Abstract
The existence of a quasi-tautomeric equilibrium in solutions of 5-hydroxy-5-phenyl-5H-pyrido[2,3-b]chromenes in sulfuric acid, which was confirmed by a linear dependence of the logarithms of the indicator ratios on acidity function HR — HO with a slope close to unity, was established. The pK values of this equilibrium correlate with the σ op and σ oR. substituent constants.
Similar content being viewed by others
Literature cited
V. M. Petrichenko and M. E. Konshin, Khim. Geterotsikl. Soedin., No. 5, 614 (1982).
V. M. Petrichenko and M. E. Konshin, Khim. Geterotsikl. Soedin., No. 6, 798 (1982).
N. C. Deno, J. J. Jaruzelski, and A. Schriesheim, J. Am. Chem. Soc., 77, 3044 (1955).
V. M. Petrichenko and M. E. Konshin, Zh. Org. Khim., 18, 2597 (1982).
N. G. Belotserkovskaya and O. F. Ginzburg, Dokl. Akad. Nauk SSSR, 185, 1098 (1964).
O. F. Ginzburg and V. V. Sinev, Izv. Sib. Otd. Akad. Nauk SSSR, Ser. Khim. Nauk, No. 7, 72 (1980).
A. I. Mikhalev and M. E. Konshin, Zh. Org. Khim., 13, 1111 (1977).
L. Hammett, Physical Organic Chemistry, McGraw-Hill (1970).
V. A. Palm, Fundamentals of the Quantitative Theory of Organic Reactions [in Russian], Khimiya, Leningrad (1977), p. 322.
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 753–755, June, 1984.
Rights and permissions
About this article
Cite this article
Petrichenko, V.M., Konshin, M.E. Quasi-tautomerism of 5-hydroxy-5-phenyl-5H-pyrido[2,3-b]chromenes in sulfuric acid. Chem Heterocycl Compd 20, 607–609 (1984). https://doi.org/10.1007/BF00508664
Received:
Revised:
Issue Date:
DOI: https://doi.org/10.1007/BF00508664