化学
选择氟
碘苯
区域选择性
三甲基硅烷
三氟甲基化
三氟甲磺酸
二甲基甲酰胺
有机化学
盐(化学)
药物化学
三氟甲基
催化作用
烷基
溶剂
作者
Wei Yu,Xiu‐Hua Xu,Feng‐Ling Qing
标识
DOI:10.1002/adsc.201500027
摘要
Abstract An efficient regioselective fluorotrifluoromethylation of unactivated alkenes has been developed. The reaction of alkenes with (trifluoromethyl)trimethylsilane (TMSCF 3 ) and Selectfluor in the presence of silver trifluoromethanesulfonate (AgOTf), cesium fluoride (CsF), and iodobenzene diacetate [PhI(OAc) 2 ] in N , N ‐dimethylformamide (DMF) at −20 °C gave the corresponding fluorotrifluoromethylated products in moderate to good yields. The silver salt turns out to be crucial for this transformation. magnified image
科研通智能强力驱动
Strongly Powered by AbleSci AI