Zobrazeno 1 - 10
of 29
pro vyhledávání: '"V. I. Musatov"'
Publikováno v:
Российский технологический журнал, Vol 10, Iss 3, Pp 85-92 (2022)
Objectives. The development of composite structures in which a strongly anisotropic magnetoelectric (ME) effect is observed is relevant for the creation of sensors that are sensitive to the direction of the magnetic field. Such an ME effect can arise
Externí odkaz:
https://doaj.org/article/9751cc7726e34bd286d75b642fcdfc13
Autor:
N. I. Zemlyana, V. V. Lipson, V. I. Musatov, O. V. Mazepa, T. L. Pavlovska, T. M. Karnozhitska
Publikováno v:
Journal of Organic and Pharmaceutical Chemistry. 16:3-10
Aim. To determine the direction of the interaction of isatins with 5-amino-pyrazoles and 2,2-dimethyl-1,3-dioxane-4,6-dione under different conditions.Results and discussion. The domino-reactions of isatins, 5-aminopyrazoles and 2,2-dimethyl-1,3-diox
Publikováno v:
Journal of Physics: Conference Series. 1515:022091
The article proposes a developed expert information system for assessing environmental risks for complexly structured and uncertain source data. The result of using the program is the desubjectivization of the decision-making process in the presence
Publikováno v:
Journal of Physics: Conference Series. 1399:055004
The article discusses methods of factor analysis to identify heterogeneity in the conditions of spatial distribution and flow formation in aquatic ecosystems. Various factor analysis algorithms were studied to take into account the conjugate action o
Autor:
V. V. Borodina, D. S. Sofronov, N. I. Zemlyanaya, M. G. Shirobokova, Svetlana V. Shishkina, Victoria V. Lipson, V. I. Musatov
Publikováno v:
Russian Journal of Organic Chemistry. 51:697-704
Domino reactions of 3-methylpyrazol-5-amine with aromatic or heterocyclic aldehydes, cyclopentanone, cyclopentane-1,3-dione or indane-1,3-dione in DMF or in alcoholic medium proceed regioselectively and lead to the formation of partially hydrogenated
Autor:
V. M. Bondarenko, V. I. Musatov, V. V. Borodina, O. O. Shishkina, N. V. Svitlichna, F. G. Yaremenko, Victoria V. Lipson
Publikováno v:
Journal of Organic and Pharmaceutical Chemistry. 12:74-80
Reactions of 3-(5-amino-1H-1,2,4-triazol-1-yl)- and 3-(2-amіno-1H-benzo[d]іmіdazol-1-yl)-3-phenylpropanehydrazides with carbonyl electrophiles such as acetylacetone, aromatic and heterocyclic aldehydes in the alcoholic medium complete by formation
Autor:
M. G. Shirobokova, Victoria V. Lipson, V. I. Musatov, L. L. Zamigailo, Svetlana V. Shishkina, O. N. Petrova, Oleg V. Shishkin
Publikováno v:
Chemistry of Heterocyclic Compounds. 49:955-967
Partly hydrogenated 4-aroyl-substituted pyrazolo[3,4-b]quinolin-5-ones and 5-aroyl-substituted pyrazolo[1,5-a]quinazolin-6-ones were obtained by three-component cyclocondensation of substituted 3(5)-aminopyrazoles with the arylglyoxal hydrates and di
Autor:
T. L. Pavlovskaya, F. G. Yaremenko, Victoria V. Lipson, V. I. Musatov, Oleg V. Shishkin, R. G. Red’kin, Svetlana V. Shishkina
Publikováno v:
Chemistry of Heterocyclic Compounds. 49:882-896
A series of new 3a',6a'-dihydro-2'H-spiro[indole-3,1'-pyrrolo[3,4-c]pyrrole]-2,4',6'(1H,3'H,5'H)- triones has been synthesized by cycloaddition of azomethine ylides, obtained from isatins and acyclic aliphatic and sulfur-containing α-amino acids, to
Autor:
M. G. Shirobokov, N. V. Svetlichnaya, V. I. Musatov, Svetlana V. Shishkina, Victoria V. Lipson, Oleg V. Shishkin
Publikováno v:
Russian Journal of Organic Chemistry. 48:273-277
The three-component condensation of 1,2-diamino-4-phenylimidazole with aromatic aldehydes and 1,3-cyclohexanediones occurred regioselectively and afforded 3-amino-1-phenyl-10-aryl-7,8-dihydroimidazo[1,5-b] cinnolin-9(5H,6H,10H)-ones.
Autor:
Svetlana V. Shishkina, M. G. Shirobokova, N. V. Svetlichnaya, V. V. Borodina, Oleg V. Shishkin, Victoria V. Lipson, V. I. Musatov
Publikováno v:
Russian Journal of Organic Chemistry. 46:1388-1398
Three-component condensation of 5(3)-amino-3(5)-methylpyrazole with aromatic aldehydes and 1,3-cyclohexanedione afforded mixtures of 3-methyl-4-aryl-2,4,6,7,8,9-hexa hydro-5H-pyrazolo[3,4-b]quinolin-5-ones and 2-methyl-9-aryl-5,6,7,9-tetrahydro pyraz