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Palladium-catalysed allylic amination in the formation of [alpha]-amino acids

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thesis
posted on 20.02.2018 by Roshan Jumnah
The review of this thesis describes palladium catalysed allylic amination in the context of the mechanism and synthetic utility. Examples of alkene geometry, regioselectivity and net retention have been illustrated as a consequence of the amination mechanism. The synthetic aspects of palladium catalysed allylic amination consists of other examples of the formation of enantiomerically enriched allylic amines and amino acids. [Continues.]

Funding

LINK Asymmetric Synthesis Studentship funded by: Loughborough University of Technology; Great Britain, Department of Trade and Industry (DTI); Engineering and Physical Sciences Research Council (EPSRC); and Lilly Research Centre.

History

School

  • Science

Department

  • Chemistry

Publisher

© Roshan Jumnah

Publisher statement

This work is made available according to the conditions of the Creative Commons Attribution-NonCommercial-NoDerivatives 2.5 Generic (CC BY-NC-ND 2.5) licence. Full details of this licence are available at: http://creativecommons.org/licenses/by-nc-nd/2.5/

Publication date

1995

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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