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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/13063
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dc.contributor.advisorMacLean, David B.en_US
dc.contributor.authorAlam, M. A.en_US
dc.date.accessioned2014-06-18T17:02:14Z-
dc.date.available2014-06-18T17:02:14Z-
dc.date.created2013-07-05en_US
dc.date.issued1964-05en_US
dc.identifier.otheropendissertations/7894en_US
dc.identifier.other8969en_US
dc.identifier.other4289353en_US
dc.identifier.urihttp://hdl.handle.net/11375/13063-
dc.description.abstractPart I. The results of an investigation of the minor alkaloids of Lycopodium flabelliforme using elution chromatography and countercurrent distribution are presented. Several alkaloids not previously reported to occur in this species were isolated and identified. A new alkaloid, hydroxy-de-N-methyl-α-obscurine, has been isolated and a structure proposed for it on the basis of physical evidence. A sufficient quantity of Lycopodium alkaloid L.5 which we have named flabellidine was isolated to permit the elucidation of its structure. Part II. A synthesis of 9-xanthenemethylamine and its rearrangement to the ring-expanded alcohol under the condition of the Demjanov reaction is described.en_US
dc.subjectChemistryen_US
dc.titleStudies in Alkaloid Chemistry: Part I. Minor Alkaloids of Lycopodium flabelliforme; Part II. Model Studies leading to a synthesis of cularineen_US
dc.typethesisen_US
dc.contributor.departmentChemistryen_US
dc.description.degreeDoctor of Philosophy (PhD)en_US
Appears in Collections:Open Access Dissertations and Theses

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