Reactions demonstrate smooth cross-coupling with aryl iodides, indicating diboron's utility in synthesis.
The reductive synthesis of fluoroalkyl copper phenanthroline complexes from fluoroalkyl iodides, using diboron as a reductant, is reported in this study. The structure of Cu(C4F9)(phen), isolated as a phosphine adduct, was confirmed by X-ray crystallography. These copper complexes underwent smooth cross-coupling with aryl iodides under mild conditions to afford fluoroalkylated arenes. Furthermore, a one-pot protocol enabled the reductive coupling of aryl iodides and fluoroalkyl iodides without the need to isolate the intermediate fluoroalkyl copper complexes.
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NISHIGUCHI et al. (2025) studied this question.
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