FISCHER SYNTHESIS OF 1-, 5-, AND 7-SUBSTITUTED 3-(N-ACYLAMINO)-2-PHENYLINDOLES

Authors

  • Н. М. Пржевальский K. A. Timiryazev Agricultural Academy, Moscow
  • Н. C. Скворцова K. A. Timiryazev Agricultural Academy, Moscow
  • И. В. Магедов K. A. Timiryazev Agricultural Academy, Moscow

Keywords:

arylhydrazines, arylhydrazones, 3-(N-acylamino)indoles

Abstract

Arylhydrazones were obtained by the reaction of arylhydrazines with ω-(N-acylamino)acetophenones and were converted into 3-(N-acylamino)-2-phenylindoles with substituents at positions 1, 5, 6, and 7 by Fischer cyclization.

How to Cite
Przheval'skii, N. M.; Skvortsova, N. S.; Magedov, I. V. Chem. Heterocycl. Compd. 2003, 39, 161. [Khim. Geterotsikl. Soedin. 2003, 189.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1023704021460

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Published

2003-02-25

Issue

No. 2 (2003)

Section

Original Papers