Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Marina A. Ezhikova"'
Autor:
Dmitry A. Gruzdev, Angelina A. Telegina, Marina A. Ezhikova, Mikhail I. Kodess, Galina L. Levit, Victor P. Krasnov
Publikováno v:
Molecules, Vol 29, Iss 18, p 4487 (2024)
Amino acids with unusual types of chirality and their derivatives have recently attracted attention as precursors in the synthesis of chiral catalysts and peptide analogues with unique properties. In this study, we have synthesized a new nido-carbora
Externí odkaz:
https://doaj.org/article/f1325d6bf3e549e59e173d8b10eba918
Autor:
Victor P. Krasnov, Irina A. Nizova, Alexey Yu. Vigorov, Tatyana V. Matveeva, Galina L. Levit, Mikhail I. Kodess, Marina A. Ezhikova, Pavel A. Slepukhin, Dmitry A. Bakulin, Ivan N. Tyurenkov, Valery N. Charushin
Publikováno v:
Molecules, Vol 28, Iss 21, p 7401 (2023)
Venous thromboembolism is a serious problem because it significantly increases the risk of developing vascular complications in elderly patients with obesity or immobilization, cancer, and many other diseases. Thus, there is a need to study new thera
Externí odkaz:
https://doaj.org/article/680523d3d06f47de83a8fc5755985268
Autor:
Marina V. Goryaeva, Olesya A. Fefelova, Yanina V. Burgart, Marina A. Ezhikova, Mikhail I. Kodess, Pavel A. Slepukhin, Vasily S. Gaviko, Victor I. Saloutin
Publikováno v:
Molecules, Vol 28, Iss 4, p 1983 (2023)
A new route to bicyclic γ-lactams was found, which was proposed as a three-component cyclization of ethyl trifluoropyruvate with methyl ketones and 1,2-, 1,3-amino alcohols. As a result, a series of trifluoromethyl-substituted tetrahydropyrrolo [2,1
Externí odkaz:
https://doaj.org/article/a0ae63583b9d49d69e41d372c492694f
Autor:
Valeriy O. Filimonov, Pavel S. Silaichev, Mikhail I. Kodess, Marina A. Ezhikova, and Andrey N. Maslivets
Publikováno v:
ARKIVOC, Vol 2015, Iss 5, Pp 259-265 (2015)
Externí odkaz:
https://doaj.org/article/26635471cf07409398a7658294d9f221
Autor:
Marina V. Goryaeva, Yanina V. Burgart, Marina A. Ezhikova, Mikhail I. Kodess, Viktor I. Saloutin
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 385-391 (2015)
The interaction of 2-ethoxymethylidene-3-oxo esters and their analogues with 5-aminotetrazole is an efficient synthetic approach to novel azaheterocycles. 2-Ethoxymethylidene-3-oxo esters bearing alkyl substituents react with 5-aminotetrazole to form
Externí odkaz:
https://doaj.org/article/f5d15db81f8f45ba87aefe4b11de779e
Autor:
Egor V. Verbitskiy, Maria S. Toporova, Mikhail I. Kodess, Marina A. Ezhikova, Maksim L. Isenov, Marina G. Pervova, Marionella A. Kravchenko, Igor D. Medvinskiy, Sergey N. Skornyakov, Gennady L. Rusinov, Valery N. Charushin
Publikováno v:
ARKIVOC, Vol 2014, Iss 5, Pp 247-270 (2014)
Externí odkaz:
https://doaj.org/article/980246937e714c5792756976aea83109
Autor:
Marina V. Goryaeva, Olesya А. Fefelova, Yanina V. Burgart, Marina А. Ezhikova, Mikhail I. Kodess, Pavel А. Slepukhin, Galina А. Triandafilova, Sergey Yu. Solodnikov, Olga P. Krasnykh, Victor I. Saloutin
Publikováno v:
Chemistry of Heterocyclic Compounds. 58:421-431
Autor:
Dmitry A. Gruzdev, Sergey A. Vakarov, Marina A. Korolyova, Ekaterina V. Bartashevich, Andrey A. Tumashov, Evgeny N. Chulakov, Marina A. Ezhikova, Mikhail I. Kodess, Galina L. Levit, Victor P. Krasnov
Publikováno v:
Organic & Biomolecular Chemistry. 20:862-869
(R)-2-Phenoxypropanoate ester was efficient chiral resolving agent in acylative KR of racemic cyclic alkylamines; highest selectivity was observed for 2-methylpiperidine with predominant formation of (R,R)-amide, which was confirmed by DFT modelling.
Autor:
M. I. Kodess, Marina G. Pervova, A. Ya. Zapevalov, Alexander V. Pestov, Marina A. Ezhikova, A. M. Semenova
Publikováno v:
Russian Chemical Bulletin. 70:933-936
Reactions of transesterification of dimethyl, diethyl and dibutyl carbonates with 2,2,3,3-tetrafluoroethyl-, 2,2,3,3,4,4,5,5-octafluorobutyl- and 2,2,3,3,4,4,5,5,6,6,7,7-dodecafluorohexyl-carbinols were investigated in the presence of various catalys
Autor:
Ekaterina O. Sinegubova, Valery N. Charushin, Vera V. Musiyak, Dmitry А. Gruzdev, Marina А. Ezhikova, Sergey А. Vakarov, Galina L. Levit, Vladimir V. Zarubaev, Victor P. Krasnov, Evgeny N. Chulakov, Alexandrina S. Volobueva, Olga А. Vozdvizhenskaya, Mikhail I. Kodess
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:498-504
A number of novel amides were synthesized by coupling of 6-[(9H-purin-6-yl)amino]hexanoic acid to heterocyclic amines. The antiviral activity of the obtained compounds, as well as of purine conjugates in which 7,8-difluoro-3-methyl-3,4-dihydro-2H-1,4