Zobrazeno 1 - 10
of 129
pro vyhledávání: '"Yuri V, Gatilov"'
Autor:
Nikolai S. Li-Zhulanov, Artem D. Rogachev, Yuri V. Gatilov, Konstantin P. Volcho, Nariman F. Salakhutdinov
Publikováno v:
Molbank, Vol 2024, Iss 1, p M1780 (2024)
The reaction of (−)-nopol mesylate with piperazine in acetonitrile under reflux, afforded symmetric 1,4-bis(2-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethyl)piperazine in a good yield. The compound was fully characterized and its structure
Externí odkaz:
https://doaj.org/article/cf5e49e7de0341da9716ea28d2a53644
Autor:
Irina V. Ilyina, Nikolai S. Li-Zhulanov, Yuri V. Gatilov, Konstantin P. Volcho, Alexander Yu. Sidorenko, Vladimir E. Agabekov, Nariman F. Salakhutdinov
Publikováno v:
Molbank, Vol 2023, Iss 4, p M1734 (2023)
The development of highly efficient methods for the synthesis of chemical products by using renewable raw materials is one of the topical areas of medicinal chemistry. The paper presents the synthesis of (2aR,2a1S,5aR,9bR)-4-isopropyl-7,8-dimethoxy-2
Externí odkaz:
https://doaj.org/article/b8bb8144a711483d9c48e071fe747f13
Publikováno v:
Molecules, Vol 29, Iss 3, p 599 (2024)
The pyrrolidine nitroxides with four bulky alkyl substituents adjacent to the N–O∙ group demonstrate very high resistance to reduction with biogenic antioxidants and enzymatic systems. This makes them valuable molecular tools for studying the str
Externí odkaz:
https://doaj.org/article/8d1d6076335a4f739d5d798f9147e472
Autor:
Vera S. Glukhacheva, Sergey G. Il’yasov, Igor V. Kazantsev, Elena O. Shestakova, Dmitri S. Il’yasov, Ilia V. Eltsov, Andrey A. Nefedov, Yuri V. Gatilov
Publikováno v:
ACS Omega, Vol 6, Iss 12, Pp 8637-8645 (2021)
Externí odkaz:
https://doaj.org/article/25836e6fc2264d15b6445724c2f31f56
Autor:
Elena O. Shestakova, Sergey G. Il’yasov, Irina A. Shchurova, Vera S. Glukhacheva, Dmitri S. Il’yasov, Egor E. Zhukov, Arkady O. Bryzgalov, Tatiana G. Tolstikova, Yuri V. Gatilov
Publikováno v:
Pharmaceuticals, Vol 15, Iss 12, p 1443 (2022)
Here, we investigated the reaction of 1,3-dipolar cycloaddition of 1,3-diazido-2-nitro-2- azapropane (DANP) to propargyl alcohol over a copper-based catalyst and identified the optimum reaction conditions that enable the synthesis of 2-nitro-1,3-bis(
Externí odkaz:
https://doaj.org/article/31882c93d32f44fa9832dcfe78f45026
Autor:
Sergey A. Dobrynin, Mark M. Gulman, Denis A. Morozov, Irina F. Zhurko, Andrey I. Taratayko, Yulia S. Sotnikova, Yurii I. Glazachev, Yuri V. Gatilov, Igor A. Kirilyuk
Publikováno v:
Molecules, Vol 27, Iss 21, p 7626 (2022)
Sterically shielded nitroxides, which demonstrate high resistance to bioreduction, are the spin labels of choice for structural studies inside living cells using pulsed EPR and functional MRI and EPRI in vivo. To prepare new sterically shielded nitro
Externí odkaz:
https://doaj.org/article/6e297bd7718949f79b7020649bc3617d
Autor:
Sergey A. Dobrynin, Igor A. Kirilyuk, Yuri V. Gatilov, Andrey A. Kuzhelev, Olesya A. Krumkacheva, Matvey V. Fedin, Michael K. Bowman, Elena G. Bagryanskaya
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2664-2670 (2019)
The unexpected formation of a highly strained polycyclic amine was observed in a one-pot synthesis from cyclopentanone, dimethyl fumarate and ammonium acetate. This multistep reaction includes 1,3-dipolar cycloaddition of dimethyl fumarate to the cyc
Externí odkaz:
https://doaj.org/article/0a3614a2426f4826a3a078eefb4143ca
Autor:
Vladislav V. Oreshko, Kseniya S. Kovaleva, Ekaterina D. Mordvinova, Olga I. Yarovaya, Yuri V. Gatilov, Dmitry N. Shcherbakov, Nikolai I. Bormotov, Olga A. Serova, Larisa N. Shishkina, Nariman F. Salakhutdinov
Publikováno v:
Molecules, Vol 27, Iss 15, p 4761 (2022)
A set of heterocyclic products was synthesized from natural (+)-camphor and semi-synthetic (−)-camphor. Then, 2-Imino-4-thiazolidinones and 2,3-dihydrothiazoles were obtained using a three-step procedure. For the synthesized compounds, their antivi
Externí odkaz:
https://doaj.org/article/c19c14fd51ec4a09af2df0d8c632568b
Autor:
Aleksandrina S. Volobueva, Olga I. Yarovaya, Marina V. Kireeva, Sophia S. Borisevich, Kseniya S. Kovaleva, Iliya Ya. Mainagashev, Yuri V. Gatilov, Margarita G. Ilyina, Vladimir V. Zarubaev, Nariman F. Salakhutdinov
Publikováno v:
Molecules, Vol 26, Iss 22, p 6794 (2021)
A number of framework amides with a ginsenol backbone have been synthesized using the Ritter reaction. We named the acetamide as Ginsamide. A method was developed for the synthesis of the corresponding amine and thioacetamide. The new compounds revea
Externí odkaz:
https://doaj.org/article/213d0b8301074d2988865ebc91dd9b70
Autor:
Sergey A. Dobrynin, Mikhail S. Usatov, Irina F. Zhurko, Denis A. Morozov, Yuliya F. Polienko, Yurii I. Glazachev, Dmitriy A. Parkhomenko, Mikhail A. Tyumentsev, Yuri V. Gatilov, Elena I. Chernyak, Elena G. Bagryanskaya, Igor A. Kirilyuk
Publikováno v:
Molecules, Vol 26, Iss 19, p 5761 (2021)
Stable free radicals are widely used as molecular probes and labels in various biophysical and biomedical research applications of magnetic resonance spectroscopy and imaging. Among these radicals, sterically shielded nitroxides of pyrrolidine series
Externí odkaz:
https://doaj.org/article/542f3f898ab04e9abcb6c47cd9269ec4