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Иловайский Алексей Игоревич

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Научная деятельность

Статьи - 77 , Доклады на конференциях - 8


Статьи (77) Подробнее

1 Budnikov A.S. , Shevchenko M.I. , Krylov I.B. , Pechen D.Y. , Alekseenko A.L. , Ilovaisky A.I. , Terent'ev A.O.
Cross-dehydrogenative C–O coupling of oximes with hydrazones: synthesis of fungicidal azo-oxime ethers
Organic Chemistry Frontiers. 2026. V.13. N1. P.31-53. DOI: 10.1039/d5qo01151e WOS Scopus OpenAlex
2 Belyakova Y.Y. , Tsykunova V.E. , Radulov P.S. , Dzhemileva L.U. , Novikov R.A. , Ilovaisky A.I. , Yaremenko I.A. , Terent’ev A.O.
One-Pot Synthesis of Aminodiperoxides from 1,5-Diketones, Geminal Bishydroperoxides and Ammonium Acetate
Molecules. 2025. V.30. N24. 4703 . DOI: 10.3390/molecules30244703 WOS Scopus OpenAlex
3 Ilovaisky A.I. , Scherbakov A.M. , Bogdanov F.B. , Miciurov D. , Chernoburova E.I. , Merkulova V.M. , Bozhenko E.I. , Dmitrenok A.S. , Salnikova D.I. , Sorokin D.V. , Khamidullina A.I. , Krasil’nikov M.A. , Zavarzin I.V. , Terent’ev A.O.
Secosteroid–2-Pyrazoline Hybrids: Design, Synthesis, Biological Evaluation and Development of Therapeutic Combinations Against ERα-Positive Breast Cancer Cells
Biomedicines. 2025. V.13. N12. 3057 . DOI: 10.3390/biomedicines13123057 WOS Scopus OpenAlex
4 Ilovaisky A.I. , Scherbakov A.M. , Miciurov D. , Chernoburova E.I. , Merkulova V.M. , Bogdanov F.B. , Salnikova D.I. , Sorokin D.V. , Krasil'nikov M.A. , Bozhenko E.I. , Zavarzin I.V. , Terent'ev A.O.
Secosteroid – 1,3,4-Oxadiazole Hybrids: Synthesis and Evaluation of Their Activity Against Hormone-Dependent Breast Cancer Cells
The Journal of Steroid Biochemistry and Molecular Biology. 2025. V.251. 106745 . DOI: 10.1016/j.jsbmb.2025.106745 Scopus OpenAlex
5 Vil’ V.A. , Barsegyan Y.A. , Chabuka B.K. , Ilovaisky A.I. , Alabugin I.V. , Terent’ev A.O.
Pd-Catalyzed C–O Bond Formation: Coupling of Aryl Boronic Acids with O-Electrophiles
ACS Catalysis. 2025. V.15. N5. P.3636-3646. DOI: 10.1021/acscatal.4c07285 WOS Scopus OpenAlex
6 Radulov P. , Skokova K. , Dmitrieva V. , Fomenkov D. , Krylov I. , Ilovaisky A. , Yaremenko I. , Terent'ev A.
Synthesis of 3,5‐Dialkoxy‐1,2‐dioxolanes by Alkoxyperoxidation of 1,3‐Diketones with Hydrogen Peroxide and Alcohols
Advanced Synthesis & Catalysis. 2025. V.367. N2. e202400951 . DOI: 10.1002/adsc.202400951 WOS Scopus OpenAlex
7 Budnikov A.S. , Krylov I.B. , Monin F.K. , Merkulova V.M. , Ilovaisky A.I. , Yan L. , Yu B. , Terent'ev A.O.
Synthesis of β-ketophosphonates through aerobic copper(II)-mediated phosphorylation of enol acetates
Beilstein Journal of Organic Chemistry. 2025. V.21. P.1192-1200. DOI: 10.3762/bjoc.21.96 WOS Scopus OpenAlex
8 Radulov P.S. , Belyakova Y.Y. , Yaremenko I.A. , Ilovaisky A.I. , Nguyen M.D. , Thi T.D. , Thanh T.T. , Terent’ev A.O.
Synthesis of hybrid compounds containing tetraoxane and triazole or imidazole moieties and their fungicidal activity
Russian Chemical Bulletin. 2024. V.73. N5. P.1312-1320. DOI: 10.1007/s11172-024-4248-0 WOS Scopus OpenAlex
9 Ilovaisky A.I. , Scherbakov A.M. , Chernoburova E.I. , Shchetinina M.A. , Merkulova V.M. , Bogdanov F.B. , Sorokin D.V. , Salnikova D.I. , Bozhenko E.I. , Zavarzin I.V. , Terent'ev A.O.
