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Palladium-Catalyzed Asymmetric Amination and Imidation of 2,3-Allenyl Phosphates
83
Citations
18
References
2005
Year
Active 1-Aminated Derivatives2,3-Allenyl PhosphatesEngineeringOrganic ChemistryOrganometallic CatalysisCatalysisStereoselective SynthesisPalladium-catalyzed Asymmetric AminationChemistryAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringZerovalent Palladium Complexes
[reaction: see text] Asymmetric amination of 2,3-allenyl phosphates with nitrogen nucleophiles such as amines, hydroxylamines, and imides can be performed efficiently using a combination of zerovalent palladium complexes and SEGPHOS or MeOBIPHEP ligand, affording the corresponding optically active 1-aminated derivatives with enantiomeric excess of up to 97% ee.
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