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https://doi.org/10.1039/c3cc46574h
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Cite Journal: Chem. Commun. |  Publication Date: Jan 1, 2014 |
 Citations: 17 |
A highly regioselective palladium-catalyzed allylic alkylation of dienyl esters with nitromethane has been developed, providing selective access to the C-5 attacked products. The structures of the ligands as well as the steric effect of the substrates are important factors in determining the regiochemical outcome of the reaction.
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