Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.605522
Title: The total synthesis of analogues of withanolide F
Author: Manicassamy, Laura
ISNI:       0000 0004 5358 6893
Awarding Body: University of York
Current Institution: University of York
Date of Award: 2014
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Abstract:
The total synthesis of analogues of withanolide F I, a highly oxygenated C-28 steroidal lactone natural product isolated from the leaves of the plant Withania adpressa is discussed herein. Chapter 1 describes the classification of the withanolides, their biological activity and previous studies towards the synthesis of the withanolides. Based on well-established chemistry, commercially available pregnenolone II was transformed into the key aldehyde III in nine steps, two steps fewer than previously published routes, with an optimised 14% yield as summarised in Chapter 2 Chapter 3 outlines the synthetic efforts towards the construction of the δ-lactone side chain in compound IV. The synthesis of 14,17-dideoxy-17-epi-withanolide F V was then completed via a straightforward acetylation-oxidation-elimination sequence from triol IV. Isomerisation of the 2,3-double bond delivered a novel analogue of withanolide F I, 3,4-dihydro-Δ3,4-14,17-dideoxy-17-epi- withanolide F VI, as reported in Chapter 4. The development of new methodology to form δ-lactone side chain IX, a key structural feature of natural products I, V and VI, from cyclic sulfone VII via the heterocyclic lactone VIII based on the Dreiding-Schmidt reaction was investigated. Chapter 5 discusses the studies towards the synthesis of strategic sulfone VII.
Supervisor: Taylor, Richard J. K. Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.605522  DOI: Not available
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