Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680579
Title: Synthesis and reactions of novel oxindoles
Author: Edeson, Steven
ISNI:       0000 0004 5916 1386
Awarding Body: University of Sheffield
Current Institution: University of Sheffield
Date of Award: 2015
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Abstract:
An important issue with the assignment of E/Z alkene geometry of 3-acylidene-oxindoles was addressed. A novel UV/Visible spectroscopic assay was developed in order to achieve this, taking advantage of contrasting electronic properties for different E/Z isomer sets. Moreover, a novel acylidene oxindole was prepared and used to provide further supporting evidence for this spectroscopic assay. Finally, the stability of related E/Z isomers was investigated, and indicated facile isomerisation to a thermodynamic minimum. A copper promoted cyclisation of o-nitrophenyl iodoacetylenes to 2-iodoisatogens was discovered. These compounds were applicable as precursors to novel isatins and consequently 3-acylidene oxindoles. The metal free aryl and alkyl cross coupling reactions of 2-iodoisatogens was developed, providing a divergent synthetic strategy to the medicinally relevant isatogen molecular group. Furthermore, an unprecedented isatogen mode of reactivity was discovered affording pseudoindoxyls, a privileged class of molecule. The mechanism for this transformation was proposed, based on control reactions and strong literature precedent.
Supervisor: Harrity, J. P. A. Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.680579  DOI: Not available
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