Статьи - Sciact

Статьи (78)

#	Публикация
21	Ryzhkov F.V. , Ryzhkova Y.E. , Elinson M.N. Python in Chemistry: Physicochemical Tools Processes. 2023. V.11. N10. 2897 . DOI: 10.3390/pr11102897 WOS Scopus OpenAlex
22	Elinson M.N. , Ryzhkova Y.E. , Vereshchagin A.N. , Ryzhkov F.V. , Kalashnikova V.M. , Korolev V.A. , Egorov M.P. Electrochemically induced assembling of isatins, kojic acid, and malonic acid derivatives into substituted spiro[indole‐3,4′‐pyran]‐2( 1 H )‐one scaffold and predicting potential protein targets Journal of Heterocyclic Chemistry. 2023. V.60. N2. P.277-290. DOI: 10.1002/jhet.4579 WOS Scopus OpenAlex
23	Ryzhkova Y.E. , Ryzhkov F.V. , Elinson M.N. , Maslov O.I. , Fakhrutdinov A.N. One-Pot Solvent-Involved Synthesis of 5-O-Substituted 5H-Chromeno[2,3-b]pyridines Molecules. 2023. V.28. N1. 64 . DOI: 10.3390/molecules28010064 WOS Scopus OpenAlex
24	Elinson M.N. , Vereshchagin A.N. , Ryzhkova Y.E. , Karpenko K.A. , Ryzhkov F.V. , Egorov M.P. Electrocatalytic Cascade Selective Approach to 3-Aryl-2' H ,3 H ,4 H -Spiro{Furo[2,3- с ]Chromene-2,5'-Pyrimidine}-2',4,4',6'(1' H ,3' H )Tetraones and Its Automatic Screening Docking Studies Polycyclic Aromatic Compounds. 2023. V.43. N9. P.8356-8370. DOI: 10.1080/10406638.2022.2149568 WOS Scopus OpenAlex
25	Ryzhkova Y.E. , Kalashnikova V.M. , Ryzhkov F.V. , Elinson M.N. 5-(1-(4-Hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)-2-oxo-2-phenylethyl)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione Molbank. 2023. V.2023. N2. M1640 . DOI: 10.3390/m1640 WOS Scopus OpenAlex
26	Ryzhkova Y.E. , Kalashnikova V.M. , Fakhrutdinov A.N. , Elinson M.N. Green multicomponent approach to novel 5‐[(2H‐Pyran‐3‐yl)(aryl)methyl]‐1,3‐dimethylpyrimidines Journal of Heterocyclic Chemistry. 2023. V.60. N4. P.576-584. DOI: 10.1002/jhet.4609 WOS Scopus OpenAlex
27	Elinson M.N. , Ryzhkova Y.E. , Ryzhkov F.V. , Kalashnikova V.M. , Maslov O.I. Stereoselective and efficient chemical transformation of aldehydes and two molecules of pyrazolin-5-one into bis(spiropyrazolone)cyclopropanes under a column chromatography-free protocol at room temperature Monatshefte Fur Chemie. 2023. V.154. N6. P.625-633. DOI: 10.1007/s00706-023-03072-5 WOS Scopus OpenAlex
28	Elinson M.N. , Vereshchagin A.N. , Ryzhkova Y.E. , Karpenko K.A. , Kalashnikova V.M. , Egorov M.P. An expedient cyclization of polyfunctional (aryl)(pyrimidinyl)(pyranyl)methanes into spiro[furo[3,2-c]pyran-2,5’-pyrimidine] scaffold Mendeleev Communications. 2023. V.33. N4. P.448-450. DOI: 10.1016/j.mencom.2023.06.002 WOS Scopus OpenAlex
29	Ryzhkova Y.E. , Elinson M.N. , Vereshchagin A.N. , Kalashnikova V.M. , Korolev V.A. , Ryzhkov F.V. , Egorov M.P. Green electrocatalytic Assembling of Salicylaldehydes, Kojic Acid, and Malonic Acid Derivatives into 2‐amino‐4H‐chromenes as Potent Anti‐inflammatory Agents ChemistrySelect. 2022. V.7. N39. e202202872 . DOI: 10.1002/slct.202202872 WOS Scopus OpenAlex
30	Elinson M.N. , Vereshchagin A.N. , Ryzhkova Y.E. , Karpenko K.A. , Ushakov I.E. , Maslov O.I. , Egorov M.P. Four-component transformation of benzaldehydes, dimethylbarbituric acid, 4-hydroxy-6-methyl-2H-pyran-2-one, and morpholine into the unsymmetrical ionic scaffold with three different heterocyclic rings Russian Chemical Bulletin. 2022. V.71. N3. P.464-473. DOI: 10.1007/s11172-022-3434-1 WOS Scopus OpenAlex
