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Nickel peroxide induced oxidation of canthaxanthin.
Lutz-Röder, A; Jezussek, M; Winterhalter, P.
Afiliación
  • Lutz-Röder A; Institut für Pharmazie und Lebensmittelchemie, Universität Erlangen-Nürnberg, Germany.
J Agric Food Chem ; 47(5): 1887-91, 1999 May.
Article en En | MEDLINE | ID: mdl-10552466
Treatment of canthaxanthin (beta,beta-carotene-4,4'-dione) (1) with nickel peroxide in dichloromethane yielded a series of cleavage products, i.e., 4-oxo-beta-ionone (2), (7E, 9E)-4-oxo-beta-apo-11-carotenal (3a), (7E, 9Z)-4-oxo-beta-apo-11-carotenal (3b), 4-oxo-beta-apo-13-carotenone (4), 4-oxo-beta-apo-14'-carotenal (5), 4-oxo-beta-apo-12'-carotenal (6), and 4-oxo-beta-apo-10'-carotenal (7). In addition, oxidized canthaxanthin derivatives, i.e., isomeric ketols all-trans-9, 10-dihydro-9-hydroxy-10-oxo-canthaxanthin (8a), (9'Z)-9, 10-dihydro-9-hydroxy-10-oxo-canthaxanthin (8b), and (13'Z)-9, 10-dihydro-9-hydroxy-10-oxo-canthaxanthin (8c) were obtained together with the tentatively identified (9'Z)-canthaxanthin-20-al (9). Structure elucidation of the reaction products was achieved by mass spectrometry and two-dimensional NMR spectroscopy.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cantaxantina / Níquel Idioma: En Revista: J Agric Food Chem Año: 1999 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cantaxantina / Níquel Idioma: En Revista: J Agric Food Chem Año: 1999 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos