A Cu-based homogeneous catalytic system was proposed for the preparation of imides from alkene-tethered amides. Here, O acted as a terminal oxidant and a cheap and easily available oxygen source. The cleavage of C[double bond, length as m-dash]C bonds and the formation of C-N bonds were catalyzed by Cu(ii) salts with proper nitrogen-containing ligands under 100 °C.
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