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.
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References
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Additional information
For communication 4, see [1].
Stravropol State University, Stavropol 355009, Russia. Russian Chemical Technology University 125190, Moscow. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1218–1222, September, 1998.
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Aksenov, A.V., Nadein, O.N., Borovlev, I.V. et al. 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. Chem Heterocycl Compd 34, 1045–1049 (1998). https://doi.org/10.1007/BF02251550
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DOI: https://doi.org/10.1007/BF02251550