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81
|
Bityukov O.V.
, Vil V.A.
, Terent’ev A.O.
Synthesis of Acyclic Geminal Bis-peroxides
Russian Journal of Organic Chemistry. 2021.
V.57. N6. P.853-878. DOI: 10.1134/s1070428021060014
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82
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Budnikov A.S.
, Krylov I.B.
, Lastovko A.V.
, Paveliev S.A.
, Romanenko A.R.
, Nikishin G.I.
, Terent'ev A.O.
Stable and reactive diacetyliminoxyl radical in oxidative C–O coupling with β-dicarbonyl compounds and their complexes
Organic and Biomolecular Chemistry. 2021.
V.19. N35. P.7581-7586. DOI: 10.1039/d1ob01269j
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83
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Mulina O.M.
, Doronin M.M.
, Terent'ev A.O.
Electrosynthesis of N-unsubstituted enaminosulfones from vinyl azides and sodium sulfinates mediated by NH4I
Tetrahedron Letters. 2021.
V.84. 153436
. DOI: 10.1016/j.tetlet.2021.153436
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84
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Bityukov O.V.
, Vil V.
, Nikishin G.
, Terent'ev A.
Alkene, Bromide, and ROH – How To Achieve Selectivity? Electrochemical Synthesis of Bromohydrins and Their Ethers
Advanced Synthesis & Catalysis. 2021.
V.363. N12. P.3070-3078. DOI: 10.1002/adsc.202100161
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85
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Vil V.A.
, Merkulova V.M.
, Ilovaisky A.I.
, Paveliev S.A.
, Nikishin G.I.
, Terent’ev A.O.
Electrochemical Synthesis of Fluorinated Ketones from Enol Acetates and Sodium Perfluoroalkyl Sulfinates
Organic Letters. 2021.
V.23. N13. P.5107-5112. DOI: 10.1021/acs.orglett.1c01643
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86
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Mulina O.M.
, Ilovaisky A.I.
, Terent'ev A.O.
Sulfenylation of Indoles Mediated by Iodine and Its Compounds
ChemistrySelect. 2021.
V.6. N38. P.10369-10378. DOI: 10.1002/slct.202102227
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87
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Alabugin I.V.
, Kuhn L.
, Medvedev M.G.
, Krivoshchapov N.V.
, Vil V.A.
, Yaremenko I.A.
, Mehaffy P.
, Yarie M.
, Terent’ev A.O.
, Zolfigol M.A.
Stereoelectronic power of oxygen in control of chemical reactivity: the anomeric effect is not alone
Chemical Society Reviews. 2021.
V.50. N18. P.10253-10345. DOI: 10.1039/d1cs00386k
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88
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Krylov I.B.
, Budnikov A.S.
, Lopat’eva E.R.
, Segida O.O.
, Paveliev S.A.
, Terent’ev A.O.
Electron-deficient N-oxyl radicals – new reagents for selective oxidative functionalization of organic substrates
Journal of physics. 2021.
V.1942. N1. 012007
. DOI: 10.1088/1742-6596/1942/1/012007
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89
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Vera A. Vil
, Gorlov E.S.
, Yu B.
, Terent'ev A.O.
Oxidative α-acyloxylation of acetals with cyclic diacyl peroxides
Organic chemistry frontiers. 2021.
V.8. N12. P.3091-3101. DOI: 10.1039/d1qo00494h
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90
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Mulina O.M.
, Doronin M.M.
, O. Terent'ev A.
Mn(OAc)3‐Mediated Sulfonylation of Vinyl Azides Resulting in N‐Unsubstituted Enaminosulfones
ChemistrySelect. 2021.
V.6. N38. P.10250-10252. DOI: 10.1002/slct.202102372
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91
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Paveliev S.A.
, Segida O.O.
, Dvoretskiy A.
, Dzyunov M.M.
, Fedorova U.V.
, Terent’ev A.O.
Electrifying Phthalimide-N-Oxyl (PINO) Radical Chemistry: Anodically Induced Dioxygenation of Vinyl Arenes with N-Hydroxyphthalimide
Journal of Organic Chemistry. 2021.
V.86. N24. P.18107-18116. DOI: 10.1021/acs.joc.1c02367
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92
|
Vil V.A.
, Barsegyan Y.A.
