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Synthesis of N-Glycosides using Azidodeoxysugars

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dc.contributor.author Vicarel, Monica L. en_US
dc.date.accessioned 2011-01-31T14:19:26Z
dc.date.accessioned 2019-09-08T02:35:37Z
dc.date.available 2011-01-31T14:19:26Z
dc.date.available 2019-09-08T02:35:37Z
dc.date.created 2006 en_US
dc.date.issued 2006 en_US
dc.identifier.other b19971278 en_US
dc.identifier.uri http://jupiter.ysu.edu/record=b1997127 en_US
dc.identifier.uri http://hdl.handle.net/1989/6277
dc.description X, 151 leaves ; ill. ; 29 cm. en_US
dc.description.abstract The following work includes methods of synthesizing N-glycosides. The main focus is the use of azides synthesized from D-glucose and D-galactose as the precursors for the synthesis of a library of analogs that have an N-glycoside linkage that could potentially be tested for biological activity towards Staphylococcus aureus Type 5 and Type 8 capsular polysaccharides. The chemistry includes a modified Staudinger approach to be used for the synthesis of amides. Also a novel approach for the construction of 1, 2, 3-triazole-linked sugars has been studied. An investigation into one-pot conversion of non-sugar alcohols to the corresponding azides has been carried out as well as the development of chemistry mentioned above using microwave irradiation. Stereoselectivity and regiospecificity in the amide and triazole chemistry will be discussed in detail. en_US
dc.description.sponsorship Youngstown State UNiversity. Department of Chemistry en_US
dc.description.statementofresponsibility by Monica L. Vicarel en_US
dc.language.iso en_US en_US
dc.relation.ispartofseries Master's Theses no. 0927 en_US
dc.subject.classification Master's Theses no. 0927 en_US
dc.subject.lcsh Glycosides. en_US
dc.subject.lcsh Chemistry, Organic. en_US
dc.subject.lcsh Staphylococcus aureus. en_US
dc.subject.lcsh Staphylococcus aureus infections--Prevention. en_US
dc.title Synthesis of N-Glycosides using Azidodeoxysugars en_US
dc.type Thesis en_US


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