Fig. 1: Enantioselective electrochemical C–H activation for full selectivity control. | Nature Catalysis

Fig. 1: Enantioselective electrochemical C–H activation for full selectivity control.

From: Enantioselective C–H annulations enabled by either nickel- or cobalt-electrocatalysed C–H activation for catalyst-controlled chemodivergence

Fig. 1: Enantioselective electrochemical C–H activation for full selectivity control.

a, Sustainability aspects of selected transition metals in comparison. b, Motivation for the development of enantioselective electrochemical C–H activation by 3d transition-metal catalysis. c, Divergent reaction pathways in alkene C–H annulations. d, Bicyclic bridged ring systems as bioisosteres for benzene derivatives. e, Selected chiral biologically active compounds containing bicyclo[2.2.1]heptane skeletons. f, Chemodivergent desymmetrizations enabled by electrocatalytic C–H activation (this work). e.r., enantiomeric ratio; d.r., diastereomeric ratio.

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