Publications

2025

154. Organic Synthesis and Catalysis Enable Facile Access to Bioactive Compounds and Drugs. S. B. Tsogoeva, K. S. Schanze. ACS Central Science, 2025, https://doi.org/10.1021/acscentsci.4c02041.

2024

153. Privileged Brønsted acid organocatalysis. S. B. Tsogoeva. Nature Catalysis, 2024, 7, 7-9.

152. Access to Artemisinin-Triazole Antimalarials via Organo-Click Reaction: High In Vitro/In Vivo Activity Against Multidrug-Resistant Malaria Parasites. L. Herrmann, M. Leidenberger, H. C. Quadros, B. W. Grau, F. Hampel, O. Friedrich, D. R. M. Moreira, B. Kappes, S. B. Tsogoeva. JACS Au, 2024, 4, 951−957 (Cover Picture).

151. A domino reaction strategy for facile and modular construction of synthetically challenging functionalized ortho-fluoroanilines. B. W. Grau, S. Kohlbauer, Y. Gu, F. Hahn, J. Lösing, C. Wangen, M. Stangier, L. Ackermann, M. Marschall, and S. B. Tsogoeva. Org. Chem. Front., 2024, DOI: 10.1039/d4qo01692k (Preprint: ChemRxiv. 2024).

150. In-Situ Electrolyte for Electrosynthesis: Scalable Anodically-Enabled One-Pot Sequence from Aldehyde to Isoxazol(in)es. A. A. Al-Romema, H. Xia, K. J. J. Mayrhofer, S. B. Tsogoeva, P. Nikolaienko. Chem. Eur. J., 2024, https://doi.org/10.1002/chem.202402696.

149. Synthesis and Photo/Radiation Chemical Characterization of a New Redox-Stable Pyridine-Triazole Ligand. A. A. Al-Romema, F. Plass, A. V. Nizovtsev, A. Kahnt, S. B. Tsogoeva. ChemPhysChem, 2024, https://doi.org/10.1002/cphc.202400273.

148. Characterization of antimalarial activity of artemisinin-based hybrid drugs. C. Quadros, L. Herrmann, J. Manaranche, L. Paloque,M. C.Borges-Silva, G. A. Dziwornu, S. D’Alessandro, K. Chibale, N. Basilico, F. Benoit-Vical, S. B. Tsogoeva, D. R. M. Moreira. Antimicrobial Agents and Chemotherapy, 2024, https://doi.org/10.1128/aac.00143-24.

147. Facile synthesis of new antiviral fluoro-quinazolines enabled by merging domino reactions. S. Kohlbauer, H. Xia, B. W. Grau, C. Wangen, F. Hahn, V. G. Nenajdenko, M. Marschall, S. B. Tsogoeva. SYNTHESIS, (dedicated to Professor H. Ila on the occasion of her 80th birthday), 2024, DOI: 10.1055/s-0043-1775411.

146. Synthesis of New Highly Functionalized Quinolines via Novel Fe(III)-Catalyzed Domino aza-Michael/Aldol/Aromatization Reaction. F. Heckmann, M. M. Ibrahim, F. Hampel, S. B. Tsogoeva. Synlett, 2024, doi: 10.1055/s-0042-1751546.

145. Dipeptide-catalysed Michael reaction under physiological conditions: Examination of potential bioorthogonality. F. Schuster, B. W. Grau, H.-G. Xu, A. Mokhir, S. B. Tsogoeva. Bioorg. Med. Chem. 2024, 103, 117650.

144. Catalytic multi-step domino and one-pot reactions. S. B. Tsogoeva, Beilstein J. Org. Chem. 2024, 20, 254–256.

Preprints

Synthesis of potent antileukemic quinazoline-thiohydantoin fused heterocycles enabled by metal-free domino reaction. L. Kersting, C. Zippel, L. Herrmann, E.-J. Seo, M. E.M. Saeed, A. Gaube, D. Tailor, A. Dheeraj, S. V. Malhotra, S. Muehlich,T. Efferth, S. B. Tsogoeva. Preprint: ChemRxiv. 2023, https://doi.org/10.26434/chemrxiv-2023-27xgq.
Autocatalytic Double sigma-Bond C(sp2 )–N Transamination Metathesis Reaction. V. Klein, F. Schuster and S. B. Tsogoeva. Preprint: ChemRxiv. 2022, https://doi.org/10.26434/chemrxiv-2022-m6k1v.

