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dc.contributor.advisorTucker, John A.
dc.contributor.authorFlintoft, Rebecca J.
dc.date.accessioned2008-07-08T20:43:03Z
dc.date.available2008-07-08T20:43:03Z
dc.date.issued1997
dc.identifier.urihttp://hdl.handle.net/10920/5585
dc.description.abstractThe successful Michael addition ofnitroethylene to various lithium ester and ketone enolates is reported. Higher and more easily purified yields are reported for the adducts of ester enolates than for the adducts of ketone enolates. In addition, a-monosubstituted ester and ketone enolates were found to react in higher yield with nitroethylene than did their a-disubstituted counterparts. The significance of these reactions is reinforced by the common misconception that nitroethylene is too unstable to produce high yields in nucleophilic addition reactions. Furthermore, these reactions support the assertion that nitroethylene may have synthetic utility as a "+CH2CH2NH2" synthon.en
dc.description.sponsorshipPharmacia and Upjohn, Inc. Medicinal Chemistry Research (Kalamazoo, MI)
dc.language.isoen_USen
dc.relation.ispartofseriesSenior Individualized Projects. Chemistry.en
dc.rightsU.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder.
dc.subject.lcshAlkylation
dc.subject.lcshKetones
dc.titleAlkylation of Ketone and Ester Enolates by Nitroethyleneen
dc.typeThesisen


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  • Chemistry Senior Individualized Projects [860]
    This collection includes Senior Individualized Projects (SIP's) completed in the Chemistry Department. Abstracts are generally available to the public, but PDF files are available only to current Kalamazoo College students, faculty, and staff.

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