-
1
-
-
0024284749
-
Absolute configuration of cis-12-oxophytodienoic acid of flaxseed: implications for the mechanism of biosynthesis from the 13(S)-hydroperoxide of linolenic acid
-
Baertschi S.W., Ingram C.D., Harris T.M., and Brash A.R. Absolute configuration of cis-12-oxophytodienoic acid of flaxseed: implications for the mechanism of biosynthesis from the 13(S)-hydroperoxide of linolenic acid. Biochemistry 27 (1988) 18-24
-
(1988)
Biochemistry
, vol.27
, pp. 18-24
-
-
Baertschi, S.W.1
Ingram, C.D.2
Harris, T.M.3
Brash, A.R.4
-
2
-
-
0001679525
-
Isolation and characterization of natural allene oxides: unstable intermediates in the metabolism of lipid hydroperoxides
-
Brash A.R., Baertschi S.W., Ingram C.D., and Harris T.M. Isolation and characterization of natural allene oxides: unstable intermediates in the metabolism of lipid hydroperoxides. Proc. Natl. Acad. Sci. U.S.A. 85 (1988) 3382-3386
-
(1988)
Proc. Natl. Acad. Sci. U.S.A.
, vol.85
, pp. 3382-3386
-
-
Brash, A.R.1
Baertschi, S.W.2
Ingram, C.D.3
Harris, T.M.4
-
4
-
-
0028332494
-
Cyclization of natural allene oxide fatty acids. The anchimeric assistance of beta, gamma-double bond beside the oxirane and the reaction mechanism
-
Grechkin A.N. Cyclization of natural allene oxide fatty acids. The anchimeric assistance of beta, gamma-double bond beside the oxirane and the reaction mechanism. Biochim. Biophys. Acta 1213 (1994) 199-206
-
(1994)
Biochim. Biophys. Acta
, vol.1213
, pp. 199-206
-
-
Grechkin, A.N.1
-
5
-
-
0031711656
-
Recent developments in biochemistry of the plant lipoxygenase pathway
-
Grechkin A.N. Recent developments in biochemistry of the plant lipoxygenase pathway. Prog. Lipid Res. 37 (1998) 317-352
-
(1998)
Prog. Lipid Res.
, vol.37
, pp. 317-352
-
-
Grechkin, A.N.1
-
6
-
-
0036890380
-
Role of structure and pH in cyclization of allene oxide fatty acids: implications for the reaction mechanism
-
Grechkin A.N., Chechetkin I.R., Mukhtarova L.S., and Hamberg M. Role of structure and pH in cyclization of allene oxide fatty acids: implications for the reaction mechanism. Chem. Phys. Lipids 120 (2002) 87-99
-
(2002)
Chem. Phys. Lipids
, vol.120
, pp. 87-99
-
-
Grechkin, A.N.1
Chechetkin, I.R.2
Mukhtarova, L.S.3
Hamberg, M.4
-
7
-
-
0033972038
-
Formation of cyclopentenones from all-(E) hydroperoxides of linoleic acid via allene oxides. New insight into the mechanism of cyclization
-
Grechkin A.N., and Hamberg M. Formation of cyclopentenones from all-(E) hydroperoxides of linoleic acid via allene oxides. New insight into the mechanism of cyclization. FEBS Lett. 466 (2000) 63-66
-
(2000)
FEBS Lett.
