Center of spectral investigations

Department of physical organic chemistry

Половяненко

Head of Center -
Cand. Sci. (Phys.-Math.) Dmitriy N. Polovyanenko
tel. (383) 330-96-61
e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

Scientific Director
Cand. Sci. (Chem) Victor I. Mamtyuk
tel. (383) 330-69-60
e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

The Center of spectral investigations (CSI) has been established on March 11, 2016 on the basis of the Laboratory of Physical Research Methods/
The Centre includes 6 groups.

Purpose:

collective use of unique expensive scientific equipment to carry out fundamental and applied research;
raising the level of experimental work in the field of molecular spectroscopy, structural and analytical research;
assistance in the implementation of scientific and scientific-applied grants and projects;
rendering services to organizations and enterprises of the Siberian region;
education and training of personnel for measurements, operation and maintenance of scientific instruments.

RESEARCH AREAS

Areas:

Analysis and identification of methods of molecular spectroscopy of organic, metal organic and inorganic substances and materials, including nanomaterials with desired properties (plastics, optical, ferromagnetic, biologically active) for science, technology and medicine
The study of natural and biological methods of molecular spectroscopy, chromatography, and microanalysis
Analysis and identification of substances and materials of synthetic, natural and anthropogenic origin, including nanomaterials
Development of physical and chemical methods of analysis of substances and materials
Creating databases of molecular spectroscopy data
independent expertise

Logistical and methodical base of Spectral Research Center allow us to study the liquid, solid and gaseous substances and carry out sample preparation of complex objects of natural, synthetic and natural origin.

STAFF

The Centre includes 6 groups:

1. Group of Nuclear Magnetic Resonance (GNMR)

№	Employee	Position	Room	Phone	Phone in.	email	Publications
№	Employee	Position	Room	Phone	Phone in.	email	by years
1	Lomanovich Alena Vladimirovna	Leading Engineer	106	330-55-04	3-50	This email address is being protected from spambots. You need JavaScript enabled to view it.
2	Salnikov Георгий Efimovich	Senior Researcher	127	330-55-04	3-25	This email address is being protected from spambots. You need JavaScript enabled to view it.
3	Krasnov Vyacheslav Ivanovich	Researcher (Cand. Chem.)	127	330-55-04	3-25	This email address is being protected from spambots. You need JavaScript enabled to view it.
4	Skorova Anna Борисовна	Leading Engineer	108	330-55-04	3-32	This email address is being protected from spambots. You need JavaScript enabled to view it.
5	Kandaurova Vera Vasilievna	technicist	106	330-55-04	3-50	This email address is being protected from spambots. You need JavaScript enabled to view it.
6	Polyanskaya Ekaterina Vladimirovna	engineer				This email address is being protected from spambots. You need JavaScript enabled to view it.
Students
7	Rumyantseva Elizaveta Andreevna	laboratory assistant

2. Group of mass spectrometry (GMS)

№	Employee	Position	Room	Phone	Phone in.	email	Publications
№	Employee	Position	Room	Phone	Phone in.	email	by years
1	Nefedov Andrey Alekseevich	Senior Researcher (Cand. Chem.). Group's Head	110	330-78-64	3-31	This email address is being protected from spambots. You need JavaScript enabled to view it.
2	Karakay Darya Aleksandrovna	Leading Engineer	110	330-78-64	3-31	This email address is being protected from spambots. You need JavaScript enabled to view it.
3	Salnikova Olga Иосифовна	Leading Engineer	110	330-78-64	3-31	This email address is being protected from spambots. You need JavaScript enabled to view it.
4	Statsenko Olga Борисовна	Leading Engineer	110	330-78-64	3-31	This email address is being protected from spambots. You need JavaScript enabled to view it.
5	Pukhnacheva Mariya Alexandrovna	engineer	110	330-78-64	3-31	This email address is being protected from spambots. You need JavaScript enabled to view it.

3. Group of Optical Spectrometry (GOS)

№	Employee	Position	Room	Phone	Phone in.	email	Publications
№	Employee	Position	Room	Phone	Phone in.	email	by years
1	Karpova Elena Viktorovna	Senior Researcher (Cand. Chem.). Group's Head	104	330-78-64	3-35	This email address is being protected from spambots. You need JavaScript enabled to view it.
2	Chuikov Igor Petrovich	Researcher (Cand. Chem.)	414 НТК	330-82-51	2-15	This email address is being protected from spambots. You need JavaScript enabled to view it.
3	Dunaevslaya Ekaterina Vladimirovna	laboratory assistant
4	Sagalaeva Natalia Ivanovna	Senior Laboratory Assistant	104	330-78-64	3-35	This email address is being protected from spambots. You need JavaScript enabled to view it.

4. Group of X-ray analysis (GXRA)

№	Employee	Position	Room	Phone	Phone in.	email	Publications
№	Employee	Position	Room	Phone	Phone in.	email	by years
1	Bagryanskaya Irina Yurievna	Leading Researcher (Doct.Chem), Group's Head	214 НТК	330-78-64	3-64	This email address is being protected from spambots. You need JavaScript enabled to view it.
2	Gatilov Yurii Vasilievich	Leading Researcher (Doct. Chem)	207 НТК	330-78-64	4-37	This email address is being protected from spambots. You need JavaScript enabled to view it.
3	Rybalova Tatyana Valerievna	Researcher	214 НТК	330-78-64	3-64	This email address is being protected from spambots. You need JavaScript enabled to view it.

5. Group of thermal analysis (GTA)

№	Employee	Position	Room	Phone	Phone in.	email	Publications
№	Employee	Position	Room	Phone	Phone in.	email	by years
1	Shundrina Inna Kazimirovna	Senior Researcher (Cand. Chem.). Group's Head	105, П-004	330-78-64	3-46, 4-03	This email address is being protected from spambots. You need JavaScript enabled to view it.

PUBLICATIONS

Laboratory staff publications (DB NIOCh)

Reviews, Articles

2023

V.A. Trukhanov, A.V. Kuevda, D.I. Dominskiy, A.L. Mannanov, T.V. Rybalova, V.A. Tafeenko, A.Yu. Sosorev, V.G. Konstantinov, M.S. Kazantsev, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
Strongly polarized surface electroluminescence from an organic light-emitting transistor
Mater. Chem. Front., 2023, Advance Article, The article was first published on 29 Nov 2022 doi:10.1039/D2QM01046A, IF=8.682
E.N. Zapolotsky, S.P. Babailov, M.V. Kniazeva, Yu.V. Strelnikova, A.S. Ovsyannikov, A.T. Gubaidullin, S.E. Solovieva, I.S. Antipin, E.S. Fomin, I.P. Chuikov
Synthesis, crystal structure and NMR-study new mononuclear paramagnetic Er (III) complex based on imine derivatives of thiacalix[4]arene
Inorganica Chimica Acta, V.545, 24 January 2023, 121267 doi:10.1016/j.ica.2022.121267, IF=3.118
E.N. Zapolotsky, S.P. Babailov, M.V. Kniazeva, Yu.V. Strelnikova, A.S. Ovsyannikov, A.T. Gubaidullin, S.E. Solovieva, I.S. Antipin, E.S. Fomin, I.P. Chuikov
Synthesis, crystal structure and NMR-study new mononuclear paramagnetic Er (III) complex based on imine derivatives of thiacalix[4]arene
Inorganica Chimica Acta, V.545, 24 January 2023, 121267 doi:10.1016/j.ica.2022.121267, IF=3.118
V. Shelkovnikov, E. Vasiliev, D. Derevyanko, A. Bukhtoyarova, V. Berezhnaya, I. Shundrina
The holographic properties of photopolymers on the base of oxygen- and sulfur-containing spirocyclic monomers
Journal of Materials Science, 2023,, V. 58, N 2, ,Pp. 983-995 doi:10.1007/s10853-022-08105-8, IF=4.682
T.T. Efremova, S.V. Morozov, E.I. Chernyak, E.V. Chumanova
Combining the genes of blue aleurone and purple pericarp in the genotype of spring bread wheat Saratovskaya 29 to increase anthocyanins in grain
Journal of Cereal Science, V. 109, January 2023, 103616 doi:10.1016/j.jcs.2022.103616, IF=4.74
И.А. Заякин, А.Я. Акыева, М.А. Сыроешкин, И.Ю. Багрянская, Е.В. Третьяков, М.П. Егоров
Синтез, структура и электрохимия нитронилнитроксилзамещенного 1,4-нафтохинона
Известия Академии наук. Серия химическая. 2023, № 1, стр. 213, IF=1.703
S.G. Il'yasov, V.S. Glukhacheva, D.S. Il'yasov, E.E. Zhukov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
Adducts of the Zinc Salt of Dinitramic Acid
Materials 2023, 16(1), 70 doi:10.3390/ma16010070, IF=3.747
M.E. Mironov, T.V. Rybalova, M.A. Pokrovski, F. Emaminia, E.R. Gandalipov, A.G. Pokrovskii, E.E. Shults
Synthesis of fully functionalized spirostanic 1,2,3-triazoles by the three component reaction of diosgenin azides with acetophenones and aryl aldehydes and their biological evaluation as antiproliferative agents
Steroids, V. 190, February 2023, 109133 doi:10.1016/j.steroids.2022.109133, IF=2.759

