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Applications of the achmatowicz rearrangement in natural product synthesis

Hobson, Stephen (2010) Applications of the achmatowicz rearrangement in natural product synthesis. PhD thesis, University of Glasgow.

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Abstract

The structurally related PM-94128 and Ajudazols A and B exhibit differing biological activities but share the isocoumarin core structure. PM-94128 belongs to a large family of compounds known as the aminodihydroisocoumarins and was isolated in 1997. It has been shown to be an inhibitor of DNA and RNA synthesis and have potent cytotoxic activity in vivo. The Ajudazols A and B were isolated in 2004 and have antifungal activity against several important food spoilers. The work that follows details the design and development of a novel method for the generation of the isocoumarin core from isobenzofuran utilizing the Achmatowicz rearrangement of a-hydroxyisobenzofurans. Spirocyclic pyrans such as Polymaxenolide are structurally complex molecules, containing large amounts of functionality. The biological activity of Polymaxenolide is unknown and there have been no total syntheses reported to date.

Item Type: Thesis (PhD)
Qualification Level: Doctoral
Keywords: Achmatowicz rearrangement, isochromanones, spirocyclic, Ajudazol, Polymaxenolide, isobenzofuran
Subjects: Q Science > QD Chemistry
Colleges/Schools: College of Science and Engineering > School of Chemistry
Supervisor's Name: Marquez, Dr. Rodolfo
Date of Award: 2010
Depositing User: Dr SJ Hobson
Unique ID: glathesis:2010-1660
Copyright: Copyright of this thesis is held by the author.
Date Deposited: 25 Mar 2010
Last Modified: 10 Dec 2012 13:44
URI: http://theses.gla.ac.uk/id/eprint/1660

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