Nickel(0)-Catalyzed [2 + 2 + 1] Carbonylative Cycloaddition of Imines and Alkynes or Norbornene Leading to γ‑Lactams
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https://figshare.com/articles/dataset/Nickel_0_Catalyzed_2_2_1_Carbonylative_Cycloaddition_of_Imines_and_Alkynes_or_Norbornene_Leading_to_Lactams/2235775
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The first nickel(0)-catalyzed [2 + 2 + 1] carbonylative cycloaddition reaction of imines and alkynes or norbornene has been achieved by employing phenyl formate as a CO source. With this method, a variety of N-benzenesulfonyl, -tosyl, and -phosphoryl-substituted γ-lactams can be prepared in good to high yields.
创建时间：
2016-02-16
