Progress Toward Troger's Base Precursors.

dc.contributor.advisorLewis, David E.
dc.contributor.authorRaupach, Elizabeth A.
dc.date.accessioned2009-02-09T16:33:55Z
dc.date.available2009-02-09T16:33:55Z
dc.date.issued2009-02-09T16:33:55Z
dc.descriptionColor poster with text and diagrams describing research by Elizabeth A. Raupach, advised by David E. Lewis.en
dc.description.abstractOur goal was to synthesize C2-symmetric flourescent Troger's base derivitives bearing substituents in the bridged diazocine ring from 4-amino-1,8-naphthalimide dyes. Our attempts at direct synthesis have been unsuccessful. As a result, we focused our attention on synthesizing a precursor 4-amino-1,8-naphthalimide with a functional group at the 3- position that would allow the dimerization of dye molecules, providing the structural framework of a Troger's base.en
dc.description.sponsorshipUniversity of Wisconsin--Eau Claire Office of Research and Sponsored Programs; Petroleum Research Fund (American Chemical Society)en
dc.identifier.urihttp://digital.library.wisc.edu/1793/32193
dc.language.isoen_USen
dc.relation.ispartofseriesUSGZE AS589en
dc.subjectTroger's base--Derivativesen
dc.subjectHeterocyclic compounds--Synthesisen
dc.subjectRing formation (Chemistry)en
dc.subjectPostersen
dc.titleProgress Toward Troger's Base Precursors.en
dc.typePresentationen

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