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Photoinduced Trifluoromethylation of Arenes and Heteroarenes Catalyzed by High-Valent Nickel Complexes.
Deolka, Shubham; Govindarajan, Ramadoss; Khaskin, Eugene; Fayzullin, Robert R; Roy, Michael C; Khusnutdinova, Julia R.
Afiliación
  • Deolka S; Okinawa Institute of Science and Technology Graduate University, Onna-son, Kunigami-gun, Okinawa, 904-0495, Japan.
  • Govindarajan R; Okinawa Institute of Science and Technology Graduate University, Onna-son, Kunigami-gun, Okinawa, 904-0495, Japan.
  • Khaskin E; Okinawa Institute of Science and Technology Graduate University, Onna-son, Kunigami-gun, Okinawa, 904-0495, Japan.
  • Fayzullin RR; Abuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of RAS, 8 Arbuzov Street, Kazan, 420088, Russian Federation.
  • Roy MC; Okinawa Institute of Science and Technology Graduate University, Onna-son, Kunigami-gun, Okinawa, 904-0495, Japan.
  • Khusnutdinova JR; Okinawa Institute of Science and Technology Graduate University, Onna-son, Kunigami-gun, Okinawa, 904-0495, Japan.
Angew Chem Int Ed Engl ; 60(46): 24620-24629, 2021 11 08.
Article en En | MEDLINE | ID: mdl-34477296
We describe a series of air-stable NiIII complexes supported by a simple, robust naphthyridine-based ligand. Access to the high-valent oxidation state is enabled by the CF3 ligands on the nickel, while the naphthyridine exhibits either a monodentate or bidentate coordination mode that depends on the oxidation state and sterics, and enables facile aerobic oxidation of NiII to NiIII . These NiIII complexes act as efficient catalysts for photoinduced C(sp2 )-H bond trifluoromethylation reactions of (hetero)arenes using versatile synthetic protocols. This blue LED light-mediated catalytic protocol proceeds via a radical pathway and demonstrates potential in the late-stage functionalization of drug analogs.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2021 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2021 Tipo del documento: Article País de afiliación: Japón