Electrochemically Induced, Metal Free Synthesis of 2-substituted chroman-4-ones

ChemistryOpen. 2024 Nov 16:e202400395. doi: 10.1002/open.202400395. Online ahead of print.

Abstract

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).