Zobrazeno 1 - 10
of 14
pro vyhledávání: '"S. V. Chashchina"'
Publikováno v:
Разработка и регистрация лекарственных средств, Vol 12, Iss 4, Pp 146-150 (2023)
Introduction. The use of anticoagulants is relevant in therapeutic, cardiological, neurological practice, geriatrics, obstetrics and gynecology, as well as in complications associated with COVID-19 infection and vaccination. In-depth studies of addit
Externí odkaz:
https://doaj.org/article/69b99fc62d654449ba57b08a0c9acea7
Publikováno v:
Pharmaceutical Chemistry Journal. 56:1188-1191
Publikováno v:
Pharmaceutical Chemistry Journal.
Publikováno v:
Pharmaceutical Chemistry Journal. 56:321-324
Publikováno v:
Russian Chemical Bulletin. 71:496-501
Autor:
A. I. Siutkina, S. V. Chashchina, R. R. Makhmudov, I. A. Kizimova, S. A. Shipilovskikh, N. M. Igidov
Publikováno v:
Russian Journal of Organic Chemistry. 57:1874-1881
Autor:
N. M. Igidov, S. V. Chashchina, M. A. Kiselev, A. I. Siutkina, I. A. Kizimova, Maksim V. Dmitriev
Publikováno v:
Russian Journal of General Chemistry. 90:182-186
Recyclization of furan-2,3-diones acylhydrazones under the action of esters, amides and nitriles of cyanoacetic acids gave the corresponding esters, amides and nitriles of 2-amino-1-R-4-oxo-5- (2-oxo-2-aryl/tert-butylethylidene)-4,5-dihydro-1H-pyrrol
Publikováno v:
Pharmaceutical Chemistry Journal. 53:1005-1008
Ritter cyclocondensation of 2-(1-naphthyl)-1,1-(R1)2-ethanols [R1 = Me, 2R1 = (CH2)4] with nitriles of general formula R2CN (acetonitrile, benzonitriles, benzyl cyanide, cyanoacetamides) and subsequent treatment of the obtained bases with HCl synthes
Autor:
A. I. Siutkina, S. V. Chashchina, N. M. Igidov, R. R. Makhmudov, I. A. Kizimova, Maksim V. Dmitriev
Publikováno v:
Russian Journal of General Chemistry. 89:2345-2352
Decyclization of N′-[5-R-2-oxofuran-3(2H)-ylidene]-2-(phenylamino)benzohydrazides under the action of heterocyclic amines leads to the formation of N-hetaryl-4-R-4-oxo-2-[2-(phenylamino)benzoyl]hydrazinylidenebutanamides. Antinociceptive and anti-i
Publikováno v:
Pharmaceutical Chemistry Journal. 53:701-705
A series of 1-(2-aminopropyl)-5-aryl-4-acyl-3-hydroxy-3-pyrrolin-2-ones were synthesized by three-component reactions of 4-substituted 2,4-dioxobutanoic acid methyl esters with mixtures of an aromatic aldehyde and 1,2-diaminopropane. Products of thei