Selective Synthesis of Pyrazol-3-yl- and Pyrazol-5-ylphosphonates
- Авторлар: Mitrofanov A.Y.1, Devnozashvili D.N.1, Beletskaya I.P.1
-
Мекемелер:
- Lomonosov Moscow State University
- Шығарылым: Том 60, № 10 (2024)
- Беттер: 1007-1016
- Бөлім: Articles
- URL: https://aspvestnik.ru/0514-7492/article/view/682481
- DOI: https://doi.org/10.31857/S0514749224100018
- EDN: https://elibrary.ru/QNKFQS
- ID: 682481
Дәйексөз келтіру
Аннотация
An approach to selective synthesis regioisomeric N-substituted pyrazolyl-3-yl- and pyrazol-5-ylphosphonates based on the reaction of aryl-substituted hydrazines with 3-oxoprop-1-yn-1-ylphosphonates has been developed.
Негізгі сөздер
Авторлар туралы
A. Mitrofanov
Lomonosov Moscow State University
Хат алмасуға жауапты Автор.
Email: mitrofanov@org.chem.msu.ru
ORCID iD: 0000-0003-3141-3599
Department of Chemistry
Ресей, Moscow, 119991D. Devnozashvili
Lomonosov Moscow State University
Email: mitrofanov@org.chem.msu.ru
ORCID iD: 0009-0007-9941-2265
Department of Chemistry
Ресей, Moscow, 119991I. Beletskaya
Lomonosov Moscow State University
Email: mitrofanov@org.chem.msu.ru
ORCID iD: 0000-0001-9705-1434
Department of Chemistry
Ресей, Moscow, 119991Әдебиет тізімі
- Fustero, S., Sánchez-Roselló, M., Barrio, P., and Simón-Fuentes, A., Chem. Rev., 2011, vol. 111, p. 6984. https://doi.org/10.1021/cr2000459
- Ji Ram, V., Sethi, A., Nath, M., and Pratap, R., The Chemistry of Heterocycles, Eds. Elsevier, 2019, p. 149.
- Ojwach, S. O. and Darkwa, J., Inorg. Chim. Acta 2010, vol. 363, p. 1947. https://doi.org/10.1016/j.ica.2010.02.014
- Withbroe, G.J., Singer, R.A., and Sieser, J.E., Org. Process Res. Dev., 2008, vol. 12, p. 480. https://doi.org/10.1021/op7002858
- Mukherjee, A. and Sarkar, A., Arkivoc, 2003, vol. 2003, p. 87. https://doi.org/10.3998/ark.5550190.0004.911
- El Boutaybi, M., Taleb, A., Touzani, R., and Bahari, Z. Mater. Today: Proc., 2020, vol. 31, p. S96. https://doi.org/10.1016/j.matpr.2020.06.249
- Halcrow, M.A., J. Chem. Soc., Dalton Trans., 2009, p. 2059. https://doi.org/10.1039/B815577A
- Pérez, J. and Riera, L., Eur. J. Inorg. Chem., 2009, vol. 2009, p. 4913. https://doi.org/10.1002/ejic.200900694
- Goulioukina, N.S., Makukhin, N.N., and Beletskaya, I.P., Russ. Chem. Rev., 2016, vol. 85, p. 667. https://doi.org/10.1070/RCR4579
- Jamali, M.F., Vaishanv, N.K., and Mohanan, K., Chem. Rec., 2020, vol. 20, p. 1394. https://doi.org/10.1002/tcr.202000091
- Goulioukina, N.S., Makukhin, N.N., Shinkarev, E.D., Grishin, Y.K., Roznyatovsky, V.A., and Beletskaya, I.P., Org. Biomol. Chem., 2016, vol. 14, p. 10000. https://doi.org/10.1039/C6OB01780K
- Kalla, R.M.N. and Kim, I., Mol. Catal., 2019, vol. 473, p. 110396. https://doi.org/10.1016/j.mcat.2019.110396
- Xiaofeng, P., Xiaofei, Z., Shunyao, L., Yunfu. L., Lefu, L., and Chunhao, Y., Org. Chem. Front., 2019, vol. 6, p. 1775. https://doi.org/10.1039/C9QO00324J
- Imen, L. and Soufiane, T., Heterocycles, 2017, vol. 94, p. 894. https://doi.org/10.3987/COM-17-13687
- Levashova, E.Yu., Zhukovsky, D.D., Dar′in, D.V., and Krasavin, M.Yu., Chem. Heterocycl. Compd., 2020, vol. 56, p. 806. https://doi.org/10.1007/s10593-020-02735-z
- Dhameja, M. and Pandey, J., Asian J. Org. Chem., 2018, vol. 7, p. 1502. https://doi.org/10.1002/ajoc.201800051
- Nájera, C., Sydnes, L.K., and Yus, M., Chem. Rev., 2019, vol. 119, p. 11110. https://doi.org/10.1021/acs.chemrev.9b00277
- Mitrofanov, A.Yu. and Beletskaya, I.P., Mendeleev Commun. 2021, vol. 31, p. 536. https://doi.org/10.1016/j.mencom.2021.07.033
- Mitrofanov, A.Yu., Bychkova, V.A., Nefedov, S.E., and Beletskaya, I.P., J. Org. Chem., 2020, vol. 85, p. 14507. https://doi.org/10.1021/acs.joc.0c00913.
- Mitrofanov, A.Yu., Bychkova, V.A., Kalugin, D.A., and Beletskaya, I.P., Synthesis, 2022, vol. 54, p. 1652. https://doi.org/10.1055/a-1690-4840
- Mitrofanov, A.Yu. and Beletskaya I.P., J. Org. Chem., 2023, vol. 88, p. 2367. https://doi.org/10.1021/acs.joc.2c02780
- Liao, L., Zhang H., and Zhao, X., ACS Catal., 2018, vol. 8, p. 6745. https://doi.org/10.1021/acscatal.8b01595
- Hsieh, M.-T., Kuo, S.-C., and Lin, H.-C., Adv. Synth. Catal. 2015, vol. 357, p. 683. https://doi.org/10.1002/adsc.201400853
- Topchiy, M.A., Zharkova, D.A., Asachenko, A.F., Muzalevskiy, V.M., Chertkov, V.A., Nenajdenko, V.G., and Nechaev, M.S., Eur. J. Org. Chem., 2018, vol. 2018, p. 3750. https://doi.org/10.1002/ejoc.201800208
- Muzalevskiy, V.M. Rulev, A.Y., Romanov, A.R., Kondrashov, E.V., Ushakov, I.A., Chertkov, V.A., and Nenajdenko, V.G., J. Org. Chem., 2017, vol. 82, p. 7200. https://doi.org/10.1021/acs.joc.7b00774
- Muzalevskiy, V.M. and Nenajdenko, V.G., Org. Biomol. Chem., 2018, vol. 16, p. 7935. https://doi.org/10.1039/c8ob02247
- Jeyaveeran, J.C., Praveen, C., Arun, Y., Prince A.A.M., and Peumal P.T., J. Chem Sci., 2016, vol. 128, p. 73. https://doi.org/10.1007/s12039-015-0993-9
Қосымша файлдар
