Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.516286
Title: Cycloaddition routes to pyrazole and pyrazoline amino acids
Author: Seager, Laura Elizabeth
ISNI:       0000 0004 2689 2334
Awarding Body: Loughborough University
Current Institution: Loughborough University
Date of Award: 2009
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Abstract:
In recent years, the design and synthesis of structures that can potentially mimic the properties of the peptide bond have been of great interest to biological chemists. We are investigating the synthesis of novel pyrazoline-based structures as potential peptide mimetics. The pyrazoline unit is assembled by 1,3-dipolar cycloaddition of nitrile imines, which are generated in situ from hydrazonyl chlorides. We have investigated two routes to afford the hydrazonyl chloride, (1) via a hydrazone and (2) via a hydrazide, both of which have resulted in the successful synthesis of the desired pyrazolines. Subsequent syntheses have been carried out using a variety of different dipoles and dipolarophiles. We have taken approach (1) and used this to synthesize a pyrazole as one major enantiomer. This pyrazole has been subject to peptide couplings to form a complete peptide mimetic. NMR studies have been carried out on the synthesized peptide mimetic to determine the degree of hydrogen bonding and β-turn characteristics.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.516286  DOI: Not available
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