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Palladium‐Catalyzed Dearomatizing Difunctionalization of Indoles and Benzofurans
36
Citations
33
References
2016
Year
Chemical EngineeringCross-coupling ReactionEngineeringPalladium‐catalyzed Dearomatizing DifunctionalizationCarbon CenterNatural SciencesDiversity-oriented SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisChemistryN ‐Boc‐indolesSynthetic ChemistryCatalytic Synthesis
Abstract A palladium‐catalyzed dearomatizing difunctionalization of N ‐Boc‐indoles and benzofurans to give tricyclic indolines and 2,3‐dihydrobenzofurans with a fully substituted carbon center is described. Product formation occurs under mild conditions at room temperature with commercially available aryl boronic acids and 2,2,6,6‐tetramethylpiperidine‐1‐oxyl (TEMPO) as a mild oxidant in good yields.
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