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New approaches for the asymmetric synthesis of pyrroloisoquinoline and isoquinoline alkaloids

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posted on 18.09.2018, 08:37 by Guy B. Streetley
Pyrroloisoquinoline (n = 1) and the pyridoisoquinoline (n = 2) ring systems (2) are found to be the major structural motif of the Erythrina and the protoberberine group of alkaloids, respectively. We have recognised that suitable bicyclic lactams (1) could act as precursors, in an intramolecular N-acyliminium ion-mediated cyclisation, resulting in a stereoselective approach to the core of the Erythrina and protoberberine ring systems. [Illustration omitted.] Access to the tetracyclic core of the Erythrina alkaloids (3) through the application of N-acyliminium ion chemistry is well established within our group. This has been demonstrated in a formal asymmetric synthesis of both enantiomers of the Erythrina alkaloid, 3- demethoxyerythratidinone (4), and described in this thesis. [Illustration omitted.] Our investigations have also involved the manipulation of this methodology toward the synthesis of the Erythrina alkaloid (-)-erysotrine (5) and the protoberberine alkaloid (-)-xylopinine (6).

History

School

  • Science

Department

  • Chemistry

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© Guy Bradwell Streetley

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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