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dc.contributor.advisorTakemura, K.H.en_US
dc.contributor.authorDi Mari, Samuel J.en_US
dc.date.accessioned2017-01-20T22:02:00Z
dc.date.available2017-01-20T22:02:00Z
dc.date.issued1962en_US
dc.identifier.urihttp://hdl.handle.net/10504/109028
dc.description.abstractFor many years, acrylonitrile has afforded the organic chemist a convenient method of introducing a three-carbon residue onto a variety of organic compounds by the so-called cyano-ethylation reaction. This reaction is generally brought about by a base-catalyzed, nucleophilic addition. The purpose of this work is to investigate and to evaluate the applicability of the readily-available diethyl 2,4-dicyanoglutaconate in a similar type of reaction. Such a reaction, if feasible, would permit the introduction of a seven-carbon residue which possesses reactive terminal functional groups. This would be of great value in synthetic organic chemistry.en_US
dc.language.isoen_USen_US
dc.publisherCreighton Universityen_US
dc.rightsA non-exclusive distribution right is granted to Creighton University and to ProQuest following the publishing model selected above.en_US
dc.titleAddition Reactions or Diethyl 2,4-dicyanoglutaconateen_US
dc.typeThesis
dc.publisher.locationOmaha, Nebraskaen_US
dc.description.noteProQuest Traditional Publishing Optionen_US
dc.contributor.cuauthorDi Mari, Samuel J.en_US
dc.degree.levelMS (Master of Science)en_US
dc.degree.disciplineChemistry (graduate program)en_US
dc.degree.nameM.S. in Chemistryen_US
dc.degree.grantorGraduate Schoolen_US


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