Skip to main content
Log in

Iminofurans chemistry: IV. Synthesis and structure of 2-N-aryl-substituted derivatives of 2-amino-4-aryl-4-oxobut-2-enoic and 2-amino-5,5-dimethyl-4-oxohex-2-enoic acids

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

Abstract

Reactions of arylamines with 4-aryl-2-hydroxy-4-oxobut-2-enoic and 2-hydroxy-5,5-dimethyl-4-oxohex-2-enoic acids gave rise to 4-aryl-2-arylamino-4-oxobut-2-enoic and 2-aryl-amino-5,5-dimethyl-4-oxohex-2-enoic acids that existed in solutions as Z- and E-isomers or in a ring form as 3-arylamino-5-tert-butyl-5-hydroxyfuran-2(5H)-ones. The probable cyclization mechanism of these compounds into 5-R-3-arylimino-3H-furan-2-one derivatives was considered.

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

References

  1. Shipilovskikh, S.A., Rubtsov, A.E., and Zalesov, V.V., Khim. Geterotsikl. Soedin., 2009.

  2. Rubtsov, A.E. and Zalesov, V.V., Zh. Org. Khim., 2003, vol. 39, p. 918.

    Google Scholar 

  3. Bukanova, E.V., Cand. Sci. (Chem.) Dissertation, Perm, 2004.

  4. Koz’minykh, V.O., Belyaev, A.O., Koz’minykh, E.N., Makhmudov, R.R., and Odegova, T.F., Khim.-Farm. Zh., 2004, vol. 38, no. 8, p. 25.

    Google Scholar 

  5. Koz’minykh, V.O. and Koz’minykh, E.N., Khim.-Farm. Zh., 2004, vol. 38, no. 2, p. 10.

    Google Scholar 

  6. Koz’minykh, V.O., Belyaev, A.O., Koz’minykh, E.N., Odegova, T.F., and Makhmudov, R.R., Khim.-Farm. Zh., 2004, vol. 38, no. 11, p. 19.

    Google Scholar 

  7. Belyaev, A.O., Cand. Sci. (Chem.) Dissertation, Perm, 2004.

  8. Koz’minykh, V.O., Bukanova, E.V., Belyaev, A.O., and Koz’minykh, E.N., Khim. Geterotsikl. Soedin., 2003, p. 1427.

  9. Gein, V.L., Kon’shina, L.O., and Andreichikov, Yu.S., Zh. Org. Khim., 1992, vol. 28, p. 2134.

    CAS  Google Scholar 

  10. Koz’minykh, E.N., Belyaev, A.O., Koz’minykh, V.O., Makhmudov, R. R., and Odegova, T.F., Khim.-Farm. Zh., 2002, vol. 36, no. 11, p. 28.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to A. E. Rubtsov.

Additional information

Original Russian Text © N.M. Igidov, A.E. Rubtsov, A.V. Tyuneva, V.V. Zalesov, A.Yu. Borodin, E.V. Bukanova, 2009, published in Zhurnal Organicheskoi Khimii, 2009, Vol. 45, No. 5, pp. 716–721.

For communication III, see [1].

Rights and permissions

Reprints and permissions

About this article

Cite this article

Igidov, N.M., Rubtsov, A.E., Tyuneva, A.V. et al. Iminofurans chemistry: IV. Synthesis and structure of 2-N-aryl-substituted derivatives of 2-amino-4-aryl-4-oxobut-2-enoic and 2-amino-5,5-dimethyl-4-oxohex-2-enoic acids. Russ J Org Chem 45, 698–704 (2009). https://doi.org/10.1134/S1070428009050091

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1070428009050091

Keywords

Navigation