Laboratory of Terpene Compounds
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N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry
of Siberian Branch of Russian Academy of Sciences


Head - Professor, Dr. Sci.(Chem) Alexey Yasil'evich Tkachev

Phone: (383) 330-88-52
internal phone: 2-17
e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

 

RESEARCH AREAS:


The basic research is focused on:

    • Development of the methods for synthesis of new optically active heteroatomic nitrogen- and sulfur- containing derivatives of lower terpenoids with the purpose creation of intermediates for the synthesis of substances with the set properties.
    • Improvement of methodology of phytochemical studies, study of secondary metabolites composition of plants of Siberia and adjacent area.

STAFF:


 

Staff

Employee Position Room Phone Phone in. email Publications
by years
1 Tkachev Alexey Vasilievich Lab's Head (Doct. Chem) 319 НТК 330-88-52 2-17 This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Pankrusina Natalia Alekseevna Senior Researcher (Cand. Chem.) 332 330-97-32 3-08 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Bizyaev Sergey Nikolaevich Researcher (Cand. Chem.) 334 330-98-55 3-70 This email address is being protected from spambots. You need JavaScript enabled to view it.
4 Vasilyev Evgeny Sergeevich Researcher (Cand. Chem.) 334 330-98-55 3-70 This email address is being protected from spambots. You need JavaScript enabled to view it.
5 Marenin Konstantin Sergeevich Researcher (Cand. Chem.) 225 330-98-55 4-01 This email address is being protected from spambots. You need JavaScript enabled to view it.
6 Domrachev Dmitry Vasilievich Junior Researcher 334, 331 330-98-55 3-70, 2-31 This email address is being protected from spambots. You need JavaScript enabled to view it.
7 Romanenko Elena Petrovna Leading Engineer 331, 332 330-97-32 2-31,3-08 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


2022
  1. Ia.S. Fomenko, M. Afewerki, M.I. Gongola, E.S. Vasilyev, L.S. Shu'pina, N.S. Ikonnikov, G.B. Shul'pin, D.G. Samsonenko, V.V. Yanshole, V.A. Nadolinny, A.N. Lavrov, A.V. Tkachev, A.L. Gushchin
    Novel Copper(II) Complexes with Dipinodiazafluorene Ligands: Synthesis, Structure, Magnetic and Catalytic Properties
    Molecules 2022, 27(13), 4072 doi:10.3390/molecules27134072, IF=4.927
  2. S.N. Bizyaev, Yu.V. Gatilov, D.V. Zubricheva, V.D. Tikhova, A.V. Tkachev
    A New Type of Terpene-Based D 2-Symmetric Macrocycles, Capable of Selectively Extracting Au, Pd and Pt from Complex Mixtures
    ChemistrySelect, V.7, N 22, June 13, 2022, e202201263 doi:10.1002/slct.202201263, IF=2.307
  3. E.P. Romanenko, D. Domrachev, A.V. Tkachev
    Variations in Essential oils from South Siberian conifers of the Pinaceae family: new data towards identification and quality control
    Chemistry & Biodiversity, V.19, N 2, February 2022, e202100755 doi:10.1002/cbdv.202100755, IF=2.745
  4. Yu.P. Ustimenko, A.M. Agafontsev, A.V. Tkachev
    Synthesis of chiral pinopyridines using catalysis by metal complexes
    Chemistry of Heterocyclic Compounds, 2022, V. 58, N 2-3, Pp 135-143 doi:10.1007/s10593-022-03066-x, IF=1.49
  5. E. Avdeeva, Ya. Reshetov, D. Domrachev, E. Gulina, S. Krivoshchekov, M. Shurupova, K. Brazovskii, M. Belousov
    Constituent composition of the essential oils from some species of the genus Saussurea DC
    Natural Product Research, 2022, V. 36, N 2, Pp 660-663 doi:10.1080/14786419.2020.1795655, IF=2.488

2021
  1. Н.И. Ткачева, С.В. Морозов, Е.В. Третьяков, А.В. Ткачев
    Обзор состояния (инвентаризация) стойких органических загрязнителей (СОЗ) в объектах окружающей среды Мурманской области
    Охрана окружающей среды и заповедное дело: электрон. журн. – 2021. - №3-4. – С. 106-127.
  2. A. Tkachev, N. Nekratova, N. Belousova, M. Shurupova, W. Letchamo
    Comparative GC-MS study of Schizonepeta multifida essential oil from Khakassia Republic shows potentials for nutraceuticals, flavor, and conservation
    Ukrainian Journal of Ecology, 2021, V.11, N ‏ ‏ 2, Pp 300-305 doi:10.15421/2021_114
  3. E.S. Vasilyev, S.N. Bizyaev, V.Yu. Komarov, A.V. Tkachev
    Bistricyclic aromatic enes annelated with nopinane fragment
    Tetrahedron, V.83, 12 March 2021, 131979 doi:10.1016/j.tet.2021.131979, IF=2.457
  4. A.M. Agafontsev, A.S. Oshchepkov, T.A. Shumilova, E.A. Kataev
    Binding and Sensing Properties of a Hybrid Naphthalimide-Pyrene Aza-Cyclophane towards Nucleotides in an Aqueous Solution
    Molecules 2021, 26(4), 980 doi:10.3390/molecules26040980, IF=4.411
  5. Н.А. Панкрушина, Т.П. Кукина
    Новые компоненты экстракта ALCEA NUDIFLORA после микроволновой экстракции
    Химия растительного сырья. 2021. № 1. С. 79-84. doi:10.14258/jcprm.2021018361
  6. Yu. A. Bryleva, Yu. P. Ustimenko, V. F. Plyusnin, A. V. Mikheilis, A. A. Shubin, L. A. Glinskaya, V. Yu. Komarov, A. M. Agafontsev , A. V. Tkachev
    Ln(III) complexes with a chiral 1H-pyrazolo[3,4-b]pyridine derivative fused with a (-)-α-pinene moiety: synthesis, crystal structure, and photophysical studies in solution and in the solid state
    New J. Chem., 2021,45, 2276-2284 doi:10.1039/D0NJ05277A, IF=3.591

2020
  1. Yu.P. Ustimenko, E.S. Vasilyev, S.N. Bizyaev, T.V. Rybalova, A.V. Tkachev
    Synthesis of chiral spirodiazafluorenes
    Chemistry of Heterocyclic Compounds, 2020, V. 56, Pp 1429-1433 doi:10.1007/s10593-020-02833-y, IF=1.519
  2. Synthesis, structure, and photoluminescent properties of lanthanide(III) complexes with a ligand based on 1,10-phenanthroline and borneol/ Yu. A. Bryleva, D. A. Piryazev, L. A. Glinskaya, A. M. Agafontsev, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1810-1822 doi:10.1134/S0022476620110141, IF=0.745
  3. COMPONENT COMPOSITION AND BIOLOGICAL ACTIVITY OF ESSENTIAL OIL OF LIGULARIA HETEROPHYLLA RUPR./ MAKUBAYEVA AIGERIM, ROMANENKO ELENA PETROVNA, ADEKENOV SERGAZY MYNZHASAROVICH, TKACHEV ALEKSEY VASIL'YEVICH// doi:10.14258/jcprm.2020038243
  4. A complex of Zn(II) with chiral nopinane-annelated 9,9′-bi-4,5-diazafluorenylidene: synthesis, structure, and properties/ T. E. Kokina, L. A. Glinskaya, D. A. Piryazev, E. S. Vasiliev, L. A. Sheludyakova, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry volume 61, pages1606–1614(2020) doi:10.1134/S0022476620100133, IF=0.745
  5. A.M. Agafontsev, T.A. Shumilova, A.S. Oshchepkov, F. Hampel, E. A. Kataev
    Ratiometric detection of ATP by fluorescent cyclophanes with bellows-type sensing mechanism
    Chemistry - A European Journal, 2020, V. 26, N 44, Special Issue: Young Chemists 2020, Pp. 9991-9997 doi:10.1002/chem.202001523, IF=4.857
  6. K.S. Marenin, A.M. Agafontsev, Yu.A. Bryleva, Yu.V. Gatilov, L.A. Glinskaya, D.A. Piryazev, A.V. Tkachev
    Stereochemistry of the Kabachnik-Fields Condensation of Terpenic Amino Oximes with Aldehydes and Dimethyl Phosphite
    ChemistrySelect, 2020, V.5 N 25, Pp 7596-7604 doi:10.1002/slct.202002369, IF=1.811
  7. T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
    Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
    Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174
  8. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
    Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
    Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
  9. Synthesis, structure, and cytotoxicity of Pd(II) and Cu(II) complexes with 1-terpenyl-3-thiosemicarbazides of pinane and para-menthane series/ Kokina T.E., Komarov V. Yu., Glinskaya L.A., Bizyaev S.N., Sheludyakova L.A., Eremina Yu. A., Klyushova L.S., Tkachev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 1, Pp 44-56 doi:10.1134/S0022476620010059, IF=0.745

