Ли-Жуланов Николай Сергеевич

Научная деятельность

Статьи - 23

Статьи (23) Подробнее

1	Li-Zhulanov N.S. , Rogachev A.D. , Gatilov Y.V. , Volcho K.P. , Salakhutdinov N.F. 1,4-Bis(2-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethyl)piperazine MolBank. 2024. V.2024. N1. P.M1780. DOI: 10.3390/m1780
2	Li-Zhulanov N.S. , Ponomarev K.Y. , Sari S. , Gülmez D. , Arikan-Akdagli S. , Krasnov V.I. , Suslov E.V. , Volcho K.P. , Salakhutdinov N.F. Myrtenyl-bispidine containing azole: synthesis and antifungal activity Mendeleev Communications. 2024. V.34. N1. P.119-121. DOI: 10.1016/j.mencom.2024.01.036 WOS Scopus
3	Li-Zhulanov N.S. , Nikolaichuk K.M. , Gatilov Y.V. , Volcho K.P. , Khvostov M.V. , Tolstikova T.G. , Salakhutdinov N.F. Chiral N-(Octahydro-2H-chromen-4-yl)-2-(dialkylamino)acetamides: Synthesis and Analgesic Activity Doklady Chemistry. 2023. V.512. N1. P.242-248. DOI: 10.1134/s0012500823600694 Scopus РИНЦ
4	Ли-Жуланов Н.С. , Кузнецова В. , Гатилов Ю.В. , Волчо К.П. , Хвостов М.В. , Толстикова Т.Г. , Салахутдинов Н.Ф. Хиральные N-(диалкилоктагидро-2H-хромен-4-ил)ацетамиды: синтез и анальгетическая активность Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2023. Т.72. №10. С.2430-2438. РИНЦ
5	Podturkina A.V. , Li-Zhulanov N.S. , Volcho K.P. , Salakhutdinov N.F. (1R,2R,6S)-2(4-(4-Isopropylbenzyl)piperazin-1-yl)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-enol MolBank. 2023. V.2023. N1. P.M1546. DOI: 10.3390/m1546 WOS РИНЦ
6	Li-Zhulanov N.S. , Zaikova N.P. , Sari S. , Gülmez D. , Sabuncuoğlu S. , Ozadali-Sari K. , Arikan-Akdagli S. , Nefedov A.A. , Rybalova T.V. , Volcho K.P. , Salakhutdinov N.F. Rational Design of New Monoterpene-Containing Azoles and Their Antifungal Activity Antibiotics. 2023. V.12. N5. P.818. DOI: 10.3390/antibiotics12050818 WOS РИНЦ
7	Li-Zhulanov N.S. , Kuznetsova V.A. , Gatilov Y.V. , Volcho K.P. , Khvostov M.V. , Tolstikova T.G. , Salakhutdinov N.F. Chiral N-(dialkyloctahydro-2H-chromen-4-yl)acetamides: synthesis and analgesic activity Russian Chemical Bulletin. 2023. Т.72. №10. С.2430-2438. DOI: 10.1007/s11172-023-4044-2 WOS Scopus РИНЦ
8	Sidorenko A.Y. , Kurban Y.M. , Kravtsova A.V. , Il'ina I.V. , Li-Zhulanov N.S. , Korchagina D.V. , Sánchez-Velandia J.E. , Aho A. , Volcho K.P. , Salakhutdinov N.F. , Murzin D.Y. , Agabekov V.E. Clays catalyzed cascade Prins and Prins-Friedel-Crafts reactions for synthesis of terpenoid-derived polycyclic compounds Applied Catalysis A: General. 2022. V.629. 118395 . DOI: 10.1016/j.apcata.2021.118395 WOS Scopus РИНЦ
9	Li-Zhulanov N.S. , Il'ina I.V. , Sidorenko A.Y. , Korchagina D.V. , Volcho K.P. , Agabekov V.E. , Salakhutdinov N.F. Cascade transformation of 4-hydroxymethyl-2-carene into novel cage methanopyrano[4,3-b]thieno[3,2-g]benzofuran derivative Mendeleev Communications. 2022. V.32. N4. P.443-445. DOI: 10.1016/j.mencom.2022.07.005 WOS РИНЦ
10	Sidorenko A.Y. , Kurban Y.M. , Il'ina I.V. , Li-Zhulanov N.S. , Korchagina D.V. , Ardashov O.V. , Wärnå J. , Volcho K.P. , Salakhutdinov N.F. , Murzin D.Y. , Agabekov V.E. Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes Applied Catalysis A: General. 2021. V.618. 118144 . DOI: 10.1016/j.apcata.2021.118144 WOS Scopus РИНЦ
11	Zaykovskaya A.O. , Kumar N. , Kholkina E.A. , Li-Zhulanov N.S. , Maki-Arvela P. , Aho A. , Peltonen J. , Peurla M. , Heinmaa I. , Kusema B.T. , Streiff S. , Murzin D.Y. Synthesis and physico-chemical characterization of Beta zeolite catalysts: Evaluation of catalytic properties in Prins cyclization of (-)-isopulegol Microporous and Mesoporous Materials. 2020. V.302. 110236 :1-11. DOI: 10.1016/j.micromeso.2020.110236 WOS Scopus РИНЦ
12	Sidorenko A.Y. , Li-Zhulanov N.S. , Maki-Arvela P. , Sandberg T. , Kravtsova A.V. , Peixoto A.F. , Freire C. , Volcho K.P. , Salakhutdinov N.F. , Agabekov V.E. , Murzin D.Y. Stereoselectivity Inversion by Water Addition in the -SO3H-catalyzed Tandem Prins-Ritter Reaction for Synthesis of 4-amidotetrahydropyran Derivatives ChemCatChem. 2020. V.12. N9. P.2605-2609. DOI: 10.1002/cctc.202000070 WOS Scopus РИНЦ
