Skip to main content
Log in

Conversion of N-(1-keto-1-aryl-2-alkyl) nitrones to 4-hydroxy-2,3,4,5-tetrahydro-1,2,4-triazines

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The reaction of N-(1-keto-1-aryl-2-alkyl)nitrones with hydrazine gives 4-hydroxy-2,3,4,5-tetrahydro-1, 2,4-triazines, the oxidation of which with lead dioxide gives 1,2,4-triazine 4-oxides.

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. E. Bellasio, F. Parravicini, A. Vigevani, and E. Testa, Gazz. Chim. Ital., 98, 1014 (1968).

    Google Scholar 

  2. L. B. Volodarskii and A. Ya. Tikhonov, Zh. Organ. Khim., 6, 307 (1970).

    Google Scholar 

  3. L. B. Volodarskii and T. K. Sevast'yanova, Zh. Organ. Khim., 7, 1687 (1971).

    Google Scholar 

  4. C. M. Atkinson and H. D. Cossey, J. Chem. Soc., C, 1805 (1962).

    Google Scholar 

  5. L. Bellamy, Infrared Spectra of Complex Molecules, Methuen (1958).

  6. H. Neunhoeffer, F. Weischedel, and V. Bohnisch, Ann., 750 12 (1971).

    Google Scholar 

  7. F. A. Daniher and B. E. Hackley, J. Org. Chem., 31, 4267 (1966).

    Google Scholar 

  8. R. Metze, Ber., 91, 1863 (1958).

    Google Scholar 

  9. C. M. Atkinson and H. D. Cossey, J. Chem. Soc., C, 1628 (1963).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 134–136, January, 1973.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sevast'yanova, T.K., Volodarskii, L.B. Conversion of N-(1-keto-1-aryl-2-alkyl) nitrones to 4-hydroxy-2,3,4,5-tetrahydro-1,2,4-triazines. Chem Heterocycl Compd 9, 123–125 (1973). https://doi.org/10.1007/BF00476169

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00476169

Keywords

Navigation