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The action of diazomethane on some picrotoxin derivatives

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dc.contributor.author Johns, R.B
dc.date.accessioned 2011-03-10T22:59:07Z
dc.date.accessioned 2022-10-25T05:07:22Z
dc.date.available 2011-03-10T22:59:07Z
dc.date.available 2022-10-25T05:07:22Z
dc.date.copyright 1930
dc.date.issued 1930
dc.identifier.uri https://ir.wgtn.ac.nz/handle/123456789/23245
dc.description.abstract Picrotoxinin C15H16O6, a nitrogen-free, physiologically active body, together with the physiologically inactive Picrotin C15H18O7 form a "molecular" compound Picrotoxin which is easily decomposed into its constituents. Picrotoxin, which was first isolated by Boullay in 1812 from the fruit of the Anamirta Cocculus, has for many years been used as a fish poison and in the treatment of barbituric poisoning. The early workers concerned themselves with the production of the pure material and the establishing of empirical formulae. It was not until after 1863 that the actual chemistry of picrotoxin was more vigorously studied. The investigators fall mainly into five groups:- Barth 1863-84 Paterno 1877-91 Angelico 1907-23 Horrmann 1910-35 Robertson 1935-39. Besides their papers there are a large number of separate publications but although Picrotoxin and both its constituents have been so intensively investigated it is only this year, 1951, that any reasonably satisfactory formulation of the structure of picrotoxinin has been put forward. 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 Picrotoxin en_NZ
dc.subject Diazomethane en_NZ
dc.title The action of diazomethane on some picrotoxin derivatives 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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