| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5219334 | Tetrahedron | 2011 | 8 Pages |
Abstract
An efficient method for the stereoselective synthesis of 3-(diarylmethylene)-2-oxindoles and 3-(arylmethylene)-2-oxindoles via carbopalladation is described. In this approach, an Ugi-4-component reaction (4-CR) adduct was used as the starting material. A one-pot sequence involving intermolecular carbopalladation C–H activation/C–C bond formation efficiently afforded the oxindole derivatives.
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