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

dc.contributor.author	Fulton, Janet Barbara
dc.date.accessioned	2011-03-16T22:34:46Z
dc.date.accessioned	2022-10-25T05:55:23Z
dc.date.available	2011-03-16T22:34:46Z
dc.date.available	2022-10-25T05:55:23Z
dc.date.copyright	1970
dc.date.issued	1970
dc.identifier.uri	https://ir.wgtn.ac.nz/handle/123456789/23352
dc.description.abstract	Ethyl 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.format	pdf	en_NZ
dc.language	en_NZ
dc.language.iso	en_NZ
dc.publisher	Te Herenga Waka—Victoria University of Wellington	en_NZ
dc.title	The reaction of 1, 2-dibromocyclohexane with beta-keto esters, and syntheses in the norcarane series	en_NZ
dc.type	Text	en_NZ
vuwschema.type.vuw	Awarded Research Masters Thesis	en_NZ
thesis.degree.discipline	Chemistry	en_NZ
thesis.degree.grantor	Te Herenga Waka—Victoria University of Wellington	en_NZ
thesis.degree.level	Masters	en_NZ
thesis.degree.name	Master of Science	en_NZ

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