Zobrazeno 1 - 10
of 125
pro vyhledávání: '"Yu. G. Shermolovich"'
Autor:
V. G. Lendel, Yu. G. Shermolovich, Sergiy S. Mykhaylychenko, М. V. Povidaichyk, M. Yu. Onysko
Publikováno v:
Scientific Bulletin of the Uzhhorod University. Series «Chemistry». 2:58-61
Carboxylic acid amides are convenient reagents for organic synthesis, and are promising building blocks for obtaining a large number of acyclic and heterocyclic compounds. Among the various aliphatic, aromatic and heterocyclic amides, fluorine-contai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1eb8325fa4fbd6db12ab670ba987b7b
https://doi.org/10.24144/2414-0260.2020.2.58-61
https://doi.org/10.24144/2414-0260.2020.2.58-61
Publikováno v:
2020 IEEE 10th International Conference Nanomaterials: Applications & Properties (NAP).
Two types of core - shell structure polymer-inorganic nanoparticles for effective $Li^{+}-$intercalation current generation were synthesized. MoS 2 was nanoscale core coated with functional polymer via polymerization initiated from the particles surf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee84013bd88b27a29efc3e5282eece2d
https://doi.org/10.1109/nap51477.2020.9309574
https://doi.org/10.1109/nap51477.2020.9309574
Autor:
N. I. Kinash, O.V. Reshetnyak, Alexander Zaichenko, K. A. Volianiuk, N. Musat, O.S. Myagkota, Yu. G. Shermolovich, G.Z. Stryganyuk, N. Ye. Mitina, O. L. Paiuk, Orest Hevus
Aim. Purposeful preparation of polymeric surfactants combining hydrophobic fluorine-containing and hydrophilic synthetic and natural blocks via radical and non-radical reactions using peroxide, epoxide and/or amino- terminal groups of the polymeric e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::228d535b3d1ca64cebd40bf407b67be7
http://dspace.nbuv.gov.ua/handle/123456789/154341
http://dspace.nbuv.gov.ua/handle/123456789/154341
Publikováno v:
Russian Journal of Organic Chemistry. 49:1572-1579
Structure of reaction products obtained from tris(diethylamino)phosphine with N,Ndialkylpolyfluoroalkanethioamides depends on the length of the polyfluoroalkyl substituent in the latter. In the case of morpholides of perfluorothiopropionic and perflu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c365174265a01b8d390a143cf9595be
https://doi.org/10.1134/s1070428013110031
https://doi.org/10.1134/s1070428013110031
Publikováno v:
Chemistry of Heterocyclic Compounds. 49:591-597
Chlorination of 4-(perfluoroalkyl)-5-(p-toluenesulfonyl)-2,6-bis(trimethylsilyloxy)pyrimidines led to the formation of 5-chloro-6-(perfluoroalkyl)-5-(p-toluenesulfonyl)pyrimidine-2,4(3H,5H)-diones, the structure of which was confirmed by NMR spectros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89ed4aab3a625b7257d4b1e2099545cb
https://doi.org/10.1007/s10593-013-1286-1
https://doi.org/10.1007/s10593-013-1286-1
Publikováno v:
ResearcherID
Methods are proposed for the preparation of fluorophosphorus-containing pyrimidines through three- component reactions of dialkyl (3,3,3-trifluoro-2-oxopropyl)phosphonates. Cyclocondensation of these phosphonates with urea and aryl aldehydes gave 6-a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7efb3cde4030abe3e5c41ed3d4c5e950
https://doi.org/10.1007/s10593-011-0863-4
https://doi.org/10.1007/s10593-011-0863-4
Autor:
S. A. But, Oleksandr S. Kanishchev, Yu. P. Bandera, A. M. Nesterenko, Vadim M. Timoshenko, Yu. G. Shermolovich
Publikováno v:
Chemistry of Heterocyclic Compounds. 43:1138-1147
Treatment of 4-aryl(benzyl)sulfonyl-5-polyfluoroalkyl-v-triazoles with NaOCl gave the 4-aryl(benzyl)-sulfonyl-2-chloro-5-polyfluoroalkyl-v-triazole derivatives which contain a chlorine atom only on the N(2) atom of the heterocycle. The structure of 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc982676cc78ca6d4d608288c5c53d26
https://doi.org/10.1007/s10593-007-0175-x
https://doi.org/10.1007/s10593-007-0175-x
Autor:
Oleksandr S. Kanishchev, Eduard B. Rusanov, Vadim M. Timoshenko, Yu. G. Shermolovich, S. A. But, Yu. P. Bandera
Publikováno v:
Chemistry of Heterocyclic Compounds. 43:887-892
1-Dimethylamino-2-(p-tolylsulfonyl)polyfluoro-1-alken-3-ones were obtained from hydrates of 3,3,3-trifluoro-1-(p-tolylsulfonyl)-2-propanone and 3,3,4,4,5,5-hexafluoro-1-(p-tolylsulfonyl)-2-pentanone under conditions of the Vilsmeier-Haack-Arnold reac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::001a40187530c66fa607e5d2f6a684c1
https://doi.org/10.1007/s10593-007-0140-8
https://doi.org/10.1007/s10593-007-0140-8
Publikováno v:
Russian Journal of Organic Chemistry. 42:261-265
Reactions of 4-fluoro-5-polyfluoroalkyl-1,2-dithiol-3-thiones with hydroxylamine and hydrazines occur with replacement of the thiocarbonyl by imino group affording oximes and hydrazones respectively. N-Alkyl-and N-aryl-3-imino-1,2-dithiolenes formed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31be04f31798cea7c52c3da9da4cfef9
https://doi.org/10.1134/s1070428002120187
https://doi.org/10.1134/s1070428002120187
Publikováno v:
Russian Journal of Organic Chemistry. 42:124-130
Chlorination of 4-fluoro-5-(1,1,2,2-tetrafluoroethyl)-1,2-dithiole-3-thione with an equimolar amount of chlorine or sulfuryl chloride gives 3-chlorosulfanyl-4-fluoro-5-(1,1,2,2-tetrafluoroethyl)-1,2-dithiolium chloride. The reaction of the title comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37081cd1f3bfa09a91ebff6bb83876e1
https://doi.org/10.1134/s1070428006010192
https://doi.org/10.1134/s1070428006010192