Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.809956
Title: Development of novel synthetic methodologies in photocatalysis
Author: Pezzetta, Cristofer
ISNI:       0000 0004 9347 3463
Awarding Body: Cardiff University
Current Institution: Cardiff University
Date of Award: 2020
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Abstract:
The last decade has seen an impressive number of studies in the field of photocatalysis: the mild conditions used for the generation of radical intermediates and the possibility to couple it with other catalytic manifolds are among the reasons of such popularity. In this thesis, the use of some photocatalytic strategies in organic synthesis is presented. The development of a dual Ni-photoredox strategy for the asymmetric synthesis of N-benzylic heterocycles, interesting drug-like compounds, is described in Chapter 2: a privileged ligand system was found for inducing chirality, and the effect of different heterocycles (in particular bearing directing groups) was addressed. A different perspective is taken in Chapter 3: in this case the focus is not on the transformation, but on PXX (peri-xanthenoxanthene) as a new photocatalyst. Possessing a relatively high reduction potential in the excited state, PXX is capable of promoting a variety of reactions, from the addition of aryl radicals to radical traps, to the organocatalytic β-arylation of cyclic ketones, to Ni-catalysed carbon-heteroatom cross-couplings. The focus moves to organocatalysis in Chapter 4, in particular to the use of chiral iminium ions as photoredox-active species: paired with 4-alkyldihydropyridines as radical precursors, an asymmetric β-alkylation of enals is thus demonstrated. ii Chapter 5 takes back themes encountered in the previous chapters to briefly introduce some attempted but not successful transformations: an organocatalytic β-fluorination of aldehydes, and a cross-coupling strategy towards an API intermediate.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.809956  DOI: Not available
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