Ni-catalyzed asymmetric hydrogenation of N-aryl imino esters for the efficient synthesis of chiral α-aryl glycines
Chiral α-amino acids find application in the fields of pharmaceutical, biological and synthetic chemistry. Here, the authors report a nickel-catalyzed asymmetric hydrogenation of N-aryl imino esters affording chiral α-aryl glycines in high yields and enantioselectivities.
Guardado en:
Autores principales: | Dan Liu, Bowen Li, Jianzhong Chen, Ilya D. Gridnev, Deyue Yan, Wanbin Zhang |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2020
|
Materias: | |
Acceso en línea: | https://doaj.org/article/f1244b61e228435dbc80c84960209471 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Ni(II)-catalyzed asymmetric alkenylations of ketimines
por: Mao Quan, et al.
Publicado: (2018) -
Pd(OAc)2-catalyzed asymmetric hydrogenation of sterically hindered N-tosylimines
por: Jianzhong Chen, et al.
Publicado: (2018) -
Dual Ni/photoredox-catalyzed asymmetric cross-coupling to access chiral benzylic boronic esters
por: Purui Zheng, et al.
Publicado: (2021) -
Nickel-catalyzed intermolecular oxidative Heck arylation driven by transfer hydrogenation
por: Honggui Lv, et al.
Publicado: (2019) -
Facilitating the transmetalation step with aryl-zincates in nickel-catalyzed enantioselective arylation of secondary benzylic halides
por: Weichen Huang, et al.
Publicado: (2019)