作者:Laurence Carroll、M? Carmen Pacheco、Ludivine Garcia、V?ronique Gouverneur                                    
                                    
                                        DOI:10.1039/b610013a
                                    
                                    
                                        日期:——
                                    
                                    Allenylsilanes reacted at room temperature in acetonitrile with Selectfluor, an electrophilic fluorinating reagent, to give secondary propargylic fluorides in moderate to good yields; mechanistically, a side-product resulting from a 1,2-silyl shift testifies to the presence of a cationic intermediate.
                                    烯丙基
硅烷在室温下与亲电
氟化试剂Selectfluor反应,在
乙腈中以中等至良好的产率生成次级炔丙基
氟化物;机理上,由1,2-
硅转移产生的副产物证明存在阳离子中间体。