Deoxyfluorination of Carboxylic Acids with CpFluor: Access to Acyl Fluorides and Amides
作者:Xiu Wang、Fei Wang、Fengfeng Huang、Chuanfa Ni、Jinbo Hu
DOI:10.1021/acs.orglett.1c00190
日期:2021.3.5
deoxyfluorination of carboxylic acids to afford various acyl fluorides. This all-carbon-based fluorination reagent enabled the efficient transformation of (hetero)aryl, alkyl, alkenyl, and alkynyl carboxylic acids to the corresponding acyl fluorides under the neutral conditions. This deoxyfluorination method was featured by the synthesis of acyl fluorides with in-situ formed CpFluor, as well as the one-pot
3,3-二氟-1,2-二苯基环丙烯(CpFluor)是一种台式稳定的氟化试剂,已用于羧酸的脱氧氟化反应中,制得各种酰基氟。这种基于全碳的氟化试剂能够在中性条件下将(杂)芳基,烷基,烯基和炔基羧酸有效转化为相应的酰基氟。这种脱氧氟化方法的特点是通过原位形成的CpFluor合成酰基氟,以及通过原位形成的酰基氟进行羧酸的一锅酰胺化反应。