Issue 11, 1996

The design, synthesis and biological evaluation of stable ozonides with antimalarial activity

Abstract

The synthesis of variously substituted 8,9,10,11-tetraoxatricyclo[5.2.1.12.6]undecan-4-ones by ozonolysis of various 8-oxabicyclo[3.2.1]oct-6-en-3-ones is described. Several of these stable ozonides exhibited activity (IC50s of 2–20 microgram cm–3) against a chloroquine-resistant strain of the malaria parasite Plasmodium falciparum.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1996, 1101-1105

The design, synthesis and biological evaluation of stable ozonides with antimalarial activity

L. de Almeida Barbosa, D. Cutler, J. Mann, M. J. Crabbe, G. C. Kirby and D. C. Warhurst, J. Chem. Soc., Perkin Trans. 1, 1996, 1101 DOI: 10.1039/P19960001101

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