P,Sligands For The Asymmetric Construction Of Quaternary Stereocenters In Palladium-Catalyzed Decarboxylative [4+2] Cycloadditions

A new hybrid P,Sligand was exploited by combining a chiral -amino sulfide and a simple diphenyl phosphite. The resultant ligand performs extremely well in a palladium-catalyzed asymmetric decarboxylative [4+2] cycloaddition reaction, thus generating multiple contiguous stereocenters and a chiral quaternary center. By doing so, a straightforward route to highly functionalized tetrahydroquinolines was developed with yields of up to 99%, as well as 98% ee and greater than 95:5 d.r. Moreover, mechanistic insights into this transformation and the possible stereocontrol are discussed.