<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-23T05:13:34Z</responseDate><request verb="GetRecord" identifier="oai:www.repository.cam.ac.uk:1810/373370" metadataPrefix="uketd_dc">https://api.repository.cam.ac.uk/server/oai/request</request><GetRecord><record><header><identifier>oai:www.repository.cam.ac.uk:1810/373370</identifier><datestamp>2024-09-12T00:41:49Z</datestamp><setSpec>com_1810_721</setSpec><setSpec>com_1810_256064</setSpec><setSpec>col_1810_218856</setSpec></header><metadata><uketd_dc:uketddc xmlns:uketd_dc="http://naca.central.cranfield.ac.uk/ethos-oai/2.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:uketdterms="http://naca.central.cranfield.ac.uk/ethos-oai/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://naca.central.cranfield.ac.uk/ethos-oai/2.0/ http://naca.central.cranfield.ac.uk/ethos-oai/2.0/uketd_dc.xsd">
   <dc:title>Modular Methods for the Synthesis of α-Tertiary and α-Branched Alkylamines via Visible-Light-Mediated Radical Generation</dc:title>
   <dc:identifier xsi:type="dcterms:DOI">https://doi.org/10.17863/CAM.111824</dc:identifier>
   <dc:creator>Smith, Milo</dc:creator>
   <uketdterms:authoridentifier xsi:type="uketdterms:ORCID">0000000284039636</uketdterms:authoridentifier>
   <uketdterms:advisor>Gaunt, Matthew</uketdterms:advisor>
   <dcterms:abstract>The efficient assembly of complex molecules from cheap and abundant feedstock materials is a central goal of organic synthesis. Alkylamines are interesting synthetic targets because they occupy a privileged position in drug discovery yet are often highly challenging to synthesise. Complex alkylamines commonly feature branching at the α-position, which can further complicate their synthesis. This thesis describes two methods for the preparation of alkylamines displaying either one (α-branched amines) or two (α-tertiary amines) α-branching substituents.

In the first method, visible-light-mediated photoredox catalysis orchestrates the formation of α-tertiary amines from alkyl primary amines, alkyl ketones, and alkene acceptors. Over 50 new α-tertiary alkylamines are reported, displaying a range of structural and functional diversity in all three components. The new method enabled a single-step synthesis of the multiple sclerosis drug fingolimod (Gilenya), and provided access to a range of unique spirocyclic tetrahydronaphthyridine and tetrahydroquinoline scaffolds. Mechanistic studies inform the proposal of a redox-neutral catalytic cycle involving generation of a key α-amino radical.

In the second method, α-branched amines are prepared from alkyl primary amines, alkyl aldehydes and alkyl iodides in an advancement of the carbonyl alkylative amination chemistry previously reported by the Gaunt group. Carbon-carbon bond formation takes place upon addition of an alkyl radical to an alkyl imine. Over 50 new a-branched alkylamines are reported, including the use of alkyl iodides bearing a pendent electrophile to enable annulation to form α-branched heterocycles in a telescoped two-step procedure. Preliminary results regarding a selective alkylation reaction at primary amines in the presence of cyclic secondary amines are also reported.</dcterms:abstract>
   <uketdterms:institution>University of Cambridge</uketdterms:institution>
   <dcterms:issued>2024-05-07</dcterms:issued>
   <dc:type>Thesis</dc:type>
   <uketdterms:qualificationlevel>Doctoral</uketdterms:qualificationlevel>
   <uketdterms:qualificationname>Doctor of Philosophy (PhD)</uketdterms:qualificationname>
   <dc:language>eng</dc:language>
   <dcterms:isReferencedBy xsi:type="dcterms:URI">https://www.repository.cam.ac.uk/handle/1810/373370</dcterms:isReferencedBy>
   <uketdterms:embargotype>embargo</uketdterms:embargotype>
   <uketdterms:embargodate>2025-09-11</uketdterms:embargodate>
   <dc:identifier xsi:type="dcterms:URI">https://apollo8-f-pro.lib.cam.ac.uk/bitstreams/71ba9e7e-6f6c-475a-99d3-4211697dbf6f/download</dc:identifier>
   <uketdterms:checksum xsi:type="uketdterms:MD5">796428aa6c5e7f0df97db5f44e8af972</uketdterms:checksum>
   <dcterms:license>https://apollo8-f-pro.lib.cam.ac.uk/bitstreams/a57b7572-4a7e-4950-8599-7a431d355ad6/download</dcterms:license>
   <uketdterms:checksum xsi:type="uketdterms:MD5">87eda9de84448d1f82354d60eee3eb5f</uketdterms:checksum>
   <dc:rights>https://www.rioxx.net/licenses/all-rights-reserved/</dc:rights>
   <dc:subject>Amines</dc:subject>
   <dc:subject>Imines</dc:subject>
   <dc:subject>Photocatalysis</dc:subject>
   <dc:subject>Photochemistry</dc:subject>
   <dc:subject>Photoredox</dc:subject>
   <dc:subject>Radicals</dc:subject>
   <dc:subject>Visible light</dc:subject>
</uketd_dc:uketddc>
</metadata></record></GetRecord></OAI-PMH>