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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2023 |
1. |
Yu. A. Kvashnin, D. V. Belyaev, M. I. Kodess, M. A. Ezhikova, G. L. Rusinov, E. V. Verbitskiy, V. N. Charushin, “Two-step synthesis of indeno[1,2-b]furazanopyrazines through combination of the S<sub>N</sub><sup>H</sup> and Heck reactions”, Mendeleev Commun., 33:6 (2023), 753–755 |
2
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2021 |
2. |
A. M. Semenova, M. A. Ezhikova, M. I. Kodess, A. Ya. Zapevalov, A. V. Pestov, “Phosgene-free synthesis of symmetric bis(polyfluoroalkyl) carbonates”, Mendeleev Commun., 31:2 (2021), 257–258 |
1
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2019 |
3. |
D. V. Belyaev, D. L. Chizhov, M. I. Kodess, M. A. Ezhikova, G. L. Rusinov, V. N. Charushin, “Synthesis of 2-(polyfluoromethyl)pyrimido-[1,2-a]benzimidazole-4-carbaldehyde derivatives”, Mendeleev Commun., 29:3 (2019), 249–251 |
5
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4. |
I. G. Ovchinnikova, G. A. Kim, E. G. Matochkina, M. I. Kodess, E. V. Nosova, G. L. Rusinov, V. N. Charushin, “Pericyclic reactions in the synthesis of new 5-aryl-5,6-dihydroquinolino[2,1-b]quinazolin-12-ones”, Mendeleev Commun., 29:2 (2019), 135–137 |
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2018 |
5. |
T. I. Filyakova, V. I. Filyakova, A. Ya. Zapevalov, M. I. Kodess, P. A. Slepukhin, V. I. Saloutin, V. N. Charushin, “3,4-Epoxyperfluorooxolane in the synthesis of new fluorine-containing furo[3,4-b]quinoxaline derivatives”, Mendeleev Commun., 28:5 (2018), 511–512 |
1
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2017 |
6. |
Yu. A. Azev, O. S. Ermakova, V. S. Berseneva, M. I. Kodess, M. A. Ezhikova, I. N. Ganebnykh, “Synthesis of the 6-oxidopyrido[1,2-a]quinoxalinium derivatives from quinoxalin-2-one and aldehydes – new examples of domino reactions”, Mendeleev Commun., 27:6 (2017), 637–639 |
5
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7. |
T. I. Filyakova, V. I. Filyakova, A. Ya. Zapevalov, M. I. Kodess, P. A. Slepukhin, V. I. Saloutin, V. N. Charushin, “New derivatives of fluorine-containing phenazines”, Mendeleev Commun., 27:3 (2017), 290–292 |
5
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8. |
Yu. A. Azev, M. I. Kodess, M. A. Ezhikova, O. S. Ermakova, V. S. Berseneva, V. A. Bakulev, “Reactions of quinoxalin-2-one with β-diketones: a new approach to 6a,7-dihydro-5H-pyrido[1,2-a]quinoxaline-6,8-diones”, Mendeleev Commun., 27:1 (2017), 97–98 |
9
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2016 |
9. |
N. N. Mochulskaya, P. A. Slepukhin, V. N. Charushin, M. I. Kodess, “Tandem A<sub>N</sub>–A<sub>N</sub> reactions in the synthesis of tetrahydrothiazolo[4,5-e][1,2,4]triazines”, Mendeleev Commun., 26:5 (2016), 375–377 |
3
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2015 |
10. |
Yu. A. Azev, O. S. Ermakova, A. M. Gibor, M. A. Ezhikova, M. I. Kodess, V. S. Berseneva, “Unusual reactions of 6-amino-1,3-dimethyluracil with some aliphatic aldehydes”, Mendeleev Commun., 25:4 (2015), 310–311 |
7
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2013 |
11. |
Yu. A. Azev, O. S. Ermakova, M. I. Kodess, M. A. Ezhikova, I. S. Kovalev, V. A. Bakulev, “Reactions of 3-phenyl-1,2,4-triazine with some C-nucleophiles”, Mendeleev Commun., 23:5 (2013), 294–296 |
5
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2011 |
12. |
V. Yu. Korotaev, A. Yu. Barkov, P. A. Slepukhin, M. I. Kodess, V. Ya. Sosnovskikh, “Unexpected spontaneous ring-contraction rearrangement of trifluoromethylated 1,2-oxazine N-oxides to 1-pyrroline N-oxides”, Mendeleev Commun., 21:5 (2011), 277–279 |
10
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13. |
V. Yu. Korotaev, A. Yu. Barkov, P. A. Slepukhin, M. I. Kodess, V. Ya. Sosnovskikh, “Diastereoselective reactions of 1,1,1-trichloro(trifluoro)-3-nitrobut-2-enes with 2-morpholinoalk-1-enes”, Mendeleev Commun., 21:2 (2011), 112–114 |
32
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14. |
V. Ya. Sosnovskikh, V. S. Moshkin, M. Yu. Kornev, M. I. Kodess, “Reactions of 3-aminoisoxazolo[4,5-c]coumarin with benzoyl chloride: the first example of a preparative 1,2,4-oxadiazole–oxazole rearrangement”, Mendeleev Commun., 21:2 (2011), 110–111 |
6
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2010 |
15. |
V. Ya. Sosnovskikh, V. S. Moshkin, M. I. Kodess, “Rearrangement of 3-aminoisoxazolo[4,5-c]coumarins into 2-aminooxazolo[4,5-c]coumarins mediated by carboxylic acid anhydrides”, Mendeleev Commun., 20:4 (2010), 209–211 |
9
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16. |
V. Yu. Korotaev, V. Ya. Sosnovskikh, M. A. Barabanov, A. Yu. Barkov, M. I. Kodess, “Stereoselective tandem [4 + 2]/[3 + 2] cycloaddition reactions of 3,3,3-trichloro(trifluoro)-1-nitropropenes and 2,3-dihydrofuran”, Mendeleev Commun., 20:1 (2010), 17–19 |
20
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2007 |
17. |
V. Yu. Korotaev, I. B. Kutyashev, V. Ya. Sosnovskikh, M. I. Kodess, “Stereoselective synthesis of N-unsubstituted pyrazolidines from 3-nitro-2-trichloromethyl-2H-chromenes and hydrazine hydrate”, Mendeleev Commun., 17:1 (2007), 52–53 |
16
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2006 |
18. |
G. L. Rusinov, P. A. Slepukhin, V. N. Charushin, O. A. Dyachenko, O. N. Kazheva, A. N. Chekhlov, E. V. Verbitskiy, M. I. Kodess, O. N. Chupakhin, “Chemistry of O- and C-adducts derived from 1,4-diazinium salts: the use of tetrahydropyrazines in the synthesis of condensed systems”, Mendeleev Commun., 16:1 (2006), 26–29 |
12
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2004 |
19. |
G. L. Levit, V. P. Krasnov, A. M. Demin, M. I. Kodess, L. Sh. Sadretdinova, T. V. Matveeva, V. A. Ol'shevskaya, V. N. Kalinin, O. N. Chupakhin, V. N. Charushin, “Kinetic resolution of 1-methyl- and 1-phenyl-3-amino-1,2-dicarba-closo-dodecaboranes via acylation with chiral acyl chlorides”, Mendeleev Commun., 14:6 (2004), 293–295 |
14
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2002 |
20. |
N. N. Volkova, E. V. Tarasov, M. I. Kodess, W. Dehaen, V. A. Bakulev, “Ring opening in di[1,2,3]triazolo-[1,3,6]thiadiazepine and -[3,1,5]benzothiadiazepine in reactions with butyllithium”, Mendeleev Commun., 12:4 (2002), 131–132 |
7
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21. |
M. G. Ponizovsky, A. M. Boguslavsky, M. I. Kodess, V. N. Charushin, O. N. Chupakhin, “Synthesis of fused quinoxalines”, Mendeleev Commun., 12:2 (2002), 68–70 |
11
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22. |
V. N. Charushin, N. N. Mochulskaya, A. A. Andreiko, M. I. Kodess, O. N. Chupakhin, “Use of tandem A<sub>N</sub>-A<sub>N</sub> reactions for the synthesis of thiazolo[4,5-e]-1,2,4-triazines”, Mendeleev Commun., 12:1 (2002), 28–30 |
9
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2001 |
23. |
Ya. V. Burgart, M. V. Pryadeina, O. G. Kuzueva, M. I. Kodess, V. I. Saloutin, O. N. Chupakhin, “Unexpected synthesis of 3,5-diethoxycarbonyl-2-pentafluorophenyl-4-phenyl-7,8,9,10-tetrafluoro-4,5-dihydrobenzo[b]oxacin-6-one”, Mendeleev Commun., 11:3 (2001), 119–120 |
2
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24. |
V. Ya. Sosnovskikh, B. I. Usachev, A. G. Blinov, M. I. Kodess, “New derivatives of dehydroacetic acid: synthesis of 2-polyfluoroalkyl-7-methylpyrano[4,3-b]pyran-4,5-diones”, Mendeleev Commun., 11:1 (2001), 36–38 |
7
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1999 |
25. |
L. V. Saloutina, A. Ya. Zapevalov, M. I. Kodess, V. I. Saloutin, O. N. Chupakhin, “A route to fluorocontaining 1,3-thiazolines via internal polyfluorooxiranes”, Mendeleev Commun., 9:6 (1999), 231–232 |
5
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