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dc.contributor.authorMorandi, Bill
dc.contributor.authorWickens, Zachary K.
dc.contributor.authorGrubbs, Robert H.
dc.date.accessioned2016-02-28T05:49:52Z
dc.date.available2016-02-28T05:49:52Z
dc.date.issued2013-01-16
dc.identifier.citationMorandi B, Wickens ZK, Grubbs RH (2013) Practical and General Palladium-Catalyzed Synthesis of Ketones from Internal Olefins. Angew Chem 125: 3016–3020. Available: http://dx.doi.org/10.1002/ange.201209541.
dc.identifier.issn0044-8249
dc.identifier.doi10.1002/ange.201209541
dc.identifier.urihttp://hdl.handle.net/10754/599374
dc.description.abstractMake it simple! A convenient and general palladium-catalyzed oxidation of internal olefins to ketones is reported. The transformation occurs at room temperature and shows wide substrate scope. Applications to the oxidation of seed-oil derivatives and a bioactive natural product (see scheme) are described, as well as intriguing mechanistic features.
dc.description.sponsorshipWe thank Scott Virgil and the Caltech Center for Catalysis for technical assistance. We gratefully acknowledge financial support from King Abdullah University of Science and Technology Center in Development, King Fahd University of Petroleum and Minerals, the NSF, and the Swiss National Science Foundation for a fellowship to B.M.
dc.publisherWiley
dc.titlePractical and General Palladium-Catalyzed Synthesis of Ketones from Internal Olefins
dc.typeArticle
dc.identifier.journalAngewandte Chemie
dc.contributor.institutionDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125 (USA)
dc.date.published-online2013-01-16
dc.date.published-print2013-03-04


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