Scientific papers

 
  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  6. Optimization of 2-alkoxyacetates as acylating agent for enzymatic kinetic resolution of chiral amines

    Oláh M., Kovács D., Katona G., Hornyánszky G., Poppe L.
    Tetrahedron (2018) 74(27): 3663-3670
    DOI: 10.1016/j.tet.2018.05.032

  7. 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: 270-278
    DOI: 10.1016/j.bej.2018.01.022

  8. 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

  9. A Peptidomimetic Antibiotic Interacts with the Periplasmic Domain of LptD from Pseudomonas aeruginosa

    Andolina G., Bencze L.-C., Zerbe K., Müller M., Steinmann J., Kocherla H., Mondal M., Sobek J., Moehle K., Malojčić G., Wollscheid B., Robinson J.A.
    ACS Chemical Biology (2018) 13(3): 666-675
    DOI: 10.1021/acschembio.7b00822

  10. 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

  11. Heterocycles 48. synthesis, characterization and biological evaluation of imidazo[2,1-b][1,3,4]thiadiazole derivatives as anti-inflammatory agents

    Cristina A., Leonte D., Vlase L., Bencze L.C., Imre S., Marc G., Apan B., Mogosan C., Zaharia V.
    Molecules (2018) 23(10): 2425
    DOI: 10.3390/molecules23102425

  12. Heterocycles 44. Synthesis, characterization and anticancer activity of new thiazole ortho-hydroxychalcones

    Coman F.-M., Mbaveng A.T., Leonte D., Bencze L.C., Vlase L., Imre S., Kuete V., Efferth T., Zaharia V.
    Medicinal Chemistry Research (2018) 27(5): 1396-1407
    DOI: 10.1007/s00044-018-2156-2

  13. Heterocycles 42. Synthesis and characterization of new thiazolo[3,2-b] [1,2,4]triazole derivatives with anti-inflammatory potential

    Cristina A., Leonte D., Vlase L., Bencze L.C., Imre S., Zaharia V.
    Farmacia (2018) 66(1): 88-96

  14. Heterocycles 43. Synthesis, characterization and antioxidant activity of some thiazole hydroxychalcones and their flavonoidic derivatives

    Constantinescu T., Leonte D., Bencze L.C., Vlase L., Imre S., Hanganu D., Zaharia V.
    Farmacia (2018) 66(4): 663-673
    DOI: 10.31925/farmacia.2018.4.16

  15. Heterocycles 46. Synthesis, characterization and biological evaluation of thiazolo[3,2-b][1,2,4]triazoles bearing benzenesulfonamide moiety

    Cristina A., Leonte D., Vlase L., Bencze L.C., Imre S., Apan B., Mogoșan C., Zaharia V.
    Farmacia (2018) 66(5): 883-893
    DOI: 10.31925/farmacia.2018.5.20