Search Results - "Karpenko, Oleksandr V."

1-R-2-([1,2,4]Triazolo[1,5-c]quinazoline-2-ylthio)etanon(ol)s: Synthesis, Bioluminescence Inhibition, Molecular Docking Studies, Antibacterial and Antifungal Activities by Antypenko, Lyudmyla M, Kovalenko, Sergiy I, Karpenko, Oleksandr V, Katsev, Andrew M, Novikov, Volodymyr P, Fedyunina, Natalia S

“…The increasing mortality due to antibacterial resistance necessitates the search for novel antimicrobial agents. Hence, series of…”
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Functionalization of 2‐Trifluoromethyl‐1H‐pyrrole: A Convenient Entry into Advanced Fluorinated Building Blocks Including all Isomeric 2‐(Trifluoromethyl)prolines by Hys, Vasyl Yu, Shevchuk, Oleksandr I., Vashchenko, Bohdan V., Karpenko, Oleksandr V., Gorlova, Alina O., Grygorenko, Oleksandr O.

“…The synthetic utility of 2‐trifluoromethyl‐1H‐pyrrole as a pharmaceutically relevant platform was demonstrated by the preparation of mono‐ and bifunctional…”
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Synthesis, Anticancer, and QSAR Studies of 2-Alkyl(aryl,hetaryl)quinazolin-4(3H)-thione's and [1,2,4]Triazolo[1,5-c]quinazoline-2-thione's Thioderivatives by Antypenko, Oleksii M., Kovalenko, Sergiy I., Karpenko, Oleksandr V., Nikitin, Vladyslav O., Antypenko, Lyudmyla M.

“…Considering the frightening high level of mortality from cancer, studies of anticancer agents are vital nowadays. The 24 thioderivatives of…”
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A New One-Step Synthesis of 1,2,4-Triazino[2,3-c]quinazolines by V. Karpenko, Oleksandr, I. Kovalenko, Sergiy, O. Chekotylo, Oleksiy, V. Shishkina, Svitlana

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Functionalization of 2‐Trifluoromethyl‐1 H ‐pyrrole: A Convenient Entry into Advanced Fluorinated Building Blocks Including all Isomeric 2‐(Trifluoromethyl)prolines by Hys, Vasyl Yu, Shevchuk, Oleksandr I., Vashchenko, Bohdan V., Karpenko, Oleksandr V., Gorlova, Alina O., Grygorenko, Oleksandr O.

“…The synthetic utility of 2‐trifluoromethyl‐1 H ‐pyrrole as a pharmaceutically relevant platform was demonstrated by the preparation of mono‐ and bifunctional…”
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Synthesis, Modification, and Anticonvulsant Activity of 3′‐R 1 ‐Spiro[indoline‐3,6′‐[1,2,4]triazino[2,3 ‐c ]quinazolin]‐2,2′(7′ H )‐diones Derivatives by Voskoboynik, Oleksii Y., Kolomoets, Oleksandra S., Nosulenko, Inna S., Berest, Galina G., Bilyi, Andrii K., Karpenko, Oleksandr V., Belenichev, Igor F., Kovalenko, Sergiy I.

“…Previously unknown 3′‐R 1 ‐5‐R 2 ‐spiro[indoline‐3,6′‐[1,2,4]triazino[2,3‐ c ]quinazoline]‐2,2′‐(7′ H )‐diones and their N‐substituted analogues were obtained…”
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Synthesis, Anticancer, and QSAR Studies of 2-Alkyl(aryl,hetaryl)quinazolin-4(3H)-thione's and [1,2,4]Triazolo[1,5-c]quinazoline-2-thione' s Thioderivatives by Antypenko, Oleksii M, Kovalenko, Sergiy I, Karpenko, Oleksandr V, Nikitin, Vladyslav O, Antypenko, Lyudmyla M

“…Considering the frightening high level of mortality from cancer, studies of anticancer agents are vital nowadays. The 24 thioderivatives of…”
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Synthesis, Modification, and Anticonvulsant Activity of 3′‐R1‐Spirotriazinoquinazolin]‐2,2′(7′H)‐diones Derivatives by Voskoboynik, Oleksii Y, Kolomoets, Oleksandra S, Nosulenko, Inna S, Berest, Galina G, Bilyi, Andrii K, Karpenko, Oleksandr V, Belenichev, Igor F, Kovalenko, Sergiy I

“…Previously unknown 3′‐R1‐5‐R2‐spiro[indoline‐3,6′‐[1,2,4]triazino[2,3‐c]quinazoline]‐2,2′‐(7′H)‐diones and their N‐substituted analogues were obtained via…”
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Synthesis, Modification, and Anticonvulsant Activity of 3′‐R1‐Spiro[indoline‐3,6′‐[1,2,4]triazino[2,3‐c]quinazolin]‐2,2′(7′H)‐diones Derivatives by Voskoboynik, Oleksii Y., Kolomoets, Oleksandra S., Nosulenko, Inna S., Berest, Galina G., Bilyi, Andrii K., Karpenko, Oleksandr V., Belenichev, Igor F., Kovalenko, Sergiy I.

“…Previously unknown 3′‐R1‐5‐R2‐spiro[indoline‐3,6′‐[1,2,4]triazino[2,3‐c]quinazoline]‐2,2′‐(7′H)‐diones and their N‐substituted analogues were obtained via…”
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Synthesis of 1-(pyrrolidin-2-ylmethyl)-1H-azoles and their piperidine-derived homologues by Zhersh Sergey, Karpenko Oleksandr, Ripenko Vasyl, Tolmachev Andrey, Grygorenko Oleksandr

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