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 |
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Hauptverfasser: | , |
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). |
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ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/chem.200802483 |