Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.791041
Title: Amide directed C(sp3)-H functionalisation of saturated amines
Author: Coomber, Charlotte E.
ISNI:       0000 0004 8500 5782
Awarding Body: UCL (University College London)
Current Institution: University College London (University of London)
Date of Award: 2019
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Abstract:
This thesis describes research towards the development of C-H activation reactions of saturated amines. Chapter 1 describes current approaches towards directed C-H activation. Chapter 2 covers approaches towards the amide directed C-H functionalisation of saturated amines. Methodology for the arylation of bicyclic amines is developed, which gives high yields of arylated products with a variety of aryl iodides and bromides. The methodology is applied to mono-, bi- and tricyclic amines with excellent yields. The reaction is improved by the introduction of a novel solvent for C-H activation, and allows for the arylation of more challenging amine substrates. It is also shown that a simple methyl substitution on the directing group can improve the yield of arylated products. Chapter 3 investigates how the directing group employed can influence both the selectivity and yields of C-H functionalisation. Different directing groups are investigated on a range of amines to establish if they can improve yield and selectivity. Chapter 4 describes efforts towards elucidating the mechanism for C-H activation. Plausible reaction intermediates are isolated. Reaction progress kinetic analysis is performed to further probe the reaction and to establish the rate dependence on the different reaction components. Same excess experiments are employed to establish the effect of the product on catalyst activity and also to determine if there is any catalyst degradation over the course of the reaction. Chapter 5 describes efforts towards sustainable amide synthesis. Direct condensation of a carboxylic acid with an amine using a borate catalyst is employed. Existing methods developed within the group are expanded to improve yields for more polar substrates, and poorly nucleophilic amines. A new ester solvent is introduced to improve solubility of these substrates and improve the sustainability and reduce cost of the process.
Supervisor: Sheppard, T. ; Porter, M. Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.791041  DOI: Not available
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