Scientific papers

 
  1. Transaminase - carbonic anhydrase bi-enzymatic cascade for preparation of (R)-1-arylethan-1-amines and (S)-1-arylethan-1-ols

    Barabás L.E., Scrob D.M., Varga A., Kiss L., Toşa M.I., Paizs C.
    Reaction Chemistry and Engineering (2023) 8(8): 2001-2010
    DOI: 10.1039/d3re00128h

  2. A robust and efficient lipase based nanobiocatalyst for phenothiazinyl-ethanol resolution

    Spelmezan C.-G., Katona G., Bencze L.C., Paizs C., Toşa M.I.
    Reaction Chemistry and Engineering (2023) 88(2): 852-862
    DOI: 10.1039/d2re00515h

  3. How to identify and characterize novel transaminases? Two novel transaminases with opposite enantioselectivity for the synthesis of optically active amines

    Gal C.A., Barabás L.-E., Varga A., Csuka P., Bencze L.C., Toşa M.I., Poppe L., Paizs C.
    Molecular Catalysis (2022) 531: 112660
    DOI: 10.1016/j.mcat.2022.112660

  4. Cross-Linked Enzyme-Adhered Nanoparticles (CLEANs) for Continuous-Flow Bioproduction

    Nagy F., Sánta-Bell E., Jipa M., Hornyánszky G., Szilágyi A., László K., Katona G., Paizs C., Poppe L., Balogh-Weiser D.
    ChemSusChem (2022) 15(2): e202102284
    DOI: 10.1002/cssc.202102284

  5. Deep eutectic solvents-a new additive in the encapsulation of lipase B from: Candida antarctica: Biocatalytic applications

    Dudu A.I., Bencze L.C., Paizs C., Toşa M.I.
    Reaction Chemistry and Engineering (2022) 7(2): 442-449
    DOI: 10.1039/d1re00469g

  6. Recent Progress in the Selective Fluorinations of Some Functionalized Cycloalkenes

    Nonn M., Paizs C., Kiss L.
    Chemical Record (2022) 22(9): e202200130
    DOI: 10.1002/tcr.202200130

  7. Cross-Linked Enzyme-Adhered Nanoparticles (CLEANs) for Continuous-Flow Bioproduction

    Nagy F., Sánta-Bell E., Jipa M., Hornyánszky G., Szilágyi A., László K., Katona G., Paizs C., Poppe L., Balogh-Weiser D.
    ChemSusChem (2022) 15(2): e202102284
    DOI: 10.1002/cssc.202102284

  8. Lipase on carbon nanotubes-an active, selective, stable and easy-to-optimize nanobiocatalyst for kinetic resolutions

    Gal C.A., Barabás L.E., Bartha Vári J.-H., Moisă M.E., Balogh-Weiser D., Bencze L.C., Poppe L., Paizs C., Toşa M.I.
    Reaction Chemistry and Engineering (2021) 6(12): 2391-2399
    DOI: 10.1039/d1re00342a

  9. Characterization of yeast strains with ketoreductase activity for bioreduction of ketones

    Csuka P., Nagy-Győr L., Molnár Z., Paizs C., Bódai V., Poppe L.
    Periodica Polytechnica Chemical Engineering (2021) 65(3): 299-307
    DOI: 10.3311/PPch.17429

  10. Robust, site-specifically immobilized phenylalanine ammonia-lyases for the enantioselective ammonia addition of cinnamic acids

    Boros K., Moisă M.E., Nagy C.L., Paizs C., Toşa M.I., Bencze L.C.
    Catalysis Science and Technology (2021) 11(16): 5553-5563
    DOI: 10.1039/d1cy00195g

  11. Green Process for the Enzymatic Synthesis of Aroma Compounds Mediated by Lipases Entrapped in Tailored Sol-Gel Matrices

    Dudu A.I., Lacatus M.A., Bencze L.C., Paizs C., Toşa M.I.
    ACS Sustainable Chemistry and Engineering (2021) 9(15): 5461-5469
    DOI: 10.1021/acssuschemeng.1c00965

  12. Substrate Tunnel Engineering Aided by X-ray Crystallography and Functional Dynamics Swaps the Function of MIO-Enzymes

    Bata Z., Molnár Z., Madaras E., Molnár B., Sánta-Bell E., Varga A., Leveles I., Qian R., Hammerschmidt F., Paizs C., Vértessy B.G., Poppe L.
    ACS Catalysis (2021) 11(8): 4538-4549
    DOI: 10.1021/acscatal.1c00266

  13. A novel phenylalanine ammonia-lyase from Pseudozyma antarctica for stereoselective biotransformations of unnatural amino acids

    Varga A., Csuka P., Sonesouphap O., Bánóczi G., Toşa M.I., Katona G., Molnár Z., Bencze L.C., Poppe L., Paizs C.
    Catalysis Today (2021) 366: 185-194
    DOI: 10.1016/j.cattod.2020.04.002

  14. Oscillations and collective behavior in convective flows

    Gergely A., Paizs C., Tötös R., Néda Z.
    Physics of Fluids (2021) 33(12): 124104
    DOI: 10.1063/5.0073347

