Pyrroloindoles. 16. Some electrophilic substitution reactions of 2,7-dicarbethoxy-1H,6H-pyrrolo[2,3-<i>e</i>]indoles

Authors

  • H. Ш. Ломадзе Iv. Dzhavakhishvili Tbilisi, State University, Tbilisi 380028
  • И. Ш. Чикваидзе Iv. Dzhavakhishvili Tbilisi, State University, Tbilisi 380028
  • Н. Л. Таргамадзe Iv. Dzhavakhishvili Tbilisi, State University, Tbilisi 380028
  • Л. Н. Kypковскaя Iv. Dzhavakhishvili Tbilisi, State University, Tbilisi 380028
  • Ш. А. Cамcония Iv. Dzhavakhishvili Tbilisi, State University, Tbilisi 380028
  • H. H. Суворов Iv. Dzhavakhishvili Tbilisi, State University, Tbilisi 380028

Abstract

Electrophilic substitutions of 2,7-dicarbethoy-1H,6H-pyrrolo[2,3-e]indole (Friedel‒Crafts acylation, nitration, bromination) take place both at position 3 of the indole ring and at positions 5 and 8 in the benzene ring.

How to Cite
Lomadze, N. S.; Chikvaidze, I. Sh.; Targamadze, N. L.; Kurkovskaya, L. N.; Samsoniya, Sh. A.; Suvorov, N. N. Chem. Heterocycl. Compd. 1994, 30, 1034. [Khim. Geterotsikl. Soedin. 1994, 1197.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01171158

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Published

1994-09-25

Issue

No. 9 (1994)

Section

Original Papers