2003
DOI: 10.1016/s0022-1139(03)00037-x
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Electrochemical partial fluorination of phenylacetic acids esters and 1-tetralone

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Cited by 13 publications
(7 citation statements)
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“…Even with this powerful fluorinating agent, the yield obtained was around 56% [4]. Quite recently Yoneda co-workers have reported 17% yield during the selective electrochemical fluorination of ethyl phenylacetate in dichloromethane using different supporting electrolytes [11]. A brief report by Cao and Fuchigami is also available [12].…”
Section: Introductionmentioning
confidence: 99%
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“…Even with this powerful fluorinating agent, the yield obtained was around 56% [4]. Quite recently Yoneda co-workers have reported 17% yield during the selective electrochemical fluorination of ethyl phenylacetate in dichloromethane using different supporting electrolytes [11]. A brief report by Cao and Fuchigami is also available [12].…”
Section: Introductionmentioning
confidence: 99%
“…F and 1 H NMR spectral data of fluorinated phenylacetic acid and its derivatives obtained during anodic fluorination of 1a-f[11,25] …”
mentioning
confidence: 99%
“…Stereo selectivity in such processes has also been reported for esters and amides [15,16]. Anodic fluorination of alkyl phenylacetates was studied by Yoneda et al in dichloromethane containing Et 3 N Á nHF, Et 4 NF Á mHF and Et 4 N Á BF 4 [17]. Shainyan et al employed anhydrous hydrofluoric acid for the anodic fluorination of benzamide and acetanilide [18].…”
Section: Introductionmentioning
confidence: 97%
“…1-Indanone and 2-indanone have also been chemically fluorinated using inorganic fluorinating agents, namely XeF 2 and CsSO 4 F [5]. Brief reports on chemical [6] as well as electrochemical fluorination [7] of tetralone are also available.…”
Section: Introductionmentioning
confidence: 99%