作者:F. L. M. Pattison、D. A. V. Peters、F. H. Dean
DOI:10.1139/v65-223
日期:1965.6.1
The addition of "BrF", using N-bromoamides in anhydrous hydrogen fluoride, to a number of aliphatic alkenes has been studied. As expected, the bromine atom in the resultant vicinal fluorobromides exhibited relatively low reactivity in nucleophilic and hydrogenolytic reactions.
已经研究了在无水氟化氢中使用 N-溴酰胺将“BrF”添加到许多脂肪族烯烃中。正如预期的那样,所得邻位氟溴化物中的溴原子在亲核和氢解反应中表现出相对较低的反应性。