Abstract
The conditions for the formation of N-substituted aromatic amines in the sulfite variant of recyclization of pyridinium salts, as well as the structural factors that affect the yields of the final substances, were investigated.
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R. S. Sagitullin, S. P. Gromov, and A. N. Kost, Dokl. Akad. Nauk SSSR, 243, 937 (1978).
A. N. Kost, A. Fadda, R. S. Sagitullin, S. P. Gromov, T. I. Petrunina, and P. A. Sharbatyan, Khim. Geterotsikl. Soedin., No. 9, 1214 (1983).
A. N. Kost, D. V. Yashunskii, S. P. Gromov, and R. S. Sagitullin, Khim. Geterotsikl. Soedin., No. 9, 1268 (1980).
Ya. F. Freimanis, in: The Chemistry of Enamino Ketones, Enamino Imines, and Enamino Thiones [in Russian], Zinatne, Riga (1974), p. 211.
R. S. Sagitullin, S. P. Gromov, and A. N. Kost, Tetrahedron, 34, 2213 (1978).
W. C. Still, M. Kahn, and A. Mitra, J. Org. Chem., 43, 2923 (1978).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1095–1098, August, 1985.
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Shkil', G.P., Khristolyubova, O.V., Lugovik, B.A. et al. Recyclization of pyridinium salts with exchange as a method for the preparation of N-substituted aromatic amines. Chem Heterocycl Compd 21, 914–917 (1985). https://doi.org/10.1007/BF00519822
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DOI: https://doi.org/10.1007/BF00519822