Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Oleg V. Zaremba"'
Autor:
Veronika R. Karpina, S. M. Kovalenko, Oleg V. Zaremba, O. V. Silin, V. V. Ivanov, S. S. Kovalenko, T. Langer
Publikováno v:
Журнал органічної та фармацевтичної хімії, Vol 17, Iss 3, Pp 5-14 (2019)
The Pim-1 enzyme from the serine/threonine protein kinase family is a likely target for the targeted therapy of tumors of hematopoietic and lymphoid tissues. Triazolopyridine is an universal scaffold upon which international scientific programs have
Externí odkaz:
https://doaj.org/article/e7d756312eed487b878994d3f9a20086
Autor:
Vladimir I. Bozhanov, Dmytro P. Bohdan, Oleksandr V. Borysov, Aleksey V. Silin, Oleg V. Zaremba, Mykola M. Avramenko, Dmitriy M. Volochnyuk, Sergey V. Ryabukhin, Konstantin S. Gavrilenko
Publikováno v:
ChemistrySelect. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ddff4d251ab55d142a3f6861e427778
https://doi.org/10.1002/slct.202104287
https://doi.org/10.1002/slct.202104287
Autor:
Eugeniy N. Ostapchuk, Oleg V. Zaremba, Oleksandr O. Grygorenko, Artem Artemenko, Yevhen Yurov, Bohdan V. Vashchenko, Oleksandr V. Hryshchuk, Yuliia Filimonova, Yevhenii M. Sokolenko
Publikováno v:
The Journal of Organic Chemistry. 84:13908-13921
An approach to di- and trihetera[3.3.n]propellanes (n = 2–4 ), advanced morpholine and piperazine analogues, is developed. The key step of the reaction sequence included a [3 + 2] cycloaddition rea...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02c630d3b9fa32937ecd078c2ea4e8f0
https://doi.org/10.1021/acs.joc.9b02067
https://doi.org/10.1021/acs.joc.9b02067
Autor:
Yevhenii M, Sokolenko, Yevhen Yu, Yurov, Bohdan V, Vashchenko, Oleksandr V, Hryshchuk, Yuliia, Filimonova, Eugeniy N, Ostapchuk, Artem, Artemenko, Oleg V, Zaremba, Oleksandr O, Grygorenko
Publikováno v:
The Journal of organic chemistry. 84(21)
An approach to di- and trihetera[3.3.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d44a062a7494a9de697b7ab2d6ab3bd0
https://pubmed.ncbi.nlm.nih.gov/31509707
https://pubmed.ncbi.nlm.nih.gov/31509707
Publikováno v:
Journal of Organic and Pharmaceutical Chemistry. 12:70-75
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c74024050043b9dadb2d95dc0ae5cc35
https://doi.org/10.24959/ophcj.14.792
https://doi.org/10.24959/ophcj.14.792
Autor:
Madina G. Kadieva, Sergiy M. Kovalenko, Sergey E. Tkachenko, Irina M. Ravnyeyko, Elena S. Golovina, Oleg D. Mitkin, Ilya Okun, Oleg V. Zaremba, Alexandre V. Ivachtchenko, Angela G. Koryakova
Publikováno v:
Bioorganic & Medicinal Chemistry. 18:5282-5290
A number of 3-(phenylsulfonyl)thieno[2,3-e][1,2,3]triazolo[1,5-a]pyrimidines were prepared and their 5-HT6 receptor binding affinity and ability to inhibit the functional cellular responses to serotonin were evaluated. 3-[(3-Chlorophenyl)sulfonyl]-N-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9885c12940216d8379c0ad034f43139
https://doi.org/10.1016/j.bmc.2010.05.051
https://doi.org/10.1016/j.bmc.2010.05.051
Autor:
Oleg V. Shishkin, Yuriy V. Sedash, Oleg V. Zaremba, Sergiy M. Kovalenko, Nikolay Yu. Gorobets, Konstantin S. Ostras, Vyacheslav N. Baumer, Svetlana V. Shishkina, Erik V. Van der Eycken, Sergey M. Desenko
Publikováno v:
Tetrahedron Letters. 51:2095-2098
A Biginelli-like three-component condensation using 3-amino-1,2,4-triazole as urea component resulted in an unexpected alternative direction of the tetrahydropyrimidine ring formation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0ff8a799d513026d0e9d05bcbb47a00
https://doi.org/10.1016/j.tetlet.2010.02.045
https://doi.org/10.1016/j.tetlet.2010.02.045
Autor:
S. S. Kovalenko, Oleksandr S. Detistov, Valentin P. Chernykh, Sergiy M. Kovalenko, Irina O. Zhuravel, Oleg V. Zaremba
Publikováno v:
Synthetic Communications. 38:3778-3784
New 5-hydroxymethyl-8-methyl-3-(3-aryl-[1,2,4]oxadiazol-5-yl)-2H-pyrano-[2,3-c]pyridin-2-ones and their esters were synthesized. The structure of obtained compounds was determined through a complete 1H NMR analysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78db32398f55e608bfef5607954c719b
https://doi.org/10.1080/00397910802219445
https://doi.org/10.1080/00397910802219445
Autor:
Olena V. Il'chenko, Oleg V. Zaremba, Sergiy M. Kovalenko, Valentin P. Chernykh, Aliaksandr A. Sherakov
Publikováno v:
Synthetic Communications. 37:2559-2568
With the purpose of searching for new biologically active compounds, a method of synthesis of new heterocyclic systems [3‐alkyl(aryl)‐2‐thioxo‐2,3‐dihydro‐1H‐benzofuro[3,2‐d]pyrimidin‐4(1H)‐ones] has been developed. The method is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d069193e5a08a72bcea48b3f08a08c49
https://doi.org/10.1080/00397910701462831
https://doi.org/10.1080/00397910701462831
Autor:
Yuriy V. Sedash, Konstantin S. Ostras, Sergiy M. Kovalenko, Svetlana V. Shishkina, Oleg V. Shishkin, Vyacheslav N. Baumer, Oleg V. Zaremba, Nikolay Yu. Gorobets, Sergey M. Desenko, Erik V. Van der Eycken
Publikováno v:
ChemInform. 41
It is demonstrated that the title compound behaves differently compared to other aminoazoles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84ed92870b40fd3add7eb949314806c1
https://doi.org/10.1002/chin.201032164
https://doi.org/10.1002/chin.201032164