Solvent-Free reaction of 3,6-Diaryl-1,2,4-Triazine-5-Carbonitriles with 2-Amino-4-aryloxazoles
- Autores: Rammohan A.1, Shtaitz Y.1, Ladin E.1, Krinochkin A.1,2, Slepukhin P.1,2, Sharutin V.3, Sharafieva E.1,4, Pospelova T.1, Kopchuk D.1,2, Zyryanov G.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
- South Ural State University
- Ural State Medical University of the Ministry of Health of Russia
- Edição: Volume 93, Nº 2 (2023)
- Páginas: 200-205
- Seção: Articles
- URL: https://journals.rcsi.science/0044-460X/article/view/144997
- DOI: https://doi.org/10.31857/S0044460X23020051
- EDN: https://elibrary.ru/QAFXCH
- ID: 144997
Citar
Resumo
Sobre autores
A. Rammohan
Ural Federal University
Email: gvzyryanov@gmail.com
Ya. Shtaitz
Ural Federal University
Email: gvzyryanov@gmail.com
E. Ladin
Ural Federal University
Email: gvzyryanov@gmail.com
A. Krinochkin
Ural Federal University;I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences
Email: gvzyryanov@gmail.com
P. Slepukhin
Ural Federal University;I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences
Email: gvzyryanov@gmail.com
V. Sharutin
South Ural State University
Email: gvzyryanov@gmail.com
E. Sharafieva
Ural Federal University;Ural State Medical University of the Ministry of Health of Russia
Email: gvzyryanov@gmail.com
T. Pospelova
Ural Federal University
Email: gvzyryanov@gmail.com
D. Kopchuk
Ural Federal University;I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences
Email: gvzyryanov@gmail.com
G. Zyryanov
Ural Federal University;I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences
Email: gvzyryanov@gmail.com
Bibliografia
- Прохоров А.М., Кожевников Д.Н. // ХГС. 2012. Вып. 8. С. 1237
- Prokhorov A.M., Kozhevnikov D.N. // Chem. Heterocycl. Compd. 2012. Vol. 48. P. 1153. doi: 10.1007/s10593-012-1117-9
- Foster Radleigh A.A., Willis M.C. // Chem. Soc. Rev. 2013. Vol. 42. P. 63. doi: 10.1039/c2cs35316d
- Gonsalves A.M.d.'A.R., Pinho e Melo T.M.V.D., Gilchrist T.L. // Tetrahedron. 1992. Vol. 48. P. 6821. doi: 10.1016/s0040-4020(01)89873-2
- Gundala S., Khasanov A.F., Kopchuk D.S., Starnovskaya E.S., Shtaitz Ya.K., Krinochkin A.P., Gorbunov E.B., Zyryanov G.V., Padmavathi V., Chupakhin O.N. // Polycycl. Arom. Compd. 2022. Vol. 42. N. 5. P. 1994. doi: 10.1080/10406638.2020.1823858
- Boger D.L., Panek J.S., Meier M.M. // J. Org. Chem. 1982. Vol. 47. N. 5. P. 895. doi: 10.1021/jo00344a031
- Sainz Y.F., Raw S.A., Taylor R.J.K. // J. Org. Chem. 2005. Vol. 70, N. 24. P. 10086. doi: 10.1021/jo0518304
- Dhar R., Huehnermann W., Kaempchen T., Overheu W., Seitz G. // Chem. Ber. 1983. Vol. 116. N. 1. P. 97. doi: 10.1002/cber.19831160111
- Fadel S., Hajbi Y., Khouili M., Lazar S., Suzenet F., Guillaumet G. // Beilstein J. Org. Chem. 2014. Vol. 10. P. 282. doi: 10.3762/bjoc.10.24
