Abstract
Abstract Various tetra-acceptor-substituted alkenes possessing unsymmetrical substituents have been effectively synthesized from vicinal tricarbonyl compounds. The alkenes have polyfunctionality and high electron deficiency. In addition, they easily react with pyrroles to give divergent pyrrolizine derivatives via the conjugate addition of pyrroles followed by intramolecular cyclization. We successfully controlled the chemoselectivity of the intramolecular cyclization (ester/ketone attack) to afford a wide range of valuable pyrrolizine derivatives.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
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
