Professur für Organische Chemie

Adresse:
Nikolaus-Fiebiger-Str. 10
91058 Erlangen


Publikationen (Download BibTeX)

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Ndreshkjana, B., Capci Karagoez, A., Klein, V., Chanvorachote, P., Muenzner, J.K., Hübner, K.,... Schneider-Stock, R. (2019). Combination of 5-fluorouracil and thymoquinone targets stem cell gene signature in colorectal cancer cells. Cell Death & Disease, 10(6). https://dx.doi.org/10.1038/s41419-019-1611-4
Foertsch, T.C., Davis, A.T., Popov, R., Von Bojnicic-Kninski, C., Held, F., Tsogoeva, S.,... Nesterov-Mueller, A. (2019). Spatial modes of laser-induced mass transfer in micro-gaps. Applied Sciences, 9(7). https://dx.doi.org/10.3390/app9071303
Guryev, A., Hahn, F., Marschall, M., & Tsogoeva, S. (2019). Visible-Light-Driven C-H Oxidation of Cyclic Tertiary Amines: Access to Synthetic Strychnos Alkaloids with Antiviral Activity. Chemistry - A European Journal, 25(16), 4062-4066. https://dx.doi.org/10.1002/chem.201900078
Mauksch, M., & Tsogoeva, S. (2019). Hückel and Möbius Aromaticity in Charged Sigma Complexes. Chemistry - A European Journal. https://dx.doi.org/10.1002/chem.201900849
Capci Karagöz, A., Leidenberger, M., Hahn, F., Friedrich, O., Hampel, F., Marschall, M.,... Tsogoeva, S. (2019). Synthesis of new betulinic acid/betulin-derived dimers and hybrids with potent antimalarial and antiviral activities. Bioorganic & Medicinal Chemistry, 27(1), 110-115. https://dx.doi.org/10.1016/j.bmc.2018.11.018
Wu, Y., Klein, V., Killian, M., Behling, C., Chea, S., Tsogoeva, S., & Bachmann, J. (2018). Novel Fully Organic Water Oxidation Electrocatalysts: A Quest for Simplicity. ACS Omega, 3(3), 2602-2608. https://dx.doi.org/10.1021/acsomega.7b01982
Fröhlich, T., Reiter, P.C., Saeed, M.E.M., Hutterer, C., Hahn, F., Leidenberger, M.,... Tsogoeva, S. (2018). Synthesis of Thymoquinone-Artemisinin Hybrids: New Potent Antileukemia, Antiviral, and Antimalarial Agents. Acs Medicinal Chemistry Letters, 9(6), 534-539. https://dx.doi.org/10.1021/acsmedchemlett.7b00412
Capci Karagöz, A., Reiter, C., Seo, E.-J., Gruber, L., Hahn, F., Leidenberger, M.,... Tsogoeva, S. (2018). Access to new highly potent antileukemia, antiviral and antimalarial agents via hybridization of natural products (homo)egonol, thymoquinone and artemisinin. Bioorganic & Medicinal Chemistry, 26(12), 3610-3618. https://dx.doi.org/10.1016/j.bmc.2018.05.041
Hahn, F., Fröhlich, T., Frank, T., Bertzbach, L.D., Kohrt, S., Kaufer, B.B.,... Marschall, M. (2018). Artesunate-derived monomeric, dimeric and trimeric experimental drugs - Their unique mechanistic basis and pronounced antiherpesviral activity. Antiviral Research, 152, 104-110. https://dx.doi.org/10.1016/j.antiviral.2018.02.013
Fröhlich, T., Kiss, A., Wolfling, J., Mernyak, E., Kulmany, A.E., Minorics, R.,... Tsogoeva, S. (2018). Synthesis of Artemisinin-Estrogen Hybrids Highly Active against HCMV, P-falciparum, and Cervical and Breast Cancer. Acs Medicinal Chemistry Letters, 9(11), 1128-1133. https://dx.doi.org/10.1021/acsmedchemlett.8b00381
Fröhlich, T., Hahn, F., Belmudes, L., Leidenberger, M., Friedrich, O., Kappes, B.,... Tsogoeva, S. (2018). Synthesis of Artemisinin-Derived Dimers, Trimers and Dendrimers: Investigation of Their Antimalarial and Antiviral Activities Including Putative Mechanisms of Action. Chemistry - A European Journal, 24(32), 8103-8113. https://dx.doi.org/10.1002/chem.201800729
Bock, C., Gangajji, P., Bönisch, S., Bauer, W., Hutterer, C., Leidenberger, M.,... Tsogoeva, S. (2017). Deeper Insight into the Six-Step Domino Reaction of Aldehydes with Malononitrile and Evaluation of Antiviral and Antimalarial Activities of the Obtained Bicyclic Products. ChemistryOpen, 6(3), 364-374. https://dx.doi.org/10.1002/open.201700005
Fröhlich, T., Ndreshkjana, B., Muenzner, J.K., Reiter, P.C., Hofmeister, E., Mederer, S.,... Tsogoeva, S. (2017). Synthesis of Novel Hybrids of Thymoquinone and Artemisinin with High Activity and Selectivity Against Colon Cancer. Chemmedchem, 12(3), 226-234. https://dx.doi.org/10.1002/cmdc.201600594
Held, F., Guryev, A., Fröhlich, T., Hampel, F., Kahnt, A., Hutterer, C.,... Tsogoeva, S. (2017). Facile access to potent antiviral quinazoline heterocycles with fluorescence properties via merging metal-free domino reactions. Nature Communications, 8. https://dx.doi.org/10.1038/ncomms15071
Ackermann, A., Capci Karagoez, A., Ghoochani, A., Buchfelder, M., Eyüpoglu, I.Y., Tsogoeva, S., & Savaskan, N. (2017). Cytotoxic profiling of artesunic and betulinic acids and their synthetic hybrid compound on neurons and gliomas. Oncotarget, 8(37), 61457-61474. https://dx.doi.org/10.18632/oncotarget.18390
Fröhlich, T., Reiter, C., Ibrahim, M.M., Beutel, J., Hutterer, C., Zeitträger, I.,... Tsogoeva, S. (2017). Synthesis of Novel Hybrids of Quinazoline and Artemisinin with High Activities against Plasmodium falciparum, Human Cytomegalovirus, and Leukemia Cells. ACS Omega, 2(6), 2422-2431. https://dx.doi.org/10.1021/acsomega.7b00310
Fingerhut, A., Wu, Y., Kahnt, A., Bachmann, J., & Tsogoeva, S. (2016). Synthesis and Electrochemical and Photophysical Characterization of New 4,4-Conjugated 2,2-Bipyridines that are End-Capped with Cyanoacrylic Acid/Ester Groups. Chemistry-An Asian Journal, 11(8), 1232-1239. https://dx.doi.org/10.1002/asia.201501324
Bock, C., Parameshwarappa, G., Bönisch, S., Neiß, C., Bauer, W., Hampel, F.,... Tsogoeva, S. (2016). Generation of Complex Azabicycles and Carbobicycles from Two Simple Compounds in a Single Operation through a Metal-Free Six-Step Domino Reaction. Chemistry - A European Journal, 22(15), 5189-5197. https://dx.doi.org/10.1002/chem.201504798
Hutterer, C., Niemann, I., Milbradt, J., Fröhlich, T., Reiter, P.C., Kadioglu, O.,... Marschall, M. (2015). The broad-spectrum antiinfective drug artesunate interferes with the canonical nuclear factor kappa B (NF-κB) pathway by targeting RelA/p65. Antiviral Research, 124, 101-109. https://dx.doi.org/10.1016/j.antiviral.2015.10.003
Held, F., Grau, D., & Tsogoeva, S. (2015). Enantioselective Cycloaddition Reactions Catalyzed by BINOL-Derived Phosphoric Acids and N-Triflyl Phosphoramides: Recent Advances. Molecules, 20, 16103-16126. https://dx.doi.org/10.3390/molecules200916103

Zuletzt aktualisiert 2019-24-04 um 10:21