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N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry
Siberian Branch of Russian Academy of Science

 

Department of Medicinal Chemistry

salahutdinov


Head - Corresponding Member of the Russian Academy of Sciences,
Doctor of Chemical Sciences, Professor
Nariman F. Salakhutdinov

phone +7 (383) 330-97-33,
Fax: +7 (383) 330-97-52,
internal phone: 3-75,
email:This email address is being protected from spambots. You need JavaScript enabled to view it.

Short history

Laboratory of physiologically active substances (up to 2012 – Laboratory of forest chemistry and natural biologically active compounds) was established as a division of the Department of Medical Chemistry, Novosibirsk Institute of Organic Chemistry SB RAS. Its personnel is based on the staff of the laboratory of cationic reactions NIOCh SB RAS (before 2004 – head Prof. V. A. Barkhash). At present, it is a unit equipped with modern scientific instruments and personnel of  high qualification. The staff of the lab has 20 employees, including two full professors and 14 PhD’s.


 

Research areas:

Research areas:



The major scientific trends

 

  • Development of new leading compounds in the most popular therapeutic areas – oncology, cardiovascular diseases, neurodegenerative diseases, analgesics, and infectious disease.
  • Reactivity study of monoterpenoids in the presence of heterogeneous catalysts. Development of effective methods of catalytic conversions of organic compounds in supercritical fluids.
  • Development of methods for the stereoselective synthesis, including new catalytically asymmetric systems.
  • Directed chemical modification of metabolites of plant and animal origin in order to obtain new semisynthetic derivatives of valuable biological properties.
  • The study of Siberian and Altai plants as a scientific basis for the development of Russian medical and preventive medications.

 

Main scientific results

 

  • A new promising agent for the treatment of Parkinson's disease, who is at the stage of pre-clinical trials, was developed. Based on polysulfur compounds, an agent having high antidepressant activity, superior to that of some commercial products, was created. Compounds perspective for the development of a new structural type of analgesics, anticonvulsants were found.
  • As a result of the reactivity study of the usnic acid which is a metabolite of a number of lichens, new highly active anti-TB and anti-influenza agents have been developed.
  • New catalytic systems for the asymmetric oxidation of sulfides to sulfoxides and asymmetric chiral addition of diethylzink to aldehydes were created. Patent collision-free methods of asymmetric synthesis of the modern anti-ulcer drug "Esomeprazole" with the use of original catalytic systems were developed.
  • As a result of phytochemical studies it was found that the roots of barberry Berberis sibirica Pall, both natural and introduced populations growing in Russia, are a practical source of isoquinoline alkaloid berberine. A technique which allows the isolation of berberine chloride with the yield up to 0.62% on the dry weight of roots was developed and patented. A review summarizing the reactions of berberine and its hydrogenated derivatives, as well as information on the biological activity of berberine and some of its derivatives was published. Methods of the direct introduction of bromine and iodine in the molecule of berberine were developed in first time.
  • New semisynthetic derivative of glycyrrhetic acid, methyl soloksolon, having anticancer and anti-inflammatory activities was obtained. Its preclinical in vitro and in vivo tests have shown a high potential of this compound as a high-performance low-toxic agent in the drug development.
  • Chemical transformations of stilbene glycosides, resveratroloside and pinostilbenoside  were performed and their derivatives were obtained. It was found that resveratroloside had cardioprotective properties comparable to those of resveratrol.

 

List of priority investigations

 

  • Scientific basis of isolation technologies of plant metabolites of Siberian flora as a raw material source promising synthons for medicinal chemistry and pharmaceutical industries.
  • Synthetic transformation of plant alkaloids, terpenoids and coumarins. The total synthesis of the substances of high pharmacological importance

 

Current projects

  • RFBR Projects:
    • Creation of a basic foundation for the development of technological methods for the synthesis of physiologically active compounds from the available monoterpenoids using supercritical solvents (11-08-00171-a);
    • Creation of anti-cancer polysulfide compounds PPAR1 inhibitors (11-04-12099-ofi-m-2011);
    • The study of the fundamental laws of interaction of monoterpenoids with aromatic aldehydes to detect antiparkinsonian agents of a new structural type (11-03-00010-a);
    • Identification of the fundamental laws of the reactivity of pinane terpenoids in the presence of acidic crystalline aluminosilicate catalysts to discover new pharmacologically active compounds (10-03-00230-a);
    • The development of selective functionalization methods of (1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol at the methyl groups to study the effects of substituents on the antiparkinsonian activity (12-03-31257 mol_a);
    • The reactivity study of carbonyl compounds of monoterpene type in the reactions with different nitrogen-containing derivatives of adamantane to find new anxiolytic agents (12-03-31392 mol_a). Integration projects:
    • A study of genetic and neurophysiological mechanisms of actions of the brain-derived neurotrophic factor and its synthetic agonists);
    • A study of metabolites of marine and plant origin as a scientific basis for the development of important drugs;
    • Integration project of SB RAS on partner basic research No 30 (2012-2013 years) "Development of long-acting form of the neurotoxin to relieve arrhythmia on in vivo model of atrial fibrillation";
    • Search and creation of products for cancer therapy based on modified natural compounds.
  • RAS and SB RAS presidium programmes:
    • The origin of life and the formation of the biosphere (Natural clays as catalysts for prebiotic reactions of chiral compounds);
    • Development of effective anticancer agents based on modified natural triterpene acids (the program "Basic Sciences for Medicine" of SB RAS);
    • Expedition project "Survey of plants of Siberia and Altai as a scientific basis for the development of domestic medicinal and preventive drugs." State contract.
    • "Preclinical studies of TB drugs based on semi-synthetic derivatives of usnic acid" (within the Federal Target Program "Development of the medical and pharmaceutical industry of the Russian Federation for the period up to 2020 and beyond"). 12411.1008799.13.002 (2012).

 

 






STAFF


Staff

Employee Position Room Phone Phone in. email Publications
by years
1 Salakhutdinov Nariman Faridovich Head of Depart. (Doct. Chem.) 310 НТК 330-97-33 3-75 This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Volcho Konstantin Petrovich Chief Researcher (Doct. Chem.) 129, 311 НТК 330-88-70 3-96, 3-01 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Lavrik Olga Ivanovna Chief Researcher (Doct. Chem.)
4 Luzina Olga Anatolievna Leading Researcher (Doct. Chem) 204 330-88-70 2-57, 2-21 This email address is being protected from spambots. You need JavaScript enabled to view it.
5 Yarovaya Olga Ivanovna Leading Researcher (Doct. Chem) 205 330-88-70 2-25 This email address is being protected from spambots. You need JavaScript enabled to view it.
6 Ardashov Oleg Vasilievich Senior Researcher (Cand. Chem.) 129 330-88-70 3-96 This email address is being protected from spambots. You need JavaScript enabled to view it.
7 Il'ina Irina Viktorovna Senior Researcher (Cand. Chem.) 129 330-88-70 3-96 This email address is being protected from spambots. You need JavaScript enabled to view it.
8 Rogachev Artem Dmitrievich Senior Researcher (Cand. Chem.) 330 330-97-47 2-36 This email address is being protected from spambots. You need JavaScript enabled to view it.
9 Salomatina Oksana Vladimirovna Senior Researcher (Cand. Chem.) П-042 330-88-70 2-55 This email address is being protected from spambots. You need JavaScript enabled to view it.
10 Sokolova Anastasiya Sergeevna Senior Researcher (Cand. Chem.) 205 330-88-70 2-25 This email address is being protected from spambots. You need JavaScript enabled to view it.
11 Khomenko Tatyana Mikhailovna Senior Researcher (Cand. Chem.) 103 330-88-70 4-46 This email address is being protected from spambots. You need JavaScript enabled to view it.
12 Dyrkheeva Nadezda Sergeevna Researcher (Cand. Chem.)
13 Zakharenko Alexandra Dmitrievna Researcher (Cand. Chem.)
14 Laev Sergey Sergeevich Researcher (Cand. Chem.) 409 НТК 2-38 This email address is being protected from spambots. You need JavaScript enabled to view it.
15 Nechepurenko Ivan Vasilievich Researcher (Cand. Chem.) 330 330-88-70; 8-983-124-30-49 2-36 This email address is being protected from spambots. You need JavaScript enabled to view it., This email address is being protected from spambots. You need JavaScript enabled to view it.
16 Patrusheva Oxana Stanislavovna Researcher (Cand. Chem.) 129 330-88-70 3-96 This email address is being protected from spambots. You need JavaScript enabled to view it.
17 Popadyuk Irina Igorevna Researcher (Cand. Chem.) П-042 330-88-70 2-55 This email address is being protected from spambots. You need JavaScript enabled to view it.
18 Fomenko Vladislav Viktorovich Researcher (Cand. Chem.) 302 330-97-47 2-02 This email address is being protected from spambots. You need JavaScript enabled to view it.
19 Komarova Nina Ivanovna Leading Engineer 308 330-97-47 2-84 This email address is being protected from spambots. You need JavaScript enabled to view it.
20 Kurbakova Svetlana Yurievna Leading Engineer 129 330-88-70 3-96 This email address is being protected from spambots. You need JavaScript enabled to view it.
21 Mainagashev Ilia Yakovlevich Leading Engineer 330 330-88-70 2-36 This email address is being protected from spambots. You need JavaScript enabled to view it.
22 Blokhin Mikhail Evgenievich engineer 204 330-88-70 2-21 This email address is being protected from spambots. You need JavaScript enabled to view it.
23 Vyazovkin Ivan Vladimirovich Leading Engineer
Students
24 Abdrakhmanova Veronika Sergeevna laboratory assistant
25 Baranova Darya Vitalievna laboratory assistant 205 330-88-70 2-25 This email address is being protected from spambots. You need JavaScript enabled to view it.
26 Okhina Alina Aleksandrovna laboratory assistant 330 330-88-70 2-36
27 Putilova Valentina Pavlovna laboratory assistant 205 330-88-70 2-25 This email address is being protected from spambots. You need JavaScript enabled to view it.
28 Mordvinova Ekaterina Borisovna laboratory assistant
PHD Students
29 Ivankin Dmitry Igorevich engineer 302, 330 330-97-47 2-02, 2-36 This email address is being protected from spambots. You need JavaScript enabled to view it.

PUBLICATIONS

Publications over the past years

 

Laboratory staff publications (DB NIOCh)

Reviews, Articles


2020
  1. 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, first published on 06 Aug 2020 doi:10.1039/D0MD00108B
  2. K. Kovaleva, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine-based thiazolidin-4-ones and 2-thioxoimidazolidin-4-ones as novel tyrosyl-DNA phosphodiesterase 1 inhibitors
    Molecular Diversity (2020), Published: 24 August 2020 doi:10.1007/s11030-020-10132-z, IF=2.13
  3. A.S. Sokolova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, N.S. Shcherbakova, A.V. Zaykovskaya, D.S. Baev, T.G. Tolstikova, D.N. Shcherbakov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Monoterpenoid-based inhibitors of filoviruses targeting the glycoprotein-mediated entry process
    European Journal of Medicinal Chemistry, 2020, V. 207, 112726 doi:10.1016/j.ejmech.2020.112726, IF=5.572
  4. Modulators of hematopoiesis disorders (a review)/ Salakhutdinov N. F., Laev S. S., Sergeevichev D. S.// Chemistry for Sustainable Development, 2020, V. 28, N 4, Pp. 343-365 doi:10.15372/KhUR2020239
  5. E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
    Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556
  6. 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
  7. O. Luzina, A. Filimonov, A. Zakharenko, A. Chepanova, O. Zakharova, E. Ilina, N. Dyrkheeva, G. Likhatskaya, N. Salakhutdinov, O. Lavrik
    Usnic Acid Conjugates with Monoterpenoids as Potent Tyrosyl-DNA Phosphodiesterase 1 Inhibitors
    Journal of Natural Products, 2020, 83, 8, 2320–2329 doi:10.1021/acs.jnatprod.9b01089, IF=3.779
  8. 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
  9. E.A. Kulikova, O.S. Kozhevnikova, A.V. Kulikov, N.G. Kolosova, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, D.V. Telegina
    Alterations of STEP46 and STEP61 Expression in the Rat Retina with Age and AMD-Like Retinopathy Development
    Int. J. Mol. Sci. 2020, 21(15), 5182 doi:10.3390/ijms21155182, IF=4.556
  10. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
    Changes in Amino Acid and Acylcarnitine Plasma Profiles for Distinguishing Patients with Multiple Sclerosis from Healthy Controls
    Multiple Sclerosis International, 2020, V. 2020, Art. Number 9010937 doi:10.1155/2020/9010937
  11. 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
  12. 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
  13. 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
  14. S.O. Kuranov, O.A. Luzina, O. Onopchenko, I. Pishel, S. Zozulya, M. Gureev, N.F. Salakhutdinov, M. Krasavin
    Exploring bulky natural and natural-like periphery in the design of p-(benzyloxy)phenylpropionic acid agonists of free fatty acid receptor 1 (GPR40)
    Bioorganic Chemistry Volume 99, June 2020, 103830 doi:10.1016/j.bioorg.2020.103830, IF=4.567
  15. Features of lipidomic profile of erythrocyte membranes and blood serum in patients with fatty liver disease/ Kkruchinina M.V., Parulikova M.V., Kurilovich S.A., Gromov A.A., Shashkov M.V., Sokolova A.S., Kruchinin V.N.// doi:10.15372/ATER20200202
  16. V.V. Chernyshov, O.I. Yarovaya, R.Yu. Peshkov, N.F. Salakhutdinov
    Synthesis of cyclic D-(+)-camphoric acid imides and study of their antiviral activity
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 763-768 doi:10.1007/s10593-020-02728-y, IF=1.491
  17. 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
  18. A.V. Markov, A.V. Sen'kova, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.I. Komarova, A.A. Ilyina, N.F. Salakhutdinov, M.A. Zenkova
    Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
    Int. J. Mol. Sci. 2020, 21(10), 3511 doi:10.3390/ijms21103511, IF=4.556
  19. A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
    Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
    ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853
  20. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
    Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
  21. 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
  22. Yu.S. Demidova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, A.A. Saraev, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
    Monoterpenoid Oximes Hydrogenation Over Platinum Catalysts
    Topics in Catalysis, 2020, V. 63, N 1-2, pages187-195 doi:10.1007/s11244-020-01234-x, IF=2.406
  23. 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
  24. A.D. Rogachev, D.V. Trebushat, A.N. Kudryashov, A.G. Pokrovsky
    Study of Sirolimus Adsorption and Preparation of Its Samples in Methanol, Acetonitrile and Their Mixtures with Water for HPLC-MS/MS Analysis
    Chromatographia, 2020, V. 83, N 2, pp 299-304 doi:10.1007/s10337-019-03835-5, IF=1.596
  25. 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
  26. Analytical Control of Impurities and Active Components in (-)-Isopulegol Derivative - Highly Potent Analgesic Agent/ Lastovka A.V, Fadeeva V.P., Il'ina I.V., Salakhutdinov N.F.// Pharmaceutical Chemistry Journal doi:10.1007/s11094-020-02176-0, IF=0.538
  27. 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
  28. E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
    Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
    Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073
  29. 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
  30. A.A. Okhina, A.D. Rogachev, O.I. Yarovaya, M.V. Khvostov, T.G. Tolstikova, A.G. Pokrovsky, V.A. Khazanov, N.F. Salakhutdinov
    Development and validation of an LC-MS/MS method for the quantitative analysis of the anti-influenza agent camphecene in rat plasma and its application to study the blood-to-plasma distribution of the agent
    Journal of Pharmaceutical and Biomedical Analysis, 2020, V. 180, 113039 doi:10.1016/j.jpba.2019.113039, IF=3.209

