Institute of Organic Chemistry

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The activity of the institute involves synthesis of organic molecules, structure elucidation and theoretical investigation. The synthetic activity aims mostly at preparation of heterocyclic compounds, carbohydrates, and polymers as well as elaboration of novel methodologies (e.g., organocatalysis, supramolecular synthesis). Investigations by NMR spectroscopy, mass spectrometry and single crystal diffractometry provide diverse possibilities for the determination of chemical structure. Furthermore, theoretical investigations are carried out in order to rationalize structures and reaction mechanisms.

Publications in 2015

Papers resulting from a collaboration among several research groups are listed for each of them.

Medicinal Chemistry Research Group

  1. Bajusz D, Rácz A, Héberger K (2015) Why is Tanimoto index an appropriate choice for fingerprint-based similarity calculations? J. Cheminformatics 7:(1) Paper 20.
    http://dx.doi.org/10.1186/s13321-015-0069-3
  2. Kelemen ÁA, Ferenczy GG, Keserű GM (2015) A desirability function-based scoring scheme for selecting fragment-like class A aminergic GPCR ligands, J. Comp.-Aided Mol. Design 29:59-66; erratum: 29:67
    http://dx.doi.org/10.1007/s10822-014-9804-5
  3. Takacs D, Csonka A, Horvath A, Windt T, Gajdacs M, Riedl Z, Hajos G, Amaral L, Molnar J, Spengler G (2015) Reversal of ABCB1-related Multidrug Resistance of Colonic Adenocarcinoma Cells by Phenothiazines. Anticancer Res. 35:3245-3251
    http://www.ncbi.nlm.nih.gov/pubmed/26026084
  4. Tarcsay A, Keseru GM (2015) Is there a link between selectivity and binding thermodynamics profiles? Drug Discovery Today 20:86-94
    http://dx.doi.org/10.1016/j.drudis.2014.09.014

Organocatalysis Research Group

  1. Jakab A, Dalicsek Z, Holczbauer T, Hamza A, Pápai I, Finta Z, Timári G, Soós T (2015) Superstable Pd(0) Complex as an Air- and Thermostable Catalyst for Suzuki Coupling Reactions, Eur. J. Org. Chem. 2015:60-66
    http://dx.doi.org/10.1002/ejoc.201403214
  2. Jakab A, Dalicsek Z, Soós T (2015) A Robust and Efficient Catalyst Possessing Electron-deficient Ligand for the Palladium-Catalyzed Direct Arylation of Heteroarenes, Eur. J. Org. Chem. 2015:56-59
    http://dx.doi.org/10.1002/ejoc.201402586
  3. Gyömöre Á, Bakos M, Földes T, Pápai I, Domján A, Soós T (2015) Moisture-Tolerant Frustrated Lewis Pair Catalyst for Hydrogenation of Aldehydes and Ketones, ACS Catalysis 5:5366-5372
    http://dx.doi.org/10.1021/acscatal.5b01299
  4. Dobi Z, Holczbauer T, Soós T (2015) Strain-Driven Direct Cross-Aldol and -Ketol Reactions of Four-Membered Heterocyclic Ketones, Org. Lett. 17:2634-2637
    http://dx.doi.org/10.1021/acs.orglett.5b01002
  5. Palkó R, Egyed O, Rokob TA, Bombicz P, Riedl Zs, Hajós Gy (2015) Transformation of Zwitterionic Pyridine Derivatives to a Spiro-Fused Ring System: Azoniabenzo[de]fluorine. Synthesis and Mechanistic Rationalization, J. Org. Chem. 80:174-179
    http://dx.doi.org/10.1021/jo5022663
  6. Varga Sz, Jakab G, Csámpai A, Soós T (2015) Iterative Coupling of Two Different Enones by Nitromethane Using Bifunctional Thiourea Organocatalysts. Stereocontrolled Assembly of Cyclic and Acyclic Structures, J. Org. Chem. 80:8990-8996
    http://dx.doi.org/10.1021/acs.joc.5b01474

