Demonstrates the synthesis of sulfur-containing amino acids via copper-catalyzed reactions, highlighting its potential applications.
Sulfur-containing amino acids play a crucial role in living organisms. Herein, we show a copper-catalyzed three-component reaction of glycine derivatives with alkenes and aryl disulfides for the synthesis of complex sulfur-containing amino acids. Remarkably, this protocol also demonstrates potential applications in late-stage site-selective modifications of glycine residues in short peptides.
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Zhu et al. (2026) studied this question.
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