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- W3164103650 endingPage "3572" @default.
- W3164103650 startingPage "3559" @default.
- W3164103650 abstract "Transition-metal catalyzed multi-component reactions have captured the attention of researchers in organic synthesis and drug synthesis due to their advantages of simple operation, easy availability of raw materials and without separation of intermediates. Among the multi-component reactions, the three-component processes have been developed into effective organic procedures. This personal account reviews our and other group's studies on the development of three-component coupling reaction for the rapid construction of two new chemical bonds simultaneously via benzylpalladium intermediates. Catalyst-switched three-component reactions of benzyl halides, activated olefins, and allyltributylstannane were successfully conducted to produce the corresponding benzylallylation products. Activation and conversion of carbon monoxide and carbon dioxide via π-benzylpalladium intermediates provide access to a wide range of unsaturated ketones and esters with excellent functional group tolerance. Meanwhile, other methods to produce benzylpalladium intermediates, including Heck insertion of alkenes into arylpalladium complexes, the oxidative addition of benzyl carbonate to palladium complexes and palladium-carbene migratory insertion, were also highlighted." @default.
- W3164103650 created "2021-06-07" @default.
- W3164103650 creator A5034305271 @default.
- W3164103650 creator A5045733530 @default.
- W3164103650 creator A5047855118 @default.
- W3164103650 date "2021-05-24" @default.
- W3164103650 modified "2023-10-11" @default.
- W3164103650 title "Palladium‐Catalyzed Three‐Component Coupling Reaction via Benzylpalladium Intermediate" @default.
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