Access to oxoquinoline heterocycles by N-heterocyclic carbene catalyzed ester activation for selective reaction with an enone
Organocatalytic ester activation is developed for a highly selective cascade reaction between saturated esters and amino enones. The reaction involves activation of the β-carbon atom of the ester as a key step. This method allows a single-step access to multicyclic oxoquinoline-type heterocycles wit...
Saved in:
Main Authors: | Fu, Zhenqian, Jiang, Ke, Zhu, Tingshun, Torres, Jaume, Chi, Robin Yonggui |
---|---|
Other Authors: | School of Biological Sciences |
Format: | Article |
Language: | English |
Published: |
2014
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/100042 http://hdl.handle.net/10220/19652 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
β-Carbon activation of saturated carboxylic esters through N-heterocyclic carbene organocatalysis
by: Xu, Jianfeng, et al.
Published: (2013) -
A highly regio- and stereoselective cascade annulation of enals and benzodi(enone)s catalyzed by N-heterocyclic carbenes
by: Fang, Xinqiang, et al.
Published: (2014) -
N-Heterocyclic carbene catalyzed radical coupling of aldehydes with redox-active esters
by: Song, Runjiang, et al.
Published: (2020) -
N-Heterocyclic carbene-catalyzed activation of esters for asymmetric reactions
by: Hao, Lin
Published: (2013) -
Carbene-catalyzed enantioselective addition of thioamides to bromoenals for access to thiazinone heterocycles
by: Liu, Changyi, et al.
Published: (2020)