  15. Flickering candle flames and their collective behavior

    Gergely A., Sándor B., Paizs C., Tötös R., Néda Z.
    Scientific Reports (2020) 10(1): 21305
    DOI: 10.1038/s41598-020-78229-x

  16. Magnetic nanoparticles with dual surface functions—efficient carriers for metalloporphyrin-catalyzed drug metabolite synthesis in batch and continuous-flow reactors

    Balogh-Weiser D., Decsi B., Krammer R., Dargó G., Ender F., Mizsei J., Berkecz R., Gyarmati B., Szilágyi A., Tőtős R., Paizs C., Poppe L., Balogh G.T.
    Nanomaterials (2020) 10(12): 2329
    DOI: 10.3390/nano10122329

  17. Solvent-Free Biocatalytic Synthesis of 2,5-bis-(Hydroxymethyl)Furan Fatty Acid Diesters from Renewable Resources

    Lăcătuş M.A., Dudu A.I., Bencze L.C., Katona G., Irimie F.-D., Paizs C., Toşa M.I.
    ACS Sustainable Chemistry and Engineering (2020) 8(3): 1611-1617
    DOI: 10.1021/acssuschemeng.9b06442

  18. Fluorescent enzyme-coupled activity assay for phenylalanine ammonia-lyases

    Moisă M.E., Amariei D.A., Nagy E.Z.A., Szarvas N., Toşa M.I., Paizs C., Bencze L.C.
    Scientific Reports (2020) 10(1): 18418
    DOI: 10.1038/s41598-020-75474-y

  19. Efficient biodiesel production catalyzed by nanobioconjugate of lipase from pseudomonas fluorescens

    Bartha-Vári J.-H., Moisă M.E., Bencze L.C., Irimie F.-D., Paizs C., Toşa M.I.
    Molecules (2020) 25(3): 651
    DOI: 10.3390/molecules25030651

  20. Conservation of the biocatalytic activity of whole yeast cells by supported sol – gel entrapment for efficient acyloin condensation

    Nagy-Győr L., Farkas E., Lăcătuș M., Tóth G., Incze D., Hornyánszky G., Bódai V., Paizs C., Poppe L., Balogh-Weiser D.
    Periodica Polytechnica Chemical Engineering (2020) 64(2): 153-161
    DOI: 10.3311/PPch.14645

  21. Effcient and stable magnetic chitosan-lipase B from candida antarctica bioconjugates in the enzymatic kinetic resolution of racemic heteroarylethanols

    Spelmezan C.G., Bencze L.C., Katona G., Irimie F.D., Paizs C., Toşa M.I.
    Molecules (2020) 25(2): 350
    DOI: 10.3390/molecules25020350

  22. Mapping the Hydrophobic Substrate Binding Site of Phenylalanine Ammonia-Lyase from Petroselinum crispum

    Nagy E.Z.A., Tork S.D., Lang P.A., Filip A., Irimie F.D., Poppe L., Toşa M.I., Schofield C.J., Brem J., Paizs C., Bencze L.C.
    ACS Catalysis (2019) 9(9): 8825-8834
    DOI: 10.1021/acscatal.9b02108

  23. The production of L- and D-phenylalanines using engineered phenylalanine ammonia lyases from Petroselinum crispum

    Tork S.D., Nagy E.Z.A., Cserepes L., Bordea D.M., Nagy B., Toşa M.I., Paizs C., Bencze L.C.
    Scientific Reports (2019) 9(1): 20123
    DOI: 10.1038/s41598-019-56554-0

  24. How to Turn Yeast Cells into a Sustainable and Switchable Biocatalyst? On-Demand Catalysis of Ketone Bioreduction or Acyloin Condensation

    Nagy-Györ L., Lăcătuş M., Balogh-Weiser D., Csuka P., Bódai V., Erdélyi B., Molnár Z., Hornyánszky G., Paizs C., Poppe L.
    ACS Sustainable Chemistry and Engineering (2019) 7(24): 19375-19383
    DOI: 10.1021/acssuschemeng.9b03367

  25. Liver-on-a-chip-magnetic nanoparticle bound synthetic metalloporphyrin-catalyzed biomimetic oxidation of a drug in a magnechip reactor

    Decsi B., Krammer R., Hegedus K., Ender F., Gyarmati B., Szilágyi A., Totos R., Katona G., Paizs C., Balogh G.T., Poppe L., Balogh-Weiser D.
    Micromachines (2019) 10(10): 668
    DOI: 10.3390/mi10100668

  26. Immobilized whole-cell transaminase biocatalysts for continuous-flow kinetic resolution of amines

    Molnár Z., Farkas E., Lakó Á., Erdélyi B., Kroutil W., Vértessy B.G., Paizs C., Poppe L.
    Catalysts (2019) 9(5): 438
    DOI: 10.3390/catal9050438

  27. "Fishing and hunting"-selective immobilization of a recombinant phenylalanine ammonia-lyase from fermentation media

