Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.500173
Title: New and efficient strategies in stereoselective heterocycle synthesis
Author: Sandon, Nicolas
Awarding Body: University of Sheffield
Current Institution: University of Sheffield
Date of Award: 2009
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
This thesis describes the development and the application of three different [3+3] annelation strategies for the formation of functionalised piperidines. Initially, the scope of the [3+3] cycloaddition reaction of Pd-trimethylenemethane and aziridines towards functionalised piperidines was investigated for its application to silyl ether substituted aziridines. These substrates appeared to be very challenging, undergoing the cycloaddition only under very rigorous conditions. Since this methodology was not trivial to repeat, a two-step strategy was explored that involved the addition of a Grignard reagent to the aziridines followed by ringclosure to the corresponding piperidines. These two procedures were found to be enantiospecific, providing good routes for the synthesis of enantiopure piperidines. The functionalisation of the exo-alkene group of these piperidines was also investigated with particular regard to the reaction diastereoselectivity. A third [3+3] annelation reaction towards the synthesis of the piperidine core has also been employed, which invoked the addition of the Bilchi Grignard reagent to the enantiopure silyl ether substituted aziridine (R)-139 to provide the corresponding acetal 263 in good yield. Acid catalysed cyclisation of the acetal produced the corresponding enantiopure tetrahydropyridine 264. The last section of this work focused on the applicability of these methods for the synthesis of natural products and highlights our attempts towards the synthesis of quinolizidine alkaloid (-)217A.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.500173  DOI: Not available
Share: