-
1
-
-
42349108638
-
Combined analysis of C-18 unsaturated fatty acids using natural abundance deuterium 2D NMR spectroscopy in chiral oriented solvents
-
DOI 10.1021/ac702443b
-
P Lesot V Baillif I Billault 2008 Combined analysis of C-18 unsaturated fatty acids using natural abundance deuterium 2D NMR spectroscopy in chiral oriented solvents Anal Chem 80 2963 2972 10.1021/ac702443b 1:CAS:528: DC%2BD1cXjtVSiu70%3D (Pubitemid 351556462)
-
(2008)
Analytical Chemistry
, vol.80
, Issue.8
, pp. 2963-2972
-
-
Lesot, P.1
Baillif, V.2
Billault, I.3
-
2
-
-
77956032713
-
Complete determination of natural site-specific enantio-isotopomeric excesses in linoleic acid using natural abundance deuterium 2D NMR in polypeptide mesophases
-
10.1039/c0cc01486a 1:CAS:528:DC%2BC3cXhtVKltLfO
-
Z Serhan L Martel I Billault P Lesot 2010 Complete determination of natural site-specific enantio-isotopomeric excesses in linoleic acid using natural abundance deuterium 2D NMR in polypeptide mesophases Chem Commun 46 6599 6601 10.1039/c0cc01486a 1:CAS:528:DC%2BC3cXhtVKltLfO
-
(2010)
Chem Commun
, vol.46
, pp. 6599-6601
-
-
Serhan, Z.1
Martel, L.2
Billault, I.3
Lesot, P.4
-
3
-
-
79251639035
-
2H NMR spectroscopy: Application to conjugated linolenic methyl esters
-
10.1007/s00216-010-4394-0 1:CAS:528:DC%2BC3cXhsVymsbrE
-
2H NMR spectroscopy: application to conjugated linolenic methyl esters Anal Bioanal Chem 399 1187 1200 10.1007/s00216-010-4394-0 1:CAS:528:DC%2BC3cXhsVymsbrE
-
(2011)
Anal Bioanal Chem
, vol.399
, pp. 1187-1200
-
-
Lesot, P.1
Serhan, Z.2
Billault, I.3
-
4
-
-
67449104516
-
Investigation of fatty acid elongation and desaturation steps in Fusarium lateritium by quantitative two-dimensional deuterium NMR spectroscopy in chiral oriented media
-
10.1074/jbc.M807826200 1:CAS:528:DC%2BD1MXktlGrsb8%3D
-
V Baillif RJ Robins S Le Feunteun P Lesot I Billault 2009 Investigation of fatty acid elongation and desaturation steps in Fusarium lateritium by quantitative two-dimensional deuterium NMR spectroscopy in chiral oriented media J Biol Chem 284 10783 10792 10.1074/jbc.M807826200 1:CAS:528: DC%2BD1MXktlGrsb8%3D
-
(2009)
J Biol Chem
, vol.284
, pp. 10783-10792
-
-
Baillif, V.1
Robins, R.J.2
Le Feunteun, S.3
Lesot, P.4
Billault, I.5
-
5
-
-
0036801997
-
Fatty acid desaturation: Variations on an oxidative theme
-
DOI 10.1016/S1367-5931(02)00365-4
-
B Behrouzian PH Buist 2002 Fatty acid desaturation: variations on an oxidative theme Curr Opinion Chem Biol 6 577 582 10.1016/S1367-5931(02)00365-4 1:CAS:528:DC%2BD38Xot1agsLc%3D (Pubitemid 35284187)
-
(2002)
Current Opinion in Chemical Biology
, vol.6
, Issue.5
, pp. 577-582
-
-
Behrouzian, B.1
Buist, P.H.2
-
6
-
-
0025323367
-
Efficient epoxidation of unsaturated fatty acids by hydroperoxide- dependent oxygenase
-
E Blée F Schuber 1990 Efficient epoxidation of unsaturated fatty acids by hydroperoxide-dependent oxygenase J Biol Chem 265 12887 12894
-
(1990)
J Biol Chem
, vol.265