2022

N.P. Isaev, A.R. Melnikov, K.A. Lomanovich, M.V. Dugin, M.Yu. Ivanov, D.N. Polovyanenko, S.L. Veber, M.K. Bowman, E.G. Bagryanskaya
A broadband pulse EPR spectrometer for high-throughput measurements in the X-band
Journal of Magnetic Resonance Open, V. 14-15, June 2023, 100092 doi:10.1016/j.jmro.2022.100092
I. Zayakin, E. Tretyakov, A. Akyeva, M. Syroeshkin, Ju. Burykina, A. Dmitrenok, A. Korlyukov, D. Nasyrova, I. Bagryanskaya, D. Stass, V.P. Ananikov
Overclocking nitronyl nitroxide gold derivatives in cross-coupling reactions
Chemistry - A European Journal, First published: 19 October 2022 doi:10.1002/chem.202203118, IF=5.19
D.V. Reshetnikov, I.D. Ivanov, D.S. Baev, T.V. Rybalova, E.S. Mozhaitsev, S.S. Patrushev, V.A. Vavilin, T.G. Tolstikova, E.E. Shults
Design, Synthesis and Assay of Novel Methylxanthine–Alkynylmethylamine Derivatives as Acetylcholinesterase Inhibitors
Molecules 2022, 27(24), 8787 doi:10.3390/molecules27248787, IF=4.927
V.V. Krisyuk, S.Urkasym. Kyzy, T.V. Rybalova, I.V. Korolkov, M.A. Grebenkina, A.N. Lavro
Structure and Properties of Heterometallics Based on Lanthanides and Transition Metals with Methoxy-β-Diketonates
Molecules 2022, 27(23), 8400 doi:10.3390/molecules27238400, IF=4.927
Effect of an Extractant on the Composition of the Lipophilic Constituents of the Extracts of Rhodiola rosea L. and on the Extracts' Activity/ T. P. Kukina, D. N. Shcherbakov, A.V. Zybkina, I. A. Elshin, V. O. Korsakov, O. I. Salnikova, P. V. Kolosov, Ts. Sandag, D. A. Karakai, E. D. Mordvinova// Russian Journal of Bioorganic Chemistry, 2022, V. 48, Pp 1461-1469 doi:10.1134/S1068162022070147, IF=1.253
Т.П. Кукина, И.А. Елшин, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, М.А. Бондарева, А.А. Нефедов, В.Ю. Чиркова, Е.А. Шарлаева, С.В. Беленькая, Д.Н. Щербаков
Состав липофильных компонентов эфирного экстракта рододендрона Адамса и активность против основной протеазы SARS COV 2
Химия растительного сырья, 2022, № 4, c. 153-162. doi:10.14258/jcprm.20220411584
A PYRIMIDINE-DERIVED DIPHOSPHINE P-MONOXIDE AND A Ag(I) COORDINATION POLYMER THEREOF: SYNTHESIS, STRUCTURE, AND LUMINESCENCE/ M. P. Davydova, I. Yu. Bagryanskaya, E. H. Sadykov, A. V. Artem'ev// Journal of Structural Chemistry, 2022, V.63, N 12, pp 2020-2027 doi:10.1134/S0022476622120137, IF=1.004
И.А. Оськина, В.И. Краснов, И.Ю. Багрянская, А.С. Виноградов, В.Е. Платонов, А.Я. Тихонов
Синтез алкилзамещенных 2-(полифториндан-5-ил)-Н--имидазол-1-олов
Журнал органической химии. 2022. Т. 58. № 12. С. 1379-1386. doi:10.31857/S0514749222120060, IF=0.861
ELECTRO-ACTIVE COPOLYMER OF METHYL METHACRYLATE AND 2((4-ACRYLOYLPIPERAZIN-1-YL)METHYL)-9H-THIOXANTHEN-9-ONE FOR MEMRISTOR MEMORY TECHNOLOGIES: ELECTROCHEMICAL AND ELECTROCHROMIC / Shundrina I.K., Bukhtoyarova A.D., Os'kina I.A., Odintsov D.S., Shundrin L.A.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 668-675. doi:10.15372/CSD2022430
STUDIES OF THE BEHAVIOUR OF PERSISTENT ORGANIC POLLUTANTS IN THE BAIKAL-SELENGA ECOSYSTEM AS AN ELEMENT OF THE IMPLEMENTATION OF THE STOCKHOLM CONVENTION/ Morozov S.V., Shirapova G.S., Ermolaeva O.A., Chernyak E.I., Tkacheva N.I., Batoev V.B., Mognonov D.M.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 600-611. doi:10.15372/CSD2022423
PHYSICOCHEMICAL INVESTIGATION OF HOMESPUN CULT OBJECTS OF THE KHANTY AND MANSI MADE AT THE END OF THE XVIII CENTURY/ Karpova E.V., Sotnikova Yu.S., Lastovka A.V., Baulo A.V., Salnikova I.V.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 585-594. doi:10.15372/CSD2022421
INVESTIGATION OF THE CHROMATOGRAPHIC BEHAVIOUR OF METABOLITES FROM BLOOD PLASMA BY HPLC-MS/MS USING A MONOLITHIC COLUMN WITH A SORBENT BASED ON 1-VINYL-1,2,4-TRIAZOLE/ Basov N.V., Rogachev A.D., Sotnikova Yu.S., Patrushev Yu.V., Pokrovsky A.G.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 571-578. doi:10.15372/CSD2022419
V.N. Kovtonyuk, Yu.V. Gatilov, P.V. Nikul'shin
Perfluorinated cyclo-tetrakis(phenylene sulfides): synthesis and structure
Mendeleev Communications, V. 32, N 6, November–December 2022, Pp. 789-791 doi:10.1016/j.mencom.2022.11.027, IF=1.837
E.O. Shestakova, S.G. Il'yasov, I.A. Shchurova, V.S. Glukhacheva, D.S. Il'yasov, E.E. Zhukov, A.O. Bryzgalov, T.G. Tolstikova, Yu.V. Gatilov
Investigation of 1,4-Substituted 1,2,3-Triazole Derivatives as Antiarrhythmics: Synthesis, Structure, and Properties
Pharmaceuticals 2022, 15(12), 1443 doi:10.3390/ph15121443, IF=5.215
A.V. Shernyukov, G.E. Salnikov, V.I. Krasnov, A.M. Genaev
Cluster halogenation of adamantane and its derivatives with bromine and iodine monochloride† Check for updates
Org. Biomol. Chem., 2022, 20(43), 8515-8527 doi:10.1039/D2OB01455F, IF=3.89
I. Philippov, Yu. Gatilov, A. Sonina, A. Vorob’ev
Oxidative [3+2]Cycloaddition of Alkynylphosphonates with Heterocyclic N-Imines: Synthesis of Pyrazolo[1,5-a]Pyridine-3-phosphonates
Molecules 2022, 27(22), 7913 doi:10.3390/molecules27227913, IF=4.927
E. Benassi, T. Vaganova, E. Malykhin, Yu. Gatilov, L. Nurtay, H. Fanc
Intermolecular Interactions in the Crystalline Structure of Some Polyhalogenated Di– and Triamino Pyridines: Spectroscopical Perspectives
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, V. 281, 15 November 2022, 121632 doi:10.1016/j.saa.2022.121632, IF=4.83
V.S. Glukhacheva, S.G. Il'yasov, E.O. Shestakova, E.E. Zhukov, D.S. Il'yasov, A.A. Minakova, I.V. Eltsov, A.A. Nefedov, A.M. Genaev
Synthesis of Nitro- and Acetyl Derivatives of 3,7,10-Trioxo-2,4,6,8,9,11-hexaaza[3.3.3]propellane
Materials 2022, 15(23), 8320 doi:10.3390/ma15238320, IF=3.747
S.A. Dobrynin, M.M. Gulman, D.A. Morozov, I.F. Zhurko, A.I. Taratayko, Yu.S. Sotnikova, Yu.I. Glazachev, Yu.V. Gatilov, I.A. Kirilyuk
Synthesis of Sterically Shielded Nitroxides Using the Reaction of Nitrones with Alkynylmagnesium Bromides
Molecules 2022, 27(21), 7626 doi:10.3390/molecules27217626, IF=4.927
R.V. Ottenbacher, D.G. Samsonenko, A.A. Nefedov, K.P. Bryliakov
Direct Regio- and Stereoselective Mono- and Polyoxyfunctionalization of Estrone Derivatives at C(sp3)-H Bonds
Journal of Catalysis, 2022, V. 415, November 2022, Pp 12-18 doi:10.1016/j.jcat.2022.09.020, IF=8.46
L. Politanskaya, Ji.Wang, N.Troshkova, I.Chuikov, I. Bagryanskayaa
One-pot synthesis of fluorinated 2-arylchroman-4-one derivatives from 2-(triisopropylsilyl)ethynylphenols and aromatic aldehydes
Journal of Fluorine Chemistry V. 263, November 2022, 110045 doi:10.1016/j.jfluchem.2022.110045, IF=2.226
A.V. Artem'ev, A.Yu. Baranov, A.S. Berezin, U.A. Lapteva, D.G. Samsonenko, I.Yu. Bagryanskaya
Trigonal Planar Au@Ag3 Clusters Showing Exceptionally Fast and Efficient Phosphorescence in Violet to Deep-Blue Region
Chemistry-A European Journal, 2022, V. 28, Iss. 60 , e202201563 doi:10.1002/chem.202201563, IF=5.02
O.V. Ardashov, D.V. Korchagina, I.Yu. Bagryanskaya, K.P. Volcho, N.F. Salakhutdinov
(1S,5R)-6,6-Dimethyl-4-(((1S,2S,5S)-2,6,6-trimethyl-4-oxobicyclo[3.1.1]heptan-2-yl)methyl)bicyclo[3.1.1]hept-3-en-2-one
Molbank 2022, 2022(4), M1465 doi:10.3390/M1465
V.Yu. Kryukov, E.I. Chernyak, N. Kryukova, M. Tyurin, A. Krivopalov, O. Yaroslavtseva, I. Senderskiy, O. Polenogova, E. Zhirakovskaia, V.V. Glupov, S.V. Morozov
Parasitoid venom alters the lipid composition and development of microorganisms on the wax moth cuticle
Entomologia Experimentalis et Applicata, V.170, Т 10, October 2022. PЗ 852-868 doi:10.1111/eea.13219, IF=2.433
Eurasian Soil Science, 2022, V. 55, Pp. 1360-1370/ D.A. Sokolov, I.S. Ivanova, S.V. Morozov, T.G. Pchelnikova, E.A. Soldatova// Eurasian Soil Science doi:10.1134/S1064229322100143, IF=1.373
E. Khusnutdinova, Z. Galimova, A. Lobov, I. Baikova, O. Kazakova, Ha Nguyen Thi. Thu, N.V.. Tuyen, Yu. Gatilov, R. Csuk, I. Serbian, S. Hoenke
Synthesis of messagenin and platanic acid chalcone derivatives and their biological potential
Natural Product Research, 2022, V. 36 (20), Pp 5189-5198 doi:10.1080/14786419.2021.1922904, IF=2.488
Ya.V. Demyanov, M.I. Rakhmanova, I.Yu. Bagryanskaya, A.V. Artem'ev
1D CuI coordination polymers based on triphenylarsine and N,N'-ditopic co-ligands: synthesis, crystal structure and TADF properties
Mendeleev Communications, 2022, 32(5), 649-651 doi:10.1016/j.mencom.2022.09.027, IF=1.837
O.I. Yarovaya, K.S. Kovaleva, S.S. Borisevich, T.V. Rybalova, Yu.V. Gatilov, E.O. Sinegubova, A.S. Volobueva, V.V. Zarubaev
Synthesis and antiviral properties of tricyclic amides derived from α-humulene and β-caryophyllene
Mendeleev Communications, 2022, 32(5), pp. 609-611 doi:10.1016/j.mencom.2022.09.013, IF=1.837
Ya.V. Demyanov, E.H. Sadykov, M.I. Rakhmanova, A.S. Novikov, I.Yu. Bagryanskaya, A.V. Artem'ev
Tris(2-Pyridyl)Arsine as a New Platform for Design of Luminescent Cu(I) and Ag(I) Complexes
Molecules 2022, 27(18), 6059 doi:10.3390/molecules27186059, IF=4.927
A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
DFT insights into superelectrophilic activation of α,β-unsaturated nitriles and ketones in superacids
Org. Biomol. Chem., 2022,20(34), 6799-6808 doi:10.1039/D2OB01141G, IF=3.89
D. V. Reshetnikov, L. G. Burova, T. V. Rybalova, E. A. Bondareva, S. S. Patrushev, A. N. Evstropov, E. E. Shults
Synthesis and Antibacterial Activity of Caffeine Derivatives Containing Amino-Acid Fragments
Chemistry of Natural Compounds, 2022, V. 58, N 5, Pp 908-915 doi:10.1007/s10600-022-03826-3, IF=0.83
Hu. Han, V.N. Kovtonyuk, Yu.V. Gatilov, R.V. Andreev
Directed synthesis of isomeric polyfluorinated dinitrotetraoxacalixarenes and bicyclooxacalixarenes
Journal of Fluorine Chemistry, 2022, V.261-262, 110022 doi:10.1016/j.jfluchem.2022.110022, IF=2.226
A.D. Kuimov, Ch.S. Becker, N.A. Shumilov, I.P. Koskin, A.A. Sonina, V.Yu. Komarov, I.K. Shundrina, M.S. Kazantsev
Synthetic approach for the control of self-doping in luminescent organic semiconductors
Mater. Chem. Front., 2022, V. 6, N 16, Pp. 2244-2255 doi:10.1039/D2QM00345G, IF=8.683
A.A. Dokuchaeva, A.a B. Mochalova, T.P. Timchenko, K.S. Podolskaya, O.A. Pashkovskaya, E.V. Karpova, I.A. Ivanov, N.A. Filatova I. Yu Zhuravleva
In Vivo Evaluation of PCL Vascular Grafts Implanted in Rat Abdominal Aorta
Polymers 2022, 14(16), 3313 doi:10.3390/polym14163313, IF=4.967
E.A. Radiush, E.A. Pritchina, E.A. Chulanova, A.A. Dmitriev, I. Yu Bagryanskaya, A.M-Z. Slawin, J. D. Woollins, N.P. Gritsan, A.V. Zibarev, N.A. Semenov
Chalcogen-bonded donor–acceptor complexes of 5,6-dicyano[1,2,5]selenadiazolo[3,4-b]pyrazine with halide ions Check for updates
New J. Chem., 2022,46(30), 14490-14501 doi:10.1039/D2NJ02345H, IF=3.924
E.S. Stoyanov, I.Yu. Bagryanskaya, I.V. Stoyanova
IR-Spectroscopic and X-ray-Structural Study of Vinyl-Type Carbocations in Their Carborane Salts
ACS Omega 2022, 7, 31, 27560-27572 doi:10.1021/acsomega.2c03025, IF=4.132
I.B. Ivshina, N.A. Luchnikova, P.Yu. Maltseva, I.V. Ilyina, K.P. Volcho, Yu.V. Gatilov, D.V. Korchagina, N.A. Kostrikina, V.V. Sorokin, A.L. Mulyukin, N.F. Salakhutdinov
Biotransformation of (-)-Isopulegol by Rhodococcus rhodochrous
Pharmaceuticals 2022, 15(8), 964; doi:10.3390/ph15080964, IF=5.215
N.A. Grigorieva, I.Yu. Fleitlikh, A.Ya. Tikhonov, V.I. Mamatyuk, E.V. Karpova, O.A. Logutenko
Recovery of indium from sulfate solutions with D2EHPA in the presence of organic proton-donor additives
Hydrometallurgy, Available online 11 June 2022, 105925 doi:10.1016/j.hydromet.2022.105925, IF=4.217
N.S. Li-Zhulanov, I.V. Il'ina, A.Yu. Sidorenko, D.V. Korchagina, K.P. Volcho, V.E. Agabekov, N.F. Salakhutdinov
Cascade transformation of 4-hydroxymethyl-2-carene into novel cage methanopyrano[4,3-b]thieno[3,2-g]benzofuran derivative
Mendeleev Communications, V. 32, N 4, July-August 2022, Pp 443-445 doi:10.1016/j.mencom.2022.07.005, IF=1.837
V.V. Oreshko, K.S. Kovaleva, E.D. Mordvinova, O.I. Yarovaya, Yu.V. Gatilov, D.N. Shcherbakov, N.I. Bormotov, O.A. Serova, L.N. Shishkina, N.F. Salakhutdinov
Synthesis and Antiviral Properties of Camphor-Derived Iminothiazolidine-4-Ones and 2,3-Dihydrothiazoles
Molecules 2022, 27(15), 4761 doi:10.3390/molecules27154761, IF=4.927
M. Babaev, E. Khusnutdinova, A. Lobov, Z. Galimova, A. Petrova, T. Rybalova, Thi Thu.Nguyen. Ha, C. Meyers, M. Prichard, O. Kazakova
Allobetulone rearrangement to lαH,19βH-ursane triterpenoids with antiviral activity
Natural Product Research, 2022, V. 36, N 13, Pp 3286-3296 doi:10.1080/14786419.2020.1855159, IF=2.488
A.Y. Glagoleva, A.V. Vikhorev, N.A. Shmakov, S.V. Morozov, E.I. Chernyak, G.V. Vasiliev, N.V. Shatskaya, E.K. Khlestkina, O.Y. Shoeva
Features of Activity of the Phenylpropanoid Biosynthesis Pathway in Melanin-Accumulating Barley Grains
Frontiers in Plant Science, 2022, V.1311, Art.Num. 923717 doi:10.3389/fpls.2022.923717, IF=6.626
A.Yu. Baranov, S.O. Slavova, A.S. Berezin, S.K. Petrovskii, D.G. Samsonenko, I.Yu. Bagryanskaya, V.P. Fedin, E.V. Grachova, A.V. Artem'ev
Controllable Synthesis and Luminescence Behavior of Tetrahedral Au@Cu4 and Au@Ag4 Clusters Supported by tris(2-Pyridyl)phosphine
Inorganic Chemistry, 2022, 61, 28, 10925-10933 doi:10.1021/acs.inorgchem.2c01474, IF=5.435
Synthesis, structure, and properties of tert-butyl perfluorobiphenyl nitroxide/ P.A. Fedyushin, A.Ya. Akyeva, M.A. Syroeshkin, T.V. Rybalova, D.V. Stass, V.A. Korolev, E.V. Tretyakov, M.P. Egorov// Russian Chemical Bulletin, 2022, V. 71, N 7, Pp 1474-1482 doi:10.1007/s11172-022-3553-8, IF=1.704
S.N. Bizyaev, Yu.V. Gatilov, D.V. Zubricheva, V.D. Tikhova, A.V. Tkachev
A New Type of Terpene-Based D 2-Symmetric Macrocycles, Capable of Selectively Extracting Au, Pd and Pt from Complex Mixtures
ChemistrySelect, V.7, N 22, June 13, 2022, e202201263 doi:10.1002/slct.202201263, IF=2.307
A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.l. Laktionov
Correction: Gostev et al. In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics. Polymers 2020, 12, 845
Polymers 2022, 14(11), 2263; doi:10.3390/polym14112263, IF=4.967
A.V. Artem'ev, A.Yu. Baranov, I.Yu. Bagryanskaya
Trigonal planar clusters Ag@Ag3 supported by (2-PyCH2)3P ligands
Inorganic Chemistry Communications, V. 140, June 2022, 109478 doi:10.1016/j.inoche.2022.109478, IF=3.428
Synthesis and study of azide-tetrazole tautomerism in 2-azido-6-phenylpyrimidin-4(3H)-one and 2-azido-4-chloro-6-phenylpyrimidine/ N. V. Aleksandrova, E. B. Nikolaenkova, Yu. V. Gatilov, D. N. Polovyanenko, V. I. Mamatyuk, V. P. Krivopalov// Russian Chemical Bulletin, 2022, V. 71, Pp 1266-1272 doi:10.1007/s11172-022-3529-8, IF=1.704
Reduction of Perfluorinated Benzocycloalkenones and Other Polyfluoroaryl Ketones to Alcohols with LiBH4/ S. Wang, D. S. Golokhvastova, Ya. V. Zonov, V. M. Karpov, T. V. Mezhenkova, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2022, V. 58, N 6, Pp 780-790 doi:10.1134/S1070428022060045, IF=0.862
A.A. Munkuev, N.S. Dyrkheeva, T.E. Kornienko, E.S. Ilina, D.I. Ivankin, E.V. Suslov, D.V. Korchagina, Yu.V. Gatilov, A.L. Zakharenko, A.A. Malakhova, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
Adamantane-Monoterpenoid Conjugates Linked via Heterocyclic Linkers Enhance the Cytotoxic Effect of Topotecan
Molecules 2022, 27(11), 3374 doi:10.3390/molecules27113374, IF=4.927
N.B. Asanbaeva, L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, M.S. Kazantsev, A.A. Dmitriev, N.P. Gritsan, N. Haro-Mares, T. Gutmann, G. Buntkowsky, E.V. Tretyakov, E.G. Bagryanskaya
Effects of Spiro-Cyclohexane Substitution of Nitroxyl Biradicals on Dynamic Nuclear Polarization
Molecules 2022, 27(10), 3252 doi:10.3390/molecules27103252, IF=4.927
S.G. Il'yasov, V.S. Glukhacheva, D.S. Il'yasov, E.E. ZhukovaIli, V. Eltsov, Yu.V. Gatilov
A novel energetic nickel coordination compound based on carbohydrazide and dinitramide
Mendeleev Communications, V. 32, N 3, May–June 2022, Pp 344-346 doi:10.1016/j.mencom.2022.05.017, IF=1.837
VOLATILE IRON(III) COMPLEXES WITH A METHOXY-SUBSTITUTED β-DIKETONATE/ S. Urkasym kyzy, T. V. Rybalova, V. Yu. Komarov, I. V. Korolkov, V. V. Krisyuk// Journal of Structural Chemistry, 2022, V. 63, № 4, Pp 524-533 doi:10.1134/S0022476622040035, IF=1.004
G.T. Sukhanov, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, K.K. Bosov, I.A. Krupnova, E.V. Pivovarova
Acidic N-dealkylation in nitrotriazolium salts
Mendeleev Communications, 2022, V. 32, N 2, Pp 215-217 doi:10.1016/j.mencom.2022.03.020, IF=1.837
A.Yu. Makarov, Yu.M. Volkova, S.B. Zikirin, I.G. Irtegova, I.Yu. Bagryanskaya, Yu.V. Gatilov, A.A. Nefedov, A.V. Zibarev
New 3,1,2,4-benzothiaselenadiazines, related π-heterocycles including Herz cations, radicals and molecular complexes, and Bunte salts
New J. Chem., 2022, ,46(7), 3687-3696 doi:10.1039/D1NJ05979C, IF=3.925
A.G. Ogienko, S.A. Myz, A.A. Nefedov, A.A. Ogienko, T.P. Adamova, O.M. Voronkova, S.V. Amosova, B.A. Trofimov, V.V. Boldyrev, E.V. Boldyreva
Clathrate Hydrates of Organic Solvents as Auxiliary Intermediates in Pharmaceutical Research and Development: Improving Dissolution Behaviour of a New Anti-Tuberculosis Drug, Perchlozon
Pharmaceutics 2022, 14(3), 495 doi:10.3390/pharmaceutics14030495, IF=6.525
L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, N.P. Gritsan, A.A. Dmitriev, M.S. Kazantsev, E.V. Zaytseva, D.A. Parkhomenko, I.V. Beregovaya, G.A. Zakabluk, E.V. Tretyakov
Multispin Systems with a Rigid Ferrocene-1,1'-diyl-Substituted 1,3-Diazetidine-2,4-diimine Coupler: A General Approach
European journal of organic Chemistry, V. 2022, N 7, February 18, 2022, e202101234 doi:10.1002/ejoc.202101234, IF=3.261
A. Paromov, I. Shchurova, A. Rogova, I. Bagryanskaya, D. Polovyanenko
Acid-Catalyzed Condensation of Benzamide with Glyoxal, and Reaction Features
Molecules 2022, 27(3), 1094 doi:10.3390/molecules27031094, IF=4.927
T.A. Vaganova, E. Benassi, Yu.V. Gatilov, I.P. Chuikov, D.P. Pishchur, E.V. Malykhin
Polyhalogenated aminobenzonitriles vs their co-crystals with 18-crown-6: amino group position as a tool to control crystal packing and solid-state fluorescence
CrystEngComm, 2022, V. 24, N 5, Pp 987-1001 doi:10.1039/D1CE01469B, IF=3.756
D.N. Shcherbakov, G.Y. Galitsyn, T.P. Kukina, N.V. Panteleeva, O.I. Salnikova, P.V. Kolosov
Prospects for comprehensive use of sea buckthorn of Novosibirsk selection
AIP Conference Proceedings, 2022, 2390(1), 030085 doi:10.1063/5.0070159
D.N. Shcherbakov, T.P. Kukina, I.A. Elshin, O.I. Salnikova, P.V. Kolosov
Deodorized Distillate of Sunflower Oil as a Source of Kaurane Compounds
AIP Conference Proceedings 2390(1), 030084, 2022. 030084-1–030084-5; doi:10.1063/5.0070161
D.N. Shcherbakov, T.P. Kukina, I.A. Elshin, N.V. Panteleeva, T.V. Teplyakova, O.I. Salnikova
GC-MS analysis of lipophilic Chaga mushroom constituents
AIP Conference Proceedings, 2022, 2390(1), 030083 doi:10.1063/5.0070158
I.Yu. Zhuravleva, E.V. Karpova, A.A. Dokuchaeva, E.V. Kuznetsova, S.V. Vladimirov, A.L. Ksenofontov, N.R. Nichay
Bovine jugular vein conduit: What affects its elastomechanical properties and thermostability?
Journal of Biomedical Materials Research Part A, 2022, V.110, N 2, Pp 394-408 doi:10.1002/jbm.a.37296, IF=4.854
G.T. Sukhanov, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, I.А. Krupnova, K.K. Bosov, E.V. Pivovarova, V.I. Krasnov
Energetic Materials Based on N-Substituted 4(5)-Nitro-1,2,3-Triazoles
Materials 2022, 15(3), 1119 doi:10.3390/ma15031119, IF=3.748
G.A. Selivanova, A.D. Skolyapova, J. Wang, E.V. Karpova, I. Shundrina, I.Yu. Bagryanskaya, E.V. Amosov
Azo dyes containing 1,3,4-thiadiazole fragment: synthesis, properties
New J. Chem., 2022, 46(4), 1929-1942 doi:10.1039/D1NJ05084B, IF=3.925
A.V. Artem'ev, Ya.V. Demyanov, M.I. Rakhmanova, I.Yu. Bagryanskaya
Pyridylarsine-based Cu(i) complexes showing TADF mixed with fast phosphorescence: a speeding-up emission rate using arsine ligands
Dalton Trans., 2022, 51(3), 1048-1055 doi:10.1039/D1DT03759E, IF=4.569
A.A. Dokuchaeva, T.P. Timchenko, E.V. Karpova, S.V. Vladimirov, I.A. Soynov, I.Y. Zhuravleva
Effects of Electrospinning Parameter Adjustment on the Mechanical Behavior of Poly-ε-caprolactone Vascular Scaffolds
Polymers, 2022, 14(2), 349 doi:10.3390/polym14020349, IF=4.967
S.P. Babailov, E.N.Zapolotsky, V.V. Kokovkin, O.G. Shakirova, I.V. Mironov, I.P. Chuikov, E.S. Fomin
Switching of shifting and relaxational NMR-thermosensor properties of iron (II) tris-(pyrazol-1-yl) methane complexes due to spin-crossover
Polyhedron, V. 212, 15 January 2022, 115611 doi:10.1016/j.poly.2021.115611, IF=2.975
A.Yu. Sidorenko, Yu.M. Kurban, A.V. Kravtsova, I.V. I'ina, N.S. Li-Zhulanov, D.V. Korchagina, J.E. Sanchez-Velandia, A. Aho, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
Clays catalyzed cascade Prins and Prins-Friedel-Crafts reactions for synthesis of terpenoid-derived polycyclic compounds
Applied Catalysis A: General, V. 629, 5 January 2022, 118395 doi:10.1016/j.apcata.2021.118395, IF=5.723
V.A. Stepanova, S.S. Patrushev, T.V. Rybalova, E.E. Shults
Cross-copling reaction to access a library of eudesmane-type methylene lactones with quinoline or isoquinoline substituent
Journal of Molecular Structure, V.1247, 5 January 2022, 131373 doi:10.1016/j.molstruc.2021.131373, IF=3.841
I.Y. Zhuravleva, A.A. Dokuchaeva, E.V. Karpova, T.P. Timchenko, A.T. Titov, SvS. Shatskaya, Yu.F. Polienko
Immobilized Bisphosphonates as Potential Inhibitors of Bioprosthetic Calcification: Effects on Various Xenogeneic Cardiovascular Tissues
Biomedicines 2022, 10(1), 65 doi:10.3390/biomedicines10010065, IF=4.757
M.E. Mironov, S.A. Borisov, T.V. Rybalova, D.S. Baev, T.G. Tolstikova, E.E. Shults
Synthesis of Anti-Inflammatory Spirostene-Pyrazole Conjugates by a Consecutive Multicomponent Reaction of Diosgenin with Oxalyl Chloride, Arylalkynes and Hydrazines or Hydrazones
Molecules 2022, 27(1), 162 doi:10.3390/molecules27010162, IF=4.927
M.A. Gromova, Yu.V. Kharitonov, S.A. Borisov, T.V. Rybalova, T.G. Tolstikova, E.E. Shul'ts
Synthetic Transformations of Higher Terpenoids. 41. Synthesis and Anti-Inflammatory Activity of 4-(Carboxyalkyl)-18-nor-isopimara-7,15-Dienes
Chemistry of Natural Compounds 2022, 58(1), Pp. 55-64 doi:10.1007/s10600-022-03596-y, IF=0.83
Reaction of 5,5′-Diaryl-1,1′-dihydroxy-2,2′-biimidazoles with Trimethyl Phosphite/ V.I. Krasnov, I.A. Os'kina, A.Ya. Tikhonov// Russian Journal of Organic Chemistry. 2021. Т. 58. № 1. Pp 70-75 doi:10.1134/S1070428022010092, IF=0.862
D.G. Trofimov, Yu.I. Glazachev, A.A. Gorodetsky, D.A. Komarov, T.V. Rybalova, I.A. Kirilyuk
4-Dialkylamino-2,5-dihydroimidazol-1-oxyls with Functional Groups at the Position 2 and at the Exocyclic Nitrogen: The pH-Sensitive Spin Labels
Gels 2022, 8(1),11 doi:10.3390/gels8010011, IF=4.432
K.M. Turdybekov, S.A. Ivasenko, D.M. Turdybekov, A.S. Makhmutova, Yu.V. Gatilov, S.M. Adekenov
ISOLATION AND STRUCTURE OF THE NEW SESQUITERPENE LACTONE 3-OXO-10β-HYDROXY-5,7&alpha(H),4,6β(H)-GUAI-1,11(13)-DIENE-6,12-OLIDE
Bulletin of the Karaganda University. Chemistry Series. 2022. № 2 (106). С. 52-60. doi:10.31489/2022Ch2/2-22-8
A.V. Artem'ev, M.P. Davydova, A.S. Berezin, D.G. Samsonenko, I.Yu. Bagryanskaya, V.K. Brel, Xiu. Hei, K.A. Brylev, O. I. Artyushin, L.E. Zelenkov, I.I. Shishkin, J. Li
New Approach toward Dual-Emissive Organic–Inorganic Hybrids by Integrating Mn(II) and Cu(I) Emission Centers in Ionic Crystals
ACS Applied Materials & Interfaces 2022, 14, 27, 31000-31009 doi:10.1021/acsami.2c06438, IF=10.383

2021

K.S. Kovaleva, O.I. Yarovaya, Yu.V. Gatilov, A.V. Slita, Ya.L. Esaulkova, V.V. Zarubaev, N.B. Rudometova, N.S. Shcherbakova, D.N. Shcherbakov, N.F. Salakhutdinov
Synthesis and Antiviral Activity of N-Heterocyclic Hydrazine Derivatives of Camphor and Fenchone
Chemistry of Heterocyclic Compounds (2021), 57, N. 4, Pp 455-461 doi:10.1007/s10593-021-02923-5, IF=1.277
D.S. Odintsov, I.K. Shundrina, D.E. Gorbunov, N.P. Gritsan, J. Beckmann, L.A. Shundrin
Spectroelectrochemical study of the reduction of 2-methyl-9H-thioxanthene-9-one and its S,S-dioxide and electronic absorption spectra of their molecular ions
Phys. Chem. Chem. Phys., 2021, 23(47), 26940-26947 doi:10.1039/D1CP04464H, IF=3.676
T.M. Khomenko, A.A. Shtro, A.V. Galochkina, Yu.V. Nikolaeva, G.D. Petukhova, S.a S. Borisevich, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
Monoterpene-Containing Substituted Coumarins as Inhibitors of Respiratory Syncytial Virus (RSV) Replication
Molecules 2021, 26(24), 7493 doi:10.3390/molecules26247493, IF=4.41
Synthesis, Structure, and Hemorheological Activity of Pentasubstituted Cyclohexanol/ I. V. Palamarchuk, Z. T. Shulgau, Sh. D. Sergazy, A. M. Zhulikeeva, Yu. V. Gatilov & I. V. Kulakov// Russian Journal of General Chemistry, 2021, V. 91, pp 2462–2468 doi:10.1134/S107036322112015X, IF=0.867
Т.П. Кукина, Д.Н. Щербаков, А.В. Зыбкина, И.А. Елшин, В.О. Корсаков, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, Е.Д. Мордвинова
Влияние экстрагента на состав липофильных компонентов экстрактов корневища Rhodiola rosea L. и активность экстрактов.
Химия растительного сырья. 2021. N 4. С. 307-317 doi:10.14258/jcprm.2021049872
Fluorination of single-walled carbon nanotubes and their application in organic photovoltaic cells as an electron acceptor/ E. S. Kobeleva, D. A. Nevostruev, M. N. Uvarov, D. E. Utkin, V. A. Zinoviev, O. A. Gurova, M. S. Kazantzev, K. M. Degtyarenko, A. V. Kulikova & L. V. Kulik// Russian Chemical Bulletin, 2021, V. 70, N. 12, pp 2427-2433 doi:10.1007/s11172-021-3363-4, IF=1.222
M.Yu. Petyuk, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
Dinuclear ReI complex based on 1,2,4,5-tetrakis(diphenylphosphino)- pyridine: synthesis and luminescence properties
Mendeleev Communications, 2021, V. 31, N 6, Pp 810-812 doi:10.1016/j.mencom.2021.11.013, IF=1.786
I.P. Koskin, Ch.S. Becker, A.A. Sonina, V.A. Trukhanov, N.A. Shumilov, A.D. Kuimov, Yu.S. Zhuravleva, Yu.O. Kiseleva, I.K. Shundrina, P.S. Sherin, D.Yu. Paraschuk, M.S. Kazantsev
Selectively Fluorinated Furan-Phenylene Co-Oligomers Pave the Way to Bright Ambipolar Light-Emitting Electronic Devices
Advanced Functional Materials, 2021, V.31, N 48, ArtNum.2104638 doi:10.1002/adfm.202104638, IF=18.808
E. Parman, M. Lokov, R. Jarviste, S. Tshepelevitsh, N.A. Semenov, E.A. Chulanova, G.E. Salnikov, D.O. Prima, Yu.G. Slizhov, I. Leito, A.V. Zibarev
Acid-Base and Anion Binding Properties of Tetrafluorinated 1,3-Benzodiazole, 1,2,3-Benzotriazole and 2,1,3-Benzoselenadiazole
ChemPhysChem, 2021, V. 22, N 22, Pp 2329-2335 doi:10.1002/cphc.202100475, IF=3.102
A.V. Artem'ev, M.Yu. Petyuk, A.S. Berezin, A.L. Gushchin, M.N. Sokolov, I.Yu. Bagryanskaya
Synthesis and study of Re(I) tricarbonyl complexes based on octachloro-1,10-phenanthroline: towards deep red-to-NIR emitters
Polyhedron, V. 209, 15 November 2021, 115484 doi:10.1016/j.poly.2021.115484, IF=3.052
A.S. Volobueva, O.I. Yarovaya, M.V. Kireeva, S.S. Borisevich, K.S. Kovaleva, I.Ya. Mainagashev, Yu.V. Gatilov, M.G. Ilyina, V.V. Zarubaev, N.F. Salakhutdinov
Discovery of New Ginsenol-like Compounds with High Antiviral Activity
Molecules, 2021, 26(22), 6794 doi:10.3390/molecules26226794, IF=4.41
O. Kazakova, L. Rubanik, A. Lobov, N. Poleshchuk, I. Baikova, Yu. Kapustina, A. Petrova, T. Korzun, T. Lopatina, A. Fedorova, T. Rybalova, D. Polovianenko, M. Mioc, C. Soica
Synthesis of erythrodiol C-ring derivatives and their activity against Chlamydia trachomatis
Steroids,V. 175, November 2021, 108912 doi:10.1016/j.steroids.2021.108912, IF=2.667
S.S. Patrushev, T.V. Rybalova, E.E. Shults
Synthetic transformations of sesquiterpene lactones. Controllable synthesis of 11,13-dihydroisoalantolactone azides and 13-(1,2,3-triazolyl)eudesmanolides
Chemistry of Heterocyclic Compounds, 2021, V.57, N 11, Pp 1116-1129, IF=1.277
Г.Т. СУХАНОВ, Ю.В. ФИЛИППОВА, И.Ю. БАГРЯНСКАЯ, А.Г. СУХАНОВА, К.К. БОСОВ, И.А. КРУПНОВА, Е.В. ПИВОВАРОВА
Синтез и свойства солей 1,3-диалкил-4-нитро-1,2,3-триазолия
Химия в интересах устойчивого развития. 2021. Т. 29. № 6. С. 702-707. doi:10.15372/KhUR2021349
Yu.V. Khoroshunova,D. A. Morozov,A. I. Taratayko,S. A. Dobrynin,I. V. Eltsov,T. V. Rybalova,Yu. S. Sotnikova,D. N. Polovyanenko,N. B. Asanbaeva,I. A. Kirilyuk
The Reactions of 6-(Hydroxymethyl)-2,2-dimethyl-1-azaspiro[4.4]nonanes with Methanesulfonyl Chloride or PPh3-CBr4
Molecules 2021, 26(19), 6000 doi:10.3390/molecules26196000, IF=4.411
Zh.S. Nurmaganbetov, V.A. Savelyev, Yu.V. Gatilov, O.A. Nurkenov, R.B. Seidakhmetova, Z.T. Shulgau, G.K. Mukusheva, S.D. Fazylov, E.E. Shults
Synthesis and analgesic activity of 1-[(1,2,3-triazol-1-yl)methyl]quinolizines based on the alkaloid lupinine
Chemistry of Heterocyclic Compounds, 2021, V. 57, Pp 911-919 doi:10.1007/s10593-021-03000-7, IF=1.276
M.S. Borisova, D.I. Ivankin, D.N. Sokolov, O.A. Luzina, T.V. Rybalova, T.G. Tolstikova, N.F. Salakhutdinov
Synthesis, antiulcerative, and anti-inflammatory activities of new campholenic derivatives-1,3-thiazolidin-4-ones, 1,3-thiazolidine-2,4-diones, and 1,3-thiazinan-4-ones
Chemical Papers, 2021, V. 75, Pp 5503–5514 doi:10.1007/s11696-021-01741-5, IF=2.097
T.V. Mezhenkova, V.V. Komarov, V.M. Karpov, Ya.V. Zonov, Yu.V. Gatilov
Reaction of perfluorotetralin with 1,2,3,4-tetrafluorobenzene in SbF5 medium: The formation of polycyclic compounds with a new carbon framework
Journal of Fluorine Chemistry, 2021, V. 250, 109882 doi:10.1016/j.jfluchem.2021.109882, IF=2.49
S.A. Dobrynin, M.S. Usatov, I.F. Zhurko, D.A. Morozov, Yu.F. Polienko, Yu.I. Glazachev, D.A. Parkhomenko, M.A. Tyumentsev, Yu.V. Gatilov, E.I. Chernyak, E.G. Bagryanskaya, I.A. Kirilyuk
A Simple Method of Synthesis of 3-Carboxy-2,2,5,5-Tetraethylpyrrolidine-1-oxyl and Preparation of Reduction-Resistant Spin Labels and Probes of Pyrrolidine Series
Molecules 2021, 26(19), 5761 doi:10.3390/molecules26195761, IF=4.41
Yu.V. Kharitonov, E.E. Shul'ts, T.V. Rybalova, A.V. Pavlova, T.G. Tolstikova
Synthetic Transformations of Higher Terpenoids. 40. Synthesis and Assessment of Analgesic Activity of N-Containing Derivatives of Lambertianic Acid Yu. V. Kharitonov, E. E. Shul’ts, T. V. Rybalova, A. V. Pavlova & T. G. Tolstikova
Chemistry of Natural Chemistry of Natural Compounds, 2021, V. 57, N 5, Pp 879-886 doi:10.1007/s10600-021-03502-y, IF=0.809
S.A. Liakhov, I.A. Schepetkin, O.S. Karpenko, H.I. Duma, N.M. Haidarzhy, L.N. Kirpotina, A.R. Kovrizhina, A.I. Khlebnikov, I.Yu. Bagryanskaya, M.T. Quinn
Novel c-Jun N-Terminal Kinase (JNK) Inhibitors with an 11H-Indeno[1,2-b]quinoxalin-11-one Scaffold
Molecules 2021, 26(18), 5688 doi:10.3390/molecules26185688, IF=4.411
E.S. Stoyanov, I.Yu. Bagryanskaya, I.V. Stoyanova
Isomers of the Allyl Carbocation C3H5+ in Solid Salts: Infrared Spectra and Structures
ACS Omega, ACS Omega 2021, 6, 37, 23691–23699 doi:10.1021/acsomega.1c01316, IF=3.512
D.S. Baranov, A.A. Popov, D.A. Nevostruev, A.A. Dmitriev, Yu.V. Gatilov, E.S. Kobeleva
One-Pot Synthesis of 2-R-Naphtho[2,3-b]thiophene-4,9-diones via Cyclization of 2-(R-Ethynyl)-1,4-naphthoquinones with Na₂S₂O₃
The Journal of Organic Chemistry, 2021, V. 86, N. 17, Pp. 11361-11369 doi:10.1021/acs.joc.1c00852, IF=4.354
I.V. Kulakov, I.V. Palamarchuk, E.B. Nikolaenkova, A.Ya. Tikhonov, Yu.V. Gatilov, A.S. Fisyuk
Study of the cyclization of N-hydroxy- and N-methoxy-N-(2-oxoalkyl)amides
Chemical Papers, 2021, V. 75, Pp 4517-4525 doi:10.1007/s11696-021-01673-0, IF=2.097
A.V. Artem'ev, M. P.Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, D.P. Pishchur
A family of Mn(ii) complexes exhibiting strong photo- and triboluminescence as well as polymorphic luminescence
Inorg. Chem. Front., 2021, V. 8, N 15, Pp 3767-3774 doi:10.1039/D1QI00556A, IF=6.569
T.A. Vaganova, Yu.V. Gatilov, S.E. Malykhin, D.P. Pishchur, M. Sukhov, B.A. Zakharov, E.V. Boldyreva, E.V. Malykhin
Co-crystals of polyhalogenated diaminobenzonitriles with 18-crown-6: effect of fluorine on the stoichiometry and supramolecular structure
CrystEngComm, 2021, V. 23, N 7, Pp 4767-4781 doi:10.1039/D1CE00530H, IF=3.545
A.O. Bryzgalov, T.A. Yakovleva, L.V. Politanskaya, I.Yu. Bagryanskaya, T.G. Tolstikova
Fluorinated 3,4-Dihydro-2H-1,4-Benzothiazin1,1-Dioxide Derivatives with Antiarrhythmic and Hypertensive Effects
American Journal of Biomedical Science & Research, 2021,13(4),328-338 doi:10.34297/AJBSR.2021.13.001882
A.S. Sokolova, O.I. Yarovaya, D.V. Baranova, A.V. Galochkina, A.A. Shtro, M.V. Kireeva, S.S. Borisevich, Y.V. Gatilov, V.V. Zarubaev, N.F. Salakhutdinov
Quaternary ammonium salts based on (-)-borneol as effective inhibitors of influenza virus
Archives of Virology, 2021, V. 166, N. 7, Pp 1965-1976 doi:10.1007/s00705-021-05102-1, IF=2.574
R.V. Ottenbacher, D.G. Samsonenko, A.A. Nefedov, E.P. Talsi, K.P. Bryliakov
Mn Aminopyridine Oxidase Mimics: Switching Between Biosynthetic-like and Xenobiotic Regioselectivity in C-H Oxidation of (-)-Ambroxide
Journal of Catalysis, 2021, V.399, July 2021, Pp 224-229 doi:10.1016/j.jcat.2021.05.014, IF=7.92
Synthesis and Structure of Antimony Complex Compounds [(4-N,N-Me2C6H4)3MeSb]I and [(4-N,N-Me2C6H4)3MeSb]2[Hg2I6]·2DMSO/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, N. А. Rodionova, I. Yu. Bagryanskaya, N. V. Pervukhina// Russian Journal of General Chemistry, 2021, V. 91, N.7, Pp 1361-1367 doi:10.1134/S1070363221070148, IF=0.868
S.M. Adekenov, A.S. Kishkentayeva, A.B. Khasenova, E.E. Shul'ts, Yu.V. Gatilov, I.Yu. Bagryanskaya
New Arylhalo-Derivatives of Grosshe
Chemistry of Natural Compounds, 2021, V. 57, N 7, Pp 685-690 doi:10.1007/s10600-021-03450-7, IF=0.809
E. Avdeeva, E. Porokhova, I. Khlusov, T. Rybalova, E. Shults, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Sukhodol, M. Belousov
Calcium Chelidonate: Semi-Synthesis, Crystallography, and Osteoinductive Activity In Vitro and In Vivo
Pharmaceuticals 2021, 14(6), 579 doi:10.3390/ph14060579, IF=5.863
E.S. Stoyanov, I.Yu. Bagryanskaya, I.V. Stoyanova
Unsaturated Vinyl-Type Carbocation [(CH3)2C=CH]+ in Its Carborane Salts
ACS Omega, 2021, 6, 24, 15834–15843 doi:10.1021/acsomega.1c01297, IF=3.512
E.V. Tretyakov, P.V. Petunin, S. Zhivetyeva, D.E. Gorbunov, N.P. Gritsan, M.V. Fedin, D.V. Stass, R.I. Samoilova, I.Yu. Bagryanskaya, I.K. Shundrina, A.S. Bogomyakov, M.S. Kazantsev, P.S. Postnikov M. E. Trusova, V.I. Ovcharenko
Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State
Journal of the American Chemical Society, 2021, 143, 21, 8164-8176 doi:10.1021/jacs.1c02938, IF=15.419
A.Yu. Sidorenko, Yu.M. Kurban, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, O.V. Ardashov, J. Wärna, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes
Applied Catalysis A: General, 2021, V. 618, 118144 doi:10.1016/j.apcata.2021.118144, IF=5.706
A. A. Munkuev,E. S. Mozhaitsev,A. A. Chepanova,E. V. Suslov,D. V. Korchagina,O. D. Zakharova,E. S. Ilina,N. S. Dyrkheeva,A. L. Zakharenko,J. Reynisson,K. P. Volcho,N. F. Salakhutdinov ,O. I. Lavrik
Novel Tdp1 Inhibitors Based on Adamantane Connected with Monoterpene Moieties via Heterocyclic Fragments
Molecules 2021, 26(11), 3128; doi:10.3390/molecules26113128, IF=4.411
M.A. Matsko, N.V. Semikolenova, V.A. Zakharov, I.E. Soshnikov, I.K. Shundrina, Wen-Hua. Sun
Formation of branched polyethylenes by ethylene homopolymerization using LNiBr2 homo- and heterogeneous precatalysts: Interpretation of the polymer structures in comparison with commercial LLDPE
Journal of Applied Polymer Science, 2021, V.138, N 20, 50436 doi:10.1002/app.50436, IF=3.125
Influence of Comonomers on the Properties of Butylene Succinate Copolyesters/ A. G. Potapov, I. K. Shundrina// Polymer Science, Series A, 2021, V. 63, N 5, Pp 465-470 doi:10.1134/S0965545X21050114, IF=1.206
Effect of Allelic Variants of Aromatic Alcohol Dehydrogenase CADim on Micromorphological and Chemical Tissue Indices in the Spring Bread Wheat Triticum aestivum L./ A. A. Konovalov, E. V. Karpova, I. K. Shundrina, E. P. Razmakhnin, I. V. Eltsov, N. P. Goncharov// Applied Biochemistry and Microbiology, 2021, V. 57, N 4, Pp. 521-532 doi:10.1134/S0003683821040086, IF=0.886
Synthesis and Molecular Structure of Hydroxy and Hydroxyimino Derivatives of Hollongdione/ I. E. Smirnova, Yu. V. Gatilov & I. Yu. Bagryanskaya// Russian Journal of Organic Chemistry, 2021, V. 57,N 4, Pp 671-674 doi:10.1134/S1070428021040266, IF=0.723
V.S. Glukhacheva, S.G. Il’yasov, I.V. Kazantsev, E.O. Shestakova, D.S. Il’yasov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
New Reaction Products of Acetylacetone with Semicarbazide Derivatives
ACS Omega 2021, 6, 12, 8637-8645 doi:10.1021/acsomega.1c00518, IF=3.512
STRUCTURE AND STEREOCHEMISTRY OF A HYDRAZONE DERIVATIVE OF HARMINE/ A. Amanzhan, P. Zh. Zhanymkhanova, I. Yu. Bagryanskaya, E. E. Shults, A. Zh. Turmukhambetov, S. M. Adekenov// Journal of Structural Chemistry, V. 62, PP 491-495 doi:10.1134/S0022476621030161, IF=1.071
I.V. Kulakov, A.L. Stalinskaya, S.Y. Chikunova, Yu.V. Gatilov
Synthesis of new representatives of 11,12-dihydro-5H-5,11-epoxybenzo[7,8]oxocino[4,3-b]pyridines – structural analogues of integrastatins A, B†
New J. Chem., 2021, V. 45, N 7, Pp 3559-3569 doi:10.1039/D0NJ06117D, IF=3.591
Yu.F. Polienko, N.M. Kuprikova, D.A. Parkhomenko, Yu.V. Gatilov, E.I. Chernyak, I.A. Kirilyuk
Synthesis of 2,5-Bis(spirocyclohexane)-Substituted Nitroxides: New Spin Labeling Agents
Tetrahedron, 2021, V. 81, 131915 doi:10.1016/j.tet.2020.131915, IF=2.457
O.A. Tarasova, N.A. Nedolya, A.I. Albanov, I.Yu. Bagryanskaya, B.A. Trofimov
Synthesis of pyrrole-ferrocene ensembles and their rearrangement into 2-(ferrocenylmethyl)-1,2-dihydro-3H-pyrrol-3-ones
Journal of Organometallic Chemistry, 2021, V. 933, 121651 doi:10.1016/j.jorganchem.2020.121651, IF=2.369
Л.М. Горностаев, Д.С. Руденко, Т.А. Руковец, О.И. Фоминых, Ю.Г. Ромашкова, Ю.В. Гатилов, В.Н. Сильников
Реакции (4e)-3-ариламино-4-(гидроксиимино)нафталин-1(4h)-онов и (4e)-2-[ариламино(алкиламино)]-4-(гидроксиимино)нафталин-1(4h)-онов с 2,2-дигидрокси-1,3-индандионом
Журнал органической химии. 2021. Т. 57. № 2. С. 194-200. doi:10.31857/S0514749221020051, IF=0.723
A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
Unusual temperature-sensitive protonation behaviour of 4-(dimethylamino)pyridine
Org. Biomol. Chem., 2021, V. 19, N 4, Pp 866-872 doi:10.1039/D0OB01893G, IF=3.876
V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
Unexpected ring opening during the imination of camphor-type bicyclic ketones
European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=3.021
V.N. Kovtonyuk, Yu.V. Gatilov, P.V. Nikul’shin, R.A. Bredikhin
Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene
Molecules 2021, 26(3), 526 doi:10.3390/molecules26030526, IF=4.411
S.S. Patrushev, L.G. Burova, A.A. Shtro, T.V. Rybalova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, E.E. Shults
Modifications of Isoalantolactone Leading to Effective Antibacterial and Antiviral Compounds
Letters in Drug Design & Discovery, 2021, V. 18 , N 7 , Pp 686 - 700 doi:10.2174/1570180817999201211193151, IF=1.15
Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=7.328
Click synthesis of triazole-linked polyazamacrocycles through selective isopimaric acid transformations/ M.A. Gromova, Yu.V. Kharitonov, T.V. Rybalova, E.E. Shults// Macroheterocycles. 2021. Т. 14. № 1. С. 105-111. doi:10.6060/mhc200817s, IF=1.2
M. Yu.Petyuk, A. S.Berezin, A. L.Gushchin, I. Yu.Bagryanskaya, A. Yu.Baranov, A. V.Artem'ev
Luminescent Re(I) scorpionates supported by tris(2-pyridyl)phosphine and its derivatives
Inorganica Chimica Acta, 2021, V.516, 120136 doi:10.1016/j.ica.2020.120136, IF=2.545
I.V. Ilyina, O.S. Patrusheva, V.V. Zarubaev, M.A. Misiurina, A.V. Slita, Ia.L. Esaulkova, D.V. Korchagina, Yu.V. Gatilov, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
Influenza antiviral activity of F- and OH-containing isopulegol-derived octahydro-2H-chromenes
Bioorganic & Medicinal Chemistry Letters, 2021, V. 31, 127677 doi:10.1016/j.bmcl.2020.127677, IF=2.823

