ABSTRACT Herein, the electrochemical S RN 1 reaction between various thianthrenium salts and β‐dicarbonyl compounds and analogues was reported. This rare example of electrochemical functionalization of thianthrenium salts allowed the formation of the arylated products in moderate to good yields. The reaction was applied to various thianthrenium salts having electron withdrawing groups and β‐dicarbonyl compounds. The study of the reaction mechanism confirmed a reduction of the electro‐poor thianthrenium salts followed by their reaction with the putative enolate species as formal nucleophile, according to a S RN 1 mechanism.
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Boudet et al. (Wed,) studied this question.
synapsesocial.com/papers/69fd7f3abfa21ec5bbf07aa6 — DOI: https://doi.org/10.1002/chem.71088
Cécile Boudet
Centre National de la Recherche Scientifique
Thibaud Brégent
Dow Chemical (Canada)
Jean‐François Brière
Centre National de la Recherche Scientifique
Chemistry - A European Journal
Centre National de la Recherche Scientifique
Université de Rouen Normandie
Normandie Université
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