Abstract

In this issue of Chem Catalysis, Zhang and co-workers demonstrate the utility of electrochemical methods to enable catalytic turnover, employing high-valent Cu for C-H bond fluorination with selectivity for more hydridic bonds. Corresponding mechanistic investigations offer a rare catalytic example of oxidation driven C-H activation.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call