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Enantioselective Cobalt-Catalyzed Hydroboration of Fluoroalkyl-Substituted Alkenes to Access Chiral Fluoroalkylboronates

Ming Hu, Boon Beng Tan, Shaozhong Ge

2022Journal of the American Chemical Society52 citationsDOIOpen Access PDF

Abstract

Selective defluoroborylation and asymmetric hydroboration reactions of fluoroalkyl-substituted terminal alkenes with pinacolborane (HBpin) have been developed with cobalt catalysts generated from Co(acac)2 and bisphosphine ligands. A variety of fluoroalkyl-substituted terminal alkenes undergo this enantioselective hydroboration, affording the corresponding chiral alkylboronates containing fluoroalkyl-substituted stereogenic carbon centers with high enantioselectivity (up to 98% ee). This asymmetric hydroboration provides a versatile foundation for the synthesis of a variety of chiral organofluorine compounds containing fluoroalkyl-substituted stereogenic carbon centers.

Topics & Concepts

HydroborationStereocenterChemistryEnantioselective synthesisCobaltCatalysisOrganic chemistryAlkeneCombinatorial chemistryFluorine in Organic ChemistryOrganoboron and organosilicon chemistryAsymmetric Synthesis and Catalysis
Enantioselective Cobalt-Catalyzed Hydroboration of Fluoroalkyl-Substituted Alkenes to Access Chiral Fluoroalkylboronates | Litcius