Publications Ewa Żymańczyk-Duda

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Ewa Żymańczyk-Duda


Żymańczyk-Duda E, Kozyra K, Brzezińska-Rodak M, Klimek-Ochab M, Baker’s yeasts driven synthesis of enantiomers of ethyl 1-hydroxy-1-(3,4-dimethoxyphenyl)methane(P-phenyl)phosphinate - possible organophosphorus CDA’s Journal of Molecular Catalysis. B, Enzymatic 2017, 1.

Górak Monika, Żymańczyk-Duda Ewa, Reductive activity of free and immobilized cells of cyanobacteria toward oxophosphonates - comparative study. Journal of Applied Phycology 2017, 29, 245.

Żymańczyk-Duda Ewa, Microbial bioconversions of biologically active P-C compounds: scope and limitations of scaling-up. Journal of Biotechnology and Biomaterials 2017, 7, 49.

Kmiecik Natalia, Żymańczyk-Duda Ewa, Enantio convergent biotransformation of O,O-dimethyl-4-oxoazetidin-2-ylphosphonate using fungal cells of Penicillium minioluteum and purified enzymes. Bioorganic Chemistry 2017, 71, 81.

Ewa Żymańczyk-Duda, Małgorzata Brzezińska-Rodak, Magdalena Klimek-Ochab, Maciej Duda, Biochemistry - Knowledge to Practical Applications - Examples Biochemstry ISBN: 978-0-9971499-2-0 2017, 1.


Majewska, P.; Serafin, M., Klimek-Ochab, M.; Brzezińska-Rodak, M.; Żymańczyk-Duda, E., Lipases and whole cell biotransformations of 2-hydroxy-2-(ethoxyphenylphosphinyl)acetic acid and its ester Bioorg. Chem. 2016, 66, 21.

Brzezińska-Rodak, M.; Klimek-Ochab, M.; Żymańczyk-Duda, E., Enzyme-mediated protoplast formation of Cuninghamella echinulata – preliminary studies BioTechnologia 2016, 97, 27.

Górak, M.; Żymańczyk-Duda, E., Reductive activity of free and immobilized cells of cyanobacteria toward oxophosphonates—comparative study J. Appl. Phycol. 2016, 1.


Zymanczyk-Duda, E.; Brzezinska-Rodak, M.; Kozyra, K.; Klimek-Ochab, M., Fungal Platform for Direct Chiral Phosphonic Building Blocks Production. Closer Look on Conversion Pathway Appl. Biochem. Biotechnol. 2015, 175, 1403.

Górak, M.; Żymańczyk-Duda, E., Application of cyanobacteria for chiral phosphonate synthesis. Green Chem. 2015, 17, 4570.

Szmigiel, B.; Żymańczyk-Duda, E.; Lochyński, S., Procedura zabiegowa eksfoliacji z zastosowaniem hydroksykwasów. Pol. J. Cosmet. 2015, 18, 119.

Górak, M.; Serafin, M.; Klimek-Ochab, M.; Żymańczyk-Duda, E., Bioocatalitic transformation of epoxy- and vinylphosphonates Chemik 2015, 69, 273.


Klimek-Ochab, M.; Mucha, A.; Żymań„czyk-Duda, E, 2-Aminoethylphosphonate Utilization by the Cold-Adapted Geomyces pannorum P11 Strain Curr. Microbiol. 2014, 68, 330.

Serafin, M.; Żymańczyk-Duda, E., Kinetic resolution of racemic mixture of 2-butyryloxy- 2-(ethoxy-P-phenylphosphinyl)acetic acid by fungi Penicillium oxalicum Chemik 2014, 68, 776.

Monika GĂłrak, Ewa Ĺťymańczyk-Duda, Sposób biokalitycznego otrzymywania (S)-2-hydroksy-2-fenyloetanofosfonianu dietylu. zgłoszenie patentowe P410414 2014, 1.

Monika GĂłrak, Ewa Ĺťymańczyk-Duda, Biokatalityczny sposób otrzymywania (S)-2-hydroksy-2-fenyloetanofosfonianu dietylu. zgłoszenie patentowe P408430 2014, 1.

Monika Górak, Ewa Żymańczyk-Duda, Application of cyanobacteria as biocatalysts for the reduction of diethyl 2-oxopropylphosphonate CHEMIK 2014, 68, 123.


Kinga Kozyra*, Magdalena Klimek-Ochab, Małgorzata Brzezińska-Rodak, Ewa Ĺťymańczyk-Duda, Direct determination of enantiomeric enrichment of chiral, underivatized aminophosphonic acids – useful for enantioselective bioconversion results evaluation Central European Journal of Chemistry 2013, 11, 1542.

Natalia Kmiecik,Magdalena Klimek-Ochab,Małgorzata Brzezińska-Rodak, PaulinaMajewska, and Ewa Żymańczyk-Duda, Chiral Phosphinate Degradation by the Fusarium Species: Scope and Limitation of the Process Biotechnology Research International 2013, 2013, 1.

Kinga Kozyra∗, Małgorzata Brzezińska-Rodak, Magdalena Klimek-Ochab, Ewa Żymańczyk-Duda, Biocatalyzed kinetic resolution of racemic mixtures of chiral alpha-aminophosphonic acids Journal of Molecular Catalysis B: Enzymatic 2013, 91, 32.

MONIKA GÓRAK*, MAŁGORZATA BRZEZIŃSKA-RODAK, MAGDALENA KLIMEK-OCHAB, EWA ŻYMAŃCZYK-DUDA, Amino acid mineralization by Serratia marcescens BioTechnologia: Journal of Biotechnology, Computational Biology and Bionanotechnology 2013, 94, 269.


