2009
DOI: 10.1016/j.jfluchem.2009.06.019
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Oxidation and chlorination reactions of perfluoroketene-N,S-acetals

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Cited by 9 publications
(1 citation statement)
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“…We envisioned that thioamide derivatives could be obtained under similar conditions. Such a procedure could serve as an alternative method for the synthesis of fluorinated thioamides . Unlike the oxydefluorination with NaOAc, the thioacetate-promoted reaction led to the formation of thioamides 5 , involving a concomitant cleavage of the N–O bond.…”
mentioning
confidence: 99%
“…We envisioned that thioamide derivatives could be obtained under similar conditions. Such a procedure could serve as an alternative method for the synthesis of fluorinated thioamides . Unlike the oxydefluorination with NaOAc, the thioacetate-promoted reaction led to the formation of thioamides 5 , involving a concomitant cleavage of the N–O bond.…”
mentioning
confidence: 99%