Usage
  • 29 views
  • 60 downloads

Oxonium Ylide Rearrangements: A Novel Approach Towards the Synthesis of the Phorbol Skeleton

  • Author / Creator
    Stewart, Craig
  • Oxonium ylides are highly reactive intermediates that can be used for the synthesis of heterocyclic and carbocyclic frameworks. These putative intermediates are almost exclusively formed from diazocarbonyl derived metallocarbenes, by attack of a pendent oxygen atom. Oxonium ylides have been shown to furnish products derived from the [1,2]-shift (Stevens rearrangement) or the [2,3]-shift in an efficient manner. Chapter 1 is a review of oxonium ylides in synthesis focusing on factors that influence the reactivity of these intermediates. Previous work has shown that the sulfur-directed Stevens rearrangement is an efficient reaction for the generation of seven and eight-membered oxa-bridged carbocycles fused to five-membered rings. Chapter 2 describes an extension of this chemistry where six-seven and six-eight membered oxa-bridged carbocyclic products were furnished in good yields. The chemo- and diastereoselectivity of these rearrangements was dependent on the configuration of the acetal stereocentre present in the diazoketone precursor. A novel approach towards the synthesis of the tigliane and daphnane diterpenes is described in Chapter 3. The tricyclic framework was generated from a highly stereoselective oxygen-directed Stevens rearrangement of an oxonium ylide. This methodology provides a straightforward route to the construction of the five-seven-six ring system found in these classes of natural products. Finally, the sulfur-directed Stevens [1,2]-shift was employed in an attempted total synthesis of the natural product (+)-phorbol in Chapter 4. Several variations of the original synthetic scheme were examined, in an effort to construct the core 6-7 ring structure. The Stevens rearrangement was found to provide the 6-7 ring system of phorbol in excellent yield. The chemo- and diastereoselectivity of this rearrangement was dependent on the configuration of the acetal centre as well as the conformation of the six-membered ring in the starting material. In the future, this advanced intermediate could be used to achieve the total synthesis of (+)-phorbol.

  • Subjects / Keywords
  • Graduation date
    2010-06
  • Type of Item
    Thesis
  • Degree
    Doctor of Philosophy
  • DOI
    https://doi.org/10.7939/R3H991
  • License
    This thesis is made available by the University of Alberta Libraries with permission of the copyright owner solely for non-commercial purposes. This thesis, or any portion thereof, may not otherwise be copied or reproduced without the written consent of the copyright owner, except to the extent permitted by Canadian copyright law.
  • Language
    English
  • Institution
    University of Alberta
  • Degree level
    Doctoral
  • Department
    • Department of Chemistry
  • Supervisor / co-supervisor and their department(s)
    • West, Frederick, G. (Chemistry)
  • Examining committee members and their departments
    • Mercer, John (Oncology)
    • Cowie, Martin (Chemistry)
    • Clark, Stephen, J. (University of Glasgow, Chemistry)
    • Lowary, Todd, L. (Chemistry)
    • Clive, Derrick, L. J. (Chemistry)