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A copper(I)‐catalyzed sulfonylative Hiyama cross‐coupling

Aurélien Adenot 1 Lucile Anthore-Dalion 1 Emmanuel Nicolas 1 Jean-Claude Berthet 1 Pierre Thuéry 1 Thibault Cantat 1 Jean‐claude Berthet 1 
1 LCMCE - Laboratoire de Chimie Moléculaire et de Catalyse pour l'Energie (ex LCCEF)
NIMBE UMR 3685 - Nanosciences et Innovation pour les Matériaux, la Biomédecine et l'Energie (ex SIS2M)
Abstract : An air-tolerant Cu-catalyzed sulfonylative Hiyama cross-coupling reaction enabling the formation of diaryl sulfones is described. Starting from aryl silanes, DABSO and aryliodides, the reaction tolerates a large variety of polar functional groups (amines, ketones, esters, aldehydes). Control experiments coupled with DFT calculations shed light on the mechanism, characterized by the formation of a Cu(I)-sulfinate intermediate via fast insertion of a SO$_2$ molecule.
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Submitted on : Friday, January 28, 2022 - 6:07:20 PM
Last modification on : Friday, April 1, 2022 - 3:57:52 AM
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Aurélien Adenot, Lucile Anthore-Dalion, Emmanuel Nicolas, Jean-Claude Berthet, Pierre Thuéry, et al.. A copper(I)‐catalyzed sulfonylative Hiyama cross‐coupling. Chemistry - A European Journal, Wiley-VCH Verlag, 2021, 27 (72), pp.18047-18053. ⟨10.1002/chem.202103371⟩. ⟨cea-03547768⟩



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