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Статьи (103) Подробнее

1	Kokuev A.O. , Sukhorukov A.Y. Azoalkene chemistry provides practical access to 5-aminopyrazoles selectively protected at the N-1 position Tetrahedron Letters. 2026. V.178. 155987 . DOI: 10.1016/j.tetlet.2026.155987 WOS Scopus OpenAlex
2	Malykhin R.S. , Nguyen D.H. , Sukhorukov A.Y. Redox-Neutral Dearomative Spirocyclization of Isoxazoline N-Oxides: A Route to Structural Analogs of Tyrosine-Derived Sponge Metabolites Journal of Organic Chemistry. 2025. V.90. N40. P.14322–14327. DOI: 10.1021/acs.joc.5c01669 WOS Scopus OpenAlex
3	Pospelov E.V. , Golovanov I.S. , Sukhorukov A.Y. , Chen J. , Zhang W. , Gridnev I.D. Mechanism of formation of active catalytic species in nickel-catalysed asymmetric hydrogenation Mendeleev Communications. 2025. V.35. N6. P.708-710. DOI: 10.71267/mencom.7818 WOS Scopus OpenAlex
4	Okladnikov I.V. , Malykhin R.S. , Lesnikov V.K. , Sukhorukov A.Y. Stabilized Sulfur Ylides as Synthetic Equivalents of the Carbyne Anion: A Domino-Type Double Annulation Approach to Indane-Fused Isoxazoline N -Oxides Organic Letters. 2025. V.27. N45. P.12687-12692. DOI: 10.1021/acs.orglett.5c04140 WOS Scopus OpenAlex
5	Zhirov A.V. , Pospelov E.V. , Sukhorukov A.Y. A Lewis/Brønsted acid-mediated route to furans from nitroalkenes and enol ethers Organic & Biomolecular Chemistry. 2025. V.23. N44. P.10159-10167. DOI: 10.1039/d5ob01200g WOS Scopus OpenAlex
6	Ushakov P.Y. , Sukhorukov A.Y. Recent advances in the application of the isoxazoline route to aldols in the synthesis of natural products Natural Product Reports. 2025. V.42. P.876-910. DOI: 10.1039/d4np00069b WOS Scopus OpenAlex
7	Pronkin D.K. , Melnikov I.N. , Meerov D.B. , Lesnikov V.K. , Sukhorukov A.Y. , Muravyev N.V. Thermal Stability of Several Organic Hydroxylamine Derivatives and a Broader Look at Explosive Hazard Identification Industrial & Engineering Chemistry Research. 2025. V.64. N2. P.1139–1151. DOI: 10.1021/acs.iecr.4c04227 WOS Scopus OpenAlex
8	Pospelov E.V. , Sinyushin K.I. , Golovanov I.S. , Lesnikov V.K. , Frolov K.V. , Nelyubina Y.V. , Sukhorukov A.Y. Transition metal(IV) complexes of nitro-substituted 2,4,9-triazaadamantane-based tris-hydroxylamines: evidence for nitrogen α-effect on stabilization of higher oxidation states Dalton Transactions. 2025. V.54. P.9530-9541. DOI: 10.1039/d5dt00812c WOS Scopus OpenAlex
9	Sukhorukov A.Y. Fundamental Role of N–O Bond-Containing Compounds in Prebiotic Synthesis JACS Au. 2025. V.5. N6. P.2420-2442. DOI: 10.1021/jacsau.5c00334 WOS Scopus OpenAlex
10	Kokuev A.O. , Sukhorukov A.Y. Copper-Catalyzed Alkynylation of In Situ-Generated Azoalkenes: An Umpolung Approach to Pyrazoles Organic Letters. 2024. V.26. N33. P.6999-7003. DOI: 10.1021/acs.orglett.4c02471 WOS Scopus OpenAlex
11	Kim N.Y. , Dukanya D. , Sethi G. , Girimanchanaika S.S. , Yang J. , Nagaraja O. , Swamynayaka A. , Vishwanath D. , Venkantesha K. , Basappa S. , Chinnathambi A. , Alharbi S.A. , Madegowda M. , Sukhorukov A. , Pandey V. , Lobie P.E. , Basappa B. , Ahn K.S. Oxazine drug-seed induces paraptosis and apoptosis through reactive oxygen species/JNK pathway in human breast cancer cells Translational Oncology. 2024. V.49. 102101 . DOI: 10.1016/j.tranon.2024.102101 OpenAlex
12	Malykhin R.S. , Sukhorukov A.Y. Reversible pH-dependent cyclization of hydroxy-substituted gem-chloronitroso compounds to isoxazoline N-oxides and 5,6-dihydro-4H-1,2-oxazine N-oxides Russian Chemical Bulletin. 2024. V.73. N5. P.1303-1311. DOI: 10.1007/s11172-024-4247-1 WOS Scopus OpenAlex
13	Pospelov E.V. , Zhirov A.V. , Kamidolla B. , Sukhorukov A.Y. Accessing Polysubstituted NH Pyrroles from Nitroalkenes via [4+2]‐Cycloaddition/Reductive Ring Contraction Strategy European Journal of Organic Chemistry. 2024. V.27. N30. e202400627 . DOI: 10.1002/ejoc.202400627 WOS Scopus OpenAlex
14	Malykhin R.S. , Aksenova S.A. , Sukhorukov A.Y. An Intramolecular Nitroso-Meerwein–Ponndorf–Verley–Oppenauer Reaction to Access Fused Pyrrolidine Scaffolds Organic Letters. 2024. V.26. N2. P.450-455. DOI: 10.1021/acs.orglett.3c03552 WOS Scopus OpenAlex
15	Ushakov P.Y. , Sukhorukov A.Y. Umpolung Approach to Aldol Products via Isoxazoline N-Oxides as Intermediates Journal of Organic Chemistry. 2024. V.89. N21. P.15590–15597. DOI: 10.1021/acs.joc.4c01671 WOS Scopus OpenAlex
16	Okladnikov I.V. , Aksenova S.A. , Ioffe S.L. , Sukhorukov A.Y. Catalytic Reductive Recyclization of Functionalized Isoxazoline N-Oxides to Pyrrolizidine-3-ones Journal of Organic Chemistry. 2024. V.89. N1. P.379-394. DOI: 10.1021/acs.joc.3c02154 WOS Scopus OpenAlex
17	Lukoyanov A.A. , Aksenova S.A. , Tabolin A.A. , Sukhorukov A.Y. 3-Halo-5,6-dihydro-4H-1,2-oxazine N-oxides as synthetic equivalents of unsaturated nitrile oxides in the [3 + 2]-cycloaddition with arynes: synthesis of substituted 3-vinyl-1,2-benzisoxazoles Organic & Biomolecular Chemistry. 2024. V.22. N18. P.3615-3621. DOI: 10.1039/d4ob00391h WOS Scopus OpenAlex
18	Malykhin R.S. , Sukhorukov A.Y. Electrophilic Intermediates in the Nef and Meyer Reactions: A Computational Study Journal of Organic Chemistry. 2024. V.89. N24. P.18109–18121. DOI: 10.1021/acs.joc.4c01933 WOS Scopus OpenAlex
19	Kokuev A.O. , Sukhorukov A.Y. Michael addition of P-nucleophiles to azoalkenes provides simple access to phosphine oxides bearing an alkylhydrazone moiety Frontiers in Chemistry. 2023. V.11. 1177680 . DOI: 10.3389/fchem.2023.1177680 WOS Scopus OpenAlex
20	Sukhorukov A.Y. Interrupted Nef and Meyer Reactions: A Growing Point for Diversity-Oriented Synthesis Based on Nitro Compounds Molecules. 2023. V.28. N2. 686 :1-20. DOI: 10.3390/molecules28020686 WOS Scopus OpenAlex