2019
  1. S.V. Morozov, N.I. Tkacheva, A.V. Tkachev
    On Problems of the Comprehensive Chemical Profiling of Medicinal Plants
    Russian Journal of Bioorganic Chemistry. - 2019. - Vol. 45, No. 7 - P. 860–875. doi:10.1134/S1068162019070070, IF=0.794
  2. Physical Activation of Extraction and Organic Synthesis Processes/ Pankrushina N. A., Lomovsky O. I., Shakhtshneider T. P// Chemistry for Sustainable Development, 2019, V. 27, № 6, P. 704-715. (In Russian) doi:10.15372/KhUR2019194
  3. E.S. Vasilyev, S.N. Bizyaev, V.Yu. Komarov, A.V. Tkachev
    Syntheses of chiral fused 4,5-diazafluorene–bis(nopinane) derivatives
    Mendeleev Commun., 2019, V. 29, N 5, Pp 584-586 doi:10.1016/j.mencom.2019.09.036, IF=2.01
  4. E. S. Vasilyev, S. N. Bizyaev, V.Yu. Komarov, Yu.V. Gatilov, A. V. Tkachev
    Chiral C2-Symmetric Diimines with 4,5-Diazafluorene Units
    Molecules 2019, 24(17), 3186 doi:10.3390/molecules24173186, IF=3.59
  5. Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110, IF=0.541
  6. T.E. Kokina, L.A. Glinskaya, L.A. Sheludyakova, Yu.A. Eremina, L.S. Klyushova, V. Yu. Komarov, D.A. Piryazev, A.V. Tkachev, S.V. Larionov
    Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (-)-camphor thiosemicarbazone
    Polyhedron, 2019, V. 163, Pp 121-130 doi:10.1016/j.poly.2019.02.020, IF=2.284
  7. A. M. Agafontsev, T. Shumilova, T.Ruffer, H. Lang, E.A. Kataev
    Anthracene-based cyclophanes with selective fluorescent responses for TTP and GTP: insights into recognition and sensing mechanisms
    Chemistry - A European Journal, 2019, V. 25, N 14, Pp 3541-3549 doi:10.1002/chem.201806130, IF=5.16
  8. A.M. Agafontsev, A. Ravi, T.A. Shumilova, A. Oshchepkov, E.A. Kataev
    Molecular receptors for recognition and sensing of nucleotides
    Chemistry - A European Journal, 2019, V. 25, N 11, Pp 2684-2694 doi:10.1002/chem.201802978, IF=5.16
  9. Luminescent Complexes of Zn(II) and Cd(II) with Chiral Ligands Containing 1,10-Phenanthroline and Natural Monoterpenoids (+)-3-Carene or (+)-Limonene Fragments/ T.E. Kokina, Yu. P. Ustimenko, M.I. Rakhmanova, L.A. Sheludyakova, A.M. Agafontsev, P.E. Plusnin, A.V. Tkachev, S.V.Larionov// Russian Journal of General Chemistry, 2019, V. 89, N 1, pp 87-95 doi:10.1134/S107036321901016X, IF=0.643

2018
  1. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, S.A. Kuznetsova, T.P. Shakhtshneider
    Effect of Microwave Irradiation on Arabinogalactan and Its Interaction with Betulin Diacetate
    Russian Journal of Bioorganic Chemistry, 2018, Vol. 44, No. 7, pp. 762-767. doi:10.1134/S1068162018070075, IF=0.838
  2. A.V. Tkachev
    Problems of the Qualitative and Quantitative Analysis of Plant Volatiles
    Russian Journal of Bioorganic Chemistry, 2018, V. 44, N. 7, P. 813-833. doi:10.1134/S1068162018070142, IF=0.837
  3. С.В. Морозов, Н.И. Ткачева, А.В. Ткачев
    Проблемы комплексного химического профилирования лекарственных растений
    Химия растительного сырья. 2018. № 4. С. 5-28. doi: 10.14258/jcprm.2018044003
  4. Yu.P. Ustimenko, A.M. Agafontsev, V.Yu. Komarov, A.V. Tkachev
    Synthesis of chiral nopinane annelated 3-methyl-1-aryl-1H-pyrazolo[3,4-b]pyridines by condensation of pinocarvone oxime with 1-aryl-1H-pyrazol-5-amines
    Mendeleev Communications, 2018, V. 28, N 6, Pp 584-586 doi:10.1016/j.mencom.2018.11.006, IF=2.098
  5. V.Yu. Kuksenok, V.V. Shtrykova, V.D. Filimonov, A.G. Druganov, A.A. Bondarev, K.S. Stankevich
    The determination of enantiomer composition of 1-((3-chlorophenyl)-(phenyl)methyl) amine and 1-((3-chlorophenyl)(phenyl)-methyl) urea (Galodif) by NMR spectroscopy, chiral HPLC, and polarimetry
    Chirality. 2018, V. 30, N 10 , Pp 1135-1143 doi:10.1002/chir.23005, IF=1.832
  6. Synthesis and structures of CuI,II complexes with a 2,2´-bipyridine derivative bearing a (+)-3-carene moiety/ T. E. Kokina. A. Glinskaya, D. A. Piryazev, A. Yu. Baranov, A. M. Agafontsev, Yu. A. Eremina, E. V. Vorontsova, A. S. Bogomyakov, D. Yu. Naumov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2018, V. 67, N 7, pp 1251-1260 doi:10.1007/s11172-018-2209-1, IF=0.781
  7. Acid-catalyzed isomerization of caryophyllene in the presence of SiO2 and Al2O3 impregnated with sulfuric acid/ E. P. RomanenkoA. V. Tkachev// Russian Chemical Bulletin, 2018, V. 67, N 6, pp 1051-1058 doi:10.1007/s11172-018-2179-3, IF=0.781
  8. A.E. Grazhdannikov, L.M. Kornaukhova, V.I. Rodionov, N.A. Pankrushina, E.E. Shults, A.S. Fabiano-Tixier, S.A. Popov, F. Chemat
    Selecting a green strategy on extraction of birch bark and isolation of pure betulin using monoterpenes
    ACS Sustainable Chem. Eng., , 2018, 6 (5), pp 6281-6288 doi:10.1021/acssuschemeng.8b00086, IF=6.14
  9. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, I.V. Eltsov, S.A. Kuznetsova, A.S. Kichkailo, T.P. Shakhtshneider
    Microwave-assisted synthesis and antitumor activity of the supramolecular complexes of betulin diacetate with arabinogalactan
    Chemical Papers, 2018, V. 72, N 5, pp 1257-1263 doi:10.1007/s11696-017-0362-x, IF=0.963
  10. Chemical profiling of Papaver Kuvajevii: Determination of the main cyanogenic glycoside - Taxifillin/ M.O. Korotkikh, A.V. Tkachev// Khimiya Rastitel'nogo Syr'ya, 2018, N 2, Pp. 71-75 doi:10.14258/jcprm.2018023506
  11. A.M. Agafoncev, T.A. Shumilova, A.V. Tkachev
    Microwave Assisted Syntheses of 4-Amino-carane-3-ols from 3,4-Epoxycarane and Heterocyclic Amines
    Current microwawe chemistry, 2018, V. 5, N 1, Pp 54 - 61 doi:10.2174/2213335604666171129154210, IF=0.212
  12. Copper(II) Complexes with Chiral Ligands Containing Fragments of Monoterpenoids and Amino Acid Esters/ Copper(II) Complexes with Chiral Ligands Containing Fragments of Monoterpenoids and Amino Acid Esters// Russian Journal of Coordination Chemistry, 2018, V. 44, N 2, pp 117-126 doi:10.1134/S1070328418020033, IF=0.674

