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 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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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 |