Halofluorination of Alkenes Using Trihaloisocyanuric Acids and HF center dot Pyridine

[摘要]：Halofluorination of alkenes with a new system (trihaloisocyanuric acids and HF center dot pyridine) results in the formation of vicinal halofluoroalkanes. The reaction is regioselective leading to Markovnikov-oriented products and the halofluorinated adducts follow anti-addition in the case of cyclohexene and 1-methylcyclohexene. Reaction yields range from 67-88%.

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