Demonstrates efficient light-driven coupling of aromatic carbonyl compounds and imines, highlighting new catalytic applications.
N,N-Dialkyl-1-pyrenylamine-based photoredox catalysts were synthesized and applied to light-driven reductive coupling reactions under blue irradiation. The catalysts exhibited comparable activity in the reductive coupling of benzaldehyde, affording the desired 1,2-diols in good yields. Extension of the substrate scope demonstrated that light-driven reductive coupling of aromatic carbonyl compounds and imines using N,N-dimethyl-1-pyrenylamine proceeded efficiently, yielding 1,2-diols and 1,2-diamine, respectively.
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Ogura et al. (2026) studied this question.
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