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An efficient synthesis of ferrocenyl substituted 1,5-diketone and cyclic <f>α,β</f>-unsaturated ketones under ultrasound irradiation
- Source :
-
Journal of Organometallic Chemistry . May2004, Vol. 689 Issue 10, p1843-1848. 6p. - Publication Year :
- 2004
-
Abstract
- Michael reactions of deoxybenzoin or dibenzyl ketone with ferrocenyl substituted chalcones catalyzed by sodium hydroxide under ultrasound irradiation can afford the corresponding Michael adducts with excellent yields. It presents a convenient, efficient and simple method for the preparation of ferrocenyl substituted 1,5-diketone compounds in the presence of ultrasound irradiation. In addition, the formation of cyclic, <f>α,β</f>-unsaturated ketones via the reactions of dibenzyl ketone with ferrocenyl substituted chalcones were found, and characterized by X-ray crystal structure analysis. [Copyright &y& Elsevier]
- Subjects :
- *BENZOIN
*KETONES
*ORGANIC compounds
*IRON compounds
*SODIUM hydroxide
Subjects
Details
- Language :
- English
- ISSN :
- 0022328X
- Volume :
- 689
- Issue :
- 10
- Database :
- Academic Search Index
- Journal :
- Journal of Organometallic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 23487456
- Full Text :
- https://doi.org/10.1016/j.jorganchem.2004.03.006