2017
  1. A.S. Kondratyev, V.D. Shteingarts, V.V. Litvak, E.V. Tretyakov, A.V. Tkachev
    Domino reaction of (2-haloethyl)polyfluorophenyl sulfides, sulfoxides, and sulfones with ammonia or amines: one-pot synthesis of 3,4-dihydro-2H-1,4-benzothiazines polyfluorinated at the benzene ring and the corresponding 1-oxides and 1,1-dioxides
    Chemistry of Heterocyclic Compounds, 2017, V. 53, N 12, P 1350-1361 doi:10.1007/s10593-018-2217-y, IF=0.893
  2. Ya.S. Fomenko, A.L. Gushchin, A.V. Tkachev, E.S. Vasilyev, P.A. Abramov, V.A. Nadolinny, M.M. Syrokvashin, M.N. Sokolov
    Fist oxidovanadium complexes containing chiral derivatives of dihydrophenanthroline and diazofluorene
    Polyhedron,2017, V. 135, Pp 96-100 doi:10.1016/j.poly.2017.07.003, IF=1.925
  3. Complexes of Cu(I) and Pd(II) with (+)-camphor and (-)-cavrone thiosemicarbazones: Synthesis, structure, and cytotoxicity of the Pd(II) complex/ T. E. Kokina, L. A. Sheludyakova, Yu. A. Eremina, E. V. Vorontsova, L. A. Glinskaya, D. A. Piryazev, E. V. Lider, A. V. Tkachev, S. V. Larionov// Russian Journal of General Chemistry, 2017, V. 87, N 10, pp 2332-2342 doi:10.1134/S1070363217100140, IF=0.552
  4. Ю.Н. Маляр, М.А. Михайленко, Н.А. Панкрушина, А.Н. Михеев, С.А. Кузнецова, Т.П. Шахтшнейдер
    Влияние микроволнового облучения на арабиногалактан и его взаимодействие с диацетатом бетулина
    Химия растительного сырья. 2017. № 4. С. 73-79
  5. S.V. Larionov, Yu.A. Bryleva, L.A. Glinskaya, V.F. Plyusnin, A.S. Kupryakov, A.M. Agafontsev, A.V. Tkachev, A.S. Bogomyakov, D.A. Piryazev, I.V. Korolkov
    Ln(III) complexes (Ln = Eu, Gd, Tb, Dy) with a chiral ligand containing 1,10-phenanthroline and (-)-menthol fragments: synthesis, structure, magnetic properties and photoluminescence
    Dalton Trans., 2017, V. 34, N 46, Pp. 11440-11450 doi:10.1039/C7DT01536D, IF=4.28
  6. А.В. Ткачев
    Проблемы качественного и количественного анализа летучих веществ растений
    Химия растительного сырья. 2017. № 3. С. 5-37.
  7. О.Н. Шмендель, Д.Л. Прокушева, Д.В. Домрачев, В.В. Величко
    Анализ продукции «Багульника болотного побеги» различных производителей
    Фармация. 2017. Т. 66. № 4. С. 7-10.
  8. N.I. Belousova, D.V. Domrachev, N.S. Fursa, M.V. Belousov
    Composition of Essential Oil from Rhododendron caucasicum
    Chemistry of Natural Compounds, 2017, V. 53, N 3, pp 574-575 doi:10.1007/s10600-017-2054-8, IF=0.46
  9. Structure and photoluminescence of Zn(II) and Сd(II) complexes with chiral bis-pyridine containing fragments of natural (–)-α-pinene/ T.E. Kokina, L.A. Glinskaya, E.S. Vasiliev, M.I. Rakhmanova, S.V. Makarova, D.A. Piryazev, I.V. Korol'kov, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2017, V. 58, N 5, pp 994-1003 doi:10.1134/S0022476617050201, IF=0.472
  10. Complexes PdCl2 with optically active hybrid ligands built of α-pinene and β-alanine molecules/ T.E. Kokina, L.A. Glinskaya, K.S. Marenin, I.V. Korol'kov, D.Yu. Naumov, A.V. Tkachev, S.V. Larionov// Russian Journal of Coordination Chemistry, 2017, V. 43, N 4, pp 213-222 doi:10.1134/S1070328417030034, IF=0.541
  11. A synthesis of tritium-labeled juvenile hormone and / I.V. Romanova, A.A. Alekseev, V.A. Richter, N.E. Gruntenko, A.M. Agafontsev, E.K. Karpova// Russian Journal of Bioorganic Chemistry, 2017, V. 43, N 2, pp 211-215 doi:10.1134/S1068162017020121, IF=0.689
  12. E.S. Vasilyev, I.Yu. Bagryanskaya, A.V. Tkachev
    Syntheses of chiral nopinane-annelated pyridines of C2 and D2-symmetry: X-ray structures of the fused derivatives of 4,5-diazafluorene, 4,5-diaza-9H-fluoren-9-one, and 9,9'-bi-4,5-diazafluorenylidene
    Mendeleev Communications, 2017, V. 27, N 2, Pp 128-130 doi:10.1016/j.mencom.2017.03.006, IF=1.741
  13. A.V. Shpatov, S.A. Popov, O.I. Salnikova, T.P. Kukina, E.N. Shmidt, B.H. Um
    Composition and Bioactivity of Lipophilic Metabolites from Needles and Twigs of Korean and Siberian Pines (Pinus koraiensis Siebold & Zucc. and P. sibirica Du Tour)
    Chemistry & Biodiversity, 2017, V. 14, N 2, Article number e1600203 doi:10.1002/cbdv.201600203, IF=1.44
  14. K.S. Marenin, Yu.V. Gatilov, A.M. Agafontsev, A.V. Tkachev
    Stereoselectivity of formation of monoterpene - Amino acids hybrid molecules in the reaction of monoterpene nitroso chlorides with α-amino acid derivatives
    Steroids, 2016, V. 117, Pp 112-119 doi:10.1016/j.steroids.2016.09.016, IF=2.282

2016
  1. N.A. Pankrushina, K.B. Rakhmetali
    Synthesis of lappaconitine N-oxide under microwave activation
    Chemistry of Heterocyclic Compounds, 2016, V. 52, N 11, pp 970-972 doi:10.1007/s10593-017-1995-y, IF=0.814
  2. T.E. Kokina, L.A. Glinskaya, A.V. Tkachev, V.F. Plyusnin, Yu.V. Tsoy, I.Yu. Bagryanskaya, E.S. Vasilyev, D.A. Piryazev, L.A. Sheludyakova, S.V. Larionov
    Chiral zinc(II) and cadmium(II) complexes with a dihydrophenanthroline ligand bearing (-)-α-pinene fragments: synthesis, crystal structures and photophysical properties
    Polyhedron, 2016, V. 117, 15 October 2016, Pp 437-444 doi:10.1016/j.poly.2016.06.018, IF=2.108
  3. A.M. Agafontsev, T.A. Shumilova, P.A. Panchenko, S. Janz, O.A. Fedorova, E.A. Kataev
    Utilizing a pH-Sensitive Dye in the Selective Fluorescent Recognition of Sulfate
    CHEMISTRY - A EUROPEAN JOURNAL, V. 22, N 42, October 10, 2016, Pp 15069-15074 doi:10.1002/chem.201602623, IF=5.77
  4. T.N. Drebushchak, V.A. Drebushchak, N.A. Pankrushina, E.V. Boldyreva
    Single-crystal to single-crystal conformational polymorphic transformation in tolbutamide at 313 K. Relation to other polymorphic transformations in tolbutamide and chlorpropamide
    CrystEngComm, 2016,18, 5736-5743 doi:10.1039/C6CE00764C, IF=3.848
  5. A.A. Gabrienko, A.V. Ewing, A.M. Chibiryaev, A.M. Agafontsev, K.A. Dubkov, S.G. Kazarian
    New insights into the mechanism of interaction between CO2 and polymers from thermodynamic parameters obtained by in situ ATR-FTIR spectroscopy
    Phys. Chem. Chem. Phys., 2016, 18(9), 6465-6475 doi:10.1039/C5CP06431G, IF=4.448
  6. T.P. Kukina, O.I. Sal'nikova, N.K. Khidyrova, M.D. Rakhmatova, N.A. Pankrushina, A.E. Grazhdannikov
    Aliphatic and Terpene Constituents of Alcea nudiflora Extracts
    Chemistry of Natural Compounds, 2016, V.52, N 2, pp 285-287 doi:10.1007/s10600-016-1615-6, IF=0.472

2015
  1. G.Z. Baisalova, N.A. Pankrushina, R.S. Erkasov, M.S. Shengene, K.K. Kulanova, A.D. Spanbayev, R.S. Orazbaeva
    Virus inhibitory activity of methanol extracts of Halimodendron halodendron Voss
    PLANTA MEDICA, 2016, V. 81, N 16, Pp 1507-1507 Аннотация к встрече: PW-52 doi:10.1055/s-0035-1565676, IF=2.151
  2. Structure of [Pd2(H2L1)Cl4] and [Pd2(H2L1)Cl4]•0,5CH2Cl2 compounds with chiral bis-α-sulfanyl oxime, a derivative of natural monoterpenoid (+)-3-carene (H2L1)/ T.E. Kokina, L.A. Glinskaya, N.B. Gorshkov, N.V. Kuratieva, I.V. Korol’kov, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2015, V. 56, N 5, pp 919-925 doi:10.1134/S0022476615050145, IF=0.508
  3. Copper(II) and silver(I) complexes with chiral N-substituted aminoacetic acid derivatives containing the natural monoterpenes (+)-3-carene and (-)-α-pinene: Synthesis and structures/ T. E. Kokina , A. M. Agafontsev, K. S. Marenin, L. A. Glinskaya, L. A. Sheludyakova, N. V. Kurat'eva, P. E. Plyusnin, M. I. Rakhmanova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2015, V. 41, N 10, pp 658-663 doi:10.1134/S1070328415100024, IF=0.484
  4. M.O. Korotkikh, N.A. Pankrushina, O.I. Sal'nikova, A.E. Sonnikova
    Alkaloids from the New Species Papaver kuvajevii
    Chemistry of Natural Compounds, July 2015, Volume 51, Issue 4, pp 803-804 doi:10.1007/s10600-015-1418-1, IF=0.509
  5. S.N. Bizyaev, Yu.V. Gatilov, A.V. Tkachev
    Syntheses of α-cyano substituted oximes from terpenic hydrocarbons via nitroso chlorides: X-ray structures of 3-cyanocaran-4-one oxime, 2-cyanopinan-3-one oxime and 1-cyano-p-menth-8-en-2-one oxime
    Mendeleev Communications, V. 25, N 2, 2015, Pp 93-95 doi:10.1016/j.mencom.2015.03.003, IF=1.34
  6. Complexes of Pd(II) and Zn(II) chlorides with anthracene-containing &aplha;-amino oxime derived from the naturally occurring monoterpenoid (+)-3-carene/ S. V. Larionov, T. E. Kokina, L. I. Myachina, L. A. Glinskaya, M. I. Rakhmanova, D. Yu. Naumov, A. V. Tkachev, A. M. Agafontsev// Russian Journal of Coordination Chemistry, March 2015, Volume 41, Issue 3, pp 162-168 doi:10.1134/S1070328415030070, IF=0.484
  7. Synthesis of glycidyl ethers derived from terpene α-amino oximes and beta-substituted alcohols on their basis/ T.A. Shumilova, A.M. Agafontsev, A.V. Tkachev// Russian Chemical Bulletin, 2015, V. 64, N 1, pp 99-106 doi:10.1007/s11172-015-0827-4, IF=0.481
  8. Н.И. Белоусова, Н.А. Некратова, А.В. Ткачев, М.Н. Шурупова
    Эфирное масло Shizonepeta multifida (Республика Хакасия)
    в Кн. «Лекарственные растения: фундаментальные и прикладные проблемы». Новосибирск: Золотой колос, 2015 (ISBN 978-5-94477-170-4) - С. 59-63.

