Abstract
A general method for the synthesis of substituted 8-amino-2-quinolono-5,6-quinones by oxidation with simultaneous animation of 6-hydroxy-2-quinolones is described. The stepwise course of the process and several properties of the compounds obtained are studied.
Similar content being viewed by others
Literature cited
G. R. Pettit and L. E. Houghton, J. Med. Chem.,11, 1080 (1968).
R. R. Holmes, J. Conrady, J. Gutherie, and R. McKay, J. Am. Chem. Soc.,76, 2400 (1954).
G. R. Pettit, W. C. Fleming, and K. D. Raulle, J. Org. Chem.,33, 1089 (1968).
W. Brackman and E. Havinga, Rec. Trav. Chim.,74, 1107 (1955).
Yu. S. Tsizin and M. V. Rubtsov, Khim. Geterotsikl. Soed., No. 1, 285 (967).
W. W. Wendlaudt and J. Haschke, Nature,195, 379 (1962).
Yu. S. Tsizin and M. V. Rubtsov, Khim. Geterotsikl. Soed., 637 (1970).
Yu. S. Tsizin and M. V. Rubtsov, Khim. Geterotsikl. Soed., 682 (1969).
A. Albert, Physical Methods in the Chemistry of Heterocyclic Compounds [Russian translation], Khimiya, Moscow-Leningrad (1966), p. 92.
M. E. Pudel', and Yu. S. Tsizin, Khim. Geterotsikl. Soed., 1112 (1970).
Author information
Authors and Affiliations
Additional information
For Communication X, see [10].
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1376–1380, October, 1970.
Rights and permissions
About this article
Cite this article
Karpova, N.B., Tsizin, Y.S. Investigation of heterocyclic quinones. Chem Heterocycl Compd 6, 1283–1287 (1970). https://doi.org/10.1007/BF00755078
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00755078