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dc.contributor.authorMorandi, Bill
dc.contributor.authorWickens, Zachary K.
dc.contributor.authorGrubbs, Robert H.
dc.date.accessioned2016-02-28T05:51:59Z
dc.date.available2016-02-28T05:51:59Z
dc.date.issued2013-07-26
dc.identifier.citationMorandi B, Wickens ZK, Grubbs RH (2013) Regioselective Wacker Oxidation of Internal Alkenes: Rapid Access to Functionalized Ketones Facilitated by Cross-Metathesis. Angew Chem 125: 9933–9936. Available: http://dx.doi.org/10.1002/ange.201303587.
dc.identifier.issn0044-8249
dc.identifier.doi10.1002/ange.201303587
dc.identifier.urihttp://hdl.handle.net/10754/599484
dc.description.abstractWacka wacka: The title reaction makes use of a wide range of directing groups (DG) to enable the highly regioselective oxidation of alkenes, and occurs predictably at the distal position. Both E and Z alkenes afford valuable functionalized ketones and cross-metathesis was shown to facilitate the preparation of the starting materials. BQ=benzoquinone.
dc.description.sponsorshipWe gratefully acknowledge financial support from the King Abdullah University of Science and Technology Centre 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.titleRegioselective Wacker Oxidation of Internal Alkenes: Rapid Access to Functionalized Ketones Facilitated by Cross-Metathesis
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-online2013-07-26
dc.date.published-print2013-09-09


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