Chemical Biology Research Group

  1. Domonkos C, Zsila F, Fitos I, Visy J, Kassai R, Bálint B, Kotschy A (2015) Synthesis and serum protein binding of novel ring-substituted harmine derivatives, RSC Adv. 5:53809-53818.
    http://dx.doi.org/10.1039/C5RA06426K
  2. Cserép GB, Demeter O, Bätzner E, Kállay M, Wagenknecht H-A, Kele P (2015) Synthesis and Evaluation of Nicotinic Acid Derived Tetrazines for Bioorthogonal Labeling, Synthesis 47:2738-2744.
    http://dx.doi.org/10.1055/s-0034-1380721
  3. Castillo G, Pribransky K, Mező G, Kocsis L, Csámpai A, Németh K, Keresztes Zs, Hianik T (2015) Electrochemical and Photometric Detection of Plasmin by Specific Peptide Substrate, Electroanalysis 27:789-798.
    http://onlinelibrary.wiley.com/doi/10.1002/elan.201400622/abstract
  4. Huber MC, Schreiber A, von Olshausen P, Varga BR, Kretz O, Joch B, Barnert S, Schubert R, Eimer S, Kele P, Schiller SM (2015) Designer amphiphilic proteins as building blocks for the intracellular formation of organelle-like compartments, Nature Mater. 14:125-132.
    http://dx.doi.org/10.1038/nmat4118
  5. Cserép G, Herner A, Kele P (2015) Bioorthogonal fluorescent labels: a review on combined forces, Methods Appl. Fluoresc. 3:042001.
    http://dx.doi.org/10.1088/2050-6120/3/4/042001

Theoretical Chemistry Research Group

  1. Jakab A, Dalicsek Z, Holczbauer T, Hamza A, Pápai I, Finta Z, Timári G, Soós T (2015) Superstable Pd(0) Complex as an Air- and Thermostable Catalyst for Suzuki Coupling Reactions, Eur. J. Org. Chem. 2015:60-66
    http://dx.doi.org/10.1002/ejoc.201403214
  2. Kortelainen M, Suhonen A, Hamza A, Papai I, Nauha E, Yliniemela-Sipari S, Nissinen M, Pihko PM (2015) Folding Patterns in a Family of Oligoamide Foldamers, Chem. Eur. J. 21:9493-9504
    http://dx.doi.org/10.1002/chem.201406521
  3. Aresta M, Dibenedetto A, Angelini A, Papai I (2015) Reaction Mechanisms in the Direct Carboxylation of Alcohols for the Synthesis of Acyclic Carbonates, Topics in Catalysis 58:2-14
    http://dx.doi.org/10.1007/s11244-014-0342-0
  4. Stirling A, Rozgonyi T, Krack M, Bernasconi M (2015) Pyrite in contact with supercritical water: the desolation of steam, Phys. Chem. Chem. Phys. 17:17375-17379
    http://dx.doi.org/10.1039/c5cp01146a
  5. Chernichenko K, Kotai B, Papai I, Zhivonitko V, Nieger M, Leskela M, Repo T (2015) Intramolecular Frustrated Lewis Pair with the Smallest Boryl Site: Reversible H-2 Addition and Kinetic Analysis, Angew. Chem. Int. Ed. 54:1749-1753
    http://dx.doi.org/10.1002/anie.201410141
  6. Lindqvist M, Borre K, Axenov K, Kotai B, Nieger M, Leskela M, Papai I, Repo T (2015) Chiral Molecular Tweezers: Synthesis and Reactivity in Asymmetric Hydrogenation, J. Am. Chem. Soc. 137:4038-4041
    http://dx.doi.org/10.1021/ja512658m
  7. Mayer I (2015) Hermitian “chemical” Hamiltonian: an alternative ab initio method, Theor. Chem. Acc. 134:86
    http://dx.doi.org/10.1007/s00214-015-1682-y
  8. Palkó R, Egyed O, Rokob TA, Bombicz P, Riedl Zs, Hajós Gy (2015) Transformation of Zwitterionic Pyridine Derivatives to a Spiro-Fused Ring System: Azoniabenzo[de]fluorine. Synthesis and Mechanistic Rationalization, J. Org. Chem. 80:174-179
    http://dx.doi.org/10.1021/jo5022663
  9. Rozgonyi T, Stirling A (2015) DFT Study of Oxidation States on Pyrite Surface Sites, J. Phys. Chem. C 119:7704-7710
    http://dx.doi.org/10.1021/acs.jpcc.5b01943
  10. Tolnai GL, Székely A, Makó Z, Gáti T, Daru J, Bihari T, Stirling A, Novák Z (2015) Efficient direct 2,2,2-trifluoroethylation of indoles via C-H functionalization, Chem. Commun. 51:4488-4491
    http://dx.doi.org/10.1039/c5cc00519a
  11. Gyömöre Á, Bakos M, Földes T, Pápai I, Domján A, Soós T (2015) Moisture-Tolerant Frustrated Lewis Pair Catalyst for Hydrogenation of Aldehydes and Ketones, ACS Catalysis 5:5366-5372
    http://dx.doi.org/10.1021/acscatal.5b01299

