Nickel-Catalyzed Asymmetric Reductive Diarylation of Vinylarenes.
Ontology highlight
ABSTRACT: A nickel-catalyzed asymmetric diarylation reaction of vinylarenes enables the preparation of chiral α,α,β-triarylated ethane scaffolds, which exist in a number of biologically active molecules. The use of reducing conditions with aryl bromides as coupling partners obviates the need for stoichiometric organometallic reagents and tolerates a broad range of functional groups. The application of an N-oxyl radical as a ligand to a nickel catalyst represents a novel approach to facilitate nickel-catalyzed cross-coupling reactions.
SUBMITTER: Anthony D
PROVIDER: S-EPMC8864584 | biostudies-literature | 2019 Mar
REPOSITORIES: biostudies-literature
ACCESS DATA