Formation of an Unusually Stable Enol by Conjugate Addition of Active Methylene Compounds to E-3-aryl-2-cyanopropenoates

dc.contributor.advisor	Lewis, David E.
dc.contributor.author	Anderson, Luke P.
dc.date.accessioned	2015-02-19T17:24:42Z
dc.date.available	2015-02-19T17:24:42Z
dc.date.issued	2014-04
dc.description	Color poster with text, diagrams, and graphs.	en
dc.description.abstract	The purpose of this study was to research the chemical transformation of the Warfarin molecule. The reactions of 4-hydroxycoumarin with substituted a-cyanocinnimate esters gives addition products that are entirely in the form of the enol tautomer, as demonstrated by the appearance of the doubly benzylic proton as a singlet rather than as a doublet (half an AB quartet).	en
dc.description.sponsorship	WiSys Technology Foundation ; University of Wisconsin--Eau Claire Office of Research and Sponsored Programs	en
dc.identifier.uri	http://digital.library.wisc.edu/1793/70567
dc.language.iso	en_US	en
dc.relation.ispartofseries	USGZE AS589	en
dc.subject	Enol tautomer	en
dc.subject	4-hydroxycoumarin	en
dc.subject	Warfarin	en
dc.subject	Posters	en
dc.title	Formation of an Unusually Stable Enol by Conjugate Addition of Active Methylene Compounds to E-3-aryl-2-cyanopropenoates	en
dc.type	Presentation	en

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