, pp. 12887-12894
-
-
Blée, E.1
Schuber, F.2
-
7
-
-
0032077678
-
Phytooxylipins and plant defense reactions
-
DOI 10.1016/S0163-7827(98)00004-6, PII S0163782798000046
-
E Blée 1998 Phytooxylipins and plant defense reactions Progr Lipid Res 37 33 72 10.1016/S0163-7827(98)00004-6 (Pubitemid 28347101)
-
(1998)
Progress in Lipid Research
, vol.37
, Issue.1
, pp. 33-72
-
-
Blee, E.1
-
8
-
-
0032496331
-
Identification of non-heme diiron proteins that catalyze triple bond and epoxy group formation
-
DOI 10.1126/science.280.5365.915
-
M Lee M Lenman A Banas M Bafor S Singh M Schweizer R Nilsson C Liljenberg A Dahlqvist P-O Gummeson S Sjödahl A Green S Stymne 1998 Identification of non-heme diiron proteins that catalyze triple bond and epoxy group formation Science 280 915 918 10.1126/science.280.5365.915 1:STN:280:DyaK1c3jvFOksw%3D%3D (Pubitemid 28215604)
-
(1998)
Science
, vol.280
, Issue.5365
, pp. 915-918
-
-
Lee, M.1
Lenman, M.2
Banas, A.3
Bafor, M.4
Singh, S.5
Schweizer, M.6
Nilsson, R.7
Liljenberg, C.8
Dahlqvist, A.9
Gummeson, P.-O.10
Sjodahl, S.11
Green, A.12
Stymne, S.13
-
9
-
-
58449111346
-
Arabidopsis thaliana CYP77A4 is the first cytochrome P450 able to catalyze the epoxidation of free fatty acids in plants
-
10.1111/j.1742-4658.2008.06819.x 1:CAS:528:DC%2BD1MXhs1KitLo%3D
-
V Sauveplane S Kandel P-E Kastner J Ehlting V Compagnon D Werck-Reichhart F Pinot 2009 Arabidopsis thaliana CYP77A4 is the first cytochrome P450 able to catalyze the epoxidation of free fatty acids in plants FEBS J 276 719 735 10.1111/j.1742-4658.2008.06819.x 1:CAS:528:DC%2BD1MXhs1KitLo%3D
-
(2009)
FEBS J
, vol.276
, pp. 719-735
-
-
Sauveplane, V.1
Kandel, S.2
Kastner, P.-E.3
Ehlting, J.4
Compagnon, V.5
Werck-Reichhart, D.6
Pinot, F.7
-
10
-
-
0037013191
-
Desaturation and hydroxylation. Residues 148 and 324 of Arabidopsis FAD2, in addition to substrate chain length, exert a major influence in partitioning of catalytic specificity
-
DOI 10.1074/jbc.M200231200
-
Broadwater J, Whittle E, Shanklin J 2002 Desaturation and hydroxylation: residues 148 and 324 of Arabidopsis fad2, in addition to substrate chain length, exert a major influence in partitioning of catalytic specificity J Biol Chem 277 15613 15620 10.1074/jbc.M200231200 (Pubitemid 34967832)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.18
, pp. 15613-15620
-
-
Broadwater, J.A.1
Whittle, E.2
Shanklin, J.3
-
12
-
-
0027317790
-
Biosynthesis of vernoleate (cis-12-epoxyoctadeca-cis-9-}noate) in microsomal preparations from developing endosperm of Euphorbia lagascae
-
DOI 10.1006/abbi.1993.1265
-
M Bafor MA Smith L Jonsson K Stobart S Stymne 1993 Biosynthesis of vernoleate (cis-12-epoxyoctodeca-cis-9-enoate) in microsomal preparations from developing endosperm of Euphorbia lagascae Arch Biochem Biophys 303 145 151 10.1006/abbi.1993.1265 1:CAS:528:DyaK3sXktVGjs7g%3D (Pubitemid 23212669)
-
(1993)
Archives of Biochemistry and Biophysics
, vol.303
, Issue.1
, pp. 145-151
-
-
Bafor, M.1
