Ball-Jones, Matthew Phillip (2017). Cascading cycloadditions for polycyclic sp\(^3\) -rich architecture. University of Birmingham. Ph.D.
Full text not available from this repository.Abstract
This thesis describes the formation of complex 3-dimensional polycyclic heterocycles via intramolecular Diels-Alder reactions of highly functionalised 4-aminooxazoles. The research presented discusses the advances made in the formation of alkene and alkyne tethered aminides alongside the synthesis of a range of 1,6- and 1,7- enynamides and the rapid transformation of such components into a densely functionalised core.
The scope of this process, using both C-2 and C-5 dienophile-tethered oxazoles is discussed and the potential of 1,6-enynamides to undergo cycloisomerisation under gold-catalysis is unveiled. Mechanisms for both the cycloisomerisation and the oxazole formation are provided, with brief investigations into inner and outer sphere processes.
The gold-catalysed formal (3+2)-dipolar cycloaddition of both aminides and dioxazoles with thioalkynes is also presented, with the production of a range of diversely functionalised 5-thiooxazoles. Preliminary investigations into the use of Bronsted acid catalysis for the synthesis of 4-thiooxazoles is discussed alongside mechanistic proposals.
Type of Work: | Thesis (Doctorates > Ph.D.) | |||||||||
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Award Type: | Doctorates > Ph.D. | |||||||||
Supervisor(s): |
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College/Faculty: | Colleges (2008 onwards) > College of Engineering & Physical Sciences | |||||||||
School or Department: | School of Chemistry | |||||||||
Funders: | None/not applicable | |||||||||
Subjects: | Q Science > QD Chemistry | |||||||||
URI: | http://etheses.bham.ac.uk/id/eprint/7986 |
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