Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.779620
Title: Sulfur-mediated C-H functionalisation in arenes and alkenes using low-cost metals
Author: Aukland, Miles
ISNI:       0000 0004 7965 3150
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:
Synthetic advances have equipped chemists with methods to selectively functionalise C-H bonds in organic molecules, thus streamlining syntheses with increased atom economy and more benign by-product generation. Unfortunately, the vast majority of developed processes utilise toxic, platinum-group metals that come from depleting stocks. The need to acquire complementary approaches with cheaper, more abundant and environmentally-friendly first-row transition-metals is well appreciated for this reason. Recently in the Procter group, an iron-mediated oxidative coupling of arenes and alkenes has been developed. Investigations in to the synthesis of pharmaceutically-relevant motifs from the products of these couplings are disclosed. Utilising the synthetic handles present in the coupling products, the synthesis of atypical antipsychotic, dibenzothiepine scaffolds has been achieved. Similarly, elaborate dihydrobenzofuran structures have been accessed using metal-catalysed cross-coupling techniques in a rapid and efficient manner. Efforts towards the development of a more general and catalytic variant of the iron-mediated coupling are also described. Also presented is an efficient protocol for the selective conversion of C-H bonds to C-C bonds using a close alliance of base-metal catalysis and Pummerer-type chemistry that operates under mild conditions; Activated sulfoxides are excellent sulfur electrophiles and can be used to activate arene and alkene C-H bonds. The resulting sulfonium salts serve as pseudohalides in nickel-catalysed cross-coupling reactions with organozinc reagents. The value and power of this developed method is then demonstrated through application to the late-stage modification of complex pharmaceuticals.
Supervisor: Procter, David ; Greaney, Michael Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.779620  DOI: Not available
Keywords: Interrupted Pummerer ; Cross-coupling ; Oxidative coupling ; Iron ; Sulfur ; Nickel Catalysis
Share: