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81
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Vereshchagin A.N.
, Frolov N.A.
, Konyuhova V.Y.
, Hansford K.A.
, Egorov M.P.
Synthesis and microbiological properties of novel bis-quaternary ammonium compounds based on 4,4′-oxydiphenol spacer
Mendeleev Communications. 2019.
V.29. N5. P.523-525. DOI: 10.1016/j.mencom.2019.09.015
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82
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Vereshchagin A.N.
, Dorofeeva E.O.
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, Korolev V.A.
, Egorov M.P.
Pyridinium bromide as a new mediator for electrochemical transformations involving CH-acids
Mendeleev Communications. 2019.
V.29. N4. P.391-392. DOI: 10.1016/j.mencom.2019.07.010
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83
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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
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84
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Vereshchagin A.N.
, Karpenko K.A.
, Elinson M.N.
, Goloveshkin A.S.
, Ushakov I.E.
, Egorov M.P.
Four-component stereoselective synthesis of tetracyano-substituted piperidines
Research on Chemical Intermediates. 2018.
V.44. N9. P.5623-5634. DOI: 10.1007/s11164-018-3444-7
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85
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Elinson M.N.
, Vereshchagin A.N.
, Korshunov A.D.
, Zaimovskaya T.A.
, Egorov M.P.
Electrochemical cascade assembling of heterocyclic ketones and two molecules of malononitrile: facile and efficient ‘one-pot’ approach to 6-heterospiro[2.5]octane-1,1,2,2-tetracarbonitrile scaffold
Monatshefte Fur Chemie. 2018.
V.149. N6. P.1069-1074. DOI: 10.1007/s00706-018-2158-2
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86
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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
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87
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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
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88
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Elinson M.N.
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, Vereshchagin A.N.
, Goloveshkin A.S.
, Bushmarinov I.S.
, Egorov M.P.
Efficient and facile ‘on-solvent’ multicomponent synthesis of medicinally privileged pyrano[3,2-c]pyridine scaffold
Research on Chemical Intermediates. 2018.
V.44. N5. P.3199-3209. DOI: 10.1007/s11164-018-3301-8
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89
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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
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90
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Elinson M.N.
, Vereshchagin A.N.
, Korshunov A.D.
, Egorov M.P.
A fast and efficient ‘on-solvent’ cascade assembling of salicylaldehydes and dimethylbarbituric acid into 5-(1,3-dimethyl-2,4-dioxo-1,3,4,5-tetrahydro-2H-chromeno[2,3-d]pyrimidin-5-yl)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-triones
Heterocyclic Communications. 2018.
V.24. N2. P.79-83. DOI: 10.1515/hc-2018-0015
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91
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Vereshchagin A.N.
, Karpenko K.A.
, Elinson M.N.
, Gorbunov S.V.
, Gordeeva A.M.
, Proshin P.I.
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, Egorov M.P.
Stereoselective one-pot synthesis of polycyanosubstituted piperidines
Monatshefte Fur Chemie. 2018.
V.149. N11. P.1979-1989. DOI: 10.1007/s00706-018-2187-x
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92
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Vereshchagin A.N.
, Karpenko K.A.
, Iliyasov T.M.
, Elinson M.N.
, Dorofeeva E.O.
, Fakhrutdinov A.N.
, Egorov M.P.
Diastereoselective multicomponent synthesis of (4RS,6SR)-4,6-diaryl-5,5-dicyano-2-methyl-1,4,5,6-tetrahydropyridine-3-carboxylates
Russian Chemical Bulletin. 2018.
V.67. N11. P.2049-2053. DOI: 10.1007/s11172-018-2327-9
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93
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Vereshchagin A.N.
, Karpenko K.A.
, Elinson M.N.
, Dorofeeva E.O.
, Goloveshkin A.S.
, Egorov M.P.
Pseudo six-component stereoselective synthesis of 2,4,6-triaryl-3,3,5,5-tetracyanopiperidines
Mendeleev Communications. 2018.
V.28. N4. P.384-386. DOI: 10.1016/j.mencom.2018.07.014
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94
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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
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95
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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
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96
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Elinson M.N.
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, 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
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97
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Vereshchagin A.N.
Classical and interdisciplinary approaches to the design of organic and hybrid molecular systems
Russian Chemical Bulletin. 2017.
V.66. N10. P.1765-1796. DOI: 10.1007/s11172-017-1950-1
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98
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Vereshchagin A.N.
, Elinson M.N.
, Anisina Y.E.
, Ryzhkov F.V.
, Goloveshkin A.S.
, Novikov R.A.
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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
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99
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Vereshchagin A.N.
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, 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
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100
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Elinson M.N.
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Electrochemical Synthesis of Heterocycles via Cascade Reactions
Current Organic Chemistry. 2017.
V.21. N15. P.1427-1439. DOI: 10.2174/1385272820666161017170200
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