1974
DOI: 10.1021/ja00812a057
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Use of tris(6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedionato)europium(III) as a shift reagent for carboxylic acids and phenols

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Cited by 11 publications
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“…However, Eu(fod)3 is sufficiently more acidic than Eu(DPM)3 so that it does not decompose in the presence of phenol, cresol, or resorcinol. Recently, Shoffner has also achieved successful results on phenolic systems using Eu(fod)3 (5).…”
mentioning
confidence: 99%
“…However, Eu(fod)3 is sufficiently more acidic than Eu(DPM)3 so that it does not decompose in the presence of phenol, cresol, or resorcinol. Recently, Shoffner has also achieved successful results on phenolic systems using Eu(fod)3 (5).…”
mentioning
confidence: 99%