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Oleg S. Eltsov

Observed names: El'tsov, O. S., El'tsov, O.S., El'tsov, Oleg S., Eltsov, O., Eltsov, O. S., Eltsov, O.S., Eltsov, Oleg, Eltsov, Oleg S., El’tsov, O. S., El’tsov, O.S., El’tsov, Oleg S., El’tsov, О. S., El’tsov, О.S., O Eltsov, O. Eltsov, O. S. ELTSOV, O. S. El"tsov, O. S. El'tsov, O. S. Eltsov, O. S. El´tsov, O. S. Elʼtsov, O. S. Elˈtsov, O. S. El’tsov, O. S. El′tsov, O. S. Yeltsov, O.S. Eltsov, Oleg Eltsov, Oleg S Eltsov, Oleg S. El'tsov, Oleg S. El´tsov, Oleg S. El’tsov, Oleg S. Eltsov, Ельцов Олег Станиславович, Ельцов, О. С., Ельцов, Олег Станиславович, О. S. El’tsov, О. С. ЕЛЬЦОВ, О. С. Ельцов, О.С. ЕЛЬЦОВ, О.С. Ельцов, Олег C. Ельцов, Олег Станиславович Ельцов
Observed institutions: Ukhta State Technical University, Ural Federal University, Brest State Technical University, Samara State Technical University, Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Samara State University, Sevastopol State University
ORCID: 0000-0002-4681-2616
Observed ORCID: 0000-0002-4681-2616
OpenAlex ID: A5076770992
Identification and analytical characteristics of synthetic cannabinoids with an indazole-3-carboxamide structure bearing a N-1-methoxycarbonylalkyl group
2015 · Vadim Shevyrin, Vladimir Melkozerov, et al. · Analytical and Bioanalytical Chemistry · 64
Regioselective synthesis of 5-trifluoromethyl-1,2,3-triazoles via CF3-directed cyclization of 1-trifluoromethyl-1,3-dicarbonyl compounds with azides
2011 · Yury A. Rozin, Johann Leban, et al. · Tetrahedron · 52
Reactions of β‐Azolylenamines with Sulfonyl Azides as an Approach to N‐Unsubstituted 1,2,3‐Triazoles and Ethene‐1,2‐diamines
2014 · Ilya Efimov, Vasiliy Bakulev, et al. · European Journal of Organic Chemistry · 51
Analytical characterization of some synthetic cannabinoids, derivatives of indole-3-carboxylic acid
2013 · Vadim Shevyrin, Vladimir Melkozerov, et al. · Forensic Science International · 45
Identification and analytical properties of new synthetic cannabimimetics bearing 2,2,3,3-tetramethylcyclopropanecarbonyl moiety
2012 · Vadim Shevyrin, Vladimir Melkozerov, et al. · Forensic Science International · 43
Switchable Synthesis of 4,5-Functionalized 1,2,3-Thiadiazoles and 1,2,3-Triazoles from 2-Cyanothioacetamides under Diazo Group Transfer Conditions
2017 · Valeriy O. Filimonov, Lidia N. Dianova, et al. · The Journal of Organic Chemistry · 38
Synthetic cannabinoids as designer drugs: New representatives of indol-3-carboxylates series and indazole-3-carboxylates as novel group of cannabinoids. Identification and analytical data
2014 · Vadim Shevyrin, Vladimir Melkozerov, et al. · Forensic Science International · 37
Synthesis, photophysical and electrochemical properties of novel 6,12-di(thiophen-2-yl) substituted indolo[3,2-b]carbazoles
2014 · Roman A. Irgashev, Anton Yu. Teslenko, et al. · Tetrahedron · 33
Nitrothiadiazolo[3,2-a]pyrimidines as promising antiglycating agents
2019 · Konstantin Savateev, Victor Fedotov, et al. · European Journal of Medicinal Chemistry · 32
A chemo- and regiocontrolled approach to bipyrazoles and pyridones via the reaction of ethyl 5-acyl-4-pyrone-2-carboxylates with hydrazines
