Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/102583
Citations
Scopus Web of ScienceĀ® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.advisorGeorge, Jonathan-
dc.contributor.authorSpence, Justin Thomas James-
dc.date.issued2016-
dc.identifier.urihttp://hdl.handle.net/2440/102583-
dc.description.abstractIn recent times, natural product synthesis has become central to many scientific fields; from chemistry, through to biology and pharmacology. As synthetic chemists, natural products are attractive targets due to their interesting and complex structures, combined with some intriguing biological properties. One field that is of particular interest is the use of a biomimetic approach towards the synthesis of complex natural products. This thesis will describe the use ortho-quinone methides and cascade reactions towards the biomimetic synthesis of the penilactones A and B, the peniphenones A-D, virgatolide B and epicolactone. The total synthesis of ent-penilactone A and penilactone B has been achieved via biomimetic Michael reactions between tetronic acids and o-quinone methides. A fivecomponent cascade reaction between a tetronic acid, formaldehyde, and a resorcinol derivative that generates four carbon-carbon bonds, one carbon-oxygen bond and two stereocenters in a one-pot synthesis of penilactone A is also reported. The total synthesis of peniphenones A-D has been achieved via Michael reactions between appropriate nucleophiles and a common ortho-quinone methide intermediate. This strategy, which was based on a biosynthetic hypothesis, minimised the use of protecting groups and thus facilitated concise syntheses of the natural products. The most complex target, the benzannulated spiroketal peniphenone A, was synthesised enantioselectively in nine linear steps from commercially available starting materials. A synthesis for the ortho-quinone methide precursor of virgatolide B has been developed. A simplified enol ether was employed for the biomimetic [4+2] cycloaddition reaction to afford a simplified virgatolide B analogue. An isomerised compound containing a cis fused ring junction, thought to arise via a [4+2] cycloaddition of an ortho-quinone methide and an endocyclic enol ether formed by acid catalysed tautomerisation in situ will also be reported. Finally, preliminary studies towards the synthesis of epicolactone have been conducted. A synthesis of the proposed key proposed biosynthetic intermediate epicoccone B has been achieved in four steps. Efforts towards the synthesis of epicoccine via our proposed cycloetherification route proved to be challenging. Furthermore, the synthesis of epicolactone through our proposed biosynthesis was not viable, which was also observed by Trauner and co-workers in their 2014 synthesis of dibefurin.en
dc.subjectnatural product synthesisen
dc.subjectbiomimetic synthesisen
dc.subjectortho-quinone methidesen
dc.titleBiomimetic synthesis of natural products via reactions of ortho-quinone methidesen
dc.typeThesesen
dc.contributor.schoolSchool of Physical Sciencesen
dc.provenanceThis electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exceptions. If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legalsen
dc.description.dissertationThesis (Ph.D.) -- University of Adelaide, School of Physical Sciences, 2016.en
dc.identifier.doi10.4225/55/582d507aea7ec-
Appears in Collections:Research Theses

Files in This Item:
File Description SizeFormat 
01front.pdf232.13 kBAdobe PDFView/Open
02whole.pdf7.69 MBAdobe PDFView/Open
Permissions
  Restricted Access
Library staff access only221.74 kBAdobe PDFView/Open
Restricted
  Restricted Access
Library staff access only30.91 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.