Supramolecular Chemistry Research Group

  1. Deák A, Jobbágy Cs, Marsi G, Molnár M, Szakács Z, Baranyai P (2015) Anion-, Solvent-, Temperature-, and Mechano-Responsive Photoluminescence in Gold(I) Diphosphine-Based Dimers, Chemistry – A European Journal 21:11495-11508
    http://onlinelibrary.wiley.com/doi/10.1002/chem.201501066/abstract
  2. Baranyai P, Marsi G, Jobbagy Cs, Domjan A, Olah L, Deak A (2015) Mechano-induced reversible colour and luminescence switching of a gold(I)-diphosphine complex, Dalton Transactions 44:13455-13459
    http://pubs.rsc.org/en/Content/ArticleLanding/2015/DT/C5DT01795E
  3. Baranyai P, Marsi G, Hamza A, Jobbágy Cs, Deák A (2015) Structural characterization of dinuclear gold(I) diphosphine complexes with anion-triggered luminescence, Structural Chemistry,
    10.1007/s11224-015-0674-9

MS Proteomics Research Group

  1. Marton L, Nagy GN, Ozohanics O, Labas A, Kramos B, Olah J, Vekey K, Vertessy BG (2015) Molecular Mechanism for the Thermo-Sensitive Phenotype of CHO-MT58 Cell Line Harbouring a Mutant CTP:Phosphocholine Cytidylyltransferase. Plos One, 10: PLOS ONE 10:e0129632
    http://dx.doi.org/10.1371/journal.pone.0129632
  2. Vékey K, Drahos L, Ludányi K (2015) Tömegspektrometria In: Sohár Pál (szerk.) A gyógyszerkutatás műszeres módszerei, Budapest, Magyar Kémikusok Egyesülete, pp. 145-170. (ISBN:978-963-9970-61-8)

