Catalytic enantioselective addition of Grignard reagents to aromatic silyl ketimines
The stereoselective addition of Grignard reagents to ketimines is potentially a straightforward route to α-chiral amines. Here the authors report a catalytic, asymmetric Grignard addition to silyl ketimines, givingN-sulfonyl protected α-chiral silyl amines with tetrasubstituted stereocentres.
Enregistré dans:
Auteurs principaux: | Jiawei Rong, Juan F. Collados, Pablo Ortiz, Ravindra P. Jumde, Edwin Otten, Syuzanna R. Harutyunyan |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Nature Portfolio
2016
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/21be2c4928f94b7f9adb7908f0ebc4c3 |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Highly enantioselective catalytic synthesis of chiral pyridines
par: Ravindra P. Jumde, et autres
Publié: (2017) -
Catalytic enantioselective addition of organometallics to unprotected carboxylic acids
par: Xingchen Yan, et autres
Publié: (2019) -
Ni(II)-catalyzed asymmetric alkenylations of ketimines
par: Mao Quan, et autres
Publié: (2018) -
Christiane Desafy-Grignard. Arthur Miller.
par: Susan Blattès
Publié: (2006) -
Synthesis of chiral anti-1,2-diamine derivatives through copper(I)-catalyzed asymmetric α-addition of ketimines to aldimines
par: Xu-Cheng Gan, et autres
Publié: (2020)