Palladium-catalyzed carbonylative cross-coupling reactions of pyridine halides and aryl boronic acids: a convenient access to α-pyridyl ketones - Normandie Université Access content directly
Journal Articles Tetrahedron Letters Year : 2001

Palladium-catalyzed carbonylative cross-coupling reactions of pyridine halides and aryl boronic acids: a convenient access to α-pyridyl ketones

Abstract

The proper choice of solvent, catalyst precursor and CO pressure enables the easy and selective transformation of mono- and dihalopyridines into phenyl pyridyl ketones in 81–95% yields. The proper choice of solvent, catalyst precursor and CO pressure enables the facile and selective transformation of mono- and dihalopyridines into phenyl pyridyl ketones.

Dates and versions

hal-02384503 , version 1 (28-11-2019)

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Samuel Couve-Bonnaire, Jean-François Carpentier, Andre Mortreux, Yves Castanet. Palladium-catalyzed carbonylative cross-coupling reactions of pyridine halides and aryl boronic acids: a convenient access to α-pyridyl ketones. Tetrahedron Letters, 2001, 42 (22), pp.3689-3691. ⟨10.1016/S0040-4039(01)00544-5⟩. ⟨hal-02384503⟩
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