Towards the total synthesis of hypoestoxide and dihypoestoxide

Cousin, Peggy (2017) Towards the total synthesis of hypoestoxide and dihypoestoxide. PhD thesis, University of Nottingham.

[img] PDF (Thesis - as examined) - Repository staff only until 18 July 2019. Subsequently available to Repository staff only - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
Download (5MB)

Abstract

The involvement of hetero Diels-Alder dimerisations in the biosynthesis of natural products has been a source of debate for many years. Hypoestoxide and dihypoestoxide are two verticillane-type diterpenoids with closely related structures. Both were isolated from the same extracts of Hypoestes rosea in Nigeria. These two natural products constitute another example of a potential hetero Diels-Alder dimerisation in biosynthesis. Therefore, this thesis reports the work towards the diterpene hypoestoxide in order to study the hetero Diels-Alder dimerisation.

The introduction emphasises the different biological properties of hypoestoxide and the isolation of dihypoestoxide. The biosynthesis of terpenes, the only previous synthesis of an isomer of hypoestoxide reported to date and the hetero Diels-Alder dimerisation in biosynthesis are described. Former Hayes group work about the stereochemical assignment of dihypoestoxide is also detailed in this part.

The results and discussion suggests a synthetic route to hypoestoxide starting from geraniol, which constitutes a sustainable source of starting material for this synthesis. Different approaches towards the formation of the exocyclic enone moiety of hypoestoxide at a later stage in the synthesis would be discussed. Challenges to remove the additional carbon at C12 position would be detailed in this part. A brief conclusion and future work in this regard are given.

Experimental procedures and full characterisation data of the different intermediates synthesised by this route are detailed.

Item Type: Thesis (University of Nottingham only) (PhD)
Supervisors: Hayes, Christopher
Stockman, R.A.
Subjects: Q Science > QD Chemistry > QD241 Organic chemistry
Faculties/Schools: UK Campuses > Faculty of Science > School of Chemistry
Item ID: 41908
Depositing User: Cousin, Peggy
Date Deposited: 18 Jul 2017 04:40
Last Modified: 19 Jul 2017 01:14
URI: http://eprints.nottingham.ac.uk/id/eprint/41908

Actions (Archive Staff Only)

Edit View Edit View