Chelation-assisted cross-coupling of anilines through in situ activation as diazonium salts with boronic acids under ligand-, base-, and salt-free conditions - Archive ouverte HAL
Article Dans Une Revue Chemistry - A European Journal Année : 2013

Chelation-assisted cross-coupling of anilines through in situ activation as diazonium salts with boronic acids under ligand-, base-, and salt-free conditions

Résumé

We describe the coupling of anilines with aryl boronic acids, under ligand-, base-, and salt-free conditions at room temperature. This new reaction proceeds through the formation of an aryl palladium alkoxo complex, which allows the transmetalation step with aryl boronic acids without any external base. Importantly, this sustainable procedure generates only environmentally friendly byproducts such as tBuOH, H2O, N2, and B(OH)3. The reaction mechanism has been deeply investigated through experimental and theoretical studies. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Dates et versions

hal-01613226 , version 1 (09-10-2017)

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R. Joncour, Nicolas Susperregui, N. Pinaud, Karinne Miqueu, E. Fouquet, et al.. Chelation-assisted cross-coupling of anilines through in situ activation as diazonium salts with boronic acids under ligand-, base-, and salt-free conditions. Chemistry - A European Journal, 2013, 19 (28), pp.9291-9296. ⟨10.1002/chem.201300858⟩. ⟨hal-01613226⟩
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