An efficient B(CF)-catalyzed multicomponent reaction of 2,3-diketoesters, amines, allenes, and nucleophiles was reported, which afforded 2α-functionalized pyrroles in moderate to good yields. The reaction features low catalyst loading, usage of a small amount of solvent, high atom economy, tunable installation of diverse functional groups at 2α-position, and water being formed as the byproduct. This is the first multicomponent reaction that combines vicinal tricarbonyl compounds with allenes.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.joc.4c01221 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!