Abstract
AbstractRacemic 2‐triazolyl or 2‐alkylethyl 9,10‐anthraquinone derivatives [(V), (X), and (XI)] are efficiently synthesized in good yields by a three‐ or four‐step procedure involving bromination, nucleophilic substitution, and CuI‐promoted 1,3‐dipolar cycloaddition or alkylation and reductive desulfonylation, respectively.
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