Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.479321
Title: Palladium-catalysed routes to the tricyclic core of the Stemona alkaloids
Author: Early, Craig
ISNI:       0000 0001 3436 9699
Awarding Body: Loughborough University
Current Institution: Loughborough University
Date of Award: 2007
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Abstract:
The Stemona alkaloids are a structurally interesting class of alkaloids isolated from the roots and rhizomes of the Stemonaceae plant family. During this project we have investigated the viability of constructing the tricyclic core of the Stemona alkaloids using a cascade Heck/carbopalladation reaction sequence, starting from an allylvinylcyclopropane building block, utilising the group's [2+3] palladium catalysed cycloaddition chemistry. [Illustration omitted.] We have briefly investigated applying our palladium catalysed [2+3] cycloaddition methodology towards doubly activated vinylcyclopropanes, preparing a selection of tetrahydrofuran and pyrrolidine precursors which underwent a Heck mediated cyclisation to yield a variety of functionalised polycycles. As well as further developing this methodology towards a tandem cycloaddition/Heck one-pot strategy. [Illustration omitted.] We have also investigated applying this methodology towards the construction of the azepine core of the Stemoamide group of Stemona alkaloids. Using the group's [2+3] cycloaddition chemistry to construct suitable pyrrolidines and subjecting them to Heck mediated cyclisations as well as investigating the viability of a tandem cycloaddition/Heck one-pot strategy.
Supervisor: Not available Sponsor: Syngenta AG
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.479321  DOI: Not available
Keywords: Chemical Sciences not elsewhere classified
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