Studies in the area of 2,3′-biquinolyl. 1. Arylation and hetarylation of 2,3′-biquinolyl dianion

Authors

  • А. B. Аксенов Stavropol' State University, Stavropol' 355009
  • И. B. Аксенова Stavropol' State University, Stavropol' 355009
  • И. B. Бoровлeв Stavropol' State University, Stavropol' 355009
  • Ю. И. Смушкевич Russian Chemical Engineering University, Moscow 125190

Abstract

The 2,3′-biquinolyl dianion, when reacting with aryl- and hetaryl halides, forms arylation products at the 4′ position, and treatment of these products with alkyl halides or water yields 1′-alkyl-4′-aryl-1′,4′-dihydro-2,3′-biquinolyls or 4′-aryl-1′,4′-dihydro-2,3′-biquinolyls, respectively. Oxidation of the latter yields 4′-aryl-2,3′-biquinolyls. The cation dependence of the arylation reaction is demonstrated.

How to Cite
Aksenov, A. V.; Aksenova, I. V.; Borovlev, I. V.; Smushkevich, Yu. I. Chem. Heterocycl. Compd. 1997, 33, 954. [Khim. Geterotsikl. Soedin. 1997, 1094.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02253168

Published

1997-08-25

Issue

Section

Original Papers