| Literature DB >> 24594178 |
Haruna Kamiya1, Emiko Yanase2, Shin-Ichi Nakatsuka1.
Abstract
The radical oxidation mechanism of anthocyanin derivatives was investigated by the reaction of cyanidin 3-O-glucoside in the presence of radical initiator 2,2'-azobis-(2,4-dimethyl)valeronitrile (AMVN) in EtOH and aqueous CH3CN. Six different oxidation products were isolated, depending on the solvent employed. These products were identified using NMR spectroscopy and multistep derivatisation reactions. Of the products obtained, two novel oxidised anthocyanin derivatives were isolated from black rice under prolonged storage. A radical reaction mechanism is proposed on the basis of these reaction products. Quantification of oxidised anthocyanins in black rice is demonstrated as a method to verify freshness of the rice.Entities:
Keywords: 2,2′-Azobis-(2,4-dimethyl)valeronitrile (AMVN); Anthocyanin; Black rice; Cyanidin 3-O-glucoside; Radical oxidation
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Year: 2014 PMID: 24594178 DOI: 10.1016/j.foodchem.2014.01.077
Source DB: PubMed Journal: Food Chem ISSN: 0308-8146 Impact factor: 7.514