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dc.contributor.advisorVan Stipdonk, Michael J.en_US
dc.contributor.authorKerstetter, Dale R.en_US
dc.date.accessioned2010-09-01T15:12:21Z
dc.date.available2010-09-01T15:12:21Z
dc.date.issued2009-12en_US
dc.identifier.othert09066en_US
dc.identifier.urihttp://hdl.handle.net/10057/2541
dc.descriptionThesis (M.S.)--Wichita State University, College of Liberal Arts and Sciences, Dept. of Chemistryen_US
dc.description.abstractThe research presented here details two studies that utilized theoretical analysis and experimentation to further the understading of peptide fragmentation. The first study was the McLafferty rearrangement, which involves transfer of a У-position hydrogen atom to a carbonyl oxygen atom through a cyclic intermediate, followed by the elimination of an alkene. The second study examined substituent effects on benzene ring terminated peptides.en_US
dc.format.extentxiii, 38 p.en_US
dc.format.extent1022044 bytes
dc.format.mimetypeapplication/pdf
dc.language.isoen_USen_US
dc.publisherWichita State Universityen_US
dc.titleMcLafferty rearrangement of peptides and substituent effects on peptide fragmentation: Theoretical and experimental investigationen_US
dc.typeThesisen_US


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