Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640974
Title: Novel oxetane-containing spirocycles and peptidomimetics
Author: Powell, Nicola Helen
ISNI:       0000 0004 5349 7233
Awarding Body: University of Warwick
Current Institution: University of Warwick
Date of Award: 2014
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Abstract:
This thesis describes work focused on the use of oxetane rings as isosteres and incorporation of this functional group into pharmaceutically relevant scaffolds. Chapter 1 describes work directed towards the synthesis of 1,5-dioxaspiro[2.3]hexanes via three different strategies, namely ring-closure to form the oxetane ring, Corey epoxidation of the corresponding 3-oxetanones, and epoxidation of the corresponding 3-methylene oxetane. Nucleophilic ring-opening of substituted 1,5-dioxaspiro[2.3]hexanes to give amino acid type isosteres is also investigated. Chapter 2 details the synthesis of novel oxetane-containing peptidomimetics. A ‘one-pot’ conjugate addition process from commercially available 3-oxetanone to give nitro dipeptide precursors in good yields was developed. Various methods for the reduction of the nitro group were explored to optimise the synthesis of the corresponding amine. Amide coupling, followed by deprotection, gave peptidomimetics containing the oxetane at the C-terminus and mid-chain in good yields over the 3 steps, whilst an N-terminus oxetane peptidomimetic was obtained in 45% yield through hydrogenation of the conjugate addition product. X-ray diffraction studies, alongside molecular dynamics simulations, provided structural insights into these new oxetane-containing peptidomimetics. Detailed experimental procedures for the synthesis of all novel compounds are described in Chapter 3.
Supervisor: Not available Sponsor: University of Warwick ; AstraZeneca (Firm)
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.640974  DOI: Not available
Keywords: QD Chemistry
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