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Solvent and Solubility Effects on Quinone Ratios

dc.contributor.advisorLove, Brian Ernesten_US
dc.contributor.authorDuffy, Brianen_US
dc.contributor.departmentChemistryen_US
dc.date.accessioned2012-09-04T18:10:57Z
dc.date.available2012-09-04T18:10:57Z
dc.date.issued2012en_US
dc.description.abstractMonoquinones and diquinones are a biologically and chemically important class of compounds that can be found in numerous natural products such as: thymoquinone, oosporein, coenzyme Q, embelin and the respective dimer, biembelin. These 1, 4-benzoquinone derivatives exhibit prominent pharmacological applications such as antibiotic, anti-tumor, anti-malarial, anti-coagulant, and anti-convulsant activity.    Though quinones can be prepared by a variety of processes, they are most commonly synthesized through the treatment of hydroquinone dimethyl ethers with ceric ammonium nitrate (CAN). However, this can lead to an unpredictable mixture of monoquinone and diquinone as the products. This project has investigated the effect of solvent and substrate water solubility on monoquinone / diquinone product ratios with the aim of being able to consistently and predictably favor one (monoquinone or diquinone) over the other.  en_US
dc.description.degreeM.S.en_US
dc.format.extent67 p.en_US
dc.format.mediumdissertations, academicen_US
dc.identifier.urihttp://hdl.handle.net/10342/4003
dc.language.isoen_US
dc.publisherEast Carolina Universityen_US
dc.subjectChemistryen_US
dc.subjectChemistry, Organicen_US
dc.subjectDiquinoneen_US
dc.subjectQuinoneen_US
dc.subjectSynthesisen_US
dc.subjectOrganic chemistry
dc.subject.lcshQuinone--Synthesis--Research
dc.subject.lcshSynthetic products
dc.titleSolvent and Solubility Effects on Quinone Ratiosen_US
dc.typeMaster's Thesisen_US

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