Regiocontrolled Heptafluoroisopropylation of Aromatic Halides by Copper(I) Carboxylates with Heptafluoroisopropyl-Zinc Reagents
                                
                                    
                                        作者:Soichiro Ono、Yuki Yokota、Shigekazu Ito、Koichi Mikami                                    
                                    
                                        DOI:10.1021/acs.orglett.8b04147
                                    
                                    
                                        日期:2019.2.15
                                    
                                    Copper(I)-mediated heptafluoroisopropylation of aryl halides (ArX: X = I, Br) is demonstrated using copper(I) carboxylates and a bis(heptafluoroisopropyl)zinc reagent Zn(i-C3F7)2(dmf)2, prepared from heptafluoroisopropyl iodide and diethylzinc. The air-tolerant solid heptafluoroisopropylzinc reagent is advantageous to conduct simple synthetic operations and successful to give the corresponding heptafluoroisopropyl
                                    使用
羧酸铜(I)和双(七
氟异丙基)
锌试剂Zn(i- C 3 F 7)2(dmf)2证明了
铜(I)介导的芳基卤化物的七
氟异丙基化(ArX:X = I,Br)。由七
氟异丙基
碘化物和
二乙基锌制备。所述耐空气的固体七
氟异丙基
锌试剂有利于进行简单的合成操作,并成功地通过
金属转移至
铜(I)中心而得到相应的七
氟异丙基
芳烃衍
生物。新开发的
铜(I)介导的七
氟异丙基化工艺可以通过
羧酸银盐推进到
铜(I)催化中,并与以前的基于自由基的工艺互补。