2019
  1. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
    Catalysis Letters, 2019, V. 149, N 12, pp 3454-3464 doi:10.1007/s10562-019-02958-6, IF=2.371
  2. 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
  3. 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
  4. A. Kulikov, N. Sinyakova, E. Kulikova, T. Khomenko, N. Salakhutdinov, V. Kulikov, K. Volcho
    Effects of Acute and Chronic Treatment of Novel Psychotropic Drug, 8- (Trifluoromethyl)-1, 2, 3, 4, 5-benzopentathiepin-6-amine Hydrochloride (TC-2153), on the Behavior of Zebrafish (Danio Rerio): A Comparison with Fluoxetine
    Letters in Drug Design & Discovery, 2019, V.16, N 12, Pp.1321-1328 doi:10.2174/1570180816666190221162952, IF=0.953
  5. O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
    Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
    Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447
  6. A. V.Lastovka,A. D.Rogachev,I. V.Il'ina,A.Kabir,K.P.Volcho,V. P.Fadeeva,A.G.Pokrovsky,N. F.Salakhutdinov,K. G.Furtonc
    Comparison of dried matrix spots and fabric phase sorptive extraction methods for quantitation of highly potent analgesic activity agent (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol in rat whole blood and plasma using LC–MS/MS
    Journal of Chromatography B, 2019, V. 1132, Art. Number 121813 doi:10.1016/j.jchromb.2019.121813, IF=2.789
  7. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
    Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
    UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
  8. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
    Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
  9. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
    Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
  10. 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
  11. Studying dependences between the chemotype structure of some natural compounds and the spectrum of their targeted activities correlated with the hypoglycemic effect/ P.M. Vasilyev, O.A. Luzina, D.A. Babkov, D.T. Appazova, N.F. Salakhutdinov, A.A. Spasov// J Struct Chem., 2019, V. 60, N 11, Pp 1827-1832 doi:10.1134/S0022476619110179, IF=0.541
  12. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  13. 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
  14. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
    Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
    Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394
  15. A.V. Markov, A.E. Kel, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: A transcriptome analysis
    Oncotarget, 2019, V. 10, N 51, Pp 5267-5297 doi:10.18632/oncotarget.27085
  16. E. Kulikova, N. Khotskin, N. Illarionova, I. Sorokin, K. Volcho, A. Kulikov
    The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
    IBRO Reports, V. 6, Supplement, September 2019, Page S492. P32.59 doi:10.1016/j.ibror.2019.07.1544
  17. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
    Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
    IBRO Reports, 2019, V. 6, Supplement, Page S115 doi:10.1016/j.ibror.2019.07.368
  18. K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
    Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256
  19. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
    Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868
  20. Synthesis and Hypoglycemic Activity of Aryl(Hetaryl)Propenoic Cyanopyrrolidine Amides/ S. O. Kuranov, M. E. Blokhin, S. A. Borisov, M. V. Khvostov, O. A. Luzina, N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, 2019, V. 45, N 5, pp 374-380 doi:10.1134/S1068162019050078, IF=0.794
  21. K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
    Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
    Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035
  22. A.V. Markov, V.O. Babich, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.F. Salakhutdinov, M.A. Zenkova
    Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
    Molecules 2019, 24(14), 2644 doi:10.3390/molecules24142644, IF=3.59
  23. 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
  24. M.V. Kruchinina, A.A. Gromov, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin
    Peculiarities of fatty acid profile of erythrocyte membranes in patients with resistant arterial hypertension: possible contribution to pathogenesis of the disease
    JOURNAL OF HYPERTENSION, 2019, V. 37 , Pp E108-E108, Sup. 1 (29th European Meeting of Hypertension and Cardiovascular Protection of the European-Society-of-Hypertension (ESH), Milan, ITALY, JUN 21-24, 2019) doi:10.1097/01.hjh.0000571388.53224.97
  25. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
    Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
    Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
  26. Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030, IF=0.636
  27. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
    Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
    Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
  28. 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
  29. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
    Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
    Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
  30. 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
  31. 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
  32. Synthesis of (1S)-(+)-camphor-10-sulfonic acid derivatives and investigations in vitro and in silico of their antiviral activity as the inhibitors of fi lovirus infections/ A. S. Sokolova, D. V. Baranova, O. I. Yarovaya, D. S. Baev, O. A. Polezhaeva, A. V. Zybkina, D. N. Shcherbakov, T. G. Tolstikova, N. F. Salakhutdinov// Russian Chemical Bulletin, 2019, V 68, N 5, pp 1041-1046 doi:10.1007/s11172-019-2517-0, IF=1.014
  33. 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
  34. 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
  35. 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
  36. Yu.N. Antonenko, L.S. Khailova, T.I. Rokitskaya, E.S. Nosikova, P.A. Nazarov, O.A. Luzina, N.F. Salakhutdinov, E.A. Kotova
    Mechanism of action of an old antibiotic revisited: Role of calcium ions in protonophoric activity of usnic acid
    Biochimica et Biophysica Acta (BBA) - Bioenergetics, V. 1860, N 4, 1 April 2019, Pp 310-316 doi:10.1016/j.bbabio.2019.01.005, IF=4.441
  37. Ju.A. Sidorova, K.P. Volcho, N.F. Salakhutdinov
    Neuroregeneration in Parkinson’s Disease: From Proteins to Small Molecules
    Current Neuropharmacology, 2019,V. 17 , N 3 , Pp. 268 - 287 doi:10.2174/1570159X16666180905094123, IF=4.568
  38. 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
  39. A.Kulikov,N.Sinyakova,E.Kulikova,N.Evglevsky,I.Kolotygin,K.Volcho,N.Salakhutdinov,V.Kulikov,A.Romaschenko,M.Moshkin
    Effects of acute and chronic treatment of STEP inhibitor, TC-2153, on the nervous system and behaviour of zebrafish (Danio rerio)
    European Neuropsychopharmacology, V. 29, Supplement 1, 2019, Pp S198-S199, P.216 doi:10.1016/j.euroneuro.2018.11.330, IF=4.468
  40. 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
  41. N. Dyrkheeva, O. Luzina, A. Filimonov, O. Zakharova, E. Ilina, A. Zakharenko, M. Kuprushkin, D. Nilov, I. Gushchina, V. Svedas, N. Salakhutdinov, O. Lavrik
    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
    Planta Medica, 2019, V. 85, N 2, Pp 103-111 doi:10.1055/a-0681-7069, IF=2.746
  42. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833

2018
  1. E.A. Kulikova, N.V. Khotskin, N.B. Illarionova, I.E. Sorokin, E.Y. Bazhenova, E.M. Kondaurova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, E. Ponimaskin, V.S. Naumenko, A.V. Kulikov
    Inhibitor of striatal-enriched protein tyrosine phosphatase, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), produces antidepressant-like effect and decreases functional activity and protein level of 5-HT2A receptor in the brain
    Neuroscience, 2018, V. 394, Pp 220-231 doi:10.1016/j.neuroscience.2018.10.031, IF=3.381
  2. 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
  3. 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
  4. V.V. Zarubaev, E.A. Pushkina, S.S. Borisevich, A.V. Galochkina, A.V. Garshinina, A.A. Shtro, A.A. Egorova, A.S. Sokolova, S.L. Khursan, O.I. Yarovaya, N.F. Salakhutdinov
    Selection of influenza virus resistant to the novel camphor-based antiviral camphecene results in loss of pathogenicity
    Virology, V. 524, November 2018, Pp 69-77 doi:10.1016/j.virol.2018.08.011, IF=3.374
  5. A.Yu. Sidorenko, I.V. Il'ina, A.V. Kravtsova, A. Aho, O.V. Ardashov, N.S. Li-Zhulanov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of chiral isobenzofurans from 3-carene in the presence of modified clays
    Molecular Catalysis, 2018, V. 459, Pp 38-45 doi:10.1016/j.mcat.2018.07.025
  6. Antimetastatic Activity of Combined Topotecan and Tyrosyl-DNA Phosphodiesterase-1 Inhibitor on Modeled Lewis Lung Carcinoma/ E. V. Koldysheva, A. P. Men'shchikova, E. L. Lushnikova, N. A. Popova, V. I. Kaledin, V. P. Nikolin, A. L. Zakharenko, O. A. Luzina, N. F. Salakhutdinov, O. I. Lavrik// Bulletin of Experimental Biology and Medicine, March 2019, V. 166, N 5, pp 661-666 doi:10.1007/s10517-019-04413-3, IF=0.546
  7. V.I. Anikeev, V.P. Sivcev, K.R. Valeev, K.P. Volcho, V.A. Sadykov, N.F. Salakhutdinov
    Highly selective reduction of nitroarenes by sc-isopropanol in the presence of zirconia in a flow reactor
    The Journal of Supercritical Fluids, V. 140, October 2018, Pp 233-237 doi:10.1016/j.supflu.2018.06.021, IF=3.122
  8. 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
  9. A.S. Sokolova, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis and antiviral activity of camphor-based 1,3-thiazolidin-4-one and thiazole derivatives as Orthopoxvirus-reproduction inhibitors
    Med. Chem. Commun,, 2018, V. 9, N 10, Pp 1746-1753 doi:10.1039/C8MD00347E, IF=2.342
  10. N.S. Li-Zhulanov, A.L. Zakharenko, A.A. Chepanova, J. Patel, A. Zafar, K.P. Volcho, N.F. Salakhutdinov, J. Reynisson, I.K. H. Leung, O.I. Lavrik
    A Novel Class of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Contains the Octahydro-2H-chromen-4-ol Scaffold
    Molecules 2018, 23(10), 2468; doi:10.3390/molecules23102468, IF=3.098
  11. A. Sidorenko, A. Kravtsova, A. Aho, I. Heinmaa, V. Agabekov, K. Volcho, N. Salakhutdinov, D. Murzin
    Acid-modified Halloysite Nanotubes as a Stereoselective Catalyst for Synthesis of 2H-Chromene Derivatives by the Reaction of Isopulegol with Aldehydes
    ChemCatChem, 2018, V. 10, N 18, Pp 3950-3954 doi:10.1002/cctc.201800974, IF=4.674
  12. А.В. Ластовка, Е.Ю. Яковлева, В.Ф. Коллегов, В.П. Фадеева, Н.Ф. Салахутдинов
    Определение остаточных органических растворителей методом газовой хроматографии в субстанции (2R,4R,4AR,7R, 8AR)-4,7-диметил-2-(тиофен-2-ил)октагидро-2H-хромен-4-ол, обладающей анальгетической активностью
    Заводская лаборатория. Диагностика материалов. 2018. Т. 84. № 9. С. 13-20. doi:10.26896/1028-6861-2018-84-9-13-20
  13. A.S. Sokolova, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, N.F. Salakhutdinov
    Discovery of a new class of inhibitors of Vaccinia virus based on (-)-borneol from Abies sibirica and (+)-camphor
    Chemistry & Biodiversity, 2018, V. 15, N 9, e1800153 doi:10.1002/cbdv.201800153, IF=1.617
  14. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  15. S.O. Kuranov, I.P. Tsypysheva, M.V. Khvostov, L.F. Zainullina, S.S. Borisevich, Yu.V. Vakhitova, O.A. Luzina, N.F. Salakhutdinov
    Synthesis and evaluation of camphor and cytisine-based cyanopyrrolidines as DPP-IV inhibitors for the treatment of type 2 diabetes mellitus
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4402-4409 doi:10.1016/j.bmc.2018.07.018, IF=2.881
  16. Synthesis of oxygen-containing heterocyclic compounds based on monoterpenoids/ O S Patrusheva, K P Volcho, N F Salakhutdinov// RUSS CHEM REV, 2018, V. 87, N 8, Pp 771-796 doi:10.1070/RCR4810, IF=3.991
  17. A.Yu. Sidorenko, A.V. Kravtsova, J. Warna, A. Aho, I. Heinmaa, I.V. Il'ina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of octahydro-2H-chromen-4-ol with analgesic activity from isopulegol and thiophene-2-carbaldehyde in the presence of acid-modified clays
    Molecular Catalysis, 2018, V. 453, Pp. 139-148 doi:10.1016/j.mcat.2018.05.007
  18. 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
  19. 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
  20. Study of the level of fatty acids in erythrocyte membranes and serum of patients with colorectal cancer in Novosibirsk/ M.V. Kruchinina, V.N. Kruchinin, Ya.I. Prudnikova, A.A. Gromov, M.V. Shashkov, A.S. Sokolova// doi:10.17650/2313-805X-2018-5-2-50-61
  21. O.A. Luzina, N.F. Salakhutdinov
    Usnic acid and its derivatives for pharmaceutical use: a patent review (2000–2017)
    Expert Opinion on Therapeutic Patents, 2018, V.28, N 6, Pp 477-491 doi:10.1080/13543776.2018.1472239, IF=2.867
  22. А.С. Донченко, В.В. Фоменко, В.Г. Васильев, В.Н. Афонюшкин, Н.А. Донченко, Ю.Н. Козлова, В.Ю. Коптев
    Изучение антагонистической активности бактерий, подавляющей синтез феназинов Pseudomonas aereginosa
    Сибирский вестник сельскохозяйственной науки, 2018. Т. 48. №.5. С. 23-29. doi: 10.26898/0370-8799-2018-5-3 doi:10.26898/0370-8799-2018-5-3
  23. 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
  24. V.Yu. Krukov, O.G. Tomilova, O.A. Luzina, O.N. Yaroslavtseva, Yu.B. Akhanaev, M.V. Tyurin, B.A. Duisembekov, N.F. Salakhutdinov, V.V. Glupov
    Effects of fluorine-containing usnic acid and fungus Beauveria bassiana on the survival and immune-physiological reactions of Colorado potato beetle larvae
    Pest Management Science, 2018, V. 74, N 3, Pp 598-606 doi:10.1002/ps.4741, IF=3.249
  25. Antiulcer and anti-inflammatory activity of the campholenic aldehyde-derived thiazolidinone/ BORISOVA Marina Sergeevna, SOKOLOV Dmitriy Nikolaevich, ZHUKOVA Natalya Anatolevna, TOLSTIKOVA Tatyana Genrikhovna, SALAKHUTDINOV Nariman Faridovich// doi:10.15372/SSMJ20180201
  26. O.V. Salomatina, I.I. Popadyuk, A.L. Zakharenko, O.D. Zakharova, D.S. Fadeev, N.I. Komarova, J. Reynisson, H.J. Arabshahi, R. Chand, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel semisynthetic derivatives of bile acids as effective tyrosyl-DNA phosphodiesterase 1 inhibitors
    Molecules, 2018, V. 23, N 3, art. number 679 doi:10.3390/molecules23030679, IF=3.098
  27. Antiulcerogenic activity of borneol derivatives/ M. S. Borisova, O. I. Yarovaya, M. D. Semenova, T. G. Tolstikova, N. F. Salakhutdinov// Russian Chemical Bulletin, 2018, V. 67, N 3, Pp 558-561 doi:10.1007/s11172-018-2110-y, IF=0.781
  28. D.S. Sergeevichev, A.A. Krasilnikova, A.G. Strelnikov, V.V. Fomenko, N.F. Salakhutdinov, A.B. Romanov, A.M. Karaskov, E.A. Pokushalov, J.S. Steinberg
    Globular chitosan prolongs the effective duration time and decreases the acute toxicity of botulinum neurotoxin after intramuscular injection in rats
    Toxicon, 2018, V. 143, Pp 90-95 doi:10.1016/j.toxicon.2018.01.013, IF=2.352
  29. 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
  30. A.A. Krasilnikova, D.S. Sergeevichev, V.V. Fomenko, A.A. Korobeynikov, M.B. Vasilyeva, A.S. Yunoshev, A.M. Karaskov, E.A. Pokushalov
    Globular chitosan treatment of bovine jugular veins: Evidence of anticalcification efficacy in the subcutaneous rat model
    Cardiovascular Pathology, V. 32, January-February 2018, Pp 1-7 doi:10.1016/j.carpath.2017.08.003, IF=2.496
  31. K.P. Volcho, S.S. Laev, G.M. Ashraf, G. Aliev, N.F. Salakhutdinov
    Application of monoterpenoids and their derivatives for treatment of neurodegenerative disorders.
    Curr Med Chem., 2018, V. 25, N 39, Pp 5327 - 5346 doi:10.2174/0929867324666170112101837, IF=3.469
  32. CHANGES OF LIPIDOM IN COLORECTAL CANCER/ Kruchinina M.V., Gromov A.A., Prudnikova Ia.I., Kruchinin V.N., Shashkov M.V., Sidelnikov V.N., Sokolova A.S., Salakhutdinov N.F.// doi:10.15372/ATER20180107
  33. D.N. Sokolov, O.A. Luzina, N.F. Salakhutdinov
    Synthesis of Sulfones and Sulfoxides Based on (+)-usnic Acid
    Chemistry of Natural Compounds, 2018, V. 54, N 1, pp 46-49 doi:10.1007/s10600-018-2256-8, IF=0.45

2017
  1. A. Kononova, A. Sokolova, S. Cheresiz, O. Yarovaya, R. Nikitina, A. Chepurnov, A.G. Pokrovsky, N. Salakhutdonov
    N-Heterocyclic borneol derivatives as the inhibitors of Marburg virus glycoprotein-mediated VSIV pseudotype entry
    Med. Chem. Commun., 2017, V. 8, N 12, Pp 2233-2237 doi:10.1039/C7MD00424A, IF=2.608
  2. 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
  3. 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
  4. 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
  5. A.V. Markov, A.V. Sen'kova, D. Warszycki, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Soloxolone methyl inhibits influenza virus replication and reduces virus-induced lung inflammation
    Scientific Reports, 2017, V. 7, Номер статьи 13968 doi:10.1038/s41598-017-14029-0, IF=4.258
  6. I.I. Popadyuk, A.V. Markov, E.A. Morozova, V.O. Babich, O.V. Salomatina, E.B. Logashenko, M.A. Zenkova, T.G. Tolstikova, N.F. Salakhutdinov
    Synthesis and evaluation of antitumor, anti-inflammatory and analgesic activity of novel deoxycholic acid derivatives bearing aryl- or hetarylsulfanyl moieties at the C-3 position
    Steroids, 2017, V. 127, Pp 1-12 doi:10.1016/j.steroids.2017.08.016, IF=2.282
  7. M.V. Trushin, R.G. Khamidullina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov
    The action of monoterpenoids with promising antiparkinsonian activity on fertility of Drosophila melanogaster
    Marmara Pharmaceutical Journal, 2017, V. 21, N 4, 2017, Pp 987-991 doi:10.12991/mpj.2017.29
  8. E.A. Kulikova, N.B. Illarionova, K.P. Volcho, T.A. Khomenko, N.F. Salakhutdinov, N.V. Khotskin, E.Y. Bazhenova, A.V. Kulikov
    The effect of TC-2153, an inhibitor of striatal-enriched protein tyrosine phosphatase, on the 5-HT2A receptors
    European Neuropsychopharmacology, 2017, V. 27, pp S654-S654, S4 (30th Congress of the European-College-of-Neuropsychopharmacology (ECNP), Paris, France, Sep 02-05, 2017) doi:10.1016/S0924-977X(17)31224-5, IF=4.238
  9. А. В. Ластовка, В. П. Фадеева, И. В. Ильина, С. Ю. Курбакова, К. П. Волчо, Н. Ф. Салахутдинов
    Исследование физико-химических свойств и разработка методики определения (2R,4R,4aR,7R,8aR)-4,7-диметил-2- (тиофен-2-ил)октагидро-2H-хромен-4-ола, обладающего высокой анальгетической активностью
    Заводская лаборатория, 2017, Т. 83, № 10, С. 11-17 doi:10.26896/1028-6861-2017-83-11-17
  10. 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
  11. A. Romanov, A. Strelnikov, D. Sergeevichev, N. Salakhutdinov, V. Fomenko, V. Shabanov, D. Losik, I. Mikheenko, A. Karaskov, E. Pokushalov
    The influence of the new pharmaceutical composition containing botulinum toxin on different pharmacological models of heart rhythm disorders
    European Heart Journal. 38 (Supplement). 2017. P1711 (ESC Congress 2017, 26-30 August, Barcelona, Spain) doi:10.1093/eurheartj/ehx502.P1711, IF=0.896
  12. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, В.М. Генералов, В.А. Рихтер, Д.В. Семенов, С.В. Морозов, А.С. Соколова, Н.Ф. Салахутдинов, М.В. Шашков, В.Н. Сидельников, В.Н. Кручинин
    Ассоциации функциональных параметров эритроцитов со структурой их мембран у мужчин г. новосибирска с атерогенными дислипидемиями и алкогольным поражением печени
    Атеросклероз. 2017. Т. 13. № 3. С. 5-13.
  13. I.I. Popadyuk, A.V. Markov, V.O. Babich, O.V. Salomatina, E.B. Logashenko, M.A. Zenkova, N.F. Salakhutdinov
    Novel derivatives of deoxycholic acid bearing aliphatic or cyclic diamine moieties at the C-3 position: synthesis and evaluation of anti-proliferative activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 16, Pp 3755-3759 doi:10.1016/j.bmcl.2017.06.072, IF=2.453
  14. 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
  15. Catalytic epoxidation of β-pinene with aqueous hydrogen peroxide/ V. V. Fomenko, O. V. Bakhvalov, V. F. Kollegov, N. F. Salakhutdinov// Russian Journal of General Chemistry, 2017, V.87, N 8, pp 1675-1679 doi:10.1134/S1070363217080059, IF=0.552
  16. E.A. Kulikova, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov
    Benzopentathiepine Derivative, 8-(Trifluoromethyl)-1,2,3,4,5-Benzopentathiepin-6-Amine Hydrochloride (TC-2153), as a Promising Anti-depressant of New Generation
    Letters in Drug Design & Discovery, 2017, V. 14, N 8, Pp 974-984 doi:10.2174/1570180814666161121112417, IF=1.169
  17. N.F. Salakhutdinov, K.P. Volcho, O.I. Yarovaya
    Monoterpenes as a renewable source of biologically active compounds
    Pure and Applied Chemistry, 2017, V.89, N 8, pp 1105-1118 doi:10.1515/pac-2017-0109, IF=2.625
  18. 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
  19. 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
  20. O.I. Artyushin, E.V. Sharova, N.M. Vinogradova, G.K. Genkina, A.A. Moiseeva, Z.S. Klemenkova, I.R. Orshanskaya, A.A. Shtro, R.A. Kadyrova, V.V. Zarubaev, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene Derivatives using Click Chemistry Methodology and Study of their Antiviral Activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V.27, N 10, Pp 2181-2184 doi:10.1016/j.bmcl.2017.03.051, IF=2.453
  21. Yu.S. Demidova, E.V. Suslov, I.L. Simakova, K.P. Volcho, E. Smolentseva, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    Promoting effect of alcohols and formic acid on Au-catalyzed one-pot myrtenol amination
    Molecular Catalysis, 2017, V. 433, Pp 414-419 (Formerly known as Journal of Molecular Catalysis A: Chemical) doi:10.1016/j.mcat.2017.02.040, IF=4.211
  22. A.S. Sokolova, O.I. Yarovaya, M.D. Semenova, A.A. Shtro, I.R. Orshanskaya, V.V. Zarubaev, N.F. Salakhutdinov
    Synthesis and in vitro study of novel borneol derivatives as potent inhibitors of the influenza A virus
    Med. Chem. Commun., 2017, 8(5), 960-963 doi:10.1039/C6MD00657D, IF=2.608
  23. S.S. Laev, N.F. Salakhutdinov, O.I. Lavrik
    Inhibitors of nuclease and redox activity of apurinic/apyrimidinic endonuclease 1/redox effector factor 1 (APE1/Ref-1)
    Bioorganic & Medicinal Chemistry, 2017, V. 25, N 9, Pp 2531-2544 doi:10.1016/j.bmc.2017.01.028, IF=2.93
  24. Modern approaches to modification of bile acids for the synthesis of compounds possessing valuable physicochemical and biological properties/ I.I. Popadyuk, O.V. Salomatina, N. F. Salakhutdinov// Russian Chemical Reviews, 2017, V. 86, N 5, Pp 388-443 doi:10.1070/RCR4683, IF=4.58
  25. A. Pavlova, O. Patrusheva, I. Il'ina, K. Volcho, T. Tolstikova, N. Salakhutdinov
    The Decisive Role of Mutual Arrangement of Hydroxy and Methoxy Groups in (3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8ahexahydro- 2H-chromene-4,8-diols in their Biological Activity
    Letters in Drug Design & Discovery, 2017, V. 14, N 5, pp. 508-514 doi:10.2174/1570180813666161102142642, IF=1.169
  26. 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
  27. М.В. Кручинина, Я.И. Прудникова, В.Н. Кручинин, В.А. Володин, М.В. Шашков, А.С. Соколова
    Возможности неинвазивной диагностики колоректального рака методами хроматографии и RAMAN-спектроскопии
    Гастроэнтерология Санкт-Петербурга, 2017. № 1. С. 86-86
  28. A.S. Sokolova, O.I. Yarovaya, A.A. Shtro, M.S. Borisova, E.A. Morozova, T.G. Tolstikova, V.V. Zarubaev, N.F. Salakhutdinov
    Synthesis and biological activity of heterocyclic borneol derivatives
    Chemistry of Heterocyclic Compounds, 2017, V. 53, N 3, pp 371-377 doi:10.1007/s10593-017-2063-3, IF=0.893
  29. K.S. Kovaleva, O.I. Yarovaya, A.V. Shernyukov, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, N.F. Salakhutdinov
    Synthesis of new heterocyclic dehydroabietylamine derivatives and their biological activity
    Chemistry of Heterocyclic Compounds, 2017, V. 53, N 3, pp 364-370 doi:10.1007/s10593-017-2058-0, IF=0.893
  30. 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
  31. A.S. Sokolova, О.I. Yarovaya, D.S. Baev, А.V. Shernyukov, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
    Aliphatic and alicyclic camphor imines as effective inhibitors of influenza virus H1N1
    European Journal of Medicinal Chemistry, 2017, V. 127, Pp 661-670 doi:10.1016/j.ejmech.2016.10.035, IF=4.519
  32. 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
  33. I.L. Simakova, Yu.S. Demidova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, A. Simakov
    Gold catalyzed one-pot myrtenol amination: Effect of catalyst redox activationOriginal Research Article
    Сatalysis Today, V. 279, Part 1, 1 January 2017, Pages 63-70 doi:10.1016/j.cattod.2016.01.044, IF=4.636
  34. M. Stekrova, P. Maki-Arvela, E. Leino, K.M. Valkaj, K. Eranen, A. Aho, A. Smeds, N. Kumar, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Two-step synthesis of monoterpenoid dioxinols exhibiting analgesic activity from isopulegol and benzaldehyde over heterogeneous catalysts
    Catalysis Today, Catalysis Today, V. 279, Part 1, 1 January 2017, Pp 56-62 doi:10.1016/j.cattod.2016.03.046, IF=4.636
  35. А.Г. Стрельников, Н.Ф. Салахутдинов
    Ботокс для сердца
    Наука из первых рук. 2017. Т. 73. № 1. С. 66-71.
  36. Usnic acid derivatives are effective inhibitors of tyrosyl-DNA phosphodiesterase 1/ A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, O.D. Zakharova, M.E. Rakhmanova, A.A. Chepanova, N.S. Dyrkheeva, O.I. Lavrik, N.F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, January 2017, Volume 43, Issue 1, pp 84-90 doi:10.1134/S1068162017010125, IF=0.689
  37. 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
  38. E. Valdman, I. Kapitsa, Е. Ivanova, T. Voronina, O. Ardashov, K. Volcho, V. Khazanov, N. Salakhutdinov
    Evolution of anti-parkinsonian activity of monoterpenoid (1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol in various in vivo models
    European Journal of Pharmacology, 2017, V. 815, Pp 351-363 doi:10.1016/j.ejphar.2017.09.022, IF=2.895

2016
  1. A.A. Shtro, V.V. Zarubaev, O.A. Luzina, D.N. Sokolov, N.F. Salakhutdinov
    Derivatives of usnic acid inhibit broad range of influenza viruses and protect mice from lethal influenza infection
    Antivir Chem Chemotherapy, V.24, N 3-4, August 2015, pp. 92-98, Published March 27, 2016 doi:10.1177/2040206616636992
  2. D. Sergeevichev, V. Fomenko, A. Dokuchaeva, E. Chepeleva, A. Korobeynikov, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Preventing Calcification and Improving Biomechanical Issues of Vein Tissues Using Chitosan
    Tissue Engineering: Part A. 2016. Vol.22, Suppl.1, S.141 DOI: 10.1089/ ten.tea.2016.5000.abstracts (conference TERMIS - Americas Conference and Exhibition, San Diego, CA, DEC 11-14, 2016), IF=3.891
  3. Sergeevichev, V. Fomenko, A. Strelnikov, A. Dokuchaeva, A. Korobeynikov, E. Chepeleva, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Denervation Properties of Botullinum Neurotoxin Type A in Complex with Chitozan
    Tissue Engineering: Part A. 2016. Vol.22, Suppl.1, S.46 DOI: 10.1089/ ten.tea.2016.5000.abstracts (conference TERMIS - Americas Conference and Exhibition, San Diego, CA, DEC 11-14, 2016), IF=3.891
  4. Chemical approach to the design of effective antidiabetic agents/ A D Rogachev, ab S O Kuranov, a N F Salakhutdinov// RUSS CHEM REV, 2016, V. 85, N 12, Pp 1313-1337 doi:10.1070/RCR4624, IF=3.687
  5. A.D. Rogachev, O.I. Yarovaya, S.V. Ankov, M.V. Khvostov, T.G. Tolstikova, A.G. Pokrovsky, N.F. Salakhutdinov
    Development and validation of ultrafast LC–MS/MS method for quantification of anti-influenza agent camphecene in whole rat blood using dried blood spots and its application to pharmacokinetic studies
    Journal of Chromatography B, Volumes 1036-1037, 15 November 2016, Pages 136-141 doi:10.1016/j.jchromb.2016.10.009, IF=2.687
  6. A.Zakharenko, O. Luzina, O.Koval, D. Nilov, I. Gushchina, N. Dyrkheeva, V. Svedas, N. Salakhutdinov, O. Lavrik
    Tyrosyl-DNA phosphodiesterase 1 inhibitors: usnic acid enamines enhance the cytotoxic effect of camptothecin
    J. Nat. Prod., 2016, 79 (11), pp 2961-2967 doi:10.1021/acs.jnatprod.6b00979, IF=3.661
  7. 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
  8. 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
  9. S.S. Laev, N.F. Salakhutdinov, O.I. Lavrik
    Tyrosyl-DNA phosphodiesterase inhibitors: Progress and potential
    Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pp 5017-5027 doi:10.1016/j.bmc.2016.09.045, IF=2.923
  10. 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
  11. Effect of New Antiviral Agent Camphecin on Behavior of Mice/ A. V. Babina, V. A. Lavrinenko, O. I. Yarovaya, N. F. Salakhutdinov// Bulletin of Experimental Biology and Medicine, January 2017, V. 162, N 3, pp 346-348 doi:10.1007/s10517-017-3612-6, IF=0.448
  12. P. Maki-Arvela, M. Barsukova, I. Winberg, A. Smeds, J. Hemming, K. Eranen, A. Torozova, A. Aho, K. Volcho, D.Yu. Murzin
    Unprecedented Selective Heterogeneously Catalysed “Green” Oxidation of Betulin to Biologically Active Compounds using Synthetic Air and Supported Ru Catalysts
    CHEMISTRYSELECT, V. 1, N 13, August 16, 2016, Pp 3866-3869 doi:10.1002/slct.201600731
  13. 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
  14. Yu.S. Demidova, E.V. Suslov, O.A. Simakova, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
    Selective one-pot carvone oxime hydrogenation over titania supported gold catalyst as a novel approach for dihydrocarvone synthesis
    Journal of Molecular Catalysis A: Chemical, V. 420, August 2016, Pp 142-148 doi:10.1016/j.molcata.2016.04.013, IF=3.957
  15. 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
  16. E.V. Sharova, G.K. Genkina, N.M. Vinogradova, O.I. Artyushin, O.I. Yarovaya, V.K. Brel
    Phosphorylation of natural productsCytisine, anabasine, and camphor using click chemistry methodology
    Phosphorus, Sulfur, and Silicon and the Related Elements, 2016, V. 191, N 11-12, Pp 1556-1557 (21st International Conference on Phosphorus Chemistry (ICPC-2016),Kazan, RUSSIA, JUN 05-10, 2016 doi:10.1080/10426507.2016.1213257, IF=0.722
  17. Biological activity of usnic acid and its derivatives: Part 2. effects on higher organisms. Molecular and physicochemical aspects/ O. A. Luzina , N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, 2016, V. 42, N 3, pp 249-268 doi:10.1134/S1068162016030109, IF=0.66
  18. 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
  19. 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
  20. M.N. Timofeeva, V.N. Panchenko, K.P. Volcho, S.V. Zakusin, V.V. Krupskaya, A. Gil, O.S. Mikhalchenko, M.A. Vicente
    Effect of acid modification of kaolin and metakaolin on Bronsted acidity and catalytic properties in the synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
    Journal of Molecular Catalysis A: Chemical, , V. 414, April 2016, Pp 160-166 doi:10.1016/j.molcata.2016.01.010, IF=3.957
  21. Biological activity of usnic acid and its derivatives: Part 1. Activity against unicellular organisms/ O. A. Luzina , N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, March 2016, V. 42, N 2, pp 115-132 doi:10.1134/S1068162016020084, IF=0.66
  22. Synthesis and cytotoxic activity of usnic acid cyanoethyl derivatives/ M. E. RakhmanovaO. A. LuzinaEmail authorM. A. PokrovskiiA. G. PokrovskiiN. F. Salakhutdinov// Russian Chemical Bulletin, February 2016, V. 65, N 2, pp 566-569 doi:10.1007/s11172-016-1338-7, IF=0.578
  23. V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Unusual transformations of aliphatic nitro compounds in a flow reactor in high-pressure isopropanol on alumina. Part 2. Formation of esters
    The Journal of Supercritical Fluids, V. 107, January 2016, Pages 179-181 doi:10.1016/j.supflu.2015.08.007, IF=2.578
  24. K.S. Kovaleva, A.A. Kononova, V.A. Korobeynikov, S.V. Cheresiz, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, O.I. Yarovaya, A.G. Pokrovsky, N.F. Salakhutdinov
    Cytotoxic and Antiviral Properties of Novel Dehydroabietylamine Salts
    Med Chem (Los Angeles) 6:10, 642-646 doi:10.4172/2161-0444.1000408

