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

Omar CHERKAOUI, Pascal NEBOIS, Houda FILLION

著者情報

キーワード: maturinone, Diels-Alder reaction, bromobenzofurandione

ジャーナルフリー

1997 年 45 巻 3 号 p. 457-458

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

詳細

抄録

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.

責任著者(Corresponding author)

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