Abstract
The reaction of 2, 3-dimethylquinoxaline and its mono-N-oxide with aromatic aldehydes and nitroso and diazo compounds has been studied. It has been found that the introduction of the N-oxide group increases the reactivity of a methyl group in the α-position with respect to it. Some properties of the compounds obtained have been studied.
Similar content being viewed by others
References
In memory of A. E. Porai-Koshits [in Russian], GKhl, Moscow and Leningrad, p. 21, 1949.
I. M. Mishina and L. S. Efros, ZhOKh, 32, 2217, 1962.
W. Borsche and W. Doeller, Ann., 537, 39, 1939.
S. N. Baranov and N. E. Plevachuk-Tarnavskaya, Ukr. khim. zh., 29, 82, 1963.
A. S. Elina, ZhOKh, 31, 1018, 1961.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Plevachuk, N.E., Baranov, S.N. Electrophilic substitution reactions in 2, 3-dimethylquinoxaline and its N-oxide. Chem Heterocycl Compd 4, 536–537 (1971). https://doi.org/10.1007/BF00486781
Issue Date:
DOI: https://doi.org/10.1007/BF00486781