Copper-catalyzed trifluoromethylation of alkenes: Synthesis of trifluoromethylated benzoxazines

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Abstract

A simple base and ligand free copper catalyzed method for the construction of trifluoromethylated benzoxazines has been developed by using Umemoto's reagent. It involves the oxidative difunctionalization of alkenes through tandem C-O and C-CF 3 bond formations. Furthermore, synthesized benzoxazines were selectively converted into trifluoromethylated allylic and (E)-vinylic benzamides by the treatment of KO t Bu and CH 3 Li, respectively.

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Jana, S., Ashokan, A., Kumar, S., Verma, A., & Kumar, S. (2015). Copper-catalyzed trifluoromethylation of alkenes: Synthesis of trifluoromethylated benzoxazines. Organic and Biomolecular Chemistry, 13(31), 8411–8415. https://doi.org/10.1039/c5ob01196e

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