Syntheses of 2,3-dihydroxycyclohexylacetic acid γ-lactones

dc.contributor.author	Browne, Alan Robert
dc.date.accessioned	2011-03-16T23:42:39Z
dc.date.accessioned	2022-10-25T06:31:12Z
dc.date.available	2011-03-16T23:42:39Z
dc.date.available	2022-10-25T06:31:12Z
dc.date.copyright	1972
dc.date.issued	1972
dc.identifier.uri	https://ir.wgtn.ac.nz/handle/123456789/23432
dc.description.abstract	Oxidation of cyclohex-2-enylacetic acid with performic acid gives 2-cis-3-trans dihydroxycyclohexylacetic acid γ-lactone. Oxidation with neutral aqueous permanganate solution gives two diols, 2-cis-3-cis-dihydroxycyclohexylacetic acid and 2-trans-3-trans-dihydroxycyclohexylacetic acid, both of which can be lactonised to the correspondingγ-lactones.	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	Syntheses of 2,3-dihydroxycyclohexylacetic acid γ-lactones	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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