Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.685193
Title: Chiral indanones and their derivatives
Author: Kerby, Paul
ISNI:       0000 0004 5924 2274
Awarding Body: University of Warwick
Current Institution: University of Warwick
Date of Award: 2015
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Abstract:
This thesis begins with an introduction to inflammation and the role of cell signalling and adhesion molecules within the body, drawing particular attention to the function of integrins and their ligands. Chapter 1 discusses the importance of the α4-integrin / paxillin interaction for α4β1-dependent cell migration and the recruitment of leukocytes. Herein, literature research into the identification of a racemic, non-cytotoxic molecule that inhibits this interaction is discussed, concluding with synthetic approaches towards the enantiomerically pure synthesis of this compound and its analogues. Chapter 2 opens with the discussion of some literature approaches to the synthesis of the indanone framework, followed by describing some initial synthetic work that was performed and the particular problems encountered with these methods. The attention of this chapter focuses on the kinetic resolution of indanones, applying both an enzymatic acylation and an oxidative kinetic resolution. The chapter demonstrates substrate viability in the aforementioned resolution techniques. Chapter 3 begins with discussing previous work in the synthesis of the target racemic compound. Following this, a detailed review of appropriate synthetic transformations is discussed, proceeding onto work towards the transformation of the enantiomerically enriched indanones into their corresponding quinolinones. The approach herein discusses some unanticipated results during this transformation.
Supervisor: Not available Sponsor: University of Warwick ; Funxtional Therapeutics
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.685193  DOI: Not available
Keywords: QD Chemistry
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