Abstract
1,1′-Diacetylferrocene was condensed with aromatic aldehydes without solvent in the presence of solid NaOH. Diacetylferrocene can give good yields of mono- or diene with either one or two molecules of a wide range of aldehydes depending only on the stoichiometry. Cyclization to ferrocenphane does not occur in this condition.
| Original language | English |
|---|---|
| Pages (from-to) | 782-785 |
| Number of pages | 4 |
| Journal | Journal of Organometallic Chemistry |
| Volume | 637-639 |
| DOIs | |
| State | Published - 3 Dec 2001 |
| Externally published | Yes |
Keywords
- 1,1′-Diacetylferrocene
- 1,1′-Dienonylferrocenes
- 1-Acetyl-1′-enonylferrocenes
- Aldol condensation
- Solid-state reaction
Fingerprint
Dive into the research topics of 'Preparation of ferrocenyl mono- and dienone derivatives through aldol condensation of 1,1′-diacetylferrocene with aromatic aldehydes in dry conditions'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver