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

Эта публикация цитируется в следующих 18 статьяx:

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Michail N. Elinson, Anatoly N. Vereshchagin, Yuliya E. Anisina, Stepan K. Krymov, Artem N. Fakhrutdinov, Alexander S. Goloveshkin, Mikhail P. Egorov, “Pot, atom and step economic (PASE) assembly of salicylaldehydes, malononitrile dimer and 4-hydroxypyridine-2(1H)-ones into medicinally relevant 5H-chromeno[2,3-b]pyridine scaffold”, Mol Divers, 24:3 (2020), 617
Nhlanhla Gracious Shabalala, Nagaraju Kerru, Suresh Maddila, Werner E. van Zyl, Sreekantha B. Jonnalagadda, “Catalyst-free synthesis of novel isopropyl 2-amino-7,7-dimethyl-4-(aryl)-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carboxylate derivatives in aqueous ethanol under ultrasound irradiation”, Chemical Data Collections, 26 (2020), 100365
Alexey A. Festa, Olga A. Storozhenko, Nikita E. Golantsov, Karthikeyan Subramani, Roman A. Novikov, Snezhana O. Zaitseva, Mikhail S. Baranov, Alexey V. Varlamov, Leonid G. Voskressensky, “Homophtalonitrile for Multicomponent Reactions: Syntheses and Optical Properties of o‐Cyanophenyl‐ or Indol‐3‐yl‐Substituted Chromeno[2,3‐c]isoquinolin‐5‐Amines”, ChemistryOpen, 8:1 (2019), 23
Michail N. Elinson, Anatoly N. Vereshchagin, Yuliya E. Anisina, Artem N. Fakhrutdinov, Alexander S. Goloveshkin, Mikhail P. Egorov, “Pot‐, Atom‐ and Step‐Economic (PASE) Multicomponent Approach to the 5‐(Dialkylphosphonate)‐Substituted 2,4‐Diamino‐5H‐chromeno[2,3‐b]pyridine Scaffold”, Eur J Org Chem, 2019:26 (2019), 4171
Michail N. Elinson, Anatoly N. Vereshchagin, Yuliya E. Anisina, Stepan K. Krymov, Artem N. Fakhrutdinov, Mikhail P. Egorov, “Selective multicomponent 'one-pot' approach to the new 5-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)chromeno[2,3-b]pyridine scaffold in pyridine–ethanol catalyst/solvent system”, Monatsh Chem, 150:6 (2019), 1073
Dmitry G. Kim, Elena V. Kalita, Vladimir V. Sharutin, Irina G. Ovchinnikova, Marina А. Ezhikova, Mikhail I. Kodess, Pavel А. Slepukhin, Anna V. Vasilenko, “Synthesis and halocyclization of 3-cyano-4,6-dimethyl-2-pyridone allyl derivatives”, Chem Heterocycl Comp, 55:6 (2019), 566
I. G. Mamedov, V. N. Khrustalev, P. V. Dorovatovskii, F. N. Naghiev, A. M. Maharramov, “Efficient synthesis of new tricyclic pyrano[3,2-c]pyridine derivatives”, Mendeleev Commun., 29:2 (2019), 232–233
M. N. Elinson, A. N. Vereshchagin, Yu. E. Anisina, S. K. Krymov, A. N. Fakhrutdinov, M. P. Egorov, “Multicomponent assembling of salicylaldehydes, kojic acid and malonic acid derivatives”, Mendeleev Commun., 29:5 (2019), 581–583
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A. N. Vereshchagin, K. A. Karpenko, M. N. Elinson, S. V. Gorbunov, Yu. E. Anisina, M. P. Egorov, “Stereoselective multicomponent synthesis of (2RS,6SR)-2,6-diaryl-3,3,5,5-tetracyanopiperidines”, Russ Chem Bull, 67:8 (2018), 1534
A. N. Vereshchagin, K. A. Karpenko, T. M. Iliyasov, M. N. Elinson, E. O. Dorofeeva, A. N. Fakhrutdinov, M. P. Egorov, “Diastereoselective multicomponent synthesis of (4RS,6SR)-4,6-diaryl-5,5-dicyano-2-methyl-1,4,5,6-tetrahydropyridine-3-carboxylates”, Russ Chem Bull, 67:11 (2018), 2049
A. N. Vereshchagin, K. A. Karpenko, M. N. Elinson, E. O. Dorofeeva, A. S. Goloveshkin, M. P. Egorov, “Pseudo six-component stereoselective synthesis of 2,4,6-triaryl-3,3,5,5-tetracyanopiperidines”, Mendeleev Commun., 28:4 (2018), 384–386
M. N. Elinson, A. N. Vereshchagin, Yu. E. Anisina, A. S. Goloveshkin, I. E. Ushakov, M. P. Egorov, “PASE facile and efficient multicomponent approach to the new type of 5-C-substituted 2,4-diamino-5H-chromeno[2,3-b]pyridine scaffold”, Mendeleev Commun., 28:4 (2018), 372–374