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Статьи (49) Подробнее

1	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 WOS Scopus OpenAlex
2	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 WOS Scopus OpenAlex
3	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
4	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 WOS Scopus OpenAlex
5	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 WOS Scopus OpenAlex
6	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 WOS Scopus OpenAlex
7	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
8	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
9	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 WOS Scopus OpenAlex
10	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
11	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 WOS Scopus OpenAlex
12	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 WOS Scopus OpenAlex
13	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 WOS Scopus OpenAlex
14	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
15	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 WOS Scopus OpenAlex
16	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 WOS Scopus OpenAlex
17	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 WOS Scopus OpenAlex
18	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
19	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 WOS Scopus OpenAlex
20	Motornov V.A. , Tabolin A.A. , Nelyubina Y.V. , Nenajdenko V.G. , Ioffe S.L. Copper-mediated oxidative [3 + 2]-annulation of nitroalkenes and pyridinium imines: efficient synthesis of 3-fluoro- and 3-nitro-pyrazolo[1,5-a]pyridines Organic & Biomolecular Chemistry. 2020. V.18. N7. P.1436-1448. DOI: 10.1039/c9ob02668a WOS Scopus OpenAlex
21	Motornov V.A. , Tabolin A.A. , Nelyubina Y.V. , Nenajdenko V.G. , Ioffe S.L. Acid‐Mediated Three Component Assembly of 4‐Fluoropyrazoles from α‐Fluoronitroalkenes, Hydrazines, and Aldehydes European Journal of Organic Chemistry. 2020. V.2020. N32. P.5211-5219. DOI: 10.1002/ejoc.202000841 WOS Scopus OpenAlex
22	Larkovich R.V. , Ponomarev S.A. , Aldoshin A.S. , Tabolin A.A. , Ioffe S.L. , Nenajdenko V.G. Diels‐Alder Reaction of β‐Fluoro‐β‐nitrostyrenes. Synthesis of Mono‐fluorinated Six‐Membered Derivatives European Journal of Organic Chemistry. 2020. V.2020. N17. P.2479-2492. DOI: 10.1002/ejoc.202000054 WOS Scopus OpenAlex
23	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 WOS Scopus OpenAlex
24	Motornov V.A. , Tabolin A.A. , Nelyubina Y.V. , Nenajdenko V.G. , Ioffe S.L. Copper-mediated oxidative [3 + 2]-annulation of nitroalkenes and pyridinium ylides: general access to functionalized indolizines and efficient synthesis of 1-fluoroindolizines Organic & Biomolecular Chemistry. 2019. V.17. N6. P.1442-1454. DOI: 10.1039/c8ob03126f WOS Scopus OpenAlex
25	Ushakov P.Y. , Khatuntseva E.A. , Nelyubina Y.V. , Tabolin A.A. , Ioffe S.L. , Sukhorukov A.Y. Synthesis of Isoxazolines from Nitroalkanes via a [4+1]‐Annulation Strategy Advanced Synthesis & Catalysis. 2019. V.361. N23. P.5322-5327. DOI: 10.1002/adsc.201901000 WOS Scopus OpenAlex
26	Ushakov P.Y. , Tabolin A.A. , Ioffe S.L. , Sukhorukov A.Y. In Situ Generated Magnesium Cyanide as an Efficient Reagent for Nucleophilic Cyanation of Nitrosoalkenes and Parent Nitronates European Journal of Organic Chemistry. 2019. V.2019. N9. P.1888-1892. DOI: 10.1002/ejoc.201801761 WOS Scopus OpenAlex
