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Iridium‐Catalyzed Asymmetric Hydrogenation of N‐Protected Indoles
146
Citations
24
References
2010
Year
Asymmetric CatalysisEngineeringNatural SciencesDiversity-oriented SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisHigh YieldHydrogenChemistryChiral NHomogeneous CatalysisChiral IndolinesMolecular CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringAsymmetric Hydrogenation
Chiral indolines substituted at C-2 or C-3 can be prepared in high yield and excellent enantioselectivity by asymmetric hydrogenation of N-protected indoles by using Ir catalysts with chiral N,P ligands. With less reactive substrates, the reaction had to be carried out at elevated temperature, but even at 60–110 °C very high enantiomeric excesses of up to 98–99 % could be obtained (see scheme).
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