Abstract
This cover picture shows a ligand‐controlled, palladium‐catalyzed migration reaction of [60]fullerene with allyloxy‐tethered aryl iodides. Using 1,2‐bis(diphenylphosphino)benzene (DPPBz) as a ligand, the chemoselectivity is switched to synthesize [60]fullerene‐fused allylbenzofurans instead of previous spirocyclic derivatives through a sequential C—O bond cleavage/allyl‐migration/intermolecular cycloaddition cascade process. Such transformation provides a unique and efficient route to rare [60]fullerene‐fused benzofurans. More details are discussed in the article by Liu et al. on page 1733—1739.image
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