Synthesis, Год журнала: 2024, Номер 56(19), С. 3045 - 3053
Опубликована: Июнь 11, 2024
Abstract Fluorinated molecules are widely used in pharmaceutical and agrochemical industries. Multifluoroalkyl-containing compounds have attracted increasing attention for their unique ability to alter the activity of drugs bioactive molecules. Herein, we report an efficient Rh(III)-catalyzed, redox-neutral, C–H multifluoroalkenylation benzamides with multifluoroalkenes, which provides a versatile protocol accessing wide range multifluoroalkenylated arenes.
Язык: Английский