, Kuhn L.
, Ekimova M.V.
, Semenov E.A.
, Korlyukov A.A.
, Terent'ev A.O.
, Alabugin I.V.
Synthesis of unstrained Criegee intermediates: inverse α-effect and other protective stereoelectronic forces can stop Baeyer–Villiger rearrangement of γ-hydroperoxy-γ-peroxylactones
Chemical Science. 2020.
V.11. N20. P.5313-5322. DOI: 10.1039/d0sc01025a
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93
|
Paveliev S.A.
, Churakov A.I.
, Alimkhanova L.S.
, Segida O.O.
, Nikishin G.I.
, Terent'ev A.O.
Electrochemical Synthesis of O ‐Phthalimide Oximes from α ‐Azido Styrenes via Radical Sequence: Generation, Addition and Recombination of Imide‐ N ‐Oxyl and Iminyl Radicals with C−O/N−O Bonds Formation
Advanced Synthesis & Catalysis. 2020.
V.362. N18. P.3864-3871. DOI: 10.1002/adsc.202000618
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|
94
|
Yaremenko I.A.
, Syromyatnikov M.Y.
, Radulov P.S.
, Belyakova Y.Y.
, Fomenkov D.I.
, Popov V.N.
, Terent'ev A.O.
Cyclic Synthetic Peroxides Inhibit Growth of Entomopathogenic Fungus Ascosphaera apis without Toxic Effect on Bumblebees
Molecules. 2020.
V.25. N8. 1954
. DOI: 10.3390/molecules25081954
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95
|
Krylov I.B.
, Paveliev S.A.
, Budnikov A.S.
, Terent’ev A.O.
Oxime radicals: generation, properties and application in organic synthesis
Beilstein Journal of Organic Chemistry. 2020.
V.16. P.1234-1276. DOI: 10.3762/bjoc.16.107
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|
96
|
Yaremenko I.A.
, Radulov P.S.
, Belyakova Y.Y.
, Demina A.A.
, Fomenkov D.I.
, Barsukov D.V.
, Subbotina I.R.
, Fleury F.
, Terentev A.O.
Catalyst Development for the Synthesis of Ozonides and Tetraoxanes Under Heterogeneous Conditions: Disclosure of an Unprecedented Class of Fungicides for Agricultural Application
Chemistry: A European Journal. 2020.
V.26. N21. P.4734-4751. DOI: 10.1002/chem.201904555
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|
|
97
|
Kammer L.M.
, Krumb M.
, Spitzbarth B.
, Lipp B.
, Kühlborn J.
, Busold J.
, Olga M Mulina
, Alexander O Terentev
, Opatz T.
Photoredox-Catalyzed Four-Component Reaction for the Synthesis of Complex Secondary Amines
Organic Letters. 2020.
V.22. N9. P.3318-3322. DOI: 10.1021/acs.orglett.0c00614
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|
98
|
Zdvizhkov A.T.
, Radulov P.S.
, Novikov R.A.
, Tafeenko V.A.
, Chernyshev V.V.
, Ilovaisky A.I.
, Terent’ev A.O.
, Nikishin G.I.
Convenient synthesis of furo[2,3-c][1,2]dioxoles from 1-aryl-2-allylalkane-1,3-diones
Mendeleev Communications. 2020.
V.30. N5. P.607-609. DOI: 10.1016/j.mencom.2020.09.018
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|
99
|
Ilovaisky A.I.
, Merkulova V.M.
, Vil V.A.
, Chernoburova E.I.
, Shchetinina M.A.
, Loguzov S.D.
, Dmitrenok A.S.
, Zavarzin I.V.
, Terent'ev A.O.
Regioselective Baeyer–Villiger Oxidation of Steroidal Ketones to Lactones Using BF3/H2O2
European Journal of Organic Chemistry. 2020.
V.2020. N3. P.402-405. DOI: 10.1002/ejoc.201901701
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|
100
|
Paveliev S.A.
, Alimkhanova L.S.
, Sergeeva A.V.
, Terent'ev A.O.
Cerium(IV) ammonium nitrate promoted synthesis of O-phthalimide oximes from vinyl azides and N-hydroxyphthalimide
Tetrahedron Letters. 2020.
V.61. N47. 152533
. DOI: 10.1016/j.tetlet.2020.152533
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