Synthesis of MONO- and BIS-Polyfluoroalcholate Derivatives Containing Aryl Ethers and Thioethers
- Authors: Soboleva E.A.1, Shelkovnikov V.V.1,2, Chernonosov A.A.3
-
Affiliations:
- Novosibirsk Institute of Organic Chemistry im. Vorozhtsova, Siberian Branch Russian Academy of Sciences
- Novosibirsk State Technical University
- Institute of Chemical Biology and Fundamental Medicine, Siberian Branch Russian Academy of Sciences
- Issue: Vol 61, No 10 (2025)
- Pages: 1503-1513
- Section: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://journals.rcsi.science/0514-7492/article/view/380887
- DOI: https://doi.org/10.7868/S3034630425100126
- ID: 380887
Cite item
Abstract
About the authors
E. A. Soboleva
Novosibirsk Institute of Organic Chemistry im. Vorozhtsova, Siberian Branch Russian Academy of Sciences
Email: lena9618745603@yandex.ru
ORCID iD: 0009-0009-2633-5734
Novosibirsk, Russia
V. V. Shelkovnikov
Novosibirsk Institute of Organic Chemistry im. Vorozhtsova, Siberian Branch Russian Academy of Sciences; Novosibirsk State Technical University
ORCID iD: 0009-0001-3364-668X
Novosibirsk, Russia; Novosibirsk, Russia
A. A. Chernonosov
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch Russian Academy of Sciences
ORCID iD: 0000-0001-8362-2443
Novosibirsk, Russia
References
- Shalaby M.A., Rizk S.A., Fahim A.M. Orog. Biomol. Chem. 2023, 21, 5317–5346. https://doi.org/10.1039/d3ob00792h
- Omar S., Shkir M., Khan M.Aj., Ahmad Z., AlFaify S. Optik. 2020, 204, 164172. https://doi.org/10.1016/j.ijleo.2020.164172
- Morsy N.M., Hassan A.S. Eur. J. Chem. 2022, 13 (2), 241-252. https://doi.org/10.5155/eurjchem.13.2.241-252.2245
- Mellado M., Sariego-Kluge R., Valdes-Navarro F., González C., Sánchez-González R., Pizarro N., Villena J., Jara-Gutierrez C., Cordova C., Bravo M.A., Aguilar L.F. Spectrochim. Acta A. 2023, 291, 122332. https://doi.org/10.1016/j.saa.2023.122332
- Cibin F.R., Doddi G., Mencarelli P. Tetrahedron. 2003, 59, 3455-3459. https://doi.org/10.1016/S0040-4020(03)00475-7
- Si Z. K., Zhang Q., Xue M. Z., Sheng Q. R., Liu Y. G. Res. Chem. Intermed. 2011, 37, 635-646. https://doi.org/10.1007/s11164-010-0236-0
- Tamilvanan M., Pandurangan A., Subramanian K., Reddy B.S.R. Polym. Adv. Technol. 2008, 19, 1218-1225. https://doi.org/10.1002/pat.1114
- Balaji R., Grande D., Nanjundan S. React. Funct. Polym. 2003, 56, 45-57. https://doi.org/10.1016/S1381-5148(03)00031-2
- Selvam P., Nanjundan S. React. Funct. Polym. 2005, 62, 179-193. https://doi.org/10.1016/j.reactfunctpolym.2004.10.003
- Selvam P., Babu K.V., Nanjundan S. Eur. Polym. J. 2005, 41, 35-45. https://doi.org/10.1016/j.eurpolymj.2004.8.015
- Li X.-D., Zhong Z.-X., Kim J. J., Lee M.-H. Macromol. Rapid Commun. 2004, 25, 1090-1094. https://doi.org/10.1002/marc.200400039
- Li X.-D., Zhong Z.-X., Lee S.H., Chang G., Lee M.-H. Appl. Phys. Lett. 2005, 86, 131912. https://doi.org/10.1063/1.1894604
- Pereira R., Silva A.M.S., Ribeiro D., Silva V.L.M., Fernandes E. Eur. J. Med. Chem. 2023, 252, 115280. https://doi.org/10.1016/j.ejmech.2023.115280
- Orlova H.A., Mahor E.Φ., Geracimova T.H. Изв. Сиб. отд. АН СССР. Сер. хим. наук. 1989, 3, 117-123.
- Соболева Е.А., Орлова Н.А., Шелковников В.В. ЖОРх. 2018, 54 (10), 1474-1480. https://doi.org/10.1134/S1070428018100081
- Бородина Е.А., Орлова Н.А., Шелковников В.В. Изв. АН. Сер. хим. 2013, 10, 2226-2233. https://doi.org/10.1007/s11172-013-0322-8
- Бородина Е.А., Орлова Н.А. ЖОРх. 2015, 51 (2), 263-270. https://doi.org/10.1134/S1070428015020207
- Шмуйлович К.С., Орлова Н.А., Береговая И.В., Шелковников В.В. Изв. АН. Сер. хим. 2011, 2, 353-358. https://doi.org/10.1007/s11172-011-0058-2
- Niedermeyer T.H.J., Strohalm M. PLOS One. 2012, 7 (9), e44913. https://doi.org/10.1371/journal.pone.0044913
Supplementary files


