Abstract
This work reports isolation of an unusual lignan with a bicyclic [2.2.2] octene skeleton, named rufescenolide (1), from stems of Cordia rufescens, along with β-sitosterol, stigmasterol, syringaldehyde, 3-β-O-D-glucopyranosyl-sitosterol, methyl caffeate, 4-methoxy-protocatechuic acid and methyl rosmarinate. Structural characterizations employed IR spectroscopic, ESIHRMS and mono and dimensional NMR spectroscopy.
Copyright © 2011 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Bridged Bicyclo Compounds / chemistry
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Bridged Bicyclo Compounds / isolation & purification*
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Caffeic Acids / chemistry*
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Cordia / chemistry*
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Hydroxybenzoates / chemistry
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Lignans / chemistry*
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Lignans / isolation & purification
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Magnetic Resonance Spectroscopy
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Molecular Structure
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Octanes / chemistry*
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Octanes / isolation & purification
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Plant Stems / chemistry
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Sitosterols / chemistry
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Sitosterols / isolation & purification
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Stigmasterol / chemistry
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Stigmasterol / isolation & purification
Substances
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Bridged Bicyclo Compounds
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Caffeic Acids
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Hydroxybenzoates
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Lignans
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Octanes
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Sitosterols
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rufescenolide
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protocatechuic acid
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gamma-sitosterol
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Stigmasterol