Synthesis of tetrafluoroethyl- and tetrafluoroethylene-containing amines by the reaction of silanes with enamines under acidic conditions

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F15%3A00443913" target="_blank" >RIV/61388963:_____/15:00443913 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1016/j.jfluchem.2014.08.004" target="_blank" >http://dx.doi.org/10.1016/j.jfluchem.2014.08.004</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.jfluchem.2014.08.004" target="_blank" >10.1016/j.jfluchem.2014.08.004</a>

Result language
angličtina
Original language name
Synthesis of tetrafluoroethyl- and tetrafluoroethylene-containing amines by the reaction of silanes with enamines under acidic conditions
Original language description
Enamines with in situ formed hydrogen fluoride underwent efficient reaction with trimethyl(1,1,2,2tetrafluoro-2-(phenylthio)ethyl)silane and trimethyl(1,1,2,2-tetrafluoro-2-(phenylsulfonyl)ethyl)silane. Radical or reductive desulfurization of the addition products provided amines containing the tetrafluoroethyl group.
Czech name
—
Czech description
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Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—

Project
<a href="/en/project/GAP207%2F11%2F0421" target="_blank" >GAP207/11/0421: Nucleophilic and radical tetrafluoroethyl and tetrafluoroethylene group transfer.</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2015
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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