Skip to main content
SpringerLink
Log in

Synthesis and properties of ω-(hydroxyaryl)alkylsulfides based on 2-isobornyl-6-methyl-4-propylphenol

  • Published:
Russian Journal of General Chemistry Aims and scope Submit manuscript

Abstract

Proceeding from 2-isobornyl-6-methyl-4-propylphenol new derivatives have been synthesized having sulfur atoms included in different functional groups. Antiradical and antioxidant activity, as well as membrane-protecting properties of the derivatives of 2-isobornyl-6-methyl-4-propylphenol in chemical and biological model systems have been investigated.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Log in via an institution

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Gorbunov, B.N., Gurvich, Ya.A., and Maslova, I.P., Khimiya i tekhnologiya stabilizatorov polimernykh materialov (Chemistry and Technology of Polymeric Materials Stabilizers), Moscow: Khimiya, 1981, p. 386.

    Google Scholar 

  2. Nechaev, A.P., Traubenberg, S.E., and Kochetkova, A.A., Pishchevaya khimiya (Food Chemistry), St. Petersburg: GIODR, 2001, p. 592.

    Google Scholar 

  3. Zarudii, F.S., Gil’mutdinov, G.Z., Zarudii, R.F., Myshkin, M.A., Gershanov, F.B., and Novikov, T.A., Pharm. Chem. J., 2001, vol. 35, no. 3, p. 162. doi 10.1023/A:1010414130628

    Article  CAS  Google Scholar 

  4. Tolstorozhev, G.B., Skornyakov, I.V., Bel’kov, M.V., Shadyro, O.I., Polozov, G.I., Sorokin, V.L., and Ksendzova, G.A., Optics Spectrosc., 2012, vol. 112, no. 5, p. 720. doi 10.1134/S0030400X12050207

    Article  CAS  Google Scholar 

  5. Chukicheva, I.Yu. and Kuchin, A.V., Ross. Khim. Zh., 2004, vol. 48, no. 3, p. 21.

    CAS  Google Scholar 

  6. Mazaletskaya, L.I., Sheludchenko, N.I., Shishkina, L.N., Kuchin, A.V., Fedorova, I.V., and Chukicheva, I.Yu., Petroleum Chem., 2011, vol. 51, no. 5, p. 348. doi 10.1134/S0965544111050100

    Article  CAS  Google Scholar 

  7. Plotnikov, M.B., Smolyakova, V.I., Ivanov, I.S., Buravlev, E.V., Chukicheva, I.Yu., Kutchin, A.V., and Krasnov, E.A., Pharm. Chem. J., 2011, vol. 44, no. 10, p. 530. doi 10.1007/s11094-011-0511-4

    Article  CAS  Google Scholar 

  8. Plotnikov, M.B., Chernysheva, G.A., Smolyakova, V.I., Ivanov, I.S., Kuchin, A.V., Chukicheva, I.Yu., and Krasnov, E.A., Vestn. Ross. Akad. Med. Nauk, 2009, vol. 11, p. 12.

    Google Scholar 

  9. Shevchenko, O.G., Plyusnina, S.N., Shishkina, L.N., Chukicheva, I.Yu., Fedorova, I.V., and Kuchin, A.V., Biol. Membrany, 2013, vol. 30, no. 1, p. 40. doi 10.7868/S0233475512060060

    CAS  Google Scholar 

  10. Prosenko, A.E., Kandalintseva, N.V., and Yagunov, S.A., Lektsii i tezisy Mezhdunar. konf. molod. uchenykh i VII shkoly akad. N.A. Emanuel “Okislenie, okislitel’nyi stress, antioksidanty” (Lectures and Abstracts of the Int. Conf. of Young Scientists and VII School of Acad. N.M. Emanuel “Oxidation, Oxidative Stress, Antioxidant”), Moscow, 2015, p. 33.

