O,S,Se-containing Biginelli products based on cyclic β-ketosulfone and their postfunctionalization von Dil, Kateryna V, Palchykov, Vitalii A

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Rh-catalyzed cyclization of carbamates–synthesis of a new heterocyclic system: tetrahydro-3H-4-oxa-2-thia-2b-azacyclopropa[cd]pentalen-3-one 2,2-dioxide von Dil, Kateryna V., Kozyriev, Yevhenii K., Palchykov, Vitalii A.

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Synthesis of 2-hexyl-5-ethylfuran-3-sulfonic acid (HEFS) – natural antithrombosis agent from Eisenia earthworms von Palchykov, Vitalii A.

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Fused chiral azaheterocycles based on monosubstituted ferrocenes von Tymoshenko, Kyrylo I., Palchykov, Vitalii A.

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Recent progress in the synthesis of morpholines von Palchykov, Vitalii A., Chebanov, Valentyn A.

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Open and rearranged norbornane derived polycyclic cage molecules as potential neuroprotective agents through attenuation of MPP+- and calcium overload-induced excitotoxicity in neu... von Egunlusi, Ayodeji O., Malan, Sarel F., Omoruyi, Sylvester I., Ekpo, Okobi E., Palchykov, Vitalii A., Joubert, Jacques

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Thiopyran-3-one 1,1-dioxides in the synthesis of heterocycles (microreview) von Kozirev, Eugene K., Palchykov, Vitalii A.

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Targeting a Cryptic Pocket in a Protein–Protein Contact by Disulfide-Induced Rupture of a Homodimeric Interface von Nguyen, Dzung, Xie, Xiulan, Jakobi, Stephan, Terwesten, Felix, Metz, Alexander, Nguyen, T. X. Phong, Palchykov, Vitalii A, Heine, Andreas, Reuter, Klaus, Klebe, Gerhard

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Dihydro-2H-thiopyran-3(4H)-one-1,1-dioxide – a versatile building block for the synthesis of new thiopyran-based heterocyclic systems von Palchykov, Vitalii A, Chabanenko, Roman M, Konshin, Valeriy V, Dotsenko, Victor V, Krivokolysko, Sergey G, Chigorina, Elena A, Horak, Yuriy I, Lytvyn, Roman Z, Vakhula, Andriy A, Obushak, Mykola D, Mazepa, Alexander V

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Cage-Like Amines in the Green Protocol of Transannular Thieno[2,3-d]Pyrimidinone Formation as Promising Anticancer Agents von Shyyka, Olga Ya, Pokhodylo, Nazariy T., Palchykov, Vitalii A., Finiuk, Nataliya S., Stoika, Rostyslav S., Obushak, Mykola D.

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Grignard Reagents and Their N‐analogues in the Synthesis of Tricyclic and Tetracyclic Cage‐like Lactams von Tkachenko, Igor V., Tarabara, Igor N., Omelchenko, Irina V., Palchykov, Vitalii A.

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The formation of the salt and neutral molecule cocrystal from equimolar solution of heliamine and bicyclo[2.2.1]hept‐5‐ene‐endo‐2,3‐dicarboxylic acid von Shishkina, Svitlana V., Isaiev, Ivan A., Urzhuntseva, Viktoriya V., Palchykov, Vitalii A.

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Synthesis of challenging 6-functionalized 1-oxaspiro[3.3]heptanes – New scaffolds for drug discovery von Kozyriev, Yevhenii K., Palchykov, Vitalii A.

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Ring-chain tautomerism of vicinal hydroxyimines bearing sulfolane moiety von Zarovnaya, Iryna S., Shishkina, Svitlana V., Palchykov, Vitalii A.

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Synthesis of new azapolycyclic scaffolds via the domino aminolysis of dicyclopentadiene diepoxide in water von Palchykov, Vitalii A., Gaponova, Rita G., Omelchenko, Iryna V., Kasyan, Liliya I.

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Synthesis and characterization of sulfolane-based amino alcohols: A combined experimental and computational study von Palchykov, Vitalii A., Zarovnaya, Iryna S., Tretiakov, Serhii V., Reshetnyak, Alyona V., Omelchenko, Iryna V., Shishkin, Oleg V., Okovytyy, Sergiy I.

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Dihydro-2 H -thiopyran-3(4 H )-one-1,1-dioxide – a versatile building block for the synthesis of new thiopyran-based heterocyclic systems von Palchykov, Vitalii A., Chabanenko, Roman M., Konshin, Valeriy V., Dotsenko, Victor V., Krivokolysko, Sergey G., Chigorina, Elena A., Horak, Yuriy I., Lytvyn, Roman Z., Vakhula, Andriy A., Obushak, Mykola D., Mazepa, Alexander V.

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Dihydro-2H-thiopyran-3(4H)-one-1,1-dioxide - a versatile building block for the synthesis of new thiopyran-based heterocyclic systemsElectronic supplementary information (ESI) avai... von Palchykov, Vitalii A, Chabanenko, Roman M, Konshin, Valeriy V, Dotsenko, Victor V, Krivokolysko, Sergey G, Chigorina, Elena A, Horak, Yuriy I, Lytvyn, Roman Z, Vakhula, Andriy A, Obushak, Mykola D, Mazepa, Alexander V

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Chemical composition and antibacterial effect of ethanolic extract of Buxus sempervirens on cryogenic strains of microorganisms in vitro von Palchykov, Vitalii A., Zazharskyi, Vladimir V., Brygadyrenko, Viktor V., Davydenko, Pavel O., Kulishenko, Oleg M., Borovik, Irina V.

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ВОНА ЗАВЖДИ ПРАЦЮВАЛА З НАТХНЕННЯМ І ВМІЛА НАДИХАТИ ІНШИХ von С. Коваленко, Валерій, О. Пальчиков, Віталій, І. Оковитий, Сергій, В. Стець, Надія

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