Zobrazeno 1 - 10
of 125
pro vyhledávání: '"Vadim V. Bardin"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 703-713 (2017)
Borates M[C6F5BF3] (M = K, Li, Bu4N) react with organolithium compounds, RLi (R = Me, Bu, Ph), in 1,2-dimethoxyethane or diglyme to give M[4-RC6F4BF3] and M[2-RC6F4BF3]. When R is Me or Bu, the nucleophilic substitution of the fluorine atom at the pa
Externí odkaz:
https://doaj.org/article/ed2cbec269db43f6a0e53de2d3ad7202
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 608-616 (2015)
Small differences in the reactivity of weakly nucleophilic potassium aryltrifluoroborates are revealed in the silver-assisted Pd-catalyzed cross-coupling of K[4-RC6F4BF3] (R = H, Bu, MeO, EtO, PrO, iPrO, BuO, t-BuO, CH2=CHCH2O, PhCH2O, PhCH2CH2O, PhO
Externí odkaz:
https://doaj.org/article/f2023903f68e4ba8929edc4cab3892bb
Publikováno v:
Russian Chemical Bulletin. 69:17-31
The results obtained by the authors and literature data on the methods of preparation, properties, and the use of ionic liquids with fluorine-containing anions are reviewed. The dependences of the physicochemical and hydrodynamic properties of the io
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::216535e42c2df03938506133c76fc33b
https://doi.org/10.1007/s11172-020-2719-5
https://doi.org/10.1007/s11172-020-2719-5
Publikováno v:
Russian Journal of General Chemistry. 90:50-61
Fluorine-containing aryldihalogenoboranes have been obtained by the reaction of boron and aluminum chlorides and bromides with potassium aryltrifluoroborates K[ArBF3] under mild conditions. In a similar way, bis(pentafluorophenyl)halogenoboranes have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2fd7a51403efeb383d6e181a2b1ea059
https://doi.org/10.1134/s1070363220010089
https://doi.org/10.1134/s1070363220010089
Autor:
Vadim V. Bardin, Nicolay Yu. Adonin
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 150:1523-1531
In search of convenient preparations of C6F5BX2 (X = Cl, Br), reactions of C6F5HgR (R = C6F5, C6H5, C2H5, Br and Cl) with BX3 were studied. Under the action of BCl3 the order of the C–Hg bond cleavage is C6F5Hg–C6H5 > C6F5–HgC2H5 > C6F5–HgC6F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13d76b0831ad8e48aed403ec122bca5a
https://doi.org/10.1007/s00706-019-02476-6
https://doi.org/10.1007/s00706-019-02476-6
Autor:
Yanina V. Burgart, Mikhail Yu. Moskalik, A. A. Tyutyunov, Valery N. Charushin, Victor I. Saloutin, Galina N. Lipunova, Lyubov N. Sobenina, Pavel V. Nikul'Shin, Andrei B. Koldobskii, Vera V. Astakhova, Daria V. Vorobyeva, Nicolay Yu. Adonin, Salekh M. Masoud, Larisa V. Politanskaya, Vasiliy M. Muzalevskiy, Bagrat A. Shainyan, E. V. Panteleeva, Sema L. Ioffe, Evgeny V. Shchegolkov, Aleksey Yu. Aksinenko, Emiliya V. Nosova, Vyacheslav Ya. Sosnovskikh, Sergei M. Igumnov, Vadim V. Bardin, Evgeny V. Tretyakov, Vladimir Eduardovich Boiko, Tatyana V. Mezhenkova, Sergey N. Osipov, Galina A. Selivanova, Dmitrii L. Obydennov, Sergey A. Usachev, Valentine G. Nenajdenko, Boris A. Trofimov, Arkady G. Makarov, Vyacheslav E. Platonov, E. S. Balenkova, Victor M. Karpov, Aleksander V. Vasilyev, Andrey V. Zibarev, Kseniya V. Belyaeva, Alexey V. Shastin, Darya O. Prima, Andrey S. Vinogradov, V. B. Sokolov, Sofia M. Morozova, Alexander D. Dilman, Yaroslav V. Zonov, Andrey A. Tabolin, Olga S. Shilova
Publikováno v:
Russian Chemical Reviews. 88:425-569
Currently, the chemistry of organofluorine compounds is a leading and rapidly developing area of organic chemistry. Fluorine present in a molecule largely determines its specific chemical and biological properties. This thematic issue covers the tren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1e3c713e514b517dfee714264b81884
https://doi.org/10.1070/rcr4871
https://doi.org/10.1070/rcr4871
Autor:
Mikhail M. Shmakov, Sergey A. Prikhod'ko, Roman Yu Peshkov, Vadim V. Bardin, Nicolay Yu Adonin
Publikováno v:
Molecular Catalysis. 521:112202
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::678d5f5b45776bacd3fd42772dce70b9
https://doi.org/10.1016/j.mcat.2022.112202
https://doi.org/10.1016/j.mcat.2022.112202
Autor:
Vadim V. Bardin
Publikováno v:
Magnetic Resonance in Chemistry. 56:1124-1130
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb46ce27194422d48eef9e46fbd64281
https://doi.org/10.1002/mrc.4755
https://doi.org/10.1002/mrc.4755
Autor:
Vadim V. Bardin
Publikováno v:
Russian Journal of General Chemistry. 89:1406-1408
The reactions of pentafluorophenylmercury derivatives with organomagnesium compounds have been studied. The interaction of pentafluorophenylmercury chloride with RMgBr (R = Et, Ph) has afforded diphenyl- and diethylmercury or phenylmercury chloride,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::decd3fe403724044e5a8cc9b91f080d7
https://doi.org/10.1134/s1070363219070090
https://doi.org/10.1134/s1070363219070090
Autor:
Vadim V. Bardin, Alexander M. Maksimov
Publikováno v:
Zeitschrift für Naturforschung B. 72:731-737
C6F5SO2Cl reacts with organolithiums and organomagnesium halides RM (R=Me, Bu, Ph; M=Li, MgX) to give mainly C6F5H and C6F5Cl. C6F5SO2Br and PhMgBr form C6F5H and (C6F5S)2. This is in contrast to known transformations of them which yield exclusively
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c0c2871b1b5c1e73e052602704a928a
https://doi.org/10.1515/znb-2017-0092
https://doi.org/10.1515/znb-2017-0092