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Biosynthesis of Lythraceae Alkaloids

dc.contributor.advisorSpenser, Ian D.
dc.contributor.authorKoo, Swe Hoo
dc.contributor.departmentChemistryen_US
dc.date.accessioned2016-01-20T18:06:05Z
dc.date.available2016-01-20T18:06:05Z
dc.date.issued1970-07
dc.description.abstract<p> The biosynthesis of the alkaloids of Decodon verticillatus, (L.)Ell, a member of the Lythraceae family, was studied by tracer methods. These alkaloids contain a phenylquinolizidine system, whose biosynthetic origin has not previously been investigated.</p> <p> Labelled samples of lysine, △^1-piperideine and phenylalanine yielded radioactive decodine and decinine, the two major alkaloids of D. verticillatus. Systematic degradations of these labelled alkaloids show that lysine, △^1-piperideine and phenylalanine serve as specific precursors. Whereas lysine and △^1-piperideine entered the quinolizidine ring, the biphenyl ring system of these alkaloids was derived from two units of phenylalanine. In a further experiment, labelled pelletierine was administered to the plants. But this experiment yielded an inconclusive result.</p>en_US
dc.description.degreeDoctor of Philosophy (PhD)en_US
dc.description.degreetypeThesisen_US
dc.identifier.urihttp://hdl.handle.net/11375/18754
dc.language.isoen_USen_US
dc.subjectbiosynthesis, lythraceae, alkaloids, units, plantsen_US
dc.titleBiosynthesis of Lythraceae Alkaloidsen_US
dc.typeThesisen_US

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