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dc.contributor.authorRiley, Andrew Philip
dc.contributor.authorDay, Victor W.
dc.contributor.authorNavarro, Hernán A.
dc.contributor.authorPrisinzano, Thomas E.
dc.identifier.citationRiley, A. P., Day, V. W., Navarro, H. A., & Prisinzano, T. E. (2013). Palladium-catalyzed Transformations of Salvinorin A, a Neoclerodane Diterpene from Salvia divinorum. Organic Letters, 15(23), 5936–5939.
dc.description.abstractTransformations that selectively modify the furan ring present in a variety of naturals products would be useful in the synthesis of biological probes but remain largely underexplored. The neoclerodane diterpene salvinorin A, isolated from Salvia divinorum, is an example of a furan-containing natural product. Following selective bromination of salvinorin A, Suzuki-Miyaura and Sonogashira couplings were accomplished in moderate to good yields without hydrolyzing the labile C-2 acetate or altering the stereochemistry of the epimerizable centers.en_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see
dc.titlePalladium-catalyzed Transformations of Salvinorin A, a Neoclerodane Diterpene from Salvia divinorumen_US
kusw.kuauthorRiley, Andrew P.
kusw.kuauthorDay, Victor W.
kusw.kuauthorPrisinzano, Thomas E.
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kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US

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