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Addition of fluoroalkyl iodides to olefins in the presence of hydrogen peroxide(H_2O_)in acetone,acetonitrile or ethanol gave the corresponding 1:1 adducts in good yields.Reaction offluoroalkyl iodide with diallyl ether(DAE)yielded tetrahydrofuran derivatives,p-Hydroquinone(p-HQ)can partly suppress the reaction.A radical initiation mechanism is proposed.
Addition of fluoroalkyl iodides to olefins in the presence of hydrogen peroxide (H_2O_) in acetone, acetonitrile or ethanol gave the corresponding 1: 1 adducts in good yield. Reaction offluoroalkyl iodide with diallyl ether (DAE) yielded tetrahydrofuran derivatives, p-Hydroquinone -HQ) can partly suppress the reaction. A radical initiation mechanism is proposed.