Abstract
Two epimeric guaianolides, both prepared from α-santonin, were 11-hydroxylated using 2-phenylsulfonyl-3-phenyloxaziridine as a reagent. Extensive use of protecting groups enabled selective acylation of the 3- and 10-hydroxy groups. © Acta Chemica Scandinavica 1996.
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CITATION STYLE
APA
Lauridsen, A., Cornett, C., Vulpius, T., Moldt, P., & Christensen, S. B. (1996). Syntheses of 11-hydroxylated guaianolides. Acta Chemica Scandinavica, 50(2), 150–157. https://doi.org/10.3891/acta.chem.scand.50-0150
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