Experimental study demonstrates switchable copper-catalyzed 1,4-polyhaloalkylcyanation of 1,3-enynes, highlighting a divergent approach to access polyhalogenated allenes via radical pathways.
We report a switchable copper-catalyzed divergent 1,4-polyhaloalkylcyanation of 1,3-enynes to construct a series of polyhalogenated allenes with high chemoselectivity and regioselectivity. The 1,4-dichloromethylcyanation of 1,3-enynes is realized by merging aminoalkyl radical-induced homolytic activation of carbon–halogen bonds with copper catalysis, while employing dtbbpy as ligands enables 1,4-trichloromethylcyanation of 1,3-enynes by hydrogen atom transfer (HAT) reactions of chloroform. Mechanistic investigations indicate that the reactions involve the selective generation of polyhalomethyl radicals by HAT or XAT process.
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Lv et al. (2026) studied this question.
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