2,3-Dichloro-1-alkylpyrazinium tetrafluoroborates: the synthesis and reactions with nucleophiles

Citation
Gl. Rusinov et al., 2,3-Dichloro-1-alkylpyrazinium tetrafluoroborates: the synthesis and reactions with nucleophiles, MENDELEEV C, (2), 2001, pp. 78-80
Citations number
10
Categorie Soggetti
Chemistry
Journal title
MENDELEEV COMMUNICATIONS
ISSN journal
09599436 → ACNP
Issue
2
Year of publication
2001
Pages
78 - 80
Database
ISI
SICI code
0959-9436(200103/04):2<78:2TTSAR>2.0.ZU;2-K
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- or disubstitution products, while the rea ction of these salts with 1,4-N,X-dinucleophiles resulted in fused heterocy clic systems.