Abstract
In the presence of phosphorus oxychloride N-acylaminoindolines rearrange to 7-α-cyanoalkyl(aralkyl)indolines. These have been converted to the corresponding amines, acids, and indoles.
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A. N. Kost, G. A. Golubeva, and Yu. N. Portnov, Dokl. Akad. Nauk SSSR, 200, 342 (1971).
N. V. Shorina, G. A. Golubeva, L. A. Sviridova, and V. N. Torocheshnikov, Khim. Geterotsikl. Soedin., No. 3, 332 (1990).
N. V. Shorina, G. A. Golubeva, L. A. Sviridova, and V. N. Torocheshnikov, Khim. Geterotsikl. Soedin., No. 3, 337 (1990).
Yu. N. Portnov and G. A. Golubeva, Khim. Geterotsikl. Soedin., No. 9, 1155 (1985).
R. Fusko and F. Sannikolo, Khim. Geterotsikl. Soedin., No. 4, 504 (1978).
V. Gevorgyan and E. Lukevics, J. Chem. Soc., Chem. Commun., 18, 1234 (1985).
A. P. Terent'ev, M. N. Preobrazhenskaya, A. S. Bobkov, and G. M. Sorokina, Zh. Obshch. Khim., 29, 2541 (1959).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1185–1189, September, 1990.
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Shorina, N.V., Golubeva, G.A., Sviridova, L.A. et al. Synthesis and reactions of 7-α-cyanoalkylindolines. Chem Heterocycl Compd 26, 988–992 (1990). https://doi.org/10.1007/BF00472477
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DOI: https://doi.org/10.1007/BF00472477