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Conformational analysis of diglycosyl disulphides containing ßS(1-1)S interglycosidic linkages

Includes bibliographical references.

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Bibliographic Details
Main Author: Matthews, Richard P
Other Authors: Naidoo, Kevin J
Format: Thesis
Language:English
Published: Department of Chemistry 2014
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access_status_str Open Access
author Matthews, Richard P
author2 Naidoo, Kevin J
author_browse Matthews, Richard P
Naidoo, Kevin J
author_facet Naidoo, Kevin J
Matthews, Richard P
author_sort Matthews, Richard P
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/6329
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:51:03.328Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
publishDateSort 2014
publisher Department of Chemistry
publisherStr Department of Chemistry
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/6329 Conformational analysis of diglycosyl disulphides containing ßS(1-1)S interglycosidic linkages Matthews, Richard P Naidoo, Kevin J Chemistry Includes bibliographical references. The conformation around the glycosidic linkage has been shown to be the single most important factor in determining the molecular shape of oligosaccharides. This property is of fundamental importance in influencing biological activity such as binding to enzymes or receptors. Therefore, knowledge of the conformational preference associated with glycosidic linkages is required. In this thesis the conformational preferences of the βS( 1-.1 ')8 glycosidic linkage within asymmetrical dissacharide mimetics have been studied using computational methods. The sulphur-sulphur torsion angle parameters contained in the CHARMM22 force field were refined based on density functional theory (OFT) calculations of dimethyl disulphide, which is a representative fragment containing the sulphur-sulphur torsion angle. The refined parameters were then used in molecular dynamics (MD) simulations of three disaccharide mimetics in vacuum, water and dimethyl sulphoxide (OM80). The resulting conformational analysis reveals that in the case of disaccharides containing unsubstituted glycosyl rings, good agreement with experimental nuclear overhauser effects (NOEs) and spin-spin coupling constants is obtained. However, for disaccharides containing substituted glycosyl rings poorer agreement with experimental data is obtained, which may suggest that further refinement of the force field is required. In addition, a natural bond orbital analysis was conducted on the 1, I' - disulphanediyl diethanol fragment to investigate the origin of the conformational preference for the +g and -g conformers of the sulphur-sulphur torsion angle. This phenomenon is shown to be as a result of a two-electron stabilising [no – σ*c-s] delocalisation from the lone pair of the oxygen atoms to the carbon-sulphur antibonding orbitals. 2014-08-13T14:26:58Z 2014-08-13T14:26:58Z 2007 Master Thesis Masters MSc http://hdl.handle.net/11427/6329 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Chemistry
Matthews, Richard P
Conformational analysis of diglycosyl disulphides containing ßS(1-1)S interglycosidic linkages
thesis_degree_str Master's
title Conformational analysis of diglycosyl disulphides containing ßS(1-1)S interglycosidic linkages
title_full Conformational analysis of diglycosyl disulphides containing ßS(1-1)S interglycosidic linkages
title_fullStr Conformational analysis of diglycosyl disulphides containing ßS(1-1)S interglycosidic linkages
title_full_unstemmed Conformational analysis of diglycosyl disulphides containing ßS(1-1)S interglycosidic linkages
title_short Conformational analysis of diglycosyl disulphides containing ßS(1-1)S interglycosidic linkages
title_sort conformational analysis of diglycosyl disulphides containing sss 1 1 s interglycosidic linkages
topic Chemistry
url http://hdl.handle.net/11427/6329
work_keys_str_mv AT matthewsrichardp conformationalanalysisofdiglycosyldisulphidescontainingßs11sinterglycosidiclinkages