Secosteroid diacylhydrazines as novel effective agents against hormone-dependent breast cancer cells
The Journal of Steroid Biochemistry and Molecular Biology. 2024. V.244. 106597 . DOI: 10.1016/j.jsbmb.2024.106597 WOS Scopus OpenAlex
10 Zaikina L.A. , Mulina O.M. , Merkulova V.M. , Ilovaisky A.I. , Vil’ V.A. , Terent'ev A.O.
Electrochemically Induced Synthesis of β‐Ketosulfones from Enol Acetates and Sodium Sulfinates
ChemistrySelect. 2024. V.9. N36. e202403708 . DOI: 10.1002/slct.202403708 WOS Scopus OpenAlex
11 Ustyuzhanin A.O. , Bityukov O.V. , Sokolovskiy P.V. , Merkulova V.M. , Ilovaisky A.I. , He L-N. , Vil' V.A. , Terent'ev A.O.
Electrochemical hydrocarboxylation of enol derivatives with CO2: access to β‑acetoxycarboxylic acids
Chemical Communications. 2024. V.60. P.8099-8102. DOI: 10.1039/d4cc02831g WOS Scopus OpenAlex
12 Ilovaisky A.I. , Scherbakov A.M. , Merkulova V.M. , Chernoburova E.I. , Shchetinina M.A. , Andreeva O.E. , Salnikova D.I. , Zavarzin I.V. , Terent’ev A.O.
Secosteroid–quinoline hybrids as new anticancer agents
The Journal of Steroid Biochemistry and Molecular Biology. 2023. V.228. 106245 :1-13. DOI: 10.1016/j.jsbmb.2022.106245 WOS Scopus OpenAlex
13 Lopat’eva E.R. , Budnikov A.S. , Krylov I.B. , Alekseenko A.L. , Ilovaisky A.I. , Glinushkin A.P. , Terent’ev A.O.
4-Disubstituted Pyrazolin-3-Ones—Novel Class of Fungicides against Phytopathogenic Fungi
Agrochemicals. 2023. V.2. N1. P.34-46. DOI: 10.3390/agrochemicals2010004 OpenAlex
14 Budnikov A.S. , Krylov I.B. , Shevchenko M.I. , Segida O.O. , Lastovko A.V. , Alekseenko A.L. , Ilovaisky A.I. , Nikishin G.I. , Terent’ev A.O.
C–O Coupling of Hydrazones with Diacetyliminoxyl Radical Leading to Azo Oxime Ethers—Novel Antifungal Agents
Molecules. 2023. V.28. N23. 7863 . DOI: 10.3390/molecules28237863 WOS Scopus OpenAlex
15 Ilovaisky A.I. , Scherbakov A.M. , Chernoburova E.I. , Povarov A.A. , Shchetinina M.A. , Merkulova V.M. , Salnikova D.I. , Sorokin D.V. , Bozhenko E.I. , Zavarzin I.V. , Terent’ev A.O.
Secosteroid thiosemicarbazides and secosteroid–1,2,4-triazoles as antiproliferative agents targeting breast cancer cells: Synthesis and biological evaluation
The Journal of Steroid Biochemistry and Molecular Biology. 2023. V.234. 106386 . DOI: 10.1016/j.jsbmb.2023.106386 WOS Scopus OpenAlex
16 Gorlov E.S. , Shuingalieva D.V. , Ilovaisky A.I. , Vil’ V.A. , Terent’ev A.O.
1-(((6-(Methoxycarbonyl)-5-oxononan-4-yl)oxy)carbonyl)cyclopropane-1-carboxylic Acid
