louisa aribi zouioueche - Catalysis

Author Information

Louisa Aribi-Zouioueche is affiliated with the Ecocompatible Asymmetric Catalysis Laboratory (LCAE) at Badji Mokhtar Annaba University, located in Annaba, Algeria. Her work predominantly revolves around the field of catalysis, with a focus on enzymatic and organocatalytic processes.

Research Contributions

Louisa Aribi-Zouioueche has made significant contributions to the field of catalysis, particularly in the areas of enzymatic synthesis and organocatalysis. Some of her notable works include the development of practical methods for synthesizing heterocyclic aromatic acetates, regio- and enantioselective ring opening of itaconic anhydride using lipase catalysis, and the efficient synthesis of valuable amides through CAL-B-mediated direct amidation. Her research extends into the synthesis of diastereoselective bis α-aminophosphonates with biological evaluations, as well as the development of novel organocatalysts and metal complexes for various catalytic applications.

Aliases

Louisa Aribi-zouioueche

Publication and Citation Metrics

Metric	Value
Total Papers	49
Total Citations	522
h-index	14

Publications:

Practical access to (S)-heterocyclic aromatic acetates via CAL-B/Na2CO3-deacylation and Mitsunobu reaction protocol

DOI: 10.1080/10242422.2022.2030726

Year: 2022

Access to valuable building blocks by the regio- and enantioselective ring opening of itaconic anhydride by lipase catalysis.

DOI: 10.1039/d2ob00047d

Year: 2022

CAL-B-mediated efficient synthesis of a set of valuable amides by direct amidation of phenoxy- and aryl-propionic acids

DOI: 10.1007/s11696-021-01636-5

Year: 2021

Fiaud's Acid, a novel organocatalyst for diastereoselective bis α-aminophosphonates synthesis with in-vitro biological evaluation of antifungal, antioxidant and enzymes inhibition potential.

DOI: 10.1016/j.bmcl.2021.128000

Year: 2021

Two Approaches for CAL-B-Catalyzed Enantioselective Deacylation of a Set of α-Phenyl Ethyl Esters: Organic Solvent with Sodium Carbonate and Micro-aqueous Medium

DOI: 10.1007/s10562-020-03525-0

Year: 2021

Enantioselective Enzymatic Synthesis of ( R )‐Phenyl Alkyl Esters and Their Analogue Amides using Fatty Acids as Green Acyl Donors.

DOI: 10.1002/slct.202103831

Year: 2021

New promising generation of phosphates α-aminophosphonates: Design, Synthesis, In-vitro biological evaluation and Computational study

DOI: 10.1016/j.molstruc.2021.131336

Year: 2021

Cobalt(II), Nickel(II) and Zinc(II) complexes based on DHA: Synthesis, X-ray crystal structure, antibacterial activity and DFT computational studies

DOI: 10.1016/j.molstruc.2020.128353

Year: 2020

Novel One‐Pot Access to Diastereoisomeric Tertiary Phospholanes Oxides by Using Enantiomerically Pure Phospholane Oxides Under Catalyst‐Free Conditions

DOI: 10.1002/slct.201903760

Year: 2020

Diastereoselective synthesis of bis(α-aminophosphonates) by lipase catalytic promiscuity

DOI: 10.1039/C8NJ06235H

Year: 2019

What Are the Advantages of Coordination Polymerization?

How to Organize Data on Google Drive?

How Does Catalysis Fit into Green Chemistry?

Who can become a member of EFCATS?

Why is Material Incompatibility a Concern?

Why are Vibrational Excited States Important in Catalysis?

What are the Limitations of Ammonia TPD?

What are Glucosyltransferases?

Why is the Ubiquitin Proteasome System Important?

What Are the Key Metrics for Catalyst Standards?

Partnered Content Networks

Relevant Topics