This process shows efficient alkynylation of N-heterocycles with unsaturated oxime esters, suggesting broad applications in organic synthesis.
A photoinduced copper-catalyzed radical cascade Sonogashira-type coupling of unsaturated oxime esters with terminal alkynes has been developed. The transformation proceeds under redox-neutral conditions via single-electron transfer (SET) from photoexcited Cu(I) acetylides, generating iminyl radicals that undergo cyclization followed by alkynylation. This strategy enables efficient construction of alkynylated N-heterocycles from readily available substrates, featuring mild conditions, broad scope, and full suppression of competing N-alkynylation. Mechanistic studies support a Cu(I)/Cu(II)/Cu(III) cycle involving photoinduced SET and radical cyclization, highlighting Cu-acetylide complexes as photoreductants in radical relay processes.
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Wang et al. (2025) studied this question.
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