Thesis (Doctoral)--University of Stockholm, 1983. / Includes articles on which author's Review is based. Includes bibliographical references.

Thesis (Ph.D.)--Aberdeen University, 2009. / Title from web page (viewed on Dec. 2, 2009). Includes bibliographical references.

Thesis (M.S.)--University of North Carolina at Greensboro, 2007. / Title from PDF title page screen. Advisor: Jason Reddick; submitted to the Dept. of Chemistry. Includes bibliographical references (p. 41-46).

In order to compare the pyrrolizidine alkaloid content of two closely related species, Senecio chrysocoma and S. paniculatus, nine populations of plants distributed between the two species, were examined. Three novel pyrrolizidine alkaloids, 7ß-angelyl-l-methylene-8∝-pyrrolizidine, 7ß-angelyl-l-methylene-8∝-pyrrolizidine and 7ß-angelyl-l-methyleneSO!-pyrrolizidine-4-oxide, as well as eight known pyrrolizidine alkaloids, 7-angelylhastanecine, 9-angelylhastanecine, 7-angelylplatynecine, 9-angelylplatynecine, 9-angelylplatynecine-4-oxide, sarracine, neosarracine and retrorsine, were isolated and identified by NMR and GC-MS techniques. Traces of five tiglyl isomers, 9-tiglylplatynecine, 9-tigl ylplatynecine-4-oxide, 7ß-tiglyl-l-methylene-8∝-pyrrolizidine, sarranicine and neosarranicine, were also isolated and tentatively identified; however, these compounds could have been artefacts of the extraction and analytical procedures. While both species of plant investigated, S. chrysocoma and S. paniculatus, were found to be morphologically different, their pyrrolizidine alkaloid content was, in fact, very similar. The presence of retrorsine in S. paniculatus plant extracts, but not in those from S. chrysocoma plants, was the only major chemical difference observed. It is perhaps significant that retrorsine was the only macrocyclic pyrrolizidine to be identified. A comprehensive, computerised database of physical data for pyrrolizidine alkaloids has been compiled, which has facilitated the identification of new pyrrolizidines and the examination of trends in proton and carbon-13 NMR data for pyrrolizidine alkaloids. A stereospecific synthesis of 7ß-angelyl-l-methylene-8∝-pyrrolizidine was undertaken toconfirm the absolute stereochemistry of the product isolated from S. chrysocoma and S. paniculatus. An inseparable 5:2 mixture of 7ß-angelyl-l-methylene-8∝-pyrrolizidine and 7ß-angelyl-l,2-didehydro-l-methyl-8∝-pyrrolizidine, together with a small amount of tiglyl isomer, was finally synthesised. The application of various chiral differentiating chromatographic and spectroscopic techniques confirmed that both the natural and synthetic products had the same stereochemistry, permitting the natural alkaloid to be identified as 7ß-angelyl-methylene-8∝-pyrrol izidine

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The total mineral ion concentration of Rooibos Tea was determined using ICP-OES. Significant concentrations of Na, K, Mg, Ca, P were found, and trace levels of Al, Fe, Mo, Sr, Zn, Ba, Cu and Pb detected. Protocatechuic acid, aspalathin and rutin were identified in Rooibos tea infusions analysed with HPLC. Analysis of tea samples by Ion Chromatography showed the presence of Cr and S042- ions. Rooibos Tea liquor had a pH of 4.6 once equilibrium had been reached. Partition coefficients (1.0 - 1.4 mm sieving fraction) for Na+, K+, Mg2+, protocatechuic acid, aspalathin, rutin, S042- and Cl were determined for infusions at 80 C using a graphical and a successive extraction method. A total mineral content method was also used to determine the partition coefficients for the mineral ions. The Na+, K+, Mg2+,SO42-, H2P04- (as P) and Cl ions as well as protocatechuic acid, aspalathin and rutin all displayed first order behavior, allowing the determination of infusion rate constants. The particle size effect was investigated at 80 C. All the mineral ions showed an increase in infusion rate constant with decreasing particle size, protocatechuic acid and aspalathin showed no trend, while the rutin infusion rate constant was independent of particle size. Calcium uptake by the leaf was observed, this was more pronounced with the smaller particle sizes. Infusion rate constants and hence diffusion coefficients were determined for the nine species for temperatures ranging from 45 to 90 C. These diffusion coefficients for the mineral ions were compared with those for the respective species in aqueous media to give hindrance factors, which were of the order of 102. Except for Cl, all hindrance factors increased with an increase in temperature. The infusion rate constants for all the species at the various temperatures were fitted to an Arrhenius equation and activation energies of infusion determined. The values were lower than those predicted theoretically. / Thesis (M.Sc.)-University of Natal, Pietermaritzburg, 1998