Zobrazeno 1 - 10
of 19
pro vyhledávání: '"V. G. Chilikin"'
Publikováno v:
ChemInform. 28
The addition of sulfur chloride pentafluoride to various terminal olefins, including those containing functional substituents, was studied. Possible side processes in these reactions are oligomerization and fluorination of the starting olefin.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a5cdf5ced86ced5aa21d77a31f2d1c9
https://doi.org/10.1002/chin.199724083
https://doi.org/10.1002/chin.199724083
Publikováno v:
Russian Chemical Bulletin. 45:2804-2806
The addition of sulfur chloride pentafluoride to various terminal olefins, including those containing functional substituents, was studied. Possible side processes in these reactions are oligomerization and fluorination of the starting olefin.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::754414e3e15641cce0e45ba0e48afe89
https://doi.org/10.1007/bf01430646
https://doi.org/10.1007/bf01430646
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 32:1306-1309
We were the first to add nitronium fluosulfate to the multiple bond of fluoroolefins to give the corresponding fluorinated β-nitroalkyl fluosulfates. The theory was expressed that the electrophilic mechanism applies to the given process.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::072aa72959a70526c3504d0a03673314
https://doi.org/10.1007/bf00953183
https://doi.org/10.1007/bf00953183
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 33:766-769
The replacement of the nitroso group in perfluoronitrosoalkanes in the presence of chlorine fluorosulfate and peroxydisulfuryl difluoride was studied. A hypothesis concerning the possible reaction mechanism was stated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcae6e2d95a76e00b2d171f4aad50c85
https://doi.org/10.1007/bf00947830
https://doi.org/10.1007/bf00947830
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 34:601-607
1. In reactions of bromine tris (fluorosulfate) with fluoroolefins the corresponding 2-bromofluoroalkyl fluorosulfates and vicinal bis (fluorosulfonyloxy) fluoroalkanes, products of addition to the multiple bond of elements of bromine monofluorosulfa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be0a2cbd1277ef0d2a476cda843f5fbc
https://doi.org/10.1007/bf00947731
https://doi.org/10.1007/bf00947731
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 34:1322-1325
The pyrolysis of adducts of 2-nitrosopolyfluoroalkyl fluorosulfates with fluoroolefins gives previously unreported fluorosulfonyloxyfluoroazomethines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e40500228511b374e22690296e0240c
https://doi.org/10.1007/bf00956119
https://doi.org/10.1007/bf00956119
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 35:810-818
1. Addition of nitrosyl fluorosulfate to the multiple bond of fluoroolefins was accomplished, and the previously unknown 2-nitrosopolyfluoroalkyl fluorosulfates were obtained. 2. It was shown that 2-nitrosopolyfluoroalkyl fluorosulfates are effective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0caa7ff8931ef63ab822073c913a59a
https://doi.org/10.1007/bf00954235
https://doi.org/10.1007/bf00954235
Publikováno v:
Chemischer Informationsdienst. 15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f7707c3ffa242d6fffa14994801e123
https://doi.org/10.1002/chin.198435161
https://doi.org/10.1002/chin.198435161
Publikováno v:
Chemischer Informationsdienst. 17
The pyrolysis of adducts of 2-nitrosopolyfluoroalkyl fluorosulfates with fluoroolefins gives previously unreported fluorosulfonyloxyfluoroazomethines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::883a3c4f5ba9f4d8687c03d459afdccb
https://doi.org/10.1002/chin.198601084
https://doi.org/10.1002/chin.198601084
Publikováno v:
Chemischer Informationsdienst. 15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a88a81385ca94efead70bd9af176822
https://doi.org/10.1002/chin.198444115
https://doi.org/10.1002/chin.198444115