Literature DB >> 27918134

Azidoperfluoroalkanes: Synthesis and Application in Copper(I)-Catalyzed Azide-Alkyne Cycloaddition.

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.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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


  3 in total

1.  Synthesis of N-perfluoroalkyl-3,4-disubstituted pyrroles by rhodium-catalyzed transannulation of N-fluoroalkyl-1,2,3-triazoles with terminal alkynes.

Authors:  Olga Bakhanovich; Viktor Khutorianskyi; Vladimir Motornov; Petr Beier
Journal:  Beilstein J Org Chem       Date:  2021-02-18       Impact factor: 2.883

2.  DFT and AFIR study on the copper(i)-catalyzed mechanism of 5-enamine-trisubstituted-1,2,3-triazole synthesis via C-N cross-coupling and the origin of ring-opening of 2H-azirines.

Authors:  Fan Yu; Zhaoman Zhou; Jiajia Song; Yanying Zhao
Journal:  RSC Adv       Date:  2021-01-13       Impact factor: 3.361

3.  Synthesis of Fluorinated Amide Derivatives via a Radical N-Perfluoroalkylation-Defluorination Pathway.

Authors:  Zhiyao Zheng; Angela van der Werf; Marie Deliaval; Nicklas Selander
Journal:  Org Lett       Date:  2020-03-25       Impact factor: 6.005

  3 in total

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