Abstract
With alkyl chlorides and alkyl phenyl ethers the dianion of 2,3′-biquinolyl forms the products from alkylation at position 4′. Their treatment with alkyl halides or water gives 1′, 4′-dialkyl-1′, 4′-dihydro-2,3′-biquinolyls or 4′-alkyl-1′,4′-dihydro-2,3′-biquinolyls respectively.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
References
A. V. Aksenov, O. N. Nadein, I. V. Borovlev, and Yu. I. Smushkevich, Khim. Geterotsikl. Soedin., No. 3, 350 (1998).
A. V. Aksenov, I. V. Aksenova, I. V. Borovlev, A. A. Bumber, A. F. Pozharskii, and Yu. I. Smushkevich, Khim. Geterotsikl. Soedin., No. 10, 1391 (1996).
A. V. Aksenov, I. V. Aksenova, I. V. Borovlev, and Yu. I. Smushkevich, Khim. Geterotsikl. Soedin., No. 8, 1094 (1997).
N. L. Holy, Chem. Rev., No. 2, 243 (1974).
A. V. Aksenov, O. N. Nadein, I. V. Borovlev, and Yu. I. Smushkevich, Khim. Geterotsikl. Soedin., No. 2, 232 (1998).
Additional information
For communication 3, see [1].
Stavropol State University, Stavropol, Russia 355009. Russian Chemical Technology University, Moscow 125190. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1214–1217, September, 1998.
Rights and permissions
About this article
Cite this article
Aksenov, A.V., Aksenova, I.V., Borovlev, I.V. et al. Investigations in the region of 2,3′-biquinolyl 4. Alkylation of the dianion of 2,3′-biquinolyl. Chem Heterocycl Compd 34, 1041–1044 (1998). https://doi.org/10.1007/BF02251549
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF02251549