This review discusses the synthesis of nitrogen-containing heterocycles through visible-light-driven reactions, highlighting their potential in pharmaceutical applications.
Nitrogen-containing heterocycles are crucial structural motifs in pharmaceuticals, natural products, and functional materials, with broad applications in medicinal chemistry. The emergence of visible-light photocatalysis has revolutionized their synthesis, offering an environmentally benign approach that operates under mild reaction conditions. Specifically, visible-light-induced domino reactions facilitate multi-step tandem transformations via mechanisms such as single-electron transfer (SET), energy transfer (EnT), or hydrogen atom transfer (HAT), minimizing intermediate isolation and purification steps. This review highlights recent advances in visible-light-induced domino reactions for the synthesis of nitrogen-containing heterocycles. It focuses on key strategies, including nitrogen-centered radical-mediated C-N bond formation and carbon-centered radical-initiated cyclization, discussing their mechanisms, current limitations, and future prospects to provide insights for advancing green synthesis and pharmaceutical science.
No takes yet. Share an insight, caveat, or question.
Li et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: