Interaction of 3-(2-pyridyl)-1,2,4-triazine-5-carbonitriles with 2-amino-4-aryloxazoles in the absence of water
- Autores: Rammohan A.1, Krinochkin A.1,2, Kopchuk D.1,2, Shtaitz Y.1, Sharafieva E.1,3, Gaviko V.1,4, Zyryanov G.1,2, Chupakhin O.1,2
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Afiliações:
- Ural Federal University
- I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences
- Ural State Medical University of the Ministry of Health of Russia
- M.N. Mikheev lnstitute of Metal Physics of Ural Branch of Russian Academy of Science
- Edição: Volume 59, Nº 9 (2023)
- Páginas: 1233-1237
- Seção: Articles
- URL: https://journals.rcsi.science/0514-7492/article/view/141692
- DOI: https://doi.org/10.31857/S0514749223090148
- EDN: https://elibrary.ru/XVBGVH
- ID: 141692
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Resumo
Sobre autores
Aluru Rammohan
Ural Federal University
A. Krinochkin
Ural Federal University;I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences
D. Kopchuk
Ural Federal University;I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences
Ya. Shtaitz
Ural Federal University
E. Sharafieva
Ural Federal University;Ural State Medical University of the Ministry of Health of Russia
V. Gaviko
Ural Federal University;M.N. Mikheev lnstitute of Metal Physics of Ural Branch of Russian Academy of Science
G. Zyryanov
Ural Federal University;I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences
Email: gvzyryanov@gmail.com
O. Chupakhin
Ural Federal University;I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences
Bibliografia
- Prokhorov A.M., Kozhevnikov D.N. Chem. Heterocycl. Compd. 2012, 48, 1153-1176. doi: 10.1007/s10593-012-1117-9
- Pabst G.R., Pfüller O.C., Sauer J. Tetrahedron. 1999, 55, 8045-8064. doi: 10.1016/S0040-4020(99)00422-6
- Shi B., Lewis W., Campbell I.B., Moody Ch.J. Org. Lett. 2009, 11, 3686-3688. doi: 10.1021/ol901502u
- Rykowski A., Branowska D., Kielak J. Tetrahedron Lett. 2000, 41, 3657-3659. doi: 10.1016/S0040-4039(00)00436-6
- Gonsalves A.M.d'A.R., Pinho e Melo T.M.V.D., Gilchrist T.L. Tetrahedron. 1992, 48, 6821-6826. doi: 10.1016/S0040-4020(01)89873-2
- Kopchuk D.S., Nikonov I.L., Khasanov A.F., Giri K., Santra S., Kovalev I.S., Nosova E.V., Gundala S., Venkatapuram P., Zyryanov G.V., Majee A., Chupakhin O.N. Org. Biomol. Chem. 2018, 16, 5119-5135. doi: 10.1039/c8ob00847g
- Krinochkin A.P., Reddy G.M., Kopchuk D.S., Slepukhin P.A., Shtaitz Y.K., Khalymbadzha I.A., Kovalev I.S., Kim G.A., Ganebnykh I.N., Zyryanov G.V., Chupakhin O.N., Charushin V.N. Mendeleev Commun. 2021, 31, 542-544. doi: 10.1016/j.mencom.2021.07.035
- Раммохан А., Криночкин А.П., Копчук Д.С., Штайц Я.К., Ковалев И.С., Савчук М.И., Зырянов Г.В., Русинов В.Л., Чупахин О.Н. ЖОрХ. 2022, 58, 127-133.
- Rammohan A., Krinochkin A.P., Kopchuk D.S., Shtaitz Ya.K., Kovalev I.S., Savchuk M.I., Zyryanov G.V., Rusinov V.L., Chupakhin O.N. Russ. J. Org. Chem. 2022, 58, 175-179. doi: 10.1134/S1070428022020026
- Mongin F., Trécourt F., Gervais B., Mongin O., Quéguiner G. J. Org. Chem. 2002, 67, 3272-3276. doi: 10.1021/jo010913r
- Zhu W., Mei X., Fu P., Wang Y., Liu P. Пат. US 20190322638A1 (2019); C.A., 2018, 169, 16904.
- Murata T., Sakakibara S., Yoshino T., Ikegami Y., Masuda T., Shimada M., Shintani T., Shimazaki M., Lowinger T.B., Ziegelbauer K.B, Fuchikami K., Umeda M., Komura H., Yoshida N. Пат. WO2002044153A1 (2002); C.A., 2002, 137, 20298.
- Diring S., Retailleau P., Ziessel R. Synlett. 2007, 3027-3031. doi: 10.1055/s-2007-990965
- Diring S., Retailleau P., Ziessel R. J. Org. Chem. 2007, 72, 10181-10193. doi: 10.1021/jo7019866
- Sandleben A., Vogt N., Hörner G., Klein A. Organometallics 2018, 37, 3332-3341. doi: 10.1021/acs.organomet.8b00559.
- Sainz Y.F., Raw S.A., Taylor R.J.K. J. Org. Chem. 2005, 70, 10086-10095. doi: 10.1021/jo0518304.
- Kozhevnikov V.N. Kozhevnikov D.N., Nikitina T.V., Rusinov V.L., Chupakhin O.N., Zabel M., König B. J. Org. Chem. 2003, 68, 2882-2888. doi: 10.1021/jo0267955
- Turner W.W., Arnold L.D., Maag H., Zlotnick A. Пат. WO2015138895A1 (2015); C.A., 2015, 163, 442905.