Total Synthesis of Maturinone through a Regioselective Diels-Alder Reaction of 5-Brominated Benzofurandione

Omar CHERKAOUI; Pascal NEBOIS; Houda FILLION

doi:10.1248/cpb.45.457

Chemical and Pharmaceutical Bulletin

Online ISSN : 1347-5223
Print ISSN : 0009-2363

Total Synthesis of Maturinone through a Regioselective Diels-Alder Reaction of 5-Brominated Benzofurandione

Omar CHERKAOUI, Pascal NEBOIS, Houda FILLION

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Keywords: maturinone, Diels-Alder reaction, bromobenzofurandione

JOURNALS FREE ACCESS

Volume 45 (1997) Issue 3 Pages 457-458

DOI https://doi.org/10.1248/cpb.45.457

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Abstract

Maturinone was efficiently prepared by means of a regiocontrolled Diels-Alder reaction between 5-bromo-2-ethoxycarbonyl-3-methylbenzo[b]furan-4, 7-dione 8 and penta-1, 3-diene.

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