Smith, M.A.2
Jonsson, L.3
Stobart, K.4
Stymne, S.5
-
13
-
-
0027716061
-
Regio- and stereoselectivity of cytochrome P-450 and peroxygenase- dependent formation of cis-12,13-epoxy-9(Z)-octadecenoic acid (vernolic acid) in Euphorbia lagascae
-
DOI 10.1006/bbrc.1993.2546
-
E Blée U Stahl F Schuber S Stymne 1993 Regio- and stereoselectivity of cytochrome P-450 and peroxygenase dependent formation of cis-12,13-epoxy-9(Z)-octadecenoic acid (vernolic acid) in Euphorbia lagascae Biochem Biophys Res Commun 197 778 784 10.1006/bbrc.1993.2546 (Pubitemid 24034637)
-
(1993)
Biochemical and Biophysical Research Communications
, vol.197
, Issue.2
, pp. 778-784
-
-
Blee, E.1
Stahl, U.2
Schuber, F.3
Stymne, S.4
-
14
-
-
79959845740
-
13C values in fructose from plant sucrose samples
-
10.1111/j.1469-8137.2011.03690.x 1:CAS:528:DC%2BC3MXhtFSqtrzN
-
13C values in fructose from plant sucrose samples New Phytol 191 579 588 10.1111/j.1469-8137.2011.03690.x 1:CAS:528:DC%2BC3MXhtFSqtrzN
-
(2011)
New Phytol
, vol.191
, pp. 579-588
-
-
Gilbert, A.1
Silvestre, V.2
Robins, R.J.3
Tcherkez, G.4
Remaud, G.5
-
15
-
-
0024381420
-
4 metabolites and precursors to radiolabeled forms of those metabolites
-
D Delorme Y Girard J Rokach 1989 Total synthesis of Leukotriene E4 metabolites and precursors to radiolabeled forms of those metabolites J Org Chem 54 3635 3640 10.1021/jo00276a025 1:CAS:528:DyaL1MXltFCqsrs%3D (Pubitemid 19204458)
-
(1989)
Journal of Organic Chemistry
, vol.54
, Issue.15
, pp. 3635-3640
-
-
Delorme, D.1
Girard, Y.2
Rokach, J.3
-
16
-
-
0004971424
-
Natural acetylenes. Part XXXII. A synthesis of crepenynic acid (octadec-9-en-12-ynoic acid)
-
Bradshaw RW, Day AC, Jones ERH, Page CB, Thaller V, Vere Hodge RA (1971) Natural acetylenes. Part XXXII. A synthesis of crepenynic acid (octadec-9-en-12-ynoic acid). J Chem Soc (C):1156-1158
-
(1971)
J Chem Soc (C)
, pp. 1156-1158
-
-
Bradshaw, R.W.1
Day, A.C.2
Erh, J.3
Page, C.B.4
Thaller, V.5
Vere Hodge, R.A.6
-
17
-
-
0034619611
-
Theoretical and experimental aspects of enantiomeric differentiation using natural abundance multinuclear NMR spectroscopy in chiral polypeptide liquid crystals
-
Sarfati M, Lesot P, Merlet D, Courtieu J (2000) Theoretical and experimental aspects of enantiomeric differentiation using natural abundance multinuclear NMR spectroscopy in chiral polypeptide liquid crystals. Chem Comm:2069-2081
-
(2000)
Chem Comm
, pp. 2069-2081
-
-
Sarfati, M.1
Lesot, P.2
Merlet, D.3
Courtieu, J.4
-
18
-
-
0037656009
-
Natural Abundance Deuterium NMR spectroscopy in polypeptide liquid crystals as a new and incisive means for the enantiodifferentiation of chiral hydrocarbons
-
10.1002/chem.200390199 1:CAS:528:DC%2BD3sXjt1GmtL0%3D
-
P Lesot M Sarfati J Courtieu 2003 Natural Abundance Deuterium NMR spectroscopy in polypeptide liquid crystals as a new and incisive means for the enantiodifferentiation of chiral hydrocarbons Chem Eur J 9 1724 1745 10.1002/chem.200390199 1:CAS:528:DC%2BD3sXjt1GmtL0%3D
