Palladium-Catalyzed Double Alkylation of 3-Aryl-2-fluoroallyl Esters with Malonate Nucleophiles through the Carbon–Fluorine Bond Cleavage
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文摘
The alkylation of (Z)-3-aryl-2-fluoroallyl acetate with the malonate anion by the [Pd(C3H5)(cod)]BF4/2,2鈥?bpy catalyst proceeds through the carbon鈥揻luorine bond cleavage, and 2 equiv of the malonate nucleophile was introduced to the allyl substrate.

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