Please use this identifier to cite or link to this item: http://hdl.handle.net/10884/502
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dc.contributor.authorFigueiredo, Paulo-
dc.contributor.authorGeorge, Florian-
dc.contributor.authorTatsuzawa, Fumi-
dc.contributor.authorToki, Kenjiro-
dc.contributor.authorSaito, Norio-
dc.contributor.authorBrouillard, Raymond-
dc.date.accessioned2012-03-06T16:02:29Z-
dc.date.available2012-03-06T16:02:29Z-
dc.date.issued1999-
dc.identifier.citationPhytochemistry 51 (1999) 125-132pt_PT
dc.identifier.urihttp://hdl.handle.net/10884/502-
dc.description.abstractThree series of structurally related anthocyanins\ extracted from the red purple ~owers of Dendrobium {Pramot|\ xLaeliocattleya cv[ Mini Purple\ Bletilla striata and Phalaenopsis all belonging to the Orchidaceae family and another series extracted from the pink ~owers of Senecio cruentus "Compositae# allowed the con_rmation of the existence of strong intramolecular copigmentation e}ects[ These interactions confer stability to the coloured forms of the molecules\ in a wide range of slightly acidic to neutral aqueous media[ Moreover\ the existence of structural relationships among the four series stressed the di}erent in~uences exerted by the diverse substituent groups[ The existence of a malonylglucoside attached to position 2 of all but three of the molecules put forward a new role for the malonyl residue\ in this particular position[pt_PT
dc.language.isoengpt_PT
dc.rightsopenAccessen
dc.subjectAnthocyaninspt_PT
dc.subjectOrchidspt_PT
dc.subjectIntramolecular copigmentationpt_PT
dc.titleNew features of intramolecular copigmentation by acylated anthocyaninspt_PT
dc.typearticlept_PT
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