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Synthesis of enaminones and enamino esters catalysed by ZrOCl2 · 8H2O

Paper ID Volume ID Publish Year Pages File Format Full-Text
52551 46877 2007 6 PDF Available
Title
Synthesis of enaminones and enamino esters catalysed by ZrOCl2 · 8H2O
Abstract

A simple, fast and efficient procedure has been developed for the synthesis of β-enaminones and β-enamino esters catalysed by zirconyl chloride octahydrate (ZrOCl2 · 8H2O). The reaction of β-diketones and β-ketoesters with primary amines was carried out efficiently under solvent-free conditions at room temperature and led to chemo- and regio-selective formations of enamine derivatives in high to excellent yields.

Keywords
1,3-Dicarbonyl compounds; Amines; Enaminones; Enamino esters; Zirconyl chloride octahydrate; Solvent-free conditions
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Synthesis of enaminones and enamino esters catalysed by ZrOCl2 · 8H2O
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Publisher
Database: Elsevier - ScienceDirect
Journal: Catalysis Communications - Volume 8, Issue 11, November 2007, Pages 1615–1620
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis
Get Full-Text Now
Don't Miss Today's Special Offer
Price was $35.95
You save - $31
Price after discount Only $4.95
100% Money Back Guarantee
Full-text PDF Download
Online Support
Any Questions? feel free to contact us