Abstract
A visible-light-promoted biaryl isocyanide insertion reaction has been developed to synthesize phenanthridine derivatives. The insertion proceeds via a radical process, and diaryliodonium salts and Umemoto’s reagent were used as radical sources. A variety of 6-arylated, as well as 6-trifluoromethylated, phenanthridine derivatives were obtained smoothly in good to excellent yields under mild conditions.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
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
