Zobrazeno 1 - 9
of 9
pro vyhledávání: '"K. V. Frosina"'
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, USSR Division of Chemical Science. 12:1627-1630
1. The nitration of hexafluorobutadiene with nitrogen dioxide was studied, and some chemical properties of the nitration products were examined. 2. The main reaction products, both in the liquid and in the gas phase, were hexafluoro-1,4-dinitro-2-but
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::122e5adae4056bf2b5d871af233d3553
https://doi.org/10.1007/bf00845790
https://doi.org/10.1007/bf00845790
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 22:1493-1496
1. A study was made of the reaction of nitrogen chlorodifluoride with the potassium salt of nitroform, cyclohexene, and vinylacetylene, at room temperature and atmospheric pressure. 2. It Is postulated that nitrogen chlorodifluoride is a molecular el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99ac0cbd74707f6007f2cf726991aa26
https://doi.org/10.1007/bf00930046
https://doi.org/10.1007/bf00930046
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 22:106-108
α,β,β-Trifluorostyrene reacts vigorously with reagents of the radical type (nitrogen tetraoxide, tetrafluorohydrazine), and reacts quite sluggishly with nucleophilic reagents (ammonia, diethylamine).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3c5ee30858145138a223f9b2496c2b6
https://doi.org/10.1007/bf00854127
https://doi.org/10.1007/bf00854127
Autor:
K. I. Pasevina, V. A. Komarov, O. V. Verenikin, A. I. Rapkin, A. V. Fokin, K. V. Frosina, T. M. Potarina
Publikováno v:
Chemischer Informationsdienst. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfa048eb73bd64346dfedcae52d47713
https://doi.org/10.1002/chin.197908133
https://doi.org/10.1002/chin.197908133
Publikováno v:
Chemischer Informationsdienst. 15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ace9ab812bc3ca078de74704263c1563
https://doi.org/10.1002/chin.198435169
https://doi.org/10.1002/chin.198435169
Publikováno v:
Chemischer Informationsdienst. 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::723c7d2ce0de3af2870dac3ec188bfad
https://doi.org/10.1002/chin.197322241
https://doi.org/10.1002/chin.197322241
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::717c0016023d8a6cae462a117a500367
https://doi.org/10.1002/chin.197139176
https://doi.org/10.1002/chin.197139176
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 33:370-371
The fluosulfate group of N-chloriminoperfluoroacyl fluosulfates is the more labile toward nucleophilic reagents. The previously unknown N-chloroperfluoroalkaneamidines and N-chlorimines of perfluoroalkanehydroxamic acids were obtained by the reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0f71f067d8e143a1d64cacfe1868b4c
https://doi.org/10.1007/bf00951073
https://doi.org/10.1007/bf00951073