9B Flavanols, Flavonols and Dihydroflavonols 469
Ta b l e 9 B. 1
(continued)
Source
Reference
Detection
(–)-Epicatechin-(4
-8)-(–)-epicatechin
3-gallate-(4
-8)-(+)- catechin
Seeds
Ricardo da Silva et al.
(1991c)
HPLC, TLC, NMR, FAB-MS after enzymatic hydrolysis, acid hydrolysis,
partial acid-catalysed degradation with phloroglucinol orphenylmethanethiol
FlavonolsQuercetin, (R1=OH, R2=H) 3-glucoside
Skin
Rib ́
ereau-Gayon(1964)
PC- Fluorescence, -UV spectroscopy, hydrolysis
Quercetin 3-glucuronide
Skin
Rib ́
ereau-Gayon(1964)
PC- Fluorescence, -UV spectroscopy, hydrolysis
Quercetin 3-glucosylgalactoside
Skin
Cheynier and Rigaud
(1986)
HPLC-UV spectrometry, -MS, -
1 H NMR, -TLC after hydrolysis
Quercetin 3-glucosylxyloside
Skin
Cheynier and Rigaud
(1986)
HPLC-UV spectrometry, -MS, -
1 H NMR, -TLC after hydrolysis
Quercetin 3-rhamnosylglucoside
Skin
Cantos et al. (2002)
HPLC-DAD, -MS-MS
Quercetin 3-rhamnosylglucoside
Leaves
Hmamouchi et al.
(1996)
HPLC-UV spectrometry, -MS, -
1 Hand
13
C NMR, -TLC after hydrolysis
Kampferol (R1=R2=H) 3-glucoside
Skin
Rib ́
ereau-Gayon(1964)
PC- Fluorescence, -UV spectroscopy, hydrolysis
Kampferol 3-glucuronide
Skin
Cheynier and Rigaud
(1986)
HPLC-UV spectrometry, -MS, -
1 H NMR, -TLC after hydrolysis
Kampferol 3-galactoside
Skin
Cheynier and Rigaud
(1986)
HPLC-UV spectrometry, -MS, -
1 H NMR, -TLC after hydrolysis
Kampferol 3-glucosylarabinoside
Skin
Cheynier and Rigaud
(1986)
HPLC-UV spectrometry, -MS, -
1 H NMR, -TLC after hydrolysis
Myricetin (R1=R2=OH) 3-glucoside
Skin
Rib ́
ereau-Gayon(1964)
PC- Fluorescence, -UV spectroscopy, hydrolysis
Myricetin 3-glucuronide
Skin
Cheynier and Rigaud
(1986)
HPLC-UV spectrometry, -MS, -
1 H NMR, -TLC after hydrolysis