NHC organocatalytic formal LUMO activation of α,β-unsaturated esters for reaction with enamides
An effective wake-up call: Stable ,β-unsaturated esters were activated by the addition of a chiral N-heterocyclic carbene (NHC) organocatalyst, and the resulting reactive Michael acceptor intermediates reacted with enamide nucleophiles to furnish optically pure products (see scheme; Ts=p-toluenesulf...
Saved in:
Main Authors: | Cheng, Jiajia, Huang, Zhijian, Chi, Robin Yonggui |
---|---|
Other Authors: | School of Physical and Mathematical Sciences |
Format: | Article |
Language: | English |
Published: |
2014
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/104220 http://hdl.handle.net/10220/19438 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
Organocatalytic activation of alkylacetic esters as enolate precursors to react with α,β-unsaturated imines
by: Hao, Lin, et al.
Published: (2014) -
NHC-catalyzed ester activation : access to sterically congested spirocyclic oxindoles via reaction of α-aryl esters and unsaturated imines
by: Hao, Lin, et al.
Published: (2014) -
Organocatalytic enantioselective γ-aminoalkylation of unsaturated ester : access to pipecolic acid derivatives
by: Xu, Jianfeng, et al.
Published: (2014) -
Carbene-catalyzed LUMO activation of alkyne esters for access to functional pyridines
by: Mou, Chengli, et al.
Published: (2020) -
Organocatalytic asymmetric aldol reaction of hydroxyacetone with β,γ-unsaturated α-keto esters: Facile access to chiral tertiary alcohols
by: Liu, C., et al.
Published: (2014)