电邮这篇文章 Synthesis of bi- and polycyclic pyrimidine derivatives
- 作者: Sokolnikova T.V.1, Proidakov A.G.1, Penzik M.V.1, Kizhnyaev V.N.1
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隶属关系:
- Irkutsk State University
- 期: 卷 60, 编号 6 (2024)
- 页面: 101-110
- 栏目: Articles
- URL: https://rjpbr.com/0514-7492/article/view/676682
- DOI: https://doi.org/10.31857/S0514749224060099
- EDN: https://elibrary.ru/QZHNEI
- ID: 676682
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详细
Based on the modification of the Biginelli reaction, various bi- and polycyclic pyrimidine derivatives (including the condensed series) were synthesized and identified, in the structure of which there are aza- and carbocyclic fragments of various nature.
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作者简介
T. Sokolnikova
Irkutsk State University
编辑信件的主要联系方式.
Email: t.golobokova@rambler.ru
ORCID iD: 0000-0003-1845-4695
Faculty of Chemistry
俄罗斯联邦, ul. K. Marksa, 1, Irkutsk, 664003A. Proidakov
Irkutsk State University
Email: t.golobokova@rambler.ru
Faculty of Chemistry
俄罗斯联邦, ul. K. Marksa, 1, Irkutsk, 664003M. Penzik
Irkutsk State University
Email: t.golobokova@rambler.ru
ORCID iD: 0000-0002-3544-9866
Faculty of Chemistry
俄罗斯联邦, ul. K. Marksa, 1, Irkutsk, 664003V. Kizhnyaev
Irkutsk State University
Email: t.golobokova@rambler.ru
ORCID iD: 0000-0003-0617-9972
Faculty of Chemistry
俄罗斯联邦, ul. K. Marksa, 1, Irkutsk, 664003参考
- Taylor R.D., MacCross M., Lawson A.D.G. J. Med. Chem. 2014, 57, 1–47. doi: 10.1021/jm4017625
- Finger V., Kufa M., Soukup O., Castagnolo D., Roh J., Korabecny J. Eur. J. Med. Chem. 2023, 246, 114946. doi: 10.1016/j.ejmech.2022.114946
- Prachayasittikul S., Pingaew R., Worachartchee-wan A., Sinthupoom N., Prachayasittikul V., Ruchirawat S., Prachayasittikul V. Mini-Reviews Med. Chem. 2017, 17, 869–901. doi: 10.2174/1389557516666160923125801.
- Zhuang J.X., Ma S.T. Chem. Med. Chem. 2020, 15, 1875–1886. doi: 10.1002/cmdc.202000378
- Шкурко О.П., Толстикова Т.Г., Седова В.Ф. Успехи хим. 2016, 85, 1056–1096. doi: 10.1070/RCR4586.
- Farghaly T.A., Harras M.F., Alsaedi A.M.R., Thakir H.A., Mahmoud H.K., Katowah D.F. Mini-Reviews Med. Chem. 2023, 23, 821–851. doi: 10.2174/1389557523666221220142911
- Buron F., Merour J.Y., Akssira M., Guillaumet G., Routie, S. Eur. J. Med. Chem., 2015, 95, 76–95. doi: 10.1016/j.ejmech.2015.03.029
- Eze C.C., Ezeokonkwo A.M., Ugwu I.D., Eze U.F., Onyeyilim E.L., Attah I.S., Okonkwo I.V. Anti-Cancer Agents Med. Chem. 2022, 22, 2822–2851. doi: 10.2174/1871520622666220318090147.
- Kuppast B., Fahmy H. Eur. J. Med. Chem., 2016, 113, 198–213. doi: 10.1016/j.ejmech.2016.02.031
- Dai X.J., Xue L.P., Ji S.K., Zhou Y., Gao Y., Zheng Y.C., Liu H.M., Liu H.M. Eur. J. Med. Chem., 2023, 249, 115101. doi: 10.1016/j.ejmech.2023.115101.
- Mohamed S.F., Abbas E.M.H., Khalaf H.S., Farghaly T.A., Abd El-Shafy D.N. Mini-Reviews Med. Chem. 2018, 18, 794–802. doi: 10.2174/1389557518666171207161542.
- Oukoloff K., Lucero B., Francisco K.R., Brunden K.R., Ballatore C. Eur. J. Med. Chem., 2019, 165, 332–346. doi: 10.1016/j.ejmech.2019.01.027.
- Scapin E., Frizzo C.P., Rodrigues L.V., Zimmer G.C., Vaucher R.A., Sagrillo M.R., Giongo J.L., Afonso C.A.M., Rijo P., Zanatta N.B. Med. Chem.Res. 2017, 26, 640–649. doi: 10.1007/s00044-017-1783-3
- Gein V.L., Prudnikova A.N., Kurbatova A.A., Dmitriev M.V. Russ. J. of General Chem. 2021, 91, 621-625. doi: 10.31857/S0044460X21040077.
- Rodante F., Catalani G., Guidotti M.J. Thermal Anal. Calorimetry. 1998, 53, 937–956. doi: 10.1023/A:1010198621609
- López-González D., Avalos-Ramirez A., Giroir-Fendler A., Godbout S., Fernandez-Lopez M., Sanchez-Silva L., Valverde J.L. Energy. 2015, 90. 1626–1635. doi: 10.1016/j.energy.2015.06.134.
- Jakab E., Till F., Várhegyi G. Fuel Process. Technol. 1991, 28, 221–238. doi: 10.1016/0378-3820(91)90076-O.
- Penzik M.V., Kozlov A.N., Zhang S., Badenko V.V., Sosnovsky I.K., Shamansky V.A. Thermochim. Acta. 2022, 711, 179209.
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