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Few unexpected results from a Suzuki–Miyaura reaction

Abstract : In the course of the synthesis of original anti-infectious compounds we focused on the palladiumcatalyzed SuzukieMiyaura arylearyl coupling reaction between 2-(3-ethoxy-5-iodo-1H-pyrazol-1-yl) pyridine and phenylboronic acid. A study of the reaction products obtained under different conditions (various ligands and solvents), not only provided us with insights to optimize this reaction but also with few side compounds, resulting from CH activation, along with the unexpected bis(3-ethoxy-1-(pyridin-2- yl)-1H-pyrazol-5-yl)palladium. Stochiometric experiments with this remarkably stable biscyclopalladated reagent and phenylhalides pointed out the occurrence of arylearyl coupling, possibly via palladium IV intermediates.
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https://hal-pasteur.archives-ouvertes.fr/pasteur-00669009
Contributor : Yves Janin <>
Submitted on : Friday, February 10, 2012 - 6:40:19 PM
Last modification on : Saturday, July 3, 2021 - 3:44:26 AM

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Elise Salanouve, Pascal Retailleau, Yves Janin. Few unexpected results from a Suzuki–Miyaura reaction. Tetrahedron, Elsevier, 2012, 68 (9), pp.2135-2140. ⟨10.1016/j.tet.2012.01.019⟩. ⟨pasteur-00669009⟩

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