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Cytochrome P450 monooxygenase systems: Diversity and plasticity for adaptive stress response

Progress in biophysics and molecular biology, 2024-11, Vol.193, p.19-34

2024

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Differentially expressed non-coding RNAs and their regulatory networks in liver cancer

Heliyon, 2023-09, Vol.9 (9), p.e19223-e19223, Article e19223

2023

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Lipid peroxidation: Reactive carbonyl species, protein/DNA adducts, and signaling switches in oxidative stress and cancer

Biochemical and biophysical research communications, 2023-12, Vol.687, p.149167-149167, Article 149167

2023

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Mapping the interconnections: a systematic review and network analysis of factors influencing teachers' technology acceptance

Frontiers in education (Lausanne), 2024-11, Vol.9

2024

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Fast and Slow Release of Catalytically Active Species in Metal/NHC Systems Induced by Aliphatic Amines

Organometallics, 2018-05, Vol.37 (9), p.1483-1492

2018

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Pd and Pt Catalyst Poisoning in the Study of Reaction Mechanisms: What Does the Mercury Test Mean for Catalysis?

ACS catalysis, 2019-04, Vol.9 (4), p.2984-2995

2019

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Revealing the unusual role of bases in activation/deactivation of catalytic systems: O-NHC coupling in M/NHC catalysis

Chemical science (Cambridge), 2018-07, Vol.9 (25), p.5564-5577

2018

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A New Mode of Operation of Pd-NHC Systems Studied in a Catalytic Mizoroki–Heck Reaction

Organometallics, 2017-05, Vol.36 (10), p.1981-1992

2017

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New class of RSO2-NHC ligands and Pd/RSO2-NHC complexes with tailored electronic properties and high performance in catalytic C–C and C–N bonds formation

Dalton transactions : an international journal of inorganic chemistry, 2023-08, Vol.52 (34), p.12067-12086

2023

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New class of RSO 2 -NHC ligands and Pd/RSO 2 -NHC complexes with tailored electronic properties and high performance in catalytic C-C and C-N bonds formation

Dalton transactions : an international journal of inorganic chemistry, 2023-08, Vol.52 (34), p.12067-12086

2023

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Preventing Pd-NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators

Catalysis science & technology, 2020-03, Vol.1 (5), p.1228-1247

2020

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New class of RSO-NHC ligands and Pd/RSO-NHC complexes with tailored electronic properties and high performance in catalytic C-C and C-N bonds formation

Dalton transactions : an international journal of inorganic chemistry, 2023-08, Vol.52 (34), p.1267-1286

2023

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The effect of the endovascular access on the effectiveness and safety of chemoembolization of the arteries of the liver with unresectable liver metastases

Kliničeskaâ praktika, 2020-02, Vol.10 (4), p.5-15

2020

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Evaluation of loads on the main joint of reactor pressure vessel under hypothetical severe accident at VVER-1200 NPP

Nuclear engineering and design, 2019-11, Vol.353, p.110222, Article 110222

2019

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Diversity Oriented Synthesis of Polycyclic Heterocycles through the Condensation of 2‑Amino[1,2,4]triazolo[1,5‑a]pyrimidines with 1,3-Diketones

Journal of organic chemistry, 2015-11, Vol.80 (21), p.10694-10709

2015

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Transition metal-free visible light induced intramolecular C–Hal/C–H bond activation leading to cyclization into pyrimido[5′,4′:3,4]pyrrolo[1,2-f ]phenanthridines

Mendeleev communications, 2024-03, Vol.34 (2), p.238-241

2024

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Moderately compact helix antennas with cutoff patterns for millimeter RTK positioning

GPS solutions, 2016-07, Vol.20 (3), p.587-594

2016

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Partially hydrogenated 2-amino[1,2,4]triazolo[1,5-a]pyrimidines as synthons for the preparation of polycondensed heterocycles: reaction with chlorocarboxylic acid chlorides

Tetrahedron, 2014-01, Vol.70 (3), p.684-701

2014

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Self-mixing interferometry for distance measurement using a semiconductor laser with current-modulated wavelength

Kompʹûternaâ optika, 2018-01, Vol.42 (1), p.54-59

2018

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Revealing the unusual role of bases in activation/deactivation of catalytic systems: O-NHC coupling in M/NHC catalysisElectronic supplementary information (ESI) available: Additional experimental data for reaction mechanisms and stoichiometry, copies of NMR spectra and Raman spectra, GC-MS and ESI-MS data, and FE-SEM/EDS data. See DOI: 10.1039/c8sc01353e

