4.6 Article

Sandmeyer-Type Trifluoromethylthiolation and Trifluoromethylselenolation of (Hetero)Aromatic Amines Catalyzed by Copper

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CHEMISTRY-A EUROPEAN JOURNAL
卷 22, 期 1, 页码 79-82

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201503524

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copper; fluorine; fluoroalkylthiolation; Sandmeyer reaction; synthetic methods

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  1. Nanokat

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Aromatic and heteroaromatic diazonium salts were efficiently converted into the corresponding trifluoromethylthio- or selenoethers by reaction with Me4NSCF3 or Me4NSeCF3, respectively, in the presence of catalytic amounts of copper thiocyanate. These Sandmeyer-type reactions proceed within one hour at room temperature, are applicable to a wide range of functionalized molecules, and can optionally be combined with the diazotizations into one-pot protocols.

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