Electrochemically induced, decarboxylative functionalization of chromone-3-carboxylic acids by N-hydroxyphthalimide esters as alkyl radical precursors was studied. Electrochemical protocol offers a sustainable and green approach, obviating the need for catalysts, relying on the direct reduction of NHPI esters using electric current. Developed protocol provides a straightforward route to the synthesis of diverse molecules with potential biological activity.
Keywords: 2-substituted chromones; Decarboxylation process; Decarboxylative alkylation; Electrochemically induced Giese reaction; Redox-Active Esters (RAEs).
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