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Reaction of oxygen and unsaturated fatty acids

  • Fatty Chemicals, New Chemistry
  • Published:
Journal of the American Oil Chemists’ Society

Abstract

Oxygen reacts readily with unsaturated fatty acids so that every time these compounds are handled there is a danger they will become contaminated with oxidation products. The products formed first are allylic hydroperoxides which are labile molecules that change rapidly to other compounds, some of which are highly flavorous. Sometimes these changes are desirable and may be promoted: frequently they are not and have to be inhibited. Instrumental procedures recently introduced—especially separation by high performance liquid chromatography and identification by1H and13C nuclear magnetic resonance spectroscopy—have led to a renewed interest in this subject. For the nonenzymic processes of autoxidation and photooxygenation we now have a better understanding of the routes leading to the first-formed allylic hydroperoxides and an improved appreciation of the structure of further oxidation products including dihydroperoxides and hydroperoxides which also contain one or more cyclic peroxide units. Direct chemical routes to several of these compounds have also been developed. Oxidation of linoleic acid by plant-derived lipoxygenases gives diene hydroperoxides similar to those produced by autoxidation, except that the former are optically active and the latter racemic. Enzymic oxidation of arachidonic acid and certain related C20 acids in animal systems produces a wide variety of prostaglandins, physiological properties. These compounds have been described as “tomorrow’s drugs”.

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References Methyl oleate—autoxidation

  1. Frankel, E. N., W. E. Neff, W. K. Rohwedder, B. P. S. Khambay, R. F. Garwood and B. C. L. Weedon, Lipids 12:901 (1977).

    Article  CAS  Google Scholar 

  2. Neff, W. E., E. N. Frankel, C. r. Scholfield and D. Weisleder, Lipids 13: 415 (1978).

    Article  CAS  Google Scholar 

  3. Neff, W. E., and E. N. Frankel, Lipids 15: 587 (1980).

    Article  CAS  Google Scholar 

  4. Frankel, E. N., Prog. Lipid Res. 19: 1 (1980).

    Article  CAS  Google Scholar 

Methyl oleate—photooxygenation (see also references 3 and 4)

  1. Chan, H.W.-S., JAOCS 54: 100 (1977).

    CAS  Google Scholar 

  2. Terao, J., and S. Matsushita, JAOCS 54: 234 (1977).

    Article  CAS  Google Scholar 

  3. Frankel, E. N., W. E. Neff and T. R. Bessler, Lipids 14: 961 (1979).

    Article  CAS  Google Scholar 

  4. Chan, H. W.-S. and G. Levett, Lipids, 12, 99 (1977).

    Article  CAS  Google Scholar 

  5. Frankel, E. N., W. E. Neff, W. K. Rohwedder, B. P. S. Khambay, R. F. Garwood and B. C. L. Weedon, Lipids 12: 908 (1977).

    Article  CAS  Google Scholar 

  6. Peers, K. E., D. T. Coxon and H. W.-S. Chan, J. Sci. Food Agric. 32: 898 (1981).

    Article  CAS  Google Scholar 

  7. Porter, N. A., B. A. Weber, H. Weenen and J. A. Khan, J. Am. Chem. Soc. 102: 5597 (1980).

    Article  CAS  Google Scholar 

  8. Porter, N. A., L. S. Lehman, B. A. Weber and K. J. Smith ibid. 103: 6447 (1981).

    Article  CAS  Google Scholar 

Methyl linoleate—photooxygenation (see also references 3, 4, 6 and 7)

  1. Thomas, M. J., and W. A. Pryor, Lipids, 15, 544 (1980).

    Article  CAS  Google Scholar 

  2. Mihelich, E. D., J. Am. Chem. Soc. 102: 7141 (1980).

    Article  CAS  Google Scholar 

  3. Frankel, E. N., W. E. Neff, E. Selke and D. Weisleder, Lipids 17: 11 (1982).

    Article  CAS  Google Scholar 

Methyl linolenate—autoxidation (see also references 3,4 and 10)

  1. Frankel, E. N., W. E. Neff, W. K. Rohwedder, B. P. S. Khambay, R. F. Garwood and B. C. L. Weedon, Lipids 12: 1055 (1977).