MS Metabolomics Research Group

  1. Jemnitz K, Szabo M, Batai-Konczos A, Szabo P, Magda B, Veres Z (2015) A Modified Procedure for Estimating the Impact of the Uptake on the Overall Biliary Clearance in Sandwich Culture of Rat Hepatocytes, Drug. Metab. Lett. 9:17-27
  2. Magda B, Márta Z, Imre T, Kalapos-Kovács B, Klebovich I, Fekete J, Szabó PT (2015) Unexpected retention behavior of baicalin: Hydrophilic interaction like properties of a reversed-phase column, J. Pharm. Biomed. Anal. 111:119-125
    www.ncbi.nlm.nih.gov/pubmed/25880242
  3. Kalapos-Kovács B, Magda B, Jani M, Fekete Zs , Szabó PT, Antal I, Krajcsi P, Klebovich I (2015) Multiple ABC transporters efflux baicalin, Phytotherapy Res., in press
    www.ncbi.nlm.nih.gov/pubmed/26400418
  4. Szalontai G, Szabó P, Besenyei G (2015) A new heterotopic Ar-BIAN ligand with a pendant P donor site, Polyhedron 92:156-165
    http://dx.doi.org/10.1016/j.poly.2015.03.008
  5. Pape VFS, Türk D, Szabó P, Wiese M, Enyedy EA, Szakács G (2015) Synthesis and characterization of the anticancer and metal binding properties of novel pyrimidinylhydrazone derivatives, J. Inorg. Biochem. 144:18-30
    http://dx.doi.org/10.1016/j.jinorgbio.2014.12.015
  6. Monostory K, Nagy A, Bűdi T, Temesvári M, Szever Zs, Szabó PT (2015) Adverse events in a newborn under valproate therapy are attributed to the loss-of-function mutations in CYP2C9 Corresponding, EBCR-15-49R1, accepted
    http://www.sciencedirect.com/science/article/pii/S2213323215000407

NMR Research Group

  1. Csikós Á, Faludi G, Domján A, Renner K, Móczó J, Pukánszky B (2015) Modification of interfacial adhesion with a functionalized polymer in PLA/wood composites, Eur. Polymer J. 68:592-600
    http://dx.doi.org/10.1016/j.eurpolymj.2015.03.032
  2. Manek E, Domján A, Madarász J, László K (2015) Interactions in aromatic probe molecule loaded poly(N-isopropylacrylamide) hydrogels and implications for drug delivery, Eur. Polymer J. 68:657-664
    http://dx.doi.org/10.1016/j.eurpolymj.2015.03.043
  3. Manek E, Domján A, Menyhárd A, László K (2015) Host-guest interactions in poly(N-isopropylacrylamide) gel: a themoanalytical approach, J. Thermal Anal. Calorim. 120:1273-1281
    http://dx.doi.org/10.1007/s10973-015-4388-4

