Publication | Closed Access
A Room-Temperature Catalytic Asymmetric Synthesis of Allenes with ECNU-Phos
161
Citations
31
References
2013
Year
Room TemperatureEngineeringBiphenyl SkeletonNatural SciencesDiversity-oriented SynthesisCatalytic SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryAsymmetric CatalysisThree-carbon Axial ChiralityEnantioselective SynthesisBiomolecular Engineering
Three-carbon axial chirality has been asymmetrically established from racemic one-carbon central chirality efficiently at room temperature: we report here the discovery of the first catalytic asymmetric carbonylation of readily available racemic propargylic carbonates to access optically active 2,3-allenoates with fairly high ee. The combination of [(π-allyl)PdCl]2 with [(R)-ECNU-Phos], a new chiral bisphosphine ligand based on a biphenyl skeleton, demonstrates high enantioselectivity. Both enantiomers of allenoates can be obtained at room temperature by applying either (R)- or (S)-ECNU-Phos.
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