Six-component reactions for the stereoselective synthesis of 3-arylidene-2-oxindoles via sequential one-pot Ugi/Heck carbocyclization/Sonogashira/nucleophilic addition = three = two

An efficient palladium-catalyzed protocol for the synthesis of 3-arylidene-2-oxindoles has been developed. In this approach, a sequential one-pot six-component reaction via Ugi/Heck carbocyclization/Sonogashira/nucleophilic addition was used for the synthesis of the desired skeleton.

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Bibliographische Detailangaben
Hauptverfasser: Bararjanian, Morteza (VerfasserIn) , Balalaie, Saeed (VerfasserIn) , Rominger, Frank (VerfasserIn) , Movassagh, Barahman (VerfasserIn) , Bijanzadeh, Hamid Reza (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: April 13, 2010
In: The journal of organic chemistry
Year: 2010, Jahrgang: 75, Heft: 9, Pages: 2806-2812
ISSN:1520-6904
DOI:10.1021/jo902713x
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/jo902713x
Volltext
Verfasserangaben:Morteza Bararjanian, Saeed Balalaie, Frank Rominger, Barahman Movassagh, and Hamid Reza Bijanzadeh
Beschreibung
Zusammenfassung:An efficient palladium-catalyzed protocol for the synthesis of 3-arylidene-2-oxindoles has been developed. In this approach, a sequential one-pot six-component reaction via Ugi/Heck carbocyclization/Sonogashira/nucleophilic addition was used for the synthesis of the desired skeleton.
Beschreibung:Gesehen am 01.12.2022
Beschreibung:Online Resource
ISSN:1520-6904
DOI:10.1021/jo902713x