Organic Letters, Journal Year: 2025, Volume and Issue: unknown
Published: April 6, 2025
Herein, we report an Fe/Co dual-catalyzed strategy for synthesizing alkenyl unnatural amino acids and peptide modifications. This approach utilizes aspartic acid glutamic derivatives as alkyl radical precursors. It avoids the use of expensive photoredox catalysts substrate preactivation while preserving chirality acids. Furthermore, this enables both modification peptides synthesis amino-acid-based drug candidates boron-neutron capture therapy (BNCT).
Language: Английский