1
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Kharitonov Y.V.
, Antipova V.I.
, Marenina M.K.
, Meshkova Y.V.
, Tolstikova T.G.
, Shults E.E.
Synthetic Transformations of Higher Terpenoids. 44#. Synthesis of New Derivatives of 18-Nor-4-Amino-8(17),13,14-Labdatriene and Evaluation of Their Cytotoxicity for MCF7, HepG2, and HeLa Tumor Cell Lines
Chemistry of Natural Compounds. 2024.
V.60. N2. P.252-262. DOI: 10.1007/s10600-024-04299-2
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2
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Kharitonov Y.V.
, Antipova V.I.
, Marenina M.K.
, Meshkova Y.V.
, Tolstikova T.G.
, Shults E.E.
Synthetic Transformations of Higher Terpenoids. 43. Synthesis and Cytotoxic Properties of New Lambertianic Acid Derivatives at the Carboxylic Group
Chemistry of Natural Compounds. 2023.
№6. С.936–947. DOI: 10.1007/s10600-023-04206-1
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3
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Харитонов Ю.В.
, Петрова Д.А.
, Шульц Э.Э.
, Покровский М.А.
, Покровский А.Г.
Синтез и оценка цитотоксичности фуранолабданоидов, содержащих 3-аминопропаноильный заместитель в фурановом цикле
ХИМИЯ В ИНТЕРЕСАХ УСТОЙЧИВОГО РАЗВИТИЯ. 2023.
№6. С.737-745. DOI: 10.15372/KhUR2023521
РИНЦ
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4
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KHARITONOV Y.V.
, PETROVA D.A.
, SHULTS E.E.
, POKROVSKII M.A.
, POKROVSKII A.G.
SYNTHESIS AND EVALUATION OF THE CYTOTOXICITY OF FURANOLABDANOIDS CONTAINING A 3-AMINOPROPANOYL SUBSTITUENT IN THE FURAN RING
ХИМИЯ В ИНТЕРЕСАХ УСТОЙЧИВОГО РАЗВИТИЯ. 2023.
V.31. N6. P.715-723. DOI: 10.15372/CSD2023521
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5
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Kharitonov Y.V.
, Shults E.E.
An Approach toward 17-Arylsubstituted Marginatafuran-Type Isospongian Diterpenoids via a Palladium-Catalyzed Heck–Suzuki Cascade Reaction of 16-Bromolambertianic Acid
Molecules. 2022.
V.27. N9. P.2643. DOI: 10.3390/molecules27092643
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РИНЦ
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6
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Gromova M.A.
, Kharitonov Y.V.
, Borisov S.A.
, Baev D.S.
, Tolstikova T.G.
, Shul’ts E.E.
Synthetic Transformations of Higher Terpenoids. 39.∗ Synthesis and Analgesic Activity of Isopimaric Acid Derivatives
Chemistry of Natural Compounds. 2021.
V.57. P.474–481. DOI: 10.1007/s10600-021-03391-1
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Scopus
РИНЦ
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7
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Gromova M.A.
, Kharitonov Y.V.
, Rybalova T.V.
, Shults E.E.
Click synthesis of triazole-linked polyazamacrocycles through selective isopimaric acid transformations
Macroheterocycles. 2021.
V.14. N1. P.105-111. DOI: 10.6060/mhc200817s
WOS
Scopus
РИНЦ
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8
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Kharitonov Y.V.
, Shul'ts E.E.
, Rybalova T.V.
, Pavlova A.V.
, Tolstikova T.G.
Synthetic Transformations of Higher Terpenoids. 40. Synthesis and Assessment of Analgesic Activity of N-Containing Derivatives of Lambertianic Acid
Chemistry of Natural Compounds. 2021.
V.57. N5. P.879-886. DOI: 10.1007/s10600-021-03502-y
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Scopus
РИНЦ
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9
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Gromova M.A.
, Kharitonov Y.V.
, Politanskaya L.,.V.
, Tretyakov E.,.V.
, Shults E.E.
A facile approach to hybrid compounds containing a tricyclic diterpenoid and fluorine-substituted heterocycles
Journal of Fluorine Chemistry. 2020.
V.236. 109554
. DOI: 10.1016/j.jfluchem.2020.109554
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Scopus
РИНЦ
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10
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Brusentseva O.I.
, Kharitonov Y.V.
, Dolgikh M.P.
, Tolstikova T.G.
, Shul'ts E.E.
Synthesis and Analgesic Activity Assessment of Furanolabdanoid Conjugates with Glucuronic Acid
Chemistry of Natural Compounds. 2020.