, vol.466
, pp. 63-66
-
-
Grechkin, A.N.1
Hamberg, M.2
-
8
-
-
0032007678
-
Biological activity and biosynthesis of pentacyclic oxylipins: the linoleic acid pathway
-
Gundlach H., and Zenk M. Biological activity and biosynthesis of pentacyclic oxylipins: the linoleic acid pathway. Phytochemistry 47 (1998) 527-537
-
(1998)
Phytochemistry
, vol.47
, pp. 527-537
-
-
Gundlach, H.1
Zenk, M.2
-
9
-
-
0002230616
-
Mechanism of corn hydroperoxide isomerase: detection of 12,13(S)-oxido-9(Z) 11-octadecadienoic acid
-
Hamberg M. Mechanism of corn hydroperoxide isomerase: detection of 12,13(S)-oxido-9(Z) 11-octadecadienoic acid. Biochim. Biophys. Acta 920 (1987) 76-84
-
(1987)
Biochim. Biophys. Acta
, vol.920
, pp. 76-84
-
-
Hamberg, M.1
-
10
-
-
0023871667
-
Fatty acid allene oxides. II. Formation of two macrolactones from 12,13(S)-epoxy-9(Z),11-octadecadienoic acid
-
Hamberg M. Fatty acid allene oxides. II. Formation of two macrolactones from 12,13(S)-epoxy-9(Z),11-octadecadienoic acid. Chem. Phys. Lipids 46 (1988) 235-243
-
(1988)
Chem. Phys. Lipids
, vol.46
, pp. 235-243
-
-
Hamberg, M.1
-
11
-
-
0034022757
-
New cyclopentenone fatty acids formed from linoleic and linolenic acids in potato
-
Hamberg M. New cyclopentenone fatty acids formed from linoleic and linolenic acids in potato. Lipids 35 (2000) 353-363
-
(2000)
Lipids
, vol.35
, pp. 353-363
-
-
Hamberg, M.1
-
12
-
-
0026451668
-
Oxylipin pathway to jasmonates: biochemistry and biological significance
-
Hamberg M., and Gardner H.W. Oxylipin pathway to jasmonates: biochemistry and biological significance. Biochim. Biophys. Acta 1165 (1992) 1-18
-
(1992)
Biochim. Biophys. Acta
, vol.1165
, pp. 1-18
-
-
Hamberg, M.1
Gardner, H.W.2
-
13
-
-
51249171444
-
Fatty acid allene oxides. II. Albumin-induced cyclization of 12,13(S)-epoxy-9(Z),11-octadecadienoic acid
-
Hamberg M., and Hughes M.A. Fatty acid allene oxides. II. Albumin-induced cyclization of 12,13(S)-epoxy-9(Z),11-octadecadienoic acid. Lipids 23 (1988) 469-475
-
(1988)
Lipids
, vol.23
, pp. 469-475
-
-
Hamberg, M.1
Hughes, M.A.2
-
14
-
-
33845801592
-
The crystal structure of Arabidopsis thaliana allene oxide cyclase: insights into the oxylipin cyclization reaction
-
Hofmann E., Zerbe P., and Schaller F. The crystal structure of Arabidopsis thaliana allene oxide cyclase: insights into the oxylipin cyclization reaction. Plant Cell 18 (2006) 3201-3217
-
(2006)
Plant Cell
, vol.18
, pp. 3201-3217
-
-
Hofmann, E.1
Zerbe, P.2
Schaller, F.3
-
15
-
-
0037195876
-
Identification of a jasmonate-regulated allene oxide synthase that metabolizes 9-hydroperoxides of linoleic and linolenic acids
-
Itoh A., Schilmiller A.L., McCaig B.C., and Howe G.A. Identification of a jasmonate-regulated allene oxide synthase that metabolizes 9-hydroperoxides of linoleic and linolenic acids. J. Biol. Chem. 277 (2002) 46051-46058
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 46051-46058
-
-
Itoh, A.1
Schilmiller, A.L.2
McCaig, B.C.3
Howe, G.A.4
-
16
-
-
3442892984
-
Silencing the jasmonate cascade: induced plant defenses and insect populations
-
Kessler A., Halitschke R., and Baldwin I.T. Silencing the jasmonate cascade: induced plant defenses and insect populations. Science 305 (2004) 665-668
-
(2004)
Science
, vol.305
, pp. 665-668
-
-
Kessler, A.1
Halitschke, R.2
Baldwin, I.T.3
-
17
-
-
0000853980
-
An efficient cyclopentenone formation via an allene oxide
-
Kim S.J., and Cha J.K. An efficient cyclopentenone formation via an allene oxide. Tetrahedron Lett. 29 (1988) 5613-5616
-
(1988)
Tetrahedron Lett.
, vol.29
, pp. 5613-5616
-
-
Kim, S.J.1
Cha, J.K.2
-
18
-
-
29244491665
-
Geometrical configuration of 12,13-epoxyoctadeca-9,11-dienoic acid, a product of the reaction catalyzed by flaxseed allene oxide synthase (CYP74A)
-
Medvedeva N.V., Latypov S.K., Balandina A.A., Mukhtarova L.S., and Grechkin A.N. Geometrical configuration of 12,13-epoxyoctadeca-9,11-dienoic acid, a product of the reaction catalyzed by flaxseed allene oxide synthase (CYP74A). Russ. J. Bioorg. Chem. 31 (2005) 595-596
-
(2005)
Russ. J. Bioorg. Chem.
, vol.31
, pp. 595-596
-
-
Medvedeva, N.V.1
Latypov, S.K.2
Balandina, A.A.3
Mukhtarova, L.S.4
Grechkin, A.N.5
-
20
-
-
0032700710
-
On the specificity of allene oxide cyclase
-
Ziegler J., Wasternack C., and Hamberg M. On the specificity of allene oxide cyclase. Lipids 34 (1999) 1005-1015
-
(1999)
Lipids
, vol.34
, pp. 1005-1015
-
-
Ziegler, J.1
Wasternack, C.2
Hamberg, M.3
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