Abstract
Anhydronium bases of 2-chloro-α-carbolines and 3,4-dihydro-Β-carbolines are formed fay Beckmann rearrangement of Β- (3-indolyl) ketone oximes. In a number of cases the formation of anhydronium bases becomes the predominant process.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
Literature cited
T. M. Efremova, K. I. Kuchkova, and A. A. Semenov, Khim. Geterotsikl. Soedin., No. 10, 1382 (1974).
K. I. Kuchkova, A. A. Semenov, and I. V. Terent'eva, Khim. Geterotsikl, Soedin., No. 2, 197 (1970).
A. A. Semenov, I. V. Terent'eva, and E. P. Styngach, Khim. Geterotsikl. Soedin., No. 1, 38 (1967).
H. C. Brown, Tetrahedron, Suppl. 8, 149 (1966).
L. Stephenson and W. K. Warburton, J. Chem. Soc., C, 1355 (1970).
J. Szmuszkovicz, J. Amer. Chem. Soc., 79, 2819 (1957).
L. G. Donaruma and V. Z. Heldt, Organic Reactions [Russian translation], Vol. 11, Moscow (1965), p. 7.
M. E. Wolf, Chem. Rev., 63, 55 (1963).
Y. Kanaoka, E. Sato, and Y. Ban, Chem. Pharm. Bull., 15, 101 (1967).
R. H. Freak and R. Robinson, J. Chem. Soc., 2013 (1938).
Author information
Authors and Affiliations
Additional information
See [1] for communication VII.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 386–391, March, 1976.
Rights and permissions
About this article
Cite this article
Kuchkova, K.I., Styngach, E.P., Rivilis, F.S. et al. Carbolines. Chem Heterocycl Compd 12, 329–333 (1976). https://doi.org/10.1007/BF00479577
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00479577