27	Aldoshin A.S. , Tabolin A.A. , Ioffe S.L. , Nenajdenko V.G. One‐Pot Synthesis of 3‐(2‐Fluoroalkenyl)indoles European Journal of Organic Chemistry. 2019. V.2019. N27. P.4384-4396. DOI: 10.1002/ejoc.201900573 WOS Scopus OpenAlex
28	Antonova Y.A. , Nelyubina Y.V. , Sukhorukov A.Y. , Ioffe S.L. , Tabolin A.A. Tandem double acylation/[3,3]-rearrangement of aliphatic nitro compounds: a route to α-oxygenated oxime derivatives Organic & Biomolecular Chemistry. 2019. V.17. N24. P.5997-6006. DOI: 10.1039/c9ob01005j WOS Scopus OpenAlex
29	Malykhin R.S. , Kokuev A.O. , Dorokhov V.S. , Nelyubina Y.V. , Tartakovsky V.A. , Tabolin A.A. , Ioffe S.L. , Sukhorukov A.Y. Nucleophilic Halogenation of Cyclic Nitronates: A General Access to 3-Halo-1,2-Oxazines Journal of Organic Chemistry. 2019. V.84. N21. P.13794-13806. DOI: 10.1021/acs.joc.9b02010 WOS Scopus OpenAlex
30	Kokuev A.O. , Antonova Y.A. , Dorokhov V.S. , Golovanov I.S. , Nelyubina Y.V. , Tabolin A.A. , Sukhorukov A.Y. , Ioffe S.L. Acylation of Nitronates: [3,3]-Sigmatropic Rearrangement of in Situ Generated N-Acyloxy,N-oxyenamines Journal of Organic Chemistry. 2018. V.83. N18. P.11057-11066. DOI: 10.1021/acs.joc.8b01652 WOS Scopus OpenAlex
31	Khotyantseva E.A. , Tabolin A.A. , Novikov R.A. , Nelyubina Y.V. , Ioffe S.L. Synthesis of unsaturated silyl nitronates via the silylation of conjugated nitroalkenes Tetrahedron Letters. 2018. V.59. N32. P.3128-3131. DOI: 10.1016/j.tetlet.2018.07.011 WOS Scopus OpenAlex
32	Aldoshin A.S. , Tabolin A.A. , Ioffe S.L. , Nenajdenko V.G. Green, Catalyst-Free Reaction of Indoles with β-Fluoro-β-nitrostyrenes in Water European Journal of Organic Chemistry. 2018. V.2018. N27-28. P.3816-3825. DOI: 10.1002/ejoc.201800385 WOS Scopus OpenAlex
33	Motornov V.A. , Tabolin A.A. , Novikov R.A. , Nelyubina Y.V. , Nenajdenko V.G. , Ioffe S.L. Fluoronitroalkenes in tandem [4 + 1]/[3 + 2]-cycloaddition: one-pot three-component assembly of fluorinated bicyclic nitroso acetals Organic Chemistry Frontiers. 2018. V.5. N17. P.2588-2594. DOI: 10.1039/c8qo00623g WOS Scopus OpenAlex
34	Tabolin A.A. , Sukhorukov A.Y. , Ioffe S.L. α‐Electrophilic Reactivity of Nitronates Chemical Record. 2018. V.18. N10. P.1489-1500. DOI: 10.1002/tcr.201800009 WOS Scopus OpenAlex
35	Tabolin A.A. , Sukhorukov A.Y. , Ioffe S.L. , Dilman A.D. Recent Advances in the Synthesis and Chemistry of Nitronates Synthesis-Stuttgart. 2017. V.49. N15. P.3255-3268. DOI: 10.1055/s-0036-1589063 WOS Scopus OpenAlex
36	Motornov V.A. , Tabolin A.A. , Novikov R.A. , Nelyubina Y.V. , Ioffe S.L. , Smolyar I.V. , Nenajdenko V.G. Synthesis and Regioselective N‐2 Functionalization of 4‐Fluoro‐5‐aryl‐1,2,3‐NH‐triazoles European Journal of Organic Chemistry. 2017. V.2017. N46. P.6851-6860. DOI: 10.1002/ejoc.201701338 WOS Scopus OpenAlex
37	Motornov V.A. , Muzalevskiy V.M. , Tabolin A.A. , Novikov R.A. , Nelyubina Y.V. , Nenajdenko V.G. , Ioffe S.L. Radical Nitration-Debromination of α-Bromo-α-fluoroalkenes as a Stereoselective Route to Aromatic α-Fluoronitroalkenes—Functionalized Fluorinated Building Blocks for Organic Synthesis Journal of Organic Chemistry. 2017. V.82. N10. P.5274-5284. DOI: 10.1021/acs.joc.7b00578 WOS Scopus OpenAlex
38	Tabolin A.A. , Ioffe S.L. Small Ring Compounds and N -oxides: Cycloadditions and Related Processes Israel Journal of Chemistry. 2016. V.56. N6-7. P.385-398. DOI: 10.1002/ijch.201500082 WOS Scopus OpenAlex
