CONDENSED TETRACYCLIC SYSTEMS WITH AN ISATIN FRAGMENT IN THE MOLECULE

Authors

  • Т. Е. Хоштария Georgian Technical University, Tbilisi 380075
  • Л. Н. Курковская Georgian Technical University, Tbilisi 380075
  • М. М. Матнадзе Georgian Technical University, Tbilisi 380075
  • М. И. Сихарулидзе Georgian Technical University, Tbilisi 380075
  • Т. О. Джаши Georgian Technical University, Tbilisi 380075
  • В. О. Ананиашвили Georgian Technical University, Tbilisi 380075
  • К. Т. Бацикадзе Georgian Technical University, Tbilisi 380075

DOI:

https://doi.org/10.1007/7390

Keywords:

isatin, indole, pyrrole

Abstract

A new method for the synthesis of the dioxodihydro-1H-benzo[b]furoindole heterocyclic systems from the corresponding isomeric amino acids with the amino groups at positions 2 and 3 is described. By this method it is possible not only to obtain the indicated  tetracyclic systems in the form of one isomer but also to interconvert them; from the tetracyclic systems with angular structure it is possible to obtain the corresponding isomers with linear structure and vice versa. The classical Sandmeyer reaction served a model for such transformations.

How to Cite
Khoshtariya, T. E.; Kurkovskaya, L. N.; Matnadze, M. M.; Sikharulidze, M. I.; Dzhashi, T. O.; Ananiashvili, V. O.; Batsikadze, K. T.  Chem. Heterocycl. Compd. 2007, 43, 1111. [Khim. Geterotsikl. Soedin. 2007, 1314.]

For this article in the English edition see DOI 10.1007/s10593-007-0171-1


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Published

2023-01-27

Issue

No. 9 (2007)

Section

Original Papers