Synthesis, structure, and biological activity of [2.2]paracyclophanes. 6. Synthesis of 2-([2.2]paracyclophan-4-yl)(benzo[<i>g</i>])indoles

Authors

  • Л. И. Крывенко Russian University of National Friendship, Moscow 117198
  • Б. Н. Анисимов Russian University of National Friendship, Moscow 117198
  • T. П. Христофорова Russian University of National Friendship, Moscow 117198
  • C. А. Солдатова Russian University of National Friendship, Moscow 117198
  • А. T. Солдатенков Russian University of National Friendship, Moscow 117198

Abstract

Cyclocondensation of 2-([2.2]paracyclophan-4-yl)-2-oxoethyltriethylammonium bromide with aniline and α-naphthylamine gives 2-(paracyclophan-4-yl)indoles and benzo[g]indole respectively.

How to Cite
Kryvenko, L. I.; Anisimov, B. N.; Khristoforova, T. P.; Soldatova, S. A.; Soldatenkov, A. D. Chem. Heterocycl. Compd. 1997, 33, 929. [Khim. Geterotsikl. Soedin. 1997, 1065.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02253163

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Published

1997-08-25

Issue

No. 8 (1997)

Section

Original Papers