Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/99263
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dc.creatorFrederico Nave
dc.creatorNatercia Teixeira
dc.creatorNuno Mateus
dc.creatorVictor de Freitas
dc.date.accessioned2023-05-23T23:09:17Z-
dc.date.available2023-05-23T23:09:17Z-
dc.date.issued2010
dc.identifier.issn0308-8146
dc.identifier.othersigarra:49114
dc.identifier.urihttps://hdl.handle.net/10216/99263-
dc.description.abstractMethylmethine bridged flavanol-anthocyanin dimeric adducts (F-A) were synthesised by hemisynthesis using catechin, acetaldehyde and F-A adducts as precursors in order to simulate putative reactions undergoing in red wine. The products obtained, catechin-methylmethine-catechin-malvidin-3-O-glucose and methylmethine-(catechin-malvidin-3-O-glucose), were analysed by HPLC-ESI-MS. The fragmentation patterns allowed the confirmation of the structures. These compounds were investigated and found in wine samples (2-year-old table wine and 10-year-old Port wine), thus confirming their formation in vino as a result of flavanol-anthocyanin adducts transformations.
dc.language.isoeng
dc.rightsrestrictedAccess
dc.subjectOutras ciências agrárias
dc.subjectOther Agrarian Sciences
dc.titleThe fate of flavanol-anthocyanin adducts in wines: Study of their putative reaction patterns in the presence of acetaldehyde
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoFaculdade de Ciências
dc.identifier.doi10.1016/j.foodchem.2010.01.060
dc.identifier.authenticusP-003-3ZN
dc.subject.fosCiências agrárias::Outras ciências agrárias
dc.subject.fosAgrarian Sciences::Other Agrarian Sciences
Appears in Collections:FCUP - Artigo em Revista Científica Internacional

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