2018-06

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Revealing the unusual role of bases in activation/deactivation of catalytic systems: O–NHC coupling in M/NHC catalysis† †Electronic supplementary information (ESI) available: Additional experimental data for reaction mechanisms and stoichiometry, copies of NMR spectra and Raman spectra, GC-MS and ESI-MS data, and FE-SEM/EDS data. See DOI: 10.1039/c8sc01353e

Chemical science (Cambridge), 2018-06, Vol.9 (25), p.5564-5577

2018

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Alkoxy base-mediated selective synthesis and new rearrangements of 1,2,4-triazolodipyrimidinones

Tetrahedron letters, 2017-02, Vol.58 (8), p.748-754

2017

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Psychogenic Erectile Dysfunction: A Multidisciplinary Problem

City Healthcare, 2023-09, Vol.4 (3), p.87-94

2023

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Partially hydrogenated 2-amino[1,2,4]triazolo[1,5-a]pyrimidines as synthons for the preparation of polycondensed heterocycles: reaction with α-bromoketones

Tetrahedron, 2015-09, Vol.71 (36), p.6259-6271

2015

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Reactivity of 2-amino[1,2,4]triazolo[1,5-а]-pyrimidines with various saturation of the pyrimidine ring towards electrophiles

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2015-11, Vol.51 (11-12), p.1039-1047

2015

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Cytochrome P450 monooxygenase systems: Diversity and plasticity for adaptive stress response

Differentially expressed non-coding RNAs and their regulatory networks in liver cancer

Lipid peroxidation: Reactive carbonyl species, protein/DNA adducts, and signaling switches in oxidative stress and cancer

Mapping the interconnections: a systematic review and network analysis of factors influencing teachers' technology acceptance

Fast and Slow Release of Catalytically Active Species in Metal/NHC Systems Induced by Aliphatic Amines

Pd and Pt Catalyst Poisoning in the Study of Reaction Mechanisms: What Does the Mercury Test Mean for Catalysis?

Revealing the unusual role of bases in activation/deactivation of catalytic systems: O-NHC coupling in M/NHC catalysis

A New Mode of Operation of Pd-NHC Systems Studied in a Catalytic Mizoroki–Heck Reaction

New class of RSO2-NHC ligands and Pd/RSO2-NHC complexes with tailored electronic properties and high performance in catalytic C–C and C–N bonds formation

New class of RSO 2 -NHC ligands and Pd/RSO 2 -NHC complexes with tailored electronic properties and high performance in catalytic C-C and C-N bonds formation

Preventing Pd-NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators

New class of RSO-NHC ligands and Pd/RSO-NHC complexes with tailored electronic properties and high performance in catalytic C-C and C-N bonds formation

The effect of the endovascular access on the effectiveness and safety of chemoembolization of the arteries of the liver with unresectable liver metastases

Evaluation of loads on the main joint of reactor pressure vessel under hypothetical severe accident at VVER-1200 NPP

Diversity Oriented Synthesis of Polycyclic Heterocycles through the Condensation of 2‑Amino[1,2,4]triazolo[1,5‑a]pyrimidines with 1,3-Diketones

Transition metal-free visible light induced intramolecular C–Hal/C–H bond activation leading to cyclization into pyrimido[5′,4′:3,4]pyrrolo[1,2-f ]phenanthridines

Moderately compact helix antennas with cutoff patterns for millimeter RTK positioning

Partially hydrogenated 2-amino[1,2,4]triazolo[1,5-a]pyrimidines as synthons for the preparation of polycondensed heterocycles: reaction with chlorocarboxylic acid chlorides

Self-mixing interferometry for distance measurement using a semiconductor laser with current-modulated wavelength

Alkoxy base-mediated selective synthesis and new rearrangements of 1,2,4-triazolodipyrimidinones

Psychogenic Erectile Dysfunction: A Multidisciplinary Problem

Partially hydrogenated 2-amino[1,2,4]triazolo[1,5-a]pyrimidines as synthons for the preparation of polycondensed heterocycles: reaction with α-bromoketones

Reactivity of 2-amino[1,2,4]triazolo[1,5-а]-pyrimidines with various saturation of the pyrimidine ring towards electrophiles

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