Palladium-Catalyzed Asymmetric Larock Isoquinoline Synthesis to Access Axially Chiral 3,4-Disubstituted Isoquinolines

Larock isoquinoline synthesis is one of the most efficient and straightforward approaches to the construction of 3,4-disubstituted isoquinolines. However, there have been no asymmetric versions for the synthesis of axially chiral isoquinolines since their initial report in 2001. Herein, we documented the first example of an asymmetric Larock isoquinoline synthesis by employing Pd(OAc)2/Walphos SL-W002–1 as the catalyst, affording the axially chiral 3,4-disubstituted isoquinolines with up to 97.5:2.5 er and 98% yield. Density Functional Theory (DFT) calculations clearly clarified the catalytic mechanism and the origin of the experimentally observed enantioselectivity.