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- W4240234864 endingPage "21406" @default.
- W4240234864 startingPage "21401" @default.
- W4240234864 abstract "Abstract A new family of carbon‐bound boron enolates, generated by a kinetically controlled halogen exchange between chlorocatecholborane and silylketene acetals, is described. These C−boron enolates are demonstrated to activate 1,3‐enyne substrates in the presence of a Pd 0 /Senphos ligand complex, resulting in the first examples of a carboboration reaction of an alkyne with enolate‐equivalent nucleophiles. Highly substituted dienyl boron building blocks are produced in excellent site‐, regio‐, and diastereoselectivity by the described catalytic cis ‐carboboration reaction." @default.
- W4240234864 created "2022-05-12" @default.
- W4240234864 creator A5027939460 @default.
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- W4240234864 creator A5075368025 @default.
- W4240234864 date "2021-08-31" @default.
- W4240234864 modified "2023-10-08" @default.
- W4240234864 title "C−Boron Enolates Enable Palladium Catalyzed Carboboration of Internal 1,3‐Enynes" @default.
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