Iridium-Catalyzed

Synthesis Enantiomer Yield NMR spectroscopy Chiral Catalyst Enantioselective Imines Hydrogenation Solvent Substrate-Directed Enantiomeric excess (ee) Pyridine Stereoselective Olefins Intramolecular N-heterocyclic carbene Reaction Conditions Asymmetric Hydrogenation C-H Activation Late-Stage Functionalization Catalyst Loading Amidation Product C-H Borylation Intermolecular Aza-Michael Addition Iridium Catalyst Trisubstituted Olefins Tetrasubstituted α-Fluoro-β-enamino Esters Efficient Access to Chiral α-Fluoro-β-amino Esters Two Adjacent Tertiary Stereocenters sp3 C-H Bonds Regioselective Cascade α,β-Unsaturated Ketones Enantioconvergent Allylation Boron-Stabilized Organozinc Reagent Benzylic Reactant Arene Ortho-silylation Formal hydroxyl-directed Cyclobutanes C(sp3)–H Borylation unactivated methyl group β-keto esters f-amphox ligands β-dehydroamino acid derivatives Monodentate phosphoramidites