Litcius/Paper detail

Enantioselective Synthesis of Axially and Centrally Chiral Styrenes via Nickel-Catalyzed Desymmetric Hydrocyanation of Biaryl Dienes

Can Li, Song‐Zhou Cai, Juntao Ye, Xianjie Fang

2024Organic Letters15 citationsDOI

Abstract

Herein, a highly regio-, enantio-, and diastereoselective nickel-catalyzed desymmetric hydrocyanation of biaryl dienes for the simultaneous construction of axial and central chiralities is presented, which offers a convenient approach to a variety of tirenes containing the union of an axially chiral biaryl and a centrally α-chiral nitrile under mild conditions using a commercially available catalyst. The synthetic utility is highlighted by the development of a novel axially chiral phosphine ligand and biphenyl-based chiral diene ligand and their potential applications in the field of asymmetric catalytic reactions.

Topics & Concepts

HydrocyanationChemistryEnantioselective synthesisCatalysisNitrileLigand (biochemistry)Combinatorial chemistryPhosphineAxial chiralityDieneNickelOrganic chemistryBiochemistryNatural rubberReceptorAxial and Atropisomeric Chirality SynthesisCatalytic C–H Functionalization MethodsAsymmetric Hydrogenation and Catalysis
Enantioselective Synthesis of Axially and Centrally Chiral Styrenes via Nickel-Catalyzed Desymmetric Hydrocyanation of Biaryl Dienes | Litcius