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
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Radical‐Mediated Hydroperfluoroalkylation of Unactivated Alkenes ; day:17 ; month:07 ; year:2023 ; extent:10
Advanced synthesis & catalysis ; (17.07.2023) (gesamt 10)
- Creator
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Sissengaliyeva, Gulsana
Dénès, Fabrice
Girbu, Vladilena
Kulcitki, Veaceslav
Hofstetter, Elena
Renaud, Philippe
- DOI
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10.1002/adsc.202300299
- URN
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urn:nbn:de:101:1-2023071715213976935456
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:47 AM CEST
Data provider
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Sissengaliyeva, Gulsana
- Dénès, Fabrice
- Girbu, Vladilena
- Kulcitki, Veaceslav
- Hofstetter, Elena
- Renaud, Philippe