Мақаланы E-mail арқылы жіберу SYNTHESIS OF 2,6-BIS(1H-IMIDAZOLE-2-YL)-4-CHLOROPYRIDINE
- Авторлар: Os'kina I.A.1, Lavrenova L.G.2, Tikhonov A.Y.1
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Мекемелер:
- Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences
- Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences
- Шығарылым: Том 61, № 3 (2025)
- Беттер: 338-340
- Бөлім: КРАТКОЕ СООБЩЕНИЕ
- URL: https://journals.rcsi.science/0514-7492/article/view/304584
- DOI: https://doi.org/10.31857/S0514749225030164
- EDN: https://elibrary.ru/evdlpm
- ID: 304584
Дәйексөз келтіру
Ашық рұқсат
Рұқсат берілді
Тек жазылушылар үшін
Аннотация
On the basis of helidamic acid, 4-chloropyridine-2,6-dicarboxamide and 4-chloropyridine-2,6-dicarbonitrile were synthesized sequentially, the interaction of which with diethyl acetal aminoacetaldehyde led to 2,6-bis(1H-imidazole-2-yl)-4-chloropyridine, a tridentate ligand.
Негізгі сөздер
Авторлар туралы
I. Os'kina
Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences
Email: oi@nioch.nsc.ru
prosp. Akad. Lavrentieva, 9, Novosibirsk, 630090 Russia
L. Lavrenova
Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciencespr. Akademika Lavrent’eva, 3, Novosibirsk, 630090 Russia
A. Tikhonov
Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciencesprosp. Akad. Lavrentieva, 9, Novosibirsk, 630090 Russia
Әдебиет тізімі
- Voss M.E., Beer C.M., Mitchell S.A., Blomgren P.A., Zhichkin P.E. Tetrahedron 2008, 64, 645–651. doi: 10.1016/j.tet.2007.11.009
- Rigsby M.L., Mandal S., Nam W., Spencer L.C., Llo- bet A., Stahl S. Chem. Sci. 2012, 3, 3058–3062. doi: 10.1039/C2SC20755A
- Shakirova O.G., Os'kina I.A., Korotaev E.V., Petrov S.A., Kuratieva N.V., Tikhonov A.Ya., Lavrenova L.G. Int. J. Mol. Sci. 2023, 24, 9853. doi: 10.3390/ijms24129853
- La Tour J.V., Wallis K.P., Le P., Hoss U. Пат. US20220202326A1 (2022). США. C.A. 2023, 179, 170111.
- Hommes P., Fischer C., Lindner C., Zipse H., Reis- sig H.-U. Angew. Chem. Int. Ed. 2014, 53, 7647–7651. doi: 10.1002/anie.201403403
- Wu K.-L., Ho S.-T., Chou C.-C., Chang Y.-C., Pan H.-A., Chi Y., Chou P.-T. Angew. Chem. Int. Ed. 2012, 51, 5642–5646. doi: 10.1002/anie.201200071
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