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