4.8 Article

Enantioselective Nickel-Catalyzed C(sp3)-H Activation of Formamides

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/ange.202209625

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  1. National Natural Science Foundation of China [22188101, 21871145]
  2. Haihe Laboratory of Sustainable Chemical Transformations and Frontiers Science Center for New Organic Matter, Nankai University [63181206]
  3. Fundamental Research Funds for the Central Universities
  4. Key Scientific Research Project in Colleges and Universities of Henan Province of China [22A150047]

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Enantioselective Ni-catalyzed C(sp(3))-H bond activation was achieved using a phosphine oxide-ligated Ni-Al bimetallic catalyst, leading to the synthesis of a series of chiral N-containing heterocycles in good yields and high enantioselectivity.
Enantioselective Ni-catalyzed C(sp(3))-H bond activation remains an elusive challenge. Herein, we used phosphine oxide-ligated Ni-Al bimetallic catalyst to realize enantioselective Ni-catalyzed aliphatic C(sp(3))-H activation of formamides, providing a series of chiral N-containing heterocycles in 40-95 % yield and 70-95 % ee.

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