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1
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Antonova Y.A.
, Tabolin A.A.
New type of a stable p-quinone methide possessing a pendant malonate moiety: synthesis and reactions with C-nucleophiles
Mendeleev Communications. 2025.
V.35. N5. P.533-536. DOI: 10.71267/mencom.7746
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2
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Pavel Ushakov
, Ivan Golovanov
, Sema Ioffe
, Andrey Tabolin
Divergent synthesis of nitrocyclopropanes and isoxazoline N-oxides from nitro compounds and vinyl sulfonium salts
Organic Chemistry Frontiers. 2024.
V.11. P.315-326. DOI: 10.1039/d3qo01664a
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3
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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
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4
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Antonova Y.A.
, Tabolin A.A.
Activation of donor-acceptor cyclopropanes under basic conditions. Ring opening of 2-(p-siloxyaryl)cyclopropane 1,1-dicarboxylates with nitro compounds and other C-nucleophiles
Organic Chemistry Frontiers. 2024.
V.11. P.6483-6494. DOI: 10.1039/d4qo01472c
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5
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Ostarkov S.N.
, Lichtenstein Y.I.
, Antonova Y.A.
, Nelyubina Y.V.
, Lesnikov V.K.
, Tabolin A.A.
Divergent Annulations of 5,6‐Dihydro‐4H‐1,2‐Oxazine N‐Oxides and Enol Diazoacetates for the Switchable Chemoselective Synthesis of Fused 1,2‐Oxazine Derivatives
European Journal of Organic Chemistry. 2024.
V.27. N45. e202400768
. DOI: 10.1002/ejoc.202400768
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6
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Antonova Y.A.
, Nelyubina Y.V.
, Ioffe S.L.
, Tabolin A.A.
[3+3]-Annulation of Cyclic Nitronates with Vinyl Diazoacetates: Diastereoselective Synthesis of Partially Saturated [1,2]Oxazino[2,3-b][1,2]oxazines and Their Base-Promoted Ring Contraction to Pyrrolo[1,2-b][1,2]oxazine Derivatives
Molecules. 2023.
V.28. N7. 3025
. DOI: 10.3390/molecules28073025
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7
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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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8
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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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9
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Motornov V.A.
, Tabolin A.A.
, Ioffe S.L.
Oxidative [3+2]-annulation of nitroalkenes and azolium ylides in the presence of Cu(ii): efficient synthesis of [5,5]-annulated N-fused heterocycles
New Journal of Chemistry. 2022.
V.46. N9. P.4134-4141. DOI: 10.1039/d1nj05332a
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10
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Fadeeva A.A.
, Ioffe S.L.
, Tabolin A.A.
Synthesis of 3‐Haloisoxazolines by Deoxygenation of 3‐Haloisoxazoline N‐Oxides under Treatment with Acetyl Bromide
ChemistrySelect. 2022.
V.7. N27. e202202267
. DOI: 10.1002/slct.202202267
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11
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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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12
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Lichtenstein Y.I.
, Golovanov I.S.
, Ioffe S.L.
, Tabolin A.A.
Tandem [3+2]-cycloaddition/homo-Baldwin rearrangement of silyl nitronates and donor-acceptor cyclopropenes. A novel approach to polysubstituted aziridines starting from nitro compounds
Tetrahedron. 2022.
V.110. 132693
. DOI: 10.1016/j.tet.2022.132693
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13
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Motornov V.A.
, Tabolin A.A.
, Nelyubina Y.V.
, Nenajdenko V.G.
, Ioffe S.L.
Copper-catalyzed [3 + 2]-cycloaddition of α-halonitroalkenes with azomethine ylides: facile synthesis of multisubstituted pyrrolidines and pyrroles
Organic & Biomolecular Chemistry. 2021.
V.19. N15. P.3413-3427. DOI: 10.1039/d1ob00146a
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14
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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
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15
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Fadeeva A.A.
, Ioffe S.L.
, Tabolin A.A.
Dehydration of isoxazoline N-oxides under electrophilic conditions – An alternative approach toward 3-haloisoxazoles
Tetrahedron Letters. 2021.
V.73. 153106
. DOI: 10.1016/j.tetlet.2021.153106
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16
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Ponomarev S.A.
, Larkovich R.V.
, Aldoshin A.S.
, Tabolin A.A.
, Ioffe S.L.
, Groß J.
, Opatz T.
, Nenajdenko V.G.
Diels–Alder reaction of β-fluoro-β-nitrostyrenes with cyclic dienes
Beilstein Journal of Organic Chemistry. 2021.
V.17. P.283-292. DOI: 10.3762/bjoc.17.27
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17
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Aldoshin A.S.
, Tabolin A.A.
, Ioffe S.L.
, Nenajdenko V.G.
An Easy Synthesis of Monofluorinated Derivatives of Pyrroles from β-Fluoro-β-Nitrostyrenes
Molecules. 2021.
V.26. N12. 3515
. DOI: 10.3390/molecules26123515
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18
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Motornov V.A.
, Tabolin A.A.
, Nenajdenko V.G.
, Ioffe S.L.
Copper‐Mediated Oxidative [3+2]‐Annulation of Nitroalkenes and Ylides of 1,2‐Diazines: Assembly of Functionalized Pyrrolo[1,2‐b]pyridazines
ChemistrySelect. 2021.
V.6. N37. P.9969-9974. DOI: 10.1002/slct.202103189
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19
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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
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20
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Fadeeva A.A.
, Ioffe S.L.
, Tabolin A.A.
Chlorination of Conjugated Nitroalkenes with PhICl2 and SO2Cl2 for the Synthesis of α-Chloronitroalkenes
Synthesis-Stuttgart. 2020.
V.52. N18. P.2679-2688. DOI: 10.1055/s-0040-1707396
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