Articles - Sciact

Articles (78)

#	Публикация
61	Ryzhkova Y.E. , Ryzhkov F.V. , Elinson M.N. 3-(4-Bromophenyl)-4-{[3-hydroxy-6-(hydroxymethyl)-4-oxo-4H-pyran-2-yl](m-tolyl)methyl}isoxazol-5(2H)-one Molbank. 2020. V.2020. N2. M1135 . DOI: 10.3390/m1135 WOS Scopus OpenAlex
62	Elinson M.N. , Ryzhkova Y.E. , Ryzhkov F.V. , Vereshchagin A.N. , Leonova N.A. , Egorov M.P. Electrochemically Induced Facile and Efficient Multicomponent Approach to Medicinally Relevant 4‐[4‐oxo‐4 H ‐pyran‐2‐yl](aryl)‐methylisoxazol‐5(2 H )‐one Scaffold ChemistrySelect. 2020. V.5. N20. P.5981-5986. DOI: 10.1002/slct.202001592 WOS Scopus OpenAlex
63	Ryzhkov F.V. , Ryzhkova Y.E. , Elinson M.N. , Vorobyev S.V. , Fakhrutdinov A.N. , Vereshchagin A.N. , Egorov M.P. Catalyst-Solvent System for PASE Approach to Hydroxyquinolinone-Substituted Chromeno[2,3-b]pyridines Its Quantum Chemical Study and Investigation of Reaction Mechanism Molecules. 2020. V.25. N11. 2573 . DOI: 10.3390/molecules25112573 WOS Scopus OpenAlex
64	Elinson M.N. , Vereshchagin A.N. , Anisina Y.E. , Krymov S.K. , Fakhrutdinov A.N. , Egorov M.P. Potassium fluoride catalysed multicomponent approach to medicinally privileged 5-[3-hydroxy-6-(hydroxymethyl)-4H-pyran-2-yl] substituted chromeno[2,3-b]pyridine scaffold Arkivoc. 2019. N2. P.38-49. DOI: 10.24820/ark.5550190.p011.002 WOS Scopus OpenAlex
65	Elinson M.N. , Vereshchagin A.N. , Anisina Y.E. , Krymov S.K. , Fakhrutdinov A.N. , Egorov M.P. Multicomponent assembling of salicylaldehydes, kojic acid and malonic acid derivatives Mendeleev Communications. 2019. V.29. N5. P.581-583. DOI: 10.1016/j.mencom.2019.09.035 WOS Scopus OpenAlex
66	Elinson M.N. , Vereshchagin A.N. , Anisina Y.E. , Krymov S.K. , Fakhrutdinov A.N. , Egorov M.P. 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 Monatshefte Fur Chemie. 2019. V.150. N6. P.1073-1078. DOI: 10.1007/s00706-019-02388-5 WOS Scopus OpenAlex
67	Elinson M.N. , Vereshchagin A.N. , Anisina Y.E. , Fakhrutdinov A.N. , Goloveshkin A.S. , Egorov M.P. Pot‐, Atom‐ and Step‐Economic (PASE) Multicomponent Approach to the 5‐(Dialkylphosphonate)‐Substituted 2,4‐Diamino‐5H‐chromeno[2,3‐b]pyridine Scaffold European Journal of Organic Chemistry. 2019. V.2019. N26. P.4171-4178. DOI: 10.1002/ejoc.201900240 WOS Scopus OpenAlex
68	Elinson M.N. , Vereshchagin A.N. , Ryzhkov F.V. , Anisina Y.E. 'Solvent-free’ and 'on-solvent’ multicomponent reaction of isatins, malononitrile, and bicyclic CH-acids: fast and efficient way to medicinal privileged spirooxindole scaffold Arkivoc. 2018. N4. P.276-285. DOI: 10.24820/ark.5550190.p010.640 WOS Scopus OpenAlex
69	Vereshchagin A.N. , Karpenko K.A. , Elinson M.N. , Gorbunov S.V. , Anisina Y.E. , Egorov M.P. Stereoselective multicomponent synthesis of (2RS,6SR)-2,6-diaryl-3,3,5,5-tetracyanopiperidines Russian Chemical Bulletin. 2018. V.67. N8. P.1534-1537. DOI: 10.1007/s11172-018-2252-y WOS Scopus OpenAlex
70	Vereshchagin A.N. , Elinson M.N. , Anisina Y.E. , Karpenko K.A. , Goloveshkin A.S. , Zlotin S.G. , Egorov M.P. High diastereoselective amine-catalyzed Knoevenagel–Michael-cyclization–ring-opening cascade between aldehydes, 3-arylisoxazol-5(4H)-ones and 3-aminocyclohex-2-en-1-ones Molecular Diversity. 2018. V.22. N3. P.627-636. DOI: 10.1007/s11030-018-9817-4 WOS Scopus OpenAlex
71	Elinson M.N. , Vereshchagin A.N. , Anisina Y.E. , Goloveshkin A.S. , Ushakov I.E. , Egorov M.P. 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 Communications. 2018. V.28. N4. P.372-374. DOI: 10.1016/j.mencom.2018.07.010 WOS Scopus OpenAlex
72	Elinson M.N. , Vereshchagin A.N. , Anisina Y.E. , Fakhrutdinov A.N. , Goloveshkin A.S. , Egorov M.P. A facile and efficient multicomponent approach to 5-[5-hydroxy- 3-(trifluoromethyl)-1H-pyrazol-4-yl]-5H-chromeno[2,3-b]pyridines Journal of Fluorine Chemistry. 2018. V.213. P.31-36. DOI: 10.1016/j.jfluchem.2018.06.008 WOS Scopus OpenAlex
73	Elinson M.N. , Vereshchagin A.N. , Anisina Y.E. , Goloveshkin A.S. , Ushakov I.E. , Egorov M.P. Multicomponent transformation of salicylaldehydes, 2-aminoprop-1-ene-1,1,3-tricarbonitrile, and pyrazolin-5-ones into substituted 2,4-diamino-5-(5-hydroxy-3-methyl-1H-pyrazol-4-yl)-5H-chromeno[2,3-b]pyridine-3-carbonitriles Russian Chemical Bulletin. 2018. V.67. N9. P.1695-1703. DOI: 10.1007/s11172-018-2278-1 WOS Scopus OpenAlex
74	Elinson M.N. , Vereshchagin A.N. , Anisina Y.E. , Egorov M.P. Efficient Multicomponent Approach to the Medicinally Relevant 5-aryl-chromeno[2,3-b]pyridine Scaffold Polycyclic Aromatic Compounds. 2017. V.40. N1. P.108-115. DOI: 10.1080/10406638.2017.1363062 WOS Scopus OpenAlex
75	Vereshchagin A.N. , Elinson M.N. , Anisina Y.E. , Ryzhkov F.V. , Goloveshkin A.S. , Novikov R.A. , Egorov M.P. Synthesis, structural, spectroscopic and docking studies of new 5C-substituted 2,4-diamino-5H-chromeno[2,3-b]pyridine-3-carbonitriles Journal of Molecular Structure. 2017. V.1146. P.766-772. DOI: 10.1016/j.molstruc.2017.06.044 WOS Scopus OpenAlex
76	Vereshchagin A.N. , Elinson M.N. , Anisina Y.E. , Ryzhkov F.V. , Novikov R.A. , Egorov M.P. PASE Pseudo-Four-Component Synthesis and Docking Studies of New 5-C-Substituted 2,4-Diamino-5H-Chromeno[2,3-b]pyridine-3-Carbonitriles ChemistrySelect. 2017. V.2. N17. P.4593-4597. DOI: 10.1002/slct.201700606 WOS Scopus OpenAlex
77	Vereshchagin A.N. , Elinson M.N. , Korshunov A.D. , Anisina Y.E. , Novikov R.A. , Goloveshkin A.S. , Bushmarinov I.S. , Zlotin S.G. , Egorov M.P. Stereoselective Michael Halogenation Initiated Ring Closure (MHIRC) Synthesis of Spirocyclopropanes from Benzylidenemalononitriles and 3-Arylisoxazol-5(4H)-ones Synlett. 2016. V.27. N17. P.2489-2493. DOI: 10.1055/s-0035-1562690 WOS Scopus OpenAlex
78	Vereshchagin A.N. , Elinson M.N. , Anisina Y.E. , Ryzhkov F.V. , Goloveshkin A.S. , Bushmarinov I.S. , Zlotin S.G. , Egorov M.P. Pot, atom and step economic (PASE) synthesis of 5-isoxazolyl-5H-chromeno[2,3-b]pyridine scaffold Mendeleev Communications. 2015. V.25. N6. P.424-426. DOI: 10.1016/j.mencom.2015.11.008 WOS Scopus OpenAlex

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