Asymmetric aldol reactions catalyzed by the promiscuous aldo–ketoreductase enzyme
The promiscuous aldo–ketoreductase (AKR) enzyme is used as a sustainable biocatalyst for the first time to catalyze asymmetric aldol reactions in aqueous medium. The reactions between aromatic aldehydes and cyclic/acyclic ketones give the corresponding products in moderate yields and enantioselectiv...
Main Authors: | Bayat, Saadi, Abd. Malek, Emilia, Mohd Yahaya, Normi, Salleh, Abu Bakar, Tejo, Bimo Ario, Abdul Rahman, Mohd Basyaruddin |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2014
|
Online Access: | http://psasir.upm.edu.my/id/eprint/36590/1/Asymmetric%20aldol%20reactions%20catalyzed%20by%20the%20promiscuous%20aldo.pdf |
Similar Items
-
Rational design of mimetic peptides based on aldo-ketoreductase enzyme as asymmetric organocatalysts in aldol reactions
by: Bayat, Saadi, et al.
Published: (2014) -
Rational design of mimetic peptides based on promiscuous aldo-ketoreductase enzyme as asymmetric catalysts in aldol and Michael reactions
by: Bayat, Saadi
Published: (2014) -
Various polar tripeptides as asymmetric organocatalyst in direct aldol reactions in aqueous media
by: Bayat, Saadi, et al.
Published: (2013) -
Asymmetric Michael reaction catalyzed by mimicked peptides
by: Bayat, Saadi, et al.
Published: (2014) -
Novel octapeptide as an asymmetric catalyst for Michael reaction in aqueous media
by: Bayat, Saadi, et al.
Published: (2013)