2014
  1. G.Zh. Baisalova, N.A. Pankrushina, D.V. Domrachev, O.I. Salnikova, R.Sh. Erkassov
    Volatile Constituents of Halimodendron halodendron Voss. Growing in Kazakhstan
    Journal of Essential Oil Bearing Plants, 2014, V.. 17, N 5, P. 886-890. doi:10.1080/0972060X.2014.935074, IF=0.187
  2. S.V. Larionov, T.E. Kokina, V.F. Plyusnin, L.A. Glinskaya, A.V. Tkachev, Yu.A. Bryleva, N.V. Kuratieva, M.I. Rakhmanova, E.S. Vasilyev
    Synthesis, structure and photoluminescence of Zn(II) and Cd(II) complexes with pyridophenazine derivative
    Polyhedron, 2014, V. 77, Pp 75-80. doi:10.1016/j.poly.2014.04.011, IF=2.46
  3. E.S. Vasilyev, A.M. Agafontsev, A.V. Tkachev
    Microwave-Assisted Synthesis of Chiral Nopinane-Annelated Pyridines by Condensation of Pinocarvone Oxime with Enamines Promoted by FeCl3 and CuCl2
    Synthetic Communications: An International Journal for Rapid Communication of Synthetic Organic Chemistry, 2014, V. 44, N 12, pp 1817-1824. doi:10.1080/00397911.2013.877145, IF=0.984
  4. Synthesis of chiral multifunctional N-terpene-containing amino acid derivatives based on simplest achiral amino acids and natural monoterpenes/ K. S. Marenin, A. M. Agafontsev, A. V. Tkachev// Russian Chemical Bulletin, March 2014, Volume 63, Issue 3, pp 759-764 doi:10.1007/s11172-014-0504-z, IF=0.509
  5. E.S. Vasilyev, A.M. Agafontsev, A.V. Tkachev
    Syntheses of Nopinane-Annelated Pyridines
    Chem. Listy – 2014. – Vol. 108 – s145.
  6. T. Shumilova, K. Marenin, A. Agafontsev, A. Tkachev
    New Approaches to Chiral Heteroatomic Auxiliaries from monoterpenes.
    Chem. Listy – 2014. – Vol. 108 – s141
  7. A. Tkachev, D. Makarova, D. Domrachev, E. Romanenko, A. Nefedov, E. Karpova
    Monitoring of key secondary metabolites of isoprenoid nature in Siberian plants
    Chem. Listy – 2014. – Vol. 108 – s119., IF=0.195
  8. М.А. Мяделец, Д.В. Домрачев, А.Н. Крикливая, Г.И. Высочина
    Зависимость состава эфирного масла monarda didyma l. ( lamiaceae) от возраста растений и характера сырья
    Химия растительного сырья. 2014. № 1. С. 215-219.

2013
  1. A.V. Shpatov, S.A. Popov, O.I. Salnikova, E.A. Khokhrina, E.N. Shmidt, B.H. Um
    Low-Volatile Lipophilic Compounds in Needles, Defoliated Twigs, and Outer Bark of Pinus thunbergii
    Natural Product Communications, 2013, V. 8, N 12, P. 1759-1762., IF=0.955
  2. D.N. Olennikov, L.M. Tankhaeva, N.A. Pankrushina, D.V. Sandanov
    Phenolic compounds of Sophora flavescens Soland. of Russian origin
    Russian Journal of Bioorganic Chemistry, 2013, V., N 7, pp 755-760 .(Original Russian Text © D.N. Olennikov, L.M. Tankhaeva, N.A. Pankrushina, D.V. Sandanov, 2012, published in Khimiya Rastitel’nogo Syr’ya, 2012, No. 4, pp. 101–108.) doi:10.1134/S106816201307011X, IF=0.523
  3. M.A. Myadelets, D.V. Domrachev, V.A. Cheremushkina
    A study of the chemical composition of essential oils of some species from the Lamiaceae L. family cultivated in the Western Siberian Region
    Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 7, pp 733-738.(Original Russian Text © M.A. Myadelets, D.V. Domrachev, V.A. Cheremushkina, 2012, published in Khimiya Rastitel’nogo Syr’ya, 2012, No. 1, pp. 111–117.) doi:10.1134/S1068162013070091, IF=0.523
  4. Complexes of PdCl2 with chiral oximes of α-(o-anisidino)caranone and α-(o-anisidino)pinanone: synthesis and crystal structures/ T. E. Kokina, L. A. Glinskaya, A. M. Agafontsev, E. V. Artimonova, L. A. Sheludyakova, I. V. Korol’kov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2013, V. 62, N 12, pp 2595-2602. doi:10.1007/s11172-013-0378-5, IF=0.423
  5. E.A. Khokhrina, A.V. Shpatov, S.A. Popov, O.I. Sal'nikova, E.N. Shmidt, B.H. Um
    Non-Volatile Compounds of Needles, Trimmed Saplings, and Outer Bark of Pinus densiflora
    Chemistry of Natural Compounds, 2013, V. 49, N 3, P. 561-565. doi:10.1007/s10600-013-0673-2, IF=0.598
  6. Synthesis of optically active Zn(II) complexes with thiosemicarbazones of (+)-camphor (L) and (-)-carvone (L1). The crystal structures of L and [Zn(L)2Cl2]/ T. E. Kokina, N. B. Gorshkov, L. A. Glinskaya, N. V. Kurat’eva, L. A. Sheludyakova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2013, V. 39, N 6, Pp 442-449. doi:10.1134/S1070328413050035, IF=0.465
  7. T.N. Drebushchak, N.A. Pankrushina, A.N. Mikheev, M.K. A. Thumm
    Crystalline products of tolbutamide decomposition in water after microwave treatment
    CrystEngComm, 2013, V. 15, N 18, P. 3582-3586. doi:10.1039/c3ce40145f, IF=3.878
  8. Composition of Essential Oils of Some Species of the Agastache Clayton ex Gronov Genus (Lamiaceae) Cultivated Under the Conditions of the Middle Urals/ M. A. Myadelets, T. A. Vorobyeva, D. V. Domrachev// Chemistry for Sustainable Development, 2013, Т. 21,. № 4, pp. 419-423. (in russian).
  9. Regulation of persistent properties of microorganisms by plant extracts of coniferous plants/ T.M. Utkina, L.P. Potehina, O.L. Kartashova, А.V.Tkachev//
  10. A.V. Shpatov, S.A. Popov, O.I. Salnikova, E.N. Shmidt, S.W. Kang, S.M. Kim, B.H. Um
    Lipophilic Extracts from Needles and Defoliated Twigs of Pinus pumila from Two Different Populations
    Chemistry & Biodiversity, 2013, V. 10, N 2, P. 198-208. doi:10.1002/cbdv.201200009, IF=1.807
  11. Synthesis and structure of palladium(II) and copper(II) complexes with chiral bis-alpha-aminooximes containing (+)-3-carene or (+)-limonene fragments and 4,4 '-methylenedianiline linker. Crystal structure of the complex [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]/ T. E. Kokina, A. V. Tkachev, L. I. Myachina, S. N. Bizyaev, L. A. Sheludyakova, L. A. Glinskaya, I. V. Korol’kov, E. G. Boguslavskii, S. V. Larionov// Russian Journal of General Chemistry, 2013, V. 83, N 2, pp 336-347 doi:10.1134/S1070363213020175, IF=0.432
  12. Synthesis, structure, and properties of nitronyl nitroxyl tetraradical with calix[4]arene framework/ E. V. Tret’yakov, V. G. Vasil’ev, A. S. Bogomyakov, G. V. Romanenko, M. V. Fedin, I. S. Antipin, S. E. Solov’eva, A. I. Konovalov, R. Z. Sagdeev, V. I. Ovcharenko// Russian Chemical Bulletin, 2013, V. 62, N 2, pp 543-547. doi:10.1007/s11172-013-0075-4, IF=0.423
  13. М.А. Мяделец, О.Ю. Васильева, Д.В. Домрачев
    Исследование химического состава эфирных масел ORIGANUM VULGARE L. с различной окраской цветков
    Химия растительного сырья, 2013, N 1, С. 129-136.

