Abstract
AbstractIn this work, a Rh(I)-catalyzed C3-alkenylation of 2,2′-bipyridine-6-carboxamide with terminal and internal alkynes was developed, providing an efficient access to a broad range of alkenylated 2,2′-bipyridine derivatives with exclusive regioselectivity and stereoselectivity. Deuterium labeling experiments indicate that an irreversible rollover C–H activation process is involved in this reaction.
Funder
National Natural Science Foundation of China
Subject
Organic Chemistry,Catalysis