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An Efficient Approach to Aromatic Aminomethylation Using Dichloromethane as Methylene Source.
Ostacolo, Carmine; Di Sarno, Veronica; Musella, Simona; Ciaglia, Tania; Vestuto, Vincenzo; Pepe, Giacomo; Merciai, Fabrizio; Campiglia, Pietro; Gomez Monterrey, Isabel M; Bertamino, Alessia.
Afiliação
  • Ostacolo C; Department of Pharmacy, University of Naples "Federico II", Naples, Italy.
  • Di Sarno V; Department of Pharmacy, University of Salerno, Fisciano, Italy.
  • Musella S; Fondazione EBRIS, Salerno, Italy.
  • Ciaglia T; Department of Pharmacy, University of Salerno, Fisciano, Italy.
  • Vestuto V; Department of Pharmacy, University of Salerno, Fisciano, Italy.
  • Pepe G; Department of Pharmacy, University of Salerno, Fisciano, Italy.
  • Merciai F; Department of Pharmacy, University of Salerno, Fisciano, Italy.
  • Campiglia P; Department of Pharmacy, University of Salerno, Fisciano, Italy.
  • Gomez Monterrey IM; Fondazione EBRIS, Salerno, Italy.
  • Bertamino A; Department of Pharmacy, University of Naples "Federico II", Naples, Italy.
Front Chem ; 7: 568, 2019.
Article em En | MEDLINE | ID: mdl-31457005
Ultrasound-promoted N-aminomethylation of indoles can be achieved in basic medium using sodium hydride and dichloromethane (DCM) as C1 donor source. This innovative amino methylation protocol results in good to excellent yields of multifunctional indole derivatives. The procedure is also applicable to other aza-heterocyclic compounds and, interestingly, affords direct access to aminomethyl-substituted aryl alcohols.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article