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dc.contributor.authorSt-Onge Carle, Myriam
dc.date.accessioned2017-09-18 15:18:58 (GMT)
dc.date.available2017-09-18 15:18:58 (GMT)
dc.date.issued2017-09-18
dc.date.submitted2017-09-06
dc.identifier.urihttp://hdl.handle.net/10012/12394
dc.description.abstractHalogenation of organic molecules is a fundamental transformation in organic chemistry. Introducing halogens into substrates can be a challenge since most methods for introducing fluorine or chlorine into molecules include the use of toxic reagents, harsh reaction conditions or expensive reagents. In recent years, hypervalent iodine compounds have garnered much interest due to their reactivity, their ease of synthesis and their mild reaction conditions, and they have been successfully employed in numerous halogenation reactions. My master’s thesis has been focused on two projects, deoxygenative chlorination using iodobenzene dichloride and denitrogenative hydrofluorination using iodotoluene difluoride.en
dc.language.isoenen
dc.publisherUniversity of Waterlooen
dc.subjectOrganic chemistryen
dc.subjectHypervalent iodineen
dc.titleUse of (Dihaloiodo)arene Reagents in Halogenation Reactionsen
dc.typeMaster Thesisen
dc.pendingfalse
uws-etd.degree.departmentChemistryen
uws-etd.degree.disciplineChemistryen
uws-etd.degree.grantorUniversity of Waterlooen
uws-etd.degreeMaster of Scienceen
uws.contributor.advisorMurphy, Graham
uws.contributor.affiliation1Faculty of Scienceen
uws.published.cityWaterlooen
uws.published.countryCanadaen
uws.published.provinceOntarioen
uws.typeOfResourceTexten
uws.peerReviewStatusUnrevieweden
uws.scholarLevelGraduateen


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