143. Autofluorescent antimalarials by hybridization of artemisinin and coumarin: In vitro/in vivo studies and live-cell imaging. L. Herrmann, M. Leidenberger, A. S. de Morais, C. Mai, A. Çapci, M. da Cruz Borges Silva, F. Plass, A. Kahnt, D. R. M. Moreira, B. Kappes, S. B. Tsogoeva. Chemical Science. 2023, 14, 12941-12952 (Front Cover, press release).

142. Autofluorescent Artemisinin-Benzimidazole Hybrids via Organo-Click Reaction: Study of Antiviral Properties and Mode of Action in Living Cells. L. Herrmann, F. Hahn, B. W. Grau, M. Wild, A. Niesar, C. Wangen, E. Kataev, M. Marschall, S. B. Tsogoeva. Chem. Eur. J. 2023, 29, e202301194.

141. The Trimeric Artesunate Analog TF27, a Broadly Acting Anti-Infective Model Drug, Exerts Pronounced Anti-SARS-CoV-2 A ctivity Spanning Variants and Host Cell Types. F. Hahn, C. Wangen, S. Häge, L. Herrmann, A. Herrmann, S. B. Tsogoeva, M. Marschall, Pharmaceutics, 2023, 15, 115.

140. Light-Driven Catalyst-Free Access to Phthalazines: Entry to Antiviral Model Drugs via Merging Domino Reactions in One-Pot. A. Guryev, F. Schuster, L. Herrmann, F. Hahn, C. Wangen, J. Hodek, J. Weber, M. Marschall, S. B. Tsogoeva, Eur. J. Org. Chem., 2023, 26, e202200994 (Front Cover) (Preprint: ChemRxiv. 2022).

2022

139. Iron-Catalyzed Olefin Metathesis: Recent Theoretical and Experimental Advances. B. W. Grau, A. Neuhauser, S. Aghazada, K. Meyer, S. B. Tsogoeva. Chem. Eur. J. 2022, https://doi.org/10.1002/chem.202201414 (Review. Dedicated to the memory of Professor Robert H. Grubbs; Frontispiece).

138. Anti-SARS-CoV-2 Inhibitory Profile of New Quinoline Compounds in Cell Culture-Based Infection Models. L. Herrmann, F. Hahn, C. Wangen, M. Marschall, S.B. Tsogoeva. Chem. Eur. J. 2022, 28, e202103861 (Front Cover and Cover Profile).

137. Visible Light-driven Metal-free C–H Functionalization: Access to New Bioactive Tetrahydroisoquinoline-Butenolide Hybrids via Domino Amine Oxidation/Vinylogous Mannich Reaction. L. Kersting, L. Kuhn, M. Anokhin, F. Schuster, C. Häberli, S. Sambyal, H. M. Sampath Kumar, J. Keiser, I. Alabugin, S. B. Tsogoeva. ChemPhotoChem, 2022, 6, e202200109 (Front Cover and Cover Profile); (Preprint: ChemRxiv. 2021).

136. Synthesis and In Vitro Study of Artemisinin/Synthetic Peroxide Based Hybrid Compounds against SARS-CoV-2 and Cancer. L. Herrmann, I. A. Yaremenko, A. Çapcı, J. Struwe, D. Tailor, A. Dheeraj, J. Hodek, Y. Y. Belyakova, P. Radulov, J. Weber, S. V. Malhotra, A. O. Terent’ev, L. Ackermann, S. B. Tsogoeva. ChemMedChem, 2022, 17, e202200005 (Preprint: ChemRxiv. 2021).

135. Lewis Acids and Heteropoly Acids in the Synthesis of Organic Peroxides. I. A. Yaremenko, P. S. Radulov, Yu. Yu. Belyakova, D. I. Fomenkov, S. B. Tsogoeva, A. O. Terent’ev. Pharmaceuticals, 2022, 15(4), 472.

