Approaches to pyranose carbohydrids /

Akula, Rakesh A.; Youngstown State University. College of Arts and Sciences.

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dc.contributor.author	Akula, Rakesh A.	en_US
dc.contributor.author	Youngstown State University. College of Arts and Sciences.	en_US
dc.date.accessioned	2011-01-31T14:20:04Z
dc.date.accessioned	2019-09-08T02:35:33Z
dc.date.available	2011-01-31T14:20:04Z
dc.date.available	2019-09-08T02:35:33Z
dc.date.created	2004	en_US
dc.date.issued	2004	en_US
dc.identifier.other	b19696000	en_US
dc.identifier.uri	http://jupiter.ysu.edu/record=b1969600	en_US
dc.identifier.uri	http://hdl.handle.net/1989/6308
dc.description	x, 127 leaves : ill. ; 29 cm.	en_US
dc.description	Thesis (M.S.)--Youngstown State University, 2004.	en_US
dc.description	Includes bibliographical references (leaves 61-64).	en_US
dc.description.abstract	The following work describes new pathways towards synthesis of sugar analogs that may act as glycomimetics for the sugars present in bacteria that make capsular polysaccharide. Two main approaches were investigated in the synthesis of N-glycosides. Staudinger and aza-Wittig reactions provided an approach towards synthesis of glucosyl imines. Another approach towards synthesis of N-glycosides involved Huisgen's 1,3-dipolar cycloaddition of azides with alkynes in the presence of Cu(l) as catalyst. These reactions were carried out in water as solvent to afford, regiospecifically, 1,4-disubsituted 1,2,3triazoles in high yields.	en_US
dc.description.statementofresponsibility	by Rakesh A. Akula.	en_US
dc.language.iso	en_US	en_US
dc.relation.ispartofseries	Master's Theses no. 0834	en_US
dc.subject.classification	Master's Theses no. 0834	en_US
dc.subject.lcsh	Glycosides--Synthesis.	en_US
dc.subject.lcsh	Polysaccharides.	en_US
dc.subject.lcsh	Azides.	en_US
dc.subject.lcsh	Triazoles.	en_US
dc.title	Approaches to pyranose carbohydrids /	en_US
dc.type	Thesis	en_US

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