This method shows successful reduction of aryl iodides and bromides with NHC-borane, indicating broad functional group compatibility.
Herein, an operationally simple photoinduced radical reduction of aryliodides and arylbromides using NHC‐borane as a reductant, without external radical initiator or photoredox catalyst, is reported. Mechanistic investigations indicate the key formation of an aryl radical, which undergoes facile reduction by NHC‐borane. The method demonstrates compatibility with a broad range of functional groups, providing a valuable tool for synthesis and isotopic labeling.
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Lalande et al. (2025) studied this question.
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