Synthesis and protonation of 2,3′-biquinolyl dianions

Authors

  • A. В. Аксенов Stavropol' State University, Stavropol' 355009
  • И. B. Аксенова Stavropol' State University, Stavropol' 355009
  • И. B. Боровлев Stavropol' State University, Stavropol' 355009
  • A. A. Бумбер Stavropol' State University, Stavropol' 355009
  • А. Ф. Пожарский Rostov State University, Rostov-on-Don 344090
  • Ю. И. Смyшкевич Russian Chemical Engineering University, Moscow 125190

Abstract

It has been shown that the reaction of 2, 3′-biquinolyls with an excess of lithium in tetrahydrofuran leads to the formation of dianions, treatment of which with water or D2O gives 1′, 4′-dihydro-2, 3′-biquinolyls or their 4′-D derivatives in good yield. Oxidation of the latter leads to 4′-D-2,3′-biquinolyl. The reduction of 2, 3′-biquinolyl has been studied.

How to Cite
Aksenov, A. V.; Aksenova, I. V.; Borovlev, I. V.; Bumber, A. A.; Pozharskii, A. F.; Smushkevich, Yu. I. Chem. Heterocycl. Compd. 1996, 32, 1196. [Khim. Geterotsikl. Soedin. 1996, 1391.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01169233

Published

1996-10-25

Issue

Section

Original Papers