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Chemical synthesis of terpenoid 0-glycosides /

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dc.contributor.author Risley, Hud L. en_US
dc.contributor.author Youngstown State University. Dept. of Chemistry. en_US
dc.date.accessioned 2011-01-31T14:18:09Z
dc.date.accessioned 2019-09-08T02:29:46Z
dc.date.available 2011-01-31T14:18:09Z
dc.date.available 2019-09-08T02:29:46Z
dc.date.created 2001 en_US
dc.date.issued 2001 en_US
dc.identifier 49554687 en_US
dc.identifier.other b18924372 en_US
dc.identifier.uri http://jupiter.ysu.edu/record=b1892437 en_US
dc.identifier.uri http://hdl.handle.net/1989/6195
dc.description viii, 93 leaves : ill. ; 29 cm. en_US
dc.description Thesis (M.S.)--Youngstown State University, 2001. en_US
dc.description Includes bibliographical references (leaves 46-47). en_US
dc.description.abstract The following work describes new synthetic routes toward terpenoid-Oglycosides. Two different approaches have been studied to add terpene functionality to the anomeric position of a D-Glucose. Firstly, a variety of glycosyl halides were investigated as intermediates to produce the C-O bond at the anomeric position. The second approach incorporated the classic Fischer glycosylation with protected and unprotected sugars reacting with terpene alcohols. en_US
dc.description.statementofresponsibility by Hud L. Risley. en_US
dc.language.iso en_US en_US
dc.relation.ispartofseries Master's Theses no. 0739 en_US
dc.subject.classification Master's Theses no. 0739 en_US
dc.subject.lcsh Glycosides. en_US
dc.subject.lcsh Terpenes. en_US
dc.title Chemical synthesis of terpenoid 0-glycosides / en_US
dc.type Thesis en_US


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