-
(2003)
Chem Eur J
, vol.9
, pp. 1724-1745
-
-
Lesot, P.1
Sarfati, M.2
Courtieu, J.3
-
19
-
-
7544250149
-
Modified z-gradient filtering as a mean to obtain phased deuterium autocorrelation 2D NMR spectra in oriented solvents
-
10.1016/j.jmr.2004.08.010 1:CAS:528:DC%2BD2cXovVClsL4%3D
-
O Lafon P Lesot D Merlet J Courtieu 2004 Modified z-gradient filtering as a mean to obtain phased deuterium autocorrelation 2D NMR spectra in oriented solvents J Magn Reson 171 135 142 10.1016/j.jmr.2004.08.010 1:CAS:528: DC%2BD2cXovVClsL4%3D
-
(2004)
J Magn Reson
, vol.171
, pp. 135-142
-
-
Lafon, O.1
Lesot, P.2
Merlet, D.3
Courtieu, J.4
-
20
-
-
0002927120
-
Deuterium NMR in the study of site-specific natural isotope fractionation (SNIF-NMR)
-
Diehl P, Fluck E, Günther H, Kosfeld R, Seelig J (eds) Springer, Berlin
-
Martin M, Martin G (1990) Deuterium NMR in the study of site-specific natural isotope fractionation (SNIF-NMR). In: Diehl P, Fluck E, Günther H, Kosfeld R, Seelig J (eds) NMR Basic Principles and Progress. Springer, Berlin, 1-63
-
(1990)
NMR Basic Principles and Progress
, pp. 1-63
-
-
Martin, M.1
Martin, G.2
-
21
-
-
2442673048
-
Exploring the analytical potential of NMR spectroscopy in chiral anisotropic media for the study of the natural abundance deuterium distribution in organic molecules
-
DOI 10.1021/ac030385e
-
P Lesot C Aroulanda I Billault 2004 Exploring the analytical potential of NMR spectroscopy in chiral anisotropic media for the study of the natural abundance deuterium distribution in organic molecules Anal Chem 76 2827 2835 10.1021/ac030385e 1:CAS:528:DC%2BD2cXjt1ajsLc%3D (Pubitemid 38657709)
-
(2004)
Analytical Chemistry
, vol.76
, Issue.10
, pp. 2827-2835
-
-
Lesot, P.1
Aroulanda, C.2
Billault, I.3
-
22
-
-
0036903763
-
2H NMR spectroscopy
-
DOI 10.1002/1439-7633(20020802)3:8<752::AID-CBIC752>3.0.CO;2-G
-
2H NMR spectroscopy ChemBioChem 3 752 759 10.1002/1439-7633(20020802)3:8<752::AID-CBIC752>3.0.CO;2-G 1:CAS:528:DC%2BD38Xmt1aqt7s%3D (Pubitemid 36004514)
-
(2002)
ChemBioChem
, vol.3
, Issue.8
, pp. 752-759
-
-
Duan, J.-R.1
Billault, I.2
Mabon, F.3
Robins, R.4
-
23
-
-
3042559899
-
Hydrogen and carbon isotopic fractionations of lipid biosynthesis among terrestrial (C3, C4 and CAM) and aquatic plants
-
DOI 10.1016/j.phytochem.2004.03.036, PII S0031942204001931
-
Y Chikaraishi H Naraoka SR Poulson 2004 Hydrogen and carbon isotopic fractionations of lipid biosynthesis among terrestrial (C3, C4 and CAM) and aquatic plants Phytochemistry 65 1369 1381 10.1016/j.phytochem.2004.03.036 1:CAS:528:DC%2BD2cXlsVaku7k%3D (Pubitemid 38844721)
-
(2004)
Phytochemistry
, vol.65
, Issue.10
, pp. 1369-1381
-
-
Chikaraishi, Y.1
Naraoka, H.2
Poulson, S.R.3
-
24
-
-
51249190983
-
Naturally occurring epoxy acids. IV. The absolute optical configuration of vernolic acid
-
10.1007/BF02668123 1:CAS:528:DyaF28Xotl2kuw%3D%3D
-
