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Palladium-catalysed routes to the tricyclic core of the Stemona alkaloids

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thesis
posted on 31.07.2018, 10:16 authored by Danial Leybourne
Heterocyclic product families include a wide and diverse range of natural and synthetic molecules, which exhibit a variety of biological activities. In particular this study will focus on the construction of the Stemona alkaloids, isolated from the roots and rhizomes of the Stemonaceae plant family. They possess the structurally novel and unique azepinoindole skeleton "B,C,D ring system." [Illustration omitted.] Studies towards the development of a novel methodology has been achieved. During our investigation we have developed a palladium(0)-catalysed [3+2]-cycloaddition strategy towards the rapid synthesis of heterocyclic skeletons, assembling polycyclic pyrrolidines and furan heterocycles from fused doubly activated vinylcyclopropanes. [Illustration omitted.] We have briefly investigated our palladium(0)-catalysed [3+2]-cycloaddition methodology towards doubly activated vinylcyclopropanes, preparing a selection of tetrahydrofuran and pyrrolidine precursors which underwent a Heck-mediated cyclisation. As well as further developing this methodology towards a tandem cycloaddition/Heck one-pot strategy. We hoped this initial ground work could be applied towards the construction of the tricyclic core of Stemona alkaloids. [Illustration omitted.]

History

School

  • Science

Department

  • Chemistry

Publisher

© Danial Leybourne

Publisher statement

This work is made available according to the conditions of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) licence. Full details of this licence are available at: https://creativecommons.org/licenses/by-nc-nd/4.0/

Publication date

2006

Notes

A Doctoral Thesis. Submitted in partial fulfilment of the requirements for the award of Doctor of Philosophy at Loughborough University.

Language

en

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