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Enantioselective Copper‐Catalyzed Three‐Component Carboboronation of Allenes: Access to Functionalized Dibenzo [<i>b,f</i>][1,4]oxazepine Derivatives
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Citations
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References
2019
Year
Chemical EngineeringChiral ProductsEngineeringNatural SciencesDiversity-oriented SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisChemistryAsymmetric CatalysisChiral Diphosphine LigandEnantioselective SynthesisChiral P
Abstract A copper‐catalyzed enantioselective three‐component difunctionalization of allenes with seven‐membered cyclic imines and bis(pinacolato)diboron (B 2 (Pin) 2 ) to approach functionalized dibenzo[ b,f ][1,4]oxazepine derivatives is developed. The chiral products are obtained in up to 81% yield, >20:1 dr, and 98% ee when either a chiral diphosphine ligand or a chiral ferrocenyl‐based P,N‐ligand is used. Furthermore, the reaction exhibits reversed diastereoselectivities when the chiral diphosphine ligand and the chiral P,N‐ligand are used respectively. magnified image
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