Halofluorination of Alkenes Using Trihaloisocyanuric Acids and HF×Pyridine
作者:Marcio de Mattos、Pierre Esteves、Lívia Crespo、Rodrigo Ribeiro
DOI:10.1055/s-0029-1220011
日期:2010.7
Halofluorination of alkenes with a new system (trihaloisocyanuric acids and HFËpyridine) 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%.