2021

134. A Noble Quest for Simplicity in the Chiral World. S. B. Tsogoeva. The New England Journal of Medicine, 2021, 385, 2579-2581.
133. Four-Step Domino Reaction Enables Fully Controlled Non-Statistical Synthesis of Hexaarylbenzene with Six Different Aryl Groups. B. Grau, M. Dill, F. Hampel, A. Kahnt, N. Jux, S. B. Tsogoeva. Angew. Chem. Int. Ed. 2021, 60, 22307-22314 (Hot Paper – Editor’s Choice; Front Cover; Phys.Org.) Preprint: ChemRxiv. 2021).
132. Controlling and Fine-Tuning Charge Transfer Emission in 2,6-Dicyanoaniline Multichromophores Prepared through Domino Reactions: Entry to a Potentially New Class of OLEDs. F. Plass, S. Bönisch, F. Held, T. Ullrich, F. Fischer, A. Guryev, A. Görling, A. Kahnt, S. B. Tsogoeva. J. Org. Chem. 2021, 86, 6111-6125 (Cover Picture).
131. Artemisinin-Derived Dimers from a Chemical Perspective. A. Çapcı, L. Herrmann, H. M. Sampath Kumar, T. Fröhlich, S. B. Tsogoeva. Medicinal Research Reviews, (Special Issue, in honor of Professor Youyou Tu’s 90^th anniversary) 2021, 41, 2927-2970 (Cover Picture).
130. Development of a PROTAC-Based Targeting Strategy Provides a Mechanistically Unique Mode of Anti-Cytomegalovirus Activity. F. Hahn, S. T. Hamilton, C. Wangen, M. Wild, J. Kicuntod, N. Brückner, J. E. L. Follett, L. Herrmann, A. Kheimar, B. B. Kaufer, W. D. Rawlinson, S. B. Tsogoeva, M. Marschall. Int. J. Mol. Sci. 2021, 22, 12858.
129. Studies of Potency and Efficacy of an Optimized Artemisinin-Quinoline Hybrid against Multiple Stages of the Plasmodium Life Cycle. H. C. Quadros, A. Çapcı, L. Herrmann, S. D’Alessandro, D. Fontinha, R. Azevedo, W. Villarreal, N. Basilico, M. Prudêncio, S. B. Tsogoeva, D. R. M. Moreira. Pharmaceuticals, 2021, 14, 1129, https://doi.org/10.3390/ph14111129.
128. The Catalysis of Ring Synthesis. S. B. Tsogoeva, G. Dong, L. Ackermann. ChemCatChem, 2021, 13, 2962-2964.
127. Chemical Hybridization of Sulfasalazine and Dihydroartemisinin Promotes Brain Tumor Cell Death. A. Ackermann, A. Çapcı, M. Buchfelder, S. B. Tsogoeva, N. Savaskan. Scientific Reports, 2021, 11: 20766.
126. Disclosure of Ground State Zimmerman-Möbius Aromaticity in Radical Anion of [6]helicene and Evidence for 4π periodic Aromatic Ring Currents in a molecular “metallic” Möbius Strip. M. Mauksch and S. B. Tsogoeva. Chem. Eur. J. 2021, 27, 14660-14671.
125. Combinatorial Drug Treatments Reveal Promising Anticytomegaloviral Profiles for Clinically Relevant Pharmaceutical Kinase Inhibitors (PKIs). M. Wild, J. Kicuntod, L. Seyler, C. Wangen, L. D. Bertzbach, A. M. Conradie, B. B. Kaufer, S. Wagner, D. Michel, J. Eickhoff, S. B. Tsogoeva, T. Bäuerle, F. Hahn, M. Marschall, Int. J. Mol. Sci. 2021, 22, 575.

