Abstract
The first dyes based on naphtho[1,8-bc]thiophen-3-(2H)-one were synthesized. The carbonyl group of these compounds has lower reactivity than the carbonyl group of naphthostyryl in condensation with arylamines.
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G. M. Oksengendler and É. P. Gendrikov, Ukr. Khim. Zh., 26, 672 (1960).
R. Herz and J. Müller, German Patent No. 545114 (1932); Chem. Zentralblatt, 2, 300 (1932).
M. A. Mostoslavskii, S. I. Saenko, and G. A. Yugai, Zh. Vses. Khim. O-va, 13, 462 (1968).
French Patent No. 2005697 (1969); Chem. Abstr., 73, 57175 (1970).
D. J. Curtin and J. W. Hausser, J. Am. Chem. Soc., 83, 3474 (1961).
A. W. Weston and R. J. Michaels, J. Am. Chem. Soc., 73, 1381 (1951).
J. R. Van Wazer, Phosphorus and Its Compounds, Interscience, New York-London (1958).
G. Becker, Introduction to the Electronic Theory of Organic Reactions [Russian translation], Mir, Moscow (1965), p. 247.
A. Weissberger and E. Proskauer, Organic Solvents [Russian translation], Inostr. Lit., Moscow (1958), p. 36.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1036–1038, August, 1976.
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Mostoslavkii, M.A., Saenko, S.I., Nazar'ko, V.G. et al. Substituted 2-aryliminonaphtho[1,8-bc]thiophene. Chem Heterocycl Compd 12, 857–859 (1976). https://doi.org/10.1007/BF00510100
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DOI: https://doi.org/10.1007/BF00510100