    Sánta-Bell E., Molnár Z., Varga A., Nagy F., Hornyánszky G., Paizs C., Balogh-Weiser D., Poppe L.
    Molecules (2019) 24(22): 4146
    DOI: 10.3390/molecules24224146

  28. Exploring the substrate scope of ferulic acid decarboxylase (FDC1) from Saccharomyces cerevisiae

    Nagy E.Z.A., Nagy C.L., Filip A., Nagy K., Gál E., Tőtős R., Poppe L., Paizs C., Bencze L.C.
    Scientific reports (2019) 9(1): 647
    DOI: 10.1038/s41598-018-36977-x

  29. “Geländer” macrocycles: Synthesis, chirality and racemisation barriers

    Lar C., Moisӑ M.E., Bogdan E., Terec A., Hӑdade N.D., Grosu I., David L., Paizs C., Grosu I.G.
    Tetrahedron Letters (2019) 60(4): 335-340
    DOI: 10.1016/j.tetlet.2018.12.047

  30. Continuous-flow enzymatic kinetic resolution mediated by a lipase nanobioconjugate

    Moisă M.E., Bencze L.C., Paizs C., Toşa M.I.
    Studia Universitatis Babes-Bolyai Chemia (2019) 64(2Tom1): 79-86
    DOI: 10.24193/subbchem.2019.2.07

  31. Click reaction-aided enzymatic kinetic resolution of secondary alcohols

    Moisă M.E., Poppe L., Gal C.A., Bencze L.C., Irimie F.D., Paizs C., Peter F., Toşa M.I.
    Reaction Chemistry and Engineering (2018) 3(5): 790-798
    DOI: 10.1039/c8re00091c

  32. Tailored Mutants of Phenylalanine Ammonia-Lyase from Petroselinum crispum for the Synthesis of Bulky l- and d-Arylalanines

    Filip A., Nagy E.Z.A., Tork S.D., Bánóczi G., Toşa M.I., Irimie F.D., Poppe L., Paizs C., Bencze L.C.
    ChemCatChem (2018) 10(12): 2627-2633
    DOI: 10.1002/cctc.201800258

  33. Eco-Friendly Enzymatic Production of 2,5-Bis(hydroxymethyl)furan Fatty Acid Diesters, Potential Biodiesel Additives

    Lăcătuş M.A., Bencze L.C., Toşa M.I., Paizs C., Irimie F.-D.
    ACS Sustainable Chemistry and Engineering (2018) 6(9): 11353-11359
    DOI: 10.1021/acssuschemeng.8b01206

  34. Chemoenzymatic Dynamic Kinetic Resolution of Amines in Fully Continuous-Flow Mode

    Farkas E., Oláh M., Földi A., Kóti J., Éles J., Nagy J., Gal C.A., Paizs C., Hornyánszky G., Poppe L.
    Organic Letters (2018) 20(24): 8052-8056
    DOI: 10.1021/acs.orglett.8b03676

  35. Co-immobilized Whole Cells with ω-Transaminase and Ketoreductase Activities for Continuous-Flow Cascade Reactions

    Nagy-Győr L., Abaházi E., Bódai V., Sátorhelyi P., Erdélyi B., Balogh-Weiser D., Paizs C., Hornyánszky G., Poppe L.
    ChemBioChem (2018) 19(17): 1845-1848
    DOI: 10.1002/cbic.201800286

  36. Covalently immobilized Trp60Cys mutant of Ω-transaminase from Chromobacterium violaceum for kinetic resolution of racemic amines in batch and continuous-flow modes

    Abaházi E., Sátorhelyi P., Erdélyi B., Vértessy B.G., Land H., Paizs C., Berglund P., Poppe L.
    Biochemical Engineering Journal (2018) 132(27): 270-278
    DOI: 10.1016/j.bej.2018.01.022

  37. Pseudomonas fluorescens Strain R124 Encodes Three Different MIO Enzymes

    Csuka P., Juhász V., Kohári S., Filip A., Varga A., Sátorhelyi P., Bencze L.C., Barton H., Paizs C., Poppe L.
    ChemBioChem (2018) 19(4): 411-418
    DOI: 10.1002/cbic.201700530

  38. Expanding the substrate scope of phenylalanine ammonia-lyase from: Petroselinum crispum towards styrylalanines

    Bencze L.C., Filip A., Bánóczi G., Toşa M.I., Irimie F.D., Gellért Á., Poppe L., Paizs C.
    Organic and Biomolecular Chemistry (2017) 15(17): 3717-3727
    DOI: 10.1039/c7ob00562h

  39. Tailored sol-gel immobilized lipase preparates for the enzymatic kinetic resolution of heteroaromatic alcohols in batch and continuous flow systems

    Moisă M.E., Spelmezan C.G., Paul C., Bartha-Vári J.H., Bencze L.C., Irimie F.D., Paizs C., Péter F., Toşa M.I.
    RSC Advances (2017) 7(83): 52977-52987
    DOI: 10.1039/c7ra10157k

