The copper-catalyzed azide–alkyne cycloaddition (CuAAC) reaction is regarded as a prime example of “click chemistry”, but the asymmetric click cycloaddition of internal alkynes still remains challenging. A new asymmetric Rh-catalyzed… Click to show full abstract
The copper-catalyzed azide–alkyne cycloaddition (CuAAC) reaction is regarded as a prime example of “click chemistry”, but the asymmetric click cycloaddition of internal alkynes still remains challenging. A new asymmetric Rh-catalyzed click cycloaddition of N-alkynylindoles with azides was developed, providing atroposelective access to C–N axially chiral triazolyl indoles, a new type of heterobiaryl, with excellent yields and enantioselectivity. This asymmetric approach is efficient, mild, robust and atom-economic, and features very broad substrate scope with easily available Tol-BINAP ligands.
               
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