Publikacje z łódzkich placówek naukowych:

  • V. V. Bakhonsky, J. Becker, G. Mlostoń, P.R. Schreiner
    "N-Alkoxyimidazolylidines (NOHCs): Nucleophilic carbenes based on oxidized imiodazolium core",
    Chem. Commun. , 2022, 58, 1538‒1541 https://doi.org/10.1039/D1CC05696D

  • H. Beer, A. Linke, J. Bresien, G. Mlostoń, M. Celeda, A. Villinger, A. Schulz
    "Synthesis of bicyclic P,S-heterocycles via addition of thioketones to a phosphorus-centered open-shell singlet biradical",
    Inorg. Chem. , 2022, 61, 2031‒2038 https://doi.org/10.1021/acs.inorgchem.1c03207

  • G. Mlostoń, K. Kula, R. Jasiński
    "A DFT study on the molecular mechanism of additions of electrophilic and nucleophilic carbenes to non-enolizable cycloaliphatic thioketones",
    Molecules, 2021, 25, e5562 https://doi.org/10.3390/molecules26185562

  • G. Mlostoń, M. Kowalczyk, A. U. Augustin, P. G. Jones, D. B. Werz
    "Lewis-acid catalyzed (3+2)-cycloadditions of donor-acceptor cyclopropanes with thioketenes",
    Eur. J. Org. Chem., 2021, 6250‒6253 https://doi.org/10.1002/ejoc.202100879

  • G. Mlostoń, M. Kowalczyk, M. Celeda, K. Gach-Janczak, A. Janecka, M. Jasiński
    "Synthesis and cytotoxic activity of lepidilines A−D: Comparison with some 4,5-diphenyl analogues and related imidazole-2-thiones",
    J. Nat. Prod., 2021, 64, 3071‒3079 https://doi.org/10.1021/acs.jnatprod.1c00797

  • Sedlák, D., Wilson, T.A., Tjarks,W., Radomska, H.S., Wang, H., Kolla, J.N., Leśnikowski, Z.J., Špičáková, A., Ali, T., Ishita, K., Rakotondraibe, L.H., Vibhute, S., Wang, D., Anzenbacher, P., Bennett, C., Bartunek, P., Coss, C.C.,
    "Structure−Activity Relationship of para-Carborane Selective Estrogen Receptor β Agonists",
    J. Med. Chem. , 2021, 64, 9330−9353 https://doi.org/10.1021/acs.jmedchem.1c00555

  • D. Kodr, C.P. Yenice, A. Simonova, D. Pavlović Saftić, R. Pohl, V. Sýkorová, M. Ortiz, L. Havran, M. Fojta, Z.J. Lesnikowski, C. K. O'Sullivan, M. Hocek
    "Carborane- or Metallacarborane-Linked Nucleotides for Redox Labelling. Orthogonal Multipotential Coding of all Four DNA Bases for Electrochemical Analysis and Sequencing",
    J. Am. Chem. Soc., 2021, 143, 7124 https://doi.org/10.1021/jacs.1c02222

  • K. Bednarska-Szczepaniak, A. Mieczkowski, A. Kierozalska, D. Pavlović Saftić, K. Głąbała, T. Przygodzki, L. Stańczyk, K. Karolczak, C. Watała, H. Rao, Z-G Gao, K.A. Jacobson, Z.J. Leśnikowski
    "Synthesis and evaluation of adenosine derivatives as A1, A2A, A2B and A3 adenosine receptor ligands containing boron clusters as phenyl isosteres and selective A3 agonists",
    Eur. J. Med. Chem., 2021, 223, 113607 https://doi.org/10.1016/j.ejmech.2021.113607

  • S. Rykowski, D. Gurda-Woźna, M. Orlicka-Płocka, A. Fedoruk-Wyszomirska, M. Giel-Pietraszuk, E. Wyszko, A. Kowalczy, P. Stączek, A. Bak, A. Kiliszek, W. Rypniewski, A. B. Olejniczak,
    "Design, Synthesis, and Evaluation of Novel 3-Carboranyl-1,8-Naphthalimide Derivatives as Potential Anticancer Agents",
    Int. J. Mol. Sci., 2021, (22), 2772 https://doi.org/10.3390/ijms22052772

  • J. Nekvinda, D. Różycka, S. Rykowsi, E. Wyszko, A. Fedoruk-Wyszomirska, D. Gurda, M. Orlicka-Płocka, M. Giel-Pietraszuk, A. Kiliszek, W. Rypniewski, R. Bachorz, J. Wojcieszak, B. Gruner, A. B. Olejniczak,
    "Synthesis of naphthalimide-carborane nad metallacarborane conjugates: anticancer activity, DNA bindibg ability",
    Bioorg. Chem. , 2020, (94), 103432

  • J. Sarnik, A. Gajek, M. Toma, J. Pawelczyk, S. Rykowski, A. Olejniczak, T. Sliwinski, R. Bielski, Z. J. Witczak,
    "(1-4)-Thiodisaccharides as anticancer agnts. Part 5. Evaluation of anticancer activity and investigation of mechanism of action",
    Bioorg. Med. Chem. Lett. , 2020, 30, 126904

  • D. Różycka, Z. J. Leśnikowski, A. B. Olejniczak,
    "Synthesis of boron cluster analogs of penicillin and their antibacterial activity",
    J. Organomet. Chem. , 2019, 881, 19-24

  • A, Mieczkowski, A. Kierozalska, M. Białek-Pietras, T. M. Goszczynski, S. Janczak, A. B. Olejniczak, M. Studzinska, E. Paradowska, Z. J. Leśnikowski,
    "Comparative study of inorganic, boron-rich cluster and organic, phenyl adenosine modifications: synthesis and properties",
    Future Med. Chem. , 2019, 11, 1267-1284

  • A.Dąbrowska, M. Matuszewski, K. Zwoliński, A. Ignaczak, A. B. Olejniczak,
    "Insight into lipophilicity of deoxyribonucleoside-boron cluster conjugates"
    Eur. J. Pharm. Sci., 2018, 111, 226-237.

  • J. Lewkowski, M. Morawska, P. Rychter, D. Rogacz, K. Lewicka, P. Dobrzyński,
    "Evaluation of Ecotoxicological Impact of New Pyrrole-derived Aminophosphonates Using Selected Bioassay Battery",
    Ecotoxicology, 2017, 26(7), 914-929 https://doi.org/10.1007/s10646-017-1821-4

  • J. Lewkowski, R. Karpowicz, M. Morawska, P. Rychter, D. Rogacz, K. Lewicka, P. Dobrzyński,
    "Ecotoxicological Impact of Ferrocene-derived Amino-phosphonates Using Bioassays Battery",
    RSC Adv., 2017, 7, 38399-38409 https://doi.org/10.1039/c7ra06079c

  • J. Lewkowski, M. Morawska, A. Kaczmarek, D. Rogacz, P. Rychter,
    "Novel N-arylaminophosphonates Bearing Pyrrole Moiety and Their Ecotoxicological Properties",
    Molecules, 2017, 22, 1132 https://doi.org/10.3390/molecules22071132

  • J. Lewkowski, M. Morawska, R. Karpowicz, P. Rychter, D. Rogacz, K. Lewicka,
    "First Synthesis and Evaluation of Eco- and Phytotoxicological Properties of Aminophosphonates Deriving from 5-Nitrofurfural",
    Chemosphere, 2017, 188 618-632 https://doi.org/10.1016/j.chemosphere.2017.09.031

  • E. M. Lewandowski, Ł. Szczupak, S. Wong, J. Skiba, A. Guśpiel, J. Solecka, V. Vrček, K. Kowalski, Y. Chen,
    "Antibacterial properities of metallocenyl-7-ADCA derivatives and structure in complex with CTX-M;-lactamase",
    Organometallics, 2017, 36, 1673-1676.

  • J. Skiba, C. Schmidt, P. Lippmann, P. Ensslen, H.-A. Wagenknecht, R. Czerwieniec, F. Brandl, I. Ott, T. Bernaś, B. Krawczyk, D. Szczukocki, K. Kowalski,
    "Substitution of metallocenes with [2.2]paracyclophane to enable confocal microscopy imaging in living cells",
    Eur. J. Inorg. Chem., 2017, 297-305.

