Electrofluoration en position benzylique dans le sulfolane
E Laurent, B Marquet, R Tardivel
Index: Laurent, Eliane; Marquet, Bernard; Tardivel, Robert Journal of Fluorine Chemistry, 1990 , vol. 49, # 1 p. 115 - 126
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Citation Number: 23
Abstract
Abstract The use of sulfolane as a solvent instead of acetonitrile in the electrofluorination of benzylic derivatives1,(R= H, Cl) gives greater yields of benzylic fluorides 2, since the formation of acetamido byproducts 4 is prevented. However, the parallel fluorination of the aromatic nucleus is not avoided under these conditions.
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