Abstract
1,4-Dihydropyrimidines were synthesized by reductive dethionation of the corresponding 2-thiono-4-aryl-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid derivatives, and some of their properties were studied.
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Literature Cited
L. A. Ignatova, S. V. Baranov, and B. V. Unkovskii, in: Reactivity of Azines, Summary of Lectures [in Russian], Novosibirsk (1979), p. 93.
B. V. Unkovskii, L. A. Ignatova, P. L. Ovechkin, and L. I. Vinogradova, Khim. Geterotsikl. Soedin., No. 12, 1690 (1970).
A. Weis and F. Frolov, Chem. Communs, No. 12, 89 (1982).
A, L. Weis, Tetrahedron Lett., 23, 449 (1982).
C. Kashima, M. Shimitzu, A. Katoh, and Y. Omote, J. Chem. Soc., Perkin 1, No. 8, 1799 (1983).
C. Kashima, M. Shimitzu, A. Katoh, and Y. Omote, Tetrahedron Lett., 24, 209 (1983).
Ya. P. Stradyn', G. Ya. Dubur, Yu. I. Beilis, Ya. R. Uldrikis, and A. F. Korotokova, Khim. Geterotsikl. Soed., No. 1, 84 (1972).
V. P. Kadysh, Ya. P. Stradyn', E. L. Khanina, G. Ya. Dubur, and D. Kh. Mutsenietse, Khim. Geterotsikl. Soedin., No. 1, 117 (1985).
K. Folkers, H. J. Harwood, and T. B. Johnson, J. Am. Chem. Soc., 54, 3751 (1932).
G. Ya. Dubur and E. L. Khanina, Khim. Geterotsikl. Soedin., No. 2, 220 (1976).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1223–1227, September, 1986.
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Khanina, E.L., Mutsenietse, D.K., Kadysh, V.P. et al. Synthesis and properties of derivatives of 1,4-dihydropyrimidine-5-carboxylic acid. Chem Heterocycl Compd 22, 990–994 (1986). https://doi.org/10.1007/BF00478132
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DOI: https://doi.org/10.1007/BF00478132