  40. A Methylidene Group in the Phosphonic Acid Analogue of Phenylalanine Reverses the Enantiopreference of Binding to Phenylalanine Ammonia-Lyases

    Bata Z., Qian R., Roller A., Horak J., Bencze L.C., Paizs C., Hammerschmidt F., Vértessy B.G., Poppe L.
    Advanced Synthesis and Catalysis (2017) 359(12): 2109-2120
    DOI: 10.1002/adsc.201700428

  41. Covalently Immobilized Lipases are Efficient Stereoselective Catalysts for the Kinetic Resolution of rac-(5-Phenylfuran-2-yl)-β-alanine Ethyl Ester Hydrochlorides

    Nagy B., Galla Z., Bencze L.C., Toşa M.I., Paizs C., Forró E., Fülöp F.
    European Journal of Organic Chemistry (2017) 2017(20): 2878-2882
    DOI: 10.1002/ejoc.201700174

  42. Aminated single-walled carbon nanotubes as carrier for covalent immobilization of phenylalanine ammonia-lyase

    Bartha-Vári J.H., Bencze L.C., Bell E., Poppe L., Katona G., Irimie F.-D., Paizs C., Toşa M.I.
    Periodica Polytechnica Chemical Engineering (2017) 61(1): 59-66
    DOI: 10.3311/PPch.10417

  43. Validated LC-MS/MS method for the concomitant determination of amoxicillin and clavulanic acid from human plasma

    Balázsi J., Paizs C., Irimie F.-D., Toşa M.I., Bencze L.C., Tőtős R.
    Studia Universitatis Babes-Bolyai Chemia (2017) 62(2Tom1): 167-178
    DOI: 10.24193/subbchem.2017.2.12

  44. Nanobioconjugates of Candida antarctica lipase B and single-walled carbon nanotubes in biodiesel production

    Bencze L.C., Bartha-Vári J.H., Katona G., Toşa M.I., Paizs C., Irimie F.-D.
    Bioresource Technology (2016) 200(2): 853-860
    DOI: 10.1016/j.biortech.2015.10.072

  45. Influence of the aromatic moiety in α- And β-arylalanines on their biotransformation with phenylalanine 2,3-aminomutase from: Pantoea agglomerans

    Varga A., Bánóczi G., Nagy B., Bencze L.C., Toşa M.I., Gellért Á., Irimie F.D., Rétey J., Poppe L., Paizs C.
    RSC Advances (2016) 6(61): 56412-56420
    DOI: 10.1039/c6ra02964g

  46. Wickerhamomyces subpelliculosus as whole-cell biocatalyst for stereoselective bioreduction of ketones

    Bódai V., Nagy-Győr L., Örkényi R., Molnár Z., Kohári S., Erdélyi B., Nagymáté Z., Romsics C., Paizs C., Poppe L., Hornyánszky G.
    Journal of Molecular Catalysis B: Enzymatic (2016) 134: 206-214
    DOI: 10.1016/j.molcatb.2016.11.003

  47. Microfluidic multiple cell chip reactor filled with enzyme-coated magnetic nanoparticles - An efficient and flexible novel tool for enzyme catalyzed biotransformations

    Ender F., Weiser D., Nagy B., Bencze C.L., Paizs C., Pálovics P., Poppe L.
    Journal of Flow Chemistry (2016) 6(1): 43-52
    DOI: 10.1556/1846.2015.00036

  48. Heterocycles 36. Single-walled carbon nanotubes-bound n,n-diethyl ethanolamine as mild and efficient racemisation agent in the enzymatic DKR of 2-Arylthiazol-4-yl-alanines

    Leonte D., Bencze L.C., Paizs C., Toşa M.I., Zaharia V., Dan Irimie F.
    Molecules (2016) 21(1): 25
    DOI: 10.3390/molecules21010025

  49. Expression and purification of recombinant phenylalanine 2,3-aminomutase from Pantoea agglomerans

    Varga A., Filip A., Bencze L.-C., Sátorhelyi P., Bell E., Vértessy B.G., Poppe L., Paizs C.
    Studia Universitatis Babes-Bolyai Chemia (2016) 61(2): 7-19

  50. Expression and purification of recombinant phenylalanine ammonia-lyase from Petroselinum crispum

    Dima N.A., Filip A., Bencze L.C., Oláh M., Sátorhelyi P., Vértessy B.G., Poppe L., Paizs C.
    Studia Universitatis Babes-Bolyai Chemia (2016) 61(2): 21-34

  51. Albumin adsorption study onto hydroxyapatite-multiwall carbon nanotube based composites

    Czikó M., Bogya E.S., Paizs C., Katona G., Konya Z., Kukovecz Á., Barabás R.
    Materials Chemistry and Physics (2016) 180(83): 314-325
    DOI: 10.1016/j.matchemphys.2016.06.012

  52. Phenylalanine Ammonia-Lyase-Catalyzed Deamination of an Acyclic Amino Acid: Enzyme Mechanistic Studies Aided by a Novel Microreactor Filled with Magnetic Nanoparticles

