Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782425
Title: Asymmetric synthesis and applications of α-aryl triketopiperazines
Author: Peczkowski, Gary Ryszard
ISNI:       0000 0004 7968 0300
Awarding Body: University of Birmingham
Current Institution: University of Birmingham
Date of Award: 2019
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Abstract:
This project aims to explore the asymmetric synthesis of α-aryl triketopiperazines and their application in synthetic transformations to access biologically relevant scaffolds. Chapter One provides a brief overview of the triketopiperazine motif including initial manipulations and its occurrence in nature. Recent work from our research group has demonstrated that triketopiperazines can undergo highly enantioselective Michael additions. Chapter Two provides an overview of these publications and the extension of this methodology to α-aryl triketopiperazines, including their synthesis and participation in asymmetric organocatalytic Michael additions. Further investigations into the transformation of the Michael addition products towards biologically relevant scaffolds are discussed in Chapter Three. This includes a novel method for access to an unusual diazabicycle and its further transformations. The application of methodology for access to quaternary α-amino acids from triketopiperazines, developed within our research group in collaboration with AstraZeneca, is discussed in Chapter Four. Chapter Five explores the triketopiperazine core as a vehicle for access to natural product scaffolds and the synthesis of a natural product possessing a triketopiperazine is also discussed.
Supervisor: Not available Sponsor: EPSRC
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.782425  DOI: Not available
Keywords: QD Chemistry
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