Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Alexander M. Maksimov"'
Autor:
Borislav V. Koshcheev, Roman A. Bredikhin, Alexander M. Maksimov, Vyacheslav E. Platonov, and Vladimir V. Shelkovnikov
Publikováno v:
ARKIVOC, Vol 2019, Iss 5, Pp 89-95 (2019)
Externí odkaz:
https://doaj.org/article/3eee36cd1d4546daa2f859f4c132876a
Autor:
Pavel V. Nikul’shin, Roman G. Fedunov, Leonid V. Kuibida, Alexander M. Maksimov, Evgeni M. Glebov, Dmitri V. Stass
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 8; Pages: 7568
We demonstrate that a series of perfluorinated para-oligophenylenes C6F5-(C6F4)n-C6F5 (n = 1–3) produce exciplexes with N,N-dimethylaniline (DMA) in degassed X-irradiated n-dodecane solutions. The optical characterization of the compounds shows tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dd8d868aecb24ce50a599aec9c5d408
Autor:
Yulia F. Polienko, Sergey A. Cherkasov, Dmitriy Parkhomenko, Denis A. Morozov, Elena G. Bagryanskaya, Alexander M. Maksimov, Igor A. Kirilyuk, Polina Kaletina, Anastasiya D. Semikina
Publikováno v:
ChemPlusChem. 86:1080-1086
In our previous work [Edeleva et al. Chem. Commun. 2019, 55, 190-193], we proposed a versatile approach to the activation of the homolysis of an aldonitrone group-containing alkoxyamine by 1,3-dipolar cycloaddition to a vinyl monomer. Both nitroxide-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68ab8411323897f5c8f7f108e0040d8b
https://doi.org/10.1002/cplu.202100266
https://doi.org/10.1002/cplu.202100266
Publikováno v:
Russian Journal of General Chemistry. 91:1316-1324
A new method for the synthesis of 4-chlorononafluoro- and 4-bromononafluorobiphenyl by the reactions of nonafluorobiphenyl-4-thiol with Cl2, PCl5, and Br2, as well as of 4,4′-dichlorooctafluorobiphenyl from octafluorobiphenyl-4,4′-dithiol, 4′-c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee7949f4d2c7599b0801b37b7f125c09
https://doi.org/10.1134/s1070363221070097
https://doi.org/10.1134/s1070363221070097
Publikováno v:
Russian Chemical Bulletin. 70:995-998
A new method for the preparation of 2,3,4,5-tetrafluorophenol from 2-[(2,3,4,5,6-pentafluorophenyl)thio]acetic acid has been proposed. It included the intramolecular cyclization of the salt of this acid in the presence of K2CO3 with the substitution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::221954c5c2c8b6eadf8eefd79789ed0a
https://doi.org/10.1007/s11172-021-3178-3
https://doi.org/10.1007/s11172-021-3178-3
Publikováno v:
Russian Journal of Organic Chemistry. 56:1911-1919
The reaction of 4-X-substituted 1-[(difluoromethyl)sulfinyl]-2,3,5,6-tetrafluorobenzenes (X = CF3, H, OMe) with methylamine and ammonia in MeCN, Et2O, and hydrocarbons occurs involves nucleophilic substitution in position 2 of the substrate. The reac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bae1c94de752a1d63b2f2608f950114
https://doi.org/10.1134/s1070428020110044
https://doi.org/10.1134/s1070428020110044
Publikováno v:
Russian Journal of General Chemistry. 90:2032-2037
Pyrolysis of a mixture of 2,5-difluoro-3,4,6-trichlorobenzenethiol with tetrafluoroethylene leads to 2,2,3,3,4,7-hexafluoro-5,6-dichloro-2,3-dihydrobenzo[b]thiophene (the major reaction product) along with 2,2,3,3,4,6-hexafluoro-5,7-dichloro-2,3-dihy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69ef965fa79f70ca72cfe7d819c5177f
https://doi.org/10.1134/s107036322011002x
https://doi.org/10.1134/s107036322011002x
Autor:
Borislav V. Koshcheev, Vyacheslav E. Platonov, Alexander M. Maksimov, Rodion V. Andreev, Roman A. Bredikhin
Publikováno v:
Arkivoc. 2020:344-361
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::baa130581cea38b1c67cada048ba5378
https://doi.org/10.24820/ark.5550190.p011.262
https://doi.org/10.24820/ark.5550190.p011.262
Autor:
Alina D. Mironova, Maksim A. Mikhaylov, Alexander M. Maksimov, Konstantin A. Brylev, Artem L. Gushchin, Dmitry V. Stass, Alexander S. Novikov, Ilia V. Eltsov, Pavel A. Abramov, Maxim N. Sokolov
Publikováno v:
European Journal of Inorganic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d19a30e8b537f8ec5e95bf6ce6ebac6b
https://doi.org/10.1002/ejic.202100890
https://doi.org/10.1002/ejic.202100890
Publikováno v:
Russian Journal of General Chemistry. 89:2378-2385
Dodecafluoro-2H,3H,5H,6H,7H-indeno[5,6-b]thiophene has been synthesized as the major product of co-pyrolysis of 6-bromo-, 6-chlorooctafluoroindane-5-thiols, or bis(6-bromo-5-perfluoroindanyl)disulfane with tetrafluoroethylene under flow conditions at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::426f654fb5bc57c7cd13d929c6004e73
https://doi.org/10.1134/s1070363219120090
https://doi.org/10.1134/s1070363219120090