13	Sidorenko A.Y. , Kravtsova A.V. , Mäki-Arvela P. , Aho A. , Il'ina I.V. , Li-Zhulanov N.S. , Korchagina D. , Volcho K.P. , Salakhutdinov N.F. , Murzin D.Y. , Sandberg T. Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes Molecular Catalysis. 2020. V.490. 110974 :1-8. DOI: 10.1016/j.mcat.2020.110974 WOS Scopus РИНЦ
14	Laluc M. , Maki-Arvela P. , Peixoto A.F. , Li-Zhulanov N. , Sandberg T. , Salakhutdinov N.F. , Volcho K. , Freire C. , Sidorenko A.Y. , Murzin D.Y. Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays Reaction Kinetics, Mechanisms and Catalysis. 2020. V.129. N2. P.627-644. DOI: 10.1007/s11144-020-01740-9 WOS Scopus РИНЦ
15	Чепанова А. , Ли-Жуланов Н.С. , Кургина Т.А. , Захаренко А.Л. , Захарова О.Д. , Волчо К.П. , Салахутдинов Н.Ф. , Лаврик О.И. Разработка ингибиторов tdpi на основе производных хроменов как потенциальных противораковых препаратов Гены и Клетки. 2020. Т.15. №53. С.68-69. РИНЦ
16	Li-Zhulanov N.S. , Pavlova A.V. , Korchagina D.V. , Gatilov Y.V. , Volcho K.P. , Tolstikova T.G. , Salakhutdinov N.F. 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. N7. P.936-941. DOI: 10.1007/s10593-020-02753-x WOS Scopus РИНЦ
17	Il'ina I.V. , Dyrkheeva N.S. , Zakharenko A.L. , Sidorenko A.Y. , Li-Zhulanov N.S. , Korchagina D.V. , Chand R. , Ayine-Tora D.M. , Chepanova A.A. , Zakharova O.D. , Ilina E.S. , Reynisson J. , Malakhova A.A. , Medvedev S.P. , Zakian S.M. , Volcho K.P. , Salakhutdinov N.F. , Lavrik O.I. Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1 Molecules. 2020. V.25. N15. 3496 . DOI: 10.3390/molecules25153496 WOS Scopus РИНЦ
18	Li-Zhulanov N.S. , Il'ina I.V. , Chicca A. , Schenker P. , Patrusheva O.S. , Nazimova E.V. , Korchagina D.V. , Krasavin M. , Volcho K.P. , Salakhutdinov N.F. Effect of chiral polyhydrochromenes on cannabinoid system Medicinal Chemistry Research. 2019. V.28. N4. P.450-464. DOI: 10.1007/s00044-019-02294-9 WOS Scopus РИНЦ
19	Li-Zhulanov N. , Maki-Arvela P. , Laluc M. , Peixoto A.F. , Kholkina E. , Sandberg T. , Aho A. , Volcho K. , Salakhutdinov N. , Freire C. , Sidorenko A.Y. , Murzin D.Y. Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays Molecular Catalysis. 2019. V.478. UNSP 110569 . DOI: 10.1016/j.mcat.2019.110569 WOS Scopus РИНЦ
20	Ardashov O.V. , Pavlova A.V. , Mahato A.K. , Sidorova Y. , Morozova E.A. , Korchagina D.V. , Salnikov G.E. , Genaev A.M. , Patrusheva O.S. , Li-Zhulanov N.S. , Tolstikova T.G. , Volcho K.P. , Salakhutdinov N.F. 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. N10. P.4337-4349. DOI: 10.1021/acschemneuro.9b00396 WOS Scopus РИНЦ
21	Chepanova A.A. , Li-Zhulanov N.S. , Sukhikh A.S. , Zafar A. , Reynisson J. , Zakharenko A.L. , Zakharova O.D. , Korchagina D.,.V. , Voleho K.P. , Salakhutdinov N.F. , Lavrik O.,.I. Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy Russian Journal of Bioorganic Chemistry. 2019. V.45. N6. P.647-655. DOI: 10.1134/S1068162019060104 WOS Scopus РИНЦ
22	Sidorenko A.Y. , Il'ina I.V. , Kravtsova A.V. , Aho A. , Ardashov O.V. , Li-Zhulanov N.S. , Volcho K.P. , Salakhutdinov N.F. , Murzin D.Y. , Agabekov V.E. Preparation of chiral isobenzofurans from 3-carene in the presence of modified clays Molecular Catalysis. 2018. V.459. P.38-45. DOI: 10.1016/j.mcat.2018.07.025 WOS Scopus РИНЦ
23	Li-Zhulanov N.S. , Zakharenko A.L. , Chepanova A.A. , Patel J. , Zafar A. , Volcho K.P. , Salakhutdinov N.F. , Reynisson J. , Leung I.K.H. , Lavrik O.I. A Novel Class of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Contains the Octahydro-2H-chromen-4-ol Scaffold Molecules. 2018. V.23. N10. 2468 . DOI: 10.3390/molecules23102468 WOS Scopus РИНЦ

Внешние ссылки

Scopus ID: 56563153400

ORCID: 0000-0003-3555-2481

ResearcherID: JUF-3385-2023