2012
  1. V.V. Martemyanov, I.M. Dubovskiy, I.A. Belousova, S.V. Pavlushin, D.V. Domrachev, M.J. Rantala, J.-P. Salminen, S.A. Bakhvalov, V.V. Glupov
    Rapid induced resistance of silver birch affects both innate immunity and performance of gypsy moths: the role of plant chemical defenses
    Arthropod-Plant Interactions, 2012, V. 6, N 4, pp 507-518. doi:10.1007/s11829-012-9202-7
  2. Comparative analysis of volatiles from needles of five-needle pines of northern and eastern Eurasia/ D.V. Domrachev, E.V. Karpova, S.N. Goroshkevich, A.V. Tkachev// RUSS J BIOORG CHEM+, 2012, V. 38, N 7, pp. 780-789. doi:10.1134/S1068162012070059, IF=0.635
  3. Crystal and molecular structure of the [Zn(HL)Cl]center dot EtOH compound, (H2L = chiral bis(menthane)propylenediaminodioxime)/ L.A. Glinskaya, Z.A. Savel’eva, S.N. Bizyaev, A.V. Tkachev, S.V. Larionov// J STRUCT CHEM+, 2012, V. 53, N 6, pp. 1111-1117. doi:10.1134/S0022476612060145, IF=0.586
  4. Nanoporous solvate of N,N-phthaloyl-glycine/ N. A. Tumanov, N. A. Pankrushina, A. A. Nefedov, E. V. Boldyreva// J STRUCT CHEM+, 2012, V. 53, N 3, pp. 606-609. doi:10.1134/S0022476612030298, IF=0.586
  5. I.E. Paukov, Y.A. Kovalevskaya, A.E. Arzamastcev, N.A. Pankrushina, E.V. Boldyreva
    Heat capacity of methacetin in a temperature range of 6 to 300 K
    J. Therm. Anal. Calorim., 2012, V. 108, N1, 243-247. doi:10.1007/s10973-011-1505-x, IF=1.603
  6. М.А. Мяделец, Д.В. Домрачев, С.В. Водолазова
    Исследование химического состава эфирных масел NEPETA SIBIRICA L., THYMUS PETRAEUS L. И SCHIZONEPETA MULTIFIDA L., произрастающих на территории республики хакасия
    Химия растительного сырья, 2012, № 4, 119-124.
  7. Phenolic compounds of Sophora flavescens Soland. of Russian origin/ D. N. Olennikov, L. M. Tankhaeva, N. A. Pankrushina, D. V. Sandanov// RUSS J BIOORG CHEM+, 2013, V.39, N 7, pp 755-760. doi:10.1134/S106816201307011X
  8. Reactions of 3-carene, limonene, and alpha-pinene nitrosochlorides with imidazole, benzotriazole, and indole/ S.N. Bizyaev, A.V. Tkachev// RUSS CHEM B+ 2012, V. 61, N 3, pp. 589-595. doi:10.1007/s11172-012-0085-7, IF=0.379
  9. A study of the chemical composition of essential oils of some species from the Lamiaceae L. family cultivated in the Western Siberian Region/ M. A. Myadelets, D. V. Domrachev, V. A. Cheremushkina// RUSS J BIOORG CHEM+, 2013, V.39, N 7, pp 733-738. doi:10.1134/S1068162013070091

2011
  1. Synthesis and properties of ZnII and CdII complexes with chiral N-derivatives of aminoacetic acid based on natural monoterpenes (+)-3-carene and (-)-α-pinene. Crystal structure of coordination polymer [Zn(HL)Cl •2H2O]n/ S.V. Larionov, T.E. Kokina, A.M. Agafontsev, K.S. Marenin, L.A. Glinskaya, I.V. Korol'kov, M.I. Rakhmanova, E.M. Uskov, P.E. Plyusnin, A.V. Tkachev// RUSS CHEM B+, 2011, V. 60, N 12, pp 2555-2563 doi:10.1007/s11172-011-0393-3, IF=0.629
  2. Synthesis, structure, and blue photoluminescence of the coordination chain polymer [Cd2(L)Cl4]n (L = 2-(3,5- dimethylpyrazol-1-yl)-4-methylquinoline)/ S.V. Larionov, Z.A. Savel'Eva, E.M. Uskov, M.I. Rakhmanova, G.V. Romanenko, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2011, V. 37, N 10, pp 719-724. doi:10.1134/S1070328411100058, IF=0.591
  3. E.S. Vasilyev, A.M. Agafontsev, V.D. Kolesnik, Yu.V. Gatilov, A.V. Tkachev
    Stereoselective functionalisation of pinopyridine with anisidines and o-phenylenediamine
    Mendeleev Commun., 2011, V. 21, N 5, 253-255. doi:10.1016/j.mencom.2011.09.007, IF=0.814
  4. Содержание алкалоидов в различных частях Sophora flavescens/ Д.В. Санданов, Н.А. Панкрушина// Хим. Природ. Соедин., 2011, № 4, 585-586. doi:10.1007/s10600-011-0029-8, IF=0.693
  5. Synthesis and properties of Cu(II) and Pd(ii) complexes with chiral bis-α-sulfanyl oxymes, the derivatives of natural monoterpene, α-pinene/ T.E. Kokina, L.A. Sheludyakova, A.V. Tkachev, E.G. Boguslavskii, A.M. Agafontsev, N.B. Gorshkov, S.V. Larionov// RUSS J ORG CHEM+, 2011, V. 47, N 8, pp. 651-1657. doi:10.1134/S1070363211080123, IF=0.393
  6. A.M. Agafontsev, N.B. Gorshkov, A.V. Tkachev
    Efficient synthesis of β-hydroxy sulfides by microwave-promoted ring opening in (+)-3-carene trans-epoxide with sodium thiolates
    Mendeleev Commun., 2011, V. 21, N 4, 192-193. doi:10.1016/j.mencom.2011.07.006, IF=0.814
  7. Crystal structure of solvate [Cd2L2Cl4]•CH2Cl2 (L = pyrazolylquinoline, the derivative of monoterpenoid (+)-3-carene) and photoluminescence of chiral complex CdLCl2/ S.V. Larionov, Z.A. Savel'eva, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, M.I. Rakhmanova, S.A. Popov, A.V. Tkachev// J STRUCT CHEM+, 201, V. 52, N 3, pp 531-537. doi:10.1134/S0022476611030127, IF=0.546
  8. Features of Chemical Reactions in the Absence of Solvents under Microwave Action/ A. N. Mikheev, V. G. Makotchenko, N. A. Pankrushina, M. O. Korotkikh, A.V. Arzhannikov, М. К. А. Thumm// Chemistry for Sustainable Development, 2011, Т. 19, № 6, 669-677.
  9. Triterpenoids in the Conferous Plants of Pinaceae Family/ T. P. Kukina, E. N. Shmidt// Chemistry for Sustainable Development, 2011, Т. 19, № 6, 655-659.
  10. М.Ю. Круглова, М.А. Ханина, Д.Л. Макарова, Д.В. Домрачев
    Исследование эфирного масла из надземной части Filipendula ulmaria (L.) Maxim
    Медицина и образование в Сибири, 2011 , № 5, статья 13
  11. A new type of polymorphic transformation in tolbutamide: Unusual low-temperature conformation ordering/ T. N. Drebushchak, N. A. Pankrushina, E. V. Boldyreva// DOKL PHYS CHEM, 2011, V. 437, N 2, pp. 61-64. doi:10.1134/S0012501611040014, IF=0.256
  12. Comparative analysis of volatiles from needles of five-needle pines of northern and eastern Eurasia/ D. V. Domrachev, E. V. Karpova, S. N. Goroshkevich, A. V. Tkachev// RUSS J BIOORG CHEM+, 2012, V. 38, N 7, pp 780-789. doi:10.1134/S1068162012070059
  13. Н.С. Фурса, П.Ю. Шкроботько, Д.Л. Макарова, Д.В. Домрачев, С.В. Панченко, И.В. Чикина, О.А. Колосова
    Изучение компонентного состава валерианового эфирного масла полученного паровой дистилляцией
    Вестник Воронежского государственного университета. Сер.: Химия, биология, фармация, 2011 , № 2, 233-239.
  14. Л.Н. Прибыткова, А.В. Ткачев, С.С. Зоркальцев, С.И. Писарева, С.В. Тузова
    Изучение химического состава и антиоксидантной активности полифенолов Artemisia santolinifolia
    Сибирский медицинский журнал (г. Томск), 2011 , Т. 26, № 1, В. 2, 65-67.
  15. В.А. Агеев, Д.Л. Макарова, Д.В. Домрачев, А.П. Родин, М.А. Ханина
    Изучение химического состава эфирного масла Aegopodium podagraria L. флоры Сибири
    Химия растительного сырья, 2011, № 1, 129-132.
  16. Synthesis and photoluminescence of the chiral compounds [ZnLCl2] • EtOH и ZnLCl2, where L is the (+)-3-Carene derivative containing pyrazoline and quinoline fragments: Crystal structure of [ZnLCl2] •EtOH/ S.V. Larionov, Z.A. Savel'Eva, R.F. Klevtsova, E.M. Uskov, L.A. Glinskaya, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2011, V. 37, N 1, pp 1-7. doi:10.1134/S1070328410121036, IF=0.591

