Enantioselective synthesis of the dioxabicyclo[3.2.1]octane core of the zaragozic acids via intramolecular Wacker-type cyclisation reactions

Patrick Perlmutter, Walailak Selajerern, Filisaty Vounatsos

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26 Citations (Scopus)

Abstract

Wacker-type cyclization reactions provide an effective entry into the dioxabicyclo[3.2.1]octane core of the zaragozic acid analogs. [on SciFinder(R)]
Original languageEnglish
Pages (from-to)2220 - 2228
Number of pages9
JournalOrganic and Biomolecular Chemistry
Volume2
Issue number15
DOIs
Publication statusPublished - 2004

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