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Atroposelective Synthesis of Axially Chiral All‐Benzenoid Biaryls by the Gold‐Catalyzed Intramolecular Hydroarylation of Alkynones
45
Citations
72
References
2016
Year
EngineeringOrganic ChemistryChemistryOrganometallic CatalysisStereoselective SynthesisCross-coupling ReactionDerivativesGold‐catalyzed Intramolecular HydroarylationDiversity-oriented SynthesisSame GoldCatalysisAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringAtroposelective SynthesisNatural SciencesCationic GoldChiral All‐benzenoid BiarylSynthetic Chemistry
The cationic gold(I)/( R )‐xyl‐binap complex was shown to catalyze the atroposelective intramolecular hydroarylation of alkynones to produce enantioenriched axially chiral all‐benzenoid biaryls, 4‐aryl‐2‐naphthol derivatives, with up to 67 % ee . The reaction of a racemic alkynone in the presence of the same gold(I) catalyst also afforded the corresponding axially chiral all‐benzenoid biaryl in excellent yield with 70 % ee .
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