2015
  1. M. Stekrova, P. Maki-Arvela, N. Kumar, E. Behravesh, A. Aho, Q. Balme, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Prins cyclization: Synthesis of compounds with tetrahydropyran moiety over heterogeneous catalysts
    Journal of Molecular Catalysis A: Chemical, V. 410, 15 December 2015, P 260-270 doi:10.1016/j.molcata.2015.09.021, IF=3.615
  2. A. Torozova, P. Maki-Arvela, N. Kumar, A. Aho, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, K.P. Volcho, N.F. Salakhutdinov, D.Y. Murzin
    Isomerization of verbenol oxide to a diol with para-menthane structure exhibiting anti-Parkinson activity
    Reaction Kinetics, Mechanisms and Catalysis, 2015, V. 116, N 2, pp 299-314 doi:10.1007/s11144-015-0903-7, IF=1.169
  3. K. Ponomarev, A. Pavlova, E. Suslov, O. Ardashov, D. Korchagina, A. Nefedov, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Synthesis and analgesic activity of new compounds combining azaadamantane and monoterpene moieties
    Medicinal Chemistry Research, 2015, V. 24, N 12, pp 4146-4156 doi:10.1007/s00044-015-1464-z, IF=1.401
  4. Synthesis and cytotoxic activity of substituted hexahydro-2H-4,6-(epoxymethano)chromen-8(5H)-ones obtained from (-)-verbenone/ I. V. Il'ina, M. A. Pokrovsky, O. S. Mikhalchenko, D. V. Korchagina, K. P. Volcho, A. G. Pokrovsky, N. F. Salakhutdinov// Russian Chemical Bulletin, 2018, V. 64, N 9, pp 2257-2260 doi:10.1007/s11172-015-1148-3, IF=0.481
  5. E.A. Kulikova, E.Y. Bazhenova, N.K. Popova, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov
    Effect of Acute Administration of 8-(Trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine Hydrochloride (TC-2153) on Biogenic Amines Metabolism in Mouse Brain
    Letters in Drug Design & Discovery, 2015, V. 12, N 10, Pp 833 - 836 doi:10.2174/1570180812666150522221634, IF=0.769
  6. A.S. Sokolova, О.I. Yarovaya, А.V. Shernyukov, Yu.V. Gatilov, Yu.V. Razumova, V.V. Zarubaev, T.S. Tretiak, А.G. Pokrovsky, O.I. Kiselev, N.F. Salakhutdinov
    Discovery of a new class of antiviral compounds: Camphor imine derivatives
    European Journal of Medicinal Chemistry, V. 105, 13 November 2015, Pp 263-273 doi:10.1016/j.ejmech.2015.10.010, IF=3.447
  7. H.J. Arabshahi, M. Rensburg, L.I. Pilkington, C.Y. Jeon, M. Song, L. Gridel, E. Leung, D. Barker, M. Vuica-Ross, K.P. Volcho, A.L. Zakharenko, O.I. Lavrik, J. Reynisson
    A synthesis, in silico, in vitro and in vivo study of thieno[2,3-b]pyridine anticancer analogues
    MedChemComm, 2015, V. 6, N 11, Pp 1987-1997 doi:10.1039/c5md00245a, IF=2.494
  8. A. Pavlova, O. Mikhalchenko, A. Rogachev, I. Il'ina, D. Korchagina, Yu. Gatilov, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Synthesis and analgesic activity of stereoisomers of 2-(3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols
    Medicinal Chemistry Research, 2015, V 24, N 11, pp 3821-3830 doi:10.1007/s00044-015-1426-5, IF=1.401
  9. E.V. Suslov, K.Yu. Ponomarev, A.D. Rogachev, M.A. Pokrovsky, A.G. Pokrovsky, M.B. Pykhtina, A.B. Beklemishev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Compounds Combining Aminoadamantane and Monoterpene Moieties: Cytotoxicity and Mutagenic Effects
    Medicinal Chemistry, V. 11, N 7, Pp 629 - 635 doi:10.2174/1573406411666150518110053, IF=1.363
  10. Inhibitory properties of nitrogen-containing adamantane derivatives with monoterpenoid fragments against tyrosyl-DNA phosphodiesterase 1/ A.L. Zakharenko, K.U. Ponomarev, E.V. Suslov, D.V. Korchagina, K.P. Volcho, I.A. Vasil'eva, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, November 2015, V. 41, N 6, pp 657-662 doi:10.1134/S1068162015060199, IF=0.535
  11. CATALYTIC SYNTHESIS OF DIOXINOL WITH ANTICONVULSANT ACTIVITY/ A.S. Torozova, E.M. Sulman, P.V. Sinitsyna, P. Maki-Arvela, K.P. Volcho, D.Yu., Murzin, I. Yu. Tiamina// Научно-технический вестник Поволжья. 2015. № 5. С. 88-90.
  12. O.V. Ardashov, Yu. S. Demidova, D.V. Korchagina, K.P. Volcho, I.L. Simakova, N.F. Salakhutdinov
    The First Synthesis of (4S,5R,6R)-5,6-Dihydroxy-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic Acid
    Helvetica Chimica Acta, V. 98, N 10, Pp 1442-1455 doi:10.1002/hlca.201500125, IF=1.138
  13. M.N. Timofeeva, V.N. Panchenko, A. Gil, S.V. Zakusin, V. V. Krupskaya, K.P. Volcho, M.A. Vicente
    Effect of structure and acidity of acid modified clay materials on synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
    Catalysis Communications, 2015, V. 69, , Pp 234-238 doi:10.1016/j.catcom.2015.07.005, IF=3.698
  14. I.V. Nechepurenko, U.A. Boyarskikh, M.V. Khvostov, D.S. Baev, N.I. Komarova, M.L. Filipenko, T.G. Tolstikova, N.F. Salakhutdinov
    Hypolipidemic Berberine Derivatives with a Reduced Aromatic Ring C
    Chemistry of Natural Compounds, 2015, V 51, N 5, pp 916-922 doi:10.1007/s10600-015-1447-9, IF=0.509
  15. V.V. Zarubaev, A.V. Garshinina, T.S. Tretiak, V.A. Fedorova, A.A. Shtro, A.S. Sokolova, O.I. Yarovaya, N.F. Salakhutdinov
    Broad range of inhibiting action of novel camphor-based compound with anti-hemagglutinin activity against influenza viruses in vitro and in vivo
    Antiviral Research, V. 120, 2015, Pp 126-133 doi:10.1016/j.antiviral.2015.06.004, IF=3.938
  16. I.I. Popadyuk, A.V. Markov, O.V. Salomatina, E.B. Logashenko, A.V. Shernyukov, M.A. Zenkova, N.F. Salakhutdinov
    Synthesis and biological activity of novel deoxycholic acid derivatives
    Bioorganic & Medicinal Chemistry, V. 23, N 15, 2015, Pp 5022-5034 doi:10.1016/j.bmc.2015.05.012, IF=2.792
  17. V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Unique shortening of carbon chain during reduction of aliphatic nitro compounds to amines in the presence of supercritical isopropanol on alumina
    The Journal of Supercritical Fluids, V.103, 2015, Pp 101-104 doi:10.1016/j.supflu.2015.04.029, IF=2.371
  18. O.B. Bekker, D.N. Sokolov, O.A. Luzina, N.I. Komarova, Yu.V. Gatilov, S.N. Andreevskaya, T.G. Smirnova, D.A. Maslov, L.N. Chernousova, N.F. Salakhutdinov, V.N. Danilenko
    Synthesis and activity of (+)-usnic acid and (-)-usnic acid derivatives containing 1,3-thiazole cycle against Mycobacterium tuberculosis
    Medicinal Chemistry Research, 2015, V. 24, N 7, pp 2926-2938 doi:10.1007/s00044-015-1348-2, IF=1.401
  19. S.S. Laev, N.F. Salakhutdinov
    Anti-arthritic agents: Progress and potential
    Bioorganic & Medicinal Chemistry, 2015, V. 23, N 13, Pp. 3059-3080 doi:10.1016/j.bmc.2015.05.010, IF=2.793
  20. O.A. Luzina, D.N. Sokolov, M.A. Pokrovskii, A.G. Pokrovskii, O.B. Bekker, V.N. Danilenko, N.F. Salakhutdinov
    Synthesis and Biological Activity of Usnic Acid Enamine Derivatives
    Chemistry of Natural Compounds, July 2015, V. 51, N 4, pp 646-651 doi:10.1007/s10600-015-1376-7, IF=0.509
  21. O. V. Ardashov, D. V. Korchagina, K. P. Volcho, N. F. Salakhutdinov
    Synthesis of 10-Carbonyl and 10-Carboxylic Derivatives of para -Mentha-1,8-Diene-5,6-Diol
    Chemistry of Natural Compounds, 2015, V. 51, N 3, pp 483-487 doi:10.1007/s10600-015-1320-x, IF=0.509
  22. A. Zakharenko, T.Khomenko, S. Zhukova, O. Koval, O. Zakharova, R. Anarbaev, N. Lebedeva, D.Korchagina, N. Komarova, V.Vasiliev, J.Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and biological evaluation of novel tyrosyl-DNA phosphodiesterase 1 inhibitors with a benzopentathiepine moiety
    Bioorganic & Medicinal Chemistry, V. 23, N 9, 2015, Pp 2044-2052 doi:10.1016/j.bmc.2015.03.020, IF=2.793
  23. INFLUENCE OF simvaglyzin ON expression AND INHIBITION of HMG-CoA reductase in rats liver/ Yu.I. Ragino, V.A. Vavilin, E.M. Stakhneva, N.F. Salakhutdinov, O.G. Safronova, A.B. Shintyapina, V.V. Lyakhovich, Yu.P. Nikitin// Атеросклероз. 2015. Т. 11. № 2. С. 14-19.
  24. S. Yu. Kurbakova, I. V. Il'ina, O. S. Mikhalchenko, M. A. Pokrovsky, D. V. Korchagina, K. P. Volcho, A. G. Pokrovsky, N. F. Salakhutdinov
    The short way to chiral compounds with hexahydrofluoreno[9,1-bc]furan framework: Synthesis and cytotoxic activity
    Bioorganic & Medicinal Chemistry, V. 23, N 7, 2015, Pp 1472-1480. doi:10.1016/j.bmc.2015.02.013, IF=2.793
  25. Yu.S. Demidova, E.V. Suslov, O.A. Simakova, I.L. Simakova, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Selective carvone hydrogenation to dihydrocarvone over titania supported gold catalyst
    Catalysis Today, Volume 241, Part B, 1 March 2015, Pages 189-194 doi:10.1016/j.cattod.2014.03.053, IF=3.893
  26. E.V. Suslov, D.V. Korchagina, M.A. Pokrovskii, A.G. Pokrovskii, K.P. Volcho, N.F. Salakhutdinov
    Synthesis and Cytotoxic Activity of Aza-Michael Reaction Products from Ethyl Sorbate and Heterocyclic Amines
    Chemistry of Natural Compounds, March 2015, Volume 51, Issue 2, pp 296-301 doi:10.1007/s10600-015-1264-1, IF=0.509
  27. Curare-like camphor derivatives and their biological activity/ A. S. Sokolova, E. A. Morozova, V. G. Vasilev, O. I. Yarovaya, T. G. Tolstikova, N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, March 2015, Volume 41, Issue 2, pp 178-185 doi:10.1134/S1068162015020156, IF=0.535
  28. M.N. Timofeeva, K.P. Volcho, O.S. Mikhalchenko, V.N. Panchenko, V.V. Krupskaya, S.V. Tsybulya, A. Gil, M.A. Vicente, N.F. Salakhutdinov
    Synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol over acid modified montmorillonite clays: Effect of acidity on the Prins cyclization
    Journal of Molecular Catalysis A: Chemical, V. 398 Pp 26-34 doi:10.1016/j.molcata.2014.11.016, IF=3.615
  29. Reduction of nitrotoluenes in supercritical isopropanol over Al2O3/ V. P. Sivcev, D. V. Korchagina, K. P. Volcho, N. F. Salakhutdinov, V. I. Anikeev// Russian Journal of Physical Chemistry A, February 2015, Volume 89, Issue 2, pp 202-206 doi:10.1134/S0036024415020314, IF=0.562
  30. А.С. Торозова, Э.М. Cульман, П. Мяки-Арвела, К.П. Волчо, Н.Ф. Салахутдинов, Д.Ю. Мурзин
    Исследование мезопористых структур МСМ-41 и МСМ-48 в синтезе биологически активного вещества для лечения болезни Паркинсона
    Вестник Тверского государственного университета. Серия: Химия. 2015. № 2. С. 31-37.
  31. A. Torozova, P. Maki-Arvela, A. Aho, N. Kumar, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Heterogeneous catalysis for transformation of biomass derived compounds beyond fuels: Synthesis of monoterpenoid dioxinols with analgesic activity
    Journal of Molecular Catalysis A: Chemical, Volume 397, February 2015, Pages 48-55 doi:10.1016/j.molcata.2014.10.023, IF=3.615
  32. A.D. Rogachev, N.F. Salakhutdinov
    Chemical Composition of Pinus sibirica (Pinaceae)
    Chemistry & Biodiversity, 2015, V. 12, N 1, pp 1-53 doi:10.1002/cbdv.201300195, IF=1.515
  33. A. Torozova, P. Maki-Arvela, N.D. Shcherban, N. Kumar, A. Aho, M. Stekrova, K. Maduna Valkaj, P. Sinitsyna, S.M. Filonenko, P.S. Yaremov, V.G. Ilyin, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Effect of acidity and texture of micro-, mesoporous and hybrid micromesoporous materials on the synthesis of paramenthanic diol exhibiting anti-Parkinson activity
    Catalysis, Structure & Reactivity, Volume 1, Issue 3, 2015, pages 146-154 doi:10.1179/2055075815Y.0000000009
  34. Comparison of Behavioral Effects of Fluoxetine, Imipramine and New Psychotropic Drug TC-2153 on Mice with Hereditary Predisposition to Catalepsy/ E. A. Kulikova , M. A.Nikhonova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, A.V. Kulikov, N.K. Popova// ZHURNAL VYSSHEI NERVNOI DEYATELNOSTI IMENI I P PAVLOVA , 2015, V.65, N 1, Pp. 105-112 doi:10.7868/S0044467715010050
  35. Anti-ulcer agents: chemical aspect of solving the problem/ L N Rogoza and N F Salakhutdinov// Russian Chemical Reviews(2015),84(1):98 doi:10.1070/RCR4430, IF=2.318

