The NARC-based approach to the enantioselective synthesis of the zaragozic acids. Synthesis of a C 5-alkoxycarbonyl-substituted 2,8-dioxabicyclo[3.2.1]octane

Patrick Perlmutter, Walailak Selajarern

Research output: Contribution to journalArticleResearchpeer-review


A direct method for the prepn. of C(5)-alkoxycarbonyl-substituted 2,8-dioxabicyclo[3.2.1]octanes is described. The key process involves a highly stereoselective NARC sequence of a nucleophilic addn. followed by ring closure. [on SciFinder(R)]
Original languageEnglish
Pages (from-to)349 - 353
Number of pages5
JournalAustralian Journal of Chemistry
Issue number4
Publication statusPublished - 2000

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