Your browser doesn't support javascript.
loading
XAT-Catalysis for Intramolecular Biaryl Synthesis.
Sephton, Thomas; Large, Jonathan M; Natrajan, Louise S; Butterworth, Sam; Greaney, Michael F.
Afiliação
  • Sephton T; School of Chemistry, University of Manchester, Manchester, M13 9PL, UK.
  • Large JM; LifeArc, Accelerator Building, Open Innovation Campus, Stevenage, SG1 2FX, UK.
  • Natrajan LS; School of Chemistry, University of Manchester, Manchester, M13 9PL, UK.
  • Butterworth S; Division of Pharmacy and Optometry, School of Health Sciences, Manchester Academic Health Sciences Centre, University of Manchester, Manchester, M13 9PL, UK.
  • Greaney MF; School of Chemistry, University of Manchester, Manchester, M13 9PL, UK.
Angew Chem Int Ed Engl ; : e202407979, 2024 May 31.
Article em En | MEDLINE | ID: mdl-38818676
ABSTRACT
Radical ipso-substitution offers an alternative to organometallic approaches for biaryl synthesis, but usually requires stoichiometric reagents such as tributyltin hydride. Here, we demonstrate that visible light photoredox catalysis can be used for ipso-biaryl synthesis, via a halogen-atom transfer (XAT) regime. Using amide substrates that promote ipso- over unwanted ortho-addition, we demonstrate smooth biaryl formation with no constraint on the electronic character of the migrating arene ring. The photoreaction can be combined in one operation to achieve a formal arylation of the inert aniline C-N bond.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article