2020

124. (Iso)Quinoline-Artemisinin Hybrids via Click Chemistry: Highly Potent Agents against Viruses. A. Çapcı, M. M. Lorion, C. Mai, F. Hahn, J. Hodek, C. Wangen, J. Weber, M. Marschall, L. Ackermann, S. B. Tsogoeva. Chem. Eur. J. 2020, 26, 12019-12026 (Cover Picture).
123. Photoracemization-based Viedma ripening of a BINOL derivative. G. Belletti, C. Tortora, I. D. Mellema, P. Tinnemans, H. Meekes, F. P. J. T. Rutjes, S. B. Tsogoeva, E. Vlieg, Chem. Eur. J. 2020, 26, 839-844 (Hot Paper – Editor’s Choice; Cover Picture).
122. Speeding up Viedma Deracemization through Water catalyzed and Reactant Self-catalyzed Racemization. C. Tortora, C. Mai, F. Cascella, M. Mauksch, A. Seidel-Morgenstern, H. Lorenz, S. B. Tsogoeva. ChemPhysChem, 2020, 21, 1775-1787 (Cover Picture).
121. Synthesis of Tamoxifen‐Artemisinin and Estrogen‐Artemisinin Hybrids Highly Potent Against Breast and Prostate Cancer. T. Fröhlich, C. Mai, R. Bogautdinov, S. N. Morozkina, A. G. Shavva, O. Friedrich, D. Gilbert, S. B. Tsogoeva. ChemMedChem, 2020, 15, 1473-1479.
120. Structural Hybridization as a Facile Approach to New Drug Candidates. H. M. S. Kumar, L. Herrmann, S. B. Tsogoeva. Bioorg. Med. Chem. Lett., (Invited Digest), 2020, 30, 127514.
119. Iron-catalyzed carbonyl metathesis reactions. B. W. Grau, S. B. Tsogoeva, Catalysts, 2020, 1092; https://doi.org/10.3390/catal10091092.
118. The artemisinin-derived autofluorescent compound BG95 exerts strong anticytomegaloviral activity based on a mitochondrial targeting mechanism. M. Wild, F. Hahn, B. Grau, L. Herrmann, A. Niesar, M. Schütz, M. M. Lorion, L. Ackermann, S. B. Tsogoeva, M. Marschall, Int. J. Mol. Sci. 2020, 21, 5578; https://doi.org/10.3390/ijms21155578
117. Target verification of artesunate-related antiviral drugs: Assessing the role of mitochondrial and regulatory proteins by click chemistry and fluorescence labeling. F. Hahn, A. Niesar, C. Wangen, M. Wild, B. Grau, L. Herrmann, A. Çapcı, A. Adrait, Y. Couté, S. B. Tsogoeva, M. Marschall. Antiviral Research, 2020, https://doi.org/10.1016/j.antiviral.2020.104861.
116. The trimeric artesunate derivative TF27 shows therapeutic and prophylactic efficacy against cytomegalovirus upon oral treatment of immunocompetent mice. M. Wild, L. D. Bertzbach, P. Tannig, C. Wangea, R. Müller, L. Herrmann, T. Fröhlich, S. B. Tsogoeva, B. B. Kaufer, M. Marschall, F. Hahn. Antiviral Research, 2020, https://doi.org/10.1016/j.antiviral.2020.104788.
115. A highly potent trimeric derivative of artesunate shows promising treatment profiles in experimental models for congenital HCMV infection in vitro and ex vivo. C. Jacquet, M. Marschall, D. Andouard, C. El Hamel, T. Chianea, S. B. Tsogoeva, S. Hantz, S. Alain. Antiviral Research, 2020, https://doi.org/10.1016/j.antiviral.2019.104700.