21	Poonacha L.K. , Ramesh R. , Ravish A. , Mohan A. , Uppar P.M. , Metri P.K. , Shivananju N.S. , Gaonkar S.L. , Gopal S. , Sukhorukov A.Y. , Pandey V. , Shubha P.B. , Basappa B. Development of Novel Indole and Coumarin Derivatives as Antibacterial Agents That Target Histidine Kinase in S. aureus Applied Microbiology. 2023. V.3. N4. P.1214-1228. DOI: 10.3390/applmicrobiol3040084 OpenAlex
22	Lesnikov V.K. , Golovanov I.S. , Nelyubina Y.V. , Aksenova S.A. , Sukhorukov A.Y. Crown-hydroxylamines are pH-dependent chelating N,O-ligands with a potential for aerobic oxidation catalysis Nature Communications. 2023. V.14. N1. 7673 . DOI: 10.1038/s41467-023-43530-6 WOS Scopus OpenAlex
23	Ozerova V.V. , Emelianov N.A. , Gutsev L.G. , Korchagin D.V. , Shilov G.V. , Dremova N.N. , Ramachandran B.R. , Sukhorukov A.Y. , Aldoshin S.M. , Frolova L.A. , Troshin P.A. Enhanced photostability of multication lead halide perovskites through the use of azaadamantane-based modifiers Materials Today Chemistry. 2023. V.30. 101590 . DOI: 10.1016/j.mtchem.2023.101590 WOS Scopus OpenAlex
24	Pospelov E.V. , Sukhorukov A.Y. Building Up a Piperazine Ring from a Primary Amino Group via Catalytic Reductive Cyclization of Dioximes International Journal of Molecular Sciences. 2023. V.24. N14. 11794 . DOI: 10.3390/ijms241411794 WOS Scopus OpenAlex
25	Pospelov E. , Zhirov A. , Kamidolla B. , Sukhorukov A. Reductive Denitrogenation of Six‐membered Cyclic Nitronates to Densely Substituted Dihydrofurans with Raney® Nickel/AcOH System Advanced Synthesis & Catalysis. 2023. V.365. N17. P.2850-2857. DOI: 10.1002/adsc.202300573 WOS Scopus OpenAlex
26	Lukoyanov A.A. , Tabolin A. , Nelyubina Y.V. , Aksenova S. , Sukhorukov A.Y. Nitronate-aryne cycloaddition as a concise route to stereochemically complex fused benzisoxazolines and amino alcohols Organic & Biomolecular Chemistry. 2023. V.21. N18. P.3871-3880. DOI: 10.1039/d3ob00235g WOS Scopus OpenAlex
27	Lesnikov V.K. , Nelyubina Y.V. , Sukhorukov A.Y. Piperazine-1,4-diol (PipzDiol): synthesis, stereodynamics and assembly of supramolecular hydrogen-bonded 2D networks New Journal of Chemistry. 2022. V.46. N42. P.20386-20394. DOI: 10.1039/d2nj03012h WOS Scopus OpenAlex
28	Okladnikov I. , Boyko Y. , Nelyubina Y. , Ioffe S. , Sukhorukov A. Asymmetric Synthesis of a Pyrrolizidinone‐Based hNK1 Antagonist through Reductive Ring Contraction of a Six‐Membered Cyclic Nitronate European Journal of Organic Chemistry. 2022. V.2022. N41. e202200796 . DOI: 10.1002/ejoc.202200796 WOS Scopus OpenAlex
29	Antonova Y.A. , Nelyubina Y.V. , Ioffe S.L. , Sukhorukov A.Y. , Tabolin A.A. Ring Closure of Nitroalkylmalonates for the Synthesis of Isoxazolines under the Acylation Conditions Advanced Synthesis & Catalysis. 2022. V.364. N15. P.2606-2612. DOI: 10.1002/adsc.202200420 WOS Scopus OpenAlex
30	Golovanov I.S. , Leonov A.V. , Lesnikov V.K. , Pospelov E.V. , Frolov K.V. , Korlyukov A.A. , Nelyubina Y.V. , Novikov V.V. , Sukhorukov A.Y. Iron(iv) complexes with tetraazaadamantane-based ligands: synthesis, structure, applications in dioxygen activation and labeling of biomolecules Dalton Transactions. 2022. V.51. N11. P.4284-4296. DOI: 10.1039/d1dt04104e WOS Scopus OpenAlex
