Publication | Closed Access
Asymmetric Catalytic 1,2‐Dihydrophosphination of Secondary 1,2‐Diphosphines – Direct Access to Free <i>P</i>*‐ and <i>P</i>*,<i>C</i>*‐Diphosphines
26
Citations
33
References
2020
Year
Cross-coupling ReactionEngineeringDirect AccessSynthesized LigandsNatural SciencesDiversity-oriented SynthesisComplete RetentionOrganic ChemistryActivated OlefinsOrganometallic CatalysisCatalysisSecondary 1,2‐DiphosphinesChemistryAsymmetric CatalysisAsymmetric Catalytic 1,2‐DihydrophosphinationEnantioselective SynthesisBiomolecular Engineering
Abstract A 1,2‐dihydrophosphination of bis(phenylphosphino)ethane with a wide range of activated olefins was achieved in a catalytic manner with enantiomeric and diastereomeric excess of up to >99% and 44% respectively. The protocol can be extended to selected substrates leading to free P ‐ and C ‐chiral 1,2‐diphosphines. The synthesized ligands can also undergo direct complexation onto palladium affording complexes with complete retention of stereo‐integrity. magnified image
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