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pubmed-article:18686962pubmed:abstractTextAn efficient tandem ring-closing dienyne metathesis of dienynes derived from cyclohex-2-enone affords the [5.3.1] carbon framework characteristic of taxanes in a single-step process. Further stereoselective functionalizations of the resulting [5.3.1] carbon framework lead to an advanced intermediate in a novel synthetic strategy for taxane analogs.lld:pubmed
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pubmed-article:18686962pubmed:articleTitleToward an efficient synthesis of taxane analogs by dienyne ring-closing metathesis.lld:pubmed
pubmed-article:18686962pubmed:affiliationDepartamento de Química Orgánica, Laboratorios del CSIC, Facultad de Química, Universidad de Santiago, 15782 Santiago de Compostela, Spain.lld:pubmed
pubmed-article:18686962pubmed:publicationTypeJournal Articlelld:pubmed
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