31	Ushakov P.Y. , Ioffe S.L. , Sukhorukov A.Y. Recent advances in the application of ylide-like species in [4 + 1]-annulation reactions: an updated review Organic Chemistry Frontiers. 2022. V.9. N19. P.5358-5382. DOI: 10.1039/d2qo00698g WOS Scopus OpenAlex
32	Malykhin R.S. , Boyko Y.D. , Nelyubina Y.V. , Ioffe S.L. , Sukhorukov A.Y. Interrupted Nef Reaction of Cyclic Nitronates: Diastereoselective Access to Densely Substituted α-Chloronitroso Compounds Journal of Organic Chemistry. 2022. V.87. N24. P.16617-16631. DOI: 10.1021/acs.joc.2c02281 WOS Scopus OpenAlex
33	Pospelov E.V. , Boyko Y.D. , Ioffe S.L. , Sukhorukov A.Y. Synthesis of Bis(β‐Oximinoalkyl)malonates and Their Catalytic Reductive Cyclization to Piperidines Advanced Synthesis & Catalysis. 2022. V.364. N15. P.2557-2564. DOI: 10.1002/adsc.202200424 WOS Scopus OpenAlex
34	Ushakov P.Y. , Ioffe S.L. , Sukhorukov A.Y. Regio- and diastereoselective access to densely functionalized ketones via the Boekelheide rearrangement of isoxazoline N-oxides Organic & Biomolecular Chemistry. 2022. V.20. N28. P.5624-5637. DOI: 10.1039/d2ob00787h WOS Scopus OpenAlex
35	Lukoyanov A.A. , Tabolin A.A. , Nelyubina Y.V. , Ioffe S.L. , Sukhorukov A.Y. Deoxygenative Arylation of 5,6-Dihydro-4H-1,2-oxazine-N-oxides with Arynes Journal of Organic Chemistry. 2022. V.87. N10. P.6838-6851. DOI: 10.1021/acs.joc.2c00515 WOS Scopus OpenAlex
36	Ushakov P.Y. , Sukhorukov A.Y. , Ioffe S.L. , Tabolin A.A. Sequential Formal [4+1]‐Cycloaddition, C−H Functionalization and Suzuki–Miyaura Cross‐Coupling for the Synthesis of Trisubstituted Isoxazolines European Journal of Organic Chemistry. 2021. V.2021. N18. P.2680-2693. DOI: 10.1002/ejoc.202100313 WOS Scopus OpenAlex
37	Malykhin R.S. , Sukhorukov A.Y. Nucleophilic Halogenation of Heterocyclic N‐Oxides: Recent Progress and a Practical Guide Advanced Synthesis & Catalysis. 2021. V.363. N13. P.3170-3188. DOI: 10.1002/adsc.202100284 WOS Scopus OpenAlex
38	Akhmirov R.T. , Ioffe S.L. , Sukhorukov A.Y. Stereoselective approach to conjugated enone oximes from aliphatic nitro compounds and sulfur ylides Mendeleev Communications. 2021. V.31. N5. P.686-689. DOI: 10.1016/j.mencom.2021.09.031 WOS Scopus OpenAlex
39	Ozerova V.V. , Zhidkov I.S. , Boldyreva A. , Dremova N.N. , Emelianov N.A. , Shilov G.V. , Frolova L.A. , Kurmaev E.Z. , Sukhorukov A.Y. , Aldoshin S.M. , Troshin P.A. Spectacular Enhancement of the Thermal and Photochemical Stability of MAPbI3 Perovskite Films Using Functionalized Tetraazaadamantane as a Molecular Modifier Energies. 2021. V.14. N3. 669 . DOI: 10.3390/en14030669 WOS Scopus OpenAlex
40	Golovanov I.S. , Malykhin R.S. , Lesnikov V.K. , Nelyubina Y.V. , Novikov V.V. , Frolov K.V. , Stadnichenko A.I. , Tretyakov E.V. , Ioffe S.L. , Sukhorukov A.Y. Revealing the Structure of Transition Metal Complexes of Formaldoxime Inorganic Chemistry. 2021. V.60. N8. P.5523-5537. DOI: 10.1021/acs.inorgchem.0c03362 WOS Scopus OpenAlex