2010
  1. _Induction of terpenoid synthesis in leaves of silver birch after defoliation caused by gypsy moth caterpillars/ V.V. Martemyanov, D.V. Domrachev, S.V. Pavlushin, I.A. Belousova, S.A. Bakhvalov, A.V. Tkachev, V.V. Glupov// Doklady Biological Sciences, 2010, V. 435, N 1, pp 407-410 doi:10.1134/S0012496610060104
  2. E.A. Korolyuk, A.V. Tkachev
    _Chemical Composition of the Essential Oil from Two Wormwood Species Artemisia frigida and Artemisia argyrophylla
    Russian Journal of Bioorganic Chemistry, 2010, V. 36, N 7, pp 884-893. doi:10.1134/S1068162010070162, IF=0.472
  3. Chiral complexes of PdCl2 with hydroxypyrazolylquinoline and pyrazolylquinoline based on the monoterpenoid (+)-3-carene: Synthesis and structures/ Z.A. Savel'eva, R.F. Klevtsova, L.A. Glinskaya, S.V. Larionov, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2010, V. 36, № 9, pp 685-692. doi:10.1134/S1070328410090083, IF=0.605
  4. On Mechanochemical Dimerization of Anthracene. Different Possible Reaction Pathways/ V. M. Tapilin, N. N. Bulgakov, A. P. Chupakhin, A. A. Politov, A. G. Druganov// J STRUCT CHEM+, 2010, V. 51, N 4, pp 635-641. doi:10.1007/s10947-010-0093-0, IF=0.453
  5. Synthesis of solvates of the copper(II) complex with chiral caryophyllane-type morpholino oxime (HL). Structure of Cu(HL)Cl2 • CHCl3/ S.V. Larionov, L.I. Myachina, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, A.M. Agafontsev, A.V. Tkachev// RUSS J COORD CHEM+, 2010, V. 36, № 8, pp 579-584. doi:10.1134/S107032841008004X, IF=0.605
  6. Synthesis of terpenoid bis-alpha-sulfanyl oximes and macrocycles on their basis/ N.B. Gorshkov, A.M. Agafontsev, A.V. Tkachev// RUSS CHEM B+, 2010, V. 59, N 7, pp 1467-1471. doi:10.1007/s11172-010-0264-3, IF=0.416
  7. Crystal structure and photoluminescence of the optically active complex [ZnL1Cl2], where L1 = pyrazolylquinoline - a derivative of monoterpenoid (+)-3-carene/ S.V. Larionov, Z.A. Savels'eva, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, S.A. Popov, A.V. Tkachev// J STRUCT CHEM+, 2010, V. 51, N 3, pp. 519-525. doi:10.1007/s10947-010-0075-2, IF=0.453
  8. N.E. Polyakov, O.A. Simaeva, M.B. Taraban, T.V. Leshina, T.A. Konovalova, L.D. Kispert, I.A. Nikitina, N.A. Pankrushina, A.V. Tkachev
    CIDNP and EPR Study of Phototransformation of Lappaconitine Derivatives in Solution
    J. Phys. Chem. B., 2010, V. 114, N 13, 4646-4651. doi:10.1021/jp909166r, IF=3.47
  9. Essential oil from Kazakhstan Artemisia species/ E.M. Suleimenov, A.V. Tkachev, S.M. Adekenov// Химия природных соединений, 2010, V. 46, N 1, 135-139 doi:10.1007/s10600-010-9548-y, IF=0.572
  10. VALERIANA OFFICINALIS: COMPONENT COMPOSITION OF VOLATILE COMPOUNDS IN THE LEAVES FROM THE OUT SKIRTS OF YAROSLAVL AND ZAPOROJIE/ P. Ju. Shkrobotko, A. V. Tkachev, M.S. Jusubov, M. V. Belousov, N. S. Fursa// Российский медико-биологический вестник им. акад. И.П. Павлова, 2010 , В. 2, 141-150.
  11. Induction of terpenoid synthesis in leaves of silver birch after defoliation caused by gypsy moth caterpillars/ V. V. Martemyanov, D. V. Domrachev, S. V. Pavlushin, I. A. Belousova, S. A. Bakhvalov, A. V. Tkachev, V. V. Glupov// Doklady Biological Sciences, 2010, V. 433, N 1, pp 407-410. doi:10.1134/S0012496610060104
  12. Supramolecular 1D assemblies of polyfluorinated arylenediamines and 18-crown-6/ S. Z. Kusov, Yu. V. Gatilov, I. Yu. Bagryanskaya, G. V. Romanenko, T. A. Vaganova, I. K. Shundrina, E. V. Malykhin// RUSS CHEM B+, 2010, V. 59, N 2, pp 382-390. doi:10.1007/s11172-010-0090-7, IF=0.416
  13. А.В. Стародубов, Д.В. Домрачев, А.В. Ткачёв
    Состав эфирного масла кедрового стланика (Pinus pumila) из Хабаровского края
    Химия растительного сырья, 2010, № 1, 81-86.

2009
  1. Chemical composition of the essential oil from two wormwood species Artemisia frigida and Artemisia argyrophylla/ E. A. Korolyuk, A. V. Tkachev// Russian Journal of Bioorganic Chemistry, 2010, V. 36, N 7, pp 884-893 doi:10.1134/S1068162010070162
  2. A.M. Agafontsev, T.V. Rybalova, Y.V. Gatilov, A.V. Tkachev
    First stereoselective cyclisation in the cembrane series: X-ray structure of (+)-(4R,8R,11S,12E,14S,16R)-11-isopropyl-4,8,14-trimethyl-14-morpholin-4-yl-3-oxa-2-azatricyclo[6.6.2.04,16]hexadeca-1,12-diene.
    Mendeleev Commun., 2009, V. 19, N 5, 246-247. doi:10.1016/j.mencom.2009.09.003, IF=0.609
  3. Synthesis, structure, and luminescence properties of complex ZnLCl2 (L is 2-(3,5-dimethylpyrazol-1-yl)-4-methylquinoline)/ Z.A. Savel'eva, S.A. Popov, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, A.V. Tkachev, S.V. Larionova// Russian Chemical Bulletin, 2009, V. 58, N 9, pp 1837-1840 doi:10.1007/s11172-009-0250-9, IF=0.469
  4. Synthesis of Pd(II) complexes containing the protonated form or molecule of 2-(3,5-dimethylpyrazol-1-yl)-4-methylquinoline (L) The crystal structure of [Pd(HL)Cl3]/ Z.A. Savel'eva, L.A. Glinskaya, R.F. Klevtsova, S.V. Larionov, S.A. Popov, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 9, pp 668-673. doi:10.1134/S1070328409090073, IF=0.533
  5. N.B. Gorshkov, A.M. Agafontsev, Yu.V. Gatilov, A.V. Tkachev
    Mannich-type three component conden-sation of a-substituted caran-4-one oximes with formaldehyde and secondary amines
    Mendeleev Commun., 2009, V. 19, N 3, 139-140. doi:10.1016/j.mencom.2009.05.008, IF=0.609
  6. Synthesis of binuclear complexes of PdCl2 with chiral α,α'-diamino-meta-xylene dioximes H2L1, H2L2, and H2L3, the derivatives of the terpenes (+)-3-carene, R-(+)-limonene, and (S)-(-)-α-pinene. Crystal structure of [Pd2(H2L1)Cl4]/ S.V. Larionov, L.I. Myachina, Z.A. Savel'Eva, L.A. Glinskaya, R.F. Klevtsova, A.V. Tkachev, A.M. Agafontsev, S.N. Bizyaev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 4, pp 286-295. doi:10.1134/S1070328409040095, IF=0.533
  7. V.S. Minkov, N.A. Tumanov, B.A. Kolesov, E.V. Boldyreva, S.N. Bizyaev
    _Phase Transitions in the Crystals of L- and DL-Cysteine on Cooling: The Role of the Hydrogen-Bond Distortions and the Side-Chain Motions. 2. DL-Cysteine
    J. Phys. Chem. B, 2009 , V. 113, N 15, 5262-5272. doi:10.1021/jp810355a, IF=4.189
  8. Synthesis and properties of the Cu(II) complexes with chiral bis{(E)-[(1S,4R)-δ7,8-1-amino-2-para-menthalidene]aminohydroxy} methane (L - A derivative of natural terpenoid (R)-(+)-limonene). Crystal structure of the [Cu(L)(μ-Cl)CuCl3] • iso-PrOH solvate/ T.E. Kokina, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, L..A. Sheludyakova, S.V. Larionov, S.N. Bisyaev, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 3, pp 200-209. doi:10.1134/S1070328409030075, IF=0.533
  9. Synthesis of binuclear complexes of PdCl2 with chiral ethylenediamine dioxime (H2L1), piperazine dioxime (H2L2), and propylenediamine dioxime (H2L3), the derivatives of the natural monoterpenoid R-(+)-limonene. The crystal structures of [Pd2(H2L1)Cl4]] and [Pd2(H2L2)Cl4]/ Z.A. Savel'Eva, L.A. Glinskaya, R.F. Klevtsova, S.V. Larionov, A.V. Tkachev, S.N. Bizyaev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 2, pp 128-135. doi:10.1134/S1070328409020079, IF=0.533

