Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Olga V. Bykhovskaya"'
Autor:
Anna G. Matveeva, Olga V. Bykhovskaya, Margarita P. Pasechnik, Anna V. Vologzhanina, Rinat R. Aysin, Sergey V. Matveev, Ivan A. Godovikov, Igor Yu. Kudryavtsev, Tatyana V. Baulina, Valery K. Brel
Publikováno v:
Mendeleev Communications. 32:588-590
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ab3e699575a9ced8854ec79ba84ab8f
https://doi.org/10.1016/j.mencom.2022.09.006
https://doi.org/10.1016/j.mencom.2022.09.006
Autor:
Lada V. Anikina, V. A. Kochmarik, Valery K. Brel, Olga V. Bykhovskaya, T. V. Baulina, I. Yu. Kudryavtsev, M. P. Pasechnik, Anna V. Vologzhanina
Publikováno v:
Russian Journal of General Chemistry. 91:2052-2060
Abstract Tris[2-(3′-cyanopropoxy)phenyl]phosphine oxide has been obtained via the alkylation of tris(2hydroxyphenyl)phosphine oxide with 4-bromobutyronitrile in the presence of K2CO3. The product structure has been elucidated by means of X-ray diff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8256dc4f7ddef3978665a866e203941d
https://doi.org/10.1134/s1070363221100194
https://doi.org/10.1134/s1070363221100194
Autor:
Rinat R. Aysin, Alexander N. Turanov, Anna G. Matveeva, Maria I. Godovikova, Vasilii K. Karandashev, I. Yu. Kudryavtsev, Olga V. Bykhovskaya, S. V. Matveev, M. P. Pasechnik, Valery K. Brel, T. V. Baulina
Publikováno v:
Russian Journal of General Chemistry. 90:2338-2349
New tripodal 1,2,3-triazole ligands based on triphenylphosphine oxide platform with different linker lengths have been synthesized, and their structure has been determined by elemental analysis, 1H, 13C, and 31P NMR spectroscopy, mass spectrometry, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11ec3bc65260641a0cda73d56d0ff4bd
https://doi.org/10.1134/s107036322012018x
https://doi.org/10.1134/s107036322012018x
Autor:
Olga V. Bykhovskaya, Igor Yu. Kudryavtsev, Anna V. Vologzhanina, S. V. Matveev, Vasilii K. Karandashev, Valery K. Brel, Anna G. Matveeva, T. V. Baulina, Alexander N. Turanov, M. P. Pasechnik
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 151:1705-1713
New hybrid tripodal propeller ligands on the triphenylphosphine oxide platform with triazole rings in the side arms and alkyl and aryl substituents in the triazole fragments have been synthesized by the click reaction. Composition and structure of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8d97ce0f327e8206c193aae88fb702d
https://doi.org/10.1007/s00706-020-02702-6
https://doi.org/10.1007/s00706-020-02702-6
Autor:
Olga V. Bykhovskaya, M. P. Pasechnik, Anna V. Vologzhanina, Igor Yu. Kudryavtsev, Anna G. Matveeva, T. V. Baulina, Valery K. Brel, S. V. Matveev
Publikováno v:
Russian Journal of General Chemistry. 89:2400-2407
A new tetrazole tripodal ligand, tris[2-(tetrazol-5-ylmethoxy)phenyl]phosphine oxide, has been obtained. Its structure in crystal and solutions has been elucidated by X-ray diffraction analysis as well as IR, Raman, and multinuclear (1H, 13C, 31P) NM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5ef70590eebff18ffca3664c383d196
https://doi.org/10.1134/s1070363219120120
https://doi.org/10.1134/s1070363219120120
Autor:
Yulia V. Nelyubina, Svetlana G. Churusova, Vladimir A. Kozlov, Olga V. Bykhovskaya, Ekaterina Yu. Rybalkina, Alexander S. Peregudov, Diana V. Aleksanyan, Zinaida S. Klemenkova, Oleg I. Artyushin
Publikováno v:
Journal of Organometallic Chemistry. 892:66-74
The reactions of 2-diphenylphosphorylaniline with 2-methylsulfanylbenzoyl chloride or 2-diphenylphosphinobenzoic acid in the presence of a coupling agent afforded new potentially tridentate ligands with different donor sets. Upon interaction with Re(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59f5ac954b3541457e61a90f2d214a2f
https://doi.org/10.1016/j.jorganchem.2019.04.020
https://doi.org/10.1016/j.jorganchem.2019.04.020
Publikováno v:
Russian Journal of General Chemistry. 87:2744-2747
A number of precursors of new tripodal ligands was obtained by hydroxyethylation of the starting tris(2-hydroxyphenyl)phosphine oxide, followed by conversion of the resulting tris[2-(2-hydroxyethoxy) phenyl]phosphine oxide to trimesylate. The treatme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68fae7fcc4912826ce1248f4b709ef9a
https://doi.org/10.1134/s1070363217110366
https://doi.org/10.1134/s1070363217110366
Publikováno v:
Russian Chemical Bulletin. 66:1256-1260
A reaction of N-allyl-substituted aminomethylene-1,1-bisphosphonates with aromatic nitrile N-oxides was used to obtain new aminomethylenebisphosphonates with one or two 3-arylisoxazoline rings at the nitrogen atom. NMR spectroscopy studies showed tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7e95d1e3f62b6c3ea5b124b2346276b
https://doi.org/10.1007/s11172-017-1881-x
https://doi.org/10.1007/s11172-017-1881-x
Publikováno v:
Russian Chemical Bulletin. 66:661-665
The Tsuji—Trost allylation of CH acids, in particular, those of the YCH2CO2Et type (Y = CO2Et, C(O)Me, CN), with allylic acetates in the K2CO3—DMF system in the presence of palladium catalysts with ligands RN(PPh2)2 (R = Ph, Pri, c-C6H11) is acco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b2c6aa5b8417c127b7098046ade5b1c
https://doi.org/10.1007/s11172-017-1788-6
https://doi.org/10.1007/s11172-017-1788-6
Autor:
Valery K. Brel, E. Yu. Rybalkina, I. M. Aladzheva, Mikhail V. Makarov, Zinaida S. Klemenkova, Olga V. Bykhovskaya
Publikováno v:
Russian Chemical Bulletin. 66:104-110
The synthesis of 3,5-bis(arylidene)piperidin-4-ones containing the 2-azidoethyl (azides 1a–d) or propargyl (acetylenes 2a–c) group at the nitrogen atom of the 4-piperidinone ring was described. The in vitro MTT assay for cytotoxicity of these com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9ec2bd39d775b0497f9f8f040c74afc
https://doi.org/10.1007/s11172-017-1707-x
https://doi.org/10.1007/s11172-017-1707-x