Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Irina Yu. Bagryanskay"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract By X-ray diffraction analysis and IR spectroscopy, it was established here that vinyl carbocations C3H5 +/C4H7 + with carborane counterion CHB11Cl11 − form stable monosolvates C3H5 +⋅C3H6/C4H7 +⋅C4H8 with molecules of alkenes C3H6/C4H8
Externí odkaz:
https://doaj.org/article/6e3e0ec4b8614a80a3b9d26e43497428
Publikováno v:
ACS Omega, Vol 6, Iss 37, Pp 23691-23699 (2021)
Externí odkaz:
https://doaj.org/article/90c0644926d84cffa460ce70a1dd946e
Autor:
Oleg V. Ardashov, Dina V. Korchagina, Irina Yu. Bagryanskaya, Konstantin P. Volcho, Nariman F. Salakhutdinov
Publikováno v:
Molbank, Vol 2022, Iss 4, p M1465 (2022)
A simple and convenient procedure for the γ, β-dimerization of verbenone was developed. The dimer was obtained during aging with KOH without a solvent. The process proceeds as the formation of the extended enolate of verbenone and its Michael addit
Externí odkaz:
https://doaj.org/article/2d35f0f9a047457b81f9463e9d1e22d2
Publikováno v:
ACS Omega, Vol 6, Iss 24, Pp 15834-15843 (2021)
Externí odkaz:
https://doaj.org/article/04aea24f619c453695ed30e8d71be19e
Publikováno v:
Molecules, Vol 28, Iss 3, p 1146 (2023)
X-ray diffraction analysis and IR spectroscopy were used to study the products of the interaction of vinyl cations C3H5+ and C4H7+ (Cat+) (as salts of carborane anion CHB11Cl11−) with basic molecules of water, alcohols, and acetone that can crystal
Externí odkaz:
https://doaj.org/article/07ff3840c01a4c708d74600c7f04a429
Autor:
Yan V. Demyanov, Evgeniy H. Sadykov, Marianna I. Rakhmanova, Alexander S. Novikov, Irina Yu. Bagryanskaya, Alexander V. Artem’ev
Publikováno v:
Molecules, Vol 27, Iss 18, p 6059 (2022)
The coordination behavior of tris(2-pyridyl)arsine (Py3As) has been studied for the first time on the example of the reactions with CuI, CuBr and AgClO4. When treated with CuI in CH2Cl2 medium, Py3As unexpectedly affords the scorpionate complex [Cu(P
Externí odkaz:
https://doaj.org/article/308cc2e9d41b462e815581ddee42b7f7
Autor:
Alexey V. Reshetov, Galina A. Selivanova, Larisa V. Politanskaya, Irina V. Beregovaya, Lyudmila N. Shchegoleva, Nadezhda V. Vasil’eva, Irina Yu. Bagryanskaya, and Vitalij D. Shteingarts
Publikováno v:
ARKIVOC, Vol 2011, Iss 8, Pp 242-262 (2011)
Externí odkaz:
https://doaj.org/article/e79a5ef562514ecc89428399be9cd79e
Autor:
Vasily E. Romanov, Irina Yu. Bagryanskaya, Dmitry E. Gorbunov, Nina P. Gritsan, Elena V. Zaytseva, Dominique Luneau, Evgeny V. Tretyakov
Publikováno v:
Crystals, Vol 8, Iss 9, p 334 (2018)
Spin-labelled compounds are widely used in chemistry, physics, biology, and material sciences, but the directed synthesis of some functionalized organic radicals is still a challenge. We succeeded in the preparation of a tetrazolyl-substituted nitron
Externí odkaz:
https://doaj.org/article/18675a2fbfa4461583290df153fa8a89
Publikováno v:
Journal of Fluorine Chemistry. 110:21-24
Reactions between perfluoro-2-methyl-2-pentene and NaN3 in acetonitrile at −20°C provided perfluoro-2-methyl-3-azido-2-pentene stable only to 0°C, which decomposed in CCl4 at 20°C to give 2,2-bis(trifluoromethyl)-3-pentafluoroethylaziridine or i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcdd3126ef50b387208b952184e1a8fb
https://doi.org/10.1016/s0022-1139(01)00395-5
https://doi.org/10.1016/s0022-1139(01)00395-5
Publikováno v:
Journal of Fluorine Chemistry. 104:263-271
Reaction of perfluoro-2-methylpent-2-ene ( 1 ) and perfluoro-5-azanon-4-ene ( 2 ) with aniline, 4-fluoroaniline, 4-methoxyaniline and 2,6-dimethylaniline in the presence of Et 3 N provides derivatives of quinoline and quinozaline, whereas reaction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf2f64d94e96a1f2f9d1d585914dd62e
https://doi.org/10.1016/s0022-1139(00)00247-5
https://doi.org/10.1016/s0022-1139(00)00247-5