Chiral γ-hydroxy-γ-lactams were versatile building blocks for the synthesis of many important bioactive compounds. Herein, we disclosed a regio- and enantioselective direct α-selective allylation of amide moiety of maleimides with potassium allyltrifluoroborates via dual-functional InIII/N,N'-dioxide complex. This protocol provides a straightforward route to optically active γ-hydroxy-γ-lactams. Additionally, alkenyloxindoles were tolerated as well, affording enantioenriched 2-allylindolin-2-ols in high yields. The gram-scale synthesis and further transformations of the products demonstrate the potential utility of this method. Based on the experimental studies and DFT calculations, a possible catalytic cycle and transition states were provided to elucidate the regio- and enantioselectivity.

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