Investigations in the region of 2,3′-biquinoline. 2. Investigation of the nucleophilic addition of organomagnesium compounds and sodium hydride to 2,3′-biquinoline

Authors

  • А. B. Акceнов Stavropol' State University, Stavropol 355009
  • O. H. Надеин Stavropol' State University, Stavropol 355009
  • И. B. Борoвлев Stavropol' State University, Stavropol 355009
  • Ю. И. Смушкевич Russian Chemical Technology University, Moscow 125190

Abstract

With sodium hydride and alkyl- and arylmagnesium halided, 2,3'-biquinaline forms the products from  addition at position 4', and with allylmagnesium chloride it forms the products from addition at position 2'. Methods were developed for the synthesis of 4'-R-1'-, 4'-dihydro- and 2'-allyl-1',2'-dihydro-2,3'-biquinolines.

How to Cite
Aksenov, A. V.; Nadein, O. N.; Borovlev, I. V.; Smushkevich, Yu. I. Chem. Heterocycl. Compd. 1998, 34, 207. [Khim. Geterotsikl. Soedin. 1998, 34, 232.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02315186

Published

1998-02-25

Issue

Section

Original Papers