Ruthenium-Catalyzed Enantioselective C–H Functionalization: A Practical Access to Optically Active Indoline Derivatives

This paper provide a new synthetic strategy to syntheis indoline derivatives by using commercial available chiral transient amine, gives a good ee( up to 94%) and also shows some potential application to some drug molecules. It provide a practical way to control the intramolecular enantioselective C-H activation. https://pubs.acs.org/doi/10.1021/jacs.9b07251