Scientific papers

 
  1. Sustainable Synthesis of Bio-Based Furanic and Aromatic Amines Using an Optimized Whole-Cell Transaminase–Decarboxylase Cascade in E. coli RARE

    Barabás Laura Edit, Tőtős Róbert, Csete Tímea Éva, Tomoiagă Raluca Bianca, Toşa Monica Ioana, Paizs Csaba
    ChemBioChem (2026) 27(13):
    DOI: 10.1002/cbic.70456

  2. Optimization of reaction parameters for the synthesis of natural aroma esters by factorial design

    Dudu Adrian Ioan, Paizs Csaba, Toşa Monica Ioana
    Reaction Chemistry and Engineering (2024) 9(11): 2994–3002
    DOI: 10.1039/d4re00265b

  3. The Biocatalytic Potential of Aromatic Ammonia–Lyase from Loktanella atrilutea

    Tomoiaga R.B., Ágoston G., Boros K., Nagy L.C., Toşa M.I., Paizs C., Bencze L.C.
    ChemBioChem (2024) 25(9): e202400011
    DOI: 10.1002/cbic.202400011

  4. Immobilization of D-amino acid dehydrogenase from Ureibacillus thermosphaericus

    Boros K., Gal L., Gal C.A., Wäscher M., Tomoiagă R.B., Toşa M.I., Pietruszka J., Bencze L.C.
    Process Biochemistry (2024) 140: 45-55
    DOI: 10.1016/j.procbio.2024.02.014

  5. 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

  6. 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

  7. 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(11): 112660
    DOI: 10.1016/j.mcat.2022.112660

  8. 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

  9. Preparation and Characterization of Doxycycline-Loaded Electrospun PLA/HAP Nanofibers as a Drug Delivery System

    Farkas N.-I., Marincaș L., Barabás R., Bizo L., Ilea A., Turdean G.L., Toşa M., Cadar O., Barbu-Tudoran L.
    Materials (2022) 15(6): 2105
    DOI: 10.3390/ma15062105

  10. 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

  11. 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

  12. 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

  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(8): 185-194
    DOI: 10.1016/j.cattod.2020.04.002

  14. Hydroxyapatite and silicon-modified hydroxyapatite as drug carriers for 4-aminopyridine

    Marincaș L., Turdean G.L., Toşa M., Kovács Z., Kovács B., Barabás R., Farkas N.-I., Bizo L.
    Crystals (2021) 11(9): 1124
    DOI: 10.3390/cryst11091124

  15. Simultaneous enrichment of grape pomace with γ-linolenic acid and carotenoids by solid-state fermentation with Zygomycetes fungi and antioxidant potential of the bioprocessed substrates

    Dulf F.V., Vodnar D.C., Toşa M.I., Dulf E.-H.
    Food Chemistry (2020) 310(12): 125927
    DOI: 10.1016/j.foodchem.2019.125927

  16. 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

  17. 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

  18. 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

  19. 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

  20. 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

  21. 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

  22. 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

  23. 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

  24. 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

  25. 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

  26. Modern diversification of the amino acid repertoire driven by oxygen

    Granold M., Hajieva P., Toşa M.I., Irimie F.-D., Moosmann B.
    Proceedings of the National Academy of Sciences of the United States of America (2018) 115(1): 41-46
    DOI: 10.1073/pnas.1717100115

  27. 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

  28. 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

  29. 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

  30. 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

  31. 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

  32. 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

  33. 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

  34. 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

  35. 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

  36. 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

  37. Total Phenolic Contents, Antioxidant Activities, and Lipid Fractions from Berry Pomaces Obtained by Solid-State Fermentation of Two Sambucus Species with Aspergillus niger

    Dulf F.V., Vodnar D.C., Dulf E.-H., Toşa M.I.
    Journal of Agricultural and Food Chemistry (2015) 63(13): 3489-3500
    DOI: 10.1021/acs.jafc.5b00520

  38. Stable hydrate of a β-lactamcarbaldehyde

    Toşa M.I., Komjáti B., Madarász J., Kolonits P., Poppe L., Nagy J.
    Studia Universitatis Babes-Bolyai Chemia (2015) 60(1): 229-238

  39. 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

  40. Candida antarctica lipases acting as versatile catalysts for the synthesis of enantiopure (R)- and (S)-1-(2-phenylthiazol-4-yl)ethanamines This paper is dedicated to the anniversary of 95th birthday of Professor Valer Fărcăşanu.

