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dc.contributor.authorSusag, Lyndia
dc.contributor.authorParvez, Masood
dc.contributor.authorMathenge, Simon G
dc.contributor.authorBenn, Michael H
dc.date.accessioned2014-04-02T07:38:38Z
dc.date.available2014-04-02T07:38:38Z
dc.date.issued2000-08
dc.identifier.citationPhytochemistry Volume 54, Issue 8, August 2000, Pages 933–935en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/pii/S0031942200001886
dc.identifier.urihttp://hdl.handle.net/11295/65730
dc.description.abstractX-ray crystallography of bisline, and the chemical interconversion of bisline and isoline (ruwenine), revealed that the structures previously assigned to these alkaloids required revision; as did that of isolinecic acid.en_US
dc.language.isoenen_US
dc.publisherUniversity of Nairobien_US
dc.subjectBisline; Isoline; Ruwenine; Ruzorine; Isolinecic acid; Pyrrolizidine alkaloids; Senecio ruwenzoriensis; Asteraceaeen_US
dc.titleStructure Revision Of Isoline (Ruwenine), Bisline And Isolinecic Aciden_US
dc.typeArticleen_US


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