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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/24454
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DC FieldValueLanguage
dc.contributor.advisorMacLean, D.-
dc.contributor.authorPerry, George-
dc.date.accessioned2019-05-27T16:20:57Z-
dc.date.available2019-05-27T16:20:57Z-
dc.date.issued1956-04-
dc.identifier.urihttp://hdl.handle.net/11375/24454-
dc.description.abstractPart (i) -The Minor Alkaloids: Annotoxine, C32H44O5N2, has now been isolated from a Canadian source. It has been separated into the alkaloids acrifoline, C16H23O2N, and annotine (alkaloid L 11), C16H21O3N. Both alkaloids have been shown to possess one hydroxyl group, one carbonyl group and one centre of unsaturation. The lack of reactivity of the third oxygen function of annotine suggests that it is present in an ether linkage. The identity of O-acetylacrifoline with alkaloid L 12 has also been proved. Part (ii) -Diphenylannotinine: Diphenylannotinine has been shown to be C28H33O3N. It possesses two hydroxyl groups, the third oxygen is present in an ether linkage. The exact nature of the ether linkage could not be ascertained on the basis of the experimental evidence.en_US
dc.language.isoenen_US
dc.subjectalkaloidsen_US
dc.subjectLycopodium annotinum L.en_US
dc.subjectdiphenylannotinineen_US
dc.subjectalkaloids of Lycopodium annotinum L.en_US
dc.subjectminor alkaloidsen_US
dc.titleThe Alkaloids of Lycopodium Annotinum L.: A Study of Diphenylannotinine and Two of the Minor Alkaloidsen_US
dc.title.alternativeThe Alkaloids of Lycopodium Annotinum L.en_US
dc.typeThesisen_US
dc.contributor.departmentChemistryen_US
dc.description.degreetypeThesisen_US
dc.description.degreeMaster of Science (MSc)en_US
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