ABSTRACT
The iodocyclofunctionalization of a series of a α,γ-dialkenyl β-enamino esters, led to the formation of the corresponding tetrahydropyrrole 1,2,3,5-tetrasubstituted, in yields ranging from 20–80%.
ACKNOWLEDGMENTS
The authors thanks the financial support from FAPESP (98/10821-0), CNPq and FINEP.