Palladium-catalyzed C-H trifluoromethylselenolation of arenes with [Me4N][SeCF3] and an oxidant
Trifluoromethylselenolation of arenes with [Me4N][SeCF3] in the presence of an oxidant through Pd-catalyzed C(sp2)-H activation under the assistance of a directing group is established for the first time. The reaction tolerates different directing groups and a variety of functional groups, enabling selective installation of a SeCF3 moiety onto the ortho positions of arenes. Mechanistic studies revealed that the CF3SeSeCF3 intermediate in situ generated from oxidation of [Me4N][SeCF3] might be the real SeCF3 reagent in the reaction.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2022 |
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Erschienen: |
2022 |
Enthalten in: |
Zur Gesamtaufnahme - volume:58 |
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Enthalten in: |
Chemical communications (Cambridge, England) - 58(2022), 66 vom: 16. Aug., Seite 9238-9241 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Liu, Lei [VerfasserIn] |
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Anmerkungen: |
Date Revised 16.08.2022 published: Electronic Citation Status PubMed-not-MEDLINE |
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doi: |
10.1039/d2cc02897b |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM344195813 |
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520 | |a Trifluoromethylselenolation of arenes with [Me4N][SeCF3] in the presence of an oxidant through Pd-catalyzed C(sp2)-H activation under the assistance of a directing group is established for the first time. The reaction tolerates different directing groups and a variety of functional groups, enabling selective installation of a SeCF3 moiety onto the ortho positions of arenes. Mechanistic studies revealed that the CF3SeSeCF3 intermediate in situ generated from oxidation of [Me4N][SeCF3] might be the real SeCF3 reagent in the reaction | ||
650 | 4 | |a Journal Article | |
700 | 1 | |a Gu, Yu-Cheng |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Cheng-Pan |e verfasserin |4 aut | |
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