Iron-catalyzed addition/cyclization cascade of activated alkenes with alcohols: access to carbonyl substituted quinoline-2,4-diones

A convenient and efficient iron-catalyzed radical addition/cyclization cascade of o -cyanoarylacrylamides with alcohols is presented for the synthesis of carbonyl substituted quinoline-2,4(1 H ,3 H )-diones in moderate to excellent yields. This transformation exhibits a wide substrate scope and sign...

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Veröffentlicht in:RSC advances 2016-01, Vol.6 (57), p.52391-52394
Hauptverfasser: Wang, Shi-Sheng, Fu, Hong, Wang, Guanlin, Sun, Meng, Li, Ya-Min
Format: Artikel
Sprache:eng
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Zusammenfassung:A convenient and efficient iron-catalyzed radical addition/cyclization cascade of o -cyanoarylacrylamides with alcohols is presented for the synthesis of carbonyl substituted quinoline-2,4(1 H ,3 H )-diones in moderate to excellent yields. This transformation exhibits a wide substrate scope and significant functional group tolerance. Iron-catalyzed radical addition/cyclization cascade of o -cyanoarylacrylamides with alcohols has been developed for the synthesis of carbonyl substituted quinoline-2,4(1 H ,3 H )-diones.
ISSN:2046-2069
2046-2069
DOI:10.1039/c6ra08976c