Abstract
AbstractChiral ligands play an essential role in transition-metal-catalyzed enantioselective transformations, in which chiral oxazoline-based scaffolds are the privileged chiral ligand. Nevertheless, 8-quinolinyl oxazoline (8-Quinox) ligands are underexplored in transition-metal-catalyzed asymmetric transformations since their development in 1998. Herein, we report an 8-Quinox ligand promoted Ni-catalyzed enantioselective reductive carbamoyl-alkylation of carbamoyl chloride tethered styrene with unactivated alkyl iodide, providing an expedient access to valuable enantioenriched oxindoles in good results.
Funder
Fundamental Research Funds for the Central Universities
Project 211
China Postdoctoral Science Foundation
National Natural Science Foundation of China
Shanghai Rising-Star Program
Natural Science Foundation of Shanghai
Cited by
6 articles.
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