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 |
thesis.degree.name |
Master of Science |
en_NZ |