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Nickel-Catalyzed Thiolation of Aryl Nitriles.

ABSTRACT: A nickel-catalyzed thiolation of aryl nitriles has been developed to access functionalized aryl thioethers. The ligand dcype (1,2-bis(dicyclohexylphosphino)ethane) as well as the base KO^t Bu (potassium tert-butoxide) are essential to achieve this transformation. This scalable and practical process involves both a C-C bond activation and a C-S bond formation. Furthermore, this reaction shows a high functional-group tolerance and enables the late-stage functionalization of important molecules.

SUBMITTER: Delcaillau T

PROVIDER: S-EPMC8456793 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Nickel-Catalyzed Coupling of Azoles with Aromatic Nitriles.

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