Progress Towards the Synthesis of Fluorescent Tröger’s bases With a Chiral Bridge

dc.contributor.authorGiebink, Anna K.Y.
dc.contributor.authorMartinez, Leah E.
dc.contributor.authorLewis, David E.
dc.date.accessioned2018-03-12T13:50:42Z
dc.date.available2018-03-12T13:50:42Z
dc.date.issued2018-03-12T13:50:42Z
dc.descriptionColor poster with text and formulas.en
dc.description.abstractJulius Tröger first synthesized Tröger’s base in 1887. The compound is obtained by the reaction between formalin and p-toluidine in the presence of concentrated hydrochloric acid. The synthesis of the first fluorescent Tröger’s bases based on the highly fluorescent 4-amino-1,8-naphthalimide fluorophore was reported in 2005. Tröger’s bases are ^-shaped chiral molecules that comprise two possible enantiomers. The molecules are C2 symmetric, and have well defined exo (convex) and endo (concave) surfaces. The cavity of the molecule provides an ideal location for the construction of the chiral host molecule.en
dc.description.sponsorshipPetroleum Research Fund administered by the American Chemical Society; University of Wisconsin--Eau Claire Office of Research and Sponsored Programsen
dc.identifier.urihttp://digital.library.wisc.edu/1793/78182
dc.language.isoen_USen
dc.relation.ispartofseriesUSGZE AS589;
dc.subjectTröger’s baseen
dc.subjectRing formation (Chemistry)en
dc.subjectPostersen
dc.titleProgress Towards the Synthesis of Fluorescent Tröger’s bases With a Chiral Bridgeen
dc.typePresentationen

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