Chemical Crystallography Research Group

  1. Resnati G, Boldyreva E, Bombicz P, Kawano M (2015) Supramolecular interactions in the solid state, IUCrJ 2, 675–690 (feature article)
    http://dx.doi.org/10.1107/S2052252515014608
  2. Bombicz P, Báthori N, Kálmán A (2015) Symmetry-controlled rearrangements in Piedfort Units (PU) of 2,4,6-triaryloxy-1,3,5-triazines, Struct Chem, 26:1611–1619 (IF: 1.837)
    http://dx.doi.org/10.1007/s11224-015-0659-8
  3. Fekete Cs, Mokrai R, Bombicz P, Nyulászi L, Kovács I (2015) η1-silolyl-FeCp(CO)2 complexes. Is there a way to sila-ferrocene?, J. Org. Chem. 799-800, 291-298 (IF: 4.721)
    http://dx.doi.org/10.1016/j.jorganchem.2015.09.023
  4. Dobi Z, Holczbauer T, Soós T (2015) Strain-Driven Direct Cross-Aldol and -Ketol Reactions of Four-Membered Heterocyclic Ketones, Org. Lett., 17 (11),2634–2637 (IF: 6.364)
    http://dx.doi.org/10.1021/acs.orglett.5b01002
  5. Sinai Á, Vangel D, Gáti T, Bombicz P, Novák Z (2015) Utilization of Copper-Catalyzed Carboarylation−Ring Closure for the Synthesis of New Oxazoline Derivatives, Org. Lett. 17, 4136−4139 (IF: 6.364)
    http://dx.doi.org/10.1021/acs.orglett.5b01860
  6. Palkó R, Egyed O, Rokob TA, Bombicz P, Riedl Zs and Hajós Gy (2015) Transformation of Zwitterionic Pyridine Derivatives to a Spiro-Fused Ring System: Azoniabenzo[de]fluorine. Synthesis and echanistic Rationalization, J. Org. Chem. 80, 174−179 (IF: 4.721)
    http://dx.doi.org/10.1021/jo5022663
  7. Bacher F, Dömötör O, Chugunova A, Nagy NV, Filipović L, Radulović S, Enyedy ÉA and Arion VB (2015) Strong effect of copper(II) coordination on antiproliferative activity of thiosemicarbazone–piperazine and thiosemicarbazone–morpholine hybrids, Dalton Trans., 44, 9071-990 (IF: 4.197)
    http://dx.doi.org/10.1039/c5dt01076d
  8. Csendes Z, Varga G, Nagy NV, Bajnóczi ÉG, Sipiczki M, Carlsond S, Canton SE, Metzinger A, Galbács G, Sipos P, Pálinkó I (2015) Synthesis, structural characterisation, and catalytic activity ofMn(II)–protected amino acid complexes covalently immobilisedon chloropropylated silica gel, Catalysis Today 241, 264–269 (IF: 3.893)
    http://dx.doi.org/10.1016/j.cattod.2013.11.066
  9. Varga E, Mika LT, Csámpai A, Holczbauer T, Kardosa Gy and Soós T (2015) Mechanistic investigations of a bifunctional squaramide organocatalyst in asymmetric Michael reaction and observation of stereoselective retro-Michael reaction, RSC Adv., 5, 95079–95086 (IF: 3.840)
    http://dx.doi.org/10.1039/c5ra19593d
  10. Kowol CR, Nagy NV, Jakusch T, Roller A, Heffeter P, Keppler BK, Enyedy ÉA (2015) Vanadium(IV/V) complexes of Triapine and related thiosemicarbazones: synthesis, solution equilibrium and bioactivity, JIB 152, 62–73, (IF: 3.444)
    http://dx.doi.org/10.1016/j.jinorgbio.2015.08.023
  11. Gráczer É, Palló A, Oláh J, Szimler T, Konarev PV, Svergun D I, Merli A, Závodszky P, Weiss MS, Vas M (2015) Glutamate 270 plays an essential role in K+-activation and domain closure of Thermus thermophilus isopropylmalate dehydrogenase, FEBS Letters 589, 240–245 (IF: 3.169)
