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Russian Journal of Organic Chemistry

, Volume 41, Issue 9, pp 1387–1391 | Cite as

New Synthesis of Formylbenzoazacrown Ethers

  • S. N. Dmitrieva
  • O. V. Tikhonova
  • S. P. Gromov
Article

Abstract

A new procedure has been developed for the synthesis of formyl-substituted benzoazacrown ethers via cyclization of halogen derivatives of aza podands by the action of sodium hydride.

Keywords

Sodium Ether Organic Chemistry Hydride Halogen 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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REFERENCES

  1. 1.
    Cation Binding by Macrocycles, Inoue, Y. and Gokel, G.W., Eds., New York: Marcel Dekker, 1990.Google Scholar
  2. 2.
    Izatt, R.M., Pawlak, K., Bradshaw, J.S., and Bruening, R.L., Chem. Rev., 1991, vol. 91, p. 1721.CrossRefGoogle Scholar
  3. 3.
    de Silva, A.P., Gunaratne, H.Q.N., Gunnlaugsson, T., Huxley, A.J.M., McCoy, C.P., Rademacher, J.T., and Rice, T.E., Chem. Rev., 1997, vol. 97, p. 1515.Google Scholar
  4. 4.
    Alfimov, M.V. and Gromov, S.P., Applied Fluorescence in Chemistry, Biology, and Medicine, Rettig, W., Strehmel, B., Schrader, S., and Seifert, H., Eds., Berlin: Springer, 1999, p. 161.Google Scholar
  5. 5.
    Valeur, B. and Leray, I., Coord. Chem. Rev., 2000, vol. 205, p. 3.CrossRefGoogle Scholar
  6. 6.
    Shinkai, S., Comprehensive Supramolecular Chemistry, Gokel, G.W., Ed., Oxford: Pergamon, 1996, vol. 1, p. 671.Google Scholar
  7. 7.
    Gromov, S.P. and Alfimov, M.V., Izv. Ross. Akad. Nauk, Ser. Khim., 1997, p. 641.Google Scholar
  8. 8.
    Mishra, A., Behera, R.K., Behera, P.K., Mishra, B.K., and Behera, G.B., Chem. Rev., 2000, vol. 100, p. 1973.Google Scholar
  9. 9.
    Yordanov, A.T. and Roundhill, D.M., Coord. Chem. Rev., 1998, vol. 170, p. 93.CrossRefGoogle Scholar
  10. 10.
    Gloe, K., Graubaum, H., Wust, M., Rambusch, T., and Seichter, W., Coord. Chem. Rev., 2001, vol. 22, p. 103.Google Scholar
  11. 11.
    Buhlmann, P., Pretsch, E., and Bakker, E., Chem. Rev., 1998, vol. 98, p. 1593.CrossRefGoogle Scholar
  12. 12.
    Gromov, S.P., Dmitrieva, S.N., and Churakova, M.V., Usp. Khim., 2005, vol. 74, p. 503.Google Scholar
  13. 13.
    Gromov, S.P., Dmitrieva, S.N., Vedernikov, A.I., and Churakova, M.V., Izv. Ross. Akad. Nauk, Ser. Khim., 2004, p. 1362.Google Scholar
  14. 14.
    Gromov, S.P., Vedernikov, A.I., and Fedorova, O.A., Izv. Ross. Akad. Nauk, Ser. Khim., 1995, p. 950.Google Scholar
  15. 15.
    Gromov, S.P., Vedernikov, A.I., and Fedorova, O.A., Izv. Ross. Akad. Nauk, Ser. Khim., 1996, p. 687.Google Scholar
  16. 16.
    Wada, F., Hirayama, H., Namiki, H., Kikukawa, K., and Matsuda, T., Bull. Chem. Soc. Jpn., 1980, vol. 53, p. 1473.Google Scholar
  17. 17.
    Stempnevskaya, I.A., Kalashnikova, S.P., and Tashmukhamedova, A.K., Uzb. Khim. Zh., 1990, p. 113.Google Scholar
  18. 18.
    Gromov, S.P., Vedernikov, A.I., and Dmitrieva, S.N., Izv. Ross. Akad. Nauk, Ser. Khim., 1999, p. 1204.Google Scholar
  19. 19.
    Gromov, S.P., Vedernikov, A.I., and Dmitrieva, S.N., Russian Patent no. 2161153, 2000; Byull. Izobret., 2000, no. 36, p. 320.Google Scholar
  20. 20.
    Gromov, S.P., Dmitrieva, S.N., Vedernikov, A.I., Kuz'mina, L.G., Churakov, A.V., Strelenko, Y.A., and Howard, J.A.K., Eur. J. Org. Chem., 2003, p. 3189.Google Scholar
  21. 21.
    Avakyan, V.G., Gromov, S.P., Vedernikov, A.I., Dmitrieva, S.N., and Alfimov, M.V., Izv. Ross. Akad. Nauk, Ser. Khim., 2004, p. 25.Google Scholar

Copyright information

© MAIK "Nauka/Interperiodica" 2005

Authors and Affiliations

  • S. N. Dmitrieva
    • 1
  • O. V. Tikhonova
    • 1
  • S. P. Gromov
    • 1
  1. 1.Photochemistry CenterRussian Academy of SciencesMoscowRussia

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