ELECTROCHEMICAL REDUCTION OF 5-OXOINDENO[1,2-<i>b</i>]PYRIDINIUM PERCHLORATES IN THE PRESENCE OF ALKYLATING AGENTS

Authors

  • Б. Туровска Latvian Institute of Organic Synthesis, Riga LV 1006
  • Д. Муцениеце Latvian Institute of Organic Synthesis, Riga LV 1006
  • В. Лусис Latvian Institute of Organic Synthesis, Riga LV 1006
  • И. Туровскис Latvian Institute of Organic Synthesis, Riga LV 1006
  • Э. Лиепиньш Latvian Institute of Organic Synthesis, Riga LV 1006
  • Я. Страдынь Latvian Institute of Organic Synthesis, Riga LV 1006

Keywords:

5,9b-dihydro-5-oxoindeno[1,2-b]pyridine, indenopyridinium perchlorates, electrochemical reduction

Abstract

It was established that 9b-substituted 5,9b-dihydroindenopyridines are formed in addition to the reduction products on preparative electrochemical reduction of 5-oxoindeno[1,2-b]pyridinium perchlorates at a mercury electrode in acetonitrile in the presence of alkylating agents.

How to Cite
Turovska, B.; Muceniece, D.; Lusis, V.; Turovskis, I.; Liepin'sh, E.; Stradins, J. Chem. Heterocycl. Compd. 2003, 39, 1600. [Khim. Geterotsikl. Soedin. 2003, 1819.]

For this article in the English edition, see DOI 10.1023/B:COHC.0000018337.96922.7d

Downloads

Published

2003-12-25

Issue

No. 12 (2003)

Section

Original Papers