Synthesis of tetrafluoroethylene-and tetrafluoroethyl-containing azides and their 1,3-dipolar cycloaddition as synthetic application

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Abstract

Tetrafluoroethylene-containing azides are accessed in two steps (one pot) from tetrafluoroalkyl bromides by metalation and reaction with electrophilic azides. Subsequent copper(i)-catalyzed azide-Alkyne cycloaddition afforded N-Tetrafluoroethyl and N-Tetrafluoroethylene 4-substituted 1,2,3-Triazoles. In addition, the protocol for the synthesis of 4,5-disubstituted 1,2,3-Triazoles is presented.

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Voltrová, S., Muselli, M., Filgas, J., Matoušek, V., Klepetářová, B., & Beier, P. (2017). Synthesis of tetrafluoroethylene-and tetrafluoroethyl-containing azides and their 1,3-dipolar cycloaddition as synthetic application. Organic and Biomolecular Chemistry, 15(23), 4962–4965. https://doi.org/10.1039/c7ob01151b

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