Conclusions
The electrolytic oxidation of the 3-nitro-1,2,4-triazole anion is realized through an intermediate radical, which splits out an H atom on reaction with the medium and reacts with benzene to give N-substituted phenyl-3-nitro-1,2,4-triazoles.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
Literature cited
V. A. Petrosyan and M. E. Niyazymbetov, Izv. Akad. Nauk SSSR, Ser. Khim., 368 (1988).
V. A. Petrosyan and M. E. Niyazymbetov, Izv. Akad. Nauk SSSR, Ser. Khim., 603 (1987).
J. Elguero, C. Marzin, and J. Roberts, J. Org. Chem.,39, 357 (1974).
P. Dvortsak, J. Reiter, T. Somorai, and P. Sohar, Magn. Reson. Chem.,23, 194 (1985).
D. Wofford, D. Forkey, and J. Russel, J. Org. Chem.,47, 5132 (1982).
G. Hawkes, E. Randall, J. Elguero, and C. Marzin, J. Chem. Soc., Perkin Trans.2, 1024 (1977).
A. Fruchier, V. Pelegrin, R. Schimpt, and J. Elguero, Org. Magn. Reson.,48, 10 (1982).
T. Shono, S. Kashimura, and H. Nogusa, Chem. Lett., 425 (1986).
L. I. Bagal, M. S. Pevzner, A. N. Frolova, and N. I. Sheludyakova, Khim. Geterotsikl. Soedin., 259 (1970).
Author information
Authors and Affiliations
Additional information
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1643–1646, July, 1988.
Rights and permissions
About this article
Cite this article
Petrosyan, V.A., Niyazymbetov, M.E., Pevzner, M.S. et al. Electrode transformations of carbanions and heteroanions. Russ Chem Bull 37, 1458–1461 (1988). https://doi.org/10.1007/BF00962762
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00962762