کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5279878 | 1385635 | 2009 | 6 صفحه PDF | دانلود رایگان |

From the polar extracts of the leaves of Quercus ilex L., two new proanthocyanidin glycosides, namely afzelechin-(4αâ8)-catechin-3-O-β-glucopyranoside (1) and afzelechin-(4αâ8)-catechin-3-O-α-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 configuration 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.
From the polar extracts of the leaves of Quercus ilex L., two new proanthocyanidin glycosides were isolated, namely afzelechin-(4αâ8)-catechin-3-O-β-glucopyranoside and afzelechin-(4αâ8)-catechin-3-O-α-rhamnopyranoside. ROESY experiments played a pivotal role in the structure elucidation.
Journal: Tetrahedron Letters - Volume 50, Issue 16, 22 April 2009, Pages 1771-1776