Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/20469
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dc.contributor.authorDhau, Jaspreet S.pt
dc.contributor.authorSingh, Avtarpt
dc.contributor.authorSingh, Amritpalpt
dc.contributor.authorDhir, Rupypt
dc.contributor.authorBrandao, Paulapt
dc.contributor.authorFelix, Vitorpt
dc.date.accessioned2017-12-07T19:48:09Z-
dc.date.issued2014pt
dc.identifier.issn0020-1693pt
dc.identifier.urihttp://hdl.handle.net/10773/20469-
dc.description.abstractA methodology for the lithiation of pyrimidine (1a) was developed and used for the synthesis of pyrimidylselenium compounds. The procedure involved prior complexation of 1a with 2.2 equiv. of BF3 center dot Et2O followed by a reaction with LDA or LTMP. The pyrazinylselenium derivatives were synthesized from the direct lithiation of pyrazine (1b) as the BF3-directed lithiation failed to give the desired products. All the synthesized compounds were characterized by elemental analysis, NMR (H-1 and C-13) and Mass spectroscopy. In addition, 2,5-bis(methylselenenyl)pyrazine (9b) was characterized by single crystal X-ray crystallography. (C) 2014 Elsevier B.V. All rights reserved.pt
dc.language.isoengpt
dc.publisherELSEVIER SCIENCE SApt
dc.relationinfo:eu-repo/grantAgreement/FCT/COMPETE/132936/PTpt
dc.rightsrestrictedAccesspor
dc.subjectBIOLOGICAL-ACTIVITYpt
dc.subjectCRYSTAL-STRUCTUREpt
dc.subjectPYRIDYLSELENIUM COMPOUNDSpt
dc.subjectORGANOSELENIUM COMPOUNDSpt
dc.subjectANTIOXIDANT ACTIVITYpt
dc.subjectCOMPLEXESpt
dc.subjectPYRIDYLpt
dc.subjectSEpt
dc.subjectTEpt
dc.subjectNANOCRYSTALSpt
dc.titleSynthesis and characterization of pyrimidyl- and pyrazinylselenium compounds: X-ray structure of 2,5-bis(methylselenenyl)pyrazinept
dc.typearticlept
dc.peerreviewedyespt
ua.distributioninternationalpt
degois.publication.firstPage359pt
degois.publication.lastPage363pt
degois.publication.titleINORGANICA CHIMICA ACTApt
degois.publication.volume421pt
dc.date.embargo10000-01-01-
dc.relation.publisherversion10.1016/j.ica.2014.06.025pt
dc.identifier.doi10.1016/j.ica.2014.06.025pt
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