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Synthesis, spectral characterization of novel Pd(II), Pt(II) π-coordination compounds based on N-allylthioureas. Cytotoxic properties and DNA binding ability

Journal of inorganic biochemistry, 2017-03, Vol.168, p.98-106

2017

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Modern Approaches to Synthetic Design of Chiral α-Tertiary Amines Based on Trifluoromethylcontaining Ketimines: A Review

Theoretical and experimental chemistry, 2022-01, Vol.57 (6), p.387-420

2022

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Effect of Pd(II) and Ni(II) coordination compounds with 4-amino-3-mercapto-5-methyl-1,2,4-triazole on the mitochondrial dehydrogenases activity

Ukrainian biochemical journal, 2015, Vol.87 (1), p.64

2015

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Development of an efficient route to CF3-substituted pyrrolopyrimidines through understanding the competition between Michael and aza-Henry reactions

Organic & biomolecular chemistry, 2015-02, Vol.13 (5), p.1420-1428

2015

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Fused pyrimidine systems: XVII. Arylsulfenylation of 5-allylpyrimidine-4(3H)-one derivatives. Synthesis of arylsulfanyl-substituted 5,6-dihydrofuro[2,3-d]- and 6,7-dihydro-5H-pyrano[2,3-d]pyrimidines

Russian journal of organic chemistry, 2017-02, Vol.53 (2), p.270-276

2017

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Effects of [(1-phenyl-5-formyl-1H-imidazol-4-yl)thio]acetic Acid on the Antioxidant Status of the Liver and Kidney in Rats with Tetrachloromethane Poisoning

Pharmaceutical chemistry journal, 2021-02, Vol.54 (11), p.1101-1105

2021

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Synthesis of Benzo[4,5]furo[3,2-b]thieno[2,3-d]pyridines —Derivatives of a New Heterocyclic System

Russian journal of organic chemistry, 2018-10, Vol.54 (10), p.1569-1572

2018

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Synthesis of 3-Chloro-4H-imidazo[5,1-c][1,4]benzothiazines and 3-Chloro-4H-5λ6-imidazo[5,1-c][1,4]benzothiazine 5,5-Dioxides

Russian journal of organic chemistry, 2018, Vol.54 (1), p.151-153

2018

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Synthesis of 2,5-dihydroimidazo[4,5-e][1,2,3]thiadiazine 1,1-dioxides—Derivatives of a novel heterocyclic system

Russian journal of organic chemistry, 2017-12, Vol.53 (12), p.1890-1892

2017

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Convenient synthesis of 3-chloroimidazo[1,5-a]quinoxalines

Russian journal of organic chemistry, 2017, Vol.53 (3), p.474-476

2017

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Convenient Synthesis of 5-Aryl-1-(1H-pyrazol-4-yl)pyrrolidin-2-ones

Russian journal of organic chemistry, 2018-06, Vol.54 (6), p.954-956

2018

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Polyfunctional imidazoles: XIV. 4-sulfonyl-5-formyl-1H-imidazoles

Russian journal of organic chemistry, 2017-10, Vol.53 (10), p.1548-1555

2017

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Fused Pyrimidine Systems: XVII. Imidazo- and Pyrimidopyrido[3,2-d]pyrimidin-4(3H)-ones

Russian journal of organic chemistry, 2018-03, Vol.54 (3), p.436-443

2018

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Halocyclization of products of allyl isothiocyanate addition to acyclic methylene active compounds

Russian journal of organic chemistry, 2017, Vol.53 (5), p.709-716

2017

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Arylation of Pyridine with 9,10-Dioxoanthracenyl-1(2)-diazonium Hydrosulfates

Russian journal of general chemistry, 2018-04, Vol.88 (4), p.836-838

2018

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Cascade cyclization of methyl 2-(azidomethyl)furan-3-carboxylates with 2-cyanoacetamides. Efficient synthesis of a new heterocyclic system, furo[3,2-e][1,2,3]triazolo- [1,5-a][1,3]diazepine

Russian journal of organic chemistry, 2017, Vol.53 (4), p.634-636

2017

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Convenient synthesis of 1-hydrazinylanthracene-9,10-diones

Russian journal of organic chemistry, 2017, Vol.53 (3), p.468-469

2017

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Synthesis of 9,10-anthracenedione diethyldithiocarbamates

Russian journal of general chemistry, 2016-12, Vol.86 (12), p.2699-2701

2016

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Electrophilic intramolecular cyclization of functional derivatives of unsaturated compounds: VIII. Cyclization of 4-aryl-N-(thiophen-3-yl)but-3-enamides by the action of polyphosphoric acid and chlorosulfanylarenes

Russian journal of organic chemistry, 2016-07, Vol.52 (7), p.987-992

2016

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Computerized Prediction, Synthesis, and Antimicrobial Activity of New Amino-Acid Derivatives of 2-Chloro-N-(9,10-Dioxo-9,10-Dihydroanthracen-1-Yl)Acetamide

Pharmaceutical chemistry journal, 2014-12, Vol.48 (9), p.582-586

2014

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Polyfunctional imidazoles: XIII.1 Addition and cyclization reactions of 1-aryl-4-chloro-5-(2-nitroethenyl)-1H-imidazoles with sulfur and nitrogen nucleophiles

Russian journal of organic chemistry, 2017, Vol.53 (3), p.407-412

2017

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Interaction of 1,5,6,8-tetrahydropyrazolo[3,4-е][1,4]diazepine-4,7-diones with some electrophilic reagents

Russian journal of organic chemistry, 2016, Vol.52 (8), p.1162-1167

2016

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Synthesis of new imidazo[1,2-a]pyrazolo[4,3-e]pyrimidin-4(6H)-one derivatives by iodocyclization of 6-alkenyl(alkynyl)-aminopyrazolo[3,4-d]pyrimidin-4(5H)-ones

Russian journal of organic chemistry, 2011-07, Vol.47 (7), p.1066-1073

2011

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Heterocyclizations of functionalized heterocumulenes with C,N-, C,O-, and C,S-binucleophiles: XII. Synthesis of alkyl 3-aryl-1,5-dioxo-2,3,5,6-tetrahydro-1H-pyrimido-[1,6-a]quinoxaline-4-carboxylates

Russian journal of organic chemistry, 2010-06, Vol.46 (6), p.890-893

2010

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Polyfunctional imidazoles: I. Synthesis of 1-substituted 4-chloro-1H-imidazole-5-carbaldehydes by Vilsmeier-Haack reaction

Russian journal of organic chemistry, 2009-08, Vol.45 (8), p.1210-1213

2009

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Synthesis, spectral characterization of novel Pd(II), Pt(II) π-coordination compounds based on N-allylthioureas. Cytotoxic properties and DNA binding ability

Modern Approaches to Synthetic Design of Chiral α-Tertiary Amines Based on Trifluoromethylcontaining Ketimines: A Review

Effect of Pd(II) and Ni(II) coordination compounds with 4-amino-3-mercapto-5-methyl-1,2,4-triazole on the mitochondrial dehydrogenases activity

Development of an efficient route to CF3-substituted pyrrolopyrimidines through understanding the competition between Michael and aza-Henry reactions

Fused pyrimidine systems: XVII. Arylsulfenylation of 5-allylpyrimidine-4(3H)-one derivatives. Synthesis of arylsulfanyl-substituted 5,6-dihydrofuro[2,3-d]- and 6,7-dihydro-5H-pyrano[2,3-d]pyrimidines

Effects of [(1-phenyl-5-formyl-1H-imidazol-4-yl)thio]acetic Acid on the Antioxidant Status of the Liver and Kidney in Rats with Tetrachloromethane Poisoning

Synthesis of Benzo[4,5]furo[3,2-b]thieno[2,3-d]pyridines —Derivatives of a New Heterocyclic System

Synthesis of 3-Chloro-4H-imidazo[5,1-c][1,4]benzothiazines and 3-Chloro-4H-5λ6-imidazo[5,1-c][1,4]benzothiazine 5,5-Dioxides

Synthesis of 2,5-dihydroimidazo[4,5-e][1,2,3]thiadiazine 1,1-dioxides—Derivatives of a novel heterocyclic system

Convenient synthesis of 3-chloroimidazo[1,5-a]quinoxalines

Convenient Synthesis of 5-Aryl-1-(1H-pyrazol-4-yl)pyrrolidin-2-ones

Polyfunctional imidazoles: XIV. 4-sulfonyl-5-formyl-1H-imidazoles

Fused Pyrimidine Systems: XVII. Imidazo- and Pyrimidopyrido[3,2-d]pyrimidin-4(3H)-ones

Halocyclization of products of allyl isothiocyanate addition to acyclic methylene active compounds

Arylation of Pyridine with 9,10-Dioxoanthracenyl-1(2)-diazonium Hydrosulfates

Cascade cyclization of methyl 2-(azidomethyl)furan-3-carboxylates with 2-cyanoacetamides. Efficient synthesis of a new heterocyclic system, furo[3,2-e][1,2,3]triazolo- [1,5-a][1,3]diazepine

Convenient synthesis of 1-hydrazinylanthracene-9,10-diones

Synthesis of 9,10-anthracenedione diethyldithiocarbamates

Electrophilic intramolecular cyclization of functional derivatives of unsaturated compounds: VIII. Cyclization of 4-aryl-N-(thiophen-3-yl)but-3-enamides by the action of polyphosphoric acid and chlorosulfanylarenes

Computerized Prediction, Synthesis, and Antimicrobial Activity of New Amino-Acid Derivatives of 2-Chloro-N-(9,10-Dioxo-9,10-Dihydroanthracen-1-Yl)Acetamide

Polyfunctional imidazoles: XIII.1 Addition and cyclization reactions of 1-aryl-4-chloro-5-(2-nitroethenyl)-1H-imidazoles with sulfur and nitrogen nucleophiles

Interaction of 1,5,6,8-tetrahydropyrazolo[3,4-е][1,4]diazepine-4,7-diones with some electrophilic reagents

Synthesis of new imidazo[1,2-a]pyrazolo[4,3-e]pyrimidin-4(6H)-one derivatives by iodocyclization of 6-alkenyl(alkynyl)-aminopyrazolo[3,4-d]pyrimidin-4(5H)-ones

Heterocyclizations of functionalized heterocumulenes with C,N-, C,O-, and C,S-binucleophiles: XII. Synthesis of alkyl 3-aryl-1,5-dioxo-2,3,5,6-tetrahydro-1H-pyrimido-[1,6-a]quinoxaline-4-carboxylates

Polyfunctional imidazoles: I. Synthesis of 1-substituted 4-chloro-1H-imidazole-5-carbaldehydes by Vilsmeier-Haack reaction

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