Научная биография: |
ИрИХ СО РАН,
Лаборатория структурных исследований,
с.н.с.
Ващенко, Александр Валентинович.
Внутримолекулярные эффекты в $N-, O-$ и $S$-винильных соединениях по данным квантовой химии и спектроскопии ЯМР : дис. ... канд. хим. наук : 02.00.04 / Иркутский ун-т. - Иркутск, 1990. - 181 с. |
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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2025 |
| 1. |
K. V. Belyaeva, L. P. Nikitina, V. S. Saliy, A. V. Afonin, I. A. Ushakov, A. V. Vashchenko, B. A. Trofimov, “One-pot assembly of functionalized (<em>m</em>-terphenyl-4'-yl)isoquinolines from 1-methylisoquinoline and electrophilic acylacetylenes”, Mendeleev Commun., 35:4 (2025), 457–460    |
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2024 |
| 2. |
B. A. Gostevsky, A. V. Vashchenko, N. F. Lazareva, “X-ray structural study of 3:1 solvate of 1-chlorosilatrane with MeCN”, Mendeleev Commun., 34:5 (2024), 745–747 |
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2019 |
| 3. |
E. Yu. Schmidt, N. V. Semenova, I. A. Ushakov, A. V. Vashchenko, B. A. Trofimov, “Diastereoselective synthesis of 5-hydroxy-3-methylalkane-1,6-diones from ketones and acetylene in two atom-economic steps”, Mendeleev Commun., 29:1 (2019), 17–18 |
3
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2018 |
| 4. |
B. A. Trofimov, K. V. Belyaeva, L. P. Nikitina, A. V. Afonin, A. V. Vashchenko, “2-(5-Arylterphenyl-4-yl)quinolines from 2-methylquinoline and 1-(het)aryl-3-phenylprop-2-yn-1-ones in just a one step: A miracle of molecular interplay”, Mendeleev Commun., 28:3 (2018), 267–269 |
5
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2017 |
| 5. |
N. V. Vchislo, E. A. Verochkina, L. I. Larina, A. V. Vashchenko, Yu. A. Chuvashev, “Reaction of 2-alkoxy- and 2-hydroxypropenals with o-phenylenediamine: a route to benzimidazoles and quinoxalines”, Mendeleev Commun., 27:2 (2017), 166–168 |
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| 6. |
S. N. Adamovich, I. A. Ushakov, A. V. Vashchenko, “Novel guanidinium salts of biologically active (het)arylchalcogenylacetic acids”, Mendeleev Commun., 27:1 (2017), 88–89 |
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2014 |
| 7. |
D. A. Shabalin, T. E. Glotova, I. A. Ushakov, M. Yu. Dvorko, A. V. Vashchenko, V. I. Smirnov, E. Yu. Schmidt, A. I. Mikhaleva, B. A. Trofimov, “2-(2-Ethynyl-1-aziranyl)-3,4-dihydro-2H-pyrrole: a one-pot assembly from isopropyl phenyl ketoxime and acetylene during the synthesis of 3H-pyrrole”, Mendeleev Commun., 24:6 (2014), 368–369 |
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