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Volumn 37, Issue 6, 2002, Pages 533-540
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Stereochemistry of the hydroperoxides formed during autoxidation of CLA methyl ester in the presence of α-tocopherol
a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
ESTERS;
HYDROGEN;
HYDROGEN PEROXIDE;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
OXIDATION;
AUTOXIDATION;
STEREOCHEMISTRY;
13 HYDROPEROXY 9,11 OCTADECADIENOIC ACID METHYL ESTER;
ALPHA TOCOPHEROL;
FREE RADICAL;
HYDROGEN;
HYDROPEROXIDE DERIVATIVE;
METHYL GROUP;
UNCLASSIFIED DRUG;
ESTER;
HYDROGEN PEROXIDE;
LINOLEIC ACID;
ARTICLE;
AUTOOXIDATION;
CARBON NUCLEAR MAGNETIC RESONANCE;
CHEMICAL BOND;
CONFORMATION;
CONJUGATION;
CORRELATION ANALYSIS;
GEOMETRY;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
ISOMER;
SPECTROSCOPY;
STEREOCHEMISTRY;
CHEMISTRY;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
OXIDATION REDUCTION REACTION;
STEREOISOMERISM;
ALPHA-TOCOPHEROL;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
ESTERS;
HYDROGEN PEROXIDE;
LINOLEIC ACID;
MAGNETIC RESONANCE SPECTROSCOPY;
OXIDATION-REDUCTION;
STEREOISOMERISM;
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EID: 0035986450
PISSN: 00244201
EISSN: None
Source Type: Journal
DOI: 10.1007/s11745-002-0929-8 Document Type: Article |
Times cited : (25)
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References (26)
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