2001
DOI: 10.1039/b006946i
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Envirocat EPZG and natural clay as efficient catalysts for transesterification of β-keto esters

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Cited by 29 publications
(14 citation statements)
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“…Of interest, the presence of suitable Brønsted and Lewis acid sites is known asa prevailing parameter governing the catalytic performance of clays toward the deep oxidation of VOCs [22]. Sofar,it is believed that Brønsted acidity (proton donor) is mainly deriving from the clay structural hydroxyl groups, while Lewis acidity (electron pair acceptor) is attributed to the aluminum (Al 3+ ) and iron (Fe 2+ and Fe 3+ ) species located in the octahedral layer and at broken edges [23,24]. Generally, both Brønsted and Lewis acid sites are common, whereas one of them might be dominant and/or catalytically beneficial [25].…”
Section: Introductionmentioning
confidence: 99%
“…Of interest, the presence of suitable Brønsted and Lewis acid sites is known asa prevailing parameter governing the catalytic performance of clays toward the deep oxidation of VOCs [22]. Sofar,it is believed that Brønsted acidity (proton donor) is mainly deriving from the clay structural hydroxyl groups, while Lewis acidity (electron pair acceptor) is attributed to the aluminum (Al 3+ ) and iron (Fe 2+ and Fe 3+ ) species located in the octahedral layer and at broken edges [23,24]. Generally, both Brønsted and Lewis acid sites are common, whereas one of them might be dominant and/or catalytically beneficial [25].…”
Section: Introductionmentioning
confidence: 99%
“…In this regard, various catalysts have been recently reported to effect this reaction as indium triiodide [23], diphenylammonium triflate [24], amberlyst-15 [25] yttria-zirconia [26] Mo-ZrO 2 [27], lithium perchlorate [28], polymer-supported lipase [29], envirocat EPZG [30], hydrotalcite [31], clays [32] and zeolites [33]. Some of these catalysts are difficult to prepare and toxic.…”
Section: Introductionmentioning
confidence: 99%
“…[33] Transesterification in Single Fluorous Phase System (Table 1, Entry 1) A test tube (50 mL) charged with ethyl 3-phenylpropionate (178 mg, 1.0 mmol), benzyl alcohol (108 mg, 1.0 mmol), 1aa (86 mg, 0.05 mmol, 5 mol %) and FC-72 (5.0 mL) was placed in a stainless pressure bottle and heated at 150 8C for 16 h. After having been cooled, toluene (5.0 mL) was added to the reaction mixture. The toluene and FC-72 layers were separated and the latter layer was washed with toluene (1.0 mL Â 2).…”
Section: Methodsmentioning
confidence: 99%