2008
  1. N. Pankrushina, I. Nikitina, E. Chernjak, C. Myz, T. Shakhtshneider, V. Boldyrev
    Solvent-free mechanochemical modification of lappakonifine and piroxicam
    Mater. Manuf. Process., 2008, V.23, N 6, 561-565. doi:10.1080/10426910802157870, IF=0.611
  2. Copper(II) and cobalt(II) complexes with a chiral 5-pyrazolone derivative obtained from the terpene (+)-3-carene: Synthesis and properties/ Z.A. Savel’eva, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, S.A. Popov, N.V. Semikolenova, A.V. Tkachev, V.A. Zakharov, S.V. Larionov// Russian Journal of Coordination Chemistry, 2008, V. 34, N 10, pp 766-771 doi:10.1134/S1070328408100102, IF=0.533
  3. V.S. Minkov, A.S. Krylov, E.V. Boldyreva, S.V. Goryainov, S.N. Bizyaev, A.N. Vtyurin
    Pressure-induced phase transitions in crystalline l- and DL-cysteine
    J. Phys. Chem. B, 2008, V. 112, N 30, 8851-8854. doi:10.1021/jp8020276, IF=4.85
  4. Экстрактивные вещества хвои ели сибирской Picea obovata Ledeb/ Э.Н. Шмидт, Г.Ф. Черненко, Т.П. Кукина, Л.М. Покровский// Химия природных соединений, Т. 44, N 4, 508-509. doi:10.1007/s10600-008-9115-y, IF=0.442
  5. T.N. Drebushchak, S.N. Bizyaev, E.V. Boldyreva
    Bis(DL-cysteinium) oxalate
    Acta Crystallogr. C, 2008, V. 64, N 6, O313-O315. doi:10.1107/S0108270108012341, IF=0.718
  6. Synthesis of 4Н--imidazole-5-carbaldoxime 3-oxides and 4Н--imidazole-5- carbonitrile 3-oxides/ I.A. Kirilyuk, D.A. Morozov, Yu.S. Tabatchikova, V.S. Medvedev, A.V. Lebedev, T.V. Rybalova, I.A. Grigor'Ev, G.V. Romanenko// Russian Chemical Bulletin, 2008, V. 57, N 7, Pp 1516-1533 doi:10.1007/s11172-008-0196-3, IF=0.537
  7. Quaternary ammonium compounds based on resin acids and rosin and their colloidal-chemical and biocidal properties/ B. A. Radbil’, S. R. Kushnir, A. B. Radbil’, E. N. Shmidt, V. F. Smirnov, N. B. Mel’nikova// Russian Journal of Applied Chemistry, 2008, V. 81, N 5, pp 874-879. doi:10.1134/S1070427208050297, IF=0.268
  8. Novel carbonyl complexes of ruthenium with α-substituted oxime derivatives of terpenes/ I.Yu. Shabalina, A.V. Golovin, V.P. Kirin, V.A. Maksakov, A.V. Virovets, A.M. Agafontsev, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2008, V. 34, N 4, Pp 286-294. doi:10.1134/S1070328408040088, IF=0.533
  9. Fe(II) complex with chiral pyrazolylquinoline L and Fe(II), Co(II), and Cu(II) complexes with achiral pyrazolylquinoline L1: Synthesis and properties. the crystal structures of [ML1Cl2] (M = Fe, Co, and Cu)/ Z.A. Savel'eva, L.A. Glinskaya, R.F. Klevtsova, S.V. Larionov, S.A. Popov, A.V. Tkachev, N.V. Semikolenova, V.A. Zakharov// Russian Journal of Coordination Chemistry, 2008, V. 34, N 4, pp 278-285 doi:10.1134/S1070328408040076, IF=0.533
  10. Synthesis and structure of Cu(II) and Pd(II) coordination compounds with chiral alpha-thiooxime, a derivative of natural terpenoid (-)-alpha-pinene/ T.E. Kokina, R.F. Klevtsova, L.A. Glinskaya, A.M. Agafontsev, A.V. Tkachev, S.V. Larionov// Russian Journal of Inorganic Chemistry, May 2008, Volume 53, Issue 5, pp 696-703., 2008, V. 34, N 5, 696-703. doi:10.1134/S0036023608050069, IF=0.533
  11. Binuclear Pd(II) complexes with chiral ethylenediaminodioxime (H2L) and bis-α-thiooxime (H2L1), the derivative of monoterpenoid(+)-3-carene. Crystal structures of [Pd2(H2L)Cl4] and [Pd2(H2L1)Cl4] •3CDCl3/ T.E. Kokina, L.I. Myachina, L.A. Glinskaya, R.F. Klevtsova, L.A. Sheludyakova, S.V. Larionov, A.V. Tkachev, S.N. Bizyaev, A.M. Agafontsev, N.B. Gorshkov// Russian Journal of Coordination Chemistry, 2008, V. 34, N 2, Pp 115-128. doi:10.1007/s11173-008-2007-7, IF=0.533
  12. Д.Л. Макарова, М.А. Ханина, В.П. Амельченко, Д.В. Домрачев, А.В. Ткачев
    Изучение химического состава эфирного масла Artemisia pontica L. флоры Сибири
    Химия растительного сырья, 2008, № 2, 55-60.
  13. Е.В. Исаева, Г.А. Ложкина, Т.В. Рязанова, А.И. Вялков, Д.В. Домрачев, А.В. Ткачев
    Хромато-масс-спектрометрическое исследование летучих компонентов вегетативной части тополя бальзамического
    Химия растительного сырья, 2008, № 1, 63-66.

2007
  1. Chirospecific analysis of plant volatiles/ A V Tkachev// Russ. Chem. Rev. 2007, 76(10) 951 doi:10.1070/RC2007v076n10ABEH003728, IF=1.717
  2. Состав эфирного масла Artemisia glauca из Западной Сибири/ Е.В. Полянская, Е.А. Королюк, А.В. Ткачёв// Хим. Природ. Соедин., 2007, N 5, 880-889. doi:10.1007/s10600-007-0187-x, IF=0.393
  3. Synthesis and structure of the [Ni(H2L)Cl]Cl complex with the chiral pentadentate nitrogen-containing ligand H2L derived from the natural terpenoid (+)-3-carene/ S. V. Larionov, L. I. Myachina, L. A. Glinskaya, R. F. Klevtsova, S. N. Bizyaev, A. V. Tkachev// Russian Chemical Bulletin, 2007, V. 56, N 9, pp 1771-1774 doi:10.1007/s11172-007-0275-x, IF=0.504
  4. Triosmium cluster with the bridging aminooxime derivative of pinane: Synthesis, crystal structure and conformational analysis/ V.S. Korenev, V.P. Kirin, V.A. Maksakov, A.V. Virovets, S.V. Tkachev, V.A. Potemkin, A.M. Agafontsev, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2007, V. 33, N 8, pp 594-600 doi:10.1134/S1070328407080088, IF=0.533
  5. Nickel(II) and copper(II) complexes with chiral bis-α-thiooxime, the derivative of natural terpenoid (+)-3-carene: Synthesis and structures/ S.V. Larionov, T.E. Kokina, A.M. Agafontsev, N.B. Gorshkov, A.V. Tkachev, R.F. Klevtsova, L.A. Glinskaya// Russian Journal of Coordination Chemistry, 2007, V. 33, N 7, pp 514-522 doi:10.1134/S107032840707007X, IF=0.418
  6. Liquid-phase noncatalytic oxidation of monoterpenoids with nitrous oxide/ E. P. Romanenko, E. V. Starokon’, G. I. Panov, A. V. Tkacheva// Russian Chemical Bulletin, 2007, V. 56, N 6, pp 1239-1243 doi:10.1007/s11172-007-0187-9, IF=0.504
  7. Transformation of 1,2,3,7atetrahydroimidazo[1,2-b]isoxazole derivatives into isoxazoles/ N. V. Chukanov, S. A. Popov, G. V. Romanenko, V. A. Reznikova// Russian Chemical Bulletin, 2007, V. 56, N 6, pp 1227-1233 doi:10.1007/s11172-007-0185-y, IF=0.504
  8. Cobalt(II) and copper(II) complexes with chiral pyrazolylquinoline, a derivative of terpenoid (+)-3-carene. Catalytic activity in ethylene polymerization reaction/ S.V. Larionov, Z.A. Savel'eva, N.V. Semikolenova, R.F. Klevtsova, L.A. Glinskaya, E.G. Boguslavskii, V.N. Ikorskii, V.A. Zakharov, S.A. Popov, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2007, V. 33, N 6, pp 436-448 doi:10.1134/S1070328407060097, IF=0.418
  9. Трехкомпонентная конденсация 6-хинолиламина с ароматическими альдегидами и циклическими 1, 3-дикетонами/ Н.Г. Козлов, К.Н. Гусак, А.В. Ткачев// Хим. Гетероцик. Соединен., 2007. № 6, 877-885. doi:10.1007/s10593-007-0120-z
  10. Е.П. Романенко, А.В. Ткачев
    Кислотно-катализируемая изомеризация оксида кариофиллена в присутствии SiO2 и Al2O3, импрегнированных серной кислотой.
    Хим. Инт. Уст. Разв., 2007, Т. 15, N 5, 581-594.
  11. Н.А. Панкрушина, И.А. Никитина, Е.И. Черняк, В.В. Болдырев
    Механохимический синтез производных природного алкалоида лаппаконитина
    Хим. Инт. Уст. Разв., 2007, Т. 15, № 2 (приложение), 149-155.
  12. C.А. Мызь, Н.А. Панкрушина, Т.П. Шахтшнейдер, А.С. Медведева, Л.П. Сафронова, В.В. Болдырев
    Механохимическое ацилирование пироксикама
    Хим. Инт. Уст. Разв., 2007, Т. 15, № 2 (приложение), 135-141.
  13. Synthesis and properties of copper(II) complexes with a chiral dioxatetraazamacrocyclic ligand based on a natural monoterpene, (+)-3-carene/ S. V. Larionov, L. I. Myachina, L. A. Sheludyakova, E. G. Boguslavskii, S. N. Bizyaev, A. V. Tkachev// Russian Journal of Inorganic Chemistry, 2007, V. 52, N 1, pp 42-45 doi:10.1134/S0036023607010081, IF=0.18