Molbank. 2023. V.2023. N2. M1651 . DOI: 10.3390/m1651 WOS Scopus OpenAlex
17 Chernoburova E.I. , Shchetinina M.A. , Korolev V.A. , Ilovaisky A.I. , Zavarzin I.V.
New stereoselective synthesis of 5α-androst-1-ene-3β,17β-diol
Russian Chemical Bulletin. 2023. V.72. N11. P.2726-2730. DOI: 10.1007/s11172-023-4078-5 WOS Scopus OpenAlex
18 Lopat’eva E.R. , Krylov I.B. , Segida O.O. , Merkulova V.M. , Ilovaisky A.I. , Terent’ev A.O.
Heterogeneous Photocatalysis as a Potent Tool for Organic Synthesis: Cross-Dehydrogenative C–C Coupling of N-Heterocycles with Ethers Employing TiO2/N-Hydroxyphthalimide System under Visible Light
Molecules. 2023. V.28. N3. 934 . DOI: 10.3390/molecules28030934 WOS Scopus OpenAlex
19 Budnikov A.S. , Lopat’eva E.R. , Krylov I.B. , Segida O.O. , Lastovko A.V. , Ilovaisky A.I. , Nikishin G.I. , Glinushkin A.P. , Terent’ev A.O.
4-Nitropyrazolin-5-ones as Readily Available Fungicides of the Novel Structural Type for Crop Protection: Atom-Efficient Scalable Synthesis and Key Structural Features Responsible for Activity
Journal of Agricultural and Food Chemistry. 2022. V.70. N15. P.4572-4581. DOI: 10.1021/acs.jafc.1c07413 WOS Scopus OpenAlex
20 Radulov P.S. , Mozzhegorov A.V. , Mulina O.M. , Yaremenko I.A. , Ilovaisky A.I. , Terent’ev A.O.
Synthesis of β-triazolyl sulfones via the reaction of vinyl sulfones with 1,2,4-triazoles under basic conditions
Russian Chemical Bulletin. 2022. V.71. N7. P.1544-1548. DOI: 10.1007/s11172-022-3562-7 WOS Scopus OpenAlex
21 Vil V.A. , Merkulova V.M. , Ilovaisky A.I. , Paveliev S.A. , Nikishin G.I. , Terent’ev A.O.
Electrochemical Synthesis of Fluorinated Ketones from Enol Acetates and Sodium Perfluoroalkyl Sulfinates
Organic Letters. 2021. V.23. N13. P.5107-5112. DOI: 10.1021/acs.orglett.1c01643 WOS Scopus OpenAlex
22 Mulina O.M. , Ilovaisky A.I. , Terent'ev A.O.
Sulfenylation of Indoles Mediated by Iodine and Its Compounds
ChemistrySelect. 2021. V.6. N38. P.10369-10378. DOI: 10.1002/slct.202102227 WOS Scopus OpenAlex
23 Ilovaisky A.I. , Merkulova V.M. , Chernoburova E.I. , Shchetinina M.A. , Salnikova D.I. , Scherbakov A.M. , Zavarzin I.V. , Terent’ev A.O.
Secosteroidal hydrazides: Promising scaffolds for anti-breast cancer agents
The Journal of Steroid Biochemistry and Molecular Biology. 2021. V.214. 106000 . DOI: 10.1016/j.jsbmb.2021.106000 WOS Scopus OpenAlex
24 Mulina O.M. , Ilovaisky A.I. , Opatz T. , Terent'ev A.O.
Photoredox-catalyzed synthesis of N-unsubstituted enaminosulfones from vinyl azides and sulfinates
Tetrahedron Letters. 2021. V.64. 152737 . DOI: 10.1016/j.tetlet.2020.152737 WOS Scopus OpenAlex
25 Mulina O.M. , Ilovaisky A.I. , Parshin V.D. , Terent'ev A.O.
Oxidative Sulfonylation of Multiple Carbon‐Carbon bonds with Sulfonyl Hydrazides, Sulfinic Acids and their Salts
Advanced Synthesis & Catalysis. 2020. V.362. N21. P.4579-4654. DOI: 10.1002/adsc.202000708 WOS Scopus OpenAlex
26 Yaremenko I.A. , Radulov P.S. , Medvedev M.G. , Krivoshchapov N.V. , Belyakova Y.Y. , Korlyukov A.A. , Ilovaisky A.I. , Terent′ev A.O. , Alabugin I.V.
