Decomposition of Novel Diazosugars: Effects on Regioselectivity

Malich, Ashley

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dc.contributor.author	Malich, Ashley	en_US
dc.date.accessioned	2013-12-16T18:53:02Z
dc.date.accessioned	2019-09-08T02:36:30Z
dc.date.available	2013-12-16T18:53:02Z
dc.date.available	2019-09-08T02:36:30Z
dc.date.issued	2008
dc.identifier	277052295	en_US
dc.identifier.other	b20382558	en_US
dc.identifier.uri	http://hdl.handle.net/1989/10789
dc.description	x, 162 leaves : ill. ; 29 cm.	en_US
dc.description.abstract	The following work describes the construction and decomposition of azidodeoxy sugars with diazoesters attached. The fate of the projected carbenoid intermediate formed in the presence of a rhodium(II) catalyst resulted in the products of inter- and intramolecular imine formation however, no C-H insertion onto the furanose platform was observed. This research also led to the formation of ketone derivatives and dimeric ethers.	en_US
dc.description.statementofresponsibility	by Ashley Marie Malich.	en_US
dc.language.iso	en_US	en_US
dc.relation.ispartofseries	Master's Theses no. 1122	en_US
dc.subject.lcsh	Sugars.	en_US
dc.subject.lcsh	Decomposition (Chemistry)--Chemistry, Organic.	en_US
dc.subject.lcsh	Carbohydrates.	en_US
dc.title	Decomposition of Novel Diazosugars: Effects on Regioselectivity	en_US
dc.type	Thesis	en_US

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