Advances in radical remote γ-functionalization of α,β-unsaturated carbonyl compounds

α,β-Unsaturated carbonyl compounds are of significant biological and industrial importance, playing a key role in pharmaceutical chemistry, particularly in drug design. γ-Enolizable carbonyl compounds exhibit unique reactivity when undergoing functionalization at the remote γ-position. Despite notable advancements, γ-functionalization of these compounds still confronts considerable unresolved challenges. Radical chemistry has emerged as a powerful tool for constructing carbon–carbon and carbon–heteroatom bonds at the γ-position. In this review, we have summarized and categorized radical γ-functionalization methods developed over the past decades, focusing on substrates such as α,β-unsaturated amides, ketones, esters, and aldehydes.