Copper-catalyzed direct C-H fluoroalkenylation of heteroarenes

Copper-catalyzed direct C-H fluoroalkenylation of heterocycles using various gem-bromofluoroalkenes as electrophiles is reported. This efficient method offers step-economical, low-cost and stereocontrolled access to relevant heteroarylated monofluoroalkenes. The synthesis of fluorinated analogues of...

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Veröffentlicht in:Organic & biomolecular chemistry 2016-01, Vol.14 (1), p.353-357
Hauptverfasser: Rousée, Kevin, Schneider, Cédric, Bouillon, Jean-Philippe, Levacher, Vincent, Hoarau, Christophe, Couve-Bonnaire, Samuel, Pannecoucke, Xavier
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Sprache:eng
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Zusammenfassung:Copper-catalyzed direct C-H fluoroalkenylation of heterocycles using various gem-bromofluoroalkenes as electrophiles is reported. This efficient method offers step-economical, low-cost and stereocontrolled access to relevant heteroarylated monofluoroalkenes. The synthesis of fluorinated analogues of biomolecules and therapeutic agents for the treatment of Duchenne muscular dystrophy as application is reported.
ISSN:1477-0520
1477-0539
DOI:10.1039/c5ob02213d