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Journal ArticleDOI

Application of clay catalysts in organic synthesis. a review

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TLDR
In this article, the application of clay catalyssts in ORGANIC SYNTHESIS is discussed. And a review of the application can be found in the Appendix.
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This article is published in Organic Preparations and Procedures International.The article was published on 2008-02-01. It has received 66 citations till now. The article focuses on the topics: Organic synthesis.

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Recent advances in engineering montmorillonite into catalysts and related catalysis

TL;DR: Montmorillonite, a ubiquitous clay mineral, has been engineered into a variety of porous and nanostructured catalysts, owing to its peculiar layered structure with characteristic surface and interc...
Journal ArticleDOI

Heterogeneous Catalytic Aqueous Phase Oxidative Cleavage of Styrenes to Benzaldehydes: An Environmentally Benign Alternative to Ozonolysis

TL;DR: In this paper, an environmentally benign heterogeneous catalytic method is described for the oxidative cleavage of styrenes to benzaldehydes by using air as a sustainable oxidant in aqueous medium.
Book ChapterDOI

Green Chemistry – Aspects for the Knoevenagel Reaction

TL;DR: The Knoevenagel reaction is considered to be a modification of the aldol reaction; the main difference between these approaches is the higher acidity of the active methylene hydrogen when compared to an -carbonyl hydrogen.
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Journal ArticleDOI

Total synthesis of marine natural products without using protecting groups

TL;DR: The preparative-scale, enantioselective, total syntheses of members of the hapalindole, fischerindoles, welwitindolinone and ambiguine families are described, each constructed without the need for protecting groups, making it possible to access other complex molecular architectures without using protecting groups.
Journal ArticleDOI

Enantioselective Total Syntheses of Welwitindolinone A and Fischerindoles I and G

TL;DR: The first total syntheses of welwitindolinone A and the most complex members of the f Fischerindole family, fischerindoles I and G, are reported.
Journal ArticleDOI

Simple Synthesis of Substituted Pyrroles

TL;DR: This method gives pyrroles with less nucleophilic multicyclic aromatic amines at room temperature using iodine-catalyzed and montmorillonite KSF-clay-induced modified Paal-Knorr methods.
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