31	Ryzhkova Y.E. , Elinson M.N. , Vereshchagin A.N. , Karpenko K.A. , Ryzhkov F.V. , Ushakov I.E. , Egorov M.P. Multicomponent Electrocatalytic Selective Approach to Unsymmetrical Spiro[furo[3,2-c]pyran-2,5′-pyrimidine] Scaffold under a Column Chromatography-Free Protocol at Room Temperature Chemistry-Switzerland. 2022. V.4. N2. P.615-629. DOI: 10.3390/chemistry4020044 WOS Scopus OpenAlex
32	Ryzhkova Y.E. , Ryzhkov F.V. , Maslov O.I. , Elinson M.N. 2,4-Diamino-5-(nitromethyl)-5H-chromeno[2,3-b]pyridine-3-carbonitrile Molbank. 2022. V.2022. N2. M1365 . DOI: 10.3390/m1365 WOS Scopus OpenAlex
33	Ryzhkova Y.E. , Ryzhkov F.V. , Fakhrutdinov A.N. , Elinson M.N. Oxidative Cyclization of 5H-Chromeno[2,3-b]pyridines to Benzo[b]chromeno[4,3,2-de][1,6]naphthyridines, Their NMR Study and Computer Evaluation as Material for LED Molecules. 2022. V.27. N13. 4156 . DOI: 10.3390/molecules27134156 WOS Scopus OpenAlex
34	Ryzhkova Y.E. , Elinson M.N. 2,4-Diamino-5-(5-amino-3-oxo-2,3-dihydro-1H-pyrazol-4-yl)-5H-chromeno[2,3-b]pyridine-3-carbonitrile Molbank. 2022. V.2022. N3. M1399 . DOI: 10.3390/m1399 WOS Scopus OpenAlex
35	Ryzhkova Y.E. , Elinson M.N. Multicomponent synthesis of 1,4-dihydropyridine-3,5-dicarbonitriles Arkivoc. 2022. N5. P.126-134. DOI: 10.24820/ark.5550190.p011.703 WOS Scopus OpenAlex
36	Elinson M.N. , Ryzhkova Y.E. , Kalashnikova V.M. , Egorov M.P. Noncatalytic on water aldol reaction of isatins with cyclic 1,3-diketones at room temperature without the need for subsequent chromatography Mendeleev Communications. 2022. V.32. N4. P.543-545. DOI: 10.1016/j.mencom.2022.07.036 WOS Scopus OpenAlex
37	Ryzhkova Y.E. , Kalashnikova V.M. , Ryzhkov F.V. , Elinson M.N. 1,3-Dimethyl-3′,5-diphenyl-1,5-dihydro-2H,5′H-spiro[furo[2,3-d]pyrimidine-6,4′-isoxazole]-2,4,5′(3H)-trione Molbank. 2022. V.2022. N1. M1317 . DOI: 10.3390/m1317 WOS Scopus OpenAlex
38	Elinson M.N. , Vereshchagin A.N. , Ryzhkova Y.E. , Karpenko K.A. , Ushakov I.E. , Goloveshkin A.S. Direct four-component assembling of arylaldehydes, dimethylbarbituric acid, 4-hydroxycoumarine, and cyclic amines into complex scaffolds with three different heterocyclic rings Monatshefte Fur Chemie. 2021. V.152. N11. P.1327-1336. DOI: 10.1007/s00706-021-02849-w WOS Scopus OpenAlex
39	Elinson M.N. , Ryzhkova Y.E. , Vereshchagin A.N. , Ryzhkov F.V. , Kalashnikova V.M. , Egorov M.P. Direct and efficient electrocatalytic multicomponent assembling of arylaldehydes, malononitrile, and pyrazolin-5-ones into spirocyclopropyl pyrazolone scaffold Monatshefte Fur Chemie. 2021. V.152. N6. P.641-648. DOI: 10.1007/s00706-021-02784-w WOS Scopus OpenAlex
40	Ryzhkov F.V. , Elinson M.N. , Ryzhkova Y.E. , Vereshchagin A.N. , Fakhrutdinov A.N. , Egorov M.P. Electrocatalytic cascade approach to the synthesis of dihydro-2'H,3H-spiro[1-benzofuran-2,5'-pyrimidines] Chemistry of Heterocyclic Compounds. 2021. V.57. N6. P.672-678. DOI: 10.1007/s10593-021-02966-8 WOS Scopus OpenAlex

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