Article ID Journal Published Year Pages File Type
66154 Journal of Molecular Catalysis A: Chemical 2012 5 Pages PDF
Abstract

Molybdate sulfuric acid (MSA) has been found as an efficient and reusable solid acid catalyst for the synthesis of new 2,3,4,5-tetrasubstituted pyrroles via a novel [2+2+1] strategy. Thus, one-pot three-component reaction of benzoin derivatives, 1,3-dicarbonyls, and ammonium acetate afforded the desired products in high yield under solvent-free conditions.

Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (89 K)Download as PowerPoint slideHighlights► MSA catalyzes efficiently the one-pot [2+2+1] strategy for the synthesis of substituted pyrroles. ► The yield of MSA-catalyzed reaction of 1,3-dicarbonyls, NH4OAc, and benzoins is high. ► This heterogeneous solid acid catalyst is recyclable. ► Electron-deficient benzoins reacted much faster than the others in the presence of MSA.

Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
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