Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647747
Title: Copper(II)-mediated oxidative coupling routes to nitrogen-heterocycles
Author: Drouhin, Pauline
ISNI:       0000 0004 5346 8344
Awarding Body: University of York
Current Institution: University of York
Date of Award: 2015
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Abstract:
Nitrogen-containing heterocycles have attracted considerable attention owing to their prevalence in numerous natural substances as well as their extensive applications in biology and pharmacology. In recent years, great efforts have been devoted to the elaboration of novel synthetic methodologies for the construction of N-heterocycles such as oxindoles and indoles. Reported in 2009 by the Taylor group, access to oxindole scaffolds has been successfully demonstrated via a copper(II)-mediated oxidative coupling approach. Following the same principle, the extension of this method to the formation of the more intricate bis-oxindole skeleton is demonstrated via the double cyclisation of bis-anilides using Cu(OAc)2·H2O as oxidant. The scope of the copper(II)-mediated cyclisation to the formation of 3H-indoles and 1H-indoles from N-aryl enamines is also described. Progress towards the total synthesis of the highly complex spirooxindole alkaloid natural product rankinidine is presented. Towards this end, the application of the copper(II)-mediated cyclisation for the formation of the oxindole core of rankinidine is presented.
Supervisor: Taylor, Richard J. K. Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.647747  DOI: Not available
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