Publication | Closed Access
Palladium-Catalyzed Synthesis of Isocoumarins and Phthalides via <i>tert</i>-Butyl Isocyanide Insertion
110
Citations
38
References
2012
Year
Combinatorial ChemistryAsymmetric CatalysisMedicinal ChemistryEngineeringBiochemistryNatural SciencesValuable LactonesLibrary SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisCyclization ReactionChemistryNatural Product SynthesisPalladium-catalyzed SynthesisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
A novel and highly efficient strategy for the synthesis of isocoumarins and phthalides through a palladium(0)-catalyzed reaction incorporating tert-butyl isocyanide has been developed. This process, providing one of the simplest methods for the synthesis of this class of valuable lactones, involves two steps including cyclization reaction and simple acid hydrolysis. The methodology is tolerant of a wide range of substrates and applicable to library synthesis.
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