Organocatalytic Enantioselective Henry Reactions
A large number of interesting organocatalytic enantioselective protocols have been explored and successfully applied in the last decade. Among them, the Henry (nitroaldol) reaction represents a powerful carbon-carbon bond-forming procedure for the preparation of valuable synthetic intermediates, suc...
Main Authors: | Raquel P. Herrera, Eugenia Marques-Lopez, Yolanda Alvarez-Casao |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2011-05-01
|
Series: | Symmetry |
Subjects: | |
Online Access: | http://www.mdpi.com/2073-8994/3/2/220/ |
Similar Items
-
Organocatalytic cascade aza-Michael/hemiacetal reaction between disubstituted hydrazines and α,β-unsaturated aldehydes: Highly diastereo- and enantioselective synthesis of pyrazolidine derivatives
by: Zhi-Cong Geng, et al.
Published: (2012-10-01) -
Recent Advances in Organocatalyzed Domino C–C Bond-Forming Reactions
by: Cleo S. Evans, et al.
Published: (2017-12-01) -
Organocatalytic and enantioselective Michael reaction between α-nitroesters and nitroalkenes. Syn/anti-selectivity control using catalysts with the same absolute backbone chirality
by: Jose I. Martínez, et al.
Published: (2015-12-01) -
Keratin Protein-Catalyzed Nitroaldol (Henry) Reaction and Comparison with Other Biopolymers
by: Marleen Häring, et al.
Published: (2016-08-01) -
Quantum Chemical Studies of Enantioselective Organocatalytic Reactions
by: Hammar, Peter
Published: (2008)