Abstract
Artemisinin [1], a potent antimalarial sesquiterpene endoperoxide, was converted via a photochemical route to its dehydro analogue, artemisitene [5]. The structure and stereochemistry of the hydroperoxide intermediate 4, produced by the action of1O2 on the enol ether 3, were established by X-ray crystallographic analysis. © 1990, American Chemical Society. All rights reserved.
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CITATION STYLE
APA
El-Feraly, F. S., Ayalp, A., Al-Yahya, M. A., McPhail, D. R., & McPhail, A. T. (1990). Conversion of Artemisinin to Artemisitene. Journal of Natural Products, 53(1), 66–71. https://doi.org/10.1021/np50067a008
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