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9
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Mishiev, R. D.; Ibragimov, D. S.; Rzaeva, Z. I.; Mamedov, E. Sh. Khim. Geterotsikl. Soedin. 1993, 271; Chem. Abstr. 1993, 119, 271275.
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15
-
-
8044242940
-
-
note
-
When refluxed for 4 h, no starting material remains, with 2 and 1 being the main products (ratio 2:1 = 2.6:1 with methyl oleate as starting material).
-
-
-
-
16
-
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8044257142
-
-
note
-
2.
-
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-
17
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0010449493
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Itakura, J.; Tanaka, H.; Ito, H. Bull. Chem. Soc. Jpn. 1969, 42, 1604.
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Ito, H.3
-
20
-
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8044226030
-
-
note
-
Authentic threo-9,10-dihydroxyoctadecanoic acid had a melting point of 92-93°C, while the erythro-isomer melted at 132-133 C.
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-
-
-
21
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-
51249179543
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-
3OD) for the erythro diastereomer. For the present configuration determination, mixtures of diol 1 and authentic erythro- or threo-9,10-dihydroxyocatadecanoic acid were prepared.
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(1979)
Lipids
, vol.14
, pp. 81
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Rakoff, H.1
Weisleder, D.2
Emken, E.A.3
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0002060240
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Christie, W. W., Ed.; The Oily Press: Dundee
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Gunstone, F. D. In Advances in Lipid Methodology - Two; Christie, W. W., Ed.; The Oily Press: Dundee, 1993; pp 1-68. Bascetta, E.; Gunstone, F. D. Chem. Phys. Lipids 1985, 36, 253. As in the case of diols (see Ref. 9), we observed two signals (separated by 0.05 ppm) for the epoxidized carbons even for the 9,10-epoxy compounds. In these references, two signals were reported only up to the 7,8-position.
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(1993)
Advances in Lipid Methodology - Two
, pp. 1-68
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Gunstone, F.D.1
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23
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0013484234
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Gunstone, F. D. In Advances in Lipid Methodology - Two; Christie, W. W., Ed.; The Oily Press: Dundee, 1993; pp 1-68. Bascetta, E.; Gunstone, F. D. Chem. Phys. Lipids 1985, 36, 253. As in the case of diols (see Ref. 9), we observed two signals (separated by 0.05 ppm) for the epoxidized carbons even for the 9,10-epoxy compounds. In these references, two signals were reported only up to the 7,8-position.
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Chem. Phys. Lipids
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Bascetta, E.1
Gunstone, F.D.2
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25
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0003010899
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For discussion of mass spectra of such compounds see: Murphy, R. C. Mass Spectrometry of Lipids (Handbook of Lipid Research 7): Plenum: New York, 1993; pp 71-130. Kleiman, R.; Spencer, G. F. J. Am .Oil Chem. Soc. 1973, 50, 31.
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Kleiman, R.1
Spencer, G.F.2
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26
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85086684427
-
-
note
-
77Se NMR and lanthanide shift experiments discussed subsequently.
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-
-
-
27
-
-
37049079732
-
-
The shift differences (in ppm) vary depending on the proximity of the functional group to C1. With increasing proximity to C1, the shift differences within the two signal groups (δ = 88 and 85) increase. Similar effects have been discussed for isolated double and triple bonds and allylic hydroxy groups in fatty compounds, see: Knothe, G.; Bagby, M. O. J. Chem. Soc., Perkin Trans. 2 1995, 615.
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Knothe, G.1
Bagby, M.O.2
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29
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84994988683
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See also Refs. 5 and 21
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77Se nucleus highly sensitive to its environment: Schroeder, T. B.; Job, C.; Brown, M. F.; Glass, R. S. Magn. Res. Chem. 1995, 33, 191. See also Refs. 5 and 21.
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Schroeder, T.B.1
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Glass, R.S.4
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84949233109
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Patai, S.; Rappoport, Z., Eds.; Wiley: New York
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Luthra, N. P.; Odom, J. D. In The Chemistry of Organic Selenium and Tellurium Compounds; Vol. 1; Patai, S.; Rappoport, Z., Eds.; Wiley: New York, 1986; pp 189-241. Duddeck, H. Prog. Nucl. Magn. Reson. Spectrosc. 1995, 27, 1.
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Odom, J.D.2
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0002565593
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Luthra, N. P.; Odom, J. D. In The Chemistry of Organic Selenium and Tellurium Compounds; Vol. 1; Patai, S.; Rappoport, Z., Eds.; Wiley: New York, 1986; pp 189-241. Duddeck, H. Prog. Nucl. Magn. Reson. Spectrosc. 1995, 27, 1.
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Duddeck, H.1
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Arbuzov, B. A.; Naumov, V. A.; Zaripov, N. M.; Pronicheva, L. D. Dokl. Akad. Nauk SSSR 1970, 195, 1333; Chem. Abstr. 1971, 74, 92295.
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Arbuzov, B.A.1
Naumov, V.A.2
Zaripov, N.M.3
Pronicheva, L.D.4
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33
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8044247805
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Arbuzov, B. A.; Naumov, V. A.; Zaripov, N. M.; Pronicheva, L. D. Dokl. Akad. Nauk SSSR 1970, 195, 1333; Chem. Abstr. 1971, 74, 92295.
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34
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37049134034
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Green, C. H.; Hellier, D. G. J. Chem. Soc., Perkin Trans. 2 1975, 190. Buchanan, G. W.; Hellier, D. G. Can. J. Chem. 1976, 54, 1428.
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Green, C.H.1
Hellier, D.G.2
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0000819940
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Green, C. H.; Hellier, D. G. J. Chem. Soc., Perkin Trans. 2 1975, 190. Buchanan, G. W.; Hellier, D. G. Can. J. Chem. 1976, 54, 1428.
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Buchanan, G.W.1
Hellier, D.G.2
-
37
-
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85086685191
-
-
note
-
3 experiments are the most definitive for distinguishing 2 a and 2b.
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-
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