Demonstrates the synthesis of chiral diaryl ethers, suggesting new pathways for effective drug design.
While transition metal-catalyzed enantioselective azide-alkyne cycloadditions are well-established for accessing 1,4-disubstituted triazoles, the direct enantioselective synthesis of chiral 1,4,5-trisubstituted triazoles from terminal alkynes via an interrupted process remains largely underdeveloped....
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Wu et al. (2026) studied this question.
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