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Unusual Selectivity of Unprotected Aziridines in Palladium-Catalyzed Allylic Amination Enables Facile Preparation of Branched Aziridines
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Citations
7
References
2004
Year
Cross-coupling ReactionEngineeringHigh LevelsOrganic ChemistryOrganometallic CatalysisCatalysisUnusual SelectivityChemistryBranched AziridinesUnprotected AziridinesStereoselective SynthesisAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringComplex Molecule Environment
Functionalized branched aziridines can be prepared in high yields and with high levels of regioselectivity using unprotected aziridines as nitrogen sources in palladium-catalyzed allylic amination. High levels of enantioselectivity can be achieved with BINAP on palladium. This methodology allows for strategic placement of an aziridine-containing fragment within a complex molecule environment for further elaboration.
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