Please use this identifier to cite or link to this item: https://repository.sustech.edu/handle/123456789/9250
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dc.contributor.authorMalla, Hassan Ali Ahmed
dc.contributor.authorMossabl, Hamid Adam Mohammed
dc.contributor.authorSupervisor - Ahmed Elsadig Mohammad Saeed
dc.date.accessioned2014-12-25T10:05:19Z
dc.date.available2014-12-25T10:05:19Z
dc.date.issued2014-07-20
dc.identifier.citationMalla,Hassan Ali Ahmed.Synthesis of some derivatives of 1,4-Naphthoquinone/Hassan Ali Ahmed Malla,Hamid Adam Mohammed Mossabl;Ahmed Elsadig Mohammad Saeed.-khartoum:Sudan University of Science and Technology,College of Science,2014.-36p. :ill;28cm.-Basheors,search .en_US
dc.identifier.urihttp://repository.sustech.edu/handle/123456789/9250
dc.descriptionBasheors,searchen_US
dc.description.abstractIn this work, 2–{5–[(2–phenylhydrazinylidene)methyl] furan–2–yl}naphthalene-1,4-dione and 2–{4-[(2– phenylhydrazinyliden)methyl]phenyl}naphthalene-1,4-dione have been synthesized by reaction of 1-(furan-2-ylmethlidene)- 2-phenylhydrazine and 1-benzylidene-2-phenylhydrazine as hydrazones with 1,4-naphthoquinone according to a well documented procedure. Access to furylnaphthoquinones from un activated quinones requires acid-inuced conditions, however oxidation coupling reaction of activated quinones proceed under neutral condition. The hydrazones were prepared from the commercially aldehydes and phenyl hydrazine.en_US
dc.description.sponsorshipSudan University of Science and Technologyen_US
dc.language.isoenen_US
dc.publisherSudan University of Science and Technologyen_US
dc.subjectChemical Scienceen_US
dc.subjectSynthesis of some derivativesen_US
dc.subjectNaphthoquinoneen_US
dc.subjectOxidation reactionen_US
dc.titleSynthesis of some derivatives of 1,4-Naphthoquinoneen_US
dc.typeThesisen_US
Appears in Collections:Bachelor of Science

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