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dc.contributor.advisorKrische, Michael J.
dc.creatorLeung, Joyce Chi Chingen
dc.date.accessioned2013-10-10T17:43:03Zen
dc.date.accessioned2017-05-11T22:34:33Z
dc.date.available2017-05-11T22:34:33Z
dc.date.issued2013-05en
dc.date.submittedMay 2013en
dc.identifier.urihttp://hdl.handle.net/2152/21527en
dc.descriptiontexten
dc.description.abstractCarbon-carbon bond forming reactions are fundamental transformations for constructing structurally complex organic building blocks, especially in the realm of natural products synthesis. Classical protocols for forming a C-C bond typically require the use of stoichiometrically preformed organometallic reagents, constituting a major drawback for organic synthesis on process scale. Since the emergence of transition metal catalysis in hydrogenation and hydrogenative C-C coupling reactions, atom and step economy have become important considerations in the development of sustainable methods. In the Krische laboratory, our goal is to utilize abundant, renewable feedstocks, so that the reactions can proceed in an efficient and atom-economical manner. Our research focuses on developing new C-C bond forming protocols that transcend the use of stoichiometric, preformed organometallic reagents, in which [pi]-unsaturates can be employed as surrogates to discrete premetallated reagents. Under transition metal catalyzed transfer hydrogenation conditions, alcohols can engage in C-C coupling, avoiding unnecessary redox manipulations prior to carbonyl addition. Stereoselective variants of these reactions are also under extensive investigation to effect stereo-induction by way of chiral motifs found in ligands and counterions. The research presented in this dissertation represents the development of a new class of C-C bond forming transformations useful for constructing synthetic challenging molecules. Development of transfer hydrogenative C-C bond forming reactions in the form of carbonyl additions such as carbonyl allylation, carbonyl propargylation, carbonyl vinylation etc. are discussed in detail. Additionally, these methods avoid the use of stoichiometric chiral allenylmetal, propargylmetal or vinylmetal reagents, respectively, accessing diastereo- and enantioenriched products of carbonyl additions in the absence of stoichiometric organometallic byproducts. By exploiting the atom-economical transfer hydrogenative carbonyl addition protocols using ruthenium and iridium, preparations of important structural motifs that are abundant in natural products, such as allylic alcohols, homoallylic alcohols and homopropargylic alcohols, become more feasible and accessible.en
dc.format.mimetypeapplication/pdfen
dc.language.isoen_USen
dc.subjectOrganometallicen
dc.subjectTransition metalen
dc.subjectCatalysisen
dc.subjectHydrogenationen
dc.subjectHydrogenativeen
dc.subjectCarbonyl additionsen
dc.subjectStereoselectiveen
dc.titleTransition metal catalyzed C-C bond formation under transfer hydrogenation conditionsen
dc.description.departmentChemistryen
dc.date.updated2013-10-10T17:43:04Zen


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