4.8 Article

Photoredox-Catalyzed α-C(sp3)-H Activation of Unprotected Secondary Amines: Facile Access to 1,4-Dicarbonyl Compounds

Journal

ORGANIC LETTERS
Volume 22, Issue 19, Pages 7460-7464

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.0c02571

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Funding

  1. National Natural Science Foundation of China [21901118, 21875109]
  2. Natural Science Foundation of Jiangsu Province [BK20190430]
  3. Fundamental Research Funds for the Central Universities [30919011217]

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A photoredox-catalyzed alpha-C(sp(3))-H activation approach of unprotected secondary amines is reported. Such transformations provide facile access to various 1,4-dicarbonyl compounds using readily available amines and alpha,beta-unsaturated compounds as feedstocks under air conditions. The substrate scope of this method is broad, and a wide array of functional groups are tolerated.

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