Asymmetric synthesis of tetrazole and dihydroisoquinoline derivatives by isocyanide-based multicomponent reactions
Asymmetric isocyanide-based multicomponent reactions are elegant, yet challenging, strategies to access valuable N-heterocycles. Here, the authors employ a chiral Mg(II) -N,N′-dioxide catalyst in three- or four-component reactions to obtain chiral tetrazoles and devise a dearomative [3+2] annulation...
Saved in:
Main Authors: | Qian Xiong, Shunxi Dong, Yushuang Chen, Xiaohua Liu, Xiaoming Feng |
---|---|
Format: | article |
Language: | EN |
Published: |
Nature Portfolio
2019
|
Subjects: | |
Online Access: | https://doaj.org/article/acf4f00c9b424b08a7574e6fbe6e3a44 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Lewis acid-catalyzed asymmetric reactions of β,γ-unsaturated 2-acyl imidazoles
by: Tengfei Kang, et al.
Published: (2020) -
The halogen bond with isocyano carbon reduces isocyanide odor
by: Alexander S. Mikherdov, et al.
Published: (2020) -
Multicomponent reactions provide key molecules for secret communication
by: Andreas C. Boukis, et al.
Published: (2018) -
Straightforward and rapid Petasis multicomponent reactions in deep eutectic solvent
by: Najmedin Azizi, et al.
Published: (2021) -
New 2-aryl-7,8-dimethoxy-3,4-dihydroisoquinolin-2-ium salts as potential antifungal agents: synthesis, bioactivity and structure-activity relationships
by: Lifei Zhu, et al.
Published: (2017)