39	Mikhaylov A.A. , Dilman A.D. , Novikov R.A. , Khoroshutina Y.A. , Struchkova M.I. , Arkhipov D.E. , Nelyubina Y.V. , Tabolin A.A. , Ioffe S.L. Tandem Pd-catalyzed C–C coupling/recyclization of 2-(2-bromoaryl)cyclopropane-1,1-dicarboxylates with primary nitro alkanes Tetrahedron Letters. 2016. V.57. N1. P.11-14. DOI: 10.1016/j.tetlet.2015.10.091 WOS Scopus OpenAlex
40	Shved A.S. , Tabolin A.A. , Novikov R.A. , Nelyubina Y.V. , Timofeev V.P. , Ioffe S.L. Six‐Membered Cyclic Nitroso Acetals: Synthesis and Studies of the Nitrogen Inversion Process of N‐Silyloxy‐3,6‐dihydro‐2H‐1,2‐oxazines European Journal of Organic Chemistry. 2016. V.2016. N33. P.5569-5578. DOI: 10.1002/ejoc.201600952 WOS Scopus OpenAlex
41	Tabolin A.A. , Gorbacheva E.O. , Novikov R.A. , Khoroshutina Y.A. , Nelyubina Y.V. , Ioffe S.L. Synthesis and chemical transformations of six/six-membered bicyclic nitroso acetals Russian Chemical Bulletin. 2016. V.65. N9. P.2243-2259. DOI: 10.1007/s11172-016-1575-9 WOS Scopus OpenAlex
42	Tabolin A.A. , Novikov R.A. , Khomutova Y.A. , Zharov A.A. , Stashina G.A. , Nelyubina Y.V. , Tomilov Y.V. , Ioffe S.L. Formal [3+3]-cycloaddition of 3-methyl-5,6-dihydro-4H-1,2-oxazine-N-oxides with cyclopropane dicarboxylates under hyperbaric conditions Tetrahedron Letters. 2015. V.56. N16. P.2102-2105. DOI: 10.1016/j.tetlet.2015.03.011 WOS Scopus OpenAlex
43	Tabolin A.A. , Ioffe S.L. Rearrangement of N-Oxyenamines and Related Reactions Chemical Reviews. 2014. V.114. N10. P.5426-5476. DOI: 10.1021/cr400196x WOS Scopus OpenAlex
44	Mikhaylov A.A. , Novikov R.A. , Khomutova Y.A. , Arkhipov D.E. , Korlyukov A.A. , Tabolin A.A. , Tomilov Y.V. , Ioffe S.L. Novel Formal [3+3] Cycloaddition of Silyl Nitronates with Activated Cyclo­propanes and Its Application in the Synthesis of Pyrroline-N-oxides Synlett. 2014. V.25. N16. P.2275-2280. DOI: 10.1055/s-0034-1378564 WOS OpenAlex
45	Shved A.S. , Tabolin A.A. , Khomutova Y.A. , Ioffe S.L. Reactions of silyl nitronates with dimethylformamide dimethyl acetal as a new general procedure for the synthesis of 2-nitroenamines Tetrahedron Letters. 2014. V.55. N45. P.6220-6223. DOI: 10.1016/j.tetlet.2014.09.071 WOS Scopus OpenAlex
46	Gorbacheva E.O. , Tabolin A.A. , Novikov R.A. , Khomutova Y.A. , Nelyubina Y.V. , Tomilov Y.V. , Ioffe S.L. Six-Membered Cyclic Nitronates as 1,3-Dipoles in Formal [3 + 3]-Cycloaddition with Donor–Acceptor Cyclopropanes. Synthesis of New Type of Bicyclic Nitrosoacetals Organic Letters. 2013. V.15. N2. P.350-353. DOI: 10.1021/ol303292c WOS Scopus OpenAlex
47	Tabolin A. , Ioffe S. , Lesiv A. , Khomutova Y. Synthesis of α-Prolinols and 2-Amino-1,5-diols from Primary Nitroalkanes and Other Simple Precursors via Intermediacy of 5,6-Dihydro-4H-1,2-oxa­zines Synthesis-Stuttgart. 2012. V.44. N12. P.1898-1906. DOI: 10.1055/s-0031-1290973 WOS Scopus OpenAlex
48	Zhmurov P.A. , Tabolin A.A. , Sukhorukov A.Y. , Lesiv A.V. , Klenov M.S. , Khomutova Y.A. , Ioffe S.L. , Tartakovsky V.A. Synthesis of phosphodiesterase IVb inhibitors 2. Stereoselective synthesis of hexahydro-3H-pyrrolo[1,2-c]imidazol-3-one and tetrahydro-1H-pyrrolo[1,2-c][1,3]oxazol-3-one derivatives Russian Chemical Bulletin. 2011. V.60. N11. P.2390-2395. DOI: 10.1007/s11172-011-0367-5 WOS Scopus OpenAlex
49	Tabolin A.A. , Lesiv A.V. , Khomutova Y.A. , Nelyubina Y.V. , Ioffe S.L. Rearrangement of 3-alkylidene-2-siloxy-tetrahydro-1,2-oxazines (ASENA). A new approach toward the synthesis of 3-α-hydroxyalkyl-5,6-dihydro-4H-1,2-oxazines Tetrahedron. 2009. V.65. N23. P.4578-4592. DOI: 10.1016/j.tet.2009.03.082 WOS Scopus OpenAlex

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