The Development of a Per-O-Benzylated 1-C-Aryl-glycal for the Synthesis of Kdo Glycosides

atmire.migration.oldid2680
dc.contributor.advisorLing, Chang-Chun
dc.contributor.authorMaillet, Robert
dc.date.accessioned2014-09-30T20:47:19Z
dc.date.available2014-11-17T08:00:51Z
dc.date.issued2014-09-30
dc.date.submitted2014en
dc.description.abstract3-Deoxy-D-manno-octulosonic acid (Kdo) is a key component of lipopolysaccharides (LPS) found in all gram-negative bacteria. The Kdo sugar exists almost exclusively in alpha-glycoside form and is essential for bacterial survival. Previously the Ling group has shown that a 1-C-aryl-3,4;6,7-diisopropylidenated heptose glycal can be a versatile donor for the synthesis beta-Kdo glycosides. The glycosylation was accomplished with high regio- and stero- selectivities by using N-iodosuccinimide (NIS). It was postulated that the reason for the observed beta-glycosylyation results arose from the presence of a fused isopropylidene ring on the top face of the glycal therefore directing via steric repulsion the formation of a the beta-Kdo glycoside. The goal of this thesis was to exchange the fused isopropylidene rings on the glycal with acyclic protecting groups so as to test if glycosylation results could be made to favor formation of a more stable and desired alpha-Kdo glycoside. Chapter 1 gives a brief introduction of bacterial polysaccharides, in particular, lipopolysaccharides (LPSs) produced by gram-negative bacteria and also Kdo monosaccharide. The biological functions and biosynthetic pathway of LPSs are also summarized. Chapter 2 provides detailed reviews on chemical methodologies reported in the literature for the synthesis of Kdo. Chapter 3 details the work of this thesis towards the development and synthesis of a per-O-benzylated 1-C-aryl-heptose glycal and its properties in glycosylations. The experimental procedures and spectroscopic data of all synthesized compounds are given in Chapter 4.en_US
dc.identifier.citationMaillet, R. (2014). The Development of a Per-O-Benzylated 1-C-Aryl-glycal for the Synthesis of Kdo Glycosides (Master's thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca. doi:10.11575/PRISM/28056en_US
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/28056
dc.identifier.urihttp://hdl.handle.net/11023/1875
dc.language.isoeng
dc.publisher.facultyGraduate Studies
dc.publisher.institutionUniversity of Calgaryen
dc.publisher.placeCalgaryen
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.
dc.subjectChemistry--Organic
dc.subject.classificationKdoen_US
dc.subject.classificationSynthesisen_US
dc.subject.classificationglycosylationen_US
dc.titleThe Development of a Per-O-Benzylated 1-C-Aryl-glycal for the Synthesis of Kdo Glycosides
dc.typemaster thesis
thesis.degree.disciplineChemistry
thesis.degree.grantorUniversity of Calgary
thesis.degree.nameMaster of Science (MSc)
ucalgary.item.requestcopytrue
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