1983
DOI: 10.1021/jo00162a034
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Aerosol direct fluorination: syntheses of perfluoro ketones

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Cited by 10 publications
(3 citation statements)
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“…helium, argon, nitrogen [32][33][34]. Of the similar importance is the fluorination in a liquid phase in the liquefied anhydrous hydrogen fluoride or 65 wt.% aqueous HF solution [35], perfluoroalkanes [36], and in low temperatures in R-11 freon [37].…”
Section: Methods Of the Fluorination And Fluorinating Agentsmentioning
confidence: 99%
“…helium, argon, nitrogen [32][33][34]. Of the similar importance is the fluorination in a liquid phase in the liquefied anhydrous hydrogen fluoride or 65 wt.% aqueous HF solution [35], perfluoroalkanes [36], and in low temperatures in R-11 freon [37].…”
Section: Methods Of the Fluorination And Fluorinating Agentsmentioning
confidence: 99%
“…Primary and secondary amines give NF 2 and NF compounds respectively and fluorination of sulphur compounds gives products in which the sulphur has been oxidised to its maximum valency state of six [149] (Table 2.4). Perfluorinations of many ethers [155], cryptands [156], polyethers [119,157], including the largest perfluoro-macrocycle [158], perfluoro [60]-crown-20 [123,159], and the first perfluorinated sugar [160], orthocarbonates [161,162], ketones [163,164], esters [124,165], phosphanes [166] and alkyl halides [167,168] have been successfully accomplished by the LaMar or aerosol processes ( Perfluorinations of many ethers [155], cryptands [156], polyethers [119,157], including the largest perfluoro-macrocycle [158], perfluoro [60]-crown-20 [123,159], and the first perfluorinated sugar [160], orthocarbonates [161,162], ketones [163,164], esters [124,165], phosphanes [166] and alkyl halides [167,168] have been successfully accomplished by the LaMar or aerosol processes ( …”
Section: E Fluorination Of Compounds Containing Functional Groupsmentioning
confidence: 99%
“…to alkanes, ethers, cycloalkanes, ketals, and ketones has been demonstrated. 1,2 We report here the extension of the process to the synthesis of perfluoroadamantane via direct fluorination of adamantane, a feat not realized by other direct fluorination methods nor by indirect fluorination methods to any significant degree.…”
mentioning
confidence: 96%