Total Synthesis of (18S)- and (18R)-Homolargazole by Rhodium-Catalyzed Hydrocarboxylation von Schotes, Christoph, Ostrovskyi, Dmytro, Senger, Johanna, Schmidtkunz, Karin, Jung, Manfred, Breit, Bernhard

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Structure-Based Design, Docking and Binding Free Energy Calculations of A366 Derivatives as Spindlin1 Inhibitors von Luise, Chiara, Robaa, Dina, Regenass, Pierre, Maurer, David, Ostrovskyi, Dmytro, Seifert, Ludwig, Bacher, Johannes, Burgahn, Teresa, Wagner, Tobias, Seitz, Johannes, Greschik, Holger, Park, Kwang-Su, Xiong, Yan, Jin, Jian, Schüle, Roland, Breit, Bernhard, Jung, Manfred, Sippl, Wolfgang

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A general strategy for the synthesis of difluoromethyl-containing pyrazoles, pyridines and pyrimidines von Iaroshenko, Viktor O., Specowius, Verena, Vlach, Katharina, Vilches-Herrera, Marcelo, Ostrovskyi, Dmytro, Mkrtchyan, Satenik, Villinger, Alexander, Langer, Peter

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Preparation data of the bromodomains BRD3(1), BRD3(2), BRD4(1), and BRPF1B and crystallization of BRD4(1)-inhibitor complexes von Hügle, Martin, Lucas, Xavier, Weitzel, Gerhard, Ostrovskyi, Dmytro, Breit, Bernhard, Gerhardt, Stefan, Schmidtkunz, Karin, Jung, Manfred, Schüle, Roland, Einsle, Oliver, Günther, Stefan, Wohlwend, Daniel

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4‑Acyl Pyrrole Derivatives Yield Novel Vectors for Designing Inhibitors of the Acetyl-Lysine Recognition Site of BRD4(1) von Hügle, Martin, Lucas, Xavier, Weitzel, Gerhard, Ostrovskyi, Dmytro, Breit, Bernhard, Gerhardt, Stefan, Einsle, Oliver, Günther, Stefan, Wohlwend, Daniel

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Beyond the BET Family: Targeting CBP/p300 with 4‐Acyl Pyrroles von Hügle, Martin, Lucas, Xavier, Ostrovskyi, Dmytro, Regenass, Pierre, Gerhardt, Stefan, Einsle, Oliver, Hau, Mirjam, Jung, Manfred, Breit, Bernhard, Günther, Stefan, Wohlwend, Daniel

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Synthesis of Fluorinated Purine and 1-Deazapurine Glycosides as Potential Inhibitors of Adenosine Deaminase von Iaroshenko, Viktor O, Ostrovskyi, Dmytro, Petrosyan, Andranik, Mkrtchyan, Satenik, Villinger, Alexander, Langer, Peter

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Synthesis of 4-Trifluoromethylpyridines by [5+1] Cyclization of 3-Hydroxy-pent-4-yn-1-ones with Urea von Iaroshenko, Viktor O., Ostrovskyi, Dmytro, Ayub, Khurshid, Spannenberg, Anke, Langer, Peter

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Efficient synthesis of purines by inverse electron-demand Diels―Alder reactions of 1-substituted-1H-imidazol-5-amines with 1,3,5-triazines von IAROSHENKO, Viktor O, MAALIK, Aneela, OSTROVSKYI, Dmytro, VILLINGER, Alexander, SPANNENBERG, Anke, LANGER, Peter

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Design and Synthesis of Polycyclic Imidazole-Containing N- Heterocycles based on CH Activation/Cyclization Reactions von Iaroshenko, Viktor O., Ostrovskyi, Dmytro, Miliutina, Mariia, Maalik, Aneela, Villinger, Alexander, Tolmachev, Andrei, Volochnyuk, Dmitriy M., Langer, Peter

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3-Methoxalylchromone--a novel versatile reagent for the regioselective purine isostere synthesis von Mkrtchyan, Satenik, Iaroshenko, Viktor O, Dudkin, Sergii, Gevorgyan, Ashot, Vilches-Herrera, Marcelo, Ghazaryan, Gagik, Volochnyuk, Dmitriy M, Ostrovskyi, Dmytro, Ahmed, Zeeshan, Villinger, Alexander, Sosnovskikh, Vyacheslav Ya, Langer, Peter

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Design, synthesis and transformation of some heteroannulated 3-aminopyridines—purine isosteres with exocyclic nitrogen atom von Iaroshenko, Viktor O., Vilches-Herrera, Marcelo, Gevorgyan, Ashot, Mkrtchyan, Satenik, Arakelyan, Knar, Ostrovskyi, Dmytro, Abbasi, Muhammad S.A., Supe, Linda, Hakobyan, Ani, Villinger, Alexander, Volochnyuk, Dmitriy M., Tolmachev, Andrei

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Tofacitinib and analogs as inhibitors of the histone kinase PRK1 (PKN1) von Ostrovskyi, Dmytro, Rumpf, Tobias, Eib, Julia, Lumbroso, Alexandre, Slynko, Inna, Klaeger, Susan, Heinzlmeir, Stephanie, Forster, Michael, Gehringer, Matthias, Pfaffenrot, Ellen, Bauer, Silke Mona, Schmidtkunz, Karin, Wenzler, Sandra, Metzger, Eric, Kuster, Bernhard, Laufer, Stefan, Schüle, Roland, Sippl, Wolfgang, Breit, Bernhard, Jung, Manfred

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Efficient synthesis of purines by inverse electron-demand Diels–Alder reactions of 1-substituted-1 H-imidazol-5-amines with 1,3,5-triazines von Iaroshenko, Viktor O., Maalik, Aneela, Ostrovskyi, Dmytro, Villinger, Alexander, Spannenberg, Anke, Langer, Peter

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Beyond the BET Family: Targeting CBP/p300 with 4‐Acyl Pyrroles von Hügle, Martin, Lucas, Xavier, Ostrovskyi, Dmytro, Regenass, Pierre, Gerhardt, Stefan, Einsle, Oliver, Hau, Mirjam, Jung, Manfred, Breit, Bernhard, Günther, Stefan, Wohlwend, Daniel

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Method for the preparation of cannabidiol von Zuhse, Ralf, Ostrovskyi, Dmytro

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METHOD FOR PREPARING CANNABIDIOL von OSTROVSKYI, Dmytro, ZUHSE, Ralf

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METHOD FOR THE PREPARATION OF CANNABIDIOL von OSTROVSKYI, DMYTRO, ZUHSE, RALF

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METHOD FOR PREPARING CANNABIDIOL von OSTROVSKYI, Dmytro, ZUHSE, Ralf

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3-Methoxalylchromone-a novel versatile reagent for the regioselective purine isostere synthesisElectronic supplementary information (ESI) available: Experimental details and 1H and... von Mkrtchyan, Satenik, Iaroshenko, Viktor O, Dudkin, Sergii, Gevorgyan, Ashot, Vilches-Herrera, Marcelo, Ghazaryan, Gagik, Volochnyuk, Dmitriy M, Ostrovskyi, Dmytro, Ahmed, Zeeshan, Villinger, Alexander, Sosnovskikh, Vyacheslav Ya, Langer, Peter

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