  • K. Kowalski, Ł. Szczupak, S. Saloman, D. Steverding, A. Jabłoński, V. Vrček, A. Hildebrandt, H. Lang, A. Rybarczyk-Pirek,
    "Cymantrene, Cyrhetrene and Ferrocene Nucleobase Conjugates: Synthesis, Structure, Computational Study, Electrochemistry and Antitrypanosomal Activity",
    ChemPlusChem., 2017, 82, 303-314.

  • I. Anisimov, S. Saloman, A. Hildebrandt, H. Lang, D. Trzybiński, K. Woźniak, D. Šakić, V. Vrček , K. Kowalski,
    "1,1'-Bis(thymine)ferrocene Nucleoside: Synthesis and Study of their Stereoselective Formation",
    ChemPlusChem, 2017, 82, 859-866.

  • J. Skiba, T. Bernaś, D. Trzybiński, K. Woźniak, G. Ferraro, D. Marasco, A. Merlino, M. Shafikov, R. Czerwieniec, K. Kowalski,
    "Mitochondria targeting with luminescent rhenium(I) complexes",
    Molecules, 2017, 22, 809-825.

  • A. Kubicka, E. Fornal, A. B. Olejniczak, A. J. Rybarczyk-Pirek, S. Wojtulewski, B. Rudolf,
    "Oxa-Michael reaction of metallocarbonyl complexes bearing the maleimidato. Reactivity studies with selected hydroxy compounds",
    Polyhedron, 2016, 107, 38-47.

  • J. Lewkowski, M. Rodriguez Moya, A. Wrona-Piotrowicz, J. Zakrzewski, R. Kontek, G. Gajek,
    "Synthesis, fluorescent properties and the promising cytotoxicity of pyrene-derived aminophosphonates",
    Beilstein J. Org. Chem., 2016, 12, 1229-1235 https://doi.org/10.3762/bjoc.12.117

  • J. Lewkowski, Z. Malinowski, A. Matusiak, M. Morawska, D. Rogacz, P. Rychter,
    "The Effect of New Thiophene-Derived Aminophosphonic Derivatives on Growth of Terrestrial Plants: A Seedling Emergence and Growth Test",
    Molecules 2016, 21, 694 https://doi.org/10.3390/molecules21060694

  • J. Lewkowski, M. Rodriguez Moya, M. Chmielak, D. Rogacz, K. Lewicka, P. Rychter,
    "Synthesis, spectral characterization of several novel 1-pyrene-derived aminophosphonates and their ecotoxicological evaluation using Heterocypris incongruens and Vibrio fisheri tests",
    Molecules, 2016, 21, 936 https://doi.org/10.3390/molecules21070936

  • K. Kowalski,
    "Ferrocenyl-nucleobase complexes: synthesis, chemistry and applications",
    Coord. Chem. Rev., 2016, 317, 132-156

  • Z.J. Leśnikowski,
    "Challenges and Opportunities for the Application of Boron Clusters in Drug Design",
    J. Med. Chem. 2016, 59, 7738-7758

  • Z.J. Leśnikowski,
    "Recent Developments with Boron as a Platform for Novel Drug Design",
    Expert Opinion on Drug Discovery, 2016, 11, 569-578

  • A. Adamska, A. Rumijowska-Galewicz, A. Ruszczynska, M. Studzińska, A. Jabłońska, E. Paradowska, E. Bulska, H. Minier-Lehmann, J. Dziadek, Z. J. Leśnikowski, A. B. Olejniczak,
    "Anti-mycobacterial activity of thymine derivatives bearing boron cluster",
    Eur. J. Med. Chem., 2016, 121, 71-81

  • J. D. Żołnierczyk, A. B. Olejniczak, A. Mieczkowski, J. Z. Błoński, Z. M. Kiliańska, T. Robak, Z. J. Leśnikowski,
    "In vitro antileukemic activity of novel adenosine derivatives bearing boron clusterr modification" ,
    Bioorgan. Med. Chem. 2016, 24, 5076-5087