Мақаланы E-mail арқылы жіберу Synthesis of (2E,4E)-2-(4-Aryl-1,3-selenazole-2-yl)-5-phenylpenta-2,4-diennitriles
- Авторлар: Frolov K.A.1,2, Krivokolysko B.S.1,2, Aksenov N.A.3, Krivokolysko S.G.1,2
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Мекемелер:
- Chemex Lab of the Dahl Lugansk State University
- St. Luke Lugansk State Medical University
- North Caucasus Federal University
- Шығарылым: Том 61, № 4 (2025)
- Беттер: 442-446
- Бөлім: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://medjrf.com/0514-7492/article/view/689664
- DOI: https://doi.org/10.31857/S0514749225040098
- EDN: https://elibrary.ru/SDXUJN
- ID: 689664
Дәйексөз келтіру
Ашық рұқсат
Рұқсат берілді
Аннотация
Upon the interaction of (2E,4E)-5-phenyl-2-cyano-2,4-pentadieneselenoamide with α-bromoketones in DMF under argon (2E,4E)-2-(4-aryl-1,3-selenazole-2-yl)-5-phenylpenta-2,4-diennitriles were obtained with yields 42-71%.
Толық мәтін
Авторлар туралы
Konstantin Frolov
Chemex Lab of the Dahl Lugansk State University; St. Luke Lugansk State Medical University
Хат алмасуға жауапты Автор.
Email: ksg-group-lugansk@mail.ru
ORCID iD: 0000-0002-8045-7582
Ресей, 20A/7, Molodyozhny Nbhd., Lugansk, 291034; 1G, 50 let Oborony Luganska Nbhd., Lugansk, 291045
Bogdan Krivokolysko
Chemex Lab of the Dahl Lugansk State University; St. Luke Lugansk State Medical University
Email: ksg-group-lugansk@mail.ru
ORCID iD: 0000-0002-3181-7609
Ресей, 20A/7, Molodyozhny Nbhd., Lugansk, 291034; 1G, 50 let Oborony Luganska Nbhd., Lugansk, 291045
Nikolay Aksenov
North Caucasus Federal University
Email: ksg-group-lugansk@mail.ru
ORCID iD: 0000-0002-7125-9066
Ресей, 1A, Pushkin St., Stavropol, 355009
Sergey Krivokolysko
Chemex Lab of the Dahl Lugansk State University; St. Luke Lugansk State Medical University
Email: ksg-group-lugansk@mail.ru
ORCID iD: 0000-0001-9879-9217
Ресей, 20A/7, Molodyozhny Nbhd., Lugansk, 291034; 1G, 50 let Oborony Luganska Nbhd., Lugansk, 291045
Әдебиет тізімі
- Iwaoka M., Arai K. Curr. Chem. Biol. 2013, 7, 2–24. doi: 10.2174/2212796811307010002
- Refaay D.A., Ahmed D.M., Mowafy A.M., Shaaban S. Med. Chem. Res. 2022, 31, 894–904. doi: 10.1007/s00044-022-02879-x
- Obieziurska-Fabisiak M., Pacuła-Miszewska A.J., Laskowska A., Scianowski J. Arkivoc. 2022, 2023 (5), 69–92. doi: 10.24820/ark.5550190.p011.908
- Makhaeva N.A., Amosova S.V., Filippov A.S., Potapov V.A., Musalov M.V. Biomolecules. 2024, 14, 1546. doi: 10.3390/biom14121546
- Dotsenko V.V., Frolov K.A., Krivokolysko S.G. Chem. Heterocyclic Comp. 2013, 49, 657–675. doi: 10.1007/s10593-013-1296-z
- Frolov K.A., Dotsenko V.V., Krivokolysko S.G. Chem. Heterocyclic Comp. 2013, 48, 1555–1561. doi: 10.1007/s10593-013-1173-9
- Pakholka N.A., Dotsenko V.V., Krivokolysko B.S., Frolov K.A., Aksenov N.A., Aksenova I.V., Shcherbakov S.V., Ovcharov S.N., Krivokolysko S.G. Russ. J. Gen. Chem. 2021, 91, 606–613. doi: 10.1134/S1070363221040058
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