LJ Morris DM Wharry 1966 Naturally occurring epoxy acids. IV. The absolute optical configuration of vernolic acid Lipids 1 41 46 10.1007/BF02668123 1:CAS:528:DyaF28Xotl2kuw%3D%3D
-
(1966)
Lipids
, vol.1
, pp. 41-46
-
-
Morris, L.J.1
Wharry, D.M.2
-
25
-
-
33748031122
-
Assignment of absolute configuration of natural abundance deuterium signals associated with (R)- and (S)-enantioisotopomers in a fatty acid aligned in a chiral liquid crystal: Enantioselective synthesis and NMR analysis
-
DOI 10.1021/ja0617892
-
V Baillif RJ Robins I Billault P Lesot 2006 Assignment of absolute configuration of natural abundance deuterium signals associated with (R)- and (S)-enantioisotopomers in a fatty acid aligned in a chiral liquid crystal: enantioselective synthesis and NMR analysis J Am Chem Soc 128 11180 11187 10.1021/ja0617892 1:CAS:528:DC%2BD28XnvVaks78%3D (Pubitemid 44300127)
-
(2006)
Journal of the American Chemical Society
, vol.128
, Issue.34
, pp. 11180-11187
-
-
Baillif, V.1
Robins, R.J.2
Billault, I.3
Lesot, P.4
-
27
-
-
0041310119
-
2H NMR: An approach to understanding metabolism and enzyme mechanism?
-
DOI 10.1023/B:PHYT.0000004301.52646.a8
-
2H distribution in natural products by quantitative NMR: an approach to understanding metabolism and enzyme mechanism? Phytochem Rev 2 87 102 10.1023/B:PHYT.0000004301.52646.a8 1:CAS:528:DC%2BD2cXptlyisg%3D%3D (Pubitemid 39012595)
-
(2003)
Phytochemistry Reviews
, vol.2
, Issue.1-2
, pp. 87-102
-
-
Robins, R.J.1
Billault, I.2
Duan, J.-R.3
Guiet, S.4
Pionnier, S.5
Zhang, B.-L.6
-
28
-
-
84892193594
-
Substrate oxidation by cytochrome P450 enzymes
-
Ortiz de Montellano PR (ed) Kluwer Academic/Plenum Publishers, New York
-
Ortiz de Montalleno PR, de Voss JJ (2005) Substrate oxidation by cytochrome P450 enzymes. In: Ortiz de Montellano PR (ed) Cytochrome P450, Structure, Mechanism and Biochemistry. Kluwer Academic/Plenum Publishers, New York, 183-245
-
(2005)
Cytochrome P450, Structure, Mechanism and Biochemistry
, pp. 183-245
-
-
Ortiz De Montalleno, P.R.1
De Voss, J.J.2
-
29
-
-
0030669437
-
Transition states of epoxidations: Diradical character, spiro geometries, transition state flexibility, and the origins of stereoselectivity
-
DOI 10.1021/ja963847x
-
K Houk J Liu NC DeMello KR Condroski 1997 Transition states of epoxidations: diradical character, spiro geometries, transition state flexibility, and the origin of stereoselectivity J Am Chem Soc 119 10147 10152 10.1021/ja963847x 1:CAS:528:DyaK2sXms1Ckurc%3D (Pubitemid 27478804)
-
(1997)
Journal of the American Chemical Society
, vol.119
, Issue.42
, pp. 10147-10152
-
-
Houk, K.N.1
Liu, J.2
DeMello, N.C.3
Condroski, K.R.4
-
30
-
-
0030909214
-
Experimental geometry of the epoxidation transition state
-
DOI 10.1021/ja963656u, PII S0002786396036566
-
DA Singleton S Merrigan J Liu K Houk 1997 The experimental geometry of the epoxidation transition state J Am Chem Soc 119 3385 3386 10.1021/ja963656u 1:CAS:528:DyaK2sXhvFGksbY%3D (Pubitemid 27213845)
-
(1997)
Journal of the American Chemical Society
