Abstract

A bulky 1-phosphabarrelene, , was obtained from the reaction of a phosphinine with benzyne; two palladium complexes of were successfully employed in the Suzuki-Miyaura coupling of several aryl chlorides with phenylboronic acid at a relatively low catalyst loading, and activated aryl chlorides were coupled at room temperature in the absence of strong bases.

Full Text
Paper version not known

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