2014
  1. А.С. Торозова, Э.М. Сульман, П.В. Синицына, П. Мяки-Арвела, К.П. Волчо, Д.Ю. Мурзин
    Применение цеолитов в процессе превращения эпоксида вербенола с образованием биологически активного вещества с обезболивающим эффектом
    В книге: Ресурсо- и энергосберегающие технологии в химической и нефтехимической промышленности VII Международная конференция Российского химического общества имени Д.И. Менделеева, посвященная 100-летию со дня рождения Л.А. Костандова. Редакционная коллегия: А.Ю. Цивадзе, Е.Г. Винокуров, Н.Р. Косинова, Н.Н. Кулов. 2015. С. 88-90.
  2. A.A. Shtro, V.V. Zarubaev, O.A. Luzina, D.N. Sokolov, O.I. Kiselev, N.F. Salakhutdinov
    Novel derivatives of usnic acid effectively inhibiting reproduction of influenza A virus
    Bioorganic & Medicinal Chemistry, V. 22, N 24, 15 December 2014, Pp 6826-6836. doi:10.1016/j.bmc.2014.10.033, IF=2.95
  3. I. Il’ina, O. Mikhalchenko, A. Pavlova, D. Korchagina, T. Tolstikova, K. Volcho, N. Salakhutdinov, E. Pokushalov
    Highly potent analgesic activity of monoterpene-derived (2S,4aR,8R,8aR)-2-aryl-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols
    Medicinal Chemistry Research, 2014, V. 23, N 12, pp 5063-5073 doi:10.1007/s00044-014-1071-4, IF=1.402
  4. А.С. Торозова, В.П. Молчанов, П. Мяки-Арвела, К.П. Волчо, Н.Ф. Салахутдинов, Д.Ю. Мурзин
    Каталитическая изомеризация эпоксида вербенола с использованием цеолитов
    Научно-технический вестник Поволжья. 2014. № 5. С. 77-80.
  5. O.S. Mikhalchenko, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Formation of the Compounds with an Epoxychromene Framework: Role of the Methoxy Groups
    Helvetica Chimica Acta, 2014, vol. 97, N 10, p. 1406-1421 doi:10.1002/hlca.201300461, IF=1.394
  6. I.V. Nechepurenko, N.I. Komarova, A.V. Shernyukov, V.G. Vasiliev, N.F. Salakhutdinov
    Smiles rearrangements in a series of berberine analogues containing a secondary acetamide fragment
    Tetrahedron Letters, V. 55, N 44, 29 October 2014, Pages 6125-6127. doi:10.1016/j.tetlet.2014.09.059, IF=2.391
  7. Effect of 2-Aminoadamantane Derivatives on Behavior of Mice in a Modified Light/Dark Test/ D. F. Avgustinovich, M. K. Fomina, E. V. Suslov, T. G. Tolstikova, K. P. Volcho, N. F. Salakhutdinov// Bulletin of Experimental Biology and Medicine, December 2014, V. 158, N 2, pp 213-218 doi:10.1007/s10517-014-2725-4, IF=0.365
  8. N.F. Salakhutdinov, S.S. Laev
    Triglyceride-lowering agents
    Bioorganic & Medicinal Chemistry, 2014, V.22, N 14, Pp 3551-3564. doi:10.1016/j.bmc.2014.05.008, IF=2.95
  9. Yu.S. Demidova, O.V. Ardashov, O.A. Simakova, I.L. Simakova, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Isomerization of bicyclic terpene epoxides into allylic alcohols without changing of the initial structure
    Journal of Molecular Catalysis A: Chemical, 2014, V. 388–389, Pp 162–166. Special Issue on Biomass Catalysis. doi:10.1016/j.molcata.2013.09.016, IF=3.678
  10. A.V. Pavlova, I.V. Il'ina, E.A. Morozova, D.V. Korchagina, S.Yu. Kurbakova, I.V. Sorokina, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    Potent Neuroprotective Activity of Monoterpene Derived 4-[(3aR,7aS)-1,3,3a,4,5,7a-Hexahydro-3,3,6-trimethylisobenzofuran-1-yl]-2-methoxyphenol in MPTP Mice Model
    Letters in Drug Design & Discovery, 2014, V. 11 N 5 pp. 611-617. doi:10.2174/1570180811666131210000316, IF=0.961
  11. A.S. Sokolova, О.I. Yarovaya, D.V. Korchagina, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, N.F. Salakhutdinov
    Camphor-based symmetric diimines as inhibitors of influenza virus reproduction
    Bioorganic & Medicinal Chemistry, 2014, V. 22, N 7, Pp 2141-2148. doi:10.1016/j.bmc.2014.02.038, IF=2.95
  12. Синтез сульфидов на основе (+)-усниновой кислоты/ О.А. Лузина, Д.Н. Соколов, Н.И. Комарова, Н.Ф. Салахутдинов// Химия природных соединений, 2014, №2, 236-240 doi:10.1007/s10600-014-0928-6, IF=0.5
  13. S. Kurbakova, I. Il'ina, A. Pavlova, D. Korchagina, O. Yarovaya, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Synthesis and analgesic activity of monoterpenoid-derived 2-aryl-4,4,7-trimethyl-4a,5,8,8a-tetrahydro-4H-benzo[d][1,3]dioxin-8-ols
    Medicinal Chemistry Research, 2014, V. 23, N 4, pp 1709-1717. doi:10.1007/s00044-013-0772-4
  14. Synthesis of hydroxy derivatives of limonene/ O V Ardashov, K P Volcho and N F Salakhutdinov// Russ. Chem. Rev. 2014, 83(4), 281-298. doi:10.1070/RC2014v083n04ABEH004383, IF=2.582
  15. V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Selective stepwise reduction of polynitroarenes using supercritical isopropanol as a source of hydrogen in a flow-type reactor in the presence of alumina
    Journal of Flow Chemistry, 2014, Vol. 4, N 3, 113-117. doi:10.1556/JFC-D-14-00004, IF=2.405
  16. M.N. Timofeeva, V.N. Panchenko, A.A. Abel, N.A. Khan, I. Ahmed, A.B. Ayupov, K.P. Volcho, S.H. Jhung
    Rearrangement of α-pinene oxide to campholenic aldehyde over the trimesate metal-organic frameworks MIL-100, MIL-110 and MIL-96
    Journal of Catalysis, 2014, V. 311, Pp 114-120. doi:10.1016/j.jcat.2013.11.006, IF=6.72
  17. V.P. Sivcev, D.V. Korchagina, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Efficient reduction of nitroarenes using supercritical alcohols as a source of hydrogen in flow-type reactor in the presence of alumina
    The Journal of Supercritical Fluids, 2014, V. 86, Pp 137-144. doi:10.1016/j.supflu.2013.12.012, IF=2.571
  18. A.V. Kulikov, M.A. Tikhonova, E.A. Kulikova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, N.K. Popova
    Antidepressant Activity of 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin- 6-amine hydrochloride (TC-2153): Comparison with Classical Antidepressants
    Letters in Drug Design & Discovery, 2014, V. 11, N 2, pp.169-173. doi:10.2174/15701808113106660079, IF=0.961
  19. M.N. Timofeeva, V.N. Panchenko, Z. Hasan, N.A. Khan, M.S. Mel'gunov, A.A. Abel, M.M. Matrosova, K.P. Volcho, S.H. Jhung
    Effect of iron content on selectivity in isomerization of alpha-pinene oxide to campholenic aldehyde over Fe-MMM-2 and Fe-VSB-5
    Applied Catalysis A: General, 2014, V. 469, Pp 427-433. doi:10.1016/j.apcata.2013.10.016, IF=3.674
  20. K. Volcho, Ardashov, O. Mikhalchenko, I. Il'ina, N. Salakhutdinov
    Synthetic Transformations of para-Menthane Monoterpenoids: New Way to Elaboration of Medicines for Mental Health
    Chem. Listy, 108, s120-s121 (2014)., IF=0.195
  21. CHROMATOGRAPHIC ANALYSIS OF THE COMPOSITION OF ENVIRONMENTALLY FRIENDLY PLANT PROTECTION PRODUCTS ON THE BASIS OF THE ABIES SIBERIAN/ Grazhdannikov A. E., Nechepurenko I.V., Komarova N. I.//
  22. O.V. Salomatina, A.V. Markov, E.B. Logashenko, D.V. Korchagina, M.A. Zenkova, N.F. Salakhutdinov, V.V. Vlassov, G.A. Tolstikov
    Synthesis of novel 2-cyano substituted glycyrrhetinic acid derivatives as inhibitors of cancer cells growth and NO production in LPS-activated J-774 cells
    Bioorganic & Medicinal Chemistry, 2014, V. 22, N 1, Pp 585-593. doi:10.1016/j.bmc.2013.10.049, IF=2.95
  23. И.В. Нечепуренко, Н.И. Комарова, О.Н. Потёмкин, Н.Ф. Салахутдинов
    Сезонная и возрастная динамика содержания берберина в интродуцированном berberis sibirica pall
    Химия растительного сырья. 2014. № 1. С. 195-202.

2013
  1. M. Stekrova, N. Kumar, P. Maki-Arvela, A. Aho, J. Linden, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Opening of monoterpene epoxide to a potent anti-Parkinson compound of para-menthane structure over heterogeneous catalysts
    Reaction Kinetics, Mechanisms and Catalysis. 2013, V. 110, N 2, pp 449-458. doi:10.1007/s11144-013-0615-9, IF=1.103
  2. M.V. Trushin, I.A. Arkharova, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov
    Genotoxicological safety assessment of a new antiparkinsonian substance ((1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol)
    World Journal of Medical Sciences, 2013, Т. 8, N 4, С. 355-358. doi:10.5829/idosi.wjms.2013.8.4.1123
  3. A.S. Sokolova, О. I. Yarovaya, А.V. Shernyukov, М.A. Pokrovsky, А.G. Pokrovsky, V.A. Lavrinenko, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, A.B. Beklemishev, N.F. Salakhutdinov
    New quaternary ammonium camphor derivatives and their antiviral activity, genotoxic effects and cytotoxicity
    Bioorganic & Medicinal Chemistry, 2013, V. 21, N 21, P: 6690-6698. doi:10.1016/j.bmc.2013.08.014, IF=2.903
  4. Transformations of alpha- and beta-ionones in the presence of Al2O3 in a supercritical solvent in a flow reactor/ V. I. Anikeev, V. P. Sivcev, K. P. Volcho, N. F. Salakhutdinov// Russian Journal of Physical Chemistry A A , 2013, V. 87, N 11, pp 1940-1942. doi:10.7868/S0044453713110046, IF=0.386
  5. Synthesis and structure determination of diastereoisomeric (1R,2R,6S)-6-[1-({[(1R,S))-1-(1-adamantyl)ethyl]amino}prop-1-en-2-yl)-3-methylcyclohex-3-ene-1,2-diols/ O. V. Ardashov, A. M. Genaev, G. E. Sal’nikov, D. V. Korchagina, K. P. Volcho, N. F. Salakhutdinov// Russian Journal of Organic Chemistry, 2013, V. 49, N 10, pp 1433-1436 doi:10.1134/S1070428013100059, IF=0.513
  6. A. V. Shernyukov, I.Ya. Mainagashev, D. V. Korchagina, A. M. Genaev, N. I. Komarova, N. F. Salakhutdinov, G. A. Tolstikov
    Synthesis of Nitrogen-Containing Derivatives of (18α,19β)-19-Hydroxy-2,3-secooleanane-2,3,28-trioic Acid 28,19-Lactone
    Helvetica Chimica Acta, 2013, V. 96, N 9, P. 1757-1781. doi:10.1002/hlca.201200492, IF=1.383
  7. M.A. Gilinsky, A.D. Rogachev, N.I. Komarova, N.F. Salakhutdinov, G.A. Tolstikov, S.E. Naumenko, T.V. Latysheva
    Cardioprotective Effect of Resveratrol and Resveratroloside
    Cardiovascular & Hematological Agents in Medicinal Chemistry., 2013, V. 11 N 3, P. 207 - 210. doi:10.2174/187152571103140120103302
  8. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A.V. Simakov, D.Y. Murzin
    One-pot myrtenol amination over Au nanoparticles supported on different metal oxides
    Applied Catalysis A: General, 2013, V. 456, P. 348-356 doi:10.1016/j.apcata.2013.06.013, IF=3.41
  9. O.V. Ardashov, A.V. Pavlova, D.V. Korchagina, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
    3-Methyl-6-(prop-1-en-2-yl) cyclohex-3-ene-1,2-diol: the Importance of Functional Groups for Antiparkinsonian Activity
    Medicinal Chemistry, 2013, V. 9, N 5, P. 731-739. doi:10.2174/1573406411309050013, IF=1.373
  10. V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Transformations of monoterpenoid ketones in supercritical isopropanol/CO2 in a continuous flow reactor in the presence of alumina. Competitive reduction of olefinic double bond and carbonyl group
    Journal of Supercritical Fluids, 2013, V. 80, P. 9-14. doi:10.1016/j.supflu.2013.03.028, IF=2.732
  11. G.V. Teplov, E.V. Suslov, V.V. Zarubaev, A.A. Shtro, L.A. Karpinskaya, A.D. Rogachev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Kiselev
    Synthesis of New Compounds Combining Adamantanamine and Monoterpene Fragments and their Antiviral Activity Against Influenza Virus A(H1N1)pdm09
    Letters in Drug Design & Discovery, 2013, V. 10, N 6, P. 477-485. doi:10.2174/1570180811310060002, IF=0.845
  12. O. Mikhalchenko, I. Il’ina, A. Pavlova, E. Morozova, D. Korchagina, T. Tolstikova, E. Pokushalov, K. Volcho, N.Salakhutdinov
    Synthesis and analgesic activity of new heterocyclic compounds derived from monoterpenoids
    Medicinal Chemistry Research, 2013, V. 22, N 6, P. 3026-3034. doi:10.1007/s00044-012-0310-9, IF=1.611
  13. M. Stekroval, N. Kumarl, P. Maki-Arvelal, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Selective Preparation of trans-Carveol over Ceria Supported Mesoporous Materials MCM-41 and SBA-15
    Materials, 2013, V.6, N 5, P. 2103-2118. doi:10.3390/ma6052103, IF=2.246
  14. The development of medical chemistry in the Siberian Branch of the Russian academy of sciences/ G. A. Tolstikov, B. A. Trofimov, N. F. Salakhutdinov// Herald of the Russian Academy of Sciences, 2013, V. 83, N 3, Pp 268-274 doi:10.1134/S1019331613020093, IF=0.214
  15. Н.Г. Власенко, М.Т. Егорычева, М.П. Половинка, Н.Ф. Салахутдинов
    Перспективные биологически активные вещества на яровой пшенице
    Защита и карантин растений, 2013, N 4, С. 36-37.
  16. Methods of the synthesis of A-seco derivatives of pentacyclic triterpenoids/ A. V. Shernyukov, N. F. Salakhutdinov, G. A. Tolstikov// Russian Chemical Bulletin, 2013, V. 62, N 4, pp 878-895. doi:10.1007/s11172-013-0120-3, IF=0.423
  17. O.V. Ardashov, A.V. Pavlova, D.V. Korchagina, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
    Antiparkinsonian activity of some 9-N-, O-, S- and C-derivatives of 3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol
    Bioorganic & Medicinal Chemistry, 2013, V. 21, N 5, P. 1082-1087. doi:10.1016/j.bmc.2013.01.003, IF=2.903
  18. Transformations of several monoterpenoids in the presence of aldehydes in supercritical solvents/ V. I. Anikeev, V. P. Sivcev, I. V. Il’ina, D. V. Korchagina, O. B. Statsenko, K. P. Volcho, N. F. Salakhutdinov// Russian Journal of Physical Chemistry A , 2013, V. 87, N 3, Pp 382-387. doi:10.1134/S0036024413030023, IF=0.386
  19. Antitumor activity of amides of dihydrobetulonic acid in vitro and in vivo/ I. V. Sorokina, I. Ya. Mainagashev, N. A. Zhukova, D. V. Korchagina, T. G. Tolstikova, V. P. Nikolin, N. A. Popova, M. A. Pokrovskii, A. G. Pokrovskii, N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 194-201 doi:10.1134/S106816201302012X, IF=0.523
  20. Synthesis of new (+)-usnic acid derivatives with the flavone structure/ D. N. Sokolov, M. E. Rakhmanova, O. A. Luzina, A. V. Shernyukov, N. F. Salakhutdinov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 212-216 doi:10.1007/s11172-013-0031-3, IF=0.423
  21. First synthesis of p-mentha-1,8-diene triol/ O. V. Ardashov, E. V. Khaid, O. S. Mikhal’chenko, D. V. Korchagina, K. P. Volcho, N. F. Salakhutdinov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 171-174 doi:10.1007/s11172-013-0025-1, IF=0.423
  22. A.V. Pozdeeva, N.I. Komarova, V.G. Vasiliev, A.D. Rogachev, N.F. Salakhutdinov, G.A. Tolstikov
    Aryloxyacetamides derived from resveratroloside and pinostilbenoside
    Mendeleev Communications, 2013, V. 23, N 1, P. 37-38. doi:10.1016/j.mencom.2013.01.013, IF=1.52

