Nickel-catalyzed hydrodefluorination/deuterodefluorination of CF3-alkenes with formic acid.
Chem Commun (Camb)
; 60(51): 6548-6551, 2024 Jun 20.
Article
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| MEDLINE
| ID: mdl-38842110
ABSTRACT
The synthesis of deuterated gem-difluoroalkenes via selective deuterodefluorination of ß-CF3-cinnamates using a nickel catalyst has been reported for the first time. Commercially available deuterated formic acid is a cheap and convenient deuterium source. The nickel-catalyst showed high selectivity for monodefluorination and avoided competitive reactions such as multiple defluorination or hydrogenation.
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MEDLINE
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En
Revista:
Chem Commun (Camb)
Asunto de la revista:
QUIMICA
Año:
2024
Tipo del documento:
Article