Visible-light-driven carboxylation improves α-amino acid synthesis in benzylamines, suggesting a novel photocatalytic approach.
α-Amino acids are vital structural motifs in both bioactive compounds and synthetic building blocks. However, the photocatalytic synthesis of α-amino acids directly from C(sp³)-H bonds and CO₂ is a long-standing challenge. Here we report a visible-light-driven C(sp³)-H bond carboxylation of benzylamine with CO₂ to synthesize substituted arylglycines. This reaction has mild reaction conditions, good functional group tolerance, and a wide substrate scope. Mechanistic studies show that carbon radicals and carbon anions as the key intermediates may be generated through a consecutive photoinduced electron transfer process.
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Cui et al. (2025) studied this question.
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