Cerium(III) chloride heptahydrate / Catalysis / 1,3-Dicarbonyl compounds / Enones / Michael reactions Cerium(III) chloride heptahydrate in the presence of sodium liquid at room temperature, the reaction can also be performed without solvents. The CeCl 3 • 7 H 2 O/NaI catalyst iodide catalyses the Mi
✦ LIBER ✦
Solvent-free reactions of alcohols with β-dicarbonyl compounds catalyzed by iron(III) chloride
✍ Scribed by Yu Yuan; Zhuangzhi Shi; Xuan Feng; Xiangnong Liu
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 142 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0268-2605
- DOI
- 10.1002/aoc.1320
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✦ Synopsis
Abstract
The direct substitution of alcohols and β‐dicarbonyl compounds was catalyzed with FeCl~3~ under solvent‐free conditions. The catalyst loading could be decreased to 0.01 mol% at high activities. It was shown that the reaction proceeded in two steps via the etherification of the alcohols. This method provided an easy and practical procedure for CC bond formation.Copyright © 2007 John Wiley & Sons, Ltd.
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