Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.564444
Title: Investigation of novel thermal cyclisation reactions and studies on their application to the synthesis of selected natural products
Author: Faggiani, Davide
Awarding Body: University of Sussex
Current Institution: University of Sussex
Date of Award: 2012
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Abstract:
The primary goal of this research project was to investigate the mechanism of a novel thermally activated cyclisation reaction discovered by Parsons et al. During these studies two novel reactions were discovered: For reaction see Abstract in pdf Reagents and Conditions: (i) Toluene 0.1M, reflux, 4h, 32%. For reaction see Abstract in pdf Reagents and Conditions: (i) Toluene, 0.01M, reflux, 4h, 53% Radical and ene pathways for the generation of these products were proposed. However, despite extensive empirical studies, no definitive proof for either mechanism was found. The breadth of the synthetic utility of the above reactions was also investigated by synthesizing various analogues. The general application of the Parsons' cyclisation to the synthesis of steroid cored and the complex natural product Jiadifenin was also investigated. Advanced intermediates were synthesised and invaluable information on reactivity was gained, however these investigations could not be completed due to time constraints
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.564444  DOI: Not available
Keywords: QD0241 Organic chemistry
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