Skip to main content
Log in

Intramolecular rearrangement of N-acetylindoxyl oxime

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

It was established that N-acetylindoxyl oxime is converted to N-acetylindoxyl acetyloxime when it is heated to 50 ° C in a mixture of acetic acid and acetic anhydride. If the reaction is carried out by refluxing, N-acetyl-2-acetoxy- 3-acetam-idoindole, which undergoes rearrangement to 1,3-diacetyl-3-acetamidooxindole when it is heated, is also formed.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Literature cited

  1. G. N. Kurilo, S. Yu. Ryabova, and A. N. Grinev, Khim. Geterotsikl. Soedin., No. 6, 832 (1979).

    Google Scholar 

  2. L. Julian and A. Magnani, J. Am. Chem. Soc., 71, 3207 (1949).

    Google Scholar 

  3. G. C. Levy and G. L. Nelson, Carbon-13 Nuclear Magnetic Resonance for Organic Chemists, New York (1972).

Download references

Author information

Authors and Affiliations

Authors

Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1068–1070, August, 1980.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Grinev, A.N., Ryabova, S.Y., Kurilov, G.N. et al. Intramolecular rearrangement of N-acetylindoxyl oxime. Chem Heterocycl Compd 16, 828–830 (1980). https://doi.org/10.1007/BF00513164

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00513164

Keywords

Navigation