Organocatalytic asymmetric allylic amination of Morita-Baylis-Hillman carbonates of isatins

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Abstract

The investigation of a Lewis base catalyzed asymmetric allylic amination of Morita-Baylis-Hillman carbonates derived from isatins afforded an electrophilic pathway to access multifunctional oxindoles bearing a C3-quaternary stereocenter, provided with good to excellent enantioselectivity (up to 94% ee) and in high yields (up to 97%). © 2012 Zhang et al.

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Zhang, H., Zhang, S. J., Zhou, Q. Q., Dong, L., & Chen, Y. C. (2012). Organocatalytic asymmetric allylic amination of Morita-Baylis-Hillman carbonates of isatins. Beilstein Journal of Organic Chemistry, 8, 1241–1245. https://doi.org/10.3762/bjoc.8.139

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