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. 2020 Oct 14;11(45):12323–12328. doi: 10.1039/d0sc05137c

The Cu-catalyzed transamidation of tertiary amides 1a.

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a

Reaction conditions: 1a (0.20 mmol), Selectfluor (0.30 mmol), CuBr2 (4 μmol, 2.0 mol% of Cu), and MeCN (1.0 mL) at 80 °C for 1 h under argon. To isolate the product as N-benzylamides, the one-pot transamidation was carried out for 3–24 h. For details, see ESI.

b

Isolated yield of ethyl 3-phenylpropionate.