This research uncovers a method to synthesize fluorinated quinoxalines using copper catalysis, suggesting efficient applications in science.
A novel copper‐catalyzed cyclization provides efficient access to fluorinated quinoxalines from o ‐phenylenediamines and diazodicarbonyl compounds. Proceeding under mild conditions with broad substrate scope, this protocol delivers diverse derivatives in moderate to good yields, offering a streamlined approach to scaffolds valuable for medicinal and materials science applications.
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Li et al. (2026) studied this question.
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