Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.779986
Title: Novel methods for the synthesis and functionalisation of sulfoximines and sulfonimidamides : new pharmacophores for the medicinal chemist's toolbox
Author: Izzo, Flavia
ISNI:       0000 0004 7965 6773
Awarding Body: University of Nottingham
Current Institution: University of Nottingham
Date of Award: 2019
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Abstract:
Sulfoximines, the monoaza analogues of sulfones, have recently gained considerable recognition as a new and versatile structural motif in the life sciences. Therefore our group, in collaboration with Bayer AG (Berlin), is investigating a simple scalable and efficient methodology to make valuable chiral sulfoximines with control of stereochemistry. In the first chapter of this report we describe a novel synthetic route towards sulfoximine synthesis. Two types of key precursors are investigated: sulfoxides and phenylalanine templates. With these substrates in hand, we investigated their use in S(O)=N transfer chemistry to obtain enantioenrieched sulfoximines. Synthetic methodology for sulfoximine preparation has progressed significantly over the last decade. In contrast, sulfonimidamides, the monoaza-analogues of sulfonamides have been neglected in the life sciences so far, even though they seem to offer very interesting properties. It can be speculated that the use of sulfonimidamides in the life sciences has been hampered substantially by the lack of commercial availability and limited synthetic methods. In this context, we also investigated a facile synthesis of NH sulfonimidamides by NH transfer to tertiary sulfinamides. Racemic NH sulfonimidamides have been prepared in yields from good to excellent in a one-pot transformation. Given the limited availability of synthetic methods to produce enantioenrieched sulfonimidamides, we expanded our work towards the synthesis of tertiary enantiopure sulfinamides, which will be used as starting material for sulfonimidamide synthesis. Sulfonimidamides, like sulfoximines, offer an additional point for substitution, the =NH group. We have now developed new methods for the functionalisation of this NH group by arylation, alkylation, trifluoromethylation, cyanation, sulfonylation, alkoxycarbonylation, and aminocarbonylation. Finally, to gain further insight into the medicinal relevant properties of sulfonimidamides, a variety of structurally diverse sulfonimidamides were analysed in the same in vitro panel.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.779986  DOI: Not available
Keywords: QD415 Biochemistry
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