Zobrazeno 1 - 10
of 41
pro vyhledávání: '"K. Yu. Suponitsky"'
Autor:
E. S. Makarova, M. V. Kabanova, S. I. Filimonov, Zh. V. Chirkova, A. A. Shetnev, K. Yu. Suponitsky
Publikováno v:
Russian Chemical Bulletin. 71:2255-2262
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afe0f75881a980772482df7078267763
https://doi.org/10.1007/s11172-022-3653-5
https://doi.org/10.1007/s11172-022-3653-5
Autor:
T. E. Khoranyan, O. V. Serushkina, I. A. Vatsadze, K. Yu. Suponitsky, K. A. Monogarov, T. K. Shkineva, I. L. Dalinger
Publikováno v:
Russian Chemical Bulletin. 71:1750-1759
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9532d607061ec3cfffc8bd0a8f3fc6a6
https://doi.org/10.1007/s11172-022-3586-z
https://doi.org/10.1007/s11172-022-3586-z
Autor:
R. P. Sukiasyan, R. A. Apreyan, A. A. Danghyan, L. S. Bezhanova, K. Yu. Suponitsky, A. K. Atanesyan
Publikováno v:
Armenian Journal of Physics. :46-52
The reaction of L–arginine with hydrochloric acid (HCl) in water solvent at 0–33°C temperature was investigated in detail in this study. In total, five compounds were successfully obtained and identified, of which L–Arg·HCl (P1), L–Arg·HCl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::162a0760f30d47d7f228250ce57e29ff
https://doi.org/10.54503/18291171-2022.15.2-3-46
https://doi.org/10.54503/18291171-2022.15.2-3-46
Publikováno v:
Russian Chemical Bulletin. 71:1034-1042
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54d4261891631056bbbcb88d2dc1d52e
https://doi.org/10.1007/s11172-022-3505-3
https://doi.org/10.1007/s11172-022-3505-3
Publikováno v:
Russian Chemical Bulletin. 71:399-403
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::944ed3de3ed1b0c28442981c2e1f1ca3
https://doi.org/10.1007/s11172-022-3425-2
https://doi.org/10.1007/s11172-022-3425-2
Autor:
K. Yu. Suponitsky, Anatolii S. Morkovnik, Lyudmila N. Divaeva, Aleksei A. Anisimov, V. G. Kartsev, Alexander A. Zubenko
Publikováno v:
Russian Journal of Organic Chemistry. 55:74-82
Structural modification of 3,4-dihydro-nor-isoharmine through expansion of the dihydropyridine ring to dihydroazepine was accomplished in two stages including pyridine-azepine recyclization of the quaternized substrate by the action of phenacyl halid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95625aac76935758b26f534c7a8a662a
https://doi.org/10.1134/s1070428019010081
https://doi.org/10.1134/s1070428019010081
Autor:
I. Yu. Chukicheva, T. A. Kolegova, K. Yu. Suponitsky, Oksana G. Shevchenko, A. V. Kutchin, O. V. Shchukina
Publikováno v:
Russian Journal of General Chemistry. 88:664-675
New isobornylphenol derivatives have been produced by introducing allyl, hydroxypropyl, and chloropropyl groups into the para-position of 2,6-diisobornylphenol and 2-isobornyl-6-(1-phenylethyl)phenol. The radical scavenging and antioxidant activity a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6278eda8c0c5b8451a4bba436ec3594
https://doi.org/10.1134/s1070363218040096
https://doi.org/10.1134/s1070363218040096
Autor:
A. N. Chernyi, Valery P. Sinditskii, Tatyana K. Shkineva, Nadezhda V. Palysaeva, Igor L. Dalinger, V. Yu. Egorshev, S.P. Smirnov, K. Yu. Suponitsky
Publikováno v:
Thermochimica Acta. 651:83-99
Physico-chemical characterization of high energetic nitropyrazoles has been conducted, including studies on the thermal decomposition under non-isothermal and isothermal conditions, burning behavior, and flame structure. The thermal stability of dini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16ee043d1d59b12812b5b0a94fba4d8e
https://doi.org/10.1016/j.tca.2017.02.019
https://doi.org/10.1016/j.tca.2017.02.019
Autor:
Evgeny V. Buravlev, K. Yu. Suponitsky, Oksana G. Shevchenko, A. V. Kutchin, I. Yu. Chukicheva
Publikováno v:
Russian Chemical Bulletin. 65:1232-1237
Bromination of 2,6-diisobornyl-4-methylphenol gave the corresponding 4-bromomethyl derivative, whose reaction with alcohols resulted in 4-alkoxymethyl-2,6-diisobornylphenols. Their toxicity, membrane protective and antioxidant activity were tested us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16de15ce0fcd1834df8dd15d7c680e64
https://doi.org/10.1007/s11172-016-1440-x
https://doi.org/10.1007/s11172-016-1440-x
Publikováno v:
Russian Chemical Bulletin. 65:811-815
The crystal and molecular structure of the reaction product of imidazolidine-2-thione and molecular iodine of the composition (C3H6N2S)2•3I2 was established by X-ray diffraction. The crystal structure is composed of strongly connected five-componen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68f09eec500f2b14c0dcf8f93f074354
https://doi.org/10.1007/s11172-016-1379-y
https://doi.org/10.1007/s11172-016-1379-y