Abstract
Separation of the water-soluble fraction of peanut skins led to the isolation of five proanthocyanidins. Based on the spectroscopic investigation and partial acid catalyzed degradation, their structures were determined to be epicatechin-(2beta-->O -->7, 4beta -->6)-[epicatechin-(4beta-->8)]-catechin (1), epicatechin-(2beta-->O -->7, 4beta-->8) epicatechin-(4beta-->8)-catechin-(4alpha-->8)-epicatechin (2), and procyanidins B2 (3), B3 (4) and B4 (5). The absolute configuration of the new compounds was determined from their circular dichroism curves and the (1)H NMR spectra of analysis of flavan-3-ols formed by thiolytic degradation of 1 and 2 in the presence of a chiral dirhodium complex (dirhodium tetra-(R)-(trifluoromethyl) phenyl acetate).
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antioxidants / pharmacology
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Arachis / chemistry*
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Biflavonoids / chemistry
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Catechin / chemistry
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Circular Dichroism
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Flavonoids / analysis
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Flavonoids / isolation & purification*
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Free Radical Scavengers / chemistry
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Free Radical Scavengers / isolation & purification*
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Free Radical Scavengers / pharmacology
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Magnetic Resonance Spectroscopy
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Phenols / isolation & purification*
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Polyphenols
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Proanthocyanidins / chemistry
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Proanthocyanidins / isolation & purification
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Rhodium / chemistry
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Sulfhydryl Reagents / pharmacology
Substances
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Antioxidants
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Biflavonoids
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Flavonoids
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Free Radical Scavengers
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Phenols
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Polyphenols
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Proanthocyanidins
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Sulfhydryl Reagents
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flavan-3-ol
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procyanidin
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Catechin
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Rhodium