Żymańczyk-Duda, E.; Klimek-Ochab, M., Stereoselective Biotransformations as an Effective Tool for the Synthesis of Chiral Compounds with P-C Bond - Scope and Limitations of the Methods. Curr. Org. Chem. 2012, 16, 1408.

Brzezińska-Rodak, M.; Klimek-Ochab, M.; Żymańczyk-Duda, E., Biocatalyzed synthesis of chiral O-phosphorylated derivative of 2-hydroxy-2-phenylethanephosphonate. Practical methods for biocatalysis and biotransformations 2 2012, 247.


Brzeziń„ska-Rodak, M.; Klimek-Ochab, M.; Żymań„czyk-Duda E.; Kafarski, P., Biocatalytic Resolution of Enantiomeric Mixtures of 1-Aminoethanephosphonic Acid Molecules 2011, 16, 5896.

Żymańczyk-Duda, E.; Brzezińska-Rodak, M.; Klimek-Ochab, M.; Lejczak, B., Application of the Beauveria bassiana Strain for the Enantioselective Oxidation of the Diethyl 1-Hydroxy-1-Phenylmethanephosphonate Curr. Microbiol. 2011, 62, 1168.

Klimek-Ochab, M.; Brzeziń„ska-Rodak, M.; Żymań„czyk-Duda, E.; Lejczak, B.; Kafarski, P., Comparative study of fungal cell disruption—scope and limitations of the methods. Folia Microbiol. 2011, 56, 469.


Brzezińska-Rodak, M.; Żymańczyk-Duda, E.; Klimek-Ochab, M.; Lejczak, B., Fungal Cells Permeabilization as a Convenient Tool of Bioreduction Enantioselectivity Control Pol. J. Chem. 2009, 83, 2113.


Żymańczyk-Duda, E.; Brzeziń„ska-Rodak, M.; Klimek-Ochab, M.; Latajka, R.; Kafarski, P.; Lejczak, B., Chiral O-phosphorylated derivative of 2-hydroxy-2-phenylethylphosphonate as a valuable product of microbial biotransformation of diethyl 2-oxo-2-phenylethylphosphonate J. Mol. Cat. B 2008, 52, 74.

Klimek-Ochab, M.; Żymańczyk-Duda, E.; Brzezińska-Rodak, M.; Majewska, P.; Lejczak, B., Effective fungal catalyzed synthesis of P-chiral organophosphorus compounds. Tetrahedron: Asymmetry 2008, 19, 450.

Ewa Żymańczyk-Duda, Biocatalyzed reactions in optically active phosphonates synthesis. Phosphorus, Sulfur, Silicon and the Related Elements 2008, 183, 1.


Brzezińska-Rodak, M.; Żymańczyk-Duda, E.; Klimek-Ochab, M.; Lejczak, B., Biocatalytical synthesis and further determination of the absolute configuration of diethyl of (R)-2-hydroxybutylphosphonate Pol. J. Chem. 2007, 81, 1911.


Brzezinska-Rodak, M.; Zymanczyk-Duda, E.; Klimek-Ochab, M.; Kafarski, P.; Lejczak, B., A simple and green procedure for the microbial effective synthesis of 1-phenylethyl alcohol in both enantiomeric forms. Biotech. Lett. 2006, 28, 511.


Żymańczyk-Duda, E.; Klimek-Ochab, M.; Kafarski, P.; Lejczak, B., Stereochemical control of biocatalytic asymmetric reduction of diethyl 2-oxopropylphosphonate employing yeasts. J. Organomet. Chem. 2005, 690, 2593.


Żymańczyk-Duda, E.; Brzezińska-Rodak, M.; Lejczak, B., Stereochemical control of asymmetric hydrogen transfer employing five different kinds of fungi in anhydrous hexane. Enzyme Microbiol. Tech. 2004, 34, 578.


Brzezińska-Rodak, M.; Żymańczyk-Duda, E.; Kafarski, P.; Lejczak, B., Application of fungi as biocatalysts for the reduction of diethyl 1-oxoalkylphosphonates in anhydrous hexane. Biotech. Prog. 2002, 18, 1287.


Gancarz, R.; Latajka, R.; Maluszek, B.; Żymańczyk-Duda, E.; Kafarski, P. , Hydrogen bonding in diethyl 2-hydroxypropylphosphonate - an example of equilibrium between intramolecular and intermolecular bonding. Magn. Res. Chem. 2000, 38, 197.

Ĺťymańczyk-Duda, E.; Kafarski, P.; Lejczak, B., Reductive biotransformation of diethyl beta-, gamma- and delta-oxoalkylphosphonates by cells of baker’s yeast Enzyme Microb. Technol. 2000, 26, 265.


Żymańczyk-Duda, E.; Lejczak, B.; Kafarski, P., Esterification of phosphonic and phosphinic acids analogues of glutamic and aspartic acids with ethyl orthoformate - scope and limitations of the method Phosphorus, Sulfur, Silicon 1996, 112, 47.

Żymańczyk-Duda Ewa, Skwarczyński mariusz, Lejczak Barbara, Kafarski Paweł, Accurate assay of enantiopurity of 1-hydroxy- and 2-hydroxyalklphosphonates esters Tetrahedron:Asymmetry 1996, 7, 1277.

Żymańczyk-Duda Ewa, Lejczak Barbara, Kafarski Paweł, Esterification of phosphonic and phosphinic acids analogues of glutamic and aspartic acids with ethyl orthoformate - scope and limitations of the method Phosphorus, Sulfur and Silicon 1996, 112, 47.


Żymańczyk-Duda Ewa, Lejczak Barbara, Kafarski Paweł, Enantioselective reduction of diethyl 2-oxoalkylphosphonates by baker's yeast. Tetrahedron 1995, 51, 11809.