- Jouha J., Buttard F., Lorion M., Berthonneau C., Khouili M., Hiebel M.-A., Guillaumet G., Brière J.-F., Suzenet F. // Org. Lett. 2017. Vol. 19. N 18. P. 4770. doi: 10.1021/acs.orglett.7b02132
- Diring S., Retailleau P., Ziessel R. // J. Org. Chem. 2007. Vol. 72. P. 10181. doi: 10.1021/jo7019866
- Diring S., Retailleau P., Ziessel R. // Synlett. 2007. Vol. 19. P. 3027. doi: 10.1055/s-2007-990965
- Prokhorov A.M., Slepukhin P.A., Rusinov V.L., Kalinin V.N., Kozhevnikov D.N. // Tetrahedron Lett. 2008. Vol. 49. N. 23. P. 3785. doi: 10.1016/j.tetlet.2008.04.008
- 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. Vol. 31. P. 542. 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. Т. 58. Вып. 2. С. 127
- 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. Vol. 58. N. 2. P. 175. doi: 10.1134/S1070428022020026
- Алуру Р., Криночкин А.П., Копчук Д.С. Штайц Я.К., Савчук М.И., Старновская Е.С., Зырянов Г.В., Русинов В.Л., Чупахин О.Н. // ЖОрХ. 2022. Т. 58. Вып. 2. С. 134
- Rammohan A., Krinochkin A.P., Kopchuk D.S., Shtaitz Ya.K., Savchuk M.I., Starnovskaya E.S., Zyryanov G.V., Rusinov V.L., Chupakhin O.N. // Russ. J. Org. Chem. 2022. Vol. 58. N 2. P. 180. doi: 10.1134/S1070428022020038
- Borowicz P., Grabowska A., Leś A., Kaczmarek L., Zagrodzki B. // Chem. Phys. Lett. 1998. Vol. 291. P. 351. doi: 10.1016/S0009-2614(98)00565-X
- Mongin F., Trécourt F., Gervais B., Mongin O., Quéguiner G. // J. Org. Chem. 2002. Vol. 67. P. 3272. doi: 10.1021/jo010913r
- Izuta S., Kosaka S., Kawai M., Miyano R., Matsuo H., Matsumoto A., Nonaka K., Takahashi Y., Omura S., Nakashima T. // J. Antibiot. 2018. Vol. 71. P. 535. doi: 10.1038/s41429-018-0028-0
- Кожевников Д.Н., Кожевников В.Н., Ковалев И.С., Русинов В.Л., Чупахин О.Н., Александров Г.Г. // ЖОрХ. 2002. Т. 38. С. 780
- Kozhevnikov D.N., Kozhevnikov V.N., Kovalev I.S., Rusinov V.L., Chupakhin O.N., Aleksandrov G.G. // Russ. J. Org. Chem. 2002. Vol. 38. N. 5. P. 744. doi: 10.1023/A:1019631610505
- Sandleben A., Vogt N., Hörner G., Klein A. // Organometallics. 2018. Vol. 37. N 19. P. 3332. doi: 10.1021/acs.organomet.8b00559
- SMART and SAINT-Plus. Versions 5.0. Data Collection and Processing Software for the SMART System. Madison: Bruker AXS Inc., 1998.
- SHELXTL/PC. Versions 5.10. An Integrated System for Solving, Refining and Displaying Crystal Structures from Diffraction Data. Madison: Bruker AXS Inc., 1998.
- Dolomanov O.V., Bourhis L.J., Gildea R.J., Howard J.A.K., Puschmann H. // J. Appl. Cryst. 2009. Vol. 42. P. 339. doi: 10.1107/S0021889808042726
- Krinochkin A.P., Shtaitz Ya.K., Rammohan A., Butorin I.I., Savchuk M.I., Khalymbadzha I.A., Kopchuk D.S., Slepukhin P.A., Melekhin V.V., Shcheglova A.V., Zyryanov G.V., Chupakhin O.N. // Eur. J. Org. Chem. 2022. Vol. 22. Art. e202200227. doi: 10.1002/ejoc.202200227
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