Zobrazeno 1 - 10
of 20
pro vyhledávání: '"T. M. Potarina"'
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 26:1983-1988
1. The addition of polyfluorinated alcohols to trifluorochloroethylene, tetrafluoroethylene, and perfluoropropylene, with the formation of the corresponding ethers, can be accomplished under mild conditions in the presence of bases in DMF solution. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13140e8a921acd1fd832c37394545c21
https://doi.org/10.1007/bf00924411
https://doi.org/10.1007/bf00924411
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 33:372-375
The corresponding acyl fluorides are formed as the result of reacting 1,1,2-trifluoro-2-chloroethyldiethylamine with fluorocarboxylic acids.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66882f2ba996895516e48ff3e2263ffe
https://doi.org/10.1007/bf00951074
https://doi.org/10.1007/bf00951074
Autor:
O. V. Verenikin, A. V. Fokin, K. V. Frosina, T. M. Potarina, K. I. Pasevina, V. A. Komarov, A. I. Rapkin
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 27:1692-1695
1. α-Hydro-β-nitroperfluoroisopropanol was obtained by the condensation of difluoronitromethane with fluoral, and also by the reduction of nitroperfluoroacetone with NaBH4+. 2. α-Hydroxy-β-nitroperfluoroisobutyric acid, as well as its amide and e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a752952ad8b56fbfa5330649cf243a8c
https://doi.org/10.1007/bf00925070
https://doi.org/10.1007/bf00925070
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 29:1684-1688
Stable α,α-dihydropolyfluoroalkyl hypochlorites were obtained by reacting ClOSO2F with fluorinated alcohols, and some of their chemical properties were studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1614b60d2fb5246961ae4e1c0a8eeebc
https://doi.org/10.1007/bf00951236
https://doi.org/10.1007/bf00951236
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 30:1285-1288
1. The synthesis and study of some properties of 5-fluorodinitromethyltetrazole and of 5-difluoronitro-methyltetrazole has been carried out. 2. Tetrazoles and their salts are alkylated predominantly in position 2.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df57410082e7e27162bb808677938754
https://doi.org/10.1007/bf01417990
https://doi.org/10.1007/bf01417990
Autor:
A. F. Kolomiets, A. V. Fokin, T. M. Potarina, V. A. Komarov, O. V. Verenikin, K. I. Pasevina, A. I. Rapkin
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 27:1375-1379
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d4586abf5fef869acef2be51514413e
https://doi.org/10.1007/bf00946875
https://doi.org/10.1007/bf00946875
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 27:2133-2135
1. The alkylation of some mercury acylates with alkyl halides in THF was studied. 2. The mercury acylates can be regarded as being intramolecular electron-donor-acceptor (EDA) complexes, in which the carbonyl oxygen atom plays the role of donor, whil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc68f46518b7b83f76c60f083f6d3574
https://doi.org/10.1007/bf00946545
https://doi.org/10.1007/bf00946545
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 30:1958-1960
When reacted with fluoroolefins, iodine fluosulfate exhibits less expressed electrophilic properties than chlorine fluosulfate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::876698c7aad1ab2b7e7e95d3a421e9e4
https://doi.org/10.1007/bf00963436
https://doi.org/10.1007/bf00963436
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 22:2739-2741
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c20a471b8077e1bc11b1fc8bd9d75396
https://doi.org/10.1007/bf00926155
https://doi.org/10.1007/bf00926155
Publikováno v:
Chemischer Informationsdienst. 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce5cbf92ab790f42585bd038c5674153
https://doi.org/10.1002/chin.198049154
https://doi.org/10.1002/chin.198049154