Fig. 3: Scope for secondary acyl enamines.
From: Enantioselective access to chiral aliphatic amines and alcohols via Ni-catalyzed hydroalkylations
The reaction was run on 0.2 mmol of acyl enamine and 0.4 mmol of alkyl iodide using DEMS (0.6 mmol) under indicated conditions unless otherwise stated. aDMMS was used instead of DEMS. bL4 was used as the ligand.