V.56. N4. P.678-687. DOI: 10.1007/s10600-020-03119-7
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Scopus
РИНЦ
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11
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Brusentzeva O.I.
, Kharitonov Y.V.
, Fadeev D.S.
, Shults E.E.
Synthesis and spectroscopic studies of furan-bridged polyazamacrocycles through 15,16-bis((prop-2-ynylamino)methyl)labdatriene transformations
Journal of Inclusion Phenomena and Macrocyclic Chemistry. 2020.
V.96. N3-4. P.245-250. DOI: 10.1007/s10847-019-00965-z
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Scopus
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12
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Gromova M.A.
, Kharitonov Y.V.
, Rybalova T.V.
, Shults E.E.
Synthetic studies on tricyclic diterpenoids: convenient synthesis of 16-arylisopimaranes
Monatshefte für Chemie Chemical Monthly. 2020.
V.151. N12. P.1817-1827. DOI: 10.1007/s00706-020-02713-3
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Scopus
РИНЦ
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13
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Gromova M.A.
, Kharitonov Y.V.
, Pokrovskii M.A.
, Bagryanskaya I.Y.
, Pokrovskii A.G.
, Shul'ts E.E.
Synthetic Transformations of Higher Terpenoids. 37. Synthesis and Cytotoxicity of 4-(Oxazol-2-Yl)-18-Norisopimaranes
Chemistry of Natural Compounds. 2019.
V.55. N1. P.52-59. DOI: 10.1007/s10600-019-02613-x
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Scopus
РИНЦ
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14
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Gromova M.A.
, Kharitonov Y.V.
, Rybalova T.V.
, Shul'ts E.E.
Synthetic Transformations of Higher Terpenoids. 38.* Synthesis of Conjugates Containing beta-Carboline and Tricyclic Diterpenoids
Chemistry of Natural Compounds. 2019.
V.55. N5. P.871-877. DOI: 10.1007/s10600-019-02836-y
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РИНЦ
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15
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Толстикова Т.Г.
, Сорокина И.В.
, Жукова Н.А.
, Морозова Е.А.
, Харитонов Ю.В.
, Миронов М.Е.
, Попов С.А.
, Шульц Э.Э.
Доступные метаболиты растений сибири как источники инновационных препаратов для медицины
ХИМИЯ В ИНТЕРЕСАХ УСТОЙЧИВОГО РАЗВИТИЯ. 2018.
Т.26. №3. С.329-344. DOI: 10.15372/KhUR20180308
РИНЦ
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16
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Gromova M.A.
, Kharitonov Y.V.
, Bagryanskaya I.Y.
, Shults E.E.
Efficient Synthesis of the N-(buta-2,3-dienyl)carboxamide of Isopimaric Acid and the Potential of This Compound towards Heterocyclic Derivatives of Diterpenoids
ChemistryOpen. 2018.
V.7. N11. P.890-901. DOI: 10.1002/open.201800205
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РИНЦ
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17
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Gromova M.A.
, Kharitonov Y.V.
, Rybalova T.V.
, Shul'ts E.E.
Synthetic Transformations of Higher Terpenoids. 36.(*) Synthesis of 13-(Oxazol-5-Yl)-15,16-Bisnorisopimaranes
Chemistry of Natural Compounds. 2018.
V.54. N2. P.293-300. DOI: 10.1007/s10600-018-2327-x
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Scopus
РИНЦ
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18
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Kharitonov Y.V.
, Shakirov M.M.
, Shults E.E.
Highly Selective Gold-Catalyzed Cycloisomerization of Furanolabdanoid Dialkynes with Alkynyl Substituents in the Furan Ring
Current Organic Synthesis. 2018.
V.15. N8. P.1147-1153. DOI: 10.2174/1570179415666180918160421
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РИНЦ
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19
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Брусенцева О.И.
, Харитонов Ю.В.
, Шульц Э.Э.
Синтетические трансформации высших терпеноидов. xxxvi. синтез гликоконъюгатов фуранолабданоидов с 1,2,3-триазольным линкером
Журнал органической химии (RUSS J ORG CHEM+). 2017.
Т.53. №1. С.42-52.
РИНЦ
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20
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Kharitonov Y.V.
, Shakirov M.M.
, Pokrovskii M.A.
, Pokrovskii A.G.
, Shu?Ts E.E.
Synthetic transformations of higher terpenoids. XXXV.* synthesis and cytotoxicity of macroheterocyclic compounds based on lambertianic acid
Chemistry of Natural Compounds. 2017.
V.53. N1. P.77-82. DOI: 10.1007/s10600-017-1915-5
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