41	Malykhin R.S. , Golovanov I.S. , Nelyubina Y.V. , Ioffe S.L. , Sukhorukov A.Y. Construction of Saturated Oxazolo[3,2-b][1,2]oxazines via Tandem [3+2]-Cycloaddition/[1,3]-Rearrangement of Cyclic Nitronates and Ketenes Journal of Organic Chemistry. 2021. V.86. N23. P.16337-16348. DOI: 10.1021/acs.joc.1c01744 WOS Scopus OpenAlex
42	Golovanov I.S. , Sukhorukov A.Y. Merging Boron with Nitrogen–Oxygen Bonds: A Review on BON Heterocycles Topics in Current Chemistry. 2021. V.379. N2. 8 . DOI: 10.1007/s41061-020-00317-3 WOS Scopus OpenAlex
43	Kokuev A.O. , Ioffe S.L. , Sukhorukov A.Y. Addition of malonic esters to azoalkenes generated in situ from α-bromo- and α-chlorohydrazones Tetrahedron Letters. 2021. V.83. 153414 . DOI: 10.1016/j.tetlet.2021.153414 WOS Scopus OpenAlex
44	Antonova Y.A. , Ioffe S.L. , Sukhorukov A.Y. , Tabolin A.A. Sequential Acylation/Silylation/Hetero‐Claisen Rearrangement of Nitroalkanes for the Synthesis of Protected Hydroxyoxime Derivatives European Journal of Organic Chemistry. 2021. V.2021. N22. P.3197-3213. DOI: 10.1002/ejoc.202100469 WOS Scopus OpenAlex
45	Sukhorukov A.Y. Editorial: Nitro Compounds as Versatile Building Blocks for the Synthesis of Pharmaceutically Relevant Substances Frontiers in Chemistry. 2020. V.8. 595246 . DOI: 10.3389/fchem.2020.595246 WOS Scopus OpenAlex
46	Semakin A.N. , Nelyubina Y.V. , Ioffe S.L. , Sukhorukov A.Y. 2,4,9‐Triazaadamantanes with “Clickable” Groups: Synthesis, Structure and Applications as Tripodal Platforms European Journal of Organic Chemistry. 2020. V.2020. N43. P.6723-6735. DOI: 10.1002/ejoc.202000832 WOS Scopus OpenAlex
47	Dorokhov V.S. , Nelyubina Y.V. , Ioffe S.L. , Sukhorukov A.Y. Asymmetric Synthesis of Merck’s Potent hNK1 Antagonist and Its Stereoisomers via Tandem Acylation/[3,3]-Rearrangement of 1,2-Oxazine N-Oxides Journal of Organic Chemistry. 2020. V.85. N17. P.11060-11071. DOI: 10.1021/acs.joc.0c01322 WOS Scopus OpenAlex
48	Sukhorukov A.Y. C−H Reactivity of the α‐Position in Nitrones and Nitronates Advanced Synthesis & Catalysis. 2020. V.362. N4. P.724-754. DOI: 10.1002/adsc.201900718 WOS Scopus OpenAlex
49	Somu C. , Mohan C.D. , Ambekar S. , Dukanya _. , Rangappa S. , Baburajeev C. , Sukhorukov A. , Mishra S. , Shanmugam M.K. , Chinnathambi A. , Awad Alahmadi T. , Alharbi S.A. , Basappa _. , Rangappa K.S. Identification of a novel 1,2 oxazine that can induce apoptosis by targeting NF-κB in hepatocellular carcinoma cells Biotechnology Reports. 2020. V.25. e00438 . DOI: 10.1016/j.btre.2020.e00438 Scopus OpenAlex
50	Sukhorukov A.Y. Catalytic Reductive Amination of Aldehydes and Ketones With Nitro Compounds: New Light on an Old Reaction Frontiers in Chemistry. 2020. V.8. 215 . DOI: 10.3389/fchem.2020.00215 WOS Scopus OpenAlex

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