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Ligand-free nickel catalyzed perfluoroalkylation of arenes and heteroarenes.
Deolka, Shubham; Govindarajan, Ramadoss; Vasylevskyi, Serhii; Roy, Michael C; Khusnutdinova, Julia R; Khaskin, Eugene.
Afiliación
  • Deolka S; Coordination Chemistry and Catalysis Unit, Okinawa Institute of Science and Technology Graduate University 1919-1 Tancha, Onna-son 904-0495 Okinawa Japan eugene.khaskin@oist.jp.
  • Govindarajan R; Coordination Chemistry and Catalysis Unit, Okinawa Institute of Science and Technology Graduate University 1919-1 Tancha, Onna-son 904-0495 Okinawa Japan eugene.khaskin@oist.jp.
  • Vasylevskyi S; Coordination Chemistry and Catalysis Unit, Okinawa Institute of Science and Technology Graduate University 1919-1 Tancha, Onna-son 904-0495 Okinawa Japan eugene.khaskin@oist.jp.
  • Roy MC; Coordination Chemistry and Catalysis Unit, Okinawa Institute of Science and Technology Graduate University 1919-1 Tancha, Onna-son 904-0495 Okinawa Japan eugene.khaskin@oist.jp.
  • Khusnutdinova JR; Coordination Chemistry and Catalysis Unit, Okinawa Institute of Science and Technology Graduate University 1919-1 Tancha, Onna-son 904-0495 Okinawa Japan eugene.khaskin@oist.jp.
  • Khaskin E; Coordination Chemistry and Catalysis Unit, Okinawa Institute of Science and Technology Graduate University 1919-1 Tancha, Onna-son 904-0495 Okinawa Japan eugene.khaskin@oist.jp.
Chem Sci ; 13(44): 12971-12979, 2022 Nov 16.
Article en En | MEDLINE | ID: mdl-36425484
ABSTRACT
We describe a "ligand-free" Ni-catalyzed perfluoroalkylation of heteroarenes to produce a diverse array of trfiluoromethyl, pentafluoroethyl and heptafluoropropyl adducts. Catalysis proceeds at room temperature via a radical pathway. The catalytic protocol is distinguished by its simplicity, and its wide scope demonstrates the potential in the late-stage functionalization of drug analogues and peptides.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Sci Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Sci Año: 2022 Tipo del documento: Article