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Electrocatalytic Formal C(sp2)-H Alkylations via Nickel-Catalyzed Cross-Electrophile Coupling with Versatile Arylsulfonium Salts.
Michiyuki, Takuya; Homölle, Simon L; Pandit, Neeraj K; Ackermann, Lutz.
Affiliation
  • Michiyuki T; Wöhler Research Institute for Sustainable Chemistry, Tammannstraße 2, 37077, Göttingen, Germany.
  • Homölle SL; Wöhler Research Institute for Sustainable Chemistry, Tammannstraße 2, 37077, Göttingen, Germany.
  • Pandit NK; Wöhler Research Institute for Sustainable Chemistry, Tammannstraße 2, 37077, Göttingen, Germany.
  • Ackermann L; Wöhler Research Institute for Sustainable Chemistry, Tammannstraße 2, 37077, Göttingen, Germany.
Angew Chem Int Ed Engl ; 63(29): e202401198, 2024 Jul 15.
Article in En | MEDLINE | ID: mdl-38695843
ABSTRACT
Producing sp3-hybridized carbon-enriched molecules is of particular interest due to their high success rate in clinical trials. The installation of aliphatic chains onto aromatic scaffolds was accomplished by nickel-catalyzed C(sp2)-C(sp3) cross-electrophile coupling with arylsulfonium salts. Thus, simple non-prefunctionalized arenes could be alkylated through the formation of aryldibenzothiophenium salts. The reaction employs an electrochemical approach to avoid potentially hazardous chemical redox agents, and importantly, the one-pot alkylation proved also viable, highlighting the robustness of our approach.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2024 Document type: Article Affiliation country: