Publications by Life Chemicals team

The CH₂O@C₆₀ complex: structural, energetic, and vibrational properties from the electron-correlation DF-LMP2 method
Dolgonos, G.A.
Struct Chem (2025). DOI: 10.1007/s11224-025-02578-4

Acyl migrations sensitive to supramolecular encapsulation
O. Lagerna, A. Shivanyuk, T. Kienko, S. Shishkina, O. Lukin, V. Fetyukhin
Chem. Commun. 2025, Advance Article. DOI: 10.1039/D5CC01417D

Spirocyclizations of Nortropanes
O.Lukin, A. Shivanyuk, G. Dolgonos, A. Gerasov, A.Mandzhulo, V. Fetyukhin
Synthesis  2025; 57(08): 1375-1401. DOI: 10.1055/a-2503-2459

Spirocyclic Hybrids of Nortropane and 1,3-Oxazinan-2-one Fragments
A. Mandzhulo, I. Vashchenko, O. Lukin, S. Shishkina, G. Dolgonos, A. Gerasov, V. Yepishev, D. Samofalova, V. Fetyukhin, A. Shivanyuk
Synthesis 2024; 56(17): 2709-2730. DOI: 10.1055/a-2335-4444

Towards Amplified Probing of Weak Intermolecular Interactions on the External Surfaces of Molecular Capsules
O. Lagerna, Dr. A. Shivanyuk, Dr. G. A. Dolgonos, Dr. S. Shishkina, T. Kienko, Dr. A. Poyarkov, I. Tarchuk, Dr. O. Lukin, Dr. V. Fetyukhin
Chemistry. A European Journal. 2024, 30 (18) DOI: 10.1002/chem.202304006

Synthesis and Antimicrobial Activity of Carbene Complexes of the Imidazole, Benzimidazole and 1,2,4-Triazole Series
G. F. Rayenko, A. S. Avksentiev, V. Sh. Saberov, E. B. Rusanov, A. B. Ryabitsky, S. V. Shishkina, O. Z. Komarovska-Porokhnyavets, V. I. Lubenets, N. I. Korotkikh
ChemistrySelect 2023, 8, e202203143. DOI: 10.1002/slct.202203143

In silico induced effect of N-ε-lysine acetylation on microtubule stability and subsequent interaction of microtubule-associated proteins
A. Rayevsky, E. Bulgakov, M. Sharifi, D. Samofalova, D. Ozheredov, P. Karpov, S. Pantano, Y. Blume.
Cell Biol. Int. 2023, 47, 1547-1557. DOI: 10.1002/cbin.12052

The nitration and bromination of 2-(pentafluorosulfanyl)-1,3-benzothiazole and 2-(trifluoromethyl)-1,3-benzothiazole
O. I. Guzyr, L. M. Potikha, S. V. Shishkina, V. N. Fetyukhin & Y. G. Shermolovich
Chemistry of Heterocyclic Compounds, 2023, 59(4/5), 304-308. DOI: 10.1007/s10593-023-03197-9

On regioselective monoacylation of abamectin and ivermectin aglycones
Iryna Vashchenko, Mariya Veselovska, Grygoriy A. Dolgonos, Oleg Lukin, Alexey Poyarkov, Tetyana Kiyenko, Martin E. Gleave, Volodymyr Fetyukhin, Alexander Shivanyuk, Francesco Gentile, Artem Cherkasov,
Tetrahedron, 2023, 149, 133713. DOI: 10.1016/j.tet.2023.133713

Vortex states in a PbTiO3 ferroelectric cylinder
S. Kondovych, M. Pavlenko, Y. Tikhonov, A. Razumnaya, I. Lukyanchuk
SciPost Phys. 14, 056 (2023) · published 30 March 2023. DOI: 10.21468/SciPostPhys.14.3.056

Two- and Three-Phase Self-assembly of Molecular Capsules
A. Shivanyuk, o. Lagerna, G. Dolgonos, V. Rozhkov, S. Shishkina, O. Lukin, A. Poyarkov, V. Fetyukhin,
ChemistrySelect, 2022, Volume7, Issue46, DOI: 10.1002/slct.202200666

Tropane-Based Dispirocyclic Oxiranes and Spirocyclic Ketones
A. Gerasov, R. Boiko, G. Dolgonos, A. Mandzhulo, A. Shivanyuk, V. Fetyukhin, O. Lukin
Synthesis 2022, Issue 01 · Volume 54 DOI: 10.1055/s-0040-1719848

Exploring the Properties of H2O@C60 with the Local Second-Order Møller-Plesset Perturbation Theory: Blue or Red Shift in C60 and H2O Fundamentals to Expect?
G. Dolgonos
ChemistrySelect Volume 6, Issue 42, p. 11583-11590 DOI: 10.1002/slct.202103004

Simple Synthesis of Complex Amines from the Diels–Alder Adducts of (–)-Cytisine
A. Chuyko, G. Dolgonos, A. Shivanyuk, V. Fetyukhin, O. Lukin
Synthesis 2021, 53. DOI: 10.1055/s-0040-1706282

Synthesis and enantiorecognition properties of stereoisomeres of inherently chiral propyloxy-octyloxy-calix[4]arene acetic acids
Oleksandr A. Yesypenko, Anastasia O. Osipova, Oleksandr O. Tribrat, Sergii O. Kravchenko, Oleg M. Usachov, Viktoriya V. Dyakonenko, Aleksey B. Ryabitskii, Vladimir V. Pirozhenko, Svitlana V. Shishkina, Alexander B. Rozhenko, Vitaly I. Kalchenko
Tetrahedron, Volume 80, 2021, 131894. DOI: 10.1016/j.tet.2020.131894

Sulfonimide-Based Dendrimers: Progress in Synthesis, Characterization, and Potential Applications
Bondareva, J.V.; Evlashin, S.A.; Lukin, O.V.
Polymers 2020, 12, 2987. DOI: 10.3390/polym12122987

Enhanced preparation of aryl and heteryl sulfur pentafluorides using mercury (II) oxide - hydrogen fluoride media as a fluorinating reagent
Guzyr, O. I.; Kozel, V. N.; Rusanov, E. B.; Rozhenko, A. B.; Fetyukhin, V. N.; Shermolovich, Y. G.
J. Fluor. Chem. 2020, 239 (June), 109635. https://doi.org/10.1016/j.jfluchem.2020.109635

A Convergent Approach to Sulfonimide-Based Dendrimers and Dendrons
Bondareva, J.; Kolotylo, M.; Rozhkov, V.; Burilov, V.; Lukin, O.
Tetrahedron Letters 2020, Available online 6 May 2020, 152011. DOI: 10.1016/j.tetlet.2020.152011

Covalent and noncovalent films made up of sulfonimide-based dendrimers
Bondareva, J.; Luchkin, S.; Dagesyan, S.; Egorov, A.; Evlashin, S.; Lukin, O.
Applied Surface Science. Published online: 18 April 2020. DOI: 10.1016/j.apsusc.2020.146345

Selective Synthesis of Exo-Spiro[2′,2′-Difluorocyclopropane-3′,2′-Tropanes]
Gerasov, A.; Dolgonos, G. A.; Mandzhulo, A. Y.; Ryabitsky, A.; Fetyukhin, V.; Lukin, O.; Shivanyuk, A.
Synthesis 2020, 52 (07), 1015–1024. DOI: 10.1055/s-0039-1691560

Diverse resistance mechanisms to the third-generation ALK inhibitor lorlatinib in ALK-rearranged lung cancer
Recondo, G.; Mezquita, L.; Facchinetti, F.; Planchard, D.; Gazzah, A.; Bigot, L.; Rizvi, A. Z.; Frias, R. L.; Thiery, J. P.; Scoazec, J.-Y., Sourisseau T., Howarth K., Deas O., Samofalova D. et al.
Clinical Cancer Research. 2020, 26 (1), 242–255. DOI: 10.1158/1078-0432.CCR-19-1104

An optimized divergent synthesis of sulfonimide-based dendrimers achieving the fifth generation
Bondareva, J.; Rozhkov, V.; Kachala, V. V.; Fetyukhin, V.; Lukin, O.
Synth. Commun. 2019, 49 (24), 3536–3545. DOI: 10.1080/00397911.2019.1676909

Reactions of T-Boc-Protected Amines with Difluorocarbene
Gerasov, A.; Shivanyuk, A.; Fetyukhin, V.; Lukin, O.
Synthesis (Stuttg). 2019, 51 (12), 2579–2583. DOI: 10.1055/s-0037-1610703

Theoretical studies of capsular complexes of C2V-symmetrical resorcin[4]arene tetraesters with tetramethylammonium cation
Dolgonos, G.; Tsukanov, A.; Psakhie, S. G.; Lukin, O.; Gurbych, O.; Shivanyuk, A.
Comput. Theor.Chem.1159 (2019), 12-17. DOI:10.1016/j.comptc.2019.05.006

Selective synthesis of N-protected exo-spiro[oxirane-3,2′-tropanes]
Mandzhulo, A.; Vashchenko, I.; Gerasov, A.; Vovk, M.; Rusanov, E.; Fetyukhin, V.; Lukin, O.; Shivanyuk, A.
Org. Chem. Front. 2019, 6 (10), 1692–1697. DOI: 10.1039/C9QO00377K

Gram-Scale Synthesis of Amines Bearing a gem-Difluorocyclopropane Moiety
Nosik, P. S.; Gerasov, A. O.; Boiko, R. O.; Rusanov, E.; Ryabukhin, S. V.; Grygorenko, O. O.; Volochnyuk, D. M.
Adv. Synth. Catal.359 (2017), 3126-3136. DOI: 10.1002/adsc.201700857

Molecular Design of near Infrared Polymethine Dyes: A Review
Bricks, J. L.; Kachkovskii, A. D.; Slominskii, Y. L.; Gerasov, A. O.; Popov, S. V.
Dye. Pigment.2015, 121, 238–255. DOI: 10.1016/J.DYEPIG.2015.05.016.

