Answers are grounded in this paper and cite their sources.
Demonstrates effective carbamoylation in peptides, highlighting a sustainable strategy for drug discovery.
Integrating amino acids/peptides into hydrazine skeletons remains a significant challenge. We report a visible-light-induced carbamoylation using DHP-tagged amino acids/peptides as radical precursors for the green synthesis of diarylhydrazine carbonyl amino acid/peptide derivatives (37 examples, up to 96% yield). This first integration of amino acid/peptide motifs into hydrazines features mild conditions, external oxidant/additive-free, broad substrate scope and excellent compatibility. It enables late-stage modification of proteins/amine-containing functional molecules, offering a sustainable strategy for peptide modification and drug discovery.
No takes yet. Share an insight, caveat, or question.
Zeng et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: