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Electrochemical methods improve molecular editing to produce isoquinolines in larger quantities, indicating potential for industrial applications.
Molecular editing and atom insertion are powerful tools for the late‐stage construction of complex molecular architectures, especially in medicinal chemistry. However, up to now, such transformations rely on harsh conditions and superstoichiometric chemical oxidants. Although electrochemical strategies for skeletal editing strongly mitigate some of these constraints, the substrate scope remains narrow. Moreover, the use of hazardous reagents in high concentrations severely limits the applicability of these strategies for scale‐up and subsequent industrial application. To overcome these bottlenecks, we herein present a manganaelectro‐catalyzed nitrogen atom insertion furnishing isoquinolines with broad functional group tolerance. Furthermore, our approach also proved suitable for recirculation flow electrolysis, including scale‐up, reflecting its potential for industrial application.
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Homölle et al. (2026) studied this question.
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