scheme3
![Asymmetric [4+2] annulation of <i>N</i>-sulfonyl ketimines: access to <i>N</i>-heterocycles bearing 1,3-nonadjacent stereocenters with a quaternary carbon center](https://image.oaes.cc/22e1aeeb-06a0-4f29-a95f-f5f36830e38f/cs4058.scheme.3.jpg)
Scheme 3. Substrate scope of aminochalcones 2a. aConditions: 1a (0.10 mmol), 2 (0.15 mmol), and catalyst (0.01 mmol) in CHCl3 (1.0 mL) at 25 °C; bIsolated yield; cDetermined by 1H NMR of the crude reaction mixture; dThe ee values were determined by chiral HPLC analysis.