Abstract
New substituted 2-ferrocenylbenzimidazole derivatives are prepared by the oxidation of corresponding Schiffs bases in situ, generated from corresponding 1,2-diamino-4-fluoro-5-(1-piperazinyl)benzenes and 2-ferrocenecarboxaldehyde using nitrobenzene.
| Original language | English |
|---|---|
| Pages (from-to) | 67-71 |
| Number of pages | 5 |
| Journal | Journal of Heterocyclic Chemistry |
| Volume | 42 |
| Issue number | 1 |
| Publication status | Published - Jan 2005 |
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ASJC Scopus subject areas
- Organic Chemistry
Cite this
Synthesis of new 2-ferrocenyl-5-fluoro-6-(4-substituted-1-piperazinyl)-1H- benzimidazoles of potential biological interest. / Abdel-Jalil, Raid J.; Voelter, Wolfgang.
In: Journal of Heterocyclic Chemistry, Vol. 42, No. 1, 01.2005, p. 67-71.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Synthesis of new 2-ferrocenyl-5-fluoro-6-(4-substituted-1-piperazinyl)-1H- benzimidazoles of potential biological interest
AU - Abdel-Jalil, Raid J.
AU - Voelter, Wolfgang
PY - 2005/1
Y1 - 2005/1
N2 - New substituted 2-ferrocenylbenzimidazole derivatives are prepared by the oxidation of corresponding Schiffs bases in situ, generated from corresponding 1,2-diamino-4-fluoro-5-(1-piperazinyl)benzenes and 2-ferrocenecarboxaldehyde using nitrobenzene.
AB - New substituted 2-ferrocenylbenzimidazole derivatives are prepared by the oxidation of corresponding Schiffs bases in situ, generated from corresponding 1,2-diamino-4-fluoro-5-(1-piperazinyl)benzenes and 2-ferrocenecarboxaldehyde using nitrobenzene.
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UR - http://www.scopus.com/inward/citedby.url?scp=17844380782&partnerID=8YFLogxK
M3 - Article
VL - 42
SP - 67
EP - 71
JO - Journal of Heterocyclic Chemistry
JF - Journal of Heterocyclic Chemistry
SN - 0022-152X
IS - 1
ER -