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Copper-Catalyzed Intramolecular C−H Oxidation/Acylation of Formyl-<i>N</i>-arylformamides Leading to Indoline-2,3-diones
205
Citations
34
References
2010
Year
Cross-coupling ReactionEngineeringTandem ReactionTransition-metal-catalyzed TransformationOrganic ChemistryCorresponding Indoline-2,3-dionesCatalysisOrganometallic CatalysisChemistryHeterocycle ChemistrySynthetic ChemistryBiomolecular Engineering
A new, efficient Cu-catalyzed intramolecular C-H oxidation/acylation method has been developed for the synthesis of substituted indoline-2,3-diones (isatins). In the presence of CuCl(2) and O(2), a variety of formyl-N-arylformamides underwent the tandem reaction to afford the corresponding indoline-2,3-diones in moderate to good yields. It is noteworthy that the reaction serves as the first example of transition-metal-catalyzed transformation for the preparation of indoline-2,3-diones.
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