Despite significant advances in C–F bond functionalization, the selective hydrogenative defluorination of monofluoroalkenes remains a considerable challenge due to competing over-reduction issues. Here, we report a practical and selective protocol for the hydrodefluorination of monofluoroalkenes, employing an inexpensive ruthenium(II) catalyst with sodium formate as a safe and convenient hydrogen source. This method enables the selective cleavage of C(sp 2 )–F bonds while minimizing overhydrogenation byproducts, thus providing efficient access to the corresponding alkenes. The reaction demonstrates broad functional group tolerance and is scalable to gram quantities.
Shu et al. (Thu,) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: