Synthesis
DOI: 10.1055/a-2759-6476
Paper
Published as part of the Special Topic Dedicated to Thieme Chemistry Journal Awardees

Radical Allylation of Vinyl Perfluorocyclic Sulfonamides Leading to 1,1,2,2,3,3-Hexafluorohex-5-ene-1-sulfonamides

Authors

  • Takaaki Maejima

    1   Department of Applied Chemistry, Yamaguchi University, Ube, Japan (Ringgold ID: RIN13150)
  • Moeri Terauchi

    1   Department of Applied Chemistry, Yamaguchi University, Ube, Japan (Ringgold ID: RIN13150)
  • Takuji Kawamoto

    1   Department of Applied Chemistry, Yamaguchi University, Ube, Japan (Ringgold ID: RIN13150)

This work was partially supported by Grants-in-Aid for Scientific Research (22K05116 and 25K00077) and JST-GteX (JPMJGX23SA and JPMJGX23S3). This work was partially carried out using research equipment shared within the MEXT Project ‘Promoting Public Utilization of Advanced Research Infrastructure’ (program for the supporting construction of core facilities) under grant JPMXS0440400023.
Supported by: Japan Society for the Promotion of Science 22K05116 ,25K00077


Graphical Abstract

Abstract

Allylation reactions are essential for the introduction of alkene functionalities into molecules, and radical allylation reactions serve as a powerful strategy to achieve this. Of the various known allylating reagents, allyl bromides offer a particularly direct and efficient approach to allylation. In this study, we report the radical allylation of vinyl perfluorocyclic sulfonamides using allyl bromides, leading to the synthesis of allylated fluoroalkyl sulfonamides.



Publication History

Received: 17 October 2025

Accepted after revision: 29 November 2025

Accepted Manuscript online:
29 November 2025

Article published online:
17 December 2025

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