One-Pot asymmetric nitro-mannich/hydroamination cascades for the synthesis of pyrrolidine derivatives: Combining organocatalysis and gold catalysis

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Abstract

The highly enantioselective preparation of trisubstituted pyrrolidine derivatives employing a one-pot nitro-Mannich/hydroamination cascade is reported. This cascade approach utilizes an asymmetric bifunctional organocatalytic nitro-Mannich reaction followed by a gold-catalyzed allene hydroamination reaction. The products are afforded in good yields and excellent diastereo- and enantioselectivities. © 2014 American Chemical Society.

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Barber, D. M., Ďuriš, A., Thompson, A. L., Sanganee, H. J., & Dixon, D. J. (2014). One-Pot asymmetric nitro-mannich/hydroamination cascades for the synthesis of pyrrolidine derivatives: Combining organocatalysis and gold catalysis. ACS Catalysis, 4(2), 634–638. https://doi.org/10.1021/cs401008v

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