Abstract
Under the influence of aqueous solutions of alkylammonium sulfites 2-(2-phenyl) ethyl)pyridinium salts undergo recyclization to 2-benzyl-N-alkylanilines. The effect of structural factors on the transamination, which takes place when a reagent with an alkyl group that differs from the alkyl group in the starting pyridinium salt is used, was investigated.
Similar content being viewed by others
Literature cited
A. N. Kost, S. P. Gromov, and R. S. Sagitullin, Tetrahedron, 37, 3423 (1981).
R. S. Sagitullin, S. P. Gromov, and A. N. Kost, Dokl. Akad. Nauk SSSR, 234, 634 (1977).
A. N. Kost, R. S. Sagitullin, and S. P. Gromov, Khim. Geterotsikl. Soedin., No. 3, 417 (1978).
R. S. Sagitullin, S. P. Gromov, and A. N. Kost, Dokl. Akad. Nauk SSSR, 243, 937 (1978).
A. N. Kost, R. S. Sagitullin, and A. A. Fadda, Khim. Geterotsikl. Soedin., No. 1, 125 (1981).
A. A. Fadda, Master's Dissertation, Moscow State University (1981).
Author information
Authors and Affiliations
Additional information
Deceased.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 63–65, January, 1983.
Rights and permissions
About this article
Cite this article
Yudin, L.G., Rumyantsev, A.N., Sagitullin, R.S. et al. Recyclization of 2-(2-phenylethyl)pyridinium salts. Chem Heterocycl Compd 19, 57–59 (1983). https://doi.org/10.1007/BF00512816
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00512816