Please use this identifier to cite or link to this item: http://hdl.handle.net/10400.1/6155
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dc.contributor.authorTursch, B.-
dc.contributor.authorDaloze, D.-
dc.contributor.authorBraekman, J. C.-
dc.contributor.authorHootele, C.-
dc.contributor.authorCravador, A.-
dc.contributor.authorLosman, D.-
dc.contributor.authorKarlsson, R.-
dc.date.accessioned2015-06-15T09:15:55Z-
dc.date.available2015-06-15T09:15:55Z-
dc.date.issued1974-
dc.identifier.issn0040-4039-
dc.identifier.otherAUT: ACR00659;-
dc.identifier.urihttp://hdl.handle.net/10400.1/6155-
dc.description.abstractIn a previous communication (2) the isolation of two defensive alkaloid, hippodamine and convergine, from the American ladybug Hippodamia convergens was reported. A preliminary chemical study (2) led to the hypothesis that hippodamine could be represented by (1), with unknown stereochemistry at carbon atom 2. Convergine was supposed to be a 3a or 6a hydroxyhippodamine.pt_PT
dc.language.isoeng-
dc.publisherPergamon- Elsevier Science, Ltd-
dc.relation.isbasedonP-008-R6V-
dc.rightsrestrictedAccess-
dc.titleChemical ecology of arthropods. 9. Structure and absolute configuration of hippodamine and convergine, two novel alkaloids from american ladybug hippodamia convergens (coleoptera- coccinellidae)-
dc.typearticle-
degois.publication.firstPage409-
degois.publication.lastPage412-
degois.publication.titleTetrahedron Letters-
dc.peerreviewedyes-
Appears in Collections:FCT2-Artigos (em revistas ou actas indexadas)

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