STUDIES IN THE CATION- INDUCED CYCLISATION OF OLEFINS

dc.contributor.authorAMUPITAN, J. 0.
dc.date.accessioned1979-02-05T10:56:24Z
dc.date.available2014-02-05T10:56:24Z
dc.date.issued1979-02-05
dc.descriptionA Thesis entitled STUDIES IN THE CATION- INDUCED CYCLISATION OF OLEFINS presented by J. 0. AMUPITAN, M.Sc. in part fulfilment of the requirements of The Victoria University of Manchester for the degree of DOCTOR OF PHILOSOPHYen_US
dc.description.abstractChapter 1 consists of a review of the role of squalene oxide in the biogenesis of triterpenoids and steroids via lanosterol. A number of non-enzymic methods of inducing such cyclisations under various conditions is also presented with greater emphasis on the more successful techniques. Chapter 2 starts with a review of the classical route to the synthesis of 2-alkylcyclohexenones via alkylation of Hagemann's ester. This is followed by a series of reactions carried out by the author leading to a novel synthetic route to the 2-alkylcyclohexenones, which is shown to be much better than the former route. A review of the Lewis acid induced cyclisation of epoxyolefins already carried out by a number of workers in our Laboratories is also presented followed by the cyclisations of epoxyolefins and alpha, Beta -unsaturated ketones carried out by the author. It is hereby demonstrated that formation of bi-, tri- and tetra- cyclic systems are feasible under suitable conditions. Chapter 3 consists of the experimental work of reactions mentioned in Chapter 2.en_US
dc.identifier.urihttp://hdl.handle.net/123456789/299
dc.language.isoenen_US
dc.subjectSTUDIESen_US
dc.subjectSTUDIESen_US
dc.subjectCYCLISATIONen_US
dc.subjectOLEFINSen_US
dc.titleSTUDIES IN THE CATION- INDUCED CYCLISATION OF OLEFINSen_US
dc.typeThesisen_US
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