Publication | Closed Access
Unprecedented Selectivity via Electronic Substrate Recognition in the 1,4‐Addition to Cyclic Olefins Using a Chiral Disulfoxide Rhodium Catalyst
98
Citations
47
References
2009
Year
Chemical EngineeringEngineeringAsymmetric Metal CatalysisOrganic ChemistryChiral DisulfoxideCyclic OlefinsCatalysisOrganometallic CatalysisChemistryHomogeneous CatalysisChelating LigandAsymmetric CatalysisElectronic Substrate RecognitionEnantioselective SynthesisCatalytic Synthesis
From zero to hero? Sulfoxides are generally not considered useful ligand entities in asymmetric metal catalysis. However, a chiral disulfoxide as a chelating ligand in the rhodium-catalyzed 1,4-addition of aryl boronic acids to cyclic, alpha,beta-unsaturated ketones and esters gives impressive catalytic results, thus opening the door to future applications of this new chiral ligand class.
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