Kharitonov Yurii Viktorovich

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Articles - 45

Articles (45) More info

1	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 WOS OpenAlex
2	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 WOS РИНЦ OpenAlex
3	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 WOS РИНЦ OpenAlex
4	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 WOS Scopus РИНЦ OpenAlex
5	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 OpenAlex
6	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 WOS Scopus РИНЦ OpenAlex
7	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 WOS Scopus РИНЦ OpenAlex
8	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 WOS Scopus РИНЦ OpenAlex
9	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 WOS Scopus OpenAlex
10	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 WOS Scopus РИНЦ OpenAlex
11	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 WOS Scopus РИНЦ OpenAlex
12	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 WOS Scopus РИНЦ OpenAlex
13	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 WOS Scopus РИНЦ OpenAlex
14	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 WOS Scopus РИНЦ OpenAlex
15	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 WOS Scopus РИНЦ OpenAlex
16	Kharitonov Y.V. , Shakirov M.M. , Shults E.E. Synthesis of Novel Labdanoid-Based Macroheterocycles Using Click-Cycloaddition Reaction Protocol Macroheterocycles. 2017. V.10. N1. P.117-122. DOI: 10.6060/mhc160959s WOS Scopus РИНЦ OpenAlex
17	Kremenko O.I. , Kharitonov Y.V. , Shul'ts E.E. Synthetic Transformations of Higher Terpenoids: XXXVI.(1) Synthesis of Furanolabdanoid Glycoconjugates with a 1,2,3-Triazole Linker Russian Journal of Organic Chemistry. 2017. V.53. N1. P.35-46. DOI: 10.1134/S1070428017010079 WOS Scopus РИНЦ OpenAlex
18	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 WOS Scopus РИНЦ OpenAlex
19	Kharitonov Y.V. , Shakirov M.M. , Shults E.E. Synthesis and spectroscopic studies of chiral macrocyclic furanolabdanoids connected on the 16,17-positions by 1,2,3-triazole rings with methylene or oxamethylene units Journal of Inclusion Phenomena and Macrocyclic Chemistry. 2016. V.84. N3-4. P.197-202. DOI: 10.1007/s10847-016-0596-1 WOS Scopus OpenAlex
20	Mironov M.E. , Pokrovsky M.A. , Kharitonov Y.V. , Shakirov M.M. , Pokrovsky A.G. , Shults E.E. Furanolabdanoid-based 1,2,4-oxadiazoles: Synthesis and cytotoxic activity ChemistrySelect. 2016. V.1. N3. P.417-424. DOI: 10.1002/slct.201600042 WOS Scopus РИНЦ OpenAlex
21	Timoshenko M.A. , Kharitonov Y.V. , Shakirov M.M. , Bagryanskaya I.Y. , Shults E.E. Synthetic Studies on Tricyclic Diterpenoids: Direct Allylic Amination Reaction of Isopimaric Acid Derivatives ChemistryOpen. 2016. V.5. N1. P.65-70. DOI: 10.1002/open.201500187 WOS Scopus OpenAlex
22	Kharitonov Y.V. , Shakirov M.M. , Shults E.E. Synthesis of Macroheterocyclic Compounds with a Furan Bridge Possessing Structural Fragments of 1,2,3-Triazoles and Natural Diterpenoids Macroheterocycles. 2015. V.8. N1. P.81-88. DOI: 10.6060/mhc141138s WOS Scopus РИНЦ OpenAlex
23	Shul'ts E.E. , Mironov M.E. , Kharitonov Y.V. Furanoditerpenoids of the Labdane Series: Occurrence in Plants, Total Synthesis, Several Transformations, and Biological Activity Chemistry of Natural Compounds. 2014. V.50. N1. P.2-21. DOI: 10.1007/s10600-014-0861-8 WOS Scopus РИНЦ OpenAlex
24	Timoshenko M.A. , Ayusheev A.B. , Kharitonov Y.V. , Shakirov M.M. , Shul'ts E.E. SYNTHETIC TRANSFORMATIONS OF HIGHER TERPENOIDS. XXXIV. PREPARATION OF CARBOXYL DERIVATIVES OF ISOPIMARIC ACID Chemistry of Natural Compounds. 2014. V.50. N4. P.673-680. DOI: 10.1007/s10600-014-1050-5 WOS Scopus РИНЦ OpenAlex
25	Kharitonov Y.V. , Shul'ts E.E. , Shakirov M.M. Synthetic Transformations of Higher Terpenoids. XXXIII. Preparation of 15,16-Dihydroisopimaric Acid and Methyl Dihydroisopimarate and their Transformations Chemistry of Natural Compounds. 2014. V.49. N6. P.1067-1075. DOI: 10.1007/s10600-014-0823-1 WOS Scopus РИНЦ OpenAlex
26	Kharitonov Y.V. , Kremenko O.I. , Shults E.E. , Shakirov M.M. , Tolstikov G.A. Synthetic transformations of higher terpenoids: XXXII. Synthesis of 16-alkenyl-substituted labdatrienes by oxidative coupling of methyl phlomisoate with alkenes Russian Journal of Organic Chemistry. 2013. V.49. N11. P.1690-1702. DOI: 10.1134/S1070428013110225 WOS Scopus РИНЦ OpenAlex
27	Kharitonov Y.V. , Shul'ts E.E. , Shakirov M.M. , Pokrovskii M.A. , Pokrovskii A.G. , Tolstikov G.A. Synthetic transformation of higher terpenoids 31. Synthesis of 1,2,3-triazolyl-containing furan labdanoids and studies of their cytotoxic activity Russian Chemical Bulletin. 2013. V.62. N9. P.2046-2055. DOI: 10.1007/s11172-013-0297-5 WOS Scopus РИНЦ OpenAlex
28	Kharitonov Y.V. , Shul'ts E.E. , Shakirov M.M. , Pokrovsky M.A. , Pokrovsky A.G. , Tolstikov G.A. Synthetic Transformations of Higher Terpenoids. XXVI. 16-Acetylaminomethyllabdanoids and Their Cytotoxicity Russian Journal of Bioorganic Chemistry. 2012. V.38. N1. P.107-115. DOI: 10.1134/S1068162011060082 WOS Scopus РИНЦ OpenAlex
29	Kharitonov Y.V. , Shul'ts E.E. , Gatilov Y.V. , Bagryanskaya I.Y. , Shakirov M.M. , Tolstikov G.A. *Synthetic transformations of higher terpenoids. XXVII. Synthesis of 7-hydroxylabdanoids and their transformations** Chemistry of Natural Compounds. 2012. V.48. N2. P.250-257. DOI: 10.1007/s10600-012-0215-3 WOS Scopus РИНЦ OpenAlex
30	Mironov M.E. , Shul'ts E.E. , Shakirov M.M. , Kharitonov Y.V. , Tolstikov G.A. Synthetic transformations of higher terpenoids: XXVIII. Diels-Alder reactions of 16-(trimethylsiloxybutadienyl) labdanoids Russian Journal of Organic Chemistry. 2012. V.48. N6. P.840-850. DOI: 10.1134/S1070428012060164 WOS Scopus РИНЦ OpenAlex
31	Kharitonov Y.V. , Shults E.E. , Shakirov M.M. , Bagryanskaya I.Y. , Tolstikov G.A. Synthetic transformations of higher terpenoids: XXIX. Gold catalyzed cycloisomerization of propargylaminomethyl substituted and propargyloxymethyl substituted furanolabdanoids Russian Journal of Organic Chemistry. 2012. V.48. N8. P.1081-1089. DOI: 10.1134/S1070428012080088 WOS Scopus РИНЦ OpenAlex
32	Kharitonov Y.V. , Shul'ts E.E. , Shakirov M.M. , Bagryanskaya I.Y. , Tolstikov G.A. First synthesis of macrocyclic furanolabdanoids via cycloaddition of diacetylenic derivatives of lambertianic acid to 1,5-diazidopentane Doklady Chemistry. 2012. V.446. P.174-179. DOI: 10.1134/S0012500812090042 WOS Scopus РИНЦ OpenAlex
33	Kharitonov Y.V. , Shul'ts E.E. , Shakirov M.M. , Tolstikov G.A. Synthetic transformations of higher terpenoids: XXV. Cross coupling of phlomisoic acid methyl ester with alkenes in the presence of oxidants Russian Journal of Organic Chemistry. 2011. V.47. N4. P.602-605. DOI: 10.1134/S107042801104021X WOS Scopus РИНЦ OpenAlex
34	Kharitonov Y.V. , Shults E.E. , Shakirov M.M. , Bagryanskaya I.Y. , Tolstikov G.A. Synthetic transformations of higher terpenoids: XXII. Reactions of lambertianic acid derivatives with organozinc reagents obtained from ethyl bromoalkanoates Russian Journal of Organic Chemistry. 2010. V.46. N9. P.1339-1347. DOI: 10.1134/S1070428010090137 WOS Scopus РИНЦ OpenAlex
