Publication | Closed Access
Synthesis of 3-Substituted Isocoumarins via a Cascade Intramolecular Ullmann-Type Coupling–Rearrangement Process
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Citations
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References
2012
Year
Combinatorial ChemistryMedicinal ChemistryCross-coupling ReactionEngineeringNatural SciencesDiversity-oriented SynthesisLibrary SynthesisOrganic ChemistryCatalysisChemistry3-Substituted IsocoumarinsHeterocycle ChemistryPharmacologyRearrangement ProcessSynthetic ChemistryBiomolecular Engineering
A simple and highly efficient strategy for the synthesis of 3-substituted isocoumarins through a copper(I)-catalyzed reaction of 1-(2-halophenyl)-1,3-diones has been developed. The procedure is based on a cascade copper-catalyzed intramolecular Ullmann-type C-arylation and rearrangement process. This methodology is tolerant of a wide range of substrates and applicable to library synthesis.
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