Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.756865
Title: Metal-free visible-light promoted generation of nitrogen-centred radicals via photoredox catalysis
Author: Davies, Jacob
ISNI:       0000 0004 7429 7222
Awarding Body: University of Manchester
Current Institution: University of Manchester
Date of Award: 2018
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
Nitrogen-centred radicals (NCRs) are powerful reaction intermediates that allow key bonds to nitrogen to be formed. However, the generation of NCRs typically requires pre-functionalised precursors that can be difficult to access and harsh reaction conditions in the formation of the NCR itself which has limited synthetic application. In this thesis, the application of visible-light mediated photoredox catalysis towards the generation of iminyl and amidyl radicals is demonstrated and the advances to NCR chemistry this has facilitated. Initial work developed electron-poor O-aryl oximes as suitable precursors for hydroimination reactions, activated via single-electron reduction under photoredox conditions. These precursors are accessible by a simple condensation reaction with the commercially available hydroxylamine and can be purified by recrystallization. The realisation of a transition metal-free protocol was made possible by using the organic dye eosin Y as the photocatalyst. This activation mode was then extended to the generation of (carb)amidyl-radicals from easy-to-make O-aryl hydroxylamides. Similar transition metal-free photoredox reaction conditions could be applied in intramolecular hydroamidation reactions allowing the preparation of lactams and cyclic (thio)carbamates. For the first time N-Boc and N-Cbz protected amidyl-radicals were utilised despite the very high electrophilic nature of these species. Finally, one of the big challenges associated with NCR chemistry was addressed; the development of multicomponent reactions for the divergent synthesis of complex N-containing molecules. Previously developed O-aryl precursors proved unsuitable and instead a novel class of alpha-imino acid precursors were identified that can be activated via oxidation under photoredox conditions. This activation mode was also rendered transition metal-free by using the Fukuzumi photoredox catalyst. These new NCR precursors proved crucial in developing a divergent methodology that allows the synthesis of up to fifteen iminofunctionalised products from a single starting material. Moreover, this methodology could be applied to the modification of complex natural products such as immunosuppressant drug mycophenolic acid and alkaloid thebaine. One could envisage such an approach may be ideal for a drug discovery type situation where changes in functionality can greater alter drug activity.
Supervisor: Greaney, Michael Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.756865  DOI: Not available
Keywords: hydroamidation ; iminofunctionalisation ; Nitrogen-centred radical ; photoredox catalysis ; hydroimidation
Share: