Article ID Journal Published Year Pages File Type
9614438 Journal of Molecular Catalysis A: Chemical 2005 6 Pages PDF
Abstract
Diels-Alder cycloaddition has been studied using amorphous silica and different ITQ-2 and MCM-41 pure silica and metal containing materials as catalysts. The introduction of transition metal atoms in the framework increases the reaction rate preserving the selectivity to the endo-endo isomer. The presence of acidic OH groups provoke the retro-Diels-Alder reaction increasing the selectivity to the endo-exo isomer.
Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
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