Friedel-Crafts arylation boosts yields of diarylmethane derivatives in a range of aldehydes, highlighting the role of photochemistry.
Photochemistry enables transformations inaccessible through ground‐state pathways. We report a sustainable and operationally simple Friedel–Crafts arylation using benzophenone oxime tosylate, in low catalyst loading, as the photoacid generator under inert conditions. The method accommodates a broad substrate scope, affording diarylmethane derivatives in good to excellent yields. Mechanistic studies elucidate key intermediates driving the transformation.
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Gkosios et al. (2025) studied this question.
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