Publication | Closed Access
Catalytic Enantioselective Synthesis of Acyclic Quaternary Centers: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Acyclic Enol Carbonates
92
Citations
40
References
2018
Year
Chemical EngineeringEngineeringLinear α-Quaternary KetonesOrganic ChemistrySelectivity RegardlessCatalysisStereoselective SynthesisChemistryCatalytic Enantioselective SynthesisOrganometallic CatalysisAsymmetric CatalysisEnantioselective SynthesisAcyclic Quaternary CentersEnolate Geometry
The first enantioselective palladium-catalyzed decarboxylative allylic alkylation of fully substituted acyclic enol carbonates providing linear α-quaternary ketones is reported. Investigation into the reaction revealed that the use of an electron-deficient phosphinooxazoline ligand renders the enolate geometry of the starting material inconsequential, with the same enantiomer of product obtained in the same level of selectivity regardless of the starting ratio of enolates. As a result, a general method toward acyclic all-carbon quaternary stereocenters has been developed.
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