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21
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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
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22
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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
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23
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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
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24
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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
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25
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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
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26
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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
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27
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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
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28
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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
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29
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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
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30
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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
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31
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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
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32
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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
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33
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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
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34
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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
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35
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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
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36
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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
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37
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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
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38
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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
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39
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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
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40
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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
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