Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts
The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate enolate intermediates is disclosed. The catalytically generated arylacetic ester enolates undergo enantioselective reactions with α,β-unsaturated imines.
Saved in:
Main Authors: | Hao, Lin, Du, Yu, Lv, Hui, Chen, Xingkuan, Jiang, Huishen, Shao, Yaling, Chi, Robin Yonggui |
---|---|
Other Authors: | School of Physical and Mathematical Sciences |
Format: | Article |
Language: | English |
Published: |
2013
|
Online Access: | https://hdl.handle.net/10356/97284 http://hdl.handle.net/10220/10637 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
Enantioselective Stetter reactions of enals and modified chalcones catalyzed by N-heterocyclic carbenes
by: Fang, Xinqiang, et al.
Published: (2014) -
β-Carbon activation of saturated carboxylic esters through N-heterocyclic carbene organocatalysis
by: Xu, Jianfeng, et al.
Published: (2013) -
Enantioselective Diels–Alder reactions of enals and alkylidene diketones catalyzed by N-heterocyclic carbenes
by: Fang, Xinqiang, et al.
Published: (2014) -
Carbene-Catalyzed Dynamic Kinetic Resolution of Carboxylic Esters
by: Chen, Xingkuan, et al.
Published: (2017) -
Oxidative γ-addition of enals to trifluoromethyl ketones : enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis
by: Mo, Junming, et al.
Published: (2013)