    Weiser D., Bencze L.C., Bánóczi G., Ender F., Kiss R., Kõkai E., Szilágyi A., Vértessy B.G., Farkas Ö., Paizs C., Poppe L.
    ChemBioChem (2015) 16(16): 2283-2288
    DOI: 10.1002/cbic.201500444

  53. Immobilization of Phenylalanine Ammonia-Lyase on Single-Walled Carbon Nanotubes for Stereoselective Biotransformations in Batch and Continuous-Flow Modes

    Bartha-Vári J.H., Toşa M.I., Irimie F.-D., Weiser D., Boros Z., Vértessy B.G., Paizs C., Poppe L.
    ChemCatChem (2015) 7(7): 1122-1128
    DOI: 10.1002/cctc.201402894

  54. Synthesis of enantiopure l-(5-phenylfuran-2-yl)alanines by a sequential multienzyme process

    Bencze L.C., Komjáti B., Pop L.-A., Paizs C., Irimie F.-D., Nagy J., Poppe L., Toşa M.I.
    Tetrahedron Asymmetry (2015) 26(18-19): 59353
    DOI: 10.1016/j.tetasy.2015.08.004

  55. Heterocycles 38. Biocatalytic synthesis of new heterocyclic mannich bases and derivatives

    Leonte D., Bencze L.C., Paizs C., Irimie F.D., Zaharia V.
    Molecules (2015) 20(7): 12300-12313
    DOI: 10.3390/molecules200712300

  56. New chemo-enzymatic approaches for the synthesis of (R)- and (S)-bufuralol

    Nagy B., Dima N., Paizs C., Brem J., Irimie F.D., Toşa M.I.
    Tetrahedron Asymmetry (2014) 25(18-19): 1316-1322
    DOI: 10.1016/j.tetasy.2014.08.002

  57. Expression and properties of the highly alkalophilic phenylalanine ammonia-lyase of thermophilic Rubrobacter xylanophilus

    Kovaćs K., Bańóczi G., Varga A., Szabó I., Holczinger A., Hornyánszky G., Zagyva I., Paizs C., V́ertessy B.G., Poppe L.
    PLoS ONE (2014) 9(1): e85943
    DOI: 10.1371/journal.pone.0085943

  58. Bisepoxide cross-linked enzyme aggregates - New immobilized biocatalysts for selective biotransformations

    Weiser D., Varga A., Kovács K., Nagy F., Szilágyi A., Vértessy B.G., Paizs C., Poppe L.
    ChemCatChem (2014) 6(5): 1463-1469
    DOI: 10.1002/cctc.201300806

  59. Surface modification of silica gels for selective adsorption of bacterial lipases

    Boros Z., Abaháziová E., Weiser D., Kovács P., Paizs C., Poppe L.
    Studia Universitatis Babes-Bolyai Chemia (2014) 59(4): 33-38
    DOI: 10.1002/ep.11897

  60. The Interaction of Nitrophenylalanines with Wild Type and Mutant 4-Methylideneimidazole-5-one-less Phenylalanine Ammonia Lyase

    Toşa M.I., Brem J., Mantu A., Irimie F.D., Paizs C., Rétey J.
    ChemCatChem (2013) 5(3): 779-783
    DOI: 10.1002/cctc.201200536

  61. Lipase-catalyzed asymmetric acylation in the chemoenzymatic synthesis of furan-based alcohols

    Hara P., Turcu M.-C., Sundell R., Toşa M., Paizs C., Irimie F.-D., Kanerva L.T.
    Tetrahedron Asymmetry (2013) 24(2-3): 142-150
    DOI: 10.1016/j.tetasy.2012.11.016

  62. Sequential enzymatic procedure for the preparation of enantiomerically pure 2-heteroaryl-2-hydroxyacetic acids

    Naghi M.A., Bencze L.C., Brem J., Paizs C., Irimie F.D., Toşa M.I.
    Tetrahedron Asymmetry (2012) 23(2): 181-187
    DOI: 10.1016/j.tetasy.2012.01.019

  63. Immobilization to improve the properties of Pseudomonas fluorescens lipase for the kinetic resolution of 3-aryl-3-hydroxy esters

    Brem J., Turcu M.C., Paizs C., Lundell K., Toşa M.-I., Irimie F.-D., Kanerva L.T.
    Process Biochemistry (2012) 47(1): 119-126
    DOI: 10.1016/j.procbio.2011.10.020

  64. Chemoenzymatic preparation of 1-heteroarylethanamines of low solubility

    Brem J., Bencze L.-C., Liljeblad A., Turcu M.C., Paizs C., Irimie F.-D., Kanerva L.T.
    European Journal of Organic Chemistry (2012) 11(17): 3288-3294
    DOI: 10.1002/ejoc.201200330

  65. Biodiesel production using enzymatic transesterification - Current state and perspectives

    Gog A., Roman M., Toşa M., Paizs C., Irimie F.D.
    Renewable Energy (2012) 39(1): 10-16
    DOI: 10.1016/j.renene.2011.08.007

