Abstract
A novel series of new 3-spiro monocyclic β-lactams 3a–i have been synthesized in high chemical yields from 9H-xanthene-9-carbonyl chloride 2 as ketene source in the [2+2] cycloaddition (Staudinger reaction) with different aromatic imines. These newly synthesized β-lactams were fully characterized and evaluated for their antimalarial activities against Plasmodium falciparum K14-resistant strain with moderate to excellent EC50 values varying from 8 up to 50 µM.
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The authors thank the Shiraz University Research Council for financial support (93-GR-SC-23).
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Jarrahpour, A., Rezaei, S., Sinou, V. et al. Synthesis of Some Novel 3-Spiro Monocyclic β-Lactams and Their Antibacterial and Antifungal Investigations. Iran J Sci Technol Trans Sci 41, 337–342 (2017). https://doi.org/10.1007/s40995-016-0033-8
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DOI: https://doi.org/10.1007/s40995-016-0033-8