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

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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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Bibliographic Details
Main Authors: Bararjanian, Morteza (Author) , Balalaie, Saeed (Author) , Rominger, Frank (Author) , Movassagh, Barahman (Author) , Bijanzadeh, Hamid Reza (Author)
Format: Article (Journal)
Language:English
Published: April 13, 2010
In: The journal of organic chemistry
Year: 2010, Volume: 75, Issue: 9, Pages: 2806-2812
ISSN:1520-6904
DOI:10.1021/jo902713x
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/jo902713x
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Author Notes:Morteza Bararjanian, Saeed Balalaie, Frank Rominger, Barahman Movassagh, and Hamid Reza Bijanzadeh
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Summary: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.
Item Description:Gesehen am 01.12.2022
Physical Description:Online Resource
ISSN:1520-6904
DOI:10.1021/jo902713x

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