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pubmed-article:12509898rdf:typepubmed:Citationlld:pubmed
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pubmed-article:12509898pubmed:dateCreated2003-1-2lld:pubmed
pubmed-article:12509898pubmed:abstractTextAn advanced intermediate in the synthesis of the phytotoxins cornexistin and hydroxycornexistin has been synthesized. Sequential palladium-mediated sp(2)-sp(3) fragment coupling and ring-closing diene metathesis have been used to construct the nine-membered carbocyclic core found in the natural products. [reaction--see text]lld:pubmed
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pubmed-article:12509898pubmed:authorpubmed-author:ClarkJ...lld:pubmed
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pubmed-article:12509898pubmed:authorpubmed-author:MarlinFrederi...lld:pubmed
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pubmed-article:12509898pubmed:pagination89-92lld:pubmed
pubmed-article:12509898pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:12509898pubmed:year2003lld:pubmed
pubmed-article:12509898pubmed:articleTitleSynthesis of the carbocyclic core of the cornexistins by ring-closing metathesis.lld:pubmed
pubmed-article:12509898pubmed:affiliationSchool of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD, UK. j.s.clark@nottingham.ac.uklld:pubmed
pubmed-article:12509898pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12509898pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed