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A generic and reproducible route to homo- and heteroannular bicyclic beta-diketones via knochel-type 1,4-conjugate additions to alpha,beta-unsaturated cycloalkenones

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JournalSynlett
DatePublished - 1 Feb 2006
Issue number2
Number of pages3
Pages (from-to)309-311
Original languageEnglish

Abstract

A generic and reproducible method for the preparation of homo- and heteroannular bicyclic beta-diketones is reported. The method employs the copper acetate mediated 1,4-conjugate addition of organozinc derivatives of iodopropionate and iodobutanoate esters to alpha, beta-unsaturated cycloalkenones, followed by intramolecular Dieckmann condensation.

    Research areas

  • annulation, enzymes, bicyclic compounds, ketones, cyclisations, 1,3-DIKETONES, REAGENTS

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