Molecules · 2010 · 56 citations · 47 references
Natural SciencesChemistryCatalysisOrganic ChemistryOrganometallic ChemistryCatalytic MaterialsCatalytic MechanismsMetal Ion CatalysisOrganic SynthesisAmination ReactionsAsymmetric CatalysisBifunctional CatalysisBifunctional CatalystsEnantioselective CatalysisEnantioselective SynthesisHydrogenationKetones
Chiral amines are one of the ubiquitous functional groups in fine chemical, pharmaceutical and agrochemical products, and the most convenient, economical, and eco-benign synthetic pathway to these amines is direct asymmetric reductive amination (DARA) of prochiral ketones. This paper shows that a wide range of aliphatic ketones can be directly aminated under hydrogenation conditions, affording chiral amines with good to excellent yields and with enantioselectivities up to 96% ee. The catalysis is effected by the cooperative action of a cationic Cp*Ir(III) complex and its phosphate counteranion.
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Enantioselective Organocatalytic Reductive Amination
Richard Storer, Diane E. Carrera, Yike Ni et al. · Journal of the American Chemical Society · 2005 · 731 citations