2018 · D. L. Obydennov, L. R. Khammatova, et al. · Organic & Biomolecular Chemistry · 22
Reactions of chromone-3-carboxylic acid and chromone-3-carboxamides with cyanoacetic acid hydrazide
2016 · Mikhail Yu. Kornev, Vladimir S. Moshkin, et al. · Mendeleev Communications · 22
Reactivity of 1,2,3-triazoles towards sulfonyl chlorides. A novel approach to 1- and 2-sulfonyl-4-azolyl-1,2,3-triazoles
2015 · Tetyana V. Beryozkina, Ilya V. Efimov, et al. · Tetrahedron · 22
Dibenzo[ f,h ]furazano[3,4- b ]quinoxalines: Synthesis by Intramolecular Cyclization through Direct Transition Metal-Free C–H Functionalization and Electrochemical, Photophysical, and Charge Mobility Characterization
2020 · Yuriy A. Kvashnin, Egor V. Verbitskiy, et al. · ACS Omega · 21
Synthetic cannabinoid 3-benzyl-5-[1-(2-pyrrolidin-1-ylethyl)-1H-indol-3-yl]-1,2,4-oxadiazole. The first detection in illicit market of new psychoactive substances
2015 · Vadim Shevyrin, Vladimir Melkozerov, et al. · Forensic Science International · 21
Novel method for the synthesis of 4-(azol-5-yl)-1,2,3-triazoles
2012 · V. A. Bakulev, I. V. Efimov, et al. · Chemistry of Heterocyclic Compounds · 21
Reactions of Thioacetamide Derivatives with Sulfonyl Azides: An Approach to Active‐Methylene N‐Sulfonylacetamidines
2015 · Lidia Dianova, Vera Berseneva, et al. · European Journal of Organic Chemistry · 20
Synthesis of A-Pentacyclic Triterpene α,β-Alkenenitriles
2014 · A. V. Pereslavtseva, I. A. Tolmacheva, et al. · Chemistry of Natural Compounds · 20
New stable form of nitroacetonitrile
2016 · Egor K. Voinkov, Evgeny N. Ulomskiy, et al. · Mendeleev Communications · 19
The tert-Amino Effect in Heterocyclic Chemistry. Synthesis of Spiro Heterocycles
2005 · E. D’yachenko, T. Glukhareva, et al. · Molecules · 19
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Dihydroxybenzoic acids as polydentate ligands in phenylantimony (V) complexes
2019 · Vladimir V. Sharutin, Olga K. Sharutina, et al. · Inorganica Chimica Acta · 18
3-Naphthoylindazoles and 2-naphthoylbenzoimidazoles as novel chemical groups of synthetic cannabinoids: Chemical structure elucidation, analytical characteristics and identification of the first representatives in smoke mixtures
2014 · Vadim Shevyrin, Vladimir Melkozerov, et al. · Forensic Science International · 18
Synthesis of new polycyclic systems based on [1,2,5]chalcogenodiazolo[3,4-b]thieno[3,2-h]quinoxalines
2023 · Yu. A. Kvashnin, E. M. Krynina, et al. · Russian Chemical Bulletin · 17
Reactions of 2-(trifluoromethyl)chromones with cyanoacetamides, ethyl cyanoacetate and diethyl malonate. Unexpected synthesis of benzo[c]coumarin derivatives
2011 · Vyacheslav Ya. Sosnovskikh, Alexander V. Safrygin, et al. · Tetrahedron Letters · 17
Antimicrobial activity of new benzazolyl N-sulfonyl amidines
2021 · Nadezhda A. Galieva, Dmitriy A. Saveliev, et al. · Mendeleev Communications · 16
New approach to unsymmetrical 1,3-diazatriphenylenes through intramolecular oxidative cyclodehydrogenation
2019 · Egor V. Verbitskiy, Oleg S. Eltsov, et al. · Tetrahedron · 16
Works count: 352
Citation count: 1,426
H-index: 19
I10-index: 53
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