Copper-catalyzed enantioselective interrupted azide–alkyne cycloaddition to access axially chiral diaryl ethers
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.
Fields of Study & Subjects
Click Chemistry and Applications
Cyclopropane Reaction Mechanisms
Axial and Atropisomeric Chirality Synthesis
Publication details
- Journal / source
- Chemical Science
- Publisher
- Royal Society of Chemistry (RSC)
- Volume
- 17
- Issue
- 23
- Pages
- 11591–11599
- Publication date
- 1 January 2026
- Language
- EN