Phenacyl azides were reacted with pyridinium ylides in the presence of Cu(OAc)2 (2 mol%) and Et3N utilizing molecular oxygen as a green oxidant to yield imidazo[1,2-a]pyridines in exclusive regioselectivity. Following the optimized protocol, 28 different fused heterocycles were synthesized in high yields (71-92%). In order to get mechanistic insight into the reaction, a few control experiments were carried out and the role of the copper salt was discussed.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1039/c5cc00815h | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!