Organosilicon derivatives based on 2-aminothiazolium cations
- 作者: Yarosh N.1, Dorofeev I.1, Zhilitskaya L.1
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隶属关系:
- Favorskii Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences
- 期: 卷 59, 编号 5 (2023)
- 页面: 588-595
- 栏目: Articles
- URL: https://journals.rcsi.science/0514-7492/article/view/145078
- DOI: https://doi.org/10.31857/S051474922305004X
- EDN: https://elibrary.ru/DQJOND
- ID: 145078
如何引用文章
详细
The reactions of 2-aminothiazole and 2-aminobenzothiazole with (iodomethyl) derivatives of silanes in the absence of a base gave the previously unknown organosilicon salts and ionic liquids of 2-aminothiazole and 2-aminobenzothiazole. Structure of the obtained compounds was proved by NMR, and UV spectroscopy methods.
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作者简介
N. Yarosh
Favorskii Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences
Email: yarosh.nina@irioch.irk.ru
I. Dorofeev
Favorskii Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences
Email: yarosh.nina@irioch.irk.ru
L. Zhilitskaya
Favorskii Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences
Email: yarosh.nina@irioch.irk.ru
参考
- Galochkina A.V., Bollikanda R.K., Zarubaev V.V., Tentler D.G., Lavrenteva I.N., Slita A.V., Chirra N., Kantevari S. Arch. Pharm. Chem. Life Sci. 2019, 352, e1800225. doi: 10.1002/ardp.201800225
- Sultanova R.M., Lobov A.N., Shumadalova A.V., Meshcheryakova S.A., Zileeva Z.R., Khusnutdinova N.S., Vakhitov V.A., Vakhitova Y.V. Nat. Prod. Res. 2021, 35, 1340-1348. doi: 10.1080/14786419.2019.16484592
- Shareef M.A., Devi G.P., Routhu S.R., Kumar C.G., Kamal A., Babu B.N. RSC Med. Chem. 2020, 11, 1178-1184. doi: 10.1039/D0MD00188K
- Alizadeh S.R., Hashemi S.M. Med. Chem. Res. 2021, 30, 771-806. doi: 10.1007/s00044-020-02686-2
- Bala R., Kumari P., Sood S., Kumar V., Singh N., Singh, K. J. Heterocycl. Chem. 2018, 55, 2507-2515. doi: 10.1002/jhet.3282
- Maghraby M.T.-E., Abou-Ghadir O.M.F., Abdel-Moty S.G., Ali A.Y., Salem O.I.A. Bioorg. Med. Chem. 2020, 28, 7115403. doi: 10.1016/j.bmc.2020.115403
- Reddy G.M., Garcia J.R., Reddy V.H., de Andrade A.M., Camilo A.Jr., Ribeiro R.A.P., de Lazaro S.R. Eur. J. Med. Chem. 2016, 123, 508-513. doi: 10.1016/j.ejmech.2016.07.062
- Giri R.S., Thaker H.M., Giordano T., Williams J., Rogers D., Sudersanam V., Vasu K.K. Eur. J. Med. Chem. 2009, 44. 2184-2189. doi: 10.1016/j.ejmech.2008.10.031
- Mao W., Ning M., Liu Z., Zhu Q., Leng Y., Zhang A. Bioorg. Med. Chem. 2012, 20, 2982-2991. doi: 10.1016/j.bmc.2012.03.008.
- Siddiqui N., Ahsan W. Med. Chem. Res. 2011, 20, 261-268. doi: 10.1007/s00044-010-9313-6
- Rezaei Z., Sarkari B., Khabnadideh S., Farjami M., Mehrjou M., Yazdi A., Riazimontazer E., Fararouei M. Anti-Infect. Agents. 2020, 18, 178-189. doi: 10.2174/2211352517666190527112955
- Bueno J.M., Carda M., Crespo B., Cuñat A.C., Cozar C., León M.L., Marco J.A., Roda N., Sanz-Cervera J.F. Bioorg. Med. Chem. Lett. 2016, 26, 3938-3944. doi: 10.1016/j.bmcl.2016.07.010.
- Kim D.-S., Chun S.-J., Jeon J.-J., Lee S.-W., Joe G.-H. Pest. Manag. Sci. 2004, 60, 1007-1012. doi: 10.1002/ps.873
- Maradiya H.R. J. Saudi Chem. Soc. 2012, 16, 69-74. doi: 10.1016/j.jscs.2010.10.021
- Elshaarawy R.F.M., Mustafa F.H.A., Sofy A.R., Hmed A.A., Janiak C. J. Environment. Chem. Engineer. 2019, 7. 102800. doi: 10.1016/j.jece.2018.11.044
- Wang X., Lv P., Zou H., Li Y., Li X., Liao Y. Industr. Engineer. Chem. Res. 2016, 55, 4911-4918. doi: 10.1021/acs.iecr.5b04630
- Xu Y., Yang L., Wang H., Zhang Y., Yang X., Pei M., Zhang G. J. Photochem. Photobiolog, A Chem. 2020, 391, 112372. doi: 10.1016/j.jphotochem.2020.112372
- Zablotskaya A., Segal I., Germane S., Shestakova I., Domracheva I., Nesterova A., Geronikaki A., Lukevics E. Chem. Heterocycl. Compd. 2002, 38, 859-866. doi: 10.1023/A:1020698107686
- Дорофеев И.А., Жилицкая Л.В., Ярош Н.О. ЖОХ. 2022, 92, 740-745.
- Dorofeev I.А., Zhilitskaya L.V., Yarosh N.О. Russ. J. Gen. Chem. 2022, 92, 806-810. doi: 10.31857/S0044460X22050092
- Шагун Л.Г., Дорофеев И.А., Жилицкая Л.В., Ярош Н.О., Ларина Л.И. ЖОрХ. 2019, 55, 1084-1088.
- Shagun L.G., Dorofeev I.А., Zhilitskaya L.V., Yarosh N.О., Larina L.I. Russ. J. Org. Chem. 2019, 55, 983-987. doi: 10.1134/S107042801907011
- Ярош Н.О., Жилицкая Л.В., Шагун Л.Г., Дорофеев И.А., Ларина Л.И. ЖОрХ. 2019, 55, 1157-1162.
- Yarosh N.О., Zhilitskaya L.V., Shagun L.G., Dorofeev I.А., Larina L.I. Russ. J. Org. Chem. 2019, 55, 1625-1629. doi: 10.1134/S0512749219080019
- Жилицкая Л.В., Ярош Н.О., Шагун Л.Г., Дорофеев И.А. ЖОХ. 2019, 89, 1239-1244.
- Zhilitskaya L.V., Yarosh N.О., Shagun L.G., Dorofeev I.А. Russ. J. Gen. Chem. 2019, 89, 1625-1629. doi: 10.1134/S1070363219080127
- Meakins G.D., Musk S.R.R., Robertson C.A., Woodhouse L.S. J. Chem. Soc. Perkin Trans. 1. 1989, 643-648. doi: 10.1039/P19890000643
- Дорофеев И.А., Жилицкая Л.В., Ярош Н.О. ЖОХ. 2021, 91, 1937-1943.
- Dorofeev I.А., Zhilitskaya L.V., Yarosh N.О. Russ. J. Gen. Chem. 2021, 91, 2447-2452. doi: 10.1134/S1070363221120136
- Reiller P., Mercier-Bion F., Gimenez N., Barre N., Miserque F. Radiochim. Acta. 2006, 94, 739-745. doi: 10.1524/ract.2006.94.9.739
- http://www.pharmaexpert.ru/PASSOnline
- Страдомский Б.В., Солодунов Ю.Ю. Экспериментальная и клиническая фармакология мазевых форм cтелланина (1,3-диэтилбензимидазолия трийодида). Ростов-на-Дону: Изд-во ЮНЦ РАН, 2013.
- Мелоян Е.К., Сафроненко А.В., Ганцгорн Е.В., Хмара Л.Е., Голубева А.О., Джабр М.А. Биомедицина. 2021, 17, 111-117.
- Meloyan E.K., Safronenko A.V., Gantsgorn E.V., Hmara L.E., Golubeva A.O., Jabr M.A. J. Biomed. 2021, 17, 111-117. doi: 10.33647/2074-5982-17-3-111-118