Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/268
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dc.contributor.authorOseni, L. A.-
dc.date.accessioned2015-09-16T12:58:02Z-
dc.date.available2015-09-16T12:58:02Z-
dc.date.issued2011-
dc.identifier.issn0975-833X-
dc.identifier.urihttp://hdl.handle.net/123456789/268-
dc.descriptionThe article is from a staff; lecturer of Department of Applied Chemistry and Biochemistry, University for Development Studies, Navrongo Campus, Navrongo, Ghanaen_US
dc.description.abstractSyntheses of α,β-unsaturated neutral Chromium Fischer carbene complexes bearing alkoxy groups as donor substituents have been explored. Treating β-bromostyrene with a base and chromium hexacarbonyl followed by alkylation with an alkyl iodide produced the alkoxystyryl carbene complexe 1 in modest yield. The results however did not show significant variation in the yield of 1 with the size of the side chain R. Owing to their resemblance to α,β-unsaturated carbonyl compounds, these compounds can provide very useful protocols for the synthesis of organic compounds.en_US
dc.description.sponsorshipInternational Journal of Current Researchen_US
dc.language.isoenen_US
dc.publisherInternational Journal of Current Researchen_US
dc.subjectα,β-unsaturation, Chromium Fischer carbene syntheses, β-bromostyreneen_US
dc.titleSYNTHESES OF NOVEL α,β-UNSATURATED CHROMIUM FISCHER CARBENE COMPLEXES USING β-BROMOSTYRENEen_US
dc.typeArticleen_US
Appears in Collections:Conference Proceedings

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