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- W2952236102 abstract "Abstract A general and simple protocol for the synthesis of α-substituted alkenylsulfones has been developed firstly via palladium-catalyzed Suzuki reactions between α-bromo ethenylsulfones and organoborons. Using a catalyst composed of Pd(OAc) 2 and SPhos, a variety of aryl, heteroaryl, and alkylboron reagents could efficiently couple with α-bromo ethenylsulfones under mild conditions. Moreover, it has been demonstrated for the first time that vinyl sulfones underwent smooth reduction by diimide generated from 2-nitrobenzenesulfonylhydrazide." @default.
- W2952236102 created "2019-06-27" @default.
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- W2952236102 date "2016-06-01" @default.
- W2952236102 modified "2023-09-24" @default.
- W2952236102 title "ChemInform Abstract: An Efficient and Straightforward Route to Terminal Vinyl Sulfones via Palladium-Catalyzed Suzuki Reactions of α-Bromo Ethenylsulfones." @default.
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- W2952236102 doi "https://doi.org/10.1002/chin.201629070" @default.
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