2020

A.Yu. Makarov, Yu.M. Volkova, L.A. Shundrin, A.A. Dmitriev, I.G. Irtegova, I.Yu. Bagryanskaya, I.K. Shundrina, N.P. Gritsan, J. Beckmann, A.V. Zibarev
Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states
Chem. Commun., 2020, 2020,56(5), 727-730 doi:10.1039/C9CC08557B, IF=5.996
T.M. Khomenko, V.V. Zarubaev, M.V. Kireeva, A.S. Volobueva, A.V. Slita, S.S. Borisevich, D.V. Korchagina, N.I. Komarova, K.P. Volcho, N.F. Salakhutdinov
New type of anti-influenza agents based on benzo[d][1,3]dithiol core
Bioorganic & Medicinal Chemistry Letters, 2020, V. 30, N 24, Art. Num. 127653 doi:10.1016/j.bmcl.2020.127653, IF=2.572
G.T. Sukhanov, I.А. Krupnova, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, K.K. Bosov, E.V. Pivovarova
Synthesis and transformations of N-butyl-3(5)-nitro-1,2,4-triazoles under the conditions of acid-catalyzed alkylation of 3(5)-nitro-1H-1,2,4-triazoles with butyl alcohols
Chemistry of Heterocyclic Compounds, 2020, V 56, Pp 1440–1448 doi:10.1007/s10593-020-02835-w, IF=1.519
Yu.P. Ustimenko, E.S. Vasilyev, S.N. Bizyaev, T.V. Rybalova, A.V. Tkachev
Synthesis of chiral spirodiazafluorenes
Chemistry of Heterocyclic Compounds, 2020, V. 56, Pp 1429-1433 doi:10.1007/s10593-020-02833-y, IF=1.519
A.V. Artem’ev, M.P. Davydova, Xi. Hei, M.I. Rakhmanova, D.G. Samsonenko, I.Yu. Bagryanskaya, K.A. Brylev, V.P. Fedin, Jia-Shiang. Chen, M. Cotlet, Ji. Li
Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
Chemistry of Materials, 2020, 32, 24, 10708-10718 doi:10.1021/acs.chemmater.0c03984, IF=9.567
M.A. Gromova, Yu.V. Kharitonov, T.V. Rybalova, E.E. Shults
Synthetic studies on tricyclic diterpenoids: convenient synthesis of 16-arylisopimaranes
Monatshefte fur Chemie - Chemical Monthly, , 2020, V. 151, N 12, Pp. 1817 - 1827 doi:10.1007/s00706-020-02713-3, IF=1.348
Bioactive Components in Methyl tert-Butyl Ether Extract of Sea Buckthorn (Hippophae rhamnoides L.) Green Waste/ T. P. Kukina, D. N. Shcherbakov, K. V. Gensh, N. V. Panteleyeva, Ye. A. Tulysheva, O. I. Sal’nikova, A. Ye. Grazhdannikov, P. V. Kolosov, G. Yu. Galitsyn// Russian Journal of Bioorganic Chemistry, 2020, V. 46, N 7, Pp 1372-1377 doi:10.1134/S1068162020070067, IF=0.681
L.V. Politanskaya, P.A. Fedyushin, T.V. Rybalova, A.S. Bogomyakov, N.B. Asanbaeva, E.V. Tretyakov
Fluorinated Organic Paramagnetic Building Blocks for Cross-Coupling Reactions
Molecules 2020, 25(22), 5427 doi:10.3390/molecules25225427, IF=3.266
V.V. Krisyuk, S. Urkasymkyzy, T.V. Rybalova, I.V. Korolkov, S.V. Sysoev, T.P. Koretskaya, B.M. Kuchumov, A.E. Turgambaeva
Volatile trinuclear heterometallic beta-diketonates: structure and thermal properties related to the chemical vapor deposition of composite thin films
Polyhedron, V. 191, 15 November 2020, 114806 doi:10.1016/j.poly.2020.114806, IF=2.342
E.V. Tretyakov, S.I. Zhivetyeva, P.V. Petunin, D.E. Gorbunov, N.P. Gritsan, I.Yu. Bagryanskaya, A.S. Bogomyakov, P.S. Postnikov, M.S. Kazantsev, M.E. Trusova, I.K. Shundrina, E.V. Zaytseva, D.A. Parkhomenko, E.G. Bagryanskaya, V. Ovcharenko
Ferromagnetically Coupled S = 1 Chains in Crystals of Verdazyl‐Nitronyl Nitroxide Diradicals
Angewandte Chemie International Edition, 2020, V. 59, N 46, Pp 20704-20710 doi:10.1002/anie.202010041, IF=12.959
S. Cherkasov, D. Parkhomenko, A. Genaev, G. Salnikov, M. Edeleva, D. Morozov, T. Rybalova, I. Kirilyuk, S.R-A. Marque, E. Bagryanskaya
NMR and EPR Study of Homolysis of Diastereomeric Alkoxyamines
Molecules 2020, 25(21), 5080 doi:10.3390/molecules25215080, IF=3.266
Conjugates of Bispidine and Monoterpenoids as Ligands of Metal Complex Catalysts for the Henry Reaction/ E. S. Mozhaitsev, K. Y. Ponomarev, O. S. Patrusheva, A. V. Medvedko, A. I. Dalinger, A. D. Rogachev, N. I. Komarova, D. V. Korchagina, E. V. Suslov, K. P. Volcho, N. F. Salakhutdinov, S. Z. Vatsadze// Russian Journal of Organic Chemistry, 2020, V.56, N 11, Pp 1969-1981 doi:10.1134/S1070428020110123, IF=0.624
L. Politanskaya, I. Bagryanskaya, E. Tretyakov, Ch. Xic
Highly efficient synthesis of novel fluorinated 3-amino-2-mercaptobenzothiazole-2(3H)-thione derivatives
Journal of Fluorine Chemistry, 2020, V.239, 109628 doi:10.1016/j.jfluchem.2020.109628, IF=2.322
B.M. Urbagarova, E.E. Shults, V.V. Taraskin, L.D. Radnaeva, T.N. Petrova, T.V. Rybalova, T.S. Frolova, A.G. Pokrovskii, Ja. Ganbaatar
Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity
Journal of Ethnopharmacology, 2020, V. 261, 1125170 doi:10.1016/j.jep.2019.112517, IF=3.69
E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B
Synthesis, Molecular, and Crystal Structure of Tris(2-carbamoylmethoxyphenyl)phosphine Oxide/ T. V. Baulina, I. Yu. Kudryavtsev, A. V. Artem’ev, I. Yu. Bagryanskaya, M. P. Pasechnik, V. K. Brel// Russian Journal of General Chemistry, 2020, V. 90, N 10, Pp 1840-1844 doi:10.1134/S1070363220100059, IF=0.716
A. D. Kuimov,Ch.S.Becker,I.P.Koskin, D. E.Zhaguparov,A.A.Sonina,I.K.Shundrina,P.S.Sherin,M. S.Kazantsev
2-((9H-fluoren-9-ylidene)methyl)pyridine as a new functional block for aggregation induced emissive and stimuli-responsive materials
Dyes and Pigments, 2020, V. 181, 108595 doi:10.1016/j.dyepig.2020.108595, IF=4.613
M.P. Davydova, I.Yu. Bagryanskaya, I.A. Bauer, M.I. Rakhmanova, V.P. Morgalyuk, V.K. Brel, A.V. Artem'ev
Green- and red-phosphorescent Mn(II) iodide complexes derived from 1,3-bis(diphenylphosphinyl)propane
Polyhedron, 2020, V. 188, 114706 doi:10.1016/j.poly.2020.114706, IF=2.343
Yu.S. Demidova, E.S. Mozhaitsev, E.V. Suslov, A.A. Nefedov, A.A. Saraeva, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, I.L. Simakova, D.Yu. Murzin
Menthylamine synthesis via gold-catalyzed hydrogenation of menthone oxime
Applied Catalysis A: General, 2020, V. 605, 117799 doi:10.1016/j.apcata.2020.117799, IF=5.6
V. Romanov, E. Tretyakov, G. Selivanova, J. Li, I. Bagryanskaya, A. Makarov, D. Luneau
Synthesis and Structure of Fluorinated (Benzo[d]imidazol-2-yl)methanols: Bench Compounds for Diverse Applications
Crystals 2020, 10(9), 786 doi:10.3390/cryst10090786, IF=2.404
I.V. Oleynik, I.K. Shundrina, I.I. Oleyinik
Highly active titanium(IV ) dichloride FI catalysts bearing a diallylamino group for the synthesis of disentangled UHMWPE
Polymers for Advanced Technologies, 2020, V. 31, N 9, Pp 1921-1934 doi:10.1002/pat.4917, IF=2.578
M.Yu. Petyuk, A.S. Berezin, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
A dinuclear Re(I) tricarbonyl complex showing thermochromic luminescence
Inorganic Chemistry Communications, 2020, V.119, 108058 doi:10.1016/j.inoche.2020.108058, IF=1.943
E.A. Chulanova, E.A. Radiush, I.K. Shundrina, I.Yu. Bagryanskaya, N.A. Semenov, J. Beckmann, N.P. Gritsan, A.V. Zibarev
Lewis Ambiphilicity of 1,2,5-Chalcogenadiazoles for Crystal Engineering: Complexes with Crown Ethers
Crystal Growth & Design, 2020, V. 20, N 9, Pp 5868-5879 doi:10.1021/acs.cgd.0c00536, IF=4.089
S. M. Adekenov, A. S. Kishkentayeva, M. M. Zhakanov, I. Y. Bagryanskaya
3-Methoxy-4,5-Methylenedioxypropiophenone and Ferocinin from Ferula kelleri
Chemistry of Natural Compounds, 2020, V. 56, N 10, Pp 896-898 doi:10.1007/s10600-020-03178-w, IF=0.652
L. Gurskaya, T. Rybalova, I. Beregovaya, E. Zaytseva, M. Kazantsev, E. Tretyakov
Aromatic nucleophilic substitution: a case study of the interaction of a lithiated nitronyl nitroxide with polyfluorinated quinoline-N-oxides
Journal of Fluorine Chemistry, 2020, V. 237, 109613 doi:10.1016/j.jfluchem.2020.109613, IF=2.322
I. Zayakin, I. Bagryanskaya, D. Stass, M. Kazantsev, E. Tretyakov
Synthesis and Structure of (Nitronyl Nitroxide-2-ido)(tert-butyldiphenylphosphine)gold(I) and -(Di(tert-butyl)phenylphosphine)gold(I) Derivatives; Their Comparative Study in the Cross-Coupling Reaction
Crystals 2020, 10(9), 770 doi:10.3390/cryst10090770, IF=2.404
D.P. Lubov, O.Yu. Lyakin, D.G. Samsonenko, T.V. Rybalova, E.P. Talsi, K.P. Bryliakov
Palladium aminopyridine complexes catalyzed selective benzylic C–H oxidations with peracetic acid
Dalton Trans., 2020, V.49, N 32, Pp 11150-11156 doi:10.1039/D0DT02247K, IF=4.174
A.V. Shpatov, T.S. Frolova, S.A. Popov, O.I. Sinitsyna, O.I. Salnikova, G. Zheng, L. Yan, N.V. Sinelnikova, L.M. Pshennikova, A.V. Kochetov
Lipophilic Metabolites from Five-needle Pines, Pinus armandii and Pinus kwangtungensis, Exhibiting Antibacterial Activity.
Chemistry & Biodiversity, 2020, V.17, N 8, e2000201 doi:10.1002/cbdv.202000201, IF=2.039
Hybrid Photopolymer Material Based on (8-Acryloyl-1,4-dithia-8-azaspiro[4.5]decan-2-yl)methyl Acrylate and Thiol-Siloxane Component for Recording Microstructures: Synthesis and Optical and Thermomechanical Properties/ D. I. Derevyanko, V. S. Basistyi, V. V. Shelkovnikov, I. K. Shundrina, A. D. Bukhtoyarova, G. E. Sal’nikov, V. N. Berezhnaya & A. A. Chernonosov// Polymer Science, Series B, 2020, V.62, N 5, Pp 509-521 doi:10.1134/S1560090420050048, IF=0.976
Reactions of 1-nitro-3,3,3-tribromomethyland 1-nitro-1,3,3,3-tetrabromomethylpropenes with aliphatic dienes/ N. A. Anisimova, E. K. Slobodchikova, M. E. Ivanova, T. V. Rybalova// Russian Journal of General Chemistry, 2020, V. 90, N 8, Pp1388-1397 doi:10.1134/S1070363220080022, IF=0.716
2-diethylaminovinyl derivatives of halogenated 1,4-quinones: synthetic and structural aspects/ S. I. Zhivetyeva, I. A. Zayakin, I. Yu. Bagryanskaya & E. V. Tretyakov// Journal of Structural Chemistryб 2020, V. 61, N 8, Pp 1253-1259 doi:10.1134/S0022476620080107 , IF=0.745
T.A. Vaganova, Yu.V. Gatilov, D.P. Pishchur, E.V. Malykhin
Polyfluorinated hydroxy and carboxy benzenes as a new type of H-donors for self-assembly with 18-crown-6 ether: synthesis, supramolecular structure and stability of co-crystals
Journal of Fluorine Chemistry, 2020, V. 236, 109577 doi:10.1016/j.jfluchem.2020.109577, IF=2.332
I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
K.S. Marenin, A.M. Agafontsev, Yu.A. Bryleva, Yu.V. Gatilov, L.A. Glinskaya, D.A. Piryazev, A.V. Tkachev
Stereochemistry of the Kabachnik-Fields Condensation of Terpenic Amino Oximes with Aldehydes and Dimethyl Phosphite
ChemistrySelect, 2020, V.5 N 25, Pp 7596-7604 doi:10.1002/slct.202002369, IF=1.811
A.A. Kotlyarova, K.Yu. Ponomarev, E.A. Morozova, D.V. Korchagina, E.V. Suslov, A.V. Pavlova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
Effect of bispidine containing monoterpenoid moieties on physical performance in mice
2020 Cognitive Sciences, Genomics and Bioinformatics (CSGB), Novosibirsk, Russia, 2020, pp. 114-117 doi:10.1109/CSGB51356.2020.9214697
A.E. Paromov, S.V. Sysolyatin, I.А. Shchurova, A.I. Rogova, V.V. Malykhin, Yu.V. Gatilov
Synthesis of oxaazaisowurtzitanes by condensation of 4-dimethylaminobenzenesulfonamide with glyoxal
Tetrahedron, 2020, V. 76, N 27, 131298 doi:10.1016/j.tet.2020.131298, IF=2.233
I. Y. Zhuravleva, Yu.F. Polienko, E. V. Karpova, T. P. Timchenko, M. B. Vasilieva, L. A. Baratova, S. S. Shatskaya, E.V. Kuznetsova, N. R. Nichay, N.Beshchasna, A. V. Bogachev-Prokophiev
Treatment With Bisphosphonates To Mitigate Calcification Of Elastin-Containing Bioprosthetic Materials
Journal of Biomedical Materials Research Part A, 2020; V. 108, N 7, Pp 1579-1588 doi:10.1002/jbm.a.36927, IF=3.525
A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687
Synthesis of Urethane-Type Polymers with Polydimethylsiloxane Blocks for the Manufacture of Fibrous Matrices by Electrospinning/ I. K. Shundrina, I. V. Oleinik, V. I. Pastukhov, L. A. Shundrin, V. S. Chernonosova & P. P. Laktionov// Polymer Science, Series B, 2020, V. 62, N 4, Pp 385-393 doi:10.1134/S1560090420040090, IF=0.976
Effect of the Means Used to Synthesize Highly Fluorinated Polyimide on the Properties of an Adsorbent Prepared on Its Basis/ E. Yu. Yakovleva, E. E. Baranovskaya, I. K. Shundrina & E. Yu. Gerasimov// Russian Journal of Physical Chemistry A, 2020, V. 94, N 7, Pp 1476-1481 doi:10.1134/S0036024420070328, IF=0.719
A.Yu. Makarov, I.Yu. Bagryanskaya, V.V. Zhivonitko
Interaction of 1,3λ4δ2,2,4-benzodithiadiazines with neutral and charged S-electrophiles: SCl2, C6F5SCl, and NS2+
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp. 968-972 doi:10.1007/s10593-020-02760-y, IF=1.519
N.S. Li-Zhulanov, A.V. Pavlova, D.V. Korchagina, Yu.V. Gatilov, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
Synthesis of 1,3-Oxazine Derivatives Based on (-)-Isopulegol using the Ritter Reaction and Study of their Analgesic Activity
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp 936-941 doi:10.1007/s10593-020-02753-x, IF=1.519
A. M. Genaev, G. E. Salnikov, K.Yu. Koltunov
Influence of Positive Charge on the NMR Parameters of Mono- and Diprotonated Forms of 4-Dimethylaminopyridine
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp 892-897 doi:10.1007/s10593-020-02749-7, IF=1.519
I.V. Il'ina, O.S. Patrusheva, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
Synthesis of Fluorinated Octahydro-2H-Chromenes in the Presence of the BF3˙Et2O-H2O Catalytic System
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp 867-874 doi:10.1007/s10593-020-02743-z, IF=1.519
A new Сu(i) iodide complex showing deep-red luminescence/ A.V. Artemev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya// Journal of Structural Chemistry, 2020, V. 61, N 7, Pp 1068-1071Journal of Structural Chemistry, 2020, V. 61, N 7, Pp 1068-1071 doi:10.1134/S0022476620070082, IF=0.745
A.V. Artem'ev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya
A NEW Cu(I) IODIDE COMPLEX SHOWING DEEP-RED LUMINESCENCE
Journal of Structural Chemistry, 2020, V. 61, N 7, pages1068-1071 doi:10.1134/S0022476620070082, IF=0.745
Synthesis of polyfluorinated tetraoxacalix[4]arenes by the interaction of pentafluoronitrobenzene with resorcinol, orcinol, and tetrafluororesorcinol/ Kovtonyuk V. N., Han H., Gatilov Yu. V.// Russian Journal of Organic Chemistry, 2020 doi:10.31857/S0514749220070058, IF=0.751
P. Fedyushin, T. Rybalova, N. Asanbaeva, E. Bagryanskaya, A. Dmitriev, N. Gritsan, M. Kazantsev, E. Tretyakov
Synthesis of Nitroxide Diradical Using a New Approach
Molecules 2020, 25(11), 2701 doi:10.3390/molecules25112701, IF=3.267
A.V. Artem'ev, A.S. Berezin, I.V. Taidakov, I.Yu. Bagryanskaya
Synthesis of dual emitting iodocuprates: can solvents switch the reaction outcome?
Inorg. Chem. Front., 2020, V. 7, N 11, Pp 2195-2203 doi:10.1039/D0QI00346H, IF=5.958
An unusual fabric from Jety-Asar-2, Eastern Aral sea region, in the context of the central asian textile tradition/ POLOSMAK N.V., KARPOVA E.V., AMOSOV E.V.// doi:10.17746/1563-0102.2020.48.3.050-058
A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties/ Davydova M.P., Rakhmanova M.I., Bagryanskaya I.Yu., Brylev K.A., Artem'ev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 6, Pp 894-898 doi:10.1134/S0022476620060086, IF=0.745
M.I. Rogovoy, M.P. Davydova, I.Yu. Bagryanskaya, A.V. Artem'ev
Efficient one-pot synthesis of diphenyl(pyrazin-2-yl)phosphine and its AgI, AuI, and PtII, complexes
Mendeleev Communications, 2020, V. 30, N 3, Pp 305-307 doi:10.1016/j.mencom.2020.05.014, IF=1.694
A.V. Markov, A.V. Sen’kova, O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova
Trioxolone Methyl, a Novel Cyano Enone-Bearing 18βH-Glycyrrhetinic Acid Derivative, Ameliorates Dextran Sulphate Sodium-Induced Colitis in Mice
Molecules 2020, 25(10), 2406 doi:10.3390/molecules25102406, IF=3.267
M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529
S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426
D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889
V.A. Logvinenko, V.P. Fadeeva, B.A. Selivanov, V.D. Tikhova, A.A. Nefedov, A.Ya. Tikhonov
Thermal decomposition of several N,N'-bis(2-hydroxyiminoalkyl)-α,α'-dinitrones
Journal of Thermal Analysis and Calorimetry, 2020, V. 140, N 2, Pp 685-693 doi:10.1007/s10973-019-08868-4, IF=2.731
I. Il'ina, E. Morozova, A. Pavlova, D. Korchagina, T. Tolstikova, K. Volcho, N. Salakhutdinov
Synthesis and analgesic activity of aliphatic ketones-derived chiral hexahydro-2H-chromenes
Medicinal Chemistry Research, 2020, V. 29, N 4, pp 738-747 doi:10.1007/s00044-020-02518-3, IF=1.783
D.S. Odintsov, I.K. Shundrina, I.A. Os'kina, I.V. Oleynik, J. Beckmann, L.A. Shundrin
Ambipolar polyimides with pendant groups based on 9H-thioxanthene-9-one derivatives: synthesis, thermostability, electrochemical and electrochromic properties
Polymer Chemistry, 2020, V. 11, N 12, Pp 2243-2251 doi:10.1039/C9PY01930H, IF=5.342
E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
A.A. Sinitsyna, S.G. Il’yasov, M.V. ChikinaIlia, I.V. Eltsov, A.A. Nefedov
A search for synthetic routes to tetrabenzylglycoluril
Chemical Papers, 2020, V. 74, N 3, pp 1019-1025 doi:10.1007/s11696-019-00941-4, IF=1.68
Synthesis and analgesic activity of 1,3,5-trisubstituted pyrazoles containing a diterpenoid moiety/ M.E. Mironov, A.I. Poltanovich , T.V., Rybalova, M.P. Dolgikh, T.G. Tolstikova, E.E Shults// Russian Chemical Bulletin, 2020, V. 69, Pp 537–546 doi:10.1007/s11172-020-2795-6, IF=1.061
M. Davydova, I. Bauer, V. Brel, M. Rakhmanova, I. Bagryanskaya, A.V. Artem'ev
Manganese(II) thiocyanate complexes with bis(phosphine oxide) ligands: synthesis and excitation wavelength-dependent multicolor luminescence
European Journal of Inorganic Chemistry, 2020, V. 2020, N 8, Pp 695-703 doi:10.1002/ejic.201901213, IF=2.529
I.F. Zhurko, S. Dobrynin, A.A. Gorodetskii, Yu.I. Glazachev, T.V. Rybalova, E.I. Chernyak, N. Asanbaeva, E.G. Bagryanskaya, I.A. Kirilyuk
2-Butyl-2-tert-butyl-5,5-diethylpyrrolidine-1-oxyls: Synthesis and Properties
Molecules 2020, 25(4), 845 doi:10.3390/molecules25040845, IF=3.267
A.A. Kotlyarova, K.Yu. Ponomarev, E.A. Morozova, D.V. Korchagina, E.V. Suslov, A.V. Pavlova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
The effect of 3,7-diazabicyclo[3.3.1]nonanes containing monoterpenoid moieties on the physical activity of mice
Journal of research in pharmacy, 2020, V. 24, N 2, Pp 196-204 doi:10.35333/jrp.2020.136
V.V. Chernyshov, O.I. Yarovaya, D.S. Fadeev, Yu.V. Gatilov, Ya.L. Esaulkova, A.S. Muryleva, K.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov
Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
Molecular Diversity, 2020, V. 24, N 1, Pp 61-67 doi:10.1007/s11030-019-09932-9, IF=2.013
E.B. Nikolaenkova, I.Yu. Bagryanskaya, A.Ya. Tikhonov
Synthesis of 2-[2-(hydroxyimino)alkyl]-1,2-oxazol-5(2Н)-ones
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 2, Pp 208-212 doi:10.1007/s10593-020-02645-0, IF=1.519
Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1, IF=1.061
T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753
QUALITY AND QUANTITATIVE COMPOSITION OF SUNFLOWER OIL DEODORIZATION DISTILLATE/ Kukina T.P., Shcherbakov D.N., Panteleyeva N. V., Sal'nikova O. I., Kolosov P.V.// doi:10.14258/jcprm.2020015909
I. Il'ina, E. Morozova, D. Korсhagina, K. Volcho, T. Tolstikova, N. Salakhutdinov
Synthesis and Analgesic Activity of Monoterpenoid Aldehyde-derived Hydro-2H-chromeneols
Letters in Drug Design & Discovery, 2020, V. 17, N 1, Pp 68-78 doi:10.2174/1570180816666181114131220, IF=1.169

