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O,S,Se-containing Biginelli products based on cyclic β-ketosulfone and their postfunctionalization

Beilstein journal of organic chemistry, 2024-08, Vol.20 (1), p.2143-2151

2024

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Calcium Modulating Effect of Polycyclic Cages: A Suitable Therapeutic Approach Against Excitotoxic-induced Neurodegeneration

Mini reviews in medicinal chemistry, 2024-01, Vol.24 (13), p.1277-1292

2024

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Rh-catalyzed cyclization of carbamates–synthesis of a new heterocyclic system: tetrahydro-3H-4-oxa-2-thia-2b-azacyclopropa[cd]pentalen-3-one 2,2-dioxide

Chemical papers, 2023-11, Vol.77 (11), p.7249-7254

2023

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Synthesis of 2-hexyl-5-ethylfuran-3-sulfonic acid (HEFS) – natural antithrombosis agent from Eisenia earthworms

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2023-07, Vol.59 (6-7), p.512-516

Palchykov, Vitalii A.

2023

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Fused chiral azaheterocycles based on monosubstituted ferrocenes

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2024-06, Vol.60 (5-6), p.212-215

2024

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Recent progress in the synthesis of morpholines

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2019-05, Vol.55 (4-5), p.324-332

2019

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Dihydro-2H-thiopyran-3(4H)-one-1,1-dioxide - a new cyclic ketomethylenic reagent for the Dimroth-type 1,2,3-triazole synthesis

Synthetic communications, 2020-06, Vol.50 (12), p.1835-1844

2020

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Open and rearranged norbornane derived polycyclic cage molecules as potential neuroprotective agents through attenuation of MPP+- and calcium overload-induced excitotoxicity in neuroblastoma SH-SY5Y cells

European journal of medicinal chemistry, 2020-10, Vol.204, p.112617, Article 112617

2020

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Thiopyran-3-one 1,1-dioxides in the synthesis of heterocycles (microreview)

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2019-05, Vol.55 (4-5), p.349-351

2019

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Targeting a Cryptic Pocket in a Protein–Protein Contact by Disulfide-Induced Rupture of a Homodimeric Interface

ACS chemical biology, 2021-06, Vol.16 (6), p.1090-1098

2021

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Dihydro-2H-thiopyran-3(4H)-one-1,1-dioxide – a versatile building block for the synthesis of new thiopyran-based heterocyclic systems

New journal of chemistry, 2018-01, Vol.42 (2), p.1403-1412

2018

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Multigram scale synthesis of 3,4- and 3,6-dihydro-2H-thiopyran 1,1-dioxides and features of their NMR spectral behavior

Synthetic communications, 2018-09, Vol.48 (17), p.2198-2205

2018

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Cage-Like Amines in the Green Protocol of Transannular Thieno[2,3-d]Pyrimidinone Formation as Promising Anticancer Agents

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2020-06, Vol.56 (6), p.793-799

2020

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Grignard Reagents and Their N‐analogues in the Synthesis of Tricyclic and Tetracyclic Cage‐like Lactams

Journal of heterocyclic chemistry, 2018-10, Vol.55 (10), p.2381-2391

2018

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The formation of the salt and neutral molecule cocrystal from equimolar solution of heliamine and bicyclo[2.2.1]hept‐5‐ene‐endo‐2,3‐dicarboxylic acid

Acta crystallographica Section B, Structural science, crystal engineering and materials, 2019-04, Vol.75 (2), p.192-200

2019

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Synthesis of challenging 6-functionalized 1-oxaspiro[3.3]heptanes – New scaffolds for drug discovery

Tetrahedron letters, 2023-06, Vol.122, p.154515, Article 154515

2023

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Ring-chain tautomerism of vicinal hydroxyimines bearing sulfolane moiety

Journal of molecular structure, 2024-12, Vol.1318, p.139166, Article 139166

2024

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Synthesis of new azapolycyclic scaffolds via the domino aminolysis of dicyclopentadiene diepoxide in water

Tetrahedron letters, 2020-07, Vol.61 (28), p.152097, Article 152097

2020

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Dihydro-2 H -thiopyran-3(4 H )-one-1,1-dioxide – a new cyclic ketomethylenic reagent for the Dimroth-type 1,2,3-triazole synthesis

Synthetic communications, 2020-06, Vol.50 (12), p.1835-1844

2020

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Multigram scale synthesis of 3,4- and 3,6-dihydro-2 H -thiopyran 1,1-dioxides and features of their NMR spectral behavior

Synthetic communications, 2018-09, Vol.48 (17), p.2198-2205

2018

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Synthesis and characterization of sulfolane-based amino alcohols: A combined experimental and computational study

