Ni-Catalyzed Carboxylation of Aziridines en Route to β-Amino Acids

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Abstract

A Ni-catalyzed reductive carboxylation of N-substituted aziridines with CO2 at atmospheric pressure is disclosed. The protocol is characterized by its mild conditions, experimental ease, and exquisite chemo- and regioselectivity pattern, thus unlocking a new catalytic blueprint to access β-amino acids, important building blocks with considerable potential as peptidomimetics.

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Davies, J., Janssen-Müller, D., Zimin, D. P., Day, C. S., Yanagi, T., Elfert, J., & Martin, R. (2021). Ni-Catalyzed Carboxylation of Aziridines en Route to β-Amino Acids. Journal of the American Chemical Society, 143(13), 4949–4954. https://doi.org/10.1021/jacs.1c01916

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