Pd-Catalyzed regioselective synthesis of 2,6-disubstituted pyridines through denitrogenation of pyridotriazoles and 3,8-diarylation of imidazo[1,2-]pyridines

Synthesis of 2,6-disubstituted pyridines from pyridotriazoles through palladium-catalyzed aerobic oxidative denitrogenative reactions has been described. Denitrogenation of arylated pyridotriazoles generates metal-carbene intermediates in situ and provides selectively 6-aryl-2-benzoylpyridines. The...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2019-09, Vol.55 (73), p.1888-1891
Hauptverfasser: Joshi, Abhisek, Semwal, Rashmi, Suresh, Eringathodi, Adimurthy, Subbarayappa
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Sprache:eng
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Zusammenfassung:Synthesis of 2,6-disubstituted pyridines from pyridotriazoles through palladium-catalyzed aerobic oxidative denitrogenative reactions has been described. Denitrogenation of arylated pyridotriazoles generates metal-carbene intermediates in situ and provides selectively 6-aryl-2-benzoylpyridines. The same conditions have been extended to regioselective C-3 and C-8 diarylation of several imidazo[1,2- a ]pyridines. Synthesis of 2,6-disubstituted pyridines from pyridotriazoles through palladium-catalyzed aerobic oxidative denitrogenative reactions has been described.
ISSN:1359-7345
1364-548X
DOI:10.1039/c9cc05953a