Nature Communications (Feb 2021)

Three-component radical homo Mannich reaction

  • Shuai Shi,
  • Wenting Qiu,
  • Pannan Miao,
  • Ruining Li,
  • Xianfeng Lin,
  • Zhankui Sun

DOI
https://doi.org/10.1038/s41467-021-21303-3
Journal volume & issue
Vol. 12, no. 1
pp. 1 – 7

Abstract

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Due to the ionic nature of its mechanism, the Mannich reaction can only use non-enolizable aldehydes as substrates. Here, the authors expand the scope of the classical Mannich reaction to enolizable aldehydes by employing a radical process resulting in a streamlined synthesis of γ-amino-carbonyl compounds.