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The reaction of 1, 2-dibromocyclohexane with beta-keto esters, and syntheses in the norcarane series

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dc.contributor.authorFulton, Janet Barbara
dc.date.accessioned2011-03-16T22:34:46Z
dc.date.accessioned2022-10-25T05:55:23Z
dc.date.available2011-03-16T22:34:46Z
dc.date.available2022-10-25T05:55:23Z
dc.date.copyright1970
dc.date.issued1970
dc.description.abstractEthyl sodioacetoacetate and trans-1,2-dibromocyclohexane react in ethanol to give, in average yield, ethyl cyclohex-2-enyl-acetate, instead of the expected product, ethyl 2-(cyclohex-2-enyl)-acetoacetate, which may, however, be obtained in poor yield using a dipolar aprotic solvent. Similar results were obtained with ethyl 2-methylacetoacetate in place of ethyl acetoacetate, and a possible explanation of these findings is suggested.en_NZ
dc.formatpdfen_NZ
dc.identifier.urihttps://ir.wgtn.ac.nz/handle/123456789/23352
dc.languageen_NZ
dc.language.isoen_NZ
dc.publisherTe Herenga Waka—Victoria University of Wellingtonen_NZ
dc.rights.holderAll rights, except those explicitly waived, are held by the Authoren_NZ
dc.rights.licenseAuthor Retains Copyrighten_NZ
dc.rights.urihttps://www.wgtn.ac.nz/library/about-us/policies-and-strategies/copyright-for-the-researcharchive
dc.subjectChemistryen_NZ
dc.subjectEthyl sodioacetoacetateen_NZ
dc.titleThe reaction of 1, 2-dibromocyclohexane with beta-keto esters, and syntheses in the norcarane seriesen_NZ
dc.typeTexten_NZ
thesis.degree.disciplineChemistryen_NZ
thesis.degree.grantorTe Herenga Waka—Victoria University of Wellingtonen_NZ
thesis.degree.levelMastersen_NZ
thesis.degree.nameMaster of Scienceen_NZ
vuwschema.type.vuwAwarded Research Masters Thesisen_NZ

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