Skip to main content
Log in

Pummerer reaction in synthesis and transformations of heterocyclic compounds (review)

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Data on the use of the Pummerer reaction in the synthesis and transformations of various heterocyclic compounds that contain oxygen, sulfur, and nitrogen as the heteroatoms are correlated.

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

Access this article

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

Instant access to the full article PDF.

Similar content being viewed by others

Literature Cited

  1. R. Pummerer, Chem. Ber., 42, 2288 (1909).

    Google Scholar 

  2. S. Oae, Topics in Organic Sulfur Chemistry. Plenary Lectures of the 8th International Symposium on Organic Sulfur Chemistry, Portoroz, Yugoslavia, June 18–23, 1978, p. 290.

  3. A. Posowsky, and K. N. Chen, J. Org. Chem., 38, 2073 (1973).

    Google Scholar 

  4. Y. Oikawa and O. Yonemitsu, J. Org. Chem., 47, 1118 (1976).

    Google Scholar 

  5. Y. Oikawa and O. Yonemitsu, J.Chem. Soc., Perkin 1, No. 13, 1479 (1976).

    Google Scholar 

  6. Y. Oikawa and O. Yonemitsu, Heterocycles, 5, 233 (1976).

    Google Scholar 

  7. D. T. Connor and M. Strandtmann, J. Org. Chem., 39, 1594 (1974).

    Google Scholar 

  8. D. T. Connor and I. R. Sorenson, J. Heterocycl. Chem., 18, 587 (1981).

    Google Scholar 

  9. Y. Oikawa and O. Yonemitsu, Tetrahedron, 30, 2653 (1974).

    Google Scholar 

  10. T. Numata and S. Oae, Chem. Ind., No. 18, 726 (1972).

    Google Scholar 

  11. S. Oae and T. Numata, Tetrahedron, 30, 2641 (1974).

    Google Scholar 

  12. T. Numata and S. Oae, Chem. Ind., No. 6, 277 (1973).

    Google Scholar 

  13. B. Stridsberg and S. Allenmark, Acta Chem. Scand., B28, 591 (1974).

    Google Scholar 

  14. B. Stridsberg and S. Allenmark, Acta Chem. Scand., B30, 219 (1976).

    Google Scholar 

  15. Y. Tamura, H. -D. Choi, H. Shindo, J. Uenishi, and H. Ishibashi, Tetrahedron Lett., 22, 81 (1981).

    Google Scholar 

  16. M. Watanabe, S. Nakamori, and H. Hasegawa, Bull. Chem. Soc. Japan, 53, 817 (1981).

    Google Scholar 

  17. S. Wolfe, P. M. Kazmaier, and H. Auksi, Can. J. Chem., 57, 2412 (1979).

    Google Scholar 

  18. H. L. Yale, J. Heterocycl. Chem., 15, 331 (1978).

    Google Scholar 

  19. D. K. Bates, R. T. Winters, and B. A. Sell, J. Heterocycl. Chem., 23, 695 (1986).

    Google Scholar 

  20. N. V. Fedorov, M. V. Shevchenko, A. V. Anisimov, and E. A. Viktorova, Khim. Geterotsikl. Soedin., No. 6, 747 (1985).

    Google Scholar 

  21. V. V. Litvinova, N. V. Fedorov, A. V. Anisimov, and E. A. Viktorova, Khim. Geterotsikl. Soedin., No. 12, 1601 (1987).

    Google Scholar 

  22. T. Numata, O. Itoh, and S. Oae, Chem. Lett., No. 8, 909 (1977).

    Google Scholar 

  23. Y. Makisumi, S. Takada, and Y. Matsukura, J. Chem. Soc., Chem. Commun., No. 20, 850 (1974).

    Google Scholar 

  24. A. G. Shultz, Tetrahedron Lett., No. 48, 4791 (1973).

    Google Scholar 

  25. D. Connor, P. Young, and M. Strandtman, J. Heterocycl. Chem., 15, 115 (1978).

    Google Scholar 

  26. R. R. King, J. Org. Chem., 45, 5347 (1980).

    Google Scholar 

  27. R. R. King, J. Org. Chem., 43, 1262 (1978).

    Google Scholar 

  28. W. E. Parham and R. Koncos, J. Am. Chem. Soc., 83, 4034 (1961).

    Google Scholar 

  29. R. B. Morin, D. C. Spry, and R. A. Mueller, Tetrahedron Lett., No. 11, 849 (1969).

    Google Scholar 

  30. E. N. Karaulova, G. D. Gal'pern, V. D. Nikitina, I. V. Cherepanova, and L. R. Barynina, Neftekhimiya, 12, 104 (1972).

    Google Scholar 

  31. W. E. Parham, L. Christensen, S. Groen, and R. Dodson, J. Org. Chem., 29, 2211 (1964).

    Google Scholar 

  32. S. Lane, J. S. Quik, and R. Tailor, Tetrahedron Lett., 25, 1039 (1984).

    Google Scholar 

  33. N. V. Fedorov, A. V. Anisimov, and E. A.Viktorova, Zh. Org. Khim., 24, 567 (1988).

    Google Scholar 

  34. R. Praefcke and Ch. Weichsel, Annalen, No. 6, 784 (1977).

    Google Scholar 

  35. W. E. Parham and M. B. Bhavsar, J. Org. Chem., 28, 2686 (1963).

    Google Scholar 

  36. M. Hori, T. Kataoka, H. Shimizu, and N. Ueda, Tetrahedron Lett., 22, 1701 (1981).

    Google Scholar 

  37. K. Yamamoto, S. Yamazaki, and I. Murata, J. Org. Chem., 52, 5239 (1987).

    Google Scholar 

  38. J. Garcia, C. Ortiz, and R. Greenhouse, J. Org. Chem., 53, 2634 (1988).

    Google Scholar 

  39. R. B. Morin, B. G. Jakson, R. A. Mueller, E. R. Lavagnino, W. B. Scanlon, and S. L. Andrews, J. Am. Chem. Soc., 85, 1896 (1963).

    Google Scholar 

  40. R. B. Morin, B. G. Jakson, R. A. Mueller, E. R. Lavagnino, W. B. Scanlon, and S. L. Andrews, J. Am. Chem. Soc., 91, 1401 (1969).

    Google Scholar 

  41. R. B. Morin and D. C. Spry, J. Chem. Soc., D, No. 6, 335 (1970).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1299–1313, October, 1989.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Fedorov, N.V., Anisimov, A.V. & Viktorova, E.A. Pummerer reaction in synthesis and transformations of heterocyclic compounds (review). Chem Heterocycl Compd 25, 1083–1096 (1989). https://doi.org/10.1007/BF00470683

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00470683

Keywords

Navigation