Publication | Closed Access
Enantioenriched Synthesis of <i>C</i><sub>1</sub>-Symmetric BINOLs: Iron-Catalyzed Cross-Coupling of 2-Naphthols and Some Mechanistic Insight
256
Citations
25
References
2010
Year
Broad Substrate ScopeChemical EngineeringCross-coupling ReactionEngineeringEnantiomeric ExcessesMechanistic InsightIron-catalyzed Cross-couplingEnantioenriched SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisChemistryAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisCatalytic Synthesis
Highly enantioselective aerobic oxidative cross-coupling of 2-naphthols with broad substrate scope was achieved using an iron(salan) complex as the catalyst. Enantiomeric excesses of the products ranged from 87 to 95%. The scope of the cross-coupling reaction was found to be different from that of the homocoupling reaction under the same reaction conditions.
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