2019

M.S. Kazantsev, A.A. Sonina, I.P. Koskin, P.S. Sherin, T.V. Rybalova, E. Benassi, E.A. Mostovich
Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals
Mater. Chem. Front., 2019, V. 3, N 8, Pp 1545-1554 doi:10.1039/C9QM00198K
E. Tretyakov, P. Fedyushin, E. Panteleeva, L. Gurskaya, T. Rybalova, A. Bogomyakov, E. Zaytseva, M. Kazantsev, I. Shundrina, V. Ovcharenko
Aromatic S_N^F-Approach to Fluorinated Phenyl tert-Butyl Nitroxides
Molecules 2019, 24(24), 4493 doi:10.3390/molecules24244493, IF=3.59
A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049
G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491
Thermal Reactions of 6-Bromo-, 6-Chloro-, and 6-(Methylsulfanyl)octaﬂuoroindane-5-thioles with Tetraﬂuorethylene. Synthesis of Dodecaﬂuoro-2H,3H,5H,6H,7H-indeno[5,6-b]thiophene/ P.V. Nikul'shin, A.M. Maksimov, Yu. V. Gatilov, V.E. Platonov// Russian Journal of General Chemistry, 2019, V. 89, N: 12, Pp 2378-2385 doi: 10.1134/S0044460X19120096 doi:10.1134/S1070363219120090, IF=0.643
V.V. Chernyshov, Y.V. Gatilov, O.I. Yarovaya, I.P. Koskin, S.S. Yarovoy, K.A. Brylev, N.F. Salakhutdinov
The first example of the stereoselective synthesis and crystal structure of a spirobicycloquinazolinone based on (–)-fenchone and anthranilamide
Acta Crystallographica Section C, V. C75, Part 12, Pp 1675-1680 doi:10.1107/S2053229619015766, IF=0.93
G.I. Borodkin, I.R. Elanov, Yu.V. Gatilov, V.G. Shubin
Direct electrophilic fluorination of naproxen with NF-reagents
Journal of Fluorine Chemistry, 2019, V. 228, 109412 doi:10.1016/j.jfluchem.2019.109412, IF=2.055
I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25
S.A. Dobrynin, I.A. Kirilyuk, Yu.V. Gatilov, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, M.K. Bowman, E.G. Bagryanskaya
Unexpected one-pot formation of the 1H-6a,8a-epiminotri-cyclopenta[a,c,e][8]annulene system from cyclopentanone, ammonia and dimethyl fumarate. Synthesis of highly strained polycyclic nitroxide and EPR study
Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2664-2670 doi:10.3762/bjoc.15.259, IF=2.595
E.P. Talsi, A.A. Bryliakova, R.V. Ottenbacher, T.V. Rybalova, K.P. Bryliakov
Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
Research, 2019, V.2019. Article ID: 4756025 doi:10.34133/2019/4756025
M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
A.L. Shatsauskas, E.R. Saibulina, Yu.V. Gatilov, A.S. Kostyuchenko, A.S. Fisyuk
Synthesis of benzo[c][1,7]naphthyridine derivatives
Chemistry of Heterocyclic Compounds, 2019, V. 55, N 11, pp 1080-1086 doi:10.1007/s10593-019-02581-8, IF=1.492
Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104, IF=0.794
Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125, IF=0.751
A.V. Lipeeva, D.O. Zakharov, Yu.V. Gatilov, M.A. Pokrovskii, A.G. Pokrovskii, E.E. Shults
Design and Synthesis of 3-(N-Substituted)aminocoumarins as Anticancer Agents from 3-Bromopeuruthenicin
ChemistrySelect, 2019, V. 4, N 34, Pp 10197-10201 doi:10.1002/slct.201901377, IF=1.716
O.V. Ardashov, A.V. Pavlova, A.K. Mahato, Yu. Sidorova, E.A. Morozova, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, O.S. Patrusheva, N. Li-Zhulanov, T.G. Tolstikova, K.P. Volcho, N. Salakhutdinov
A novel small molecule supports the survival of cultured dopamine neurons and may restore the dopaminergic innervation of the brain in the MPTP mouse model of Parkinson's disease
ACS Chemical Neuroscience, 2019, V. 10, N 10, Pp 4337-4349 doi:10.1021/acschemneuro.9b00396, IF=3.861
A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934
N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69
V.A. Savel'ev, A.A. Kotova, T.V. Rybalova, E.E. Shults
Regioselective Synthesis of 1,3,5-Trisubstituted Pyrazoles Containing an Anthranilic Acid Motif
Chemistry of Heterocyclic Compounds, 2019, V. 55, N 10, pp 943-955 doi:10.1007/s10593-019-02561-y, IF=1.492
Е.В. Карпова, И.К. Шундрина, Е. Орлова, А. Коновалов
Ароматические и минеральные вещества в тканях образцов яровой мягкой пшеницы Triticum aestivum L., различающихся по устойчивости к бурой ржавчине (возбудитель Puccinia triticina Erikss.)
Химия растительного сырья, 2019, 4, стр. 87-95 doi:10.14258/jcprm.2019045238
Study of Plant Coumarins: XVII. Synthesis and Transformations of 6-Carboxamidocoumarins/ E.E.Shults, D.O. Zakharov, A.V. Lipeeva, Yu.V. Gatilov, A.G. Makarov// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1518-1526 doi:10.1134/S1070428019100099, IF=0.751
A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
T.A. Vaganova, Yu.V. Gatilov, E. Benassi, I.P. Chuikov, D.P. Pishchur, E.V. Malykhin
Impact of molecular packing rearrangement on solid-state fluorescence: polyhalogenated N-hetarylamines vs. their co-crystals with 18-crown-6
CrystEngComm, 2019, V. 21, N 39, Pp 5931-5946 doi:10.1039/C9CE00645A, IF=3.381
E. S. Vasilyev, S. N. Bizyaev, V.Yu. Komarov, Yu.V. Gatilov, A. V. Tkachev
Chiral C₂-Symmetric Diimines with 4,5-Diazafluorene Units
Molecules 2019, 24(17), 3186 doi:10.3390/molecules24173186, IF=3.59
P.V. Petunin, D.E. Votkina, M.E. Trusova, T.V. Rybalova, E.V. Amosov, M.N. Uvarov, P.S. Postnikov, M.S. Kazantsev, E.A. Mostovich
Oxidative addition of verdazyl halogenides to Pd(PPh3)4
New J. Chem., 2019, V.43, N 38, Pp15293-15301 doi:10.1039/C9NJ03361K, IF=3.69
A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795
M.A. Gromova, Yu.V. Kharitonov, T.V. Rybalova, E.E. Shul'ts
Synthetic Transformations of Higher Terpenoids. 38.* Synthesis of Conjugates Containing β-Carboline and Tricyclic Diterpenoids
Chemistry of Natural Compounds, 2019, V. 55, N 5, pp 871-877 doi:10.1007/s10600-019-02836-y, IF=0.566
Aliphatic and triterpenoic products of ether extracts saponification of POPULUS NIGRA L/ T. P. Kukina, I. A. Elshin , O. I. Salnikova , I. V. Eltsov// doi:10.14258/jcprm.2019034951
G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049
A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429
A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine/ A. V. Artem'ev, A. S. Beresin, I. Yu. Bagryanskaya// Journal of Structural Chemistry, 2019, V. 60, N 6, pp 967-971 doi:10.1134/S0022476619060118, IF=0.541
V.N. Kovtonyuk, Yu.V. Gatilov, G.E. Salnikov, E.V. Amosov
Polyfluorinated tetraoxacalixarenes and bicyclooxacalixarenes. Interaction of pentafluorobenzonitrile with resorcinol, orcinol and tetrafluororesorcinol
Journal of Fluorine Chemistry, 2019, V. 222-223, Pp 59-67 doi:10.1016/j.jfluchem.2019.04.011, IF=2.055
A.M. Genaev, L.N. Shchegoleva, G.E. Salnikov, A.V. Shernyukov, L.A. Shundrin, I.K. Shundrina, Z. Zhu, K.Yu. Koltunov
Acid-Catalyzed vs. Thermally Induced C1-C1' Bond Cleavage in 1,1'-Bi-2-naphthol. An Experimental and Theoretical Study
J. Org. Chem., 2019, V. 84, N 11, Pp 7238-7243 doi:10.1021/acs.joc.9b00915, IF=4.745
T.M. Khomenko, D.V. Korchagina, D.S. Baev, P.M. Vassiliev, K.P. Volcho, N.F. Salakhutdinov
Antimicrobial Activity of Substituted Benzopentathiepin-6-amines
Journal of Antibiotics, 2019, V. 72, pp 590-599 doi:10.1038/s41429-019-0191-y, IF=2.446
E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
Z. Zhu, A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
Mechanistic investigation of superelectrophilic activation of 1,1'-bi-2-naphthols in the presence of aluminum halides
Org. Biomol. Chem., 2019, V. 17, N 16, Pp 3971-3977 doi:10.1039/C9OB00640K, IF=3.49
Synthesis and analgesic activity of octahydro-2H-chromenols, derivatives of aliphatic ketones/ I. V. Il'ina, D. V. Korchagina, E. A. Morozova, T. G. Tolstikova, K. P. Volcho, N. F. Salakhutdinov// Russian Chemical Bulletin, 2019, V. 68, N 5, pp 1061-1066 doi:10.1007/s11172-019-2520-5, IF=1.014
Synthesis, hypolipidemic and antifungal activity of tetrahydroberberrubine sulfonates/ I. V. Nechepurenko, E. D. Shirokova, M. V. Khvostov, T. S. Frolova, O. I. Sinitsyna, A. M. Maksimov, R. A. Bredikhin, N. I. Komarova, D. S. Fadeev, O. A. Luzina, T. G. Tolstikova, N. F. Salakhutdinova// Russian Chemical Bulletin, 2019, V. 68, N 5, pp 1052-1060 doi:10.1007/s11172-019-2519-y, IF=1.014
Effect of Aliphatic Diols and Dicarboxylic Acids on the Properties of Ethylene Succinate Copolyesters/ A. G. Potapov, I. K. Shundrina// Polymer Science, Series A, 2019, V. 61, N 5, pp 544-554 doi:10.1134/S0965545X19050146, IF=0.984
On the Reaction of 2-Benzylamino-1,4-naphthoquinones with Nitrosylsulfuric Acid/ L. M. Gornostaev, E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, O. I. Fominykh, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2019, V. 55, N 5, pp 608–614 doi:10.1134/S1070428019050051, IF=0.751
V.Yu. Shuvalov, A.S. Rupp, A.K. Kuratova, A.S. Fisyuk, A.A. Nefedov, G.P. Sagitullina
Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
SYNLETT, 2019, V. 30, N 8, Pp 919-923 doi:10.1055/s-0037-1612416, IF=2.418
E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953
V.V. Shelkovnikov, I.Yu. Kargapolova, S.V. Korotaev, N.A. Orlova, T.V. Rybalova, I.P. Chuikov
Three-color luminescent transformation of the julolidine pyrylo/pyridocyanine dyes in the adsorbed state
Journal of Photochemistry and Photobiology A: Chemistry, 2019, V. 375 , Pp 181-190 doi:10.1016/j.jphotochem.2019.02.022, IF=3.261
E.S. Mozhaitsev, A.L. Zakharenko, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, I.A. Vasil’eva, A.A. Chepanova, E. Black, J. Patel, R. Chand, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
Anti-Cancer Agents in Medicinal Chemistry, 2019, V. 19 , N 4 , Pp 463-472 doi:10.2174/1871520619666181207094243, IF=2.18
V. Romanov, I. Bagryanskaya, N. Gritsan, D. Gorbunov, Yu. Vlasenko, M. Yusubov, E. Zaytseva, D. Luneau, E. Tretyakov
Assembly of Imidazolyl-Substituted Nitronyl Nitroxides into Ferromagnetically Coupled Chains
Crystals 2019, 9(4), 219 doi:10.3390/cryst9040219, IF=2.061
N.S. Li-Zhulanov, I.V. Il’ina, A. Chicca, P. Schenker, O.S. Patrusheva, E.V. Nazimova, D.V. Korchagina, M. Krasavin, K.P. Volcho, N.F. Salakhutdinov
Effect of chiral polyhydrochromenes on cannabinoid system
Medicinal Chemistry Research, 2019, V. 28, N 4, pp 450-464 doi:10.1007/s00044-019-02294-9, IF=1.72
Exploration of SNF-Approach toward Functionalized Nitronyl Nitroxides/ P. Fedyushin, L. Gurskaya, E. Panteleeva, B. Koshcheev, A. Maksimov, T.V. Rybalova, E. Zaytseva, E. Tretyakov// doi:10.17677/fn20714807.2019.02.04
A.V. Shernyukov, A.M. Genaev, G.E. Salnikov, V.G. Shubin, H.S. Rzepa
Elevated reaction order of 1,3,5-tri-tert-butylbenzene bromination as evidence of a clustered polybromide transition state: a combined kinetic and computational study
Org. Biomol. Chem., 2019, V. 17, N 15, pp 3781-3789 doi:10.1039/C9OB00607A, IF=3.49
Zh. Zhu, G.E. Salnikov, K.Yu. Koltunov
Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides
Tetrahedron Letters, 2019, V. 60, N 12, Pp 857-859 doi:10.1016/j.tetlet.2019.02.026, IF=2.259
A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, O.A. Tarasova, I.Yu. Bagryanskaya, N.A. Nedolya
Chemoselective mechanochemical route toward a bright TADF-emitting CuI-based coordination polymer
Inorg. Chem. Front., 2019, V. 6, N 3, Pp 671-679 doi:10.1039/C8QI01302K, IF=5.934
Synthesis of diazaadamantanes from 1,5-dimethylbispidinone and some natural ketones/ Suslov E.V.1, Ponomarev K. Yu.1, Korchagina D.V.1, Volcho K.P.1,2, Salakhutdinov N.F.// Russian Chemical Bulletin, 2019, V. 68, N 3, pp 601-605 doi:10.1007/s11172-019-2461-z, IF=1.014
D.O. Prima, A.G. Makarov, I.Yu. Bagryanskaya, A.E. Kolesnikov, L.V. Zargarova, D.S. Baev, T.F. Eliseeva, L.V. Politanskaya, A.Yu. Makarov, Yu.G. Slizhov, A. V. Zibarev
Fluorine-Containing n-6 and Angulaand Linear n-6-n' (n, n' = 5, 6, 7) Diaza-Heterocyclic Scaffolds Assembled on Benzene Core in Unified Way
ChemistrySelect, 2019, V. 4, N 8, Pp 2383-2386 doi:10.1002/slct.201803970, IF=1.716
A.V. Artem.ev, E.A. Pritchina, M.I. Rakhmanova, N.P. Gritsan, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
Dalton Trans., 2019, V. 48, N 7, Pp 2328-2337 doi:10.1039/C8DT04328K, IF=4.052
V.Yu. Shuvalovv, A.S. Rupp, A.S. Fisyuk, A.K. Kuratova, A.A. Nefedov, G.P. Sagitullina
Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
ChemistrySelect, 2019, V. 4, N 5, Pp 1696-1699 doi:10.1002/slct.201803515, IF=1.716
A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
Fabrication of High-Aspect-Ratio Microstructures on Tetraacrylate/Acrylamide Monomers Using Synchrotron Radiation/ D. I. Derevyanko, N. A. Orlova, V. V. Shelkovnikov, I. K. Shundrina, B. G. Goldenberg, V. P. Korolkov// High Energy Chemistry, 2019, V. 53, N 2, pp 136-142 doi:10.1134/S0018143919020048, IF=0.634
S.M. Adekenov, P.Zh. Zhanimkhanova, Zh.S. Nurmaganbetov, A. Amanzhan, S.V. Chernov, A.Zh. Turmukhambetov, I.Yu. Bagryanskaya, Yu.V. Gatilov, E.E. Shults
Synthetic modifications of carboline alkaloid harmine: synthesis of 8-substituted derivatives
Chemistry of Heterocyclic Compounds, 2019, V. 55, N 2, pp 135-141 doi:10.1007/s10593-019-02429-1, IF=1.492
Generation of Perfluoroand 1-Chloroperfluoroindanyl and -Benzocyclobutenyl Cations with Perfluoroalkyl Groups in the Aliphatic Ring/ T.V. Mezhenkova, V.M. Karpov, Ya.V. Zonov , I.P. Chuikov// Russian Journal of Organic Chemistry, 2019, V. 55, N 2, pp 193–201 doi:10.1134/S1070428019020118, IF=0.751
R.Yu. Peshkov, Ch. Wang, E.V. Panteleeva, T.V. Rybalova, E.V. Tretyakov
Radical Anions of Aromatic Carbonitriles as Reagents for Arylation of Fluorinated Benzonitriles
J. Org. Chem., 2019, 84 (2), pp 963-972 doi:10.1021/acs.joc.8b02904, IF=4.745
N. Pushkarevsky, E. Chulanova, L. Shundrin, A. Smolentsev, G. Salnikov, E. Pritchina, A. Genaev, I. Irtegova, I. Bagryanskaya, S. Konchenko, N. Gritsan, J. Beckmann, A. Zibarev
Radical Anions, Radical-Anion Salts and Anionic Complexes of 2,1,3-Benzochalcogenadiazoles (S, Se, Te)
Chemistry - A European Journal, Chemistry - A European Journal, 2019, V. 25, N 3, Pp 806-816 doi:10.1002/chem.201803465, IF=5.16
O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, R.K. Glaznev, I.E. Gerasimov, Y.K. Naganovsky, I.K. Shundrina, A.Yu. Snegirev, R. Vinu
Kinetics of Thermal Decomposition of PMMA at Different Heating Rates and in a Wide Temperature Range
Thermochimica Acta, 2019, V. 671, Pp 17-25 doi:Thermochimica Acta, Available online 30 , IF=2.251
The Xiongnu Gold from Noin-Ula (Mongolia)/ N.V. Polosmak, S.S. Shatskaya, M.V. Zadorozhnyy, L.P. Kundo, E.V. Karpova// Archaeology, Ethnology and Anthropology of Eurasia, 2019, V. 47, N 1, Pp 83-94 doi:10.17746/1563-0110.2019.47.1.083-094
A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
M.A. Gromova, Yu.V. Kharitonov, M.A. Pokrovskii, I.Yu. Bagryanskaya, A.G. Pokrovskii, E.E. Shul'ts
Synthetic Transformations of Higher Terpenoids. 37. Synthesis and Cytotoxicity of 4-(Oxazol-2-Yl)-18-Norisopimaranes
Chemistry of Natural Compounds, 2019, V. 55, N 1, pp 52-59 doi:10.1007/s10600-019-02613-x, IF=0.567
Antimony Complexes {[2,6-(OME)2C6H3]3SBCH2C(O)OET}2[HG2I6]2- and {[2,6-(OME)2C6H3]3SBME}2+[HgI4]2- ˙ DMSO : Synthesis and Structure/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, I. Yu. Bagryanskaya, N. V. Pervukhina, I. V. El'tsov, N. V. Kurat'eva// Russian Journal of Inorganic Chemistry, 2019, V. 64, N 1, pp 28-35 doi:10.1134/S0036023619010078, IF=0.822
Reactions of 1,4-naphthoquinone and 5-hydroxy-1,4-naphthoquinone with ninhydrin/ L.M. Gornostaev, O.I. Fominyh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A. Stashina// Russian Chemical Bulletin, V. 68, N 1, pp 86-91 doi:10.1007/s11172-019-2420-8, IF=1.014
P. Fedyushin, E. Panteleeva, I. Bagryanskaya, K. Maryunina, K. Inoue, D. Stass, E. Tretyakov
An approach to fluorinated phthalonitriles containing a nitronyl nitroxide or iminonitroxide moiety
Journal of Fluorine Chemistry, 2019, V. 217, Pp 1-7 doi:10.1016/j.jfluchem.2018.10.016, IF=2.055