    Google Scholar 

  11. Terakh, E.I., Prosenko, A.E., Nikulina, V.V., and Zaitseva, O.V., Russ. J. Appl. Chem., 2003, vol. 76, no. 2, p. 253. doi 10.1023/A:1024602729156

    Article  CAS  Google Scholar 

  12. Prosenko, A.E., Terakh, E.I., Gorokh, E.A., Nikulina, V.V., and Grigor’ev, I.A., Russ. J. Appl. Chem., 2003, vol. 76, no. 2, p. 248. doi 10.1023/A:1024650612317

    Article  CAS  Google Scholar 

  13. Author’s Certificate 1072420, 1983.

  14. RF Patent 1007405, 1993.

  15. RF Patent 2367420, 2009.

  16. Han, C.-C. and Balakumar, R., Tetrahedron Lett., 2006, vol. 47, p. 8255. doi 10.1016/j.tetlet.2006.09.093

    Article  CAS  Google Scholar 

  17. Kandalintseva, N.V., Prosenko, A.E., Dyubchenko, O.I., and Stoyanov, E.S., J. Org. Chem., 2001, vol. 37, no. 9, p. 1249. doi 10.1023/A:1013163000911

    CAS  Google Scholar 

  18. Khomchenko, A.S., Cand. Sci. (Chem.) Disseratation, Novosibirsk, 2010.

  19. Tsepalov, V.F., Kharitonova, A.A., Gladyshev, T.P., and Emanuel, N.M., Kinet. Katal., 1977, vol. 18, no. 5, p. 1261.

    CAS  Google Scholar 

  20. Aleksandrov, A.L. and Denisov, A.A., Izv. Akad. Nauk SSSR, Ser. Khim., 1969, no. 8, p. 1652.

    Google Scholar 

  21. Tsepalov, V.F. and Slyapintokh, V.Ya., Kinet. Katal., 1962, vol. 3, p. 870.

    CAS  Google Scholar 

  22. Takebayashi, J., Chen, J., and Tai, A., Adv. Protocols in Oxidative Stress, Meth. Mol. Biol., 2010. 594, p. 287.

    Article  CAS  Google Scholar 

  23. Ko, F.N., Hsiao, G., and Kuo, Y.H., Free Radic. Biol. Med., 1997, vol. 22, p. 215.

    Article  CAS  Google Scholar 

  24. López-Revuelta, A., Sánchez-Gallego, J.I., Hermandez-Hernandez, A., Sánchez-Yague, J., and Llanillo, M., Chem. Biol. Interact., 2006, vol. 161, p. 79.

    Article  Google Scholar 

  25. Banerjee, A., Kunwar, A., Mishra, B., and Priyadarsini, K.I., Chem. Biol. Interact., 2008, vol. 174 (2), p. 134.

    Article  CAS  Google Scholar 

  26. Costa, R.M., Magalhães, A.S., Pereira, J.A., Andrade, P.B., Valentao, P., Carvalho, M., and Silva, B.M., Food Chem. Toxicol., 2009, vol. 47, p. 860.

    Article  CAS  Google Scholar 

  27. Wang, C., Qin, X., Huang, B., He, F., and Zeng, C., Biochem. Bioph. Res. Commun., 2010, vol. 402, p. 773.

    Article  CAS  Google Scholar 

  28. Asakawa, T. and Matsushita, S., Lipids., 1980, vol. 15, p. 137.

    Article  CAS  Google Scholar 

  29. Berg, J.A., Kamp, J.A.F., Lubin, A.H., Roelofsen, A., and Kuypers, F.A., Free Radic. Biol. Med., 1992, vol. 12, no. 6, p. 487.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Institute of Chemistry, Komi Scientific Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, Syktyvkar, Komi Republic, 167982, Russia

    I. Yu. Chukicheva, O. V. Sukrusheva, O. A. Shumova & A. V. Kuchin

  2. Emanuel Institute of Biochemical Physics of Russian Academy of Sciences, Moscow, Russia

    L. I. Mazaletskaya

  3. Institute of Biology, Komi Scientific Center, Ural Branch, Russian Academy of Sciences, Komi Republic, Syktyvkar, Russia

    O. G. Shevchenko

Authors
  1. I. Yu. Chukicheva
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. O. V. Sukrusheva
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. O. A. Shumova
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. L. I. Mazaletskaya
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. O. G. Shevchenko
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. A. V. Kuchin
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to O. V. Sukrusheva.

Additional information

Original Russian Text © I.Yu. Chukicheva, О.V. Sukrusheva, O.A. Shumova, L.I. Mazaletskaya, O.G Shevchenko, А.V. Kuchin, 2016, published in Zhurnal Obshchei Khimii, 2016, Vol. 86, No. 9, pp. 1487–1494.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Chukicheva, I.Y., Sukrusheva, O.V., Shumova, O.A. et al. Synthesis and properties of ω-(hydroxyaryl)alkylsulfides based on 2-isobornyl-6-methyl-4-propylphenol. Russ J Gen Chem 86, 2052–2058 (2016). https://doi.org/10.1134/S1070363216090127

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1070363216090127

Keywords

Search

Navigation