Optimization of microwave-assisted Michael addition reaction catalyzed by L-proline in ionic liquid medium using response surface methodology
Michael addition reactions of aldehyde to β-nitrostyrene catalyzed by L-proline were investigated by using controlled, monomode microwave-assisted technique in a closed vessel system. Ionic liquid 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([bmim]NTf2) was used as the reaction med...
Main Authors: | Omar, Emmy Maryati, Abdul Rahman, Mohd Basyaruddin, Abd. Malek, Emilia, Tejo, Bimo Ario, Ni, Bukuo, Headley, Allan D. |
---|---|
Format: | Article |
Language: | English |
Published: |
Taylor & Francis
2014
|
Online Access: | http://psasir.upm.edu.my/id/eprint/34775/1/Optimization%20of%20microwave-assisted%20Michael%20addition%20reaction%20catalyzed%20by%20L-proline%20in%20ionic%20liquid%20medium%20using%20response%20surface%20methodology.pdf |
Similar Items
-
The role of neutral anions in ionic liquid as solvent media for the reactivity and stereoselectivity towards asymmetric Michael addition reaction of n-pentanal with B-nitrostryrene catalyzed by L-Proline
by: M. Omar, Emmy, et al.
Published: (2019) -
Development of proline-based chiral ionic liquid organocatalyst for asymmetric Michael reaction under microwave irradiation
by: Omar, Emmy Maryati
Published: (2013) -
Asymmetric Michael reaction catalyzed by mimicked peptides
by: Bayat, Saadi, et al.
Published: (2014) -
Ionic Liquid-Supported (ILS) (S)-Pyrrolidine Sulfonamide for Asymmetric Michael addition reactions of Aldehydes with Nitroolefins.
by: Abdul Rahman, Mohd Basyaruddin, et al.
Published: (2011) -
Novel octapeptide as an asymmetric catalyst for Michael reaction in aqueous media
by: Bayat, Saadi, et al.
Published: (2013)