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.
Original language | English (US) |
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Pages (from-to) | 3198-3202 |
Number of pages | 5 |
Journal | Angewandte Chemie - International Edition |
Volume | 58 |
Issue number | 10 |
DOIs | |
State | Published - Mar 4 2019 |
Keywords
- alkenes
- aryl bromides
- asymmetric catalysis
- diarylation
- nickel
ASJC Scopus subject areas
- Catalysis
- General Chemistry