Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801586
Title: Expedient methods for the stereoselective glycosylation of carbohydrates
Author: Williams, Ryan
Awarding Body: University of Bristol
Current Institution: University of Bristol
Date of Award: 2020
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
Carbohydrates are a widely abundant class of biological compounds that play pivotal roles in medicine, cellular function and nutrition. Despite the ubiquity of carbohydrates in living systems, their efficient synthesis presents a significant challenge. Major reasons for this include the difficulties in controlling the stereochemistry of the glycosylation reaction and the laborious, time-consuming nature of oligosaccharide preparation. This thesis describes efforts to overcome these challenges through new technologies that expedite glycosylation reactions and subsequent product purification. A library of glycosyl donors and acceptors was prepared. Using these substrates, a cooperative thiourea-Brønsted acid dual organocatalytic glycosylation strategy for the synthesis of 2-deoxyglycosides was probed. Experiments were performed to uncover mechanistic information about the organocatalytic reaction. Subsequently, a palladium catalysed glycosylation protocol for the preparation of 2-deoxyglycosides was developed. After optimisation of the model reaction, the tolerance of the method for various glycosyl acceptors was assessed through a substrate screen. Generally, high product yields were obtained with excellent α selectivity. A probable mechanism is discussed. Continuous flow glycosylation reactions were then explored. Initially, a flow glycosylation protocol using a gold(I) catalyst was surveyed. Some promising results were discovered, however, the system proved inconsistent and ultimately unsuitable for the flow regime. Ionic liquid supported glycosylations in flow were then explored for the first time. After reaction optimisation, excellent yields of glycosylation product were obtained in just 15 seconds residence time, with no requirement for column chromatography. Application of the optimal reaction conditions to several other glycosyl donors and acceptors proved challenging due to unexpected protecting group reactivity leading to side products and irreproducibility of results. Nonetheless, mixtures of β-1,2-glucans were successfully prepared using this method, whilst a novel glycosyl donor featuring an orthogonal carbonate protecting group was identified as a key scaffold for the synthesis of β-1,6-glucans.
Supervisor: Galan, Carmen Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.801586  DOI: Not available
Share: