Cyclocondensation of methyl 5-methyl-1-(2-oxo-2-phenylethyl)-1H-pyrazole-3-carboxylate as a method for constructing a new 18-member nitrogenic macroheterocycle
- 作者: Kharaneko A.O.1, Pekhtereva T.M.1, Kharaneko O.I.1, Morkovnik A.S.2
-
隶属关系:
- Litvinenko Institute of Physical Organic and Coal Chemistry
- Institute of Physical and Organic Chemistry, Southern Federal University
- 期: 卷 61, 编号 5 (2025)
- 页面: 544-551
- 栏目: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://journals.rcsi.science/0514-7492/article/view/318339
- DOI: https://doi.org/10.31857/S0514749225050047
- ID: 318339
如何引用文章
详细
作者简介
A. Kharaneko
Litvinenko Institute of Physical Organic and Coal Chemistry
Email: antonhar08@rambler.ru
ul. R. Luxemburg, 70, Donetsk, 283114 Russia
T. Pekhtereva
Litvinenko Institute of Physical Organic and Coal Chemistryul. R. Luxemburg, 70, Donetsk, 283114 Russia
O. Kharaneko
Litvinenko Institute of Physical Organic and Coal Chemistryul. R. Luxemburg, 70, Donetsk, 283114 Russia
A. Morkovnik
Institute of Physical and Organic Chemistry, Southern Federal Universityprosp. Stachki, 194/2, Rostov-on-Don, 344090 Russia
参考
- Vinogradov A.A., Yin Y., Suga H., J. Am. Chem. Soc. 2019, 141, 4167–4181. doi: 10.1021/jacs.8b13178
- Peacock H., Suga H. Trends Pharmacol. Sci. 2021, 42 (5), 385–397. doi: 10.1016/j.tips.2021.02.004
- Ushakov E.N., Alfimov M.V., Gromov S.P., Macroheterocycles. 2010, 3 (4), 189–200. doi: 10.6060/mhc2010.4.189
- Ullah F., Khan T.A., Iltaf J., Anwar S., Khan M.F.A., Khan M.R., Ullah S., Fayyaz ur Rehman M., Mustaqeem M., Kotwica-Mojzych K., Mojzych M., Appl. Sci. 2022, 12, 1102. doi: 10.3390/app12031102
- Marsault E., Peterson M. L., J. Med. Chem. 2011, 54, 1961–2004. doi: 10.1021/jm1012374
- Gilissen P.J., White P.B., Berrocal J.A., Vanthuyne N., Rutjes F.P.J.T., Feringa B.L., Elemans J.A.A.W., Nolt R.J.M. Nat. Commun. 2020, 11, 5291–5301. doi: 10.1038/s41467-020-19123-y
- Beletskaya I.P., Averin A.D., Pleshkova N.A., Borisen- ko A.A., Serebryakova M.V., Denat F., Guilard R. Synlett. 2005, 1, 87–90. doi: 10.1055/s-2004-836040
- Ишмуратов Г.Ю., Яковлева М.П., Мингалеева Г.Р., Толстиков А.Г. Макрогетероциклы. 2011, 4 (4), 270–310. [Ishmuratov G.Yu., Yakovleva M.P., Mingale- eva G.R., Tolstikov A.G. Macroheterocycles. 2011, 4 (4), 270–310.] doi: 10.6060/mhc2011.4.06
- Lawson A.D.G., MacCoss M., Heer J.P. J. Med. Chem. 2018, 61 (10), 4283–4289. doi: 10.1021/acs.jmedchem.7b01120
- Харанеко А.О., Харанеко О.И. ЖОрХ. 2018, 54, 738–742. [Kharaneko A.O. Kharaneko O.I. Russ. J. Org. Chem. 2018, 54, 742–746.] doi: 10.1134/S1070428018050111
- Харанеко А.О., Пехтерева Т.М., Харанеко О.И. ЖОрХ. 2020, 56, 118–128. [Kharaneko A.O., Pekhtereva T.M., Kharaneko O.I. Russ. J. Org. Chem. 2020, 56, 95–104.] doi: 10.1134/S1070428020010169
- Харанеко А.О. ЖОрХ. 2017, 53, 727–734. [Kharane- ko A.O. Russ. J. Org. Chem. 2017, 53, 738–745.] doi: 10.1134/S1070428017050153
- Харанеко А.О., Пехтерева Т.М., Харанеко О.И. ЖОрХ. 2020, 56, 619–627. [Kharaneko A.O., Pekhtereva T.M., Kharaneko O.I. Russ. J. Org. Chem. 2020, 56, 654–661.] doi: 10.1134/S1070428020040144
- Харанеко А.О., Пехтерева Т.М., Харанеко О.И. ЖОрХ. 2020, 56, 118–128. [Kharaneko A.O., Pekhtereva T.M., Kharaneko O.I. Russ. J. Org. Chem. 2020, 56, 95–104.] doi: 10.1134/S1070428020010169
- Харанеко А.О., Харанеко О.И. ЖОрХ. 2019, 55, 341–346. [Kharaneko A.O., Kharaneko O.I. Russ. J. Org. Chem. 2019, 55, 291–295.] doi: 10.1134/S1070428019030023
- Shutaleva A.D., Fesenko A.A., Yankov A.N., Tafeen- ko V.A., Chernyshev V.V. J. Mol. Struct. 2017, 1150, 349–357. doi: 10.1016/j.molstruc.2017.08.096
- Ramakrishnan A., Chourasiya S.S., Bharatam P.V. RSC Adv. 2015, 5 (69), 55938–5947. doi: 10.1039/c5ra05574a
- Sharma A., Jad Y., Siddiqui M.R.H., Torre B.G., Albericio F., El-Faham A. J. Chem., 2017, Article ID 5702962. doi: 10.1155/2017/5702962
- Granovsky A.A., Firefly, version 8, http://classic.chem.msu.su/gran/firefly/index.html
- Schmidt M.W., Baldridge K.K., Boatz J.A., Elbert S.T., Gordon M.S., Jensen J.H., Koseki S., Matsunaga N., Nguyen K.A., Su S., Windus T.L., Dupuis M., Montgomery J.A. J. Comput. Chem. 1993, 14 (11), 1347–1363. doi: 10.1002/jcc.540141112
- CrysAlisPro, version 1.171.38.41, Rigaku Oxford Diffraction, Oxford, 2015.
- Sheldrick G.M., Acta Crystallogr., Sect. A: Found. Adv. 2015, 71, 3–8. doi: 10.1107/S2053273314026370
- Sheldrick G.M., Acta Crystallogr., Sect. C: Struct. Chem. 2015, 71, 3–8. doi: 10.1107/S2053229614024218
- Dolomanov O.V., Bourhis L.J., Gildea R.J., Ho- ward J.A.K., Puschmann H.J. Appl. Crystallogr. 2009, 42, 339–341. doi: 10.1107/S0021889808042726
补充文件
