1998
DOI: 10.1016/s1381-1169(98)00029-6
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Zeolite-catalysed rearrangements in organic synthesis

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Cited by 43 publications
(12 citation statements)
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“…The replacement of these conventional catalysts by heterogeneous reusable acid catalysts is promoting an important effort in heterogeneous catalysis research, mainly in the field of zeolites. Zeolites [4][5][6][7][8][9][10] and other acid heterogeneous catalysts such as the sulfonic resin Nafion [9] have been studied as catalytic systems in the Fries rearrangement of phenyl acetate. Rapid deactivation observed in zeolites, either in gaseous or liquid phase, evidence the need for a greater size pore system.…”
Section: Introductionmentioning
confidence: 99%
“…The replacement of these conventional catalysts by heterogeneous reusable acid catalysts is promoting an important effort in heterogeneous catalysis research, mainly in the field of zeolites. Zeolites [4][5][6][7][8][9][10] and other acid heterogeneous catalysts such as the sulfonic resin Nafion [9] have been studied as catalytic systems in the Fries rearrangement of phenyl acetate. Rapid deactivation observed in zeolites, either in gaseous or liquid phase, evidence the need for a greater size pore system.…”
Section: Introductionmentioning
confidence: 99%
“…has been achieved (Scheme 15) [134]. The arenesulfonic acid-centers located within the structure of SBA-15 show high catalytic performance as compared to other homogeneous [135] and heterogeneous acid catalysts [136][137][138][139][140]. This high activity is accompanied with a remarkable stability without leaching of sulfur species during the reaction.…”
Section: Acetylation and Acetoxylation Reactionsmentioning
confidence: 98%
“…For instance, the Claisen rearrangement of allyl aryl ethers 10 followed by intramolecular hydroxyalkylation of the resulting olefin afforded 2-methyldihydrobenzofuran (11) (Scheme 6) [55]. For instance, the Claisen rearrangement of allyl aryl ethers 10 followed by intramolecular hydroxyalkylation of the resulting olefin afforded 2-methyldihydrobenzofuran (11) (Scheme 6) [55].…”
Section: Furans and Related Compoundsmentioning
confidence: 99%