Abstract
Copper complexes, generated by the treatment of CuCl2 with EtMgCl, catalyze a reductive coupling reaction of perfluoroarenes with 1,3-dienes via C–F bond cleavage, in which the internal carbon of 1,3-dienes preferably reacts with perfluoroarenes giving rise to branched allylated perfluoroarenes as a major coupling product.
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