Journal of molecular structure, 2018-04, Vol.1157, p.149-158

2018

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ВОНА ЗАВЖДИ ПРАЦЮВАЛА З НАТХНЕННЯМ І ВМІЛА НАДИХАТИ ІНШИХ

Journal of Chemistry and Technologies, 2023-01, Vol.30 (4), p.490-501

2023

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Dihydro-2 H -thiopyran-3(4 H )-one-1,1-dioxide – a versatile building block for the synthesis of new thiopyran-based heterocyclic systems

New journal of chemistry, 2018, Vol.42 (2), p.1403-1412

2018

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Dihydro-2H-thiopyran-3(4H)-one-1,1-dioxide - a versatile building block for the synthesis of new thiopyran-based heterocyclic systemsElectronic supplementary information (ESI) available: Spectral data, in silico screening data. See DOI: 10.1039/c7nj03846a

2018-01

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Chemical composition and antibacterial effect of ethanolic extract of Buxus sempervirens on cryogenic strains of microorganisms in vitro

Chemical Data Collections, 2020-02, Vol.25, p.100323, Article 100323

2020

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O,S,Se-containing Biginelli products based on cyclic β-ketosulfone and their postfunctionalization

Calcium Modulating Effect of Polycyclic Cages: A Suitable Therapeutic Approach Against Excitotoxic-induced Neurodegeneration

Rh-catalyzed cyclization of carbamates–synthesis of a new heterocyclic system: tetrahydro-3H-4-oxa-2-thia-2b-azacyclopropa[cd]pentalen-3-one 2,2-dioxide

Synthesis of 2-hexyl-5-ethylfuran-3-sulfonic acid (HEFS) – natural antithrombosis agent from Eisenia earthworms

Fused chiral azaheterocycles based on monosubstituted ferrocenes

Recent progress in the synthesis of morpholines

Dihydro-2H-thiopyran-3(4H)-one-1,1-dioxide - a new cyclic ketomethylenic reagent for the Dimroth-type 1,2,3-triazole synthesis

Open and rearranged norbornane derived polycyclic cage molecules as potential neuroprotective agents through attenuation of MPP+- and calcium overload-induced excitotoxicity in neuroblastoma SH-SY5Y cells

Thiopyran-3-one 1,1-dioxides in the synthesis of heterocycles (microreview)

Targeting a Cryptic Pocket in a Protein–Protein Contact by Disulfide-Induced Rupture of a Homodimeric Interface

Dihydro-2H-thiopyran-3(4H)-one-1,1-dioxide – a versatile building block for the synthesis of new thiopyran-based heterocyclic systems

Multigram scale synthesis of 3,4- and 3,6-dihydro-2H-thiopyran 1,1-dioxides and features of their NMR spectral behavior

Cage-Like Amines in the Green Protocol of Transannular Thieno[2,3-d]Pyrimidinone Formation as Promising Anticancer Agents

Grignard Reagents and Their N‐analogues in the Synthesis of Tricyclic and Tetracyclic Cage‐like Lactams

The formation of the salt and neutral molecule cocrystal from equimolar solution of heliamine and bicyclo[2.2.1]hept‐5‐ene‐endo‐2,3‐dicarboxylic acid

Synthesis of challenging 6-functionalized 1-oxaspiro[3.3]heptanes – New scaffolds for drug discovery

Ring-chain tautomerism of vicinal hydroxyimines bearing sulfolane moiety

Synthesis of new azapolycyclic scaffolds via the domino aminolysis of dicyclopentadiene diepoxide in water

Dihydro-2 H -thiopyran-3(4 H )-one-1,1-dioxide – a new cyclic ketomethylenic reagent for the Dimroth-type 1,2,3-triazole synthesis

Multigram scale synthesis of 3,4- and 3,6-dihydro-2 H -thiopyran 1,1-dioxides and features of their NMR spectral behavior

Synthesis and characterization of sulfolane-based amino alcohols: A combined experimental and computational study

ВОНА ЗАВЖДИ ПРАЦЮВАЛА З НАТХНЕННЯМ І ВМІЛА НАДИХАТИ ІНШИХ

Dihydro-2 H -thiopyran-3(4 H )-one-1,1-dioxide – a versatile building block for the synthesis of new thiopyran-based heterocyclic systems

Dihydro-2H-thiopyran-3(4H)-one-1,1-dioxide - a versatile building block for the synthesis of new thiopyran-based heterocyclic systemsElectronic supplementary information (ESI) available: Spectral data, in silico screening data. See DOI: 10.1039/c7nj03846a

Chemical composition and antibacterial effect of ethanolic extract of Buxus sempervirens on cryogenic strains of microorganisms in vitro

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