Publication | Closed Access
Allylic Imidate Rearrangements Catalyzed by Planar Chiral Palladacycles
98
Citations
96
References
2010
Year
Allylic Imidate RearrangementCross-coupling ReactionEngineeringAlkene MetathesisPlanar Chiral IronPlanar Chiral PalladacyclesAsymmetric SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisChemistryAsymmetric CatalysisEnantioselective SynthesisBiomolecular Engineering
The discovery that palladacycles are efficient catalysts for the allylic imidate rearrangement has resulted in the successful application of several such complexes to this reaction based on planar chiral iron and cobalt containing metallocenes. These palladacycles enable the efficient and highly enantioselective synthesis of a wide variety of protected allylic amines, which are valuable building blocks for use in asymmetric synthesis.
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