2018

A.V. Artem'ev, I.Yu. Bagryanskaya
[Cu4I73-]n: A novel 1-D iodocuprate aggregate
Journal of Molecular Structure, 2018, V. 1173, Pp. 743-749 doi:10.1016/j.molstruc.2018.07.006, IF=2.011
M.A. Gromova, Yu.V. Kharitonov, I.Yu. Bagryanskaya, E.E. Shults
Efficient Synthesis of the N-(buta-2,3-dienyl)carboxamide of Isopimaric Acid and the Potential of This Compound towards Heterocyclic Derivatives of Diterpenoids
ChemistryOpen, 2018, V. 7, N 11, Pp 890-901 doi:10.1002/open.201800205, IF=2.801
K.S. Kovaleva, F.I. Zubkov, N.I. Bormotov, R.A. Novikov, P.V. Dorovatovskii, V.N. Khrustalev, Yu.V. Gatilov, V.V. Zarubaev, O.I. Yarovaya, L.N. Shishkina, N.F. Salakhutdinov
Synthesis of D-(+)-camphor-based N-acylhydrazones and their antiviral activity
Med. Chem. Commun., 2018, V. 9, N 12, Pp 2072-2082 doi:10.1039/C8MD00442K, IF=2.342
Z. Zhu, A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
Superelectrophilic activation of 1-nitronaphthalene in the presence of aluminum chloride. Reactions with benzene and cyclohexane
Org. Biomol. Chem., 2018, V.16, N 47, Pp 9129-9132 doi:10.1039/C8OB02653J, IF=3.423
Thermal Reactions of Polyfluoro-ortho-chloroarenethiols with Tetrafluoroethylene/ P. V. Nikul'shin, A. M. Maksimov, Yu. V. Gatilov, V. E. Platonov// Russian Journal of General Chemistry, 2018, V. 88, N 12, pp 2486-2497 doi:10.1134/S107036321812006X, IF=0.658
A. Ogienko, S. Myz, A. Ogienko, A. Nefedov, A.S. Stoporev, M.S. Mel'gunov, A.S. Yunoshev, T. Shakhtshneider, V.V. Boldyrev, E. Boldyreva
Cryosynthesis of co-crystals of poorly water-soluble pharmaceutical compounds and their solid dispersions with polymers. “Meloxicam - succinic acid” system as a case study
Cryst. Growth Des. 2018, 18, 12, 7401-7409 doi:10.1021/acs.cgd.8b01070, IF=3.971
A.D. Rogachev, O.I. Yarovaya, A.V. Fatianova, V.A. Lavrinenko, E.V. Amosov, V.V. Zarubaev, A.G. Pokrovsky, N.F. Salakhutdinov
Untargeted search and identification of metabolites of antiviral agent camphecene in rat urine by liquid chromatography and mass spectrometry and studying their distribution in organs following peroral administration of the compound
Journal of Pharmaceutical and Biomedical Analysis, 2018, V. 161, Pp 383-392 doi:10.1016/j.jpba.2018.09.003, IF=2.831
R. Ottenbacher, E. Talsi, T. Rybalova, K.P. Bryliakov
Enantioselective Benzylic Hydroxylation of Arylalkanes with H2O2 in Fluorinated Alcohols in the Presence of Chiral Mn Aminopyridine Complexes
ChemCatChem, 2018, V.10, N 22, Pp 5323-5330 doi:10.1002/cctc.201801476, IF=4.673
G.A. Selivanova, A.D. Skolyapova, R.I. Dralyuk, E.V. Karpova, I.K. Shundrina, I.Yu. Bagryanskaya, E.V. Amosov, T.V. Basova, E.V. Tretyakov
Solid-phase transitions of polymorphs of 4-(4-N,N-dialkylaminophenyl)azobiphenyl-2,3'4'-tricarbonitriles and their analogues
Thermochimica Acta, 2018, V. 669, Pp 88-98 doi:10.1016/j.tca.2018.08.022, IF=2.188
Yu.A. Ten, O.G. Salnikov, S.A. Amitina, D.V. Stass, T.V. Rybalova, M.S. Kazantsev, A.S. Bogomyakov, E.A. Mostovich, D.G. Mazhukin
The Suzuki–Miyaura reaction as a tool for modification of phenoxyl-nitroxyl radicals of the 4H-imidazole N-oxide series
RSC Adv., 2018, V. 8, N 46, Pp 26099-26107 doi:10.1039/C8RA05103H, IF=2.936
Nitrimines: VII. Reaction of S,S′-Dimethyl-N-nitroimidodithiocarbonate with Alkali. Synthesis of S-Methyl-N-nitrothiocarbamate and Its Salts/ A. M. Astakhov, D. V. Antishin, А. А. Nefedov, G. E. Salnikov, E. S. Buka// Russian Journal of Organic Chemistry, 2018, V. 54, N 11, pp 1638-1642 doi:10.1134/S1070428018110039, IF=0.654
A.I. Taratayko, T.V. Rybalova, V.A. Reznikov
Synthesis of paramagnetic spiropyran derivatives
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A. A. Sonina, I.P. Koskin, P.S. Sherin, T. V. Rybalova, I. K. Shundrina, E. A. Mostovich, M. S. Kazantsev
Crystal packing control of a trifluoromethyl-substituted furan/phenylene co-oligomer
Acta Crystallographica Section B, 2018, V. 74, N 5, Pp 450-457 doi:10.1107/S2052520618011782, IF=6.467
Molecular and Supramolecular Structure of 8-(Trifluoromethyl)Benzo[f][1,2,3,4,5] Pentathiepin-6-Amine - A Representative of Condensed Arene Pentathiepines/ T. V. Rybalova, A. D. Rogachev, T. M. Khomenko, K. P. Volcho, N. F. Salakhutdinov// Journal of Structural Chemistry, 2018, V. 59, N 7, pp 1753-1758 doi:10.1134/S0022476618070326, IF=0.521
А.П. Крысин, А.А. Нефедов, Т.Я. Гаврикова, А.С. Кильметьев
О реакции полисульфидов 2-трет-бутилфенола с каучуком и гептеном-1 в инертной атмосфере и на воздухе
Химия в интересах устойчивого развития. 2018. Т. 26. № 4. С. 403-410. doi:10.15372/KhUR20180407
S.A. Dobrynin, Yu.I. Glazachev, Yu.V. Gatilov, E.I. Chernyak, G.E. Salnikov, I.A. Kirilyuk
Synthesis of 3,4-Bis-(hydroxymethyl)-2,2,5,5-tetraethylpyrrolidin-1-oxyl via 1,3-Dipolar Cycloaddition of Azomethine Ylide to Activated Alkene
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P.V. Petunin, E.A. Martynko, M.E. Trusova, M.S. Kazantsev, T.V. Rybalova, R.R. Valiev, M.N. Uvarov, P.S. Postnikov, E. Mostovich
Verdazyl radical building blocks: synthesis, structure and Sonogashira cross-coupling reactions
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N.A. Semenov, D.E. Gorbunov, M.V. Shakhova, G.E. Salnikov, I.Yu. Bagryanskaya, V.V. Korolev, J. Beckmann, N.P. Gritsan, A.V. Zibarev
Donor-Acceptor Complexes between 1,2,5-Chalcogenadiazoles (Te, Se, S) and the Pseudo Halides CN- and XCN- (X = O, S, Se, Te)
Chemistry - A European Journal, 2018, V.24, N 49, Pp 12983-12991 doi:10.1002/chem.201802257, IF=5.16
И.Ю. Журавлева, Е.В. Карпова, Л.А. Опарина, Н. Кабос, А.Л. Ксенофонтов, А.С. Журавлева, Н.Р. Ничай, А.В. Богачев-Прокофьев, Б.А. Трофимов, А.М. Караськов
Ксеноперикард, консервированный дии пентаэпоксидами: молекулярные механизмы сшивки и механические свойства биоматериала
Патология кровообращения и кардиохирургия. 2018. Т. 22. № 3. С. 56-68. doi:10.21688-1681-3472-2018-3-56-68
V.E. Romanov, I.Yu. Bagryanskaya, D.E. Gorbunov, N.P. Gritsan, E.V. Zaytseva, D. Luneau, E.V. Tretyakov
A Crystallographic Study of a Novel Tetrazolyl-Substituted Nitronyl Nitroxide Radical
Crystals 2018, 8(9), 334 doi:10.3390/cryst8090334, IF=2.144
I.V. Kulakov, I.V. Palamarchuk, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
Synthesis, structure and biological activity 3- (arylmethyl) aminopyridine-2 (1H) -ones and 1H-pyrido[2,3-b][1,4]oxazin-2(3H)-ones
Journal of Molecular Structure, V.1166, 15 August 2018, Pp. 262-269 doi:10.1016/j.molstruc.2018.04.036, IF=2.011
A.I. Titkov, I.K. Shundrina, R.M. Gadirov, A.V. Odod, A.E. Kurtsevich, Yu.M.Yukhin, N.Z. Lyakhov
Thermal and laser sintering of a highly stable inkjet ink consisting of silver nanoparticles stabilized by a combination of a short chain carboxylic acid and a polymeric dispersant
Materials Today: Proceedings, 2018, V. 5, N 8, Part 2, Pp 16042-16050 (14th International Conference on Nanosciences & Nanotechnologies (NN17) 4–7 July 2017 | Thessaloniki, Greece) doi:10.1016/j.matpr.2018.05.049
M.B. Bushuev, V.P. Krivopalov, E.B. Nikolaenkova, K.A. Vinogradova, Yu.V. Gatilov
Hysteretic spin crossover in isomeric iron(II) complexes
Dalton Trans., 2018, V. 47, N 29, Pp 9585-9591 doi:10.1039/C8DT02223B, IF=4.099
E.V. Zaytseva, Yu.V. Gatilov, D.G. Mazhukin
The synthesis of new functionalized 1,3,5-triazine-based stable bi- and trinitroxides of the 2,5-dihydroimidazole series
Arkivoc, 2018, part v, 359-374 doi:10.24820/ark.5550190.p010.614, IF=1.048
Модификация аминогруппы полифторированных арилендиаминов в реакциях с альдегидами и хинонами/ Т.А. Ваганова, И.П. Чуйков, Е.В. Малыхин// Fluorine notes, 2018, V.119, N 4, Cc 5-6 doi:10.17677/fn20714807.2018.04.03
L. Politanskaya, Z. Duan, I. Bagryanskaya, I. Eltsov, E. Tretyakov, Chanjuan. Xi
Highly efficient synthesis of polyfluorinated 2-mercaptobenzothiazole derivatives
Journal of Fluorine Chemistry, 2018, V. 212, Pp 130-136 doi:10.1016/j.jfluchem.2018.06.001, IF=1.879
V.V. Krisyuk, S. Urkasym-Kyzy, T.V. Rybalova, I.A. Baidina, I.V. Korolkov, D.L. Chizhov, D.N. Bazhin, Yu.S. Kudyakova
Isomerization as a tool to design volatile heterometallic complexes with methoxy-substituted β-diketonates
JJournal of Coordination Chemistry, 2018, V. 71, N 14, Pp 2194-2208 doi:10.1080/00958972.2018.1479746, IF=1.703
I.K. Shundrina, D.S. Odintsov, I.A. Os'kina, I.G. Irtegova, L.A. Shundrin
Synthesis, electrochemical reduction and radical anions of 2-{[bis(4-amino(nitro)phenyl)]aminomethyl}-9H-thioxanthene-9-one derivatives
European Journal of Organic Chemistry, 2018, V. 2018, N 26, Pp 3471-3480 doi:10.1002/ejoc.201800525, IF=2.882
S.I. Zhivetyeva, I.A. Zayakin, I.Yu. Bagryanskaya, E.V. Zaytseva, E.G. Bargyanskaya, E.V. Tretyakov
Interaction of a lithiated nitronyl nitroxide with polyfluorinated 1,4-naphthoquinones
Tetrahedron, 2018, V. 74, N 28, Pp 3924-3930 doi:10.1016/j.tet.2018.05.075, IF=2.377
A.L. Zakharenko, E.S. Mozhaitsev, E.V. Suslov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
Synthesis and Inhibitory Properties of Imines Containing Monoterpenoid and Adamantane Fragments Against DNA Repair Enzyme Tyrosyl-DNA Phosphodiesterase 1 (Tdp1)
Chemistry of Natural Compounds, 2018, V. 54, N 4, pp 672-676 doi:10.1007/s10600-018-2443-7, IF=0.449
L. Politanskaya, T. Rybalova, O. Zakharova, G. Nevinsky, E. Tretyakov
p-Toluenesulfonic acid mediated one-pot cascade synthesis and cytotoxicity evaluation of polyfluorinated 2-aryl-2,3-dihydroquinolin-4-ones and their derivatives
Journal of Fluorine Chemistry, 2018, V.211, Pp 129-140 doi:10.1016/j.jfluchem.2018.04.005, IF=1.879
A.D. Skolyapova, G.A. Selivanova, E.V. Tretyakov, I.Yu. Bagryanskaya, V.D. Shteingarts
Synthesis of polyfluorinated aminoquinolines via nitroquinolines
Journal of Fluorine Chemistry, 2018, V. 211, Pp 14-23 doi:10.1016/j.jfluchem.2018.04.006, IF=1.879
I.V. Ilyina, V.V. Zarubaev, I.N. Lavrentieva, A.A. Shtro, I.L. Esaulkova, D.V. Korchagina, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
Highly potent activity of isopulegol-derived substituted octahydro-2H-chromen-4-ols against influenza A and B viruses
Bioorganic & Medicinal Chemistry Letters, 2018, V. 28, N 11, Pp 2061-2067 doi:10.1016/j.bmcl.2018.04.057, IF=2.371
A.V. Karakulov, E.A. Karpova, V.G. Vasiliev
Ecological and geographical variation of morphometric parameters and flavonoid composition of Rhododendron parvifolium
Turczaninowia, 2018, V. 21, N 2, Pp 133-144 doi:10.14258/turczaninowia.21.2.14
Tris(2,6-dimethoxyphenyl)antimony Diazide: Synthesis and Structure/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, I. Yu. Bagryanskaya, N. V. Pervukhina// Russian Journal of Inorganic Chemistry, 2018, V. 63, N 6, pp 781-785 doi:10.1134/S0036023618060086, IF=0.709
The content of biologically active polyphenols Lonicera Caerulea Subsp. Pallasll in Natural Conditions and the introduction/ I.G. Boyarskikh, K.G. Vasiliev, T.A. Kukushkina// Khimiya Rastitel'nogo Syr'ya, 2018, N 2, Pp 89-96 doi:10.14258/jcprm.2018023452
O.T. Dyan, P.A. Zaikin, D.S. Fadeev, Y.V. Gatilov, G.I. Borodkin
1,1-Difluoronaphthalen-2(1H)-ones as building blocks for fluorinated tetraphenes
Journal of Fluorine Chemistry,2018, V. 210, Pp 88-93 doi:10.1016/j.jfluchem.2018.03.008, IF=1.879
S. Bothe, J. Nowag, V. Klimavicius, M. Hoffmann, T.I. Troitskaya, E.V. Amosov, V.M. Tormyshev, I. Kirilyuk, A. Taratayko, A.A. Kuzhelev, D. Parkhomenko, E.G. Bagryanskaya, T. Gutmann, G. Buntkowsky
Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization
J. Phys. Chem. C, 2018, 122 (21), pp 11422-11432 doi:10.1021/acs.jpcc.8b02570, IF=4.484
A.V. Artem'ev, E.P. Doronina, I.Yu. Bagryanskaya, L.V. Klyba
Bis(dicyclohexylselenophosphinyl)selenide, [Cy2P(Se)]2Se: Synthesis, molecular structure and application for self-assembly of a tetrahedral Cu(I) cluster
Journal of Molecular Structure, 2018, V. 1160, Pp 208-214 doi:10.1016/j.molstruc.2018.02.007, IF=2.011
G. Audran, E.G. Bagryanskaya, I.Yu. Bagryanskaya, M. Edeleva, P. Kaletina, S.R-A. Marque, D. Parkhomenko, E.V. Tretyakov, S.I. Zhivetyeva
The effect of the oxophilic Tb(III) cation on Csingle bond-ON bond homolysis in alkoxyamines
Inorganic Chemistry Communications, 2018, V. 91, Pp 5-7 doi:10.1016/j.inoche.2018.02.019, IF=1.81
Synthesis and Structure of Cyclohexenes Functionalized by Nitro and Trifluoro(chloro)methyl Groups/ N. A. Anisimova, E. K. Slobodchikova, V. M. Berestovitskaya, M. E. Ivanova, A. A. Kuzhaeva, T. V. Rybalova// Russian Journal of General Chemistry, 2018, V. 88, N 5, Pp 883-891 doi:10.1134/S1070363218050079, IF=0.658
Hexa(isothiocyanato)chromates(III) of Some Yttrium Group Lanthanide(III) and Europium Complexes with Nicotinic Acid: Synthesis and Crystal Structures/ E. V. Cherkasova, N. V. Pervukhina, N. V. Kuratieva, I. Yu. Bagryanskaya, T. G. Cherkasova// Russian Journal of Inorganic Chemistry, 2018, V. 63, N 5, pp 626-630 doi:10.1134/S003602361805011X, IF=0.709
Configurational Stability of 1,1'-Bi-2-naphthol in Superacid System HSO3F-SBF5-SO2ClF/ G. E. Salnikov, A. M. Genaev, A. V. Shernyukov, Z. Zhu, N. V. Tkachenko, K. Yu. Koltunov// Russian Journal of Organic Chemistry, 2018, V. 54, N 5, pp 792-794 doi:10.1134/S1070428018050214, IF=0.655
M.S. Kazantsev, A.A. Beloborodova, A.D. Kuimov, I.P. Koskin, E.S. Frantseva, T.V. Rybalova, I.K. Shundrina, C.S. Becker, E.A. Mostovich
Synthesis, luminescence and charge transport properties of furan/phenylene co-oligomers: The study of conjugation length effect
Organic Electronics, , 2018, V. 56, May 2018, Pages 208-215 doi:10.1016/j.orgel.2018.01.010, IF=3.68
L. Gurskaya, I. Bagryanskaya, E. Amosov, M. Kazantsev, L. Politanskaya, E. Zaytseva, E. Bagryanskaya, A. Chernonosov, E. Tretyakov
1,3-Diaza[3]ferrocenophanes functionalized with a nitronyl nitroxide group
Tetrahedron, 2018, V. 74, N 15, Pp 1942-1950 doi:10.1016/j.tet.2018.02.062, IF=2.377
Yu.S. Demidova, E.V. Suslov, I.L. Simakova, E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
One-pot monoterpene alcohol amination over Au/ZrO₂ catalyst: Effect of the substrate structure
Journal of Catalysis, 2018, V. 360, Pages 127-134 doi:10.1016/j.jcat.2018.01.020, IF=6.759
D. Sadyrbekov, T. Saliev, Yu. Gatilov, I. Kulakov, R. Seidakhmetova, T. Seilkhanov, S. Askarova
Spatial Structure and Antimicrobial Activity of Cyclopropane Derivative of Limonene
Natural Product Communications, 2018, V. 13, N 4, Pp: 387-388 WOS:000433651900001, IF=0.809
A.O. Finke, M.E. Mironov, A.B. Skorova, E.E. Shults
Copper-catalyzed 1,3-dipolar cycloaddition reaction of spirosolanederived azide for the preparation of modified solasodine alkaloid
Chemistry of Heterocyclic Compounds, 2018, V. 54, N 4, pp 411-416 doi:10.1007/s10593-018-2284-0, IF=1.201
I.V. Kulakov, D.N. Ogurtsova, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
Synthesis, Structure, and Some Transformations of Novel 1,5-methanonaphtho[1,2-g][1,3,5]oxadiazocine Derivatives
Journal of Heterocyclic Chemistry, 2018, V. 55, N 4, Pp 923-928 doi:10.1002/jhet.3119, IF=1.141
M.A. Gromova, Yu.V. Kharitonov, T.V. Rybalova, E.E. Shul'ts
Synthetic Transformations of Higher Terpenoids. 36.* Synthesis of 13-(Oxazol-5-Yl)-15,16-Bisnorisopimaranes
Chemistry of Natural Compounds, 2018, V. 54, N 2, pp 293-300 doi:10.1007/s10600-018-2327-x, IF=0.45
Reaction of Perfluorobenzocyclobutene with Excess Pentafluorobenzene in SbF5/ T.V. Mezhenkova, V.R. Sinyakov, V.M. Karpov, Ya.V. Zonov, Yu.V. Gatilov, V.E. Platonov// Russian Journal of Organic Chemistry, 2018, V. 54, N 4, pp 545-553 doi:10.1134/S107042801804005X, IF=0.655
A.Yu. Makarov, I.Yu. Bagryanskaya, Yu.M. Volkova, M.M. Shakirov, A.V. Zibarev
Salts of Sterically-Hindered Chalcogen-Varied Herz Cations Including Those with New Anions [Te₃Cl₁₄]^2- and [Te₄Cl₁₈]^2- Anions
European Journal of Inorganic Chemistry, 2018, V. 2018, N 11, Pp 1322-1332 doi:10.1002/ejic.201701470, IF=2.507
V.S. Glukhacheva, S.G. Il'yasov, A.A. Obraztsov, Yu.V. Gatilov, I.V. Eltsov
A New Synthetic Route to Heteroanthracenes
European Journal of Organic Chemistry, 2018, V. 2018, N 10, Pp 1265-1273 doi:10.1002/ejoc.201701689, IF=2.882
D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767
Molecular and Crystal Structure of 2-Amino-Polyfluorophenyl-4,4,5,5-Tetramethyl-4,5-Dihydro-1H-Imidazol- 3-Oxide-1-Oxyls/ E.V. Tretyakov, T.V. Makhneva, L.V. Politanskaya, I.Yu. Bagryanskaya, D.V. Stass// Journal of Structural Chemistry, 2018, V. 59, N 3, pp 689-696 doi:10.1134/S0022476618030289, IF=0.521
А.П. Крысин, В.П. Фадеева, О.Н. Никуличева, А.А. Нефедов
Решение алгоритма: фенольные антиоксиданты - путь к улучшению механических свойств полимерных материалов
Химия в интересах устойчивого развития. 2018. Т. 26. № 2. С. 149-155 doi:10.15372/KhUR20180205
P.A. Fedyushin, R.Yu. Peshkov, E.V. Panteleeva, E.V. Tretyakov, I.V. Beregovaya, Yu.V. Gatilov, V.D. Shteingarts
Purposeful regioselectivity control of the Birch reductive alkylation of biphenyl-4-carbonitrile
Tetrahedron, 2018, V. 74, N 8, Pages 842-851 doi:10.1016/j.tet.2017.12.046, IF=2.377
A.V. Artem'ev, M.R. Ryzhikov, I.V. Taidakov, M.I. Rakhmanova, E.A. Varaksina, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
Bright green-to-yellow emitting Cu(I) complexes based on bis(2-pyridyl)phosphine oxides: synthesis, structure and effective thermally activated-delayed fluorescence
Dalton Trans., 2018, V.47, N 8, Pp 2701-2710 doi:10.1039/C7DT04758D, IF=4.099
K.Yu. Ponomarev, E.V. Suslov, A.L. Zakharenko, O.D. Zakharova, A.D. Rogachev, D.V. Korchagina, A. Zafar, J. Reynisson, A.A. Nefedov, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
Aminoadamantanes Containing Monoterpene-derived Fragments as Potent Tyrosyl-DNA phosphodiesterase 1 Inhibitors
Bioorganic Chemistry, V.76, February 2018, Pp. 392-399 doi:10.1016/j.bioorg.2017.12.005, IF=3.929
T.A. Vaganova, Yu.V. Gatilov, D.P. Pishchur, I.P. Chuikov, E.V. Malykhin
Controlled self-assembly of π-stacked/H-bonded 1D crystal structures from polyfluorinated arylamines and 18-crown-6 (2:1).Associate vs. co-former fluorescence properties
CrystEngComm, 2018, V. 20, N 6, Pp 807-817 doi:10.1039/C7CE01851G, IF=3.304
Synthesis of Nickel Nanoparticles by the Reduction of Its Salts Using the Modified Polyol Method in the Presence of Sodium Polyacrylates with Various Molecular Weights/ O. A. Logutenko, A. I. Titkov, A. M. Vorob'ev, I. K. Shundrina, Yu. M. Yukhin, N. Z. Lyakhov// Russian Journal of General Chemistry, 2018, V. 88, N 2, pp 288-294 doi:10.1134/S1070363218020160, IF=0.658
X-Ray Diffraction Study of Perfluoro- 9,10-Diphenylanthracene and Perfluoro- 9,10-Diphenyldihydroanthracenes/ Yu. V. Gatilov, T.V. Mezhenkova, V.M. Karpov// Journal of Structural Chemistry, 2018, V. 59, N 2, pp 449-454 (doi: 10.1134/S0022476618020282) doi:10.1134/S0022476618020282, IF=0.521
S.I. Zhivetyeva, E.V. Tretyakov, I.Yu. Bagryanskaya
Synthesis of novel phosphonium betaines and bis-betaines derived from hexafluoro-1,4-naphthoquinone
Journal of Fluorine Chemistry, V. 206, February 2018, Pp. 19-28 doi:10.1016/j.jfluchem.2017.11.010, IF=1.879
Yu.V. Yushkova, E.I. Chernyak, Yu.V. Gatilov, V.G. Vasil'ev, S.V. Morozov, I.A. Grigor'ev
Synthesis, Structure, Antioxidant Activity, and Water Solubility of Trolox Ion Conjugates
Saudi Pharmaceutical Journal, 2018, V. 26, N 1, Pp 84-92 doi:10.1016/j.jsps.2017.10.008, IF=3.11
Nitro derivatives of 2,1,3-benzothiadiazole 1-oxides: synthesis, structural study, and NO release/ L. S. Konstantinova, E. A. Knyazeva, Yu. V. Gatilov, S. G. Zlotin, O. A. Rakitin// Russian Chemical Bulletin, 2018, V. 67, N1, pp 95-101 doi:10.1007/s11172-018-2042-6, IF=0.781
Oximation of 2-(R1-Amino)-4-(R2-imino)naphthalen-1(4H)-ones/ L. M. Gornostaev, T. A. Rukovets, E. V. Arnold, Yu. G. Khalyavina, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2018, V. 54, N 1, pp 78-86 doi:10.1134/S1070428018010062, IF=0.655

