Six-Component Reactions for the Stereoselective Synthesis of 3-Arylidene-2-oxindoles via Sequential One-Pot Ugi/Heck Carbocyclization/Sonogashira/Nucleophilic Addition
Abstract
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- Dataset
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- arylidene
- skeleton
- Sequential
- Stereoselective Synthesis
- sequential
- approach
- synthesis
- Carbocyclization
- Arylidene
- Ugi
- AdditionAn
- carbocyclization
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Last time updated on 16/03/2018
This paper was published in The Francis Crick Institute.
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