    http://dx.doi.org/10.1016/j.febslet.2014.12.005
  12. Jakab A, Dalicsek Z, Holczbauer T, Hamza A, Pápai I, Finta Z, Timári G, Soós T (2015) Superstable Palladium(0) Complex as an Air- and Thermostable Catalyst for Suzuki Coupling Reactions, Eur. J. Org. Chem. 60–66 (IF: 3.065)
    http://dx.doi.org/10.1002/ejoc.201403214
  13. Ghosh S, Pandey NK, Banerjee P, Chaudhury K, Nagy NV, Dasgupta S (2015) Copper(II) directs formation of toxic amorphous aggregates resulting in inhibition of hen egg white lysozyme fibrillation under alkaline salt-mediated conditions, Journal of Biomolecular Structure and Dynamics 33 (5) 991-1007 (IF: 2.919)
    http://dx.doi.org/10.1080/07391102.2014.921864
  14. Ghosh S, Pandey NK, Bhattacharya S, Roy A, Nagy NV, Dasgupta S (2015) Evidence of two oxidation states of copper during aggregation of hen egg white lysozyme (HEWL), International Journal of Biological Macromolecules 76, 1-9 (IF: 2.858)
    http://dx.doi.org/10.1016/j.ijbiomac.2015.02.014
  15. Ilkei V, Bana P, Tóth F, Palló A, Holczbauer T, Czugler M, Sánta Zs, Dékány M, Szigetvári Á, Hazai L, Szántay Jr. Cs, Szántay Cs, Kalaus Gy (2015) Tetrahedron, on-line (IF: 2.641)
    http://dx.doi.org/10.1016/j.tet.2015.10.020
  16. Schneider Gy, Görbe T, Mernyák E, Wölfling J, Holczbauer T, Czugler M, Sohár P, Minorics R, Zupkó I (2015) Synthesis of novel 17-(5’-iodo)triazolyl-3-methoxyestrane epimers via Cu(I)-catalyzed azide–alkyne cycloadditon, and an evaluation of their cytotoxic activity in vitro, Steroids 98, 153–165 (IF: 2.639)
    http://dx.doi.org/10.1016/j.steroids.2015.02.018
  17. Szalontai G, Szabó P, Besenyei G, (2015) A new heterotopic Ar-BIAN ligand with a pendant P donor site, Polyhedron 92, 156–165 (IF: 2.011)
    http://dx.doi.org/10.1016/j.poly.2015.03.008
  18. Faigl F, Deák Sz, Erdélyi Zs, Holczbauer T, Czugler M, Nyerges M and Mátravölgyi B (2015) New Atropisomeric Amino Alcohol Ligands for Enantioselective Addition of Diethylzinc to Aldehydes, Chirality 27:216–222 (IF: 1.886)
    http://dx.doi.org/10.1002/chir.22415
  19. Bagi P, Fekete A, Kállay M, Hessz D, Kubinyi M, Holczbauer T, Czugler M, Fogassy E, Keglevich Gy (2015) A Case Study on the Resolution of the 1-i-Butyl-3-methyl-3-phospholene 1-Oxide via Diastereomeric Complex Formation Using TADDOL Derivatives and via Diastereomeric Coordination Complexes Formed from the Calcium Salts of O,O’-Diaroyl-(2R,3R)- tartaric Acids, Heteroatom Chemistry 26, 1, 79-90 (IF: 1.076)
    http://dx.doi.org/10.1002/hc.21218
  20. Bombicz P (2015) X-ray crystallography, Crystallography Reviews 22(1), 79-81 (Book Review)
    http://dx.doi.org/10.1080/0889311X.2015.1082129
  21. Kálmán A (2015) Mester és tanítvány: Sir Lawrence Bragg (1890–1971) és Náray-Szabó István (1899–1972) Magyar Kémikusok Lapja 284-286
  22. Bombicz P, Fábián L, Kálmán A (2015) Egykristály-röntgendiffrakció In: Sohár Pál (szerk.) A gyógyszerkutatás műszeres módszerei, Budapest, Magyar Kémikusok Egyesülete, 2015. pp. 171-222. (könyv fejezet) (ISBN:978-963-9970-61-8)