2017

A.V. Artem'ev, Ju.A. Eremina, E.V. Lider, O.V. Antonova, E.V. Vorontsova, I.Yu. Bagryanskaya
Luminescent Ag(I) scorpionates based on tris(2-pyridyl)phosphine oxide: Synthesis and cytotoxic activity evaluation
Polyhedron, 2017, V. 138, Pp 218-224 doi:10.1016/j.poly.2017.09.041, IF=1.925
V. Romanov, A. Vorob'ev, I. Bagryanskaya, D. Parkhomenko, E. Tretyakov
1,3-Dipolar Cycloaddition of a Nitronyl Nitroxide-Substituted Alkyne to Heteroaromatic N-Imines
Australian Journal of Chemistry, 2017, 70(12) 1317-1320 doi:10.1071/CH17476, IF=1.327
A. V. Artem'ev, V. A. Kuimov, E. A. Matveeva, I. Yu. Bagryanskaya, A. I. Govdi, S. F. Vasilevsky, M.I. Rakhmanova, D. O. Samultsev, N. K. Gusarova, B. A. Trofimov
A new access to tri(1-naphthyl)phosphine and its catalytically active palladacycles and luminescent Cu(I) complex
Inorganic Chemistry Communications, 2017, V. 86, 2017, Pp 94-97 doi:10.1016/j.inoche.2017.09.008, IF=1.639
K.Yu. Ponomarev, E.A. Morozova, E.V. Suslov, D.V. Korchagina, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
Synthesis and Analgesic Activity of 5,7- and 6-Substituted Diazaadamantanes Containing Monoterpene Moieties
Chemistry of Natural Compounds, 2017, V. 53, N 6, Pp 1131-1136 doi:10.1007/s10600-017-2216-8, IF=0.46
O.S. Patrusheva, A.V. Pavlova, D.V. Korchagina, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
Synthesis and Analgesic Activity of 4,7-Dimethyl-3,4,4a,5,8,8a-Hexahydro-2-Chromen-4,8-Diols Containing Alkyl-Substituted Aromatic Moieties
Chemistry of Natural Compounds, 2017, V. 53, N 6, Pp 1066-1071 doi:10.1007/s10600-017-2202-1, IF=0.46
L.S. Konstantinova, I.V. Baranovsky, E.A. Pritchina, M.S. Mikhailov, I.Yu. Bagryanskaya, N.A. Semenov, I.G. Irtegova, G.E. Salnikov, K.A. Lyssenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin
Fused 1,2,3-Thiaselenazoles Synthesized from 1,2,3-Dithiazoles through Selective Chalcogen Exchange
Chemistry - A European Journal, 2017, V. 23, N 67, Pp 17037-17047 doi:10.1002/chem.201703182, IF=5.316
Development and Validation of a Method for Determination of a New Effective Inhibitor of Influenza Virus H1N1 in Blood Plasma/ A. S. Sokolova, O. I. Yarovaya, A. A. Nefedov, N. F. Salakhutdinov// Pharmaceutical Chemistry Journal, 2018, V. 51, N 12, pp 1102-1105 doi:10.1007/s11094-018-1748-y, IF=0.444
P.A. Abramov, K. A. Brylev, A.Yu. Vorob'ev, Yu. V. Gatilov, G. I. Borodkin, N. Kitamura, M. N. Sokolov
Emission tuning in Re(I) complexes: Expanding heterocyclic ligands and/or introduction of perfluorinated ligands
Polyhedron, 2017, V.137, Pp 231-237 doi:10.1016/j.poly.2017.08.046, IF=1.925
V.Yu. Shuvalov, I.V. Eltsov, N.A. Tumanov, E.V. Boldyreva, A.A. Nefedov, G.P. Sagitullina
[6]-[9]Metacyclophanes: a New Synthesis, Crystal Structures, NMR- and UV-Research
European Journal of Organic Chemistry, 2017, V. 2017,N 36, Pp 5410-5416 doi:10.1002/ejoc.201700946, IF=2.834
E. Tretyakov, A. Keerthi, M. Baumgarten, S. Veber, M. Fedin, D. Gorbunov, I. Shundrina, N. Gritsan
The Design of Radical Stacks: Nitronyl-Nitroxide-Substituted Heteropentacenes
ChemistryOpen, 2017, V. 6, N 5, Pp 642-652 doi:10.1002/open.201700110, IF=2.917
I.V. Kulakov, A.A. Karbainova, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
Synthesis and Analgesic Activity of bis(3,4-dihydroquinoxalin-2(1H)-one) and bis(3,4-dihydro-2H-1,4-benzoxazin-2-one) Derivatives
Chemistry of Heterocyclic Compounds, 2017, V.53, N 10, pp 1094-1097 doi:10.1007/s10593-017-2178-6, IF=0.893
E. Suslov, V.V. Zarubaev, A.V. Slita, K. Ponomarev, D. Korchagina, D.M. Ayine-Tora, J. Reynisson, K. Volcho, N. Salakhutdinov
Anti-Influenza Activity of Diazaadamantanes Combined with Monoterpene Moieties
Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 19, Pp 4531-4535 doi:10.1016/j.bmcl.2017.08.062, IF=2.453
A.M. Sheveleva, A.V. Anikeenko, A.S. Poryvaev, D.L. Kuzmina, I.K. Shundrina, D.I. Kolokolov, A. G. Stepanov, M.V. Fedin
Probing Gas Adsorption in Metal-Organic Framework ZIF-8 by EPR of Embedded Nitroxides
J. Phys. Chem. C, Just Accepted Manuscript doi:10.1021/acs.jpcc.7b06884, IF=4.535
Yu.M. Deryabina, T.A. Kornakova, N.L. Bazhina, V.D. Tikhova
Comparative Infrared Spectra Analysis of One Territory Soil Humic Acids by IR-EXPERT Computer System
IInt. J. Green. Pharm. 2017 (Suppl); 11(3), pp S465-S469 (http://greenpharmacy.info/index.php/ijgp/article/view/1158) doi:10.22377/ijgp.v11i03.1158
D.O. Prima, D.S. Baev, E.V. Vorontsova, T.S. Frolova, I.Yu. Bagryanskaya, Yu.G. Slizhov, T.G. Tolstikova, A.Yu. Makarov, A.V. Zibarev
New cancer cells apoptosis agents: Fluorinated aza-heterocycles
AIP Conference Proceedings, V. 1882, N 1, 020057 (2017) (Proceedings of the International Conference on Physics of Cancer: Interdisciplinary Problems and Clinical Applications (PC IPCA’17), 23-26 May 2017, Tomsk, Russia) doi:10.1063/1.5001636
A.V. Artem'ev, I.Yu. Bagryanskaya, E.P. Doronina, P.M. Tolstoy, A.L. Gushchin, M.I. Rakhmanova, A.Yu. Ivanov, A.O. Suturina
A new family of clusters containing a silver-centered tetracapped [Ag@Ag4(μ3-P)4] tetrahedron, inscribed within a N12 icosahedron
Dalton Trans., 2017,46, 12425-12429 doi:10.1039/C7DT02597A, IF=4.28
High-temperature adsorption layers based on fluoridated polyimide and diatomite carrier/ E.Yu. Yakovleva, I.K. Shundrina, E.Yu. Gerasimov// Russian Journal of Physical Chemistry A, 2017, V. 91, N 9, pp 1797-1804 doi:10.1134/S0036024417090321
T.P. Kukina, I.A. Elshin, O.I. Sal'nikova
Comparative Analysis of Aliphatic, Phenolcarboxylic, and Triterpenic Acids from Populus nigra and Salix alba Barks
Chemistry of Natural Compounds, 2017, V. 53, N 5, pp 941-943 doi:10.1007/s10600-017-2162-5, IF=0.46
D.O. Prima, E.V. Vorontsova, A.G. Makarov, A.Yu. Makarov, I.Yu. Bagryanskaya, T.F. Mikhailovskaya, Yu.G. Slizhov, A.V. Zibarev
Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis
Mendeleev Communications, 2017, V. 27, N 5, Pp 439-442 doi:10.1016/j.mencom.2017.09.002, IF=1.741
N.A. Pushkarevsky, P. A. Petrov, D.S. Grigoriev, A.I. Smolentsev, L.M. Lee, F. Kleemiss, G.E. Salnikov, S.N. Konchenko, I. Vargas-Baca, S. Grabowsky, J. Beckmann, A.V. Zibarev
Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
Chemistry - A European Journal, 2017, V. 23, N 46, Pp 10987-10991 doi:10.1002/chem.201703018, IF=5.316
K. Ponomarev, E. Morozova, A. Pavlova, E. Suslov, D. Korchagina, A. Nefedov, T. Tolstikova, K. Volcho, N. Salakhutdinov
Synthesis and Analgesic Activity of Amines Combining Diazaadamantane and Monoterpene Fragments
Medicinal Chemistry, 2017, V. 13 , N 8, Pp 773 - 779 doi:10.2174/1573406413666170525124316, IF=2.331
I.V. Kulakov, A.L. Shatsauskas, M.V. Matsukevich, I.V. Palamarchuk, T.M. Seilkhanov, Y.V. Gatilov, A.S. Fisyuk
A New Approach to the Synthesis of Benzo[ c ][1,7]naphthyridin-4(3 H )-ones
Synthesis (Germany), 2017, 49(16): 3700-3709 doi:10.1055/s-0036-1590470, IF=2.65
T.A. Vaganova, V.I. Rodionov, I.P. Chuikov, E.A. Chochrina, E.V. Malykhin
Selective one-pot synthesis of aminopolyhalobenzonitriles from polyhalobenzotrichlorides in anhydrous ammonia
Journal of Fluorine Chemistry, Volume 200, August 2017, Pages 84-90 doi:10.1016/j.jfluchem.2017.06.005, IF=2.101
V. Shelkovnikov, G. Selivanova, G. Lyubas, S. Korotaev, I. Shundrina, E. Tretyakov, E. Zueva, A. Plekhanov, S. Mikerin, A. Simanchuk
Second-order nonlinear optical properties of composite material of an azo-chromophore with a tricyanodiphenyl acceptor in a poly(styrene-co-methyl methacrylate) matrix
Optical Materials, 2017, V. 69, Pp 67-72 doi:10.1016/j.optmat.2017.04.008, IF=2.237
A.N. Blaznov, E.V. Atyasova, I.K. Shundrina, V.V. Samoilenko, V.V. Firsov, A.S. Zubkov
Thermomechanical characterization of BFRP and GFRP with different degree of conversion
Polymer Testing, 2017, V. 60, Pp 49-57 doi:10.1016/j.polymertesting.2017.03.011, IF=2.463
I. Il'ina, A. Pavlova, D. Korchagina, O. Ardashov, T. Tolstikova, K. Volcho, N. Salakhutdinov
Synthesis and analgesic activity of monoterpenoid-derived alkyl-substituted chiral hexahydro-2H-chromenes
Medicinal Chemistry Research, 2017, V. 26, N 7, pp 1415-1426 doi:10.1007/s00044-017-1847-4, IF=1.276
T.P. Kukina, D.N. Shcherbakov, K.V. Gensh, E.A. Tulysheva, O.I. Salnikova, A.E. Grazhdannikov, E.A. Kolosova
Bioactive Components of Sea Buckthorn Hippophae rhamnoides L. Foliage
Russian Journal of Bioorganic Chemistry, 2017, Vol. 43, No. 7, pp. 747-751, IF=0.689
V.N. Kovtonyuk, Yu.V. Gatilov
Polyfluorinated oxacalixarenes. Interaction of perfluoro-m-xylene with resorcinol and tetrafluororesorcinol
Journal of Fluorine Chemistry, 2017, V. 199, Pp 52-59 doi:10.1016/j.jfluchem.2017.04.010, IF=2.101
P.A. Zaikin, O.T. Dyan, D.S. Fadeev, Yu.V. Gatilov, G.I. Borodkin
1,1-Difluoronaphthalene-2(1H)-ones in Diels-Alder Reaction
Journal of Fluorine Chemistry, 2017, V. 199, Pp 20-29 doi:10.1016/j.jfluchem.2017.04.008, IF=2.101
T.M. Khomenko, V.V. Zarubaev, I.R. Orshanskaya, R.A. Kadyrova, V.A. Sannikova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
Anti-influenza activity of monoterpene-containing substituted coumarins
Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 13, Pp 2920-2925 doi:10.1016/j.bmcl.2017.04.091, IF=2.453
A.E. Paromov, S.V. Sysolyatin, Y.V. Gatilov
An Acid-Catalyzed Cascade Synthesis of Oxaazatetracyclo [5.5.0.03,11.05,9]dodecane Derivatives
Journal of Energetic Materials, 2017, V.35, N 3, Pp. 363-373 doi:10.1080/07370652.2016.1194499, IF=1.557
А.А. Коновалов, И.К. Шундрина, Е.В. Карпова, И.В. Ельцов, Е.А. Орлова, Н.П. Гончаров
Влияние лигнификации и минерализации тканей листа на устойчивость к бурой ржавчине растений мягкой пшеницы
Вавиловский журнал генетики и селекции, 2017, Т. 21, N 6, Сс. 686-693 doi:10.18699/VJ17.286
Hexafluorosilicates of cobalt(II) complexes with dimethylsulfoxide and dimethylformamide/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, N.V. Kurat'eva, V.V. Medvedev, E.S. Tatarinova, E.V. Cherkasova// Russian Journal of Inorganic Chemistry, June 2017, V. 62, N 6, pp 760-765 doi:10.1134/S003602361706002X, IF=0.787
E.V. Sokol, O.A. Kozmenko, H.N. Khoury, S.N. Kokh, S.A. Novikova, A.A. Nefedov, I.A. Sokol, P. Zaikin
Calcareous sediments of the Muwaqqar Chalk Marl Formation, Jordan: Mineralogical and geochemical evidences for Zn and Cd enrichment
Gondwana Research, 2017, V. 46, Pp 204-226 doi:10.1016/j.gr.2017.03.008, IF=6.959
S.S. Patrushev, T.V. Rybalova, I. D. Ivanov, V.A. Vavilin, E.E. Shults
Synthesis of a new class of bisheterocycles via the Heck reaction of eudesmane type methylene lactones with 8-bromoxanthines
Tetrahedron, 2017, V. 73, N 19, Pp 2717-2726 In Press, Accepted Manuscript - Note to users doi:10.1016/j.tet.2017.03.016, IF=2.651
P.A. Zaikin, O.T. Dyan, D.V. Evtushok, A.N. Usoltsev, E.V. Karpova, G.I. Borodkin, V.G. Shubin
Solvent-free Fluorination of Electron Rich Aromatic Compounds with F-TEDA-BF4 Reagent: Toward "Dry" Processes
European Journal of Organic Chemistry, 2017, V. 2017, N 17, Pp 2469-2474 doi:10.1002/ejoc.201700179, IF=2.834
A.A. Beloborodova, V.S. Minkov, D.A. Rychkov, T.V. Rybalova, E.V. Boldyreva
First Evidence of Polymorphism in Furosemide Solvates
Cryst. Growth Des., 2017, 17 (5), pp 2333-2341 doi:10.1021/acs.cgd.6b01191, IF=4.54
D.S. Fadeev, I.P. Chuikov, V.M. Karpov, V.I. Mamatyuk
The Investigation of NMR parameters of the heptafluoroindenyl cation
Journal of Fluorine Chemistry, V. 197, May 2017, Pages 1-5 doi:10.1016/j.jfluchem.2017.02.002, IF=2.101
K.S. Kovaleva, O.I. Yarovaya, D.S. Fadeev, N.F. Salakhutdinov
One-pot synthesis of 1,5,3-oxathiazepanes via the three-component condensation of primary amines, formaldehyde and 2-mercaptoethanol
Tetrahedron Letters, 2017, V. 58, N 19, Pp 1868-1870 doi:10.1016/j.tetlet.2017.03.090, IF=2.193
G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, S.R.A. Marque, D. Parkhomenko, E. Tretyakov, S. Zhivetyeva
Zinc(II) Hexafluoroacetylacetonate Complexes of Alkoxyamines: NMR and Kinetic Investigations. First Step for a New Way to Prepare Hybrid Materials
ChemistrySelect, 2017, V. 2, N 12, Pp 3584-3593 doi:10.1002/slct.201700678
G.E. Salnikov, A.M. Genaev, A.V. Shernyukov, V.G. Shubin
Protonation of ninhydrin and indan-1,2,3-trione revisited: A combined theoretical and experimental study
Journal of Molecular Structure, 2017, V. 1134, Pp 1-5 doi:10.1016/j.molstruc.2016.12.057, IF=1.753
I.K. Shundrina, M.A. Matsko, K.I. Baskakova, L.G. Echevskaya, M.I. Nikolaeva, L.A. Shundrin, V.A. Zakharov
Dynamic mechanical analysis of ethylene/1-hexene copolymers: The effect of the catalyst type on the short-chain branching distribution and properties of the amorphous and crystalline phases
Journal of Applied Polymer Science, 2017, V. 134, N 14, Article number 44638 doi:10.1002/app.44638, IF=1.86
T.A. Vaganova, Y.V. Gatilov, S.E. Malykhin, D.P. Pishchur, Y.V. Larichev, V.I. Rodionov, E.V. Malykhin
Design and supramolecular structure of crystal associates of polyfluoroarylenediamines and 18-crown-6 (2:1)
Journal of Molecular Structure, V. 1133, 5 April 2017, P. 122-134 doi:10.1016/j.molstruc.2016.11.091, IF=1.753
E.V. Tretyakov, P.A. Fedyushin, E.V. Panteleeva, D.V. Stass, I.Yu. Bagryanskaya, I.V. Beregovaya, A.S. Bogomyakov
Substitution of a Fluorine Atom in Perfluorobenzonitrile by a Lithiated Nitronyl Nitroxide
J. Org. Chem., 2017, 82 (8), pp 4179-4185 doi:10.1021/acs.joc.7b00144, IF=4.848
A.D. Skolyapova, G.A. Selivanova, E.V. Tretyakov, T.F. Bogdanova, L.N. Shchegoleva, I.Yu. Bagryanskaya, L.Yu. Gurskaya, V.D. Shteingarts
Interaction of polyfluorinated 2-chloroquinolines with ammonia
Tetrahedron, 2017, V. 73, N 9, Pp 1219-1229 doi:10.1016/j.tet.2017.01.026, IF=2.651
M.S. Kazantsev, A.A. Beloborodova, E.S. Frantseva, T.V. Rybalova, V.G. Konstantinov, I.K. Shundrina, D.Yu. Paraschuk, E.A. Mostovich
Methyl substituent effect on structure, luminescence and semiconducting properties of furan/phenylene co-oligomer single crystals
CrystEngComm, 2017,19, 1809-1815 doi:10.1039/C6CE02565J, IF=3.108
S.A. Prikhod'ko, A.Yu. Shabalin, V.V. Bardin, I.V. Eltsov, I.K. Shundrina, V.N. Parmon, N.Yu. Adonin
1-Alkyl-3-methylimidazolium 4-organyloxy-2,3,5,6-tetrafluorophenyltrifluoroborates as a new platform for ionic liquids with specific properties
RSC Adv., 2017,7, 17497-17504 doi:10.1039/C7RA01709J, IF=3.108
S.M. Adekenov, Zh.R. Shaimerdenova, Yu.V. Gatilov, G.A. Atazhanova
Two New Sesquiterpene Lactones from Artemisia halophila
Chemistry of Natural Compounds, 2017, V. 53, N 2, pp 284-289 doi:10.1007/s10600-017-1971-x, IF=0.46
E.V. Nazimova, A.A. Shtro, V.B. Anikin, O.S. Patrusheva, I.V. Il'ina, D.V. Korchagina, V.V. Zarubaev, K.P. Volcho, N.F. Salakhutdinov
Influenza Antiviral Activity of Br-Containing [2R,4R(S),4aR,7R,8aR]-4,7-Dimethyl-2-(Thiophen-2-YL)Octahydro-2H-Chromen-4-Ols Prepared from (–)-Isopulegol
Chemistry of Natural Compounds, 2017, V. 53, N 2, pp 260-264 doi:10.1007/s10600-017-1966-7, IF=0.46
T.A. Vaganova, A.I. Plekhanov, A.E. Simanchuk, S.L. Mikerin, E.V. Spesivtsev, E.V. Karpova, T.S. Frolova, E.V. Malykhin
Synthesis and characterization of novel polyhalogenaromatic polyimide material for electro-optic applications
Journal of Fluorine Chemistry, 2017, V. 195, Pp 70-78 doi:10.1016/j.jfluchem.2017.01.010, IF=2.101
E.S. Vasilyev, I.Yu. Bagryanskaya, A.V. Tkachev
Syntheses of chiral nopinane-annelated pyridines of C₂ and D₂-symmetry: X-ray structures of the fused derivatives of 4,5-diazafluorene, 4,5-diaza-9H-fluoren-9-one, and 9,9'-bi-4,5-diazafluorenylidene
Mendeleev Communications, 2017, V. 27, N 2, Pp 128-130 doi:10.1016/j.mencom.2017.03.006, IF=1.741
Cobalt(II) hexaiododimercurate(II) complex with ε-caprolactam: Synthesis and crystal structure/ A.V. Tikhomirova, I.Yu. Bagryanskaya, N.V. Pervukhina, T.G. Cherkasova// Russian Journal of Inorganic Chemistry, February 2017, V. 62, N 2, pp 187-190 doi:10.1134/S0036023617020206, IF=0.787
Double complex [Mn2(C11H13N3O)6(H2O)2][Cr(NH3)2(NCS)4]4: Synthesis and crystal structure/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, A.L. Vornakov, E.V. Cherkasova, N.V. Kuratieva// Russian Journal of Inorganic Chemistry, February 2017, V. 62, N 2, pp 182-186 doi:10.1134/S003602361702005X, IF=0.787
A.A. Shatrova, D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.S. Fadeev, L.V. Kulik
Novel Anthrathiophene-Based Small Molecules as Donor Material for Organic Photovoltaics: Synthesis and Light-Induced EPR Study
Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 425-438 doi:10.1515/zpch-2016-0832, IF=1.327
Luminophores of the luminous fungus Neonothopanus nambi/ Y.P. Zernov, T.V. Kobzeva, T.Y. Dranova, D.V. Stas, A.A. Alekseev, A.A. Nefedov// Biophysics (Russian Federation), V, 62, N 2, 1 March 2017, Pp 265-270 doi:10.1134/S0006350917020300
A.V. Shpatov, S.A. Popov, O.I. Salnikova, T.P. Kukina, E.N. Shmidt, B.H. Um
Composition and Bioactivity of Lipophilic Metabolites from Needles and Twigs of Korean and Siberian Pines (Pinus koraiensis Siebold & Zucc. and P. sibirica Du Tour)
Chemistry & Biodiversity, 2017, V. 14, N 2, Article number e1600203 doi:10.1002/cbdv.201600203, IF=1.44
A.S. Kuzmich, T.M. Khomenko, S.N. Fedorov, T.N. Makarieva, L.K. Shubina, N.I. Komarova, D.V. Korchagina, T.V. Rybalova, K.P. Volcho, N.F. Salakhutdinov
Cytotoxic and cancer preventive activity of benzotrithioles and benzotrithiole oxides, synthetic analogues of varacins
Medicinal Chemistry Research, 2017, V. 26, N 2, pp 397-404 doi:10.1007/s00044-016-1759-8, IF=1.276
A.V. Artem'ev, N.A. Kolyvanov, L.A. Oparina, N.K. Gusarova, A.O. Sutyrina, I.Y. Bagryanskaya, B.A. Trofimov
Four-Component Reaction between Secondary Phosphines, Primary Amines, Aldehydes, and Chalcogens: A Facile Access to Functionalized α-Aminophosphine Chalcogenides
Synthesis (Germany), 2017, V. 49, N 3, Pp 677-684 doi:10.1055/s-0036-1588127, IF=2.65
I. Bagryanskaya, M. Fedin, D. Gorbunov, N. Gritsan, L. Gurskaya, M. Kazantsev, Yu. Polienko, D. Stass, E. Tretyakov
A Nitroxide Diradical Containing a Ferrocen-1,1'-diyl-substituted 1,3-Diazetidine-2,4-diimine Coupler
Tetrahedron Letters, 2017, V. 58, N 5, Pp 478-481 doi:10.1016/j.tetlet.2016.12.068, IF=2.193
Yu.M. Volkova, A.Yu. Makarov, S.B. Zikirin, A.M. Genaev, I.Yu. Bagryanskaya, A.V. Zibarev
3,1,2,4-Benzothiaselenadiazine and related heterocycles: synthesis and transformation into Herz-type radicals
Mendeleev Communications, 2017, V. 27, N 1, Pp 19-22 doi:10.1016/j.mencom.2017.01.005, IF=1.741
E. A. Chulanova, E.A. Pritchina, L. A. Malaspina, S. Grabowsky, F. Mostaghimi, J. Beckmann, I. Yu. Bagryanskaya, M. V. Shakhova, L. S. Konstantinova, O.A. Rakitin, N. P. Gritsan ,A. V. Zibarev
New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction
Chemistry - A European Journal, 2017, V. 23, N 4, Pp 852-864 doi:10.1002/chem.201604121, IF=5.316
A.M. Genaev, G.E. Salnikov, A.V. Shernyukov, Z. Zhu, K.Yu. Koltunov
Protonation Behavior of 1,1'-Bi-2-naphthol and Insights into Its Acid-Catalyzed Atropisomerization
Org. Lett., 2017, 19 (3), pp 532-535 doi:10.1021/acs.orglett.6b03696, IF=6.578
E. Karpova, A. Nefedov, V. Mamatyuk, N. Polosmak, L. Kundo
Multi-analytical approach (SEM-EDS, FTIR, Py-GC/MS) to characterize the lacquer objects from Xiongnu burial complex (Noin-Ula, Mongolia)
Microchemical Journal, Volume 130, January 2017, Pages 336-344 doi:10.1016/j.microc.2016.10.013, IF=3.33
K.S. Marenin, Yu.V. Gatilov, A.M. Agafontsev, A.V. Tkachev
Stereoselectivity of formation of monoterpene - Amino acids hybrid molecules in the reaction of monoterpene nitroso chlorides with α-amino acid derivatives
Steroids, 2016, V. 117, Pp 112-119 doi:10.1016/j.steroids.2016.09.016, IF=2.282
D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, Y.V. Gatilov, L.V. Kulik
Diaza-analogs of benzopyrene and perylene containing thienyl and 4-(phenylamino)phenyl groups: Synthesis, characterization, optical and electrochemical properties
Dyes and Pigments, 2017, V. 136, Pp 707-714 doi:10.1016/j.dyepig.2016.09.026, IF=3.473
G.A. Atazhanova, A.V. Gering, F.T. Mukasheva, P.E. Sakenova, Yu.V. Gatilov, V.S. Korneev, S.M. Adekenov
Chemical Study of Pulicaria salviifolia
Chemistry of Natural Compounds, 2017, V. 53, N 1, pp 178-180 doi:10.1007/s10600-017-1943-1, IF=0.46
Furfural nitrosemicarbazone salts/ V. S. Glukhacheva, S. G. Il'yasov, G. V. Sakovich, Yu. V. Gatilov// Russian Chemical Bulletin, January 2017, V. 66, N 1, pp 83-85 doi:10.1007/s11172-017-1703-1, IF=0.528
Yu.S. Demidova, E.V. Suslov, I.L. Simakova , E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
Selectivity control in one-pot myrtenol amination over Au/ZrO2 by molecular hydrogen addition
Journal of Molecular Catalysis A: Chemical, V. 426, Part A, January 2017, Pages 60–67 doi:10.1016/j.molcata.2016.10.034, IF=3.957
A.I. Titkov, N.V. Bulina, A.S. Ulihin, I.K. Shundrina, E.V. Karpova, E.Yu. Gerasimov, Yu.M. Yukhin, N.Z. Lyakhov
N-Lauroylsarcosine capped silver nanoparticle based inks for flexible electronics
Journal of Materials Science: Materials in Electronics, January 2017, V. 28, N 2, pp 2029-2036 doi:10.1007/s10854-016-5762-0, IF=2.19

