Radical‐Mediated Hydroperfluoroalkylation of Unactivated Alkenes

Abstract: The direct hydroperfluoroalkylation of a wide range of unactivated alkenes has been achieved at room temperature with readily available iodoperfluoroalkanes using 4‐tert‐butylcatechol as a source of hydrogen atom and triethylborane. The hydrotrifluoromethylation could also be achieved under these conditions using gaseous trifluoromethyl iodide. An experimentally simple two‐step, one‐pot hydrotrifluoromethylation process using the easy‐to‐use trifluoromethanesulfonyl chloride as the source of trifluoromethyl radicals has also been developed. Using these two approaches, a broad range of substrates, including isoprenoid natural products, were efficiently derivatized.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Radical‐Mediated Hydroperfluoroalkylation of Unactivated Alkenes ; day:17 ; month:07 ; year:2023 ; extent:10
Advanced synthesis & catalysis ; (17.07.2023) (gesamt 10)

Creator
Sissengaliyeva, Gulsana
Dénès, Fabrice
Girbu, Vladilena
Kulcitki, Veaceslav
Hofstetter, Elena
Renaud, Philippe

DOI
10.1002/adsc.202300299
URN
urn:nbn:de:101:1-2023071715213976935456
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
14.08.2025, 10:47 AM CEST

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Associated

  • Sissengaliyeva, Gulsana
  • Dénès, Fabrice
  • Girbu, Vladilena
  • Kulcitki, Veaceslav
  • Hofstetter, Elena
  • Renaud, Philippe

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