Novel transformation activates C–C bonds in benzene using rare-earth metallacycles, suggesting new pathways for arene reactivity.
Activation of inert C–C bonds in arenes remains a formidable challenge in synthetic chemistry. Despite advances in arene C–C bond activation, metathesis transformations of aromatic C–C bonds remain largely unexplored. Recently, we uncovered a rare-earth metal-enabled intramolecular metathesis between a benzene C–C bond and a C–C single bond, assisted by the high reactivity and synergistic effect of rare-earth metallacycles. Mechanistic studies reveal a stepwise [2+2] cycloaddition/cycloreversion sequence via a fused tricyclic intermediate. This transformation expands the chemical space of arene reactivity, providing a rare example of aromatic ring-opening metathesis through a noncarbene pathway.
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Liu et al. (2025) studied this question.
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