Skip to main content
Log in

S(2)- or N(3)-Substituted 2-Mercapto-5-(4-pyridyl)-1,3,4-oxadiazoles

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

New S(2)- or N(3)-substituted 2-mercapto-5-(4-pyridyl)-1,3,4-oxadiazoles have been obtained and characterized. The direction of substitution depends on the structure of the initial reactants and the reaction conditions. The synthesis of several thiosemicarbazides has been effected from isonicotinic acid hydrazide.

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. H. Liszkiewicz, T. Glowiak, M. W. Kowalska, M. Rutkowska, A. Szelag, J. Barczynska, L. Kedzierska-Gozdzik, F. Blaszczyk, and W. Dziewiszek, Pol. J. Chem., 73, 321 (1999).

    Google Scholar 

  2. A. Rutavicius, S. Valyulene, and Z. Kuodis, Khim. Geterotsikl. Soedin., 966 (2000).

  3. V. Yakubkene and P. Vainilavicius, Khim. Geterotsikl. Soedin., 1125 (1998).

  4. S. I. Yakimovich, V. I. Nikolaev, and O. A. Afonina, Zh. Org. Khim., 15, 922 (1979).

    Google Scholar 

  5. A. Rutavicius and V. Mozolis, Trud. Akad. Nauk LitSSR, Ser. B, 5(126), 81 (1981).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rutavicius, A., Kuodis, Z. S(2)- or N(3)-Substituted 2-Mercapto-5-(4-pyridyl)-1,3,4-oxadiazoles. Chemistry of Heterocyclic Compounds 38, 852–858 (2002). https://doi.org/10.1023/A:1020646123616

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1020646123616

Navigation