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Alkaline degradations of picrotoxinin derivatives

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dc.contributor.author Coombe, Reginaid George
dc.date.accessioned 2010-11-17T19:32:47Z
dc.date.accessioned 2022-10-10T20:23:32Z
dc.date.available 2010-11-17T19:32:47Z
dc.date.available 2022-10-10T20:23:32Z
dc.date.copyright 1957
dc.date.issued 1957
dc.identifier.uri https://ir.wgtn.ac.nz/handle/123456789/21583
dc.description.abstract These and similar remarks were made during the first flush of enthusiasm heralding the new quantum applications to chemistry. That these hopes were ill founded soon became apparent with the realisation that in real molecules insuperable mathematical difficulties are involved in obtaining a rigorous solution which is a prerequisite in calculating the required information. So the familiar pattern continued, basing conclusions on experimental observations and modification of theory accordingly. Although Robinson Nature, 1947, 160, 815 has described morphine as the star performer of the team of molecular acrobats, it is felt that the picrotoxin series has strong claims to make on this score. The apparently straightforward substance, picrotoxin, early shown to be an equimolecular compound Sielisch Annalen, 1912, 391, 1, Bakunin and Giordani, Rend. Accad. Sci. Fis. Mat. Napoli, 1924 (iii) 30, 166 of picrotin and picrotoxinin, has proved a very puzzling structural problem, and although known for almost a century and a half, and despite the efforts of many competent workers in the field, it is only now that the solution is finally being obtained. 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 Alkaline degradations of picrotoxinin 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
thesis.degree.name Master of Science en_NZ


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