The Cu-catalyzed, formal aza-[3 + 2] cycloaddition reaction of pyridine derivatives with α-diazo oxime ethers in trifluoroethanol was used to synthesize imidazopyridines via the release of molecular nitrogen and elimination of alcohol. These methods enabled modular synthesis of a wide range of N-heterobicyclic compounds such as imidazopyridazines, imidazopyrimidines, and imidazopyrazines with an α-imino Cu-carbenoid generated from the α-diazo oxime ethers and copper.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.joc.7b01714 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!