Investigations in the region of 2,3′-biquinolyl 5. Investigation of the reaction of stabilized C-nucleophiles with 1-alkyl-3-(2-quinolyl)quinolinium halides

Abstract

The regioselectivity of the nucleophilic addition of stabilized C-nucleophiles to 1-alkyl-3-(2-quinolyl)quinolinium halides was investigated. The reaction of the latter with enolates, indolesodium, and cyanide ion leads to 4′-substituted 1′-alkyl-1′, 4′-dihydro-2,3′-biquinolyls.

How to Cite
Aksenov, A. V.; Nadein, O. N.; Borovlev, I. V.; Smushkevich, Yu. I. Chem. Heterocycl. Compd. 1998, 34, 1045. [Khim. Geterotsikl. Soedin. 1998, 34, 1218.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02251550