, vol.119
, Issue.14
, pp. 3385-3386
-
-
Singleton, D.A.1
Merrigan, S.R.2
Liu, J.3
Houk, K.N.4
-
31
-
-
0018103875
-
Secondary deuterium isotope effects on olefin epoxidation by cytochrome P-450
-
DOI 10.1016/0006-2952(78)90099-0
-
RP Hanzlik GO Shearer 1978 Secondary deuterium isotope effects on olefin epoxidation by cytochrome P-450 Biochem Pharmacol 27 1441 1444 10.1016/0006-2952(78)90099-0 1:CAS:528:DyaE1MXot1Orsg%3D%3D (Pubitemid 8401742)
-
(1978)
Biochemical Pharmacology
, vol.27
, Issue.10
, pp. 1441-1444
-
-
Hanzlik, R.P.1
Shearer, G.O.2
-
32
-
-
0033588022
-
Lipoxygenases: Occurrence, functions, catalysis, and acquisition of substrate
-
DOI 10.1074/jbc.274.34.23679
-
AR Brash 1999 Lipoxygenases: occurrence, functions, catalysis, and acquisition of substrate J Biol Chem 274 23679 23682 10.1074/jbc.274.34.23679 1:CAS:528:DyaK1MXlsVOnsrc%3D (Pubitemid 29390284)
-
(1999)
Journal of Biological Chemistry
, vol.274
, Issue.34
, pp. 23679-23682
-
-
Brash, A.R.1
-
33
-
-
55249126573
-
Kinetic isotope effects in the oxidation of arachidonic acid by soybean lipoxygenase-1
-
10.1016/j.bmcl.2008.08.108 1:CAS:528:DC%2BD1cXhtlOht7jN
-
C Jacquot S Peng WA van der Donk 2008 Kinetic isotope effects in the oxidation of arachidonic acid by soybean lipoxygenase-1 Bioorg Med Chem Lett 18 5959 5962 10.1016/j.bmcl.2008.08.108 1:CAS:528:DC%2BD1cXhtlOht7jN
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 5959-5962
-
-
Jacquot, C.1
Peng, S.2
Van Der Donk, W.A.3
-
36
-
-
0036523376
-
2H NMR spectroscopy of the fatty acids of capsaicinoids
-
DOI 10.1002/1439-7633(20020301)3:2/3<212::AID-CBIC212>3.0.CO;2-R
-
S Markai PA Marchand F Mabon E Baguet I Billault RJ Robins 2002 Natural deuterium distribution in branched-chain medium-length fatty acids is nonstatistical: A site-specific study by quantitative H-2 NMR spectroscopy of the fatty acids of capsaicinoids ChemBioChem 3 212 218 10.1002/1439- 7633(20020301)3:2/3<212::AID-CBIC212>3.0.CO;2-R 1:CAS:528: DC%2BD38Xis1Kit7Y%3D (Pubitemid 36004497)
-
(2002)
ChemBioChem
, vol.3
, Issue.2-3
, pp. 212-218
-
-
Markai, S.1
Marchand, P.A.2
Mabon, F.3
Baguet, E.4
Billault, I.5
Robins, R.J.6
-
37
-
-
33744524007
-
The prediction of isotopic patterns in phenylpropanoids from their precursors and the mechanism of the NIH-shift: Basis of the isotopic characteristics of natural aromatic compounds
-
DOI 10.1016/j.phytochem.2006.03.014, PII S0031942206001622
-
H-L Schmidt RA Werner W Eisenreich C Fuganti G Fronza G Remaud RJ Robins 2006 The prediction of isotopic patterns in phenylpropanoids from their precursors and the mechanism of the NIH-shift: Basis of the isotopic characteristics of natural aromatic compounds Phytochemistry 67 1094 1103 10.1016/j.phytochem.2006.03.014 1:CAS:528:DC%2BD28XlsVelsrw%3D (Pubitemid 43818034)
-
(2006)
Phytochemistry
, vol.67
, Issue.11
, pp. 1094-1103
-
-
Schmidt, H.-L.1
Werner, R.A.2
Eisenreich, W.3
Fuganti, C.4
Fronza, G.5
Remaud, G.6
Robins, R.J.7
|