2019

114. Artemisinin‐(Iso)Quinoline Hybrids by C‐H Activation and Click Chemistry: Combating Multidrug‐Resistant Malaria. A. Çapcı, M. M. Lorion, H. Wang, N. Simon, M. Leidenberger, M. C. Borges Silva, D. R. M. Moreira, Y. Zhu, Y. Meng, J. Y. Chen, M. Lee, O. Friedrich, B. Kappes, J. Wang, L. Ackermann, S. B. Tsogoeva, Angew. Chem. Int. Ed., 2019, 58, 13066-13079 (Hot Paper – Editor’s Choice; Cover Picture, Highlighted by Nature, Featured in ACIE Special Issue Science Forum 2019), press release.
113. Facile Access to Challenging ortho-Terphenyls via Merging Two Multi-Step Domino Reactions in One-Pot: A Joint Experimental/ Theoretical Study. B. W. Grau, S. Bönisch, A. Neuhauser, F. Hampel, A. Görling, S. B. Tsogoeva, ChemCatChem, 2019, 11, 3982-3992 (Invited Article; Special Issue “Women of Catalysis”).
112. Biomimetic non-heme iron-catalyzed epoxidation of challenging terminal alkenes using aqueous H₂O₂ as an environmentally friendly oxidant. A. Fingerhut, J. Vargas-Caporali, M. Antonio Leyva-Ramírez, E. Juaristi, S. B. Tsogoeva, Molecules, 2019, 24, 3182; doi:10.3390/molecules24173182 (Special Issue “Organic Transformations Promoted by 3d Metal Complexes: Synthetic Applications and Mechanisms”).
111. Combination of 5-Fluorouracil and Thymoquinone Targets Stem Cell Gene Signature in Colorectal Cancer Cells. B. Ndreshkjana, A. Çapci, V. Klein, P. Chanvorachote, J. K. Muenzner, K. Huebner, S. Steinmann, K. Erlenbach-Wünsch, C. I. Geppert, A. Agaimy, F. Ballout, C. El-Baba, H. Gali-Muhtasib, A. Hartmann, S. B. Tsogoeva, R. Schneider-Stock, Cell Death & Disease, 2019, 10:379.
110. Visible‐Light‐Driven C‐H Oxidation of Cyclic Tertiary Amines: Access to Synthetic Strychnos Alkaloids with Antiviral Activity. A. A. Guryev, F. Hahn, M. Marschall, S. B. Tsogoeva. Chem. Eur. J., (dedicated to Professor H. Ila on the occasion of her 75th birthday), 2019, 25, 4062-4066.
109. Hückel and Möbius Aromaticity in Charged Sigma Complexes. M. Mauksch, S. B. Tsogoeva. Chem. Eur. J. (dedicated to Professor Tim Clark on the occasion of his 70th birthday), 2019, 25, 7457-7462.
108. Synthesis of New Betulinic acid/Betulin-derived Dimers and Hybrids with Potent Antimalarial and Antiviral Activities. A. Çapcı Karagöz, M. Leidenberger, F. Hahn, F. Hampel, O. Friedrich, M. Marschall, B. Kappes, S. B. Tsogoeva. Bioorg. Med. Chem. 2019, 27, 110-115.
107. In vivo proof-of-concept for two experimental antiviral drugs, both directed to cellular targets, using a murine cytomegalovirus model. E. Sonntag, F. Hahn, L. D. Bertzbach, L. Seyler. C. Wangen, R. Müller, P. Tannig, B. Grau, M. Baumann, E. Zent, G. Zischinsky, J. Eickhoff, B. B. Kaufer, T. Bäuerle, S. B. Tsogoeva, M. Marschall. Antiviral Research, 2019, 161, 63-69.
106. Spatial modes of laser-induced mass transfer in microgaps. T. Foertsch, A. T. Davis, R. Popov, C. von Bojničić-Kninski, F. E. Held, S. B. Tsogoeva, F. F. Löffler, A. Nesterov-Mueller, Appl. Sci. 2019, 9, 1303; doi:10.3390/app9071303.

