Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.495332
Title: Studies towards the total synthesis of labiatin A
Author: Vignard, David
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 2008
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Abstract:
This thesis is concerned with studies towards the total synthesis of labiatin A using metal carbenoid chemistry. The work described herein shows the most recent contribution to this field from our research group. Chapter I provides an introduction to metal carbenoids and their uses in organic synthesis. In particular, the synthesis of diazo carbonyl compounds, their decomposition by metal catalysts leading to the formation of metal carbenoids and the reactions involving metal carbenoids is described. A retrosynthesis of labiatin A involving the use of two metal-carbenoid transformations- intramolecular C-H insertion reaction and oxonium ylide formation followed by [2,3]-sigmatropic rearrangement- is presented. In Chapter II, the successful applications of these two reactions to the enantioselective synthesis of the tricyclic core of labiatin A is described. This is followed by the description of the different attempts to complete the synthesis of labiatin A. Finally, the exploration of a modified approach to the total synthesis of labiatin A is described. Chapter III provides the analytical support to this thesis.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.495332  DOI: Not available
Keywords: QD Chemistry
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