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Towards a Metal-catalyzed Annulation Route to Pyridines and N-Hydroxy Pyrroles

dc.contributor.authorWhitmore, Kenneth M.
dc.contributor.supervisorBeauchemin, André
dc.date.accessioned2012-03-27T20:16:29Z
dc.date.available2012-03-27T20:16:29Z
dc.date.created2012
dc.date.issued2012
dc.degree.disciplineSciences / Science
dc.degree.levelmasters
dc.degree.nameMSc
dc.description.abstractDespite progress in the metal-catalyzed synthesis of aromatic heterocycles, annulation routes towards 6-membered heterocycles remain underdeveloped. Specifically, routes towards pyridines are rare in spite of the prevalence of this moiety in novel drug candidates. Our initial efforts towards pyridines featured oximes as competent nucleophiles in the intramolecular, 6-exo dig annulation of alkynes using Brønsted acid catalysis. Two of the oxidation states required for subsequent aromatization are contained within the oxime via loss of water. An extension of this chemistry is presented and discussed, and involves the intramolecular metal-catalyzed 6-endo dig annulation of analagous alkynyl-oximes. Additionally, the discovery of a 5-exo dig annulation of related systems is discussed.
dc.embargo.termsimmediate
dc.faculty.departmentChimie / Chemistry
dc.identifier.urihttp://hdl.handle.net/10393/22675
dc.identifier.urihttp://dx.doi.org/10.20381/ruor-5561
dc.language.isoen
dc.publisherUniversité d'Ottawa / University of Ottawa
dc.subjectPyridine
dc.subjectHeterocycle
dc.subjectN-Hydroxy Pyrrole
dc.subjectAnnulation
dc.subjectCatalysis
dc.subjectMetal
dc.titleTowards a Metal-catalyzed Annulation Route to Pyridines and N-Hydroxy Pyrroles
dc.typeThesis
thesis.degree.disciplineSciences / Science
thesis.degree.levelMasters
thesis.degree.nameMSc
uottawa.departmentChimie / Chemistry

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