Transition-metal catalyzed redox triggered C-C bond forming reactions via carbonyl addition

dc.contributor.advisorKrische, Michael J.
dc.creatorZhang, Wandi
dc.date.accessioned2019-07-16T18:39:58Z
dc.date.available2019-07-16T18:39:58Z
dc.date.created2019-05
dc.date.issued2019-05
dc.date.submittedMay 2019
dc.date.updated2019-07-16T18:39:59Z
dc.description.abstractCarbon-carbon (C–C) bonds construct the skeleton of all organic molecules. Hence, the development of new efficient methods of C–C bond formation is of great significance in organic chemistry. Since the discovery of the Grignard reaction, carbonyl addition has been an established method for C–C bond formation. In classical carbonyl additions, premetalated reagents or stoichiometric metallic reductants are required. By taking advantage of the native reducing capability of alcohols, our lab has developed methods that exploit alcohols and π-unsaturates to generate transient electrophile-nucleophile pairs to directly convert lower alcohols to higher alcohol. Efforts have been focused on the development of transition metal-catalyzed redox-triggered coupling reactions of primary alcohols and aldehydes to π-unsaturates as well as aryl iodides. Modern methods to construct new C-C bonds in highly selective manner via carbonyl addition were undertaken.
dc.description.departmentChemistry
dc.format.mimetypeapplication/pdf
dc.identifier.urihttps://hdl.handle.net/2152/75167
dc.identifier.urihttp://dx.doi.org/10.26153/tsw/2273
dc.language.isoen
dc.subjectTransition metal catalysis
dc.subjectCarbonyl addition
dc.subjectC-C bond forming reaction
dc.titleTransition-metal catalyzed redox triggered C-C bond forming reactions via carbonyl addition
dc.typeThesis
dc.type.materialtext
thesis.degree.departmentChemistry
thesis.degree.disciplineChemistry
thesis.degree.grantorThe University of Texas at Austin
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy

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