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This article is cited in 10 scientific papers (total in 10 papers)
2,3-Dichloro-1-alkylpyrazinium tetrafluoroborates: the synthesis and reactions with nucleophiles
G. L. Rusinova, P. A. Slepukhina, V. N. Charushinb, O. N. Chupakhina a I. Ya. Postovsky Institute of Organic Synthesis, Urals Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
b Department of Organic Chemistry, Urals State Technical University, Ekaterinburg, Russian Federation
Abstract:
The alkylation of 2,3-dichloropyrazine with the Meerwein reagents R3O+BF4− (R=Me or Et) afforded 1-alkyl-2,3-dichloropyrazinium tetrafluoroborates, which were transformed into mono.mono- or disubstitution products, while the reaction of these salts with 1,4-N,Xdinucleophiles resulted in fused heterocyclic systems.
Citation:
G. L. Rusinov, P. A. Slepukhin, V. N. Charushin, O. N. Chupakhin, “2,3-Dichloro-1-alkylpyrazinium tetrafluoroborates: the synthesis and reactions with nucleophiles”, Mendeleev Commun., 11:2 (2001), 78–80
Linking options:
https://www.mathnet.ru/eng/mendc4227 https://www.mathnet.ru/eng/mendc/v11/i2/p78
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