    Radu A., Moisă M.E., Toşa M.I., Dima N., Zaharia V., Irimie F.D.
    Journal of Molecular Catalysis B: Enzymatic (2014) 107(11): 114-119
    DOI: 10.1016/j.molcatb.2014.05.007

  41. Molecular cloning and characterization of a thermostable esterase/lipase produced by a novel Anoxybacillus flavithermus strain

    Chiş L., Hriscu M., Bica A., Toşa M., Nagy G., Róna G., Vértessy B.G., Irimie F.D.
    Journal of General and Applied Microbiology (2013) 59(2): 119-134
    DOI: 10.2323/jgam.59.119

  42. pH-Profiling of thermoactive lipases and esterases: Caveats and further notes

    Hriscu M., Chiş L., Toşa M., Irimie F.D.
    European Journal of Lipid Science and Technology (2013) 115(5): 571-575
    DOI: 10.1002/ejlt.201200305

  43. 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

  44. 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

  45. Heterocycles 32. Efficient kinetic resolution of 1-(2-arylthiazol-4-yl) ethanols and their acetates using lipase B from Candida antarctica

    Hapău D., Brem J., Moisă M., Toşa M.-I., Irimie F.D., Zaharia V.
    Journal of Molecular Catalysis B: Enzymatic (2013) 94: 88-94
    DOI: 10.1016/j.molcatb.2013.05.005

  46. 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

  47. 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

  48. Recombinant Anoxybacillus flavithermus T1 esterase/lipase: Optimization of expression and recovery

    Chiş L.-M., Hriscu M., Chirilă F., Lupan I., Toşa M., Irimie F.D.
    Environmental Engineering and Management Journal (2012) 11(11): 1915-1922

  49. Chemoenzymatic synthesis of highly enantiomerically enriched secondary alcohols with a thiazolic core

    Pop L., Lassalas P., Bencze L.C., Toşa M.I., Nagy B., Irimie F.D., Hoarau C.
    Tetrahedron Asymmetry (2012) 23(6-7): 474-481
    DOI: 10.1016/j.tetasy.2012.03.014

  50. 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

  51. 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

  52. 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

  53. 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

  54. 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

  55. 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

  56. 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

  57. 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

  58. 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

  59. 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

  60. 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

  61. 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

  62. New ways for old structures

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

  63. Quantification of ibuprofen and pseudoephedrine in human plasma by LC/MS/MS for pharmacokinetic studies

    Marcovici A.M., Toşa M.-I., Vlase O., Leucuţa S.E., dan Irimie F.
    Studia Universitatis Babes-Bolyai Chemia (2009) 4(SPEC.ISSUE 2): 171-179

  64. 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

  65. Formyl-and acetylindols: Vibrational spectroscopy of an expectably pharmacologically active compound family

    Billes F., Podea P.V., Mohammed-Ziegler I., Toşa M., Mikosch H., Irimie D.-F.
    Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy (2009) 74(5): 1031-1045
    DOI: 10.1016/j.saa.2009.08.044

  66. 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

  67. 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

  68. 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

  69. 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

  70. 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

  71. Experimental and quantum chemical study on the vibrational spectroscopy of N-methylphenothiazines: Part 1

    Endrédi H., Billes F., Toşa M., Majdik C., Irimie F.D.
    Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy (2006) 63(2): 349-360
    DOI: 10.1016/j.saa.2005.05.021

  72. 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

  73. 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

  74. 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

  75. 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

  76. 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

  77. 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

  78. 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

  79. 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

  80. 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

  81. 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

  82. 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

  83. 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

  84. 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

  85. 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