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Introducing Cationic Selenium-Containing Triazapentadiene Ligand Framework: Synthesis, Coordination Chemistry, and Antifungal Activity

Inorganic chemistry, 2024-07, Vol.63 (30), p.13924-13937

2024

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Impact of Climate Change on Ruderal Communities in the Conditions of Ukraine

Ekológia Bratislava, 2023-03, Vol.42 (1), p.39-46

2023

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Iridium Halide Complexes [1,1‐X2‐8‐SMe2‐1,2,8‐IrC2B9H10]2 (X = Cl, Br, I): Synthesis, Reactivity and Catalytic Activity

European journal of inorganic chemistry, 2017-10, Vol.2017 (38-39), p.4635-4644

2017

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Synthesis, crystal structure and catalytic activity in reductive amination of dichlorido(η 6 - p -cymene)(2′-dicyclohexylphosphanyl-2,6-dimethoxybiphenyl-κ P )ruthenium(II)

Acta crystallographica. Section E, Crystallographic communications, 2018-04, Vol.74 (4), p.487-491

2018

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Application of FT-IR Spectroscopy for Investigation of Pink Water Remediation by Pine Bark

The open biotechnology journal, 2015, Vol.9 (1), p.67-75

2015

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Two different faces of the triangular cluster Rh3Cp3(μ2-CO)3 towards metalloelectrophiles: Structural and theoretical study

Journal of organometallic chemistry, 2020-10, Vol.924, p.121432, Article 121432

2020

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Stipo pulcherrimae-Festucetalia pallentis Pop 1968 of calcareous petrophytic steppes in Ukraine

Hacquetia, 2021-12, Vol.20 (2), p.303-325

2021

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Sodium hypophosphite mediated reductive amination of carbonyl compounds with ,-dialkylformamides

New journal of chemistry, 2023-04, Vol.47 (14), p.6532-6535

2023

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Indenyl rhodium complexes. Synthesis and catalytic activity in reductive amination using carbon monoxide as a reducing agent

Journal of organometallic chemistry, 2018-07, Vol.867, p.106-112

2018

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Syntaxonomy of chalk outcrop vegetation of the order Thymo cretacei-Hyssopetalia cretacei

Hacquetia, 2018-06, Vol.17 (1), p.85-109

2018

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Syngas as a synergistic reducing agent for selective reductive amination-a mild route to bioactive amines

New journal of chemistry, 2023-06, Vol.47 (22), p.1514-1518

2023

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Sodium hypophosphite mediated reductive amination of carbonyl compounds with N , N -dialkylformamides

New journal of chemistry, 2023-04, Vol.47 (14), p.6532-6535

2023

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A Family of Cagelike Mn-Silsesquioxane/Bathophenanthroline Complexes: Synthesis, Structure, and Catalytic and Antifungal Activity

Inorganic chemistry, 2023-09, Vol.62 (38), p.15537-15549

2023

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Indenyl Rhodium Complexes with Arene Ligands: Synthesis and Application for Reductive Amination

Organometallics, 2018-08, Vol.37 (15), p.2553-2562

2018

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Cover Feature: Synthesis of Nitriles from Aldehydes with Elongation of the Molecule with Two Carbon Atoms (Eur. J. Org. Chem. 1/2019)

European journal of organic chemistry, 2019-01, Vol.2019 (1), p.3-3

2019

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Ruthenium‐Catalyzed Reductive Amidation without an External Hydrogen Source

European journal of organic chemistry, 2018-01, Vol.2018 (4), p.557-563

2018

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Biotransformation of pink water TNT on the surface of a low-cost adsorbent pine bark

Biodegradation (Dordrecht), 2015-09, Vol.26 (5), p.375-386

2015

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Alkyl formates as reagents for reductive amination of carbonyl compounds

Mendeleev communications, 2020-01, Vol.30 (1), p.112-113

2020

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Synthesis of Nitriles from Aldehydes with Elongation of the Molecule with Two Carbon Atoms

European journal of organic chemistry, 2019-01, Vol.2019 (1), p.32-35

2019

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Effect of pine bark on the biotransformation of trinitrotoluene and on the bacterial community structure in a batch experiment

Environmental technology, 2014-10, Vol.35 (19), p.2456-2465

2014

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Synthesis, crystal structure and catalytic activity in reductive amination of di-chlorido-(η 6 - p -cymene)(2'-di-cyclo-hexyl-phosphanyl-2,6-di-meth-oxy-biphen-yl-κ P )ruthenium(II)

Acta crystallographica. Section E, Crystallographic communications, 2018-04, Vol.74 (Pt 4), p.487-491

2018

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Introducing Cationic Selenium-Containing Triazapentadiene Ligand Framework: Synthesis, Coordination Chemistry, and Antifungal Activity

Impact of Climate Change on Ruderal Communities in the Conditions of Ukraine

Iridium Halide Complexes [1,1‐X2‐8‐SMe2‐1,2,8‐IrC2B9H10]2 (X = Cl, Br, I): Synthesis, Reactivity and Catalytic Activity

Synthesis, crystal structure and catalytic activity in reductive amination of dichlorido(η 6 - p -cymene)(2′-dicyclohexylphosphanyl-2,6-dimethoxybiphenyl-κ P )ruthenium(II)

Application of FT-IR Spectroscopy for Investigation of Pink Water Remediation by Pine Bark

Two different faces of the triangular cluster Rh3Cp3(μ2-CO)3 towards metalloelectrophiles: Structural and theoretical study

Stipo pulcherrimae-Festucetalia pallentis Pop 1968 of calcareous petrophytic steppes in Ukraine

Sodium hypophosphite mediated reductive amination of carbonyl compounds with ,-dialkylformamides

Indenyl rhodium complexes. Synthesis and catalytic activity in reductive amination using carbon monoxide as a reducing agent

Syntaxonomy of chalk outcrop vegetation of the order Thymo cretacei-Hyssopetalia cretacei

Syngas as a synergistic reducing agent for selective reductive amination-a mild route to bioactive amines

Sodium hypophosphite mediated reductive amination of carbonyl compounds with N , N -dialkylformamides

A Family of Cagelike Mn-Silsesquioxane/Bathophenanthroline Complexes: Synthesis, Structure, and Catalytic and Antifungal Activity

Indenyl Rhodium Complexes with Arene Ligands: Synthesis and Application for Reductive Amination

Cover Feature: Synthesis of Nitriles from Aldehydes with Elongation of the Molecule with Two Carbon Atoms (Eur. J. Org. Chem. 1/2019)

Ruthenium‐Catalyzed Reductive Amidation without an External Hydrogen Source

Biotransformation of pink water TNT on the surface of a low-cost adsorbent pine bark

Alkyl formates as reagents for reductive amination of carbonyl compounds

Synthesis of Nitriles from Aldehydes with Elongation of the Molecule with Two Carbon Atoms

Effect of pine bark on the biotransformation of trinitrotoluene and on the bacterial community structure in a batch experiment

Synthesis, crystal structure and catalytic activity in reductive amination of di-chlorido-(η 6 - p -cymene)(2'-di-cyclo-hexyl-phosphanyl-2,6-di-meth-oxy-biphen-yl-κ P )ruthenium(II)

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