Synthesis of novel benzoylated indoles

Authors

  • Ш. А. Самсония Iv. Dzhavakhishvili Tbilisi, State University, Tbilisi 380028
  • И. Ш. Чикваидзе Iv. Dzhavakhishvili Tbilisi, State University, Tbilisi 380028
  • Э. О. Гогричиани Iv. Dzhavakhishvili Tbilisi, State University, Tbilisi 380028
  • H. Ш. Ломадзе Iv. Dzhavakhishvili Tbilisi, State University, Tbilisi 380028
  • Н. Л. Tаргaмaдзе Iv. Dzhavakhishvili Tbilisi, State University, Tbilisi 380028

Abstract

It has been shown that Friedel‒Crafts p-nitrobenzoylation of 2,2′-dicarbethoxybis(5-indoyl)methane occurs at the bridging group. From the products of p-nitrobenzoylation of 2-carbethoxy-5-methylindole, 2-carbethoxy-5-hydroxy-indole and 2,7-dicarbethoxy-1H,6H-pyrrolo[2,3-e]indole there were obtained corresponding amines and an oxime.

How to Cite
Samsoniya, Sh. A.; Chikvaidze, I. Sh.; Gogrichiani, É. O.; Lomadze, N. Sh.; Targamadze, N. L. Chem. Heterocycl. Compd. 1994, 30, 1039. [Khim. Geterotsikl. Soedin. 1994, 1202.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01171159

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Published

1994-09-25

Issue

No. 9 (1994)

Section

Original Papers