1973
DOI: 10.1016/s0022-1139(00)82862-6
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Fluoroketenes VII. Synthesis and reactivity of trifluoromethylfluoroketene, perfluoroacryloyl fluoride, perfluoromethacryloyl fluoride, methyl perfluoroacrylate and methyl perfluoromethacrylate

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Cited by 57 publications
(41 citation statements)
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“…Higher perfluoroolefins can also be employed [216]. The methyl ethers are valuable intermediates, which can be converted to acid fluorides with sulfur trioxide [217] or other Lewis acids [218]. Primary and secondary perfluorinated alkoxides (see Chap.…”
Section: Partially Fluorinated Ethersmentioning
confidence: 99%
“…Higher perfluoroolefins can also be employed [216]. The methyl ethers are valuable intermediates, which can be converted to acid fluorides with sulfur trioxide [217] or other Lewis acids [218]. Primary and secondary perfluorinated alkoxides (see Chap.…”
Section: Partially Fluorinated Ethersmentioning
confidence: 99%
“…Examples of additions of difluorocarbene to substrates as electron deficient as a,b-unsaturated carbonyl compounds are few and far between [24,25]. Therefore, studies were carried out in order to obtain comparative reactivity data for this new difluorocarbene reagent.…”
Section: Comparative Reactivity/selectivity Of Tfda-derived Difluorocmentioning
confidence: 99%
“…19 F NMR spectra were recorded at 282.2 and 470.3 MHz, using an internal standard of trichlorofluoromethane. In spectra of certain complex spin systems, line spacings reported as Js may not be true coupling constants.…”
Section: Methodsmentioning
confidence: 99%
“…Despite many attempts, 14 has never been isolated, and has only been trapped as derivatives 15 and 16 (Scheme 3) [18,19].…”
Section: Ketene Formationmentioning
confidence: 99%
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