Enantio‐ and Regioselective NiH‐Catalyzed Reductive Hydroarylation of Vinylarenes with Aryl Iodides
Yuli He, Chuang LIU, Lei Yu, Shaolin Zhu
Abstract
A highly enantio- and regioselective hydroarylation process of vinylarenes with aryl halides has been developed using a NiH catalyst and a new chiral bis imidazoline ligand. A broad range of structurally diverse, enantioenriched 1,1-diarylalkanes, a structure found in a number of biologically active molecules, have been obtained with excellent yields and enantioselectivities under extremely mild conditions.
Topics & Concepts
RegioselectivityChemistryCatalysisArylHalideLigand (biochemistry)Combinatorial chemistryReductive eliminationMoleculeStereoisomerismOrganic chemistryReceptorBiochemistryAlkylCatalytic C–H Functionalization MethodsSynthesis and Catalytic ReactionsAsymmetric Hydrogenation and Catalysis