Highly selective transition-metal-free transamidation of amides and amidation of esters at room temperature
Transamidation reactions usually require transition metal catalysts and/or harsh conditions. Here, the authors show a general and operationally-simple protocol for the transamidation of amides and amidation of esters by highly selective acyl cleavage with non-nucleophilic amines under mild condition...
Guardado en:
Autores principales: | Guangchen Li, Michal Szostak |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2018
|
Materias: | |
Acceso en línea: | https://doaj.org/article/cc76dc0e7b4347d29b67230c62c50468 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
A two-step approach to achieve secondary amide transamidation enabled by nickel catalysis
por: Emma L. Baker, et al.
Publicado: (2016) -
Direct amidation of esters with nitroarenes
por: Chi Wai Cheung, et al.
Publicado: (2017) -
Catalytic amidation of natural and synthetic polyol esters with sulfonamides
por: Hua Liu, et al.
Publicado: (2019) -
Synthesis of amides and esters containing furan rings under microwave-assisted conditions
por: Janczewski Łukasz, et al.
Publicado: (2021) -
Amide nitrogen pyramidalization changes lactam amide spinning
por: Yuko Otani, et al.
Publicado: (2019)