How to Build Rigid Oxygen-Rich Tricyclic Heterocycles from Triketones and Hydrogen Peroxide: Control of Dynamic Covalent Chemistry with Inverse α-Effect
Journal of the American Chemical Society. 2020. V.142. N34. P.14588-14607. DOI: 10.1021/jacs.0c06294 WOS Scopus OpenAlex
27 Zdvizhkov A.T. , Radulov P.S. , Novikov R.A. , Tafeenko V.A. , Chernyshev V.V. , Ilovaisky A.I. , Terent’ev A.O. , Nikishin G.I.
Convenient synthesis of furo[2,3-c][1,2]dioxoles from 1-aryl-2-allylalkane-1,3-diones
Mendeleev Communications. 2020. V.30. N5. P.607-609. DOI: 10.1016/j.mencom.2020.09.018 WOS Scopus OpenAlex
28 Ilovaisky A.I. , Merkulova V.M. , Vil V.A. , Chernoburova E.I. , Shchetinina M.A. , Loguzov S.D. , Dmitrenok A.S. , Zavarzin I.V. , Terent'ev A.O.
Regioselective Baeyer–Villiger Oxidation of Steroidal Ketones to Lactones Using BF3/H2O2
European Journal of Organic Chemistry. 2020. V.2020. N3. P.402-405. DOI: 10.1002/ejoc.201901701 WOS Scopus OpenAlex
29 Terent’ev A.O. , Mulina O.M. , Ilovaisky A.I. , Kokorekin V.A. , Nikishin G.I.
Ammonium iodide-mediated electrosynthesis of unsymmetrical thiosulfonates from arenesulfonohydrazides and thiols
Mendeleev Communications. 2019. V.29. N1. P.80-82. DOI: 10.1016/j.mencom.2019.01.027 WOS Scopus OpenAlex
30 Mulina O.M. , Ilovaisky A.I. , Terent'ev A.O.
Oxidative Coupling with S–N Bond Formation
European Journal of Organic Chemistry. 2018. V.2018. N34. P.4648-4672. DOI: 10.1002/ejoc.201800838 WOS Scopus OpenAlex
31 Vil V.A. , Yaremenko I.A. , Ilovaisky A.I. , Terent'ev A.O.
Peroxides with Anthelmintic, Antiprotozoal, Fungicidal and Antiviral Bioactivity: Properties, Synthesis and Reactions
Molecules. 2017. V.22. N11. 1881 . DOI: 10.3390/molecules22111881 WOS Scopus OpenAlex
32 Terent'ev A.O. , Mulina O.M. , Pirgach D.A. , Ilovaisky A.I. , Syroeshkin M.A. , Kapustina N.I. , Nikishin G.I.
Electrosynthesis of vinyl sulfones from alkenes and sulfonyl hydrazides mediated by KI: Аn electrochemical mechanistic study
Tetrahedron. 2017. V.73. N49. P.6871-6879. DOI: 10.1016/j.tet.2017.10.047 WOS Scopus OpenAlex
33 Vil V.A. , Yaremenko I.A. , Ilovaisky A.I. , Terent'ev A.O.
Synthetic Strategies for Peroxide Ring Construction in Artemisinin
Molecules. 2017. V.22. N1. 117 . DOI: 10.3390/molecules22010117 WOS Scopus OpenAlex
34 Zdvizhkov A.T. , Terent’ev A.O. , Radulov P.S. , Novikov R.A. , Tafeenko V.A. , Chernyshev V.V. , Ilovaisky A.I. , Levitsky D.O. , Fleury F. , Nikishin G.I.
