Abstract
The alkoxy radicals that are derived from cyclic hemiacetals have been generated through the visible-light-promoted reaction of the corresponding N-alkoxyphthalimides with Hantzsch ester as the reductant. The alkoxy radicals subsequently undergo β-scission of the C-C bond to generate carbon-centered radicals, which are trapped by alkynyl-, alkenyl-, or allylsulfones.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have