Acylation of N-phenyl-2-(indol-3-yl)succinimides

Authors

  • C. Л. Богза L. M. Litvinenko Institute of Physical Organic and Coal Chemistry, National Academy of Sciences of Ukraine, 340114 Donetsk
  • K. И. Кобраков A. N. Kosygin Moscow State Textile Academy
  • М. Ю. Зубрицкий L. M. Litvinenko Institute of Physical Organic and Coal Chemistry, National Academy of Sciences of Ukraine, 340114 Donetsk
  • С. Ю. Cyйков L. M. Litvinenko Institute of Physical Organic and Coal Chemistry, National Academy of Sciences of Ukraine, 340114 Donetsk
  • B. И. Дуленко L. M. Litvinenko Institute of Physical Organic and Coal Chemistry, National Academy of Sciences of Ukraine, 340114 Donetsk

Abstract

Treatment of N-phenyl-2-(1-R-indol-3-yl)succinimides with acetyl perchlorate leads to acylation of the benzene ring of the indole substituent.

How to Cite
Bogza, S. L.; Kobrakov, K. I.; Zubritskii, M. Y.; Suikov, S. Yu.; Dulenko, V. I. Chem. Heterocycl. Compd. 1997, 33, 74. [Khim. Geterotsikl. Soedin. 1997, 85.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02290750

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Published

1997-01-25

Issue

No. 1 (1997)

Section

Original Papers