    Article  CAS  Google Scholar 

  2. Chan, H. W.-S., J. A. Matthew and D. T. Coxon, Chem. Commun. 235 (1980).

  3. Neff, W. E., E. N. Frankel and D. Weisleder, Lipids 16: 439 (1981).

    Article  CAS  Google Scholar 

Methyl linolenate—photooxygenation (see also references 3-7)

  1. O’Connor, D. E., E. D. Mihelich and M. C. Coleman, J. Am. Chem. Soc. 103: 223 (1981).

    Article  CAS  Google Scholar 

  2. Coxon, D. T., K. R. Price and H. W.-S. Chan, Chem. Phys. Lipids 28: 365 (1981).

    Article  CAS  Google Scholar 

  3. Neff, W. E., E. N. Frankel and D. Weisleder, Lipids 17: 780 (1982).

    Article  CAS  Google Scholar 

  4. Frankel, E. N., W. E. Neff and D. Weisleder, Chem. Commun. 599 (1982).

Chemical synthesis

  1. Corey, E. J., A. Marfat, J. R. Falck and J. O. Albright, J. Am. Chem. Soc. 102: 1433 (1980).

    Article  CAS  Google Scholar 

  2. Corey, E. J., J. O. Albright, A. E. Barton and S. Hashimoto, Ibid. 102: 1435 (1980).

    Article  CAS  Google Scholar 

  3. Porter, N. A., B. A. Weber, H. Weenen and J. A. Khan, Ibid. 102: 5597 (1980).

    Article  CAS  Google Scholar 

  4. Porter, N. A., D. H. Roberts and C. B. Zeigler Jr. Ibid. 102: 5912 (1980).

    Article  CAS  Google Scholar 

  5. Porter, N. A., A. N. Roe and A. T. McPhail, Ibid. 102: 7574 (1980).

    Article  CAS  Google Scholar 

  6. Frankel, E. N., D. Weisleder and W. E. Neff, Chem. Commun. 766 (1981).

  7. Bascetta, E., Ph.D. thesis, University of St. Andrews, 1983.

Enzymic oxidation—plant systems

  1. Veldink, G. A., J. F. G. Vliegenthart and J. Boldingh, Prog. Chem. Fats Other Lipids 15: 131 (1977).

    Article  CAS  Google Scholar 

  2. Zimmerman, D. C., and P. Feng, Lipids 13: 313 (1978).

    Article  CAS  Google Scholar 

  3. Vick, B. A., P. Feng and D. C. Zimmerman, Lipids 15: 468 (1980).

    Article  CAS  Google Scholar 

  4. Feng, P., B. A. Vick and D. C. Zimmerman, Lipids 16: 377 (1981).

    Article  CAS  Google Scholar 

  5. Van Os, C. P. A., G. P. M. Rijke-Schilder, H. van Halbeek, J. Verhagen and J. F. G. Vliegenthart, Biochim. Biophys. Acta, 663: 177 (1981).

    Google Scholar 

Enzymic oxidation—animal systems

  1. Nelson, N. A., R. C. Kelly and R. A. Johnson, Chem. Eng. News, 16 Aug.: 30 (1982).

  2. Ackroyd, J., and F. Scheinmann, Chem. Soc. Rev. 11: 321 (1982).

    Article  CAS  Google Scholar 

  3. Kikuchi, M., and Y. Tsukitani, Tetrahedron Lett. 23: 5171 (1982); Kobayashi, M., T. Yasuzawa, M. Yoshihara, H. Akutsu, Y. Kyogoku and I. Kitigawa, Ibid. Tetrahedron Lett. 23: 5331 (1982).

    Article  CAS  Google Scholar 

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Gunstone, F.D. Reaction of oxygen and unsaturated fatty acids. J Am Oil Chem Soc 61, 441–447 (1984). https://doi.org/10.1007/BF02678811

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