Cobalt‐Catalyzed N‐Arylation of Nitrogen Nucleophiles in Water

Cobalt ′n′ cross‐coupling! A facile and practical strategy catalyzed by CoCl2⋅6 H2O has been developed for the N‐arylation of nitrogen nucleophiles with substituted aryl halides in water. The protocol is very simple and requires only mild conditions. A variety of nitrogen nucleophiles, including pyr...

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Veröffentlicht in:Chemistry : a European journal 2009-03, Vol.15 (13), p.3072-3075
Hauptverfasser: Teo, Yong‐Chua, Chua, Guan‐Leong
Format: Artikel
Sprache:eng
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Zusammenfassung:Cobalt ′n′ cross‐coupling! A facile and practical strategy catalyzed by CoCl2⋅6 H2O has been developed for the N‐arylation of nitrogen nucleophiles with substituted aryl halides in water. The protocol is very simple and requires only mild conditions. A variety of nitrogen nucleophiles, including pyrazole, indole, and 7‐azaindole, undergo catalysis to afford N‐arylated products in moderate to good yields (up to 86 %; see scheme). Cobalt ′n′ cross‐coupling! A facile and practical strategy catalyzed by CoCl2⋅6 H2O has been developed for the N‐arylation of nitrogen nucleophiles with substituted aryl halides in water. The protocol is very simple and requires only mild conditions. A variety of nitrogen nucleophiles, including pyrazole, indole, and 7‐azaindole, undergo catalysis to afford N‐arylated products in moderate to good yields (up to 86 %; see scheme).
ISSN:0947-6539
1521-3765
DOI:10.1002/chem.200802483