4.8 Article

Palladium-Catalyzed C(sp3) C(sp2) Cross-Coupling of (Trimethylsilyl)methyllithium with (Hetero)Aryl Halides

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ORGANIC LETTERS
卷 17, 期 9, 页码 2262-2265

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b00905

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  1. Netherlands Organization for Scientific Research (NWO-CW)
  2. National Research School Catalysis (NRSC-C)
  3. European Research Council (ERC) [227897]
  4. Royal Netherland Academy of Arts and Sciences (KNAW)
  5. Ministry of Education Culture and Science [024.601035]

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The palladium-catalyzed direct cross-coupling of a range of organic chlorides and bromides with the bifunctional C(sp(3))-(trimethylsilyl)methyllithium reagent is reported. The use of Pd-PEPPSI-IPent as the catalyst allows for the preparation of structurally diverse and synthetically versatile benzyl- and allylsilanes in high yields under mild conditions (room temperature) with short reaction times.

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