| Literature DB >> 27918134 |
Zsófia E Blastik1, Svatava Voltrová1, Václav Matoušek2, Bronislav Jurásek1, David W Manley1, Blanka Klepetářová1, Petr Beier1.
Abstract
We report an efficient and scalable synthesis of azidotrifluoromethane (CF3 N3 ) and longer perfluorocarbon-chain analogues (RF N3 ; RF =C2 F5 , n C3 F7 , n C8 F17 ), 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.Entities:
Keywords: azides; click reactions; fluorine; perfluoroalkanes; triazoles
Year: 2016 PMID: 27918134 DOI: 10.1002/anie.201609715
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336