Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618887
Title: Unique approaches towards the synthesis of polycyclic sesquiterpene targets
Author: Gordon, Malcolm Roger
ISNI:       0000 0004 5355 6678
Awarding Body: University of Strathclyde
Current Institution: University of Strathclyde
Date of Award: 2014
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Abstract:
A programme of work towards the total synthesis of the natural product sesquithuriferone has been performed, with significant advances towards the realisation of this overall goal achieved. From this perspective, two main synthetic strategies have been investigated towards the synthesis of a common early-stage intermediate, critical to the construction of the core tricyclic scaffold. In this regard, both of these preparative pathways were explored simultaneously, with the aim of developing a robust and versatile route through to the natural product target. The first of these approaches involved the development of a novel [3+3]-sigmatropic rearrangement, to provide access to range of substituted cyclopentanones. Towards this aim, significant progress has been achieved, with late stage compounds having been prepared. Initial studies concentrated specifically on the synthesis of a novel (Sf(B-lactone key to the synthesis of sesquithuriferone. Additionally, a novel strategy to acce ss a range of substituted systems of structural similarity has been developed and, within the body of this research, a number of preparative pathways designed to access these systems have been explored. As each of the individual routes have been investigated, short optimisation studies have been pursued. The second route towards the synthesis of the common intermediate involved an umpolung conjugate addition strategy. Towards this aim, a robust and versatile set of protocols have been developed to provide access to both the racemic and asymmetric variants of this compound. Towards the construction of the key tricyclic core of sesquithuriferone, a Pauson-Khand approach was pursued. In this regard, a wide range of structural derivatives were synthesised and examined, under a spectrum of standard protocols, to identify an optimal structure to facilitate this key organometallic annulation. Upon completion of this optimisation programme, a range of synthetic strategies were explored towardthe completion of the desired natural target. Significant progress towards this goal has been achieved, with the preparation of several late stage compounds completed. In addition, through the development of this route towards sesquithuriferone, several points of diversity have been identified and investigated with the aim of assessing if the identified synthetic strategy under investigation could be applicable to the synthesis of other members of the same family of natural compounds.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.618887  DOI: Not available
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