Publication | Closed Access
Copper‐Catalyzed Direct Trifluoro‐ and Perfluoroalkylselenolations of Boronic Acids with a Shelf‐Stable Family of Reagents
73
Citations
59
References
2017
Year
Chemical EngineeringDirect Trifluoro‐EngineeringShelf‐stable FamilyVinylboronic AcidsBoronic AcidsOrganic ChemistryOrganometallic CatalysisCatalysisAvailable CatalystChemistryCopper‐catalyzed Direct PerfluoroalkylselenolationSynthetic ChemistryCatalytic Synthesis
Abstract Herein the copper‐catalyzed direct perfluoroalkylselenolation of aryl‐ and vinylboronic acids is described for the first time. The key to success is the design of new shelf‐stable perfluoroalkylselenolating reagents, namely perfluoroalkyl tolueneselenosulfonates. The reaction occurs at room temperature in the presence of commercially available catalyst and ligand in catalytic quantities. magnified image
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