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Photoredox/Nickel-Catalyzed Single-Electron Tsuji-Trost Reaction: Development and Mechanistic Insights.
Matsui, Jennifer K; Gutiérrez-Bonet, Álvaro; Rotella, Madeline; Alam, Rauful; Gutierrez, Osvaldo; Molander, Gary A.
Afiliación
  • Matsui JK; Department of Chemistry, University of Pennsylvania, Roy and Diana Vagelos Laboratories, Philadelphia, PA, 19104-6323, USA.
  • Gutiérrez-Bonet Á; Department of Chemistry, University of Pennsylvania, Roy and Diana Vagelos Laboratories, Philadelphia, PA, 19104-6323, USA.
  • Rotella M; Department of Chemistry and Biochemistry, University of Maryland, College Park, MD, 20742, USA.
  • Alam R; Department of Chemistry, University of Pennsylvania, Roy and Diana Vagelos Laboratories, Philadelphia, PA, 19104-6323, USA.
  • Gutierrez O; Department of Chemistry and Biochemistry, University of Maryland, College Park, MD, 20742, USA.
  • Molander GA; Department of Chemistry, University of Pennsylvania, Roy and Diana Vagelos Laboratories, Philadelphia, PA, 19104-6323, USA.
Angew Chem Int Ed Engl ; 57(48): 15847-15851, 2018 11 26.
Article en En | MEDLINE | ID: mdl-30307672
ABSTRACT
A regioselective, nickel-catalyzed photoredox allylation of secondary, benzyl, and α-alkoxy radical precursors is disclosed. Through this manifold, a variety of linear allylic alcohols and allylated monosaccharides are accessible in high yields under mild reaction conditions. Quantum mechanical calculations [DFT and DLPNO-CCSD(T)] support the mechanistic hypothesis of a Ni0 to NiII oxidative addition pathway followed by radical addition and inner-sphere allylation.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Propanoles / Electrones / Níquel Idioma: En Revista: Angew Chem Int Ed Engl Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Propanoles / Electrones / Níquel Idioma: En Revista: Angew Chem Int Ed Engl Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos