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4. Formation of alpha- and gamma-ketols from 18O-labelled linoleic acid hydroperoxides by corn germ hydroperoxide isomerase. Gerritsen M; Veldink GA; Vliegenthart JF; Boldingh J FEBS Lett; 1976 Aug; 67(2):149-52. PubMed ID: 955114 [No Abstract] [Full Text] [Related]
5. The enzymic conversion of linoleic acid hydroperoxide by flax-seed hydroperoxide isomerase. Veldink GA; Vliegenthart JF; Boldingh J Biochem J; 1970 Nov; 120(1):55-60. PubMed ID: 5494229 [TBL] [Abstract][Full Text] [Related]
6. Degradation of linoleic acid hydroperoxides by a cysteine . FeCl3 catalyst as a model for similar biochemical reactions. II. Specificity in formation of fatty acid epoxides. Gardner HW; Kleiman R Biochim Biophys Acta; 1981 Jul; 665(1):113-24. PubMed ID: 7284409 [TBL] [Abstract][Full Text] [Related]
7. Enzymic reactions of fatty acid hydroperoxides in extracts of potato tuber. I. Comparison 9D- and 13L-hydroperoxy-octadecadienoic acids as substrates for the formation of a divinyl ether derivative. Galliard T; Matthew JA Biochim Biophys Acta; 1975 Jul; 398(1):1-9. PubMed ID: 238639 [TBL] [Abstract][Full Text] [Related]
8. Formation of ketols from linolenic acid 13-hydroperoxide via allene oxide. Evidence for two distinct mechanisms of allene oxide hydrolysis. Grechkin AN; Kuramshin RA; Safonova EY; Latypov SK; Ilyasov AV Biochim Biophys Acta; 1991 Nov; 1086(3):317-25. PubMed ID: 1742324 [TBL] [Abstract][Full Text] [Related]
9. Degradation of linoleic acid hydroperoxides by a cysteine . FeCl3 catalyst as a model for similar biochemical reactions. III. A novel product, trans-12,13-epoxy-11-oxo-trans-9-octadecenoic acid, from 13-L (S)-hydroperoxy-cis-9,trans-11-octadecadienoic acid. Gardner HW; Crawford CG Biochim Biophys Acta; 1981 Jul; 665(1):126-33. PubMed ID: 7284410 [No Abstract] [Full Text] [Related]
10. Hydroperoxides of alpha-ketols. Novel products of the plant lipoxygenase pathway. Grechkin AN; Kuramshin RA; Latypov SK; Safonova YYu ; Gafarova TE; Ilyasov AV Eur J Biochem; 1991 Jul; 199(2):451-7. PubMed ID: 1906404 [TBL] [Abstract][Full Text] [Related]
11. The formation of cis-3-nonenal, trans-2-nonenal and hexanal from linoleic acid hydroperoxide isomers by a hydroperoxide cleavage enzyme system in cucumber (Cucumis sativus) fruits. Galliard T; Phillips DR; Reynolds J Biochim Biophys Acta; 1976 Aug; 441(2):181-92. PubMed ID: 8126 [TBL] [Abstract][Full Text] [Related]
12. Allene oxide cyclase: a new enzyme in plant lipid metabolism. Hamberg M; Fahlstadius P Arch Biochem Biophys; 1990 Feb; 276(2):518-26. PubMed ID: 2306110 [TBL] [Abstract][Full Text] [Related]
13. Conversion of linoleic acid hydroperoxide to hydroxy, keto, epoxyhydroxy, and trihydroxy fatty acids by hematin. Dix TA; Marnett LJ J Biol Chem; 1985 May; 260(9):5351-7. PubMed ID: 3988758 [TBL] [Abstract][Full Text] [Related]
14. Hydroperoxide-dependent epoxidation of unsaturated fatty acids in the broad bean (Vicia faba L.). Hamberg M; Hamberg G Arch Biochem Biophys; 1990 Dec; 283(2):409-16. PubMed ID: 2275553 [TBL] [Abstract][Full Text] [Related]
15. Biosynthesis of 12-oxo-10,15(Z)-phytodienoic acid: identification of an allene oxide cyclase. Hamberg M Biochem Biophys Res Commun; 1988 Oct; 156(1):543-50. PubMed ID: 3178850 [TBL] [Abstract][Full Text] [Related]
16. Stereospecific biosynthesis of (9S,13S)-10-oxo-phytoenoic acid in young maize roots. Ogorodnikova AV; Gorina SS; Mukhtarova LS; Mukhitova FK; Toporkova YY; Hamberg M; Grechkin AN Biochim Biophys Acta; 2015 Sep; 1851(9):1262-70. PubMed ID: 26008579 [TBL] [Abstract][Full Text] [Related]
17. Characterization of metabolic pathway of linoleic acid 9-hydroperoxide in cytosolic fraction of potato tubers and identification of reaction products. Kimura H; Yokota K Appl Biochem Biotechnol; 2004; 118(1-3):115-32. PubMed ID: 15304744 [TBL] [Abstract][Full Text] [Related]
18. Products of linoleic hydroperoxide-decomposing enzyme of alfalfa seed. Esselman WJ; Clagett CO J Lipid Res; 1974 Mar; 15(2):173-8. PubMed ID: 4208994 [TBL] [Abstract][Full Text] [Related]
20. [Carbonyl compounds from the reaction of barley isomerase with linoleic acid hydroperoxides. Their development from the 9- or the 13-hydroperoxide-isomer (author's transl)]. Heimann W; Timm U Z Lebensm Unters Forsch; 1977 Sep; 165(1):12-4. PubMed ID: 919789 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]