Oxidative decarboxylation of some bicyclo[4,1,0] heptene carboxylic acids

dc.contributor.author	Galloway, Neil
dc.date.accessioned	2011-03-16T22:31:46Z
dc.date.accessioned	2022-10-25T05:40:39Z
dc.date.available	2011-03-16T22:31:46Z
dc.date.available	2022-10-25T05:40:39Z
dc.date.copyright	1979
dc.date.issued	1979
dc.identifier.uri	https://ir.wgtn.ac.nz/handle/123456789/23319
dc.description.abstract	The behaviour of a series of bicyclo[4,1,0]hept-3-ene-1,6-dicarboxylic acids with lead tetraacetate has been examined. Only monodecarboxylation was observed leading to isobenzofuranones. This has been rationalised by invoking carboxylate-assisted opening of the three-membered ring. Preliminary studies of a series of bicyclo[4,l,0]hept-3-ene-1-monocarboxylic acids have been carried out. Ring-cleaved products are again observed and benzyl acetates have been characterised.	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	Oxidative decarboxylation of some bicyclo[4,1,0] heptene carboxylic acids	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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