  66. Preparation of unnatural amino acids with ammonia-lyases and 2,3-aminomutases

    Poppe L., Paizs C., Kovács K., Irimie F.-D., Vértessy B.
    Methods in Molecular Biology (2012) 794(3): 3-19
    DOI: 10.1007/978-1-61779-331-8_1

  67. Chemoenzymatic one-pot synthesis of both (R)- and (S)-aryl-1,2-ethanediols

    Bencze L.C., Paizs C., Toşa M.I., Irimie F.D., Rétey J.
    ChemCatChem (2011) 3(2): 343-346
    DOI: 10.1002/cctc.201000295

  68. Lipase mediated sequential resolution of aromatic β-hydroxy esters using fatty acid derivatives

    Brem J., Naghi M., Toşa M.-I., Boros Z., Poppe L., Irimie F.-D., Paizs C.
    Tetrahedron Asymmetry (2011) 22(16-17): 1672-1679
    DOI: 10.1016/j.tetasy.2011.09.005

  69. Lipase-catalyzed kinetic resolutions of racemic 1-(10-ethyl-10H- phenothiazin-1,2, and 4-yl)ethanols and their acetates

    Brem J., Pilbák S., Paizs C., Bánóczi G., Irimie F.-D., Toşa M.-I., Poppe L.
    Tetrahedron Asymmetry (2011) 22(8): 916-923
    DOI: 10.1016/j.tetasy.2011.05.009

  70. Sequential use of regio- and stereoselective lipases for the efficient kinetic resolution of racemic 1-(5-phenylfuran-2-yl)ethane-1,2-diols

    Bencze L.C., Paizs C., Toşa M.I., Irimie F.D.
    Tetrahedron Asymmetry (2011) 22(6): 675-683
    DOI: 10.1016/j.tetasy.2011.03.006

  71. Lipases A and B from Candida antarctica in the enantioselective acylation of ethyl 3-heteroaryl-3-hydroxypropanoates: Aspects on the preparation and enantiopreference

    Brem J., Liljeblad A., Paizs C., Toşa M.I., Irimie F.-D., Kanerva L.T.
    Tetrahedron Asymmetry (2011) 22(3): 315-322
    DOI: 10.1016/j.tetasy.2011.01.027

  72. Lipase-catalyzed synthesis of both enantiomers of 3-chloro-1-arylpropan-1- ols

    Pop L.A., Czompa A., Paizs C., Toa M.I., Vass E., Mátyus P., Irimie F.-D.
    Synthesis (2011) 22(18): T49711SS
    DOI: 10.1055/s-0030-1260149

  73. CaL-B a highly selective biocatalyst for the kinetic resolution of furylbenzthiazole-2-yl-ethanols and acetates

    Bencze L.C., Paizs C., Toşa M.I., Trif M., Irimie F.D.
    Tetrahedron Asymmetry (2010) 21(16): 1999-2004
    DOI: 10.1016/j.tetasy.2010.06.010

  74. Lipase-catalyzed kinetic resolution of racemic 1-(10-alkyl-10H- phenothiazin-3-yl)ethanols and their butanoates

    Brem J., Toşa M.-I., Paizs C., Munceanu A., Matković-Čalogović D., Irimie F.-D.
    Tetrahedron Asymmetry (2010) 21(16): 1993-1998
    DOI: 10.1016/j.tetasy.2010.06.007

  75. Synthesis of enantiomerically enriched (R)- and (S)-benzofuranyl- and benzo[b]thiophenyl-1,2-ethanediols via enantiopure cyanohydrins as intermediates

    Bencze L.C., Paizs C., Toşa M.I., Vass E., Irimie F.D.
    Tetrahedron Asymmetry (2010) 21(4): 443-450
    DOI: 10.1016/j.tetasy.2010.01.018

  76. Substituent effects on the stereochemical outcome of the baker's yeast-mediated biotransformation of α-hydroxy- and α-acetoxymethyl-5-phenylfuran-2-yl-ethanones

    Bencze L.C., Paizs C., Toşa M.I., Irimie F.D.
    Tetrahedron Asymmetry (2010) 21(3): 356-364
    DOI: 10.1016/j.tetasy.2010.02.004

  77. Enzyme-catalyzed synthesis of (R)- and (S)-3-hydroxy-3-(10-alkyl-10H-phenothiazin-3-yl)propanoic acids

    Brem J., Toşa M.I., Paizs C., Vass E., Irimie F.D.
    Tetrahedron Asymmetry (2010) 21(3): 365-373
    DOI: 10.1016/j.tetasy.2010.02.006

  78. 2-amino-3-(5-phenylfuran-2-yl)propionic acids and 5-phenylfuran-2-ylacrylic acids are novel substrates of phenylalanine ammonia-lyase

    Paizs C., Toşa M.I., Bencze L.C., Brem J., Irimie F.D., Rétey J.
    Heterocycles (2010) 82(2): 1217-1228
    DOI: 10.3987/COM-10-S(E)60

  79. New ways for old structures

    Irimie F.D., Paizs C., Toşa M., Podea P.
    Studia Universitatis Babes-Bolyai Chemia (2009) 4(1): 7-16

