Publication | Closed Access
Trifluoromethylation/Difluoromethylation‐Initiated Radical Cyclization of <i>o</i>‐Alkenyl Aromatic Isocyanides for Direct Construction of 4‐Cyano‐2‐Trifluoromethyl/Difluoromethyl‐Containing Quinolines
46
Citations
66
References
2020
Year
Broad Substrate ScopeChemical EngineeringEngineeringPhotoredox ProcessPhotochemistryNatural SciencesDiversity-oriented SynthesisFluorous SynthesisRadical CyclizationOrganic ChemistryDirect ConstructionOrganometallic CatalysisCatalysisChemistryHeterocycle ChemistryHalogenationRadical‐triggered CyclizationVisible‐light Photoredox Catalysis
Abstract In this study, a radical‐triggered cyclization of o ‐alkenyl aromatic isocyanides prepared from accessible starting materials is developed. The reaction provides a general and efficient method for the synthesis of 4‐CN‐2‐CF 3 /CF 2 H‐containing quinolines under copper or visible‐light photoredox catalysis in a one‐pot synthetic procedure. This protocol demonstrates good to high yields, broad substrate scope, and good functional group tolerance. magnified image
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