Abstract
AbstractCarbon dioxide is an ideal C1 source in organic synthesis as a precursor for the carboxyl group. With the development of photocatalysis, the carboxylation reactions with CO2 incorporation could be carried out in a more environmental and sustainable manner without the addition of stoichiometric metallic reductants. This minireview summarizes the recent development in light‐induced carboxylation of organic (pseudo)halides and analogues with CO2 via C−X (X=Br, Cl, O, N, etc.) bond cleavage.
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