2012
  1. Cyclization of citronellal in a supercritical solvent in a flow reactor in the presence of Al2O3/ V.I. Anikeev, I.V. Il'ina, K.P. Volcho, N.F. Salakhutdinov// RUSS J PHYS CHEM A+, 2012, V. 86, N 12, pp.1917-1919. doi:10.1134/S0036024412120035, IF=0.458
  2. Синтез аналогов берберинбромида, содержащих фрагмент третичных амидов уксусной кислоты в 9-О-положениии/ И.В. Нечепуренко, Н.И. Комарова, В.Г. Васильев, Н.Ф. Салахутдинов// Хим. Природ. Соедин., 2012, № 6, 924–929. doi:10.1007/s10600-013-0461-z, IF=1.29
  3. D.N. Sokolov, V.V. Zarubaev, A.A. Shtro, O.A. Luzina, N.I. Komarova, N.F. Salakhutdinov, O.I. Kiselev
    Anti-viral activity of (-)- and (+)-usnic acids and their derivatives against influenza virus A(H1N1)2009
    Bioorg. Med. Chem. Lett., V. 22, N. 23, 7060-7064. doi:10.1016/j.bmcl.2012.09.084, IF=2.553
  4. V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Transformations of acetophenone and its derivatives in supercritical fluid isopropanol/CO2 in a continuous flow reactor in the presence of alumina
    J. Supercri.l Fluid., 2012, V. 70, 35–39. doi:10.1016/j.supflu.2012.05.012, IF=2.859
  5. Нитрование и получение секо-производных аллобетулина/ А.В. Шернюков, И.Я. Майнагашев, Д.В. Корчагина, Ю.В. Гатилов, Н.Ф. Салахутдинов, Г.А. Толстиков// Хим. Природ. Соедин., 2012, № 5, 732-736. doi:10.1007/s10600-012-0392-0, IF=1.29
  6. Synthesis of Betulin Derivatives: N '{N-[3-OXO-20(29)-Lupen-28-OYL]-9-Aminononanoyl}3-Amino-3-Phenylpropionic Acid/ S.V. Sysolyatin, V.N. Surmachev, V.V. Malykhin, A.I. Kalashnikov, I.A. Surmacheva, E.G. Sonina, A.S. Dubkov, G.A. Tolstikov, E.E. Shul'ts, N.F. Salakhutdinov, U.M. Dzhemilev// PHARM CHEM J+, 2012, V. 46, N 8, pp. 473-477. doi:10.1007/s11094-012-0828-7, IF=0.372
  7. A. Zakharenko, D. Sokolov, O. Luzina, M. Sukhanova, S. Khodyreva, O. Zakharova, N. Salakhutdinov, O. Lavrik
    Influence of Usnic Acid and its Derivatives on the Activity of Mammalian Poly(ADP-ribose)polymerase 1 and DNA Polymerase β
    Med. Chem., 2012, V. 8, № 5, 883-893. doi:10.2174/1573406411309050013, IF=1.496
  8. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, А.И. Шевела, В.В. Власов
    Комплексный подход к лечению асептического некроза головки бедренной кости
    Фундаментальные исследования, 2012, № 8, 193-196.
  9. Synthesis and Anxiolytic Activity of 2-Aminoadamantane Derivatives Containing Monoterpene Fragments/ I.G. Kapitsa, E.V. Suslov, G.V. Teplov, D.V. Korchagina, N.I. Komarova, K.P. Volcho, T.A. Voronina, A.I. Shevela, N.F. Salakhutdinov// PHARM CHEM J+, 2012, V. 46, N 5, pp. 263-265. doi:10.1007/s11094-012-0775-3, IF=0.372
  10. Usnic acid: preparation, structure, properties and chemical transformations/ D.N. Sokolov, O.A. Luzina, N.F. Salakhutdinov// RUSS CHEM REV+, 2012, V. 81, N 8, pp. 747-768. doi:10.1070/RC2012v081n08ABEH004245, IF=2.644
  11. Вторичные метаболиты лишайника Cladonia stellaris/ М.П. Половинка, Н.И. Комарова, Д.В. Корчагина, Д.Н. Соколов, О.А. Лузина, Н.Г. Власенко, А.А. Малюга, Е.В. Романова, Н.Ф. Салахутдинов// Хим. Природ. Соедин., 2012, № 3, 356-359. doi:10.1007/s10600-012-0259-4, IF=1.29
  12. Синтез ауронов на основе усниновой кислоты/ Д.Н. Соколов, О.А. Лузина, А.В. Шернюков, Н.Ф. Салахутдинов// Хим. Природ. Соедин., 2012, № 3, 350-355. doi:10.1007/s10600-012-0258-5, IF=1.29
  13. Синтез простых эфиров пиразольных производных (+)-усниновой кислоты/ Д.Н. Соколов, О.А. Лузина, Н.Ф. Салахутдинов// Хим. Природ. Соедин., 2012, № 3, 345-349. doi:10.1007/s10600-012-0257-6, IF=1.29
  14. A.V. Kulikov, M.A. Tikhonova, E.A. Kulikova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, N.K. Popova
    A new synthetic varacin analogue, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), decreased hereditary catalepsy and increased the BDNF gene expression in the hippocampus in mice
    Psychopharmacology, 2012, V. 221, N 3, 469–478. doi:10.1007/s00213-011-2594-8, IF=4.77
  15. М.П. Половинка, Н.Г. Власенко, А.А. Малюга, М.Т. Егорычева, Н.Ф. Салахутдинов
    Новые комплексные препараты на основе экстрактов лиственницы и лишайника – эффективное средство повышения урожайности яровой пшеницы
    Химия в интересах устойчивого развития, 2012, № 6, 713-720.
  16. T.G. Tolstikova, A.V. Pavlova, E.A. Morozova, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov
    The analgesic activity of 8- ( trifluoromethyl)-1,2,3,4,5-benzopentathiepine-6-amine and its hydrochloride
    Lett. Drug Des. Discov., 2012, V. 9, N 5, 513-516. doi:10.2174/157018012800389296, IF=0.871
  17. А.Г. Шушарин, М.П. Половинка, В.В. Морозов
    Новый способ лечения синовита и кисты Бейкера у пациентов с ревматоидным артритом
    Международный журнал прикладных и фундаментальных исследований, 2012. № 4, 61-62. full text
  18. А.Г. Шушарин, М.П. Половинка, В.П. Прохоренко, В.В. Морозов
    Лечение асептического некроза головки бедренной кости инъекциями перфторана в сочетании с лазеротерапией
    Международный журнал прикладных и фундаментальных исследований, 2012, № 4, 51-52.
  19. А.Г. Шушарин, М.П. Половинка, В.П. Прохоренко, В.В. Морозов
    Опыт лечения асептического некроза головки бедренной кости, стартовавшего после операции эндопротезирования
    Международный журнал прикладных и фундаментальных исследований, 2012, № 4, 44-46.
  20. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, В. Морозов
    Случаи асептического некроза головки бедренной кости у пациентов с рецидивирующим генитальным герпесом: клинический пример, опыт лечения
    Международный журнал прикладных и фундаментальных исследований, 2012, № 4, 28-29.
  21. Н.Ф. Салахутдинов
    Создание академиком Г.А. Толстиковым Отдела химии природных и биологически активных соединений в Новосибирском институте органической химии СО РАН
    Известия Уфимского научного центра РАН, 2012, № 4, 118-120.
  22. О.С. Михальченко, К.П. Волчо, Т.Г. Толстикова, Н.Ф. Салахутдинов
    Синтез гетероциклических соединений взаимодействием альдегидов с монотерпеноидами в присутствии монтмориллонитовых глин
    Известия Уфимского научного центра РАН, 2012, № 4, 53-79.
  23. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, А.И. Шевела, В.В. Власов
    Лечение асептического некроза ТБС с применением локальной инъекционной терапии под УЗ-контролем
    Современные проблемы науки и образования, 2012, № 4, URL: http://www.science-education.ru/104-6807
  24. В.В. Фоменко, С.С. Лаев
    Как победить атеросклероз
    Наука из первых рук, 2012, № 4 (46), 26-31.
  25. M.M. Kutuzov, A.L. Zakharenko, M.V. Sukhanova, S.N. Khodyreva, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Polysulfide compounds as inhibitors of the key base excision repair enzymes
    Biopolym. Cell, 2012, V. 28, N 3, 239–241. doi:10.7124/bc.28.3
  26. A.L. Zakharenko, O.V. Salomatina, M.V. Sukhanova, M.M. Kutuzov, E.S. Ilina, S.N. Khodyreva, V. Schreiber, N.F. Salakhutdinov, O.I. Lavrik
    Glycyrrhetinic acid and its derivatives as inhibitors of poly(ADP-ribose)polymerases 1 and 2, apurinic/apyrimidinic endonuclease 1 and DNA polymerase β
    Biopolym. Cell, 2012, V. 28, N 3, 223–228. doi:10.7124/bc.28.3
  27. Взаимодействие изоцемброла со спиртами на глине/ О.И. Яровая, Д.В. Корчагина, Н.Ф. Салахутдинов, Г.А. Толстиков// Хим. Природ. Соедин., 2012, № 1, 54-57. doi:10.1007/s10600-012-0158-8, IF=1.29
  28. Взаимодействие некоторых производных гликозидов резвератрола с гипохлоритами в различных средах/ А.Д. Рогачев, Н.И. Комарова, А.В. Поздеева, Д.В. Корчагина, В.Г. Васильев, Н.Ф. Салахутдинов, Г.А. Толстиков// Хим. Природ. Соедин., 2012, № 1, 5-11. doi:10.1007/s10600-012-0146-z, IF=1.29
  29. Screening of Usnic Acid Derivatives as Potential Synergists of the Entomopathogenic Fungus Beauveria bassiana for the Control of Colorado Potato Beetle/ Kryukov V.Yu.1, Luzina O.A.2, Yaroslavtseva O.N.1, Polovinka M.P.2, Salakhutdinov N.F.2, Glupov V.V.// Agricultural Chemistry
  30. Oxidation of alpha-pinene by atmospheric oxygen in the supercritical CO2-ethyl acetate system in the presence of Co(II) complexes/ V.I. Anikeev, I.V. Il'ina, S.Yu. Kurbakova, A.A. Nefedov, K.P. Volcho, N.F. Salakhutdinov// RUSS J PHYS CHEM A+, 2012, V. 86, N 2, pp.190-195. doi:10.1134/S0036024412010049, IF=0.458
  31. Chiral schiff bases synthesized from terpenes of pinane series in asymmetric metall complex oxidation of sulfi des/ I.V. Il'ina, E.A. Koneva, D.V. Korchagina, G.E. Sal'Nikov, A.M. Genaev, K.P. Volcho, N.F. Salakhutdinov// RUSS J ORG CHEM+. 2012, V.48, N 2, pp. 214-220. doi:10.1134/S1070428012020108, IF=0.648
  32. I.V. Il'ina, V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    The Meerwein-Ponndorf-Verley type reaction in a mixture of supercritical isopropanol/CO2 in a continuous flow reactor in the presence of alumina
    J. Supercri.l Fluid., 2012, V. 61, 115–118. doi:10.1016/j.supflu.2011.10.004, IF=2.859
  33. Synthesis of new chiral schiff bases from (+)-2-carene/ E.A. Koneva, D.V. Korchagina, A.M. Genaev, K.P. Volcho, N.F. Salakhutdinov// RUSS J ORG CHEM+, 2012, V.48, N 1, pp. 32-39. doi:10.1134/S1070428012010058, IF=0.648

2011
  1. К.P. Volcho, I.V. Il'ina, N.F. Salakhutdinov, V.I. Anikeev
    Reactivity of verbenol and verbenone epoxides in supercritical solvents
    ARKIVOC, 2011, (viii), 134-140. doi:10.3998/ark.5550190.0012.809, IF=1.95
  2. I.V. Il'ina, S.Yu. Kurbakova, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Meerwein-Ponndorf-Verley reduction of aldehydes formed in situ from α- and β-pinene epoxides in a supercritical fluid in the presence of alumina
    J. Saudi Chem. Soc., 2011, V. 15, N 4, 313-317. doi:10.1016/j.jscs.2011.07.010
  3. Взаимодействие (+)-усниновой кислоты и некоторых ее производных с диазометаном/ Д.Н. Соколов, О.А. Лузина, Д.В. Корчагина, М.П. Половинка, Н.Ф. Салахутдинов// Природ. Соедин., 2011, № 5, 623–627. doi:10.1007/s10600-011-0041-z, IF=0.693
  4. Synthesis of chalcones derived from (+)- and (-)-usnic acids/ D.N. Sokolov, O.A. Luzina, M.P. Polovinka, N.F. Salakhutdinov, G.A. Tolstikov// RUSS CHEM B+, 2011, V. 60, N 11, pp 2406-2411. doi:10.1007/s11172-011-0370-x, IF=0.629
  5. Acid-catalyzed transformations of diepoxy derivatives of terpinolene/ O. V. Salomatina, O. I. Yarovaya, D. V. Korchagina, Yu. V. Gatilov, V. A. Barkhash// RUSS J ORG CHEM+, 2011, V. 47, N 10, pp 1479-1486. doi:10.1134/S1070428011100046, IF=0.634
  6. N.F. Salakhutdinov, L.N. Rogoza, G.A. Tolstikov
    Hypercholesteremia: Chemical Aspect of Approach
    Curr. Med. Chem., 2011. V. 18, N 26, pp 4076-4105. doi:10.2174/092986711796957248, IF=4.63
  7. T.M. Khomenko, D.V. Korchagina, N.I. Komarova, K.P. Volcho, N.F. Salakhutdinov
    Synthesis of 6-Amino-benzopentathiepines by Reactions of 4-Nitro-benzyldithiol-2-ones with NaHS
    Lett. Org. Chem., 2011, V. 8, N 3, 193-197. doi:10.2174/157017811795038331, IF=0.785
  8. Turpentine-based flotation agents in copper-nickel ore flotation/ S.A. Kondrat'ev, V.I. Rostovtsev, O.I. Yarovaya, N.F. Salakhutdinov// J MIN SCI+, -2011, V. 47, N 4, pp 514-521. doi:10.1134/S1062739147040149, IF=0.389
  9. LDLR Up-Regulatory Activity of Berberine and Its Bromo and Iodo Derivatives in Human Liver HepG2 Cells/ I.V. Nechepurenko, U.A. Boyarskikh, N.I. Komarova, M.P. Polovinka, M.L. Filipenko, G.I. Lifshits, N.F. Salakhutdinov, G.A. Tolstikov// DOKL CHEM, 2011, V. 439, N 1, pp. 204-208. doi:10.1134/S0012500811070093 Part: 1, IF=0.256
  10. Terpenes in Superacids: Synthesis-Related Possibilities/ M. P. Polovinka, N. F. Salakhytdinov// Chemistry for Sustainable Development, 2011, Т. 19, № 6, 619-632.
  11. O.V. Ardashov, A.V. Pavlova, I.V. Il'ina, E.A. Morozova, D.V. Korchagina, E.V. Karpova, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
    Highly potent activity of (1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol in animal models of Parkinson's disease
    J. Med. Chem., 2011, V. 54, N 11, 3866-74. doi:10.1021/jm2001579, IF=5.206
  12. Восстановление 2,3-секо-28-оксо-19β,28-эпокси-18α-олеан-2,3-дикарбоновой кислоты и её циклического ангидрида/ А.В. Шернюков, И.Я. Майнагашев, Д.В. Корчагина, Ю.В. Гатилов, Н.Ф. Салахутдинов, Г.А. Толстиков// Хим. Природ. Соедин., 2011, № 2, 218-223. doi:10.1007/s10600-011-9891-7, IF=0.693
  13. Взаимодействие (+)-усниновой кислоты и некоторых ее производных с борогидридом натрия/ Д.Н. Соколов, О.А. Лузина, М.П. Половинка, Н.Ф. Салахутдинов// Хим. Природ. Соедин., 2011, № 2, 188–190. doi:10.1007/s10600-011-9882-8, IF=0.693
  14. "Bius" - an Efficient Tool to Increase the Crop Capacity of Spring Wheat and Potatoes/ M. P. Polovinka, N. G. Vlasenko, A. A. Malyuga, M. T. Egorycheva, N. F. Salakhutdinov, G.A. Tolstikov// Chemistry for Sustainable Development, 2011, Т. 19, № 6, 637-642.
  15. O.V. Ardashov, V.V. Zarubaev, A.A. Shtro, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Kiselev
    Antiviral activity of 3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol and its derivatives against influenza A(H1N1)2009 virus
    Lett. Drug Des. Discov., 2011, V. 8, N 4, 375-380. doi:10.2174/157018011794839411, IF=0.667
  16. А.Г. Шушарин, В.В. Морозов, М.П. Половинка
    Медицинское тепловидение – современные возможности метода
    Современные проблемы науки и образования, 2011 , № 4, URL: www.science-education.ru/98-4726
  17. E.A. Koneva, E.V. Suslov, D.V. Korchagina, A.M. Genaev, K.P. Volcho, N.F. Salakhutdinov
    Catalytic asymmetric addition of diethylzinc to benzaldehyde using α-pinene-derived ligands
    The Open Catalysis Journal, 2011, V. 4, 107-112.
  18. Effect of a new potential psychotropic drug, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride, on the expression of serotonin-related genes in the mouse brain/ A.V. Kulikov, M.A. Tikhonova, N.K. Popova, T.M. Khomenko, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, E.A. Kulikova// MOL BIOL+, -2011, V. 45, N 2, pp 251-257. doi:10.1134/S0026893310061044, IF=0.653
  19. E.B. Logashenko, O.V. Salomatina, A.V. Markov, D.V. Korchagina, N.F. Salakhutdinov, G.A. Tolstikov, V.V. Vlasov, M.A. Zenkova
    Synthesis of Pro-Apoptopic Activity of Novel Glycyrrhetinic Acid Derivatives
    ChemBioChem, 2011, V. 12, N 5, 784-794. doi:10.1002/cbic.201000618, IF=3.944
  20. I.V. Il’ina, K.P. Volcho, O.S. Mikhalchenko, D.V. Korchagina, N.F. Salakhutdinov
    Reactions of Verbenol Epoxide with Aromatic Aldehydes Containing Hydroxy or Methoxy Groups in the Presence of Montmorillonite Clay
    Helv. Chim. Acta, 2011, V. 94, N 3, 502-513. doi:10.1002/hlca.201000269, IF=1.284

