Abstract
AbstractA mild and efficient nickel‐catalyzed 2,2‐difluoroethylation of (hetero)aryl halides with readily available 2‐chloro‐1,1‐difluoroethane has been developed. The reductive cross‐coupling reaction is synthetically simple and exhibits good functional group tolerance. This approach provides a facile access to synthesize 2,2‐difluoroethylated molecules for drug discovery.
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