2018

105. Synthesis of artemisinin-derived di/tri-mers and dendrimers, investigation of their activity against P. falciparum and cytomegalovirus, and insights into their mechanisms of action. T. Fröhlich, F. Hahn, L. Belmudes, M. Leidenberger, O. Friedrich, B. Kappes, Y. Couté, M. Marschall, S. B. Tsogoeva. Chem. Eur. J., 2018, 24, 8103-8113 (Hot Paper – Editor’s Choice; Frontispiece, Highlighted in Chemistry Views, 2018).
104. Three-Component Domino Knoevenagel/Vinylogous Michael Reaction: Entry to Challenging o-Terphenyls. D. Grau, B. W. Grau, F. Hampel, S. B. Tsogoeva, Chem. Eur. J., 2018, 24, 6551-6556 (Hot Paper – Editor’s Choice; Frontispiece).
103. Synthesis of artemisinin-estrogen hybrids highly active against HCMV, P. falciparum, cervical and breast cancer. T. Fröhlich, A. Kiss, J. Wolfling, E. Mernyak, Á. E. Kulmány, R. Minorics, I. Zupkó, M. Leidenberger, O. Friedrich, B. Kappes, F. Hahn, M. Marschall, G. Schneider, S. B. Tsogoeva. ACS Med. Chem. Lett., 2018, 9, 1128-1133.
102. Access to new highly potent antileukemia, antiviral and antimalarial agents via hybridization of natural products (homo)egonol, thymoquinone and artemisinin. A. Çapcı Karagöz, C. Reiter, E.-J. Seo, L. Gruber, F. Hahn, M. Leidenberger, V. Klein, F. Hampel, O. Friedrich, M. Marschall, B. Kappes, T. Efferth, S. B. Tsogoeva. Bioorg. Med. Chem. 2018, 26, 3610-3618.
101. Spin-paired Solvated Electron Couples in Alkali-Ammonia Systems. M. Mauksch and S. B. Tsogoeva, Phys. Chem. Chem. Phys. (PCCP), 2018, 20, 27740-27744.
100. Strict Correlation of HOMO Topology and Magnetic Aromaticity Indices in d‐Block Metalloaromatics. M. Mauksch, S. B. Tsogoeva. Chem. Eur. J., 2018, 24, 10059-10063.
99. Novel fully organic water oxidation electrocatalysts: A quest for simplicity. Y. Wu, V. Klein, M. S. Killian, C. Behling, S. Chea, S. B. Tsogoeva, J. Bachmann. ACS Omega, 2018, 3, 2602-2608.
98. Synthesis of Thymoquinone–Artemisinin Hybrids: New Potent Antileukemia, Antiviral, and Antimalarial Agents. T. Fröhlich, C. Reiter, M. E. M. Saeed, C. Hutterer, F. Hahn, M. Leidenberger, O. Friedrich, B. Kappes, M. Marschall, T. Efferth, S. B. Tsogoeva, ACS Med. Chem. Lett., 2018, 9, 534-539.
97. Artesunate-derived monomeric, dimeric and trimeric experimental drugs – their unique mechanistic basis and pronounced antiherpesviral activity. F. Hahn, T. Fröhlich, T. Frank, L. D. Bertzbach, S. Kohrt, B. B. Kaufer, T. Stamminger, S. B. Tsogoeva, M. Marschall, Antiviral Research, 2018, 152, 104-110.
96. Treatment of Multidrug-Resistant Leukemia Cells by Novel Artemisinin-, Egonol-, and Thymoquinone-Derived Hybrid Compounds. L. Gruber, S. Abdelfatah, T. Fröhlich, C. Reiter, V. Klein, S. B. Tsogoeva, T. Efferth. Molecules, 2018, 23, 841; DOI: 10.3390/molecules23040841.

