Search filters

List of works by Ewa Żymańczyk-Duda

(S)-Thienyl and (R)-Pirydyl phosphonate Derivatives Synthesized by Stereoselective Resolution of Their Racemic Mixtures With <i>Rhodotorula mucilaginosa</i> (DSM 70403) - Scaling Approaches

scientific article published on 11 November 2020

2-Aminoethylphosphonate utilization by the cold-adapted Geomyces pannorum P11 strain

scientific article published on 27 October 2013

A simple and green procedure for the microbial effective synthesis of 1-phenylethyl alcohol in both enantiomeric forms

scientific article published in April 2006

Accurate assay of enantiopurity of 1-hydroxy- and 2-hydroxyalkylphosphonate esters

Application of fungi as biocatalysts for the reduction of diethyl 1-oxoalkylphosphonates in anhydrous hexane

scientific article published in November 2002

Application of the Beauveria bassiana strain for the enantioselective oxidation of the diethyl 1-hydroxy-1-phenylmethanephosphonate.

scientific article published on 15 December 2010

Biocatalytic resolution of enantiomeric mixtures of 1-aminoethanephosphonic acid

scientific article published on 14 July 2011

Biocatalyzed Reactions in Optically Active Phosphonate Synthesis

Biocatalyzed kinetic resolution of racemic mixtures of chiral α-aminophosphonic acids

Biogenic synthesis of silica nanoparticles from corn cobs husks. Dependence of the productivity on the method of raw material processing

scientific article published on 18 March 2020

Chiral O-phosphorylated derivative of 2-hydroxy-2-phenylethylphosphonate as a valuable product of microbial biotransformation of diethyl 2-oxo-2-phenylethylphosphonate

Chiral phosphinate degradation by the fusarium species: scope and limitation of the process

scientific article published on 10 November 2013

Comparative study of fungal cell disruption--scope and limitations of the methods

scientific article

Cyanobacteria as Valuable Tool in Biotechnology

scientific article published on 20 October 2021

Direct determination of enantiomeric enrichment of chiral, underivatized aminophosphonic acids — useful for enantioselective bioconversion results evaluation

Effective fungal catalyzed synthesis of P-chiral organophosphorus compounds

Enantio convergent biotransformation of O,O-dimethyl-4-oxoazetidin-2-ylphosphonate using fungal cells of Penicillium minioluteum and purified enzymes

scientific article published on 24 January 2017

Enantioselective reduction of diethyl 2-oxoalkylphosphonates by baker's yeast

First biological conversion of chiral heterophosphonate derivative - Scaling and paths of conversion discussion

scientific article published on 30 January 2019

Fungal platform for direct chiral phosphonic building blocks production. Closer look on conversion pathway

scientific article published on 16 November 2014

Fungal synthesis of chiral phosphonic synthetic platform - Scope and limitations of the method

scientific article published on 2 February 2018

Half-Preparative Scale Synthesis of (S)-1-Phenylethane-1,2-Diol as a Result of 2-Phenylethanol Hydroxylation with Aspergillus niger (IAFB 2301) Assistance

scientific article published on 10 June 2020

Lipases and whole cell biotransformations of 2-hydroxy-2-(ethoxyphenylphosphinyl)acetic acid and its ester.

scientific article published on 2 March 2016

Nanosilica synthesis mediated by Aspergillus parasiticus strain

scientific article published on 01 March 2018

Preface

scientific article published on 03 July 2019

Reductive activity of free and immobilized cells of cyanobacteria toward oxophosphonates-comparative study

scientific article published on 15 September 2016

Reductive capabilities of different cyanobacterial strains towards acetophenone as a model substrate - Prospect of applications for chiral building blocks synthesis

scientific article published on 26 February 2019

Stereochemical control of asymmetric hydrogen transfer employing five different kinds of fungi in anhydrous hexane

article by Ewa Żymańczyk-Duda et al published May 2004 in Enzyme and Microbial Technology

Stereochemical control of biocatalytic asymmetric reduction of diethyl 2-oxopropylphosphonate employing yeasts