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Rearrangement of 1-acetylindoxyl oxime into 1-acetyl-2-acetoxy-3-iminoindoline hydrosulfate

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

1-Acetyl-2-acetoxy-3-iminoindoline hydrosulfate was obtained by rearrangement of 1-acetylindoxyl oxime by the action of concentrated H2SO4. The hydrolysis and oxidative dimerization reactions of the above iminoindoline hydrosulfate were investigated.

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Literature Cited

  1. A. N. Grinev, S. Yu. Ryabova, G. N. Kurilo, and K. F. Turchin, Khim. Geterotsikl. Soed., No. 8, 1068 (1980).

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Authors and Affiliations

  1. S. Ordzhonikidze All-union Scientific Research Chemical-Pharmaceutical Institute, 119815, Moscow

    V. S. Velezheva, S. Yu. Ryabova & L. M. Alekseeva

Authors
  1. V. S. Velezheva
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  2. S. Yu. Ryabova
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  3. L. M. Alekseeva
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 329–331, March, 1990.

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Velezheva, V.S., Ryabova, S.Y. & Alekseeva, L.M. Rearrangement of 1-acetylindoxyl oxime into 1-acetyl-2-acetoxy-3-iminoindoline hydrosulfate. Chem Heterocycl Compd 26, 279–281 (1990). https://doi.org/10.1007/BF00472543

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  • DOI: https://doi.org/10.1007/BF00472543

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