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https://doi.org/10.1021/ol500121z
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Cite Journal: Organic Letters |  Publication Date: Jan 30, 2014 |
 Citations: 25 |
Affiliation: Nihon University
The alkylation of (Z)-3-aryl-2-fluoroallyl acetate with the malonate anion by the [Pd(C3H5)(cod)]BF4/2,2'-bpy catalyst proceeds through the carbon-fluorine bond cleavage, and 2 equiv of the malonate nucleophile was introduced to the allyl substrate.
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