Transformation of 2-allyl-1,3-diketones to bicyclic compounds containing 1,2-dioxolane and tetrahydrofuran rings using the I 2 /H 2 O 2 system
Tetrahedron Letters. 2016. V.57. N8. P.949-952. DOI: 10.1016/j.tetlet.2016.01.061 WOS Scopus OpenAlex
35 Elinson M.N. , Vereshchagin A.N. , Bobrovsky S.I. , Nasybullin R.F. , Ilovaisky A.I. , Merkulova V.M.
Pseudo four-component reaction of salicylaldehydes and cyclic ketones with two molecules of malononitrile: A facile and efficient way to synthesize 4-[2-(dicyanomethylene)cyclic or heterocyclic]-2-amino-4H-chromenes
Comptes Rendus Chimie. 2016. V.19. N3. P.293-298. DOI: 10.1016/j.crci.2015.11.002 WOS Scopus OpenAlex
36 Elinson M.N. , Vereshchagin A.N. , Nasybullin R.F. , Bobrovsky S.I. , Ilovaisky A.I. , Merkulova V.M. , Bushmarinov I.S. , Egorov M.P.
General approach to a spiro indole-3,1′-naphthalene tetracyclic system: stereoselective pseudo four-component reaction of isatins and cyclic ketones with two molecules of malononitrile
RSC Advances. 2015. V.5. N62. P.50421-50424. DOI: 10.1039/c5ra03452c WOS Scopus OpenAlex
37 Tashkin V.Y. , Gavrilchik A.N. , Ilovaisky A.I. , Apell H.-J. , Sokolov V.S.
Electrogenic binding of ions at the cytoplasmic side of the Na+,K+-ATPase
Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology. 2015. V.9. N2. P.92-99. DOI: 10.1134/s1990747815020105 WOS Scopus OpenAlex
38 Ilovaisky A.I. , Medvedev M.G. , Merkulova V.M. , Elinson M.N. , Nikishin G.I.
Green Approach to the Design of Functionalized Medicinally Privileged 4‐Aryl‐1,4‐dihydropyrano[2,3‐c]‐pyrazole‐5‐carbonitrile Scaffold
Journal of Heterocyclic Chemistry. 2014. V.51. N2. P.523-526. DOI: 10.1002/jhet.1737 WOS Scopus OpenAlex
39 Elinson M.N. , Ryzhkov F.V. , Merkulova V.M. , Ilovaisky A.I. , Nikishin G.I.
Solvent-free multicomponent assembling of aldehydes, N,N′-dialkyl barbiturates and malononitrile: fast and efficient approach to pyrano[2,3-d]pyrimidines
Heterocyclic Communications. 2014. V.20. N5. P.281-284. DOI: 10.1515/hc-2014-0114 WOS Scopus OpenAlex
40 Elinson M.N. , Merkulova V.M. , Ilovaisky A.I. , Chizhov A.O. , Barba F. , Batanero B.
Electrocatalytic Fast and Efficient Aldol Addition of Pyrazoline-5-ones to Isatine
Journal of The Electrochemical Society. 2014. V.161. N6. P.G48-G53. DOI: 10.1149/2.104406jes WOS Scopus OpenAlex
41 Elinson M.N. , Merkulova V.M. , Ilovaisky A.I. , Nikishin G.I.
Cascade Assembling of Isatins and Barbituric Acids: Facile and Efficient Way to 2′′H‐Dispiro[indole‐3,5′‐furo[2,3‐d]pyrimidine‐6′,5′′‐pyrimidine]‐2,2′,2′′,4′,4′′,6′′‐(1H,1′H,1′′H,3′H,3′′H)‐hexone Scaffold
Journal of Heterocyclic Chemistry. 2013. V.50. N5. P.1236-1241. DOI: 10.1002/jhet.1699 WOS Scopus OpenAlex
42 Kokorekin V.A. , Terent’ev A.O. , Ramenskaya G.V. , Grammatikova N.É. , Rodionova G.M. , Ilovaiskii A.I.
Synthesis and Antifungal Activity of Arylthiocyanates
Pharmaceutical Chemistry Journal. 2013. V.47. N8. P.422-425. DOI: 10.1007/s11094-013-0973-7 WOS Scopus OpenAlex
43 Terent'ev A.O. , Krylov I.B. , Timofeev V.P. , Starikova Z.A. , Merkulova V.M. , Ilovaisky A.I. , Nikishin G.I.
Oxidative C-O Cross‐Coupling of 1,3‐Dicarbonyl Compounds and Their Heteroanalogues with N‐Substituted Hydroxamic Acids and N‐Hydroxyimides
Advanced Synthesis & Catalysis. 2013. V.355. N11-12. P.2375-2390. DOI: 10.1002/adsc.201300341 WOS Scopus OpenAlex