Functional Pharmacology Research Group

  1. Kardos J, Szabó Z, Héja L (2015) Framing neuro-glia coupling in antiepileptic drug design. J Med Chem, in press, IF: 5.480.
    http://www.ncbi.nlm.nih.gov/pubmed/26372259
  2. Szebényi K, Füredi A, Kolacsek O, Pergel E, Bősze Zs, Bender B, Vajdovich P, Tóvári J, Homolya L, Szakács G, Héja L, Enyedi Á, Sarkadi B, Apáti Á, Orbán TI (2015) Generation of a homozygous transgenic rat strain stably expressing a calcium sensor protein for direct examination of calcium signaling. Sci Rep 5: 12645, IF: 5.078.
    http://www.ncbi.nlm.nih.gov/pubmed/26234466
  3. Keszthelyi T, Holló G, Nyitrai G, Kardos J, Héja L (2015) Bilayer charge reversal and modification of lipid organization by dendrimers as observed by sum-frequency vibrational spectroscopy. Langmuir 31: 7815-7825, IF: 4.384.
    http://www.ncbi.nlm.nih.gov/pubmed/26099064
  4. Pál I, Kardos J, Dobolyi Á, Héja L (2015) Appearance of fast astrocytic component in voltage-sensitive dye imaging of neural activity. Mol Brain 8: 1-20, IF: 4.35.
    http://www.ncbi.nlm.nih.gov/pubmed/26043770
  5. Hofer KT, Kandrács Á, Ulbert I, Pál I, Szabó C, Héja L, Wittner L (2015) The hippocampal CA3 region can generate two distinct types of sharp wave-ripple complexes, in vitro. Hippocampus 25: 169-186, IF: 4.302.
    http://www.ncbi.nlm.nih.gov/pubmed/25209976
  6. Kékesi O, Ioja E, Szabó Zs, Kardos J, Héja L (2015) Recurrent seizure-like events are associated with coupled astroglial synchronization. Front Cell Neurosci 9: 215, IF: 4.175.
    http://www.ncbi.nlm.nih.gov/pubmed/26150770
  7. Kovács Z, Kardos J, Kékesi KA, Juhász G, Lakatos R, Héja L (2015) Effects of nucleosides on glia-neuron interactions: open up new vistas in development of more effective antiepileptic drugs. Curr Med Chem 22: 1500-1514, IF: 3.715.
    http://www.ncbi.nlm.nih.gov/pubmed/25666791
  8. Kovács Z, Kékesi KA, Juhász G, Barna J, Héja L, Lakatos R, Dobolyi A (2015) Non-adenosine nucleoside inosine, guanosine and uridine as promising antiepileptic drugs: a summary of current literature. Mini Rev Med Chem 14: 1033-1042, IF: 3.186
    http://www.ncbi.nlm.nih.gov/pubmed/25382017
  9. Kardos J, Héja L (2015) How membrane proteins work giving autonomous traverse pathways? Struct Chem DOI 10.1007/s11224-015-0601-0, IF: 2.198
    http://link.springer.com/article/10.1007%2Fs11224-015-0601-0
  10. Kardos J, Jemnitz K, Jablonkai I, Bóta A, Varga Z, Visy J, Héja L (2015) The Janus facet of nanomaterials. BioMed Res Int 2015: 317184, IF: 2.076
    http://www.ncbi.nlm.nih.gov/pubmed/26075225
  11. Jemnitz K, Szabó M, Bátai-Konczos A, Szabó P, Magda B, Veres Z (2015) A modified procedure for estimating the impact of the uptake on the overall biliary clearance in sandwich culture of rat hepatocytes. Drug Metab Lett 9: 17-27 IF: 1.85
    http://www.ncbi.nlm.nih.gov/pubmed/25600202
  12. Lőrincz T, Jemnitz K, Kardon T, Mandl J, Szarka A (2015) Ferroptosis is involved in acetaminophen induced cell death. Pathology & Oncology Research, 21: 1115-1121, IF: 1.806
    http://www.ncbi.nlm.nih.gov/pubmed/25962350
  13. Jablonkai I (2015) Herbicide metabolism in weeds: selectivity and herbicide resistance. In Herbicides (Eds.: Andrew Price, Lina Sarunaite, Jessica Kelton) InTech Open Access Publisher – ISBN 978-953-51-4413-7, in press.

Instrumentation Center

  1. Pashynska V, Stepanian S, Gomory A, Vekey K, Adamowicz L (2015) Competing intermolecular interactions of artemisinin-type agents and aspirin with membrane phospholipids: Combined model mass spectrometry and quantum-chemical study, Chem. Phys. 455:81-87
    http://www.sciencedirect.com/science/article/pii/S0301010415001159
  2. Feher K, Gomory A, Skoda-Foldes R (2015) A modular synthesis of 1,4,5-trisubstituted 1,2,3-triazoles with ferrocene moieties, Monatshefte fur Chemie 146:1455-1463
    http://link.springer.com/article/10.1007/s00706-015-1490-z
  3. Pocsfalvi G, Stanly C,Vilasi A, Fiume I, Capasso G, Turiák L, Buzas EI, Vékey K (2015) Mass spectrometry of extracellular vesicles, Mass Spectrometry Reviews, in press
    http://onlinelibrary.wiley.com/doi/10.1002/mas.21457/abstract
  4. Palkó R, Egyed O, Rokob TA, Bombicz P, Riedl Zs, Hajós Gy (2015) Transformation of Zwitterionic Pyridine Derivatives to a Spiro-Fused Ring System: Azoniabenzo[de]fluorine. Synthesis and Mechanistic Rationalization, J. Org. Chem. 80:174-179
    http://dx.doi.org/10.1021/jo5022663