bonds under ligand and solvent-free conditions are highly selective to the presence of copper. While bromoarenes undergo C-N (or -O) coupling in stoichiometric presence of copper, heteroaryl bromides require only catalytic amounts of copper(I) salts depending on the position of bromo substituents. Such selectivity coupled with ligand and solvent-free protocols appear promising from the viewpoint of ecology and economy and are more attractive as compared to the existing protocols.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.47B(11) [November 2008]en_US
dc.subjectCu catalysten_US
dc.subjectBromopyridinesen_US
dc.subjectC-N couplingen_US
dc.subjectC-O couplingen_US
dc.subjectligand-free conditionsen_US
dc.titleRole of copper in catalyzing aryl and heteroaryl-nitrogen (or -oxygen) bond formation under ligand-free and solvent-free conditionsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.47B(11) [November 2008]

Files in This Item:
File Description SizeFormat 
IJCB 47B(11) 1701-1706.pdf83.37 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.