Please use this identifier to cite or link to this item: http://ithesis-ir.su.ac.th/dspace/handle/123456789/4160
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dc.contributorSineenart ATTANONCHAIen
dc.contributorสินีนาฏ อรรถนนท์ชัยth
dc.contributor.advisorPunlop Kuntiyongen
dc.contributor.advisorพัลลภ คันธิยงค์th
dc.contributor.otherSilpakorn University. Scienceen
dc.date.accessioned2022-12-13T04:32:21Z-
dc.date.available2022-12-13T04:32:21Z-
dc.date.issued25/11/2022
dc.identifier.urihttp://ithesis-ir.su.ac.th/dspace/handle/123456789/4160-
dc.descriptionMaster of Science (M.Sc.)en
dc.descriptionวิทยาศาสตรมหาบัณฑิต (วท.ม)th
dc.description.abstractIndolizidine alkaloids are chemical constituents which can isolated from a variety of terrestrial and marine plants and animals.Indolizidine alkaloids possess 1-azabicyclo [4.3.0] nonane system as the core structure.This alkaloids have been used for a wide range of pharmacology with a various biological activities. It was isolated from plant in families Asclepiadaceae, Convolvulaceae (morning glory), Orchidaceae (orchid), Fabaceae (or Leguminosae) and Pandanaceae. In this research, we will discuss synthetic studies of two members of non-aromatic indolizidine containing alkaloids which are tashiromine, a 5-hydroxymethylindolizidine alkaloid and indolizidine 167B via N-acyliminium ion cyclization as a key step.en
dc.description.abstract-th
dc.language.isoen
dc.publisherSilpakorn University
dc.rightsSilpakorn University
dc.subjectTashiromineen
dc.subjectIndolizidine 167Ben
dc.subjectN-acyliminium ion cyclizationen
dc.subject.classificationChemistryen
dc.titleSynthesis of non-aromatics indolizidine alkaloidsen
dc.titleการสังเคราะห์นอนอะโรมาติก อินโดลิซิดีน อัลคาลอยด์th
dc.typeThesisen
dc.typeวิทยานิพนธ์th
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