posted on 2022-03-29, 01:39authored byWendy L. Loa-Kum-Cheung
Nature generates huge diversity in molecular frameworks by using the simplest route, starting from abundantly available precursors. The biogenesis of natural products provides valuable information for the design of efficient routes for complex natural products based on structural analysis and biosynthetic pathways. Chapter 1 investigates the diastereoselective biomimetic synthesis of the natural products mikimopine and cucumopine, based on their biogenesis from the Pictet-Spengler reaction between the naturally abundant precursors !-ketoglutaric acid and L-histidine. Chapter 2 and 3 then focus on the structurally diverse and complex family of natural products, known as the oroidin alkaloids. In Chapter 2, a comprehensive review of the oroidin alkaloids isolated thus far, is first provided. The biogenesis of all the currently known oroidin alkaloids has been analysed and this has led, for the first time, to a unifying theory for their formation in Nature. Haloperoxidase enzymes are thought to play an important role in the biosynthesis of these marine natural products. Taking this into account, our proposed biogenesis explains the formation of every oroidin alkaloid from the reactive intermediate epoxide or bromonium ion of the precursor oroidin or dihydrooroidin, and forms the basis of a biomimetic approach towards the synthesis of these fascinating and biologically active alkaloids. Our efforts towards this, are described in Chapter 3, first by exploring the epoxide route and then the bromonium ion route, and have led to the synthesis of some natural and unnatural oroidin alkaloids. Chapter 4 then moves away from the topic of biomimetic synthesis and describes the synthesis ofhemicyanine hybrids of the fluorescent natural product epicocconone. The photophysical properties of these novel near infra-red dyes are reported and their potential in the detection of biomolecules demonstrated. Finally the experimental andappendices for the whole thesis are provided in Chapter 5 and 6 respectively.
History
Table of Contents
Chapter 1. Diastereoselective biomimetic synthesis of natural products mikimopine and cucumopine -- Chapter 2. Biogenesis of the oroidin alkaloids -- Chapter 3. Biomimetic approach towards the synthesis of oroidin alkaloids from their biogenetic precursor(s) -- Chapter 4. Investigation of the bromonium ion route -- Chapter 4. Synthesis of epicconone-hemicyanine hybrids for near infra-red fluorescence -- Chapter 5. Experimental.
Notes
Includes bibliographical references
Empirical thesis.
Awarding Institution
Macquarie University
Degree Type
Thesis PhD
Degree
PhD, Macquarie University, Faculty of Science and Engineering, Department of Chemistry and Biomolecular Sciences
Department, Centre or School
Department of Chemistry and Biomolecular Sciences
Year of Award
2014
Principal Supervisor
Peter H. Karuso
Rights
Copyright Wendy L. Loa-Kum-Cheung 2014.
Copyright disclaimer: http://www.copyright.mq.edu.au