2017

95. Facile access to potent antiviral quinazoline heterocycles with fluorescence properties via merging metal-free domino reactions. F. E. Held, A. A. Guryev, T. Fröhlich, F. Hampel, A. Kahnt, C. Hutterer, M. Steingruber, H. Bahsi, C. von Bojničić-Kninski, D. S. Mattes, T. C. Foertsch, A. Nesterov-Mueller, M. Marschall, S. B. Tsogoeva, Nature Commun., 2017, 8: 15071 (Highlighted by Nature Commun. in “Synthetic and Medicinal Chemistry” Themed Collection; Featured by Science Magazine; Research in Germany; Science Newsline; Technology Networks; EurekAlert! Science News; Phys.Org; Health Medicinet; Jura Forum; Bionity.com).
94. Deeper Insight into the Six-Step Domino Reaction of Aldehydes with Malononitrile and Evaluation of Antiviral and Antimalarial Activities of the Obtained Bicyclic Products. C. M. Bock, G. Parameshwarappa, S. Bönisch, W. Bauer, C. Hutterer, M. Leidenberger, O. Friedrich, M. Marschall, B. Kappes, A. Görling, S. B. Tsogoeva. ChemistryOpen, 2017, 6, 364-374 (Cover Picture).
93. Synthesis of Novel Hybrids of Quinazoline and Artemisinin with High Activities Against Plasmodium falciparum, Human Cytomegalovirus and Leukemia Cells. T. Fröhlich, C. Reiter, M. M. Ibrahim, J. Beutel, C. Hutterer, I. Zeitträger, H. Bahsi, M. Leidenberger, O. Friedrich, B. Kappes, T. Efferth, M.Marschall, S. B. Tsogoeva, ACS Omega, 2017, 2, 2422-2431.
92. Iron-catalyzed olefin metathesis with low-valent iron alkylidenes. M. Mauksch and S. B. Tsogoeva. Chem. Eur. J. (paper dedicated to Professor Roald Hoffmann on occasion of his 80th birthday), 2017, 23, 10264-10269.
91. Cytotoxic profiling of artesunic and betulinic acids and their synthetic hybrid compound on neurons and gliomas. A. Ackermann, A. Çapcı Karagöz, A. Ghoochani, M. Buchfelder, I. Eyüpoglu, S. B. Tsogoeva, N. Savaskan, Oncotarget, 2017, DOI: 10.18632/oncotarget.18390.
90. 4N electron aromatic cycles in polycyclic hydrocarbons. M. Mauksch and S. B. Tsogoeva, Phys. Chem. Chem. Phys. (PCCP), 2017, 19, 14066-14072.
89. Synthesis of Novel Hybrids of Thymoquinone and Artemisinin with High Activity and Selectivity Against Colon Cancer. T. Fröhlich, B. Ndreshkjana, J. K. Muenzner, C. Reiter, E. Hofmeister, S. Mederer, M. Fatfat, C. El-Baba, H. Gali‑Muhtasib, R. Schneider-Stock, S. B. Tsogoeva. ChemMedChem, 2017, 12, 226-234.
88. Synthesis of (R)-modafinil via organo- and non-heme iron-catalyzed sulfoxidation using hydrogen peroxide as environmentally benign oxidant. F. E. Held, K.A. Stingl, S. B. Tsogoeva. SYMMETRY, 2017, 9(6), 88; DOI: 10.3390/sym9060088 (Cover Picture).
87. A new architecture of high spin organics based on Baird’s rule of 4n electron triplet aromatics. M. Mauksch and S. B. Tsogoeva, Phys. Chem. Chem. Phys. (PCCP), 2017, 19, 4688-4694 (Featured by Advances in Engineering).
86. Synthesis of Substituted 1,2,3-Triazoles via Metal-Free Click Cycloaddition Reactions and Alternative Cyclization Methods. H. B. Jalani, A. Çapcı Karagöz, S. B. Tsogoeva. SYNTHESIS (Special Issue to celebrate the 70th birthday of Professor Dieter Enders), 2017, 49, 29-41.

2016

85. Generation of Complex Azabicycles and Carbobicycles from Two Simple Compounds in a Single Operation via a Metal-Free Six-Step Domino Reaction. C. M. Bock, G. Parameshwarappa, S. Bönisch, C. Neiss, W. Bauer, F. Hampel, A. Görling, S. B. Tsogoeva, Chem. Eur. J. (paper dedicated to Professor Lutz F. Tietze), 2016, 22, 5189-5197 (Hot Paper – Editor’s Choice; Cover Picture; see also the Feature ARTICLE).
84. Artemisinin-Derived Dimers: Potent Antimalarial and Anticancer Agents. T. Fröhlich, A. Çapci Karagöz, C. Reiter, S. B. Tsogoeva, J. Med. Chem. (Invited Perspective), 2016, 59, 7360-7388.
83. In Vivo and In Vitro Optimization of Screening Antimalarial Hits toward Lead Molecules for Preclinical Development. T. Fröhlich and S. B. Tsogoeva, J. Med. Chem. (Invited Viewpoint), 2016, 59, 9668-9671.