Copper(II)-Catalyzed Enantioselective Addition of Aryl Amines to Isatin-Derived N-Boc-Ketimines for the Synthesis of Acyclic N,N′-Ketals

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Here, we demonstrated a copper(II)-catalyzed enantioselective addition of aryl amines to isatin-derived N -Boc-ketimines using chiral O–N–N tridentate ligands derived from BINOL and proline. Generally, the chiral acyclic N, N ′-ketals were obtained in high yields (up to 98%) and excellent ee values (up to 98%). Various aryl amines could be tolerated and a gram-scale reaction was also possible. Further, an X-ray diffraction experiment confirmed that the configuration of isatin-derived N -Boc ketimine should be ( Z ). Confirmation of the configuration of the ketimine would make it easier to understand the rationale for stereofacial selective activation of the electrophile with either organo- or Lewis acid–based catalysts.

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