Isoxazoline analogues of artemisinin were obtained in low yield and low diastereoselectivity from the 1,3-dipolar cycloaddition of nitrile oxides. Alternatively, starting from the aldehyde 7, a number of transformations - Wittig reaction and reduction, Henry reaction and cyanohydrin formation - were achieved in significantly higher yields. In the cases where a new stereocenter was introduced this occured diastereoselectively. © 2007 by MDPI.
CITATION STYLE
Van Neck, T., Van Mierloo, S., & Dehaen, W. (2007). Functionalisation of artemisinin and its ring-contracted derivatives. Molecules, 12(3), 395–405. https://doi.org/10.3390/12030395
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