Abstract
The first cyclization/decarboxylation reaction of isatins with acyl chlorides promoted by 4-dimethylaminopyridine (DMAP) was described and a series of desired 3-alkenyl-oxindoles were obtained in good yields (up to 80%) and E/Z selectivities (up to 6.4/1). This protocol provided a new and feasible access to 3-alkenyl-oxindoles.
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
