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STRUCTURE AND CONFORMATIONAL ANALYSIS OF 5,5-BIS(BROMOMETHYL)-2-PHENYL-1,3-DIOXANE
Khazhiev, S.Y., Khusainov, M.A., Khalikov, R.A., Tyumkina, T.V., Meshcheryakova, E.S., Khalilov, L.M., Kuznetsov, V.V. (2018)
, 13С NMR spectroscopy and X-ray analysis. The molecule exists in the chair conformation
ГИДРОЛИЗ ИНУЛИНА В ПРИСУТСТВИИ ЙОДА
INULIN HYDROLYSIS IN THE PRESENCE OF IODINE
МУЛЛАГИЛЬДИНА, К.И., ИВАНОВ, С.П., КОНКИНА, И.Г., ЛОБОВ, А.Н., ДАУТОВА, Л.А., КОЗЛОВ, В.Н., МАКСЮТОВ, Р.Р., МУРИНОВ, Ю.И., ФАЙЗРАХМАНОВ, И.С., Mullagildina, K.I., Ivanov, S.P., Konkina, I.G., Lobov, A.N., Dautova, L.A., Kozlov, V.N., Maxytov, R.R., Murinov, Yu. I., Fayzrakhmanov, I.S. (2019)
NMR SPECTROSCOPY
Structure and Conformational Analysis of 5,5-Bis(bromomethyl)-2-[4-(dimethylamino)phenyl]-1,3-dioxane
Khazhiev, SY, Khusainov, MA, Khalikov, RA, Kataev, VA, Tyumkina, TV, Meshcheryakova, ES, Khalilov, LM, Kuznetsov, VV (2021)
for fine organic synthesis and a potential bactericidal compound, was investigated by H-1 and C-13 NMR
INVESTIGATION OF THE SOLUTION PHASE CHEMILUMINESCENCE OF 1,2,4-TRIAZOLE DERIVATIVES
Kayumova, R.R., Muslukhov, R.R., Abdullin, M.F., Klen, E.E., Khaliullin, F.A., Magadeeva, G.F., Mamykin, A.V., Khursan, S.L. (2014)
of the reaction products. The possible reaction products were determined by NMR spectroscopy, mass spectrometry
РАЗРАБОТКА МЕТОДОВ ОПРЕДЕЛЕНИЯ ПОДЛИННОСТИ 2-[1-ИЗОБУТИЛ-3-МЕТИЛ-7-(1,1-ДИОКСОТИЕТАНИЛ-3) КСАНТИНИЛ-8-ТИО]УКСУСНОЙ КИСЛОТЫ
DEVELOPMENT OF METHODS FOR DETERMINING THE AUTHENTICITY OF 2-[1-ISOBUTYL-3-METHYL-7-(1,1-DIOXOTHIETANYL-3) XANTHINYL-8-THIO]ACETIC ACID
Маматов, Ж.К., Mamatov, Zh.K. (2020)
infrared spectroscopy
STRUCTURE AND CONFORMATIONAL ANALYSIS OF 5,5-BIS(BROMOMETHYL)-2,2-DIPHENYL-1,3-DIOXANE
KHAZHIEV, S.Y., KHUSAINOV, M.A., KUZNETSOV, V.V., KHALIKOV, R.A., KATAEV, V.A., TYUMKINA, T.V., MESHCHERYAKOVA, E.S., KHALILOV, L.M. (2020)
The structure of 5,5-bis(bromomethyl)-2,2-diphenyl-1,3-dioxane was studied by 1H and 13C NMR
Synthesis and Antiaggregant Activity of 2-[3-Methyl-1-Ethylxanthinyl-8-Thio]Acetic Acid Salts Containing a Thietane Ring
Khaliullin, F.A., Shabalina, Y.V., Samorodov, A.V., Kamilov, F.K., Timirkhanova, G.A., Murataev, D.Z. (2018)
thietane ring, with yields of 44 - 96%. The structures of these compounds were confirmed by IR and NMR
SYNTHESIS OF PYRINIDINE-2,4(1Н,3Н)-DIONE DERIVATIVES CONTAINING N-ALKYL SUBSTITUENTS
Raskildinaa, G.Z., Valieva, V.F., Ozdena, I.V., Meshcheryakova, S.A., Spirikhin, L.V., Zlotskiia, S.S. (2017)
disubstituted uracils. The structure of the synthesized compounds was studied by H1 and 13С NMR spectroscopy
Synthesis and diverse biological activity profile of triethyl-ammonium isatin-3-hydrazones
Bogdanov, A, Tsivileva, O, Voloshina, A, Lyubina, A, Amerhanova, S, Burtceva, E, Bukharov, S, Samorodov, A, Pavlov, V (2022)
in the aromatic fragment have been synthesized. Their structure and composition were confirmed by NMR-and IR-spectroscopies
СИНТЕЗ ПРОИЗВОДНЫХ ПИРИМИДИН-2,4(Ш,3Щ-ДИОНОВ, СОДЕРЖАЩИХ N-АЛКИЛЬНЫЕ ЗАМЕСТИТЕЛИ
Synthesis of pyrinidine-2,4(1H,3H)-dione derivatives containing N-alkyl substituents
RASKILDINA, G.Z., VALIEV, V.F., OZDEN, I.V., ZLOTSKII, S.S., MESHCHERYAKOVA, S.A., SPIRIKHIN, L.V., Раскильдина Г.З.,, Валиев В.Ф.,, Озден И.В.,, Мещерякова С.А.,, Спирихин Л.В.,, Злотский С.С. (2017)
disubstituted uracils. The structure of the synthesized compounds was studied by H1 and 13С NMR spectroscopy

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