30556-86-6Relevant articles and documents
Convenient synthesis of monodisperse fluorinated nonionic surfactants containing two hydrophilic hydroxylated moieties
Guittard, Frederic,De Givenchy, Elisabeth Taffin,Szoenyi, Francois,Cambon, Aime
, p. 7863 - 7866 (1995)
New fluorinated nonionic surfactants containing two monodisperse oligo(oxyethylene) tails and having a hydroxyl group in the terminal position were easily obtained, with good yields, a purity higher than 95%, a high solubility in water and show interesting surface properties for their physicochemical application: low surface tensions and noteworthy critical micelle concentrations.
Nouvelles methodes de preparation des 2-F-alkylethylamines
Szoenyi, F.,Guennouni, F.,Cambon, A.
, p. 85 - 92 (1991)
2-F-Alkylethylamines are difficult to obtain on the laboratory scale and their preparation without the formation of secondary products has never been reported.In this work we demonstrate that it is possible to obtain these compounds univocally and with easy to use methods.The spectral data of these compounds are reported for the first time.
Synthese des 2-F-alkylethylamines: optimisation de l'obtention des azotures de 2-F-alkyletyle et de leur reduction en amines
Trabelsi, H.,Szoenyi, F.,Michelangeli, N.,Cambon, A.
, p. 115 - 118 (1994)
2-F-Alkylethylamines are very important intermediates in organic fluorine chemistry.In this work, it has been demonstrated that it is possible to combine the advantages of two techniques, i.e. phase-transfer catalysis and the use of water as a dispersing medium, in the reduction of 2-F-alkylethyl azides, and hence simplify significantly the synthesis of such amines from 2-F-alkylethyl iodides.
Light-fluorous TEMPO: reagent, spin trap and stable free radical
Dobbs, Adrian P.,Jones, Peter,Penny, Mark J.,Rigby, Stephen E.
supporting information; experimental part, p. 5271 - 5277 (2009/11/30)
The synthesis of two light-fluorous TEMPO derivatives is reported, along with their fluorous-organic solvent partition coefficients and their ESR spectra. Applications of the fluorous-TEMPO reagents in oxidation reactions and as radical traps are discussed.
Novel light-fluorous TEMPO reagents and their application in oxidation reactions
Dobbs, Adrian P.,Penny, Mark J.,Jones, Peter
scheme or table, p. 6955 - 6958 (2009/04/07)
The synthesis of two light-fluorous TEMPO derivatives is reported, along with their application in oxidation reactions.
