Effect of Microwaves in the Chiral Switching Asymmetric Michael Reaction
Highly enantioselective Michael reactions of malonates with cyclic enones are achieved in remarkably less time under microwave irradiation using newly developed heterobimetallic catalysts.
Main Authors: | S. Velmathi, S. Narasimhan |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2003-02-01
|
Series: | Molecules |
Subjects: | |
Online Access: | http://www.mdpi.com/1420-3049/8/2/256/ |
Similar Items
-
Novel Chiral Switching Ligands for Enantioselective Asymmetric Reductions of Prochiral Ketones
by: S. Velmathi, et al.
Published: (2001-11-01) -
Asymmetric cyclopentannulation reactions: scope and limitation
by: Schanen, Patrick
Published: (2003) -
Chiral Aminophosphines as Catalysts for Enantioselective Double-Michael Indoline Syntheses
by: Ohyun Kwon, et al.
Published: (2012-05-01) -
Beneficial Contribution of Biosourced Ionic Liquids and Microwaves in the Michael Reaction
by: Katia Bacha, et al.
Published: (2020-07-01) -
Michael Additions of Amines to Methyl Acrylates Promoted by Microwave Irradiation
by: Irma Linzaga, et al.
Published: (2008-02-01)