Synthetic Modification of 1,3-Thiazolidin-4-One 1,1-Dioxides
Listunov, D.; Popov, K.; Volovenko, Y.; Popov, S.
Phosphorus. Sulfur. Silicon Relat. Elem.2013, 188 (12), 1792–1798. DOI: 10.1080/10426507.2013.787998

Conformational structure of the unsymmetrical monomethine cyanine bearing 2-azaazulene and 2-benzothiazole residues as terminal groups: Experimental and quantum-chemical investigation
A.B. Ryabitskii, J.L. Bricks, A.D. Kachkovskii, A.N. Chernega, Y.G. Vlasenko
J. Mol. Str. 982 (2010) 79. DOI: 10.1016/j.molstruc.2010.08.010

One-pot synthesis of diethyl 4,4’-(1,4-phenylene)bis-[6-(halomethyl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylates] and their bispyrrolocyclization
I.O. Lebedyeva, M.V. Povstyanoy, V.M. Povstyanoy, O.G. Panasyuk, E.S. Guban’, A.B. Ryabitskii
Monatsh. Chem. 141 (2010) 997–1000. DOI: 10.1007/s00706-010-0354-9

Studies of 2‐Azaazulenium Derivatives: The Natures of Electron Transitions in the 2‐Azaazulenium Cation and in Monomethine Cyanine Dyes Bearing 2‐Azaazulenium Moieties as Terminal Groups
Julia Bricks, Aeksey Rabitskii, and Alexei Kachkovskii
Chem. Eur. J. v. 16, 29 (2010) 8773-8784. DOI: 10.1002/chem.201000366

Ternary Condensation of Biginelli Thiones, Chloroacetic Acid, and Aldehydes as an Effective Approach towards Thiazolo[3,2-a]pyrimidines and 5-Arylidenethiazolidine-2,4-diones
Iryna O. Lebedyeva, Mykhaylo V. Povstyanoy, Aleksey B. Ryabitskii, and Vyacheslav M. Povstyanoy
J. Heterocyclic Chem. 47 (2010) 368. DOI: 10.1002/jhet.323

Interaction of 4-substituted 5-carbethoxy-6-chloromethylpyrimidin-2-one with hydrazines and hydrazide derivatives: synthesis and structure
I.O. Lebedyeva, M.V. Povstyanoy, A.B. Ryabitsky, and O.G. Panasyuk
Ukr. Khim. Zhur. 76 (2010) 46.

Octafluoro-4,40-bipyridine and its derivatives: Synthesis, molecular and crystal structure
Alexey V. Gutov , Eduard B. Rusanov, Alexey B. Ryabitskii, Alexander N. Chernega
J. Fluor. Chem. 131 (2010) 278–281. DOI: 10.1016/j.jfluchem.2009.11.022

The aza Arndt–Eistert reaction based on N-trifluoromethylsulfonylarenecarboximidoyl chlorides
L.M.Yagupolskii, I.I.Maletina, L.V.Sokolenko, Y.G.Vlasenko, M.V. Drozdova, V.V.Polovinko
J. Fluor. Chem. 2009, v. 131, p. 238-247. DOI: 10.1016/j.jfluchem.2009.10.019

Crystalline and Molecular Design of Functionalized Viologens
A. V. Gutov, E. B. Rusanov, A. B. Ryabitskii, I. F. Tsimbal, and A. N. Chernega
Russ. J. General Chem. v. 79, 9 (2009) 1910. DOI: 10.1134/S1070363209090175

Studies of 2-Azaazulenium Derivatives: The Natures of Electron Transitions in the 2-Azaazulenium Cation and in Monomethine Cyanine Dyes Bearing 2-Azaazulenium Moieties as Terminal Groups
Julia Bricks, Aleksey Ryabitskii, and Alexei Kachkovskii
Eur. J. Org. Chem. (2009) 3439. DOI: 10.1002/ejoc.200900204

3-aminopyrrole-2,5-diones 3*. Synthesis of benzenehexa-carboxylic acid trimethylimide and 1,1′-dimethyl-4-methylamino-[3,3′]bipyrrolyl-2,5,2′,5′-tetraone by the reaction of 1-methyl-3-methylaminopyrrole-2,5-dione with hydrogen chloride
S. V. Chepyshev, Yu. N. Chepysheva, A. B. Ryabitsky, and A. V. Prosyanik
Chem. Het. Comp. v. 45, 7 (2009) 823. DOI: 10.1007/s10593-009-0355-y

2-Aminopyrrole-2,5-diones 2. Vinyl nucleophilic substitution of the alkylamino group in 1-alkyl-3-alkylaminopyrrole-2,5-diones by arylamines
S. V. Chepyshev, Yu. N. Chepysheva, A. B. Ryabitskii, and A. V. Prosyanik
Chem. Het. Comp. v. 44, 5 (2008) 523. DOI: 10.1007/s10593-008-0071-z