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The Stobbe condensation with cyclohexanone and decarboxylation studiesHunt, Richard Henry, January 1949 (has links)
Thesis (Ph. D.)--University of Wisconsin--Madison, 1949. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.
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The effect of solvent and ligand on the metal ion catalyzed oxalacetate decarboxylation: an equilibrium and kinetics study in dioxane-water mixed solvents /Mao, Hsiang-kuen January 1978 (has links)
No description available.
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Mechanistic studies in the bicyclo [2,2,1] heptyl seriesPincombe, Christopher Fletcher. January 1973 (has links) (PDF)
No description available.
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General Base Catalyzed Deprotonation of a Thiamin-derived Intermediate: Evidence for Sequential Proton Transfer in Pyridine Catalyzed DecarboxylationRathgeber, Steven 15 February 2010 (has links)
The conjugate acid of pyridine had been found to catalyze decarboxylation of alpha-mandelylthiamin (MTh). It was proposed this occurs by association between the substrate and pyridinium ion in a pi-stacked complex prior to cleavage of the C-C bond. Despite the evidence for selective acid catalyzed decarboxylation of MTh with pyridine and its derivatives, the nature of proton transfer occuring after the C-C bond breaks and before the final products form had not been investigated. General base catalyzed deprotonation of hydroxybenzylthiamin (HBnTh) has been applied as a model for the reverse reaction of acid-catalyzed decarboxylation. Kinetic analysis of this process suggests the acceleration by a preassociated pyridinium ion and the product-determining step in the decarboxylation of MTh are facilitated by independent sequential proton transfers.
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General Base Catalyzed Deprotonation of a Thiamin-derived Intermediate: Evidence for Sequential Proton Transfer in Pyridine Catalyzed DecarboxylationRathgeber, Steven 15 February 2010 (has links)
The conjugate acid of pyridine had been found to catalyze decarboxylation of alpha-mandelylthiamin (MTh). It was proposed this occurs by association between the substrate and pyridinium ion in a pi-stacked complex prior to cleavage of the C-C bond. Despite the evidence for selective acid catalyzed decarboxylation of MTh with pyridine and its derivatives, the nature of proton transfer occuring after the C-C bond breaks and before the final products form had not been investigated. General base catalyzed deprotonation of hydroxybenzylthiamin (HBnTh) has been applied as a model for the reverse reaction of acid-catalyzed decarboxylation. Kinetic analysis of this process suggests the acceleration by a preassociated pyridinium ion and the product-determining step in the decarboxylation of MTh are facilitated by independent sequential proton transfers.
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Water assisted decomposition reactions of thionyl halides and ketoprofenYeung, Chi-shun., 楊智淳. January 2010 (has links)
published_or_final_version / Chemistry / Master / Master of Philosophy
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The effect of oxidation on the 2- and 3- positions on the decarboxylation of certain polyanhydrouronic acidsMorris, John 08 1900 (has links)
No description available.
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Mechanistic studies in the bicyclo [2,2,1] heptyl seriesPincombe, Christopher Fletcher January 1973 (has links)
iv, 210 leaves : ill. ; 26 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (Ph.D.)--University of Adelaide, Dept. of Organic Chemistry, 1973
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Mechanistic studies in the bicyclo [2,2,1] heptyl series.Pincombe, Christopher Fletcher. January 1973 (has links) (PDF)
Thesis (Ph.D.) -- University of Adelaide, Dept. of Organic Chemistry, 1973.
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Oxidative decarboxylation of N, N-dialkyl [alpha]-amino acidsOrvis, Roy Lynn, January 1966 (has links)
Thesis (Ph. D.)--University of Wisconsin, 1966. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.
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