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dc.contributor.authorTicli, Vincenzo
dc.date.accessioned2020-11-17T18:59:34Z
dc.date.available2020-11-17T18:59:34Z
dc.identifier.urihttp://hdl.handle.net/10464/14970
dc.description.abstractDiscussed in this thesis is the synthesis of a C10-benzyloxy unnatural derivative of narciclasine. The described approach involves the use of homochiral cyclohexadiene diols, products of the biocatalytic transformation of aromatic compounds, as precursors to ring C, and of highly oxygenated aromatic molecules to construct ring A. The document also reports a detailed account of the protocols studied for the intramolecular formation of ring B. Experimental data and spectral data are provided for the novel compounds.en_US
dc.language.isoengen_US
dc.publisherBrock Universityen_US
dc.subjectnarciclasine amaryllidaceae biocatalysis total synthesisen_US
dc.titleApproaches towards C-10-hydroxylated analogues of narciclasineen_US
dc.typeElectronic Thesis or Dissertationen_US
dc.degree.namePh.D. Chemistryen_US
dc.degree.levelDoctoralen_US
dc.contributor.departmentDepartment of Chemistryen_US
dc.degree.disciplineFaculty of Mathematics and Scienceen_US
refterms.dateFOA2021-08-12T01:37:48Z


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