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Journal of Enzyme Inhibition and Medicinal Chemistry Volume 25, 2010 - Issue 1
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Research Article

Synthesis and leishmanicidal activity of 2,3,4-substituted-5-imidazolones

Khalid Mohammed KhanH. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, PakistanCorrespondence[email protected] [email protected]
,
Uzma Rasool MughalH. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan
,
Nida AmbreenH. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan
,
SamreenH. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan
,
Shahnaz PerveenPCSIR Laboratories Complex, Karachi, Pakistan
&
M. Iqbal ChoudharyH. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan
Pages 29-37 | Received 15 Jan 2009, Accepted 25 Mar 2009, Published online: 23 Dec 2009

References

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  • Salma U, Mazhar M, Imtiaz-ud-Din, Ali S, Khan KM. In vitro antileishmanial activities of germatarnyl and silicon incorporated diorganotin derivatives: synthesis and spectroscopic properties. J Enzyme Inhib Med Chem 2009;23:413–19.
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  • (a) A ratio of 1:10 of oxazolone to PPA was used to get E-isomer; (b) Rao YS. A new stereospecific synthesis of the E isomers of 2-phenyl-4-arylmethylene-2-oxazolin-5-ones. J Org Chem 1976;41:722–725.
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