Abstract
The reaction of a 2-aminoindole with arylidenemalonic and arylidenecyanoacetic esters was studied. The effect of substituents in the benzene ring of the arylidenemalonic ester on the reaction pathway is demonstrated.
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Yu. N. Portnov, V. G. Zabrodnyaya, S. N. Bulaga, and V. G. Voronin, Summaries of Papers Presented at the First All-Union Conference on the Chemistry, Biochemistry, and Pharmacology of Indole Derivatives [in Russian], Tbilisi (1986), p. 123.
T. V. Mel'nikova, A. N. Kost, R. S. Sagitullin, and N. N. Borisov, Khim. Geterotsikl. Soedin., No. 11, 1273 (1973).
A. N. Kost and R. S. Sagitullin, Vestnik Moskovsk. Univ., Ser. 2, Khim., 20, No. 6, 516 (1979).
R. S. Sagitullin, A. N. Kost, E. D. Matveeva, and N. I. Nemudrova, Khim. Geterotsikl. Soedin., No. 7, 920 (1970).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 899–902, July, 1992.
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Portnov, Y.N., Bulaga, S.N. & Zabrodnyaya, V.G. Reaction of a 2-aminoindole with difunctional compounds. Chem Heterocycl Compd 28, 746–749 (1992). https://doi.org/10.1007/BF00474486
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DOI: https://doi.org/10.1007/BF00474486