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◆ Chemical Science2026-01-01· Enantioselective synthesis

Copper-catalyzed enantioselective interrupted azide–alkyne cycloaddition to access axially chiral diaryl ethers

Ruixue Wu, Lan Chen, Yihan Chen, Qimin Wu, Qirui Chen, Aijun Lin, Hequan Yao, Qiuyu Li, Shang Gao

原始摘要(英文原文)· Original abstract
Bu is essential for the inhibition of protonated byproducts. The orthogonal reactivity of the residual terminal alkyne and amine groups within the products provides versatile platforms for downstream chemistry, enriching the structural diversity of axially chiral diaryl ethers.
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Copper-catalyzed enantioselective interrupted azide–alkyne cycloaddition to access axially chiral diaryl ethers — 科研速览 Science Skim