Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.778789
Title: Novel approaches toward the synthesis of pseudaminic acid
Author: Fields, Alexander Matthew
ISNI:       0000 0004 7964 5177
Awarding Body: University of Sheffield
Current Institution: University of Sheffield
Date of Award: 2019
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Abstract:
Pseudaminic acid is a carbohydrate glycoside which is found on post-translationally glycosylated bacterial flagella. Disturbance of the biosynthetic pathway for this sugar nullifies the pathogenicity of the bacteria A. caviae, H. pylori & C. jejuni. In order to explore this possibility, attempts were made to develop a novel synthetic route. Parallel to efforts to synthesis the side chain of pseudaminic acid, L-allo-threonine, N-chiral imines derived from cheap and readily available (2S)-ethyl lactate were prepared and subjected to Lewis acid-mediated trimethylsilylcyanide additions as part of new methodology for robust and facile asymmetric Strecker reactions. 2,3-anti¬-β-Hydroxy-α-aminonitriles were prepared in excellent yield (77%, 4 steps) and good diastereoselectivity (90 : 10). L-allo-threonine was accessed and further functionalised to Garner-like cyclic aldehydes which were used as substrates for a doubly diastereoselective nitroaldol reaction to construct the carbon chain of pseudaminic acid. These reactions proceeded with mild selectivity and conversion. Models for the addition to both Garner aldehydes and N-chiral imines were discussed in detail.
Supervisor: Jones, Simon Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.778789  DOI: Not available
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