  80. The effect of electromagnetic fields on baker's yeast population dynamics, biocatalytic activity and selectivity

    Sandu D., Lingvay I., Lányi S., Micu D.D., Popescu C.L., Brem J., Bencze L.C., Paizs C.
    Studia Universitatis Babes-Bolyai Chemia (2009) 4(2): 195-201

  81. Enzyme-catalyzed synthesis of (R)- and (S)-3-heteroaryl-3-hydroxy-propanoic acids and their derivatives

    Brem J., Paizs C., Toşa M.I., Vass E., Irimie F.D.
    Tetrahedron Asymmetry (2009) 20(4): 489-496
    DOI: 10.1016/j.tetasy.2009.02.001

  82. The putative coenzyme B12-dependent methylmalonyl-CoA mutase from potatoes is a phosphatase

    Paizs C., Diemer T., Rétey J.
    Bioorganic Chemistry (2008) 36(6): 261-264
    DOI: 10.1016/j.bioorg.2008.06.002

  83. Chemoenzymatic synthesis of (R)- and (S)-1-heteroarylethanols

    Toşa M.I., Podea P.V., Paizs C., Irimie F.D.
    Tetrahedron Asymmetry (2008) 19(17): 2068-2071
    DOI: 10.1016/j.tetasy.2008.08.023

  84. Baker's yeast-mediated synthesis of (R)- and (S)-heteroaryl-ethane-1,2-diols

    Podea P.V., Paizs C., Toşa M.I., Irimie F.D.
    Tetrahedron Asymmetry (2008) 19(16): 1959-1964
    DOI: 10.1016/j.tetasy.2008.07.030

  85. Lipase-catalyzed kinetic resolution of racemic 1-heteroarylethanols-experimental and QM/MM study

    Toşa M., Pilbák S., Moldovan P., Paizs C., Szatzker G., Szakács G., Novák L., Irimie F.-D., Poppe L.
    Tetrahedron Asymmetry (2008) 19(15): 1844-1852
    DOI: 10.1016/j.tetasy.2008.07.004

  86. Chemoenzymatic preparation of enantiopure l-benzofuranyl- and l-benzo[b]thiophenyl alanines

    Podea P.V., Toşa M.I., Paizs C., Irimie F.D.
    Tetrahedron Asymmetry (2008) 19(4): 500-511
    DOI: 10.1016/j.tetasy.2008.01.031

  87. Investigation of the mechanism of action of pyrogallol-phloroglucinol transhydroxylase by using putative intermediates

    Paizs C., Bartlewski-Hof U., Rétey J.
    Chemistry - A European Journal (2007) 13(10): 2805-2811
    DOI: 10.1002/chem.200601053

  88. Inhibition of histidine ammonia lyase by heteroaryl-alanines and acrylates

    Katona A., Toşa M.I., Paizs C., Rétey J.
    Chemistry and Biodiversity (2006) 3(5): 502-508
    DOI: 10.1002/cbdv.200690053

  89. The interaction of heteroaryl-acrylates and alanines with phenylalanine ammonia-lyase from parsley

    Paizs C., Katona A., Rétey J.
    Chemistry - A European Journal (2006) 12(10): 2739-2744
    DOI: 10.1002/chem.200501034

  90. Chemoenzymatic one-pot synthesis of enantiopure L-arylalanines from arylaldehydes

    Paizs C., Katona A., Rétey J.
    European Journal of Organic Chemistry (2006) 12(5): 1113-1116
    DOI: 10.1002/ejoc.200500902

  91. NIR surface enhanced Raman spectroscopy and bands assignment by DFT calculations of non-natural β-amino acids

    Iliescu T., Maniu D., Chis V., Irimie F.D., Paizs Cs., Toşa M.
    Chemical Physics (2005) 310(1-3): 189-199
    DOI: 10.1016/j.chemphys.2004.10.034

  92. Biocatalytic enantioselective preparation of phenothiazine-based cyanohydrin acetates: Kinetic and dynamic kinetic resolution

    Paizs C., Tähtinen P., Toşa M., Majdik C., Irimie F.-D., Kanerva L.T.
    Tetrahedron (2004) 60(46 SPEC. ISS.): 10533-10540
    DOI: 10.1016/j.tet.2004.06.136

  93. Kinetic resolution of 1-(benzofuran-2-yl)ethanols by lipase-catalyzed enantiomer selective reactions

    Paizs C., Toşa M., Bódai V., Szakács G., Kmecz I., Simándi B., Majdik C., Novák L., Irimie F.-D., Poppe L.
    Tetrahedron Asymmetry (2003) 14(13): 1943-1949
    DOI: 10.1016/S0957-4166(03)00358-6

  94. Preparation of novel phenylfuran-based cyanohydrin esters: Lipase-catalysed kinetic and dynamic resolution

    Paizs C., Tähtinen P., Lundell K., Poppe L., Irimie F.-D., Kanerva L.T.
    Tetrahedron Asymmetry (2003) 14(13): 1895-1904
    DOI: 10.1016/S0957-4166(03)00286-6

