| Literature DB >> 33543179 |
Luciana Cicco1, Jose A Hernández-Fernández2, Antonio Salomone3, Paola Vitale4, Marina Ramos-Martín2, Javier González-Sabín5, Alejandro Presa Soto2, Filippo M Perna4, Vito Capriati4, Joaquín García-Álvarez2.
Abstract
An efficient and selective N-functionalization of amides is first reported via a CuI-catalyzed Goldberg-type C-N coupling reaction between aryl iodides and primary/secondary amides run either in Deep Eutectic Solvents (DESs) or water as sustainable reaction media, under mild and bench-type reaction conditions (absence of protecting atmosphere). Higher activities were observed in an aqueous medium, though the employment of DESs expanded and improved the scope of the reaction to include also aliphatic amides. Additional valuable features of the reported protocol include: (i) the possibility to scale up the reaction without any erosion of the yield/reaction time; (ii) the recyclability of both the catalyst and the eutectic solvent up to 4 consecutive runs; and (iii) the feasibility of the proposed catalytic system for the synthesis of biologically active molecules.Entities:
Year: 2021 PMID: 33543179 DOI: 10.1039/d0ob02501a
Source DB: PubMed Journal: Org Biomol Chem ISSN: 1477-0520 Impact factor: 3.876