Litcius/Paper detail

Nickel-Catalyzed Dynamic Kinetic Asymmetric Reductive Arylation of Aldehydes with Heterobiaryl Triflates

Xinran Ding, Chuan Wang

2025Organic Letters15 citationsDOI

Abstract

In this context, we report a nickel-catalyzed dynamic kinetic asymmetric reductive arylation of aldehydes with racemic heterobiaryl triflates, offering a series of axially chiral heterobiaryls bearing a centrally chiral secondary alcohol moiety in a highly diastereo- and enantioselective manner. The simultaneous control of both axial and central stereogenic elements of the products lies in the stereoselective nucleophilic addition of the configurationally labile hetereobiaryl nickel complex to the formyl group of aldehydes.

Topics & Concepts

ChemistryCatalysisNickelKinetic energyCombinatorial chemistryReductive eliminationOrganic chemistryPhysicsQuantum mechanicsAxial and Atropisomeric Chirality SynthesisCatalytic C–H Functionalization MethodsAsymmetric Hydrogenation and Catalysis
Nickel-Catalyzed Dynamic Kinetic Asymmetric Reductive Arylation of Aldehydes with Heterobiaryl Triflates | Litcius