1992
DOI: 10.1016/s0022-1139(00)80183-9
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Synthèse des isocyanates de 2-F-alkyléthyle

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Cited by 36 publications
(10 citation statements)
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“…3-Perfluoroalkylpropanoic acids were obtained by carboxylation of the corresponding organomagnesium compound of 2-perfluoroalkylethyl iodide. 10 The intermediate (2,3-dihydrothieno[3,4-b] [1,4]dioxin-2-yl)methanol was obtained in six steps from thiodiglycolic acid 11 with an overall yield of 34% and 2-(1H-pyrrol-1-yl)ethanol by action of the pyrrolyl potassium salt on 2-chloroethanol. 12 9-Fluorenemethanol was commercially available.…”
Section: Resultsmentioning
confidence: 99%
“…3-Perfluoroalkylpropanoic acids were obtained by carboxylation of the corresponding organomagnesium compound of 2-perfluoroalkylethyl iodide. 10 The intermediate (2,3-dihydrothieno[3,4-b] [1,4]dioxin-2-yl)methanol was obtained in six steps from thiodiglycolic acid 11 with an overall yield of 34% and 2-(1H-pyrrol-1-yl)ethanol by action of the pyrrolyl potassium salt on 2-chloroethanol. 12 9-Fluorenemethanol was commercially available.…”
Section: Resultsmentioning
confidence: 99%
“…Unless specified as dry, the solvents were unpurified reagent grade. The procedure for the preparation of 2-F-alkylpropanoic acids are described elsewhere [17]. Perfluorinated raw materials were given by Atofina.…”
Section: Methodsmentioning
confidence: 99%
“…etc. could be extended to ETFE cotelomer iodides with minor modification [33][34][35][36][37][38]. However, there are major difficulties associated with, particularly with regard to the poor solubility of the ETFE cotelomer iodides in some of the organic solvents used as medium for these transformations.…”
Section: Surface Protection Derivatives From Etfe Cotelomer Iodidesmentioning
confidence: 99%