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dc.contributor.advisorGlazener, Everett R.
dc.creatorFlannery, Richard Edward
dc.date.accessioned2020-01-08T17:44:38Z
dc.date.available2020-01-08T17:44:38Z
dc.date.created1971
dc.date.issued1971
dc.identifier.urihttps://hdl.handle.net/1969.1/DISSERTATIONS-171045
dc.description.abstractβ-Diketones such as acetyl- and benzoylacetone have previously been alkylated at their methyl group instead of at their more acidic methylene group by employing, as intermediates, their dicarbanions instead of their monocarbanions. The alkylating agents in the previous cases contained carbon, hydrogen, and halogen. The present study extends the usefulness of this reaction to include haloacetals and halodioxolanes. The reactions of the halodioxolanes with disodioacetylacetone were found to be dependent on the structure of the alkylating agent. 2- (Bromo- or chloromethyl) -2- methyl-1, 3-dioxolane (XXV, X = Br or Cl, n =1 ) ...en
dc.format.extent119 leavesen
dc.format.mediumelectronicen
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.rightsThis thesis was part of a retrospective digitization project authorized by the Texas A&M University Libraries. Copyright remains vested with the author(s). It is the user's responsibility to secure permission from the copyright holder(s) for re-use of the work beyond the provision of Fair Use.en
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subject.classification1971 Dissertation F585
dc.titleAlkylation of [beta]-Diketone dicarbanions with haloacetals and halodioxolanes to form [gamma]-derivativesen
dc.typeThesisen
thesis.degree.disciplineChemistryen
thesis.degree.grantorTexas A&M Universityen
thesis.degree.nameDoctor of Philosophyen
thesis.degree.levelDoctoralen
dc.contributor.committeeMemberBoone, James L.
dc.contributor.committeeMemberEarle, James H.
dc.contributor.committeeMemberHawkins, Leslie V.
dc.type.genredissertationsen
dc.type.materialtexten
dc.format.digitalOriginreformatted digitalen
dc.publisher.digitalTexas A&M University. Libraries


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