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Photoredox-Nickel Dual-Catalyzed C-Alkylation of Secondary Nitroalkanes: Access to Sterically Hindered α-Tertiary Amines.
Rezazadeh, Sina; Martin, Maxwell I; Kim, Raphael S; Yap, Glenn P A; Rosenthal, Joel; Watson, Donald A.
Afiliación
  • Rezazadeh S; Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716, United States.
  • Martin MI; Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716, United States.
  • Kim RS; Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716, United States.
  • Yap GPA; Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716, United States.
  • Rosenthal J; Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716, United States.
  • Watson DA; Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716, United States.
J Am Chem Soc ; 145(8): 4707-4715, 2023 Mar 01.
Article en En | MEDLINE | ID: mdl-36795911
The preparation of tertiary nitroalkanes via the nickel-catalyzed alkylation of secondary nitroalkanes using aliphatic iodides is reported. Previously, catalytic access to this important class of nitroalkanes via alkylation has not been possible due to the inability of catalysts to overcome the steric demands of the products. However, we have now found that the use of a nickel catalyst in combination with a photoredox catalyst and light leads to much more active alkylation catalysts. These can now access tertiary nitroalkanes. The conditions are scalable as well as air and moisture tolerant. Importantly, reduction of the tertiary nitroalkane products allows rapid access to α-tertiary amines.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos