|
61
|
Ryzhkova Y.E.
, Ryzhkov F.V.
, Elinson M.N.
, Vereshchagin A.N.
, Egorov M.P.
Pseudo-four-component synthesis of 5-(4-hydroxy-2-oxo-1,2-dihydropyridin-3-yl)-substituted 5H-chromeno[2,3-b]pyridines and estimation of its affinity to sirtuin 2
Arkivoc. 2020.
N6. P.193-208. DOI: 10.24820/ark.5550190.p011.220
WOS
Scopus
OpenAlex
|
|
62
|
Ryzhkov F.V.
, Elinson M.N.
, Ryzhkova Y.E.
, Vereshchagin A.N.
, Goloveshkin A.S.
, Egorov M.P.
Stereoselective domino assembling of five molecules: one-pot approach to (2R',3S,4'R)-2',4'-diaryl-1',4'-dihydro-2'H-spiro[indoline-3,3'-pyridines]
Comptes Rendus Chimie. 2020.
V.23. N2. P.159-168. DOI: 10.5802/crchim.13
WOS
Scopus
OpenAlex
|
|
63
|
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
|
|
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
|