  95. Optically active 1-(benzofuran-2-yl)ethanols and ethane-1,2-diols by enantiotopic selective bioreductions

    Paizs C., Toşa M., Majdik C., Moldovan P., Novák L., Kolonits P., Marcovici A., Irimie F.-D., Poppe L.
    Tetrahedron Asymmetry (2003) 14(11): 1495-1501
    DOI: 10.1016/S0957-4166(03)00222-2

  96. Raman, infrared, and surface-enhanced Raman spectroscopy in combination with ab initio and density functional theory calculations on 10-isopropyl-10H-phenothiazine-5-oxide

    Bolboaca M., Iliescu T., Paizs Cs., Irimie F.D., Kiefer W.
    Journal of Physical Chemistry A (2003) 107(11): 1811-1818
    DOI: 10.1021/jp021731j

  97. Candida antarctica lipase A in the dynamic resolution of novel furylbenzotiazol-based cyanohydrin acetates

    Paizs C., Toşa M., Majdik C., Tähtinen P., Irimie F.D., Kanerva L.T.
    Tetrahedron Asymmetry (2003) 14(5): 619-627
    DOI: 10.1016/S0957-4166(03)00025-9

  98. Baker's yeast mediated preparation of (10-alkyl-10H-phenothiazin-3-yl)methanols

    Toşa M., Paizs C., Majdik C., Moldovan P., Novák L., Kolonits P., Szabó É., Poppe L., Irimie F.-D.
    Journal of Molecular Catalysis - B Enzymatic (2002) 17(6): 241-248
    DOI: 10.1016/S1381-1177(02)00015-2

  99. Separation of N-alkyl phenothiazine sulfones by HPTLC using an optimum mobile phase

    Cimpoiu C., Hodisan S., Toa M., Paizs C., Majdik C., Irimie F.-D.
    Journal of Pharmaceutical and Biomedical Analysis (2002) 28(2): 385-389
    DOI: 10.1016/S0731-7085(01)00626-4

  100. Synthesis of optically active 3-substituted-10-alkyl-10H-phenothiazine-5-oxides by enantioselective biotransformations

    Toşa M., Paizs C., Majdik C., Novák L., Kolonits P., Irimie F.-D., Poppe L.
    Tetrahedron Asymmetry (2002) 13(2): 211-221
    DOI: 10.1016/S0957-4166(02)00077-0

  101. Bioorganic synthesis of some (5-benzothiazol-2-yl-furan-2-yl)-methanols in cell catalysis using Saccharomyces cerevisiae

    Irimie F.-D., Paizs C., Majdik C., Toşa M., Mişca R., Silaghi-Dumitrescu R.
    Heterocyclic Communications (2002) 8(5): 489-492
    DOI: 10.1515/HC.2002.8.5.489

  102. Chemo-enzymatic preparation of hydroxymethyl ketones

    Paizs C., Toşa M., Majdik C., Bódai V., Novák L., Irimie F.-D., Poppe L.
    Journal of the Chemical Society. Perkin Transactions 1 (2002) 21: 2400-2402
    DOI: 10.1039/b206851f

  103. Selective oxidaton methods for preparation of N-alkylphenothiazine sulfoxides and sulfones

    Toşa M., Paizs C., Majdik C., Poppe L., Kolonits P., Silberg I.A., Novák L., Irimie F.-D.
    Heterocyclic Communications (2001) 7(3): 277-282
    DOI: 10.1515/HC.2001.7.3.277

  104. Bioreduction with bakers' yeast of π - Deficient heterocyclic aldehydes

    Irimie F.D., Afloroaei C., Toşa M., Paizs C.
    Heterocyclic Communications (1999) 5(3): 253-256
    DOI: 10.1515/HC.1999.5.3.253

  105. ESR study of the dynamics of adsorbed nitroxide radicals on porous surfaces in the dehydration process

    Damian G., Cozar O., Miclăus V., Paizs Cs., Znamirovschi V., Chis V., David L.
    Colloids and Surfaces A: Physicochemical and Engineering Aspects (1998) 137(1-3): 1-6
    DOI: 10.1016/S0927-7757(97)00092-7

  106. Bakers' yeast-mediated reductions of some nitro-dibenzofurans

    Irimie F.-D., Paizs C., Toşa M.-I., Afloroaei C., Miclăuş V.
    Heterocyclic Communications (1997) 3(6): 549-553
    DOI: 10.1515/HC.1997.3.6.549

  107. Oxidarea metanolului la formaldehidă pe catalizatori oxidici de Mo-Fe I. Modelul matematic de bilanţ de masă

    Toşa C., Miclăuş V., Toşa M., Pop A., Paizs C.
    Revista de Chimie (1997) 48(4): 284-290

  108. Oxidarea metanolului la formaldehidă pe catalizatori oxidici de Mo-Fe II. Modelarea matematică şi analiza procesului

    Pop A., Paizs C., Toşa C., Toşa M., Miclăuš V.
    Revista de Chimie (1997) 48(7): 616-620