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CIRCULAR DICHROISM OF LIPOXYGENASE-1 FROM SOYBEANSSPAAPEN LJM; VELDINK GA; LIEFKENS TJ et al.1979; BIOCHIM. BIOPHYS. ACTA; NLD; DA. 1979; VOL. 574; NO 2; PP. 301-311; BIBL. 20 REF.Article

A quantitative optical and EPR study on the interaction between soybean lipoxygenase-1 and 13-L-hydroperoxylinoleic acidSLAPPENDEL, S; VELDINK, G. A; VLIEGENTHART, J. F. G et al.Biochimica et biophysica acta. 1983, Vol 747, Num 1-2, pp 32-36, issn 0006-3002Article

Formation of acyclic α- and γ-ketols and 12-oxophytodienoic acid from linolenic acid 13-hydroperoxide by a flax enzyme preparation. Evidence for a single enzyme leading to a common allene epoxide intermediateCROMBIE, L; MORGAN, D. O.Journal of the Chemical Society. Chemical communications. 1988, Num 8, pp 558-560, issn 0022-4936Article

SHORT-LIVED RADICALS PRODUCED IN THE COURSE OF THE REACTIONS OF 13-L-HYDROPEROXYLINOLEIC ACID WITH FERROUS IONS DETECTED BY SPIN TRAPPING AND CONTINUOUS FLOW ESR SPECTROSCOPYAOSHIMA H; TANIGUCHI H.1983; ANALYTICAL LETTERS; ISSN 0003-2719; USA; DA. 1983; VOL. 16; NO 4; PP. 301-308; BIBL. 11 REF.Article

CONTRACTION OF THE CANINE BASILAR ARTERY FOLLOWING LINOLEIC, ARACHIDONIC, 13-HYDROPEROXYLINOLEIC, OR 15-HYDROPEROXYARACHIDONIC ACIDKOIDE T; NODA Y; HATA SI et al.1981; PROC. SOC. EXP. BIOL. MED.; ISSN 0037-9727; USA; DA. 1981; VOL. 168; NO 3; PP. 399-402; BIBL. 15 REF.Article

AUTOXIDATION OF POLYUNSATURATED LIPIDS. FACTORS CONTROLLING THE STEREOCHEMISTRY OF PRODUCT HYDROPEROXIDESPORTER NA; WEBER BA; WEENEN H et al.1980; J. AMER. CHEM. SOC.; USA; DA. 1980; VOL. 102; NO 17; PP. 5597-5601; BIBL. 29 REF.Article

DECOMPOSITION OF LINOLEIC ACID HYDROPEROXIDES. II: BREAKDOWN OF METHYL 13-HYDROPEROXY-CIS-9-TRANS-11-OCTADECADIENOATE BY RADICALS OR COPPER II IONSSCHIEBERLE P; GROSCH W.1981; Z. LEBENSM.-UNTERS. FORSCH.; ISSN 0044-3026; DEU; DA. 1981; VOL. 173; NO 3; PP. 192-198; ABS. GER; BIBL. 27 REF.Article

DECOMPOSITION OF LIPID HYDROPEROXIDE BY SAYBEAN LIPOXYGENASE-1 UNDER AEROBIC CONDITIONS STUDIED BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY AND THE SPIN TRAPPING METHOD = ETUDE DE LA DEGRATION DES HYDROPEROXYDES LIPIDIQUES PAR LA LIPOXYGENASE-1 DE SOJA DANS DES CONDITIONS D'AEROBIE, PAR CHROMATOGRAPHIE EN PHASE LIQUIDE DE HAUTE PERFORMANCE ET PAR LA METHODE DE PIEGEAGE DU SPINAOSHIMA H; KAJIWARA T; HATANAKA A et al.1981; AGRIC. BIOL. CHEM.; ISSN 0002-1369; JPN; DA. 1981; VOL. 45; NO 10; PP. 2245-2251; BIBL. 34 REF.Article

THE MECHANISM OF THE REARRANGEMENT OF LINOLEATE HYDROPEROXIDESCHAN HWS; LEVETT G; MATTHEW JA et al.1979; CHEM. PHYS. LIPIDS; NLD; DA. 1979; VOL. 24; NO 3; PP. 245-256; BIBL. 20 REF.Article

