Article ID Journal Published Year Pages File Type
5279878 Tetrahedron Letters 2009 6 Pages PDF
Abstract

From the polar extracts of the leaves of Quercus ilex L., two new proanthocyanidin glycosides, namely afzelechin-(4α→8)-catechin-3-O-β-glucopyranoside (1) and afzelechin-(4α→8)-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.

Graphical abstractFrom the polar extracts of the leaves of Quercus ilex L., two new proanthocyanidin glycosides were isolated, namely afzelechin-(4α→8)-catechin-3-O-β-glucopyranoside and afzelechin-(4α→8)-catechin-3-O-α-rhamnopyranoside. ROESY experiments played a pivotal role in the structure elucidation.Download full-size image

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Physical Sciences and Engineering Chemistry Organic Chemistry
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