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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2024 |
| 1. |
M. N. Elinson, A. N. Vereshchagin, Yu. E. Ryzhkova, F. V. Ryzhkov, “Electrochemical transformations of CH-acids”, Mendeleev Commun., 34:2 (2024), 145–155   |
2
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2021 |
| 2. |
М. Н. Элинсон, Ю. Е. Рыжкова, Ф. В. Рыжков, “Мультикомпонентный дизайн хромено[2,3-b]пиридиновых систем”, Усп. хим., 90:1 (2021), 94–115  ; M. N. Elinson, Yu. E. Ryzhkova, F. V. Ryzhkov, “Multicomponent design of chromeno[2,3-b]pyridine systems”, Russian Chem. Reviews, 90:1 (2021), 94–115  |
33
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2017 |
| 3. |
M. N. Elinson, F. V. Ryzhkov, A. N. Vereshchagin, A. D. Korshunov, R. A. Novikov, M. P. Egorov, “'On-solvent' new domino reaction of salicylaldehyde, malononitrile and 4-hydroxy-6-methylpyridin-2(1H)-one: fast and efficient approach to medicinally relevant 4-pyridinyl-2-amino-4H-chromene scaffold”, Mendeleev Commun., 27:6 (2017), 559–561 |
18
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2016 |
| 4. |
M. N. Elinson, F. V. Ryzhkov, A. N. Vereshchagin, T. A. Zaimovskaya, V. A. Korolev, M. P. Egorov, “Multicomponent assembling of isatins, malononitrile and 4-hydroxy-6-methylpyridin-2(1H)-ones: one-pot efficient approach to privileged spiro[indoline-3,4'-pyrano[3,2-c]pyridine]-2,5'(6'H)-dione scaffold”, Mendeleev Commun., 26:5 (2016), 399–401 |
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2015 |
| 5. |
A. N. Vereshchagin, M. N. Elinson, Yu. E. Anisina, F. V. Ryzhkov, A. S. Goloveshkin, I. S. Bushmarinov, S. G. Zlotin, M. P. Egorov, “Pot, atom and step economic (PASE) synthesis of 5-isoxazolyl-5H-chromeno[2,3-b]pyridine scaffold”, Mendeleev Commun., 25:6 (2015), 424–426 |
51
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| 6. |
M. N. Elinson, F. V. Ryzhkov, T. A. Zaimovskaya, M. P. Egorov, “Non-catalytic solvent-free synthesis of 5,6,7,8-tetrahydro-4H-chromenes from aldehydes, dimedone and malononitrlie at ambient temperature”, Mendeleev Commun., 25:3 (2015), 185–187 |
13
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2014 |
| 7. |
M. N. Elinson, F. V. Ryzhkov, R. F. Nasybullin, T. A. Zaimovskaya, M. P. Egorov, “Sodium acetate catalyzed multicomponent approach to medicinally privileged 2-amino-4H-chromene scaffold from salicylaldehydes, malononitrile and cyanoacetates”, Mendeleev Commun., 24:3 (2014), 170–172 |
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