INDOLE DERIVATIVES. 141. SYNTHESIS AND INVESTIGATION OF NEW 2-ARYLINDOLES

Authors

  • Ш. А. Самсония I. Javakhishvili Tbilisi State University, Tbilisi 380028
  • И. Ш. Чикваидзе I. Javakhishvili Tbilisi State University, Tbilisi 380028
  • Т. Г. Нариндошвили I. Javakhishvili Tbilisi State University, Tbilisi 380028
  • H. Н. Суворов I. Javakhishvili Tbilisi State University, Tbilisi 380028

Keywords:

arylindoles, indolization, azo coupling, formylation, nitrosation

Abstract

2-(Diphenylmethan-4-yl)- and 2-(dibenzyl-4-yl)indoles have been synthesized by the Fischer reaction. Reactions carried out included azo coupling, formylation, and nitrosation. The corresponding 3‑substituted derivatives were obtained.

How to Cite
Samsoniya, Sh. A.; Chikvaidze, I. Sh.; Narindoshvili, T. G.; Suvorov, N. N. Chem. Heterocycl. Compd. 2001, 37, 827. [Khim. Geterotsikl. Soedin. 2001, 899.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1012439205723

Published

2001-07-25

Issue

Section

Original Papers