Abstract
The condensation of 2-tosylaminoindole and 1-methyl-2-tosylaminoindoline with aromatic aldehydes gives primarily trans-3-arylidene derivatives, which exist in two tautomeric forms in solution.
Similar content being viewed by others
Literature cited
R. S. Sagitullin, A. N, Kost, E. D. Matveeva, and N. I. Nemudrova, Khim. Geterotsikl. Soedin., 920 (1970).
A. N. Kost, R. S. Sagitullin, T. V. Mel'nikova, and G. V. Kaplun, Khim. Geterotsikl. Soedin., 1368 (1972).
R. W. Daisley and J. Walker, J. Chem. Soc., C, 3357 (1971).
A. N. Kost, R. S. Sagitullin, V. I. Gorbunov, and N. N. Modyanov, Khim. Geterotsikl. Soedin., 359 (1970).
A. S. Bailey and A. J. Buckley, J. Chem. Soc., Perkin I, 1943 (1973).
J. Kebrle and K. Hoffmann, Helv. Chim. Acta, 39, 116 (1956).
A. S. Bailey and A. J. Buckley, J. Chem. Soc., Perkin I, 1602 (1973).
R. E. Harman, G. Wellman, and S. K. Gupta, J. Org. Chem., 38, 11 (1973).
C. Tacconi and E. Marinonr [sic], Res. Sci., 38, 1239 (1968).
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 343–347, March, 1976.
Rights and permissions
About this article
Cite this article
Kost, A.N., Sagitullin, R.S. & Men'shikov, V.V. Condensation of 2- tosylaminoindole with aromatic aldehydes. Chem Heterocycl Compd 12, 292–296 (1976). https://doi.org/10.1007/BF00479567
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00479567