Catalysis and Zeolites 1999
DOI: 10.1007/978-3-662-03764-5_6
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Zeolite Effects in Organic Catalysis

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Cited by 15 publications
(11 citation statements)
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“…There are excellent, almost exhaustive overviews of organic reactions catalyzed by zeolites (1)(2)(3)(4). Instead of pursuing completeness, this chapter intends to illustrate zeolite effects on fine chemicals transformations with a series of wellselected and recent examples.…”
Section: Introductionmentioning
confidence: 98%
“…There are excellent, almost exhaustive overviews of organic reactions catalyzed by zeolites (1)(2)(3)(4). Instead of pursuing completeness, this chapter intends to illustrate zeolite effects on fine chemicals transformations with a series of wellselected and recent examples.…”
Section: Introductionmentioning
confidence: 98%
“…The advantages of zeolites over other solids are, according to Espeel et al, 4 their great acid strength and practically unlimited applicability to different types of catalysis. The main weaknesses are that they are very sensitive to deactivation by irreversible adsorption or pore blockage by heavy products, and also the incompatibility in size of molecules resulting from the fine chemicals area and the cages of the micropores.…”
mentioning
confidence: 99%
“…The main weaknesses are that they are very sensitive to deactivation by irreversible adsorption or pore blockage by heavy products, and also the incompatibility in size of molecules resulting from the fine chemicals area and the cages of the micropores. 4 Metals supported on zeolites are prepared by incorporating the transition metal either by cation exchange or an impregnation procedure and then reducing the transition metal. The design of the supported catalyst is based mainly on the knowledge of the interaction and location of the active phase on the support.…”
mentioning
confidence: 99%
“…[2] Among them, heterogeneously catalysed Friedel±Crafts alkylation reactions are receiving a great deal of attention even for large scale processes. [3] Catalytic and stereoselective alkylation of indoles via 1,4-addition to electron-deficient double bonds is an important organic reaction that affords products that may be transformed into valuable building blocks.…”
mentioning
confidence: 99%
“…Firstly, by selecting the batch 1,4-addition of 2-methylindole (1) to 2-cyclohexen-1-one (2) as the model reaction, a range of solid acids were screened as catalysts (Scheme 1). [6] From the data collected in Table 1 it emerges that, although in the absence of promoting agent the reaction did not occur in significant extents over 24 h reaction time, commercial ion-exchange sulfonic resins such as Amberlyst-15, 35, 36 and 40, employed at 20% wt, allowed 3 to be isolated in high yields (61 ± 76%).…”
mentioning
confidence: 99%