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A New Type of Chiral Sulfinamide Monophosphine Ligands: Stereodivergent Synthesis and Application in Enantioselective Gold(I)‐Catalyzed Cycloaddition Reactions
272
Citations
45
References
2014
Year
EngineeringNew TypeOrganic ChemistryChemistryChiral Sulfinamide MonophosphinesMedicinal ChemistryNovel OrganocatalystsStereodivergent SynthesisMing-phos LigandsOrganometallic CatalysisStereoselective SynthesisCatalysisPharmacologyAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringSo-called Ming-phos LigandsNatural SciencesChiral Sulfinamide Monophosphine
A simple, new type of chiral sulfinamide monophosphines, the so-called Ming-Phos ligands, is reported; these ligands could be easily prepared from inexpensive and commercially available starting materials. The Ming-Phos ligands performed well in the enantioselective gold-catalyzed cycloaddition reaction of 2-(1-alkynyl)-alk-2-en-1-ones with nitrones. Both enantiomers of the products could be obtained in good yields and with excellent diastereo- and enantioselectivity through transformations that were catalyzed by gold complexes derived from two diastereomers of Ming-Phos ligand M5 (Ar=1-naphthyl).
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