2016

Photopolymerization kinetics of a thiol-enol composition determined via recording/playback of a transmission holographic diffraction grating/ V. V. Shelkovnikov, D. I. Derevyanko, L. V. Ektova, N. A. Orlova, V. A. Loskutov, E. V. Vasil'iev, E. V. Karpova// Polymer Science Series B, 2016, V. 58, N 5, pp 519-528 doi:10.1134/S1560090416050109, IF=0.736
Remains of tapestry from a Xiongnu (Early 1st Century AD) Burial in Mound 22 at Noin-Ula/ N.V. Polosmak, E.A. Karpova// ARCHAEOLOGY ETHNOLOGY AND ANTHROPOLOGY OF EURASIA,, 2016, V/. 44 № 4 , Pp.76-82 doi:10.17746/1563-0110.2016.44.4.076-082
A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, A.O. Sutyrina, I.Yu. Bagryanskaya, P.M. Tolstoy, A.L. Gushchin, A.S. Mazur, N.K. Gusarova, B.A. Trofimov
Luminescent CuI thiocyanate complexes based on tris(2-pyridyl)phosphine and its oxide: from mono-, di- and trinuclear species to coordination polymers
New J. Chem., 2016,40, 10028-10040 doi:10.1039/C6NJ02087A, IF=3.276
S.I. Zhivetyeva, O.D. Zakharova, L.P. Ovchinnikova, D.S. Baev, I.Yu. Bagryanskaya, V.D. Shteingarts, T.G. Tolstikova, G.A. Nevinsky, E.V. Tretyakov
Phosphonium betaines derived from hexafluoro-1,4-naphthoquinone: Synthesis and cytotoxic and antioxidant activities
Journal of Fluorine Chemistry, V. 192, Part A, December 2016, Pp 68-77 doi:10.1016/j.jfluchem.2016.10.014, IF=2.213
T.V. Mezhenkova, V.M. Karpov, I.V. Beregovaya, Ya.V. Zonov, I.P. Chuikov, V.E. Platonov
Generation of perfluorinated 1-alkylbenzocyclobuten-1-yl and 1-alkylindan-1-yl cations. On paradoxical stabilizing influence of an electron-withdrawing perfluoroisopropyl group on the relative stabilities of the cations
Journal of Fluorine Chemistry, 2016, V. 192, Part A, Pp 31-40 doi:10.1016/j.jfluchem.2016.10.009, IF=2.213
G. Audran, E. Bagryanskaya, I. Bagryanskaya, P. Bremond, M. Edeleva, S.R. Marque, D. Parkhomenko, E. Tretyakov, S. Zhivetyeva
C-ON bond homolysis of alkoxyamines triggered by paramagnetic copper(II) salts
Inorg. Chem. Front., 2016,3, 1464-1472 doi:10.1039/C6QI00277C, IF=4.532
T. Khomenko, A. Zakharenko, T. Odarchenko, H.J. Arabshahi, V. Sannikova, O. Zakharova, D. Korchagina, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
New inhibitors of tyrosyl-DNA phosphodiesterase I (Tdp 1) combining 7-hydroxycoumarin and monoterpenoid moieties
Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pp 5573-5581 doi:10.1016/j.bmc.2016.09.016, IF=2.923
O.S. Patrusheva, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, S.A. Boldyrev, I.V. Ilyina, S.Yu. Kurbakova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
Anti-influenza activity of monoterpene-derived substituted hexahydro-2H-chromenes
Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pages 5158-5161 doi:10.1016/j.bmc.2016.08.037, IF=2.923
T.E. Kokina, L.A. Glinskaya, A.V. Tkachev, V.F. Plyusnin, Yu.V. Tsoy, I.Yu. Bagryanskaya, E.S. Vasilyev, D.A. Piryazev, L.A. Sheludyakova, S.V. Larionov
Chiral zinc(II) and cadmium(II) complexes with a dihydrophenanthroline ligand bearing (-)-α-pinene fragments: synthesis, crystal structures and photophysical properties
Polyhedron, 2016, V. 117, 15 October 2016, Pp 437-444 doi:10.1016/j.poly.2016.06.018, IF=2.108
Chromosomal localization of aromatic alcohol dehydrogenase fast-migrating isoenzyme Aadh1F (CAD1-F) gene in Triticum aestivum L. bread wheat/ A. A. Konovalov, I.K. Shundrina, E. V. Karpova, N. P. Goncharov, E. Ya. Kondratenko// Russian Journal of Genetics, October 2016, V. 52, N 10, pp 1110-1116 doi:10.1134/S1022795416080056
A.S. Kihkentayeva, E.E. Shults, Yu.V. Gatilov, S.S. Patrushev, S. Karim, G.A. Atazhanova, S.M. Adekenov
Synthetic Transformations of Sesquiterpene Lactones 10*. Synthesis of 13-Arylguaianolides
Chemistry of Heterocyclic Compounds, October 2016, V. 52, N 10, pp 788-796 doi:10.1007/s10593-016-1967-7, IF=0.815
1-Bromo-3,3,3-trifluoro-1-nitropropene: Synthesis and reaction with phenyl azide/ N. A. AnisimovaEmail authorE. K. SlobodchikovaA. A. KuzhaevaE. V. Stukan’I. Yu. BagryanskayaV. M. Berestovitskaya// Russian Journal of Organic Chemistry, October 2016, Volume 52, Issue 10, pp 1379-1384 doi:10.1134/S1070428016100018, IF=0.759
Formation of ω-(4-oxo-1,4-dihydropyridin-2-yl)alkanamides in the Beckmann rearrangement of spiro-fused cycloalkanone oximes/ V. A. Savel'ev, A. Ya. Tikhonov, T. V. Rybalova// Russian Journal of Organic Chemistry, October 2016, Volume 52, Issue 10, pp 1379-1384 doi:10.1134/S1070428016100134, IF=0.759
M.S. Kazantsev, E.S. Frantseva, L.G. Kudriashova, V.G. Konstantinov, A.A. Mannanov, T.V. Rybalova, E.V. Karpova, I.K. Shundrina, G.N. Kamaev, M.S. Pshenichnikov, E.A. Mostovich, D.Yu. Paraschuk
Highly-emissive solution-grown furan/phenylene co-oligomer single crystals
RSC Adv., 2016,6(95), 92325-92329 doi:10.1039/C6RA23160H, IF=3.289
A.B. Burdukov, M.A. Vershinin, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, A.S. Belov, Ya.Z. Voloshin, A.A. Nefedov
Using Minisci Reaction for Modification of the tris-Dioximate Metal Clathrochelates: Free-Radical Substitution at the Glyoximate Fragment of an Iron(II)-Encapsulating Cage Framework
Macroheterocycles, 2016, 9(4), 413-417 doi:10.6060/mhc161182b, IF=0.804
A.B. Burdukov, R. Sipos, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, M.A. Vershinin, E.G. Boguslavsky, D.B. Kal'nyi,S. L. Selektor, A.V. Shokurov,Ya. Z. Voloshin, A.A. Nefedov
Synthesis, X-Ray Structure and (Spectro)electrochemical Study of an Electrochromic Iron(II) Chlathrochelate with Tuned Redox Properties
Macroheterocycles 2016 9(3) 257-262 doi:10.6060/mhc160537b, IF=0.804
A.V. Pavlova, E.V. Nazimova, O.S. Mikhal'chenko, I.V. Il'ina, D.V. Korchagina, O.V. Ardashov, E.A. Morozova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
Synthesis and Analgesic Activity of 4,7-Dimethyl-3,4,4a,5,8,8a-Hexahydro-2H-Chromen-4,8-Diols Containing Thiophene Substituents
Chemistry of Natural Compounds, , 2016, V. 52, N 5, pp 813-820 doi:10.1007/s10600-016-1785-2, IF=0.472
E.P. Talsi, T.V. Rybalova, K.P. Bryliakov
Ti-Salalen Mediated Asymmetric Epoxidation of Olefins with H₂O₂: Effect of Ligand on the Catalytic Performance, and Insight into the Oxidation Mechanism
Journal of Molecular Catalysis A: Chemical, 2016, V. 421, 2016, Pages 131-137 doi:10.1016/j.molcata.2016.05.019, IF=3.957
G.I. Borodkin, I.R. Elanov, Yu.V. Gatilov, V.G. Shubin
Promotional effect of ionic liquids in electrophilic fluorination of methylated uracils
RSC Advances, 2016, V. 6, N 6, Pp 60556-60564 doi:10.1039/C6RA10850D, IF=3.289
A. Sokolova, A. Pavlova, N. Komarova, O. Ardashov, A. Shernyukov, Yu. Gatilov, O. Yarovaya, T. Tolstikova, N. Salakhutdinov
Synthesis and analgesic activity of new α-truxillic acid derivatives with monoterpenoid fragments
Medicinal Chemistry Research, 2016, V. 25, N 8, pp 1608-1615 doi:10.1007/s00044-016-1593-z, IF=1.435
Ya.V. Zonov, V.M. Karpov, T.V. Mezhenkova, T.V. Rybalova, Yu.V. Gatilov, V.E. Platonov
Transformations of perfluorinated 1,2-dialkyl-, 1,1- and 1,2-alkylphenylbenzocyclobutenes to indan-2-one and isochromene derivatives under the action of CO/SbF5
Journal of Fluorine Chemistry, 2016, V. 188, August 2016, Pp 117-125 doi:10.1016/j.jfluchem.2016.06.014, IF=2.213
A.G. Potapov, I.K. Shundrina
The influence of different fillers on mechanical and physical properties of high-molecular-weight biodegradable aliphatic polyesters
Polymer Science Series A, July 2016, V. 58, N 4, pp 585-592 doi:10.1134/S0965545X1604012X, IF=0.759
L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, O.A. Tarasova, V.A. Shagun, I.Yu. Bagryanskaya, B.A. Trofimov
Unexpected acid-catalyzed ferrocenylmethylation of diverse nucleophiles with vinyloxymethylferrocene
Tetrahedron, 2016, V. 72, N 29, Pp 4414-4422 doi:10.1016/j.tet.2016.06.012, IF=2.644
O.P. Korobeinichev, M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, Y. Hu
Counterflow flames of ultrahigh-molecular-weight polyethylene with and without triphenylphosphate
Combustion and Flame, 2016, V. 169, July 2016, Pp 261-271 doi:10.1016/j.combustflame.2016.04.019, IF=4.168
A.M. Sheveleva, M.Yu. Ivanov, I.K. Shundrina, A.D. Bukhtoyarova, E.G. Bagryanskaya, M.V. Fedin
Continuous Wave and Time-Resolved Electron Paramagnetic Resonance Study of Photoinduced Radicals in Fluoroacrylic Porous Polymer Films
J. Phys. Chem. C, 2016, 120 (27), Pp 14767-14773 doi:10.1021/acs.jpcc.6b05016, IF=4.508
E. Nazimova, A. Pavlova, O. Mikhalchenko, I. Il'ina, D. Korchagina, T. Tolstikova, K. Volcho, N. Salakhutdinov
Discovery of highly potent analgesic activity of isopulegol-derived (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol
Medicinal Chemistry Research, 2016, V. 25, N 7, pp 1369-1383 doi:10.1007/s00044-016-1573-3, IF=1.435
Synthesis of polyfluorinated A3B tetraoxacalix[4]arenes/ V.N. Kovtonyuk, Yu.V. Gatilov// Russian Journal of Organic Chemistry, 2016, V. 52, N 7, pp 946-949 doi:10.1134/S1070428016070046, IF=0.759
A.V. Artem'ev, N.K. Gusarova, A.O. Sutyrina, Y.V. Gatilov, B.A. Trofimov
Synthesis of tris[2-(2-furyl)ethyl]phosphine its chalcogenides and PdII complex
Mendeleev Communications, 2016, V. 26, N 4, Pp 314-316 doi:10.1016/j.mencom.2016.07.016, IF=1.404
D.S. Baranov, Y.V. Gatilov
Cyclization of 2-(3-R-prop-2-ynyloxy)-4-phenyliminonaphthalen- 1(4H)-ones into 2-R-methylidene-6-phenylamino-2,3-dihydronaphtho[2,1-b]-1,4-dioxines
Mendeleev Communications, 2016, V. 26, N 4, Pp 282-284 doi:10.1016/j.mencom.2016.07.004, IF=1.404
A.V. Artem'ev, N.K. Gusarova, I.Yu. Bagryanskaya, Yu.V. Gatilov, A.O. Sutyrina
First heteroleptic diselenophosphinate and thioselenophosphinate nickel(II) complexes with N-donor co-ligands
Polyhedron, V. 111, 17 June 2016, Pp 79-85 doi:10.1016/j.poly.2016.03.024, IF=2.108
E. Karpova, V. Vasiliev, V. Mamatyuk, N. Polosmak, L. Kundo
Xiongnu burial complex: A study of ancient textiles from the 22nd Noin-Ula barrow (Mongolia, first century AD)
Journal of Archaeological Science, V. 70, June 2016, Pp 15-22 doi:10.1016/j.jas.2016.04.001, IF=2.255
M.E. Mironov, I.Yu. Bagryanskaya, E.E. Shults
Synthesis of 3-trimethylsiloxy-1-(furan-3-yl)butadiene and its reactions with dienophiles
Chemistry of Heterocyclic Compounds, , 2016, V. 52, N 6, pp 364-373 doi:10.1007/s10593-016-1897-4, IF=0.814
Structure of molecular cocrystals of 18-crown-6 and polyhalogeno-meta-phenylenediamines/ T. A. Vaganova, Yu. V. Gatilov, V. I. Rodionov, E. V. Malykhin// Journal of Structural Chemistry, 2016, V. 57, N 6, pp 1225-1234 doi:10.1134/S002247661606024X, IF=0.536
Reaction of aryl(diarylphosphoryl)methanols with alkyl propiolates. Regio- and stereoselective synthesis of functional vinyl ethers/ N. I. Ivanova, P. A. Volkov, K. O. Khrapova, L. I. Larina, I. Yu. Bagryanskaya, N. K. Gusarova, B. A. Trofimo// Russian Journal of Organic Chemistry, June 2016, V. 52, N. 6, pp 772-776 doi:10.1134/S1070428016060026, IF=0.759
L.S. Konstantinova, I.V. Baranovsky, I.G. Irtegova, I.Y. Bagryanskaya, L.A. Shundrin, A.V. Zibarev, O.A. Rakitin
Fused 1,2,3-Dithiazoles: Convenient Synthesis, Structural Characterization, and Electrochemical Properties
Molecules 2016, 21(5), 596 doi:10.3390/molecules21050596, IF=2.464
Valve-containing xenovenous conduit: terra incognita or tabula rasa?/ I.Yu. Zhuravleva, E.V. Karpova, E.V. Kuznetsova, A.S. Yunoshev, A.A. Korobeynikov, T.P. Timchenko, N.R. Nichay, I.A. Soynov, A.V. Gorbatykh// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 90-101
Structure of ultrahigh molecular weight polyethylene-air counterflow flame/ M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev// Combustion, Explosion, and Shock Waves, May 2016, V. 52, N 3, pp 260-272 doi:10.1134/S0010508216030023, IF=0.604
I.V. Kulakov, D.N. Ogurtsova, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov
Synthesis and structure of novel ylidene derivatives of methanobenzo[g]thiazolo[2,3-d][1,3,5]oxadiazocine
Chemistry of Heterocyclic Compounds, 2016, V. 52, N. 5, pp 331-336 doi:10.1007/s10593-016-1886-7, IF=0.814
S.M. Adekenov, A.I. Makubaeva, D.N. Kokkozov, E.N. Kanafin, V.S. Korneev, Yu.V. Gatilov, A.S. Kishkentaeva, G.A. Atazhanova
Chemical Composition of Artemisia aralensis
Chemistry of Natural Compounds, 2016, V. 52, N3, pp 417-420 doi:10.1007/s10600-016-1662-z, IF=0.472
I.V. Il'ina, K.P. Volcho, D.V. Korchagina, N.F. Salakhutdinov
The Convenient Way for Obtaining Geranial by Acid-Catalyzed Kinetic Resolution of Citral
Helvetica Chimica Acta, 2016, V. 99, N 5, Pp 373-377 doi:10.1002/hlca.201500266, IF=1.87
O.S. Mikhalchenko, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
A practical way to synthesize chiral fluoro-containing polyhydro-2H-chromenes from monoterpenoids
Beilstein J. Org. Chem. 2016, 12, 648-653 doi:10.3762/bjoc.12.64, IF=2.697
I.Yu. Bagryanskaya, L.V. Politanskaya, E.V. Tretyakov
Frequently used, but still unknown: Terbium(III) tris-hexafluoroacetylacetonate dihydrate
Inorganic Chemistry Communications, April 2016, V. 66, Pp 47-50 doi:10.1016/j.inoche.2016.02.009, IF=1.761
Supramolecular architecture of crystals of perfluorinated 3-alkylphthalides/ T. V. Rybalova, Yu. V. Gatilov, Ya. V. Zonov, V. M. Karpov// Journal of Structural Chemistry, 2016, V. 57, N 4, pp 777-783 doi:10.1134/S0022476616040223, IF=0.536
V.I. Supranovich, A.Yu. Vorob'ev, G.I. Borodkin, Yu.V. Gatilov, V.G. Shubin
Study on selectivity in the reaction of 2-substituted pyridinium-N-imines with dimethyl acetylenedicarboxylate
Tetrahedron Letters, V. 57, N 10, 9 March 2016, Pp 1093-1096 doi:10.1016/j.tetlet.2016.01.092, IF=2.346
G.A. Selivanova, E.V. Tretyakov, E.V. Amosov, I.Yu. Bagryanskaya, V.G. Vasiliev, E.V. Vasilyev, V.D. Tikhova, E.V. Karpova, T.V. Basova, D.V. Stass, V.D. Shteingarts
X-Ray induced phase transitions in 4-((4-(dibutylamino)phenyl)diazenyl)-biphenyl-2,3',4'-tricarbonitrile
Journal of Molecular Structure, V. 1107, 5 March 2016, Pp 242-248 doi:10.1016/j.molstruc.2015.11.060, IF=1.779
T.P. Kukina, O.I. Sal'nikova, N.K. Khidyrova, M.D. Rakhmatova, N.A. Pankrushina, A.E. Grazhdannikov
Aliphatic and Terpene Constituents of Alcea nudiflora Extracts
Chemistry of Natural Compounds, 2016, V.52, N 2, pp 285-287 doi:10.1007/s10600-016-1615-6, IF=0.472
T.F. Mikhailovskaya, A.G. Makarov, N.Yu. Selikhova, A.Yu. Makarov, E.A. Pritchina, I.Yu. Bagryanskaya, E.V. Vorontsova, I.D. Ivanov, V.D. Tikhova, N.P. Gritsan, Y.G. Slizhov, A.V. Zibarev
Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine
Journal of Fluorine Chemistry, V. 183, March 2016, Pp 44-58 doi:10.1016/j.jfluchem.2016.01.009, IF=2.213
D.V. Trukhin, O.Yu. Rogozhnikova, T.I. Troitskaya, V.G. Vasiliev, M.l K. Bowman, V.M. Tormyshev
Facile and High-Yielding Synthesis of TAM Biradicals and Monofunctional TAM Radicals
Synlett, 2016, 27(06), Pp 893-899 doi:10.1055/s-0035-1561299, IF=2.322
D.S. Baranov, D.S. Fadeev
Synthesis of 2-octyloxy-7H-benzo[e]perimidin-7-one and 3-substituted 3H-benzo[e]perimidine-2,7-diones
Mendeleev Communications, V. 26, N 2, March-April 2016, Pp 174- 176 doi:10.1016/j.mencom.2016.03.032, IF=1.404
S.P. Babailov, P.A. Stabnikov, I.V. Korolkov, N.V. Pervukhina, O.S. Koshcheeva, I.P. Chuikov
Structure and Paramagnetic Properties of Tris-Pivaloyltrifluoracetonate Thulium(III) Complexes with 18-Crown-6 by X-Ray Analysis and NMR
Polyhedron, V.105, 17 February 2016, Pp 178-185 doi:10.1016/j.poly.2015.12.014, IF=2.108
M.A. Timoshenko, Yu.V. Kharitonov, M.M. Shakirov, I.Yu. Bagryanskaya, E.E. Shults
Synthetic Studies on Tricyclic Diterpenoids: Direct Allylic Amination Reaction of Isopimaric Acid Derivatives
ChemistryOPEN, V. 5, N 1, pp 65-70, February 2016 doi:10.1002/open.201500187, IF=3.585
Т.П. Кукина, Д.Н. Щербаков, К.В. Геньш, Е.А. Тулышева, О.И. Сальникова, А.Е. Гражданников, Е.А. Колосова
Биоактивные компоненты древесной зелени облепихи HIPPOPHAE RHAMNOIDES L.
Химия растительного сырья. 2016. № 1. С. 37-42. doi:10.14258/jcprm.2016011100
Reaction of 3-(R-methylidene)-2-ethoxylindolenines with N,N'-binucleophiles/ V. P. Borovik, Yu. V. Gatilov, O. P. Shkurko// Russian Journal of Organic Chemistry, 2016, V. 52, N 2, pp 228-234 doi:10.1134/S1070428016020123, IF=0.759
D.S. Fadeev, I.P. Chuikov, V.I. Mamatyuk
A study of NMR parameters of para-substituted polyfluorinated benzyl cations and their precursors
Journal of Fluorine Chemistry, V. 182, February 2016, Pp 53-60 doi:10.1016/j.jfluchem.2015.12.003, IF=2.213
B.A. Trofimov, L.V. Andriyankova, L.P. Nikitina, K.V. Belyaeva, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
(Imidazol-2-yl)methyl-1,3-propanediones: Regioselective C–H Functionalization of the Imidazole Ring by Acylacetylene/Aldehyde Pairs
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2016, V. 2016, N 6, Pp 1199-1204 doi:10.1002/ejoc.201501617, IF=3.68
B.A. Trofimov, L.P. Nikitina, K.V. Belyaeva, L.V. Andriyankova, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
Insertion of 1,3-diphenylprop-2-yn-1-one into imidazo[4,5-b]pyridines in the presence of water: one-pot synthesis of pyrido[2,3-b][1,4]diazocin-9-ones
Mendeleev Communications, 2016, V.26, N 1, Pp 16-18 doi:10.1016/j.mencom.2016.01.007, IF=1.404
A.V. Artem'ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, B.G. Sukhov, A.O. Sutyrina, E.A. Matveeva, S.F. Vasilevsky, A.I. Govdi, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
Reaction of elemental phosphorus with &alpa;-methylstyrenes: one-pot synthesis of secondary and tertiary phosphines, prospective bulky ligands for Pd(II) catalysts
Tetrahedron, V. 72, N 4, 28 January 2016, Pp 443-450 doi:10.1016/j.tet.2015.11.009, IF=2.644
Y.V. Tarasenko, T.V. Abramova, V.I. Mamatuk, V.N. Silnikov
Effective Synthesis of Fluorescently Labeled Morpholino Nucleoside Triphosphate Derivatives
Nucleosides, Nucleotides and Nucleic Acids, 2016, V. 35, N 1, Pp 32-42 doi:10.1080/15257770.2015.1114125, IF=0.875
A.V. Shernyukov, A.M. Genaev, G.E. Salnikov, H.S. Rzepa, V.G. Shubin
Noncatalytic bromination of benzene: A combined computational and experimental study
Journal of Computational Chemistry, V. 37, N 2, 15 January 2016, Pp 210-225 doi:10.1002/jcc.23985, IF=3.648
Microwave-Assisted Synthesis of Phthalocyanine Zinc Complexes Derived from Aminotricyanobiphenyl-Based Azo Dyes/ G.A. Selivanova, E. V. Amosov, V. G. Vasilyev, E. A. Lukyanets, E. V. Tretyakov, V.D. Shteingarts// Macroheterocycles 2016 9(1) 80-88 doi:10.6060/mhc151192s, IF=0.804
А.Н. Блазнов, Е.В. Атясова, Н.В. Бычин, И.К. Шундрина, Н.Н. Ходакова, В.В. Самойленко
Влияние степени отверждения связующего на температуру стеклования композитных материалов
Южно-Сибирский научный вестник, 2016, № 1 (13), С. 13-20.
A.V. Artem'ev, N.A. Chernysheva, S.V. Yas'ko, N.K. Gusarova, I.Yu. Bagryanskaya, B.A. Trofimov
Straightforward Solvent-Free Synthesis of Tertiary Phosphine Chalcogenides from Secondary Phosphines, Electron-Rich Alkenes, and Elemental Sulfur or Selenium
HETEROATOM CHEMISTRY, V. 27, N 1, 2016, Pp. 48-53 doi:10.1002/hc.21300, IF=1.202
M.B. Bushuev, D.P. Pishchur, V.A. Logvinenko, Yu.V. Gatilov, I.V. Korolkov, I.K. Shundrina, E.B. Nikolaenkova, V.P. Krivopalov
A mononuclear iron(II) complex: cooperativity, kinetics and activation energy of the solvent-dependent spin transition
Dalton Trans., 2016,45(1), 107-120 doi:10.1039/C5DT03750F, IF=4.177
S.P. Babailov, I.P. Chuikov, A.I. Kruppa
Activation Energies of Intermolecular Dynamics in Ethylenediaminetetraacetate Complexes with Lanthanides: An Effect of the “Gadolinium Break”
Inorganica Chimica Acta, V. 439, 1 January 2016, Pp 117-122 doi:10.1016/j.ica.2015.10.009, IF=1.917
И.Г. Боярских, А.И. Сысо, В.Г. Васильев, Т.И. Сиромля
Содержание полифенольных соединений, микро- и макроэлементов в стеблях и листьях LONICERA CAERULEA SUBSP. PALLASII (CAPRIFOLIACEAE)
Растительные ресурсы. 2016. Т. 52. № 1. С. 135-150

DEVICES:

1. Group of Nuclear Magnetic Resonance (GNMR)

- спектроскопия ядерного магнитного резонанса (ЯМР)>
- спектроскопия электронного парамагнитного резонанса (ЭПР) и ЭПР-томография

Devices:

Bruker Avance 300
Bruker Avance 400
Bruker Avance 600
Bruker DRX 500

2. Group of mass spectrometry (GMS)

- газовая хроматография
- газовая хромато-масс-спектроскопия (с приставкой термодесорбции)
- жидкостная хроматография
- жидкостная хромато-масс-спектрометрия

Devices:

Agilent LC 1100 DAD
Agilent LC 1200 + Bruker micro TOF-Q
Agilent LC 1100 + MSD G2707
Agilent 7200 GC-QTOF
Agilent GC-MSD 6890/5973
HP GC-MSD 5890/5971
Thermo Electron DFS GC-MS

3. Group of Optical Spectrometry (GOS)

- ИК-Фурье и КР- спектроскопия
- УФ-Вид спектроскопия
- флуоресцентная спектроскопия
- поляризационная спектроскопия
- электронная микроскопия (с приставкой термодесорбции и элементным анализатором)

Devices:

Varian Cary Eclipse Optical Activity PolАAr 3005
Electron microscope Hitachi ТМ-1000 + EDS SFIFT
Bruker IR+IR-microscope
Vector 22 + IFS-66
Bruker Raman Sеnterra
НР Uv-Vis 8453А DAD
Varian Uv-Vis-NIR Cary 5000
Varian Cary Eclipse
Optical Activity PolАAr 3005
Electron microscope Hitachi ТМ-1000 + EDS SFIFT

4. Group of X-ray analysis (GXRA)

- X- ray diffraction analysis

Devices:

Bruker X-ray САРРА-АРЕХ
Bruker X-ray P4

5. Group of thermal analysis (GTA)

- thermal analysis: thermogravimetry and differential scanning calorimetry
- dynamic thermomechanical analysis

Devices:

Thermoanalyzer STA 409
Dynamic mechanical DMA-2420

6. Group of service of scientific equipment (GSSE)

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Department of physical organic chemistry

Purpose:

1. Group of Nuclear Magnetic Resonance (GNMR)

2. Group of mass spectrometry (GMS)

3. Group of Optical Spectrometry (GOS)

4. Group of X-ray analysis (GXRA)

5. Group of thermal analysis (GTA)

Laboratory staff publications (DB NIOCh)

1. Group of Nuclear Magnetic Resonance (GNMR)

2. Group of mass spectrometry (GMS)

3. Group of Optical Spectrometry (GOS)

4. Group of X-ray analysis (GXRA)

5. Group of thermal analysis (GTA)

6. Group of service of scientific equipment (GSSE)

Scientific Departments