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. 2021 Jun 26;60(31):17211–17217. doi: 10.1002/anie.202103269

Table 2.

Palladium‐catalyzed iodination of aryl and vinyl carboxylic acids.[a] Inline graphic

graphic file with name ANIE-60-17211-g002.jpg

[a] Reaction conditions: vinyl carboxylic acid (0.25 mmol), 1‐iodobutane (2, 0.275 mmol), Pd2(dba)3 (5 mol %), Xantphos (10 mol %), 1,8‐bis(dimethylamino)naphthalene (proton sponge, 0.275 mmol), 1‐(chloro‐1‐pyrrolidinylmethylene)pyrrolidinium hexafluorophosphate (PyCIU, 0.35 mmol), toluene (2.5 mL), 120 °C, 16 h. [b] GC yield using n‐dodecane as internal standard. [c] Starting from benzoyl chloride (0.25 mmol) without PyCIU and proton sponge.