The
exploitation of microwave irradiation in radical reactions,
in which formamide was used as both the solvent and reagent, enabled
the development of an ultrafast methodology for amidation via carbamoyl
radicals. The synthesis of novel functionalized isoquinoline-1,3-diones
in only 10 s is described for the first time. A very efficient and
environmentally benign methodology was developed. Mild conditions,
very short reaction time, low energy consumption, high atom economy,
use of an inexpensive and green catalyst, nonanhydrous conditions,
high selectivity, and nontoxic solvents are some advantages of this
method. The low value of the E factor (6.1) reflects
the low waste generation, making this method very attractive for industrial
applications.