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
- Авторлар: Kharaneko A.O.1, Pekhtereva T.M.1, Kharaneko O.I.1, Morkovnik A.S.2
-
Мекемелер:
- Litvinenko Institute of Physical Organic and Coal Chemistry
- Institute of Physical and Organic Chemistry, Southern Federal University
- Шығарылым: Том 61, № 5 (2025)
- Беттер: 544-551
- Бөлім: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://journals.rcsi.science/0514-7492/article/view/318339
- DOI: https://doi.org/10.31857/S0514749225050047
- ID: 318339
Дәйексөз келтіру
Аннотация
Авторлар туралы
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
Әдебиет тізімі
- 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
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