CYSTEINE ADDS TO LIPID HYDROPEROXIDE.GARDNER HW; KLEIMAN R; WEISLEDER D et al.1977; LIPIDS; U.S.A.; DA. 1977; VOL. 12; NO 8; PP. 655-660; BIBL. 17 REF.Article

THERMAL DECOMPOSITION OF INDIVIDUAL POSITIONAL ISOMERS OF METHYL LINOLEATE HYDROPEROXIDE: EVIDENCE OF CARBON OXYGEN BOND SCISSION.CHAN HWS; PRESCOTT FAA; SWOBODA PAT et al.1976; J. AMER. OIL CHEMISTS' SOC.; U.S.A.; DA. 1976; VOL. 53; NO 9; PP. 572-576; BIBL. 21 REF.Article

Quantification of carbonyls produced by the decomposition of hydroperoxidesSALDIA, B; HAMMOND, E. G.Journal of the American Oil Chemists' Society. 1989, Vol 66, Num 8, pp 1097-1102, issn 0003-021XArticle

Photolyse von 13(S)-Hydroperoxy-9(Z), 11(E)-octadecadiensäuremethylester in Gegenwart von Sauerstoff ― Analuse der niedermolekularen Reaktionsprodukte = Photolyse de (S)-hydroperoxy-13 (Z, E)-octadiène-9,11oate de méthyle en présence d'oxygène. Analyse des produits de réaction de faible masse moléculaire = Photolysis of methyl-13(S)-hydroperoxy-9(Z), 11(E)-octadecacadienoate in presence of oxygen. Analysis of the low molecular reaction productsSCHIEBERLE, P; GROSCH, W.Fette, Seifen, Anstrichmittel. 1985, Vol 87, Num 2, pp 76-80, issn 0015-038XArticle

Oxidation of lipids. IX: Decomposition of methyl lineolate and methyl lineolate hydroperoxides in solutionYAMAMOTO, Y; SAEKI, N; HAGA, S et al.Bulletin of the Chemical Society of Japan. 1984, Vol 57, Num 11, pp 3177-3181, issn 0009-2673Article

A simple method for preparation of pure isomers of methyl linoleate hydroperoxide by dry silica gel column chromatographyMIYASHITA, K; CHIBA, T; HATA, K et al.Yukagaku. 1985, Vol 34, Num 12, pp 1029-1031, issn 0513-398XArticle

Acid-catalyzed transformation of 13(S)-hydroperoxylinoleic acid into epoxyhydroxyoctadecenoic and trihydroxyoctadecenoic acidsGARDNER, H. W; NELSON, E. C; TJARKS, L. W et al.Chemistry and physics of lipids. 1984, Vol 35, Num 2, pp 87-101, issn 0009-3084Article

The effect of dietary lipid hydroperoxide on lymphoid tissues in miceOARADA, M; ITO, E; TERAO, K et al.Biochimica et biophysica acta. 1988, Vol 960, Num 2, pp 229-235, issn 0006-3002Article

Formation of fluorescent substances in the reaction of the hydroperoxide isomers of methyl linoleate and amylamineIIO, T; YODEN, K; TABATA, T et al.Chemical and pharmaceutical bulletin. 1987, Vol 35, Num 12, pp 5015-5019, issn 0009-2363Article

Acid catalysis of a linoleic acid hydroperoxide: formation of epoxides by an intramolecular cyclization of the hydroperoxide groupGARDNER, H. W; WEISLEDER, D; NELSON, E. C et al.Journal of organic chemistry. 1984, Vol 49, Num 3, pp 508-515, issn 0022-3263Article

DECOMPOSITION OF LINOLEIC ACID HYDROPEROXIDES BY RADICALS. I: STRUCTURES OF PRODUCTS OF METHYL 13-HYDROPEROXY-CIS, TRANS-9,11-OCTADECADIENOATESCHIEBERLE P; TSOUKALAS B; GROSCH W et al.1979; Z. LEBENSMITTEL-UNTERS. U. -FORSCH.; DEU; DA. 1979; VOL. 168; NO 6; PP. 448-456; ABS. GER; BIBL. 30 REF.Article