2010
  1. A highly effective antiparkinsonian drug of a new structural type/ T. G. Tolstikova, A. V. Pavlova, Ye. A. Morozova, O. V. Ardashov, I. V. Il’ina, K. P. Volcho, N. F. Salakhutdinov, G. A. Tolstikov// Doklady Biological Sciences, 2010, V. 433, N 1, pp 398-399. doi:10.1134/S0012496610060074
  2. Hydrogenation and conformational analysis of (1R,2R,6S)-3-methyl-6-(1-methylethenyl)cyclohex-3-ene-1,2-diol/ O.V. Ardashov, A.M. Genaev, I.V. Il'ina, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, G.A. Tolstikov// RUSS J ORG CHEM+, 2010, V. 46, N 12, pp 1786-1789. doi:10.1134/S1070428010120043, IF=0.524
  3. N.F. Salakhutdinov, G.A. Tolstikov
    Diquaternized Curarelike Myorelaxants: Structure and Biological Activity
    Mini-Rev. Med. Chem., 2010, V. 10, N 13, 1248-1262. doi:10.2174/13895575110091248, IF=2.97
  4. Окисление усниновой кислоты/ Д.Н. Соколов, О.А. Лузина, М.П. Половинка, Д.В. Корчагина, Ю.В. Гатилов, Н.Ф. Салахутдинов// Химия природных соединений, 2010, V. 46, N 5, 616-618. doi:10.1007/s10600-010-9727-x, IF=0.572
  5. I.V. Il’ina, K.P. Volcho, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, E.V. Karpova, N.F. Salakhutdinov
    Unusual Reactions of (+)-Car-2-ene and (+)-Car-3-ene with Aldehydes on K10 clay
    Helv. Chim. Acta, 2010, V. 93, 2135-2150. doi:10.1002/hlca.201000145, IF=1.434
  6. New Chiral Ligands Based on (+)-α-Pinene/ E.A. Koneva, D.V. Korchagina, Yu.V. Gatilov, A.M. Genaev, A.P. Krysin, K.P. Volcho, A.G. Tolstikov, N.F. Salakhutdinov// RUSS J ORG CHEM+, 2010, V. 46, N 8, pp 1109-1115. doi:10.1134/S1070428010080014, IF=0.524
  7. Reaction of sabinene with aldehydes in the presence of montmorillonite K10 clay/ I.V. Il'ina, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, G.A. Tolstikov// RUSS J ORG CHEM+, 2010, V. 46, N 7, pp 1002-1005. doi:10.1134/S1070428010070079, IF=0.524
  8. Reaction of (-)-cis-verbenol epoxide with aromatic aldehydes over montmorillonite K10 clay/ I.V. Il'ina, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov// RUSS J ORG CHEM+, 2010, V. 46, N 7, pp 998-1001. doi:10.1134/S1070428010070067, IF=0.524
  9. STUDY OF ANTIATHEROGENIC EFFECTS OF SIMVAGLYZIN ON RABBIT'S HYPERCHOLESTEROLEMIA MODEL/ Yu.I. Ragino, V.А. Vavilin, N.F. Salakhutdinov, S.I. Makarova, Е.М. Stakhneva, О.G. Safronova// Атеросклероз, 2010, Т. 6, № 1, 5-11.(in russian)
  10. "Bioklad" as Efficient Protectant of the Seeds of Spring Wheat/ M. T. Egorycheva, N. G. Vlasenko, M. P. Polovinka, N. F. Salakhutdinov// Chemistry for Sustainable Development, 2010, V.18., № 6, pp.729-733. (in russian)
  11. Inhibitors of NO-Synthases: the Chemical Aspect of the Problem/ Yu. S.Kosenkova, M. P. Polovinka, N. F. Salakhutdinov// Chemistry for Sustainable Development, 2010, V.18., № 6, pp.669-690. (in russian)
  12. Complex of CuII with a chiral Schiff base (H2L) derived from the natural monoterpene (+)-6h-pinene. Synthesis and the properties of the complex and its solvate with acetonitrile. Crystal structure of [Cu(HL)Cl]•H2O/ T.E. Kokina, R.F. Klevtsova, L.A. Glinskaya, E.G. Boguslavskii, E.A. Koneva, K.P. Volcho, S.V. Larionov// RUSS CHEM B+, 2010, V. 59, N 4, pp 712-716. doi:10.1007/s11172-010-0151-y, IF=0.416
  13. Reaction of (-)-carvone with phenylmethanethiol in the presence of basic Cs β-zeolite/ E.V. Suslov, K.P. Volcho, D.V. Korchagina, N.F. Salakhutdinov// RUSS J ORG CHEM+, 2010, V. 46, N 4, pp 503-505. doi:10.1134/S1070428010040093, IF=0.524
  14. Hydroxyketones of para-Menthane Series as Promising Analgetics/ A.V. Pavlova, T.G. Tolstikova, E.A. Morozova, O.V. Ardashov, I.V. Ilyina, K.P. Volcho, N.F. Salakhutdinov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp.423-455. (in russian)
  15. Effect of the Nature of Exchange Cation in Montmorillonite Clay on the Direction of Transformations of Verbenol Epoxide/ I.V. Ilyina, S.Yu. Kurbakova, K.P. Volcho, N.F. Salakhutdinov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp.457-460. (in russian)
  16. Antituberculous Activity of Natural and Synthetic Compounds/ L.N. Rogoza, N.F. Salakhutdinov G.A.Tolstikov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp.423-455. (in russian)
  17. V.I. Anikeev, I.V. Il'ina, K.P. Volcho, A. Yermakova, N.F. Salakhutdinov
    Reactivity of α-pinene epoxide in supercritical solvents
    J. Supercrit. Fluid., 2010, V. 52, N 1, 71–75. doi:10.1016/j.supflu.2009.11.003, IF=2.638
  18. Synthesis and biological activity of novel glycyrrhetic acid derivatives/ O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova, V.V. Vlasov, G.A. Tolstikov// Doklady Chemistry, 2010, V. 430, N 2, pp 35-38. doi:10.1134/S0012500810020011 Part: 2, IF=0.204
  19. The thermolysis of &alpha-pinene and verbenone epoxides in supercritical solvents/ V.I. Anikeev, A. Ermakova, I.V. Il'Ina, K.P. Volcho, N.F. Salakhutdinov// RUSS J PHYS CHEM A+, 2010, V. 84, № 7, pp 1112-1117. doi:10.1134/S0036024410070058, IF=0.437
  20. Berberin: Chemistry and Biological Activity/ I. V.Nechepurenko, N. F. Salakhutdinov , G. A. Tolstikov// Chemistry for Sustainable Development, 2010, V.18., № 1, pp.1 – 23. (in russian).

2009
  1. (4S,5R,6R)-para-mentha-1,8-dien-5,6-diol is a new highly effective anticonvulsant agent/ T.G. Tolstikova, A.V. Pavlova, M.P. Dolgikh, I.V. Il'ina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, G.A. Tolstikov// Doklady Biological Sciences, 2009, V. 429, N 1, pp 494-496. doi:10.1134/S0012496609060039
  2. Natural Montmorillonite Clay as Prebiotic Catalyst/ I.V. Il'ina, E.V. Suslov, T.M. Khomenko, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov// PALEONTOLOGICAL JOURNAL, 2009, V. 43, N 8, pp 958-964 doi:10.1134/S0031030109080139, IF=0.368
  3. Chemical modification of usnic acid: III. Reaction of (+)-usnic acid with substituted phenylhydrazines/ O.A. Luzina, M.P. Polovinka, N.F. Salakhutdinov, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2009, V. 45, N 12, pp 1783-1789 doi:10.1134/S1070428009120069, IF=0.556
  4. Spirocyclization of 2,3-seco-19 beta,28-epoxy-28-oxo-18 alpha-olean-2,3-dicarboxylic anhydride with benzylamines/ A.V. Shernyukov, I.Ya. Mainagashev, D.V. Korchagina, Yu.V. Gatilov, N.F. Salakhutdinov, G.A. Tolstikov// Doklady Chemistry, 2009, V.429,N 1, pp 286-289 doi:10.1134/S0012500809110081, IF=0.231
  5. Аминопроизводные усниновой кислоты/ А.А. Тазетдинова, О.А. Лузина, М.П. Половинка, Н.Ф. Салахутдинов, Г.А. Толстиков// Хим. Природ. Соедин., 2009, №. 6, 672. doi:10.1007/s10600-010-9502-z, IF=0.467
  6. Synthesis, composition, and properties of products formed in interaction of ortho-tert-butylphenol with sulfur monochloride/ A. P. Krysin, T. G. Egorova, N. I. Komarova, V. G. Vasil’ev, L. M. Pokrovskii// Russian Journal of Applied Chemistry, 2009, V. 82, N 11, pp 1965-1969 doi:10.1134/S1070427209110123, IF=0.291
  7. Unusual products of the reactions of verbenone and verbenol with N-bromosuccinimide in the presence of water/ O.V. Ardashov, I.V. Il'ina, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov// Russian Journal of Organic Chemistry, 2009, V. 45, N 10, pp 1452-1455. doi:10.1134/S1070428009100054, IF=0.556
  8. Asymmetric Oxidation of 4-Nitro-6-trifluoromethyl-1,2,3-benzotrithiole/ T.M. Khomenko, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov// Russian Journal of Organic Chemistry, 2009, V. 45, N 9, pp 1402-1404 doi:10.1134/S1070428009090140, IF=0.556
  9. T.M. Khomenko, T.G. Tolstikova, A.V. Bolkunov, M.P. Dolgikh, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    8-(Trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine: Novel Aminobenzopentathiepine Having in vivo Anticonvulsant and Anxiolytic Activities
    Lett. Drug Des. Discov., 2009, V. 6, N 6, 464-467. doi:10.2174/157018009789057544, IF=0.786
  10. Synthesis of new chiral schiff bases from (+)-3-carene and their use in asymmetric oxidation of sulfides catalyzed by metal complexes/ E.A. Koneva, K.P. Volcho, D.V. Korchagina, N.F. Salakhutdinov, A.G. Tolstikov// Russian Journal of Organic Chemistry, 2009, V. 45, N 6, pp 815-824 doi:10.1134/S1070428009060037, IF=0.556
  11. L.N. Rogoza, N.F. Salachutdinov, G.A. Tolstikov
    Natural and synthetic antimycobacterial compounds.
    Mini-Reviews in Organic Chemistry. 2009. V.. 6. N 2, pp 135-151. doi:10.2174/157019309788167657, IF=1.449
  12. Синтез гетероциклических соединений с использованием основного цеолита Csβ/ Е.В. Суслов, Д.В. Корчагина, К.П. Волчо, Н.Ф. Салахутдинов// Хим. Гетероцикл. Соедин., 2009, Т. 45, № 5. 711-718. doi:10.1007/s10593-009-0296-5, IF=0.462
  13. Выделение и идентификация 4',6-диметокси-7-гидрокси-изофлавона - компонента культивируемых in vitro корней Hedysarum theinum/ И.В. Нечепуренко, Н.И. Комарова, И.Н. Кузовкина, М.Ю. Вдовитченко, М.П. Половинка, Н.Ф. Салахутдинов// Хим. Природ. Соедин., 2009, № 3, 357–358. doi:10.1007/s10600-009-9327-9, IF=0.467
  14. Ю.С. Косенкова, М.П. Половинка, Д.В. Корчагина, Н.И. Комарова, Н.Ю. Курочкина, В.А. Черемушкина, Н.Ф. Салахутдинов
    Сезонная динамика накопления риккардина С в Primula macrocalyx Bge.
    Химия в интересах устойчивого развития, 2009, Т.17, N 5, С. 507-511.
  15. Ю.С. Косенкова, М.П. Половинка, Д.В. Корчагина, Н.И. Комарова, Н.Ф. Салахутдинов
    Получение эфиров риккардина С- потенциальных ингибиторов NO-синтазы
    Химия в интересах устойчивого развития, 2009, Т. 17, N 5, С. 495-506.
  16. Asymmetric oxidation of sulfides catalyzed by titanium and vanadium complexes in the synthesis of biologically active sulfoxides/ K.P. Volcho, N.F. Salakhutdinov// Russian Chemical Reviews, 2009, V. 78, N 5, pp 457-464. doi:10.1070/RC2009v078n05ABEH004023, IF=1.832
  17. O.A. Luzina, M.P. Polovinka, N.F. Salakhutdinov, G.A. Tolstikov
    Schmidt reaction of usnic acid
    Chemistry of Natural Compounds, 2009, V. 45, N 2, pp 251-252. doi:10.1007/s10600-009-9267-4, IF=0.467
  18. О.В. Саломатина, Д.В. Корчагина, Н.Ф. Салахутдинов, Г.А. Толстиков
    Получение метилового эфира 2-циано-3,12-диоксо-11-дезоксо-18βH-глициретт-1(2),11(9)-диеновой кислоты
    Химия в интересах устойчивого развития, 2009. Т. 17. N 3, С. 297-303.
  19. А.Д. Рогачев, Н.И. Комарова, Д.В. Корчагина, М.П. Долгих, И.В. Сорокина, Д.С. Баев, Т.Г. Толстикова, В.В. Фоменко, Н.Ф. Салахутдинов
    Некоторые пренилированные фенолы рододендрона Адамса Rhododendron adamsii: выделение, модификация и фармакологические испытания
    Химия в интересах устойчивого развития, 2009. Т.17. N 2, C. 191-198.
  20. С.С. Лаев, В.В. Фоменко, Н.И. Комарова, Д.В. Корчагина, Н.Ф. Салахутдинов
    Реакции эпоксида β-пинена с некоторыми аминами под воздействием микроволнового излучения
    Химия в интересах устойчивого развития, 2009. Т. 17. N 2, С. 161-166.
  21. Изучение структуры олигомерных проантоцианидинов корней Hedysarum Theinum методами тиолиза и MC MALDI-TOF/ И.В. Нечепуренко, Н.И. Комарова, Ю.В. Герасимова, В.В. Коваль, М.П. Половинка, Д.В. Корчагина, Н.Ф. Салахутдинов// Хим. Природ. Соедин. , 2009, №1, 30-36. doi:10.1007/s10600-009-9216-2, IF=0.467
  22. Определение количественного содержания основных флавоноидов листьев и стеблей Rhododendron adamsii методом ВЭЖХ./ Н.И. Комарова, А.Д. Рогачев, Е.И. Черняк, С.В. Морозов, В.В. Фоменко, Н.Ф. Салахутдинов// Хим. Природ. Соедин. ,, 2009, №. 1, 26-29. doi:10.1007/s10600-009-9215-3, IF=0.467
  23. Synthetic transformations of higher terpenoids: XVIII. Synthesis of optically active 9,10-anthraquinone derivatives/ E.E. Shul'ts, D.S. Oleinikov, I.V. Nechepurenko, M.M. Shakirov, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2009, V. 45, N 1, pp 87-101 doi:10.1134/S1070428009010126, IF=0.556
  24. Diels-alder reactions with cyclic sulfones: VIII. Organic catalysis in the synthesis of spiro[1-benzothiophene-4,5 '-pyrimidine]-2 ',4',6'-trione 1,1-dioxides and 2 '-thioxospiro[1-benzothiophene-4,5 '-pyrimidine]-4 ',6 '-dione 1,1-dioxides/ E.E. Shul'ts, G.N. Andreev, M.M. Shakirov, N.I. Komarova, I.Y. Bagryanskaya, Yu.V. Gatilov, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2009, V. 45, N 1, pp 87-101 doi:10.1134/S1070428009010126, IF=0.556

