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- W4386091255 abstract "Abstract An iridium‐catalyzed remote site‐switchable hydroarylation of alkenes was reported, delivering the products functionalized at the subterminal methylene and terminal methyl positions on an alkyl chain controlled by two different ligands, respectively, in good yields and with good to excellent site‐selectivities. The catalytic system showed good functional group tolerance and a broad substrate scope, including unactivated and activated alkenes. More importantly, the regioconvergent transformations of mixtures of isomeric alkenes were also successfully realized. The results of the mechanistic studies demonstrate that the reaction undergoes a chain‐walking process to give an [Ar−Ir−H] complex of terminal alkene. The subsequent processes proceed through the modified Chalk–Harrod‐type mechanism via the migratory insertion of terminal alkene into the Ir−C bond followed by C−H reductive elimination to afford the hydrofunctionalization products site‐selectively." @default.
- W4386091255 created "2023-08-24" @default.
- W4386091255 creator A5001940565 @default.
- W4386091255 creator A5005228021 @default.
- W4386091255 creator A5050166160 @default.
- W4386091255 creator A5051565228 @default.
- W4386091255 creator A5053771024 @default.
- W4386091255 creator A5076288007 @default.
- W4386091255 date "2023-08-31" @default.
- W4386091255 modified "2023-10-18" @default.
- W4386091255 title "Iridium‐Catalyzed Remote Site‐Switchable Hydroarylation of Alkenes Controlled by Ligands" @default.
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