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Studies towards a scalable synthesis of N-acetyl-L-fucosamine

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dc.contributor.author Conway, Ryan P.
dc.contributor.other Youngstown State University. Department of Chemistry.
dc.date.accessioned 2021-10-14T17:36:26Z
dc.date.available 2021-10-14T17:36:26Z
dc.date.issued 2007
dc.identifier.other B20213979
dc.identifier.other 190693639
dc.identifier.uri https://jupiter.ysu.edu:443/record=b2021397
dc.identifier.uri http://hdl.handle.net/1989/16626
dc.description xii, 241 leaves : ill. ; 29 cm. Thesis (M.S.)--Youngstown State University, 2007. Includes bibliographical references (leaves 78-80). en_US
dc.description.abstract The following describes two attempted syntheses of the rare sugar N-acetyl-L-fucosamine (L-FucNAc) from the inexpensive and readily available L-rhamnose. The syntheses will each involve a protection, oxidation, and reduction strategy in the inversion of the stereochemistry about two sterocenters in L-rhamnose, as well as the introduction of nitrogen at the C-2 position. N-Acetyl-L-fucosamine is one of three carboydrate components of the capsular polysaccharide (CP) of Staphylococcus aureus, which protects the bacterium from the body's immune response. The termination of the CP may provide alternative therapies against S. aureus and possibly other pathogens. en_US
dc.description.sponsorship Youngstown State University. Department of Chemistry. en_US
dc.language.iso en_US en_US
dc.relation.ispartofseries Master's Theses;no. 0963
dc.subject Staphylococcus aureus infections -- Prevention. en_US
dc.subject Sugars. en_US
dc.subject Carbohydrates -- Synthesis. en_US
dc.title Studies towards a scalable synthesis of N-acetyl-L-fucosamine en_US
dc.type Thesis en_US


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