2006
  1. E. P. Romanenko and A. V. Tkachev
    Identification by GC-MS of cymene isomers and 3,7,7-trimethylcyclohepta-1,3,5-triene in essential oils
    Chem. Nat. Compd. (Хим. Природ. Соедин.), 2006, V. 42, N 6, 699-701. doi:10.1007/s10600-006-0256-6, IF=0.31
  2. A. V. Tkachev, A. M. Gur'ev and M. S. Yusubov
    Acorafuran, a new sesquiterpenoid from Acorus calamus essential oil
    Chem. Nat. Compd. (Хим. Природ. Соедин.), 2006, V. 42, N 6, 696-698. doi:10.1007/s10600-006-0255-7, IF=0.31
  3. Complexes [Cu(H2L)](NO3)2 and [Cu(H2L)Cl]2[CuCl2]Cl·0.5H2 (H2L is chiral bis(menthane) propylenediaminodioxime): Synthesis and structure/ Z. A. Savel'eva, R. F. Klevtsova, L. A. Glinskaya, V. N. Ikorskii, S. N. Bizyaev, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2006, V. 32, N 11, pp 784-791 doi:10.1134/S1070328406110030, IF=0.54
  4. Ni(II) complexes with optically active bis(menthane), pinano-para-menthane ethylenediaminodioximes and pinano-para-menthane, bis(pinane) propylenediaminodioximes: Synthesis, structures, and properties/ Z. A. Savel’eva, S. N. Bizyaev, L. A. Glinskaya, R. F. Klevtsova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2006, V. 32, N 10, pp 723-732 doi:10.1134/S1070328406100058, IF=0.54
  5. Verbanone in the synthesis of amidoketones from o-menthane series/ S. S. Koval'skaya, N. G. Kozlov, A. V. Tkachev// Russian Journal of Organic Chemistry, 2006, V. 42, N 8, pp 1141-1145 doi:10.1134/S1070428006080069, IF=0.419
  6. Verbanone in the synthesis of amidoketones from o-menthane series/ S. S. Koval'skaya, N. G. Kozlov, A. V. Tkachev// Russian Journal of Organic Chemistry, 2006, 42, N 8, pp 1141-1145 doi:10.1134/S1070428006080069, IF=0.419
  7. T.N. Drebushchak, N.A. Pankrushina, T.P. Shakhtshneider, S.A. Apenina
    4-Benzoyloxy-2-methyl-N-(2-pyridyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide
    Acta Crystallogr. C, 2006, V. 62, N 7, o429-o431. doi:10.1107/S0108270106020567, IF=0.779
  8. Catalytic oxidation of α-pinene with tert-butyl hydroperoxide in the presence of Fe-pillared montmorillonite/ E. P. Romanenko, E. A. Taraban, A. V. Tkachev// Russian Chemical Bulletin, 2006, V 55, N 6, pp 993-998 doi:10.1007/s11172-006-0368-y, IF=0.589
  9. A.E. Goncharov, A.A. Politov, N.A. Pankrushina, O.I. Lomovskii
    Isolation of lappaconitine from Aconitum septentrionale roots by adsorption
    Chem. Nat. Compd. (Хим. Природ. Соедин.), 2006, V. 42, N 3, 336-339. doi:10.1007/s10600-006-0114-6, IF=0.31
  10. D.V. Domrachev, A.V. Tkachev
    Absolute configuration of Birkenal, a nor-Sesquiterpene Aldehyde from Essential Oil of Betula pubescens Buds
    Chem. Nat. Compd. (Хим. Природ. Соедин.), 2006, V. 42, N 3, 304-306. doi:10.1007/s10600-006-0105-7, IF=0.31
  11. D.T. Sadyrbekov, E.M. Suleimenov, E.V. Tikhonova, G.A. Atazhanova , A.V. Tkachev, S.M. Adekenov
    Component composition of essential oils from four species of the genus Achillea growing in Kazakhstan
    Chem. Nat. Compd. (Хим. Природ. Соедин.), 2006, V. 42, N 3, 294-297. doi:10.1007/s10600-006-0102-x, IF=0.31
  12. Cu(II) complexes with chiral ethylenediaminodioxime and propylenediaminodioxime, the derivatives of monoterpenoid α-pinene: Synthesis and structures/ S. V. Larionov, Z. A. Savel'eva, L. A. Glinskaya, R. F. Klevtsova, L. A. Sheludyakova, S. N. Bizyaev, A. V. Tkachev// Russian Journal of Coordination Chemistry, 2006, V. 32, N 5, pp 350-358 doi:10.1134/S1070328406050071, IF=0.54
  13. E.V. Deeva, T.V. Glukhareva, A.V. Tkachev, Yu.Yu. Morzherin
    Stereoselective synthesis of spirofused 3-substituted 2,3,4,4a,5,6-hexahydro-6H-benzo[c]quinolizine using the tert-amino effect
    Mendeleev Commun., 2006, V. 16, N 2, 82-83. doi:10.1070/MC2006v016n02ABEH002247, IF=0.709
  14. Co(III) complexes with optically active bis(menthane), pinano-para-menthane, carano-para-menthane, and bis(carane) propylenediaminodioximes/ S. V. Larionov, A. V. Tkachev, Z. A. Savel’eva, L. I. Myachina, L. A. Glinskaya, R. F. Klevtsova, S. N. Bizyaev// Russian Journal of Coordination Chemistry, l 2006, V. 32, N 4, pp 250-260 doi:10.1134/S107032840604004X, IF=0.54
  15. A.V. Tkachev, E.A. Korolyuk, W. Letchamo
    Chemical Screening of Volatile Oil-bearing Flora of Siberia IX. Variations in Chemical Composition of the Essential Oil of Heteropappus altaicus Willd. (Novopokr.) Growing Wild at Different Altitudes of Altai Region, Russia.
    J. Essent. Oil Res., 2006, V. 18, N 2, 149-151. doi:10.1080/10412905.2006.9699048, IF=0.37
  16. A chiral pentadentate macrocyclic ligand (L) based on the natural monoterpene (-)-α-pinene and the seven-coordinate cobalt compound [CoL(NO3)]NO3/ S. V. Larionov, A. V. Tkachev, L. I. Myachina, S. N. Bizyaev, L. A. Glinskaya, R. F. Klevtsova// Doklady Chemistry, 2006, V. 411, N 1, pp 206-211 doi:10.1134/S0012500806110048, IF=0.239
  17. Synthesis of 4-[(p-alkylanilino-palkylphenyl)methyl]4-butyl-1,2-diphenylpyrazolidine-3,5-diones/ N. G. Kozlov, S. V. Rubis, A. V. Tkachev, L. I. Basalaeva// Russian Journal of General Chemistry, 2006, V. 76, N 2, pp 307-310 doi:10.1134/S1070363206020241
  18. A.V. Tkachev, E.A. Korolyuk, W. Konig, Y.V. Kuleshova, W. Letchamo
    Chemical Screening of Volatile Oil-Bearing Flora of Siberia VIII: Variations in Chemical Composition of the Essential Oil of Wild Growing Seseli buchtormense (Fisch. ex Sprengel) W. Koch from Different Altitudes of Altai Region.
    J. Essent. Oil Res., 2006, V. 18, N 1, 100-103. doi:10.1080/10412905.2006.9699399, IF=0.37
  19. A.V. Tkachev, E.A. Korolyuk, W. Letchamo
    Volatile Oil-Bearing Flora of Siberia VIII: Essential Oil Composition and Antimicrobial Activity of Wild Solidago virgaurea L. from the Russian Altai.
    J. Essent. Oil Res., 2006, V. 18, N 1, 46-50. doi:10.1080/10412905.2006.9699382, IF=0.37

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