Publikace na Ústřední knihovna |
2017
Abstrakt
We report an efficient and scalable synthesis of azidotrifluoromethane (CF3N3) and longer perfluorocarbonchain analogues (RFN3; R-F= C2F5, (C3F7)-C-n, (C8F17)-C-n), which enables the direct insertion of CF3 and perfluoroalkyl groups into triazole ring systems. The azidoperfluoroalkanes show good reactivity with terminal alkynes in copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC), giving access to rare and stable N-perfluoroalkyl triazoles.
Azidoperfluoroalkanes are thermally stable and the efficiency of their preparation should be attractive for discovery programs.