2008
  1. The cholesterol lowering properties of the complex compound simvastatin with glycyrrhizic acid (simvaglyzin) in experimental models/ V. A. Vavilin, N. F. Salakhutdinov, Yu. I. Ragino, N. E. Polyakov, M. B. Taraban, T. V. Leshina, E. M. Stakhneva, V. V. Lyakhovich, Yu. P. Nikitin, G. A. Tolstikov// Biochemistry (Moscow) Supplement Series B: Biomedical Chemistry, 2008, V/ 2, N 4, pp 373-380 doi:10.1134/S1990750808040070
  2. Transformations of Terpenoids on Acidic Clays/ // doi:10.2174/157019308786242151, IF=2
  3. О.В. Бахвалов, В.В. Фоменко, Н.Ф. Салахутдинов
    Современные способы эпоксидирования α- и β-пиненов, 3-карена и лимонена
    Химия в инстересах устойчивого развития, 2008, Т. 16, № 6, 643-701.
  4. Derivatives of Pinane Amino Acids as New Anticonvulsants/ T. G. Tolstikova, E. A. Morozova, A. V. Pavlova, A. V. Bolkunov, M. P. Dolgikh, E. A. Koneva, K. P. Volcho, N. F. Salakhutdinov, G. A. Tolstikov// Doklady Chemistry, 2008, V. 422, N 2, pp 248-250 doi:10.1134/S0012500808100029, IF=0.442
  5. E.A. Koneva, K.P. Volcho, Yu.V. Gatilov, D.V. Korchagina, G.E. Salnikov, N.F. Salakhutdinov
    Synthesis of the Derivatives of the Optically Active β-Amino Acids from (+)-2-Car-2-ene
    Helvetica Chimica Acta, 2008, V. 91, N 10, Pp 1849-1856. doi:10.1002/hlca.200890197, IF=1.514
  6. Жирнокислотный состав и вторичные метаболиты малополярных экстрактов надземной части Primula macrocalyx Bge/ Ю.С. Косенкова, М.П. Половинка, Н.И. Комарова, Д.В. Корчагина, С.В. Морозов, А.И. Вялков, Н.Ф. Салахутдинов// Химия природных соединений, 2008, Т. 44, N 5, 457-460. doi:10.1007/s10600-008-9145-5, IF=0.442
  7. Antioxidant and endothelium-stabilizing effects of simvaglyzin on rabbits with experimental hypercholesterolemia/ Yu.I. Ragino, V.A. Vavilin, N.F. Salakhutdinov, S.I. Makarova, E.M. Stakhneva, O.G. Safronova, V.V. Lyakhovich, Yu.P. Nikitin, G.A. Tolstikov// Bulletin of Experimental Biology and Medicine, 2008, V. 146, N 2, pp 206-209 doi:10.1007/s10517-008-0252-x, IF=0.248
  8. Synthesis of optically active omeprazole by catalysis with vanadyl complexes with chiral Schiff bases/ E.A. Koneva, T.M. Khomenko, S.Yu. Kurbakova, N.I. Komarova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, G.A. Tolstikov, A.G. Tolstikov// Russian Chemical Bulletin, 2008, V. 57, N 8, Pp 1680-1685. doi:10.1007/s11172-008-0221-6, IF=0.537
  9. Е.М. Стахнева, В.А. Вавилин, Н.Ф. Салахутдинов, О.Г. Сафронова, С.И. Макарова, М.В. Иванова, Ю.И. Рагино
    Липидснижающий и антиоксидантный эффекты симваглизина при экспериментальной гиперхолестеринемии
    Регионарное кровообращение и микроциркуляция, 2008, Т. 7, № 2, 52-53.
  10. Е.В. Суслов, Д.В. Корчагина, В.В. Самуков, К.П. Волчо, Н.Ф. Салахутдинов
    Влияние модификации цеолита Csβ хиральными веществами на ход реакции 5,5,8-триметилнона-3,7-диен-2-она с малононитрилом
    Химия в инстересах устойчивого развития, 2008, Т. 16, № 4, 441–447.
  11. Study of cholesterol-lowering effect and safety of simvaglisin on rabbit model of hypercholesterolemia/ Yu.I. Ragino, E.M. Stakhneva, O.G. Safronova, Yu.P. Nikitin, V.A. Vavilin, S.I. Makarova, N.F. Salakhutdinov, G.A. Tolstikov// Bulletin of Experimental Biology and Medicine, 2008, V. 145, N 3, pp 317-319 doi:10.1007/s10517-008-0079-5, IF=0.248
  12. Низкомолекулярные фенольные соединения корней копеечника чайного Hedysarum theinum Krasnob/ И.В. Нечепуренко, М.П. Половинка, Н.И. Комарова, Д.В. Корчагина, Н.Ф. Салахутдинов, С.Б. Нечепуренко// Химия природных соединений, 2008, Т. 44, N 1, 26-28. doi:10.1007/s10600-008-0009-9, IF=0.442
  13. New chiral Schiff bases derived from (+)- and (-)-α-pinenes in the metal complex catalyzed asymmetric oxidation of sulfides/ E.A. Koneva, K.P. Volcho, D.V. Korchagina, N.I. Komarova, A.I. Kochnev, N.F. Salakhutdinov, A.G. Tolstikov// Russian Chemical Bulletin, 2008, V. 57, N 1, Pp 108-117. doi:10.1007/s11172-008-0017-8, IF=0.537
  14. An efficient procedure for the synthesis of Esomeprazole using a titanium complex with two chiral ligands/ T.M. Khomenko, K.P. Volcho, N.I. Komarova, N.F. Salakhutdinov// Russian Journal of Organic Chemistry, 2008, V. 44, N 1, pp 124-127. doi:10.1007/s11178-008-1016-9, IF=0.51
  15. Acid-catalyzed transformations of pinane terpenoids. New prospects/ I.V. Il'ina, K.P. Volcho, N.F. Salakhutdinov// Russian Journal of Organic Chemistry, 2008, V. 44, N 1, pp 1-23. doi:10.1134/S1070428008010016, IF=0.51

2007
  1. Y.S. Kosenkova, M.P. Polovinka, N.I. Komarova, D.V. Korchagina, N.Y. Kurochkina, V.A. Cheremushkina, N.F. Salakhutdinov
    Riccardin C, a bisbibenzyl compound from Primula macrocalyx
    Chem. Nat. Compd. (Хим. Природ. Соедин.), 2007, V. 43, N 6, 712-713. doi:10.1007/s10600-007-0241-8, IF=0.393
  2. O.V. Ardashov, I.V. Il’ina, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Unusual α-hydroxyaldehyde with a cyclopentane framework from verbenol epoxide
    Mendeleev Commun., 2007, V. 17, N 5, 303-305. doi:10.1016/j.mencom.2007.09.020, IF=0.712
  3. Plant metabolites of the Siberian flora. Chemical transformations and the scope of practical application/ E. E. Shults, V. A. Raldugin, K. P. Volcho, N. F. Salakhutdinov, G. A. Tolstikov// Russ. Chem. Rev., 2007, 76(7), 655 doi:10.1070/RC2007v076n07ABEH003717, IF=1.717
  4. Chemical modification of usnic acid - 2. Reactions of (+)-usnic acid with amino acids/ O. A. Luzina, M. P. Polovinka, N. F. Salakhutdinov, G. A. Tolstikov// Russian Chemical Bulletin, 2007, V. 56, N 6, pp 1249-1251 doi:10.1007/s11172-007-0189-7, IF=0.504
  5. Chemical modification of usnic acid 1. Reaction of (+)-usnic acid with perfluoroolefins/ G. G. Furin, O. A. Luzina, R. I. Sokuev, M. P. Polovinka, N. F. Salakhutdinov, G. A. Tolstikov// Russian Chemical Bulletin, 2007, V. 56, N 6, pp 1244-1248 doi:10.1007/s11172-007-0188-8, IF=0.504
  6. O.V. Salomatina, T.G. Kuznetsova, D.V. Korchagina, E.A. Paukshtis, E.M. Moroz, K.P. Volcho, V.A. Barkhash, N.F. Salakhutdinov
    Effects of the Properties of SO4/ZrO2 Solid Catalysts on the Products of Transformation and Reaction Mechanism of R-(+)-limonene Diepoxides
    J. Mol. Catal. A: Chemical, V. 269, N 1-2, 72-80. doi:10.1016/j.molcata.2007.01.005, IF=2.51
  7. А.Д. Рогачев, С.В. Морозов, А.И. Вялков, В.В. Фоменко, Н.Ф. Салахутдинов
    Фитохимическое исследование рододендрона Адамса Rhododendron adamsii Rehder. Количественное содержание жирных кислот в листьях и стеблях
    Хим. Инт. Уст. Разв., 2007, Т. 15, № 5, 575-579.
  8. Г.Г. Фурин
    Новое в интенсификации процесса получения полифтораро¬матичес¬ких соединений действием фторида калия на полихлорарены
    Хим. Инт. Уст. Разв., 2007, Т. 15, № 5, 525-538.
  9. Synthesis of epoxy dinitriles from citral and their acid-catalyzed transformations/ K. P. Volcho, O. I. Yarovaya, S. Yu. Kurbakova, D. V. Korchagina, V. A. Barkhash, N. F. Salakhutdinov// Russian Journal of Organic Chemistry, 2007, V. 43, N 4, pp 511-517 doi:10.1134/S1070428007040045, IF=0.492
  10. Г.Г. Фурин, А.Н. Ильин, А.А. Ильин
    Основные тенденции развития методов получения полифторолефинов
    Хим. Инт. Уст. Разв., 2007, Т. 15, № 4, 401-415.
  11. Promising prospects for using partially fluorinated alcohols as O-nucleophilic reagents in organofluoric synthesis/ A. A. Il'in, A. N. Il'in, Yu. L. Bakhmutov, G. G. Furin, L. M. Pokrovskii// Russian Journal of Applied Chemistry, 2007, V. 80, N 3, pp 405-418 doi: 10.1134/S1070427207030123, IF=0.187
  12. Л.Н. Рогоза, Н.Ф. Салахутдинов, Г.А. Толстиков
    Синтез макроциклических производных полиметиленаминов и их аналогов
    Хим. Инт. Уст. Разв., 2007, Т. 15, N 3, 385-400.
  13. Т.Г. Толстикова, Г.Г. Фурин, М.П. Долгих, А.А. Ильин
    Первичная токсичность фторсодержа-щих органических соединений сферы практического назначения
    Хим. Инт. Уст. Разв., 2007, Т. 15, № 3, 309-316.
  14. I.V. Il'ina, K.P. Volcho, D.V. Korchagina, V.A. Barkhash, N.F. Salakhutdinov
    Reactions of Allyl Alcohols of the Pinane Series and of their Epoxides in the Presence of Montmorillonite Clay
    Helv. Chim. Acta, 2007, V. 90, N 2, 353-368. doi:10.1002/hlca.200790042, IF=1.549
  15. S.S. Laev, L.Yu. Gurskaya, G.A. Selivanova, I.V. Beregovay, L.N. Shchegoleva, N.V. Vasil'eva, M.M. Shakirov, V.D. Shteingarts
    N-Acetylation as a means to activate polyfluoroarylamines for selectyive ortho-hydrodefluorination by zinc in aqueous ammonia: a concise route to polyfluorobenzo Azaheterocycles
    Eur. J. Org. Chem., 2007, N 2, 306-316. doi:10.1002/ejoc.200600684, IF=2.769
  16. Компоненты этилацетатного экстракта корней Hedysarum Theinum/ И.В. Нечепуренко, М.П. Половинка, О.И. Сальникова, Л.М. Покровский, Н.И. Комарова, Н.Ф. Салахутдинов, С.Б. Нечепуренко// Хим. Природ. Соедин., 2007, N 1, 6-9. doi:10.1007/s10600-007-0052-y, IF=0.393
  17. Transformations of (-)-myrtenal epoxide over askanite-bentonite clay/ I. V. Il'ina, K. P. Volcho, D. V. Korchagina, V. A. Barkhash, N. F. Salakhutdinov// Russian Journal of Organic Chemistry, 2007, V. 43, N 1, pp 56-59 doi:10.1134/S1070428007010058, IF=0.492
  18. Г.Г. Фурин
    Синтез и применение продуктов взаимодействия серного ангидрида с перфторолефинами
    Хим. Инт. Уст. Разв., 2007, Т. 15, № 1, 11-23.

2006
  1. New chiral ligands from myrtenal and caryophyllene for asymmetric oxydation of sulfides catalyzed by metal complexes/ T. M. Khomenko, O. V. Salomatina, S. Yu. Kurbakova, I. V. Il’ina, K. P. Volcho, N. I. Komarova, D. V. Korchagina, N. F. Salakhutdinov, A. G. Tolstikov// Russian Journal of Organic Chemistry, 2006, V. 42, N 11, pp 1653-1661 doi:10.1134/S1070428006110091, IF=0.419
  2. C.C. Лаев, В.В. Фоменко, Т.М. Юрьева, Т.П. Минюкова, Н.Ф. Салахутдинов
    Гидрирование некоторых природных терпенов на катализаторах CuO-Al2O3 и NiO-Cr2O3
    Химия в интересах устойчивого развития, 2006, Т. 14, № 5, 523-528.
  3. Л.Н.Рогоза, Н.Ф.Салахутдинов, Г.А.Толстиков
    Синтез линейных производных полиметиленаминов природного происхождения и их аналогов
    Химия в интересах устойчивого развития, 2006, Т. 14, № 5, 497-521.
  4. Effect of the synthetic resorcinol derivative of caryophyllene on cholesterol biosynthesis and the functional activity of immune system cells/ E. N. Kudinova, N. F. Salakhutdinov, V. V. Fomenko, N. N. Vol’skii, O. M. Perminova, O. N. Khoshchenko, Y. Ch. Shwarts, M. I. Dushkin// Pharmaceutical Chemistry Journal, 2006, V. 40, N 10, pp 540-543 doi:10.1007/s11094-006-0188-2, IF=0.209
  5. Reactions of perfluoro(2-methylpent-2-ene) and perfluoro(5-azanon-4-ene) with primary amines containing a 2,6-di-tert-butylphenol fragment/ G. G. Furin, A. P. Krysin, N. I. Protsuk, V. A. Lopyrev// Russian Journal of Organic Chemistry, 2006, V. 42, N 10, pp 1429-1434 doi:10.1134/S1070428006100034, IF=0.419
  6. Transformations of diepoxy derivatives of limonene in homogeneous acidic media/ O. V. Salomatina, O. I. Yarovaya, D. V. Korchagina, Yu. V. Gatilov, M. P. Polovinka, V. A. Barkhash// Russian Journal of Organic Chemistry, 2006, V. 42, N 9, pp 1313-1320 doi:10.1134/S1070428006090107, IF=0.419
  7. E.V. Suslov, T.M. Khomenko, I.V. Il’ina, D.V. Korchagina, N.I. Komarova, K.P. Volcho, N.F. Salakhutdinov
    Asymmetric Induction in Catalyzed Synthesis of Organic Compounds as an Important Stage in the Evolution of Life on Earth
    Paleontological J., 2006, V. 40, № 4, S532–S537. doi:10.1134/S0031030106100133, IF=0.36
  8. Сравнительный анализ химического состава эфирных масел листьев и стеблей Rhododendron adamsii rehder, Rhododendronaureum georgi и Rhododendron dauricum l/ А.Д. Рогачев, В.В. Фоменко, О.И. Сальникова, Л.М. Покровский, Н.Ф. Салахутдинов// Хим. Природ. Соедин., 2006, Т. 42, № 4, 344-347. doi:10.1007/s10600-006-0172-9, IF=0.31
  9. The study of photoisomerisation of 1-aryloxyanthraquinones by NMR spectroscopy and UV spectrophotometry/ S. P. Babailov, L. S. Klimenko, I. Ya. Mainagashev// Journal of Structural Chemistry, 2006, V. 47, N 4, pp 663-667 doi:10.1007/s10947-006-0353-1, IF=0.37
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    New Chiral Basic Heterogeneous Catalyst Based on Css Zeolite
    Mendeleev Commun., 2006, V. 16, N 4, 202-204. doi:10.1070/MC2006v016n04ABEH002244, IF=0.709
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    Antioxidant and redox properties of supramolecular complexes of carotenoids with beta-glycyrrhizic acid
    Free Radical Bio. Med., 2006, V. 40, N 10, 1804-1809. doi:10.1016/j.freeradbiomed.2006.01.015, IF=5.399
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