Publication | Closed Access
Cascade Synthesis of 3-Alkylidene Dihydrobenzofuran Derivatives via Rhodium(III)-Catalyzed Redox-Neutral C–H Functionalization/Cyclization
71
Citations
47
References
2015
Year
C-h Functionalization/cascade CyclizationChemical EngineeringPropargyl CarbonatesEngineeringCross-coupling ReactionEfficient RhodiumRedox-neutral C–h Functionalization/cyclizationOrganic ChemistryOrganometallic CatalysisCatalysis3-Alkylidene Dihydrobenzofuran DerivativesChemistryCascade SynthesisSynthetic Chemistry
An efficient rhodium(III)-catalyzed coupling reaction of N-phenoxyacetamides with propargyl carbonates to yield 3-alkylidene dihydrobenzofuran derivatives via C-H functionalization/cascade cyclization has been developed. This transformation represents a redox-neutral process and features the formation of three new bonds under mild conditions.
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