Dmitry S. Kopchuk

ORCID: 0000-0002-0397-4033
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About
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Research Areas
  • Synthesis and Characterization of Heterocyclic Compounds
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Synthesis and Biological Evaluation
  • Chemical Reaction Mechanisms
  • Synthesis and Reactivity of Heterocycles
  • Luminescence and Fluorescent Materials
  • Molecular Sensors and Ion Detection
  • Lanthanide and Transition Metal Complexes
  • Synthesis and Reactions of Organic Compounds
  • Magnetism in coordination complexes
  • Cyclization and Aryne Chemistry
  • Fluorine in Organic Chemistry
  • DNA and Nucleic Acid Chemistry
  • Chemical Reactions and Mechanisms
  • Metal complexes synthesis and properties
  • Synthesis and biological activity
  • Supramolecular Chemistry and Complexes
  • Porphyrin and Phthalocyanine Chemistry
  • Quinazolinone synthesis and applications
  • Click Chemistry and Applications
  • Catalytic C–H Functionalization Methods
  • Chemical synthesis and alkaloids
  • Phenothiazines and Benzothiazines Synthesis and Activities
  • Radical Photochemical Reactions

Ural Federal University
2016-2025

Institute of Organic Synthesis
2016-2025

Russian Academy of Sciences
2015-2025

Ural Branch of the Russian Academy of Sciences
2015-2024

A.V. Topchiev Institute of Petrochemical Synthesis
2019

Lomonosov Moscow State University
2019

Mechanochemical approaches in an organic synthesis have received increased interest because of their wide applications green methodologies.

10.1039/c9gc03414e article EN Green Chemistry 2019-12-23

The key types of low-molecular-mass chemosensors for the detection nitroaromatic compounds representing energetic substances (explosives) are analyzed. coordination and chemical properties these structural features their complexes with considered. causes methods attaining high selectivity recognition demonstrated. primary attention is paid to use visual explosives this class by colorimetric photometric methods. Examples using photo- chemiluminescence purpose described. A separate section...

10.1070/rc2014v083n09abeh004467 article EN Russian Chemical Reviews 2014-09-30

Abstract This review aims to report recent advances on decarboxylative reactions of amino acids catalyzed by transition metals or non‐metals and the growing opportunities they present in construction complex chemical scaffolds for applications encompassing natural product synthesis, synthetic methodology development, functional materials. Different have been highlighted such as radical, photoredox metal metal‐free coupling reactions. etc. The is divided into two main sections: one deals with...

10.1002/adsc.201801331 article EN Advanced Synthesis & Catalysis 2018-12-06

Abstract Cross dehydrogenative coupling (CDC) reactions have become a convenient synthetic strategy for the synthesis of various (het)aromatic scaffolds. In recent times ball milling has emerged as powerful tool to perform in greener way. The current review highlights applications cross under towards useful molecules more efficient and manner. magnified image

10.1002/adsc.202200296 article EN Advanced Synthesis & Catalysis 2022-06-16

Pyrene-containing water-soluble probes for the fluorescent detection of nitroaromatic compounds (NACs), such as explosive components (2,4-DNT and 2,4,6-TNT) herbicides (2,4-dinitrocresol, 2,4-DNOC), in aqueous media are reported. In probes, introduction surface-active hydrophilic "heads" at periphery lipophilic (i.e., hydrophobic) pyrene "tails" resulted formation highly micelle-like aggregates/pre-associates solutions concentrations ≤10(-5) m. The enhanced fluorescence quenching herein...

10.1002/asia.201501310 article EN Chemistry - An Asian Journal 2016-01-12

The interactions between substituted 5-<italic>R</italic>-3-(pyridyl-2)-1,2,4-triazines with <italic>in situ</italic> generated aryne intermediates have been studied.

10.1039/c8ob00847g article EN Organic & Biomolecular Chemistry 2018-01-01

A convenient approach towards 5-(aryl/alkyl)amino-1,2,4-triazines and α-arylamino-2,2′-bipyridines was developed following <italic>ipso</italic>-substitution of a cyano-group by amino groups and, finally, aza-Diels-Alder reaction with 1-morpholynocyclopentene.

10.1039/c6ra26305d article EN cc-by-nc RSC Advances 2017-01-01

An efficient solvent-free procedure for the synthesis of pillar[6]arenes has been developed.

10.1039/c5gc01505g article EN Green Chemistry 2015-08-24

Abstract The Friedel‐Crafts reaction represents one of the most efficient tools for formation carbon‐carbon bonds and direct derivatization aromatic compounds. Asymmetric arylation imines involving has received much interest recently. present review summarizes works on asymmetric by different approaches including their development to date. is divided into three main sections: addition arenes in presence chiral catalysts; containing tails coupling aryl boronic acids imines. magnified image

10.1002/adsc.202000548 article EN Advanced Synthesis & Catalysis 2020-07-03

Abstract This work describes a solvent‐free approach towards “push‐pull” fluorophores based on 5‐aryl‐2,2′‐bipyridines bearing the residues of various anilines at α‐position edge pyridine cycle. We have also studied possibility varying (het)aromatic‐substituents C5 position resulted 2,2′‐bipyridines as well substituents in aniline residues. The structures products were confirmed 1 H and 13 C NMR spectroscopic data, mass spectrometry, elemental analysis X‐ray diffraction analysis....

10.1002/slct.201800220 article EN ChemistrySelect 2018-04-24
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