Direct amidation of esters with nitroarenes
Direct conversion of esters to amides, while attractive, is often limited to activated esters or highly nucleophilic amines. Here the authors report a nickel-catalysed reductive coupling between unactivated esters and nitroarenes, giving a direct route to aromatic amides.
Guardado en:
Autores principales: | Chi Wai Cheung, Marten Leendert Ploeger, Xile Hu |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/10b081dbcf634db29252db615d5ffd3a |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Amine synthesis via iron-catalysed reductive coupling of nitroarenes with alkyl halides
por: Chi Wai Cheung, et al.
Publicado: (2016) -
Erratum: Amine synthesis via iron-catalysed reductive coupling of nitroarenes with alkyl halides
por: Chi Wai Cheung, et al.
Publicado: (2016) -
Highly selective transition-metal-free transamidation of amides and amidation of esters at room temperature
por: Guangchen Li, et al.
Publicado: (2018) -
Catalytic amidation of natural and synthetic polyol esters with sulfonamides
por: Hua Liu, et al.
Publicado: (2019) -
Facile access to nitroarenes and nitroheteroarenes using N-nitrosaccharin
por: Roxan Calvo, et al.
Publicado: (2019)