9B Flavanols, Flavonols and Dihydroflavonols 469
Ta b l e 9 B. 1(continued)SourceReferenceDetection(–)-Epicatechin-(4-8)-(–)-epicatechin3-gallate-(4-8)-(+)- catechinSeedsRicardo da Silva et al.(1991c)HPLC, TLC, NMR, FAB-MS after enzymatic hydrolysis, acid hydrolysis,partial acid-catalysed degradation with phloroglucinol orphenylmethanethiolFlavonolsQuercetin, (R1=OH, R2=H) 3-glucosideSkinRib ́ereau-Gayon(1964)PC- Fluorescence, -UV spectroscopy, hydrolysisQuercetin 3-glucuronideSkinRib ́ereau-Gayon(1964)PC- Fluorescence, -UV spectroscopy, hydrolysisQuercetin 3-glucosylgalactosideSkinCheynier and Rigaud(1986)HPLC-UV spectrometry, -MS, -1 H NMR, -TLC after hydrolysisQuercetin 3-glucosylxylosideSkinCheynier and Rigaud(1986)HPLC-UV spectrometry, -MS, -1 H NMR, -TLC after hydrolysisQuercetin 3-rhamnosylglucosideSkinCantos et al. (2002)HPLC-DAD, -MS-MSQuercetin 3-rhamnosylglucosideLeavesHmamouchi et al.(1996)HPLC-UV spectrometry, -MS, -1 Hand13C NMR, -TLC after hydrolysisKampferol (R1=R2=H) 3-glucosideSkinRib ́ereau-Gayon(1964)PC- Fluorescence, -UV spectroscopy, hydrolysisKampferol 3-glucuronideSkinCheynier and Rigaud(1986)HPLC-UV spectrometry, -MS, -1 H NMR, -TLC after hydrolysisKampferol 3-galactosideSkinCheynier and Rigaud(1986)HPLC-UV spectrometry, -MS, -1 H NMR, -TLC after hydrolysisKampferol 3-glucosylarabinosideSkinCheynier and Rigaud(1986)HPLC-UV spectrometry, -MS, -1 H NMR, -TLC after hydrolysisMyricetin (R1=R2=OH) 3-glucosideSkinRib ́ereau-Gayon(1964)PC- Fluorescence, -UV spectroscopy, hydrolysisMyricetin 3-glucuronideSkinCheynier and Rigaud(1986)HPLC-UV spectrometry, -MS, -1 H NMR, -TLC after hydrolysis