35	Mironov M.E. , Kharitonov Y.V. , Shul'ts E.E. , Shakirov M.M. , Gatilov Y.V. , Tolstikov G.A. Synthetic transformations of higher terpenoids: XXIII. Synthesis of diterpenoid-based dihydroisoindolones Russian Journal of Organic Chemistry. 2010. V.46. N12. P.1869-1882. DOI: 10.1134/S107042801012016X WOS Scopus РИНЦ OpenAlex
36	Mironov M.E. , Kharitonov Y.V. , Shul'ts E.E. , Shakirov M.M. , Bagryanskaya Y. , Tolstikov G.A. *Synthetic transformations of higher terpenoids. XXI. preparation of phlomisoic acid and its N-containing derivatives** Chemistry of Natural Compounds. 2010. V.46. N2. P.233-241. DOI: 10.1007/s10600-010-9577-6 WOS Scopus РИНЦ OpenAlex
37	Kharitonov Y.V. , Shults E.E. , Shakirov M.M. , Tolstikov G.A. Synthetic transformations of higher terpenoids: XIX. Synthesis of 1,7-epoxyisoindolones and 7,9a-epoxythiazolo[2,3-a]isoindolones from terpenoids Russian Journal of Organic Chemistry. 2009. V.45. N5. P.637-649. DOI: 10.1134/S1070428009050017 WOS Scopus РИНЦ OpenAlex
38	Kharitonov Y.V. , Shul'ts E.E. , Shakirov M.M. , Tolstikov G.A. Synthetic transformations of higher terpenoids: XVII. Intramolecular cyclization of N-furfuryl Amides of the labdane series Russian Journal of Organic Chemistry. 2008. V.44. N4. P.516-523. DOI: 10.1134/S1070428008040088 WOS Scopus РИНЦ OpenAlex
39	Kharitonov Y.V. , Shul'ts E.E. , Shakirov M.M. , Tolstikov G.A. Synthetic transformations of higher terpenoids: XV. Transformations of azlactone derived from 16-formyllambertianic acid methyl ester Russian Journal of Organic Chemistry. 2007. V.43. N6. P.839-851. DOI: 10.1134/S1070428007060073 WOS Scopus РИНЦ OpenAlex
40	Kharitonov Y.V. , Shul'ts E.E. , Shakirov M.M. , Tolstikov G.A. Synthetic transformations of higher terpenoids: XIV. Heterocyclization reactions of 15,16,18-ricarboxylabdadiene. New nitrogen-containing diterpenoids Russian Journal of Organic Chemistry. 2006. V.42. N5. P.707-718. DOI: 10.1134/S1070428006050113 WOS Scopus РИНЦ OpenAlex
41	Kharitonov Y. , Shults E. , Shakirov M. , Tolstikov G. Synthetic transformations of higher terpenoids: X. Intramolecular cyclization of N-allyl- and N-propargyl-16-dialkylammoniomethyl-12-furfuryl-13,14,15,16-tetranorlabdanoid bromides Russian Journal of Organic Chemistry. 2005. V.41. N8. P.1145-1157. DOI: 10.1007/s11178-005-0307-7 WOS Scopus РИНЦ OpenAlex
42	Kharitonov Y. , Shults E. , Shakirov M. , Tolstikov G. New nitrogen-containing labdanoids from lambertianic add Doklady Chemistry. 2004. V.395. P.43-46. DOI: 10.1023/B:DOCH.0000021273.00956.30 WOS Scopus РИНЦ OpenAlex
43	Tolstikova T.G. , Sorokina I.V. , Dolgikh M.P. , Kharitonov Y.V. , Chernov S.V. , Shul'ts E.E. , Tolstikov G.A. Search for new drugs: Neurotropic activity of lambertianic acid adducts with N-substituted maleinimides Pharmaceutical Chemistry Journal. 2004. V.38. N10. P.532-534. DOI: 10.1007/s11094-005-0003-5 Scopus РИНЦ OpenAlex
44	Kharitonov Y. , Shults E. , Shakirov M. , Tolstikov G. Synthetic transformations of higher terpenoids: VIII. [4+2]-cycloaddition reactions of lambertianic acid Russian Journal of Organic Chemistry. 2003. V.39. N1. P.57-74. DOI: 10.1023/A:1023490528591 WOS Scopus РИНЦ OpenAlex
45	Kharitonov Y. , Shults E. , Shakirov M. , Tolstikov G. Unusual cleavage of products of [4+2] cycloaddition of thiol-2-en-4-one-1,1-dioxide with beta-substituted furans Doklady Chemistry. 2001. V.381. N1-3. P.332-335. DOI: 10.1023/A:1012936909862 WOS Scopus РИНЦ OpenAlex

Identifiers

Scopus ID: 7006798336

ORCID: 0000-0001-8234-5130

Elibrary ID: 55818