<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Karioti, Anastasia</style></author><author><style face="normal" font="default" size="100%">Bilia, Anna Rita</style></author><author><style face="normal" font="default" size="100%">Gabbiani, Chiara</style></author><author><style face="normal" font="default" size="100%">Messori, Luigi</style></author><author><style face="normal" font="default" size="100%">Skaltsa, Helen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Proanthocyanidin glycosides from the leaves of Quercus ilex L. (Fagaceae)</style></title><secondary-title><style face="normal" font="default" size="100%">Tetrahedron Letters</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Circular dichroism</style></keyword><keyword><style  face="normal" font="default" size="100%">Fagaceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Oak-leaves</style></keyword><keyword><style  face="normal" font="default" size="100%">Proanthocyanidin glycosides</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</style></keyword><keyword><style  face="normal" font="default" size="100%">ROESY</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><publisher><style face="normal" font="default" size="100%">Elsevier Ltd</style></publisher><volume><style face="normal" font="default" size="100%">50</style></volume><pages><style face="normal" font="default" size="100%">1771-1776</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">From the polar extracts of the leaves of Quercus ilex L., two new proanthocyanidin glycosides, namely afzelechin-(4a?8)-catechin-3-O-b-glucopyranoside (1) and afzelechin-(4a?8)-catechin-3-O-a-rhamnopyranoside (2), were isolated in addition to catechin (3), proanthocyanidin B3 (4), prodelphinidin C (5), dehydrodicatechin A (6), quercetin (7) and six known ﬂavonol glucosides with their acylated derivatives (8–13) and ellagic acid (14). The structures of all isolated compounds were established by spectroscopic means, mainly 1D and 2D NMR, as well as LC/MS and HR-MS spectrometric analyses. The absolute con- ﬁguration of compound 1 was determined by CD measurements. The proanthocyanidin glycosides are especially interesting, as they possess the sugar in the upper unit of the dimer, which is rare for this type of compounds.</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Karioti, A.</style></author><author><style face="normal" font="default" size="100%">Bilia, A. R.</style></author><author><style face="normal" font="default" size="100%">Skaltsa, H.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A novel dimeric proanthocyanidin 3-O-glucoside from Quercus ilex L. (Fagaceae)</style></title><secondary-title><style face="normal" font="default" size="100%">PLANTA MEDICA</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Circular dichroism</style></keyword><keyword><style  face="normal" font="default" size="100%">Fagaceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Oak-leaves</style></keyword><keyword><style  face="normal" font="default" size="100%">Proanthocyanidin glycosides</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus ilex</style></keyword><keyword><style  face="normal" font="default" size="100%">ROESY</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2007///</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">73</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">ity at room temperature in order to deactivate any enzymes and avoid polymerizations and oxidations. Final extraction was carried out using MeOH and MeOH/H2O 8/2. A fast fractionation of the residue was done using VLC over silica gel followed by repeated cc over Sephadex LH-60 and Sephadex LH-20. Fractionations were monitored with HPLC-DAD-MS. The structures of the isolated compounds were established by means of 1D &amp; 2D NMR.</style></abstract><issue><style face="normal" font="default" size="100%">9</style></issue></record></records></xml>