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41
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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
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42
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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
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43
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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
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44
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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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45
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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
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46
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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
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47
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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
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48
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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
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49
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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
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50
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Pospelov E.V.
, Golovanov I.S.
, Ioffe S.L.
, Sukhorukov A.Y.
The Cyclic Nitronate Route to Pharmaceutical Molecules: Synthesis of GSK’s Potent PDE4 Inhibitor as a Case Study
Molecules. 2020.
V.25. N16. 3613
. DOI: 10.3390/molecules25163613
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51
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Sukhorukov A.Y.
Umpolung of Enamines: An Overview on Strategies and Synthons
Synlett. 2020.
V.31. N05. P.439-449. DOI: 10.1055/s-0037-1610741
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52
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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
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53
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Sukhorukov A.Y.
Recent Advances in the Stereoselective Synthesis of Pyrrolizidin‐3‐ones
В сборнике
Synthetic Approaches to Nonaromatic Nitrogen Heterocycles.
– John Wiley & Sons Ltd..,
2020.
– C.179-223. – ISBN 9781119708704. DOI: 10.1002/9781119708841.ch8
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54
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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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55
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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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56
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Naumovich Y.A.
, Ioffe S.L.
, Sukhorukov A.Y.
Michael Addition of P-Nucleophiles to Conjugated Nitrosoalkenes
Journal of Organic Chemistry. 2019.
V.84. N11. P.7244-7254. DOI: 10.1021/acs.joc.9b00924
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57
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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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58
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Malykhin R.S.
, Golovanov I.S.
, Ioffe S.L.
, Sukhorukov A.Y.
Tandem Deoxygenation/Halogenation of N -Oxides Under Acylation Conditions: Scope and In Situ IR Spectroscopic Study
European Journal of Organic Chemistry. 2019.
V.2019. N26. P.4139-4148. DOI: 10.1002/ejoc.201900131
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59
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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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60
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Komendantova A.S.
, Fakhrutdinov A.N.
, Menchikov L.G.
, Sukhorukov A.Y.
, Zavarzin I.V.
, Volkova Y.A.
Cyclization of β‐Chlorovinyl Thiohydrazones into Pyridazines: A Mechanistic Study
European Journal of Organic Chemistry. 2019.
V.2019. N2-3. P.527-536. DOI: 10.1002/ejoc.201801118
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