Abstract
A Pd(0)-catalyzed cascade cyclization of methylenecyclopropanes (MCPs) involving an intramolecular Heck-type reaction and β-H eliminations has been disclosed in this paper. The reaction proceeds smoothly through an unprecedented ring-opening pattern of MCPs via a cyclopropene intermediate and a vinylpalladium carbene species seemingly, furnishing spirocyclic compounds containing fluorene and 1,2-dihydronaphthalene moieties in moderate to good yields.
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
