Pyridine sulfinates as general nucleophilic coupling partners in palladium-catalyzed cross-coupling reactions with aryl halides

Pyridine rings are ubiquitous in drug molecules; however, the pre-eminent reaction used to form carbon–carbon bonds in the pharmaceutical industry, the Suzuki–Miyaura cross-coupling reaction, often fails when applied to these structures. This phenomenon is most pronounced in 2-substituted pyridines,...

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Bibliographic Details
Main Authors: Markovic, T, Rocke, B, Blakemore, D, Mascitti, V, Willis, M
Format: Journal article
Published: Royal Society of Chemistry 2017