Indolopyridines with a hetero atom at a position of fusion. 7. Electrophilic substitution in 5,6-dihydroindolo[2,1-<i>a</i>]isoquinoline

Authors

  • Ж. Нтаганда Russian University of National Friendship, Moscow 117198
  • C. А. Солдатовa Russian University of National Friendship, Moscow 117198
  • Б. Н. Анисимов Russian University of National Friendship, Moscow 117198
  • Х. А. P. Аларкон Russian University of National Friendship, Moscow 117198
  • А. T. Солдатенков Russian University of National Friendship, Moscow 117198

Abstract

Halogenation, acylation, azo coupling, and alkylaminomethylation of 5,6-dihydroindoto[2,1-a]isoguinoline were carried out at the C(11) position (pyrrole fragment). In dibromination, the second bromine atom was introduced into the C(9) position (indole part of the molecule).

How to Cite
Ntaganda, G.; Soldatova, S. A.; Anisimov, B. N.; Alarkon Kh. A. R.; Soldatenkov, A. T. Chem. Heterocycl. Compd. 1994, 30, 196. [Khim. Geterotsikl. Soedin. 1994, 217.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01165011

 

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Published

1994-02-25

Issue

No. 2 (1994)

Section

Original Papers