7,7-dimethylnorcarone as a synthetic intermediate for chamic acid

dc.contributor.author	Heyworth, Rex Malcolm
dc.date.accessioned	2011-03-10T22:50:28Z
dc.date.accessioned	2022-10-25T04:24:05Z
dc.date.available	2011-03-10T22:50:28Z
dc.date.available	2022-10-25T04:24:05Z
dc.date.copyright	1961
dc.date.issued	1961
dc.identifier.uri	https://ir.wgtn.ac.nz/handle/123456789/23148
dc.description.abstract	The aim of this thesis is to show how the structure of the two naturally occurring substances, chamic acid, and chaminic acid can be verified synthetically by using an intermediate of the 7,7-dimethylbicyclo-[4,1,0] - heptan-2-one (7,7-dimethylnorcarone) type. The main object of the present work is to find a method for synthesising this intermediate. The route chosen consists of saturating the benzene ring of a suitably substituted derivative of benzoic acid with the view to eventually closing the ring giving rise to a bicyclic compound containing the cyclopropane and the cyclohexanone ring systems. The probable stereochemistry of chamic acid is also discussed.	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.subject	Chamic acid	en_NZ
dc.subject	Chaminic acid	en_NZ
dc.subject	Structure	en_NZ
dc.title	7,7-dimethylnorcarone as a synthetic intermediate for chamic acid	en_NZ
dc.type	Text	en_NZ
vuwschema.type.vuw	Awarded Research Masters Thesis	en_NZ
thesis.degree.grantor	Te Herenga Waka—Victoria University of Wellington	en_NZ
thesis.degree.level	Masters	en_NZ

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