44 Elinson M.N. , Ilovaisky A.I. , Merkulova V.M. , Barba F. , Batanero B.
General approach to spiroacenaphthylene pentacyclic systems: direct multicomponent assembling of acenaphthenequinone and cyclic carbonyl compounds with two molecules of malononitrile
Tetrahedron. 2013. V.69. N34. P.7125-7130. DOI: 10.1016/j.tet.2013.06.015 WOS Scopus OpenAlex
45 Elinson M.N. , Medvedev M.G. , Ilovaisky A.I. , Merkulova V.M. , Zaimovskaya T.A. , Nikishin G.I.
Solvent-free cascade assembling of salicylic aldehydes and malononitrile: rapid and efficient approach to 2-amino-4H-chromene scaffold
Mendeleev Communications. 2013. V.23. N2. P.94-95. DOI: 10.1016/j.mencom.2013.03.014 WOS Scopus OpenAlex
46 Elinson M.N. , Merkulova V.M. , Ilovaisky A.I. , Chizhov A.O. , Barba F. , Batanero B.
Electrocatalytic Aldol Addition of Cyclic 1,3-Ketoesters to Isatins: Acetone as a Solvent for the Efficient and Facile Electrochemically Induced Way to 3-Substituted-3-Hydroxyindol-2-One Scaffold
Journal of The Electrochemical Society. 2012. V.159. N11. P.G123-G127. DOI: 10.1149/2.021211jes WOS Scopus OpenAlex
47 Elinson M.N. , Ilovaisky A.I. , Merkulova V.M. , Belyakov P.A. , Barba F. , Batanero B.
General non-catalytic approach to spiroacenaphthylene heterocycles: multicomponent assembling of acenaphthenequinone, cyclic CH-acids and malononitrile
Tetrahedron. 2012. V.68. N29. P.5833-5837. DOI: 10.1016/j.tet.2012.05.005 WOS Scopus OpenAlex
48 Elinson M.N. , Ilovaisky A.I. , Merkulova V.M. , Zaimovskaya T.A. , Nikishin G.I.
Non-Catalytic Thermal Multicomponent Assembling of Isatin, Cyclic CH-Acids and Malononitrile: An Efficient Approach to Spirooxindole Scaffold
Mendeleev Communications. 2012. V.22. N3. P.143-144. DOI: 10.1016/j.mencom.2012.05.010 WOS Scopus OpenAlex
49 Elinson M.N. , Merkulova V.M. , Ilovaisky A.I. , Barba F. , Batanero B.
Electrocatalytic tandem Knoevenagel–Michael addition of barbituric acids to isatins: Facile and efficient way to substituted 5,5′-(2-oxo-2,3-dihydro-1H-indole-3,3-diyl)bis(pyrimidine-2,4,6-(1H,3H,5H)-trione) scaffold
Electrochimica Acta. 2011. V.56. N24. P.8219-8223. DOI: 10.1016/j.electacta.2011.06.059 WOS Scopus OpenAlex
50 Elinson M.N. , Ilovaisky A.I. , Merkulova V.M. , Zaimovskaya T.A. , Nikishin G.I.
Electrocatalytic multicomponent assembling of aldehydes, N-alkyl barbiturates and malononitrile: an efficient approach to pyrano[2,3-d]pyrimidines
Mendeleev Communications. 2011. V.21. N3. P.122-124. DOI: 10.1016/j.mencom.2011.04.002 WOS Scopus OpenAlex

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СИНТЕЗ β-КЕТОФОСФОНАТОВ ЧЕРЕЗ АЭРОБНОЕ МЕДЬ (II) –КАТАЛИЗИРУЕМОЕ ФОСФОРИЛИРОВАНИЕ ЕНОЛАЦЕТАТОВ
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5 Печень Д.Ю. , Будников А.С. , Шевченко М.И. , Крылов И.Б. , Иловайский А.И. , Терентьев А.О.
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Внешние ссылки

ORCID: 0000-0003-2204-2191
Scopus ID: 6602848609
РИНЦ ID: 49946
ResearcherID: AAO-2858-2020